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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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06-22-2007, 03:44 AM | #1 | |||
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I know sweating is part of the deal. But for the last month is almost continual!! I was never one to sweat, even during my sports days. But now, it runs down my back and on my face....(not real attractive!) Does anyone know how I can deal with this? I thought maybe the meds, but I am down to only taking carbamazepine (for epilepsy) , lyrica, and zopiclone (for sleeping). It's driving me nutz!!
I have tried cold drinks, cool baths, but it just comes back with a vengance. My doc is "un-knowing" about Rsd, is there a med for sweating? Thanks for any help.... Hippy |
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"Thanks for this!" says: | loretta (07-06-2009) |
06-22-2007, 06:52 AM | #2 | |||
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There are several medicines for excessive sweating...Robinul and Robinul-forte, and Clonodine. I have never used these products, I just found this info out by googling it, lol.
The data was meant for Neuropathy patients, so I think we can "assume" it would work for us as well. But I've always been told that it can be extremely dangerous to stop yourself from sweating... you need to sweat to regulate your body temp. I have the same issues you do, both from the rsd and from aids. I just change shirts a LOT more often than I used to.
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"Thanks for this!" says: | loretta (07-06-2009) |
06-22-2007, 09:40 AM | #3 | ||
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hello,
just wanted to let you know that i too sweat buckets! what fun, right? anyway, my doc prescribed the clonidine patch. what a difference! it completely stopped the excessive sweating, especially helpful for my night sweats. hope this helps, jenny |
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"Thanks for this!" says: | loretta (07-06-2009) |
06-22-2007, 12:09 PM | #4 | |||
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Magnate
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I never sweated before RSD and now I can take a bath in my own sweat. My nights are horrible. I've delt with it now for about 5 years and I didn't know there was anything out there to help. I am going to ask my Dr. about one of them. Mine hasn't let up in the whole 5 years.
Ada |
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"Thanks for this!" says: | loretta (07-06-2009) |
06-22-2007, 01:13 PM | #5 | |||
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"TheOne", Jenny, Ada
Thank you so much! It's bad enough that sleep has been taken away, and to fight the pain....but, sweating too?? I am in a flare at the moment, so I am just feeling a little bit PO'd at it all. There's nothing worse than an angry, sweaty, hurty Hippy...sheesh. But thanks to you all, I will seek help and let the "un-knowing" know what might help to stop it. Hippy |
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06-23-2007, 12:37 AM | #6 | ||
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Until I started on CLONIDINE, I was sweating day and night. My sheets and clothes were always so wet I'd get chills.
I don't know how it works but it sure helps a lot. Before the clonidine I used Xanax to calm the SNS and it helped for a little while but they always returned. I hope you find something that helps you. Hope |
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"Thanks for this!" says: | loretta (07-06-2009) |
06-23-2007, 01:12 AM | #7 | |||
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Hi Hippy! I really don't sweat as much.. when Im in the sun which is not long at all. (Don't wanna ruin my pretty face) LOL Seriously, I use baby powder or plain 'ol corn starch is the best! Good luck sweetie.. Oh "Gold Bond powder" is Great too! love, Desi
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