I had tears of joy for you reading this, followed by tears of utter anguish. My husband was diagnosed with CRPS in December of 2013 after a botched surgery to repair a ligament following a workplace injury. To say that his treatment has been slow and ineffective would be the understatement of the century. In November of 2014 he had a QME with an impartial doctor who said he had many ideas for his treatment- none of which he could carry out. He mentioned a "cranial massage" which at the time sounded totally absurd to me. I hadn't given it a second thought until reading your post. He even included that in his report to the IC and nothing was done. Reading that nearly a year ago we may have been given a solution to lessen his pain and possibly even improve or cause a complete relapse of his situation is utterly devastating. And yet, I have so, so much hope after reading your post. THANK YOU and congratulations on your success!