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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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