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Gail Rae Hudson

Very good "Part 2" post, Mona! I like this way this sums everything up while providing yet more indepth information. Good series.

Deb Peterson

I'll never forget our first visits to the neuropsychologist, who claimed she couldn't see any sign of depression in my mother. I almost fell off my chair. I suspected that I might be in some denial about the dementia, but I KNEW in no uncertain terms that she was depressed, too. So reading this piece was very enlightening, Mona. My mother is now being treated for depression and it does make a difference. Another reason it might be hard to detect in many AD sufferers, I think, is because they are part of a generation that was not encouraged to "let it all hang out." Both of my parents have always had their shoulders to the grindstone, in more ways than one.

Excellent points about coordinating patient and caregiver need, too.

Karma

Wow, this really scares me. I suffer from depression....Many of the residents at my mom's "memory care" facility seem to have some signs of depression, but a lot of Alzheimer's symptoms go along with depression symptoms - sleep disturbances, being confused ->nervous. My mom started crying regularly, according to one of the care managers, in the afternoons when family isn't there. My grandmother though gets anti-depressants, and they don't solve her symptoms of being very upset and confused and crying and being agitated.

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  • The Tangled Neuron started as a personal site chronicling my search for answers on my father's dementia. Although it's too late to help Dad, I hope to provide the information other people with memory loss, their families and caregivers need to make decisions, identify resources and find new ways to live with memory loss. Inclusion of links, advertisements and content generated by others does not imply endorsement. Remember, nothing on this site is meant as a substitute for professional medical advice or for using your own judgment!

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