







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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At Thailand’s Vivo Bene Dementia Resort, pampering is the priority. This special report for 60 MINUTES asks, why can’t there be facilities like Vivo Bene in Australia?

Researchers studying Australians with type 2 diabetes found those taking the first-line treatment medication metformin had significantly slower cognitive decline compared to those who did

VIDEO: See why the
 wonderful Alzheimer’s activities program, “Creative Aging: Dance Like Nobody’s Watching” has been a smash success for people with Alzheimer’s, as well as caregivers.

Here’s Teddy Mac and his son Simon singing Oklahoma – one of his showstoppers – from a few years ago.
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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yup, these people have lives they are living well, despite it all!
This is one of the Precious video for me, I really love this.
Great article.
This is great. I lived with my father for 11 years following my mothers death, nearly eight years of that time we lived with the diagnosis. He wanted a time line. His doctors response was that everyone was different and that he would not put him in a box as far as his abilities or life expectancy, just as he would not put his Autistic child in a box. I was so grateful for that. He passed nearly eight years after diagnosis. I so wish I knew what I know now about the desease having been his caregiver until his death. I was the
fortunate child, the one who had the time to know the man, not just Daddy.