The Natural Repertory of Prof.

William
Nelson

Edited by Professor Emeritus Desire Dubounet, IMUNE

ISBN 978-615-5169-68-7

1
 The Natural Repertory

Of

Prof. William Nelson

An In-Depth Understanding of
Nelsonian Homeopathy

Including a Catalogue of all two-hundred

Nelsonian Homeopathic Remedies
 The Natural Repertory of Prof. William Nelson

1985, 1990 Academy of Applied Quantum

Bio-Technologies.
Rio Rancho, New Mexico

Revised edition, 2008, William J. Cunningham

White Dove Healing Arts, Ltd.

All rights reserved. No part of this publication may be

reproduced or transmitted in any form or by any means
electronic or mechanical, including photocopying,
recording, or any other information retrieval system,
without permission in writing from:

White Dove Healing Arts, Ltd.

10959 Lynne Avenue, Lafayette, Colorado 80026

Telephone (303) 828-4439

 TABLE OF CONTENTS
Introduction ______________________________________________________________________ 1
TM
Quantum Quality Control ~ QQC ___________________________________________________ 4
Combination Homeopathy___________________________________________________________ 8
Regarding the Remedies____________________________________________________________ 10
Homeopathy______________________________________________________________________ 15
Possible Mechanisms of Homeopathic Information Transfer________________________________ 22
The Hormetic Philosophy___________________________________________________________ 29
Nosodes_________________________________________________________________________ 34
Isodes __________________________________________________________________________ 46
The Liquitrophic Philosophy_________________________________________________________ 55
The Anodyne Philosophy___________________________________________________________ 77
The Combination Philosophy________________________________________________________ 83
The Restorative Philosophy__________________________________________________________ 94
Sarcodes ________________________________________________________________________ 96
Oriental Herbal Philosophy__________________________________________________________ 106
Chinese Herbology and Homeopathy__________________________________________________ 115
The Miasm Philosophy_____________________________________________________________ 123
The Psychological Philosophy________________________________________________________ 127
Imponderable Homeopathy__________________________________________________________ 131
Allersodes_______________________________________________________________________ 138
The Dehabituate Philosophy_________________________________________________________ 157
Vitamins and Powdered Products_____________________________________________________ 159
Screening Groups Used in the Academy of Applied Quantum Biotechnology
Computer Program_________________________________________________________________ 164
List of Homeopathic Remedies with Similar Herbal Action_________________________________ 188
An Advanced Treatise in Quantum Biology_____________________________________________ 198
Alphabetical List of Health Disorders and Chromosome Locations___________________________ 214
Lectins__________________________________________________________________________ 231
Venoms_________________________________________________________________________ 239
Gemmotherapy____________________________________________________________________ 259
Classical Hahnemanian Singulars_____________________________________________________ 262
A New Perspective on Research______________________________________________________ 264
Metabolic Pathways _______________________________________________________________ 301
 TABLES AND CHARTS

Periodic Table Crystal Structure______________________________________________ 12

Duplication Study__________________________________________________________ 25

Comparison Chart: New Homeopathy Allopathy________________________________ 26

Inflammation: Part of the Defense Phase of Life__________________________________ 27

Chromosome Homeopathic___________________________________________________ 230

Snake Venoms Containing NGF_______________________________________________ 245

Distribution of Hemorrhagic, Lethal and Proteolytic Activities in Snake Venoms________ 247

Effect of Venoms from Different Species of Snakes on the Histamine (H) and Serotonin (S)
Content of Isolated Rabbit Platelets_____________________________________________ 248

Summary of Immunopathology, Histopathology, and Electro-microscopic findings of the

Kidney in Snakebite_________________________________________________________ 254

Renal Failure with Known Lesions in Various Snakebites___________________________ 255

 DR. RECOMMENDS PLEDGE

First, do no harm

We pledge to provide safe products and to educate practitioners in

understanding their efficacy and using them safely.

Help ease misery and suffering

We pledge to test and develop the highest quality products, and to

educate practitioners in relieving causes of disease and to
stimulate recovery.

Respect the natural process of Gods living world

We pledge to remember that we do not know and that nature does

know, thus, we shall use as natural a healing process as possible.

Provide research, consulting and education in natural, homeopathic and

nutritional healing

We pledge to broaden confidence through the realization that

natural healing methods are superior to synthetic ones in the long
run and often in the short term.

***
 INTRODUCTION

A repertory is a compilation of the homeopathics used by a

practitioner, and many have been written by homeopaths throughout the
ages. This particular one is the Natural Repertory of Dr. William Nelson.
With this book, homeopathy enters into the modern age in regard to
toxicity, hormones, amino acids, minerals, vitamins, sarcodes, nosodes,
allersodes, isodes, and classical homeopathy. This is by far, to date, the
most extensive repertory ever compiled by any homeopath.
Within these pages, there are many remedies that are used for the
entire human condition. For every known disease, we have developed
nosodes, sarcodes, isodes, allersodes, and classical treatments. Within
this document, we propose a new vision of statistical analysis that will
modernize homeopathy and bring it into the new age of modern
medicine.
We also offer a new definition of homeopathy here, one that is broader;
from reversal (which is not apropos to all of homeopathy) to herbology,
naturopathy, and all forms of natural medicine. Our new definition will
show how homeopathy is the science of using the body to respond,
rather than using external means, which is the philosophy of allopathy.
Allopathy tries to artificially reduce symptoms, which can sometimes
make the patient dependent on an external agent. In homeopathy, it is
about working with a natural entity to try to balance the patients
metabolism. At times, allopathy is used but only in its most gentle form
in trying to stimulate the body to achieve balance by itself. We can fight
symptoms allopathically while trying to produce harmony and natural
health in the patient. Homeopathy is equivalent to system balance, and
allopathy implies an external treatment of the symptoms.
Within these pages, we present a new era of homeopathy, a new era of
understanding and expansion of homeopathy from its limited confines to
a broader based, total m edical system.
1
 Many classic homeopaths may not completely understand everything
within this treatise. They may struggle and try to rationalize against
using the remedies. We only can hope that they will embrace the vision
and understand how homeopathy can be used in dramatic, new ways.
We feel history is being expanded within these pages, allowing the
homeopath to broaden their base of understanding to encompass the
total concept of biology and medicine.
We welcome the open-minded reader to this exciting, new concept of
homeopathic thinking.

2
 Protocol for Wellness

Relieve or diminish the causes of disease as much as possible, and

improve on ones lifestyle.

Treat the organs of involvement by rebuilding, draining, de-toxing,

and reconstructing. Use sarcodes (glandulars) and the correct
structure and flow.

Re-establish the balance of flow through adjustment, yoga,

acupuncture, acupressure, electric field work, polarity techniques,
etc.

Relieve symptoms by balancing homeostasis through homeopathy.

The use of combination homeopathics makes it safe and easy.

Use nutrition, exercise, affirmation, massage, and stress reduction

programs.

Our next challenge concerns the politics of free choice. We need to

develop a safe system in which we can train and watch over these
different wellness consultants, and to encourage the people of the United
States to freely choose wellness intervention over crisis intervention.

3
 Quantum Quality Control ~ QQCTM

Quantum Quality Control or Double QC (QQCTM) is a trademark of Dr.

Nelsons, developed by him to determine the finest quality control that
can be utilized in the development of homeopathics. Walter Shewhart
came up with the idea of superb quality control as the hallmark of a good
business that would last through financial difficulties. He offered this
technology to the Americans in the 1950s and early 60s, and American
industry scoffed at him. W. Edward Deming collaborated with Shewhart
and when the boom markets were not interested in incentives for quality,
he eventually left America and found a welcome home in the Japanese
market where quality control became the pinnacle of Japanese
businesses. This helped the small nation which was recovering after the
devastation of the World War to become a new economic power
dominating the car market and electronics industries as well as many
others through the utilization of quality control.
Many surmise that purchases from the Orient are junk but these are
rarely from Japan; more often they are from Taiwan or Hong Kong. The
Japanese try to excel in quality control and make it a hallmark of their
industry. Quality is the best way to build a business and quality control
is the best tool. Using this model, we try to develop a quality control
technique for homeopathy that would allow us to produce the finest
homeopathic products.
A complete description of this double QC process is included in the
Quantum Vibrational Medicine of Dr. Nelson, in which the analysis of the
different techniques and how they came about are explained. We go into
the magnetic, static and conductance patterns and the trivector fields
produced by bio-quantum homeopathics, and we explain the logical
capacities of these homeopathics. Looking at the polymorphic state or
liquid crystal effect is also well discussed in the book.

4
 We wish to briefly discuss quality control to help doctors understand
how Dr. Recommends can develop the finest homeopathics in the world.
Many techniques are used, including superb intake or initial acceptance
criteria to allow only the finest quality herb, hormone, enzyme, sarcode,
nosode, isode or allersode. This way there is control each step of the
process through the shape, structure, electrodynamics, Kirlian
photography, and other dramatic means. Below are some profiles used to
develop this QQCTM process.
The QQCTM process includes developing the best statistical information
on the product in a clinical setting, to make sure that the products not
only fit our QQCTM process but also work in patient populations,
guaranteeing safety and efficacy.
Dr. Recommends has developed the finest in homeopathy, as well as
the most extensive remedy list in the industry today. With these different
compounds we have the finest medical pharmaceutical house in the
world for the widest variety of ailments. We insist on:

Statistical evaluation of clinical results to confirm safety and

efficacy
Raw material intake must begin with the best
Kirlian photography to confirm bio-energy field stability
Trivector analysis to confirm polymorphic liquid crystal state
Cryogenic photography to confirm polymorphic liquid crystal state
Spectro-photometry and atomic absorption to confirm bio-photon
absorption and release
Culture to confirm safety
Chromatography to confirm safety
Pro bono programs to give back by helping the poor
Education for the doctor and the public

5
 On the first page is the Dr. Recommends pledge which includes safety
first, then efficacy. We revere nature in all that we do even though we
realize that sometimes we must use synthetic pharmaceuticals to break
up the damage done before. We revere the natural process in every way
possible.
We also provide education. A repertory can only outline products, and
not really spell out their use. To obtain more information the reader is
pointed to a list of books by Dr. Nelson that can be found at
http://www.whitedovehealing.com/training/books.htm. (White Dove
Healing Arts, Ltd.) Many of these books are on video and audio tape,
which will help the practitioner with the wide range of health issues and
encourage the use of some of these simple homeopathic techniques thus
increasing cure rate, and helping patients in many new ways. It is hoped
that these books offer data needed to continue broadening the ability to
cure, so that diseases on earth can be a thing of the past by helping to
provide simple, natural, safe, medical solutions.
These techniques are utilized only by Dr. Recommends for quality
control management to develop the finest homeopathics. Only by using
the finest quality products can homeopaths truly succeed. The people of
the world want natural medicines and a medical philosophy that works
with the body, not against it. Homeopaths now need to maximize their
results and can do so if the industry will focus on quality.
The Dr. Recommends Quantum Quality Control consists of
spectrophotometry and atomic absorption, electrolyte potential, Kirlian
field analysis, bacteria and fungal cultures, rickettsia and viral detection,
trivector analysis, cryogenic photography, and pilot and clinical testing.
This thorough policy of product control provides the quality of product
that everyone deserves.
Double QC is the process of quality control which will assure the finest
energetic remedies. The Nelsonian manufacturing process gives a more
active homeopathic. Sea life, brain hormones, and enzymes are mixed
6
into each batch and an electrical potential current is run through the
base alcohol and water to produce the finest homeopathics in the world.

The eight steps in Quantum Quality Control ~ QQCTM

Raw materials intake (make sure you begin with the best)
Kirlian photography (confirm bio-energy field stability)
Trivector analysis (confirm electronic, magnetic, capacitance state)
Cryogenic photography (confirm polymorphic liquid crystal state)
Spectrophotometry and atomic absorption (confirm bio-photon
absorption and release)

Culture (confirm safety no micro-organism growth)

Chromatography (confirm safety proper protein, hormone and
enzyme existence)

Statistical evaluation of clinical results (confirm safety and efficacy)

7
 Combination Homeopathy

Classic homeopathy uses singular compounds in their basic form

which were devised by Samuel Hahnemann. Hahnemann never realized
the important fact that all the compounds he was using were
combinations of many other compounds and elements. Apis mellifica is a
very complex combination that nature has developed into a single energy
pattern. There are over 50,000 known compounds in this singular
remedy.
The very principle of nature is combination in which many elements
are blended into life. If we were to blend Apis mellifica with Lachesis, two
biological compounds, we would get a new entity unlike each of them
separately. Their effects might be amplified, cancelled or synergistically
changed. The skill is to treat the combination as a new entity that needs
scientific validation.
Combination homeopathy involves one to blend or prepare different
remedies for broader based action which most classic homeopathic
combinations are used for. For just one patient we might take a specific
group of allergens, isodes, nosodes, or sarcodes and combine them in a
way that produces a combination specifically for the patient. The
scientific art in combination homeopathy is covered in Quantum
Vibrational Medicine.
Much of combination homeopathy was developed to make the
principles of homeopathy easy for practitioners to use. With combination
homeopathy, doctors no longer have to remember the profile of each
individual entity. They can remember simple terms such as pain, heat
improves or pain, cold improves. The practitioner only has to know two
different concepts in the face of pain; heat and cold.
Combination homeopathy offers safety as well as an increased band of
efficacy over most singular homeopathics. The argument for combination
homeopathy includes several justifiable concepts that most singular
8
homeopaths may not truly know about. Most singular homeopaths argue
circularly, and may never have tried combinations because they have
superstitious or vague beliefs that only Hahnemann truly understood
homeopathy, not even considering the fact that the world has changed
dramatically since his time. This belief is often fostered by minds that
resist new thinking and scientific improvements. This way of thinking
and lack of science has held homeopathy back long enough.
Dr. Nelson has devised many combination homeopathics that are easy
to use by practitioners. These homeopathics are tested in statistical
ways. If we look into the chapter called A New Perspective on Research,
in Bio-Quantum Matrix, we can read some new statistical information that
will prove the safety and efficacy of such formulas. In The Experimental
Data on Homeopathy clinical tests validate results that prove
homeopathys effectiveness. These many combinations teach homeopaths
to use homeopathy in broader ways.
Combination homeopathy offers the best techniques to entice
allopathic medical doctors into the homeopathic camp as it can be
taught very quickly and easily. A list of the many different combination
remedies used by Dr. Recommends is included here. It goes way beyond
homeopathic lines that existed before.
We welcome the reader and practitioner to a new world of homeopathy
and a deep understanding of how to utilize the combinations more
significantly.
After presenting this list, different types of remedies used for
circulation, nerve disorders, digestion problems, immunology, and other
types of sicknesses will be covered. This will allow the practitioner some
viable shortcuts in using homeopathy.

9
 Regarding the Remedies

The Dr. Recommends combination remedies are developed with several

advantageous points in mind. They are as follows:

Ease of use: Designed for the busy doctor to learn about and use.
Guaranteed safety: Engineered to be safe first dont hurt.
Effectiveness: Passed crucial quantum quality control procedures
that surpass other homeopathics in the world.
Affordable: Easily affordable.
High quality service: Delivery on special order items beats most
regular deliver.
FDA registered: Registered with the FDA (National Drug Code/
NDC numbers) and are also registered in Canada (Drug
Identification Number/DIN), Australia, and the Common Market.
World wide distribution.

This catalog contains the most dramatic homeopathic remedies ever

engineered. The Dr. Recommends remedies are scientifically formulated
and contain many trace elements from the Polymorphic Periodic Table
developed by Dr. James Isaacs. Trace elements have profound biological
effects by producing stimulating and stabilizing effects on the body.
Trace element therapies are used in conjunction with scientifically
developed sarcodes, nosodes and isodes. The shape and atomic structure
of these elements are used in making the Dr. Recommends remedies the
most effective homeopathics in the world.
Dr. Recommends remedies use very high potencies, along with lower
potencies, in a homochord blend. This unique, scientific combining of the
homochords guarantee their safety and effectiveness. To ensure the
quality of the product, Dr. Recommends remedies are quantum quality

10
controlled using the QQCTM techniques. This produces the finest and
most profound healing combinations. Dr. Recommends remedies are
made with the Nelsonian manufacturing process which activates
electrical, synergistic, polymorphic and energetic potentials.
Unfortunately, the Nelsonian process increases the energy so well that
electronic duplicators and imprinters cannot duplicate these formulas.
The Dr. Recommends remedies are designed to blend with each other
and work together for health. Any contraindication to the mixing of these
remedies will be noted. These remedies are safe and easy to use.

11
 Periodic Table Crystal Structure

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
H He
1 Hex Hex

Li Be B C N O F Ne
2 Cub Hex Rhom Hex Hex Cub Cub Cub

3 Na Mg
Cub Hex
Al Si
Cub Cub
P S Cl Ar
Mono Ortho Ortho Cub

K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr
4 Cub Cub Hex Hex Cub Cub Cub Cub Hex Cub Cub Hex Ortho Cub Rhom Hex Ortho Cub

5 Rb
Cub
Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te
Cub Hex Hex Cub Cub Hex Hex Cub Cub Cub Hex Tet Tet Rhom Hex
I Xe
Ortho Cub

Cs Ba * Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn
6 Cub Cub Hex Cub Cub Hex Hex Cub Cub Cub Rhom Hex Cub Rhom Mono ? Cub

Fr Ra ** Rf Db Sg Bh Hs Mt Uun Uuu Uub

7 Cub Cub ? ? ? ? ? ? ? ? ?

* La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu
Hex Cub Hex Hex Hex Rhom Cub Hex Hex Hex Hex Hex Hex Cub Hex

** Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr
Cub Cub Ortho Ortho Ortho Mono Hex ? ? ? ? ? ? ? ?

Crystal Structure Abbreviations

Hex Hexagonal
Rhom Rhombohedral
Cub Cubic
Mono Monoclinic
Ortho Orthorhombic
Tet Tetragonal
? Unknown

http://www.chemicalelements.com/show/crystalstructure.html

12
 HOW THE COMBINATION REMEDIES ARE USED

Homeopathy can be used as nutritional supplementation. If we use

a homeopathic compound such as Vitamin B to supplement the
bodys deficiency syndrome, then homeopathy is used in a
nutritional sense. A concentrated source of B-12 which is diluted,
one part to ten, six times, arrives at a 6x. This is approximately
equal to the RDA of B12, 5 micrograms. Homeopathic remedies
made for nutritional supplementation can be found in the
Liquitrophics and Vitamin sections. Vitamins in the minimal dose
can also be used to regulate metabolism of the vitamins. The
theories of Dr. Royal Lee, the Father of Natural Vitamins, proved
that low doses of natural, high quality vitamins can do the job
better than mega dose, synthetic vitamins.
Homeopathy can be used to help stimulate the body. If a low dose
homeopathic of Belladonna is used, it is possible to achieve the
low-dose pharmacological action. This will trigger the body to
stimulate its own healing. The vast difference between homeopathy
and allopathy is that homeopathy does not incur dependence, but
rather uses the minimal dose philosophy and gently shifts the
patient towards restoring health. Homeopathy stimulates the body
where allopathy works against the symptoms.
Homeopathy can be used in classic ways to help reverse
symptoms. Homeopathy can help reverse symptoms and stimulate
the body to return to the balance of its cybernetic systems.
Homeopathy encourages homeostasis and cure without side
effects. In homeopathy, the symptoms are messengers of
underlying imbalances; whereas allopathy works in synthetic ways
to only control symptoms.
Homeopathy works to encourage energetic stabilization.
Homeopathy encourages energetic stabilization by encouraging
13
 correct tissue development with sarcodes, reducing allergic
reactivity with allersodes, increasing hormetic detox with nosodes,
stabilizing synthetic reactions with isodes and producing healing
effects with imponderables and classic remedies.

Classification of the Remedies

Dr. Recommends remedies are classified in the following manner:

Over the counter (OTC). This category does not require a
prescription from a medical doctor. It is sold to the public and it is
safe to use. It does not require professional training to be obtained.
Professional Use. This category includes such practitioners as
licensed naturopaths, massage therapists, or other professionals
who do not have a license to dispense pharmaceuticals.
Rx. The remedies in this category can only be prescribed by a
licensed medical professional within the states.

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 Homeopathy

The theory and practice of homeopathy is strange to those of us who

are accustomed to conventional Western medicine. But we all sense the
rightness of a healing system which conceives of all symptoms as parts of
a larger whole, which appears to stimulate the bodys natural healing
force rather than attack its parts. Homeopathy seems to work with us,
not on us. It assists our innate biological intelligence to be healthy. When
we break a bone, it is our innate intelligence that repairs it. In fact, our
bodies can heal themselves of dramatic diseases. Homeopathy
encourages and maximizes our innate intelligence to cure ourselves.
At one time, homeopathy was the number one form of medicine in the
United States. Allopathy rose to precedence when the culture turned
towards the economically driven development of synthetic chemicals and
turned its back on natural healing techniques. Now homeopathy is
experiencing regeneration in the United States. The rise in iatrogenic
diseases and synthetic chemical problems has reintroduced the
importance of choosing natural healing techniques.
Homeopathy is the science of healing from within, or prompting the
organism to heal itself. Homeopathics are used to stimulate the organism
toward its own state of homeostasis (balance). Homeopathy is a concept
of minimal dose which Samuel Hahnemann, the Father of Homeopathy,
discovered while trying to determine the smallest amount of a
pharmacological agent that could gently nudge the patient back into the
biological cybernetics of health. Using a feather to stimulate such a
balance is the principle of homeopathy.
Throughout history, disease has been viewed from two fundamentally
different perspectives: One, as a malfunction of specific components of
the body, where symptoms are seen as the disease itself, and two, where
symptoms are a result of a deeper disturbance or imbalance of the
person as a whole, and where symptoms are simply the outward
15
manifestation. Disease is the blockage of the flow of life, and symptoms
are the bodys way of dealing with the blockage. Symptoms just point the
way towards natural homeostasis and homeopathic cure.
Perspective number one is the basis underlying modern orthodox
medicine. Whatever symptoms arise, they are counteracted by drugs,
e.g., an antihistamine for a histamine reaction, an analgesic for pain,
steroids for inflammation, an MAO inhibitor for depression, an
antipyretic for fever, etc. In allopathy, 95 percent of all pharmacology
works against symptoms and against the body. However, perspective
number two is an ancient concept which underlies the entire holistic
health movement, including homeopathy. Nature is revered and utilized
to balance the system. The innate intelligence is worked with, not
against. With homeopathy, side effects are relatively unknown.
Symptoms are not the disease, they merely accompany the disease.
Symptoms are evidence of disease. But treating symptoms is like killing
the messenger for bringing bad news. In fact, by treating symptoms you
are suppressing the bodys natural responses and inhibiting the healing
process, interfering with life.
As far back as 190 years ago, long before the term holistic health was
coined, homeopaths recognized the inseparability of body and mind.
Homeopaths have always stressed the importance of assessing the
totality of the person. Homeopathic medicines thus have physiological
activity. Violinist Yehudi Menuhin once said, Homeopathy is one of the
rare medical approaches which carries no penalties only benefits. In
theory, there is no reason why orthodox medicine should not embrace
homeopathy as an ally.

16
 Significance of Homeopathy

There is a growing consensus in the world that the massive

expenditures on medical research have failed to demonstrate any
significant improvement in societys level of health. The incidence of
major chronic diseases like cancer, diabetes and heart disease has
continued to climb, and medical costs have soared beyond the means of
the average person. More and more, doctors and lay people alike are
searching for alternatives.
Homeopathy offers a time tested method which satisfies the need for a
more economical and non-toxic therapy. It encompasses all areas of
medical care prevention, emergency and acute care, and chronic
disease treatment. Homeopathy offers the individual and society
improved health, productivity, and enjoyment of life.

17
 Advantages of Combination Homeopathic Therapy

Combination homeopathic remedies are safe, effective and

compatible with all types of medical, surgical, psychological,
physical and nutritional therapies.

Homeopathy is the safest method for treating infants, children,

elderly patients and individuals who have an allergic history of
drug reaction.

Combination homeopathic remedies provide a wider range of

utility.

Combination homeopathics offer increased safety due to fewer side

effects.

Iatrogenic or toxic reactions are rare.

Fatal poisoning is unheard of.

Recovery is usually progressive.

Disorders for which no specific medication is available may

respond to homeopathics.

Homeopathy can rescue the medical establishment from its drug

addiction.

The expense is minimal.

Homeopathy stimulates the body into a healing process it goes

beyond just treating the symptoms.

Combination homeopathy is easy to learn and to use.

18
 AMERICA IS PREPARED MEDICALLY FOR EVERYTHING

We have:
The most hospitals
The most drug stores
The most pharmacists
The most nursing homes
The most medical doctors
The most medical schools
The most surgical operations
The most clinical laboratories
The most nurses and nurses aides
The most education about disease
The most publicity about diseases
The most sick insurance policies
The most medical scientific research
The most pharmaceutical companies
The most sick insurance companies
The most physician office laboratories
The most medical research in the world
The most health societies and associations
The most radio and television sick talk about disease
The most federal government medical agencies
A USDA, FDA, HCFA, CDC AND SURGEON GENERAL
The most State and local health agencies

WITH

THE WORLDSS HIGHEST MEDICAL COSTS

EVERYTHING BUT GOOD HEALTH

Any serious proposal that is genuinely designed to prevent disease

will be sure to meet with stubborn opposition from those who have a
vested interest in disease. Prevention, if genuine, would put the
disease treaters out of business. Without the sick man the entire
medical industry would collapse, consequently, it becomes necessary
that there shall always be a sick man. - Herbert Sheldon

BUT IT DOESNT HAVE TO BE.

19
 PREVENTION OF DISEASE

Every person can prevent disease. Every person can attract disease.
The list of diseases below can create more suffering and affect more
lives and more people than earthquakes, floods or other natural
disasters in the United States. Yet man devotes more time and money
to control natural disasters than to prevent disease.
The cause for most of the non-infectious diseases listed below can
be food related.

One does not have to be

One of the 1 million who will be diagnosed with cancer this
year
One of the 1 million who die of cancer each year.
One of the 1 million who die of heart disease
One of the 400,000 new cases of skin cancer each year.
One of the 126,000 new cases of colon cancer each year.
One of the 99,000 new cases of uterine cancer each year.
One of the 38,000 new cases of bladder cancer each year.
One of the 45 million who suffer headaches.
One of the 35 million who suffer from allergy.
One of the 7 million who have coronary artery disease.
One of the 37 million who suffer from hypertension.
One of the 9 million who suffer from asthma.
One of the 1.6 million suffering from gout.
One of the 100 million who suffer from chronic back pain.
One of the 36 million who suffer from hearing loss.
One of the 24.5 million who have cataracts.
One of the 26 million who suffer from gallstones.
One of the 6.5 million who suffer from osteoporosis.
One of the 225,000 to undergo angioplasty.
One of the 35 million to suffer from candidiasis.
One of the 35 million to undergo surgery each year.
One of 36 million who cant afford sick insurance.
One of the 6.9 million currently confined to a nursing home
for long term nursing care. The projection for the year 2040
is 18 million.

20
 Dangers of Homeopathic Utilization

Masking a major disorder: This may provoke a patient to not

seek proper medical care. If symptoms persist, seek medical
attention; always work with a doctors supervision for maximum
safety. Try to choose a physician who is reverent of nature and
reluctant to use synthetics.

Alcohol sensitivities: If alcohol sensitive, the homeopathic drops

may be put into a 3 oz. glass of warm water. Allow 1 minute for
alcohol to evaporate. If the problem persists, alcohol sensitive
persons may get remedies in pills without alcohol.

Provings: This is a symptom caused by a homeopathic, and it is

usually mild in appearance. If the homeopathic is terminated
and symptoms abate in 24 hours, it could be a proving; if
symptoms continue after 24 hours, then it is unlikely they were
caused by the homeopathic. It is natural for modest symptoms
to be exhibited during the healing and cleansing of the body.
When symptoms grow in intensity or for a prolonged length of
time seek professional help.

The Food and Drug Administration (FDA) recognizes the

Homeopathic Pharmacopoeia of the United States (HPUS) regulations,
which indicate how remedies should be made, dispensed and utilized
by homeopathic practitioners. The remedies in this catalog are
registered with the FDA, following HPUS guidelines.

21
 POSSIBLE MECHANISMS OF HOMEOPATHIC
INFORMATION TRANSFER

Homeopathy is a medical art used for centuries to treat illness. But

what are the ways in which a homeopathic can work? Please see the
list below:

Pharmacology: Low potency products which in dilute form

follow two laws:
Arundt-Schultz Law A very small dose of a poison has
reverse effects of the larger mega dose, i.e., homeopathic
belladonna relieves the redness and dryness that raw
belladonna produces.
Law of Initial Values As the quantity of substance is
proportionately reduced the potent effectiveness can elevate,
paradoxically reverse, or reduce depending on the substance
itself.
Imprinting of a message into the polymorphic structure of the
carrier water and alcohol mixture. Here the clath-rate structure
of water is changed to receive a message and transfer this
message to a patient. The receptors for this message would be
on the cell membrane and be similar to olfactory receptors of
the nose. This might explain the ability of strong odors to block
homeopathy.
Quantic storage of information in the quantic states of the
electrons, atoms, and molecules of the carrier fluid. This
transfer would be disrupted by sunlight, x-ray, or other photon
or particle release. Homeopathics are sensitive to the same.
Energy is needed for this shift and possibly could be supplied
by succussion. (There seems to be a minimum of times a
product needs to be succussed: 10 to 15 times).

22
 Energetic and electrical pattern of the homeopathic. By
analyzing the spectral reactions of the homeopathic to
conductance, electrons, inductance (magnetic relativity), and
capacitance (static reactance). This gives a trivector analysis of
the electrical signature of the homeopathic.
Storage might take place in dimensions beyond the 1st, 2nd, 3rd,
and 4th. Some shift of matter in dimensions 4, 5, and 6 might
be a possible place for memory storage of a homeopathic. This
might explain the imponderables of homeopathy or the power of
energy healing. This is measured by correlating the virtual
biophotons of a homeopathic.

In the second mode, the memory ability of water and alcohol is

mentioned. This phenomena can be studied through photon scattering
tests, nuclear magnetic resonance and simplest of all, freezing. If the
water holds a plastic amorphous memory in liquid form as it enters solid
form, this shape should have some effect on the ice patterns. A freezer
that maintains -5c within 1 degree was used to crystallize the
substances. The homeopathics used were less than 5% alcohol to allow
proper freezing. They were put into 1 in. circular 1/8 in. deep trays, and
then allowed to cool in the refrigerator for 2 hours at +5c before insertion
into the freezer at -5c. After 12 hours, the disks were frozen and allowed
investigation. Patterns would form on the homeopathics. There was
indeed some shape transfer even beyond 25x where probabilities of
product existing are minuscule.
Another easy way to measure energetic homeopathics is through
Kirlian photography. This involves simply placing the product in a highly
charged electrical field through a container or rare electron gasses. The
electric charge fluoresces the gas, but the homeopathic acts as a prism to
direct the charge and each homeopathic produces its own fingerprint or
pattern of colors to identify it. These charged particles will be enhanced
23
by the polymorphic shape of the water, the quantic states of the sub-
molecular bodies and perhaps by the quasi-dimensional memory. It is
also interesting to note that so called duplicated remedies show no
fingerprint under freezing or Kirlian photography.

Duplicated Remedies and Homoepathic Information Transfer

As has been discussed, there are several possible modes of information

transfer. Duplicators work on a supposed magnetic transfer. In the first
mode, which involves chemical action, magnetics would not work for
information transfer. In the second and third modes, the mechanical
force of succussion could change electron or molecular quantic states.
Magnetics cannot effect this change. If magnetics could indeed do so,
then homeopathy would be useless. The magnetic interference from a
T.V. set or a telephone unit would change the information. Transport of a
homeopathic through the magnetic lines of the earth would change the
information and nullify homeopathic effectiveness.
As mentioned, duplicated remedies show no change in freezing
patterns or in Kirlian photography. Duplicated remedies are probably
advanced placebo at best. To test this supposition, an experiment was
performed with double blind capacity.
Procedure: 35 patients were chosen from a naturopathic Doctors
practice. All patients were using certain homeopathics on a regular basis
and knew what results to expect. Some patients used a Candida nosode
to control bloating or other bodily symptoms; others used Belladonna or
Lachesis. All were familiar with their remedys effect.
Each patient was given either a regular homeopathic or a duplicated
remedy. Each patient was also given either a placebo sugar pill, or a pill
with 5mg. Narcan (Naloxone). Naloxone is used to block endorphin
response and has been found to block the placebo effect in placebo
responsive patients. Patient profiles were chosen to exclude those with
24
symptoms of pain as Naloxone can increase pain perception. The test
was double blind with neither patient nor practitioner knowing which
formula was given. Patients were given questionnaires to evaluate the
efficacy of the remedy. Results of the effectiveness are shown in the
accompanying diagram.
Results: The tests show that the duplicated remedy performed
significantly lower than the real remedy. The placebo blocking Narcan
pill significantly lowered efficacy (63% is approximately the predicted
placebo effect).
Perhaps the information transfer of mode number 4 (multi-dimensional
transfer) could account for the transfer of duplicators; Narcan with its
endorphin blocking action might also block other dimensional
information transfer. Even so, the study shows a markedly decreased
efficacy with the duplicated remedy. Radionic remedies have no
pharmacology, quantic state or polymorphic state, thus, they are not
homeopathics and homeopathy is continually blamed for radionic
remedies that fail.
Here again, quality is often not paramount to homeopaths. Some prefer
the greater monetary reward duplicators or imprinters provide. This lack
of focus on quality and maximization of effectiveness could erode our
industry. Only through quality and dedication to developing and
delivering the finest homeopathics can we truly succeed. If you want the
best, at affordable prices, Dr. Recommends remedies are for you.

DUPLICATION STUDY
Placebo Duplicated Real
(Imprinted) Homeopathic
Placebo 55% 63% 97%
Narcan 10% 11% 96%

25
 COMPARISON CHART
NEW HOMEOPATHY
Very small chance of side effects
Minimal cost
Safe for children and elderly
Non-addictive
Works by letting patient reestablish
homeostasis
Little if any malpractice, due to
safety
Philosophy: bodys reactions are an
intelligent attempt to deal with
toxicity and other disease-causing
conditions
Easy to use
Safe for environment, natural
Tries to cure
Tries to treat whole body
metabolically
The patient is an individual
Symptoms are only a part of a
complex set of problems
Pain is Gods gift, and lifes way of
telling us about underlying
problems
Stimulates immune system
Sensitive to energetic problems of
the body
ALLOPATHY
Very great chance of side effects
Usually high costs
Warning of risks if not used
correctly
Creates dependency
Works by externally blocking,
stimulating, or interfering with the
body
Major malpractice suits. Iatrogenic
disease is on the increase
Philosophy: Body is stupid and
malfunctions often; it then needs to
be stimulated, blocked, or fooled by
the doctor and his synthetic
medication
Takes years of experience
Manufacturing hurts environment
Tries to sedate reactions
Tries to reduce patients to mere
symptoms
The patient is a set of symptoms
Symptoms are bearers of bad news,
and we should kill the messenger
Pain is the enemy and must be
covered up. Improperly reduces
inflammation
Weakens immune system.
Ignores energetic nature of the
body
26
 INFLAMMATION
Part of the Defense Phase of Life
Sympathetic, Acidosis, Hyaluronidase, Hydrolysis, Tissue Bouillon,
Hypertony, Histamine

Homeopathy/Naturopathy Allopathy
Holistically Driven Symptom Driven

Defense Management Suppression

Restoration of Homeostasis Chemotherapeutics
Release of Etiology Antibiotics, Antipyretics
Minimal Dose Steroids, Anti-Inflammatories
NSAID

Precipitate Develops as
System Balance Restored
Biology/Reacts to Synthetic
Compounds/Mega-Doses of
Drugs/Builds Dependency

System Release of Auto Produces Wild (Illegal/Improper)

Toxins Peptides (Overdose of Drugs)
Reduced Cascades Induces Anti-Body Cascade

Proper Anti-Body Release Produces Improper

Auto Anti-Bodies

Cure Produces Auto Aggression Diseases:

Lupus, Arthritis, Asthma, etc.

27
 HOMEOPATHIC INSTRUCTION

Take nothing by mouth 10 15 minutes prior to and following

dosage. This includes food, drink, cigarettes, chewing gum,
toothpaste, etc.

Limit caffeine or nicotine in any form, such as soda pop, coffee,

chocolate, cigarettes. If necessary use one hour after taking a
homeopathic

Limit mint in any form, such as candy mints, mint toothpaste,

mint mouthwash.

No camphor, as in muscle and joint rubs. Avoid moth ball fumes.

If dental drilling or trauma to mouth occurs, use topically for 48

hours.

Limit breathing of strong smells, such as paint thinner,

eucalyptus, cigarette smoke (especially menthol).

Limit raw garlic, onions and strong spices to one hour after taking
a homeopathic. Cooked garlic is ok.

Place drops under the tongue and hold for 10 seconds to allow for
absorption.

Keep homeopathics out of direct sunlight and x-ray.

Homeopathics may generally be taken at the same time with other

suggested homeopathics.

Homeopathics should not be mixed with Liquitrophics and should

be taken 20 minutes apart.

CAUTION: Alcohol sensitivities If a person is sensitive to alcohol, put

the drops into a 3 oz. glass of warm water. Allow one minute for alcohol
to evaporate. Pills are also available without alcohol. By following these
guidelines, you will give the remedies the greatest opportunity to
succeed.

28
 THE HORMETIC PHILOSOPHY

Over the last hundred years, man has drastically increased his toxic
exposure through the development of synthetics. Present day scientists
have found in a new study of hormesis that tickle doses, small trace
doses of a toxin, can have stimulatory effects on the body. Hormesis
stimulates a cells defense system. In hormesis the homeostatic balance
is tipped, forcing the body to take measures to protect itself or the effect
where a toxic substance acts like a stimulant in small doses but acts as
an inhibitor in large doses.
The Dr. Recommends hormetic remedies cover a wide variety of toxic
conditions including asbestos poisoning, beauty shop toxins,
environmental toxins, industrial toxins, mercury amalgams and more.
The Dr. Recommends formulas are safe yet powerful in their ability to
stimulate the individual to detoxify without inducing a healing crisis. The
high-end potencies used in the Dr. Recommends remedies are
counterbalanced by the lower dose remedies mixed in the homochords.
These highly engineered hormetic remedies can be used for increased
safety and effectiveness, producing a more stable and safer remedy for
doctors to use with their patients.

29
 HORMETIC REMEDIES

AMEBA-FUGE (1 fl. oz.)

Catalog No. 0005
Indication: Ameba infections
Ingredients: Diloxanide Furoate Metronidazole 3x. Artemisia
absinthium, Bismuthum Metallicum, Allium sativum, Ipecacuanha 6x.
Ammonium Phosphoricum 6x, 12x. Ferrum phosphoricum 6x, 12x, 30x.
Ameba, Entamoeba histolytica, Naegleria fowleri 24x, 40x, 75x, 120x,
300x, 500x.

ASBESTOS (1 fl. oz.)

Catalog No. 0006
Indication: Asbestos sensitivity, Assists in detox
Ingredients: Zincum Valerianicum 5x. Lung sarcode 6x, 12x, 30x, 60x,
100x. Iodium 12x. Silicea 12x, 30x, 60x. Asbestos 25x, 60x, 100x,
350x, 500x.

BACTERIA-FUGE (1 fl. oz.)

Catalog No. 0007
Indication: Bacterial infections
Ingredients: Hydrastis canadensis 3x, 6x, 12x, 30x, 100x. Zincum
Metallicum 4x, 12x. Aloe socotrina 6x. Allium sativum, Arum
maculatum 12x. Mercurius Vivus 16x. Broad-based Bacillinum,
Pyrogenium, Anthracinum, Staphysagria 16x-30x, 100x. Diphtherinum,
Streptococcinum, Staphylococcinum, Pneumococcinum, Syphilinum,
Botulinum, Tuberculinum 16x-30x, 100x, 500-1000x. Eucalyptol 20x.
Lac caninum, Lac vaccinum 30x.

COSMETIC MATERIALS (1 fl. oz.)

Catalog No. 0008
Indication: Cosmetic material sensitivity, Assists in detox
Ingredients: Natrum Carbonicum 4x. Manganum Metallicum 6x.
Formalinum 10x, 30x, 100x, 500x. Nitricum Acidum, Phosphoricum
Acidum, Hypophysis, Sulphur 12x. Miscellaneous Beauty Shop Toxins
30x, 60x, 100x, 750x, 1100x. Kali Cyanatum 20x, 30x, 60x, 100x.

30
DENTAL MATERIALS (1 fl. oz.)
Catalog No. 0004
Indication: Dental material sensitivity, Assists in detox
Ingredients: Caries, Gingivitis, Periodontitis 16x, 20x, 30x. Root Ostitis
20x, 30x. Argentum Metallicum, Mercurius Solubilis, Aurum
Metallicum, Platinum Metallicum, Dental Materials (Amalgams,
Composites, Bonding Resins, Dentin Bonders, Cavity Liners, Metals,
Ceramics, Cements, Temporary Restoratives, Root Canal Materials,
Anesthetics, Denture Materials, Flourides) 30x, 60x, 100x, 500x, 1000x.

ENVIRONMENTAL POLLUTANTS (1 fl. oz.)

Catalog No. 0011
Indication: Water and air pollution sensitivity, Assists in detox
Ingredients: Zincum Metallicum 3x. Chlorophyllum 5x. Manganum
Metallicum 5x, 12x. Taraxacum officinale 6x, 12x, 30x. Formalinum 8x,
12x, 30x, 100x, 500x. Petroleum 16x, 20x, 30x, 60x, 100x, 500x, 1000x.
Air Pollution 50x, 155x, 700x. Water Pollution 50x, 500x.
Hydrocarbonum 60x.

FOOD ADDITIVES (1 fl. oz.)

Catalog No. 0001
Indication: Food additive sensitivity, Assists in detox
Ingredients: Berberis vulgaris, Plantago major 3x, 6x, 12x, 30x. Zincum
Metallicum, Lycopodium clavatum, Selenium Metallicum 6x, 30x.
Graphites, Taraxacum officinale, Arctium 8x, 12x. Petroleum 13x, 24x,
100x, 500x. Miscellaneous Food Additives 30x, 60x, 100x, 500x, 1000x.

FUNGI-FUGE (1 fl. oz.)

Catalog No. 0012
Indication: Fungal infections
Ingredients: Tabebuia impetiginosa, Equisetum arvense 3x. Natrum
Muriaticum 4x. Colostrum 6x, 12x. Bovine Glandulars: Thymus, Liver,
Lymph, Spleen 5x, 12x, 30x, 60x, 100x. Manganum Metallicum,
Selenium Metallicum, Zincum Metallicum, Allium sativum 6x. Bovista
6x, 12x. Usnea barbata, Amanita muscaria, Saccharomyces, Ustilago
maidis, Borax 6x, 12x, 30x. Apis mellifica 12x. Graphites 16x, 30x.
Chlorinum, Iodium 20x, 30x, 100x. Candida albicans, Candida
parapsilosis, Blastomyces, Molds, Epidermophyton, Chlamydia,
Geotrichum 30x, 60x, 100x, 500x, 1000x, 50m. Mercurius Solubilis,
Salarinum, Antibiotics 50x, 100x.

31
HALOGENS (1 fl. oz.)
Catalog No. 0010
Indication: Chlorine or fluorine sensitivity, Assists in detox
Ingredients: Zincum Metallicum, Selenium Metallicum 6x. Chlorinum,
Bromium, Fluorine 6x, 12x, 30x, 40x, 100x, 500x, 1000x. Diatomum
12x, 30x, 60x. Mercury 100x.

INDUSTRIAL POLLUTANTS (1 fl. oz.)

Catalog No. 0013
Indication: Industrial pollution sensitivity, Assists in detox
Ingredients: Taraxacum officinale, Chlorophyllum, Plantago major 4x,
12x, 30x. Selenium Metallicum 6x. Silicea 7x. Plumbum Metallicum
12x. Zincum Metallicum, Iodium 30x, 60x, 100x. Industrial Toxins 40x,
40c, 40m.

INSECTICIDES (1 fl oz.)
Catalog No. 0002
Indication: Insecticide sensitivity, Assists in detoxification.
Ingredients: Taraxacum officinale, Plantago major 3x. Carduus
marianus 4x. Natrum Muriaticum 6x. Cholecystokinin,
Acetylcholinesterase, Acetylcholine 20x, 30x, 60x, 100x. Organo
Phosphates, Miscellaneous Synthetic Insecticides and Herbicides 30x,
60x, 100x, 500x, 1000x.

METALS (1 fl. oz.)

Catalog No. 0014
Indication: Metal sensitivity, Assists in detox
Ingredients: Plantago major 4x, 6x-12x. Silicea 6x, 12x, 30x. Kali
Muriaticum, Kali Phosphoricum, Liver Sarcode, Kidney Sarcode: 6x,
12x, 30x, 60x, 100x. Aluminum Metallicum, Aurum Metallicum,
Cadmium Metallicum, Beryllium Metallicum, Niccolum Metallicum,
Mercurius Vivus, Amalgam, Argentum Metallicum, Plumbum Metallicum,
Stannum Metallicum, Selenium Metallicum, Rubidium, Radon, Radium,
Cobaltum Metallicum, Molybdenum, Antimony, Uranium, Bismuthum
Metallicum, Platinum Metallicum 30x-30c, 30m.

RADIATION (1 fl. oz.)

Catalog No. 0003
Indication: Radiation sensitivity, Assists in detox
Ingredients: Sodium Alginate 2x. Citrus limonum 3x. Hydrangea
arborescens 4x. Iodium, Sarcodes: Adrenalinum, Brain, Thyroidinum
6x, 12x, 30x, 60x, 100x. Imponderables: X-ray, Color TV, Microwave,
Gamma Radiations 6x, 12x, 30x. Phosphorus 12x. Radium Bromatum
22x, 60x, 100x, 500x, 1000x. EMR Spectrum 100x.

32
SYNTHETIC CHEMICALS (1 fl. oz.)
Catalog No. 0009
Indication: Synthetic pharmaceutical sensitivity, Assists in detox
Ingredients: Natrum Muriaticum 3x. Kali Nitricum 6x. Platinum
Metallicum 8x. Plumbum Metallicum, Graphites, Lac defloratum 8x,
12x, 30x, 100x. Vaccinotoxinum 16x, 30x, 60x. Pharmaceutical Toxins
60x, 100x, 500x, 1000x.

VERMI-FUGE (1 fl. oz.)

Catalog No. 0015
Indication: Intestinal parasite infections
Ingredients: Absinthium 3x, 6x. Sulphur 4x. Rhamnus purshiana,
Cinchona officinalis, Juglans nigra, Ferrum Phosphoricum 6x.
Magnesium Metallicum 7x. Cymbopogon citratus 8x. Mercurius
Solubilis 12x. Nosodes of Various Helminths, Nematodes and Intestinal
Parasites 12x-30x, 60x, 100x, 500x, 1000x.

VIRAL-FUGE (1 fl. oz.)

Catalog No. 0016
Indication: Viral infections
Ingredients: Trifolium pratense, Echinacea purpurea, Natrum
Muriaticum, Asclepias tuberosa, Ferrum Iodatum, Zincum Metallicum
3x. Ferrum Phosphoricum 4x. Lac Vaccinum, Euphrasia officinalis 6x.
Thuja occidentalis 6x, 12x, 30x, 60x, 100x. Camphora, Calcarea
Arsenicica, Arium Virus, Ichthyolum, Selenium Metallicum 12x.
Vaccinotoxinum, Morinum, Variolinum, Miscellaneous Influenzinum,
Psorinum, Vincetoxicum 12x, 30x, 60x, 100x, 500x, 1000x, 50m. Aurum
Metallicum, Platinum Metallicum, Uranium 60x-100x.

33
 NOSODES

Nosodal therapy involves using disease-causing or disease-containing

tissues and diluting them to cause reversal effects. This is the basic
principle of vaccination and homeopathy. Diseased tissue can be used to
alleviate disease conditions. This is the science of nosodal homeopathy. A
nosode is a homeopathic or diluted and energized form of the diseased
entity.
Within this treatise, a list of the following are included: bacteria,
worms, viruses, fungi, protozoa, rickettsia, and many other tissues; as
well as medical nosodes of various diseases and diseased tissues. Also
included are: dental toxins that allow the dentist to use different disease-
causing dental material from the nosodal tray.
There is a wide range of nosodal factors used by modern homeopaths.
Those known to Dr. Nelson are contained in this document. To reference
some experimental data behind nosodal homeopathy we point the reader
to The Experimental Data on Homeopathy, by Dr. William Nelson. Within
the pages of that document one can read about how nosodal homeopathy
is used to reverse disease conditions.
Homeopathy offers a safe alternative to vaccination which has very
similar modes of operation. Even new ideas of DNA and RNA theory can
be ascertained with this new homeopathy.

34
VIRUSES

CONJUNTIVITIS, VIRAL MALARIA

COMMON WARTS AND MONILA ALBACANS VIRAL
CONDOMYLOMA COMPONENT
COXSACKIE NOSLAMINT
DIPTHERIA PLANTERS WARTS
EPSTEIN BARR POLIO MYELITIS
ESCHERICOLI VIRAL Q FEVER
COMPONENT RETRO-VIR
FAEKALALK RHINOPNEUMONIA
HEPATITIS A ROCKY MOUNTAIN SPOTTED
HEPATITIS B FEVER
HERPES PROGENTALIS SWINE INFLUENZA
HERPES SIMPLEX TRICHINOSIS
HERPES ZOSTER V GRIPPE
HUMAN PAPPILOMA VIRUS VAPCH GRIPPE
INFECTIOUS MONONUCLEOSIS VA2 GRIPPE
INFLUENCINIUM VA2 LGRIPPE
INFLUENZA V2 GRIPPE
INFLUENZA (BERIN 55) V3 GRIPPE
INFLUENZA 83 V4 GRIPPE
INFLUENZA 84 V5 GRIPPE
INFLUENZA 85 V20 GRIPPEV50 GRIPPE
INFLUENZA 86 V60 GRIPPEV76 GRIPPE
INFLUENZA 87 RETROVIRUS1RETROVIRUS10
INFLUENZA 88 VIRUS

35
FUNGUS

ADNEXITIS CRYPTOTOCCUS 4
ASPERGILLUS, FLAVUS, CRYPTOTOCCUS 5
FUMIGATUS, GLAUCUS, CYRTOCOCUS NEOFORMS
NIGER, TERRUS EPIDERMOPHYTON 1
BLASTOMYCOCES 1 EPIDERMOPHYTON 2
BLASTOMYCOCES 2 EPIDERMOPHYTON 3
BLASTOMYCOCES 3 EPIDERMOPHYTON 4
BLASTOMYCOCES 4 FUNGUS FLORA
CANDIDA ALBICANS HISTOPLASMOSIS 1
CANDIDA GLABRATA HISTOPLASMOSIS 2
CANDIDA GUILLIER HISTOPLASMOSIS 3
CANDIDA KRUSEI HISTOPLAMSOSIS 4
CANDIDA LAUERENTI HISTOPLASMOSIS 5
CANDIDA LIPOLYTI NEOFORMS 1
CANDIDA LUSITANI NEOFORMS 2
CANDIDA ORIENTALIS NEOFORMS 3
CANDIDA PARAPSILOSA PNEUMOCYSTOSIS
CANDIDA PSEUDOTROPICALIS SACROMYCOSES 1
CANDIDA RUGOSA SACROMYCOSES 7
CANDIDA STELLATO SCEREVISI
CANDIDA TAMATA TINEA CURTIS
CANDIDA TROPICALIS TINEA CURVIS
CRYPTOTOCCUS 1 TINEA PEDIS
CRYPTOTOCCUS 2 TYCO SPORON
CRYPTOTOCCUS 3

36
BACTERIA

ACTINOMYSOSIS
ADNEXITIS
AEROBACTER
AMOEBA
AMOEBA HEPAR ABSCESSUS
ANTHRAX
ASCARIDINUM
BAC. GARTNER
BAC. MORGAN
BACILLUS ANTHRACIS ANTHRAX, MALIGNANT PUSTULE
BACTEROIDES
BARTONELLOSIS
BIFIDUS
BOTULINUM
BRUCELLOSIS
CARIES
CAUCAUOUS
CHLAMYDIA TRACHOMATIS
CHOLERA
DYSENTERY
ECOLI
ENCEPHALITIS
ENTEROCOCCINUM
FRANCISELLA TULARENIS TULAREMIA
GASTROENTEROCOLI
HAEMOPHILUS INFLUENZA
KAWASAKI
KLEBSIELLA PNEUMONIAE
LEGIONELLA
LISTERIA MONOCYTOGENES
LYMES
MELIOIDOSIS
MENINGOCOCCINUM
MORBILLINUM
MYCOPLASMA PNEUMONIAE
MYOBACTERIUM LEPRAE LEPROMATOUS LEPROSY
NEISSERIA GONORRHOEAE
NOCARDIA
NOS. ELEPHANTIASIS
NOS. FISHPYROGENIUM (FRESHWATER)
NOS. RHINOPNEUMONITIS
OXYUREN
PEPTOSTREPTOCOCCUS ANAER.
PLASMODIUM SPP. MALARIA
37
BACTERIA, cont.

PNEUMOCCIN
PNEUMOCOCCUS
PROGENIUM
PROPIONIBACTERIUM ACNES ACNE
PROTEUS
PSEUDOMONAS
PYOCYANEUS
R. MOOSERI
R. QUINTANA TRENCH FEVER
R. RICKETTESII
RICKETTSIA PROWAZEKII
RUBEOLA
SAB ACIDOPHILUS/BIFIDUS
SALMONELLA TP
SCARLATINUM
SHIGA KRUSE
SHIGELLA PARADYSENTERIAE
SPRILLUL MINUS RAT-BITE FEVER
STAPHYL AUREUS
STAPHYL PYOGENES IMPETIGO
STAPHYLOCOCCIN
STAPHYLOCOCCUS EPIDERMIDIS ACNE
STREPTOBACILLUS MONILIFORMIS RAT-BITE FEVER
STREPTOCOCCIN
STREPTOCOCCUS HAEMOLYTICUS
SYPHILIS
TERSENIA PESTIS PLAGUE
TETANUS
THERMAL BACTERIA
TOXOPLASMOSIS
TREPONEMA CARATEUM PINTA
TREPONEMA PALLIDUM SYPHILIS (SECONDARY)
TREPONEMA PERTENUE YAWS
TRICHINELLA SPIRALIS, MAN
TUBERCULINUM
TULEREMIA
TYPHOIDINUM
TYPHUS
VACCININUM

38
NOSODES, DENTAL

ASTRO 1180 KETAC-CEM

AUTOPOLYMERISAT LIFE
(AUTOACRYLAT) LUCITONE 199
BARRIER MARCAINE
BIO C MOLYBDENUM
BIO H NOBILIUM
C & B METABOND NOS. ACUTE BACTERIAL
CARBOCAINE 2% OSTITIS OF THE JAW
CARBOCAINE 3% NOS. ACUTE PULPITIS
CARBOXYLAT-CEMENT NOS. APICAL GRANULOMA
CAVIT-G NOS. CARIES
CERAMCO II NOS. CHRON. BACT. OSTITIS
COMPOS FULL MATERIAL OF JAW
COMPSPAN OPAQUE NOS. CHRON. PULPITIS
COMPSPAN RESIN NOS. CORYNEBACTERIUM
CONCEPT NOS. CYST EPITHELIAL
CONQUEST DF NOS. DENTAL SACK
COPALITE NOS. EAR SCLEROSIS
COPPERAMALGAM NOS. EPULIS
DEGUNDENT G NOS. EXUDATIVE OSTITIS
DENTAL GOLD NOS. FATTY OSTITIS OF JAW
DG-63 NOS. FISTULA DENTALIS
DICOR NOS. FOLLICLUARE CYST
DISPERSAL NOS. FUNDUS ABSCESS
CURELON NOS. GANGRANOSE PULPA
DYCAL NOS. GINGIVITIS
E-2713 NOS. GRANULMOA PURULENT
EBA NOS. JAW OSTITIS
FIRMILAY NOS. NECROTIC GINGIVITIS
FLECKS NOS. OSTEOSCLEROSIS
GC DENTIN CEMENT OF THE JAW
GEL KAM NOS. PARODONTOSE
GINGIVITIS NOS. PAROTIS DENTAL
GLUMA PART 3 CALCULI
GUTTA PERCHA NOS. PARULIS (STAPH. AUX.)
HELIOBOND NOS. PARULIS (STREPTOC.
HELIOMOLAR MUC.)
HERCULITE XR NOS. PERIODONTAL FIBROM
HYDROXYAPATITE NOS. PERIODONTAL POCKET
HYDROXYLINE NOS. PERIODONTITIS
HP-3 NOS. PULPAL STONE
IN-CERAM NOS. RADICULAR CYST
JELENKO O NOS. ROOT CANAL TX
JET ACRYLIC NOS. ROOT GRANULOMIUM
39
NOSODES, DENTAL, cont.

