Thank you.
I guess what I'm struggling with this morning is that we've heard that it's a small number of people who have actually had diagnosis and treatment and it was referred to just Dr. Zamboni's work. The number is upward of a thousand people now. I think Dr. Maggisano was clear in saying that let's not just do an interesting academic exercise, that we do have to test.
Why did the MS Society's announcement of research spending a few days ago aim exclusively at finding a statistical association of CCSVI in MS patients and not at allocating a single cent to actual treatment of CCSVI when all studies done to date have found that association?