To everyone in this forum, a Merry Christmas. To patients and doctors. To those who think CCSVI could be a promoter of MS and to those who think CCSVI is not real. To those delving into alternative possibilities of jaw or spinal misalignment and realignment. To Cheer, HappyPoet, EJC, DrSclafani, blossom, uprightdoc, DrCumming, Endovasc, phlebologist, mrhodes, David1949, eric593, MarkW, codefellow, pelopidas, Donnchadh, tiredloulou, and the list goes on. Merry Christmas. To the researchers and the researched. To those who cannot afford treatment. To those whose veins have been harmed by treatment. To those who have had successful treatment, and wish it were so for everyone.
Back in 2009, I first heard about CCSVI when resting up after Thanksgiving festivities. Then, after Christmas festivities, again I needed to rest for a few days, but it gave me time to come back here, and to read and read and read, and to understand. To anyone who is first learning of CCSVI now, over this Christmastime, may it be a worthwhile journey.
Last edited by Cece
on Sat Dec 31, 2011 12:24 pm, edited 1 time in total.