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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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Junior Member
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Hello Dears,
I just spent an hour typing this question, then lost it, so this is going to be short. My keyboard is deficient: the punctuation keys want to be French, so this ![]() I got my SCS in 07 and it is my favourite thing. I would never give it up. Because I am (now, since RSD) so thin they opted to put the battery in my right hip-upper buttock area and gradually since then my 2003 compressed disk (lower spine, hipbone level) injury has been flaring up more and more. I also had a rotated pelvis at the same time. I chose a job requiring physical activity because I am an idiot and now I have been home for nearly three unpaid weeks. It started with penumonia, then at precisely the same moment a rabid UTI developed and my back went out to the point that I am using 1-2 canes to walk. I have not had to use a cane in years. I had donated mine to the Salvation Army. I have osteopenia at the disk site, and scoliosis and am wondering if, with the battery, if it is just too much and if it would be better if the battery were moved around front ![]() ![]() For those who have a front placed battery, is it comfortable ![]() ![]() Any fellow experiences appreciated. Thank you kindly ![]()
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One cannot learn unless those who know tell.
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