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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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Thank you Daniella and Kathy,
I truly appreciate your honesty. Today for me has been a bad day and I am sorry if messages bring anyone down. I love my PM doctor. I have been to what I considered the best at Vanderbilt University and they did not help me like he has. He has at least provided some relief. Yesterday we tried something new, peripheral nerve blocks. I had 3 injections near and at the elbow, into the median, ulnar and radial. My hand and forearm were numb for the most part of the day (which was nice), then about 8 pm I noticed that I had not had any spasms in my hand. I was very excited that finally something was working. I was wrong. I woke up at midnight with pain like before I even started the meds. I don't know what triggered it to be this bad again. Was it because the doctor had to touch my arm? Anyway, I should have never gotten my hopes up, I should know better by now. I read this study done on RSD and peripheral nerve blocks and the results seemed so great on everyone. If only! |
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"Thanks for this!" says: | loretta (05-13-2010) |
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Junior Member
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"Thanks for this!" says: | loretta (05-13-2010) |
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Magnate
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There is quite a bit of information on this website.
Anyone newly diagnosed (which I'd categorize you as) with RSD should: 1. Be proactive about treatment, but do your research first. 2. Be optimistic that remission is a possibility, but accept that there is no set timetable for when that remission will occur. 3. Seek mental health resources for you and your husband. |
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"Thanks for this!" says: |
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