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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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Senior Member
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Hi Abrown,
Pain control has made a big difference for me while I have waited and waited for WC to approve 10 day outpatient ketamine infusions and for a spot in a physician's office for the treatments. Have you tried something like Fentanyl patches, which deliver opiod meds to your system all the time? I recently titrated off of them, just to prove to myself that I could, and to see what kind of pain my body was still in. It was really ugly. So I am back on them. They work extremely well I discovered. I also take a muscle relaxer and Ambien CR to sleep at night. Those meds usually work also, and when they don't, I keep oral Oxycodones nearby to help. Other meds I am on include Cymbalta, Topamax and high blood pressure meds because of the pain. I've been sick now for 3 and a half years. It's taken a long time for me to work out the meds and to figure out the best system for dealing with the pain. My personal care physician is awesome because he has helped me with most of what I have needed. Many times I find that physical activity is a good diversion, too. My headaches don't hurt as bad if I go out and take a walk. And vitamins have helped with my energy levels - make sure you are getting enough Vit C and Calcium and Iron, etc. I take a lot of supplements, many I found out about on this board. Try to get to the very best doctor that you can in your area to help you with your RSD. Get rid of the SCS when you can (if that's what you want). Help yourself the best you can. I hope my message has helped you a little. Please keep us informed on how you are doing. XOXOXO Sandy Quote:
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