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Letters to the editor where published in the May 27th issue of Maclean's but only the printed magazine and not the on-line one. Here they are. They have been edited down from their original form. https://www.facebook.com/notes/ccsvi-ontario/letters-to-the-editor-published-in-the-may-27th-issue-of-ma...

In light of the FDA 'raids', 'surprise visits' or whatever else we'd like to call it. Posted on CCSVI Ontario:

CANADA. . . please write to your MPs before Wednesday, November 30, 2011 to support Kirsty Duncan's Bill C-280 . . . a national strategy for CCSVI.

"Will Your Eyes Change from Black to Blue?" by C.C.S.V.I. Ontario on Wednesday, August 31, 2011 at 10:19am Will your Eyes Change from Black to Blue? I am one of the lucky ones. I had the money, and the strength to fight my way overseas, when you, my Government, my health care system failed me. My im...

Yes, the AGM is today and I'm anxiously waiting to hear from those I know who attended. I went to the hotel where the panel discussion on CCSVI was being held yesterday. As you know, Dr. Sclafani couldn't get out of NY due to weather. After the meeting, I and a few others had the pleasure of meeting...

Hi Everyone,

I just wanted to do an update on C.C.S.V.I. Ontario.

We have changed over from a facebook "Group" to a facebook "Page". If you'd like to join and help advocate, please join us at:

http://www.facebook.com/pages/CCSVI-Ont ... 3851427194

Thank you!
a

For those on facebook, we've started a new group called CCSVI Ontario focusing on politicians, doctors and science.
Please have a look and join, if you like!
http://www.facebook.com/?ref=home#!/hom ... 5662683837

That's dear ole' Colin Rose. (note sarcasm)

He is anti-ccsvi. He loves to poke his head into CCSVI groups until the moderators ban him. He seems to love the attacks and rebutals. I believe his facebook wall is open for that reason only.

He loves to stir the pot.

Hi all,
If you are in and around the Toronto area, another rally is being planned for Global CCSVI Day.

It's at Queen's Park on May 5th between 12:00 - 2:00 pm.

Come and join us if you can! Come and be loud and proud!

Let me pick on just one of the 'expert' panels. . . Dr. Rubin sat on the original 'expert' panel that advised the Health Minister to not proceed with pan-canadian trials because there wasn't enough evidence. Now, he will sit on yet another panel to create an after-care protocol for a condition and t...

leetz, yes, that letter was sent by one of the MSSC 'top' neuros to a patient who inquired about CCSVI. He is on their advisory counsel and has received millions in research money and is tied up with big pharma. . . . big surprise. He has already made up his mind that this is a hoax yet they gave hi...

Dr. Sclafani,
Could you explain R versus L entry for CCSVI treatment? I understand L is preferred for catching MT Syndrome but are there other reasons and is it more dangerous than going in through the R side?
thank you in advance!
a

If you're Canadian and are having trouble getting a referral to get tested, I know a doctor who is willing to write referrals those those who CANNOT obtain one from their doctor(s).
PM me and I'll send you his info.
tx
a

I was treated in Albany as well. I think as doctors gain experience and also learning from us, they adjust what the 'criteria' is that gets treated. Both my jugulars were mildly stenosed at about 40% and I was still treated. My azygos was also ballooned. He doesn't wait for the 50% stenosis mark or ...

Just saw this updated reminder on facebook. THREE days left and he now has 150 reports. . . . More please! Mark Lane is reminding everyone that we ONLY HAVE 2 DAYS LEFT for all those Canadians who have had angio/venoplasty as treatment for CCSVI or MS to send a 1-2 page testimony of your experiences...