Mark Lane is requesting that all those Canadians who have had angio/venoplasty as treatment for CCSVI or MS to send a 1 page testimony of your experiences pre and post op to mark@marklane.ca. Please include your name and contact information. This anecdotal evidence will be presented first hand to the provinicial Health Ministers on the 12 Sept in NL.
23 minutes ago · Comment · Like · View Feedback (3)Hide Feedback (3) · Flag
Joan Beal and Sally Winship like this..
CCSVI in Multiple: Sclerosis great idea and initiative, Mark--
11 minutes ago ·
URGENT!! Request 'Mark Lane' CCSVI Facebook!! LAST CHANCE!!
URGENT!! Request 'Mark Lane' CCSVI Facebook!! LAST CHANCE!!
A very positive and potentially motivating idea..
Last edited by PCakes on Fri Sep 10, 2010 1:46 pm, edited 5 times in total.
- garyak
- Family Elder
- Posts: 314
- Joined: Sun May 30, 2010 2:00 pm
- Location: grande prairie , alberta,canada
- Contact:
Consider using "urgent" in the title? This is an important post. Dr. Kirsty Duncan is also calling for Canadians who have had the procedure to collaborate and document , as a group, our post procedure results;
http://www.insidetoronto.com/community/ ... als-for-ms
http://www.insidetoronto.com/community/ ... als-for-ms
fantastic idea
Wow, I like this idea. I might steal it for us Americans too. Thinking....
- 1eye
- Family Elder
- Posts: 3780
- Joined: Wed Mar 17, 2010 3:00 pm
- Location: Kanata, Ontario, Canada
- Contact:
The Canadians will do their usual Catbert-ian thing, and fiddle with their 'MS' observations for many years after the rest of the world has settled the issues very convincingly. Life for the former 'MS' patient will be made as miserable as possible. Getting Liberated will continue, at least in Canada, to be as difficult as ten years' worth on back-tax returns, followed by acquiring Canadian citizenship, refugee status, aboriginal status, and a license to practice medicine if you got your degree in Elbonia.
It's the way we do things, because
We...
are...
Canadians.
It's the way we do things, because
We...
are...
Canadians.
This unit of entertainment not brought to you by FREMULON.
Not a doctor.
"I'm still here, how 'bout that? I may have lost my lunchbox, but I'm still here." John Cowan Hartford (December 30, 1937 – June 4, 2001)
Not a doctor.
"I'm still here, how 'bout that? I may have lost my lunchbox, but I'm still here." John Cowan Hartford (December 30, 1937 – June 4, 2001)
- cheerleader
- Family Elder
- Posts: 5361
- Joined: Mon Sep 10, 2007 2:00 pm
- Location: southern California
Mark has 150 testimonies to present to the health ministry on Sept. 13. C'mon Canada...send this man your stories. He's the real deal
link to Mark's story
cheer
link to Mark's story
cheer
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
Guys, I think surgical canada is a good source to reach people who had the procedure. I am sure not all of them are internet savvy. So, try contacting them to reach out to people ...
A new scientific truth does not triumph by convincing its opponents and making them see the light, but rather because its opponents eventually die and a new generation grows up that is familiar with it
- Max Planck
- Max Planck
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