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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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I went to the ER for basically the same thing. I specifically asked for a doc at the ER that knew something about RSD. I had to wait quite a while for him, but it was worth it. He told me that it was the Vegus nerves that the RSD was effecting. Meds given Gabapentin, Valium, Percocet, and if it the pain gets out of hand then IV Dilaudid. The trick as I know you know, is to stay ahead of the pain, otherwise it takes more big gun drugs to turn it back around. As far as a permanent solution… I do not know of one. But I do understand. It effects my teeth, gums, jaw, eyes, neck… absolutely no fun. So sorry hon. Hope you get relief soon!
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Your info is greatly appreciated! It's by far the worst area I've ever had to deal with spread. |
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"Thanks for this!" says: | Vrae (09-20-2012) |
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Elder
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I haven't been to the er since being diagnosed with rsd.
I don't want them to think I am seeking drugs as I am already on all kinds of medications....I figure there's not much more they can do for me. I usually just suffer though whatever is going on, take my meds, go to bed, and wait to see what tomorrow brings. Sigh.... Abbie
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My avatar pic is my beautiful niece Ashley! . Rest in Peace 3/8/90 ~~ 4/2/12
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"Thanks for this!" says: | pooh_ac (09-23-2012) |
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Junior Member
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Be cautious of the sympauthetic nerv block. weigh your options carefully.i understand your options are limited but I say this because I had a sympathetic nerve block and I regret it wendy day.not to say you will because as we all know everyone responds differently I would just be cautious.i wish you the best.
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