Cheer, the link worked fine for me and it was great to hear your voice on the program.. I'd read your letter on ccsvi in multiple sclerosis so that was not news to me, although I admired the calm and erudite manner in which you replied to the rubbish written by Corcoran.
Thanks for the link, it is now on the ms-ccsvi-uk fan page on facebook.
Michele, warrior4MS, mother and champion for Ella, the MSer. The solution is out there we just have to ask the right questions.