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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board

Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index

I have extensive experience with Ketamine - when I first thought i had RSD, my GP had a compounding pharmatist work up a cream with Ketamine, Amitriptoline and one other ingredient. It took away my burning pain totally and enabled me to wear my brace, but unfortunately I used it too often and developed an alergic reaction after three months which was very itchy and made the burning pain worse. We tried my staying off it for two month, the rash came back as soon as I used it again we tried different carriers, no dice; we tried reducing the amount; taking out the other stuff; nothing worked. So, yes it works, yes probably goes into your blood stream, but if you get someone to compound it for you do not use it more than twice a day and maybe you will not develop an allergy. I was using it three or four times a day, thinking that if I kept the pain away, my body might get used to that and stop sending the messages etc. etc. I would give it a try at lower percentage. In fact, now that I have been off it for three years, I might give it another go at a very low dosage. I think mine was 10% - I would get that in half. Laura

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