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 08-25-2012, 08:58 AM #1
latemodel1 latemodel1 is offline
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Looking for someone with crps that has had a ketamine infusion. I have crps after a surgery in my left hand and wrist. I have permanent nerve damage.Has ketamine helped folks that have had a surgery that the results are not positive. my doctor is looking at spinal cord stimulation but im scared after this mess that I have been left with. thanks in advance
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Old 08-27-2012, 05:17 AM #2
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Check out ketamine Klub on facebook. There are lots of people on there who have had ketamine and can answer alot of questions.

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Originally Posted by latemodel1 View Post
Looking for someone with crps that has had a ketamine infusion. I have crps after a surgery in my left hand and wrist. I have permanent nerve damage.Has ketamine helped folks that have had a surgery that the results are not positive. my doctor is looking at spinal cord stimulation but im scared after this mess that I have been left with. thanks in advance
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GOD help me be faithful in the midst of my suffering. Alt1268
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Old 09-01-2012, 11:23 PM #3
ElsieGrant ElsieGrant is offline
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If you are still looking to talk to someone who has had Ketamine infusions I have had at least 8 in the course of a year. They really were the only thing that came close to helping but in the end the results were too low and they didn't last long enough to justify the risk and they had to be stopped. Feel feel to email me *edit* and I will do my best to answer any questions you have about my experience with the Ketamine treatments. I am 22 and I have had RSD for 9 years. I am also on Facebook as of today and new to NeuroTalk, I saw your post and thought I might be of some help.

Last edited by Koala77; 09-02-2012 at 12:48 AM. Reason: Personal details removed. You may contact Elsie via PM
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Old 09-11-2012, 06:45 PM #4
betsykk betsykk is offline
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I agree that KK on FB has the best resources...dozens of patients who have had K, documents, doctors, insurance codes and more.
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