This is BEAUTIFUL and so meaningful to those of us who have RSD/CRPS. I am a new friend, Paula in Florida and I have had RSD for 16 years now and it has been NO fun for me or my family ( as ya'll well know) I did have a Spinal Cord Stimulator implanted in October of 07 and it does help me with the pain. It is my second one ( the first one didn't work) I am still in the pain mode though, and I worry that my stimulator will stop working at any time. I hated the narcotics for so many years and now that I am off ALL of them, I'm soo afraid that I'll have to start them again...I do NOT want that. prayer is my daily companion, and I'm certain that it is yours, as well. It does help!!
We ALL need friends to talk to about this horrid disease. I am also a nurse and I totally understand what it has done to me and so many other people , whom I have come to know, who also suffer with RSD/CRPS. If I can ever help ya'll in ANY way, Please feel free to write me. I'm ALWAYS available.
A Friend INDEED, Paula