Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

 
 
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Old 03-27-2007, 01:55 PM #10
InHisHands InHisHands is offline
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Join Date: Dec 2006
Posts: 808
15 yr Member
InHisHands InHisHands is offline
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Join Date: Dec 2006
Posts: 808
15 yr Member
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Quote:
Originally Posted by artist View Post
Hi Vanessa,

Worrying, that breathing problem - I'm wondering when you were last checked out for things other than RSD...sometimes the RSD can be so overwhelming that it masks other things that might be going wrong. Many of us, sad to say, have other conditions coexisting with RSD, and some of the conditions overlap as far as symptoms go... perhaps you should ask the doc to check you out next time you're there, just in case.

But, btw, I agree with Di that when PT starts to present its own problems, the time has come to ease up; she's right, not all PT is good for RSD - I'm not saying they're getting it wrong, at all - just that the body can only cope with so much, and you've gotta give the brain a chance to cope too.

You're a real trooper, though, I take my hat off to you - and I love your enthusiasm - sometimes, though, we need to stand back, take a breather and rethink a little. Maybe time for a small pause - in general, I mean, not just the PT?

Just a thought, do take care, we love having you here,
all the best

Thanks for the sweet caring words, and for the kind advice, Artist.

I am going to mention the whole breathing thing to my Dr., and see what she thinks. I didn't even think about it being something other than the pain... because it happens when my pain is through the roof.

I have since changed the way I do all my PT- I take breaks so that my muscles don't do that strange contraction thing... it has helped, and I realize that I can only tolerate so much. I do know that all PT isn't good for RSD, but there is some that is. My physical therapist has worked on changing the whole program so that it is tailored for me, not for just an RSD patient, but for my RSD. Some of the things I was doing there we both realized needed to go and they were serving no purpose (and just increasing my pain).
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