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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board

Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index

My husband hasn't even seen Dr. Schwartzman yet. When he was first diagnosed in May 06, we called to make an appt. with Dr. S. and they said it was a 2 year wait. Well, not knowing a lot at that time about RSD we didn't make the appt. I guess we thought he would get better. This June, after his SCS stopped controlling his pain he called again and was given an appt. for Oct. 2008. I don't understand how they can make an RSD patient wait that long. Ketamine is what we want to look into. His PM is in Abington, Rosenthal, et al. Nice people, but I think they have reached the end of the road. They are the ones who suggested this T2 thing. I too have looked for doctors who have knowledge of RSD. No luck. I live 30 miles west of Philly. There was Dr. Harbut I think his name is in Hershey but by the time I found out about him he had already moved out of Pa. I wonder if my husband's PM can/will do lidocaine infusion. What is that like? Inpatient? Side effects?

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