Dr. Brandes---CCSVI in Canada

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

Dr. Brandes---CCSVI in Canada

Postby cheerleader » Wed Nov 17, 2010 11:55 am

A recap, one year since the CTV news program--
(almost 2 years for those of us on TIMS)

Where do we go from here?
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
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Postby CCSVIhusband » Wed Nov 17, 2010 12:18 pm

Great article ...
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Postby Blaze » Wed Nov 17, 2010 12:49 pm

It continues to boggle my mind that an oncologist like Dr. Brandes is so strongly in our corner while the neurologists are so dismissive and Canadian IRs and vascular surgeons, except Dr. McDonald and Dr. Godley, are so incredibly silent.
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Postby bruce123 » Wed Nov 17, 2010 1:03 pm

A good article with some excellent references, linked the way they do it in Wikipedia. It's very handy to access some of the early media coverage. It's good to be reminded of items such as Dr. Freedman's "hoax" comment.

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Postby MrSuccess » Wed Nov 17, 2010 6:54 pm

another well spoken doctor ..... willing to accept information put before him.

I still cannot believe how far the CCSVI discovery has grown - in such a short time frame .

As we know ..... there is lot's of activity going on ..... that should start fairly soon to show their investigational reports .

good work everyone ....

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Postby welshman » Wed Nov 17, 2010 8:37 pm

It's so good to know that there are at least a couple of people in Canada with some intelligence :D
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