April 30 Presentation by BNAC researchers

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.
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Nick
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Post by Nick »

Nick wrote:Bump and grind. 8)
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1eye
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ctv

Post by 1eye »

Please note that tomorrow night there will be a follow-up report on W5. Click on the link for more information:


http://www.facebook.com/event.php?eid=115607475136662

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Post by Rokkit »

This keeps getting bumped, but I keep not being able to figure out what action I'm supposed to take. I visited the direct-ms site for details as indicated in the first post but didn't find any mention of it.
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dlb
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Re: April 30 Presentation by BNAC researchers

Post by dlb »

This is a copy of Nick's first post & this Direct MS link takes you directly to the poster for the info session being held tonight in Calgary. Hope that helps...
Nick wrote:Ladies and Gents

Direct-MS will be hosting a presentation in Calgary, Canada on April 30, 2010 to be given by Dr’s Zivadinov and Weinstock-Guttman, leading researchers on CCSVI in North America. Please visit our site for more details. As we have done with past speakers, we will be recording the event and will have the presentation available as a webcast on our website in the presentations section sometime after the occurrence.

Cheers
Nick
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Post by Rokkit »

A ha! I never clicked on the direct-ms link cuz I thought it was just the home page. I always clicked on the presentations link which went to a page with no apparent CCSVI connection. My fault.
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Billmeik
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Post by Billmeik »

so did anybody go? What was said?
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dlb
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Post by dlb »

I went & I really enjoyed the presentations by Zivadinov & Weinstock-Guttman. Kind of a layman's version of much that was explained in that teleconference from Toronto. I think they are compassionate & caring and I was a little disappointed that they were verbally attacked in the Q&A session. These researchers are not the people that set the board rules. I felt a little bad about that for them. That is just my opinion. Thanks Direct-MS for bringing them in to the area for us to learn!
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cheerleader
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Post by cheerleader »

Reports on Facebook say it was a very scientific evening, lots of info on the research, and great presentations to OVER 900 PEOPLE. wow.
I think it's important for MS patients to understand these doctors are the researchers...NOT caretakers or treatment facilitators. I tried t explain that on FB, but there's so much interest in getting a diagnosis and treatment now, it's tough. Sorry the doctors had to deal with that energy-
also sorry I couldn't come up and attend.
Go Dr. Embry, Nick and Direct-MS. Thanks for being leaders-
cheer
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
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