Since CRPS started I began to have "the sweats," both hot and cold. Throughout the summer I was freezing with a heating pad and a heated blanket. I think I mentioned that my sister came to visit me wearing tank tops and carrying a fan. We were a weird sight.

In my case I know it isn't the meds since the cold/hot thing started prior to me taking any. LDN has helped with the pain and color changes, but not much with body temp regulation-maybe in time it will get better. I cannot bear wearing binding clothing, especially a bra! Heavy or bulky clothing makes me antsy.

There is so much more to this disease. I feel like even though I am improving in one area I am falling apart in others.