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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board


Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index


Re: Sweats/Chills
May 25, 2003
Like Soxy I deal with the skin sensitivity also. The Chils, Sweats and the rashes I get are all related to RSD. My Dr's give me a Stronger Hydrocortizone cream for my rash plus the Aveno skin care line helps me with the itchies all over. I hate the sweats/chills the worst. I am past menopaus. had that done many yrs back in my 30"s and take meds for hot flashes. This associated with RSD is much worse the normal hot flashes. I try to wear cool clothes so that when I have the chills I can grab a sweater/jacket/blanket then throw it off when the hots come back. They sure come back with a vengence sometimes don't they. I have more problems with pain waking me up then chills/sweats.

I wish us all a nice calm day with a low pain day

Angels do exist, there all around watching us all.

Stickgirl
Re: Sweats/Chills
Dec 24, 2006
My hands are constantly sweating from the RSD.

I am constantly feeling like my arms, hands, shoulders are burning up :blob_fire (while on the outside my skin is freezing cold). I get really warm/ flushed quite a bit and then all of a sudden I'll be freezing! :eek:

Tempature changes are part of RSD/ CRPS... it is like your body's tempature is way reset... Example: When I feel 70 degree water with my right arm it feels warm, while on my left arm it feels warm!


About the skin sensitivity: I also experience that. If someone just brushes by me the pain is AWFUL and I sometimes scream/ cry from the lightest touch. I know what that's like and I am working hard on desensitization for that.





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