Worldwide Information and News Regarding Reflex Sympathetic Dystrophy Syndrome / Complex Regional Pain Syndrome.

Please share with your friends, family and anyone who is affilicted with this condition.

Check back often as we post new information as it becomes available.

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One response to “About

  1. I have RSD/CRPS developed after surgery on my { R } foot, spread through out my whole body over time. It shall be 17 yrs. in June 2015, when I first developed this condition. I spent the 1st yr. in a wheel chair, then was able to walk with aid of a Cane, eventually walked on my own. Now I’m not mobile albeit doing my best to stay as mobile as possible. I have had kidney issue’s, Vertigo, Shingles, Breathing, Thyroid, and I also tried the SCS implant which did not work for me. Plus a number of other problems which stem all from this condition. If anyone has a question feel free to ask. I’m considering the implant of the Morphine pump, the Dr’s have suggested for quite some time I have it. I now have came to the cross road where something more needs to be done. If anyone reads this and has knowledge concerning the Pump please contact me–leave a reply how long you have had on implanted and what your experience has been. Thank You, gentle hugs, Brenda

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