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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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02-05-2013, 12:55 PM | #1 | ||
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I've an app' tomorrow and everything has been tried you name it all the opiates/nerve pain killers/anti-convulsants/nerve blocks etc
Now I'm worried what my GP will think when I suggest this, I've scowered the whole web ever since having this and Ketamine is the only thing that has a consistent high pain relief rate feedback I can only just use my hands so something needs to happen now as it's getting much worse Last edited by bfff2020; 02-05-2013 at 02:15 PM. |
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02-05-2013, 05:53 PM | #2 | ||
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Do you have any other professionals involved in your care? Pain Management doc, etc.?
A GP may not be very knowledgeable about that treatment. I have a GP on my team, but he is not my primary doctor for treating my CRPS. |
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02-05-2013, 07:32 PM | #3 | ||
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I'm in pain management but there's a four month wait until I see them next, saw them once and they didn't even discuss pain relief - useless, they went through a bunch of stuff and said there's nothing more they could do and I wouldn't accept that notion so they offered me acupuncture we'll see
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