A group of researchers in Italy is proposing a revolutionary new theory about Multiple Sclerosis. They’ve offered some compelling evidence that MS is primarily a vascular disease, and that the neurologic damage seen in MS patients has its genesis in blood flow problems within the veins of those patients. They're calling this theory Chronic Cerebrospinal Venous Insufficiency, or CCSVI for short.
The Italian researchers, led by Dr. Paolo Zamboni, imaged the veins leading from the brain and spinal cord of several hundred MS patients, and found that virtually all of them showed evidence of a narrowing or blockage of these vital vascular pathways. Specifically, they found blockages or stenosis in the jugular and/or azygos veins of the MS patients they studied, findings not seen in healthy control subjects or in patients with other vascular or neurolgic conditions.
These researchers theorize that these blockages constrict the flow of blood leaving the central nervous system, causing a reflux of blood back into the brain and/or spine. This reflux leads to edema and inflammation, which in turn leads to an immune response, which then leads to the lesions that are the hallmark of Multiple Sclerosis.
A group of patients who congregate online at ThisisMS.com have become convinced that there is significant merit to this theory. Here is a link to a thread on that site which contains all of the research behind the CCSVI theory, and discussions pertinent to it. One of these patients managed to contact a highly respected vascular doctor at Stanford University, Dr. Michael Dake,. who looked over the research materials and agreed that there might indeed be something to this radical approach.
Dr. Dake and his colleagues have themselves begun imaging the vascular systems of MS patients, and have found results similar to those of the Italian researchers. The Stanford group has gone so far as to start surgically clearing the blocked veins of MS patients, by placing stents at the sites of the blockages.
The researchers in Italy have also been clearing the blockages that they've found, and plan on holding a news conference announcing their findings and results sometime early this summer.
Needless to say, this theory, and the data behind it, flies in the face of accepted scientific thought about Multiple Sclerosis. I'm not entirely convinced that this hypothesis explains all the complexities and wide range of disease presentations seen in MS patients, but the evidence certainly seems compelling enough to warrant further serious investigation.
Personally, I've never quite bought into the "autoimmune" theory of the disease, and I would welcome the paradigm shift that these new ideas might bring about. It's time for mainstream researchers to start looking beyond accepted MS dogma, which thus far has brought us treatments that are only partially effective, and often highly toxic. Surely, there must be a better approach to treating MS than suppressing the intricately complex human immune system.
There is precedent to this kind of radical shift in ideas about a disease. For decades, gastric ulcers with thought to be caused by diet and stress, until researchers discovered that they are actually caused by a bacteria that can be treated quite successfully with antibiotics. Poking at theories that have been accepted as fact can sometimes lead to startling results.
New! Update on "MS as Vascular Disease", posted 8/28/09.
Update 11/21/09! Canadian television has done a video news report on CCSVI. Click here for the link.
Update 11/30/09! CCSVI: Separating Fact from Fiction. Click here.


27 comments:
Excellent information. I just recently came across the study. It is very interesting. It seems that researchers refuse to think outside the box.
excellent job marc!!
This could also explain the heat sensitivity related to MS, as the restricted blood flow doesn't take the heat away from the brain fast enough, and also the fatiguing, as again the blood is not taking away the metaolic byproducts fast enough.
May help explain why oxygen therapy (which is known to reduce inflammation and increase vascularisation) can help in MS
Hi Marc,
Please take a look at my blog and pick up your award.
Please pass it on to five blogs of your choice.
Love Herrad
This is fascinating. I have spinal arthritis with a host of other confusing diagnoses and don't really want to suppress my immune system as a "cure." I wonder then if MS would belong to the realm of autonomic illnesses.
Was just thinking...suppressing the immune system with the TNF inhibitors actually causes MS for some people. I don't know why.
sorry i dont buy into your thinking that ms is vascular disease. I was tested for vascular disease and found i dont have it but do have ms disease.
Hello Marc, A colleague and I just stumbled across your blog and our lives are deeply affected by ms. I was wondering how you heard of this research or how Dr Dake heard of the research taking place with this Dr Zamboni?
Anonymous: if you follow the link in the above post, it will take you to thisisMS.com, where there is a forum devoted to this theory. It's a terrific resource on all of the research that's been done, and there are personal accounts of several MS patients who have recently undergone surgery to correct their vascular abnormalities. Just click on the sentence that begins "Here is a link to..."
I also have ms at now and only 38,I WORK AS NURSE IN THE OR,IT IS AMAZING HOW WELL I FEEL AFTER DR.DAKE PUT MY STENT IN TWO WEEKS AGO.I HAVE SOOOOO MUCH ENERGY,AND NO MORE HEADACHES.EVERYONE WITH MS SHOULD GET THIS IT WORKS.I FEEL GREAT. THANKS TO DR.DAKE . BRIDGETT
Hi Bridgett,
I would like to know about cost of this surgery/ treatment for a person who is not US citizen and what is the process to get this planned and scheduling with Dr. Dake.
