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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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Hi Jo*mar - I was just going to ask if TENS was the same thing as stim (which we had at PT) then I saw your post - I guess they're different. I'll ask my PT if he also has a TENS machine - good idea. My daughter's pain doc gave us something called a Hivamat, which helped a little bit, mainly in keeping flares away. I think that's something different, though, but it's also an electrical-type thing.
Hi Brambledog, re Calmare - I have a little different understanding about it and wanted to share a few links, since it was mentioned. My understanding is that although it's similar to a TENS unit, it's substantially different; different enough that it has its own unique and separate U.S. patent : http://www.uspto.gov/web/patents/pat...-20130219.html. Also, it's different enough that one of the most prestigious health organizations in the U.S., the Mayo Clinic, has several official clinical trials underway; here's one : http://clinicaltrials.gov/ct2/show/N...rambler&rank=1 . These are both U.S. government websites; not Calmare sites. Anyway, whatever it is, it put my daughter into remission, and she didn't have to get a SCS! I'm still learning about and studying all sorts of different treatments (including TENS, which is why I started this thread), because I know we're talking remission, not cure, with RSD, but I do know that this treatment did wonders for my daughter. Hi Az-Di, My daughter was scheduling her SCS when we came across a mention of Calmare and tried it, so we know at least a little what you're feeling ![]() Could you guys please share a little more how the TENS works? Where do you put the pads (?) in relation to what is hurting the most and/or the original injury site? How often can you use it? Thanks for sharing - it's so good to get people's experience with things! Last edited by SloRian; 06-17-2013 at 04:37 PM. |
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