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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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Junior Member
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Hi.. My name is Bri & I am new to this site & happy to have found it. I was diagnosed with crps/rsd in my left foot over a year ago, it has since spread to my right foot. It took many doctors to finally figure out what was going on. I have had injections, tried many different meds & a month ago I had an SCS put in(I also posted in the SCS forum). I was wondering if any one else has tried an SCS for rsd? My dr thought I was a good candidate for it & I had great success with the trial but not so much with the permanent. I am beginning to regret my decision & wonder if I have created more problems for myself
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"Thanks for this!" says: | RSD ME (03-31-2014) |
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Thread | Forum | |||
I'm new to this site | New Member Introductions | |||
New to Site. Need RSD help. | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
New to site and RSD | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
new to site | New Member Introductions |