Research on the Alzheimer’s Disease relation to its caregivers

Research on the Alzheimer’s Disease relation to its caregivers

This is an assignment that focuses on the investigation of the Alzheimer’s Disease relation to its caregivers. The paper also analyzes various aspects on the caregiver side of view.

Investigation of the Alzheimer’s Disease relation to its caregivers

H‌‌‍‌‌‍‍‍‌‍‍‌‍‍‍‌‌‌‍ere is my literature introduction from last paper and the problem that ultimately led me to my research topic. In this literature review,

I aim to differentiate if men and women caregivers are impacted as it relates to caregiver burden and burns out while caring for loved ones suffering from Alzheimer’s Disease. I want to discover all the factors that contribute to whether men or women would be impacted more than the other as it relates to caregiver burden. Burden leads to burnout of the caregiver. Still, I want to find interventions in the literature, that are trying to address the impact that before the responsibility is too much to handle.

Problem Alzheimer’s disease is an ongoing epidemic in the aging population. It continues to be a prevalent problem as this population grows. The disease attacks the brain’s nerve cells, causing memory loss, behavioral changes, confusion, and deterioration of language skills. Alzheimer’s disease affects more than 5 million Americans, 65 and older. (Wennberg,2015). This disease not only causes problems with the carrier, but there is a significant impact that is associated with being the caregiver. Specifically an informal caregiver that may be being launched into this role unexpectedly. The role of an informal caregiver can be tasking, expensive, draining, and rewarding, but these factors can all occur at different stages.

Investigation of the Alzheimer’s Disease relation to its caregivers

In the past, many people have conducted research surrounding this disease. It should continue as many families continue to deal with the hardship of the care needed. This is in addition to support a loved one with Alzheimer’s disease. What information is available to help those in a position to cope with it, and should as a society. We should be concerned about the factors that attach to caregiver burnout. Caregiver burnout and burden are part of critical social issues as this could not only affect the care recipient, an aged person with significant cognitive decline, but it also affects the caregiver’s health.

The goal will be to conduct proper research to help find interventions for informal caregivers. This is to ensure the dignity and safety of both the caregiver and care recipient. My current research question is. How are the resources available to informal caregivers caring for loved one suffering Alzheimer’s dementia. Also, to help‌‌‍‌‌‍‍‍‌‍‍‌‍‍‍‌‌‌‍ combat burden and improve the overall quality of care provided to the care recipient?