Today I would like to introduce you to (or maybe you are already familiar with) RSDSA. This website has been a great reference point for me over the past couple years. RSDSA was founded in 1984, and it’s mission is to
“provide support, education, and hope to everyone affected by CRPS/RSD while we drive research to develop better treatment and a cure.”
This website has a wealth of articles on the condition, ongoing research studies, available treatments, stories from people affected with RSD/CRPS, info on support groups, and much much more. For a reasonable fee of $20 ($25 for international dues), you gain a 1-year membership of RSDSA. You will receive quarterly news letters, info on you can to get connected with others affected with CRPS/RSD, stay up-to-date with CRPS/RSD related literature and events. I highly recommend that you take browse through this website and hope you find it find it helpful as you or a loved one navigates through life with CRPS/RSD.