Introduction
The purpose of this topic is to expand research on Dementia/Alzheimer’s Disease from the standpoint of the caregiver perspective. The disease was named after Dr. Alois Alzheimer, a doctor and an academic, who wrote his first paper on clinical dementia. His first study was on a woman by the name of Ms. Frau Auguste. Dr. Alzheimer had been the patient for 5 years until she died in 1905 from the chronic illness known as Dementia/Alzheimer’s (Kennard, 2006).
Because of the support that married couple caregivers have, the instances of Alzheimer’s disease in the latter are comparatively easier to address.
Literature review
Table 1. Literature used for the research
Analysis
The term “Alzheimer/ dementia” is traditionally used as an umbrella term for symptoms of cognitive decline, including sclerosis, yet it is not considered a clinical diagnosis until an underlying disorder has been defined (Psych Central, 2014). “Dementia” is also applied to the symptoms that have been triggered by brain function alterations. The symptoms of the given disease include, but are not restricted to, reiterating the same question; loss of spatial orientation skills; inability to follow basic directions; losing the track of time, forgetting people’s names; complete disregard of one’s safety, hygiene, or nutrition. The pace of dementia progress varies depending on the patient’s health issues (National Institute on Aging, 2014).
Conclusion
Because of different rates in the loss of caregivers’ abilities, parents affected with Alzheimer’s must have someone by their side, whose behavioral and communicational patterns they can follow. Thus, Alzheimer’s treatment is more efficient in married couples.
Reference List
Fuller, F. J. (1992). Health of elderly male dependent-care agents for a spouse with Alzheimer’s disease. Ann Arbor, MI: ProQuest.
Hayes, M. J. (2003). Negotiating and managing intimacy when the gendered self is threatened: Living and loving with Alzheimer’s disease. Ann Arbor, MI: ProQuest.
Kennard, C. (2006). Did Dr. Alzheimer discover Alzheimer’s disease?
Li, J. (2006). Effects of psychological stress and cytokine genes on humoral immune response to tetanus toxoid adsorbed in family caregivers of Alzheimer’s disease patients. . Ann Arbor, MI: ProQuest.
O’Donnell, M. E. (1997). The lived experience of uncertainty for spouse caregivers of people with Alzheimer’s disease. Ann Arbor, MI: ProQuest.
National Institute on Aging (2014). Alzheimer’s Disease Education and Referral Center.
Psych Central (2014). Learn. Share. Grow. What is dementia? Web.
Yaeger, T. D. (1990). Factors influencing family caregivers’ utilization of adult day care for persons with Alzheimer’s disease. Ann Arbor, MI: ProQuest.