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CRPS - anyone suffering with complex regional pain syndrome
Chronic Pain | Last Active: Apr 27 4:59am | Replies (349)Comment receiving replies
I have CRPS. I’m sorry to hear you do, too. I went to an anesthesiologist who specializes in pain management. I could not get any type of medication to work on my body. My CRPS is in my legs. In March I had a permanent spinal cord stimulator implanted in my spine. I am using the Boston Scientific one. It has taken some time to adjust to it however, I do not regret putting this in at all! I strongly recommend it.
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Just a follow up to my implant. It’s a miracle! I am moving so much better and the pain is drastically reduced! I’ve started water aerobics from the waist down. Going three days a week. After the scar tissue fuses around the wires in the spine I’ll be able to do more with my upper torso. Almost daily I’m feeding better! Waking. Cleaning the house! My normal routine plus exercises now. Once the swelling went down around the battery there was a huge improvement!