[Kstrong3]

Originally Posted by RSD_Angel

I have a GREAT doc that i see if you are willing to come up to NY!!! He even had RSD himself so he knows exaclty what we are talking about!!

Let me know if you want his name and everythng!


Amber

Amber , Please send the name of the MD you are seeing.

Also, does anyone have any experience with any MD's in NYC?

My sister has RSD for 14 years and until 1 month ago was being managed pretty well w/ dilaudid in her implanted pain pump and working out every day. She has started having severe pain in her foot and it is traveling up to her pelvis and rectum.

[Jomar]

bumping up for new member

[alaska49]

Originally Posted by Kstrong3

Also, does anyone have any experience with any MD's in NYC?

My sister has RSD for 14 years and until 1 month ago was being managed pretty well w/ dilaudid in her implanted pain pump and working out every day. She has started having severe pain in her foot and it is traveling up to her pelvis and rectum.

I have experience with a doctor in NYC his name is DR Richman and he is at the Hospital for Special Surgery. He is in thier pain department. I just got done with a procedure with him in which he also did the 5 day in-patient ketamine and he was wonderful.

Niki

[loretta]

Hi kstrong3 and welcome,
If you look up RSDSA on the web and punch in the zip code for part of New York, it will give you name and phone number of a RSD support group leader. Then you could ask for references in New York. RSDSA is a national organization for our disorder and is great for helping people like yourself. I'm sure you could get some phone numbers from the New York RSDers. Wish you well. Take care, loretta