Guest guest Posted February 12, 2011 Report Share Posted February 12, 2011 I beg to differ from what this Dr. said.I've had RSD for 17+YEARS now and I've had SEVERAL conversations with different Dr.'s over the years as my doctors have changed for one reason or the other. The PAIN PUMP CAN work, but NOT everyone who gets it works out 100% of the time and it's sometimes needed to be removed. (I've looked into this and that's the info I was given-it's not an opinion). There's also a Stimulator that's also implanted, attached to the Spine and sends a very light electrical current to the Sympathetic Nerves as it comes down from the brain before it gets to the affected limbs and other area(s) to prevent such a HORRIBLE pain sensation. This is pretty much by memory, as I've looked into this a few years ago intensely and I may be slightly incorrect somewhere as my memory is faulty, but for the most part it's accurate. More info on these 2 methods of pain relief can be found on the RSD website- the National/International Foundation for all concerned: patients,Dr.'s,groups,caregiver(s),spouses,friends,family members,etc. the website: http://www.rsds.org/index2.html and you'll find complete information there. Quote Link to comment Share on other sites More sharing options...
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