Thanks for the cheer! I will keep posting my progress.
Lisa, I'm sure you will get your call soon:) I would love to exchange info and hopefully we can meet!
He only asked a few basic questions, and then answered a few of mine. We discused my symptoms. We talked about the progress he has made with the procedure. I explained my feelings about CCSVI. We briefly discussed my neuro (who has a packet of info on CCSVI, but had his nurse call to tell me he couldn't support it). I felt Dr. Dake's frustration, (not sure if that is the right way to describe it?) with the neurologic community. He mentioned being told not to get "our" hopes up.
Wow............ to me that says volumes about neuros, drug companies, and MS.
I explained that if there is a part of my anatomy which is compromised or not working right, I want it fixed.
Mark, I am sure I'll have plenty of questions before I go, lol! I am excited to join the club!!!
Have a wonderful day everyone
I know I will
PS: I have been skipping my copaxone shots a lot, and now I think I'm done.