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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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Treatment for moderate to severe Alzheimer’s is available in an extended-release formulation. Learn how Namenda XR (generic memantine) offers a more convenient way to take this Alzheimer’s medication.

Love & kindness are never wasted. They always make a difference. They bless the one who receives them, and they bless you, the giver.

There are over 80 types of dementia besides Alzheimer’s. Teepa Snow, dementia expert, explains why knowing the right type is so important and why so few people with dementia really do.

As Mom can no longer speak and give consent, Saskia can’t get power of attorney or access her Mom’s medical records. See Saskia explain the importance of early diagnosis.
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!!!