I saw a new doctor this past Thursday who seems to know a lot more about RSD. He wants to do a nerve test and go from there. Mom said as of right nw things are loking good that I most likely don't have RSD, but she wants to see how the nerve test goes. Thanks everyone fr the advice and help, having somewhere to put things into words makes a big difference. Mom has also sat with me and read some posts. She thinks it's great that there is a place where people with RSD can talk and said this would have made her experience better when she was first diagnsed because she could have found someone who understood what she was going thrugh.