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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board

Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index

Hi Michelle and Cathy,
Michelle, When i called Dr. S office a month ago. They referred me to the RSD foundation and i got some names. It is too bad that i have to wait for 15 months to be able to see him. I suppose i need to fly in and perhaps making some plan to stay over. Today i went to see a pain management doc who said i don't have RSD because he could not see the temp change or skin texture change or muscle weakness or dsytrophy, etc although i definately have the dry and wrinkly skin and blocthy red color on my hands and of course the burning and oversensitive palms. I told me my feet are going through the same process. He only offered bio-feedback and not even a nerve. This doc is the Kaiser doc and that was the place that mess me with the painful IV. Very frustrating to say the least.
Cathy, go ahead to make an appt with Dr. S. In the mean time, find a doc who can treat you. Perhaps you will get a full remission. One of my friends got the full remission.
Good Luck!

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