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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)

fmichael in Calif re:CRPS

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Unread 11-29-2012, 08:45 PM   #11
CRPSsongbird
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Originally Posted by sallysue View Post
Dear Michael - I finally sent you the PM. My life has just been upside down since the first injury (venipuncture Feb 27, 2012). And my pain has worsened significantly over time. Thank you. Sallysue

Sally,
I'm sop sorry to hear of your continued/worsened pain. i hope you can find relief. I my self am looking for a good Pain Management Doc....Not so much luck. The anti seizure drugs give me AWFUL side effects that make daily life intolerable. And I fear taking antidepressants as the ones I was on a few years ago made me suicidal (lexapro ssri's) . Also my current PN Doctor is kinda of limited in what he can do as he seems totally against narcotic pains meds, and is only suggesting a Sympathetic blockade (Phentolamine?). I am trapped in this cycle of pain and ignorance........grr But i hope you feel "better" and at LEAST we can have each other to talk to ....
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Unread 11-30-2012, 03:20 PM   #12
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Michael - You are obviously popular based on the number viewing this message strand! Wish you could help find a cure soon for all of us with this horrid condition. Just sent you a follow-up detailed PM Friday. thank you! SS
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Unread 12-01-2012, 08:58 AM   #13
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Originally Posted by sallysue View Post
Michael - You are obviously popular based on the number viewing this message strand! Wish you could help find a cure soon for all of us with this horrid condition. . .
Funny, but I addressed this the other day in a private musing, which with any luck, probably bears repeating. So, with your encouragement, my now expurgated and otherwise expanded thoughts on cures - at least on the subject of fresh or "acute" cases of CRPS and those "cures" which are out there right now but have yet to be widely adopted - appear at the start of a new thread, available "cures" for acute CRPS - requiring only $$$ for large studies.

And with that, my thanks, I appreciate the support.

Mike
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