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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Old 02-17-2013, 08:54 AM #11
cinders999 cinders999 is offline
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cinders999 cinders999 is offline
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Quote:
Originally Posted by catra121 View Post
Based on your post I think you know the answer to your own question and it is the same as I would do: you need to find another doctor. A doctor who is not well informed about RSD, doesn't believe it exists, and isn't willing to listen to their patient about their needs and limitations is NOT a good doctor. Plain and simple and I wouldn't trust my care to them and I don't think that you should either. Find another doctor. Take care and good luck.
I agree with catra, sounds like they have got their medical degree but not what it takes to be a true doctor!
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Old 02-17-2013, 12:07 PM #12
dmt1961 dmt1961 is offline
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Hi Alaska. I would suggest seeking a new doctor but if she can help with the sarcoidosis then maybe having your RSD doctor consult this new doctor would change her point of view. Would he be willing to speak her and vice versa?
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