NOS. ULCERATIVE GINGIVITIS PURE ALLOY

NUPRO NEUTRAL REXILLIUM V
OCCLUSIN ROOT GRANULOMIUM
OLYMPIA RX-IV
OPTEC DENTIN SCOTCHBOND II
OPTEC HSP SCOTCHPREP
OPTEC U-BOND SEALAPEX
ORAL MUCOCUTANEUS SILUX PLUS
PAPILOMA SODIUM FLUORIDE
P-10 SPC PERIODONTO COMPLEX
P-50 STAINLESS STEEL
PALLADIUM SILVER TERM
PERTAC TICONIUM
PHOSPHATE-CEMENT TITANIUM
POLYMERISAT (ACRYLAT) TITANIUM ALLOY
PORSELITE DUAL TRIADVLC
POST-COM II VINYLPOLYMERISAT
PRISMA APH VITA VMK 68
PRISMA DENTIN VITADUR N
PRISMA U-BOND 3 VITRA BOND
PROFILE 2-1
PROTEMP XR BAND
PULP CANAL SEALER XR DENTIN
PULPDENT XYLOCAINE 2%
ZOE 2200
ZONE

40
NOSODES, MEDICAL

ACID PHOSPHATES CONTARACTA SENILIS

ALBUMIN, COWMILK CO2 CONTENT
ALKALINE PHOSPHATASE COPPER SERUM
ALPHA GLOBULIN CPK
ALPHA1 GLOBULIN CR. WHOLE BLOOD
ALPHA2 GLOBULIN CU. WHOLE BLOOD
ALUMINUM SERUM CREATINE
ALUMINUM WHOLE BLOOD CREATINI
AMPYCILLIN DIFFERENTIAL TESTS
ARTERIAL OXYGEN AFTER ENCEPHALOMELOMALACIA
PURE OXYGEN ENDOMETRITIS
ARTERIAL OXYGEN TUBERCULOSSA
SATURATION EOSINOPHIL
ASTHMA BRONCHITIS FASTING BLOOD SUGAR
BASOS GALACTOSE IN BLOOD
BETA GLOBULIN GAMMA GLOBULIN
BICARBONATE SERUM GLOBULIN
BLEEDING TIME GLUCOSE
BLOOD AMMONIA HEMOGLOBIN
BLOOD LACTATE LEVEL HEPATITIS
BLOOD PYRUVATE LEVEL IRON SERUM
BLOOD UREA NITRATE IRON WHOLE BLOOD
LEVEL LACTIC DEHYDROGENASE
BLOOD VOLUME LDH
BUN LEAD SERUM
CADMIUM SERUM LEAD WHOLE BLOOD
CADMIUM WHOLE BLOOD LIPID TRIGLYCER
CALCIUM SERUM LIPOPROTEIN SERUM
CALCIUM WHOLE BLOOD LUPUS
CALCULI PROSTATAE LUPUS ERYTHEMATOSIS
CALCULI RENALES LYMPHS
CALCULI RENALES MANGANESE
OXALIC ACID MERCURY SERUM
CALCULI VESICALES MERCURY WHOLE BLOOD
CAPILLARY FRAGILITY MN. WHOLE BLOOD
CATARACTA BRUNESCENS MONOS
CATARACTA COMPLICAT MULTIPLE SCLEROSIS
CELL MORPHOLOGY NERUALGIE
CHOLESTEROL NEUROFIBROM
CHOLESTEROL ESTER NICKEL SERUM
SERUM NICKEL WHOLE BLOOD
CHROMIUM SERUM NODULAR PROSTATIC
CHRONIC CYSTITIS AND HYPERPLASIA
ENDOMETRIOSIS NOS. BLADDER BIHARZIOSIS
41
NOSODES, MEDICAL, cont. SODIUM SERUM
SODIUM WHOLE BLOOD
NOS. BLADDER POLYP SPIROMETRIC STUDIES
NOS. BLADDER Tbc THROMBIN TIME
NOS. CYSTOPYELITIS TIMED VITAL CAPACITY
NOS. FIBROADENOM TONSILLA
MAMMA TONSILLA PHARYNGEA
NOS. KIDNEY PAPILOMA TOTAL BILIRUBIN
NOS. MAMMA FIBROMATOSIS TOTAL LIPIDS
NOS. MASTITIS TOTAL LUNG CAPACITY
NOS. MASTOPATHIA CYSTICA TOTAL PROTEIN
NOS. OXALIC ACID URICA TRANSAMINASES
NOS. PERIORCHITIS TRICHOMONAS VAGINITIS
NOS. PROSTATA-ADENOM T3 VERTEBRAE
NOS. SOLITARY CYST (KIDNEY) T4 VERTEBRAE
NOS. TESTICULAR FISTULA Tbc T7 VERTEBRAE
NOS URETHRITIS POST MASC URIC ACID
PARTIAL THROMBOPLASTIN VAGINITIS
TIME VITAL CAPACITY
PHOSPHATE SERUM WBC
PHOSPHATE WHOLE BLOOD WILSON
PHOSPHOLIPIDS ZINC SERUM
PLASMA KETONES ZINC WHOLE BLOOD
PLATELET COUNT 2 HOUR POSTPRANDIAL
PLEURITIS BLOOD SERUM
POTASSIUM SERUM
POTASSIUM WHOLE BLOOD
PROGRESSIVE MUSCULAR
DYSTROPHIE
PROTHROMBIN CONSUMPTION
PROTHROMBIN TIME
PSA
PSORIASIS
RED BLOOD COUNT
RESIDUAL VOLUME

RETICULOCYTE
SE. WHOLE BLOOD
SEGS PMN
SELENIUM SERUM
SGOT
SGPT
SINUSITIS FLONTALIS
SINUSITIS MAXILLARIS
42
PARASITES

AMIDOSTOMUM ANSERIS, BIRD

ANCYLOSTOMA CANIUM, DOG, CAT
ANCYLOSTOMA DUODENALE, MAN
ANCYLOSTOMA TUBAEFORME, CAT
ANGIOSTRONGYLUS CANTONENSIS, MAN
ANGIOSTRONGYLUS VASORUM, DOG
ANOPLOCEPHALA MAGNA, HORSE
APOPHALLUS DONICUS, DOG, CAT
ASCARIDIA GALLI, BIRD
ASCARIS LUMBRICOIDES, MAN
ASCAROPS STRONGYLINA, PIG
ASPICULIRIS TETRAPTERA, MOUSE, RAT
CAPILLARIA AEROPHILA, CAT, DOG
CAPILLARIA BREVIPES, BIRD
CAPILLARIA FELIS-CATI, CAT
CAPILLARIA OBSIGNATA, BIRD
CAPILLARIA PLICA, DOG
CAPILLARIA PUTORII, DOG, CAT
CATATROPIS VERRUCOSA, BIRD
CHILOMASTIX MESNILI, MAN
CYATHOSTOMA SPP., HORSE
CYSTICAULUS OCREATUS, SHEEP
DAVAINEA PROGLOTTINA, BIRD
DELAFONDIA VULGARIS, HORSE
DICROCOELIUM LANCEATUM, MAN
DICTYOCAULUS FILARIA, SHEEP
DIENTAMOEBA FRAGILIS, MAN
DIOCTOPHYMA RENALE, DOG
DIPHYLLOBOTHRIUM LATUM, MAN, DOG, CAT
DIPYLIDIUM CANINUM, MAN, DOG, CAT
DIROFILARIA IMMITIS, DOG
ECHINOCOCCUS GRANULOSUS, DOG
ECHINOCOCCUS MULTILOCULARIS, DOG
ECHINOSTOMA RECURVATUM, BIRD
ECHINOSTOMA REVOLUTUM, BIRD
ENDOLIMAX NANA, MAN
ENTAMOEBA COLI, MAN
ENTAMOEBA GINGIVALIS, MAN
ENTAMOEBA HISTOLYTICA, MAN
ENTEROBIUS VERMICULARIS, MAN
FASCIOLA HEPATICA, MAN
GIARDIA LAMBLIA
GRAPHIDIUM STRIGOSUM, HARE

43
PARASITES, cont.

HABRONEMA MUSCAE, HORSE

HAEMONCUS CONTORTUS, SHEEP
HAEMONCUS PLACEI, CATTLE
HETERAKIS GALLINARUM, BIRD
HYDATIGERA TAENIAEFORMIS, DOG, CAT
HYMENOLEPIS DIMINUTA, MAN
HYMENOLEPIS NANA, MAN
IODAMOEBA WILLIAMS, MAN
MARSHALLAGIA MARSHALLI, MAN
MESOCESTOIDES LINEATUS, DOG, CAT
MESOSTEPHANUS SP., CAT
METASTRONGYLINAE, PIG
MEULTBRAU
MUELLERIUS CAPILLARIS, SHEEP
MULTICEPS GAIGERI, DOG
MULTICEPS MULTICEPS, DOG
MULTICEPS SERIALIS, DOG
MULTICEPS SMYTHI, DOG
NECATOR AMERICANUS, MAN
NEMATODIRUS FILICOLLIS, CATTLE
NEMATODIRUS SPATHIGER, CATTLE
NEMATOSPIROIDES DUBIA, RAT, MOUSE
NIPPOSTRONGYLUS BRASILIENSIS, RAT, MOUSE
OESOPHAGOSTOMUM DENTATUM, PIC
OLLULANUS TRICUSPIS, DOG, CAT
ONCHOCERCA, MAN
OPISTORCHIS FELINEUS, MAN
PARAMPHIS CERVI, CATTLE
PROBSTMAYRIA VIVIPARA, HORSE
PROSTHOGONUMUS OVATUS, BIRD
PROTOSTRONGYLUS RUFESCENS, SHEEP
RAILLIETINA ECHINOBOTHRIDA, BIRD
SCHISTOSOMA BOVIS, CATTLE
SCHISTOSOMA HAEMATOBIUM, MAN
SCHISTOSOMA MANSONI, MAN
SPIROCERCA LUPI, DOG
STEPHANURUS DENTATUS, PIG
STRONGYLOIDES STERCORALIS, MAN, DOG, CAT
STRONGYLUS EQUINUS, HORSE
SYNGAMUS TRACHEA, BIRDS
SYPHACIA MURIS, RAT, MOUSE
SYPHACIA OBVELATA, MOUSE, RAT
TAENIA CERVI, DOG
TAENIA CRASSICEPS, DOG
44
PARASITES, cont.

TAENIA HYDATIGENA, DOG, CAT

TAENIA KRABBEI, DOG
TAENIA OVIS, DOG
TAENIA PISIFORMIS, DOG, CAT
TAENIA SAGINATUM, MAN
TAENIA SOLIUM, MAN
THELAZIA RHODESII, CATTLE
TOXASCARIS LEONINA, DOG
TOXOCARA CANIS, DOG
TOXOCARA CATI, CAT
TRICHINELLA SPIRALIS, MAN
TRICHOMONAS HOMINIS, MAN
TRICHOSTRONGYLUS AXEI, CATTLE
TRICHOSTRONGYLUS TENUIS, BIRDS
TRICHURIS SERRATA, CAT
TRICHURIS TRICHIURA, MAN
TRICHURIS VULPIS, DOG
TROPISURUS FISSIINUS, BIRD
UNCINARIA STENOCEPHALA, DOG, CAT

45
 ISODES

It is stated in The Experimental Data on Homeopathy by Dr. William

Nelson, that isodal homeopathy includes using different synthetic
compounds that can cause disease, even including body secretions. The
form of isodal therapy that we will concentrate on is that of different
synthetic compounds and pollutants that can cause disease. Dr. Nelson
has devised many combinations known as xenobiotics that deal with
broad-based detoxification. There is also a large list of pollutants that
can be developed in homeopathic form and various combinations for
trained homeopaths to use.
In this chapter there is a long list of pollutants and disease-causing
factors caused from heavy metals, insecticides, food additives, etc.,
included. This challenging form of homeopathy offers exciting new ways
to deal with an increasingly polluted world. Many of these compounds
have the potential to be extremely dangerous and must have strict
controls which are exercised by Dr. Recommends. It is necessary to make
sure that the items rendered by licensed doctors are safe to use. The
pledge of Dr. Recommends is to make safety very important.
Welcome reader to an exciting new world of expanded homeopathy, a
world that was unknown to Hahnemann as many of these chemicals did
not exist during his time, but they are a big part of the structure of
disease today. Our patients must be cleansed and detoxified of these
noxious chemicals. In The Experimental Data on Homeopathy, evidence is
offered for homeopathys effectiveness in this area. The new field of
hormesis research also offers additional evidence for isodal homeopathys
ability to help the patient.

46
POLLUTANTS I

ABIETIC ACID ALUMINUM FLUORIDE

ABRIN ALUMINUM FORMATE
ACENAPHTHENE ALUMINUM METHYL
ACERDOL ALUMINUM PICRATE
ACETAL ALVARTHR
ACETAMIDE ALYPIN
ACETAMIDINE AMATOL
HYDROCHLORIDE AMINOMETHANE
ACETATE RAYON AMINOPTERIN
ACETOACET-o-CHLORANILIDE AMINOPYRINE
ACETOACETIC ACID AMMONIA-d3
ACETOGUANAMINE AMMONIA GAS
ACETONE PEROXIDE AMMONIUM ARSENATE
ACETONE SEMICARBAZONE AMMONIUM AZIDE
ACETULAN AMMONIUM BICHROMATE
ACETYL IODIDE AMMONIUM BIFLUORIDE
ACETYL TRIETHYL CITRATE AMMONIUM BINOXALATE
ACETYBUTYROLACTONE AMMONIUM BROMATE
ACETYLENE AMMONIUM CHLORATE
ACETYLENE TETRACHLORIDE AMMONIUM CHLOROOSMATE
ACETYLSALICYLIC ACID AMMONIUM
ACRIDINE CHLOROPALLADITE
ACROLEIN AMMONIUM CYANIDE
ACTINIUM AMMONIUM EMBELATE
ADIPIC ACID AMMONIUM FLUOGALLATE
ADIPONITRILE AMMONIUM PICRATE
ALDRIN AMMONIUM SELENITE
ALIZARIN AMMONIUM THIOCYANATE
ALKALOID SALTS AMYL ALCOHOL
ALLOXANTIN AMYL NITRITE
ALLYL AMINE AMYL SILICATE
ALLYL CHLORIDE AMYLOFORM
ALLYL CHLOROPHENYL ANABASINE
CARBONATE ANILINE
ALLYL FLUORIDE ANILINE BRILLIANT GREEN
ALLYL FORMATE ANILINE FLUORIDE
ALLYL IODIDE ANILINE GREEN
ALLYL THIOUREA ANILINE HYDROCHLORIDE
ALLYLENE ANILITE
ALUMINUM BROMIDE ANISOLE
ALUMINUM BROMATE ANTHRAROBIN
ALUMINUM CARBIDE ANTIMONY TRIETHYL
ALUMINUM CHLORATE ANTIPYRINE
ALUMINUM CHLORIDE APHRODINE, YOHIMBINE
47
POLLUTANTS I, cont.

APOMORPHINE BEETHLE
ARSANILIC ACID BENZALDEHYDE
ARSENIC BENZEDRINE
ARSENIC TRISELENIDE BENZENE
ARSENIC TRISULFIDE BENZENE HEXACHLORIDE
ARSENOBENZENE BENZHYDROL
ARSINE BENZIDINE
ASCARIDOLE BENZIL
ASPIRIN BENZOIC ACID
ATROPINE BENZOIN
AUROUS CYANIDE BENZYL MRCAPTAN
AUTUNITE BENZYLAMINE
AZOBENZENE BERYL
AZOCHLORAMIDE BERBERINE
n-AMYLENE BETA RAYS
o-AMINOETHYLBENZENE BETEL
p-AMINOBENZOIC ACID BIMETHYL
sec-AMYL ACETATE BISMUTH
sec-n-AMYL ALCOHOL BISULFITES
2-ACETAMIDOFLUORENE BITHIONOL
2-AMINOETHANOL BORAX
BARBITUATES BORAZOLE
BARIUM ARSENIDE BORIC ACID
BARIUM CARBIDE BOROCAINE
BARIUM CHLORIDE BROMATES
BARIUM CHROMATE BROMIDES
BARIUM CYANIDE BUTYLATED HYDROXYANISOLE
BARIUM MYRISTATE n-BUTYL GLYCIDYL ETHER
BARIUM NITRATE DI-TERT-BUTYL p-CRESOL
HIGH EXPLOSIVES

48
POLLUTANTS II

BROMINE CHLORAL HYDRATE

BROMOPHORM CHLORATES
BROMOPICRIN CHLORAZINE
BRUCINE CHLORDANE
BUTANE CHLOREX
BUTANOL ALCOHOL CHLORIC ACID
BUTYL ALCOHOL CHLORINATED NAPHTHALENES
BUTESIN CHLORINE DIOXIDE
BUTOXYL CHLORINE HYDRATE
BUTYLAMINE CHLORINE TRIFLUORIDE
BUTYN CHLOROACETONE
BUTYRIC ACID CHLOROALDEHYDE
BUTYRONE CHLORHYDO
2-BUTYNE CHLORIDES
CACODYL CHLORINE
CADMIUM SERUM CHLOROBENZENE
CAFFEINE CHLOROBENZOL
CALCIMINE CHLOROBUTANOL
CALCITE CHLOROETHENE
CALCIUM CYANAMIDE CHLOROETHYNE
CALCIUM HYDROXIDE CHLOROFORMIUM
CAMPHENE CHLOROPICRIN
CAMPHOR CHLOROPRENE
CANNABIS CYCLOHEXANE
CANTHARIDES m-CHLOROANILINE
CAPROIC ACID m-CHLORONITROBENZENE
CAPRYLIC ACID m-CHLOROPHENOL
CARBAMIDE o-CHLOROPHENOL
CARBITOL m-CHLOROPHENYL
CARBOLIC ACID ISOCYANATE
CARBOLINEUM o-CHLOROPHENYL ISOCYANATE
CARBON TETRACHLORIDE p-CHLORO-o-NITROANILINE
CARBONYLS 2-CHLORO-6-NITROTOLUENE
CARBORUNDUM DECALIN
CARBOWAX DEMETON
CARNAUBA WAX DIBORANE
CELLOIDIN DICOBALT OCTACARBONYL
CELLULOID DIETHYL CARBONATE
CERIUM DIETHYL SULFATE
CESIUM DIETHYLAMINE
CETAB DIETHYLENE GLYCOL
CEVADINE DIETHYLPHOSPHINE
CHELIDONINE DIHYDROPYRAN
CHLORAL DIIODOACETYLENE
49
POLLUTANTS II, cont.

DIIODOFORMOXIME ETHYL OXALATE

DIKETENE ETHYL SILICATE
DIMETHYL BERYLLIUM ETHYL TRICHLOROSILANE
DIMETHYL ETHER ETHYLAMINE
DIMETHYL SULFATE ETHYLBENZENE
DIMETHYLDIOXANE ETHYLDICHLOROARSINE
DINITRO-o-sec-BUTYL PHENOL ETHYLENE CHLOROBROMIDE
DINITROCHLOROHYDRIN ETHYLENE GLYCOL
DINITRODICHLOROBENZENE ETHYLENEDIAMINE
DINITROGEN TRIOXIDE ETHYLIDENE CHLORIDE
DIONIN FERBAM
DIPHENYL FERRIC NITRATE
DIPHENYLCYANOARSINE FERRIC OXALATE
DIPHOSGENE FERRIC SULFIDE
DITAINE FIBERGLASS
o-DIMETHYL PHTHALATE FLUOACETATES
ECGONINE FLUOBERYLLATES
EMERY FLUORIDES
EPHEDRINE HCL FLUOROACETIC ACIDE
ETHYL ACETATE FLUOSILICATES
ETHYL ACRYLATE FLUOSULFONIC ACID
ETHYL ALCOHOL FORMALDEHYDE
ETHYL BROMIDE DEHYDROGENASE
ETHYL BUTYL KETONE FORMIC ACID
ETHYL ETHER FORMYL FLUORIDE
ETHYL FLUOROSULFONATE FURAN
ETHYL IODIDE FURFURAL
ETHYL ISOTHIOCYANATE GAMBOGE
ETHYL MERCAPTAN GASOLINE
ETHYL NITRATE

50
POLLUTANTS III

GILSONITE LACQUERS
SLYCERYL DIACETATE LACTIC ACID
GLYOXAL LANTHANUM SULFATE
GRANITE DUST LAUDANINE
HANANE LEAD AZIDE
HENNA LITHIUM ORATATE (PILL)
HEPTAFLUOROUTYRIC ACID LUMINAL
HEPTANE LUPERCO
HEPTYL ACETATE LUPERSOL
HEXACHLOROACETONE LUPININE
HEXACHLOROMETHYL ETHER LYCONINE
HEXACHLORONAPHTHALENE NICKEL ARSENIDE
HEXACHLOROPROPENE NICKEL CARBIDE
HEXAETHYL TETRAPHOSPHATE NICKEL CARBONYL
HEXENE-1 NICKEL CHLORATE
HYDRAZINE NICKEL CHLORIDE
HYDRAZOIC ACID NICKEL IODIDE
HYDROCHLORIC ACID NICKEL NITRATE
HYDROFLUORIC ACID NICKEL PEROXIDE
HYDROFLUOSILICIC ACID NICKEL SULFATE
HYDROGEN PEROXIDE NICOTINE
HYDROGEN SELENIDE NICOTINE SULFATE
HYDROXYLAMINE NIRVANOL
HYPOIODOUS ACID NITRIC ACID
p-HYDROQUINONE NITRIC OXIDE
INDIUM NITRITES
IODIC ACID NITROBENZENE
IODOFORM NITROETHANE
IPECAC NITROGEN CHLORIDE
IROKO NITROGLYCERIN
IRON PENTACARBONYL NITRONAPHTHALENE
ISOAMYL ACETATE NITROPRUSSIDES
ISOAMYL FORMATE NITROSYL BROMIDE
ISOBUTYL ALCOHOL NITROSYL SULFURIC ACID
ISOOCTANE NITRYL CHLORIDE
ISOPRENE NORNICOTINE
ISOPROPYL ALCOHOL p-NITROPHENOL
ISOPROPYL ETHER OCTACHLORO-CAMPHENE
ISOPROPYLAMINE OCTADECYL
JUNIPER BERRIES TRICHLOROSILANE
KAPOK OCTAMETHYL
KEROSENE PYROPHOSPHORAMIDE
KETENE OCTANE
KRYOFIN OCTYL ALDEHYDE
51
POLLUTANTS III, cont.

OLEFINS
OLEUM
OPIUM
ORRIS
ORTOL
OXALATES
OXALIC ACID
OXALYL CHLORIDE

52
POLLUTANTS IV

OZONE PYRROLIDINE
PARAFORMALDEHYDE QUARTZ
PARALDEHYDE QUINOLINE
PARATHION QUINONE
PELARGONIC MORPHOLIDE RADON
PENTACHLOROMETHYL ETHER RESOURCINOL
PENTACHLORONAPHTHALENE RICIN
PENTACHLOROPHENOL RICININE
PENTASOL ROSIN
PERBENZOIOC ACID ROTENONE
PERCHLORATES RUBIDIUM
PERCHLORIC ACID RUTHENIUM
PERCHLOROETHYLENE SAFROLE
PERIODIC ACID SALICYLICANILIDE
PERONINE SAPONINS
PEROXY SULFURIC ACID SARIN
PERTHANE SILANES
PHENACAINE HYDROCHLORIDE SILICA
PHENOTHIAZINE SILICON CHLORIDE
PHENOTHIOXIN SISAL
PHENYL CARBYLAMINE SODIUM CHLORATE
CHLORIDE SODIUM ETHYL XANTHATE
PHENYL MUSTARD OIL SODIUM HYDROXIDE
PHENYLHYDRAZINE SODIUM NITROPRUSSIDE
PHENYLTRICHLOROSILANE SODIUM PEROXIDE
PHOSGENE SOMAN
PHOSPHINE SORBIC ACID
PHYSOSTIGMA SPARTEINE
PICRIC ACID STANNANE
POTASSIUM IODIDE STRONTIUM
POTASSIUM NITRITE STROPHANTHIN
POTASSIUM PERSULFATE STRYCHNINE
PROCAINE HYDROCHLORIDE STYRENE OXIDE
PROPIOLACTONE SULFUR DIOXIDE
PROPIONYL CHLORIDE SULFUR TRIOXIDE (ALPHA)
PROPYL ALDEHYDE SULFURIC ACID
PROPYLENE SULFUROUS ACID
PROPYLENE ETHER TABUN
PROPYLENE OXIDE TAR, DEHYDRATED
PROTACTINIUM TAR, LIQUID
PTOMAINES TARTARIC ACID
PYRETHRUM FLOWERS TELLURIUM
PYRIDINE TETRACHLORONAPHTHALENE
PYROGALLOL TETRACHLOROSILANE
53
POLLUTANTS IV, cont.

TETRAETHYL PYROPHOSPHATE VINYL ETHER

TETRAETHYLTHIURAM SULFIDE VINYLTRICHLOROSILANE
TETRAHYDROFURAN WARFARIN
TETRAHYDRONAPHTHALENE WELDING FUMES
TETRANITROMETHANE WHISKY
TETRYL XENON
THALLIUM XYLIDINE
THEBAINE m-XYLYL BROMIDE
THEOPHORIN m-XYLYL CHORIDE
THIOCETIC ACID m-XYLYNE
THIOGLYCOLIC ACID YOHIMBINE
THIOGLYCOLLATES ZIRCONIUM
THIONYL CHLORIDE FLUORIDE
THIONYL FLUORIDE
THIOPHOSPHORYL FLUORIDE
THIOSEMICARBAZONE
THORIUM
TIGLIC ACID
TITANIUM TETRACHLORIDE
TOLUENE
TOXAPHENE
TREMETOL
TRI-o-CRESYL PHOSPHATE
TRICHLOROACETYL CHLORIDE
TRICHLOROSILANE
TRIFLUORONITROSOMETHANE
TRIISOBUTYLALUMINUM
TRIMETHYLAMINE
TRINITROANISOLE
TRINITROTULUENE
TRISODIUM PHSOPHATE
TRITIUM
TUMERIC
TURPENTINE
o-TOLUIDINE
p-THOIXENE
ULTRAVIOLET RADIATION
UNDECANAL
URANIUM
URIC ACID
URUSHIOL
VANADIUM
VARNISH
VINYL CHLORIDE
54
 THE LIQUITROPHIC PHILOSOPHY

In the development of a nutritional science we find that the body does

indeed need vitamins, enzymes, coenzymes and a multitude of other
factors to survive, including protein, carbohydrates, fats, water, air, and
exercise. In the field of homeopathy we often deal with just subtle
energies, but homeopathy need not always be so dilute. Many
homeopathics can be utilized in low concentrations at mother tinctures
of 1x, 2x, 3x, or 4x to supply chemical properties to the system for
chemical effects.
The Dr. Recommends Liquitrophics remedies supply the vitamins,
minerals, enzymes, alkaloids and hormones needed by the body to
regulate biological activities.
The Liquitrophics remedies are not in pill form, but in liquid form to
maximize the surface area and to trigger the digestive system for
absorption at the point in which it works best; the mouth. Inside the
nasal pharynx area are many nerve structures running to the brain that
help trigger the digestive system for maximum absorption and utilization
of the remedy.
The liquid formulation of these remedies maximizes their effectiveness.
This means less can be used in much safer dosages. The Dr.
Recommends Liquitrophics remedies are developed to be safe for
children within their specific context and are quality controlled within
the QQCTM standards.

55
 LIQUITROPHIC REMEDIES

ADRENO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0096
Indication: Weak adrenal glands, hypoadrenia
Ingredients: Panax Quinquefolium 2x. Sarcodes: Adrenal, Spleen,
Pantothenic Acid, Lobelia cardinalis, Rosa canina 3x. Coffea cruda,
Paullinia sorbilis 3x, 6x. Ephedra vulgaris 3x, 6x, 12x. Ascorbic acid,
Magnesia Phosphorica, Adrenalinum 4x. Arachidonic Acid 5x, 12x, 30x,
60x, 1000x. Sarcodes: Pituitary, Hypothalamus 6x.
Adrenocorticotrophin 6x, 12x, 30x.

AMINO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0097
Indication: Supplies amino acids and minerals
Ingredients: Panax quinquefolium, Hydrocotyle asiatica, Polygonum
punctatum, Fucus disticus, Undaria pinnatifida, Gigartina papillata,
Porphyra, Arame, Rhodymenia, Alaria esculenta 2x.

ARTHRO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0102
Indication: Connective tissue repair, joint strain or sprains
Ingredients: Calendula officinalis, Echinacea purpurea, Symphytum
officinale, Rhododendron chrysanthum 3x. Shark and Bovine Muscle,
Ligament, Cartilage 3x, 6x. Ruta graveolens 4x. Collagen, Elastin 4x,
12x, 60x, 100x, 500x. Silicea 5x, 6x, 12x. Hypericum perforatum,
Euphrasia officinalis, Aceticum Acidum, Arnica montana 6x. Glycine,
Alanine, Serine, Proline 6x, 12x, 30x, 60x. Formica rufa 20x.

B LIQUITROPHIC (4 fl. oz.)

Catalog No. 0098
Indication: Mental depression, pellagra, vaso constriction
Ingredients: Hordeum vulgare, Saccharomyces cerevisiae, Angelica
archangelica 3x. Sarcodes: Liver, Heart 3x. Vitamins: B1 - B20, 3x, 4x,
12x, 30x, 60x, 100x. Beta vulgaris, Raphanus sativus 4x, 5x, 6x, 16x.
Natrum Pyruvate 6x, 12x, 30x.

C LIQUITROPHIC (4 fl. oz.)

Catalog No. 0123
Indication: Supplies Vitamin C, infection resistance
Ingredients: Citrus limonum, Malpighia punicifolia, Rosa canina,
Solanum tuberosum 1x. Calcium Ascorbate, Citrus aurantium, Bone
Marrow 2x. Agaricus bisporus, Petroselinum sativum, Capsicum
Annuum 3x. Ascorbatase 6x.

56
CARDIO LIQUITROPHIC (4 fl. oz.)
Catalog No. 0107
Indication: Heart repair, infarction risk
Ingredients: Crataegus Oxyacantha, Plantago major, Kali Muriaticum,
Kali Phosphoricum 3x. Cytisus scoparius 4x, 6x, 12x, 30x. Sarcodes:
Thyroidinum, Heart, Vagus Nerve, Cardiac Plexus 4x, 6x, 30x, 100x.
Cactus grandiflorus 5x. Digitalis purpurea, Natrum Muriaticum,
Carnitine, Valeriana officinalis, Lecithin 6x. Alanine, Methionine,
Proline, Leucine 6x, 12x, 30x, 60x.

DERMA LIQUITROPHIC (4 fl. oz.)

Catalog No. 0119
Indication: Skin repair, psoriasis
Ingredients: Equisetum arvense, Iris germanica, Berberis vulgaris,
Mahonia aquifolium 3x. Thuja occidentalis, Nux vomica 6x. Sassafras
officinale, Chondrus crispus, Mentha piperita 6x, 12x, 30x, 60x, 100x.
Hypericum perforatum 10x. Mercurius Solubilis, Petroleum 12x.
Graphites 16x.

FEM LIQUITROPHIC (4 fl. oz.)

Catalog No. 0106
Indication: Balance the female system
Ingredients: Rubus idaeus, Dioscorea villosa, Glycyrrhiza glabra,
Trillium erectum, Liatris spicata 2x. Caulophyllum thalictroides, Ignatia
amara 6x. Sarcodes: Ovary, Uterus, Mammary, Pituitary,
Hypothalamus 6x, 12x, 30x.

G LIQUITROPHIC (4 fl. oz.)

Catalog No. 0101
Indication: Brain repair, dementia, poor memory
Ingredients: Ginkgo biloba 2x. Glycerinum, Taurine 3x. Brain Sarcodes
3x, 6x, 12x, 30x, 60x, 100x. Vitamin B2, B6, B15, Niacinamide, Choline,
PABA, Inositol, Biotin, Folic Acid, Scutellaria lateriflora, Convallaria
majalis, Tyrosine, Glutamine, Glutamic Acid, Phosphatydl Choline 4x.
Datura stramonium 8x, 12x. Oxytocin 12x, 30x, 60x, 100x, 500x.

GLUCO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0125
Indication: Diabetes, hyperglycemia
Ingredients: Aletris farinosa, Ignatia amara, Rhamnus purshiana,
Diabatina 2x. Geranium maculatum, Convallaria majalis 3x.

57
HEMO LIQUITROPHIC (4 fl. oz.)
Catalog No. 0099
Indication: Blood cell repair, anemia
Ingredients: Ferrum Gluconate, Ferrum Phosphoricum, Ferrum
Sulphuricum, Ferrum Muriaticum, Trifolium pratense, Panicum
miliaceum, Fagopyrum esculentum, Beta vulgaris, Panax quinquefolium,
Hydrocotyle asiatica, Polygonum punctatum, Pyridoxine,
Cyanocobalamin, Thiamine, Riboflavin, Folicum Acidum 3x, 12, 60,
500x. Hemoglobin 4x. Sarcodes: Spleen, Bone Marrow, Pituitary, Liver
6x. Intrinsic Factor 6x, 12x, 30x, 60x. Erythropoietin 6x, 12x, 30x, 60x,
100x. Tyrosine, Histidine 30x, 60x, 1000x.

HEMO-A LIQUITROPHIC (4 fl. oz.)

Catalog No. 0126
Indication: Auto-immune disorders
Ingredients: Cucumis sativus 1x. Phytolacca decandra 2x. Sarcode:
Thymus 3x. Trifolium pratense, Sarcodes: Adenoids, Tonsils, Appendix
4x. Vaccinotoxinum 30x, 100x.

HEPATO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0112
Indication: Liver repair, liver toxicity
Ingredients: Cucurbita, Beta vulgaris, Raphanus sativus, Arctium,
Plantago major 2x. Bupleurum, Verbena hastata 2x, 6x. Ascorbicum
Acidum 3x. Sarcodes: Liver, Gallbladder 3x, 6x, 12x, 30x, 60x, 100x.
Podophyllum peltatum 4x. Glycine, Methionine, Proline, Cytochrome,
Flavoprotein, NAD, NADP, Inositol, Choline 5x, 10x, 30x, 100x. Natrum
Sulphuricum 6x. Natrum Muriaticum 14x. Creatine Phosphokinase,
Glutamic-oxaloacetic transaminase, Lactic Dehydrogenase 16x, 30x, 60x,
100x.

LIENO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0120
Indication: Spleen repair
Ingredients: Sarcode: Spleen 3x. Quercus robur 4x. Ceanothus
americanus 6x. Helianthus annuus 6x, 12x. Natrum Muriaticum 6x,
12x, 30x. Germanium, Arctium lappa, Myeloperoxidase 6x, 12x, 30x,
60x, 100x.

58
LIPID LIQUITROPHIC (4 fl. oz.)
Catalog No. 0105
Indication: Fatty acid deficiencies
Ingredients: Oil from: Canola, Olive, Sesame Seed, Safflower, Sunflower,
Wheat Germ, Garlic, Carrot, Lemon, Orange, Borage, Linseed (Flax Seed),
Cod Liver, Lecithin (from Soybean), Lettuce, Evening Primrose, Rose
Hips, Pumpkin Seed, Cinnamon, Apple Seed, Senna, Myrrh, Barley,
Apricot Kernel, Currants, Australian Tea Tree, Grape Seed, Hazel Nut.

LYMPHO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0114
Indication: Lymphatic repair, cleansing
Ingredients: Echinacea purpurea, Trifolium pratense 2x. Arctium,
Capsicum annuum, Citrus limonum 3x. Sarcodes: Lymph, Spleen,
Mammary, Thymus 3x, 6x, 12x, 30x, 60x, 100x. Hydrastis canadensis
5x. Sarcodes: Adenoids, Tonsils, Appendix 5x, 12x, 30x, 60x, 100x.

NEO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0103
Indication: Degenerative tissue
Ingredients: Vinca minor, Carduus marianus, Phytolacca decandra,
Plantago major 2x. Sanguinaria canadensis, Viscum album, Amygdala
amara 3x. Carduus benedictus, Taxus baccata 3x, 6x, 12x, 30x, 60x,
100x. Rhamnus cathartica, Glycyrrhiza glabra 6x.

NEPHRO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0110
Indication: Kidney repair, detoxification of protein waste
Ingredients: Hydrangea arborescens 2x. Eupatorium purpureum,
Pareira brava, Pisum sativum, Taraxacum officinale 3x. Natrum
Phosphoricum 3x, 6x, 12x, 30x, 60x, 100x. Kali Carbonicum, Natrum
Nitricum 4x, 6x, 12x, 30x, 60x, 100x. Berberis vulgaris, Uva ursi,
Sarcodes: Kidney, Bladder 6x, 12x, 30x, 60x, 100x, 500x. Urea,
Ammonium, Rennin, Aldosterone 24x, 40x, 60x, 100x.

59
OSTEO LIQUITROPHIC (4 fl. oz.)
Catalog No. 0100
Indication: Bone repair, cold & flu
Ingredients: Bone Meal, Liquid Calcium, Lactuca sativa 3x, 6x, 12x, 60x,
100x, 1500x. Calcarea Fluorica, Calcarea Sulphurica, Calcarea
Phosphorica, Calcarea Muriatica, Calcarea Carbonica, Manganum
Metallicum, Magnesium Metallicum, Equisetum arvense, Juglans nigra,
Vitamin D, D2, D3, A, F 4x, 8x, 12x, 60x, 100x. Niccolum Metallicum
5x, 12x, 30x, 60x, 100x. Osteoclasts, Osteoblasts 6x, 12x, 30x, 60x,
100x. Thyrocalcitonin 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Sarcodes:
Bone, Thyroidinum, Parathyroid, Liver, Kidney, Skin 6x, 30x, 60x, 100x,
1000x. Fluorine, Molybdenum 12x, 30x, 100x.

OXY LIQUITROPHIC (4 fl. oz.)

Catalog No. 0109
Indication: Oxygenator and energizing aid
Contraindication: Flower, yeast, bee pollen allergies
Ingredients: Bee Pollen, Flower Pollen, RNA-DNA from Yeast 2x.
Amygdala amara, Laminaria, Medicago sativa, Symphytum officinale 3x.
Vitamins B12-B18, Chelated Zinc 6x. Oxytocin, Carbonic Anhydrase,
Hemoglobin, Taurine 6x, 12x, 60x, 100x.

PITUI LIQUITROPHIC (4 fl. oz.)

Catalog No. 0116
Indication: Pituitary repair, Assists in detox
Ingredients: Amygdala amara 3x. Cimicifuga racemosa, Sarcode:
Hypothalamus 3x, 6x, 12x, 30x. Sarcodes: Pituitary Anterior, Pituitary
Posterior 4x. Caulophyllum thalictroides 6x. Arginine, Lysine, Ornithine
6x, 12x, 30x. Adrenocorticotrophin 6x, 12x, 30x, 60x, 100x.

PROPEPSIA LIQUITROPHIC (4 fl. oz.)

Catalog No. 0104
Indication: Stimulates and balances digestive enzyme release
Ingredients: Pancreatinum 2x. Bromelain, Papain, Coriandrum sativum,
Cinnamomum, Eugenia caryophyllata, Berberis vulgaris, Herbal Bitters,
Mentha piperita, Ananas comosus 3x. Sarcodes: Parotid, Stomach,
Pancreas, Liver, Small and Large Intestine, Vagus Nerve 6x.
Pancreozymin-cholecystokinin, Lysozyme, Pepsinogen, Trypsinogen,
Chymotrypsin, Lipase, Amylase, Cellulase, Protease, 6x, 12x, 30x, 60x,
100x, 500x.

60
PULMO LIQUITROPHIC (4 fl. oz.)
Catalog No. 0113
Indication: Lung repair
Ingredients: Eucalyptus globulus 2x. Sarcode: Lung 3x. Adrenalinum
4x. Sanguinaria canadensis 6x. Carbon Dioxide, Ferrum Metallicum,
Zincum Metallicum, Oxygen, Carbonic Anhydrase, Verbascum thapsus,
Curare 6x, 12x, 30x, 60x, 100x. Belladonna 12x.

SEROTO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0117
Indication: Parkinsonian symptoms, depression
Contraindication: High blood pressure
Ingredients: Musa paradisiaca, Medicago sativa, Scutellaria lateriflora,
Valeriana officinalis, Nerium odorum, Magnesia Phosphorica, GABA,
Choline Chloride, Inositol, Niacinum, Pyridoxine 3x, 6x, 12x, 30x, 60x,
100x. Serotonin, Dopamine 4x, 12x, 60x, 100x. 5-Hydroxy-L-
Tryptophan, Niacinamide 6x, 12x, 30x, 60x, 100x. Amygdala amara 30x,
100x.

THYMO LIQUITROPHIC (4 fl. oz.)

Catalog No. 0121
Indication: Thymus repair
Contraindication: Disease involving excess white blood cell count
Ingredients: Sarcode: Thymus 3x. Thymol, Natrum Muriaticum 6x.
Phytolacca decandra, Arctium lappa 6x, 12x, 30x.

THYRO LIQUITROPHIC (1 fl. oz.)

Catalog No. 0122
Indication: Thyroid repair
Contraindication: Hyperthyroid conditions
Ingredients: Olive Oil, Canola Oil, Sesame Oil. Thyroidinum 3x, 5x, 6x,
12x, 30x, 100x. Lac defloratum 4x, 6x, 8x. Fucus vesiculosus 6x, 12x,
30x. Molybdenum 8x. Plumbum Metallicum, Mercurius Vivus,
Argentum Metallicum, Platinum Metallicum, Alumina, Bismuthum
Metallicum, Carboneum, Selenium Metallicum, Stannum Metallicum,
Silicea, Sulphur 30x, 60x, 100x.

61
 LIQUITROPHIC INSTRUCTION

Liquitrophics may be taken with meals, although they should not

be mixed with piping hot foods over 106 degrees F.

Refrigerate after opening.

Liquitrophics and homeopathics should be taken 20 minutes

apart.

Do not store Liquitrophics in sunlight.

Liquitrophics may be taken at the same time with other

Liquitrophics. The exception to this would be that Lipid
Liquitrophic and Thyro Liquitrophic should not be mixed with
other homeopathics or Liquitrophics.

CAUTION: Alcohol sensitivities: If a person is sensitive to alcohol, put

the dosage into a 3 oz. glass of warm water. Allow one minute for the
alcohol to evaporate.

By following these guidelines, you will give the remedies the greatest
opportunity to succeed.

62
AMINO ACIDS
ALANINE (L-ALANINAMIDE)
ARGININE (L-ARGININAMIDE)
ASPARAGINE (NA-T-BOC-N-Y-XANTHYL-L-ASPARAGINE)
ASPARTIC ACID (L-ASPARTIC ACID AMIDE)
ASPARTIC ACID (P-NITROPHENYL ESTER)
CYSTEINE
GLUTAMIC ACID
GLUTAMINE
GLYCINAMIDE
GLYCINE
HISTIDINE
ISOGLUTAMINE
ISOLEUCINE
L-LYSINE
L-METHIONINE
L-TAURINE
LEUCINE
METHIONINE
N-CBZ-EZ-AMINO-N-CAPROIC ACID
N-CBZ-D-3-(2-NAPHTHYL) ALANINE
N-CBZ-L-HOMOSERINE
N-CBZ-Y-AMIN0-N-BUTYRIC ACID
N-T-BOC-L-HOMOSERINE
N-T-BOC-Y-AMINOBUTYRIC ACID
NORLEUCINE
NORVALINE
ORNITHINE
PHENYLALANINE
PROLINE
PYROGLUTAMIC ACID
SARCOSINE
SERINE
STATINE
THREONINE
TRYPTOPHAN
TYROSINE
VALINE

63
LIPIDS

Fatty Acid Anhydrides

C 2:0 Acetic
C 4:0 Butyric
C 6:0 Caproic
C 8:0 Caprylic
C 10:0 Capric
C 12:0 Lauric
C 14:0 Myristic
C 16:0 Palmitic
C 17:0 Heptadecanoic
C 18:0 Stearic
C 18:1, cis-9 Oleic
C 18:1, trans-9 Elaidic
C 18:2, cis-9, 12 Linoleic
C 20:0 Arachidonic
C 22:1, cis-11 11-Eicosenoic
C 22:0 Behenic

Diglycerides

C 6:0 Dicaproin, 1,3 isomer

C 8:0 Dicaprylin, 1,2-, 1,3-and mixed isomers
C 10:0 Dicaprin, 1, 2-, 1, 3- and mixed isomers
C 12:0 Dilaurin, 1, 2-, 1, 3- and mixed isomers
C 14:0 Dimyristin, 1, 2-, 1, 3- and mixed isomers
C 15:0 Dipentadecanoin, 1, 3-isomer
C 16:0 Dipalmitin, 1,2-, 1,3- and mixed isomers
C 18:0 Disteaarin, 1, 2-, 1, 3- and mixed isomers
C 18:1, cis-9 Diolein, 1,2- 1,3- and mixed isomers
C 18:1, cis-9, C2:0 1-Oleoyl-2-Acetyl
C 18:1, trans-9 Dielaidin, 1,3-isomer
C 18:2, cis-9, 12 Dilinolein, 1,3-isomer
C 20:0 Diarachidin, 1,3-and mixed isomers
C 20:1, cis-11 Di-11-Eicosenoin, mixed isomers
C22:1, cis-13 Dierucin, mixed isomers

64
LIPIDS, cont.
Monoglycerides

C 8:0 1-Monocapryloyl-rac-glycerol
C 10:0 1-Monodecanoyl-rac-glycerol
C 12:0 1-Monolauroyl-rac-glycerol
C 14:0 1-Monomyristoyl-rac-glycerol
C 16:0 1-Monopalmitoyl-rac-glycerol
C 16:1, cis-9 1-Monopalmitoleoyl-rac-glycerol
C 18:0 1-Monostearoyl-rac-glycerol
C 18:1, cis 9 1-Monooleoyl-rac-glycerol
C 18:1, trans-9 Monoelaidin
C 18:2, cis-9, 12 1-Monolinoleoyl-rac-glycerol
C 18:3, cis-9,12,15 1-Monolinoleoyl-rac-glycerol
C 20:1, cis-11 Mono-11-eicosenooin, 1-isomer
C 22:1, cis-13 Monoerucin, 1-isomer

65
Lipids, cont.

Triglycerides

C 2:0 Triacetin
C 4:0 Tributyrin
C 6:0 Tricaproin
C 8:0 Tricaprylin
C 9:0 Trinonanoin
C 10:0 Tricaprin
C 12:0 Trilaurin
C 13:0 Tritridecanoin
C 14:0 Trimyristin
C 14:1, cis-9 Trimyristolein
C 15:0 Tripentadecanoin
C 16:0 Tripalmitin
C 16:1, cis-9 Trielaidin
C 17:0 Triheptadecanoin
C 18:0 Tristearin
C 18:1, trans-9 Trielaidin
C 18:1, cis-9 Triolein
C 18:1, cis-6 Tripetroselinin
C 18:2, cis-9, 12 Trilinolelaidin
C 18:3, cis-9, 12, 15 Trilinolenin
C 19:0 Trinonadecanoin
C 20: Triarachidin
C 20:1, cis-5, 8, 11, 14 Triarachidonin
C 22:0 Tribehenin
C 22:1, cis-13 Trierucin
C 24:1, cis-15 Trinervonin

66
HORMONES

ACETYL CHOLINASE
ACETYL CHOLINE
ADRENAL PEPTIDE E
ADRENALIN
ADRENOCORTICOTROPIC HORMONE (ACTH: CORTICOTROPIN A)
ALDOSTERONE
AMASTATIN
ANGIOTENSIN (CONVERTING ENZYME INHIBITOR)
ANGIOTENSIN I
ANGIOTENSIN II (HYPERTENSIN II)
ANGIOTENSIN III INHIBITOR
ANGIOTENSINOGEN (FRAGMENT)
ANTI-PAIN
ANTI-REPRODUCTIVE TRIPEPTIDE
ATRIOPEPTIN I
ATRIOPEPTIN II
ATRIOPEPTIN III
BEAUVERICIN
BRADYKININ
BRADYKININ POTENTIATOR C
B-CASOMORPHIN
B-LIPOTROPIN FRAGMENTS
BRADYKININ POTENTIATOR B
CAERULEIN
CALCITONIN (THYRO)
CHOLECYSTOKININ
CHYMOSTATIN
CORTICOTROPIN RELEASING FACTOR
DERMORPHIN
DYNORPHIN A (PORCINE)
CYNORPHIN B (PORCINE)
ELASTIN CHEMOTACTIC FRAGMENT
ELEDOISIN
ENKEPHALINAMIDE
EPINEPHRINE
ERYTHROPOIETIN
ESTROGEN
a-ENDORPHIN
GALANIN
GASTRIC INHIBITORY POLYPEPTIDE
GASTRIN
GASTRIN RELEASING PEPTIDE
GASTRIN I FRAGMENTS
GASTRIN II

67
HORMONES, cont.

GLUCAGON
GLUTATHIONE
GROWTH HORMONE
GROWTH HORMON RELEASING FACTOR
INSULIN
KALLIDIN
KATACALCIN
KEMPTIDE
KENTSIN
KETOSTEROIDS (ALL)
KYOTORPHIN
L-ALANYLGLYCYL-L-SERYL-L-GLUTAMIC ACID
L-METHIONYL-L-LEUCYL-L-PHENYLALANINE
L-TYROSYLGLYCYLCLYCINE
L-VALYLGLYCYL-L-SERYL-L-GLUTAMIC ACID
LEUCINE ENKEPHALIN-LYS
LEUPEPTIN
LEUTINIZING HORMONE
LEUTINIZING RELEASING HORMONE
METHIONINE ENKEPHALINE
MINERAL CORTICOID
MORPHICEPTIN
MOTILIN
a-MELANOCYTE STIMULATING HORMONE
a1-MATING FACTOR
(D-TRP2)-METHIONINE ENKEPHALIN
N-ACETYL-L-METHIONYL-L-LEUCYL-L-PHENYLALANYL-L-METHIONINE
N-FORMYL-L-METHIONYL-L-LEUCYL-L-PHENYLALANINE METHYL
N-FORMYL-L-METHIONYL-L-LEUCYL-L-TYROSINE
N-FORMYL-L-METHIONYL-L-PHENYLALANYL-L-LYSINE N-FORMYL
N-FORMYL-L-NORLEUCYL-L-LEUCYL-L-PHENYLALANINE
N-T-BOC-L-LEUCYL-L-PHENYLALANINE
N-T-BOC-L-METHIONYL-L-LEUCYL-L-PHENYLALANINE
N-T-BOC-L-METHIONYL-L-LEUCYL-L-TYROSINE
NEOENDORPHIN
NERVE GROWTH FACTOR
NEUROMEDIN C
NEUROTENSIN
NOREPINEPHRINE
a-NEOENDORPHIN
OXYTOCIN
PANCREATIC POLYPEPTIDE
PANCREOZYMIN
PARATHYROID HORMONE
68
PEPTIDE YY
PITUITARY DIURETIC HORMONE (POSTERIOR)
PITUITARY RELEASE (ANTERIOR)
PRESSINOIC ACID
PROCTOLIN
PROENKEPHALIN
PROGESTERONE
PROLACTIN
RENIN
RENIN INHIBITOR
SCHIZOPHRENIA RELATED PEPTIDE
SECRETIN
SOMATOSTATIN
SOMATOSTATIN 25
SOMATOSTATIN 28
SYNDYPHALIN-20
TESTOSTERONE
THYMOPOIETIN 32-36
THYMOSIN
THYROCALCITONIN
THYROID STIMULATING HORMONE
VAL-GLY-VAL-ALA-PRO-GLY
VASOPRESSIN
VASOTOCIN
XENOPSIN
YEAST a-FACTOR

69
HOMRONES/BIOACTIVE PEPTIDES

Adrenocorticotropic Hormone (ACTH: Corticotropin A)

Angiotensin I
Angiotensin II (Hypertensin II)
Angiotensin III
Angiotensin III Inhibitor
Angiotensin-Converting Enzyme Inhibitor (pGlu-Trp-Pro-Arg-Pr9o-Gin-
lie-Pro-Pro)
Angiotensinogen (Fragment 1-14)
Renin
Bradykinin (Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg)
Bradykinin Potentiator B (pGlu-Gly-Leu-Pro-Pro-Arg-Pro-Lys-11e-Pro-
Pro)
Bradykinin Poetntiator C (pGlu-Gly-Leu-Pro-Pro-Gly-Pro-Pro-11e-Pro-
Pro)

CHEMOTACTIC PEPTIDES

N-Acetyl-L-Methionyl-L-Lefucyl-L-Phenylalanine
L-Alanylglycyl-L-Seryl-L-Glutamic Acid (Eosinophil chemotactic factor of
anaphylaxis)
N-t-BOC-L-Methionyl-L-Leucyl-L-Phenylalanine (Chemotactic peptide
antagonist)
N-t-BOC-L-Phenylalanyl-D-Leucyl-L-Phenylalanyl-D-Leucyl-L-
Phenylalanin
(Chemotactic peptide inhibitor)
N-Formyl-L-Methionyl-L-Leucyl-L-Phenylalanine Methyl Ester (A potent
chemotactic peptide for human blood monocytes)
N-Formyl-L-Methionyl-L-Leucyl-L-Phenylalanyl-L-Lysine (Acetate salt)
N-Formyl-L-Methionyl-L-Leucyl-L-Tyrosine (Dicyclohexylammonium salt)
N-Formyl-L-Norleucyl-L-Leucryl-L-Phenylalanine (Chemotactic peptide)
N-Formyl-L-Norleucyl-L-Leucyl-L-Phenylalanyl-L-Tyrosine
L-Methionyl-L-Leucyl-L-Phenylalanine (Acetate Salt Exhibits very weak
chemotactic properties)
Val-Gly-Val-Ala-Pro-Gly (Elastin chemotactic fragment)
L-Valylglycyl-L-Seryl-L-Glutamic Acid (Esinophil chemotactic factor of
anaphylaxis)
Dynorphin A (Porcine)
Dynorphin B (Porcine)
a-Endorphin
Leucine Enkephalin
Leucine Enkephalin-Lys
Enkephalinamide
Methionine Enkephaline (Tyr-Gly-Gly-Phe-Leu-Lys)
[D-Trp 2]-Methionine Enkephalin
70
Proenkephalin
Syndyphalin
Syndyphalin-20
L-Tyrosylglycylglycine

ENZYME INHIBITORS

Amastatin
Angiotensin-Converting Enzyme Inhibitor
Antipain
Chymostatin
Leupeptin

GASTROINTESTINAL PEPTIDES

Caerulein
Cholecystokinin
Galanin
Gastric Inhibitory Polypeptide
Gastrin
Gastrin I Fragments
Gastrin II (Sulfated)
Gastrin Releasing Peptide (Porcine)
Glucagon (Crystalline)
Pancreatic Polypeptide
Pancreozymin
Peptide YY
Secretin
Growth Hormone Releasing Factor (1-44)
a-Melanocyte Stimulating Hormone
Neurotensin

OPIOID PEPTIDES

Adrenal Peptide E
B-Casomorphin
Dermorphin
Kyotorphin
Morphiceptin
Oxytocin
Pressinoic Acid
Vasopressin
Vasotocin
Somatostatin
Somatotstatin 25
71
Somatostatin 28 (Fragment 1-14)

MISCELLANEOUS

Amastatin
Antipain
Beauvericin
Calcitonin
Cholecystokinin
Corticotropin Releasing Factor
Elastin Chemotactic Fragment
Eledoisin
Erythropoietin
Glucagon
Glutathione
Insulin
Katacalcin
Kentsin
Neuromedin C
Pancreozymin
Proctolin
Proenkephalin
Thymosin a
Thyrocalcitonin
Xenopsin

72
ENZYMES
ACETYL CHOLINE ESTER
ACETYLESTERASE
ACID MALTASE POMPES DISEASE
ACID PHOSPHATASE
ADENOSINE 5-DIPHOSPHATE
ALKALINE PHOSPHATASE
ALAKALINEPROTEASE
ALDOASE
ALPHA 1, 4 GLUCOSIDASE POMPES DISEASE
AMINO ACID DECARBOXYLASES
AMINO ACID OXIDASE
AMINOBUTYRIC ACID TRANSAMINASE
AMYLO-1, 6 GLUCOSIDASE CORIS DISEASE
ANGIOTENSIN-CONVERTING ENZYME INHIBITOR
ARGINASE
ARGININE DECARBOXYLASE
ASCORBATE OXIDASE
ASPARAGINASE
ASPARTIC ACID DECARBOXYLASE
ATPase
a-AMYLAST
b-AMYLASE
BILE ACID DEHYRDROGENASE
BUTYL CHOLINESTERASE
CALCULASE
CANDIDA PSEUDOTROPICALIS
CANDIDA UTILIS
CARBONIC ANHYDRASE
CARBOXYPEPTIDASE A
CARNITINE PALMITOYLTRANSFERASE MYOPATHY
CAROBXYPEPTIDASE B
CATALASE
CELLULASE
CHOLESTEROL
OXIDASE
CHOLINE KINASE
CHOLINESTERASE, ACETYL
CHLOROPEROXIDASE
CHOLESTEROL ESTERASE
CHOLINE ACETYLTRANSFERASE
CHOLINE OXIDASE
CHOLINESTERASE, BUTYRYL
CHYRO TRYPSIN
COENZYME A DEHYDROGENASE

73
ENZYMES, cont.
COLLAGENASE
CORTISONE REDUCTASE
CREATINASE
CREATININASE
CREATININE PHOSPHOKINASE
CYTOCHROME b2
CYTOCHROME C REDUCTASE
a-CHYMOTRYPSIN
DEOXYRIBONUCLEASE (ATP DEPENDENT)
DEOXYRIBONUCLEASE 1
DEOXYRIBONUCLEASE 2
DEOXYRIBONUCLEIC ACID LIGASE
DEOXYRIBONUCLEIC ACID POLYMERASE
DEXTRANASE
DNA LIGASE
DNA POLYMERASE
DOPAMINE B-MYDROXYLAST
ELASTASE
ENTEROKINASE
FORMALDEHYDE DEHYDROGENASE
FUCOSE DEHYDROGENASE
GABASE
GLUTAMINASE
GLUTATHIONE PEROXIDASE
BLUATHIONE REDUCTASE
GLUCOSE DEHYDROGENASE
GLUTAMIC DECARBOXYLASE
GLUTAMIC DEHYDROGENASE
GLYCEROL DEHYDROGENASE
GLYCOGEN PHOSPHORYLASE
GLYCOGEN SYNTHETASE
HISTAMINE
HISTIDASE
HYALURONIDASE
HYDROXYPYRUVATE REDUCTASE
HYDROXYSTEROID DEHYDROGENASE
INVERTASE
ISOAMYLASE
ISOCITRATE LYASE
ISOMALTASE
LACTASE
LACTATE DEHYDROGENASE
LACTATE 2-MONOOXYGENASE

74
ENZYMES, cont.
LACTIC DEHYDROGENASE
LACTOPEROXIDASE
LDH
LECITHINASE A
LECITHINASE B
LECITHINASE C
LECITHINASE D
LEUCINE DEHYDROGENASE
LIPASE
LIPOXIDASE
LYSIN
LYSINE DECARBOXYLASE
LYSOZYME
LYTIC ENZYMES
MALATHION HYDROLASE
MALTASE
MERCURIPAPAIN
MONOAMINE OXIDASE
MYLEO PEROXIDASE
MYOPHOSPHORYLASE McARDLES DISEASE
MYOSIN
NADASE
NEURAMINIDASE
NUCLEASE
OTNIHINE DECARBOXYLASE
OXALATE OXIDASE
PANCREATIN
PANCREOZYMIN
PAPAIN
PARATHION HYDROLASE
PECTINASE
PECTOLYASE
PENICILLINASE
PEP CARBOXYLASSE
PEPSIN
PEPSINOGEN
PEPTIDASE
PEROXIDASE
PHOSPHATASE, ACID
PHOSPHODIESTERASE
PHOSPHOFRUCTOKINASE MYOPATHY
PHOSPHOLIPASE A2
PHOSPHORYLASE

75
ENZYMES, cont.
PHYTASE
PROSTAGLANDID DEHYDROGENASE
PROTEASE
PYRUVATE DEHYDROGENASE
PYRUVATE KINASE
PYRUVATE OXIDASE
PYTALIN
TRYPSIN
RENIN
RENNIN
RIBONUCLEASE
SACCHARASE
SBP BROMELAIN PAPIN
STEROID DEHYDROGENASE
SUCRASE
TRYPSIN
TRYPSINOGEN
TRYPTOPHAN
TYROSINASE
URICASE
VANILMANDELIC ACID DEHYDROGENASE
VITAMIN C ASE
XANTHINE OXIDASE

76
 THE ANODYNE PHILOSOPHY

Anodyne is the medical word for a remedy used to treat pain

conditions. The neurology of pain involves many sensory neurons and
their ability to project neurological signals through the nervous
system to the brain, which then perceives these signals as pain. The
physiology of pain is akin to the physiology of neurology and
perception. Pain results when there is an over or under balance in the
neurons of any area resulting in an energetic overload.
The Dr. Recommends anodyne remedies are formulated to help in a
wide variety of pain conditions. They are not designed to cover up the
pain, nor are they designed as pain killers. They are designed to help
in healing the factors behind the pain and to stimulate the organism
into a healing process, thereby reducing the amount of pain through
natural means. Anodyne formulas give us a broad-based collection of
easy-to-use remedies to help many types of pain conditions in the
body and are quality controlled within the QQCTM guidelines.
Pain is not the enemy; pain is indeed the messenger of a problem
and must not be fought against. It is the purpose of homoeopathy to
work with the pain.
If pain persists, it is a further indication that there is a serious
underlying condition and the patient should be referred to a
professional who can treat the patient effectively.

