Hi Erica and Welcome to Neurotalk
I don't know, but if you go to RSDSA (our national organization) and there is a space for your zipcode. Put that in and if there is a support group close to you, it will give you a name and phone number of the closest one to you. Hope there is!!
You are always welcome to PM (Private message) me and ask anything. I've had RSD 15 years and full body.
RSDSA has a lot of good information and so does rsdrx.com Dr. Hooshmand is retired but has his website up. Under puzzles List there are 146 questions and his answers.= very infrormative.
Hope the best- your friend, loretta tell us about yourself and concerns, and this is a wonderful group of supportive,caring friends. soft hugs