By Steven H. Zarit, Ronda C. Talley
Assisting a person with Alzheimer’s sickness or one other disease that factors dementia is extremely hard and annoying for the relations. Like many disabling stipulations, Alzheimer’s sickness results in trouble or lack of ability to hold out universal actions of everyday life, and so kin take over various initiatives starting from coping with the person’s funds to supporting with intimate actions comparable to bathing and dressing.
Key assurance in Caregiving for Alzheimer’s illness and similar Disorders includes:
Early prognosis and kinfolk dynamics
Emotional wishes of caregivers
Developmentally acceptable long term take care of individuals with Alzheimer’s
Family caregivers as participants of the Alzheimer’s therapy Team
Legal and moral matters for caregivers
Faith and spirituality
The economics of taking good care of people with Alzheimer’s disease
Cultural, racial, ethnic, and socioeconomic problems with minority caregivers
Advances in Alzheimer’s sickness research
Caregiving for Alzheimer’s affliction and comparable Disorders bargains a wealth of insights and concepts for researchers, practitioners, and graduate scholars around the caregiving fields, together with psychology, social paintings, public well-being, geriatrics and gerontology, and medication in addition to public and schooling coverage makers.
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Additional resources for Caregiving for Alzheimer's Disease and Related Disorders: Research Practice Policy
The goal of this chapter is to explore the potential impact of early diagnosis, advances in genetics, and prevention models on AD caregivers. An examination of what is currently known in these areas will be followed by discussion of the research, education, practice, and policy needs these trends have created. Finally, we will speculate about future directions in AD caregiving that may result from early diagnosis and prevention efforts. Throughout this chapter, the term families will be used for convenience.
In its strategic plan for years 2001–2005, the National Institute on Aging has emphasized an Alzheimer’s Disease Prevention Initiative (National Institute on Aging, 2001). This initiative grew, in part, out of analyses that showed that if the average onset age of AD could be delayed just 5 years, the number of cases in 2050 would be reduced by 50% (Brookmeyer, Gray, & Kawas, 1998). This reduction in cases is predicated on the fact that AD occurs in people who live beyond the median expected survival.
Journal of Medical Genetics, 34, 63–72. Wackerbarth, S. , & Johnson, M. M. (2002). The carrot and the stick: Benefits and barriers in getting a diagnosis. Alzheimer Disease and Associated Disorders, 16, 213–220. Chapter 2 Psychosocial Interventions to Address the Emotional Needs of Caregivers of Individuals with Alzheimer’s Disease Mary Mittelman Alzheimer’s disease (AD) poses unique difficulties for many families. The time from the onset of symptoms of the illness to death is typically 5–15 years.
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