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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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New Member
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I am new to this site for posting but I have been viewing this site for a while.
I am so happy to see such an active site. Thank you all for sharing I have gained a lot of information and comfort from you postings!!!!!! I have a SCS and can tell you of my own journey with it. Your first question was regarding spreding. I have had spred since the SCS. I was told that it could possibly stop or slow the spreding but is not a deffinate. As far as recovery time it was much longer that I was led to believe. It was 5-6 weeks before I was aloud to start returning to unrestricted activities. No driving, no lifting, no bending, etc... I have some relief from the permanent stimulator (ANS rechargable), I feel I had more relief when I had the trial stim. I have had my pain meds increased since having the permanent stim. but keep in mind everyone is different. I am inpressed by your vigor in standing up for your self!!! I hope this is helpful. jclg |
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