Thanks & Regards
MAnoj
Does anyone have contact information for Dr Drake or Dr Zivadinvo? I couple recent articles state they are looking to recruit people in Canada and the US.
Thanks!
Lisa
Big Parma is going to be very angry that a rather simple medical procedure can basically cure MS.
There goes their billions of dollars in toxic drugs that they sell to poor individuals struck with MS.
God bless Dr. Zamboni and his vision to see above and beyond what others didn't recognize.
We need more radical researches who are couragious to go against accepted trends.
I AM A CANADIAN IN CHESTERMERE ALBERTA WITH MS FOR 23 YEARS THANK GOODNESS FOR DR. ZAMBONI'S THINKING OUTSIDE OF THE BOX HE DESERVE A PRIZE. VAL M
hi my name is sandra blyth my little boy sam has ms sam is 6 years old,sam was diagnosed with ms this august when he was 5...we live in scotland..im excited about this news..it sadly has not made any headlines here in scotland my email address is sandrablyth@live.com if anyone wants to contact me.
My wife has had MS for 40. We have been using alternative methods for years with some succes. Apparently the MS Society frowns on this amazing and relatively simple procedure and is advising against it. They instead should be funding research for these doctors and see how far they can go with this. After watching for 40 years I am convinced that the MS Society is in bed with the drug companies and will do anything to stop any doctor who would try something new or alternative. It is nothing but a big money industry with nothing to do with curing the patients.
I so agree when people are saying that the MS Society does not want people to try the new Liberation Treatment. All the drug companies want is our money like I mean come on people give us our life back.
Response from MS society to CCSVI?
Where is it ? Other than the "wait and see", they are scared of going out of business. That is thier goal isn't it?
This would mean there is a solution and the donations from the drug companies would not be needed.
This, along with LDN, should be covered and supported by the networks. But it's not!
Action talks..Where is Obama healthcare? This solution would enable more people to generate tax revenue and and ease the pressure of expensive drugs on insurance companies.
Hi,my name is dave.I have been living with MS for almost 20 years now.I agree with the comment that healthcare is tied in with the we don't want a cure drug companys.does anyone know that the drug companys bring in more money than the IRS at tax time each year,it's true! think about it,is it better to find cures for illness?
sad but true, take care
Hi, my name is Marc. The Virginia Mason Clinic in Seattle treated my MS since it was dicovered some 15 yrs. ago. The department of neurology experimented with me for years with Avonex, Ribif and then with Novantrone, all to no avail. Virginia Mason ripped me off in excess of $100,000. With no positive results from the clinic, I finally decided to obtain an opinion from a neurologist at the Mayo Clinic. The good doctor sadly shook his head when he listened to my story. "To be brutally honest", he confided, "there is no successful treatment, as yet, for MS. All the money you spent on medications and doctors' visits was to support the medical industry, nothing else. Continue taking Tegretol to relieve your headaches. Otherwise, live a healthy life as best you can. MS is not a killer desease." (paraphrased).
MS is money making for doctors and MS societys the cure they dont want any of us to have
MS does kill
WHY DO YOU SAY MS KILLS, DO YOU KNOW SOMETHING I DON'T!!!
My wife has had MS since childhood, but diagnosed only 25 years ago when she was 40.
We have followed the progress of MS treatments and even tried Betaseron until her white blood cell count became too low. She is now quadriplegic, on a ventilator, fed through a PEG tube.
The different "kinds" of MS may reflect different causes / illnesses, rather than just different progression patterns. Remissions occur frequently enough to convince some that what they did / took recently helped cure them.
Belief and the placebo effect also play a role in making it difficult to determine what is a cure and what is not.
If there were a simple and inexpensive way to cure MS, we would know it, even if no one stood to make a profit from it. When it is found, the word will get out.
Few of you would work long hours for nothing, and it is not a bad thing that scientists and investors hope to get paid, too. Most of them would like to see MS cured, as they would have succeeded, and they could move on to other things.
Months ago "Bridgitt" told us how wonderful she felt soon after the CCSVI operation. Where is she now? As with bee venom and special diets, we are not learning of long-term cures and successful double-blind experiments.
I have some hope that adult stem cells will produce some useful results, but even here I note that we get initial enthusiastism followed by silence months later.
A guarded optimism seems most appropriate.
Seven years after being diagnosed my wife's life is slipping away , she lives with constant pain , struggles to swallow , can hardly walk even with assistance . The current line of drugs have no effect . We need a breakthrough here.
It is a killer , just slowly .
F - South Africa
Dear F South Africa, is there a medical practitioner in SA you know of who carries out the CCSVI treatment?
Steve UK
Dear F - South Africa,
We eased my wife's MS pain with regular morphine sulfate (oral, actually by gastric tube) and helped her mood with Prozac.
"Better living through chemistry," until we find something better.
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