I don't see why you need to start bugging anybody. Why as a patient would you want to run around promoting this when the data eventually will speak for itself along with peer reviews and other articles. After all you may think it is all clear cut, but many things may appear that way and more data is still needed.
BZW I have submitted my data to Stanford and am waiting for a date with them and will have the surgery, but I sure would have wanted to wait for better data if I was just diagnosed. Now having had MS for many years and having researched this and other treatments for years I am fine with my choice, but I would not recommend this for newly diagnosed.