I have RSD/CRPS and have had it for 4 years and have been told there is nothing more that can be done for it. I have been rated 25% whole body disabled and I would think someone has more to say or do out there than what ive gone through with my treatment. Anyone have any ideas/comments or suggestions? Im in the midwest- so not here, I guess they are out of ideas. I dont want to live the rest of my life this way if i have a shot of not having to, who would (right!).