77
 ANODYNE REMEDIES

ABDOMINAL ANODYNE (1 fl. oz.)

Catalog No. 0017
Indication: Cramping, Pre-appendicitis
Ingredients: Ferrum Metallicum, Chamomilla 3x. Bismuthum
Metallicum, Borax 4x. Lycopodium clavatum 5x. Carbo Vegetabilis, Solar
Plexus, Vagus Nerve, Bovine Stomach Tissue, Natrum Sulphuricum 6x,
12x, 30x, 60x, 100x. Bromium 7x. Sulphur 8x, 30x, 60x. Muriaticum
Acidum, Platinum Metallicum, Alumen 12x, 30x, 60x, 100x. Plumbum
Metallicum, Mercurius Vivus, Nux vomica 30x, 60x, 100x.

ANODYNE-ACD (1 fl. oz.)

Catalog No. 0286
Indication: Pain from acid conditions
Ingredients: Natrum Bicarbonate 3x. Full spectrum Fatty Acids, Coca,
Ferrum Metallicum 5x. Antimonium Tartaricum 6x. Chemoreceptors 6x,
12x, 30x. Sepia, Muriaticum Acidum 8x, 16x, 30x. Oxalicum Acidum,
Uricum Acidum 16x, 30x. Endorphins 20x, 60x, 100x.

ANODYNE-ALK (1 fl. oz.)

Catalog No. 0287
Indication: Pain from alkaline conditions
Ingredients: Ascorbicum Acidum, Smilax 3x. Coca 5x. Zincum
Metallicum, RNA-DNA, Magnesium Thiosulfate, Propionaldehyde 6x.
Chemoreceptors 6x, 12x, 30x. Natrum Bicarbonate 8x, 16x, 30x.
Causticum, Calcarea Sulphurica, Calcarea Phosphorica, Calcarea
Magnesia 12x. Endorphins 20x, 60x, 100x.

ANODYNE-AUTOX (1 fl. oz.)

Catalog No. 0288
Indication: Pain from self-made toxins, injury
Ingredients: Smilax 3x. Symphytum officinale 4x. Arnica montana 4x,
10x, 30x. Calendula officinalis 5x, 15x, 30x. Isotonic Plasma 6x, 20x.
Mechanoreceptors 6x, 12x, 30x. Aurum Metallicum, Carbo Animalis 12x.
Endorphins, Gate Receptors (Spine & Brain) 20x, 60x, 100x.
Vaccinotoxinum 60x, 100x, 500x, 1000x.

78
ANODYNE-C (1 fl. oz.)
Catalog No. 0058
Indication: Pain where cold improves
Ingredients: Pulsatilla 4x. Natrum Sulphuricum 6x. Dulcamara 6x, 12x,
30x. Ferrum Metallicum 6x, 12x, 30x, 100x. Sarcodes: Temperature
Sensor Nerve Cells 6x, 12x, 30x, 60x, 100x. Arsenicum Metallicum 8x.
Rhododendron chrysanthum 12x. Echinacea purpurea, Lachesis mutus
12x, 30x, 100x. Aluminium Metallicum, Aurum Metallicum, Bismuthum
Metallicum, Borax, Plumbum Metallicum, Silicea 16x, 20x, 50x, 100x.

ANODYNE-ELC (1 fl. oz.)

Catalog No. 0289
Indication: Pain provoked by exposure to electric or energetic fields,
television, microwaves, etc.
Ingredients: Euphrasia officinalis, Pilocarpus 3x. Agate 4x, 5x, 6x.
Cuprum Metallicum 6x, 12x. Electromagnetic Nerve Receptors 6x, 12x,
30x, 60x, 100x. Full spectrum EMR, Full spectrum magnetic oscillations
6x, 12x, 30x, 60x, 100x, 500x, 1000x. Glonoine 12x, 30x. Corallium
Nigra 30x.

ANODYNE-NT (1 fl. oz.)

Catalog No. 0050
Indication: Pain where no touch improves
Ingredients: Zincum Metallicum 3x. Selenium Metallicum 4x, 6x, 30x,
100x. Bryonia 5x. Nux vomica 6x. Zincum Metallicum 6x, 12x, 30x,
60x. Sarcodes: Kruski Cells (Pressure Sensors) 6x, 12x, 30x, 60x, 100x.
Silicea 6x, 12x, 30x, 100x. Arsenicum Album, Gelsemium sempervirens,
Plumbum Metallicum, Lachesis mutus 8x, 12x, 30x.

ANODYNE-T (1 fl. oz.)

Catalog No. 0049
Indication: Pain where touch improves
Ingredients: Coffea cruda 3x. Belladonna 4x. Bryonia, Aconitum
napellus 5x. Spigelia marilandica 6x. Sarcodes: Kruski Cells (Pressure
Sensors) 6x, 12x, 30x, 60x, 100x. Bismuthum Metallicum, Magnesia
Phosphorica 12x. Iodium 16x-24x. Borax 16x-30x.

CEPHALO ANODYNE (1 fl. oz.)

Catalog No. 0036
Indication: Sub-orbital, migraine, temporal headache
Ingredients: Iris versicolor, Chrysanthemum parthenium, Salix nigra 2x.
Sanguinaria canadensis 3x. Endorphins 6x, 12x, 30x. Ammonium
Carbonicum 5x. Silicea, Manganum Metallicum, Cimicifuga racemosa
6x. Bovine Pituitary Glandular, Antimonium, Arsenicum Metallicum
12x. Cuprum Metallicum, Graphites, Iodium 16x.

79
ANODYNE-G (1 fl. oz.)
Catalog No. 0048
Indication: General pain
Ingredients: Salix alba 3x, 6x. Selenium Metallicum, Zincum Metallicum,
Vitamins A, C, E 6x. Acetaminophen, Ibuprofen, Acetylsalicylic Acid
6x-30x. Arsenicum Metallicum, Arum maculatum 6x, 12x, 30x.
Sarcodes: Major Nerves 6x, 12x, 30x, 60x, 100x. Barium, Mercurius
Vivus 30x.

ANODYNE-H (1 fl. oz.)

Catalog No. 0057
Indication: Pain where heat improves
Ingredients: Kali Carbonicum, Bryonia, Manganum Metallicum 6x.
Sarcodes: Temperature Sensor Nerve Cells 6x, 12x, 30x, 60x, 100x.
Sulphur, Zincum Metallicum 6x, 100x. Borax 8x, 12x. Belladonna, Apis
mellifica, Ruta graveolens, Rhus toxicodendron 12x, 30x. Fluorine, Arnica
montana 12x, 30x, 100x. Arsenicum Metallicum 12x, 30x, 100x, 500x.
Mercurius Vivus 30x.

ANODYNE-M (1 fl. oz.)

Catalog No. 0051
Indication: Pain where motion improves
Ingredients: Valeriana officinalis 1x. Pulsatilla 2x. Dioscorea villosa 3x.
Kali Iodatum 4x, 6x, 12x, 70x. Ignatia amara, Oxalicum Acidum 5x.
Rhus toxicodendron 6x. Phosphorus 8x, 12x, 25x. Cuprum Metallicum
12x, 30x. Sarcodes: Nerve Sensors of Proprioceptors 12x, 30x, 60x, 100x.
Silicea 100x, 500x.

ANODYNE-NM (1 fl. oz.)

Catalog No. 0052
Indication: Pain where no motion improves
Ingredients: Magnesia Phosphorica 3x, 6x. Bryonia 8x. Manganum
Metallicum 8x, 12x, 30x. Kreosotum, Nux vomica 9x. Sarcodes: Nerve
Sensors of Proprioceptors 12x, 30x, 60x, 100x. Platinum Metallicum 20x,
50x, 100x. Mercurius Vivus 30x, 60x, 100x.

ANODYNE-NT (1 fl. oz.)

Catalog No. 0050
Indication: Pain where no touch improves
Ingredients: Zincum Metallicum 3x. Selenium Metallicum 4x, 6x, 30x,
100x. Bryonia 5x. Nux vomica 6x. Zincum Metallicum 6x, 12x, 30x,
60x. Sarcodes: Kruski Cells (Pressure Sensors) 6x, 12x, 30x, 60x, 100x.
Silicea 6x, 12x, 30x, 100x. Arsenicum Album, Gelsemium sempervirens,
Plumbum Metallicum, Lachesis mutus 8x, 12x, 30x.

80
ANODYNE-T (1 fl. oz.)
Catalog No. 0049
Indication: Pain where touch improves
Ingredients: Coffea cruda 3x. Belladonna 4x. Bryonia, Aconitum
napellus 5x. Spigelia marilandica 6x. Sarcodes: Kruski Cells (Pressure
Sensors) 6x, 12x, 30x, 60x, 100x. Bismuthum Metallicum, Magnesia
Phosphorica 12x. Iodium 16x-24x. Borax 16x-30x.

CEPHALO ANODYNE (1 fl. oz.)

Catalog No. 0036
Indication: Sub-orbital, migraine, temporal headache
Ingredients: Iris versicolor, Chrysanthemum parthenium, Salix nigra 2x. Sanguinaria
canadensis 3x. Endorphins 6x, 12x, 30x. Ammonium Carbonicum 5x. Silicea,
Manganum Metallicum, Cimicifuga racemosa 6x. Bovine Pituitary Glandular,
Antimonium, Arsenicum Metallicum 12x. Cuprum Metallicum, Graphites, Iodium 16x.

FACIAL ANODYNE (1 fl. oz.)

Catalog No. 0031
Indication: Facial pain, Symptoms relating to Bell's Palsy
Ingredients: Salix nigra 3x. Aconitum napellus 4x. Zincum Metallicum, Manganum
Metallicum, Silicea, Belladonna 6x. Argentum Metallicum 8x. Phosphorus, Chromium
12x. Trigeminal Nerve 16x, 30x, 60x, 100x, 500x.

INTERCOSTO ANODYNE (1 fl. oz.)

Catalog No. 0059
Indication: Intercostal neuralgia
Ingredients: Ruta graveolens 6x, 12x. Arsenicum Album 12x. Intercostal Cartilage, Rib
Glandular 12x, 30x. Antimonium, Plumbum Metallicum, Rhus toxicodendron 30x.

LARGE JOINT ANODYNE (1 fl. oz.)

Catalog No. 0044
Indication: Large joint discomfort, knees, elbows, shoulders
Ingredients: Bryonia 4x. Magnesium Metallicum, Manganum Metallicum, Calcarea,
Arnica montana, Sulphuricum Acidum 6x. Zincum Metallicum 6x, 12x, 30x, 60x, 100x,
500x, 1000x. Niccolum Metallicum 8x. Ledum palustre 10x. Sulphur 12x. Ligament,
Cartilage 12x, 30x. Strontium 20x.

LUMBO ANODYNE(1 fl. oz.)

Catalog No. 0070
Indication: Low back pain
Ingredients: Niacinamide 3x. Nux vomica, Atropinum 4x. Rhus toxicodendron 5x.
Nicotinum 6x. Sarcodes: Kidney, Liver, Lumbar and Sacral Vertebrae, Sciatic and
Femoral Nerve 6x, 12x, 30x, 60x, 100x. Arnica montana 30x, 100x.

81
SCIATIC ANODYNE (1 fl. oz.)
Catalog No. 0060
Indication: Sciatic, Low back pain
Ingredients: Manganum Metallicum 4x, 12x, 30x, 60x, 100x, 1000x. Sarcode: Sciatic
Nerve 6x, 12x. Magnesia Phosphorica 8x. Atropinum 12x. Aconitum napellus 12x.
Arsenicum Album 30x.

SMALL JOINT ANODYNE (1 fl. oz.)

Catalog No. 0045
Indication: Small joint pain in fingers, toes
Ingredients: Lithium Carbonicum 2X, 12x. Atropinum 4x. Calendula officinalis,
Nitricum Acidum, Magnesium Metallicum, Manganum Metallicum, Calcarea 6x.
Rhododendron chrysanthum 6x, 12x, 30x, 60x, 1000x. Zincum Metallicum 6x, 12x, 30x,
60x, 100x, 500x, 1000x. Niccolum Metallicum 8x. Platinum Metallicum, Sulphur 12x.
Ligament, Cartilage 12x, 30x. Ammonium Phosphoricum 12x, 30x, 100x. Strontium,
Plumbum Metallicum 20x. Natrum Sulphuricum, Nux vomica 30x.

THORACIC ANODYNE (1 fl. oz.)

Catalog No. 0067
Indication: Acute chest pains
Ingredients: Crataegus oxyacantha, Cactus grandiflorus, Scilla maritima 2x. Kali
Carbonicum, Kalmia latifolia, Spigelia marilandica 3x. Digitalis purpurea 4x. Arsenicum
Album, Phosphorus 5x. Manganum Metallicum 6x, 12x, 30x, 60x, 100x. Selenium
Metallicum 8x. Creatine Phosphokinase, Rennin, Histaminum 12x, 20x, 60x, 100x.
Zincum Metallicum, Platinum Metallicum 12x, 30x, 60x.

82
 THE COMBINATION PHILOSOPHY

Combination homeopathy is the most popular type of homeopathy

used in the world today. Combination ingredients are chosen based on a
symptomatic picture. Therefore, combinations can be engineered for
broader based ranges of effectiveness, whereas, singular homeopathics
usually have profoundly small realms of utilization. Combination
homeopathy is easy to learn, as a minimal amount of training is needed
for the doctor to perceive the symptomatic picture that is presented.
In nature, everything exists in a combination form. Thus, Apis
mellifica, or honey bee, is a very complex combination that nature has
brought together to yield one energetic substance. This is the law of
synergy the sum of the whole is greater than that of the parts.
Combining is the secret of life.
This type of synergy is culminated in the Dr. Recommends combination
remedies. The combination remedies have been developed with QQCTM
techniques, to ensure that the blending of the ingredients have a
synergistic effect and become a new singular formula. The Dr.
Recommends combination remedies are safe and effective formulas that
will minimize healing crises and help to reduce risk to the patient. The
combination remedies also utilize the best of trace element work in
achieving their glandular activity.

83
 COMBINATION REMEDIES

ARRHYTH-1 (1 fl. oz.)

Catalog No. 0043
Indication: Irregularities of the pulse
Ingredients: Crataegus oxyacantha, Valeriana officinalis, Kali
Phosphoricum, Amni visnaga, Leonurus Cardiac, Cytisus scoparius,
Sumbul 2x. Heart, Nerium oleander 3x. Zincum Metallicum 5x. Iberis
amara 6x. Sulphur, Platinum Metallicum 12x.

ARTHRO 1 (1 fl. oz.)

Catalog No. 0032
Indication: Joint stiffness and pain
Ingredients: Angelica archangelica, Du Huo 2x. Magnesia Phosphorica
2x, 3x, 6x. Dong Quai, Cnidium, Achyranthes, Gambir, Kali Muriaticum,
Manganum Metallicum, Yucca filamentosa 3x. Cartilage 3x, 6x, 12x.
Rhus toxicodendron 5x. Arsenicum Metallicum 6x. Hordeum vulgare 8x.
Oxalicum Acidum 8x, 12x. Arnica montana 8x, 100x, 1000x.
Antimonium, Borax, Baryta, Arsenicum Metallicum, Platinum
Metallicum, Sulphur, Elastin, Elastase, Collagen, Collagenase 12x.

CEPHALO-LD (1 fl. oz.)

Catalog No. 0064
Indication: Learning disabilities, Mental clarity
Ingredients: Convallaria majalis 2x, 6x. Cistus canadensis, Impatiens,
Clematis erecta 6x, 12x, 30x, 60x, 100x, 500x, 1000x. Bovine Brain
Tissue 6x, 12x. Sepia 8x. Phosphorus 10x. Zincum Metallicum,
Belladonna 12x. Plumbum Metallicum, Platinum Metallicum 25x, 75x,
100x. Mercurius Vivus 25x, 75x, 100x, 500x. Bovine Kidney Glandular,
Lycopodium clavatum 30x.

CEPHALO-M (1 fl. oz.)

Catalog No. 0065
Indication: Stimulates blood flow to brain, Memory
Ingredients: Euphrasia officinalis, Rosmarinus officinalis 2x. Salvia
officinalis 2x, 6x. Artemisia vulgaris, Asparagus officinalis 3x. Ilex
paraguariensis 5x. Convallaria majalis, Allium sativum, Calcarea
Phosphorica 6x. Brain 6x, 12x, 30x, 60x, 100x. Baryta Carbonica 8x.
Sulphur, Silicea, Selenium Metallicum, Zincum Metallicum 12x, 100x,
1000x. Plumbum Metallicum 30x.

84
CEPHALO-SD (1 fl. oz.)
Catalog No. 0172
Indication: Memory, Brain power
Ingredients: Gingko biloba, Choline, Phosphatydl Choline 2x. Taurine,
Tyrosine 3x. Niacin, Niacinamide, Biotin 4x. Phenylalanine 5x. Nerve
Growth Factor 6x. Brain Sarcode 6x, 12x, 30x, 60x, 100x. Vitamins:
B1-B20 8x. Paullinia cupana 3x.

COUGH SYRUP (4 fl. oz.)

Catalog No. 0027
Indication: Cough
Ingredients: Laurocerasus, Spongia tosta, Rumex crispus, Belladonna,
Ipecacuanha, Drosera rotundifolia 3x. Mentha, Adrenalinum, Ligusticum
porteri 4x. Convallaria majalis, Alumen, Bromium, Ferrum
Phosphoricum, Zincum Metallicum, Manganum Metallicum, Magnesia
Phosphorica, Baryta, Bismuthum Metallicum, Dextromethorphan 6x.
Sarcodes: Cough Center, Lung 6x, 12x, 30x, 60x, 100x. Arsenicum
Metallicum 8x. Stannum Metallicum 9x. Platinum Metallicum, Sulphur
12x, 24x, 30x, 60x.

CoQ (1 fl. oz.)

Catalog No. 0300
Indication: Deficiencies of CoQ
Ingredients: Sesame Seed oil, Avocado oil, Biotin, Folic acid, CoQ10 3x.
CoA, CoQ6, CoQ7, CoQ9, Ascorbic palmitate 6x, 12x, 24x, 30x.

DERMA-A (1 fl. oz.)

Catalog No. 0018
Indication: Comedones, Pustules, Blackheads, Whiteheads
Ingredients: Selenium Metallicum, Zincum Metallicum 4x. Cimicifuga
racemosa 6x, 12x, 24x. Lymph 6x, 12x, 30x. Natrum Muriaticum 6x,
200x. Argentum Metallicum, Aurum Metallicum, Gelsemium
sempervirens, Iodium, Manganum Metallicum 8x. Placenta 9x. Kali
Bromatum, Alumen, 12x, 24x, 60x. Juglans nigra 12x, 30x. Ledum
palustre, Hepar Sulphuris Calcareum, Mercurius Vivus 30x, 60x, 100x.

85
DERMA-I (1 fl. oz.)
Catalog No. 0020
Indication: Itching
Ingredients: Sarcodes: Liver, Lymph 3x, 6x, 12x, 30x, 60x, 100x.
Selenium Metallicum, Zincum Metallicum, Borax, Magnesium
Metallicum, Manganum Metallicum, Pangamicum Acidum 4x. Silicea,
Graphites, Calcarea Carbonica 6x. Alumen, Arsenicum Metallicum,
Baryta, Bismuthum Metallicum, Cuprum Metallicum, Stannum
Metallicum, Nitricum Acidum 8x. Muriaticum Acidum, Sulphuricum
Acidum 8x, 12x, 30x, 60x. Iodium, Phenylalanine, Tyrosine,
Phenylpyruvic Acid 12x, 30x, 60x. Phenylalanine Hydroxylase,
Glutamic-oxaloacetic Transaminase, Creatine Phosphokinase, Lactate
Dehydrogenase 60x, 100x, 500x.

EAR DROPS (1 fl. oz.)

Catalog No. 0173
Indication: Ear ache and excess ear wax (external use)
Ingredients: Olive Oil, Sesame Seed Oil. Verbascum thapsus 1x.
Anthemis nobilis 2x. Plantago major 3x. Vanilla, Ferrum Phosphoricum
4x, 6x.

ENTERO-B (1 fl. oz.)

Catalog No. 0047
Indication: Bowel flora disorders
Ingredients: Large Intestine Sarcode, Colostrum 4x. Manganum
Metallicum 6x. Natrum Muriaticum 6x, 100x, 1000x. Argentum
Metallicum, Arsenicum Metallicum, Arum maculatum, Lactobacillus 12x.
Bacteroidum 30x.

ENTERO-C (1 fl. oz.)

Catalog No. 0035
Indication: Constipation
Ingredients: Senna, Cascara sagrada, Zincum Metallicum 3x. Borax,
Ferrum Metallicum 6x. Alumina, Phosphorus 8x. Sulphur, Barium,
Aurum Metallicum, Antimonium, Arsenicum Metallicum 12x. Iodium
16x. Lycopodium clavatum 30x.

EU-STRESS (1 fl. oz.)

Catalog No. 0023
Indication: Stress
Ingredients: Apis mellifica 2x, 6x. Royal Jelly 3x. Adrenalinum 3x, 6x,
12x, 30x, 60x, 100x. Citrullus, Cistus canadensis, Impatiens, Clematis
erecta, Zincum Metallicum, Ferrum Metallicum, Silicea 6x.
Hypothalamus, Amygdala amara 6x, 12x, 30x, 60x, 100x. Vanadium
Metallicum 8x, 12x, 30x. Lithium Carbonicum 12x, 30x, 60x.
Neurotensin 16x, 30x, 60x, 100x.
86
FEM-B (1 fl. oz.)
Catalog No. 0068
Indication: Balance female organ systems
Ingredients: Caulophyllum thalictroides 2x, 6x. Rubus idaeus,
Cimicifuga racemosa 6x. Sarcodes: Ovary, Corpus Luteum, Uterus,
Mammary, Hypothalamus, Pituitary, Adrenal, Estrogen, Progesterone 6x,
12x, 30x, 100x, 500x, 1000x. Mercurius Vivus, Petroleum, Baryta,
Sulphur 20x.

FEM-M (1 fl. oz.)

Catalog No. 0046
Indication: Menopausal conditions
Ingredients: Chamomilla 3x, 30x, 100x, 500x, 1000x. Cimicifuga
racemosa, Sanguinaria canadensis, Ovarian Sarcode 6x. Silicea 8x.
Borax, Graphites, Iodium, Phosphorus, Estrogen 12x. Lachesis mutus
16x.

FEM-PMS (1 fl. oz.)

Catalog No. 0066
Indication: Premenstrual cramping, Irritability and depression
Ingredients: Chamomilla, Vitamin B6 3x. Caulophyllum thalictroides 3x,
6x. Cimicifuga racemosa 4x. Magnesia Phosphorica, Magnesia
Carbonica, Natrum Muriaticum 6x. Manganum Metallicum 6x, 12x, 30x.
Estrogen, Progesterone 6x, 12x. Natrum Carbonicum 12x. Phosphorus
30x. Platinum Metallicum 30x, 100x.

GASTRO-I (1 fl. oz.)

Catalog No. 0062
Indication: Stomach lining ulcerations
Ingredients: Oryza sativa, Panicum miliaceum, Triticum repens, Poria,
Raphanus sativus, Brassica, Zingiber officinale, Glycyrrhiza glabra,
Disodium Phosphate 2x. Borax 6x. Sarcodes: Stomach, Small Intestine
6x, 12x, 30x, 60x, 100x. Calcarea Carbonica 8x. Carbo Vegetabilis 8x,
12x, 30x. Mercurius Vivus, Arsenicum Metallicum 30x. Plumbum
Metallicum 100x. Sulphur, Cuprum Metallicum, Selenium Metallicum
200x.

GLUCO-H (1 fl. oz.)

Catalog No. 0038
Indications: Hypoglycemia
Ingredients: Oenothera biennis 3x. Chromium Metallicum 6x. ATP,
Insulin, Pancreas 6x, 12x, 30x. Plumbum Metallicum, Antimonium
Metallicum, Arsenicum Metallicum 20x. Nux vomica 30x. Saccharum
Officinale 30x, 200x, 1000x.

87
GLUCO-I (1 fl. oz.)
Catalog No. 0029
Indication: Hereditary tendency toward diabetes
Ingredients: Lycopodium clavatum, Selenium Metallicum, Zincum
Metallicum, Sulphur, Chromium, Alumen 6x. Sarcodes: Hypothalamus,
Posterior Pituitary, Kidney, Pancreas 6x, 12x, 30x, 60x, 100x. Argentum
Metallicum, Bismuthum Metallicum, Barium 12x. DNA, Insulin 12x,
60x, 100x, 1000x. Gelsemium sempervirens, Iodium, Plumbum
Metallicum 20x. Uranium, Phosphoricum Acidum 30x. Radium
Bromatum, ATPase, Antidiuretic Hormone 60x. Glucose, Glycogen
1000x.

HEMO-L (1 fl. oz.)

Catalog No. 0299
Indication: White blood cell disorders
Ingredients: Ceanothus americanus 2x. Nux vomica, Thuja occidentalis
3x. Ipecacuanha 4x, 6x, 12x. Leukemia Nosode 6x, 8x, 12x, 30x, 60x,
100x, 1000x. Hapalochlaena maculata, Sarcodes: Lymph, Spleen 6x,
12x, 30x, 60x, 100x. Leukocytes 12x, 30x, 60x, 100x. Phosphorus,
Natrum Muriaticum 30x, 60x, 100x.

HYPERTHYRO 1 (1 fl. oz.)

Catalog No. 0039
Indication: Iodine sensitivity, Over-active thyroid
Ingredients: Selenium Metallicum, Vitamin A 2x. Bovine Pituitary
Glandular 6x. Thyroidinum 12x, 24x, 30x. Sulphur, Arsenicum
Metallicum 16x. Mercurius Vivus, Molybdenum 20x. Iodium, Natrum
Muriaticum 30x. TSH 30x.

HYPERTONIA 2 (4 fl. oz.)

Catalog No. 0108
Indication: High blood pressure
Ingredients: Valeriana officinalis 2x. Citricum Acidum, Kali Bitartrate
3x. Rauwolfia serpentina, Fucus vesiculosus 4x. Kali Muriaticum, Kali
Phosphoricum 4x, 5x, 6x, 12x. Rhamnus purshiana, Allium sativum,
Rennin, Sarcodes: Mid Brain, Kidney, Liver, Collective Arterial 6x.
Vasopressin, Angiotensin I, II, Neurotensin 8x, 12x, 30x, 60x, 100x,
500x.

HYPOTONIA 1 (1 fl. oz.)

Catalog No. 0040
Indication: Low blood pressure
Ingredients: Crataegus oxyacantha 2x. Nerium oleander, Laurocerasus,
Cytisus scoparius 3x. Zincum Metallicum, Natrum Sulphuricum 6x.
Chromium 8x. Angiotensin 12x.

88
IMMUNOPOIE (1 fl. oz.)
Catalog No. 0041
Indication: Stimulates immune system
Ingredients: Petroselinum sativum, Natrum Muriaticum 3x. Bovine
Glandulars: Thymus, Bone Marrow, Liver, Spleen, Adenoids, Tonsils 5x,
6x, 12x, 30x, 100x. Aurum Metallicum, Argentum Metallicum, Sulphur
12x. Appendix 15x, 30x, 100x. Mercury Amalgam 100x, 500x, 1000x.
Saccharinum 100x

INFLU-F (1 fl. oz.)

Catalog No. 0033
Indication: Flu and fever like symptoms
Ingredients: Euphrasia officinalis, Ulmus fulva 2x. Pulsatilla 2x, 6x,
12x. Dulcamara 3x. Ferrum Phosphoricum, Ruta Graveolens 4x.
Zincum Metallicum, Bismuthum Metallicum, Adrenalinum, Thuja
occidentalis, Hyssopus officinalis 6x. Aconitum napellus 6x, 8x, 12x.
Belladonna 8x. Rhus toxicodendron, Camphora, Manganum Metallicum,
Phosphorus, Iodium 12x.

INFLU-I (1 fl. oz.)

Catalog No. 0034
Indication: Intestinal flu symptoms
Ingredients: Chamomilla, Marrubium vulgare 1x. Mentha piperita,
Lavandula officinalis, Ocimum basilicum, Citrus limonum, Populus
candicans 2x. Pogostemon patchouli 3x. Zincum Metallicum,
Symphytum officinale 6x. Sulphur, Argentum Metallicum, Iodium,
Manganum Metallicum, Alumen, Phosphorus 12x.

ME 1 (1 fl. oz.)
Catalog No. 0030
Indication: Epstein Barr related conditions
Ingredients: Zincum Metallicum, Natrum Muriaticum, Natrum
Phosphoricum, Natrum Sulphuricum, Natrum Carbonicum 6x.
Antimonium, Lithium 12x. Epstein Barr Virus, Mononucleosis,
Hemolytic Influenza, Hemolytic Streptococcus, CMV 16x, 24x, 30x, 100x.

METABOLIC 1 (1 fl. oz.)

Catalog No. 0157
Indication: Metabolic disorders
Ingredients: All Glandulars 5x-30x, 60x-100x, 500x, 1000x. All Cell
Salts 6x-12x, 30x-500x, 1000x. All Amino Acids 10x-30x, 50m. All Parts
of Krebs Cycle 12x-30x, 50m. RNA/DNA 30x-100x, 50m. Chromosomes
12x, 30x, 60x, 100x, 500x, 1000x. Collective Miasms: Psorinum,
Sycosis, Syphilinum 500x, 1000x, 2000x, 50m.

89
MUCOUSLYSIS (4 fl. oz.)
Catalog No. 0115
Indication: Mucous conditions
Ingredients: Plantago major, Urtica dioica, Equisetum arvense 1x.
Eucalyptus globulus 2x. Lobelia cardinalis, Vinca minor, Ephedra
vulgaris 3x. Calcarea Iodata 5x. Sarcodes: Lymph, Pancreas 6x, 12x,
30x, 60x, 100x. Arsenicum Iodatum 8x. Mucin 30x, 60x, 100x.

mRNA (4 fl. oz.)

Catalog No. 0290
Indication: Resets mesenger RNA for intercellular regulation
Ingredients: Mercaptoethanol 12x, 30x, 60x, 100x, 500x, 1000x. mRNA
100x, 500x, 1000x.

NASO-I (1 fl. oz.)

Catalog No. 0061
Indication: Rhinitis, Sinusitis
Ingredients: Natrum Muriaticum, Manganum Metallicum, Zincum
Metallicum 4x, 6x, 12x. Allium cepa, Allium sativum 6x. All Sinuses 6x,
12x, 30x, 60x, 100x. Pulsatilla 12x. Sulphur, Aluminium Metallicum,
Mercurius Vivus, Stannum Metallicum, Bromium, Borax 30x, 100x.

NEO-P (1 fl. oz.)

Catalog No. 0028
Indication: Degenerative tissue
Ingredients: Naja tripudians 5x, 12x, 30x. Zincum Metallicum, Calcarea
Phosphorica, Sulphur, Antimonium 6x, 12x, 30x, 60x, 100x. Bovine
Glandulars 6x, 16x. Viscum album 6x, 12x, 100x. Cuprum Metallicum,
Arsenicum Metallicum 8x, 12x, 30x. Interferon: Alpha, Beta, Gamma,
Interleuken: I, II, III 12x, 24x, 30x. Taxus baccata 12x-30x. Carcinum
12x, 30x, 100x, 500x, 1000x.

NEURO-R (4 fl. oz.)

Catalog No. 0056
Indication: Stress and nerval over-stimulation
Ingredients: Panax quinquefolium, Zincum Valerianicum, Lecithin 3x,
12x, 30x. Serotonin 5x. Cistus canadensis, Impatiens, Clematis erecta
6x. Pulsatilla, Magnesia Phosphorica, Passiflora incarnata, Valeriana
officinalis, Coffea cruda, Lithium Carbonicum, GABA 6x, 12x.
Acetylcholine 6x, 12x, 30x, 60x, 100x. Aconitum napellus, Selenium
Metallicum 8x. Arsenicum Iodatum, Endorphins, Neurotensin 12x, 30x,
60x. Gelsemium sempervirens 18x, 24x, 30x. Cuprum Metallicum,
Aluminium Metallicum 30x, 100x.

90
PROSTA-I (1 fl. oz.)
Catalog No. 0054
Indication: Inflamed prostate
Ingredients: Bee Pollen, Zincum Metallicum 3x. Prostate 6x, 12x, 30x,
60x, 100x, 500x, 1000x. Capsicum annuum 6x, 12x. Natrum
Sulphuricum 6x, 12x, 30x. Baryta Carbonica, Pulsatilla 12x. Plumbum
Metallicum, Platinum Metallicum, Cadmium Metallicum 12x, 30x, 60x,
100x, 500x. Tuberculinum, Thuja occidentalis 16x, 30x, 100x, 1000x.

PULMO-A (1 fl. oz.)

Catalog No. 0024
Indication: Asthmatic-like conditions
Ingredients: Arsenicum Album 4x, 6x, 8x. Bryonia 2x, 6x, 12x.
Adrenalinum 3x, 6x. Zincum Metallicum, Silicea, Carbo Vegetabilis 6x.
Lung Sarcode 6x, 12x, 30x, 60x, 100x. Lithium Carbonicum 8x.
Camphora 12x, 30x. Histamine 16x, 24x, 30x. Belladonna, Natrum
Muriaticum 30x. NADP, NAD, NADH 60x, 100x, 500x. Natrum
Sulphuricum 200x.

PULMO-P (1 fl. oz.)

Catalog No. 0053
Indication: Pulmonary infections and accompanying pain
Ingredients: Asclepias tuberosa 3x. Bovine Lung Tissue, Sepia,
Cinchona officinalis 6x. Silicea 6x, 12x, 30x. Picricum Acidum 8x.
Arsenicum Iodatum, Bryonia 12x. Sulphur 12x, 30x. Selenium
Metallicum 12x, 30x, 100x. Cuprum Metallicum, Stannum Metallicum,
Aurum Metallicum, Platinum Metallicum 18x, 30x. Calcarea Carbonica,
Lycopodium clavatum, Phosphorus 30x. Mercurius Vivus 100x, 500x.

PURATIVE (1 fl. oz.)

Catalog No. 0124
Indication: Cleans microorganism infestations from the body
Ingredients: Hydrastis canadensis 1x. Citrus paradisi semen 2x. Aloe
socotrina, Benzoin 3x. Chrysanthemum coccineum, Vitamins: A, C, E
4x.

REN-P (1 fl. oz.)

Catalog No. 0055
Indication: Excess urinary protein, Enzymatic disturbance
Ingredients: Kidney 6x, 12x. Vita Mar 8x. Phosphorus, Ledum palustre
12x. Albumin, Petroleum 12x, 30x. Mercurius Vivus 20x, 30x, 100x.
Silicea, Sulphur, Zincum Metallicum 30x.

91
RENLAPIS (1 fl. oz.)
Catalog No. 0063
Indication: Kidney pain, Gravel urine
Ingredients: Crataegus oxyacantha 2x, 6x. Sarsaparilla 3x. Digitalis
purpurea 3x, 6x. Nitricum Acidum, Berberis vulgaris, Lycopodium
clavatum 6x. Kidney Sarcode 6x, 12x, 30x, 60x, 100x. Bismuthum
Metallicum, Borax 8x. Stannum Metallicum 10x. Lithium, Selenium
Metallicum 12x. Oxalicum Acidum, Uricum Acidum 30x.

SARCOESIS (1 fl. oz.)

Catalog No. 0019
Indication: Inflammatory and swelling conditions
Ingredients: Chrysanthemum parthenium 2x. Zincum Metallicum,
Verbascum thapsus 3x. Urtica dioica 4x. Apis mellifica 4x, 6x, 12x,
30x. Adrenalinum 4x, 6x, 12x, 30x, 60x, 100x. Belladonna 5x, 6x, 12x,
30x. Crotalus horridus 6x. Silicea, Triosteum perfoliatum 6x, 12x.
Natrum Muriaticum, Magnesia Phosphorica, Kali Sulphuricum, Lymph
6x, 12x, 30x, 60x, 100x. Hepar Sulphuris Calcareum 8x, 16x, 30x.
Lachesis mutus 12x, 30x. Chymotrypsin, Histidine, Histamine, ATPase
Lysozyme, 12x, 30x, 60x, 100x. Glucose-6-Phosphatase, Coenzyme A
Dehydrogenase 30x, 60x, 100x. Biopterin, Hepar Suis 100x, 500x,
1000x

SHARK CARTILAGE (1 fl. oz.)

Catalog No. 0118
Contains the nutritional factors of shark cartilage
Ingredients: Shark Cartilage 3x, 6x, 12x, 30x. Thymol, Sarcode:
Thymus 4x, 6x, 12x. Sarcode: Lymph 5x, 15x, 30x. Natrum
Muriaticum, Mentha piperita 6x. Silicea 12x, 30x, 60x.

THERACEPHALIC (1 fl. oz.)

Catalog No. 0026
Indication: Brain circulation after stroke or injury
Ingredients: Scutellaria lateriflora 3x. Convallaria majalis 3x, 6x, 12x.
Taurine, Tyrosine 3x, 12x, 60x. Thyroidinum 5x. Magnesia
Phosphorica, Manganum Metallicum 6x, 12x, 30x, 60x, 100x.
Variolinum 12x, 30x, 60x, 100x. Stannum Metallicum 8x. Sarcodes:
Brain, Arterial Wall 12x, 30x, 60x, 100x.

92
THERACIRCULO (1 fl. oz.)
Catalog No. 0025
Indication: Circulatory disorders
Ingredients: Niacinum, Niacinamidum 2x. Adrenalinum, Camphora 4x.
Aorta Valve, Ferrum Metallicum 6x, 12x, 30x. Thrombin, Proteolytic
Enzymes 8x, 24x, 30x, 100x. Stannum Metallicum 8x, 24x, 50x.
Sulphur, Heloderma, Aesculus hippocastanum, Crotalus horridus 12x.
Tabacum 12x, 24x. Arterial Tissue 12x, 30x. Baryta 20x. Arnica
montana 100x.

TRAUMATIC 1 (1 fl. oz.)

Catalog No. 0042
Indication: Injuries, Rebuilds cellular tissue
Ingredients: Echinacea purpurea 3x. Arnica montana 3x, 6x, 12x, 100x,
1000x, 50lm. Sulphur 3x, 12x. Calendula officinalis 3x, 12x, 30x, 100x,
1000x, 50lm. Symphytum officinale 5x, 12x, 30x, 60x, 100x. Bone
Marrow 6x, 12x, 30x, 60x, 100x, 500x. Niccolum Metallicum 10x, 30x,
100x. Rhus toxicodendron, Barium, Bromium, Bismuthum Metallicum
12x, 30x, 60x, 100x. Arsenicum Metallicum 100x.

VENA-H (1 fl. oz.)

Catalog No. 0037
Indication: Hemorrhoidal conditions
Ingredients: Aesculus hippocastanum 2x. Collinsonia canadensis 3x.
Nux vomica 4x. Lycopodium clavatum, Sulphur 5x. Cuprum
Metallicum, Nitricum Acidum, Graphites, Veins 6x. Liver Aliesterase,
Proteolytic Enzyme, Chymotrypsin, Vanadium Metallicum 8x.

VIR-H (1 fl. oz.)

Catalog No. 0069
Indication: Herpes, Cold sores
Ingredients: Silicea 5x. Selenium Metallicum, Euphrasia officinalis,
Trifolium pratense 6x. Sulphur, Antimonium Crudum, Arsenicum
Metallicum, Iodium 12x. Plumbum Metallicum 16x. Herpes simplex I,
II, III, Herpes zoster, Herpes progenitalis 16x, 24x, 30x, 100x. Thuja
occidentalis 30x.

93
 THE RESTORATIVE PHILOSOPHY

Sarcode remedies have been used for many years in homeopathy to

help rebuild and correct tissues when organ structures are in disease
states. Damage caused by disease states in organs can result in
malfunctioning on an organic level. The Dr. Recommends restorative
remedies help the tissues to rebuild. Energetic students have shown
that a potent glandular can rectify an energetic imbalance where there
is no organic disturbance. This is covered in The Experimental Data on
Homeopathy by Dr. William Nelson, and shows the uses and proposed
mechanisms of sarcodal homeopathy.
Sarcodal homeopathy offers the safest and most gentle form of
homeopathy. Results are often the slowest to be seen due to the
correct rebuilding of the degenerative cells in the organs. The
restorative remedies will work more quickly and successfully in
younger patients than in older ones. In the older patient, these
remedies can at times be utilized to stimulate cleansing and to
stabilize and reduce the risk of a healing crisis.
The Dr. Recommends restorative homeopathics are engineered in
homochords of differing potencies. Maximum efficiency is achieved
with a combination of 4x, 6x, 12x, 30x, 60x, 100x, 500x, and 1000x.
This allows the body to respond to the frequency of dilution which
works best to rebuild tissues. The restorative remedies are safe and
effective and quality controlled by the QQCTM techniques to ensure
efficacy.

94
 RESTORATIVE REMEDIES

Ingredients: New Zealand or American Ursa and Bovine Glandulars

4x, 6x, 12x, 30x, 60x, 100x, 500x, and 1000x.

Bone and Bone Marrow

Brain
Cervical
Cranial, Sacral
Ear
Eye
Gallbladder
Heart, Lung
Kidney, Ovarian, Adrenal
Kidney, Prostate, Adrenal
Liver, Gallbladder
Lymph, Spleen, Mammary
Major Nerves
Muscle, Ligament, Cartilage
Orchic
Pancreas, Stomach
Pineal, Pituitary, Hypothalamus
Sinuses
Skin and Mucous Membrane
Small and Large Intestine
Thoracic
Thyroid, Thymus, Parathyroid

95
 SARCODES

Sarcodal homeopathy involves using healthy glandular tissue from a

healthy organism to treat sick conditions within the body. For an
expanded view of sarcodes and the experimental context behind them
read The Experimental Data on Homeopathy, by Dr. William Nelson. In
the text it outlines exactly how sarcodal homeopathy works. Sarcodal
homeopathy promotes growth and development of healthy glandular
tissue.
Within this treatise, many different sarcodes will be classified that can
be used by a knowledgeable homeopath. The list of sarcodal tissues used
here is very large and may be beyond the grasp of some homeopaths. We
have a variety of tissues being used by homeopaths in many ways. Since
these sarcodal tissues help to rebuild tissue, help tissue to organize
properly, and increase the probability of the presence of healthy tissue
over old tissue, it is possible to see how homeopathy can be used.
Sarcodal tissue can go beyond mere tissue to secretions; which include
hormones, enzymes, coenzymes, RNA, DNA, and others. Thus, we can
see from the long list a wide range of sarcodal tissues that can be
brought beyond just tissue to include secretions of the body. This vast
array of secretions is broadened to include as many different hormones
and enzymes known by Dr. Nelson at this time.

96
SARCODES I

ADENOIDS
ADRENAL
ADRENAL GLANDULAR
APPENDIX
AUDITORY NERVE
BONE MARROW
BOWEL FLORA
BRAIN
CEREBRUM
CORPUS CALLOSUM
CORPUS LEUTEUM
CYSTERNA CHYLI
EMOTIONS
ESONOPHIL
FRONTAL LOBE
GALLBLADDER
HEART
HYPOTHALAMUS
ILEO CECAL VALVE
INTRINSIC FACTOR
ISLE OF LANGERHANS
KIDNEY
LARGE INTESTINE
LIMBIC SYSTEM
LIVER
LEUCOCYTE
LUNG
LYMPHOCYTE
MAMMARY GLANDS
MEDULA
MICHELLE BALANCE
MID BRAIN
MONOCYTE
MOUTH
NERVES OF ABDOMEN (PERIPHERAL SPINAL NERVES)
OCCIPITAL
OCULOMOTOR 3 (CRANIAL NERVES)
OLFACTORY HAIRS (CILIA) (SMELL)
OLFACTORY MUCOSA (SMELL)
OLFACTORY NEURONS (SMELL)
OLFACTORY PLATE (SMELL)
OLFACTORY TRACT (SMELL)
OLFACTORY 1 (CRANIAL NERVES)

97
SARCODES I, cont.

OPTIC CHIASMA (RELATED STRUCTURES-BRAIN STEM)

OPTIC DISC (LAYERS OF THE EYE: RETINA-EYE)
OPTIC NERVE (EYE)
OPTIC 2 (CRANIAL NERVES)
ORGAN OF CORTI (INTERNAL EAR-EAR)
OTIC (GANGLIA-PARASYMP)
OTOLOTHS (EQUILIBRIUM: MACULA-EAR)
OVAL WINDOW (INTERNAL EAR-EAR)
OVARIES
PAIN (SENSORY)
PANCREAS
PARATHYROID
PARIETAL LOBE
PELVIC/PERINEAL VISCERA (POSTGANGLIONIC NEURONS-AUTOSYMP)
PERINEURIUM (MOTOR NERVES)
PERSONALITY (BRAIN)
PINEAL
PITUIPOSTERIOR
PITUITANTERIOR
PITUITARY
POLYMORPH
PONS (HINDBRAIN-BRAIN STEM)
PONS (MOTOR NERVES)
PONTINE CISTERN (SUBARACHNOID SPACES-CERE FLUID)
PORE CANAL (TASTE BUDS-TASTE)
POST GANGLIONIC AXONS (AUTOSYMP)
POST GANGLIONIC CELL BODIES (AUTOSYMP)
POSTERIOR FUNICULUS (SPINAL CORD-WHITE MATTER)
POSTERIOR HORNS (SPINAL CORD-GRAY MATTER)
POSTERIOR MEDIAN SULCUS (SPINAL CORD)
POSTERIOR RAMUS (MOTOR NERVES)
PRECENTRAL GYRUS (MOTOR NERVES)
PREGANGLIONIC AXONS (AUTOSYMP)
PREGANGLIONIC CELL BODIES (AUTOSYMP)
PREVERTEBRAL GANGLIA (AUTOSYMP)
PREVERTEBRAL GANGLIA (POSTGANGLIONIC NEURONS-AUTOSYMP)
PRINCIPAL SPEECH AREA (FRONTAL LOBE-CEREBRUM)
PROSTAGLANDIN
PTERYGOPALATINE (GANGLIAPARASYMP)
PUPIL (EYE)
PYRAMIDS (MYELENCEPHALON-BRAIN STEM)
RECEPTOR CELLS (TASTE BUDS-TASTE)
RECKLESS (EMOTION)
RETICULAR FORMATION
98
SARCODES I, cont.

RETINAL ARTERIES (LAYERS OF THE EYE: RETINA-EYE)

RHINENCEPHALIN
SACCULE/UTRICLE (INTERNAL EAR-EAR)
SEMICIRCULAR CANALS (INTERNAL EAR-EAR)
SEMICIRCULAR DUCTS (INTERNAL EAR-EAR)
SENSORY AREA (PARIETAL LOBE-CEREBRUM)
SKELETAL MUSCLES (MOTOR NERVES)
SKIN (MOTOR NERVES)
SMALL INTESTINE
SPINAL CORD (RELATED STRUCTURES-BRAIN STEM)
SPINAL NERVES (MOTOR NERVES)
SPINAL NERVES (POSTGANGLIONIC NEURONS-AUTOSYMP)
SPLANCHNIC NERVE (AUTOSYMP)
SPLANCHNIC NERVE (PREGANGLIONIC NEURONS-AUTOSYMP)
SPLEEN
STALK OF HYPOPHYSIS (RELATED STRUCTURES-BRAIN STEM)
STAPES (MIDDLE EAR-EAR)
STOMACH
STOMACH ACID
SUBARACHNOID SPACE (ARACHNOID-MENINGES)
SUBMANDIBULAR (GANGLIA-PARASYMP)
SUPERFICIAL FASCIA (MOTOR NERVES)
SUPERIOR CEREBELLAR PEDUNCLE (MIDBRAIN-BRAIN STEM)
SUPERIOR CISTERN (SUBARACHNOID SPACES-CERE FLUID)
SUPERIOR COLLICULI (MIDBRAIN-BRAIN STEM)
SUPPORTING CELLS (EQUILIBRIUM: CRISTA-EAR)
SUPPORTING CELLS (INTERNAL EAR-EAR)
SUPPORTING CELLS (SMELL)
SUPPORTING CELLS (TASTE BUDS-TASTE)
SUSPENSORY LIGAMENT (EYE)
SWEAT GLANDS (TO SKIN AUTOSYMP)
SYMPATHETIC CHAIN (POSTGANGLIONIC NEURONS-AUTOSYMP)
SYMPATHETIC CHAIN OF GANGLIA (AUTOSYMP)
TECTORIAL MEMBRANE (INTERNAL EAR-EAR)
TEMPORAL LOBE
TEMPORAL MANDIBULAR JOINT
TENTORIUM CEREBELLI (DURA MATTER-MENINGES)
TESTIS
THALAMUS (DIENCEPHALON)
THIRD VENTRICULE (DIENCEPHALON)
THORACIC DUCT
THORACIC VISCERA (POSTGANGLIONIC NERUONS-AUTOSYMP)
THYMUS
THYROID
99
SARCODES I, cont.

TMJ
TONSILS
TOUCH-PRESSURE (SENSORY)
TRIGEMINAL (PERIPHERAL SPINAL NERVES)
UTERUS
VAGUS NERVE
VALVE OF HOUSTON
WBC

100
SARCODES II

1ST 12TH CRANIAL NERVES

FRONTAL BONE
INFA CONCHA VERTEBRAE
INTESTINE, SMALL/LARGE
LYMPH, SPLEEN, MAMMARY
MAXILLAE
M1
3RD 6TH NERVE
OCCIPITAL
OCCIPITAL CONDYLES
OCCIPUT
OLFACTORY NERVE
OPTICAL NERVE
PALATINE BONE
PARIETAL BONE
SACROILIAC
SACRUM
SPHENOID
SQUAMA
STOMACH, PANCREAS
TEAR DUCTS
TEMPORAL BONE
TRIGEMINAL 5 (CRANIAL NERVES)
TROUCHLEAT 4 (CRANIAL NERVES)
TYMPANIC MEMBRANE (EXTERNAL EAR-EAR)
VAGUS NERVE
VENTRAL ROOT (MOTOR NERVES)
VENTRAL (ANTERIOR) ROOT (SPINAL CORD-SPINAL NERVES)
C1-C7 VERTEBRAE
L1-L5 VERTEBRAE
T1-T12 VERTEBRAE
VESTIBULAR PATHWAY (PERIPHERAL SPINAL NERVES)
VESTIBULE (INTERNAL EAR-EAR)
VESTIBULOCOCHLEAR 8 (CRANIAL NERVES)
VISCERAL AFFERENT PATHWAY (PERIPHERAL SPINAL NERVES)
VISUAL AREA (OCCIPITAL LOBE-CEREBRUM)
VITREOUS BODY (LAYERS OF THE EYE: SPACES/FLUID-EYE)
VOMER BONE
WHITE COMMISSURES (SPINAL CORD-WHITE MATTER)
WHITE RAMUS COMMUNICANS (AUTOSYMP)
ZYGOMA BONE

101
SARCODES III

ABDOMINAL VISCERA (POSTGANGLIONIC NEURONS-AUTOSYMP)

ABDUCENS 6 (CRANIAL NERVES)
ACCESSORY 11 (CRANIAL NERVES)
AGGRESSION
AMYGDALA (DIENCEPHALON)
ANGER (EMOTION)
ANTERIOR CORTICOSPINAL TRACT (MOTOR NERVES)
ANTERIOR CUTANEOUS DIVISION (MOTOR NERVES)
ANTERIOR FUNICULUS (SPINAL CORD-WHITE MATTER)
ANTERIOR HORNS (SPINAL CORD-GRAY MATTER)
ANTERIOR MEDIAN FISSURE (SPINAL CORD)
ANTERIOR RAMUS (MOTOR NERVES)
ANXIETY (EMOTION)
ARRECTOR PILI (TO SKIN-AUTOSYMP)
ASSOCIATION NEURON (MOTOR NERVES)
ASSOCIATION TRACTS (SUBDIVISIONS OF WHITE MATTER-CEREBRUM)
AUDITORY AREA (TEMPORAL LOBE-CEREBRUM)
AUDITORY (EUSTACHIAN) VERSTIBULE (MIDDLE EAR-EAR)
AURICLE (EXTERNAL EAR-EAR)
AUTISTIC (EMOTION)
AXONS (MOTOR NERVES)
AXONS (PREGANGLIONIC NEURONS-AUTOSYMP)
AXONS EYE, NASAL, ORAL, ETC. (POSTGANGLIONIC AXONS-PARASYMP)
AXONS HEAD & NECK (POSTGANGLIONIC NEURONS-AUTOSYMP)
AXONS S2, S3, & S4 (PREGANGLIONIC NEURONS-PARASYMP)
AXONS 3, 7, 9, 10 CRANIAL NERVES (PREGANG. NEURONS-
PARASYMP)
BASILAR MEMBRANE (INTERNAL EAR-EAR)
BLOOD VESSELS (TO SKIN-AUTOSYMP)
BONY LABYRINTH (INTERNAL EAR-EAR)
CARELESS (EMOTION)
CAUDATE NUCLEUS (BASAL NUCLEI-CEREBRUM)
CAUDATE NUCLEUS (DIENCEPHALON)
CELL BODIES (POSTGANGLIONIC AXONS PARASYMP)
CELL BODIES (POSTGANGLIONIC NEURONS- AUTOSYMP)
CELL BODIES (PREGANGLIONIC NEURONS AUTOSYMP)
CELL BODIES (PREGANGLIONIC NEURONS PARASYMP)
CENTRAL CANAL
CENTRAL CANAL (VENTRICLES-CERE FLUID)
CENTRAL SULCUS (MAJOR FISSURES-CEREBRUM)
CEREBELLUM (HINDBRAIN-BRAIN STEM)
CEREBRAL AQUEDUCT (MIDBRAIN-BRAIN STEM)
CEREBRAL AQUEDUCT (VENTRICLES-CERE FLUID)
CEREBRAL PEDUNCLE (MIDBRAIN-BRAIN STEM)
102
SARCODES III, cont.

CEREBRAL PEDUNCLE (MOTOR NERVES)

CHOROID PLEXUS (CERE FLUID)
CILIARY (GANGLIA-PARASYMP)
CILIARY BODY
CILIARY PROCESSES (LAYERS OF THE EYE: CHOROID-EYE)
CIRCUMVALLATE (PAPILLAE-TASTE)
COCHLEA (INTERNAL EAR-EAR)
COCHLEAR (PERIPHERAL SPINAL NERVES)
COCHLEAR DUCT (INTERNAL EAR-EAR)
COGNITION (BRAIN)
COMMISSURE (SUBDIVISIONS OF WHITE MATTER-CEREBRUM)
CONFUSION (EMOTION)
CONJUNCTIVA (EYE)
CORNEA (LAYERS OF THE EYE: SCLERA-EYE)
CORONA RADIATA (MOTOR NERVES)
CORONA RADIATA (PROJECTION TRACTS-CEREBRUM)
CORPUS CALLOSUM (DIENCEPHALON)
CUPOLA (EQUILIBRIUM: CRISTA-EAR)
CUTANEOUS DIVISION (MOTOR NERVES)
CRIBRIFORM PLATE (SMELL)
DELUSION (EMOTION)
DEPRESSION (EMOTION)
DORSAL ROOT (MOTOR NERVES)
DORSAL (POSTERIOR) ROOT (SPINAL CORD-SPINAL NERVES)
DORSAL ROOT GANGLION (SPINAL CORD-SPINAL NERVES)
EFFECTOR (MOTOR NERVES)
EMR (SENSORY)
ENDOLYMPHATIC DUCT (INTERNAL EAR-EAR)
ENDONEURIUM (MOTOR NERVES)
EPINEURIUM (MOTOR NERVES)
EPITHALAMUS (DIENCEPHALON)
EXTERNAL AUDITORY MEATUS (EXTERNAL EAR-EAR)
FACIAL 7 (CRANIAL NERVES)
FACILATATING EFFECT (MOTOR NERVES)
FALX CEREBRI (DURA MATER-MENINGES)
FEAR (EMOTION)
FILIFORM (PAPILLAE-TASTE)
FILUM TERMINALE (PIA MATTER-MENINGES)
FOURTH VENTRICLE (HINDBRAIN-BRAIN STEM)
FOURTH VENTRICLE (MYELENCEPHALON-BRAIN STEM)
FOVEA CENTRALIS (LAYERS OF THE EYE: RETINA-EYE)
FUNGIFORM (PAPILLAE-TASTE)
GLOSSOPHARYNGEAL 9 (CRANIAL NERVES)
GRAY COMMISSURES (SPINAL CORD-GRAY MATTER)
103
SARCODES III, cont.

GRAY RAMUS COMMUNICANS (AUTOSYMP)

GREAT CISTERN (SUBARACHNOID SPACES-CERE FLUID)
HAIR CELLS (EQUILIBRIUM: CRISTA-EAR)
HAIR CELLS (EQUILIBRIUM: MACULA-EAR)
HAIR CELLS (INTERNAL EAR-EAR)
HAPTIC (SENSORY)
HEAT-COLD (SENSORY)
HYPOGLOSSAL 12 (CRANIAL NERVES)
HYPOPHYSIS (DIENCEPHALON)
HYPOTHALAMUS (DIENCEPHALON)
INCUS
INFERIOR COLLICULI (MIDBRAIN-BRAIN STEM)
INHIBITING EFFECT (MOTOR NERVES)
INTERMEDIATE ZONE (SPINAL CORD-GRAY MATTER)
INTERNAL CAPSULE (DIENCEPHALON)
INTERNAL CAPSULE (MOTOR NERVES)
INTERNAL CAPSULE (PROJECTION TRACTS-CEREBRUM)
INTERPENDUNCULAR CISTERN (SUBARACHNOID SPACES-CERE
FLUID)
INTERVENTRICULAR FORAMEN (VENTRICLES-CERE FLUID)
INTRAMURAL (GANGLIA-PARASYMP)
JOY (EMOTION)
LATERAL CORTICOSPINAL TRACT (MOTOR NERVES)
LATERAL CUTANEOUS DIVISION (MOTOR NERVES)
LATERAL FISSURE (MAJOR FISSURES-CEREBRUM)
LATERAL FUNICULUS (SPINAL CORD-WHITE MATTER)
LATERAL HORNS (SPINAL CORD-GRAY MATTER)
LATERAL RETICULOSPINAL (MOTOR NERVES)
LATERAL VENTRICLE (DIENCEPHALON)
LATERAL VENTRICLES (SUB CORTICAL AREAS-CEREBRUM)
LATERAL 3RD (VENTRICLES-CERE FLUID)
LATERAL 4TH (VENTRICLES-CERE FLUID)
LENS (EYE)
LENTICULA NUCLEUS (BASAL NUCLEI-CEREBRUM)
LENTICULA NUCLEUS (DIENCEPHALON)
LONGITUDINAL FISSURE (MAJOR FISSURES-CEREBRUM)
LUMBAR CISTERN (SUBARACHNOID SPACES-CERE FLUID)
LUST (EMOTION)
MALLEUS (MIDDLES EAR-EAR)
MAMMILLARY BODIES (RELATED STRUCTURES-BRAIN STEM)
MEDICAL RETICULOSPINAL (MOTOR NERVES)
MEDICAN/LATERAL APERTURES (CERE FLUID)
MEDULLARY PYRAMIDS (MOTOR NERVES)
MIDDLE CEREBELLAR PEDUNCLES (HINDBRAIN-BRAIN STEM)
104
SARCODES III, cont.

