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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board

Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index

Re: Sweats/Chills
Dec 26, 2006
Hi everyone:wave:

Boy someone did some research. This post was started in 2003!! I was looking through some of the names, and I guess this was way before my time.

I think we all have sweats and chills. I remember after my neck surgery, when I started going back to physical therapy, I would litterally soak the sheets in a matter of minutes. :rolleyes: That's when I was first dx'd with RSD. I also read some earlier posts about sweating so bad like you feel like you were getting ill. This used to happen to me alot at first. That happens when you are in so much pain, that is a good sign that your meds need an adjustment. My feet will feel like they are on fire on the top, but on the bottom they feel ice cold, and my doctor when examining me said it was the opposite. :dizzy: It's just the central nervous system misfiring.

I guess the best way to combat this, is by dressing in layers. I know it's hard to find the right fabrics that don't irritate the skin. Splothcy skin is a sign of RSD as well. It's called motteling. And I hate the sweating part too! Does anyone else go through alot of lotion? I drink plenty of water, but I think from sweating so much it dries the skin out. Just curious! Aloha Skooze

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