Thanks Renee,

I would really care to know how your experience is if you follow through! Please do keep us posted. I am finding that those of us with RSD/CRPS that has gone on for "years" do have many autoimmune issues. I did also post that I have tested positive for some genetic mutations that tie into neuro and vascular disease... and I'm following up with extensive autoimmune testing. No one has a road map yet for what to do, but we are providing a great start. Bravo Renee and all of you who push through the barriers to understanding and treatment. May we all keep each other informed. So far, my biggest marker is MTHFR in relation... it is common in the population and strongly affects the ANS. While perhaps not curable,it can be treatable!

Best for all,

Hana