CCSVI MS UPDATED
It has been just six years since the Professor Zamboni posted his CCSVI theory on the internet suggesting that MS is in fact a blood circulation disorder of the brain. Since then scientific research has revealed that disruption of ANY fluid bathing the central nervous system (blood, cerebrospinal, glymphatic) can cause “MS” symptoms. This site is intended to share the “liberation” I feel as an MSer who no longer needs to fear inevitable doom.
I launched my “MS Cure Enigmas” site as follows.
“In Multiple Sclerosis blood vessels "deformed" by childhood stress cannot accommodate the blood flow. I believe the auto-immune activity is secondary to the true cause of MS, blood refluxes which injure the brain and spinal cord. The origin of the refluxes may be structural 1) CCSVI stenosis (as proposed by Professor Zamboni) and/or cerebrospinal fluid pressure or 2) it may be a stress reaction to toxicity.
Epidemiological studies on MS show that those who grow up close to the equator have less chance to develop MS than those living in latitudes closer to the poles. It is the latitude where one lives before age 15 that counts, not where one lives subsequently. It is therefore thought that the lack of sunlight leading to a Vit D deficiency is a factor in susceptibility to MS.
But perhaps an equally important explanation of the geographical factor is Winter Cold.
The shoulders and neck typically tense up under stress thus restricting circulation to and from the brain. Cold weather stiffens the muscles. Winters bring the body aches of colds and flus. Illness itself (e.g. Clamydia Pneumoniae, Mononucleosis) may damage the cell walls and valves of the vascular system.
It is also said that MS patients tend to be high powered, ambitious people. Tensed up in other words. MS cases cluster in northern Europe and North America. Let’s say growing up in a culturally demanding family environment (or in any case stressful) while subject to Cold weather and frequent colds and flus actually compresses and deforms the circulatory system in the child’s developing body. By the time he/she reaches age 15, the damaged blood vessels can no longer accommodate the blood flow. MS first appears in adolescents, seldom in children. Let’s compare the deformity to ancient Chinese footbinding where the tiny child’s foot cannot support the adult woman.
Food intolerances, especially to wheat and dairy products, can further compound the stress. The Neolithic agricultural revolution dates back not much more than 10,000 years, a blink of the eye in terms of biological evolution. Bowel problems are a sure sign of food “stress”. The significant increase in MS cases in Japan over the past 30 years points to food toxicity as root cause.
And the disadvantage of being female. While originally there was no difference in MS incidence between the sexes, over the past 50 years women’s share has increased to the point where up to three out of four MSers are female. What changed 50 years ago? The advent of birth control pills and hormonal therapies which are known to impact the vascular system adversely.
Maybe the real story behind MS is the damage to the blood vessels caused by growing up in a 1) driven, ambitious or otherwise stressful family environment compounded by 2) a climate of Cold winters which contribute to 3) frequent viral illnesses compounded by 4) an intolerance to the wheat and lactose of a Neolithic diet.”
Return to the present. Frankly, that analysis is O.K. but it’s slightly off the mark, ignoring vital factors. What’s missing? Why should the blood vessels in MSers be so weak that mere muscle tension can disrupt blood circulation? Recent research by Professor Zamboni has found that the endothelium – inner vein wall - cells are absent in the Internal Jugular veins of MS subjects. Without walls the veins could collapse like a flimsy garden hose. Why are these cells missing? Childhood illness, poor nutrition owing to food sensitivities, insufficient Vitamin D ( a form of vein rickets perhaps? A genetic factor specific to MS reinforces the need for Vitamin D.) Whatever the reason, a damaged endothelium is the vital factor.
And Latitude? It's the Sun which brings health through Vitamin D AND the release of Nitric Oxide. Nitric Oxide is a vasodilator critical to the development and function of the vascular system (read endothelium again). (Research into Cardiovascular disease – not MS or CCSVI – led to these insights.) It is NOT the nerves which impact the blood flow so much as the blood flow which impacts the nerves. A properly functioning vein wall so critical to blood circulation depends on a healthy life style (diet, supplements, exercise, stress reduction, UV rays). These factors missing during the critical growth period could well lead to a deformed, poorly developed vascular system. The evidence pointing to MS as a circulatory system disease is overwhelming. And the epidemiological factors fall into place.
