Caregiving for Alzheimer’s Disease and Related Disorders: by Glenn E. Smith PhD, Angela Lunde BA (auth.), Steven H.

By Glenn E. Smith PhD, Angela Lunde BA (auth.), Steven H. Zarit, Ronda C. Talley (eds.)

Assisting an individual with Alzheimer’s affliction or one other sickness that reasons dementia is very challenging and demanding for the family members. Like many disabling stipulations, Alzheimer’s disorder results in hassle or lack of ability to hold out universal actions of lifestyle, and so kin take over quite a few initiatives starting from handling the person’s funds to assisting with intimate actions akin to bathing and dressing.

Key assurance in Caregiving for Alzheimer’s sickness and comparable Disorders includes:

Early analysis and kin dynamics
Emotional wishes of caregivers
Developmentally acceptable long term take care of individuals with Alzheimer’s
Family caregivers as contributors of the Alzheimer’s remedy 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 ailment research

Caregiving for Alzheimer’s disorder and comparable Disorders deals a wealth of insights and concepts for researchers, practitioners, and graduate scholars around the caregiving fields, together with psychology, social paintings, public health and wellbeing, geriatrics and gerontology, and drugs in addition to public and schooling coverage makers.

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Extra resources for Caregiving for Alzheimer’s Disease and Related Disorders: Research • Practice • Policy

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These problems can be exacerbated by the fact that many spouse caregivers feel that they must provide all the care for their ill spouse. In addition, family members and friends may not be used to offering help or providing emotional support for the caregiver. People who care for a parent, as opposed to a spouse with dementia, face different caregiving challenges. Adult child caregivers are more likely to have multiple responsibilities, including jobs, marriage, and child rearing. They must also face the emotional challenge of the role change associated with caring for their parents who formerly were in the position of having to care for them.

As a result, spouse caregivers may have placed greater reliance on the companionship and emotional support of their husband or wife with dementia than younger caregivers. The caregiving spouse can become socially isolated when dementia erodes the ability of the ill spouse to understand his or her needs, to communicate effectively, or to participate in activities they may have formerly enjoyed together. These problems can be exacerbated by the fact that many spouse caregivers feel that they must provide all the care for their ill spouse.

Journal of Internal Medicine. 256:183–194. Petersen, R. C. ). (2002). Mayo Clinic on Alzheimer’s disease. Rochester, MN: Mayo Clinic Heath Information. Petersen, R. , Smith, G. , Waring, S. , Ivnik, R. , Tangalos, E. , & Kokmen, E. (1999). Mild cognitive impairment: Clinical characterization and outcome. Archives of Neurology, 56, 303–308. Petersen, R. , Stevens, J. , Tangalos, E. , Cummings, J. , & DeKosky, S. T. (2001). Practice parameter: Early detection of dementia: Mild cognitive impairment (an evidence-based review).

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