I have to strongly agree with the other replys here. My heart goes out to you. I do know the feeling of not being able to think clearly and I only have CRPS/RSD in one hand and arm! But all the meds.............
Again to agree with everyone else I think you should find another opinion.
It was the best thing I ever did because luckily I found a Dr. very familiar with CRPS (she had it herself).
The best advice I was given by a physical therapist is "You must be your own best advocate" with this.
I'm not normally very assertive but now I tell myself to do for myself what I wish someone would do for me.
Call Pain Management Clinics and ask if any Dr.s are familiar with CRPS/RSD and if you find one do whatever you can to get in there.
PLEASE fight for yourself!
Wishing you all the best