A point also missing from my original paper is the observed atrophy of brain grey matter as the disease progresses. Blood refluxes damage the myelin white matter which are revealed as MRI lesions during early stage relapses. Eventually the relapses recede, the lesions disappear as the grey matter deteriorates. I believe every effort must be made to stop the blood reflux, stop the relapses and nourish the grey matter as well as the myelin sheath, the earlier the better. Optimal nutrition, supplements, blood circulation therapies and venoplasty itself if the stenosis is serious all serve this end.
Finally, the Epstein-Barr virus remains dormant throughout the life of MSers after an initial Mononucleosis infection. Did the initial infection damage the endothelium? Does periodic activation of the virus trigger “attacks”? Or do the “attacks” re-activate the virus because poor perfusion through damaged endothelium leads to oxygen deficiency?
That being said, the most grievous omission in my paper is Primary Progressive MS, indeed Progression in general. I’ve come to think that the 10% PPMS cases exhibit primarily obstructed cerebrospinal fluid (CSF) or direct pressure on the spinal cord itself, (NOT stenosed veins) owing to a damaged, degenerated spine. And the more common RRMS (RelapseRemissionMS) is transformed into the Progressive form as the disease process damages the spine and body structure in general.. (See January 21, 2015 Blog “How RRMS progresses to SPMS”). Once that happens, venoplasty effectiveness may be limited.
The MS-UK site’s succinct definition of PPMS.
Primary Progressive MS (PPMS) concerns about 10 to 15% of MS cases. In contrast to RRMS (RelapseRemission) cases, the PPMS disease progresses continually without respite after striking an older population (age 40’s to 50’s). Unlike RRMS, there is little to no inflammation, there are fewer brain lesions, the lesions which do exist present fewer inflammatory cells, and more are found on the spinal cord than in the brain which leads to mobility problems. While PPMS cases exhibit less inflammation, there appears to be greater damage to the axons.”
And an additional interesting detail. While RRMS strikes women 2 to 3 times more than men (think veins), PPMS is thought to strike principally men (think accidents, child sports injuries).
PPMS patients are not included in MS drug research and treatment because both target the myelin damaging inflammation of RelapseRemission MS observed on the MRI, that is to say, the blood reflux (CCSVI).
And now we arrive at a real irony. Dr. Damadian invented the precursor to this famous MRI so necessary to the MS medical industrial complex. He recently invented the FONAR cine (fluid circulation) Upright MRI which has revealed that many MS patients exhibit obstruction of cerebrospinal fluid in the neck (cervicals). In other words it’s a body structure issue for these patients, not an auto-immune disorder. Treatment calls for skeletal adjustments, an Osteopath or a Chiropractor, perhaps even surgery.
Let’s re-define MS categories. We have two basic forms of Multiple Sclerosis. 1) CCSVI MS concerns defective veins. 2) Structural MS concerns elements of the body structure - bones, muscles, arteries. In both cases the blood and cerebrospinal fluid circulation are obstructed or slowed. Effective treatments differ, in the one case the veins need to be addressed, in the second the body structure.
Scientific studies confirm these observations. For example February 13, 2015 PLOS ONE* published a double blind study revealing that it takes twice as long for blood to flow from the heart through the brain and back to the heart in MSers than in normals, this regardless of the MSers condition. In other words, poor perfusion is a marker for MS. There it is, what we needed to know. The Answer.
And the Answer suggests Solutions.
END OF PART ONE
Professor Zamboni initially proposed using the Sonogram to diagnose veins running from the brain towards the heart – the Internal Jugular Veins and the Vertebral Veins. Once the stenoses in the veins were observed he recommended opening the stenoses with balloon venoplasty as well as the chest azygos vein if indicated. In his paper “CCSVI – A New paradigm and therapy for multiple sclerosis” posted on July 25, 2010, the Interventional Radiologist Salvatore J.A. Sclafani, MD refers to Dr. Zamboni’s work by writing “Chronic cerebrospinal venous insufficiency (CCSVI) is a hemodynamic condition in which cerebrospinal drainage is altered and inhibited. Outflow obstructions of the internal jugular veins (IJVs), vertebral veins, and/or azygos vein ( AZV) and their tributaries result in stasis or reflux of these outflow veins and redirection of flow through vicarious circuits…”
Dr. Sclafani has performed over 500 venoplasties for CCSVI and has found the condition in many more vein types than initially proposed by Dr. Zamboni. He recommends use of the Intravenous Ultrasound (IVUS) to allow the Doctor to best judge the size of the balloon – too small the vein re-stenoses, too large the vein wall may be damaged resulting in thrombosis. For him the gold standard for CCSVI diagnosis is the IVUS venoplasty itself, the sonogram being inconclusive. The FDA put a stop to CCSVI treatment for MS outside of research trials in May 2012 which has retarded development of appropriate stents and improvements of the procedure. (That is to say, insurance won’t pay for treatment which remains available for those in the USA able to pay.) Worldwide a common experience of MSers undergoing venoplasty is relief once the veinous obstruction is overcome and subsequent disappointment when the vein restenoses, maybe immediately, maybe several months later.
