Hi everyone. I am taking a proactive approach to my MS treatment. I have sent my history and MRI's to Dr Michael Dake at Stanford University Hospital. He is currently testing and treating CCSVI (chronic cerebrospinal venous insufficiency). He called me Monday night and we went over everything about the testing and procedure. I am now awaiting a call from Alexandra his scheduler for my testing date and to see what or if insurance will pay. I know it's not a cure, but it is a step in the right direction. More to come later.