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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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What’s it like having early-onset dementia? Find out today from Jason, who shares his answers with viewers who have asked about his experiences and those of his wife Leslie.
VIDEO: See how one lady faced the stigma of Alzheimer’s and rose above its storm clouds. Learn why she continues to take part in her community and how she lives life with dementia to the fullest.
Harvard’s Dr. Rudolph Tanzi is edging Alzheimer’s research forward with a string of breakthroughs. He’s one of today’s most talked-about Alzheimer’s researchers. Watch Rudy Tanzi talk about the inspiration for his life’s work.
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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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!!!