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