Welcome and sincere sympathy for your RSD. I prefer RSD myself. I've seen 3 pain management doctors who say CRPS, and 2 others who say RSD. Many nurses look like a deer in headlights when you say CRPS but then go "ohhh" when you say RSD.
Either way it is so good to have this forum as a support group because we are so misunderstood by so many other people in our world. This disease affects is all a little differently yet, we all seen to understand the weird inconsistencies of the pain and mobility issues.
I'm interested in what is giving you some rellief.
I just had my SCS trial placed in today and I will place my experience in a different post.