People going to this site gain a lot knowledge on what is going on in the world of MS. But what we do not get is a lot a feedback good or bad and in between regarding their CCSVI, Stem cell or drug treatments. We seem to lack a continued experience both short or long term. I think people should post their experiences good and bad. There is a lot treatments out there and people should know what to expect. We have not heard any more from people who had the treatments in the last year. Did they still work? or not etc.