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 10-28-2012, 10:42 PM #13
painman2009 painman2009 is offline
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Join Date: Feb 2011
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painman2009 painman2009 is offline
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Join Date: Feb 2011
Posts: 362
10 yr Member
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Quote:
Originally Posted by LIT LOVE View Post
I'd look at a doc that is not a traditional pm doc. Preferably someone with ESD experience. There is a whole host of issues that come with seeing a pm that mean reduced care IMO.

I have also learned to concentrate on the most urgent matters at every appointment. I pick my battles. Is it urgent to change dosages or type of meds? This can add 10 minutes or so to an appointment.

What other options have you been offered or discussed for a treatment plan? What do you want? Ketamine infusions may help you. Blocks may help you. If you have an extra couple thousand to spend, HBOT might be a good choice, etc. (Doubtful WC will pay for it.)
I have naut to spend. and I have dscussed hbot, he also said pain pump(surgery I wont agree) acs (again surgery, as well as a batery up my cooly, I wont agree) he also did a quck mention of amputation.. obviously I will not agree to lose a limb. he did the lumbar blocks.. (a lot) no help at all, I've also had sterid injections, lydicain, cortizonwe injections.. all no help some made it worse.
I presently have a tens unit.. I use for strict back injury as it does noting for the RSD. the PM wont discuss the creams for topical use, I tried aqua therapy till I could no longer afford it.( i think it was helping just keep cardio good)
also PT plus all these wonderfully awful drugs..
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