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Areas of communication that promotes hope: Taking time to talk Giving information Click to edit Master subtitle style Demonstrating caring behaviors Being friendly, respectful and honest
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In a pilot study, patients were asked to describe their idea of a good communicator. Most of them mentioned: Being a good listener or being available to listen to their particular concerns Asking simple questions Using open, not leading questions
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We communicate our support to others both verbally and non-verbally, and there must be consistency between these two forms if we are to be perceived as GENUINE. Try to relate to dying people on a personal as well as a professional level. Benjamin (1981) emphasized the necessity of congruence between verbal and non-verbal communication in effective counseling. 4/21/12
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PROMOTING HOPE
Nurses can help patients cope with these anxieties, not with false reassurance but by encouraging them to talk about their fears and by providing appropriate medical information. It is important that, in the earlier stages of advanced disease, patients are able to put their illness into perspective, so that they can participate in other aspects of life. 4/21/12 can help patients to Nurses
PROMOTING HOPE
Maintenance of the individuals perception of control over loss is essential to preserving hope. In a study of what dignity means to those who are terminally ill, McClement identified factors that support and undermine dignity in these patients. One aspect of the patients dignity-conserving list is continuity of self. The implication for staff is 4/21/12 that they should view
People with verbal communication difficulties can experience emotional distress caused by loneliness, lack of self-esteem or depression. These people may include those who have had a stroke or who suffer from learning difficulties. Kopp noted that language impairments or problems with hearing could often occur in settings where 4/21/12 people were nursed. elderly
Ham (1991) suggested that, if people with dementia are not aware of their condition at an early stage, they cannot make choices about their future care. Time to come to terms with the diagnosis may enable them to make any financial, spiritual and medical decisions while they are still able to do so. Viewing dementia as a disability rather than a 4/21/12 allows us to view the disease
Staff often depend on families to communicate with children when a family member is seriously ill. Sheldon (1994) found that parents may underestimate their childrens needs, partly in the belief that they are protecting them and partly because they themselves are exhausted and 4/21/12 distressed by preparing
The familys ability to support children will depend on pre-existing communication and coping styles. The Clinical Standards Board for Scotland outlined the need for children to be given information to help them understand the likely outcome of the patients illness. Sheldon noted that greater emphasis is now 4/21/12 being placed on including
Macpherson and Cooke introduced a workbook for families of hospice patients to help parents better understand their childrens knowledge of the patients illness and to begin to explore their childrens thoughts and feelings. It provided opportunities to interact and build relationships with the staff. However, the authors noted that it was important to fully inform parents about the workbook as it raised issues about 4/21/12 death and dying that might be unacceptable to