MIDDLE CEREBELLAR PEDUNCLES (MYELENCEPHALON-BRAIN STEM)

MOTOR AREA (FRONTAL LOBE-CEREBRUM)
MOTOR CELL BODIES (SPINAL CORD-SPINAL NERVES)
MOVEMENT (SENSORY)
MUSCLES OF THE EYEBALL (EYE)
MUSCULAR BRANCH (MOTOR NERVES)
MUSCULAR BRANCHES (MOTOR NERVES)
NERVE FIBERS (EQUILIBRIUM: CRISTA-EAR)
NERVE FIBERS (EQUILIBRIUM: MACULA-EAR)
NERVE FIBERS (TASTE BUDS-TASTE)
NERVES OF HEAD & FACE (PERIPHERAL SPINAL NERVES)
NERVES OF LOWER LIMBS (PERIPHERAL SPINAL NERVES)
NERVES OF THORAX (PERIPHERAL SPINAL NERVES)
NERVES OF UPPER LIMBS (PERIPHERAL SPINAL NERVES)

105
 ORIENTAL HERBAL PHILOSOPHY

The Chinese did not have a system of succussion, nor did they have a
system of homeopathic dilution, but their pharmacology was much akin
to homeopathic processes. Many herbs were diluted to find safer levels of
activity. This titration allowed for strong herbs to be used more safely.
The Chinese have studied the medicinal effects of herbs for thousands
of years. Specific directions were developed on how to pick the herbs,
preserve the herbs, and how to prepare the herbal remedy. Often, these
remedies were made in dilute quantities, sometimes as low as one part
per trillion, which is equivalent to a 9x. They understood how certain
herbs could be made more dilute and still achieve pharmacological
effectiveness. Nature provides many energetic factors beyond mere
chemistry. Subtle energetic effects, mineral balance, electrical regulation
abilities, and more are stable in dilution. Dilution also offers safety in
compliance with the minimal dose concept of medicine. Many Chinese
herbs have excellent effects in low-potency homeopathic form.
The Dr. Recommends oriental herb remedies combine the compatibility of
herbology and homeopathy. This is to insure safety first, while
guaranteeing effectiveness. Many compounds can be increased in
energetic potency as we make them more and more dilute, while
preserving their activity. The oriental herb formulas are quality controlled
through QQCTM techniques.

Source: http://www.myhealthandharmony.com/category_s/33.htm

106
 Quality of Herbs

America has often come under fire because of an inability to supply

good quality herbs. This is largely due to the fact that American herbs
can be picked at any time, in any place. In following the Chinese
protocol, herbs are picked at precise times and in precise ways so that
the pharmacological activity of the herb is preserved. Dr. Recommends
buys many of its herbs from the Chinese, Japanese and Korean markets.
Still, that is not enough; each of these herbs must undergo quality
control methods to make sure that the pharmacological activity of the
herb is above the satisfactory level and at the highest level of potency in
developing the natural pharmaceuticals.
Next in developing quality control techniques beyond the chemistry
and beyond the range of 12x, Dr. Recommends developed Kirlian
photography methods of analysis, freezing studies of the crystalline
structure of the liquid crystal effect of water, trivector analysis to analyze
the magnetic, dielectric static and conductance fields of the different
homeopathics to understand the energetic nature of these compounds;
and patient reactivity modes, challenging them on skin resistance,
voltage, and other directed activity. As well, Dr. Recommends has
researched a photo-multiplier, and has measured the photons coming off
of these fields; and how these different compounds affect living tissue
with their electromagnetic radiation through the mitogenic process.
The development of a quality control process was paramount in
developing a way to create the most precise, safe and effective remedies
for doctors to use with their patients.
Dr. Recommends realized that this needed to have a global expression,
and has developed manufacturing in Ireland and Canada. Dr.
Recommends has developed a global strategy to supply doctors and
practitioners throughout the USA, Europe, and Canada with product,

107
guaranteeing the safety and effectiveness, the reverence for nature, and
the education. Current seminar development is happening in all of these
countries; educating doctors in how to develop diagnostic protocol and
healing therapeutic regimes for their patients, using these natural
products.
For the doctor who wants natural, homeopathic pharmaceuticals, Dr.
Recommends is ready to serve with the highest level of quality and
service all directed through the company pledge for safety, effectiveness,
quality control, natural healing, reverence of nature, and education of
both patient and doctor. Dr. Recommends welcomes you to a new
standard and level of quality control and service.

108
 ORIENTAL HERBAL REMEDIES

ANTHELMINTIC (1 fl. oz.)

Catalog No. 0127
Indication: Purgative for worms and intestinal parasites
Ingredients: Meliae Toosendan Fructus, Quisqualis Fructus, Cucurbitae
Semen, Torreyae Semen, Omphalia, 3x, 6x, 12x, 30x.

ANTI-ASTHMATIC (1 fl. oz.)

Catalog No. 0135
Indication: Wind and cold effects, chills and fever, Exterior symptom
complex, Regulates energy for lungs
Ingredients: Perillae Folium, Astragali Radix, Ephedrae Herba,
Cinnamomi Cortex, Armeniacae Semen, Glycyrrhizae Radix, Paeoniae
Radix, Zizyphi Fructus 3x, 6x, 12x, 30x.

ANTI-PHLOGISTIC (1 fl. oz.)

Catalog No. 0129
Indication: Protects body from wind, cold, dampness, Improves chi
Ingredients: Schizonepetae Herba, Ledebouriellae Radix, Notopterygii
Rhizoma, Angelicae Dahuricae Radix , Ligustici Rhizoma, Bupleuri Radix,
Peucedani Radix, Platycodi Radix, Poria, Menthae Herba, Glycyrrhizae
Radix, Aurantii Fructus 3x, 6x, 12x, 30x.

ANTI-PYRETIC (1 fl. oz.)

Catalog No. 0137
Indication: Fever, Febrifugal, Expels toxic heat, wind, chills from exterior
Ingredients: Forsythiae Fructus, Menthae Herba, Platycodi Radix,
Lonicerae Flos, Schizonepetae Herba, Arctii Fructus 3x, 6x, 12x, 30x.

ANTI-RHEUMATIC (1 fl. oz.)

Catalog No. 0138
Indication: Dispels wind, cold, dampness to improve rheumatic pain,
Activates blood flow in collateral channels
Ingredients: Aconiti Carmichaeli Preparata Radix, Angelicae Dahuricae
Radix, Olibanum, Myrrha, Lumbricus, Clematidis Radix, Draconos Os
3x, 6x, 12x, 30x.

109
BLOOD (1 fl. oz.)
Catalog No. 0133
Indication: Replenishes blood, Restores vitality, Maximizes acupuncture
system development of blood
Ingredients: Ginseng Radix, Rehmanniae Radix, Angelicae Dahuricae
Radix, Atractylodis Lanceae Rhizoma, Cinnamomi Cortex, Paeoniae
Radix, Arctii Fructus, Trifolium pratense, Spinacea oleracea 3x, 6x, 12x,
30x.

BONE (1 fl. oz.)

Catalog No. 0175
Indication: Degenerative conditions, Unstable chi
Ingredients: Myrrha, Lonicerae Flos, Scutellaria lateriflora, Taraxacum
officinale, Magnoliae Officinalis Cortex, Juglans nigra, Tang Kuei,
Akebiae Caulis Fructus, Echinacea purpurea, Shark Cartilage, Sarcode:
Bone/Bone Marrow, Equisetum arvense, Beta vulgaris 3x, 6x, 12x, 30x.

CARMINATIVE (1 fl. oz.)

Catalog No. 0130
Indication: Relieves gas and stagnation of food, Dispels congestion of
toxic energy from stomach and bowels
Ingredients: Citri Immaturi Pericarpium, Magnoliae Liliflorae Flos,
Linderae Radix, Rhei Rhizoma, Pharbitis Semen 3x, 6x, 12x, 30x.

COLD AND FLU (1 fl. oz.)

Catalog No. 0162
Indication: Colds, Flu, Expels heat, cold and wind from interior
Ingredients: Lonicerae Flos, Forsythiae Fructus, Arctii Fructus, Menthol,
Glycerinum, Glycine, Schizonepetae Herba, Echinacea purpurea,
Placenta, Zingiber officinale 3x, 6x, 12x, 30x.

DIGESTIVE STIMULATOR (1 fl. oz.)

Catalog No. 0131
Indication: Invigorates stomach, spleen, lung, heart, Reinforces middle
burner
ngredients: Ginseng Radix, Codonopsis Pilosulae Radix, Astragali Radix,
Glycyrrhizae Radix, Hordei Germinatus Fructus, Atractylodis Lanceae
Rhizoma, Polygonati Rhizoma 3x, 6x, 12x, 30x.

ESOPHAGUS (1 fl. oz.)

Catalog No. 0163
Indication: Degenerative conditions, Unstable chi, Balances upper
warmer
Ingredients: Salvia officinalis, Scutellaria Barbatae Herba , Zizyphi
Fructus, Rhei Rhizoma, Achyranthis Radix, Zingiber officinale,
Ammonium Nitricum 3x, 6x, 12x, 30x.
110
EXPECTORANT (1 fl. oz.)
Catalog No. 0136
Indication: Clears lungs of mucous, Dispels heat in lungs
Ingredients: Anemarrhenae Rhizoma, Mori Radicis Cortex, Trichosanthis
Semen, Gardeniae Fructus, Poria, Citri Immaturi Pericarpium 3x, 6x,
12x, 30x.

FEMALE (1 fl. oz.)

Catalog No. 0134
Indication: Regulates menstrual disturbances, Restores vitality and
energy to blood of female
Ingredients: Codonopsis Pilosulae Radix, Atractylodis Lanceae Rhizoma,
Angelicae Dahuricae Radix, Rehmanniae Radix, Poria, Cyperi Rhizoma,
Zizyphi Fructus, Ligustici Rhizoma, Glycyrrhizae Radix 3x, 6x, 12x, 30x.

HEPATIC (1 fl. oz.)

Catalog No. 0128
Indication: Removes stagnant energy from liver, Restores liver chi
Ingredients: Magnoliae Officinalis Cortex, Curcumae Rhizoma,
Aquilariae Lignum, Verbena hastata, Bupleuri Radix, Corydalidis Tuber
3x, 6x, 12x, 30x.

HYPERTENSIVE (1 fl. oz.)

Catalog No. 0140
Indication: Alleviates heat in liver, Corrects deficiency in yin of liver,
Balances excess yang
Ingredients: Haematitum, Pinellia Tuber, Achyranthis Radix, Rauwolfiae
Verticillatae Radix 3x, 6x, 12x, 30x.

KIDNEY (1 fl. oz.)

Catalog No. 0164
Indication: Degenerative conditions, Unstable chi, Removes toxic energy
from ancestral meridians.
Ingredients: Lobelia inflata, Imperatae Rhizoma, Dioscorea batatis
Rhizoma, Lygodii Spora, Desmodii Herba, Haematitum,
Cirsii Japonica 3x, 6x, 12x, 30x.

LARGE INTESTINE (1 fl. oz.)

Catalog No. 0165
Indication: Degenerative conditions, Unstable chi, Removes wind from
large intestine
Ingredients: Oldenlandiae Herba, Lonicerae Flos, Scutellaria Barbatae
Herba, Taraxacum officinale, Sophorae Flos, Sanguisorbae Radix,
Magnoliae Officinalis Cortex, Akebiae Caulis, Citrus trifoliata, Salviae
Miltorrhizae Radix 3x, 6x, 12x, 30x.

111
LAXATIVE (1 fl. oz.)
Catalog No. 0141
Indication: Relieves constipation due to spleen fluid deficiency, Dispels
toxic energy from large intestine, Boosts liver chi
Ingredients: Cannabis Semen, Rhei Rhizoma, Armeniacae Semen,
Magnoliae Officinalis Cortex, Rhamnus purshiana , Capsicum
frutescens, Rhei Rhizoma 3x, 6x, 12x, 30x.

LIVER (1 fl. oz.)

Catalog No. 0166
Indication: Degenerative conditions, Unstable chi, Removes toxic energy
liver
Ingredients: Archangelica , Salviae Miltorrhizae Radix, Carathami Flos,
Scutellariae Barbatae Herba, Echinopsis Radix, Akebiae Caulis, Paeoniae
Radix, Gardeniae Fructus, Amoni Semen, Angelica Sinensis 3x, 6x, 12x,
30x.

LUNG (1 fl. oz.)

Catalog No. 0167
Indication: Degenerative conditions, Unstable chi, Removes heat from
lung
Ingredients: Mori Folium, Coicis Semen, Trichosanthis Radix,
Sargassum, Pumex, Houttuyniae Herba, Armeniacae Semen, Laminariae
Thallus, Lepidii Semen, Stemonae Radix, Salviae Miltorrhizae Radix,
Glycyrrhizae Radix, Imperatae Rhizoma 3x, 6x, 12x, 30x.

LYMPH (1 fl. oz.)

Catalog No. 0168
Indication: Degenerative conditions, Unstable chi, Removes excess yin
from interior
Ingredients: Myrrha, Aconiti Carmichaeli Praeparata Radix, Angelicae
Dahuricae Radix, Ephredrae Herba, Echinacea purpurea 3x, 6x, 12x,
30x.

MENTAL (1 fl. oz.)

Catalog No. 0132
Indication: Invigorates kidney meridian, Senility, Old age, Balances
excess yin
Ingredients: Cornu Cervi, Hippocampus, Epimedii Herba, Ginseng Radix,
Cynomorii Herba, Angelicae Dahuricae Radix 3x, 6x, 12x, 30x.

112
PREVENTATIVE (1 fl. oz.)
Catalog No. 0169
Indication: Tonifies and improves immunity, Balances yin and yang
irregularities
Ingredients: Wisteria chinensis, Trapa natans, Terminalia Chebulae
Fructus, Coicis Semen 3x, 6x, 12x, 30x.

SEDATIVE (1 fl. oz.)

Catalog No. 0139
Indication: Nourishes blood of liver, Expels heat from heart, Fatigue,
Insomnia
Ingredients: Coptidis Rhizoma, Cinnabaris, Valeriana officinalis, Zizyphi
Fructus, Glycyrrhizae Radix, Zizyphi Spinosi Semen, Tritici Fructus 3x,
6x, 12x, 30x.

STOMACH (1 fl. oz.)

Catalog No. 0170
Indication: Degenerative conditions, Unstable chi, Balances middle
warmer
Ingredients: Solanum nigrum, Salviae Miltorrhizae Radix, Scutellariae
Barbatae Herba, Pteris Herba, Raphni Semen 3x, 6x, 12x, 30x.

UTERINE (1 fl. oz.)

Catalog No. 0171
Indication: Degenerative conditions, Unstable chi
Ingredients: Cinnamomi Cortex, Carthami Flos, Phellodendri Cortex,
Ostraea Testa, Astragali Radix, Lonicerae Flos, Gentianae Scabrae Radix,
Aconiti Carmichaeli Praeparata Radix, Linderae Radix, Violae Herba 3x,
6x, 12x, 30x.

113
CHINESE-AMERICAN HERBALS

Achyranthes Laminaria Rhubarb

Aconite (Processed) Leonurus Salvia
Aconite (Roasted) Lepidium Sanguisorba
Akebia Licorice Sargassum
Anemone Lily Schizandra
Angelica Lindera Schizonepeta
Anteater Scales Lonicera Scute
Apricot Seed Lotus Embryo Scute Herba
Arctium Lotus Receptacles Smilax
Areca Seed Lotus Seed Sophora
Asparagus Lycium Fruit Stemona
Astragalus Lygodium Sterculia
Cardamon Magnolia Bark Tang-Kuei
Carthamus Magnolia Flower Terminalia
Centipeda Malt Thlaspi
Chih-Shih Mentha Thymifolia
Chrysanthemum Morus Bark Trichosanthes Fruit
Cirsium Morus Branch Trichossanthes Seed
Clematis Morus Leaves Tsao-ko
Coix Myristicae Tsao-Tou-Kou
Cyperus Myrrh Tussilago
Cuttle Bone Oldenlandia Viola
Dioscorea Omphalia Xanthium
Dragon Bone Oryza
Fennel Peony
Forsythia Phellodendron
Gardenia Placenta
Gentiana Plantago
Glehnia Pumice
Haematite Pyrite
Hoelen Raphanus
Houttuynia Rauwolfia
Imperta
Jujube

This is a brief list of the most used Chinese herbal homeopathics.

Others are available upon request made as homocords (3x, 6x, 12x, 30x)
of the herbal.

114
 CHINESE HERBOLOGY AND HOMEOPATHY

In the chapter on the scientific explanation of homeopathy it was

explained that there are several different pharmacological dynamics
which allowed for homeopathy to occur at low-dose ratios; those of 12x
or below.
The Arndt-Schultz law indicated how poisons in certain compounds
would have a paradoxical shift in activity as they were made more and
more dilute. This means that whatever the effect of a poison is in raw
dose, as it is made more and more dilute there is a paradoxical shift, or a
reversal of what the compound does.
As we have proved several times in the Quantum Biology, the Quantum
Biology Workbook, and other publications, homeopathy is not just like
treating like. Oftentimes homeopathy is treating via the pharmacological
agent within the herb. Thus the indications of the homeopathic remedy
are very similar, if not identical to the indications suggested by the active
ingredients of the original herb. With this in mind, just what is
homeopathy vs. allopathy? To offer a new definition for homeopathy
which encompasses the old definition, we can see that a homeopath is
truly trying to stimulate the organism of the human body to respond and
heal itself. In allopathy, an outside intervention via a drug is meant to
sedate, stimulate, block, deceive, or do some type of unnatural process.
Thus, the organism becomes dependent on the outside stimulus, such as
when an MAO inhibitor is used to stop depression; the persons own
development of monoamine oxidase becomes deficient. If we use an anti-
histamine to fight histamine release, then the persons own development
of histamine can be deficient.
Allopathy seeks to build dependence. The key for the allopath is the
hope that the allopathic medication will pick up some slack, and that the
patient will heal himself while the allopathic medication is operating. In
other words, he hopes that the patient can find his own biological
115
solution while the anti-histamine is working. But the anti-histamines
and most of the allopathic synthetic medications, of course, do not cure;
they only stimulate externally, relying on the forces of nature to cure the
body in the interim.
In homeopathy, there are many different principles at play that are
trying to encourage the body to heal itself, rather than stimulating it to
heal itself. This is the concept of the minimal dose which Hahnemann
believed in; trying to find the smallest amount of a homeopathic or
pharmacological agent that could gently nudge the patient back into the
biological cybernetics of health. Using a feather to stimulate such a
balance is the principle of homeopathy.
In using the Arndt-Schultz law for poisons such as Belladonna, Apis
mellifica, Hepar sulph, etc., we can see that this principle illustrates that
what a poison does in raw dose is opposite to a homeopathic form of the
poison. It can be observed in snake venoms and other biological poisons
that they have the ability to mend and heal different enzyme pathways.
In herbs which are not poisons, we can also see a homeopathic
principle where a compound is used to apply a gentle nudge to the
patient to return to health. In Chinese herbalism, if a patient had too
much heat in the body, such as fever, the herbalist would use a
refrigerant. If a patient had a problem with constipation, then an herbal
laxative would be used.
We see these different propositions as being akin to homeopathy in
that we would try to use the least possible amount of refrigerant or
whatever product to accomplish the job of bringing the patient back to
stability, just as a homeopath might use Eyebright, or might use adrenal
tissue to help in a weak adrenal case. This is also applied to the concept
of Chinese herbalism.
The new definition of homeopathy is one of gentle stimulation of the
body to heal itself rather than to be dependent on an outside
pharmacological intervention. This broader definition of homeopathy will
116
allow us to re-evaluate the different herbals and natural compounds that
used to be in the natural compendium, and bring them back into the
medical repertoire. In using the different compounds of the herbal
repertoire we can see that this is much akin to a homeopathic
philosophy. The dilution process is merely to seek a minimal dose of
these items, so that we can accomplish the positive effects and minimize
the negative effects of the herbs. Thus, homeopathy allows for many
different factors:
1) Homeopathy can be nutritional supplementation. If we use a
homeopathic compound such as Vitamin A or Vitamin B to supplement
the bodys deficiency syndrome, then homeopathy can be used in a
nutritional sense. If we were to take a concentrated source of B-12 and
dilute it one part to ten, six times, to arrive at a 6x, we would see that
this 6x is approximately equal to the RDA of B-12. Some of the minute
doses of vitamins that people use can be reflected in the compounds of
homeopathy. Such homeopathic compounds made for nutritional
supplementation are in the Liquitrophic line made by Dr. Recommends.
These different liquitrophic were developed for nutritional
supplementation in using the minimal dose philosophy, and also using
the highest quality of vitamins known to man; that of vitamins made by
nature, not the synthetic vitamins made by mans technology. This line
was basically a variation of Royal Lees ideas of protomorphology and
nutrition using natural compounds such as snow pea for kidney
development, wheat grass for B Vitamins, natural wheat germ for
Vitamin E, and the whole series of natural Vitamin C factors for Vitamin
C. These compounds have been blended into natural liquids for vitamin
supplementation, and are a superior line to some of the Standard
Process Formulas. The Standard Process Formulas use different
unnatural pills, as nature does not provide pill trees and capsule bushes.
Using these liquids, we can increase the surface area over one million
times. We can start the digestive process in the mouth with the help of
117
the brain and all the innervations that go into the nasal pharynx, so that
the nervous system can properly prepare for absorption and utilization.
By doing this, it has been possible to increase the effectiveness and the
mode of delivery of the Standard Process Formulas while capturing an
increase in the potency.
2) Homeopathy can be used to help stimulate the body. So if we use
caffeine or Belladonna at low dose, we can achieve some of the low-dose
pharmacological action; trying to trigger the body to do its own healing.
The vast difference here between homeopathy and allopathy is that we do
not try to incur dependence with homeopathy, but rather use the
minimal dose, and gently shift the patient to being able to accomplish his
own health.
3) Homeopathy can be used in many classic ways to help reverse
symptoms, and stimulate the body to return to the balance of its
cybernetic systems. This chapter is dedicated, however, to the idea of
using herbs in high concentrations and low potencies of 2x, 3x, and 4x
for pharmacological and homeopathic action.
Let us return to the analysis of the Chinese herb philosophy.
Belladonna contains atropine, and the pharmacological effects of it are
that it makes us red as a beet, dry as a bone, and mad as a hatter. This
is the anti-cholinergic effect of the pharmacology of the atropine in the
Belladonna compound. Belladonna is a poison. If taken in large enough
doses it will cause death. If we make the Belladonna solution more and
more dilute, and more and more dilute, we will see, if we chart the
pharmacological effects of Belladonna, that at a certain point it will cause
a paradoxical shift, and it will reverse redness, reverse dryness, and
reverse madness. Thus, if a patient were to come to us who was red as a
beet, dry as a bone, and mad as a hatter, we might suggest a 6x, 9x, or
possibly higher potencies of Belladonna to reverse these processes.
The Arndt-Schultz law, as pointed out in the chapter on pharmacology,
states that a compound that is a poison will always have a reversal. A
118
compound that is not a poison will follow Wilders Law of Initial Values.
This tells us that as a nonpoisonous compound is made more dilute we
might see an increase in its pharmacological activity of what the raw
dose of the formula does, we might see an inverse, or we might see no
effect whatsoever. An example of this would include most of the sarcodal
tissues including thyroid and adrenal. Here we will see that the effect of
these sarcodal tissues is stimulation or a hormonal effect. If we use raw
adrenaline, we will see that it has a stimulating effect on the body. If we
use a more and more dilute form of the adrenaline - 6x, 12x, etc., we will
often see a similar increase in the same type of stimulation capacity. We
rarely see reverses in the sarcodal formulas.
Many herbs also follow this potentiation cycle, such as Eyebright,
which if taken in raw doses makes the eyes bright; hence its name. It
was named Eyebright because herbalists found that it helped conditions
of the eye. As we make it more and more dilute we see that the
homeopathic use of Eyebright, even in dilute quantities of 16x, 30x, and
above, will help improve eyes and vision. If it were all reversal, we would
only use Eybright when a patient came in whose vision was too good. If a
patient said, I see too well, then homeopathic Eyebright would be used.
But this is not the case; homeopathic Eyebright is used to improve
vision. Many herbs have increased or equal health value in homeopathic
form. It is wrong to merely value compounds by their dosages, as in
synthetic pharmacology. Many Chinese herbs can have excellent effects
in low-potency homeopathic form.
As stated in the Law of Initial Values, some things will be reversal if
they tend towards poisons, and some things will be potentiating of their
original effects. Also, some items will have no effect at all as they are
made more and more dilute.
In the study of Chinese herbalism, we see a very profound description
of an excellent natural pharmacology. We can see that the Chinese have
studied the medicinal effects of herbs for thousands of years, and that
119
specific directions were developed in how to pick these herbs, preserve
them, and then prepare certain remedies. Often these remedies were
made in dilute quantities, sometimes as low as one part per trillion,
which is equivalent to a 9x. The Chinese understood how certain items
could be made more dilute and still achieve pharmacological
effectiveness. To assume that the only active ingredients are chemical in
these Chinese herbs is to make the same mistake the synthetic chemical
companies make. Nature provides many energetic factors beyond mere
chemistry. Subtle energetic effects, mineral balance, electrical regulation
abilities, and more are stable in dilution. Dilution also offers safety in
compliance with the minimal dose concept of medicine.
The Chinese did not have a system of succussion, nor did they have a
system of homeopathic dilution, but their pharmacology was much akin
to some of these processes. Many herbs were diluted to find safer levels
of activity. This titration allows for strong herbs to be used safely.
One of the problems of the herbal industry in America is the lack of
preciseness in how an herb should be picked and processed. In China,
an herb is picked at precise times of the year using precise methods, so
that the pharmacological activity of the herb is assured. In America,
however, the herbal industry for the last fifty years has been much less
precise. Without a precise pharmacopoeia, unknowing American
distributors of herbs might pick them at non-pharmacologically active
periods of their cycle. Without care for quality control, many companies
pass on irregular or impotent products without safety or efficacy. This
has led to the demise of the herbal industry in America; whereas, the fine
quality control processes of the herbs in China has led to the high
success of Chinas sphere of medical influence. In 1962, the FDA
abolished the natural compendium of herbs and natural remedies. We
might look at several theories for its demise, but indeed, some of this
lack of quality control is a factor.

120
 In developing an herbal protocol to mix with homeopathics, wise
manufacturers including Dr. Recommends have had to develop severe,
exacting quality control criteria for accepting different herbals ordered
from American or other herbal suppliers. These types of quality control
techniques include product surveys, product assays, and product
determination in methods such as spectrophotometer, atomic
absorption, chromatography, culture analysis, and other forms of
chemical procedures to determine pharmacological activity. Dr.
Recommends has been able to develop the finest quality control analysis
protocol to assure the highest form of potency for the different herbs
utilized.
The Chinese literature is filled with herbal references, and information
about how these herbs can be used medicinally to help patients in a wide
variety of ways. It is Dr. Recommends idea that many of these herbs can
also be put into homeopathic dilution, and used in a similar process.
This is to insure safety first while guaranteeing effectiveness. We do not
see this as contradictory to the homeopathic process in any way. In fact,
Wilders Law of Initial Values tells us that many of these compounds,
once understood, can be increased in energetic potency as we make them
more and more dilute, while preserving activity. Dr. Recommends has
developed a pilot study and statistical protocols to determine the
absolute effectiveness and safety of the different compounds. Clinical
trials are an important part of the Dr. Recommends quality control
protocol.
Dr. Recommends started with the idea that Chinese herbology and
homeopathy were compatible in their format, and could be blended. The
first type of blending in this technology was through a system of oriental
herb formulas directed toward different organ systems, which were called
Oriental Herbs for Organs. A list of these different products is included.

121
These were taken from the book, Treating Cancer with Chinese Herbs, by
Hong-Yen Hsu. In this book, several cancer treatment modalities were
noted for a variety of different organ system types of cancer. These
treatment modalities were developed by doctors in Shanghai, China.
They used many different types of herbal therapies which Dr.
Recommends sought to blend into formulas for treatment of similar
degenerative problems.
After twenty-five years of commerce with these products, the remarks
by many doctors have confirmed that this is not only a safe system of
treatment, it is a very effective one as well. The herbs in those different
formulas were put into formulas at low potencies of 2x, 3x, and
sometimes 4x, equivalent to the dilution methods used by the doctors in
China. In fact, the dilutions are almost equivalent to the treatments used
in China.
The success of these formulas has led Dr. Recommends to develop
other formulas following the Chinese herbal system. These are developed
with the Chinese herbal acupuncture modality of treatment. In
developing these herbal formulas, Dr. Recommends tries to use herbal
remedies from all over the world, including those from the Amazon rain
forest where certain herbs have been studied and used by Amazon tribes
for years. In making up these formulas, Dr. Recommends has used herbal
formulas from the Amazon, China, Korea, America, South America,
Europe, Russia, and many other places.

Bibliography
Lee, R. Hanson, W. Protomorphology. Lee Foundation for Nutritional
Research, 1947. Milwaukee, Wisconsin.

Hsu, Hong-Yen. Treating Cancer with Chinese Herbs. The Oriental

Healing Arts Institute, 1982. Long Beach, California.

122
 THE MIASM PHILOSOPHY

In classical homeopathy, a miasm is thought to be a tendency toward a

disease pattern that is passed on from one generation to the next.
Sometimes, these disease tendencies can produce a variety of conditions
that can be inherited from our ancestors. Hahnemann found that
miasms such as sycosis (a type of gonorrhea), syphilis, and psora, could
be transmitted through genetic inheritance. We now know that there are
other types of miasm links. Miasms work on very high vibrational levels;
thus, the miasm formulas need to be in a very high homochord state to
help in breaking up the miasm tendency in the patient. This is achieved
through the QQCTM process.
We caution the young initiate in homeopathy; using these remedies
takes some degree of skill and training.

123
 MIASM REMEDIES

MIASM-ALLER (1 fl. oz.)

Catalog No. 0154
Indication: Allergies
Ingredients: Encephalitis, Typhus, Malaria, Anthrax, Toxoplasmosis,
Venereum, Cold Virus, Allergic Reactivity Sarcodes: Adrenal, Pancreas,
Liver 12x, 30x, 100x, 500x, 1000x.

MIASM-CAN (1 fl. oz.)

Catalog No. 0155
Indication: Degenerative diseases
Ingredients: Melanoma, Sarcoma, Myeloma, Neurofibroma, Carcinoma,
Tumor 12x, 30x, 100x, 500x, 1000x.

MIASM-CF (1 fl. oz.)

Catalog No. 0156
Indication: Chronic fatigue, Tiredness, Exhaustion
Ingredients: Brucellosis, Epstein Barr, Mononucleosis, Cytomegalovirus,
Tularemia, Streptococcus fecalis, Elephantiasis, Coxsackie,
Neuromyasthenia, Candida albicans 12x, 30x, 100x, 500x, 1000x.
Echovirus 12x, 17x, 30x, 100x, 500x, 1000x. Pseudomonas 12x, 17x,
30x, 100x, 500x, 1000x. Borrelia burgdorferi 13x, 30x, 100x, 500x,
1000x. Malaria, Pestinum 15x, 30x, 100x, 500x, 1000x. Spirillum
minus 16x, 30x, 100x, 500x, 1000x.

MIASM-CHOL (1 fl. oz.)

Catalog No. 0151
Indication: Cholera, Intestinal disorders
Ingredients: Ameba 15c, 30c, 100c; Cholera, Dysentery (Bacillus
dysenteriae), Pyrogenium, 20x, 30x, 100x, 500x, 1000x.

MIASM-FNG (1 fl. oz.)

Catalog No. 0152
Indication: Fungus, Yeast sensitivity
Ingredients: Amanita muscaria, Saccharomyces, Candida albicans,
Molds, Epidermophyton, Chlamydia 12x, 30x, 100x, 500x, 1000x.
Blastomyces 17x, 30x, 100x, 500x, 1000x. Candida parapsilosis 19x,
30x, 100x, 500x, 1000x.

124
MIASM-LEP (1 fl. oz.)
Catalog No. 0146
Indication: Leprosy, Skin disorders
Ingredients: Leprosy, DNA, RNA, Myrrh, Verbascum thapsus 12x, 30x,
100x, 500x, 1000x.

MIASM-MEN (1 fl. oz.)

Catalog No. 0153
Indication: Mental disorders
Ingredients: Encephalitis, Nocardia, Bacteria, Virus, Imponderables:
Guilt, Shame, Jealousy, Rage, Hatred, Prejudice, Incest, Greed,
Judgmental, Obsession, Depression, Aggression 12x, 30x, 100x, 500x,
1000x. Meningitis, Trichinosis 15x, 30x, 100x, 500x, 1000x.

MIASM-MZL (1 fl. oz.)

Catalog No. 0147
Indication: Measles, Dermatitis
Ingredients: DNA, RNA, Chamomilla, Trifolium pretense, Pulsatilla 12x,
30x, 100x, 500x, 1000x; Morbillinum (Rubeola) 20x, 30x, 100x, 500x,
1000x.

MIASM-PSO (1 fl. oz.)

Catalog No. 0143
Indication: Psora, Skin disturbances
Ingredients: Psorinum, Staphylococcus, Streptococcus, Tuberculinum,
DNA, RNA, Calcarea Carbonica, Medorrhinum, Kali Muriaticum,
Pulsatilla, Bryonia 12x, 30x, 100x, 500x, 1000x.

MIASM-SYC (1 fl. oz.)

Catalog No. 0144
Indication: Sycosis, Skin disorders
Ingredients: Syphilinum, Nocardia, DNA, RNA, Natrum Muriaticum,
Petroleum, Sulphur, Natrum Sulphuricum, Zincum Valerianicum, Apis
mellifica 12x, 30x, 100x, 500x, 1000x. Medorrhinum, Chlamydia
trachomatis 16x, 30x, 100x, 500x, 1000x.

MIASM-SYP (1 fl. oz.)

Catalog No. 0142
Indication: Syphilis, Skin disorders, Sexual disturbances
Ingredients: Syphillinum, DNA, RNA, Lymes, Antimonium Crudum, Kali
Muriaticum, Mercurius Solubilis, Mercurius Vivus, Hepar Sulphuris
Calcareum 12x, 30x, 100x, 500x, 1000x.

125
MIASM-TB (1 fl. oz.)
Catalog No. 0148
Indication: Tuberculosis
Ingredients: Tuberculosis, Pneumonia, Bronchiecyasis, Pertussis, DNA,
RNA, Natrum Sulphuricum, Aconitum napellus 12x,
30x, 100x, 500x, 1000x.

MIASM-TET (1 fl. oz.)

Catalog No. 0145
Indication: Tetanus, TMJ disorders
Ingredients: Tetanus, TMJ, DNA, RNA, Botulinum, Shigella, Calcarea
Phosphorica, Calcarea Sulphurica 12x, 30x, 100x, 500x, 1000x.

MIASM-VAC (1 fl. oz.)

Catalog No. 0149
Indication: Vaccine
Ingredients: Vaccinotoxinum, Varicella, Parotitis, Polio, Grippe,
Influenza, Diphtheria, Measles, Tetanus 12x, 30x, 100x, 500x, 1000x.

MIASM-VIR (1 fl. oz.)

Catalog No. 0150
Indication: Virus sensitivity
Ingredients: Apium Virus, Ichthyolum, Vaccinotoxinum, Morinum,
Variolinum, Misc. Influenzinum, Vincetoxicum, Retrovirus 12x, 30x,
100x, 500x, 1000x. Psorinum 16x, 30x, 100x, 500x, 1000x.

126
 THE PSYCHOLOGICAL PHILOSOPHY

The Dr. Recommends psychological homeopathic formulas use a

combination of homeopathic ingredients to help stabilize psychological
conditions found in the patient population. These psychological
conditions run the range of depression, anxiety, mania, etc. It must be
pointed out that these patients systems are often complicated by other
allopathic treatment that can diminish the homeopathic results.
The Dr. Recommends psychological remedies are not complete therapy
in and of themselves. Any type of psychological treatment should include
a referral to a psychologist, counselor, or other professional trained in
this area. These remedies are an adjunctive therapy and should never be
used as a primary or a singular method of treatment.

127
 PSYCHOLOGICAL REMEDIES

PSY-ADJ (1 fl. oz.)

Catalog No. 0301
Indication: Adjustment disorders
Ingredients: Ustilago maidis, Antipyrine 2x. Caladium seguinum 3x.
Digitalis purpurea, Arundo mauritanica, Glonoine, Xerophyllum
asphodeloides 6x. Anhalonium 12x. Kreosotum 24x. Lachesis mutus
30x. Phosphorus, Nux vomica 30x, 60x, 100x.

PSY-ANX (1 fl. oz.)

Catalog No. 0302
Indication: Anxiety
Ingredients: Oxytropis lambertii 3x. Natrum Muriaticum, Borax 4x.
Alumina 5x. Causticum 6x. Plumbum Metallicum 8x. Sepia 12x.
Lilium tigrinum 30x. Chamomilla, Coffea tosta 30x, 60x, 100x.

PSY-DELR (1 fl. oz.)

Catalog No. 0303
Indication: Delirium
Ingredients: Chamomilla 1x. Helleborus, Chininum Sulphuricum,
Passiflora incarnata, Scopolamine 2x. Datura stramonium 3x.
Aconitum napellus 4x. Ranunculus bulbosus 4x, 30x, 60x, 100x. Rhus
toxicodendron, Operculina, Kali Bromatum, Absinthium 6x. Lachesis
mutus 8x. Belladonna 30x, 60x, 100x.

PSY-DEM (1 fl. oz.)

Catalog No. 0159
Indication: Dementia
Ingredients: Damiana 1x. Apium graveolens, Calcarea Phosphorica 3x,
1000x. Hyoscyamus niger 4x. Zincum Metallicum, Phosphoricum
Acidum, Baryta Carbonica, Calcarea Carbonica 6x. Aurum Iodatum 8x.
Picricum Acidum 10x. Lilium Tigrinum 12x, 30x. Phosphorus 12x, 30x,
60x, 100x. Stannum Metallicum, Alumina, Iodium, 30x, 60x, 100x.
Sulphur, Plumbum Metallicum, Antimonium, Mercurius Vivus,
Bismuthum Metallicum, Iodium 30x, 60x, 100x, 500x.

PSY-DEP (1 fl. oz.)

Catalog No. 0158
Indication: Depression
Ingredients: Vitamin B3, B5, B6 4x. Lithium Carbonicum, CCK 6x.
Sarcode: Brain 6x, 12x. Caulophyllum thalictroides 12x, 30x. Ignatia
amara 12x, 30x. Sepia 12x. Serotonin 16x. Mercurius Vivus, Silicea,
Plumbum Metallicum, Iodium, Sulphur 60x, 100x, 1000x, 2000x.

128
PSY-DEP/EX (1 fl. oz.)
Catalog No. 0304
Indication: Depression (Extrovert)
Ingredients: Pulsatilla 3x. Caulophyllum thalictroides 3x, 6x, 12x, 60x.
Cimicifuga racemosa 6x. Natrum Muriaticum, Ferula asafoetida 12x.
Lachesis mutus 16x. Sepia 16x, 30x, 60x. CCK 30x, 60x. Agaricus
muscarius, Silicea 30x, 60x, 100x.

PSY-DEP/IN (1 fl. oz.)

Catalog No. 0305
Indication: Depression (Introvert)
Ingredients: Passiflora incarnata 2x. Pulsatilla 3x. Nux vomica 3x, 6x,
12x, 60x. Natrum Muriaticum 12x. CCK 12x, 30x. Sulphur, Petroleum
60x. Ruta graveolens, Causticum 30x, 60x, 100x, 200x.

PSY-DIS (1 fl. oz.)

Catalog No. 0306
Indication: Dissociative disorders
Ingredients: Cyclamen 3x. Thuja occidentalis, Sepia 6x, 12x. Datura
stramonium 30x. Anacardium occidentale, Lachesis mutus, Nitricum
Acidum, Hyoscyamus niger 200x. Cimicifuga racemosa, Gelsemium
sempervirens 30x, 60x, 100x, 200x.

PSY-HYS (1 fl. oz.)

Catalog No. 0160
Indication: Hysteria
Ingredients: Valeriana officinalis, Pulsatilla 2x. Castoreum, Picricum
Acidum 5x. Asafoetida, Asterias rubens, Ignatia amara, Zincum
Metallicum 6x. Mygale 9c. Moschus 12x. Alumina, Aurum Metallicum,
Graphites, Sulphur 30x, 60x, 100x, 1000x

PSY-MANIA (1 fl. oz.)

Catalog No. 0307
Indication: Mania
Ingredients: Salix nigra 1x. Murex 3x, 30x. Atropinum 8x, 30x.
Cantharis 12x. Belladonna 12x, 100x. Panax quinquefolium 20x.
Absinthium, Aconitum, Baptisia tinctoria 30x. Natrum Muriaticum,
Spongia tosta, Passiflora incarnata 30x, 60x, 100x, 200x.

129
PSY-MOOD (1 fl. oz.)
Catalog No. 0161
Indication: Mood disorders
Ingredients: Chamomilla 1x. Aurum Muriaticum 2x. Borax, Aloe
socotrina 3x. Capsicum annuum 4x. Agaricus, Baptisia tinctoria,
Bryonia, Mancinella 6x. Phosphorus 9x. Sulphur, Aluminium
Metallicum, Stannum Metallicum, Mercurius Vivus, Iodium 30x, 60x,
100x, 500x, 1000x.

PSY-PER (1 fl. oz.)

Catalog No. 0308
Indication: Personality disorders
Ingredients: Echinacea purpurea 3x. Rhus toxicodendron, Podophyllum
peltatum 6x. Thuja occidentalis 6x, 12x, 30x. Sulphur 30x, 50x.
Picricum Acidum 60x. Phosphorus, Natrum Muriaticum, Bryonia 30x,
60x, 100x.

PSY-SCHZ (1 fl. oz.)

Catalog No. 0309
Indication: Schizophrenia
Ingredients: Aesculus hippocastanum, Medicago sativa 2x. Helonias
dioica 2x, 6x. Cypripedium pubescens 4x. Abrotanum, Aethusa
cynapium 6x. Radium, Sepia 30x. Apis mellifica, Phosphorus,
Belladonna, Nux vomica 30x, 60x, 100x.

130
 IMPONDERABLE HOMEOPATHY

Imponderable homeopathy is the science of using different vibrational

entities and transferring them into a water and diatomaceous earth
mixture. This mixture acts as a mother tincture, and can absorb negative
or positive energies if exposed to them for fifteen minutes or longer.
Thus, if the emotional vibrations of greed are exposed to diatomaceous
earth and water, it can become a mother tincture of the imponderable
known as greed. The most famous type of imponderable homeopathy is
x-ray. X-rays are exposed to diatomaceous earth and alcohol, producing
a mother tincture. This can then be utilized to detoxify a person who has
been exposed to radiation.
Within this range of imponderable homeopathics there is the potential
to treat a wide range of intellectual, vibrational, and energetic problems.
Included within this text is a long list of some vibrational homeopathics
that are used by the Dr. Recommends pharmaceutical company. This
range of imponderable homeopathics can be used with some exciting new
perspectives on homeopathy.
Another imponderable homeopathic series is the Bach remedies. These
remedies were developed by Dr. Edward Bach in England, many years
ago to help a wide spectrum of emotional issues. These remedies consist
of flower essences derived from many plants and flowers.
The science of Bach philosophy is extensive. The preparation of the
remedies is of the homeopathic manner. The essences are diluted and
then mixed with water and alcohol for patient consumption. For this
reason, we have decided to add them to our Repertory and put them into
this chapter; not because of the nature of their manufacture, but
because of the nature of their use.
These flower essences are made in a very rational, scientific way, but
the process is not entirely comprehensible. Each entity seems to work on

131
a variety of emotional and physiological functions within the patient.
Thus, the pattern of work is imponderable.
Aided by new biochemical techniques and a vastly expanded
understanding of immunology and neurochemistry, researchers have
recently conducted new scientific studies at leading universities,
hospital, and research facilities throughout the country, clearly linking
mental and emotional stress as a primary factor in nearly all physical
disorders. These studies show that emotions, acting through the brain,
can affect nervous system function, hormone levels, and immunological
responses, thereby changing a persons susceptibility to a host of organic
illnesses.
Source:
http://query.nytimes.com/gst/fullpage.html?sec=health&res=9B06EFDA1E38F937A15
756C0A965948260&n=Top/News/Health/Diseases,%20Conditions,%20and%20Health
%20Topics/Cancer

Stress and related disorders have grown to become a major concern to

us all. However, stress in and of itself is not the problem. The problem is
in just how well we handle stress. The more mentally and emotionally
centered and balanced we are, the more effectively we are able to deal
with stress in our lives. To this end, we chose to put these remedies and
their repertory into this section of the book.

132
 BACH REMEDIES

Agrimony: For those not wishing to burden others with their troubles
and who cover up their suffering behind a cheerful faade. They are
distressed by argument or quarrel, and may seek escape from pain and
worry through the use of drugs or alcohol.

Aspen: For those who experience vague fears and anxieties of unknown
origin, they are often apprehensive.

Beech: For those who while desiring perfection, easily find fault with
people and things. Critical and at times intolerant, they may overact to
small annoyances or idiosyncrasies of others.

Centaury: For those who are over anxious to please, often weak willed
and easily exploited or dominated by others. As a result they may neglect
their own particular interests.

Cerato: For those who lack confidence in their own judgment and
decisions. They constantly seek the advice of others and may often be
misguided.

Cherry Plum: For fear of losing mental and physical control, of doing
something desperate. May have impulses to do things thought or known
to be wrong.

Chestnut Bud: For those who fail to learn from experience, repeating the
same patterns or mistakes again and again.

Chicory: For those who are overfull of care for others and need to direct
and control those close to them. Always finding something to correct or
put right.

Clematis: For those who tend to live in the future, lack concentration;
are daydreamers, drowsy or spacey, and have a halfhearted interest in
their present circumstances.

Crab Apple: For those who may feel something is not quite clean about
themselves, or have a fear of being contaminated. For feelings of shame
or poor self image. For example, thinking oneself not attractive for one
reason or another. When necessary, may be taken to assist in
detoxification; for example, during a cold or while fasting.

Elm: For those who at times may experience momentary feelings of

inadequacy, being overwhelmed by their responsibilities.
133
BACH REMEDIES, cont.

Gentian: For those who become easily discouraged by small delays or

hindrances. This may cause self doubt.

Gorse: For feelings of hopelessness and futility. When there is little hope
of relief.

Heather: For those who seek the companionship of anyone who will
listen to their troubles. They are generally not good listeners and have
difficulty being alone for any length of time.

Holly: To be used when troubled by negative feelings such as envy,

jealousy, suspicion, revenge, vexations of the heart, and states indicating
a need for more love.

Honeysuckle: For those dwelling in the past, nostalgia, homesickness;

always talking about the good old days when things were better.

Hornbeam: For the Monday morning feeling of not being able to face the
day. For those feeling that some part of the body or mind needs
strengthening, and for constant fatigue and tiredness.

Impatiens: For those quick in thought and action who require all things
to be done without delay. They are impatient with people who are slow
and often prefer to work alone.

Larch: For those who despite being capable, lack self confidence or feel
inferior. Anticipating failure, they refuse to make a real effort to succeed.

Mimulus: For fear of known things, such as heights, water, the dark,
other people, or being alone, etc.

Mustard: For deep gloom which comes on for apparently no known

reason; sudden melancholia or heavy sadness which lifts just as
suddenly.

Oak: For those who struggle on despite despondency from hardships,

even when ill and overworked; they never give up.

Olive: For mental and physical exhaustion, sapped vitality with no

reserve. This may come after an illness or personal ordeal.

134
BACH REMEDIES, cont.

Pine: For those who feel they should do or should have done better, who
are self-reproachful or blame themselves for the mistakes of others.
Hardworking people who suffer much from the faults they attach to
themselves, they are never satisfied with their success.

Red Chestnut: For those who find it difficult not to be overly concerned
or anxious for others, always fearing something wrong may happen to
those they care for.

Rescue Remedy: The most well known formula in the Back Remedy
system. It has a positive calming and stabilizing effect in an extremely
broad range of stressful situations, which include nervousness, anxiety,
accidents, bereavement, and times of great fright, anguish, and
desperation. Even minor everyday stresses, such as arguments, taking
exams, making speeches, job interviews or other similar stressful
situations are reportedly greatly helped.

Rock Rose: For those who experience states of terror, panic and
hysteria; also when troubled by nightmares.

Rock Water: For those who are very strict with themselves in their daily
living. They are hard masters to themselves, struggling toward some ideal
or to set an example for others. This would include strict adherence to a
living style or to religious, personal, or social disciplines.

Scleranthus: For those unable to decide between two things, first one
seeming right then the other. Often presenting extreme variations in
energy or mood swings.

Star of Bethlehem: For grief, trauma, loss. For the mental and
emotional effect during and after a trauma.

Sweet Chestnut: For those who feel they have reached the limits of their
endurance. For those moments of deep despair when the anguish seems
to be unbearable.

Vervain: For those who have strong opinions and who usually need to
have the last word; always teaching or philosophizing. When taken to an
extreme, they can be argumentative and overbearing.

135
BACH REMEDIES, cont.

Vine: For those who are strong willed. Leaders in their own right who are
unquestionably in charge. However, when taken to an extreme they may
become dictatorial.

Walnut: Assists in stabilizing emotional upsets during transition periods,

such as puberty, adolescence, and menopause. Also helps one to break
past links and emotionally adjust to new beginnings such as moving,
changing or taking a new job, beginning or ending a relationship.

Water Violet: For those who are gentle, independent, aloof, and self-
reliant, who do not interfere in the affairs of others; and when ill or in
trouble prefer to bear their difficulties alone.

White Chestnut: For constant and persistent unwanted thoughts, such

as mental arguments, worries or repetitious thoughts that prevent peace
of mind and disrupt concentration.

Wild Oat: For the dissatisfaction with not having succeeded in ones
career of life goal. When there is unfulfilled ambition, career uncertainty
or, boredom with ones present position or station in life.

Wild Rose: For those who, for no apparent reason, have resigned
themselves to their circumstances. Having become indifferent, little effort
is made to improve things or find joy.

Willow: For those who have suffered some circumstance or misfortune

which they feel was unfair or unjust. As a result, they become resentful
and bitter toward life or toward those who they feel were at fault.

Source:
http://www.healingartsspa.com/bach_flower_remedies.htm
http://bowentherapy.homestead.com/bachflowers.html

136
 VIBRATIONAL REACTANTS

AGGRESSION 2000-2500 HERTZ

ANGER 2500-3000 HERTZ
ANXIETY 3000-3500 HERTZ
AUTISTIC 3500-4000 HERTZ
AWARENESS 4000-4500 HERTZ
BLUE 4500-5000 HERTZ
CARELESS 5000-5500 HERTZ
CHAKRA, BASE 5500-6000 HERTZ
CHAKRA, BROW 6000-10000 HERTZ
CHAKRA, CROWN HESITATION
CHAKRA, HEART HYPER GAMMA RADIATION
CHAKRA, STOMACH INDIGO
CHAKRA, THROAT INFRARED
CONFUSION JEALOUSY
COSMOS JOY (EMOTION)
50 CYCLES LA
60 CYCLES VERTEBRAE
75 CYCLES LEFT SPIN
100 CYCLES LUST
150 CYCLES MI
DELUSION MICROWAVE
DEPRESSION NEGATIVE MAGNETIC
1ST DIMENSION NEGATIVE STATIC
2ND DIMENSION ORANGE
3RD DIMENSION PASSIVITY
4TH DIMENSION POSITIVE MAGNETIC
5TH DIMENSION POSITIVE STATIC
6TH DIMENSION POWER
7TH DIMENSION PROJECTION
8TH DIMENSION RADIO
9TH DIMENSION RATIONALIZATION
10TH DIMENSION RE
DO RECKLESS
EELF RED VISIBLE
ELF RIGHT SPIN
FA SADNESS
FEAR SO
GAMMA RAYS TI
GRAVITATION ULTRAVIOLET
GREED VIOLET
GREEN VISIBLE
0-500 HERTZ WORRY
500-1000 HERTZ X-RAYS
1000-1500 HERTZ YELLOW
1500-2000 HERTZ

137
 ALLERSODES

In treating allergies, it was found that small amounts of allergy-causing

agents can be used to help reverse the anti-body cascade and other
allergic factors within the body. This type of desensitization can be used
with oral antigens or injectibles. Modern medicine has used this type of
allergy treatment for several decades. Dr. Recommends has developed a
large range of allersodes including inhalant and food allersodes. Within
the scope of allersodes there are also phenolics which help break up the
sensitivities to different phenol rings; bodily secretions, including
hyluronidase; natural anti-histamines, including adrenaline; and other
liver enzymes that help the body to naturally reduce allergic reactivity.
Dr. Nelson has developed a large list of allersodes included here. To see
the research on the effectiveness of these allergy compounds we point the
reader to The Experimental Data on Homeopathy. Within this text, it is
possible to see proof of how allergy homeopathy can be used to
desensitize our patients.

138
ANIMAL HAIR (1 oz.)
Catalog No. 0291
Oral Antigen Combination
Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x.
1-3 Cyclohexanedione 8x. Cat Hair, Dog Hair, Horse Hair 9x, 12x, 30x,
60x, 100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a
tincture of purified water and non-allergenic alcohol.

DAIRY (1 oz.)
Catalog No. 0292
Oral Antigen Combination
Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x.
1-3 Cyclohexanedione 8x. Cheeses, Cow's Milk, Goat's Milk, Ice Cream,
Butter 9x, 12x, 30x, 60x, 100x. Histaminum 30x, 60x, 100x, 500x. In a
tincture of purified water and non-allergenic alcohol.

GRAIN (1 oz.)
Catalog No. 0293
Oral Antigen Combination
Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x.
1-3 Cyclohexanedione 8x. Wheat, Corn, Barley, Millet, Rice 9x, 12x, 30x,
60x, 100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a
tincture of purified water and non-allergenic alcohol.

MOLD/HOUSE DUST (1 oz.)

Catalog No. 0294
Oral Antigen Combination
Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x.
1-3 Cyclohexanedione 8x. Mildew, Molds, Household Dust 9x, 12x, 30x,
60x, 100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a
tincture of purified water and non-allergenic alcohol.
139
OLFACTORY SENSITIVITY (1 oz.)
Catalog No. 0295
Oral Antigen Combination
Ingredients: Rosa canina flos, Taraxacum officinale, Solidago virgaurea,
Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x. 1-3
Cyclohexanedione, Formaldehyde 8x. Miscellaneous Synthetic Aromatic
Compounds 8x, 12x, 30x, 100x, 1000x. Olfactaid 12x. Formaldehyde
Dehydrogenase 16x, 30x, 60x. Histaminum 30x, 60x, 100x, 500x. In a
tincture of purified water and non-allergenic alcohol.

POLLEN (1 oz.)
Catalog No. 0296
Oral Antigen Combination
Ingredients: Beta Glucuronidase, Adrenalinum 4x. Hyaluronidase 6x.
1-3 Cyclohexanedione 8x. Flowers, Trees, Grasses 9x, 12x, 30x, 60x,
100x, 500x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a tincture of
purified water and non-allergenic alcohol.

SULFIDE SENSITIVITY (1 oz.)

Catalog No. 0297
Oral Antigen Combination
Ingredients: Trifolium pratense, Beta Glucuronidase, Adrenalinum 4x.
Hyaluronidase 6x. 1-3 Cyclohexanedione 6x. Salicylicum Acidum,
Salicinum, Sodium Bisulfide, Tartrazine, Monosodium Gluconate 8x,
12x, 30x, 100x, 1000x. Histaminum 30x, 60x, 100x, 500x. In a tincture
of purified water and non-allergenic alcohol.

140
 INHALANT REACTANTS

ACACIA
ACTINOMYCES ISRAELII
AGARICUS MUSC.
ALDER, RED, WHITE
ALFALFA
ALLSCALE
ALERNARIA TENIUS
ASH, ARIZONA, GREEN, OREGON, WHITE
ASPEN, QUAKING
ASPERGILLUS, FLAVUS, FUMIGATUS, GLAUCUS, NIGER, TERRUS
BAHIA
BARLEY, CULTIVATED
BARLEY SMUT, LOOSE
BAYBERRY
BEEFWOOD
BENT, CREEPING
BERMUDA GRASS
BIRCH, MIXED, RED, RIVER, WHITE
BLASTOMYCES DERMATITIDIS
BLUE, ANNUAL, CANADA, KENTUCKY
BLUEGRASS
BOTRYTIS
BOX ELDER
BROMEHUNG
BROMWEED
CANADA BLUEGRASS
CANDIDA (MONILA) ALBICANS
CARELESSWEED
CEDAR, MOUNTAIN, PINCHOT, RED
CEPHALOSPORIUM, COMMON, ROSEUM
CHAETOMIU
CHESS, SOUTHERN
CHINESE ELM
CLADOSPORIUM FULVUM
CLAVICEPS, PASPALI, PURPUREA
CLOVER, SWEET
COCKLEBUR
CORN, CULTIVATED, POLLEN
CORN SMUT
COSMOS
COTTONWOOD
COTTONWOOD, MIX, COMMON, ARIZONA, EASTERN, WESTERN
CRAWLING INSECT

141
INHALANT REACTANTS, cont.

CURVALIARIA SPICIFERA
CYPRESS, BALD, ARIZONA
DAHLIA
DANDELION
DERMATOPHILUS CONGOLENSIS
DOCK, RUMEX MIX, SOUR, YELLOW
ELM, AMERICAN, CEDAR, CHINESE, SLIPPERY
EUCALYPTUS
FIR, DOUGLAS
FIREBUSH
FIVE GRASS MIX
FLOWER POLLEN
FLYING INSECT
FUSARIUM SOLANI
GELASINOSPORA CEREALIS
GEOTRICHUM CANDIDUM
GLIOCLADIUM FIMBRIATUM
GOLDERNROD
GRAIN
GRAMMA, BLUE
GRASS, BERMUDA
GRASS, BROME, CANARY, JOHNSON, JUNE, OAT, ORCHARD, QUACK
GREASEWOOD
GUM, BLACK, SWEET
HACKBERRY
HAY
HAZELBERRY
HAZELNUT, AMERICAN
HELMINTHOSPORIUM SATIVUM
HEMLOCK, WESTERN
HEMP, COMMON
HICKORY, MIXED, PIGNUS, SHELLBARK
HISTOPLASMA, CAPSULATUM, FARCIMINOSUM
HONEYSUCKLE
HORMODENDRUM CLAD
HOUSE
IODINE BUSH
IRIS VERSICOLOR
JERUSALEM OAK
JOHNSON GRASS SMUT
JUNIPER
LAMBSQUARTER
LOMBARDY POPLAR
MAGNOLIA
142
INHALANT REACTANTS, cont.

