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When Diagnosing Alzheimer’s, Diagnose the Caregiver’s Health, Too

PAY EXTRA ATTENTION to the care-partner's health during Alzheimer's. With a quick inquiry, nurses and doctors can easily spot caregivers needing enhanced support. Find out how simple & essential this can be.
Nurse checking with an Alzheimer's caregiver

Caregiving for an Alzheimer’s patient can be especially burdensome for spousal and family caregivers, who at the time of their loved one’s Alzheimer’s diagnosis, suffer from their own problems, according to a University of Eastern Finland study.

Caregiver Stress and Psychological Load

The study analyzed the psychological stress of family caregivers during a three-year period following the Alzheimer’s diagnosis. The study constitutes part of the ALSOVA project involving 236 persons diagnosed with Alzheimer’s disease and their family caregivers. The study participants were voluntarily recruited from the memory disorder clinics of three Finnish central and university hospitals. The patients participating in the study were at the onset diagnosed with a very mild or mild form of Alzheimer’s disease.

The results indicate that the heaviest psychological stress was experienced by family caregivers who at the time of diagnosis suffered from depressive symptoms. “The occurrence of even mild depressive symptoms predicted a psychological load on the family caregiver irrespective of, for example, the progression of the disease,” says Researcher Tarja Välimäki of the Department of Nursing Science.

Check Caregiver’s Health at Time of Diagnosing Alzheimer’s

The study also found that the psychological stress of spousal caregivers was greater already at the onset of the study than that of other family caregivers, and that the psychological stress of spousal caregivers also increased during the follow-up.

According to the study researchers, the results suggest that it is wise to pay attention also to the family caregiver’s health at the time of the Alzheimer’s diagnosis. “A depression inquiry carried out by, for example, a memory nurse would make it possible to recognize family caregivers who need enhanced support.”

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carmar
carmar
May 7, 2018 12:37 pm

So who will care about the care giver? I had no one.

Anonymous
Anonymous
Reply to  carmar
May 7, 2018 2:17 pm

Having no one either – – I turned to the Alzheimer's Association. Their social workers and class givers helped me find hope again. Other caregivers that I met at meetings reached out to me and made the struggle a little easier. There are people "out there" willing to help.

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Peter Berger

With experience in dementia caregiving, public education, and Alzheimer’s-focused writing—and a professional research background shaped in what many consider one of the world’s top laboratories—I work to make complex findings clear, practical, and genuinely helpful for families and professionals providing care.

This site was inspired by my Mom’s autoimmune dementia.

It is a place where we separate out the wheat from the chafe, the important articles & videos from each week’s river of news. Google gets a new post on Alzheimer’s or dementia every 7 minutes. That can overwhelm anyone looking for help. This site filters out, focuses on and offers only the best information. it has helped hundreds of thousands of people since it debuted in 2007. Thanks to our many subscribers for your supportive feedback.

The site is dedicated to all those preserving the dignity of the community of people living with dementia.

Peter Berger, Editor

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Welcome

Alzheimer’s & Dementia Weekly was inspired by my mother’s journey with autoimmune dementia and my dad’s with Parkinson’s dementia.

Walking beside them opened my eyes to the confusion, the courage, and the deep humanity found in families and professionals caring for someone they love.

Since its debut in 2007, this site has had one clear mission:
to separate the wheat from the chaff — to highlight only the most essential articles, studies, tools, and videos from the overwhelming river of dementia-related information.
(At last count, Google receives a new post on Alzheimer’s or dementia every seven minutes.) For anyone seeking clarity or support, that constant flow can be exhausting and discouraging.

Alzheimer’s Weekly filters, translates, and explains what matters most, helping hundreds of thousands of families, clinicians, and care teams around the world make sense of the latest research and best practices.

This site is dedicated to everyone who works—often quietly and tirelessly—to preserve dignity in the community of people living with dementia.


About the Editor

With experience in dementia caregiving, public education, and Alzheimer’s-focused writing—and a professional research background shaped in what many consider one of the world’s top laboratories—I work to make complex findings clear, practical, and genuinely helpful for both families and professionals providing care.

My goal is simple:
Translate the best science into guidance that lightens the load, strengthens understanding, and helps every person with dementia live with dignity.

Peter Berger
Editor, Alzheimer’s Weekly

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