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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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Junior Member
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Hi everyone,
I was told by 2 doctors that i have RSD. Last December i had a slip and fall accident on the ice and i broke the tib/fib in 3 places. They had to put 2 bolts, 11 pins and a plate in to hold my ankle and leg together. Since then i've been in terrible pain, Swelling and discoloration to my foot and lower leg and very senesitive to touch along with being cold all the time. I've been too so many doctors and they all tell me they can't help me and i don't know where to turn i was told that this spreads very fast and i can tell a difference in it everyday. i hardly have any range of motion in my foot because i've tried for almost a year to get a doctor to treat me and no luck. I live in upper michigan (harrison, Mi) and at this point i cant take it my family doctor has no idea what to do but make me wait for different doctors that all tell me the same thing (i cant help you).. Does anyone know of any doctors that caan help that are in michigan or anywhere for that matter.... Thank You Betty |
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#2 | ||
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Junior Member
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Hi everyone,
I was told by 2 doctors that i have RSD. Last December i had a slip and fall accident on the ice and i broke the tib/fib in 3 places. They had to put 2 bolts, 11 pins and a plate in to hold my ankle and leg together. Since then i've been in terrible pain, Swelling and discoloration to my foot and lower leg and very senesitive to touch along with being cold all the time. I've been too so many doctors and they all tell me they can't help me and i don't know where to turn i was told that this spreads very fast and i can tell a difference in it everyday. i hardly have any range of motion in my foot because i've tried for almost a year to get a doctor to treat me and no luck. I live in upper michigan (harrison, Mi) and at this point i cant take it my family doctor has no idea what to do but make me wait for different doctors that all tell me the same thing (i cant help you).. Does anyone know of any doctors that caan help that are in michigan or anywhere for that matter.... Thank You Betty |
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#3 | |||
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Wisest Elder Ever
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There are some studies coming out of Britain and France about using high dose Vit C for ankle/wrist surgery/trauma patients.
They found when given for 50 days or so at onset of the surgery there was significant reduction in RSD formation. Now, you are post surgical for some time, so I don't know if it would help you. 1000mg Vit daily... Ester C is easiest to tolerate. We've had a Vitamin C thread here recently too: http://neurotalk.psychcentral.com/sh...hlight=vitamin If I were you, I'd look into this, since it is not a huge invasive thing, or a serious drug treatment. Consult with your doctor if you can take this amount of Vit C based on your medical records and history and treatments already. This is one example to be found on PubMed: http://www.ncbi.nlm.nih.gov/pubmed/19840748 There are several other papers going back to 2000 on this topic as well.
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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