For anyone that has received the treatment-
Who has seen a physiotherapist?
Who has embarked upon a physio-therapy program, what are your improvements, if any?
PHYSIO-POST LIBERATION
Can't really contribute to that but wanted to mention that physios seem to be a good way to "spread the message". I have two friends who are physiotherapists, I told them bout CCSVI. They were very interested and told their MS patients about. Now one of them is on her way to liberation treatment (or maybe already done, they have a medical confidentiality, too). Seems that physios are good multipliers because they are in contact with PwMS but don't have the "pressure" about CCSVI as they can't do anything but tell about. They're not in the professional position to say "do this" or "don't do this" (just "google this" ;) ) or about deciding wether it's true.
"There is only one good, knowledge, and one evil, ignorance." Socrates