Read the stories

my lost youth

Posted on Oct 12, 2012 by Farid Abi Daoud from Nova Scotia

So I only figured out I had MS about 2 months ago, though I`ve been feeling symptoms for three years. I was always an elite athlete, I played rep soccer on team nova scotia and I ran track in provincials. Going into high school I… Read more.

Update to story posted on Apr 14, 2011--Angioplasty for All

Posted on Aug 11, 2012 by Lori Batchelor from British Columbia

While out on a "cruise" on my scooter with my husband, we ran into--no I didn't hurt him (standard joke reply)--a fellow who remembered me from before treatment because I used to have a big sign attached calling for Canada to allow treatment for CCSVI.… Read more.

No Financila Help for those who need CCSVI follow ups

Posted on Aug 6, 2012 by Linda brown from Ontario

On May 18,2011 my husband Rodney had the Liberation treatment in California. His two brothers paid all our expenses and for the procedure. I won"t go into detail except to say that the results were remarkable and he has a new lease on life. Recently… Read more.

Angioplasty Decision

Posted on May 29, 2012 by Anna Macy from British Columbia

Angioplasty Decision
An article in Daily Kos (July 2010) completely changed my life by introducing Professor Zamboni’s idea that Multiple Sclerosis is a blood circulation disorder. Using self help and alternative therapies to control and even heal the disease based on his insight, I… Read more.

CCSVI / LILELY LINKED TO MY MS

Posted on Feb 15, 2012 by Ward

I was diagnosed with PPMS IN 2008.
44 Years of age.

CCSVI proceedure done Feb 2011.


I had CCSVI tests done in Vancouver which showed that I did indeed have major restrictions in my Jugular and… Read more.

ccsvi

Posted on Feb 8, 2012 by sherzad

my wife had a procedure done on Jun 30 20011 in california,New port beach. Before she was walking with a walker, after the procedure about 30 minute later they told us to go. after 2 hour she had to go to the emergency room, she… Read more.