MAPLE, SOFT, HARD

MARIGOLD
MARSHELDER, BURWEED, NARROWLEAF, ROUGH
MEADOW FESCUE
MESQUITE
MEXICAN TEA
MICROSPORUM, AUDOUINII, CANIS, GYPSEUM
MONOTOSPORA
MUCOR, CORYMBIFERA, MUCEDO, PLUMBEUS
MUGWART, COMMON
MULBERRY, PAPER, RED, WHITE
MYCOGONE ALBA
NARCISSUS
NASTRUTIUM
NEUROSPORA, SITOPHILA
NIGROSPORA, SPHAERICA
NOCARDIA ASTEROIDES
OAK, BLACK, BLACKJACK, BUR, LIVE, POST, RED, WHITE
OAKBLACK
OAT, CULTIVATED
PAEONIA OFFICINALIS
PENICILLUM, CHRYSOGENUM, NOTATUM, RUBRUM
PIGWEED
PLANTAIN, ENGLISH
POVERTY WEED
QUAILBUSH
RABBITBUSH
RAGWEED, DESERT, FALSE, GIANT, SHORT, SLENDER, WESTERN
WOOLY, MIX
REDTOP
RHIZOPUS NIGRICANS
RHODOTORULA MUCILAGINOSA
RINKEL
ROSE
RUSSIAN THISTLE
RYE, CULTIVATED
RYE GRASS, COMMON, ITALIAN, PERENNIAL
SAFE, DRAGON, PASTURE, PRAIRIE, MIX
SAGEBRUSH, COMMON
SALTBUSH, ANNUAL
SCOPULARIOPSIS
SHADSCALE
SHEEP SORREL
SORGHUM, GRAIN
143
INHALANT REACTANTS, cont.

SORGHUM, SMUT
SPONDYLOCLANDIUM ATROVIRENS
SPOROTRICHUM PRUINOSUM
STACHYBOTRYS ATRA
SUGAR BEET POLLEN
SUNFLOWER
SYNTHETIC FABRIC
TOBACCO
WEED POLLEN MIX
WESTERN WATER HEMP
WHEAT, CULTIVATED, GRASS
WINGSCALE
WINTERFAT
WORMWOOD, ANNUAL, COMMON

144
PHENOLS I
ACC ACETALDEHYDE
ACETIC ACID
ACETONE
ADENINE
AFLATOXINS
ALDEHYDE
ALLYL BUTYRATE
ALLYL TIGLATE
AMSOLE
AMYGDALIN
ANETHOLE
APIOL
ARGININE
ASPARAGINE
d1-ALANINE
BENZALDEHYDE
BENZOIC ACID
BENZOTHIAZOLE
BENZYL
BENZYL BUTYRATE
BENZYL TIGLATE
BHA
BHT
BIOFLAVENOIDS
BRAIN SUBSTANCE
BUTANOIC ACID
BUTYRIC ACID
d-BIOTIN
CAFFEIC ACID
CAFFEINE
CALCIUM AMINO ACID CHELATE
CALCIUM OROTATE
CAMPHOR
CANDIDA
CAPSAICIN
CAROTENE
CARYOPHYLLENE
CHALCONE
CHLOROGENIC ACID
CINEOL
CINNAMALDEHYDE
CINNAMIC ACID
CONIFERYL ALCOHOL
COUMARIN

145
PHENOLS I, cont.

DECANOIC ACID
DOPAMINE
ELLAGIO ACID
EPHEDRINE HCL
ESTERS (30 TYPES)
ESTROGEN
ETHYL BUTYRATE
ETHYL HEPTANOATE
ETHYL HEXANOATE
ETHYL OCTANOATE
EHTYL PROPIONATE
ETHYL PYRUVATE
ETHYL VALERATE
EUGENOL
FD&C BLUE NO. 1
FD&C BLUE NO. 2
FD&C GREEN NO. 3
FD&C RED NO. 2
FD&C RED NO. 3
FD&C RED NO. 40
FD&C VIOLET NO. 1
FD&C YELLOW NO. 6
FOLIC ACID
FORMALDEHYDE DEHYDROGENASE
FURFURAL
FURFURYL BUTYRATE
FURFURYL HEPTANOATE
FURFURYL HEXANOATE
FURFURYL OCTANOATE
FURFURYL PENTANOATE
FURFURYL PROPIONATE
GABA
GALLIC ACID
GENISTEIN (BIOCHANIN A)
GERMANIUM
GLUTIN
GLYCINE
1-GLUTAMIC ACID
HEART SUBSTANCE
HEMOGLOBIN
HESPERETIN
HISTAMINE
HYDROCINNAMIC ACID

146
PHENOLS I, cont.

HYPOTHALAMUS SUBSTANCE
n-HEXYL BUTYRATE
n-HEXYL TIGLATE
ICOLEUCINE
INDOLE
INOSINE
INOSITOL
ISOASCORBIC ACID
ISOPROPYL BUTYRATE
ISOPROPYL TIGLATE
KIDNEY SUBSTANCE
alpha-KETO GLUTARIC ACID
L-CARNITINE HYDROCHLORIDE
L-DOPA
L-GLUTAMINE + GLUTAMIN ACID
L-GLUTATHIONE
L-LYSINE (PILL)
LACTIC ACID
LACTOSE
LEUCINE
LIMONEN
LINALOOL
LIPASE BLENDS
LYMPHATIC SUBSTANCE
MALIC ACID
MALTOSE
MALVIN
MANGANESE AMINO ACID CHELATE
MANNAN
MENTHOL
METHIONINE
METHYL BUTYRATE
METHYL SALICYLATE
METHYL TIGLATE
MINADIONE
MOLYBDENUM AMINO ACID CHELATE
MONO AMMONIUM GLYCYRRHIZINATE
N, N-DIMETHYLGLYCINE HYDROCHLORIDE
NARINGENIN
NICOTINE
NOREPINEPHRINE
OCTACOSANOL
OCTANOIC ACID
OCTAPAMINE
147
PHENOLS I, cont.

ORCHIC SUBSTANCE
OVARIAN SUBSTANCE
PABA
PANCREATIN
PANCRELIPASE
PENTOSE
PHENETHYL 2-METHYLBUTYRATE
PHENYLALANINE
PHENYLISOTHIO
PHLORIDZIN
PINENE

148
ALLERSODES
ACC
Acetaldehyde
Acetic Acid
Acetone
Adenine
Aflatoxins
dl-Alanine
Aldehyde
Allyl Butyrate
Allyl Tiglate
Amygdalin
Anethole
Apiol
Arginine
Asparagine
Benzaldehyde
Benzoic Acid
Benzothiazole
Benzyl
Benzyl Butyrate
Benzyl Tiglate
BHA
BHT (Buylated Hydroxytoluene)
d-Biotin
Bioflavenoids
Brain Substance
Butanoic Acid
Butyric Acid
Caffeic Acid
Caffeine
Calcium Chelate
Camphor
Candida
Capsaicin
Carotene
L-Carnitine Hydrochloride
Caryophyllene
Chalcone
Chlorogenic Acid
Cineol
Cinnamic Acid
Coniferyl Alcohol
Coumarin
Decanoic Acid

149
ALLERSODES, cont.
N, N-Dimethylglycine Hydrochloride
L-Dopa
Dopamine
Ellagic Acid
Ephedrine HCl
Esters (30 types)
Estrogen
Ethyl Butyrate
Ethyl Heptanoate
Ethyl Hexanoate
Ethyl Octanoate
Ethyl Propionate
Ethyl Pyruvate
Ethyl Valerate
Eugenol
FD&C Blue No. 1
FD&C Blue No. 2
FD&C Green No. 3
FD&C Red No. 2
FD&C Red No. 3
FD&C Red No. 40
FD&C Yellow No. 5
FD&C Yellow No. 6
FD&C Violet No. 1
Folic Acid
Formaldehyde
Furfural
Furfural Butyrate
Furfural Heptanoate
Furfural Hexanoate
Furfural Octanoate
Furfural Pentanoate
Furfural Propionate
GABA (Gamma-Amino Butyric Acid)
Gallic Acid
Genistein (Biochanin A)
Germanium
1-Glutamic Acid
1-Glutamine
L-Glutathione
Glutin
Glycine
Glycyrrhizinate
Heart Substance

150
ALLERSODES, cont.

Hemoglobin
Hesperetin
Histamine
Hydrocinnamic Acid
Hypothalamus Substance
Indole
Inosine
Inositol
Isoascorbic Acid
Isoleucine
Isopropyl Butyrate
Isopropyl Tiglate
alpha-Keto Glutaric Acid
Kidney Substance
Lactic Acid
Lactose
Leucine
Limonene
Linalool
Lipase Blends
Lymphatic Substance
Lysine
Malic Acid
Maltose
Malvin
Manganese Chelate
Mannan
Menadione
Methionine
Menthol
Methyl Butyrate
Methyl Salicylate
Methyl Tiglate
Molybdenum Chelate
Naringenin
Nicotine
Norepinephrine
Octacosanol
Octanoic Acid
Octopamine
Orchic Substance
Ovarian Substance
PABA (Para Amino Benzoic Acid)
Pancreatin
151
ALLERSODES, cont.

Pancrelipase
Pentose
Phenethyl 2-Methylbutyrate
Phenylalanine
Phenylisothio
Phloridzin
Pinene
Piperine
Piperonal
Pituitary Substance
Progesterone
Propyl Butyrate
Propyl Tiglate
Putresine
Pyrrole
Pyridoxal-5-Phosphate
Pyridoxine Hydrochloride (Vitamin B-6)
Phytic Acid
Pyruvic
Quercetin
Red Bone Marrow
Riboflavin (Vitamin B-2)
Rutin
Safrole
Salsolinol
Serotonin
Skatol
Spleen Substance
Succinic Acid
Suprarenal/Adrenal Substance
Suprarenal Cortex
Taurine
Thiamine Hydrochloride (Vitamin B-1)
Thujone
Thymol
Thymine
Thyroid
Trypsin
Tryptophan
Tyramine
Tyrosine
Ubiquinone 50
Uric Acid
Uterus Substance
152
ALLERSODES, cont.

Valeraldehyde
Vanillin
d-Xylose

153
ALLERGINS, ANTIGENS, FOODS
Almond Meal
Angora (Goat Mohair)
Apple
Banana
Bean
Birch Mix
Brewers Yeast
Broccoli
Cabbage
Carrot
Cat
Cattle
Cauliflower
Celery
Cheese
Cheddar Mix
Chicken
Chocolate
Citrus
Coffee
Corn Pollen
Cotton Seed
Cotton Wood
Cucumber
Dock Sorrel
Dog
Dust Mix (House)
Dust Mix (Mattress)
Dust Mix (Rug)
Dust Mix (Upholstery)
Eastern Oak
Egg White (Chicken)
Elm Mix
Feathers (Chicken, Goose, Duck)
Flax Seed
Flower Pollen I
Fruit Juice
Garlic
Grain Mill Dust (Corn)
Grain Mill Dust (Wheat)
Grass (Alfalfa)
Grass (Golden Rod)
Grass (Kentucky Blue)
Grass (Meadow Fescue)

154
ALLERGINS, ANTIGENS, FOODS, cont.

Grass (Orchard)
Grass (Perennial Rye)
Grass (Red Clover)
Grass (Red Top)
Grass (Sweet Vernal)
Grass (Timothy)
Green Pepper
Hair Spray
Hickory Mix
Horse
Juniper
Kapok
Kelp-Iodine
Lemon
Lettuce
Maple Mix
Milk
Mold Mix
Mulberry
Mushroom
Nut Mix (Almond)
Nut Mix (Brazil)
Nut Mix (Cashew)
Nut Mix (Coconut)
Nut Mix (English Walnut)
Nut Mix (Peanut)
Nut Mix (Pecan)
Onion
Orange
Penicillium (Chrysogenum)
Penicillium (Digitatum)
Penicillium (Notatuer)
Penicillium (Roquefort)
Perfume Mix
Pollen (Amaranthus)
Pollen (Chenopodium)
Pollen (Cockle Burr)
Pollen (Daisy)
Pollen (Dandelion)
Pollen (Grass)
Pollen (Honey Suckle)
Pollen (Marsh Elder)
Pollen (Mugwort)
Pollen (White)
155
ALLERGINS, ANTIGENS, FOODS, cont.

Red Meat
Rice
Sage
Salmon
Scale Mix
Sesame
Sheep Wool
Shellfish (Clam)
Shellfish (Crab)
Shellfish (Oyster)
Shellfish (Scallop)
Shellfish (Shrimp)
Soybean
Spinach
Strawberry
Tobacco
Tomato
Western Oak Mix

156
 THE DEHABITUATE PHILOSOPHY

In our society today, addictions have become a dramatic problem in the

cultures disease structure. Many people have addictive tendencies and
can become addicted to a variety of things, not just illegal drugs, but
caffeine, tobacco, alcohol, sugar, sex, stress, and other things.
The Dr. Recommends dehabituate remedies have been designed for
homeopathic stimulation of the organism to deal with the addictions and
discharge them in simple, natural ways. The dehabituate remedies have
been engineered for safety through the QQCTM techniques. These
remedies are only designed as an adjunct therapy to a more complete
addiction reduction system.
We recommend Alcoholics Anonymous, Gamblers Anonymous, or any
other twelve-step programs that help people deal with these addictive
tendencies.

157
 DEHABITUATE REMEDIES

SMOKING DEHABITUATE 1 (1 fl. oz.)

Catalog No. 0021
Indication: Systemic stimulation to help reduce smoking. Use during
first 3 to 4 weeks as a nicotine supplement (Do not use beyond suggested
dosage.)
Ingredients: Nicotinum 3x. Calcarea Phosphorica, Zincum Metallicum
4x. Lobelia cardinalis, Selenium Metallicum 6x. Bladder 6x, 12x, 30x,
60x, 100x. Hypothalamus 6x, 12x, 30x, 60x, 100x. Lung 6x, 12x, 30x,
60x, 100x. Beta-Endorphin 6x, 30x. Coffea Tosta 6x, 30x, 100x. Nux
vomica 12x. Tabacum 12x, 16x, 24x, 100x. Saccharinum 16x, 100x.
Plumbum Metallicum 18x

SMOKING DEHABITUATE 2 (1 fl. oz.)

Catalog No. 0022
Indication: Systemic stimulation to help reduce smoking. Use after first
month as a detox and for relapse prevention.
Ingredients: Zincum Metallicum, Calcarea Phosphorica 4x. Silicea,
Lobelia inflata, Selenium Metallicum 6x. Sarcodes: Lung,
Hypothalamus, Bladder 6x-12x, 30x, 60x, 100x. Endorphins 6x, 30x,
100x, 500x, 1000x. Coffea 6x, 30x, 100x. Nux vomica 12x. Tabacum
12x, 16x, 24x, 100x, 500x, 1000x. Saccharinum 16x, 50m. Plumbum
Metallicum 18x, 100x, 1000x. Nicotinum 30x.

158
 VITAMINS

The Dr. Recommends vitamin and mineral products can be used in a

therapeutic practice. The sciences of nutritional medicine and
orthomolecular biology have shown that compounds can be used to help
patients in attaining balance. The science of nutritional deficiency and
excess must be dealt with.
The following products can be utilized to supplement patients diets,
and also to help in orthomolecular ways through the stabilization of
enzyme pathways, hormonal utilization, and vitamin integrity. These
formulas are designed to work with the body naturally by assisting the
nutritional intake of the patient and supplementing the needed vitamins
and enzymes.

159
 LIQUID VITAMINS

A-Z LIQUID (4 fl. oz.)

Natural Source of Full-Range Essential Vitamins
Ingredients: Aloe vera, Medicago sativa, Calcium Ascorbate, Panax
quinquefolium 1x. Caryophyllus aromaticus, Ribes nigrum., Angelica
archangelica 2x. Apis mellifica, Chromium, Selenium Metallicum 3x.
In a tincture of water and non-allergenic alcohol.

DRINKER'S VITAMIN (4 fl. oz.)

Supplies Vitamins and Minerals depleted by alcohol
Ingredients: Magnesium, Calcium Gluconate, B-Complex, Eggshell,
Saccharomyces cerevisiae, Bee Pollen, Angelica archangelica 2x. Liver
Sarcode, Tang Kuei, Oldenlandia affinis, Baptisia tinctoria, Prunus
armeniaca 3x. In a tincture of water and non-allergenic alcohol.

SMOKER'S VITAMIN (4 fl. oz.)

Supplies Vitamins and Minerals depleted by smoking
Ingredients: Ascorbic Acid, Beta Carotene 1x. Taraxacum officinale,
Petroselinum sativum, Spinacia oleracea, Urtica dioica, Equisetum
arvense 2x. Beta vulgaris, Paeonia officinalis, Carthamus tinctorius,
Selenium Metallicum, Commiphora myrrha 3x. Ephedra sinica 4x.
In a tincture of water and non-allergenic alcohol.

HOMEOPATHIC CATALYST WATER (4 fl. oz.)

Increases osmotic capacity
NOTE: Should NOT be used by diabetics.
Ingredients: Purified water, Non-allergenic alcohol, Chlorophyll,
Magnesium, Stearic Acid, Natural Organic Tree Sap, Equisetum.

160
VITAMINS

ADERMINE HCL
ANEURINE
ANEURINE PYRO PHOSPHATE
ARACDONIC ACID
p-AMINOBENZOIC ACID
BETA-CAROTENE
BIOFLAVINOIDS
CALCIFEROL
CAPROIC ACID
COENZYME Q6
COENZYME Q7
COENZYME Q8
COENZYME Q9
COENZYME Q10
COLLAGEN
CYTOCHROME
CYTOCHROME FAD
DESTHIOBIOTIN
DICHLOROFOLIC ACID
ELASTIN
ERGO CALCIFEROL
ERGOSTEROL
FAD
FERODOXIN
GLUTATHIONE
GSG GLUTATHIONE
HYDROXO COBALAMINE
LIBOAMIDE
LINOLEIC ACID
LINOLENIC ACID
LIPOIC ACID
NADP
NAPATHO QUINONE
NICOTINIC ACID
ORTHO QUINONE
PHYKO BIOTIN
PORPHYRIN
PTEROYLGLUTAMIC ACID
PYCOCYANIN CYANIN
RETINAL
RETINOL
RETINOL ACETATE
RETINOL PALITATE
THIOCTIC ACID
161
TOCOPHEROL
TRIGONELLINE
UBIQUINONE ALL
UBIQUINONE -30
UBIQUINONE-35
UBIQUINONE-40
UBIQUINONE-45
UBIQUINONE-50
VITAMIN A
VITAMIN A2
VITAMIN A3
VITAMIN B1
VITAMIN B2
VITAMIN B3
VITAMIN B4
VITAMIN B5
VITAMIN B6
VITAMIN B7
VITAMIN B 8
VITAMIN B9
VITAMIN B10
VITAMIN B11
VITAMIN B12
VITAMIN B13
VITAMIN B14
VITAMIN B15
VITAMIN B16
VITAMIN B17
VITAMIN B18
VITAMIN B19
VITAMIN B20
VITAMIN C
VITAMIN D
VITAMIN D2
VITAMIN D3
VITAMIN E
VITAMIN F-ALL
VITAMIN K
VITAMIN U

162
 POWDERED PRODUCTS

In keeping with the Dr. Recommends philosophy which involves

digestion starting in the mouth, there are various powdered products
available that contain different minerals, vitamins, enzymes and other
ingredients that are not easily made into liquids. They have long shelf
lives in powdered form, and can be utilized by patients for detoxification
and other things for long periods of time, safely and efficiently.
Many of the powders can be stirred into juices or other liquids by the
patient and taken as part of his/her daily regime. These must be used
with the help of a trained practitioner or skilled professional to help the
patient in treatment.

POWDERS

ACTIVATED CHARCOAL POWDER (6 oz.)

Ingredients: Activated Charcoal Powder.

ANTACID POWDER (6 oz.)

Ingredients: Kali Bicarbonate, Natrum Bicarbonate, Calcium Carbonate,

Magnesium Phosphorica, Natrum Muraticum, Kali Muraticum, Silicea.

CLEANSING & SKIN POULTICE (6 oz.)

Applied to skin to draw out toxins, Intestinal Cleanse

Ingredients: Organic Bentonite, Activated Charcoal, Orsa Clay,
Equisetum arvense, Symphytum officinale, Arnica montana, Myristica
fragrans, Magnesia Sulphurica, Natrum Muriaticum, Capsicum annuum.

DISODIUM PHOSPHATE POWDER (6 oz.)

Ingredients: Disodium Phosphate, Magnesia Sulphurica.

MUSTARD POULTICE (6 oz.)

Ingredients: Bentonite, Brassica nigra, Brassica alba, Sanguinaria

Canadensis, Symphytum officinale, Urtica dioica, Arctium lappa, Carica
papaya, Activated Charcoal, Capsicum frutescens.

163
 Screening Groups Used in the Academy of Applied Quantum
Biotech Computer Programs

Listed here are some screening groups used in the Academy of

Applied Quantum Biotech computer programs with biofeedback
instrumentation for bio-computer analysis. These compounds can be
used and purchased as homeopathics.

THE SCREENING GROUPS

Congenital 1 Syphilinum
Syphlitic miasm
Medorrhinum
Gonococcinum
Papilloma Virus

Congenital 2 Tuberculinum Kock

Tuberculinum Bovinum
Tuberculinum Avis
Bacillinum
Retrovirus

Congenital 3 Tuberculinum Klebs

Tuberculinum Denys
Tuberculinum Rosen
Tuberculinum
Marmoret
Ricketsia

Upper Respiratory Bacteria 1 Staphlococcus Aureus

Strept B haemolyticus
Pneumococcus
Haemophilus influenza
Tersina Pestis

164
Bowel Nosodes 1 E. Coli
Proteus
Pseudomonas (Bac.
pyocyanus)
Klebsiella pneumoniae
Thermal Baccilli

Bowel Nosodes 2 Staph abdominalis

Strept faecalis
Enterococcus
Bacteroides
Pseudomonas

Bowel Nosodes 3 Typhiodinum sp.

Shigella dysenteriae
Cholera
Pasturella
Giardia

Bowel Nosodes 4 Tularemia

Clostridium welchii
Shigella sonnei

Bowel Nosodes 5 Acidophilous

Bifidus
Bulgaricus
Caucaucous
Lacto Baccilus (All)

Upper Respiratory Viruses Adenovirus

Rhinovirus
Coronavirus
Respiratory syncytial
virus
Retro Virus HLV 1-2
HLV 3-4-5
HLV 6-7-8
HLV 9-10-11-12
ARC

165
Influenzal Screen Influenza, all
varieties
Influenza A
Influenza B
Influenza current
year (79/80)

Enteric Viruses Retrovirus

Polio
Coxackie
Echo virus

Liver Viruses Hepatitis A

Hepatitis B
Hepatitis C
Cytomegalovirus
Epstein-Barr virus

Childhood Viruses Parotidinum

Rubella
Morbillinum
Roseola infantum
Herpes (All)

Protozoal Screen Malaria

Toxoplasmosis
Entamoeba histolytica
Strongaloides
Amoeba (All)

Fungal Screen #1 Tines

Aspergillus
Coccidiomycosis
Histoplasmosis
Blasto Hominus
(Mycosis)

Fungal Screen #2 Cryptococcus

Aspergillus
Sacromyces
Mycosis
Tycosporon

166
Fungal Screen #3 Candida Albicans
Candida Rugosa
Candida Stellerata
Candida Tropicalis
Candida Krusei

Venereal Group Syphilinum

Medorrhinum
Chlamydia
trachomitis
Mycoplasma (All)
Papiloma

Uric Acid Metabolic Group Acid uricum

Hypoxanthine
Kreatine
Glutamine
Oxalic Acidum

Lipid Group Screen Cholesterinum

Blycerinum
Acid acetessigsour-
aethylester (acetic
acid ethylester)
Acetone
Triglyceridus

Liver Miscellaneous Brucella abortus

Listeria monocytogenes
Leptospirosis
Tularemia
Glandular Fever

Urinary Tract Irritants Acid citricum

Acid sorbicum
Acid benzoicum
Terebinthina
Allergic Irritant

167
Nephrolithiasis Screen Acid oxalicum
Acid uricum
Calcarea
phosphoricum
Calcarea sulfuricum
Acid Nitricum
(Proteins)

Vaginitis Screen Candida albicans

Trichomonus
vaginalis
Haemophilus
vaginalis
Strep faecalis
Allergic Vaginitis

Accessory Lung Pathogens Chlamydia

psittacosis
Mycopolasma
pneumoniae
Parainfluenza viruses
Actinomycosis Israeli
Crypto Cystitis
Aspergillus
Histoplasmosis

Respiratory Tract Irritants Tobacco smoke

Auto exhaust fumes
Acid sulfurous
Asbestos
Allergic Irritant

Stimulant Screen #1 Coffee cruda

Tobacco smoke
Caffeine
Tea (Thea Chinese)
Sugar

168
Stimulant Screen #2 Salt
Animal fat
Theo-bromine
Adrenal stress protein

Salicylate Screen Acid salicylicum

Acid acetyl salicylicum
Food dyes
Sodium bisulfide

Heavy Metals 1 Arsenicum album

Plumbum metallicum
Cadmium met.
Merc. sol.
Molybdenum

Heavy Metals 2 Stannum met.

Aluminum
Cuprum metallicum
(copper)
Niccolum metallicum
(nickel)
Antimony

Heavy Metals #3 Barium

Germanium
Gold
Vanadium
Silver

Heavy Metals #4 Plutonium

(Radioactive) Uranium
Radium
Radon
Cesium

Parasite Screen #1 Giardia lambia

Enterobius
vermicularis
Ascaris lumbriocoides
Oxyures vermicularis
Blastohominus

169
Parasite Screen #2 Ancylostoma
Chilomastix
Diphylidium
Endolimax
Necator Americanus

Parasite Screen #3 Fasciola hepatica

Dicrocdelium
lanceatum
Hymenocepis
Schistosoma
Teania

Nerual Viruses Vaccininum

Variolinum
Varicella
Herpes zoster
Meningitis (Viral)

Neurotoxins 1 Tetanus
Botulinum
Q-fever
Scarlatinum
Salmonella

Neurotoxins 2 Hydrophobinum
Distemperinum
Arbovirus
Tick fever
Candida Albicanus

Herpes Group Herpes Simplex I

Herpes Simplex II
Herpes Simplex
Herpes Progenitalis
Herpes Zoster

Adrenal Screen Diptherinum

Toxoplasmosis
Tularemia
Meningecoccinum
Pseudomonas

170
Food Additive Screen Acid salycylicum
Butylated
hydroxyanasol
Sodium nitrate
Monosodium glutamate
Synthetic Chemicals
Addex

Dermatology Irritants Rhus tox

Niccolum metallicum
Petroleum
Benzoin
Hydro carbons (All)

Toxic Bowel Metabolites Indol

Skatol
Mercaptan
Thioether
Sulphur

Antibiotic Screen Penicillin

Erythromycin
Tetracycline
Sulfanilimide
Chemex
Synthetic Chemicals

Epidermals House dust

House dust mite
Cat/Dog hair
Feathers
House dust scale

Pollen Mix Grass mix 1, 2, 3

Tree mix
Weed mix
Flower Pollen
Grains

Mold Spore Mix Mold mix A

Mold mix B
T.O.E.
Candida albicans
FNG
Fungifuge

171
Phenol Group Acid carbolicum
Acid benzoicum
Creosole
Kreosotum
Phenols (All)

Hydrocarbon Group Ethyl alcohol

Petroleum
Kerosene
Diesel
Envrox, Enviro.
Industrial Pollutants

Miscellaneous Chemicals Formaldehyde

Acetone
Acid sulfurosum
Benzenium
Industriox
Industrial pollutants

Mutagen/Carcinogen Group Methylcholanthrene

Nitrosamine
Benzene
Chloroform
Phosphorous
compounds

Pesticides 1 Halogenated Hydrocarbons D.D.T.

Lindane
Hexachlorbenzol
Heptachlor
Insecticides

Pesticide 2 Organophosphates Malathion

Parathion
DDVP
Diazanon
Addex
Insecticides

Pesticide 3 Carbamates Dithiocarbamate

Aldicarb

172
Pesticide 4 Miscellaneous Paraquat
2, 4, 5, t-Ester
Dinitrokresol
Diquat

Dental Materials 1 Chrom Cobart

Molybdenum
Gold
Silver amalgam
Palladium
Amalgam
Dental Materials

Dental Materials 2 Phosphate cement

Carboxylate cement
Polymerisat
Zinc oxydatum
Phenol/Cresol

Gingival Screen Gingivitis

Ulcer gingivitis
Necrotic gingivitis
Amoebic gingivitis

Periodontal Screen Zahnfleistasche

Paradontose
Zahnsacken
Periodontitis
Parulis (Strep muc.)
Parulis (Staph aur.)

Pulpitis Screen Gangranose pulpa

Acute pulpitis
Chronic pulpitis
Toxic pulpitis

Periapical Screen Odonton Fudus

Root canal granuloma
Gangran granuloma
Radicular cyste

173
Jaw Lesion Screen Jaw ostitis
Exudative ostitis
Acute bacterial ostitis
Chronic bacteria ostitis
Infective ostitis
Injury ostitis

Foci Screen #1 Foci in right lower jaw

Foci in left lower jaw
Foci in right upper jaw
Foci in left upper jaw
Foci in cranium

Foci Screen #2 Foci in cranial vertebrae

Foci in cervical
vertebrae
Foci in thoracic
vertebrae
Foci in lumbar
vertebrae
Foci in sacral vertebrae

Foci Screen #3 Foci in palatine tonsils

Foci in adenoids
Foci in pharyngeal
tonsils
Foci in tubal tonsil
Foci in laryngeal tonsil

Foci Screen #4 Foci in maxillary sinus

Foci in cavernous sinus
Foci in sphenoidal sinus
Foci in ethmoid cell
Foci in frontal sinus

Foci Screen #5 Lesions in body

Foci in head area
Foci in right upper
quadrant
Foci in left upper
quadrant
Foci in right lower
quadrant
Foci in left lower
quadrant

174
Foci Screen #6 Right side brain
Foci in frontal lobe
Foci in temporal lobe
Foci in parietal lobe
Foci in occipital lobe
Foci in midbrain

Foci Screen #7 Left side brain

Foci in frontal lobe
Foci in temporal lobe
Foci in parietal lobe
Foci in occipital lobe
Foci in midbrain

Foci Screen #8 Neurological

Foci in (Ans) para-
sympathetic nerves
Foci in (Ans)
sympathetic nerves
Foci in (Cns) motor
nerves
Foci in (Cns) sensory
nerves
Foci in cranial nerves

Foci Screen #9 Digestive dist.

Foci in stomach
Foci in small intestine
Foci in large intestine
Foci in liver
Foci in pancreas

175
 INDICATED SCREENING GROUPS
FOR THE MERIDIANS AND VESSELS OF ELECTROACUPUNCTURE
ACCORDING TO DR. REINHOLD VOLL

SPLEEN

Sp4 Congenital 1, 2, 3
Liver viruses
Enteric viruses
Protozoan group
Heavy metals 1, 2

Sp3 Hepatitis viruses

Enteric viruses
Dental materials
Heavy metals 1, 2

PANCREAS

Pn1 Hepatitis viruses

Enteric viruses
Childhood viral
illnesses
Toxic bowel
metabolites
Bowel nosodes 1-4

Pn2 Upper respiratory

bacteria 1
Uric acid metabolite
group
Pn3 Childhood viruses
Hepatitis viruses
Enteric viruses
Bowel nosodes 1-4

Pn4 Lipid metabolic group

Heavy metals 1, 2
Childhood viruses

176
STOMACH Congenital 1, 2, 3
Upper respiratory
bacteria 1
Enteric viruses
Heavy metals 1, 2
Dental materials 1

LIVER Liver viruses

Enteric viruses
Congenital 1, 2, 3
Protozoal group
Bowel nosodes 1-4
Liver miscellaneous
Fungal group
Insecticide groups
Salicylate combo
Common antibiotics
Stimulant screen

GALL BLADDER Bowel nosodes 1-4

Lipid metabolite group
Protozoan group
Intestinal parasites

KIDNEY

Ki1 & Ki2 Bowel nosodes 1, 2

Nephrolithiasis group
Urinary tract irritants
Congenital 1, 2, 3

Ki2a & Ki3 U.R.I. bacteria 1, 2

Congenital 1, 2, 3
Heavy metals 1, 2
Food testing
Common stimulant
group

177
UROGENITAL

B1 67 Bowel nosodes 1, 2
Congenital 1, 2, 3
Venereal screen
Urinary tract irritants

B1 65, 64 (male) Congenital 1, 2, 3

Venereal screen
Protozoan group
Vaginitis group
Bowel group 1, 2

B1 65, 64 (female) Congenital 1, 2, 3

Venereal screen
Protozoan group
Vaginitis group
Bowel group 1, 2

LUNG Congenital 1, 2, 3
U.R.I. bacteria 1, 2
U.R.I. viruses
Influenzal group
Bowel nosodes 1, 2
Enteric viruses
Accessory lung
pathogens
Respiratory tract
irritants
Salicylate screen
Fungus screen

LARYNX/HYPOPHARYNX Use above nosode

screen as for Lung

LARGE INTESTINE Parasite screen

Protozoan screen
Congenital 1, 2, 3
Bowel nosodes 1-4
Enteric viruses
Liver viruses
Mutagen/Carcinogen
screen
Heavy metals 1, 2
Toxic bowel
metabolites

178
SMALL INTESTINE Congenital nosodes
1, 2, 3
Bowel nosodes 1-4
Enteric viruses
Liver viruses
Stimulant screen
Parasite screen
Protozoal screen

HEART Congenital 1, 2, 3
Influenzal screen
Enteric viruses
Liver viruses
Upper respiratory
viruses
Upper respiratory
bacteria 1, 2
Protozoal screen
Neurotoxin screen
Neural viruses
Herpes group
Heavy metals 1, 2
Common stimulants
Insecticide screen
Childhood viruses

NERVOUS SYSTEM Congenital1, 2, 3

Neural viruses
Neurotoxins screen
Childhood viruses
Protozoal screen
Enteric viruses
Liver viruses
Influenzal screen
Upper respiratory
viruses
Heavy metals 1, 2
Insecticides

179
MENINGES

ND 1b Congenital 1, 2, 3
Upper respiratory
viruses
Upper respiratory
bacteria 1, 2
Protozoal screen
Bowel nosodes 1-4

ND 1a Basic autonomic
screening protocol
Hydrocarbon group
Phenol group
Miscellaneous group
Food additive group
Stimulant group
Antibiotic group
Respiratory irritant
group
Toxic bowel
metabolites
Dental materials 1, 2
Root canal group
Heavy metal group 1, 2
Pesticide group 1-4
plus all nosode
groups for
Nervous System
groups

CIRCULATION Congenital 1, 2, 3
Upper respiratory
bacteria 2
Enteric viruses
Liver viruses
Heavy metals 1, 2
Dental materials
Mutagen/Carcinogen
screen
Neurotoxins 1, 2

180
ENDOCRINE - Triple Warmer Meridian

Tw1 (adrenal) Congenital 1, 2, 3

Tw1 (gonads) Adrenal screen
Refer to nosodes B1 65,
64 for male and female

Tw2 (Thyroid) Congenital 1, 2, 3

(Parathyroid) Upper respiratory
(Thymus) viruses
Enteric viruses
Upper respiratory
bacteria 1, 2
Heavy metals 1, 2
Dental materials 1

Tw3 (Pituitary) Congenital 1, 2, 3

(Pineal) Upper respiratory
viruses
Enteric viruses
Influenzal screen
Heavy metals 1, 2
Dental materials 1

ALLERGY VESSEL

Allergy 1 Food screens

Urinary tract irritants
Insecticide screens
Food additive screen
Dermatology
irritants
Stimulant screen
Parasite screen

ADG 1a Basic autonomic

screening protocol
Heavy metals 1, 2
Dental materials 1, 2

ADG 2 Pollen screen

Mold screen
Epidermal screen
Food screening

181
ADG 3 Pollen screen
Mold screen
Epidermal screen
Insect stings
Dental materials 1, 2

SKIN Congenital 1, 2
Childhood viruses
Upper respiratory
bacteria 1, 2
Refer to pancreas
Refer to liver
Dermatology irritant
screen
Mold screen
Food screens
Heavy metals 1, 2
Dental materials 1, 2
Toxic bowel metabolites

JOINT DEGENERATION & Congenital 1, 2, 3

FIBROID DEGENERATION Upper respiratory
(Connective Tissue) bacteria 1, 2
Enteric viruses
Liver viruses
Bowel nosodes 1-4
Dental pure culture
nosodes

LYMPHATIC VESSEL Congenital 1, 2, 3

Lyl, Lyl-La, Lyla (Tonsils, Pharynx, Middle Ear) viruses
Upper respiratory
bacteria 1, 2
Influenzal screen
Dental materials 1, 2
Dental pure culture
nosodes
Bowel nosodes 1

182
Ly3 (Nose and Paranasal Sinuses) Congenital 1, 2, 3
U. R. I. viruses
U. R. I. bacteria 1, 2
Influenza screen
Bowel nosode group 1
Remember to refer to
ADG 3, ND3a & Twla

Ly2a (Eyes) Congenital 1, 2, 3

U. R. I. viruses
U. R. I. bacteria 1, 2
Bowel nosodes 1
Enteric viruses
Protozoal screen
Fungal screen

Ly2 (Dental) Dental materials 1, 2

Root canal screen
Gingival screen
Pulpitis screen
Periodontal screen
(remember Tw2)
Periapical screen
Upper respiratory
bacteria 1
Dental pure culture
nosodes
Bowel nosodes 1
Jaw lesion screen

183
 AN OPERANT DEFINITION OF HOMEOPATHY

Homeopathy has been cloaked in mystery and misunderstanding, in

that there are many principles which have not fully done justice to the
complete range of homeopathic action. Many proponents use
homeopathy in vastly different ways making the field look confused and
irregular.
One of the misconceptions is that it is assumed that all things are
reversal in homeopathy that what a substance causes in a large dose it
will reverse in a minute dose. This is not always so, and we will dedicate
this chapter to that topic.
As is pointed out in the chapter on snake venoms, the Arndt-Schultz
law allows for the principle that what a poison might do at a raw dose, an
extreme dilution of that poison will often time produce a paradoxical
reversal of activity. If a patient were having a heart arrhythmia or
irregularity, rattle snake venom, which causes a proteolytic effect on
tissues and also has a cardio toxic effect on the heart muscles,
oftentimes in small quantities, can help reverse the arrhythmia and
stabilize the heart. The chapter on venoms and poison goes into this in
detail.
Dr. James P. Isaacs, in his book entitled Complementarity in Biology:
Quantization of Molecular Motion. (James P. Isaacs, John C. Lamb: John
Hopkins Press: Baltimore, 1969), points out another law of pharmacology
which is Wilders law of initial value. In Wilders law, if a substance is not
a poison, as we make it more and more dilute, one of three things will
happen: 1) it still could have a reversal, 2) there might be an increase in
the original effect, or 3) nothing may happen at all. This is Wilders law of
initial value. It is often used in pharmacology to chart out dose response
curves.
Many herbals, plants, glandulars, minerals, etc., are used in
homeopathy and are not poisonous. Some of these will not always have

184
reversal effects. A classic example often noted in the literature is that of
Eyebright. Eyebright is an herb used in homeopathy and herbal
remedies. The name was coined because of the products positive effect
on vision and the optic system. It helps make eyes bright. That is the
herbal indication for Eyebright. The homeopathic indication for it is
exactly the same. It is also used for vision problems, and to help patients
with optical disturbances. If everything in homeopathy were truly all
reversal, we would only use Eyebright on the patients who had vision
that was too perfect, because then the reversal effect of Eyebright in
homeopathic form would be that it would interfere with vision. This is
not the case.
It is also not the case in many types of sarcodal formulas. Thyroid
tissue has been demonstrated to have positive effects on the thyroid
system, and the thyroid hormone from the tissue can be utilized in cases
of hypothyroidism to stabilize thyroid function. In homeopathic form this
same thyroid tissue, as a sarcode, has the exact same indications. It can
also be utilized in the hypothyroid condition in which the patient has a
weak thyroid gland.
Examples of sarcodal remedies abound in this non-reversal action.
Adrenaline tissue, brain tissue, endocrine systems, heart tissue and the
like, all have the same indications homeopathically as they do in
glandular technology when used in raw dose. In all of these cases the
glandulars (sarcodes) are used to stabilize function. Thus, they can be
used in hyper or hypo cases. In the case of hyperthyroidism or
hypothyroidism, the thyroid sarcode might be used which helps stabilize
tissue. But it is not always reversal.
The sarcodal remedies, as we proved in the chapter on sarcodes, will
have a stabilizing effect in rejuvenating or increasing the probability that
healthy tissues will ensue in the organism. As the organism produces
new tissues in the thyroid, the cervical, the vertebrae, or wherever in the
body, the homeopathic sarcodal therapy can help to insure that healthy

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tissues will be built instead of unhealthy ones. The sarcodal forms of
homeopathics do not follow what is thought about homeopathy; that it is
all reversal of action.
Another example in homeopathy is the indications of calendula.
Calendula, which is taken from the marigold plant, has been used by
herbalists for centuries, if not eons, for different injuries. The
homeopathic indications for calendula are equivalent. Oftentimes
homeopaths will find that the dilute form of calendula can, in certain
cases, have increased activity in treatment of injuries, and trauma
conditions.
James Tyler Kent writes that homeopathic calendula cannot be denied
its ability to help in accident or injury cases. Another example is
Dioscoria villosa, known as wild yam. The herbal therapeutics of it is that
it is hepatic, stomachic, atonic, expectorant, anti-spasmodic, a sedative,
and an anti-asthmatic. Its herbal uses include colic, jaundice,
hardening/blocking of the liver, nausea (in pregnant women), cholera,
neuralgia, hiccups, whooping cough, bronchitis, etc. Homeopathic
indications are for painful afflictions of the abdomen, pelvic viscera,
feeble digestive powers, colic, gallstones, heart spasms, uterine colic,
back pain, and cramps. There are almost identical indications for the
homeopathic as for the herbal.
We now look at the herb Caulophyllum also known as squawroot or
blue cohosh. It is used as an anti-spasmodic, nervine tonic, diuretic,
anti-rheumatic, and anti-inflammatory. It is known as womans best
friend for the reason that it has a powerful effect on stabilizing womens
systems, and helping in the alleviation of cramps. This remedy is
excellent for spasms, epilepsy, uterine inflammation, and the like. If
everything worked in reversal, we would use the cohosh for the opposite
indications of its herbal.

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 Let us now look at the homeopathic indications. Oscar E. Boerickes
repertory calls it Caulophyllum, and it is a womans remedy. During
labor, when pains are present, the patient is exhausted and fretful. This
remedy is excellent in its ability to help birthing pains. It is good for the
stomach, dyspepsia, and all problems of the female system. It increases
stability of menses and leucorrhea, and works for stiff joints, etc. Here is
another example that the herbal recommendations are the same as the
homeopathic. Even using this in dramatically dilute form, at 30x, and
40x, there is stability in its action.
Another example is Blue Vervain, in Latin; Verbena. Its herbal
indications are that of a nervine tonic, anti-spasmodic, diaphoretic, and
beneficial for the stomach; astringent, fever-fugue, and antiseptic. Its
uses are for dyspepsia, indigestion, all liver conditions, kidney/bladder
complaints, amenorrhea, dysmenorrhea, hysteria, epilepsy, chorea,
nervous exhaustion, insomnia, diarrhea, nervous system, nervous
depression, weakness, spasms, and irritation. It promotes the absorption
of blood, and helps in pain and bruises. It is tremendously helpful for the
liver, insomnia, epilepsy, hallucinations, and mental exhaustion. Find
below a list of some of the formulas in the HPUS (Homeopathic
Pharmacopeia of the United States) which have similar indications
herbally as well as homeopathically.
As we go through the HPUS we will see that 65% or more of the HPUS
has similar indications herbally and homeopathically, making the two
modalities almost equal. By building this new definition into homeopathy
we can utilize the best of homeopathy, as well as naturopathy and herbal
therapy to help the American public demystify some of the homeopathic
reactions. This will give needed publicity as well as simplicity to allow
them to choose the system of homeopathy as a medical modality.
As can be seen from the dose-response curve in Figures 1, 2, and 3,
there are dramatic differences between the Arndt-Schultz principle of
poisons and Wilders law of initial value.

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LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Abelmoschus Aquilegi
Abies Nigra Aquilegia Vulgaris
Abrotanum Aralia Dispida
Achyranthes Calea Aralia Quinquefolia
Actae Spicata Arbutus Andrach
Adamas Areca Catechu
Adelheidsquelle Artemisia Vulgaris
Adonis Virnalis Arum Dracontium
Adrenaline Arum Italicum
Aesculus Glabra Arum Maculatum
Aesculus Hippocastanum Arum Triphyllum
Agave Americana Arundo Mauritanica
Agave Tequilana Asclepias Incarnata
Agnus Castus Asclepias Syriaca
Agrimonia Eupatoria Asimina Triloba
Agrostemma Githago Asparagus Officin
Aletris Farinosa Aspidosperma
Alfalfa Asperula Odorata
Alisma Plantago Avena Sativa
Allium Sativum Barosma
Alnus Glutinosa Bellis Perennis
Aloe Socotrina Berberis Aquifolium
Alstonia Constricta Berberis Vulgaris
Alstonia Scholaris Berberis Vulgaris, Fructus
Althaea Officinalis Beta Vulgaris
Ammi Visnaga Bixa Orellana
Ampelopsis Quinquefolia Boldo
Amygdalus Persica Borago Officinalis
Anagallis Arvensis Branca Ursina
Ananassa Brassica Napus
Anchusa Officinalis Buxus Sempervirens
Anemone Nemorosa Cacao
Anemopsis California Cactus Grande
Anethum Graveolens Cahinca
Angelica Archangelica Cajuputum
Angelica Atropurpurea Calcarea Acetica
Angophora Lanceolata Calcarea Lactica
Anthenis Nobilis Calendula Officinalis
Apium Graveolens Calotropis Gigantea
Apocynum Andro Calthapalustris
Aqua Marina Canlophylum

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LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION
Canchalagua
Canna Anjustifolia
Carduus Benedictus
Carduus Marianus
Carum Carvi
Cascara
Cascarilla
Castanea Vesca
Castoreum
Catalpa Bignonioides
Cataria Nepeta
Ceanothus
Ceanothus Americanus
Cedron
Celtis Occidentalis
Cephalanthus Occidentalis
Cerasus Virginiana
Cereus Bonplandii
Cereus Serpentinus
Cetraria Islandica
Chamomilla
Cheiranthus Cheiri
Chelidonium Majus
Chelidonium Majus, Radix
Chelone Glabra
Chenopodium Anthelminticum
Chenopodim Vulvaria
Chimaphila Maculata
Chimaphila Umbellata
Chionanthus Virginica
Chrysanthemum Leucanthemum
Cicer Arietinum
Cichorium Intybus
Cimicifuga Racemosa
Cineraria Maritima
Cinnamomum
Cistus Canadensis
Citrus Decumana
Citrus Limonum
Citrus Vulgaris
Clematis Virginiana
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Clematis Vitalba, Folia
Coccus Cacti
Cochlearia Armoracia
Cochlearia Officinalis
Collinsonia Canadensis
Comocladia Dentata
Conchiolinum
Condurango
Convolvulus Arvensis
Copaiva Officinalis
Cornus Alternifolia
Cornus Circinata
Cornus Florida
Crocus Sativa
Crataegus
Cucurbita Citrullus
Cucurbita Pepo, Flos
Cucurbita Pepo, Semen
Cuphea petiolata
Cydonia Vulgaris
Cynara Scolymus
Cypripedium Pubescens
Cytisus Scoparius
Daphne Indica
Dictamnus Albus
Dioscorea Villosa
Dirca Palustris
Dolichos Pruriens
Draba Verna
Drosera Rotundifolia
Dulcamara, Flos
Echinacea Angustifolia
Elaeis Guineensis
Elaterium
Epiiedra Vulgaris
Epigaea Repens
Epilobium Palustre
Epiphegus Virginiana
Equisetum Arvense
Erechtites Hieracifolia
Erigeron Canadensis
LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Eriodictyon Californicum Glycerinum

Erodium Glycogenum
Eryngium Aquaticum Glycyrrhiza Glabra
Eryngium Maritimum Gnaphalium Leontopodium
Erythraea Centaurium Gossypium Herbaceum
Ethylicum Granatum
Eugenia Caryophyllata Gratiola Officinalis
Eugenia Jambosa Grindelia
Euonymus Atropurpureus Guaco
Euonymus Europaeus Guaiacum
Eupatorium Aromaticum Guatteria Gaumeri
Eupatorium Cannabinum Gymnocladus Canadensis
Eupatorium Perfoliatum Haematoxylon Campechianum
Eupatorium Purpureum Hamamelis Virginiana
Euphrasia Officinalis Haronga Madagascariensis
Fagopyrum Esculentum Helianthus Annuus
Fagus Sylvatica Heliotropium Peruvianum
Ferula Glauca Helonias Dioica
Ficus Religiosa Hedeoma
Filix Mas Helleborus
Foeniculum Vulgare Hepatica Triloba
Fragaria Vesca Hoang-Nan
Franciscea Uniflora Homarus
Fraxinus Americana Hura Crepitans
Fraxinus Excelsior Hydrangea Arborescens
Fucus Vesiculosus Hydrastis
Galanthus Nivalis Hydrastis Canadensis
Galega Officinalis Hydrocotyle
Galium Aparine Hydrocotyle Asiatica
Galphimia Glauca Hydrophyllum Virginianum
Gambogia Hypericum
Gaultheria Procumbens Iberis Amara
Genista Tinctoria Ilex Aquifolium
Gentiana Lutea Ilex Paraguariensis
Gentiana Quinquefolia Illicium Anisatum
Geranium Maculatum Imperatoria Ostruthium
Geranium Robertianum Inula Helenium
Geum Rivale Iris Florentina
Geum Urbanum Iris Foetidissima
Ginkgo Biloba Iris Germanica
Glechoma Hederacea Iris Tenax

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LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Iris Versicolor Magnesia Grandiflora

Jacaranda Caroba Mandragora Officinarum
Jalapa Mangifera Indica
Juglans Cinerea Marrubium Bulgare
Juniperus Communis Matica
Juniperus Virginiana Melissa Officinalis
Justicia Adhatoda Menispermum Canadense
Kamala Mentha Piperita
Karaka Mentha Pulegium
Kousso Mentha Viridis
Laburnum Anagyroides Mentholum
Lacerta Agilis Menyanthes Trifoliata
Lachnanthes Tinctoria Mezereum
Lamium Album Millefolium
Lappa Major Mimosa Humilis
Lathyrus Sativus Mitchella Repens
Lecithin Momordica Balsamina
Lemna Minor Musa Sapientum
Leonurus Cardiaca Myosotis
Lepidium Bonariense Myrica Cerifera
Leptandra Virginica Myristica Sebifera
Lespedeza Captiata Myrrha
Levisticum Officinale Myrtus Communis
Liatris Spicata Nabalus Serpentarius
Lilium Tigrinum Narcissus Pseudo-Narcissus
Linaria Vulgaris Nasturtium Aquaticum
Linum Usitatissimum Negundo
Lonicera Periclymenum Nepeta Cataria
Lonicera Xylosteum Nux Moschata
Lophophytum Leandri Nymphaea Odorata
Luffa Operculata Ocimum Basilicum
Lupulinum Ocimum Canum
Lycopersicum Esculentum Oenothera Biennis
Lycopodium Clavatum Oleander
Lycopus Virginicus Oleum Carvi
Lysimachia Nummularia Ononis Spinosa
Macrotinum Onopurdum
Magnesia Carbonica Opuntia Vulgaris
Magnesia Muriatica Oreodaphne
Magnesia Oxydata Origanum Majorana
Magnesia Sulfurica Ornithogalum Umbellatum

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LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Ostrya Primula Vulgaris

Ovi Gallinae Pellicula Prunus Padus
Oxalis Acetosella Prunus Spinosa
Oxydendrum Arboreum Prunus Virginiana
Paeonia Officinalis Ptelea Trifoliata
Pareira Brava Pulsatilla
Parietaria Officinalis Pulsatilla Nuttalliana
Paronichia Illecebrum Pyrus Americana
Parthenium Quassia Amara
Passiflora Incarnata Quebracho
Pastinaca Sativa Quercus Robur
Paullinia Pinnata Ranunculus
Paullinia Sorbilis Ratanhia
Pecten Rap Hanns
Pediculus Capitis Rhododenrom
Penthorum Sedoides Rhus Aromatica
Persea Americana Resina Laricis
Petroselinum Sativum Rhamnus Californica
Phaseolus Rhamnus Cathartica
Phellandrium Aquaticum Rhamnus Purshiana
Physalis Alkekengi Rheum Officinale
Phytolacca Ricinus Communis
Pichi Robinia Pseudoacacia
Pimenta Officinalis Rosa Canina
Pimpinella Saxifraga Rosa Damascena
Pinus Lambertiana Rosmarinum Officinalis
Pinus Sylvestris Rubia Tinctorum
Piper Methysticum Rumex Acetosa
Piper Nigrum Rumex Crispus
Piscidia Erythrina Rumex Obtusifolius
Plantago Major Russula Foetens
Platanus Ruta Graveolens
Plectranthus Fruticosus Sabadilla
Plumbago Littoralis Sabal Serrulata
Polygonum Punctatum Salix Alba
Polygonum Sagittatum Salix Nigra
Populus Candicans Salix Purpurea
Potentilla Anserina Salvia Officinalis
Pothos Foetidus Sambucus Canadensis
Primula Obconica Sambucus Nigra
Primula Veris Sambucus Nigra

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LIST OF HOMEOPATHIC REMEDIES WITH SIMILAR HERBAL ACTION

Sanicula Thlaspi Bursa Pastoris

Sarracenia Purpurea Thuja Occidentalis
Sarsaparilla Tilia Europaea
Sassafras Officinale Tormentilla
Schinus Molle Torula
Scolopensrium Vulgare Trifolium Pratense
Scutellaria Lateriflora Trifolium Repens
Sedum Acre Trillium Pendulum
Semper Vivum Tectorum Triosteum Perfoliatum
Senecio Aureus Triticum Repens
Senecio Jacobaea Tropaeolum Majus
Senega Officinalis Turnera
Senna Tussilago Farfara
Sepia Tussilago Petasites
Sinapis Ulmus Fulva
Sinapis Nigra Uricum Acidum
Skookum Chuck Urtica Dioica
Solanum Carolinense Urtica Urens
Solanum Mammosum Usnea Barbata
Solidago Virgaurea Uva Ursi
Spartium Scoparium Valeriana Officinalis
Spigelia Marilandica Verbascum Thapsus
Spilanthes Oleracea Verbena Hastata
Spinacia Verbena Officinalis
Spiraea Ulmaria Viburnum Opulus
Stellaria Media Viburnum Prunifolium
Sterculia Acuminata Viola Odorata
Sticta Pulmonaria Viola Tricolor
Stigmata Maidis Wiesbaden
Stillingia Sylvatica Wyethia Helenioides
Sumbul Symphoricarpus Xanthoxylum Fraxineum
Racemosus
Symphytum Officinale Yucca Filamentosa
Taraxacum Officinale, Radix Yohim Binum
Taxus Baccata Zingiber Officinale
Teucrium Marum
Teucrium Scorodonia
Thaspium Aureum
Thymus Serryllum
Thea Sinensis
Theobrominum

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 SUMMARY

As can be seen from this brief list of examples, much of homeopathy is

not always reversal; much of it is very similar to the action of herbal
therapy.
In herbal homeopathy, the minimal dose of an herb can achieve an
effect. Herbology and homeopathy might join forces to become a more
powerful form of medicine.
In 1962, the FDA developed a new Food and Drug Cosmetic Act, which
let homeopathy in the HPUS, as well as the USP (United States
Pharmacopeia). In 1962, they did not include the Natural Compendium
of Herbs which was supplied before 1962. This was because of an
inability of herbalists to agree and to actively support themselves in the
development of their Natural Compendium.
Now we are going to provide a new description and definition of
homeopathy which includes herbal precepts and reinstate herbalism
under our new HPUS guidelines. Since homeopathy and herbalism share
so much, and since the HPUS provides a legal backdrop for doctors to
have NDC (National Drug Code) coded formulas within the HPUS, it is
possible to include these different herbs and their activity within our
guidelines.
Homeopathy need not always involve using dramatically dilute
substances. Mother tinctures, 1x, 2x, and 3x, are often high
concentrations and yet this is still homeopathy.
Let us explore the description of an opposite to homeopathy, which is
allopathy. In allopathy we are working against the body, just as the
allopath might use an antihistamine when the patient has a histamine
response. By using an outside intervention the practitioner intervenes
with the body so that the body will have time to heal itself. Thus, if there
is a histamine response due to some causative factor, the allopath would
use an antihistamine to help block the histamine, hoping that he/she

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provides enough of a buffer to stall, so that the body can overcome the
disease. Allopathy is not dealing with the true cause (rarely is the cause
of the disease the fact that the person is deficient in the antihistamine or
other drug). Oftentimes, histamine release is prompted by allergic
activity, nutritional disturbances, chemical imbalances, and the like. The
patient can sometimes build a dependence on these allopathic
medications, as they will help the symptom, not the disease, and thus,
will build dependence. This can often be beneficial to the synthetic
chemical companies, but not to the patient.
Allopathy seeks to provide an outside intervention from the smart
doctor to the stupid patients body, to try to sedate, block, stimulate,
trick or fool the system with a synthetic pharmacological agent. Allopathy
can be seen as a heterogeneous type of medicine in which the
intervention comes not from within the system, but from outside the
system. In homeopathy, however, we provide the minimal dose of activity
from our agents to allow the human system of the patient to achieve its
balance through its own cybernetic feedback control.
Homeopathy develops healing forces from within, or homogeneously,
whereas allopathy does it from outside, or heterogeneously. The
homeopath tries to work with the patients body to stimulate it towards
healing and homeostasis balance. The principle of homeostasis implies
that the body will seek to try to balance its activity along the lines of a
certain degree of function. Thus, in maintaining calcium balance, the
parathyroid and thyroid hormones will help to regulate calcium,
oftentimes by taking calcium out of the bone to maintain serum calcium
or by appetite control to drive the appetite toward different foods to
balance our calcium intake. A very intricate sense of balance is needed
for the extremely complex job of homeostasis.
The whole principle of homeopathy relies on the study of homeostasis.
In homeopathy, an herb is used only to provide the stimulus for the body
to heal itself. The minimal dose is sought. Thus, Eyebright might help to

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supply the needed nutrition and the needed pharmacological agents to
help the patients body to rejuvenate its optical system, and achieve
health. This implies a homogenous stimulation of homeostasis which is
homeopathy.
Our definition of homeopathy is: Homeopathy is the medical art of
gently stimulating the patients body toward balance and homeostasis.

