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-   Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)
-   -   Ketamine (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/11753-ketamine.html)

optimumeg 01-22-2007 07:25 PM

Ketamine
 
I was wondering how many people here have taken ketamine, how well it works for you, and how hard it was to get it from a doctor? Also, what type of doctor did you have to go through to get it?

I am very interesting in getting Ketamine so my allydonia and hyperalgesia go away.

CZZ74 01-22-2007 09:06 PM

Hi I have had the ketamine
 
Hi , I have had the ketamine - two 5day hospital infusion in ICU and 23 - 2 Day Booster Infusions. Yes , they have helped me. but Not as a cure. They did remove 13lbs of fluid from my legs and lowered my daily pain level from an 7-8 to a 6, still with of course flares. But the boosters improve my quality of life significantly for about 4 weeks after. Unfortunately, I have a very bad case of full body rsd. I need to go every two months and you just cant go that often. NOw I am waiting my first 4 monnth spread and the pain is back to and 8 even with many many pain meds. So yes ketamine works for me. I dont have my life back but it improves the quality. I have had alot of ketamine. The edema is now building in my right leg, orginal injury site. I dont know if I will make the 4 month interval. But I am trying. Hope this information helps. CZ ( in the meantime I am starting HBot next week) I have great hopes for this as long term use of the ketamine is a scary. Oh very important- it helped immensly with my alloydinya. I am in my fourth year.

artist 01-25-2007 03:02 AM

bumping up....


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