Hello Elizabeth, I have had CRPS II for almost 6 years now, like most others it wasnt diagnosed right away nor treated. The result of the 2 1/2 year delay caused lots of anxiety,depression and the diseaase spread from the hand it started in to both arms,shoulders and mid back. Late last year I injured my right knee..you guessed it, now I have full body RSD. Last year was the worst for me, my wife of 10 years couldnt take having a sick husband and left me to fend for myself. I was a wonderful husband and provider, because I had many days I could not keep up or help with everything I was too much of a burden for her.Since all of this happened I ended up in a Psychcare hospital and then followed up with outpatient care for a year now, that has helped more than anything.

 As for a spinal cord stimulator, I have heard lots of bad and very little good,since a surgury triggered my RSD my decision was easy...no more cutting on me, my arms n hands have had 7 nerve surgury's....number 6 triggered the disease and 7 made it worse. What I would do if I were you I would ask your Dr for names of patients who he has implanted with this device and then ask them, ask as many people as you need to help you decide. If you would like to talk more to me contact me directly  at [email protected]

Good luck and god bless

Frank