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.
Duration : 0:3:3
the Doctor said …
the Doctor said that my neurologist could put my on the Drugs
1 in a 1000 chance of dieing from them and 30% effective and £30k a year 24 people died last year from Tysabri
$28400 per year!!!! the liberation treatment costs $14000 from poland and cures you!!!!!
Hi, I am an MS’er. …
Hi, I am an MS’er. and I read with inrterest the stories.
The complexeties of MS mean that this is possibly one of the factors.
I am on LDN, with GREAT improvements, but this story remindes me that at the same time as I wentr onto LDN I was also onto Warferine as I had a DVT. Blood monitored every 6 weeks, to check ‘viscosity’ , does this fit in with the CCSVI idea??
well I am not stopping either treatment to see.
Terl
Thank you for …
Thank you for making the video. We are seeing history being made. Essential Health Clinic in Glasgow plan to bring Scanning to UK ?mid 2010.
Virginia Bottomley as Health Minister late 80’s, gave set a precedent and pit IN WRITING that any treatment , including COMPLIMETARY is payable BY THE NHS if grounds are shown that there is benefit. I think that still stands actually. RADIO CLYDE’s Tiger Tim SCOTLAND is going to Poland in March and proba.bly have a News Team to televise the event,
Thanks for the …
Thanks for the heads up!
Just read about a …
Just read about a breakthrough here in the UK…needless to say that it looks like the health service and the doubters,will drag their feet ….not commiting to pulling out all the stops to help sufferers.
Lets hope that voices will be heard.
Am I a sufferer ? No….but there are so many people who are,and the number is growing, Best thing to do,is find a cure,and a reason ! Makes sence ! In the end the NHS will save money ! That will make then do something ……perhaps !
gekiryudojo check …
gekiryudojo check out HKINTHEUK vids on CCSVI.
Or join our action group here in the UK if you really want to make a difference:
Find the best …
Find the best vascular surgeons in your area and show them the scientific articles. Ask them to monitor CCSVI and think about the number of MS patients who might want this therapy IF it is proven, as we suspect.
If you are brave, sign up for a proper clinical trial. It is critical for this to be a real cure, for it to stand the smell test.
I am very optimistic about CCSVI, and I wish the best to all fellow MSrs.
yea i second your …
yea i second your comment but that is not going to happen coz people are 2 greedy 2 much
Hi Thanks for your …
Hi Thanks for your video, and all the information. I have such Hi hopes now.. and I am going in the morning to get my Tysabri. I will talk this all over with my Neurologist, here at USC in Ca. And I will Make a new video about my own findings. As USC is a cutting edge Research Hospital, and Hopefully I’ll have some new news on CCSVI by Tomar evening. TTYL Violet.
Google “inclined …
Google “inclined bed therapy” for ms.
Or check out my video on this subject.
Kind regards
Andrew
Thanks for the …
Thanks for the comment!
I know of a …
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.
that there is a …
that there is a correlation, I never told her to look pacifically at the left jugular she found it! the rest makes sense to me
, I have a large …
, I have a large plaque on the left side of my brain had optic neuritis in the left eye 3 times, tinnitus in the left ear
The relapse this year affected my right arm and leg that is controlled by the left hemisphere I could go on but it doesnt take a genius to realise
I’ve have it …
I’ve have it Defiantly since 2001 and I think from 1995, CCSVI
is quite probably the cause As far as I’m concerned I had a Doppler ultrasound just over a week ago and the technionSonographer kept losing the left Jugular vain, and said it needs more investigation,
I am sorry to hear …
I am sorry to hear you have MS but hang in there. Keep doing your research. Looks like you have some good info
This makes me …
This makes me really sad…. It’s a hard thing to have MS because you never know what can happen. By boyfriend was diagnosed when he was 16 and is now 23. he strugles having it, he try’s to deny it and when I herd about the liberation treatment I Was Very excited! It will come soon if everyone express’s how much we need it! keep ur hopes up!!!
I agree with that! …
I agree with that! If this is the cure or the ultimate treatment for MS. The pharmaceutical industry tends to loose Billions of dollars. Not millions. So don’t go looking for any MS societies or Neurologists to go jumping on any band wagon soon.
meanwhile instead …
meanwhile instead of embracing it, people are content to pump any old crap into our veins to relieve the symptoms while others mill around worried about losing their Jobs that is the MS (tea and sympathy) society (who are not Doctors) and the neurologists who also have come up with Nil! in decades.
QED this is a time to wake up to the fact that Dr Zamboni
has done something big here nmore than the rest have done!
Well I had an …
Well I had an ultrasound 2 days ago and guess what! there is something wrong with my left Jugular vain and it will need further investigation said the sonographer (she had difficulty seeing the left Jugular and there was something going on with it !) as for knowing what causes MS this is the first thing anyone has come up with for years
that makes sense, oh and Works!!!
We still might be a …
We still might be a long way off on knowing what causes MS. In my own opinion I feel that we are born with it. Genetics has a lot to do with it. But this Liberation treatment seems to be the treatment or maybe even the cure that we have all been looking for. I feel that this is on the right track.
the impossible is …
the impossible is sometimes easier than the difficult. never ever let your dreams die. it will be possible during our lifetime. God bless and keep the FAITH.
Call the National …
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!
My next one is in …
just a few short hours to go!
My next one is in full production and is all information
Thank you Trevor! …
Thank you Trevor! One of the best videos! Keep up the fight!
Take care,
Bill