I was diagnosed with RSD in 1994. From then to 1999 I was in the hospital for nerve blocks and numerous surgeries such as gall bladder taken out, fingers on right hand wired open and I have a urinary ostomy. My RSD is atypical and my Neurologist feels that is because I have a nerve disease that they can't figure out what it is. My mobility has went down hill quickly. I now have RSD though my whole body. It would be nice to be able to vent and ask questions about things I'm going though physically. I am pretty much homebound and I don't get much interaction with people in person or by phone. It would be nice to see if others have some issues I do and for me to share some things that help me and maybe would help others with the same things. I look forward to talking with others that understand what I'm going through.