Hi, I was diagnosed with Rsd/Crps in November 2011. I have had aggressive treatments and after several months of agony, I actually feel like my condition is improving some. I am looking for fellow sufferers who have lived with this condition for a long time and would like to get some tips on what has worked for them over the years, as from what I have researched it is probably going to be with me for the rest of my life as no known cure. Nice to meet all of you.