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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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When a hurricane hits Florida — or anywhere that has a very large population of people with dementia, there are special preparations that should be made by those living with dementia. Check these dementia-in-a-storm readiness lists.

A monthly, 40-minute phone call from a non-clinical professional may suppress or reverse the trajectory of depression so frequently experienced by family members caring for
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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.
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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Each year, I write a letter to the Congressional Delegation from my state asking (more tike pleading) them to visit my wife who is in Final Stage Alzheimer’s and is in a nursing home. She went to their offices at the conclusion of the Alzheimer’s Association Advocacy Forum in 2010. Two years later she was in Long Term Care. If they are to see the REAL face of Alzheimer’s, they’d have to come to her or any of the others in the final stage of this horrible disease. To date, over the years, none has accepted my invitation and it would be a profile in courage if any did. Hopefully, Kim Campbell will extend a similar invitation to her National representatives and will be more successful than I have been.
There ARE NO SURVIVORS WALKs FOR ALZHEIMER’S!! That’s a sad fact that MUST change!!!