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The most important thing a newly diagnosed Parkinson's patient can do is to 
find a support group.  I know that it can be hard to see how PD affect those 
who suffer long term disease, but people in a support group generally know 
where the best movement disorder specialists practice.  It is the one regret 
I have when I look back on my husband's PD journey (which lasted 28 years). 
We wasted years looking for the 'right' neurologist when that fellow 
practiced right under our noses not more than 15 miles away.  My husband 
suffered unnecessarily because he was afraid to go to a support group.
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God bless
Mary Ann Ryan (CG Jamie 68/28 with PD, died 11/20/07)
www.bentwillowfarm.org 

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