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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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#11 | ||
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Guest
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Put it off as long as you can got appointment to see Professer om 19th Dec to see if he's willing to experiment on me
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#12 | |||
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Junior Member
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Hi,
I am new to the forum so can't post any links yet. I have read about a course of high dose vitamin C prior to surgery being helpful to prevent spread of crps. The other comments regarding anesthesiologist's involvement is something I have read about before too. I hope you do not need need need the surgery as there is always the risk. This is one reason I have refused the Spinal Cord Stimulator - I do know of many who have benefited from SCS for many years, but for me, I said "no thanks". Best of luck to you, and please keep us posted on how things go. Please google "Vitamin C prior to surgery to prevent spread of crps" and you will find some information about it. Aloha, Jenny |
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#13 | ||
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Member
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Thanks for the replies. Jenny, I have also read about the vitamin C and have been taking it everyday. I read it should be taken for a year before the surgery. I am trying to go completely holistic and have been talking to my health food persons. I also was recommended the spinal cord stimulator, but also refulsed it. I have too much trouble with other infections and side effects. I walk with a cane and do ok, but the cold weather causes me to tighten up a bit. I usually walk with crutches when walking alot. I know this is something I need to bear and will take it one day at a time. I am grateful for the people on this site and for all the encouragement. Hugs and Prayers
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#14 | ||
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Member
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