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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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ketamine ;don't do it!!!!!

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Old 01-12-2013, 07:42 PM #1
daylilyfan daylilyfan is offline
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If I could afford it I might consider it. However, my doc at Clev Clinic said I've had RSD to long (12 years) that I am not a good candidate. Yet, I heard of another doc there that does the infusions no matter how long a person has had RSD.
Last edited by daylilyfan; 01-12-2013 at 11:23 PM.
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Old 01-15-2013, 12:32 AM #2
flo53 flo53 is offline
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many treatments out there are out of reach for many rsd people, but there are new developments on the horizon that will be affordable for many to alleviate their pain. I am an advocate for what is bio friendly to our bodies. Giving our bodies nutrition, rest, destressing, having a positive mind, movement and getting out. I have had rsd for 1 year now and I am feeling much better. you don't need drugs, you need to use what is non invasive.
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Old 01-15-2013, 06:33 PM #3
LIT LOVE LIT LOVE is offline
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Quote:
Originally Posted by flo53 View Post
many treatments out there are out of reach for many rsd people, but there are new developments on the horizon that will be affordable for many to alleviate their pain. I am an advocate for what is bio friendly to our bodies. Giving our bodies nutrition, rest, destressing, having a positive mind, movement and getting out. I have had rsd for 1 year now and I am feeling much better. you don't need drugs, you need to use what is non invasive.
All these things are a good idea, up until the last sentence. YOU didn't need drugs. Many docs hesitate to even make a firm RSD diagnosis within a short period of time--part of the problem with getting early aggressive treatment in the "window" for best chance at remission. The response to that problem has been diagnosing some patients too quickly.

Ketamine has changed the lives of many RSD patients.
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Old 01-15-2013, 06:57 PM #4
loretta loretta is offline
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Originally Posted by daylilyfan View Post
If I could afford it I might consider it. However, my doc at Clev Clinic said I've had RSD to long (12 years) that I am not a good candidate. Yet, I heard of another doc there that does the infusions no matter how long a person has had RSD.
Hi daylillyfan, who is your doc at the clev clinic? Is Stanton-Hicks still there? I'm considering seeing a doc that hicks mentered there. Thanks, loretta
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