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On November 8, the Parkinsn Information Exchange Network will have been
offering information and support for those of us with pd and our
caregivers for 10 years.

I have had several people ask me how we are going to celebrate this.
John Cottingham and I decided to put the question to all of you.  Any
and all suggestions will be welcome.

We would also like some feedback as to the role PIEN plays in your
day-to-day living with pd.  How did you find us?  How long have you been
a member?  What do you find is most useful?  How can we improve?

Put your thinking caps on, folks and let's decide on the best way to
celebrate 10 years of sharing and caring.

Barb

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