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PostPosted: Thu Feb 17, 2011 5:07 pm 
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CCSVI presentation by Dr. Bill Code
His presentation begins at 22 min 20 sec.
http://www.ustream.tv/recorded/12720508

Sorry but you have to sit through a commercial first.


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PostPosted: Thu Feb 17, 2011 6:57 pm 
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Location: Kanata, Ontario, Canada
Very highly recommended, even though he does sell Emu oil on the side, He doesn't disclose. Does that make him dishonest? I think he just doesn't do commercials, so you won't hear anything about it, other than that it is an antioxidant. Good luck trying to get some, anyway.

He spoke about many things, and has a credibility many doctors should envy, Don't believe me, watch it for yourself. Anybody seen a transcript?

He is a (former) SP'MS' patient who had the Procedure,

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"Try - Just A Little Bit Harder" - Janis Joplin
CCSVI procedure Albany Aug 2010
'MS' is over - if you want it
Patients sans/without patience


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PostPosted: Thu Feb 17, 2011 7:27 pm 
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Location: Houston, TX
Thanks David1949,

good azygos info at 1:16:40

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If you can't explain it simply, you don't understand it well enough. - Al Einstein


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PostPosted: Thu Feb 17, 2011 8:17 pm 
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Location: Montana, USA
Hi 1eye and David1949,

Great talk, but I wish the sound was better. I still learned a few new things though.

I have a great source for Emu Oil. I have been to Joe & Clover's Emu Ranch personally. They live in the same small town that I do in Montana. Wonderful people and a wonderful product.

http://www.wildroseemu.com/pages/aboutus.asp

Respectfully,
Lora


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PostPosted: Thu Feb 17, 2011 8:30 pm 
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Location: Vancouver, Wa
Thanks David1949. Very educational and well worth watching.


Bob


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PostPosted: Fri Feb 18, 2011 12:21 am 
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Location: LeftCoast Canada
Superb. Required viewing. I will send him an email of thanks right now!

PN


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PostPosted: Fri Feb 18, 2011 9:57 am 
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Location: Cornwall, Ontario Canada
Here is the website to get the emu oil from B.C. / Canada

http://songlines.ca/


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PostPosted: Sat Feb 19, 2011 1:20 pm 
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Watched it last night through laughs and tears.

Thanks a million David1949.


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PostPosted: Sat Feb 19, 2011 2:13 pm 
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Wow, it's long, but well worth watching. Dr Code thinks there may be a link between hemochromatosis and MS (see question 2hrs 16Minutes onward).
MS and hemochromatosis run in my family so I've been researching this fror a while.
I got rid of all my symptoms by reducing my iron levels by phlebotomy.
Prior to my first phleb I was sleeping 20hrs a week in the afternoons, and had elevated transferrin saturation and high ferritin, and the effect was immediate for me. Prior to that I had developed a lot of the symptoms my sister has, she has had MS for 20 years and like me carries the hemochromatosis gene.


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PostPosted: Sat Feb 19, 2011 6:33 pm 
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Location: southern California
Dr. Code is a great guy. He was in southern CA, and stopped at our home for a visit earlier today. Jeff and I enjoyed his company--he is a bright, articulate and fired up advocate for CCSVI research. Look for more news stories on him in the near future in the Canadian media.
cheer

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Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
dual stents placed 5/09
CCSVI in MS


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