Hi
With regard to your CCSVI experience, which country are you in ? Here in the UK, they have only agreed to trials for CCSVI in MS sufferers, maybe because the guy who discovered it was only looking at MS people (the rest of us get NO options!!) that smacks of inequality to me. I don’t think they have grasped that CCSVI is an entity unto itself and not exclusive to MS sufferers,
Regards
Barbara
(UK)