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Re: CCSVI + angioplasty

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Thank you for sharing your experience. This is great news! I am hoping to find

a doctor who would do the same procedure here in Seattle. All the best!

>

> I just wanted to share my experience of getting the proper diagnosis for

ccsvi. I had three tests which indicated no stenosis including a ct scan,

ultrasound , and mrv of the neck. I was told not to pursue but I asked to

perform one more test to verify stenosis of the azygous vein. When the venogram

was performed , they found stenosis of the azygous but also stenosis of the

right jugular vein. The doctor became a believer and performed the angioplasty.

The diagnosis used was venous stenosis not ccsvi. The angioplasty was strictly

ballooning and no stents placed. A reporter covered the story and will be

posted in a well known paper in the USA. My doctors included a vascular surgeon

and interventional radiologist. Dr. Simon , an amazing doctor, performed

the venogram and the angioplasty. He was very excited about the new theory.

The procedures wereperformed at Jfk medical center in Edison, NJ. Please note

the venogram is the best test to verify stenosis. Otherwise, like me , you will

not find results. I will continue on Ldn but I do believe in Dr. Zamboni's

theory of CCSVI. I wish you all the best and I hope we all cured of this

horrible monster known as ms. Between the Ldn and the angioplasty, I believe

that I am cured.

>

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