Like most MSer’s who saw the W5 report on CCSVI in November 2009, I was excited by the possibility of a treatment that might alleviate some of my symptoms.

I was just checking my old emails and that’s when I started sending out my first emails on this – a year and a half – and wow – what an intense 18 months this has been!!!

And now, earlier this week, on Monday April 11, 2011, I too became one of the 12,000+ MSer’s worldwide who have been treated for CCSVI.

This site is about where I was treated, my experience, pre-op and post-op care, comments on drugs, pictures of my angioplasty, and places to stay. Just follow the links on the left.

If you have any further questions you can email me at bradencorby [at] shaw.ca

In Joy
Braden