Is the MS Society now promoting CCSVI treatment for MSers?

It's hard to believe, but these "liberation testimonials" are on the web site of the MS Society of Canada: http://ccsvi.ca/story/16/it-is-so-unbelieveable-i-m-in-awe.html.  Have they truly done an about face on this issue?  An argument is raging in Facebook, where some of those who have been fighting against the MSSC to get CCSVI studied are understandably cynical and suspicious.  But could this be the actual turning point?