My Neurologist at Johns Hopkins is one of the researchers & is selecting patients to participate. My next appt is in November and I am planning to discuss it with him then.

I haven't researched it--would be very interested in learning what others think.

Is it approved in USA yet & are there many Dr's that do it?
I have only heard/read of a Dr that does it in Germany & his wait list is long & it is very expensive. He also has strict guidelines on when he will do it. Think it is about $60,000 Aus to do it + airfare, accom & take a carer etc.
Still no guarantee it will work & only do it on people in early stage ms.

I'm going to discuss it with my Dr,but I don't want to stop Tecfidera. It's working so welll