This thread is exactly why I am comforted when I visit this forum...it seems that everyone has had this experience and if you haven't, you are very lucky...I am done, for the time being, with neurologists and pain management...the stress and anguish that I was put through has not been worth it to me.....I have a diagnosis and been through the med changes and I feel that my MD does a way better job than any other person I have been to. I don't want a spinal block, because I already have cerebral palsy and the ketamine infusions are out because no one near me does them...the only thing that I want is to be able to take care of my family, my house and my dogs. I feel like I am at an "even" point in this disorder and even though my RSD has spread, it's no different than it was a year ago...it is somewhat under control through my current regimen of medicine, Wii Fit Plus, and epsom salt baths

Big hugs and prayers go out to you!:grouphug: