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Is smaller really better? Necessary?

Posted by RichardTaylor at 21st December, 2009


Hello

The reductionist have captured or interest, our minds, our heats, and our wallets! They have convinced us that in order to cure the brain of the symptoms of dementia we need to reduce the causes of the symptoms to the smallest amount of human tissue/fluid we can change by swallowing pills and/or shooting various chemicals into our blood stream. How small must we go to change the symptoms? Right now, we are tracking individual cells and their components. Some study individual proteins. Others are going even smaller, looking at our genes and DNAAnd assuming we do find the real causes of each of the many, many symptoms of dementia, how are we going to undo/alter/prevent them? How, how much and how expensive will this process be for those of us experiencing this or that symptom? What side effects of these treatments can we reasonably expect to experience?

Hands in the audience if you truly see light at the end of this tunnel. Stand up if you think we have the turned for the home stretch. Speak up if you believe that just because we say something, it must, or at least will someday be true - someday!?

As for the rest of us - there is still today to enjoy. There is still a purposeful and purpose filled life to live. There is still love to give and receive. There are still songs to be sung, people to meet, need things to enjoy.

Richard

“Dance like no one is watching. Sing like no one is listening. Love like you’ve never been hurt and live like it’s heaven on Earth.” - Mark Twain

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Category : Blogs

Comments

Judy Crager January 5, 2010

Dearest Richard,
I have been reading and “using you” for nearly a year now in the Dementia Care training class that I do at our Long Term Care facility and I recommend your writings to our families in our Alzheimer’s support group, as well. You get the point across so clearly from the person with dementia’s perspective about what is needed and how we as caregivers can help.
Regarding today’s blog…I wish I had an answer. It may seem that everyone is looking in different places and in different ways to find a cause, then a treatment for this disease. I just hope that they are all communicating and sharing notes.
I lost my husband 5 years ago to fronto-temporal dementia, probably Pick’s disease, and was so frustrated at the lack of even having a “real” diagnosis to go with what he had - let alone any sort of treatment option.
You are doing valuable work, Richard, please keep on fighting the good fight. Best wishes to you, your wife and the rest of your family.

Tracy February 11, 2010

Dear Richard,
I am just finding about you as i am working with a 62 yo woman psych. –
-I amencouraging her to read about the disease, —yours seems perfect, tho I am not sure she can follow it…but it inspires me to help her find a voice and pursue her own interests, with help of course.
Meanwhile,
Is the Dec 09 your latest newsletter? ..I will be sharing this with her spouse as well and wanted most current of your updates .

Thanks for all you are doing tohelp us support alz clients.
Tracy

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