Hi

Thanks for sharing that info with us.

I checked out the link - it appears that Jannie has been successful on a state level only, so that the new pain law is effective in Michigan.

I am a member of RSDSA (in Milford, CT, the director is Jim Broatch) but not the National Pain Foundation. I will have to check it out!

Diana, I am so sorry that you are having a tough time right now, I hope the dives help you. Did you say you have tried Lidocaine and/or Ketamine yet? I know you have had RSD for over 20 years. I am getting my first Lidocaine infusion in a few weeks, the blocks were becoming less with each successive one. They only do it for an an hour at a time, the subcutaneous actually sounds better....but I have to go with what it offered by my PM for now. Have you ever made an appt with Dr. S at Drexel in Philly?

Take care, Sandy