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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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Senior Member
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I've researched about HBOT too, but being on the good ole NHS, they don't offer it, and the cost is way out of my price league. I'd love to try it, the science is sound, there have been some good results, and plenty of folk seem to get something out of it...
DJhasty, it would be brilliant if you did a diary about your HBOT, I'll be fascinated to see how it goes for you - and I'll keep my fingers crossed that you achieve some pain reduction. That would be worth any amount of time and hassle ![]() Good luck. Bram.
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CRPS started in left knee after op in Aug. 2011 Spread to entire left leg and foot, left arm, right foot. Coeliac since 2007. Patella femoral arthritis both knees. Keep smiling! . |
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#2 | |||
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OMG DJ! You're really having a rough time of this! I'm very interested in knowing how the HBOT goes for you! I really hope it provides relief for you.
I've no idea if my insurance will or will not cover it. I'm stuck in limbo for where to go next. HBOT and/or Calmare are on the agenda. Please do keep us posted. ![]() |
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"Thanks for this!" says: | Djhasty (08-26-2013) |
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#3 | |||
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Thanks Bram and AZ-Di. HBOT is not covered by Medicare either. HBOT is considered Off-Label, meaning the FDA has not approved it for the treatment of CRPS. We will have to cover this ourselves. It was difficult to decide just what treatment to put our money on. HBOT is the least invasive and somewhat helpful. We are hoping for the best.
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Djhasty - CRPS Type II with migraine, Dystonia and spasticity - Diagnosis 2010 following - Injury 2004 L5S1; 2nd metatarsal left foot fracture; left hip fracture |
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There was a lady here who had good success with this with her daughter. She made a thread on it - give it a search :-) Let us know if you try it!
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"Thanks for this!" says: | Djhasty (08-27-2013) |
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