Avis Favaro online tomorrow ??

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

Avis Favaro online tomorrow ??

Postby ozarkcanoer » Tue Nov 24, 2009 4:54 pm

I just looked at the Facebook page and there is a notification of an online Q&A with Avis Favaro tomorrow. Does anyone know how to join this online session ?
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Postby Arcee » Tue Nov 24, 2009 5:17 pm

I don't, but whoever does, please tell her that her professionalism is much appreciated. If you watched that follow snip from the newscast, she ends by saying it is "an honor" to report on this. And it is a blessing that she has.
diagnosed RR in spring '04
1 stent placed in left jugular vein 7/15/09
on and off Copaxone
allergric to interferons and Tysabri
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Postby ozarkcanoer » Tue Nov 24, 2009 5:28 pm

:oops: :oops:

OK, I'm joining the Facebook generation finally, Luddite that I am, LOLOL.

So the online with Avis Favaro is on Facebook with a link to the Globe and Mail... unless I've royally messed up again. My husband got me signed up. (sigh), I've been avoiding Facebook forever, LOL.
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Postby euphoniaa » Tue Nov 24, 2009 6:08 pm

http://www.theglobeandmail.com/news/nat ... le1375643/

Here's a link to the site - I got it from the thread that chrishasms posted earlier today about funding. This is what it says about joining the "online discussion", but I'm not sure if it explains completely.

We are pleased to welcome the CTV correspondent behind the W5 feature The Liberation Treatment: A whole new approach to MS for an online discussion Wednesday, Nov. 25 at 11 a.m. ET.

Medical/health correspondent Avis Favaro will take your questions about her documentary and the treatment described by the president of the MS Society of Canada as "exciting" and "potentially paradigm shifting.”

Join the conversation on this page Wednesday. You can also leave a question in advance through our comment function.
Dx'd with MS & HNPP (hereditary peripheral neuropathy) 7/03 but must have had MS for 30 yrs before that. I've never taken meds for MS except 1 yr experiment on LDN. (I found diet, exercise, sleep, humor, music help me the most.)
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Postby ozarkcanoer » Tue Nov 24, 2009 6:14 pm

Thanks, euphonia... so embarassed :oops: :oops: I'm just getting old, LOL. I didn't need to join Facebook after all !! Oh well, one small step for me in a confusing world. :D :D
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