I was diagnosed with RSD in April. Two years ago I had surgery on my neck and now RSD has developed. I have it in my neck, back, both arms and now my feet and ankles. I have a good doctor but am now running into insurance issues. I have had to quit working and my dr.'s office does not want to contract with a new company right now. There are only two pain specialist in San Antonio listed on this insurance; one does not treat RSD, the other dr.'s office will not return my calls. I know my doctor would be very concerned but I can not get past the office staff. He would like to put in a neuro stimultor. I feel this is the best course of action as my symptoms are worsening. Where do I get more infomation, support and advocates? I truly feel lost. This is taking a huge toll on my family and my life is diminished by over fifty percent. Does anyone have any advice?