Some dictums of homeopathy:

The human body is complex beyond our understanding, so we

must work reverently with it to encourage health and balance from
within.

Disease results from violation of natural law, and disease

symptoms are a message from the body as it attempts to deal with
the causative agent. Symptoms are beacons and traffic signals
which point to cures. Symptoms are not the enemy as believed by
allopaths.

Cure must come from removing or reducing the cause of disease,

and then stimulating balance and homeostasis.

The healing of nations shall come from the leaves of the field. Only
nature knows the intimate details of cure, and only nature can
manufacture truly curative agents.

Homeopathy, herbology, acupuncture, and naturopathy have more

in common than originally believed. Together with other similar
modalities they represent a new era in medicine.

Our broadened viewpoint of homeopathy lets the techniques of

herbology to be used to their fullest proficiency. This allows the different
herbal manufacturers to have a professional naturopathic and
homeopathic philosophical governmental agency through the HPUS to
guide them in quality control and legal direction. This broad-based
definition of homeopathy has existed for years, and yet because of the
mystery of homeopathy in like treating like, oftentimes it is categorized

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as only like treating like. With this new, broader definition, and by
utilizing the forces of different homeopathic practitioners and
manufacturers to propagate this definition to the American public, they
can get a better idea of how homeopaths are able to help in dramatic
ways to stabilize and balance their bodies. Our herbal repertoire also will
bring Chinese herbals into the system and let legally controlled
manufacturers supply quality Chinese herbs with a proper national drug
code to doctors.
It is hoped that this chapter and the rest of this Natural Repertory will
help to clear up some of the myths and misunderstandings in regard to
homeopathy in its practical use. Homeopathy represents an inexpensive
modality of medicine which is safe and effective in treating a wide variety
of medical ills. In the 1990s, the American culture was severely
threatened economically, and overburdened by a medical system that
clung to allopathic synthetic pharmacology and surgery. These measures
are not only drastically expensive and environmentally unsafe, but they
are not cures. Allopathy is needed in medicine as a last resort in keeping
some patients alive. The baby must not be thrown out with the bath
water. Allopathy will always be a part of medicine. But allopaths should
learn the fallacies of their techniques. They do not seek to bring patients
to balance or cure. They only seek to develop dependency on different
items in the lost hope that patients bodies can regain balance before the
synthetic drugs do their damage to kidneys, liver, nerves and digestion.
Allopaths treat symptoms. To this end, homeopathy offers economic
solutions, the development of safe and effective modalities, and help in
returning to a system of reverence for the natural process of our bodies
and the natural process of the ecological system of the world.
One day medicine might overcome its egocentric biases, and teach all
techniques and philosophies together under one true medicine. A new
day will dawn in which healers will learn to appreciate each other and
help patients, rather than propagate egos.

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 AN ADVANCED TREATISE IN QUANTUM BIOLOGY
The Quantic Link to DNA

The father of quantum theory was Erwin Schrdinger. He believed that

there was a definite link between quantum theory and DNA. As we have
reviewed several parts of biological literature in this book, we now would
like to review a brief introduction on quantum theory and genetic coding.
Here we see the best demonstration of a quantum biological function, as
the formation of the DNA code does not utilize half-steps; it makes
distance coding jumps. There are distinct patterns in the DNA code that
allow for exacting patterns. In hereditary techniques we can see that
there is a preciseness of transfer which yet has some degree of
indeterminacy. As we have discussed in the Quantum Biology and in this
workbook, there must be a metabolic side as well as a reproductive side
to our matrix, so that the metabolism can respond to a wide variety of
different types of environmental conditions. But the genetic coding would
have to have very limited, predictable and distinct types of jumps. It
would have to be a more precise and closed process. We have already
discussed this in some detail (see Quantum Biology). Now, let us review
some of the literature which has led to our understanding of DNA
function.
In the early days, there were three categories of food: oleaginous (fats),
saccharinous (carbohydrates), and albuminous (protein). The
development of protein was a key factor in the development of life. It is
protein which is analyzed in our treatise on DNA. Jns Jakob Berzelius
proposed the names of cystein and glycine as he was doing research on
amino acids. In 1838, he coined the word protein, which is Greek for
primary substance. He found that this was the basic unit of all
albuminous material. Gerardus Johannes Mulder, also working in the
very early 1800s, continued some of the Berzelius work. He proposed a

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basic albuminous substance with an empirical formula C40H62N10O12; this
combined with many other formulas produced some of the basic proteins
of life.
In the 1890s, Emil Fischer, who was once a student of August Kekul,
found that there were dextro and levo types of polymers. He was the first
to find that there was a chirality, or handedness to nature. He then
found that this handedness also applied to protein compounds.
In the 1850s, Thomas Graham found crystalloids and colloids, and
studied their functions. Colla came from the Greek for glue. Theodor
Svedberg contributed evidence to the theory that proteins were
homogenous. Using Avogadros number and the weight of the large
colloidal particles, he determined their diffusion rate and sedimentation
as a constant in the earths gravitational field, producing up to 500 times
the force of gravity. He then separated these colloidal factors, and helped
to further the concept of homogeneity.
By 1936, Linus Pauling and Alfred Mirsky put forth the idea that
polypeptide chains of native proteins could be folded and held together
between the N/h group and the oxygen atom of the C//O group of
peptide bonds. Many different scientists, including Corey and Perutz,
started working with these large chemicals and proposed some of the
different fashions which led to the discovery of the helix.
John Kendrew was the first to find the three-dimensional structure of
myoglobin which has an approximate molecular weight of 17,500. He
found that 75% of myoglobin has a helical polypeptide chain. Thus, the
helix was further brought into science.
The three-dimensional structure of insulin was discovered in 1969, by
Dorothy Crowfoot Hodgkin, working at Oxford University. Other bio-
molecules were found, such as cholesterol, calciferol, penicillin, and B-
12, using x-ray photographs of the diffusion patterns of the insulin
crystal. Dorothy Hodgkin was able to propose the structure of this very
complex molecule. Insulin was the first native protein to be synthesized.

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 In 1966, Robert Bruce Merrifield developed insulin by means of a
machine which was designed to carry out polypeptide synthesis.
Synthetic chemistry was well underway, and the precept of synthetic
chemistry to this day has been that of placing the calcium, carbon, and
hydrogen in the right spots. This was achieved by looking at the x-ray
photographs and diffraction patterns, doing spectrographic analysis, and
other different functions. But they were not able to discern the type of
energy that existed in the quantic bonds, or of the electrons in their
outer rings. Nature still has many secrets.
Some of the different quantic energy patterns of the natural substances
still were unknown to these synthetic developers. The synthetic
developers sought to develop synthetic compounds but found that they
were not as effective as natural entities. This did not hinder them in the
least; they achieved extreme financial success through their synthesis.
They were able to develop and manufacture compounds and live off
rather rich royalties as these synthetic compounds were sold as
medicines. As they reduced the complex world of natural biology into
synthetic components they developed more and more compounds. Many
were to follow after insulin.
Lets take a look at some of the first work that was done with insulin. It
was founded to be only 3.4% effective at best in the early crystalline
structure designed by Merrifield. Later, in the 1960s, scientists started to
dispel the idea that organic substances were different from the synthetic
matter which they were developing. Because of the limits of their thought
and the limits of their techniques of measurement these compounds
appeared to be equal. This is not the case in the 1990s. With our
sophisticated energy equipment and methods of discerning the energy
patterns and electrical responses of compounds, we now find that nature
does indeed have some rather complex safeguards and complex secrets
which the synthetic chemical companies have yet to divine.

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 In 1986, Carl Popper delivered an address to the Royal Society. In this
address he told the attendees, who included many of the fathers of
synthetic molecular biology, that biochemical organizations and
processes could never be understood in chemical terms alone. Because of
this, Popper proposed that organic evolution would never be explained by
chemical or Darwinian Theory and that chemical reductionism for the
environment proposed many different risks, as we put many of these
synthetic chemicals into our environment and our bodies. In fact, due to
the large number of chemicals which have been put into our bodies,
perhaps Carl Poppers warning has come too late. Many dramatic
problems have resulted from iatrogenic poisoning of the planet and
iatrogenic diseases which were caused by synthetic compounds.
Dramatic damage has resulted from ignorance and profiteering.
Mans ability to understand is always limited by his ability to measure
the results of his work. At every point in science the scientists assume
that their measurements are complete, therefore their knowledge must
be complete. As new discoveries are made and more sophisticated
measurement techniques are developed this philosophy opens the door
to deeper and deeper understanding. With the advent of quantum theory
and the idea of the Heisenberg Uncertainty Principle we now realize that
true knowledge cannot be attained, and that we cannot in any way
manufacture the same compounds developed by nature. Our attempts at
this are merely guesses, perhaps good guesses but still, nature holds
secrets as we continue to explore biology to the end of our days. Only
nature truly knows.
In 1893, Albrecht Kossel, doing physiological research identified
chromatin as a nucleoprotamine. This was found to be a nucleoprotein,
and was some of the beginning work needed in looking at RNA and DNA
function.
Nucleic acid sugars and their phosphate-bonded brothers were written
about by Phoebus Levene in 1905. Levene, working with Walter A.

201
Jacobs, classified sugar of yeast nucleic acids as D-Ribose. This is linked
to the bases by a glycosidic bond. They termed these nucleosides.
Adenosine, guanosine, cytidine, and uridine, when esterified by
phosphates, became adenylic acid, guanylic acid, cytidylic acid, and
uridylic acid. It was Levene who later found that this sugar is RNA and
DNA was not a hexose, but a pentose.
Early determinations of the molecular weight of DNA gave values of the
order of 103. In 1938, Frederick Sanger proposed that its weight was 106.
Levene also was able to confirm this new molecular weight in 1938.
In 1944, at the Rockefeller Institute Hospital, Oswald Avery came up
with the first strong evidence that DNA was really the key to transferring
genetic characteristics in microbes. Avery also proposed some of the DNA
enzymes, such as DNA depolymerase and deoxyribonuclease. These
enzymes were found to deactivate DNA, but were later key in the process
of unfolding and unwinding the DNA to set genetics in motion.
In 1945, DNA was found to have light absorption in the area of 260
nanometers, and to have some mitogenic-like production of UV. These
purines and pyrimidines were also found to have strong light
relationships; both absorption and production.
Erwin Chargaff in 1950 was able to show some of the strong light
spectrophoto reaction of the different components of DNA and DNA itself.
From this, the research finding adenine, guanine, cytosine, and thymine,
or A, G, C, and T, led to the discovery of the different Chargaff rules.
First, the total of purines and pyrimidines are quantitatively equi-
molecular; that is, A + G = T + C. Second, the molecular quantities of
adenine and thymine individually are equal: A = T. Third, the amounts of
guanine and cytosine are molecularly equivalent; G = C. A relation of the
preceding rules comes to the final rule in which A + C = G +T. Later, it
was found that uracil took the place of thymine in the RNA components
of the cell. These rules echo our quantum rules in many ways.

202
 Many people around 1950 were struggling to find ways of
understanding this. But it was Crick and Watson at Cambridge who best
improved on Paulings research, using the Chargaff rules and developing
a consensus idea of the structure of DNA. They proposed a double helix.
This opened the door for dramatic understanding.
The mechanics of this process could be easily understood by the
mechanically-minded scientists of the time. Yet, this type of mechanical
process did not appear in any other chemical process. Chemical
processes were known to be statistical, or involving random development
of compounds which were pushed and pulled apart through entropic or
thermodynamic processes. This strand of DNA does not do this; it is not
a randomized process. It pulls apart and pushes together in a very
precise maze. The actual mechanisms of this push and pull were not
studied by these scientists; they liked the idea of the chemistry involved.
But now, we can ask the question: Through what processes is DNA
pushed/pulled apart? The answer leads to quantum dynamics. Our
quantic analysis matrix can be superimposed on the DNA action.
Research blossomed into the concept of the mechanics of DNA. As
Isaacs has told us, the E. coli is an example of a type of near vion from
cells, meaning the base amount of matter needed to actually make up a
living unit which could metabolize and reproduce on its own. Inside the
E. coli is a doublestranded DNA chromosome which contains 4 x 106
base pairs. It will reproduce at maximum rate of 750 base pairs per
second. This is at a given unwound replicating fork region. So it will take
about forty minutes to reproduce a complete chromosome. If the
conditions are right, E. coli will divide into two daughter cells every
twenty minutes. This is the nature of vionic activity.
In 1953, Paul Zamecnik, working at Harvard University, tried to put
radioactive isotopes of different amino acids into a bacteria colony. This
was an attempt to trace the radioactive polypeptides through the
different ribosomes. The experiment was a failure because by putting in

203
the different radioactive isotopes the RNA functioning came to a halt. It
could only be brought back by bringing in a fresh, natural selection of
the amino acids. Thus, DNA has some ability to possibly know that the
items involved are radioactive. This would be reinforced by our quantum
theories; if a radioactive particle were put into this process, the biology
would soon be able to know it and halt its progress. Biology and life
operate on many levels including sub molecular. The process would be
able to notice radioactivity as an irregularity.
This makes us wonder about the different radioactive tracing
experiments in which radioactive iodine was put into the body by
experimenters who found that it goes to the thyroid; and then it was
assumed that all iodine would go to the thyroid. All we know from that
experiment is that radioactive iodine goes to the thyroid. We do not know
where normal iodine goes. This is another limitation of quantic theory.
Tracing experiments have led to many faulty conclusions in biology.
Electron microscopists started to come up with ideas of transcription
and translation of the ability to handle RNA and DNA. But basically, at
the relative body temperature E. colis DNA is transcribed at a rate of
around sixteen nucleotides per second into the messenger RNA strand.
The messenger RNA strand has an average length of 2,000 to 3,000
nucleotides. The half-life of the messenger RNA strand is about 90
seconds. So the ten to fifteen ribosomes which are in the process of
translating with a given messenger RNA and forming a polyribosome
become attached to the strand during the period of transcription from
the DNA. Polypeptides formed by each ribosome of a polyribosome
system are the same. The formation time of a polypeptide is around ten
seconds under certain prime conditions.
The growing E. coli bacteria contain some 15,000 ribosomes. They
make up 25% of the cell mass. The ribosome is approximately 20
nanometers across and has a molecular weight of 2.7 x 106.

204
 By 1966, many of the details of the genetic code were worked out, 61
out of the total 64 triplet codons.
From the late 1950s, the sequence of amino acids in proteins with a
specific function, such as insulin, hemoglobin, or cytochrome c, were
determined and catalogued by a range of organisms followed a decade
later by corresponding determination of nucleic acid sequences. In
analyzing the sequences then available, Zuckerkandl and Pauling (1965),
pointed out that a present-day protein contains its own ancestral history
in its quantic organization, and that similarities of homologous
polypeptide chains along with the accepted fossil record provide
evolutionary data of three types.
The probable amino acid sequence of the ancestral polypeptide
from which the chains compared had diverged.

The approximate epoch at which the divergence started.

The lines of descent through which the alterations in amino acid

sequence proceeded.

The vast extent of data storage and processing that was proved in our
quantic chapter easily allows for this process.
Zuckerkandl and Pauling calculated a mean substitution rate for a
hemoglobin polypeptide of one amino acid every 14.5 million years from
the 18 residue differences attained in comparison of the horse and the
human chain. It was known that the and the chains of the
human hemoglobin tetramer (22) show 78 differences so one can
surmise that the two polypeptides originally split from a common origin
by gene duplication at least 565 million years ago. Originally, the
common point was monomeric hemoglobin consisting of a single
polypeptide chain. This chain has a more modern representation in the
blood of primitive jawless fish (the lamprey and the hagfish, which lack
the advantage of cooperative oxygen uptake and release that emerged
with the evolution of the hemoglobin tetramer).

205
 A similar technique to that of Zuckerkandl and Pauling with their
construct of a molecular evolutionary clock was put forward by Motoo
Kimura. They used a Poisson distribution. Thus, the events of low
probability in a vast population like the decay of radioactive isotopes
used to calibrate the geological evolutionary clock are mathematically
calculated. Kimura posted that for two homologous polypeptides made of
n residues with varying amino acids at d sites due to bifurcation over a

time t, the rate of evolutionary amino acid substitution per site per years,
kaa, is given by the relation

2tkaa = -1n(1 d/n) - -2.31og(1 d/n).

This equation, applied to a series of sequenced polypeptides with a
common biochemical role such as the chain of vertebrate hemoglobin
will result in a constant value of kaa of the order of 10-9 residue
replacements per site per year, a unit that M. Kimura termed the pauling
or the molecular evolutionary unit (MEU). This is allowed for in our
bioquantic matrix. Life must allow for some minute variations to occur in
its reproduction accounting system. Varying slightly for a given type of
protein, the value of the kaa varies readily for proteins of contrasting
functional types by three orders of magnitude. This ranges from the
rapidly evolving fibrinopeptides (8.3 MEU) to the well conserved histone
proteins (0.009 MEU). The fibrinopeptides are key in the formation of
blood clots, and only a minuscule part of the polypeptide has an
essential function. The amino acids of the other segments freely undergo
substitution without the benefits of selective control. This process
involved no drastic functional changes. Comparatively, histone
polypeptides are essential in the conservation of the genetic material,
making up the nucleosome particles where the double-stranded DNA
supercoils in the eukaryote nucleus to provide the nucleoprotein
chromatin whereby a string of beads form.

206
 The MEU, or one Pauling, is a definite quantic type of function. Our
bioquantic matrix must tolerate some limited variations. These variations
can result in genetic improvements from genetic bifurcation (see
Fractals in Quantum Biology). But, for these variations to last they
must result in increased productivity. Increased productivity comes from
cooperation with the environment, not superiority. So Darwin was wrong
about survival of the fittest. Now, we can say that there is survival of the
adaptive and cooperative.
The histone proteins are stabilized and conserved. They have only two
differences out of about 100 amino acids in the H4 polypeptide between
calf thymus and the pea plant even though animals and plants split
apart some 1.2 billion years ago.
Contrasts of the mRNA sequences coding for the histone H4
polypeptide in two sea urchin species demonstrates that the synonymous
mutation rate in the DNA transcribed is as high as that of the fast
evolving fibrinopeptides. The degeneracy of the genetic code is eminent
for the third position (3 end) of the coding base triplets. Here the
transitional mutations (U/C) or (A/G) are mostly inert. Comparison of
the mRNA sequences coding for the and the polypeptide chains of
mammalian haemoglobin demonstrate that natural selection has lowered
the rates of surviving base changes in the first and second positions of
the triplet codons which are approximately equal+ to one-quarter or less
of the mutational rate found for the third codon position. Quantum
theory is consistent with such processing. Schrdinger was right in
assuming that genetics is a quantic activity. Genetics or reproduction
requires an exacting and limited process. Metabolism requires vast
responsiveness.
The archaebacteria characteristically thrive in extreme environments,
hot sulphurous vents, salt marshes, or anaerobic organic-rich muds.
Archaebacteria are ancient, as the term archae implies. They have

207
heterogeneity of their 16S rRNA sequences due to divergence over aeons.
As Isaacs points out jumps in species and genes also must follow quantic
law. The indices of those 16s rRNA sequences distinguish three major
divisions:
The methanogens and halophiles
Thermoplasma, a group containing a single organism
A heterogeneous group of sulphur-dependent
thermoacidophiles, probably the most ancient of the
prokaryotes

These bacteria can live under acidic conditions (pH 1-6) and at elevated
temperatures (60-95 C). Sulfolobus oxidizes sulphur to sulphate while
others reduce sulphate to sulphide, like Archaeoglobus which develops
small quantities of methane as well. These are some of the extremes of
life, or conditions in which the matrix of life can operate.
The 16S tRNA sequences of the eubacteria indicated that, while Gram
positive organisms form a distinct group of related species, gram negative
organisms are much more diverse. The break into nine groups is defined
by a common coefficient of 0.2-0.3 within a group. Most Gram negative
bacteria belong to the purple bacteria group which has not only the
colored photosynthetic organisms but also many colorless analogues.
Samples of these analogues are E. coli and other enteric bacteria. The
green photosynthetic bacteria also go into two distinct groups ~
Sulphur (hydrogen sulphide substrate)
Non-sulphur (organic substrate) types
which are not closely related (SAB 0.18). The cyanobacteria consist of a
coherent group, and they are similar to the chloroplast organelles of
eukaryotic red and green algae, and green plants (SAB values of 0.25
0.30). If a quantum leap is performed in the genetic code of bacteria,
then this will result in a new type of bacteria.
The sulphate-reducing bacteria which use the oxygen of the sulphate
for a primitive form of respiration comprise a Gram negative eubacterial

208
group. A type of bacteria in this group, Desulfovibrio sulfodismutans, can
attain free energy from the disproportionation of sulphite or thiosulfate to
sulphide and sulphate. This is an inorganic fermentation process
similar to the redox disproportionation of glucose to ethanol and carbon
dioxide (Bak and Cypionka 1987).
Thus, we can plot genetic changes on a hermitian matrix. This allows
us to develop new energetic laws of biology.
The eukaryote organelles, the mitochondrion, and the chloroplast all
share a prokaryote size (1 m). They are vions that contain their own
DNA. These vions also have a circular double strand as in bacteria, and
ribosomes of the bacterial type. The 165 rRNA sequences of the
organelles tell us that the mitochondria belong to the purple group of
eubacteria and the chloroplasts to the group of cyanobacteria.
Indigenous DNA in the organelles and the sameness of their 16S rRNA
sequences to those of extant eubacteria led to the theory that
mitochondria and chloroplasts evolved by a process of endosymbiosis.
This theory hypothesized that ancestral eukaryote with a vacuole
nutrient method of securing nutrients into a membrane-bounded vacuole
once engulfed a purple-group aerobic bacterium generating ATP through
the respiratory chain. As the guest supplied ATP, the host archae-
eukaryote provided back to the guest proto-mitochondrion the materials
required for its maintenance and ATP production. So, mutual vionic
patterns merged for symbiotic cooperation. The phagocytosis of a
cyanobacterium into a vacuole led to the development of the chloroplast,
which supplied carbohydrate to its host. In return, the cyanobacteria
supplied a life-support system. The two membranes around the organelle
are leftovers of the endosymbiotic beginnings. The inner membrane
represents the cytoplasmic membrane of the eubacterial guest. The outer
membrane corresponds to that lining supplied from the vacuole of the
host eukaryote. In vionic coupling sometimes functions can be presented

209
dually. Quantum laws can still be obeyed. Backup systems are
abounding in biology.
Possible relatives of the ancestral eukaryote, as many as a thousand
species, have no mitochondria or other organelles. These species split
from vion tendency to form the archaezoa subdivision of the eukaryotes,
just as the metakaryota, which contain mitochondria, is an example of a
vion. Sequenced representatives of the archaezoa are minute parasites of
the metamonada and the microsporidia. These vions contain bacterial
sized ribosomes with 16S rRNA in the smaller subunit. They dont have
the 18S rRNA found in the higher eukaryotes. The 16S rRNA sequences
of a microsporidia and a metamonada species differ greatly from
mitochondrion containing eukaryotes, the metakaryota. This suggests
an early vionic divergence. The archaezoa and the metakaryota split
before the age (1.4 billion years) of the larger microfossils (10 m) which,
on account of their size probably represent the remains of organelle
equipped eukaryotes (CavalierSmith 1989). We can see this vionic
divergence in our matrix.
Biochemically, the eukaryotes share similarities with both the
eubacteria and the archaebacteria. The translation of mRNA into a
polypeptide starts with methionine in the eukaryotes as it does in the
archaebacteria. But translation starts with N formylmethionine in the
eubacteria. Elongation of the polypeptide chain is stopped by dipthera
toxin in the eukaryotes and the archaebacteria but not in the eubacteria.
Chloramphenicol stops the elongation in eubacteria but not in
eukaryotes or archaebacteria. The lipids of the cytoplasmic membrane in
both eubacteria and eukaryotes contain the diesters of L-
glycerophosphate with straight-chain fatty acids. In contrast, the
archaebactrial lipids are composed of the diethers of D-glycerophosphate
with phytanol and other branched-chain alcohols. The variance of vionic

210
technique in metabolism responsiveness is pointed out here. The quantic
interchange of environmental forces can have a wide range of activity.
The analysis of DNA and its function has received extreme scrutiny
from the scientific community over the last twenty-five years. Many
different abilities of DNA have been described and experimentally
ascertained.
One of the most recent advances in DNA is that of gene splicing,
wherein genetic engineering can be accomplished by taking out a bad
gene and splicing a healthy gene into the DNA. This dramatic new
research offers great potential for medicine in correcting metabolic or
genetic disorders.
Modern medicine has also developed the technique of splicing the gene
into a virus and allowing the virus to penetrate into the cell membrane,
and to create a new gene code which will replace the diseased code with
a healthy genetic code.
But with all this dramatic research being done with DNA, scientists
have done little to account for the phenomenon of how the transmission
of genetic data can be accomplished. For this, we can go to Schrdinger
and his description of the quantum abilities of DNA. This we have
outlined in the chapters of his book to give a basic understanding.
Our description of the quantum philosophy and the quantum
dynamics will let us find and be predictive of the long range forces in
biology that account for the function of DNA. The development of the
matrices will also help explain some of the DNA functioning.

211
 SUMMARY - THE QUANTIC LINK TO DNA

We reviewed the literature and the thought processes which

arrived at the different philosophical understanding of DNA,
leading to todays use of chromosomal therapy in medicine.

We outlined the possible ways that Schrdinger was right about

DNA working on quantum levels. Genetic transfer of the DNA is
accomplished by quantum dynamics.

We outlined a basic mathematical precept to understand this

quantic link to DNA. Thus, we attempted to explain genetics
through quantum theory.

A proposition was outlined on how DNA function can be further

analyzed, not just from the chemical dynamics, but also from an
energetic, quantum dynamics to further understand how to correct
these situations in the future. A possible new DNA therapy is
hinted at by using chromosomal homeopathy.

Bibliography

Bak, F. Cypionka, H. A novel type of energy metabolism involving

fermentation of inorganic sulphur compounds. Nature. 1987; 326:891-
892.

Cavalier-Smith, T. Molecular phylogeny. Archaebacteria and Archezoa.

Nature. 1989; 339(6220):100-1.

Zuckerkandl, E. Pauling, L. Evolutionary divergence and convergence in

proteins, 1965; 97-166 In: Evolving Genes and Proteins, edited by V.
Bryson and H.J. Vogel. Academic Press, New York.

212
 THE HUMAN GENOME
How to interpret the index and map

Disorders that appear within square brackets [ ] represent non-diseases

mainly genetic variations that lead to apparently abnormal laboratory
test values (e.g., dysalbuminemic euthyroidal hyperthyroxinemia).
Disorders printed inside boxes in the map represent allelic disorders,
which can result in multiple, quite dissimilar disorders from the various
mutations in the same gene. Disorders printed within braces { } represent
genetic mutations that make affected individuals susceptible to a specific
disease, infection or other condition (e.g., coronary artery disease). A
question mark ? before the disorder means that confirmation of a gene or
locus is uncertain or in dispute. Although all known or suspected genetic
disorders appear in the index, some do not appear on the map if their
chromosomal location is particularly controversial. Moreover, on the
ideogram of chromosome X, some disorders have been left out to
conserve space. These excluded disorders are included in the index and
marked with an asterisk *. Disorders printed in bold were added to the
list in the past year. Those printed underlined have been changed in
location on the chromosomes in the past year. Finally, each disorder in
the index is followed by one of three numbers in parentheses that
indicates whether the mutation was located by mapping (1) wild-type
gene, (2) the disease phenotype, or (3) both approaches.

213
 ALPHABETICAL INDEX OF HEALTH DISORDERS
AND CHROMOSOME LOCATION

Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency (1) 8q21

Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency (3) 6p21.3
3-hydroxyacyl-CoA dehydrogenase deficiency (1) Chr.7
*46, XY female (2) xp22.2-p21.3
Aarskog-Scott syndrome (2) Xq13
?Abetaa Lipoproteinemia 2p24
[Acanthocytosis 1 form] (1) 17q21-q22
Acatalasemia (1) 11p13
Acetyl-CoA carboxylase deficiency (1) 17q21
Acid-maltase deficiency, adult (1) 17q23
Acoustic neuroma (2) 22q11.21-q13.1
?Acrokeratoelastoidosis (2) 2p
ACTH deficiency (1) 2p25
Acute alcohol intolerance (1) 12q24.2
Acute Lymphoblastic Leukemia (2) 9p22-p21
Acute Promyelocytic Leukemia (1) 17q21.1
Acute Promyelocytic Leukemia (2) 15q22
Acyl-CoA Dehydrogenase, medium chain, deficiency of (1) 1p31
Acyl-CoA Dehydrogenase, short chain, deficiency of (1) 12q22-qter
Adenylosuccinase deficiency (1) Chr.22
Adrenal hyperplasia II (1) 1p13
Adrenal hypoplasia, primary (2) Chr.10
Adrenocortical carcinoma (2) Xp21.3-p21.2
Adrenoleukodystrophy (2) 11p15.5
Adrenomyeloneruopathy (2) Xq28
[AFP deficiency, congenital] (1) Xq28
Agammaglobulinemia, type 2, X-linked (2) 4q11-q13
*Agammaglobulinemia, X-Linked (2) Xq21.3-q22
Aicardi syndrome (2) Xq22

214
Albinism (3) 11q14-q21
Albinism-deafness syndrome (2) Xq26.3-q27.1
?Aldolase A deficiency (1) 16q22-q24
Allan-Herndon syndrome Xq21
Alpha-1-antichymotrypsin deficiency (1) 14q32.1
Alpha-NAGA deficiency (1) 22q11
Alport syndrome (3) Xq22
Alzheimers disease, type I (3) 21q21.3-q22.05
*Amelogenesis imperfecta (1) Xp22.3-p22.1
[AMP deaminase deficiency, erythrocyte] (1) 1p21-p13
Amyloid neuropathy, familial, several allelic types (3) 18q11.2-q12.1
Amyloidosis, cerebroaterial, Dutch type (1) 21q21.3-q22.05
Amyloidosis, Finnish type (1) 9q34
Amyloidosis, Iowa form (2) 11q23
{?Amyloidosis, secondary, susceptibility to} 1q12-q23
Amyotrophic Lateral Sclerosis (2) 21q21.1-q22.3
?Anal canal carcinoma (2) 11q22-qter
Analbuminemia (1) 4q11-q13
Anemia, congenital due to deficiency of gastric intrinsic factor (1) Chr.11
Anemia, sideroblastic/hypochromic (3) Xp21-q21
Aneurysm, familial (2) 2q31
Angelman syndrome (2) 15q11-q13
Angioedema, hereditary (1) 11q11-q13.1
Anhidrotic ectodermal dysplasia (2) Xq12.2-13.1
Aniridia of WAGR syndrome (2) 11p13
Aniridia-1 (2) 2p25
Aniridia-2 (2) 11p13
Anterior segment mesenchymal dysgenesis (2) 4q28-q31
Antithrombin III deficiency, (3) 1q23-q25
ApoA-I and apocC-III deficiency, combined (1) Chr.11
Apolipoprotein B-100, defective (1) 2p24
[Apoliproprotein H deficiency] (1) Chr.17
Argininemia (1) 6q23
Argininosuccinicaciduria (1) 7cen-q11.2
Arteriohepatic dysplasia (2) 20p11.2
Aspartylglucosaminuria (3) 4q23-q27
Ataxia-telangiectasia (2) 11q22-q23
Atopy (2) 11q12-q13
Atransferrinemia (1) 3q21
Atrial septal defect, secundum type (2) 6p21.3
Autonomic failure due to DBH deficiency (1) 9q34

215
?Batten disease, 1 form (1) 15q24-q25
Batten disease (2) 16p11
Becker muscular dystrophy (3) Xp21.2
Beckwith-Wiedemann syndrome (2) 11pter-p15
Bernard-Soulier syndrome (1) 17pter-p12
?Bloom syndrome (1) Chr.19
?Bloom syndrome (2) Chr.12
*Borjeson-Forssman-Lehmann syndrome (2) Xp26-q27
?Branchiootic syndrome (2) 8q13.3
?Breast cancer (1) 17p13.3
Breast cancer, ductal (2) 1p36
Breast cancer, ductal (2) Chr.13
Breast cancer, early onset (2) 17q21
Brody myopathy (1) Chr.16
Burkitts Lymphoma 8q24.1
?C1q deficiency (1) 1p
?C1q deficiency (1) 1p
C1r/Cis deficiency, combined (1) 12p13
C1r/Cis deficiency, combined (1) 12p13
C2 deficiency (3) 6p21.3
C3 deficiency (1) 19p13.3-p13.2
C3b inactivator deficiency (1) 4p25
C4 deficiency (3) 6p21.3
C4 deficiency (3) 6p21.3
C5 deficiency (1) 9q34.1
C6 deficiency (1) 5p13
C7 deficiency (1) 5p13
C8 deficiency, type I (2) 1p22
C9 deficiency, type II (2) 1p22
C9 deficiency (1) 5p13
?Campomelic dysplasia with sex reversal (2) 5q33.1
?Campomelic dysplasia with sex reversal (2) 8q21.4
Carbamoylphosphate synthetase I deficiency (1) 2p
[Carbonic anhydrase I deficiency] (1) 8q22
?Cardiomyopathy (1) 2q35
?Carotid body tumor-1 (2) 13q34
Cate eye syndrome (2) 22q11
?Cataract, anterior polar (2) 14q24
?Cataract, anterior polar (2) 2p25
Cataract, Coppock-Like (3) 2q33-q35
Cataract, Marner type (2) 16q22.1

216
Cataract, zonular pulverulent (2) 1q22
*?Cataracts, congenital total (2) Xp
Central core disease of muscle (2) 19q12-q13.2
Cerebral amyloid angiopathy (1) Chr.20
Cerebrotendinous xanthomatosis (2) 2q33-qter
[CEPT-deficiency] (1) 16q21
Charcot-Marie-Tooth disease, slow nerve conduction type Ia (2) 17p11.2
Charcot-Marie-Tooth disease, slow nerve conduction type Ib (2) 1q21.2-q23
Charcot-Marie-Tooth disease, X-linked dominant (2) Xq13
Charcot-Marie Tooth disease X-linked recessive 1 (2) Xq22.2
?Chediak-Higashi syndrome (2) 1q43
Cholesteryl ester storage disease (1) 10q24-q25
*Chondrodysplasia punctata, X-Linked dominant (2) Xq28
Chondrodysplasia punctata, X-Linked recessive (2) Xpter-p22.32
Choroideremia (2) Xq21.2
Chronic granulomatous disease due to deficiency of NCF-1 (1) 7q11.23
Chronic granulomatous disease due to deficiency of NCF-2 (1) 1q25
Chronic infections (1) 10q11.2-q21
Citrullinemia (1) 9q34
Cleft palate, X-linked (2) Xq21
CMO II deficiency (1) 8q21
*Coffin-Lowry syndrome (2) Xp22.2-p22.1
?Coloboma of iris (2) 2pter-p25.1
Colorblindness, blue monochromatic (3) Xq28
Colorblindness, blue monochromatic (3) Xq28
Colorblindness, blue monochromatic (3 Xq28
Colorblindness, deutan (3) Xq28
Colorblindness, protan (3) Xq28
Colorblindness, tritan (2) 7q22-qter
Colorectal adenoma (1) 12p12.1
?Colorectal cancer (1) 12p12.1
Colorectal cancer (1) 18q23.3
Colorectal cancer (3) 17p13.1
Colorectal cancer, familial (2) 5q22-q23
Combined C6/C7 deficiency (1) 5p13
?Combined variable hypogammaglobulinemia (1) 14q32.33
Conductive deafness with stapes fixation (2) Xq13-q21.1
Coproporphyria (1) Chr.9
{Coronary artery disease, susceptibility to} (1) 6q27
Cortisol resistance (1) 5q31
CR1 deficiency (1) 1q32

217
Craniosynostosis (2) 7p21.3-p21.2
[Creatine kinase, brain type, ectopic expression of] (2) 14q32
Creutzfeldt-Jakob disease (2) 20pter-p12
?Cryptorchidism (2) Xp21
[Cystathioninuria] (1) Chr.16
Cystic fibrosis (2) 7q31.3-q32
Debrisoquine sensitivity (1) 22q11.2-q12.2
Dentinogeneis imperfecta-1 (2) 4q13-q21
Diabetes insipidus, nephrogenic (3) Xq28
Diabetes insipidus, neurohypophyseal (1) 20pter-p12.21
?Diabetes mellitus, insulin dependent (2) 6p21.3
Diabetes mellitus, insulin-resistant, with acanthosis nigricans (1) 19p13.3-p13.2
Diabetes mellitus, rare form (1) 11p15.5
?Diaphragmatic hernia (2) 1q32.3-q42.3
Diastrophic dysplasia (2) 5q22-q34
DiGeorge syndrome (2) 22q11
Diphenylhydatoin toxicity (1) 1q22-qter
[Diphtheria, susceptibility to} (1) 5q23
?Dubin-Johnson syndrome (2) 13q34
Duchenne muscular dystrophy (3) Xp21.2
[Dysalbuminemic hyperthyroxinemia] (1) 4q11-q13
[Dysalbuminemic hyperzincemia] (1) 4q11-q13
Dysfibrinogenemia, alpha types (1) 4q28
Dysfibrinogenemia, beta types (1) 4q28
Dysfibrinogenemia, gamma types (1) 4q28
Dyskeratosis congenital (2) Xq28
?Dyslexia-1 (2) 15q11
Dysplasminogenemic thrombophilia (1) 6q26-q27
Dysprothrombinemia (1) 11p11-q12
[Dystransthyretinemic hyperthyroxinemia] (1) 18q11.2-q12.1
Ehlers-Danlos syndrome, type IV (3) 2q31
Ehlers-Danlos syndrome, type VIIA1 (3) 17q21.3-q22.05
Ehlers-Danlos syndrome, type VIIA2 (3) 7q21.3-q22.1
?Ehlers-Danlos syndrome, type X (3) 2q34-q36
[Elliptocytosis, Malaysian-Melanesian type] (1) 17q21-q22
Elliptocytosis-1 (3) 1p36.2-p34
Elliptocytosis-2 (2) 1q21
Elliptocytosis-3 (2) 14q22-q23.2
Emery-Dreifuss muscular dystrophy (2) Xq28
Emphysema (1) 14q32.1
Emphysema due to alpha-2-macroglobulin deficiency (1) 12p13.3-p12.3

218
Emphysema-cirrhosis (1) 14q32.1
Enolase deficiency (1) 1pter-p36.13
?Eosinophilic myeloproliferative disorder (2) 12p13
Epidermolysis bullosa dystrophica, recessive (3) 11q11-q23
Epidermolysis bullosa Ogna type (2) 8q24
Epidermolysis bullosa progressiva (2) Unassigned Link
?Epidermolysis bullosa simplex, Koebner type 1q21-q24
Epilepsy, juvenile myoclonic (2) 6p21.3
Epilepsy, progressive myoclonic (2) 21q22.3
?Erythremia (1) 7q21-q22
Erythremias, alpha- (1) 16pter-p13.3
Erythremias, beta- (1) 11p15.5
Erythroblastosis fetalis (1) 1p36.2-p34
Erythrokeratodermia variabilis (2) 1p36.2-p34
*[Euthyroidal hyper- and hypothyroxinemia] (1) Xq21-q22
Ewing Sarcoma (2) 22q12
Exertional myoglobinuria due to deficiency of LDH-A (1) 11p15.4
Fabry disease (3) Xq22
Facioscapulohumeral muscular dystrophy (2) 4q34-qter
Factor H deficiency (1) 1q32
Factor V deficiency (1) 1q23
Factor VII deficiency (1) 13q34
Factor X deficiency (1) 13q34
Factor XI deficiency (1) 4q35
Factor XII deficiency (1) 5q33-qter
Factor XIIIA deficiency 6p25-p24
Factor XIIIB deficiency 1q31-q32.1
?Familial Mediterranean fever (1) 9q32-q33
?Fanconi anemia (1) 1q41-q42
Fanconi anemia-1 (2) 20Q
Favism (1) Xq28
?Fetal alcohol syndrome (1) 12q24.2
?Fetal hydantoin syndrome (1) 1p22-qter
Fletcher factor deficiency (1) 4q35
*Focal dermal hypoplasia (2) Xp22.31
Fragile X syndrome/Martin-Bell syndrome (2) Xq27.3
Friedreich ataxia (2) 9q13-q21.1
Fructose Intolerance (1) 9q22
?Fryns syndrome (2) 1q24-q31.2
Fucosidosis (1) 1p34
Fumarase deficiency (1) 1q42.1

219
G6PD deficiency (1) Xq28
Galactokinase deficiency (1) 17q21-q22
Galactose epimerase deficiency (1) 1pter-p32
Galactosemia (1) 9p13
Galactosialidosis (1) 20q13.1
Gardner syndrome (2) 5q22-q23
Gaucher disease (1) 1q21
Gerstmann-Straussler disease (2) 10q21-q22
Glanzmann thrombasthenia, type A (1) 20pter-p12
Glanzmann thrombasthenia, type B (1) 17q21.32
Glaucoma, congenital (2) 17q21.1-q21.3
Glioblastoma multiforme (2) Chr.11
Glutaricaciduria, type II (1) 10p12-q23.2
Glutaricaciduria, type IIc (1) 15q23-q25
Glutathioninuria (1) Chr.19
Glycerol kinase deficiency (2) 22q11.1-q11.2
Glycogen storage disease VII (1) Xp21.3-p21.2
*Glycogen storage disease, X-Linked hepatic (2) Xp22
[Glyoxalase II deficiency] (1) 16p13
GM1-Gangliosidosis (1) 3p21-p14.2
GM2-Gangliosidosis, juvenile, adult (1) 15q22-q25.1
GM2- Gangliosidosis, AB variant (1) Chr.5
Goeminne TKCR syndrome (2) Xq28
Goiter, adolescent multinodular (1) 8q24.2-q24.3
?Goldenhar syndrome (2) 7p
*Gonadal dysgenesis, XY female type F (2) Xp22-p21
Gonadoblastoma (2) 11p13
*?Gonadotropin deficiency (2) Xp21
Granulomatous disease, autosomal, due to deficiency of CYBA 16q24
Granulomatous disease, chronic, X-Linked (2) Xp21.1
Greig craniopolysyndactyly syndrome (2) 7p13
*?Growth hormone deficiency, X-Linked (2) Xq21.3-q22
?Gynecomastia, familial, due to increased aromatase activity (1) 15q21.1
Gyrate atrophy of choroids and retina with ornithinemia, B6
responsive or unresponsive (1) 10q26
Harderoporphyria (1) Chr9
Hb H mental retardation syndrome (2) 16pter-p13.3
Heinz body anemias, alpha- (1) 16pter-p13.3
Heinz body anemias, beta- (1) 11p15.5
Hemochromatosis (2) 6p21.3
Hemodialysis-related amyloidosis (1) 15q21-q22

220
Hemolytic anemia due to ADA excess (1) 20q13.11
Hemolytic anemia due to adenylate kinase deficiency (1) 9q34.1
Hemolytic anemia due to bisphosphoglycerate mutase deficiency (1) 7q31-q34
Hemolytic anemia due to G6PD deficiency (1) Xq28
Hemolytic anemia due to glucosephosphate isomerase deficiency (1) 19cen-q12
Hemolytic anemia due to glutathione peroxidase deficiency (1) 11-q12
Hemolytic anemia due to glutathione reductase deficiency (1) 8p21.1
Hemolytic anemia due to hexokinase deficiency (1) 10p11.2
Hemolytic anemia due to PGK deficiency (1) Xq13
Hemolytic anemia due to phosphofructokinase deficiency (1) 21q22.3
Hemolytic anemia due to triosephosphate isomerase deficiency (1) 12p13
Hemophilia A (3) Xq28
Hemophilia B (3) Xq27.1-q27.2
Hemorrhagic diathesis due to antithrombin Pittsburgh (1) 14q32.1
Hemorrhagic diathesis due to PAI1 deficiency (1) 7q21.3-q22
?Hepatic lipase deficiency (1) 15q21-q23
?Hepatocarcinoma (2) 2q14-q21
Hepatocellular carcinoma (3) 4q32.1
[Hereditary persistence of alpha-fetoprotein] (3) 4q11-q13
?Hereditary persistence of fetal hemoglobin (3) 11p15.5
*[Hereditary persistence of fetal hemoglobin, Swiss type (2) Xp11.23
Hers disease, or glycogen storage disease VI (1) Chr.14
Heterocellular hereditary persistence of fetal hemoglobin (2) 11p15
*?Heterocellular hereditary persistence of fetal hemoglobin (2) Xq28
!Hex A pseudodeficiency! (1) 15q22-q25.1
?H syndrome (2) 13q34
[Histidinemia] (1) 12q22-q23
?Holoprosencephaly (2) 2p21
?Holoprosencephaly (2) 21q22.3
?Holoprosencephaly (2) 7q36
?Holt-Oram syndrome (2) 14q23-q24.2
?Holt-Oram syndrome (2) 20p13
Homocystinuria, B6-responsive and nonresponsive types (1) 21q22.3
HPFH, deletion type (1) 11p15.5
HPFH, nondeletion type A (1) 11p15.5
HPFH, nondeletion type G (1) 11p15.5
HPRT-related gout (1) Xq26-q27.2
Huntingtons disease (2) 4p16.3
Hurler syndrome (1) 4p16.3
Hurler-Scheie syndrome (1) 4p16.3

221
Hydrocephalus, X-Linked (2) Xq28
Hydrops fetalis, 1 form (1) 19cen-q12
Hyperammonemia due to CTPase deficiency (1) 1pter-q12
Hyperbetalipoproteinemia (1) 2p24
Hypercholesterolemia, familial (3) 19p13.2-p13.1
?Hyperglycinemia, isolated nonketotic, type I (2) 9p22
?Hypergonadotropic hypogonadism (1) 19q13.32
?Hyperimmunoglobulin G1syndrome (2) 14q32.33
Hyperkalemic periodic paralysi (3) 17q23.1-q25.3
?Hyperleucinemia-isoleucinemia or hypervalinemia (1) 12pter-q12
Hyperlipoproteinemia I (1) 8p22
Hyperlipoproteinemia, type Ib (1) 19q13.1
Hyperlipoproteinemia, type III (1) 19q13.1
[Hyperphenylalaninemia, mild] (3) 12p24.1
[?Hyperproglucagonemia] (1) 2q36-q37
Hyperproinsulinemia, familial (1) 11p15.3
Hypertriglyceridemia, 1 form (1) 11q23
Hypertrophic cardiomyopathy, 1 form (3) 14q12
?Hypervalinemia or hyperleucine-isoleucinemia (1) Chr.19
Hypobetalipoproteinemia 11q23
Hypobetalipoproteinemia (1) 2p24
[Hypoceruloplasminemia, hereditary] (1) 3q21-q24
Hypofibrinogenemia, gamma types (1) 4q28
?Hypogonadotropic hypogonadism due to GNRH deficiency (1) 8p21-q11.2
Hypomagnesemia, X-Linked primary (2) Xp22
?Hypomelanosis of Ito (2) 15q11-q13
?Hypomelanosis of Ito (2) 9q33-qter
Hypoparathyroidism, familial (1) 11p15.3-p15.1
*Hypoparathyroidism, X-Linked (2) Xq26-q27
?Hypophosphatasia, adult (1) 1p36.1-p34
Hypophosphatasia, infantile (3) 1p36.1-p34
Hypophosphatemia, hereditary (2) Xp22.2-p22.1
?Hypophosphatemia with deafness (2) Xp22
Hypoprothrombinemia (1) 11p11-q12
Hypothyroidism, hereditary congenital, 1 or more types (1) 8q24.224.3
Hypothyroidism, nongoitrous (1) 1p22
Hypothyroidism, nongoitrous, due to TSH resistance (1) 14q31
?Ichthyosis vulgaris (1) 1q21
Ichthyosis, X-Linked (3) Xpter-p22.32
Immunodeficiency, X-Linked, with hyperIgM (2) Xq24-q27
*Incontinentia pigmenti, familial (2) Xq27-q28

222
Incontinentia pigmenti, sporadic type (2) Xp11.21
Infertile male syndrome (1) Xcen-q13
[Inosinie triphosphatase deficiency] (1) 20p
Interferon, alpha, deficiency (1) 9p21
Interferon, immune, deficiency (1) 12q24.1
?Isolated growth hormone deficiency due to defect in GHRF (1) 20p11.23qter
Isolated growth hormone deficiency, Illig type with absent GH and
Kowarski type with bioinactive GH (3) 17q22-q24
Isovalericacidemia (1) 15q14-q15
?Jacobsen syndrome 11q
Kallmann syndrome X22.3
Kennedy disease (2) Xq21.3-q22
?Kniest dysplasia (1) 12q13.11-q13.2
?Kostmann agranulocytosis (2) 6p21.3
Krabbe disease (1) 14q21-q31
?Lactase deficiency, adult (1) Chr.2
?Lactase deficiency, congenital (1) Chr.2
?Lactoferrin-deficient neutrophils 3q21-q23
Langer-Giedon syndrome (2) 8q24.11-q13.2
Langer-Saldino achondrogenesis-hypochondrogenesis (1) 12q13.11-q13.2
Laron dwarfism (1) 5p13-p12
?Laryngeal adductor paralysis (2) 6p21.3p21.2
{Lead poisoning, susceptibility to} (1) 9q34
?Leiomyomata, multiple hereditary cutaneous (2) 18p11.32
Leprechaunism (1) 19p13.3-p13.2
Lesch-Nyhan syndrome (3) Xq26-27.2
?Letterer-Siwe disease (2) 13q14-q31
Leukemia, acute lymphoblastic (1) 19p13.3.-p13.2
?Leukemia, acute lymphocytic, with 4/11 translocation (3) 4q21
Leukemia, acute myeloid, M2 type (1) Xpter-p21
Leukemia, acute T-cell (2) 11p13
Leukemia, chronic myeloid (3) 22q11.21
Leukemia, chronic myeloid (3) 9q34.1
Leukemia, T-cell acute lymphocytic (2) 10q24
Leukemia/Lymphoma, B-cell, 1 (2) 11q13.3
Leukemia/Lymphoma, B-cell, 2 (2) 18q21.3
Leukemia/Lymphoma, B-cell, 3 (2) 19q13
Leukemia/Lymphoma, T-cell, (2) 1p32
Leukemia/Lymphoma, T-cell, (2) 14q32.1
Leukemia/Lymphoma, T-cell, (2) 2q34
Leukemia/Lymphoma, T-cell, (3) 14q11.2

223
Leukocyte adhesion deficiency (2) 21q22.3
Li-Fraumeni syndrome (1) 17p13.1
Lipoamide dehydrogenase deficiency (1) 7q31-q32
Lipoid adrenal hyperplasia, congenital (1) Chr.15
Lipoma (2) 12q13-q14
Liver cell carcinoma (1) 11p14-p13
Long QT syndrome (2) 11p15.5
Lowes syndrome Xq25
Lupus erythematosus, systemic (1) 1q23-q24
Lymphoproliferative syndrome, X-linked (2) Xq25
?Lynch cancer family syndrome II (2) 18q11-q12
?Lysosomal acid phosphatase deficiency (1) 11p12-p11
Macrocytic anemia of 5q syndrome II (2) 5q12-q32
Macular dystrophy, atypical vitelliform (2) 8q24
Macular dystrophy,?vitelline type (2) 6p25-qter
?Major mental illness (2) 11p21-q22
?Male infertility due to acrosin deficiency (2) 22q13-qter
?Male infertility, familial 11p13
?Male pseudohermaphroditism due to defective LH (1) 19q13.32
Malignant hyperthermia (2) 19q13.1-q13.3
Malignant melanoma, cutaneous (2) 1p36
Manic-depressive illness, X-Linked (2) Xq28
Mannosidosis (1) 19p13.2-q12
Maple syrup urine disease (1) 19q13.1-q13.2
Maple syrup urine disease, type II (1) 1p31
Maple syrup urine disease, type III (3) 6p22-p21
Marfan syndrome (2) 15q-q21.3
Maroteaux-Lamy syndrome (1) 5q11-q13
Martin-Bell syndrome/Fragile X syndrome (2) Xq27.3
NASA syndrome (2) Xq28
McArdle disease (1) 11q13
*[McLeod phenotype] (2) Xp21.2-p21.1
Medullary thyroid carcinoma (2) 10q21.1
?Megacolon (2) 13q22.1-q32.1
?Megaloblastic anemia 5q11.1-q13.2
?Megalocomea, X-Linked (2) Xq21.3-q22
Meningioma (2) 22q12.3-qter
Meningioma (3) 22q12.3-q13.1
Menkes disease (2) Xq12-q13
Mental retardation of WAGR (2) 11p13
*Mental retardation, X-Linked nonspecific, I (2) Xp22

224
*Mental retardation, X-Linked nonspecific, II (2) Xq11-q12
*Mental retardation-skeletal dysplasia (2) Xq28
Metachromatic Leukodystrophy (1) 22q13.31-qter
Metachromatic Leukodystrophy due to deficiency of SAP-1 (1) 16pter-p13.3
Methemoglobinemia, enzymopathic (1) 11p15.5
Methylmalonicaciduria, mutase deficiency type (1) 6p21
?Microcephaly, true (2) 1q31-q32.1
Miller-Dieker Lissencephaly syndrome (2) 17p13.3
MODY, 1 form (3) 11p15.5
Mucolipidosis II (1) 4q21-q23
Mucolipidosis III (1) 4q21-q23
Mucopolysaccharidosis I (1) 4p16.3
*Mucopolysaccharidosis II (2) Xq28.1
Mucopolysaccharidosis IVB (1) 3p21-p14.2
Mucopolysaccharidosis VII (1) 7q22
Multiple endocrine neoplasia II (2) 11q13
Multiple endocrine neoplasia II (2) 10q21.1
Multiple endocrine neoplasia III (2) 10q21.1
?Multiple exostoses (2) 8q23-q24.1
?Multiple Lipomatosis (2) 12q13-q14
?Muscle glycogenosis (1) Xq12-q13
Myeloperoxidase deficiency (1) 17q21.3-q23
Myoadenylate deaminase deficiency (1) 1p21-p13
Myopathy due to CTPase deficiency (1) 1pter-q12
Myopathy due to phosphoglycerate mutase deficiency 7p13-p12.3
Myotonic dystrophy (2) 19q13.2-q13.3
Myotubular myopathy, X-Linked (2) Xq28
Myxoid Liposarcoma (2) 12q13-q14
*?N syndrome Xp23.3-p21.1
Nail-patella syndrome (2) 9q34
*Nance-Horan syndrome (2) Xp22.3-p21.1
Neuroblastoma (2) 1p32
Neuroepithelioma (2) 22q12
Neurofibromatosis, von Recklinghausen (2) 17q11.2
Neutropenia, immune (2) 1q23-q24
?Nevoid basal cell carcinoma syndrome (2) 1p
Niemann-Pick disease (1) 11p15.4-15.1
*Nightblindness, congenital stationary, type I (2) Xp11.3
Norries disease (2) Xp11.4
Norum disease (3) 16q22.1
Nucleoside phosphorylase deficiency, immunodeficiency due to (2) 14q13.1

225
*Ocular albinism, Forsius-Eriksson type (2) Xp11-q11
Ocular albinism, Nettleship-Falls type (2) Xp22.3
?Optic atrophy, Kjer type (2) 2p
Ornithine transcarbamylase deficiency (3) Xp21.1
Orofacial cleft (2) 6pter-p23
Oroticaciduria (1) 3q13
Osteoartrosis, precocious (3) 12q13.11-q13.2
Osteogenesis imperfecta, 2 or more clinical forms (3) 17q21.31-q22.05
Osteogenesis, retinoblastoma-related (2) 7q21.3-q22.1
Osteosarcoma, retinoblastoma-related (2) 13q14.1
Ovarian carcinoma (2) 9p24
*Ovarian failure, premature (2) Xq26-q27
Oxalosis I (1) 2q36-q37
?Paget disease of bone (2) 6p21.3
{?Parkinsonism, susceptibility to} (1) 22q11.2q12.2
Paroxysmal nocturnal hemoglobinuria (1) 11p14-p13
Pelizaeus-Merzbacher disease (3) Xq22
?Pendred syndrome (2) 8q24
Periodontitis, juvenile (2) 4q11-q13
Persistent Mullerian duct syndrome (1) 19p13.3-p13.2
Phenylketonuria (3) 12q24.1
Phenylketonuria due to dihydropteridine reductase deficiency (1) 4p15.31
*Phosphoribosylpyrophosphate synthetase-related gout (1) Xq22-q24
?Phosphorylase kinase deficiency of liver and muscle (2) 16q12-q13.1
?Piebaldism (2) 4q12
PK deficiency hemolytic anemia (1) 1q21-q22
[Placental lactogen deficiency] (1) 17q22-q24
Placental steroid sulfatase deficiency (3) Xpter-p22.32
Plasmin inhibitor deficiency (1) 18p11.1-q112
Plasminogen activator deficiency (1) 8p12
Plasminogen deficiency, types I and II (1) 6q26-q27
Plasminogen Tochigi disease (1) 6q26-q27
Platelet alpha/delta storage pool deficiency (1) 1q21-q24
{Polio, susceptibility to} (2) 19q12-q13.2
Polycystic kidney disease (2) 16p13.31-p13.12
Polycystic ovarian disease (1) 17q11-q12
Polyposis coli, familial (2) 5q22-q23
Pompe disease (1) 17q23
Porphyria, acute hepatic (1) 9q34
Porphyria, acute intermittent (1) 11q23.2-qter
Porphyria, congenital erythropoietic (1) 10q25.2-q26.3

226
Porphyria, cutanea tarda (1) 1p34
Porphyria, hepatoerythropoietic (1) 1p34
Porphyria variegata (2) 14q32
Postanesthetic apnea (1) 3q25.2
Prader-Willi syndrome (2) 15q11
*Progressive cone dystrophy (2) p21.1-p11.3
Prolidase deficiency (1) 19cen-q13.11
*Properdin deficiency, X-Linked (3) Xp11.4
Propionicacidemia, type I or pccA type (1) 13q32
Propionicacidemia, type II or pccB type (1) 3q13.3-q22
Protein C deficiency (1) 2q13-q14
Protein S deficiency (1) 3p11.1-q11.2
Pseudohermaphroditism, male, with gynecomastia (1) 17q11-q12
Pseudohypoaldosteronism (1) 4q31.1
Pseudohypoparathyroidism, type Ia (1) 2oq13.2-q13.3
Pseudo-Zellweger syndrome (1) 3p23-p22
?Pyridoxine dependency with seizures (1) 2q
Pyropoikilocytosis (1) 1q21
Pyruvate carboxylase deficiency (1) 11q
*Pyruvate dehydrogenase deficiency (1) Xp22.2-p22.1
?Rabson-Mendenhall syndrome (1) 19p13.3-p13.2
?Ragweed sensitivity (2) 6p21.3
Reifenstein syndrome (1) Xcen-q13
Renal cell carcinoma (2) 3p14.2
[Renal glucosuria] (2) 6p21.3
?Retinal cone dystrophy-1 (2) 6p25-q25
?Retinal cone-rod dystrophy (2) 18q21-q22.2
Retinitis pigmentosa, autosomal dominant (3) 3q21-q24
Retinitis pigmentosa-2 (2) Xp11.3
Retinitis pigmentosa-3 (2) Xp21.3
Retinoblastoma (2) 13q14.1-q14.2
?Retinol binding protein, deficiency of (1) 10q23-q24
Retinoschisis (2) Xp22.3-p22.1
*?Rett syndrome (2) Xp
Rhabdomyosarcoma (2) 11p15.5
Rhabdomyosarcoma, alveolar (2) 2q37
Rh-null disease (1) 3cen-q22
?Rh-null hemolytic anemia (1) 1p36.2-p34
Rieger syndrome (2) 4q23-q27
?Rothmund-Thomson syndrome (2) Chr.18
Salivary gland pleomorphic adenoma (2) 8q12

227
Sandhoff disease (1) 5q13
Sanfilippo syndrome D (1) 12q14
*Sarcoma, synovial (2) Xp11.2
Scheie syndrome (1) 4p16.3
*SCID, X-Linked (2) Xq13.1-q21.1
Sclerotylosis (2) 4q28-q31
Seizures, benign neonatal (2) Chr.20
Severe combined immunodeficiency due to ADA deficiency (1) 20q13.11
Severe combined immunodeficiency due to IL-2 deficiency (1) 4q26-q27
Severe combined immunodeficiency (SCID), HLA class II-negative type (1) 19p13
?Sialidosis (1) Chr.10
?Sialidosis (2) 6p21.3
Sicle cell anemia (1) 11p15.5
?Situs inversus viscerum (2) 14q32
?SLE (1) 1q32
Small-cell cancer of lung (2) 3p23-p21
?Smith-Lemli-Opitz syndrome (2) 7q23-qter
Smith-Magenis syndrome (2) 17p11.2
Spastic paraplegia, X-Linked, uncomplicated (2) Xq21-q22
Spherocytosis, recessive (1) 1q21
Spherocytosis-1 (3) 14q22-q23.2
Spherocytosis-2 (3) 8p11.2
Spinal muscular atrophy II (2) 5q11.2-q13.3
Spinal muscular atrophy III (2) 5q11.2-q13.3
Spinocerebellar-ataxia 6p21.3-p21.2
Spondyloepiphyseal dysplasia congenital (3) 12q13.11-q13.2
*Spondyloepiphyseal dysplasia tarda (2) Xp22
Stickler syndrome (3) 12q13.11-q13.2
Sucrose intolerance (1) 3q25-q26
?Susceptibility to amyloid in FMF (1) 11pter-p12
Tay-Sachs disease (1) 15q22-q25.1
Testicular feminization (1) Xcen-q13
Thalassemias, alpha- (1) 16pter-p13.3
Thalassemias, beta- (1) 11p15.5
Thrombocytopenia, X-Linked (2) Xp21-p11
Thrombophilia due to elevated HRG (2) 3p14-qter
Thrombophilia due to excessive plasminogen activator inhibitor (1) 7q21.3-q22
Thrombophilia due to heparin cofactor II deficiency (1) Chr.22
Thyroid hormone resistance (3) 3p24.3
Thyroid iodine peroxidase deficiency (1) 2pter-p12
Thyroid papillary carcinoma (1) 10q11-q12

228
Thyrotropin-releasing hormone deficiency (2) Chr.3
Torsion dystonia (2) 9q32-q34
Torsion dystonia-parkinsonism, Filipino type (2) Xq21
?Tourette syndrome (2) 18q22.1
Transcobalamin II deficiency (1) 22q11.2-qter
[Transcortin deficiency](1) 14q31-q32.1
?Treacher Collins mandibulofacial dysostosis 5q11
Trichorhinophalangeal syndrome, type I (2) 8q24.2
Trypsinogen deficiency (1) 7q32-qter
Tuberous sclerosis-1 (2) 9q33-q34
Tuberous sclerosis-2 (2) 11q23
Tyrosinemia, type I (1) 15q23-q25
Tyrosinemia, type II (1) 16q22.1-q22.3
Urolithiasis, 2,8-dihydroxyadenine (1) 16q24
Usher syndrome, type-2 (2) 1q32
van der Woude syndrome (2) 1q32
Vitamin D dependency, type I (2) 12q14
{Vivax malaria, susceptibility to} (1) 1q21-q22
von Hippel-Lindau syndrome (2) 3p26-p25
von Willebrand disease (1) 12pter-p12
Waardenburg syndrome, type I (2) 2q37.3
?Watson syndrome (2) 17q11.2
Werdnig-Hoffmann disease (2) 5q11.2-q13.3
*Wieacker-Wolff syndrome (2) Xq13-q21
Wilms tumor (2) 11p13
Wilms tumor, type 2 (2) 11p15.5
Wilson disease (2) 13q14-q21
Wiskott-Aldrich syndrome (2) Xp11.3-p11.2
Wolf-Hirschhorn syndrome (3) 4p16.1
Wolman disease (1) 10q24-q25
?Xeroderma pigmentosum (1) 1q41-q42
?Xeroderma pigmentosum, 1 form (1) 19q13.2-q13.3
Xeroderma pigmentosum, group A (1) 9q34.1
Xeroderma pigmentosum, group B (1) 2q21
Xeroderma pigmentosum, group F (2) Chr.15
?Xeroderma pigmentosum, one type (1) Chr.13
Zellweger syndrome (2) 7q11.23

229
 DR. RECOMMENDS METABOLIC 1
A CHROMOSOME HOMEOPATHIC

Chromosome
No.

