Dr. Bill Code writes about his CCSVI angioplasty

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

Dr. Bill Code writes about his CCSVI angioplasty

Postby cheerleader » Fri Jan 14, 2011 5:13 pm

Dr. Bill Code has MS and has been investigating CCSVI for over a year. Here is his personal story--testing in Buffalo (where he showed 4/5 of the Zamboni criteria), treatment in California and recovery back home in Canada.

In short, I believe CCSVI is the “real deal” and is a part of the critical puzzle for the signs and symptoms of MS. Historically, coronary artery bypass grafting and coronary angioplasty were developed for symptomatic relief of chest pain. Why not angioplasty CCSVI for relief of fatigue, headaches, neuropathic pain, sleep disturbance, muscle spasm and balance problems in MS?



http://www.drbillcode.com/ccsvi.html
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
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Postby CRHInv » Fri Jan 14, 2011 7:15 pm

Thanks Cheer!
That is quite an article. He hits on so many good points and I thought the information on using an anti-inflamatory diet was very interesting.
dx 4/09 * Stanford appointment 11/09/09 * One stent left, low jugular 11/10/09!<br />One year from treatment, I have my life back.  Placebo schmebo.
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Postby ikulo » Fri Jan 14, 2011 7:29 pm

I found this sentence to be of greatest interest:

In fact, some of us will require a stent in the azygos if the heart muscle impinges on the azygos vein up against the front of the vertebral column.
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Postby Cece » Fri Jan 14, 2011 7:38 pm

ikulo wrote:I found this sentence to be of greatest interest:

In fact, some of us will require a stent in the azygos if the heart muscle impinges on the azygos vein up against the front of the vertebral column.

But wouldn't a stent there then impinge on the heart muscle?
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Postby Blaze » Sat Jan 15, 2011 9:36 am

Great perspective. I hope Dr. Code will consider joining Dr. Scalafani's thread for docs.
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Postby Billmeik » Sat Jan 15, 2011 11:04 am

great info
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Postby cheerleader » Sat Jan 15, 2011 11:11 am

Glad you liked his writing! I thought it was terrific too. Clear and concise.

Dr. Code is a wonderful gentleman, articulate spokeperson, and has been writing about his MS since he was first diagnosed. He hasn't visitied this site, but I'll encourage him to come over and join the doctors' thread. He's just started Facebooking, and is active thru his website as well. We had a very long phone conversation on the science of CCSVI and the need to get more doctors involved worldwide. His viewpoint will help---
cheer
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
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