We all know the lack of impact of his posters at ECTRIMS.
Hmm, not so sure there was a lack of impact. From what I heard, they got a lot of attention. People were interested. Not an easy thing to measure.
I certainly wish more were happening regarding testing, and that others will continue to step up and do interventions for CCSVI. But I think the neurologists especially need to see published data on results as well as clinical trials. And I am all for advocating, doing a ton of it myself, but just wanted to say that I think there is a lot bubbling going on, impact in a way, while the wait for some key information continues.