Another issue overlooked at the outset was the skeletal factor, that pressure ON the vein by a bone, muscle or artery may be obstructing blood flow rather than a valve problem (for example) IN the vein. In this case venoplasty is inappropriate and even potentially damaging.
So before even considering venoplasty I believe one should be examined for skeletal obstructions. The ideal equipment is the FONAR upright Cine MRI invented by Dr. Damadian. Unfortunately, obstructions in cerebrospinal fluid flow are less likely to be observed MRIs when the patient is recumbent. Also, Neurologists are looking for brain/spinal lesions considered markers for disease activity rather than the condition of cerebro-spinal fluid flow. For diagnosis of CSF flow there are apparently 15 FONAR sites in the US and one in London. (http://www.fonar.com/news/052114.htm
At this time, Chiropractors familiar with spinal structural conditions are probably best equipped to study, diagnose and even treat skeletal obstructions of blood and cerebrospinal fluid flow through the central nervous system. Dr Michael Flanagan “upright doc” on the Thisisms.com website (CCVBP) recommends use of the COX Technic Flexion-Distraction tables (the most advanced is now version 8) to treat spinal conditions. NUCCA (National Upper Cervical Chiropractic Association) Chiropractors specialize in treating the Cervicals and the Atlas Orthogonal (C1). Some Dentists believe that MSers should have their TMJ (Temporomandibular Joint Disorders) treated to relieve fluid flow through the brain. I myself think the entire head/neck/back structure needs to be calibrated, that treating the jaw in isolation cannot possibly overcome a structural imbalance. Besides, this kind of dental work is expensive for incomplete results.
To change the subject, yesterday I broke down and took an antibiotic for a bladder infection. The homeopathy treatment seemed to be working, but then I went out for the day, didn’t drink much, it was very hot, and the infection took off. (This kind of infection is my “canary in the coal mine”. I was doing great until I spent the week-end with someone who I now realize is very toxic for me. The infection so informs me. Homeopathy works on the principle that while we are constantly submerged in germs, the beasties can do us harm only when we are psychologically vulnerable. The correct remedy should overcome this vulnerability. I must in future change my approach to this disagreeable individual so I don’t get sick in the first place.)
I don’t like taking antibiotics because they trigger MS symptoms. Why? I always assumed that they perturb the immune system. Now I think they simply act like a toxin which creates body tension. After a bad experience with an inclined bed (see post “ Inclined Bed Warning” Jan. 5, 2015) I’ve concluded that the origin of my current left foot symptom is pressure on the spine and/or cerebro-spinal fluid. So the slightest tension impedes fluid circulation. (Homeopathy works by relieving that tension.) Foods can act as toxins, glutens being a classic example. The flu can cause the entire body to seize up in cramps which seem to shut down my entire body’s fluid circulation leading to terrible MS symptoms. I don’t think one need look any further than that basic principle. And work from there.
I ask my husband every day to briefly massage my upper back, both of us standing, and then massage down the length of my back to the lumbars. He grumbles but can see that I’m doing better so he does it. And every morning I give myself a TENS acupressure treatment. (See TENS Acupressure post). I take a walk (with a cane) every day. I swim if I can or use a portable bike apparatus. And I get an osteopathic or acupuncture treatment once a month. (I’ve resumed Homeopathic treatment. The Osteopath was pleasantly shocked by the suppleness of my body following a course of homeopathy.)
Osteopaths are the ideal therapists to get the fluids circulating. I’ve come to think Progression is caused by blocked cerebrospinal fluid in the spine, that mobility deficiencies originate in the spine. My Osteopath thinks MSers need the combined skills of a Chiropractor – to free any obstructions by manipulating the skeleton – and an Osteopath to get the fluids circulating. This would include the newly discovered Glymphatic fluid which cleanses the brain during sleep.
In the meantime, anyone who seriously seeks to heal MS can’t ignore nutrition. Let’s start by looking at the MS healing recipe cooked up by Ashton Embry, PhD for his son Matt who describes it on his site http://www.mshope.com.
