Rich, I've read and chatted with a few folks who showed signs of RSD but it turned out to be trapped nerves instead. As soon as those nerves were released their symptoms vanished. As mentioned by others the trick is to find a specialist who knows RSD/CRPS and this can be time consuming, in which it was with my wife's case, took 4 years for her. You could cut to the chase and check this group out---http://www.rsdhealthcare.org/ They have a good reputation but I believe they do not except insurance. So, I believe the way it works is you pay them, and if approved your insurance then pays you. I hope everything turns out roses for you and good luck.

jim