MSLDAY ~ I am so happy you quoted this....
Now if my brain could digest & methodically understand & speak it.
My pain management doc doesnt want me to have any more TOS surgeries due to the CRPS but how long can my system hold out to Botox Chemodenerviation procedures 4 x's a year for the TOS pain & not increase the CRPS.
I have pretty much full body CRPS 10+ years now including it now affecting my stomach. I read here so many people say it has affected their organs. I can so relate. Its so incredibly frustrating that CRPS cannot be used for my SSDI doc & W/C defense. FM & RSD is not spoken in court & result in approvals these days in California.
Quote:
Originally Posted by Mslday
That is a good question Pete, something I was never too clear on either. Here is what I found, it is from the most up to date Medifocus Guidebook on Reflex Sympathetic Dystrophy.
MsL
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