RNA Control 13 Nerval Disease

1A RNA Control 13A Nerval Disease
2 RNA Control 14 Nerval Disease
2A RNA Control (Tactile) 14A Nerval Disease
3 RNA Control (Vision) 15 Nerval Disease
3A RNA Control (Hearing) 15A Nerval Disease
4 RNA Control 16 MS
4A RNA Control 16A MD
5 RNA Control 17 Digestive
5A RNA Control 17A Kidney Problems
6 Bone Disturbance 18 Kidney Problems
6A Bone Disturbance 18A Kidney Problems
7 Skin Disturbance 19 Liver Problems
7A Skin Disturbance 19A Liver Problems
8 Lipid Metabolism 20 Liver Problems
8A Cholesterol Control 20A Pancreas
9 Cholesterol Control 21 Pancreas
9A Cholesterol Control 21A Pancreas
10 Blood Disturbance 22 Brain
10A Blood Disturbance 22A Brain
11 Downs Syndrome (Alzheimers) 23 Sex System
11A Downs Syndrome (Alzheimers) 23A Addiction
12 Immune System 24 Extra Chromosome (Sociopath)
12A Immune System

230
 LECTINS

Lectins are proteins or glycoproteins of non-immune origin that

agglutinate cells and/or precipitate complex carbohydrates. The
agglutination activity of these highly specific carbohydrate-binding
molecules is usually inhibited by a simple monosaccharide, but for some
lectins di, tri, and even polysaccharides are required.
Lectins are isolated from a wide variety of natural sources, including
seeds, plant roots and bark, fungi, bacteria, seaweed and sponges,
mollusks, fish eggs, body fluids of invertebrates and lower vertebrates
and from mammalian cell membranes. The precise physiological role of
lectins in nature is still unknown, but they have proved to be very
valuable in a wide variety of applications in vitro, including:

Blood groupings and erythrocyte poly agglutination studies

Mitogenic stimulation of lymphocytes
Lymphocyte subpopulation studies
Fractionation of cells and other particles
Isolation, purification and structural studies of carbohydrate
containing molecules
Histochemical studies of normal and pathological conditions

Source: http://www.answers.com/topic/lectin?cat=health /
http://books.google.com/books?id=9xWhUBTdDqgC&pg=PA30&lpg=PA30&dq=lectins
+are+proteins+or+glycoproteins+of+%22non+immune%22+origin+that+agglutinate+cell
s&source=web&ots=5zlpr6hyyU&sig=nCH_vu506zeDKX5XEuwc_LyXXgQ

231
 Common Name

Asparagus Pea Limulin

Avocado Mung Bean
Black Locust Mushroom
Broad Bean Osage Orange
Camels Foot Tree Pagoda Tree
Chick Pea Pea, Garden
Concanavalin A Peanut
Coral Tree (Israel) Pokeweed
Eel Potato
Elder Red Kidney Bean
False Acacia Red Marine Algae
Fava Bean Roman Snail
Furze Scarlet Runner Bean
Gorse Siberian Pea Tree
Green Marine Algae Snail, Garden
Hairy Vetch Soybean
Horse Gram Spindle Tree
Horseshoe Crab Sweet Pea
Jack Bean Thorn Apple
Japanese Wisteria Tomato
Jimson Weed Wheat Germ
Laburnum, Scotch Winged Bean
Lentil Winged Pea
Lima Bean

232
OLIGO ELEMENTS

FIRE DIATHESIS III

Manganese-Cobalt

EARTH DIATHESIS V
Zinc-Nickel-Cobalt, Zinc-Copper

METAL DIATHESIS II
Manganese-Copper

WATER DIATHESIS IV
Copper-Gold-Silver

WOOD DIATHESIS I
Manganese

IODINE
LITHIUM
MAGNESIUM
SULPHUR
ZINC

OLIGO DEOXYRIBONUCLEOTIDE

URACIL
CYTOSINE
ADENINE
THYMINE
INOSINE
GUANINE

233
MINERALS
ALUMINUM
BORON
CALCIUM
CARBON
CHLORINE
CHROMIUM
BOCALT
COPPER
HYDROGEN
IODINE
IRON
MAGNESIUM
MANGANESE
MOLYBDENUM
NICKEL
NITROGEN
OXYGEN
PHOSPHOROUS
POTASSIUM
SELENIUM
SILICON
SODIUM
SULPHER
TIN
VANADIUM
ZINC

234
 METALLIC ELEMENTS

ALUMINUM MERCURY
AMERICUM MOLYB
ANTIMONY NEODYMIUM
ARGON NEON
ARSENIC NIOBIUM
BARIUM OSMIUM
BERYLLIUM PLATINUM
BISMUTH PLUTONIUM
BROMINE POLONIUM
CADMIUM POTASSIUM
CALCIUM RADIUM
CERIUM RADON
CESIUM RUBIDIUM
CHROMIUM SB
COBALT SCANADIUM
COPPER SELENIUM
FLOURINE SILVER
GALANIUM SODIUM
GALLIUM STRONTIUM
GERMANIUM TECHNETIUM
GOLD TELLURIUM
HAFNIUM THORIUM
HELIUM TIN
IODINE TITANIUM
IRIDIUM TUNGSTEN
IRON URANIUM
KRYPTON VANADIUM
LANTHANUM W
LEAD XENON
LITHIUM YTTRIUM
MAGNESIUM ZINC
MANGANESE ZIRCONIUM
MENDELEVIUM

235
 PHENOLICS

Acetaldehyde: Petrochemical sensitivity, (perfumes, flavors, dyes,

plastics, synthetic rubber), alcoholism, spreading phenomenon of
allergies to foods, sugar, metabolism, and yeast.

Acetylcholine Chloride: Parasympathetic stimulant (neurotransmitter)

lowers blood pressure; chronic fatigue, depression, phobias,
schizophrenia.

Apiol: PHS, obesity, infertility, gout, arthritis, hypothalamus-pituitary

axis, homosexuals.

Ascorbic Acid: Allergic shiners, antioxidant, anxiety, bleeding gums and

gum disease, cataracts, chemical sensitivity, collagen disease, dental
caries, diarrhea, easy bruising, edema, fatigue, frequent infections, fruit
intolerance, high cholesterol level, hyperactivity, hypertension, light
sensitivity, loss of appetite, mental problems, muscle soreness, open
angle glaucoma, premature aging, slow wound healing, stiff and tender
joints, weakness in connective tissue.

Butylatedhydroxytoluene (BHT): Aggression, belligerence, depression,

hyperactivity, temper outbursts.

Caffeic Acid: Constricts capillary walls, stimulates ACTH release

(decreasing thymus weight), allergic rhinitis, pharyngeal drainage, otitis,
asthma.

Chlorogenic Acid: Allergies to pollens, dust, molds; skin rashes,

congestion and headaches, asthma, hay fever.

Cinnamic Acid: Bladder dysfunction, cystitis, enuresis, skin problems,

(acne, eczema, psoriasis), congestion, asthma, chronic fatigue,
hypoglycemia, cravings for fruit.

Coniferyl Alcohol: Allergies to evergreens, headaches.

Coumarin: Constricts capillary walls, inhibits clotting, estrogen effect

asthma, hay fever, digestive problems, low back and cervical neck pain,
chronic fatigue.

Dopamine: Neurotransmitter, arrhythmia, Parkinsonism, anxiety,

depression, dyslexia, autism, schizophrenia.

Estrogen: PMS, cyclic changes, (closely associated with Vitamin D),

effeminate traits in males.

236
PHENOLICS, cont.

Gaba: Lowers blood pressure, inhibitory transmitter in brain, anger,

hostility.

Gallic Acid: Related to racing heart, anti-cancer (in 80% foods-universal

reactor), chronic sinusitis, rhinitis, craving sweets, musculo-skeletal
problems (low back pain), chronic fatigue, hyper-activity.

Histamine: Released from injured cells, increases pore size, dilates

capillaries, hay fever, vertigo.

Indole: Bloating, constipation, asthma, allergic rhinitis, sinus

congestion, chronic fatigue, common in milk drinkers and children.

L-Dopa: Arrhythmia, stimulates ACTH release (decreasing thymus

weight), Parkinsonism, chronic anxiety, depression.

Malvin: Red to purple coloring in food, arthritis, psoriasis, asthma,

epilepsy, MS, dyslexia, autism, hyperactivity.

Mannan: Constitutes 30-50% of yeast cell wall, suppresses T-lymphocyte

production, chronic hives, angio-edema.

Menadione: Related to Vitamin K production, liver dysfunction, fatigue,

easy bruising, chronic nosebleeds, chronic colitis, diarrhea, varicose
veins, arthritis.

Norepinephrine: Stimulates sympathetic nervous system (fight or flight),

raises blood pressure, maintains freedom from depression, agoraphobia.

Octopamine: Petrochemical sensitivities.

Phenylalanine: Building block for dopamine, cinnamic acid, caffeic acid,

coumarin and coniferyl alcohol, headaches, blurred vision, poor appetite,
depression, sleep disorders.

Phenylisothiocyanate: MD, diarrhea, chronic arrhythmia, hypertension,

thyroid dysfunction.

Phloridzin: Strengthens vascular system, blocks absorption of glucose in

kidneys (glucosuria), sugar cravings, collagen diseases.

Piperine: Stomach disorders.

237
Progesterone: PMS, menopausal stress, temporarily raises cholesterol
levels.

Pyrole: Gas, bloating, anxiety, depression, mauve factor in

schizophrenia.

Quercetin: In 78% of foods. Hay fever, suppresses histamine release,

chelates with metals to prevent oxidation of Vitamin C and adrenaline,
decreases vascular fragility, stimulates adrenaline release, decreasing
thymus weight, reduces overall metabolism, reduces temperature and
oxygen consumption, suppresses thyroid activity, linked with male
impotence.

Rutin: Increases vascular strength, hay fever, rhinitis, reduces

permeability of capillary walls.

Salsolinol: Alcoholism, chocoholism, headaches, throat discomfort,

general weakness, mental fog, obsessive-compulsive behavior.

Serotonin: Neurotransmitter, sensory perception, temperature

regulation, decreases bleeding, increases peristaltic motion, insomnia,
memory loss, depression, dyslexia, mental retardation, obsessive,
compulsive, aggressive, suicidal (lower serotonin level, higher aggression,
and more violent suicide).

Taurine: Stimulates liver function and bile flow, related to viruses in

liver and environmental toxicity.

Tryptophan: Antidepressant, sleep disorders, bloating, constipation,

increases peristalsis, decreases bleeding, skin inflammations.

Phenylpropanolamine: Aids in the elimination of environmental

sensitivities.

238
 VENOMS

Many different types of venom have been used historically in different

medicines by many cultures. Snake venom in particular has gotten much
attention throughout the ages. The snake was thought to represent death
but also to represent aspects of life. It has been part of mythology in
almost every culture.
The symbol for healing, the staff with the snake around it, is used by
the American Medical Association as its signature. Many aspects of
healing are connected to snakes.
Venoms were found to have many different effects for both medicine
and biology. As early as 1737, Geoffroy and Hunault observed that the
blood from cats and dogs bitten by vipers did not coagulate. In 1787,
Felice Fontana found that when he injected a rabbit in the jugular vein
with a small quantity of the same venom, this caused immediate death.
On opening the vessels he found that the blood was coagulated.
This was later solved in 1899, by M. Phisalix, who found that there
were two distinct types of activity in this viper venom. One was an anti-
coagulant at high doses, and the other a coagulant at low doses. This
was part of the first evidence that some compounds could have various
effects at different potencies. The amount of dilution could sometimes
accomplish an influx or a distinct difference of action in potencies or
dilutions. This was later developed as the Arndt-Schultz law of
pharmacology which states that what a poison does at a raw dose, a
dilute form of that poison will affect inversely, or paradoxically.
Dr. Isaacs remarks that the effect between alpha receptors and beta
receptors in the body is not a factor of different compounds that
stimulate results, but different amounts of the same compound. Different
dilutions can have different effects on neural transmitter points within
the body which is key to the understanding of homeopathy, especially
when looking at different snake and insect venoms.

239
 In 1854, Brainard found that venom in blood taken from animals
bitten by crotalidae did not cause coagulation. In 1860, Mitchell found
that the toxic secretion of the Crotalus adamanteus prevented blood from
clotting in vitro. In 1893, Martin cited that the venom of elapidae (an
example of which is the Pseudechis porphyriacus and the Notechis
scutatus) coagulated blood in the vessels when injected at high doses;
but at low doses it rendered the blood unable to coagulate. The venom of
an Indian cobra when tested at any dose was found to inhibit blood
coagulation in vivo and in vitro. This was found to be true in 1895, by D.
D. Cunningham, in 1898, by Stephens and Meyers, in 1904, by Rogers.
In 1901, George Lamb classified a dissertation of venoms according to
their action on plasma. He noted in his article that Russells pit viper
venom coagulated citrated plasma. This plasma does not in itself
spontaneously coagulate. F. Noc confirmed these findings, and
discovered that the venom of Asian and African elepidae prevented the
coagulation of citrated plasma to which calcium chloride had been added
for protection.
In 1904, Paul Morawitz proposed that there was an essential element
of the transformation of fibrinogen to fibrin which allows for the
formation of different blood clots. The serozyme of serum acting on the
cytozyme from the platelets caused thrombin to form. Thrombin was
found to be the factor reacting on fibrinogen.
In 1910, Noc presumed that some venom induced coagulation by the
contribution of active thrombin to the blood. J. Mellanby found that
coagulation of these venoms was increased by the addition of calcium.
In 1912, Maurice Arthus put forth the idea that crotalidae acted as if it
contained thrombin, whereas Russells pit viper venom accelerated the
transformation of prothrombin to thrombin.
In 1905, C. J. Martin was able to demonstrate that the coagulating
factors of venoms did not pass through dialysis membranes.

240
 In 1904, Paul Morawitz introduced the idea of the enzyme capacities of
these different venoms, and their ability to act very similarly to the
digestive juices.
The capacity of these venoms to have enzymatic action in the body was
then determined. These venoms could be deadly if the enzyme activity
was too intense such as in the case of Russells pit viper which causes
thrombosis.
Cortalus was a very strong enzyme; whereas elapidae was found to be
weak proteolytically, but strong in its other enzyme activity.
In 1912, C. Delezenne claimed that the venom of Lachesis contained
akinase which activated pancreatic juice. Later in 1919, he observed in
experiments that the toxic secretion of snakes was able to cause catalytic
breakdown of nucleic acids.
By the beginning of the twentieth century, classification of the different
distinguishing properties of snake venoms was possible. Some acted as if
they had ferments, or protein enzyme-like substances. Some were toxic.
Some had diastases.
In 1887, Henry Seawall, at the University of Michigan, Ann Arbor, was
the first one in the United States to observe that a type of venom serum
could be developed. He injected pigeons with small amounts of venom;
not enough to cause death. Weeks later, the same pigeons, when injected
with a larger quantity of the venom were able to resist the venoms
effects.
Hahnemans work with some snake venoms pointed out their reversal
functions. This brief document is an attempt to discuss some of these
venoms and their use in medicine today.
Snakes can use their venom in many different ways. Often, the
purpose of venom is to hunt and digest. People bitten by a snake usually
have respiratory, circulatory, neurological, cardiac and coagulation
problems. The enzymes in the venom will start digestion of the tissues of

241
the victim so that the digestive system of the snake, which is not
extremely strong, can get a head start on the digestive process.
These venoms have strong pharmacological activity with a highly
specific mode of action. Most of the contents of these venoms are
proteins. Low molecular weight compounds such as peptides, nucleotides
and metal ion are also often present.

CLASSICS OF NEUROTOXINS

In the neurotoxin development there are two pharmacological classes

of neurotoxins: 1) those which are post-synaptic, and 2) those which are
pre-synaptic. Curare is an example of a post-synaptic neurotoxin. It
binds to the nicotinic acetylcholine receptors, and prevents the
depolarizing action of acetylcholine. These toxins are usually referred to
as curare-like toxins. Pre-synaptic toxins inhibit the release of
acetylcholine, and their toxicity is much higher than that of the post-
synaptic toxins.
Another type of toxin is the membrane toxins which change the
permeability of the membrane. They are often cardio-toxins, lytic factors,
cytotoxins, etc. These names indicate the types of membranes they affect.
Membrane toxins have been isolated only from elapid venoms. These
membrane toxins work by penetrating into the hydrophobic layer of the
membrane. Many of these toxins have phospholipase types of structures.
A secondary hypothesis is that the membrane might be disrupted by the
interaction of the disulfides in the toxin and the sulpha-hydro groups in
the membrane. These toxin-induced permeability changes can have
many biochemical and pharmacological activities. They might be
hemolytic which would allow for the disruption of red blood cells; or
cytotoxic, where they might induce a type of leukemia or lymphocytoma.
There is a depolarizing effect of the different membranes which can cause
peripheral nerve problems, contracture, paralysis, ventricular fibrillation

242
and systolic arrest of the heart muscle. They might interfere with
transport mechanisms such as inhibition of the accumulation of anions,
amino acids, or glucose into the tissues of thyroid, kidney, small
intestine, etc. There can be effects on membrane activity and membrane
enzymes. This might provide inactivation of magnesium, sodium,
potassium, and possibly even ATPase. All of these require intact
membranes in order to function properly. Certain of these toxins can
liberate calcium from muscle fibers and produce tetany.
Some plants share some of these membrane toxins. An example is
mistletoe which is a parasitic plant of the family Loranthaceae. Mistletoe
toxins are very basic, and they have an isoelectric point of about pH11.
They are very stable, and heating an ocular solution to 100 C for thirty
minutes has no influence on their toxicity. This mistletoe toxin consists
of 46 amino acids in the peptide chain, cross-linked by three disulfides.
These toxins in low concentration of ten micrograms per milliliter will
produce depolarization and contraction in rabbit papillary and frog
skeletal muscles, and the effects can be reversed by calcium. So it is
suggested that the toxins bind to the cell membrane, and thus displace
calcium.
Let us proceed to analyze some of the different toxins provided by
different venoms. One is crotoxin which is the main neurotoxin of the
South American rattlesnake Crotalus durissus terrificus. This is a very
powerful toxin which affects certain neurons and muscular structure.
Specifically, the toxin from this snake produces problems in the neck
and can contribute to nuchal rigidity. This has caused the South
American rattlesnake to be called the neck breaker, because of its effect
on neck muscles. Homeopathic crotoxin has been used quite successfully
on neck and cervical conditions.
The Australian tiapan, Oxyuranus scutellatus has extremely potent
venom. It exhibits a low phospholipase activity, and has an effect similar

243
to curare. The Australian tiger snake venom has strong effects in being
able to bind calcium, and it is inactivated in the presence of bromine.
Enhydrina schistosa, known as the common sea snake, has venom
which produces myoglobinuria and muscle movement pains. Mice die
rapidly of respiratory failure at high doses; whereas, at low doses,
respiratory conditions can be treated.
The venom of the Bungarus multicinctus has three different neurotoxic
reactions, all of which produce a post-synaptic type of neuromuscular
block. This bungaro toxin has a huge ability to inhibit choline uptake in
the synaptic cleft, blocking the synthesis of acetylcholine which leads one
to believe that it could be important in the homeopathic treatment of
cholinergic diseases such as Alzheimers.
The venom of different rattlesnakes contains a convulxin which
induces convulsions in the intended victim. An example of a cardiotoxin
comes from the Mohave rattlesnake venom. A compound known as
Mohave is known to have dramatic cardiological effects. It is thought that
this venom is also a phospholipase type of toxin.
All types of Crotalus, especially the western diamond back rattlesnake,
contain myocardial depressor proteins which suppress and produce a
myocardial anesthesia or a myocardial depression in the animal.
Some of the different rattlesnakes have a potent hypotensive peptide
known as hypotensin which can dramatically reduce arterial pressure.
Another interesting compound often found in snake venoms is that of
NGF (nerve growth factor). NGF is an agent which regulates growth and
differentiation of neurons in the sympathetic and in some cases sensory
neural tissue. There are three principal characteristics of NGF: 1) the
holofiber outgrowth from dorsal root or sympathetic ganglia; 2) the
sympathetic ganglion enlargement in neonatal mice characterized by
hyperplasia and hypertrophy; and 3) the immuno-sympathectomy, the
destruction of sympathetic chain ganglia by the in vivo injection of anti-
serum to NGF.

244
 Snake Venoms Containing NGF

Viperidae Bothrops jararaca

Bitis gabonica Crotalus adamanteus
Echis carinatus Crotalus atrox
Echis coloatus Crotalus horridus
Vipera ammodytes Crotalus terrificus
Vipera aspis Elapidae
Vipera russellii Dendroaspis viridis
Crotalidae Naja melanoleuca
Agkistrodon piscivorus Naja naja
Ancistrodon contortrix Naja nigrocollis
lactocinctus
Ancistrodon rhodostoma Sepedon haemachatus

Oftentimes, this nerve growth factor occurs in the cobra family. Cobra
venom seems to contain the highest amount of NGF of all the snake
venoms.
The venom of the Black Mamba, Dendroaspiaspsis jamesoni, causes
marked depolarization of membranes and inhibits the excitability of
skeletal muscles. This can effect cardiac and respiratory function;
whereas, the cobra venom is primarily neuro-toxic and causes
degenerative tissue to form. The venom of the families of the viper and
rattlesnake are primarily related to hemorrhages and coagulation
disturbances. The enzyme effect of these different venoms can start lysis
in red cells as well as other cells of the body. This is to prepare the
intended victim for digestion. Cobra venom lowers the red blood cell
count in victims, but this alone does not seem to produce lethal effects.
The most powerful hemolytic snake is the Pseudechis papuans, also
known as the Papuan black snake. People bitten by this snake often
produce red or black urine which results from the breakup of red blood
cells. The hemolysis effects are profoundly proteolytic, and this venom
offers homeopathy some interesting challenges.

245
 Venoms of the viper family are potent in their ability to digest different
cells. In fat, small tears in the blood vessels can occur as a result of this
venom. The action of the proteolytic enzyme in the venom can also
produce necrosis. The venoms of the rattlesnake viper family can have
strong necrotizing effects. Oftentimes necrosis is seen at the site of the
bite in the human victims who survive these snake bites. The proteolytic
effects kill cells homeopathically. It can restore life to necrotized areas, as
in peripheral circulatory disease.
Edema and swelling occur after many different snake bites because
they start histamine cascades. A chart on some of the hemorrhagic and
proteolytic effects of snake venom is shown below.

246
 Distribution of Hemorrhagic, Lethal and Proteolytic Activities
in Snake Venoms

(Ohsaka, A. et al., 1960)

Hemorrhagic Lethal Proteolytic LD50

Snake Venom activity activity activity /
MHD(g) LD50(g) (units/mg) MHD

A. contortrix 1.90 200 33.7 105

contortrix
A. contortrix mokasen 1.20 125 48.1 104
A. piscivorus 0.80 60.0 41.5 75
piscivorus
A. halys 0.14 16.0 35.8 114
Bothrops atrox 2.11 5.6 44.5 2.7
Bothrops jararaca 0.75 18.5 74.0 25
C. adamanteus 0.04 18.5 9.76 462
C. atrox 0.43 45.0 83.6 105
C. durissus terrificus 18.0 3.6 39.2 0.2
C. viridis viridis 0.56 21.0 39.5 38
T. flavoviridis 0.20 54.0 33.0 270
T. flavoviridis 1.15 160 37.8 139
tokarensis
T. elegans 0.30 71.0 13.0 237
T. okinavensis 1.38 140 69.0 102
Vipera russellii 21.0 2.2 5.56 0.1
Vipera ammodytes 0.47 7.4 41.7 16
Vipera palestinae 0.54 7.1 4.96 13
Cuasus rhombeatus 0.81 250 0.26 309
Bitis arietans 0.15 15.0 18.7 100
Bitis gabonica 0.04 13.5 11.7 338
Ophiophagus hannah 0.84 54.0 12.0 64
Bungarus fasciatus 100a 18.5 0.06 0.18
Naja melanoleuca 100 6.0 7.00 0.06
Naja naja atra 100a 8.0 0.12 0.08
Naja naja 100 5.6 2.85 0.06

Key:
A: Agkistrodon
C: Crotalus
T: Trimeresurus

247
 This type of histamine release is compounded by other toxins. Many
rattlesnakes have strong histamine releasing proteins which help to
complicate the involvement of their venoms. A list of the different venoms
and their effect on histamine and serotonin content is shown below.

Effect of Venoms from Different Species of Snakes on the Histamine

(H) and Serotonin (S) Content of Isolated Rabbit Platelets

(Markwardt, F. et al., 1966)

Venom Concentration Effect a Effect a

(g/ml H S
Naja flava, N. haje 100 0 0
N. naja, N. n. oxiana
N. nigricollis 100 ++ ++
Bungarus fasciatus 100 0 0
Dendroaspis viridis 100 0 0
Bitis arietans 100 0 0
Echis carinatus 100 0 0
Vipera ammodytes
V. berus, V. russellii 100 0 0
Agkistrodon piscivorus 100 0 0
A. contortrix 100 + 0
Bothrops alternate 100 0 0
B. neuwiedii 100 0 0
B. cotiara, B. insularis 10 + 0
B. jararacussu 10 + +
B. jararaca 10 ++ +
Crotalus adamanteus
C. atrox, C. viridis 100 0 0
Lachesis muta
Sistrurus catenatus 100 ++ ++
Crotalus horridus 10 ++ ++
C. durissus terrificus 10 + +
C. durissus terrificus 1 ++ ++
C. durissus terrificus 0.1 + +

a 0 = no release: ++ = over 50% release: + = less than 50% release.

248
 Another area to explore is the liberation of pharmacologically active
substances by different snake venoms. Snake venoms can activate and
release histamine, serotonin (five-hydroxytryptamine), and bradykinin.
Some slow-reacting substances can be released such as prostaglandins
and lysophosphatides, catecholamines such as adrenaline, chetosteroids,
and finally, anaphylatoxin. Anaphylaxis can also be stimulated by certain
venoms, or treated with dilute forms of same.
Another dangerous fact about snake venoms is their nephrotoxicity.
The kidney is affected in almost all types of snake bites. Venom can
produce renal lesions including glomerulitis, glomeronephritis, arthritis,
interstitial nephritis, tubular necrosis, cortical necrosis, and renal
infarct. Renal failure is oftentimes the most common result, as well as
hematuria, myoglobinuria, hemoglobinuria, and proteinuria.
Probably the most frequently used remedy in homeopathy from snake
venom is Lachesis. This venom comes from Lachesis trigonocephalous, a
large South American snake from three to fourteen feet long. Its
poisonous venom was first used by Dr. Constantine Hering of
Philadelphia. The Lachesis is prepared at 6x and higher; proportions
below 6x may be dangerously toxic.
In its raw form this can produce a poisonous condition of the blood
which causes hypersensitivity in the body. The patient usually reports
that he cannot bear anything tight around the throat. This is known as a
left-sided remedy, as it usually affects the left side in its raw form. There
is a general aggravation of conditions after sleep which indicates
Lachesis must be used. Blueness of the skin and eruptions can appear.
Some of the other homeopathic indications are loquacity where the
patient jumps from one subject to another; jealousy, fear of being
poisoned, and sometimes the patient imagines that he is under some
superhuman control. Headache over the left eye accompanying a cold,
with the headache worsening in the heat of the sun might also indicate
that Lachesis may be needed.

249
 Facial erysipelas that first appear as red and then dark bluish or
purplish, with more on the left side, can also indicate the need for
Lachesis. Watery discharge from the left nostril, throbbing headache
relieved when the discharge appears; dry tongue protruded with
difficulty, cracked tongue at the tip which is brown on the dorsum, great
difficulty in swallowing, high fever, exhaustion, a craving for oysters,
horribly offensive diarrhea, ovarian trouble (often pain in the left ovary),
menses which are scanty, feeble, black or offensive; and pain in the hips
(bearing down on the left ovary, better when flow is established) are some
of the conditions which can indicate that Lachesis is needed.
Crotalus, the rattlesnake venom, is a classic homeopathic which Dr.
Hering also wrote about. Its homeopathic indications are often a
yellowness of the skin from disintegration of the blood and a tendency to
hemorrhage. In yellow fever, crotalus is often indicated in the stage of
black vomit when there is low delirium, yellow skin, and oozing of blood
from every orifice.
Naja is aother classic homeopathic venom found in the cobra Naja
tripudians. It is often used in degenerative diseases as well as in valvular
diseases of the heart, with a dry, teasing cough present.
Another is the elaps, a type of Elaps corallinus. This is the coral snake
venom which was first introduced homeopathically by Dr. Benot Jules
Mure of Brazil. Some initial homeopathic indications for elaps are:
sniffles in children, stuffed up nose, and a great sense of coldness in the
stomach from cold water.
Another type of venom used in classical homeopathy is the Bufo rana,
or the South American toad. Many South American toads have sweat
that contains neurotoxins. These are noted to affect the sexual system,
and Bufo rana has been used widely for sexual deviance and for many
other types of cases as well. Bufo rana has been used to help encourage
sexuality and to treat cases of frigidity. Its usual dose in those cases is
100x or above.

250
 The Colorado River toad venom is known to cause epilepsy, as many of
the different toad venoms do. Homeopathic treatment of epileptic
conditions consists of different toad venoms.
Sepia succus is an inky secretion released by the cuddle fish when it is
pursued by its enemies. The cuddle fish releases it as a dummy target,
allowing the cuddle fish to go unnoticed. This Sepia product has been
widely used in homeopathy for many kinds of conditions. The five general
characteristics of sepia are: 1) weakness, 2) yellow complexion, 3)
bearing-down sensation, 4) violent motion that relieves the symptoms 5)
the amelioration of symptoms at midday. The mental symptoms of sepia
include weak memory, helplessness, susceptibility to excitement,
susceptibility to terror, despair, fear of being alone (the person wants
company desperately), and headaches (more common in the morning),
increasing as the day goes by, relieved by sleep or violent motion. The
patient who is sad and tearful with headache feels better in open air.
Menstrual headache can also be noted.
Blue Octopus venom produces blood disorders similar to leukemia. It is
powerful homeopathically in the treatment of leukemia
Many spider venoms are of value for homeopathic use. The tarantula
venom, known as Tarantula hispaa, helps in cases of restlessness. The
patient needing this will always be in constant motion, even though
motion aggravates most of the symptoms. The person must be doing
something all the time. This venom becomes very useful with patients
who are hysterical.
Tarantula cubensis relieves the atrocious pain that accompanies a
sloughing carbuncle.
Black Spider venom, also known as Mygale lasiodora, is used in chorea
where there is twitching of the facial muscles, irregular convulsive
movements of one side of the body, words are jerked out, and the
movements cease during sleep but return more violently in the morning.

251
 Theridion, spider venom from Theridion curassavicum or the orange
spider is found in the West Indies. This venom can produce throbbing
pains over the left eye which is aggravated in the heat of the sun. Noise
aggravates it as well. This pain is associated with vertigo, and often
times, nausea. It is worsened by closing the eyes, motion or jarring, or
walking across the floor. There is extreme sensitivity to noise. This
venom is very good for conditions of cardiac anxiety.
The cross spider, known as Aranea diadema, is a large black spider of
the central United States. Two particular symptoms directing one to
aranea are numbness of the parts of the body supplied by the ulnar
nerve, and boring, digging pain in the oscalcis.
Black widow venom gives dramatic help for many neurological
conditions, especially peripheral neuropathy.
Scorpion venoms are powerful in homeopathy. They usually cause
paralysis, pains and weakness, and can be used to reverse some of those
same conditions.
Even the venom from the ant can have homeopathic effects. Ant venom
is very rich in formic acid, and this causes inflammation and irritation;
thus, ant venom can help reverse such conditions.
The venom of the honey bee, Apis mellifica, is highly important in
homeopathy as it produces certain types of conditions. The characteristic
symptoms of Apis are: 1) drowsiness, 2) edema, 3) thirst, 4) intolerance of
heat, 5) stinging pains, 6) aggravation in the afternoon (between 4:00 and
6:00) and 7) bruised sensations. Meningitis can often be treated with
Apis. Oftentimes the patient is fidgety, awkward, clumsy, and silly;
laughs, drops things, and is often very jealous.
Wasp venom can have very powerful implications in homeopathy, as
can the Spanish fly or cantharis.
With this brief review of venoms that nature offers, some intriguing
protein compounds can be utilized. Many of these venoms follow the
Arndt-Schultz principle and have reverse action in small, dilute

252
homeopathic forms, whereas many of these venoms can be utilized in low
doses to accomplish other tasks. There are hundreds of thousands of
insects, spiders, snakes, and animals that carry different venoms. These
venoms have had dramatic potential in shaping medicine. They offer
medicine profound techniques in treating the myriad of diseases found in
the human being.
This is another reason why it is such a tragedy to destroy our rain
forests. Many of the people going to the rain forests are looking just for
plants, herbs, and fungi that might be used in pharmaceuticals, not
realizing that some of the most potent pharmacological acting agents in
the rain forests come from the venoms of these different insects and
animals which are becoming extinct. We must stop cutting down the rain
forests and look in as many different places as we can to find ways to let
nature heal. Nature can heal, and man can destroy.
This short treatise has been only a brief introduction to some of the
pharmacological ways that venoms can be used in homeopathy.

253
 Summary of Immunopathology, Histopathology, and Electron-microscopic findings of the Kidney in Snakebite

Immunopathology Histopathology Electron-microscopy

Location of deposits

Type of Glomerular Arteriolar Arterial Proliferation Tubular Necrotizing Thrombophlebitis Glomerular Glomerular Tubular
capillary wall wall of glomerular necrosis and arteritis electron- basement degeneration,
Snake mesangial regeneration dense membrane necrosis and
cells deposits alteration regeneration
Russells 1gM C3(=) C3(+) + ++ + + + - +
viper (+ to ++)
C3(=)
Green 1gM (trace to C3(=) No + to ++ + - + +b - +
+) deposit
pit viper C3(=)
Fibrin a
Cobra 1gM (+) C3 (=) No + - - - + + -
C3 deposit
(+ to ++)

- = Negative
+ = Mild
++ = Moderate
a
= Focal deposition
b
= With deposition of fibrin

255
Renal Failure with Known Lesions in Various Snakebites

Snake Renal Lesion

Crotalus terrificus Tubular necrosis

Cryptophis nigrescens Tubular necrosis

Sea snake Tubular necrosis
Russells viper Tubular necrosis
Echis carinatus Cortical necrosis
Borthrops jararaca Cortical necrosis
Agkistrodon hypnale Cortical necrosis
Bitis arietans Proliferative
glomerulonephritis

Cases with renal failure without known snake or renal

lesions are not included.

255
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258
 GEMMOTHERAPY

Gemmotherapy consists of making herbal remedies from the buds or

shoots of young plants. These remedies cleanse cells of toxins through
digestion, urinary tract, lung, and skin. Some of the remedies can be
found below.

Abies Pectinata: Decalcification and rickets, dental caries

Acer Campestres: Sequelly of poliomyelitis and paralysis, Herpes Zoster
Aesculus Hippocastanum: Hemorrhoids
Alnus Glutinosa: Sequelly of cerebral hemorrhage, cerebral infarction,
chronic rhinitis
Alnus Incana: Arthritis
Ampelopsis Weitchii: Chronic rheumatism, rheumatoid arthritis
Betula Pubescens: Intellectual overwork, psych-asthenia
Carpinus Betulus: Spasmodic and chronic rhino-pharyngitis, spasmodic
cough
Castanea Vesca: Venous congestion
Cedrus Libani: Dry eczema, ichthyosis, pruritus
Cercis Siliquastrum: Improves arterial circulation
Citrus Limonum: In the presence of an increase in blood fibrinogen
levels
Cornus Sanguinea: Enhanced coagulation
Corylus Avellana: Emphysema and pulmonary fibrosis
Crataegus Oxyacantha: Cardiac insufficiency, precordial pain,
tachycardia, sequelly of infarction
Fagus Sylavaatica: Renal insufficiency, renal lithiasis
Ficus Carica: Obsessional and anxiety neurosis, gastric and peptic
ulcers
Fraxinum Excelsior: Acute and chronic gout
Ilex Aquifolium: Gout or urethema

259
GEMMOTHERAPY, cont.

Juglans Regia: Varicose ulcers, skin infections (impetigo, infected

eczema)
Juniperus Communis: Major hepatic insufficiency and cirrhotic
syndromes
Olea Europaea: Hypertension, arteriosclerosis, hypercholesterolemia
Pinus Montana: Chronic rheumatism, vertebral osteoarthrosis,
osteroarthrosis of the hips and knees
Platanus Orientalis: Urticaria with accompanying inflammation, itching,
and discomfort
Pulus Nigra: Obliterative arterial disease of the lower limbs and
associated trophic disturbances
Prunus Amygdalus: Vascular sclerosis, hypertension
Quercus Pedonculata: Increases the bodily defense mechanisms
Ribes Nigrum: Allergic problems, chronic coryza, hay fever, migraine
Rosa Canina: Migraine and headache
Rosmarinus Officinalis: Hepatic insufficiency, biliary colic, biliary
dyskinesia
Rubus Fructicosus: Female problems, menstrual disturbances, pelvic
pain, metritis and vaginitis
Secale Cereale: Hepatic insufficiency
Sequoia Gigantea: Prostatic hypertrophy and adenoma, uterine fibroids
Sorbus Domestica: Venous problems, sequelly of phlebitis, haemogliasis
Syringa Vulgaris: Arterial sclerosis or improved arterial circulation
Tamaris Gallica: Various types of hypercholesterolemia
Tilia Tomentosa: Nerve sedative, tranquilizer, insomnia, neuralgia
Ulmus Campestris: Weeping eczema, acne and impetigo

260
GEMMOTHERAPY, cont.

Vaccinium Vitis: Intestinal syndromes, chronic E. coli infections

Viburnum Lantana: Simple and complicated asthma
Vitus Vinifera: Bone metabolism and inhibits proliferative deformities
such as osteophytes
Zea Mais: Favors post infarction healing of cardiac tissue and produces a
fall in blood transaminase levels
Source: http://homeoinfo.com/08_non-
classical_topics/is_it_homeopathy/gemmotherapy.php

261
 CLASSICAL HAHNEMANIAN SINGULARS

Acetonum Cactus Grande

Acetyl Choline Chloride Caulophyllum
Acid Cic-Aconite Cell Salts (All)
Acid Citricum Chamomilla
Acid Fumaricum Cehlidonium
Acid Glutaminicum Chlorcamphor Menthol
Acid Malic Chlormphenicol
Acid Pyruvicum Chloroformium
Acid Succinicum Chlortetracycline
Adipinic Acid Cholesterinum
Allergy Malus Chromium Oxide
Aloe Cina
Alpha-Ketoglutaaric Acid Cinchona
Alumina Congo Red
Ammonium Carb. Cortisone
Ammonium Phos. Crataegus
Anacardium Cysteinum
Apis Mel. Cystinum
Arnica Digitalis
Arsenicum Alb. Dimethyl terephthalate
Bar. Oxalsusccinicum Diphenylamine
Belladonna Diphenylhydantoin
Bentonite Di-Sodium Phosphate
Benzinum Crudum DNA
Benzpyrene Echinacea
Berberis Estradiolbenzoate
Bilirubinum Ethylene Glycol
Bryonia Ethylene Oxide
Bufo Rana Evening Primrose
Butter Yellow Formaldehyde Dehydrogenase
Calendula Formaldehyde Sol.
Cantharis Formic Acid
Caprolactam Fumaria
Caprylic Acid Fucus Vesiculosus
Capsicum Germanium
Carbo An. Glutaminum
Carbo Veg. Glycerinum
Carboneum Tetrachloratum Glycocollum
Cardus Mar. Glycogen
Carrageenan (Type 1, Glyoxal
Lycopodium) Graphites
Carrageenan (Type 5, Hamamelis Virginica
Lycopodium) Harnsaure (Acid. Uric)

262
Classical Hahnemanian
Singulars, cont.

Hepa Sulph. Petroleum

Hexamethylentetramin Phenacetinum
Hirudinum Phenylalanine
Histidinum Phosphorous
Hyaluronidase Phytolacca
Hydrangea Plasma (Horse) Prophlthiouracil
Hypoxanthinum Pulsatilla
Ignatia Rauwolfia
Indican Rhus Tox.
Indolum Ruta Grav.
Insulinum Sepia
Interferon Serotonin
Ipeca Silicae (Equisetum)
Iris Versicolor SolidagoSpigelia
Isoniazide Spongia
Isotonic Plasma Staphisagria
Jodoformium Sulfanilamidum
Juglans Sulfur
Kali Carb. Superheated Vegetable Fat
Kreatinum Tetracycline
Lachesis Thioacetamid
Lithium Nitrate Thuj
Lycopodium Tryptophanum
Macrodantin Ubiquinone
Mag Phos. Urea
Mercurius Urtica
Methylethylketon Vaccinnum
Naja Viscum Album (Gr. on Abies
Natrum Muriaticum Alba)
Natrum Sulph. Viscum Album (Gr. on Acer
Nux Vomica Camp.)
Oleander Viscum Album (Gr. on Populus)
Paraffinum Viscum Album (All)
Penicillinum Vitamin D
Peptonum

263
 A NEW PERSPECTIVE ON RESEARCH

In 1991, U.S. News and World Report published a series of articles

about alternatives to medical techniques, and how they are getting more
and more attention by doctors throughout America. More doctors were
turning to alternative techniques in light of the inability to get lasting
results via synthetic allopathy and surgical intervention. As the populace
starts to look for more natural techniques with fewer side effects,
alternative medicine practitioners have been developing natural types of
therapies, and improving their skills with these natural modalities. This
underground medical group has developed some wonderful techniques to
deal with a wide variety of medical problems.
It is important to note that every field of endeavor in society will have
evolution in its thought and philosophies. There can be no eternal
stagnation in the philosophy or psychology of any group.
Through the years medical philosophy has created many different
foundations which have yielded over time. Medicine started with very
natural philosophies and became more statistical and analytical after the
development of statistics by Poincare. Synthetic chemistry came along
and offered its processes, and the dramatic amount of profitability which
could be incurred from patenting such items further helped to develop
the synthetic cause, thus leading to an allopathic philosophy primarily
based on synthetic chemistry and surgical intervention. This is the basic
mind set which has developed in medicine over the last fifty years and
which is now starting to yield to other fields of endeavor. Some of them
are electronics, physics, energetics, naturopathy, and homeopathy.
There is a new psychology of medicine which will develop over the next
five to ten years, and will have a softer philosophy, making up for some
of the mistakes made in the past due to synthetic allopathy.
As we observe this process of the psychological evolution in medical
philosophy, it is important to note that it parallels the psychological

264
evolution of the minds of men. This chapter is dedicated to a new
concept of medical psychology and philosophy. The opponents of this
development will try to cling to old style ideations, and they will also
secure themselves in the arrogant, obstinate stance of being judgmental.
This attitude might stop them from reading and getting the benefits that
this treatise has to offer. We hope that they can soften their hearts and
minds to allow a new psychology and philosophy to develop freely.
In this U.S. News and World Report article, several different modalities
were addressed: acupuncture, biofeedback, homeopathy, nutrition,
naturopathy and others. Please see full-text article below.

BIG CLAIMS, NO PROOF

A look at farther-out cures, from aromas to reflexology

Mainstream doctors may wonder why anyone with heart

disease would take herbs instead of a beta blocker. Yet
the claims for alternative healing are intriguing, if
largely unproven. Here's a guide to six treatments.

HOMEOPATHY

WHAT IT IS. A medical system based on the teachings

of Samuel Hahnemann, a German doctor who in the
1800s believed that symptoms such as fevers should
not be suppressed because they represent the body's
efforts to repel disease.

THE CLAIM. Diseases can be cured only by using drugs

that echo the symptoms. A feverish person, for example,
would be given a drug that would raise body
temperature. And the drugs should be administered in
doses so diluted they are practically undetectable.

THE EVIDENCE. An analysis of 105 controlled though

sometimes poorly executed studies published worldwide
found ''positive'' results for homeopathy treatments in
81 trials, according to a report in last February's British
Medical Journal. The results provide a basis for
continued research, the authors conclude -- with better-
done trials.

265
HERBALISM

WHAT IT IS. An ancient system of medicine in which

preparations of leaves, stems, seeds and roots are
consumed or rubbed on the body.

THE CLAIM. Herbal remedies contain natural

ingredients as potent as synthetic drugs but often safer.

THE EVIDENCE. Plant extracts can indeed be valuable;

researchers constantly seek out new possibilities. May's
Proceedings of the Society for Experimental Biology and
Medicine, for example, reports that Andrographis
paniculata, an herb used in China to cure hepatitis,
dysentery and meningitis, also hampers reproduction in
lab tests of the human immunodeficiency virus, which
causes AIDS. But a report in Allergy last year found that
herbal treatments for rashes made symptoms worse.

NATUROPATHY

WHAT IT IS. A therapy dating to 19th-century Germany

that relies on air, sunshine, water, heat, massage and
herbs to cure both the body and the mind.

THE CLAIM. Illnesses from colds to typhoid can be

cured by purging the body of poisons, accomplished
through fasting, salt-water baths, breathing and
relaxation exercises -- even psychotherapy.

THE EVIDENCE. Few controlled trials have produced

conclusive results.

AROMATHERAPY

WHAT IT IS. An ancient Chinese form of herbal

medicine that seeks to cure illnesses with the aromatic
oils of plants.

THE CLAIM. Plant essences are massaged into the skin,

used as bath oils, inhaled and, in very rare cases, even
ingested.

THE EVIDENCE. Scents can indeed evoke strong

emotions. Recent studies also show that certain scents,
like peppermint, can increase workers' productivity and

266
 vanilla's aroma can be relaxing. But whether scents can
cure diseases like gastrointestinal disorders, as is
claimed, is as yet unproven.

MAHARISHI AYUR-VEDA

WHAT IT IS. A form of natural healing based on ancient

Indian texts recently translated for Westerners by
Maharishi Mahesh Yogi, who introduced the world to
transcendental meditation.

THE CLAIM. All illness results from ''imbalances'' in

such functions as respiration, circulation and
metabolism and can be treated through meditation,
massage and herbal medicines.

THE EVIDENCE. In May, the Journal of the American

Medical Association ran a three-page letter -- not a
study -- from proponents citing positive findings from a
range of investigations. One U.S. study found that so-
called Ayurvedic herbal compounds reduced the
incidence of breast cancers in ''up to 88 percent'' of
experimental animals. It will take many solid studies to
make doctors overlook Ayur-Veda's mystical precepts.

REFLEXOLOGY

WHAT IT IS. A massage technique that attempts to

treat diseases and keep the ''life force'' in balance. Its
origins can be traced to ancient China.

THE CLAIM. Areas on the soles and sides of the feet

govern ''energy channels'' that extend throughout the
body. By massaging specific spots on the foot, a
reflexologist can sense and unblock clogged channels.

THE EVIDENCE. No controlled clinical trials are

described in medical journals.

Reference

Podolsky, Doug. U.S. News & World Report. Big Claims, No

Proof. 23 September 1991. Vol. 111, Issue 13, p77.

267
 The critique of homeopathy was that there were not enough apparent
clinical trials. It is the purpose of this article to question the very
foundation of clinical trials as the end all deciding factor in whether
procedure or medical belief is acceptable or worthwhile in medicine.
The factor of clinical trials means that once an item or drug is chosen it
can be put to a clinical test in the patient population to see if it really
does that for which it was originally designed.
To do a clinical trial, a randomly selected group of patients, possessing
whatever traits we would be looking for (such as diabetes, high blood
pressure, or any other type of medical illness) would be selected. Then, a
controlled population or group is selected. We now give the substance,
the therapy, to a certain number, known as the effect group, and the
control group would get a placebo, or some other type of comparative
therapy regime. We now do a statistical manipulation at the end of this
study, whatever time line it might be, to see if the purported remedy
would work better than placebo in the study. Comparative statistics
would be used to evaluate whether the substance performed well versus
the placebo or control group. This is an over-simplification of a statistical
clinical trial.
The purpose and the basis of our study is to challenge the Null
hypothesis. The Null hypothesis: the two groups which are being
statistically challenged will be equivalent, and will not show any
difference. If the Null hypothesis is disproved, and the two groups are
different, then we can assume that there is statistical evidence that one
group outperforms the other by some criteria.
The problem with modern medical statistical analysis is that if the two
groups are proved equal, and the Null hypothesis is not disproved, then
the assumption is that the two therapies are equivalent. This is not what
the Null hypothesis states, as it was originally set up for analysis. The
true conclusion is that the groups differed, but the difference in the two
groups could not be detected by the limitations of our measurements.

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 Thus, in determining that synthetic vitamins are equivalent to natural
vitamins in the statistical studies we must clarify that the Null
hypothesis does not state that the two groups are equivalent; just that
the sophistication of our measurement skills is not sufficient to measure
the difference. This is the true conclusion which can be achieved from
the Null hypothesis. But oftentimes in science the Null hypothesis is
abused as in assuming that two groups are equivalent, when actually
there might be a problem with accuracy skills.
As we have pointed out, reductionism is often a problem in science, not
the solution. In doing these types of studies we see the errors of
reductionism at their finest.

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 PROBLEMS WITH CLINICAL TRIALS

Reductionism. Reducing the complex patient to simple

measurements. This makes attained information suspect and
weak. Medicine becomes cold, impersonal, and statistical.
Compassion cannot be reflected by statistics.

Never long enough. Effects of a synthetic medication can result in

genetic damage generations later.

Overconfidence and misinterpretation of the Null hypothesis. If a

study of natural vs. synthetic vitamins shows no difference in
results, it does not occur to researchers that they or their ability to
measure could be in error.

Most always benefits the one who can afford to fund the study.
Experimenter effect.

Trials will always reward and reinforce the philosophy of those

performing them. Allopathy is preferred; homeopathy and
naturopathy are ignored.

Quantity does not dispel quantity. Publish or perish rule pushes

paper out of educational institutions which just perpetuates the
allopathic delusion.

Inability to accept the truth that allopathy is hurting patients in

vast numbers. Iatrogenic malpractice suits resulting from synthetic
drugs top fifteen billion dollars a year. We must realize that our
clinical trial process is a failure, and replace it.

These errors of reductionism result in errors of decision-making within

the medical establishment. As we take these individuals with rampant,
variant problems, different conditions of liver function, kidney function,
skin conditions, ethnic backgrounds, and the like, we then take these
populations and reduce them to one type of criteria. We reduce the
complexity of their human diversity to a simple variable of blood
pressure, hormone level in the blood, range of motion, or whatever type
of statistical measurement technique we use.

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 There are possibly millions, if not millions of millions of variables which
can be measured in the human body. The body is vastly complex. No
known study has ever measured all of the variables possible to achieve a
total analysis. Every known study has been reductionistic in some way.
It is necessary to realize the inadequacy of statistical information, and
not revere them or put them on the pedestal created by modern science.

SOLUTIONS TO CLINICAL TRIAL PROTOCOLS

Realization of the inadequacy of any clinical trial to give perfect

conclusions. Incorporate compassion, education, and love back
into medicine.

Nature has designed chemicals and complex compounds such as

herbs and glandulars for millions and millions of years.
Naturopathy comes with its own long-term background study.

Realize that the Null hypothesis only says that this study showed,
not proved, no effect.

Reduce restrictions on orphan drug funding and encourage more

natural drug testing by reducing philosophical criticisms.

Broaden our philosophy of medicine to revere the natural process

and acknowledge the unknown in biology.

Give equal funding to studies on homeopathy and naturopathy at

educational institutions.

Broaden our medical philosophy to include quantum theory,

energetics, homeopathy and naturopathy. Teach doctors that there
is a safer and more compassionate way to do medicine. First dont
hurt must be brought back into medicine. Clinical trials should
only be a small part of medical consideration, and not deified.

As has been stated several times, the concept of reductionism is the

fallacy, the error of science. Not that reductionism is totally bad; it must
be a part of our decision-making process. But to make it the only part,
the pinnacle, the demigod of medicine, is where the error lies. Using

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reductionistic studies to shape medical protocol has resulted in a
medical establishment which is about to collapse under the weight of
iatrogenic diseases and malpractice payments.
In science, the Null hypothesis is often talked about, meaning that we
try to prove an experiment with the Null hypothesis. As an example, our
hypothesis might be that digitalis can help heart patients. The Null
hypothesis is that digitalis does nothing, and actually is no different from
a placebo. To test our Null hypothesis we work up a random-sample
group, wherein two populations will receive different treatments. One will
get digitalis and one will get a placebo. If both groups experience equal
results, then the Null hypothesis is proven; there is no difference
between the groups or the interventions. This basic assumption is
incorrect in the true management of science. In the true management of
experimental science and statistical management we will find that all
that we know from this study is that the study could not prove any
difference between these two materials. It is wrong to assume that the
two materials are the same just because this study did not prove them to
be different.
In 1982, the Journal of the American Medical Association published an
article about hyperactive children. (Consensus Conf: Defined diets and
childhood hyperactivity. JAMA 1982; 248(3)290-292.) One group was
given lemonade made with a processed white sugar and the other was
given lemonade made with saccharin. It was found that there was no
basic difference between the two groups, and that the Null hypothesis
was achieved. Many of the medical doctors who reported on this study
and who were quoted on Lifetime Medical Network said that from this
study they could conclude that there were no problems regarding
hyperactivity generated by sugar. That was an irregular conclusion. The
actual conclusion is that there is no difference between saccharin and
processed sugar, but the study did not involve any natural sugars or
fruit sweeteners.

