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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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#1 | ||
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I had problems with anything that touched my fingers and hands. I too had to wear gloves in frozen areas or outside in warm/hot weather too. I haven't had the "bruising" but do have the redness. Things that I have found that helps are biofreeze and lidocaine gel. I hope that helps
shunique |
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#2 | ||
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I have a lot of problems with my hands. I have full body RSD and when I have a flair up my hands feel like I am touching the sides of hot pot on the stove. They are sensative to touch. I have had RSD for 8 years. Just recently my hands have started to swell and are painful when closing them. I have used biofreeze on my hands, arms,legs and feet. I see a chiropractor 3 sometimes 5 times a week. He use an activator to adjust me not his hands. I know his adjustments have kept me off of a lot of medications. I tried that way and didn't like the side effects. I'm new to this web site and I look forward to talking with everyone and learning new ways to cope. |
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#3 | ||
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I can relate with the pain and sensitivity. I too have rsd all over my body and am stage 4 with extreme nerve damage too. I have lost most use of my left hand/arm-no ulna nerve response and getting worse. I have had pain for over 10 yrs and out of work for 5. I look forward to talking to you and hope you have low pain days
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