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thank you, Linda, for making my day with your kind comments.  Your support
gives me the strength  to carry on.

Ray

-----Original Message----- 
From: Linda
Sent: Friday, October 05, 2012 12:18 AM
To: [log in to unmask]
Subject: Re: back, neck and leg pain

Thanks for your input, Ray.  And many, many thanks for the articles you
post.  You are the best source of information on this disease I have found
anywhere.  So glad I found you and this list!      Linda
----- Original Message ----- 
From: "Rayilyn Brown" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Thursday, October 04, 2012 10:22 PM
Subject: Re: back, neck and leg pain


> Linda
>
> I have had PD 16 years and can't remember when my pain started, but it has
> gotten  bad this  last year.  My right hip area hurts when I walk probably
> because my left leg is drawn up and I'm on my left toes.   When I sit or
> don't  move I'm OK, so I'm convinced it is PD; also it varies,  I never
> know just what it will be like.  I get leg pain when I move in bed.
>
> In my opinion, I think you are wise to be wary of invasive procedures.  It
> sounds like you have a number of things going on at once.
>
> I think I'm learning what it is  like to turn to stone.
>
> Ray
>
> -----Original Message----- 
> From: Linda
> Sent: Thursday, October 04, 2012 3:09 PM
> To: [log in to unmask]
> Subject: back, neck and leg pain
>
> I would appreciate some input from other people with Parkinson's in regard
> to the issue of pain. I have been told that I have degenerative disk
> disease with a narrowing of the spinal column in the lumbar area. I was
> also told that my left knee was bone on bone in 2006 and would need a
> replacement sometime in the future. I was diagnosed with fibromyalgia in
> 1997's and diagnosed with Parkinson's disease in May of 2010.
>
> It seems like there are so many factors that I am very hesitant to do or
> have done any invasive measures such as knee replacement or back surgery
> because I feel like it will not resolve enough of the pain issues to be
> worth the risk and the attempted rehabilitation. The neurologist I have
> just been seeing recently made the statement that the pain would not be
> from Parkinson's. I'm not sure if she thinks that pain is not a part of
> the disease or that she feels that the pain I described wouldn't be from
> the disease. My current back pain appeared to become acute after swimming
> a few days in a row. It felt very good in the water to twist and turn my
> body but after that, movement became more difficult than my pain level
> increased radically.
>
> It was very helpful to be on this list and receive the information about
> briefings through the Parkinson's organization. I was able to get the
> briefing on Parkinson's and pain and found that most informative. I plan
> to be reviewing many of those articles. The recent stem cell article was
> also very interesting.
>
> I would appreciate any input from others as to their experiences and
> thoughts on the little bit of information that I have given here.
>
> Thanks, Linda
>
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