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Bill/Aletta & Sally

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Hello everyone:

Reading through the posts for the last three days, I

came across Sally's today. It so reminded me of the

message I sent a few y ears back when Bill was first

diagnosed. At the time, many of you responded with

information and questions to ask the many doctors we

were seeing. I am sure Sally will get the same

support. We must remember that this is an insidious

disease, and not very well known. Family and friends

are of little help. This site is very, very important.

My Bill was in such denial that he would have never

thought of posting, but now he looks over my shoulder

and asks, " What are they saying? Anything new? "

So, both the caregiver and the ill person benefit.

I'd hate to see Bill not post since his assistance has

been invaluable to us. His knowledge and experience

saw us through quite a few hard times. I believe my

Bill would not be doing as well as he is if we hadn't

had this site.

As they say in the Twelve Step Programs- Take what you

need and leave the rest.

Does anyone remember the Mother Theresa quote we used

to have. Maybe it is time to bring it back again.

And reach out to Sally for the support and help she

needs at this moment.

Hug

Hope

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