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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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#11 | |||
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Senior Member
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A pro pos of Vrae's post, when I saw Dr. Fugedy in June, he said he has successfully treated someone with TMJ by using the inhibitory cathodal signal from tDCS on the trigeminal nerve. Sounds like it could be worth a shot here.
Mike
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I have learned that to be with those I like is enough. - Walt Whitman |
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"Thanks for this!" says: | Vrae (09-30-2012) |
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#12 | ||
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Member
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Thanks im glad your flair has settled down! I dont have lido patches because they never worked for me. I did have extra steriods and took them today to see if it helps take down some of the inflamation and i will try and keep my talking limited.
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#13 | ||
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Member
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The RSD defenly attacked my vocal chords. I was in a TERRIBLE flair for almost a full week. Im out of the flair now, but my voice has not returned to normal and its been 2 weeks now. I assume its now a pemanent thing. Ive been in alot of stress as my little brother is extremely sick right now in the hospital, so im sure thats not helping at all. But i can say this is absoutly crap!
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#14 | ||
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Magnate
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Please don't give up yet. If you can avoid talking for a week or two, it might make the difference. If you respond to blocks and/or K, that might help as well. (I did do a course of steroids along the way, and if I had had my normal meds, they should have helped.) |
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#15 | ||
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New Member
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When I first had my injury before given the DX: RSD ~ I told every Dr since day one my tongue feels like i have pizza burn on it, nonstop. It's been for over 4 months now, i felt like i was crazy but reading this and knowing it can effect your mouth makes me feel better ( sane ) lol
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