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 Just because the study tells us that there are no differences does not
mean that differences do not exist. One such example of bad science has
happened over the last fifty years: during this time scientists have found
from their studies that there is no difference between natural and
synthetic compounds.
Thus, a natural vitamin was found to have the same effect as a
synthetic in that the two did not prove different in studies performed.
These studies were reductionistic and flawed. Just because their studies
could not find any difference does not mean that there were no
differences.
The basic misuse of the Null hypothesis has generated a tremendous
income for synthetic pharmaceutical companies who develop synthetic
compounds by the train-car load. Studies that do show differences
between the natural and synthetic compounds are quickly discounted by
the chemical companies. This brings us to a political ideation of who can
make a true judgment on the correctness of a study, and oftentimes the
philosophy of the judge will affect his decision.
In America, it is complicated by the issue of freedom of choice. If a
person truly wishes to have natural entities, and only natural entities
put into his/her body, this is his/her choice. These natural compounds
are dispensed under the same guidance of the Food and Drug
Administration to guarantee safety and efficacy. Yet, synthetic chemical
companies wish to inhibit the choice of the population and force on it
synthetic compounds.
Many drugs get through clinical trials and later are found to cause
sickness in the patient population. Every year, ten to twenty
medications, on the average, are taken off the shelves of pharmacists
because the clinical trials were not thorough enough in finding out some
of the different problems. Prozac was released into the medical system,
and now much evidence is pointing to the fact that people taking Prozac

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might develop unstable thinking. Prozac might possibly even contribute
to provoking a user to kill other people in fits of anger.
Thalidomide was made available after clinical trials proved its success
in handling morning sickness. But thalidomide produced babies born
with flipper like appendages, and other gross genetic defects. One of my
professors remarked at that time that it was a blessing that
thalidomide caused these deformed flippers and great aberrant
dysfunctions of genetic material. I inquired what he meant by blessing.
He said that the blessing was that it was a violent enough reaction that it
got taken off the market quickly. What if the effect of thalidomide was
that it just lowered ones I.Q. five or ten points? We might not have
discovered that until several generations later. Thalidomide was taken off
the market, altered, and released back on the market as Benedictine.
Benedictine had just that effect, it lowered the IQ ten points, and was
later taken off the market in the late 1980s because of its ability to alter
genetic functioning and cause a wide variety of learning disabilities and
other disturbances.
The thalidomide problems were horrible, but were not pervasive
throughout the population. The Benedictine problems were much less
horrible, but were much more pervasive, as it affected literally millions of
children in America.
The following is a list of drugs that were taken off the market after it
was found that their original clinical trials were not thorough enough to
indicate some of the problems with them. Perhaps this list will convince
the reader that clinical trials are not sufficient to protect the public.

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Acetazolamide
Acetyldigitoxin
Alkavervir
Allopurinol
Alseroxylon
Aminophylline
Aminosalicylate Sodium
Amitriptyline Hydrochloride
Amodiaquine Hydrochloride
Ampicillin/Ampicillin Trihydrate
Anileridine Hydrochloride
Anisotropine Methylbromide
Atropine Sulfate
Azathioprine
Bacampicillin Hydrochloride
Bendroflumethiazide
Benzthiazide
Benztropine Mesylate
Betazole Hydrochloride
Bethanechol Chloride
Bretylium Tosylate
Bromodiphenhydramine Hydrochloride
Brompheniramine Maleate
Butabarbital Sodium
Calcium; Meglumine; Metrizoic Acid
Calcium Metrizoate
Captopril
Carphenazine Maleate
Carprofen
Cefadroxil
Cephalexin
Cephradine
Ceruletide Diethylamine
Chlophedianol Hydrochloride
Chloramphenicol
Chloramphenicol; Polymyxin B Sulfate
Chloramphenicol; Prednisolone
Chlordiazepoxide Hydrochloride
Chlorhexidine Bluconate
Chlormerodrin, HG-197
Chloroquine Phosphate
Chloroquine Phosphate; Primaquine phosphate
Chlorothiazide
Chlorpheniramine Maleate
Chlorphentermine Hydrochloride
Chlorpromazine Hydrochloride

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Chlorpropamide
Chlorthalidone
Chlorzoxazone
Chymopapain
Cisplatin
Clindamycin Hydrochloride
Clorazepate Dipotassium
Codeine Phosphate; *Multiple*
Colchicine; probenecid
Cortisone Acetate
Cryptenamine Acetates
Cryptenamine Tannates
Cyclobenzaprine Hydrochloride
Cyclothiazide
Cycrimine Hydrochloride
Cyproheptadine Hydrochloride
Cysteine Hydrochloride
Decamethonium Bromide
Demeclocycline Hydrochloride
Deserpidine
Desoximetasone
Desoxycorticosterone Acetate
Dexamethasone
Dexamethasone Sodium Phosphate
Dexbrompheniramine Maleate
Dexbrompheniramine Maleate; Pseudoephedrine Sulfate
Dextroamphetamine Sulfate
Diatrizoate Meglumine
Diazepam
Diazoxide
Dibucaines Hydrochloride
Dicloxacillin Sodium
Dicumarol
Diethylpropion Hydrochloride
Diethylstilbestrol
Difenoxin Hydrochloride: *Multiple*
Diflorasone Diacetate
Digitoxin
Digoxin
Dihydroergotamine Mesylate; Heparin Sodium; Licocaine
Hydrochloride
Dimenhydrinate
Dinoprost Tromethamine
Diphemanil Methylsulfate
Diphenhydramine Hydrochloride
Disulfiram

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Dopamine Hydrochloride
Doxepin Hydrochloride
Doxyclycine Hyclate
Dromostanolone Propionate
Dydrogesterone
Dyphylline
Epinephrine; Etidocaine
Hydrochloride
Epinephrine; Lidocaine
Hydrochloride
Ergocalciferol
Ergoloid Mesylates
Erythromycin
Estradiol Valerate; Testosterone
Enanthate
Estrogens, Conjugated
Estrogens, Esterified
Estrone
Ethchlorvynol
Ethinyl Estradiol
Ethinyl Estradiol; Norethindrone
Ethoxzolamide
Ethylestrenol
Ethynodiol Diacetate; Mestranol
Etidocaine Hydrochloride
Ferrous Citrate, FE-59
Fluocinolone Acetonide
Fluorometholone
Fluphenazine Hydrochloride
Fluprednisolone
Folic Acid 1 mg
Gallium Citrate, GA-67
Gemfibrozil
Blutethimide
Glycopyrrolate
Gonadorelin Hydrochloride
Gonadotropin Chorionic
Guanabenz Acetate
Halcinonide
Haloperidol
Heparin Sodium
Hetacillin
Hetacillin Potassium
Hexachlorophene
Hexocyclium Methysulfate
Hexylcaine Hydrochloride

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Homatropine Methylbromide
Hydralazine Hydrochloride
Hydrochlorothiazide
Hydrochlorothiazide;
Labetalol Hydrochloride
Hydrochlorothiazide; Methyldopa
Hydrochlorothiazide; Pindolol
Hydrochlorothiazide; Reserpine
Hydrochlorothiazide; Spironolactone
Hydrochlorothiazide; Triamterene
Hydrocodone Bitartrate; *Multiple*
Hydroflumethiazide
Hydroxocobalamin
Hydroxystilbamidine Isethionate
Hydroxyzine Hydrochloride
Hydroxyzine Pamoate
Ifosfamide
Imipramine Hydrochloride
Indocyanine Green
Indomethacin
Insulin Suspisophane
Purified Pork
Insulin Susp Protamine Zinc
Purified Pork
Insulin Zinc Susp, Extended
Biosynthetic Human
Iodipamide Sodium
Iodoxamate Meglumine
Isoetharine Hydrochloride
Isoniazid
Isoproterenol Hydrochloride
Isoproterenol Sulfate
Isosorbide Dinitrate
Lactulose
Levallorphan Tartrate
Levodopa
Levopropoxyphene Napsylate, Anhydrous
Lidocaine Hydrochloride; Oxytetracycline
Liothyronine Sodium
Liotrix (T4; T3)
Lithium Carbonate
Loperamide Hydrochloride
Loxapine Succinate
Mannitol
Mazindol
Mebutamate

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Meclizine Hydrochloride
Meclofenamate Sodium
Mefenamic Acid
Mefloquine Hydrochloride
Menadiol Sodium Diphosphate
Menadione
Mepenzolate Bromide
Meperidine Hydrochloride
Meprednisone
Meprobamate
Mestranol; Norethindrone
Mestranol; Norethynodrel
Metharbital
Methicillin Sodium
Methixene Hydrochloride
Methocarbamol
Methotrexate Sodium
Methoxsalen
Methyclothiazide
Methylprednisolone
Methylprednisolone; Neomycin Sulfate
Methyltestosterone
Methyprylon
Metoclopramide Hydrochloride
Metrizamide
Minocycline Hydrochloride
Minoxidil
Molindone Hydrochloride
Naloxone hydrochloride
Netilmicin Sulfate
Niacin 500 mg.
Nitrofurantoin
Nitrofurantoin Sodium
Nystatin 500,000 IU.
Orphenadrine Citrate
Oxandrolone
Oxazepam
Oxybutynin Chloride
Oxyphenbutazone
Oxyphenonium Bromide
Oxytetracycline Hydrochloride
Oxytocin
Paramethadione
Pargyline Hydrochloride
Paramomycin Sulfate
Penbutololl Sulfate

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Penicillin G Benzathine
Penicillin G Potassium
Penicillin G Procaine
Penicillin G Sodium
Penicillin V Potassium
Pentazocine hydrochloride
Pentobarbital Sodium
Pentolinium Tartrate
Perphenazine
Phendimetrazine Tartrate
Phenindoine
Phenmetrazine Hydrochloride
Phenprocoumon
Phentermine Hydrochloride
Phentermine Resin Complex
Phenyl Aminosalicylate
Phenylpropanolamine Hydrochloride; *Multiple*
Phenytoin Sodium
Phytonadione
Piperacetazine
Piperazine Citrate
Pipobroman
Potassium Aminosalicylate
Potassium Chloride
Pralidoxime Chloride
Prednisolone
Prednisolone Acetate
Prednisolone Sodium Phosphate
Prednisone
Prilocaine Hydrochloride
Procainamide hydrochloride
Procaine Hydrochloride
Procaine Merethoxylline; Theophylline
Prochlorperazine Edisylate
Prochlorperazine Maleate
Progesterone
Promazine Hydrochloride
Promethazine Hydrochloride
Propantheline Bromide
Propoxyphene Hydrochloride
Propoxyphene Hydrochloride; *Multiple*
Propranolol Hydrochloride
Propyliodone
Propylthiouracil
Protamine Sulfate
Pseudoephedrine Hydrochloride

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Pseudoephedrine Hydrochloride; Triprolidine Hydrochloride
Pyridoxine Hydrochloride
Pyrvinium Pamoate
Quinestrol
Quinidine Gluconate
Quinidine Sulfate
Rescinnamine
Reserpine
Saralsin Acetate
Secobarbital Sodium
Selenomethionine, SE-75
Sodium Iodide, I-123
Sodium Iodide, I-131
Sodium Monofluorophosphate
Sodium Succinate
Somatropin, Biosynthetic
Streptomycin Sulfate
Succinylcholine Chloride
Sulfabenzamide; Sulfacetamide; Sulfathiazole
Sulfadiazine
Sulfameter
Sulfamethizole
Sulfamethoxazole
Sulfaphenazole
Sulfasalazine
Sulfinpyrazone
Sulfisoxazole Diolamine
Sulfoxone Sodium
Suprofen
Technetium TC-99M Albumin Aggregated
Technetium TC-99M Sodium
Pertechnetate
Temazepam
Testolactone
Testosterone Propionate
Tetracycline Hydrochloride
Thalidamide
Theophylline
Thioridazine Hydrochloride
Thyroglobulin
Timolol Maleate
Tioconazole
Tolazamide
Tolbutamide
Trazodone Hydrochloride
Triamcinolone Acetonide

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Triazolam
Trichlormethiazide
Triclofos Sodium
Tridihexethyl Chloride
Triflupromazine Hydrochloride
Trihexyphenidyl Hydrochloride
Trimeprazine Tartrate
Trimethoprum
Trimipramine Maleate
Tripelennamine Hydrochloride
Triprolidine Hydrochloride
Trisulfapyrimidines
Troleandomycin
Ursodiol
Verapamil Hydrochloride
Veratrum Viride
Vinblastine Sulfate
Fincristine Sulfate
Viomycin Sulfate
Warfarin Potassium
Warfarin Sodium
Xenon, XE-133

Some forms of these compounds were restricted after clinical trails

showed them to be safe. There has been tremendous iatrogenic (doctor-
induced) damage done to the people of the United States. Clinical drug
trials are not at fault here, but the medical establishments worshipping
of these clinical drug trials are. Every drug on this list went through the
same clinical trials that the medical establishment uses as its criteria.
This decision-making process of taking clinical trials and making them
the demigod of the industry is at fault. People are being hurt because of
faulty logic in medicine. These trials are expensive and can be purchased
by rich patent-seeking synthetic chemical companies. This author
realizes that challenging the establishments heart will not be taken
lightly, and will not be without violent attacks.
If the legal damages that have been incurred by these iatrogenic
compounds are looked at, it is possible to see that there are literally
billions of dollars every year paid out by drug companies in medical

282
malpractice and iatrogenic damage suits. The vast amount of damage
caused by this industry is incredible; an industry which takes in
approximately one hundred billion dollars of income pays out literally ten
to twenty billion dollars a year in malpractice settlements. This still
leaves an eighty billion dollar profit margin in an industry which spends
very little in actual product manufacturing. The largest amount of
expenditure by any drug company is that of research, development, and
clinical trials of laboratory studies.
It is this very research and development of the whole cognitive plan of
allopathic medication that is being challenged. The allopathic medication
philosophy is one that works against the body, or develops a compound
to sedate a symptom. If the person has a histamine response, an anti-
histamine is given; if the person has depression, an MAO inhibitor may
be given. In every case of allopathic utilization, it is assumed that the
bodys function is irregular and foolish, and some type of synthetic
irregularity which can upset the cybernetic balancing system of the body
develops.
The legal issues of medical practice are also stacked against alternative
practitioners. In 1990, of the 570,000 doctors in the United States, 1,437
were put on probation, or had their licenses suspended or revoked. That
represents .3% of the doctor population. In 1989, there were 1,500, and
9 practitioners who were likewise reprimanded. Very few of these
practitioners were actually prosecuted for unprofessional conduct by
aligning themselves with alternative practices. The majority of these
medical doctors were dealt with because of alcohol abuse, drug abuse,
and sexual abuse of patients; some of them for allopathic malpractice.
Very few of them were actually dealt with because of alternative theories.
In most states, a medical doctor is bound to perform therapies and
diagnostic techniques which are medically accepted.
In 1990, the Alaska State Medical Board may not base a finding of
professional incompetence solely on the basis that a licensees practice is

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unconventional or experimental in the absence of demonstrable physical
harm to the patient. Source: www.healthy.net/public/legal-
lg/regulations/MPA.HTM)
If the doctor is not hurting anybody with an experimental or
unconventional technique, he/she would not have his license revoked.
Strong evidence would have to be found that the patient had been
harmed in order to challenge the doctor. Many of these so-called
unconventional therapies are accepted by a vast majority of doctors, and
there is no one form of medicine that is accepted above all others.
Medicine abounds with many techniques that are not fully, scientifically
evaluated or properly challenged. Oftentimes, doctors who use these
unconventional techniques are challenged by traditional medical doctors
on the basis of only one or two cases. Many doctors have had their
practices disrupted because of one or two cases where unconventional
therapy did not quite abate the patients complaint.
Doctors see patients dying every day. Hospitals abound with patients
whose therapies and diagnostic accuracy have led to their demise. Robert
S. Mendelsohn, in his book, Confessions of a Medical Heretic, (Chicago:
Contemporary Books. 1979), wrote that when the doctors in a group of
hospitals in a certain local community went on strike, there was a major
change in the death rate it dropped dramatically. Fewer people died
when doctors stopped practicing some accepted medical techniques.
In another case in Denver, Colorado, the state charged parents for not
using traditional medicine when their child died from a disease that was
assumed to be treatable at a local hospital. The parent was a Christian
Scientist who believed more in prayer than in drugs. If the ratio of
children who survive with Christian Scientist parents vs. the ratio of
children who survive overall in hospitals is looked at, there is a
tremendous degree of variance. Children died at a greater rate in
hospitals than they did from having Christian Scientist parents. In the
world today, The United States is fifteenth overall in birth mortality,

284
meaning that there are fourteen countries where newborns have a better
chance of survival than in the United States. These countries are those
that depend more on natural medicine, homeopathy, and prevention
techniques. Perhaps these types of analyses can open up the closed
minds of the so-called traditional statisticians to realize that perhaps
there is an alternative.
Legal judgments can be based on incomplete scientific ideas. It must
be accepted that the science of medicine is a pseudo-science; it is not an
exact philosophy. With this in mind, we should be slow to write laws that
prohibit or discourage different philosophies of medicine.
Practitioners and patients have the right to make choices. Medical
boards and peer groups are not needed to challenge practitioners who try
to take philosophies and practices and push them into areas where they
do not have strong scientific validity. The laws of each state for the
practice of medicine are vital, and medical board inquiries are essential
in developing better and better qualities of medicine. Yet in the proof that
a doctor is doing something wrong with unconventional techniques, as in
the case of Warren Levin, who was challenged because of two separate
instances, it should become quickly apparent that one should not jump
to conclusions on one or two cases of impropriety. No doctor in the land
could withstand such a shifted bias. Whereas one or two cases out of the
thousands seen over a ten-year period should put a persons practice on
the line. Statistics must be looked at as well, and looked at for a certain
percentage, wherein a doctor might be brought out in front of a peer
group, and the peer group also should be able to express different
opinions.
Many people with medical minds are firmly entrenched in
reductionism, synthetic chemistry and surgery, who make tremendous
amounts of money for the industries that they promote. Yet people die
every day of iatrogenic diseases resulting from surgery and synthetic
drugs. Society has found a way to let these doctors off the hook, and yet

285
they put doctors who do unconventional therapies on the hook. It is
possible that this challenge might be directed to help destroy a natural
medicine industry which would challenge the incomes of the synthetic
drug companies.
Investigative books, including: Murder by Injection: The Story of the
Medical Conspiracy against America, by Eustace Mullins (P.O. Box 1105,
Staunton, Virginia 24401: National Council for Medical Research, 1988).
Off the Pedestal: New women in the Art of Homer, Chase, and Sargent,
edited by Holly Pyne Connor. New Brunswick, N.J.: Rutgers University
Press, 2006, Mendelsohns series, and many others, are bringing to light
the vast medical cover-up that has been promulgated by allopathic
minds seeking to tyrannize and influence the minds of men. We need to
deepen our philosophy of medicine, get into quantum physics, and try to
understand biology at many different levels. These levels will include the
ideas of statistical analysis, peer group philosophies, and scientific
development of energetic phenomena.
In the Quantum Biology Workbook, a heavy-duty physics statement is
made using the highest levels of mathematics, physics and science
known to our society. We conclude that allopathy is an irregular choice,
and that the factors of clinical trials in reductionistic science are
incomplete in their ability to protect the people using pharmaceutical
products. We can see from this advanced physics and this upper level
science that homeopathy and naturopathy are much more logical choices
to use in developing medical techniques.
As we go through different clinical trials that have been done in this
book, we also review the literature of other research that has been done
in naturopathy and homeopathy. We can see that in almost every
attempt to utilize naturopathic and homeopathic techniques success is
achieved. It is very rare in the literature to find a homeopathic or
naturopathic study that failed to show a large degree of efficacy and
safety.

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 Jos Kleijnen, Paul Knipschild, and Gerben ter Riet, in their article in
the British Medical Journal, Clinical Trials of Homeopathy, (BMJ 1991;
302(6772), 316-323), assayed over 105 clinical trials of homeopathy from
around the world. They concluded that 81 of the trials showed positive
scientific undeniable results; 24 of them could be challenged. They
concluded that there was a legitimate case for further evaluation.
Full text article can be found at:
www.pubmedcentral.nih.gov/picrender.fcgi?artid=1668980&blobtype=pdf
According to the Null hypothesis in the case of homeopathy there is
dramatic evidence of efficacy. Homeopathy works according to the
scientific literature. With this type of data contained in these books and
in this type of report it would seem that the use of homeopathy not only
should be warranted, but that using an allopathic drug, which could
produce a side effect or risk, might become a case of medical impropriety.
I dont believe that medicine can wait for homeopathy to be challenged
over twenty years time.
Homeopathy and naturopathy as an industry throughout the world
outsell allopathic medications by almost three to one. This is because of
the large amount of sales that are done in India, Pakistan, Bangladesh,
China, etc. Out of this entire world market, which amounts to perhaps
ten billion dollars in sales (it costs much less to manufacture and sell
homeopathic products than allopathic ones), malpractice and different
settlements measure in the thousands of dollars throughout the entire
world. There are hardly any suits against naturopathic and homeopathic
doctors, although when this does happen they are usually very small.
Out of a ten billion dollar industry, less than one percent of one percent
of one percent of one percent of its total capital generation is paid out in
malpractice, compared to our allopathic counterparts, who pay in the
neighborhood of fifteen to twenty percent a year in settlements.
The justification for homeopathy need not come completely from
clinical trials. Without using clinical trials its possible to look at the

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world market and see that homeopathy works. It makes sense. One can
look at the returns on malpractice insurance which shows how many
people were hurt, and see that homeopathy works, whereas synthetic
chemistry hurts. The statistics bear this out. One can look at these
statistics and see that allopathy needs to be challenged, and that the
process of using clinical trials and revering the publication/print process
as the end all answer must be challenged in order to proceed any further
with medicine. Reductionistic clinical trials are the problem, not the
solution.
It must be realized that the mind of the observer interferes with the
experiment. This is a basic premise of quantum theory which allopathy is
not putting into use. The basic treatise of this book has proven that
quantum theory must be considered as a meaningful step into biology.
In quantum theory, the mind state of the observer will influence the
outcome. In the preparation of clinical trials, the power of mental
philosophy and the mind state of the person behind them must be
recognized. The development of modern chemistry, which pinnacled in
synthetic processes, gave these people a severe mind set, a mind set
based on chemical analysis, not energy, physics, and other sciences. This
predominantly chemical-based philosophy will interfere with their
observational ability. Hence, it is possible to see the action of this
philosophical backdrop in their pursuit of medical truth. This has led to
chemical solutions, surgical solutions, and allopathic ideation.
Another philosophical and psychological problem behind this medical
juggernaut is the idea of allopathic superiority to nature. As was pointed
out in Quantum Biology, it is basically akin to the philosophy of allopathy
and synthetic chemicals that the observer knows more than the situation
he or she observes, in that the medical doctor knows more about biology
than the patients body. The patients body, thus, becomes flawed and
stupid in the eyes of the experimenter. If there is a histamine reaction,
an anti-histamine is given to the stupid body; if there is depression, the

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stupid body is given an MAO inhibitor; if there is fever, the stupid
body is given an anti-pyretic. In other words, the concept of allopathy is
that something is wrong with the body and that outside intervention
from a superior intellectual source will help correct the problem. This
also is a seriously flawed philosophy and psychological backdrop to
which all of the medical experiments are then interred.
With homeopathy and naturopathy as a basis in medicine, we can
develop a different foundation. Our foundation will revere the natural
process, and realize our inability to know intimately such a process. We
would want to intervene on the process very little, and try to stimulate
the process back to its own natural balance using natural mechanisms
and gentle nudges to help stimulate the organism to achieve its own
balance. The organism has the superior knowledge of biology.
If we take such a philosophy, and reevaluate the last hundred years of
medical research, we can see that some of the conclusions drawn from
allopathy were severely flawed. An overview of the medical research will
show us that many of the experiments performed were reductionistic and
philosophically inadequate.
Part of this book has been written with the idea that there is an
evolution in human thought, and that human thought has evolved from
many different states. It is wrong for us to think that human thought
and social conditions have stayed the same through the years. The early
tribes and societies had very weak ideas of philosophy and the ideation of
a king becoming part god showed some of the limitations of their
thinking. Early societies did not have the ideation of spatial organization
to allow them to do proper art perspectives. This was a developmental
process. There was a developmental process in the ideas of psychology
and philosophy, in the idea of science, and in the concepts of religion
and theology.
Every form of human thought will evolve and change through the ages,
just as medicine will evolve and change through the impact of this book

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and thousands more like it. They will challenge the ideas behind medical
thought and philosophy and bring about new ones that include a soft
approach, and a gentleness and humility toward what is not known. As
we develop and achieve this new type of mental thought we will be able to
embrace an old philosophy of medicine. We will be able to find this old
philosophy, ignored by technology and achieve a new way. The thesis
and the antithesis will blend into a new form of truth. The thesis is that
of naturopathy and homeopathy; the antithesis is allopathy and surgery.
These two will blend to achieve a new form of thought in which the
doctor, being educated and knowledgeable in all of these different
philosophies will have more directed choices, and will be able to affect
more safety and efficacy with his patients.
It is this authors purpose to challenge the conclusion of the article in
the U.S. News and World Report. Perhaps more long-term studies need to
be adapted to allopathic thought (long-term meaning over a period of ten
generations). To say that more clinical trials need to be done in
homeopathy is to state a truth, but to say that before homeopathy
should be used by the masses, this needs to be done is to state an
untruth. Grossly incorrect is this proposition to make homeopathy spend
massive amounts of money on ridiculous reductionistic trials.
Homeopathy is a legal entity in America and should not be forced into
major expenditures in clinical trials which would do nothing to increase
safety or efficacy. It is the opinion of these synthetic drug companies that
if they could force homeopathy into such trials, they could perhaps
destroy homeopathy, because it does not make the large amounts of
money that allopathy does. Homeopathy would not have the money to
afford such trials. Homeopathy by definition is not a money-making
proposition. It is, however, curative.
These trials are irregular with modern mathematics and modern
medicine, and they will not give us the complete results we thought they
would. Statistics lie, and statisticians deceive.

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 The FDA was formed by Dr. Clayton to protect homeopathy. He lobbied
for years and years for a federal organization that could protect the
American people in their choices of food and drugs. He sought to help in
protecting the philosophy of homeopathy. Within two weeks after
founding the FDA, Dr. Clayton died. The FDA has acknowledged the
Homeopathic Pharmacopeia of the United States, and it is a legally
accepted in America. The Homeopathic Pharmacopeia of the United
States (HPUS) has never commanded enough money to generate
popularity.
Allopathic philosophy and its use of clinical trials have sought to
tyrannize peoples minds and change their perspectives. It has hoped
that doctors would make allopathic choices of drugs, rather than
homeopathic choices. This type of tyranny over the minds of people is
what the founders of our country sought to defend against.
In 1991, President George W. Bush developed a thyroid condition which
produced heart palpitations. This author wrote him a letter. In that
letter, I said (in paraphrase):

Mr. President:

As President of the United States, I recognize that you have a

lot of pressure to choose an allopathic therapy for your
condition. At this time of war, (written just after the Gulf War), I
can imagine the tremendous amount of stress and tension that
you were going through, and I can also fathom how it has
probably produced a hyperthyroid condition that has now gone
out of control. In your choice of therapy, Mr. President, you as
an American citizen have the right to choose many different
types of medicines.

Your can choose chiropractic treatment for your condition,

and perhaps adjustment of the nerves might provide a balance
to the thyroid and alleviate stress. You can choose acupuncture
treatment, and an acupuncturist might try to balance the
meridian flow and help to sedate the irritation of the nerves of
the heart, and sedate the body and balance its energies. You
can choose nutrition, and seek a diet to help relax and balance

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your metabolism. You can also choose homeopathic therapy,
and take a homeopathic which we have shown to be not only
safe, but also effective in many cases of treating hyperthyroid
conditions. You could choose naturopathy in the District of
Columbia, and seek natural therapies for your condition. You
also can choose allopathic medicine, which works against the
body. I realize, Mr. President, the tremendous amount of
pressure on you to choose allopathic medication. Because of
your position as United States President, if you were to choose a
chiropractor, acupuncturist, homeopath, or other doctor, you
might rock a very large economic boat, and threaten an
entrenched philosophy of medicine.

The Queen of England, in a very similar position, has made

the choice of homeopathy, Mr. President. She, The Queen of
England and her family are only treated by homeopathic
physicians; they are not treated in allopathic ways at all. They
have rocked the big boat for many, many years. Even in light of
extreme pressure, the logic and success of homeopathy
outweighs the finances of allopathy.

Along with this letter, I send two bottles of Hyperthyro-1

homeopathic which we were able to blend. We did some pilot
studies and found that it was safe and effective in these cases.
Many similar cases of hyperthyroidism have been cured by this
remedy.

So, Mr. President, you as an American citizen have the

freedom of choice, to choose any of these different endeavors. I,
as an American citizen have the freedom of choice, to write this
letter, and to voice what type of therapy I might have chosen.
Had I been in your position, Mr. President, I would have chosen
homeopathy and alternative natural therapies. [President Bush
could also have chosen naturopathic treatment, since
naturopathy is legal within the confines of Washington, D.C.]

But also, Mr. President, as an American citizen I will fight for

you to have the right to choose. If you choose allopathy, even if I
dont agree or approve, I will fight to protect that choice. I hope,
Mr. President that you will also fight to protect my choice. There
are several forces in the allopathic community who so value
clinical trails, and so value their process and their philosophy
that they seek to tyrannize the minds of men. And Mr.
President, you can walk down to the Jefferson Memorial, where
written around the top of the inside of the memorial, in big
letters carved in stone, is a quote by Thomas Jefferson: I have

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 sworn on the altar to oppose any tyranny over the minds of
men. Mr. President, freedom of choice has never been more
threatened than it is now by allopathic mental tyranny.

Homeopathy entered into 1992 with some baggage as well. The people
doing homeopathy in the United States were, most of the time, unable
and unwilling to do highly sophisticated quality control. Oftentimes, the
manufacturers did not comply with legal regulations set out by the FDA.
Even the 211 CFRs (Code of Federal Regulations) were not utilized by
unregistered homeopathic companies. Homeopathy must build quality
control techniques such as those used at Dr. Recommends; pilot studies,
clinical trials, safety and effectiveness analysis, culture techniques, and
chromatography. Quality control techniques of the energetic process
must be done as well, such as the REGAE (Rare Electron Gas Allopathic
Evaluation) capacitance rating, inductance rating, conductance rating,
and polymorphic shaping studies to understand the crystalline effects.
These are some of the techniques that must be done in a true quality
control way, as well as total legal compliance. As yet, the homeopathy
industry as a whole does neither. To meet the challenge of our new
thinking, and to direct homeopathy back into the medical mainstay, it
will have to meet these challenges head on, change, and bring itself into
reputability.
As we have seen from our exploration, reductionism was probably more
of a problem than a solution in science. We need to use our
reductionistic trials; we also need to develop holistic, individualized
concepts of medicine for more safety and effectiveness without just using
short-term clinical trials. Nature knows protection. We only hope that the
freedom of choice be kept alive in America. Many people I have known
have left America in search of freedom of medical choice. We can only
hope that freedom of choice be reestablished as the basic tenet of the
American justice system. Our capitalistic philosophy has produced a
successful past for our patentable, synthetic, chemical brethren. But

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now the logic and reason of homeopathy and naturopathy must earn at
least the freedom of choice. Perhaps this philosophy will earn more. As
Victor Hugo once said, There is only one thing more powerful than all
the armies of the world, and that is an idea whose time has come.
Natural medicines time has come. Watch out, allopathy.
Deepak Chopras book, Quantum Healing: Exploring the Frontiers of
Mind/Body Medicine, New York: Bantam Books, 1989, offers supportive
information for what is discussed here. He speaks of the idea of quantum
healing which must involve compassion, and a new form of
understanding that goes beyond the physical area into quantic
dimensions. This is very important for us to realize. In his book, he
makes a point about how a certain patient was picnic-deficient, and
needed to have nice, enjoyable picnics to restore him to health. Chopra
puts into view a mystical connection with another world, and explains it
in different Asian terms. These terms he later relates to as quantum
factors of types of energy.
In our treatise, we also find that there is something that affects this
indeterminacy, or quantic principle. We have called it a God
Consciousness, a nature within Quantum Biology. We truly believe that
Chopras referral to a God Consciousness and a quantic understanding
is the same as what we are implying. There must be some type of greater
power that dictates the precision with which biology pursues.
Chopra puts some of our scientific perspectives into more human
terms as he relates different cases, and how the cases go beyond classic
medical understanding. Many other researchers of late have followed a
similar path, and found challenging ways of critiquing modern medicines
statistical type of logic. We must point out in this document that if there
is a God Consciousness, an ability of will, happiness, joy, compassion,
caring, sharing and touch to help people, it will not fit into any model
that could be measured with statistical pre-test/post-test, clinical, drug
trial data. Clinical trials need to be part of our concept, but not deified.

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We need to use them to help determine safety and help to interpret our
range of effectiveness, but they still should be within the guidelines of
nature.

PROBLEMS BEHIND THE MEDICAL DILEMMA

Arrogance; a belief in superiority over biology

Persecution for the belief in nature and homeopathy

Judgmentalism; psychological over-reaction against other natural

philosophies. Preferred doctors of high influence are almost always
allopaths who are ignorant of homeopathy

Greed; synthetic companies profit mostly from patented unnatural

compounds

Lack of personal responsibility in healthcare

Belief that medical technology will save someone after years of an

unhealthy lifestyle

Crisis philosophy; seeking medical help only after all else fails

Insurance costs

Malpractice costs and medical fears

Lack of a true biology and no philosophical base

Quantity based medicine, not quality based

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 SOLUTIONS TO THE MEDICAL DILEMMA

Humility, reverence for natures process, understanding of

quantic philosophy

Proper study will show homeopathic and naturopathic

credibility

Proper peer group process: allowing a group of like-minded

doctors to evaluate the amount of harm done, if any

Protecting natural formulas with more strict copyrights that

allow natural based pharmaceutical companies to benefit from
their research

Building personal responsibility into medical education at every

level

Educating for prevention and early treatment procedures

Building a low-cost system of wellness counselors who can

intervene and help in early and simple health care problems,
reserving doctors and hospitals for crisis care

Reducing insurance costs by using homeopathy and

naturopathy and also escalating insurance costs for:

Obesity
Smoking
Alcohol abuse
Drug addiction

Letting the ones who incur the most medical costs pay them.
This will discourage bad health habits.

Malpractice results mostly from synthetic allopathic drugs and

surgery. Changing to homeopathy and naturopathy will show
dramatic results.

Appreciation and reverence for the unknown builds a quantum

philosophy for medicine.

Building everything for quality, not quantity. This will take more
cash initially, but will be cheaper in the long run.

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 Now, let us be more specific as to what might be needed to actually set
the criteria of how to approve new combination homeopathics, or new
combination drugs. First, we will need to depend on safety as our
primary goal. We need to look for safety first, or as Hippocrates said,
First, dont hurt. This needs to be our absolute guideline for everything
we do. We have to imagine that everything we do could get to the youth
of our society, as I think that everything could get to my five year old
daughter. The thought of anything happening to this small child is
absolutely, totally intolerable. First dont hurt.
Safety first is an absolute guideline. It is unfortunate that in the late
1950s the president of the American Medical Association (AMA), said in a
public address that the AMA no longer had to guarantee safety first; they
had to biopsy, x-ray, sedate, stimulate, stab, cut, and otherwise defame
the body in order to do medicine. This idea will be intolerable in our new
medicine as it forms. Safety first must be insured every step of the way.
In a recent report, it was said that there is a possibility that the
plankton at the South Pole might be in a condition of iron deficiency, and
that if the plankton had an exposure to iron, they might be able to
develop the ozone needed to compensate for the ozone deficiency of the
South Pole. His treatise makes very sound, scientific sense, and all the
science regarding the plankton around the South Pole has been done in
a superior manifest way. But yet, the scientific community is hesitant to
make such a maneuver, fearing the consequences of what one tanker-
load of iron might do at the South Pole.
This same type of fear of what this might do to the ecology of the entire
world is not shared by the synthetic chemical companies, as they engage
ever increasing numbers of synthetic chemicals that do not exist in the
world, and they are putting these into the exosphere of our planet. This
has been happening for over fifty years. Our new medicine will absolutely
insist on proof that safety within the smallest amount of parameters
must be guaranteed before we can proceed. We should no longer dump

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synthetic, never-occurring un-natural compounds into the environment
in the percentage that they have been in the past.
We must set policies as to what we are going to do, and this policy has
to be geared through the idea that only nature knows. Only through
such humility can science actually address the issues of biology and
medicine. The arrogant idea that if, we do not know its function we
should cut it out, allowed for the destruction of adenoids, tonsils,
appendix, spleen, thymus, etc. This type of arrogance must cease. Nature
knows, and nature had a plan for the adenoids, tonsils and appendix,
even though we did not know it. To assume that it is not needed because
we do not understand it, is the absolute arrogance of science. We must
have humility and a reverence towards science to be able to proceed in
any way, shape or form. Clinical trials are not enough; we must have a
guaranteed policy of understanding nature and natures own in order to
proceed into the new dimensions of medicine and biology
The alternative industry has done very little to offer any type of
scientific inquiry regarding statistics as its guideline. We will need to
develop pilot studies that guarantee effectiveness in safety, primarily.
These types of statistical endeavors will have to be replicated by many
different doctors in many different ways; not with the same criteria as
drug trial studies, but in something similar that will guarantee the
worlds safety and the worlds effectiveness of such remedies. These pilot
studies need to use the statistics of the day, and will have to be at a
razor-sharp edge to prove safe and effective.
As we continue to revere nature, and understand that only nature truly
knows, we will have to develop this into a hallmark of our biology. This
will allow homeopathy and all its nosodes, allersodes isodes, sarcodes,
etc., to explode into the scene of medicine. We also need to have the
philosophy and the psychology to understand that behavioral medicine,
psychological intervention, the psycho-immunological link and other
factors are also very much needed for us to have a true medicine. We

298
need to take Chopras advice, and develop a science and a medicine of
compassion, caring, sharing, touch, and healing to carry us into the new
era of medicine.
We will need to have a constant field input to allow doctors who are
using such medications to critique their actions in an ever changing
environment, realizing that what the action of any homoeopathic or drug
might be might change as the population evolves, in light of an ever
changing reactivity to the environment. Statistics will play an ever larger
part, but yet will not be deified in light of philosophy. The philosophy
that nature knows must be revered, not the statistics of clinical trials.
We must realize what nature and God Consciousness can do in the
field of biology and medicine. Only then, can we truly shape a new
medicine through these different guidelines, concentrating on safety at
all costs. We need effectiveness, but never at the cost of safety; revering
nature and education, so that the doctors, the populace, the society at
large can share in our appreciation and harmony of the natural flow of
medicine. To this end this book is written.

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 SUMMARY

A review of the insurance literature and true success stories on

naturopathy and homeopathy vs. synthetic allopathy have
conclusively proven that there is a severe problem in the field of
synthetic allopathy. Synthetic allopathy pays billions of dollars in
damages each year. Millions more are hurt by this technology who
do not seek damages. Those who are helped do not outweigh the
damages. The solution for this could be the new wave of
homeopathy and naturopathy into general areas of medicine.

There were profiteering issues behind the surge of synthetic

allopathy that were spearheaded by reductionism as a mechanism
of directing research. Now with the skills developed through
mathematics and quantum theory, it is possible to see that the
field of reductionistic research leaves dramatic problems for
medicine.

A new system of research must be developed for medicine. Some

ideas for a new system were presented within this chapter.

Medicine must learn not to deify statistical reductionistic papers,

and must learn to develop a reverence for the natural process
rather than synthetic dynamics.

Freedom of choice must return to the world system of medicine.

Systems of medicine such as chiropractic, naturopathy,

homeopathy, acupuncture, behavioral medicine and biofeedback
are legal systems.

Synthetic allopathy seeks to tyrannize the minds of men against

these other medical beliefs.

We must oppose any such tyranny over the minds of men.

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 METABOLIC PATHWAYS

This section includes a list of the cellular energy components utilized

in cellular metabolism and energy regulation. Sometimes an irregularity
of function can be corrected with a homeopathic of the enzyme or
component.

Alcohol dehydrogenase
Glycerol-3-phosphate dehydrogenase
D-Xylulose reductase
L-Xylulose reductase
D-Iditol dehydrogenase
Glucuronate reductase
UDP glucose dehydrogenase
Histidinol dehydrogenase
Shikimate dehydrogenase
Lactate dehydrogenase
D-Lactate dehydrogenase
Glycerate dehydrogenase
3-Hydroxybutyrate dehydrogenase
3-Hydroxyisobutyrate dehydrogenase
Mevaldate reductase
Hydroxyethylglutaryl-CoA reductase (NADPH)
3-Hydroxyacyl-CoA dehydrogenase
Malate dehydrogenase
Malate dehydrogenase (oxaloacetate-decarboxylating)
Malate dehydrogenase (decarboxylating)
Isocitrate dehydrogenase (NAD+)
Phosphogluconate dehydrogenase
Phosphogluconate dehydrogenase (decarboxylating)
L-Gulonate dehydrogenase
Glucose-6-phosphate dehydrogenase
Ribitol dehydrogenase
3-Hydroxpropionate dehydrogenase
Tartronate-semialdehyde reductase
Glyoxylate reductase (NADP+)
Hydroxypyruvate reductase
Malate dehydrogenase (NAPD+)
Phosphoglycerate dehydrogenase
3-Oxo-[acyl-carrier-protein] reductase
Retinol dehydrogenase
IMP:NAD+oxidoreductase

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L-Gulonolactone oxidase
Choline dehydrogenase
Glycerol-3-phosphate dehydrogenase
Aldehyde dehydrogenase
Benzaldehyde dehydrogenase (NADP+)
Betaine-aldehyde dehydrogenase
Aspartate-semialdehyde dehydrogenase
Glyceraldehyde-phosphate dehydrogenase
IMP dehydrogenase
Succinate-semialdehyde dehydrogenase (NAD (P) +)
Malonate semialdehyde dehydrogenase (acetylating)
Glycoadehyde dehydrogenase
Succinate-semialdehyde dehydrogenase
2-Oxiosovalerate dehydrogenase
Benzaldahyde dehydrogenase (NAD+)
Aminoadipate-demialdehyde dehydrogenase
Aminomuconate-semialdehyde dehydrogenase
Retinal dehydrogenase
Xanthine dehydrogenase
Glutamate-semialdehyde dehydrogenase
Xanthine oxidase
Pyruvate dehydrogenase (lipoamide)
2-Oxobutyrate synthase
Dihydrouracil dehydrogenase (NAD+)
Dihydrouracil dehydrogenase (NADP+)
Acyl-CoA dehydrogenase (NADP+)
Enoyl-[acyl-carrier-protein] reductase
Enoyl-[acyl-carrier-protein] reductase (NADPH)
Prephenate dehydrogenase (NADP+)
Orotate reductase
Coproporphyrinogen oxidase
Succinate dehydrogenase
Butryl-CoA dehydrogenase
Acyl-CoA dehydrogenase
Glutaryl-CoA dehydrogenase
Alanine dehydrogenase
Glutamate dehydrogenase
Serine dehydrogenase
Valine dehydrogenase (NADP+)
Leucine dehydrogenase
D-aspertate oxidase
L-amino acid oxidase
Glycine dehydrogenase
Amine oxidase (pyridoxal-containing)
Ethanolamine oxidase
Pyrroline-2-carboxylate reductase

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Pyrroline-5-carboxylate reductase
Saccaropine dehydrogenase (NAD+, lysine-forming)
Saccharopine dehydrogenase
L-Pyrroline-5-carboxylate dehydrogenase
Sarcosine oxidase
Sarcosine dehydrogenase
Dimethyglycine dehydrogenase
L-Pipecolate dehydrogenase
Cystine reductase (NADH)
Dihydrolipoamide reductase (NAD+)
Hypotaurine dehydrogenase
Sulphite oxidase
Sulphite reductase (ferredoxin)
L-Ascorbate-cytochrome b5 reductase
Ascorbate oxidase
Catechol 1, 2-dioxygenase
Catechol 2, 3-dioxygenase
Homogentisare 1, 2-dioxygenase
3-Hydroxyanthranilate 3, 4-dioxygenase
Tryptophan 2, 3-dioxygenase
Cycsteine dioxygenase
B-Carotene 15, 15 dioxygenase
4-Hydroxphenylpyruvate dioxygenase
myo-Inositol oxygenase
Benzoate 1, 2-dioxygenase
Y-Butyrobetaine-2-oxogluterate dioxygenase
Proline, 2-oxogluterate dioxygenase
Trimethylysine, 2-oxogluterate dioxygenase
Anthranilate 1, 2-dioxygenase (deaminating, decarboxylating)
Imidazoleacetate 4-monooxygenase
Kynurenine 3-monooxygenase
Phenylalanine 4-monooxygenase
Tyrosine 3-monooxygenase
Monophenol monooxygenase
Prostaglandin synthase
Acyl-CoA desaturase
Squalene monoxyenase (2, 3-epoxidising)
Ribonucleoside-diphosphate reductase
Nicotinamide methyltransferase
Guanidinoacetate methyltransferase
Dimethylthetin-homocysteine methyltransferase
Acetylserotonin methyltransterase
Betaine-homocysteine methyltransferase
Homocysteine methyltransferase
Tetrahydropteroyltriglutamate methyltransferase
Phosphatidylethanolamine methyltransderase

303
Glycine methyltransferase
Noradrenaline N-methyltransferase
Thymidylate synthase
Serine hydroxymithyltransferase
Phosphoribosyglycinamide formyltransferase
Phosphoribosylaminoimidazole-carboxamie formyltransferase
Glutamate formiminotransferase
Methylmalonyl-CoA carboxyltransferase
Aspartate carboamoyltransferase
Ornithine carbamoyltransferase
Glycine amidinotransferase
Transketolase
Transaldolase
Amino-acid acetyltransferase
Glucosaminephosphate acetyltransferase
Arylamine acetyltransferase
Choline acetyltransferase
Phosphate acetyltransferase
Acetyl-CoA acetyltransferase
Dihydrolipoamide acetyltransferase
Glycerophosphate acyltransferase
Acetyl-CoA acyltransferase
Diacylglycerol acyltransferase
Carnitine palmitoyltransferase
Lysolecithin acetyltransferase
Sphingosine acyltransferase
Lysine acetyltransferase
Glutamate acetyltransferase
S-Aminolaivulinate synthase
[Acyl-carrier-protein] acetyltransferase
[Acyl-carrier-protein] malonytransferase
3-Oxoacyl-[acyl-carrier-protein] synthase
Serine palmitoyltransferase
1-Acylglycerolphosphate acyltransferase
Phosphorylase
Amylosucrase
Glycogen (starch) synthase
Sucrose synthase
Glucuranosyl-transferase
Starch synthase
Lactose synthase
Sphingosine B-galactosyltransferase
Cellulose synthase (GDP-forming)
Glucomannan 4-B-D-mannosyltransferase
UDP galactose-N-acylsphingosine galactosyltransferase
UDP-N-Acetylglucosamine glycoprotein N-acetyl-glucosaminyltransferase

304
UDP galactose-ceramide galactosyltransferase
GDP-fucose-lactose fucosyltransferase
Purine nucleoside phosphorylase
Pryimidine-nucleoside phosphorylase
Thumidine phosphorylase
Hypoxanthine phosphoribosyltransferase
Uracil phosphoribosyltransferase
Orotate phosphoribosyltransferase
Nicotinate phosphoribosyltransferase
Amidophosphoribosyltransferase
ATPP-phosphoribosyltransferase
Anthranilate phosphoribosyltransferase
Nocotinatemonomucleotide pyrophosphorylase (carboxylating)
Dimethyltransferase
Methionine adenosyltransferase
Geranyltransferase
Amonopropyltransferase
Farnesyltransferase
Spermine synthase
Aminotransferase
Aspartate aminotransferase
Alanini aminotransferase
Glycine aminotransferase
Tyrosine aminotransferase
Leucine aminotransferase
Histidinol-phosphate aminotransferase
Acetylornithine aminotransferase
Ornithine-oxo-acid aminotransferase
Glutamine fructose 6-phosphate aminotransferase
Succinyl-diaminopimelate aminotransferase
B-Alanine-pyruvate aminotransferase
Aminobutyrate aminotransferase
L-3-Aminoisobutyrate aminotransferase
4-Hydroxyglutamate transaminase
Tryptophan aminotransferase
Valine-isoleucine aminotransferase
L-Lysine 6-aminotransferase
2-Aminoadipate aminotransferase
Branched-chain-amino-acid aminotransferase
Serine-pyruvate aminotransferase
Phosphoserine aminotransferase
Glutamate synthase
Glucokinase
Ketohexokinase
Fructokinase
Galactokinase

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Mannokinase
6-Phosphofructokinase
Ribokinase
Ribulodinase
Xylulokinase
NAD+kinase
Dephospho-CoA kinase
Triokinase
Glycerol kinase
Glycerate kinase
Choline kinase
Pantothenate kinase
Pantetheine kinase
Mevalonate kinase
Homoserine kinase
Pyruvate kinase
D-Ribulokinase
L-Xylulokinase
N-Acylmannosamine kinase
myo-Inositol-kinase
Shikimate kinase
Pyrophosphate-serine phosphotransferase
Acetate kinase
Phosphoglycerate kinase
Aspartate kinase
Formate kinase
Carbamoyl-phosphate synthase (glutamine)
Creatine kinase
Phosphomevalonate kinase
Nucleoside-phosphate kinase
Nucleosidediphosphate kinase
dTMP kinase
Cytidylate kinase
Phosphoglucomutase
Acetylglucosamine phosphomutase
Phosphoglycerosmutase
Ribosephosphat pyrophosphokinase
Pantetheinephosphate adenylyltransferase
RNA nucleotidyltransferase
DNA nucleotidyltrnasferase
Glucose-1-phosphate guanylyltransferase
Ethanolaminephosphate cytidylyltransferase
Galactose-1-phosphate uridylyltransferase
Hexose-1-phosphate guanylyltransferase
GTP-mannose-1-phosphate guanylyltransferase
Ethanolaminephosphate cytidylyltransferase

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Cholinephosphate cytidylyltransferase
Nicotinatemononucleotide adenylyltransferase
Mannose-1-phosphate guanylyltransferase
UDP acetylglucosamine pyrophosphorylase
Glucose-1-phosphate thyidylyltransferase
Glucose-1-phosphate guanylyltransferase
Phosphatidate cytidylyltransferase
Acylmeuraminate cytidylyltransferase
Ethanolaminephosphotransferase
Cholinephosphotransferase
Ceramide cholinephosphotransferase
Blycerophosphate phosphatidyltransferase
CDP diglyceride-serine o-phosphatidyltransferase
CDP diglyceride-inositol phosphatidyltransferase
Phospho-N-acetylmuramoyl-pentapeptide transferase
Propionate CoA-transferase
3-Oxoacid CoA-transferase
3-Oxoadipate CoA-transferase
Triacylglycerol lipase
Phospholipase A2
Lysophospholipase
Acetylcholinesterase
Aldonolactonase
3-Oxoadipate enol-lactotase
Acylcarnitine hydrolase
6-Phosphogluconolactotase
Phospholipase A1
Acetyl-CoA hydrolase
3-Hydroxyisobutyryl-CoA hydrolase
Phosphoserine phosphatase
Phosphatidate phosphatase
5 Nucleotidase
Glucose-6-phosphatase
Hexosediphosphatase
Histidinolphosphatase
1L-myo-Inositol-1-phosphatase
Phosphatidylglycerophospatase
N-Acylneuraminate-9-phosphatase
Nucleotidase
Glycerophosphinicochopane diesterase
Phospholipase C
Phospholipase D
Phosphatidylinositol phosphodieterase
Sphingomyelin phosphosphesterase
B-galactosidase
B-fructofuranosidase

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Adenosylhomocysteinase
Asparaginase
Glutaminase
Ureidosuccinase
Formylaspartate deformatase
Aryl-formamidase
Acetylornithine deacetylase
Glutaminase
Ureidosuccinase
Formylaspartate deformatase
Aryl-formamidase
Succinyl-diaminopimelatase desuccinylase
Citrullinase
Pantothensase
Acylsphingosine deacylase
Hippurate hydrolase
Dihydropyrimidinase
Dinydor-orotase
Allantoinase
Imidazolonepropionase
Arginase
Formiminoaspartate deiminase
Arginine deiminase
AMP deaminase
IMP cyclohydrolase
dCMP deaminase
Phosphoribosyl-AMP cyclohydrolase
Adenosinetriphosphatase
Nucleoside triphosphatase
Fumarylaetoacetase
Kynureninase
Phosphoamidase
Carboxylyase
Pyruvate decarboxylase
Oxaloacetate decarboxylase
Acetoacetate decarboxylase
Aspartate 4-decarboxylase
Glutamate decarboxylase
Ornithine decarboxylase
Diaminopimelate decarboxylase
Phosphoribosylaminoimidazole carboxylase
Histidine decarboxylase
Orotidine-5 phosphate decarboxylase
Aromatic L-amino-acid decarboxylase
Cysteine sulphinate decarboxylase
Phosphoenolpyruvate carboxylase

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Di-phosphomevalonate decarboxylase
Keto-L-glutonate decarboxylase
Phosphopantothenoyl-cysteine decarboxylase
Uroporphyrinogen decarboxylase
Phosphoenolpyruvate carboxykinase (pyrophosphate)
Ribulosebisphosphate carboxylase
Propionyl-CoA carboxylase
Phenylpyruvate decarboxylase
Aminocarboxymuconate-semialdehyde decarboxylase
Tartronate-semialdehyde synthase
Indole-3-glycerol-phosphate synthase
Phosphoenolpyruvate carboxykinase (ATP)
Phosphatidylserine decarboxylase
Aldehyde lyase
Phosphoketolase
Ketopantoaldolase
Fructose-bisphosphate aldolase
Phospho-2-keto-3-deoxy-heptonate aldolase
Isocitrate lysase
Malate synthase
Hydroxymithylglutaryl-CoA lyase
Citrate (si) synthase
ATP citrate (pro-3S)-lyase
4-Hydroxy-2-oxoglutarate aldolase
Acetolactate synthase
N-Acylneuraminate-9-phosphate synthase
Homocirtate synthase
Anthranlate synthase
Tryptophanase
Fumarate hydratase
Aconitate hydratase
Citrate dehydratase
Dihydroxyacid dehydratase
5-Dehydroquinate dehydratase
Enolase
Phosphogluconate dehydratase
L-Serine dehydratase
Threonine dehydratase
Enoyl-CoA hydratase
Methylglutaconyl-CoA hydratase
Imidazoleglycerolphosphate dehydratase
Tryptophan synthase
Cystathionine B-synthase
Porphobilinogen synthase
Mesaconate hydratase
dTDP glucose 4, 6-dehydratase

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GDP-manose 4,6-dehydratase
Urocanate hydratase
Prophenate dehydratase
Dihydrodipicolinate synthase
3-Hydroxyoctanoyl-[acyl-carrier-protein] dehydratase
D-3-Hydroxydecanoyl-[acyl-carrier-protein] dehydratase
Threonine synthase
Cystathionine Y-synthase
Aspartate ammonia-lyase
Methylaspartate ammonia-lyase
Histidine ammonia-lyase
Uroporphyrinogen I synthase
Argininosuccinate lyase
Adenylosuccinate lyase
Cystathionine Y-lyase
Cystathionine B-lyase
Adenylate-cyclase
Ribulosephosphate 3-epimerase
UDP-glucose 4-epimerase
L-Ribulosephosphate 4-epimerase
UDP-glucinonate epimerase
UDP-acetylglucosamine 4-epimerase
UDP-acetylglucosamine 2-epimerase
Methylmalonyl-CoA racemase
Maleylacetoacetate isomerase
Retinal isomerase
Triosephosphate isomerase
Arabinose isomerase
L-Arabinose isomerase
Xylose isomerase
Ribosephosphate isomerase
Mannosephosphate isomerase
Glucosephosphate isomerase
D-Lyxose ketol-isomerase
N-(5 Phospho-D-ribosylformimino)-5-amino-1-(5 phosphoribosyl)-4-
imidazolecarboxamide isomerase
Glucose isomerase
Glucosaminephosphate isomerase (glutamine-forming)
Isopentenyldiphosphate isomerase
Muconolactone isomerase
Phosphoglycerate phosphomutase
Phosphoacetylglucosamine mutase
Phosphomannomutase
Methylasartate mutase
Methylmalonyl-CoA mutase
Chorismate mutase
Lanosterol-cyclase

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Muconate cycloisomerase
myo-Inositol-1-phosphate synthase
Succinyl-CoA-synthase
Asparagine synthetase
Glutamine synthetase
Asparagine synthetase
NAD+synthetase
Pantothenate synthetase
Y-Glutamylcysteine synthetase
Glutathione synthase
Phosphopantothenoyl-cysteine synthetase
Phosphoribosylaminoimidazole-succinocarboxamide synthase
UDP-N-acetylmuramoylalilne synthetase
UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-D-alanyl-D-alanine
synthetase
Phosphoribosylaminoimidazole synthetase
GMP synthetase
CTP synthetase
Adenylosuccinate synthase
Argininosuccinate synthase
5-Phosphoribosylamine synthetase
Phosphoribosylglycinamide synthetase
NAD+synthetase (glutamine-hydrolysing)
GMP synthetase (glutamine-hydrolysing)
Phosphoribosylformylglycinamidine synthetase
Carbomoyl phosphate synthetase
Pyruvate carboxylase
Acetyl-CoA carboxylase
Propionyl-CoA carboxylase
Propionyl-CoA carboxylase
Methylcrotonoyl-CoA carboxylase

See metabolic pathways below.

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For more on Metabolic Pathways:

http://www.sigmaaldrich.com/Area_of_Interest/Life_Science/Metabolom
ics/Key_Resources/Metabolic_Pathways.html?cm_mmc_o=TBBTkwCjCF
wfz_BkBFbglCjC55gCjCFwfz_Bkbg%205zftczYl

http://www.expasy.ch/cgi-bin/show_thumbnails.pl

http://www.gwu.edu/~mpb/

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 Dr. Recommends is dedicated to developing statistical data banks to
prove the efficacy of homeopathy to standard medicine and the world.
Many studies have been done by Dr. Nelson in developing experimental
and clinical proof for the efficacy and safety of homeopathy.

DISCLAIMER

If conditions persist, and are not responding properly to the

homeopathic program, we encourage the doctor to make other referrals
so that the condition will not deteriorate. Allopathic medicine has some
dramatic benefits that can help with different disease structure in their
crisis stages.
Many patients do not go to doctors until they are in a crisis stage.
Homeopathy might be too slow in working. We usually suggest that the
patient use the remedies for two to four weeks if the condition allows. If
results are not attained, the doctor should make a referral for more
dramatic therapies. These should be discussed with a bio-physician who
has an appreciation for the rules of nature.
Homeopathic remedies are designed to work as an adjunct and support
to standard medical therapies. They are not meant as a replacement. If
symptoms persist, consult a medical doctor. If pregnant or lactating
consult your physician.

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 Continuing Education Units
______________________________________
When you, the reader, finish reading the booklet
you are allowed to credit yourself
with the same number of CEUs
that you spent in hours reading the book.

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