Dr. Sandy McDonald, Mark Haacke & libertated testify

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.

Dr. Sandy McDonald, Mark Haacke & libertated testify

Postby Brightspot » Fri May 28, 2010 11:14 pm

Next meeting of the Canadian Parliamentary Sub Committee on Neurological Health will be on June 1st.

Testifying will be Dr. Sandy McDonald, Mark Haacke, Steven Garvie (Liberated Canadian MS Patient), and someone called Lianne Webb.

Looing forward to reading the minutes!!

I understand that Dr. Kirsty Duncan (MP and opposition Health Critic) continues to push the government for the answers to some pretty urgent questions about when Canadians can expect to get screening and treatment for CCSVI in our own country under our own pulbicly funded medical system.
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Postby whyRwehere » Fri May 28, 2010 11:26 pm

Sounds good, look forward to hearing how it goes...
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Postby eric593 » Sat May 29, 2010 12:11 am

Is this around the 45 day limit mark where the government has to provide answers to Dr. Duncan's earlier questions?

I quote Dr. McDonald in all my letter-writing pleas to government, College, Society of Phlebology, etc. I look forward to more of his eloquence. I wish we could get more people in the vascular field involved in advocating on our behalf and explaining why it's needed to fix our veins because BLOCKED VEINS IS BAD REGARDLESS OF DETERMINING WHAT THEIR EFFECT ON OUR MS IS.
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Postby Fernie12 » Sat May 29, 2010 8:48 pm

HERE HERE! Let's show up in force, all you Ottawans!
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Postby dialed_in » Sun May 30, 2010 7:45 am

Lianne Webb is another patient of Dr. McDonald's

http://www.ctv.ca/servlet/ArticleNews/s ... ?s_name=W5
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Postby Chrystal » Sun May 30, 2010 9:41 am


Demonstration for immediate CCSVI testing & treatment

Date: Tuesday, June 1, 2010
Time: 11:00am - 3:00pm
Location: Subcommittee on Neurologial Diseases
Street: Room 752, 131 Queen St.
City/Town: Ottawa, ON


Please come to the meeting to support Dr.Sandy McDonald and Mark Haake who will be testifying in front of the government's Neurological Subcommittee . This is a CRUCIAL meeting for our fight to allow people with MS to have the right to vascular care, just like every other Canadian.

We need to be there in large numbers.

The meeting is Tuesday, June 1, 2010. The meeting will be 1.5 to 2 hours, but plan on being there longer.

Please go to Facebook to register: http://www.facebook.com/event.php?eid=111916645519132

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