CCSVI Multiple sclerosis Breakthrough/cure

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http://www.cbc.ca/video/#/News/TV_Shows/The_National/ID=1344104506
US scientists are testing a radical new theory that multiple sclerosis (MS) is caused by blockages in the veins that drain the brain.
The University of Buffalo team were intrigued by the work of Italian researcher Dr Paolo Zamboni who claims 90% of MS is caused by narrowed veins.
He says the restricted drainage, visible on scans, injures the brain leading to MS.
He has already widened the blockages in a handful of patients.
The US team want to replicate his earlier work before treating patients.
Experts welcomed the research saying it was important to confirm the basic science before evaluating any therapy.
MS is a long-term inflammatory condition of the central nervous system which affects the transfer of messages from the nervous system to the rest of the body.


The Buffalo team, led by Dr Robert Zivadinov, plan to recruit 1,100 patients with MS and 600 other volunteers as controls who are either healthy or have neurological diseases other than MS.
Using Doppler ultrasound, they will scan the patients to see if they can find any blockages within the veins of the neck and brain.
If they can prove Dr Zamboni's theory of "chronic cerebrospinal venous insufficiency", they say it will change our understanding of MS.
Rewriting science
Margaret Paroski, who is chief medical officer at Kaleida Health, where the Buffalo researchers are based, said the work could overturn prevailing wisdom that the damage in MS is predominantly the result of abnormal immune responses.
"When I was in medical school, we thought peptic ulcer disease was due to stress. We now know that 80% of cases are due to a bacterial infection.
"Dr Zivadinov's work may lead to a whole different way of thinking about MS."
Dr Zamboni, of the University of Ferrara, believes the blockages are the cause rather than the consequence of MS and that they allow iron from the blood to leak into the brain tissue, where it causes damage.
He has performed procedures similar to angioplasty to unblock the veins and get the blood flowing normally again.
He claims this "liberation procedure" can alleviate many of the symptoms of MS and is due to publish his findings in the Journal of Vascular Surgery.
In an interview with CTV News in Canada he said: "I found the evidence of narrowing - narrowing of the veins just in MS patients.
"I'm fully convinced that this is very, very important for people."
Early days
Kevin Lipp, an MS patient from the US, has been symptom-free since being treated by Dr Zamboni.
He said: "It's only been 10 months. If nothing happens in the next two to three years, we'll know it's working."
The BBC has heard anecdotally of other surgeons in Europe testing out the same treatment.
The MS Society said more research was needed to see if this was an avenue that should be explored further.
"This is not something patients can expect as a treatment now. This is experimental work and is being tested. We need to know more about its safety and effectiveness."
Helen Yates, of the MS Resource Centre, said: "There is no doubt that this area warrants a great deal more study.
"This could represent a completely novel approach to MS research which, if proven to be relevant, could be a "sea change" in the understanding of the mechanisms involved in the condition."

"I found the evidence of narrowing - narrowing of the veins just in MS patients"

Dr Zamboni
Subject: 20 Years Ago - Dr. Zamboni

20-Years ago:
Dr. Zamboni studied Sardinian children who had jugular venous malformations (So-Called Primary Venous Aneurysms pub.1990) 20 years later, 90% of this group had CDMS.

MS takes many years to develop. Just as Budd Chiari (a venous disease of the liver) is diagnosed in young adults. Shall we wait another 20 years?




Also from brand new studies:
Every MS patient tested has some form of jugular venous occlusion and reflux- in the US, Poland and Italy. Papers are now being accepted and in press.

Category:

Education

Tags:

• CCSVI
• MS
• multiple
• sclerosis
• Cure

[gekiryudojo]

one year later No Relapse No more Symptoms No more MS just living with the damage from before the liberation but I can deal with that! happy Days!

[gekiryudojo]

I am Liberated!!! and so is my Wife! on 15th 0ct! on the same Day in Nis Serbia

[mamadawnna]

I will be treated on Oct 1/2010, people tell me not to get my hopes up but this give me hope.  Thankyou.

[gekiryudojo]

@mamadawnna thanks your welcome I am in Serbia Belgrade for 5 weeks and will be Liberated as well as my Wife soon! good luck to you!

[gekiryudojo]

@mamadawnna I am Liberated!!! and so is my Wife! on 15th 0ct! on the same Day in Nis Serbia

[2008IQ]

I´ve been diagnosed with MS since 2007, and a couple of months ago took the neck scan (having heard about this), in hope they´d find blockages there, but to my disappointment they found nothing. No abnormalities of bloodflow, narrowings or blockages. Everything seemed ok there. Back to square one. I sincerely hope for a cure for this shitty condition, but this one didn´t seem to be it. At least for me. I´m a male 37.

[gekiryudojo]

@2008IQ what type have you got? RR MS? you never said ,all MS is different and yes there are a lot with MS but no CCSVI, I am still being investigated you may still have it but not in the Neck

[gerredward]

I know of a Canadian with who went to Italy in the summer and Dr.Zamboni did the operation on him. He was in much pain before and walking with a cane. He says he now feels normal again, plays tennis and thanks God for the miracle. All of us must open our eyes & put preassure on the U.S. Government to stop this bs and get some results for our people in trouble.

[9gabbycats]

Call the National Multiple Sclerosis Society @ 1-800-344-4867 and tell them to put you on the interested party list and TELL OUR DOCTORS TO START SENDING THEIR PATIENTS FOR AN MRV AND AT LEAST START CHECKING FOR CCSVI! Please pass this along! Thay are taking names and numbers and stories!

[AWDESIGNS8]

@mamadawnna thats all people has is hope never give up hope love april

[violetmatthers]

Ms is so awful :( I hate the fog, the numbness the pain sooo much. But at least we have new hope Violet

[apsugovs32]

oin my group on facebook... ccsvi and the liberation treatment in the USA. help me fight

[shenzycacy]

@2008IQ yeah i know how that feels... but im 17 :( just gotta keep fighting it though...!! together we stand strong ! and fight and fight and find a cure for everyone!!

together we stand STRONG !! X

[2008IQ]

@gekiryudojo Ive had 2 different diagnoses from 2 different docs. 1st one told me it was PP MS, since I´ve never had clear relapses or remissions, the worsening has been generally progressive. The 2nd doc interviewed me again, and changed the diagnosis to (sorry I´m not sure about the right terms in english) "the wave type" of MS. Took Betaferon first, now Tysabri. Using a cain. Scanning my spinal area or feet for blockages (my suggestion) would be "a waste of your money", the doc said.