CCSVI presentation by Dr. Bill Code

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

CCSVI presentation by Dr. Bill Code

Postby David1949 » Thu Feb 17, 2011 4:07 pm

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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Postby 1eye » Thu Feb 17, 2011 5:57 pm

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,
"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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Postby AlmostClever » Thu Feb 17, 2011 6:27 pm

Thanks David1949,

good azygos info at 1:16:40
If you can't explain it simply, you don't understand it well enough. - Al Einstein
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Postby Ruthless67 » Thu Feb 17, 2011 7:17 pm

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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Postby orion98665 » Thu Feb 17, 2011 7:30 pm

Thanks David1949. Very educational and well worth watching.


Bob
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Postby PointsNorth » Thu Feb 17, 2011 11:21 pm

Superb. Required viewing. I will send him an email of thanks right now!

PN
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Postby Bizzy » Fri Feb 18, 2011 8:57 am

Here is the website to get the emu oil from B.C. / Canada

http://songlines.ca/
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Postby mavis » Sat Feb 19, 2011 12:20 pm

Watched it last night through laughs and tears.

Thanks a million David1949.
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Postby Bethr » Sat Feb 19, 2011 1:13 pm

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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Postby cheerleader » Sat Feb 19, 2011 5:33 pm

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
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
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