A report looking at the client population of those who have Alzheimer's disease.
Written in 2005; 1,527 words; 4 sources; APA; $ 50.95
Paper Summary:
This report identifies and recognizes the population of individuals dealing with the condition of Alzheimer's disease (AD). The paper describes the impact that a diagnosis of AD can have on the person diagnosed and the caretakers of that person, the type of support and service people with AD and their families receive and the inadequacies of that service and what can be done to improve the service and support.
From the Paper:
"Alzheimer's Disease not only affects millions of individuals in America, but it is also one of the leading causes of death in the old population. And providing long-term care for Alzheimer's can be problematic in terms of both personal and economic cost, as the disease does not show improvement as it progresses and is even not covered by many supplemental insurance plans because it is cost-prohibitive. Medicare and other insurance options must be tailored to treat Alzheimer's with attention not just to the older client population who are suffering from the disease, but to support staff and family member who must also cope with it. A holistic pattern should be expanded in this respect to give care to the client population suffering from Alzheimer's as well as their spouses, who may be emotionally and mentally effected, family, who may be daunted by the prohibitive nature of the disease, and healthcare professionals, who may see the disease as unbeatable and respond inappropriately in the level of care being given to the client themselves."
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