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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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02-04-2008, 06:55 PM
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Hi Amber,
WOW, I think I would have been a bit upset myself. So, VENT AWAY GIRL, VENT AWAY!! Has your doctor ever sent you to a "Pain Management" doctor? Has he discussed the possibility of having the Spinal Cord Stimulator or SCS? I also have Full Body RSD, along with Fibromyalgia, MS, and Full Body Osteoporosis with high risk for fractures, and am going through the process now of setting up for the trial run with the SCS, and was told if that doesn't work, than all I could do would be the pain pump. So I was wondering if you tried it and didn't like it, or if that option was ever offered. I am not sure about the Ketamine, but like you I have heard numerous others who are one it. I don't think all of them could be on clinical trials, but maybe so?? Well I hope you found enough chocolate and another pepsi, or had someone bring you some, and are feeeeeeeeeeeling a little bit better now. Love, Peace & Blessings, Marla Last edited by Chemar; 02-04-2008 at 07:13 PM. Reason: font size edited :) |
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