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