As a simple MS'er watching numerous debates on CPAC, I thought it would be an idea to have a thread on CCSVI Toronto run for the week to help those involved with the debate have access and knowledge at the ready from the ones that have kept this in the public eye since November 21 2009. The day CCSVI was introduced to us all who have MS around the world.

Many times during debates they run out of points and facts to make in their arguments of tabled Bills. Such was the case with Bill C-20 this morning.

Let this be our way of helping Kirsty and other Members of Parliament have the facts and questions at the ready just by taking a look at Facebook and the people that know more about CCSVI than the Professionals that we are supposed to be under their care and have nothing to offer us but useless medications that cost Thousands of Dollars to the Taxpayer and taken us from our places of employment and hurt our family relationships.

We know CCSVI Toronto and so many wonderful groups using social media tools, have been at the forefront in the sharing of information on this CCSVI journey. Let's help our friend Kirsty Duncan and other Members of Parliament have access to the facts and make our voices heard whilst Bill C280 is debated in the house of Commons on Thursday December 8, 2011 @18:30 EST.

May the Members of Parliament have a good debate on Bill C-280 (An Act to establish a National Strategy for Chronic Cerebrospinal Venous Insufficiency) as it will only keep information flowing over the Holiday break. Who knows maybe 1 of your points might be brought up by a member of Parliament in attendance Thursday.

Jamie

BILL C-280:

An Act to establish a National Strategy for Cerebrospinal Venous Insufficiency

http://tinyurl.com/7hrdgs4