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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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#1 | ||
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Magnate
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Angel rsd did you recieve any benefits from this and was it the 2-4 hour one and any side effects?
Galena thank you for the hopeful story I appreciate it |
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#2 | |||
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YW Daniella!
![]() Hugs, Karen
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Laugh until you cry, don't cry until you laugh. Living, loving and laughing with RSD for 14 years and counting. |
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#3 | ||
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Magnate
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I looked into HBOT and was going to do it and may but this doc thinks it won't do much. He did suggest acupuncture though not in the areas effected and I talked to the lady yesterday so we will see. I think I will start with this iv and the new meds and go from there. Thanks again
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#4 | |||
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daniella,
i had wonderful results with the lidocaine iv's.....for 5 years i was functional, in little pain, and had few sympathetic symptoms. tho my pain doc did have some patients who had the iv's once a month, i did better with a different approach....i would have 3 treatments spread out over 8 or 9 days, and then none for 3 months......the first one never gave me more than 10 or 12 hours of pain relief, the second would last for a day or 2 and third was good for about 8 or 9 weeks. as of 3 years ago, my insurance company will no longer pay for ANY sort of lidocaine treatment and i have had a serious increase in all symptoms since then....i wish with all my heart that i could have the treatments done again, but we can't get approval for it. if your insurance will cover it, then u might want to give it a try.....it doesn't work for everyone, but it seems to work very well for the people it does help. good luck with the treatments.
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best to all, liz |
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#5 | |||
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Liz,
I'm so sorry this happened to you. I don't get it. Why won't they want to keep paying for something that actually works for you? Is it because they know that you'd need it for a long period of time? Is it just the financial side they're worried about? That's terrible. What treatment are you on now?
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All the best, Marleen ===================== Work related (car) accident September 21, 1995, consequences: - chondromalacia patellae both knees - RSD both legs (late diagnosis, almost 3 years into RSD) & spread to arms/hands as of 2008 |
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#6 | ||
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Magnate
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I am so sorry Liz that your insurance stopped paying that is horrible. I have heard others with a similar problem. They find something that works and then the insurance makes them stop or switch. I am scheduled for Tues. I am fearful because my body with all the other problems besides RSD I have though the doctors know that I do they are not sure why. I will keep everyone updated. I hope you can fight the insurance company or find something that works for you again. Many thoughts and thanks
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#7 | |||
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Quote:
carrie
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hope this finds all in less pain . rsd DX 99 had since 98 full body and organ involement,fibro ,pelvic pain ,etc,,,,,, please check out our website to help bring awareness to RSD! . |
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"Thanks for this!" says: | daniella (04-27-2009) |
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#8 | ||
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I had one hour of the lido IV infusion. I had no pain for my entire body for only 15 minutes. It was heaven. Unfortunately, pain has gradually return after the infusion stopped. Does insurance cover this treatment? I wonder whether or not i should try for longer period.
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#9 | ||
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Danelia,
Did you have pudenda nerve issues? Numb |
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#10 | ||
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Magnate
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I hear it is very limited amount of time of relief. I think this doctor is usuing it as more of dx of what is causing my pain more. I have peripheral neuropathy and rsd. Not what you stated but who knows anymore. So many doctors and so many opinions.
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