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Dear Joe,

It is good to get to know you.  The description of your symptoms  leading up
to your diagnosis is quite similar to mine and I'm sure to many here  on this
list.

I'm sorry to hear of the loss of your wife Lori.  This is one of the  most
difficult losses any of us will ever face in our lives.

I realized after I'd sent my mail to you that I had probably overwhelmed  you
with the many organizations I'd listed.  I guess I was trying to give  you a
head start in finding the sources that I've found so helpful over  time.  If
you haven't already, check out the National Parkinson  Foundation's web site as
a beginning.  They have up-to-the minute info on  research and drugs.  You
can also register with their "Ask the  Doctor", "Ask the Dietician" and "Ask the
Surgeon"  After registering, you  can e-mail them a question and you will
receive a response to your question via  e-mail. Questions are answered on a
daily basis along with  those of the other members.  Oh yes, you can contact them
and  request their packet of Parkinson's publications.  I've found these very
helpful when I have a question from time to time.

If you would like more info about the other groups I'd mentioned, I'd be
happy to direct you to their sites and/or give you a brief synopsis of their
mission.

If you have a chance, watch 60 Minutes this evening for their segment on
"GDNF."  It involves a drug trial for Parkinson's patients.

Take care,

Dee


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