also Watch this it takes a few seconds to load. www.cbc.ca 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 1100 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 …
Tag: ccsvi, cure, MS, Multiple, sclerosisDottor T. Il divulgatore scientifico
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.
Thanks for the comment!
Google “inclined bed therapy” for ms.
Or check out my video on this subject.
Kind regards
Andrew
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.
yea i second your comment but that shit is not going to happen coz people are 2 greedy 2 much
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.
gekiryudojo check out HKINTHEUK vids on CCSVI.
Or join our action group here in the UK if you really want to make a difference:
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 !
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. 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 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 heads up!
@cbschu My brother has MS and we are looking for a clinic or hospital where he can have the test (CCSVI) done, unfortunately, here in Canada they refuse to issue the test when required for MS treatment, our government ordered all clinics even privite institutions to refuse all CCSVI request (even if he has a doctor order). We are looking for a clinic in Plattsburgh NY to have the test done as this location is an hour drive for us . NEED HELP PLEASE THANK YOU.
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.
@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
@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.
@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
oin my group on facebook… ccsvi and the liberation treatment in the USA. help me fight
Ms is so awful
I hate the fog, the numbness the pain sooo much. But at least we have new hope Violet
I will be treated on Oct 1/2010, people tell me not to get my hopes up but this give me hope. Thankyou.
@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!
I am Liberated!!! and so is my Wife! on 15th 0ct! on the same Day in Nis Serbia
@mamadawnna I am Liberated!!! and so is my Wife! on 15th 0ct! on the same Day in Nis Serbia
@mamadawnna thats all people has is hope never give up hope love april
go on here and look at people that been healed in the Name of Jesus
Awesome video! I don’t know what its like to have MS but my mom has MS, she was diagnosed in 1997 with RR MS and as of 3 years ago she has SP MS (Secondary Progressive), she is 52 years old.
We are scheduled for her Liberation Treatment in San Diego California at the David Hubbard Foundation, and Del Mar Vein Care.
I am so excited for her! I’ve heard nothing but positive outcomes of the CCSVI Treatment and I am looking forward to seeing how she feels afterwards!!
Tina