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Social Effects Of Alzheimer's Disease

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Currently, Alzheimer’s disease is the sixth leading cause of death in the United States taking the over 80 thousand lives per year (Center for Disease Control, 2015), and as population continues to age, more people will develop Alzheimer’s. Therefore, a global epidemic is imminent and without a cure or a way to slow down the disease, it is something to be concerned about. However, this a disease that affects more people than just those who suffer from it. It is predicted that by 2050, the prevalence of Alzheimer’s will quadruple (Brookmeyer, Johnson, Ziegler-Graham & Arrighi, 2007). As the disease progresses, patients will need advanced care. This poses a burden to our society, as it will create an enormous strain on the health care system, …show more content…
Alzheimer’s is a devastating disease and those affected by it suffer as they continue to lose their memories and their ability to carry out basic living functions. Alzheimer’s Disease is the most common type of dementia accounting for 60% to 80% of the cases (Alzheimer’s Association, 2014, e49). As defined by the Alzheimer’s Association (2014) dementia is an overall term for diseases and conditions characterized by a decline in memory or other thinking skills that affects a person’s ability to perform everyday activity. Alzheimer’s was first discovered over 100 years ago but research into its symptoms, causes, risk factors and treatment has gained momentum only in the last 30 years (Alzheimer’s Association, 2014, e48). Even with the development of technology, and the surge of information on the subject, there is still much to be discovered about Alzheimer’s. The exact biological changes that cause Alzheimer’s, why it progresses at different rates, and how the disease can be prevented, slowed or stopped are the main focus of current Alzheimer’s …show more content…
Caregivers are known to present symptoms of depression and the feeling of burden. The Alzheimer’s Association (2014) discusses the public health impact of Alzheimer’s disease, including prevalence and incidence, mortality rates, costs of care, and overall effect on caregivers and society. Their report provides important information on the role of caregivers to people with Alzheimer’s. They inform that most of the caregivers to people with Alzheimer’s are immediate family members, relatives, or friends. The Alzheimer’s Association (2014) established that in the year 2013 unpaid caregivers to patients with Alzheimer’s disease provided over 17.7 billion hours of informal care. They also looked at who is providing care for these individuals and “found that 65% of caregivers are women; 21% were aged 65 years and older; 44% had some college education or had received a degree; 64% were currently employed, a student, or a homemaker; and 71% were married or in a long-term relationship” (Alzheimer’s Association, 2014, p. e64). Although the help provided by family members of people with Alzheimer’s disease is similar to the help provided by caregivers of people with other conditions, dementia caregivers tend to provide more extensive

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