Oops. A lawyer from the MS Society of Canada just sent Matt Embry a threatening letter. He is to revise his site, which in their opinion too closely resembles their own, OR ELSE. Well, of course he did take his site down and is now revising it. Who wants to do battle with Godzilla? Who is doing business here, the MS Society of Canada or Matt Embry? Why do MSers have to put up with all these vested interests? I recommend Matt’s site as a starting point.
After studying patient testimony worldwide, Matt went to Poland in 2010 where a Sonogram revealed that his jugulars were “blocked” 100% on one side, 50% on the other. He underwent venoplasty and enjoyed the restored blood flow for about 3 months after which the veins apparently restenosed. He didn’t want to take the risk of having stents inserted. (It was mainly his brain congestion rather than mobility issues which the venoplasty corrected.) He now keeps the blood flowing through intense cardiovascular exercise. In other words, the veins must narrow or collapse or the valves “stick”, but exercise will open them, they are not actually obstructed. I use swimming and a portable “bicycle” device as well as osteopathy or massage or acupuncture to get the same results.
I walk with a cane and am certainly not in the shape he is. That’s why I mention healing options such as osteopathy. I believe everyone can get some relief no matter what their condition. Even a simple non-professional massage should help. Think of moving the blood from the heart, up through the brain and back down to the heart, think of speeding up the flow. Think positive action, relief of stagnation. I really do feel better since I began to work on my “fluid mechanics”. My head is no longer congested.
Back to diet.
I believe proper diet serves 4 purposes: 1) to prevent body stress - on the vascular system i.e. the blood reflux and/or on the cerebro-spinal fluid 2) to heal and reinforce the endothelium of the vascular system at the cellular level 3) to nourish the brain cells (white matter, myelin sheath, axons, grey matter) especially important if there has been some brain damage and 4) to re-inforce the immune system in order to de-activate a latent virus or bacteria (probably Epstein-Barr virus – cause of Mononucleosis - for me).
I describe my diet under the Paleo-Macrobiotic title. CCSVI Alliance website provides a diet as does MS Diet for Women. They all follow the same general principles. Eliminating glutens tends to be a real stumbling block (which I can understand). The first time I read an MS diet article by a young man who was high-stepping next to his empty wheelchair (January 1983), I didn’t want to believe eliminating glutens could be so important. Well, I was wrong.
Thisisms.com under CCSVI
1. “Dr. Sclafani Answers some Questions” for Venoplasty
2. “upright doc”under “CCSVI and CCVBP”for skeletal issues (Dr. Michael Flanagan)
3. “cheerleader” (Joan Beal) 2015 ISNVD** abstracts online
All available in Veins and Lymphatics publication--
http://www.pagepressjournals.org/index. ... /view/5398 **International Society of Neurovascular Diseases
MSHope (currently being revised)
Marie A. Rhodes’ book CCSVI as the Cause of Multiple Sclerosis is an outstanding general resource.
I am suggesting these sites for information only - a starting point in your own research.
Even though Dr. Zamboni's insight has come a bit late for me, it has given me a new lease on life. I used to live in constant fear of a debilitating relapse. Now I know what to do to head off a breakdown. Having embarked once again on my diet I feel better and hopeful of improvement in the future. I know that anything which improves blood/brain fluid circulation (swimming, acupuncture, acupressure, massage, kinesiology, osteopathic, chiropractic, any energy therapy – AND fifteen minutes of Sun a day) will make me feel better and prevent a relapse. As I’ve gotten control over the blood reflux into the brain, I’ve come to see the importance of keeping my spine strong and stabilized. Optimal nutrition and supplements and oxygen can keep my blood vessels as well as the brain’s grey matter healthy. And I need to be ever vigilant in avoiding illnesses which might trigger the latent EBV virus.
I hope other Multiple Sclerosis patients will reflect on their own history and that my experience will be of use in their Healing.
July 1, 2015
(Version 1 - February 15, 2012. Version 2 – June 8, 2013. Version 3 August 1, 2014. See under pages more...)
Anna Macy is an American writer living in Paris.
She can be reached at email@example.com
*Cerebral Circulation Time is Prolonged and Not Correlated with EDSS in Multiple Sclerosis Patients: A Study Using Digital Subtracted Angiography
Tags: MS, CCSVI, Dr. Zamboni, Dr. Sclafani, Dr Flanagan, Dr. Damadian, FONAR MRI, EBV, cerebro-spinal fluid