Care of Alzheimer Patient Issues in the Family Research Paper

A Care of Alzheimer Patient Issues in the Family - Research Paper Example I strongly hypothesize that most families and members of the society, in general, do not have the potential and ability to identify the early symptoms of the disease so that early intervention regimes can be implemented, are unable to cope with the increasing demands of caring for an Alzheimer’s patient and themselves often coped poorly under the circumstances of having an Alzheimer’s patient within the household. I also hypothesize that some families do not pay due care and attention that is demanded by these patients. If so, my question is what these clients/ families and the community in general needs most from the human service provider and organization. Alzheimer’s disease, thought to be a consequence of the increase in the production/ accumulation of a specific protein (beta-amyloidal protein) which causes nerve cell damage, is a progressive disease of the brain featuring memory retardation and disturbances in other cognitive/ mental functions such as language and perception of reality. On average, symptoms of Alzheimer’s are noticed by families three years before a conclusive diagnosis is done. While not an inevitable part of aging, Alzheimer prevalence increases significantly after the age of 65 years (Zarka, 2011). The disease develops when the toxic protein, beta amyloidal, accumulates in the brain in the form of plaques which are thought to be in turn toxic to neurons, disrupting messages within the brain by damaging connections between brain cells. The brain cells finally die and information recalling or assimilation disrupted hence.