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OHSU has some of the top brain guys & gals in the country.   I see the head
of the center (actually head of the VA center aslo) Dr. Nutt.  In the Oregon
City area Dr. Phipps and Dr. Ashe are very good also.  Have Fun!
\Randy


Games to entertain your brain.
http://www.stargraphics.com

Star Graphics Corp
10943 S Forest Ridge Ln
Oregon City, OR 97045
----- Original Message -----
From: "S.Wilson" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Monday, November 21, 2005 1:33 PM
Subject: Re: Neuros


>I am mostly a listner on the Caregiver for PD list.
> My Husband Iven was diaagnose with PD in 2003.
> We live in Portland OR and have Kaiser, our neuro is Dr. Gancher.
>
> Iven just retired and I will hopefully late next year.  Iven is doing okay
> right now and wwe plan to RV for a while so are thinking of changing
> Health Benefits .. to probably Blue Cross....so by any chance do you know
> how we would find a "good"  pd neuro in the Portland area...
> We have Oregon Health Science University Hospital and I know they do some
> research and there a doctors listed ... but how to find a good one baffels
> me.
>
> All the issue I read especially  doctoring one is really overwhelming yet
> so important for the future.
>
> Any insite you could provide would be really great.
>
> Sue CG for IVEN   62/2003
>
> Charles Meyer <[log in to unmask]> wrote: Dear Sheri.
> Hi and welcome to the list am a 60 year old retired physician.. I have
> had PD   since 1989.,  and DBS surgery.  I see DR Gallagher at UWH.  I
> have been involved the Madison Area support group with for most of the
> 16 years.  Who is your neurologist.?   Where are you located?  I am in
> Middleton.. I also belong to an informal group which meets once a month
> where we get together and just talk about how we are doing.   Possibly
> we could get together and and talk   in person or by phone.  You can
> reach me  at 608-833-9336.
>
> Charlie
>
>
> Charles T. Meyer MD
>
>
> Sheri Harper wrote:
>
>>Hi, my name is Sheri, the University of Wisconsin gave me the information
>>on your group. I am 57 and have been dealing with Parkinsons like symptons
>>for the last couple of years. I was finally diagnosed just a few months
>>ago. I am presently on medication and seem to be doing much better. I am
>>very interested in getting all the information I can about PD. My daughter
>>is a RN and has been a great help. I have also joined a support group, but
>>missed the first meeting. I am looking forward to the next meeting which I
>>will be attending. I think any time you can meet new people in your area
>>it is a good thing!!!!
>>
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>>In the body of the message put: signoff parkinsn
>>
>>
>>
>
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>
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