Hello all, I have a daughter that has suffered with RSD for 14yrs she is now 21. She has suffered horrible with this condition. Her name is Ashley *edit*.
I also have RSD, not nearly as bad as most. They found mine within the first 4 months. I had 27 nerve blocks, trial SCS and now the pain pump. I don't talk a lot about my RSD, we all know how having one person with RSD goes with people judging and being rude. Just think how it goes when there are 2. We live in Calie and are always looking for others to help, support, and share.
*edit* We gotta stick together and find the answer to RSD.
Peace and less pain hugs.