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thanks Kathleen.  I tried several support groups and did not care for them. 
Same thing when I had cancer - it was very depressing!!
Ray
Rayilyn Brown
Director AZNPF
Arizona Chapter National Parkinson Foundation
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----- Original Message ----- 
From: "Kathleen Cochran" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Saturday, November 15, 2008 8:00 AM
Subject: Re: I have just been diagnosed with Parkinson's


>I believe support groups are not for everyone and can be counterproductive.
> A positive attitude is of paramount importance in living with this 
> disease,
> and support groups can undermine that. It's next to impossible to look at
> someone whose condition is worse than yours and not imagine that this is
> your future. That is not only dispiriting, but also wrong. PD is 
> notoriously
> variable in symptoms and progression from one person to the next. You 
> can't
> predict based on someone else's experience what your course will be.
>
> That said, some people thrive on support groups.
>
> I also think those who love and care for PD patients may benefit from
> support groups at least as much as patients do.
>
> Kathleen
>
> 2008/11/14 Gerry Haines <[log in to unmask]>
>
>>
>> In a message dated 11/12/2008 2:00:33 A.M. Eastern Standard Time,
>> [log in to unmask] writes:
>>
>> 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.
>>
>>
>>
>> Been there have done that.  Have to agree, except I think a good  neuro. 
>> is
>> first., I lost my husband  in April, after 22 years of  dealing with this
>> disease.  I have advocated, spoken, been everywhere  trying to find a 
>> cure.
>>  I run
>> a support group, and they are wonderful, but  Brig would not go either 
>> for
>> the
>> first 7 years.  Just please take an active  part.
>>
>>
>> Gerry Haines
>> Pennsylvania State Coordinator.
>> Parkinson's Action Network
>> "Do  something good for someone you least like today."
>> St. Anthony of  Padua
>>
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