Hi, I've registered although I haven't posted with my story yet. However, I couldn't resist responding to this these posts on rsd and sweating, etc. I have rsd that is everywhere now(long story) and it's gotten so that I can't even go anywhere because by the time I get there, I have sweat dripping all over as if I came out of the shower and didn't dry off. I have to watch what my clothes are made out of and what color they are so that they don't look as if I spilled a bucket of water down my back. In spite of the wetness my skin is cold and clammy. I've done this for years and it's become such a problem that I just wear cotton pjs and don't leave the house except for docs and hosp. I'm now back in my electric w/c from bilateral below the knee amputations and even though I deal with everything fairly well, I've decided that from now on " mohammad needs to come to the mountain" from now on instead of the other way around. It's just too much. I just stay home, keep up with my hobbies and entertain my grandkids. I certainly empathize with you all in a big way though. I'll try to post my neuro and health story, as well as my good things, when I have more energy and less pain. by the way, I followed this site several years ago, and my neurologist mentioned it to me and it reminded me it was still there. I'm so glad. susan from ky