Thread: Rsd/crps
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Old 10-23-2012, 08:15 PM
alaska49 alaska49 is offline
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Join Date: May 2009
Location: Pennsylvania
Posts: 221
15 yr Member
alaska49 alaska49 is offline
Member
 
Join Date: May 2009
Location: Pennsylvania
Posts: 221
15 yr Member
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Your story sounds just like mine as I got my RSD from 3 reconstructive surgeries to my foot also. The third surgery it spread full body and within 3 months I was in wheelchair, couldnt use my hands, swallow, hold up my head. Its been 9 years now 6 with it full body and internal. I have seen over 200 doctors in 5 states the best treatment I found was the ketamine, not just the infusions but nassal spray and lossanges for home. I still have a long way to go in recovering but just dont give up there is some kind of help out there. Being in ohio I just warn you not to go to the pain program in cleveland clinic they treat every pain condition even back pain and headaches like its all made up and if you stop thinking of it, it will go away. I thank cleveland clinic was the worste hospital I found for helping RSD. Although stanton hicks was good.

Niki
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