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 07-25-2013, 12:51 AM #8
Dubious Dubious is offline
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Join Date: Jan 2009
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Dubious Dubious is offline
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Join Date: Jan 2009
Location: Paradise
Posts: 855
15 yr Member
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Quote:
Originally Posted by AZ-Di View Post
O.K. so I'm all over the place on deciding whether or not to get the permanent SCS. I had the trial removed on July 11th. After that I was not ready to decide ANYTHING!
I went for a consultation about "Calmare" therapy and I was leaning that way. I presented the info. to my pain Dr. (she wants perm. SCS) and she was not impressed. Of course they are in different camps and neither bellieves in what the other is doing.
Anyway, now I suspect the CRPS is spreadiing.
Does anyone have experience with either treatment helping to prevent the spread?
I posted this in the SCS subforum as well.
Many thanks to SloRian for the info. on the Calmare clinic (I went to the Scottsdale AZ location). I found them and was impressed.
I've had an appendectomy and a hernia repair (opposite side) since my onset of CRPS. I now have periodic intense deep, burning pain at times regionally now that was never realized before. Thankfully it is not very often but when it occurs, stops me in my tracks and doubles me over....
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