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  • Dr. Hemangi of Noble continues: “These are early days and certainly all evidence that the combination of liberation and stem cell therapies working together at this point is anecdotal. However I am not aware of other medical facilities in the world that offer the synthesis of both to MS patients on an approved basis and it is indeed a rare opportunity for MS patients to take advantage of a treatment that is quite possibly unique in the world”. Log on to ccsviclinic. ca for more information.

  • I've been around enough to see several highly touted "cures" for MS all of which turned out to be ineffective or worse (I've seen a few get really messed up by some "cures".). MSers are a desperate population and you can sell them anything. But you cannot cure something that you do not know the cause for. The early trials for CCSVI were not encouraging. Anything works with early MS incl healthy lifestyle. BEWARE!

  • this is crazy!!! Rick Simpson HAVE cure but they don't alow him to have licence for it. This is TRULY crazy! Why no one talk about that? Crazy!!!!

  • For all of you, if you belive that CCSVI is an option for your treatment of MS, be aware that it's still EXPERIMENTAL. It doesnt mean it doesnt work, it's just that there is not enough  evidence YET. You should as MS patients know, that MS is based on relapses, so dont count for granted that a symptom free period means MS free. I advice you to try CCSVI to add to the pool of patients treated to find the truth about CSVI, but not to expect a 100% cure while on it.

  • If you’re diagnosed with Multiple Sclerosis, cheer up because the cure for MS is already discovered, and it’s called “CCSVI,” or “The Liberation Treatment!” This cure was discovered by “Dr. Zamboni!” You can search this here on You Tube. Just search: “CCSVI,” “Liberation Treatment,” and/or “Doctor Zamboni!” You can also log on Face Book and check”CCSVI in Multiple Sclerosis!” Feel better!

  • @MSpinalcord This will cure ms every bit as well as as snake venom and hyperbaric oxygen therapies did. More cures from salesmen.

  • @Crosscheque

    What are you talking about!? I'm, certainly, not a salesman; I’m a human-being with heart and compassion. I was diagnosed with Multiple Sclerosis, and I had the CCSVI procedure done myself. All the horrible signs of MS, which I experienced, are improving as I’m getting better and better. All I want to do is to inform those diagnosed with MS that there is an effective treatment that can cure them from this horrible disease. How is that I'm being a salesman, Crosscheque!?

  • Scientist discovered that All NON-Africans have bet. 1%-4% of Neanderthals DNA while 'pure' Africans(sub-saharan) don't have it. It seems like MS is very rare among 'pure' Africans compared to 60% of African Americans who have caucasian blood. I am just wondering if the Neanderthal DNA might have something to do with it. I guess there is an advantage to being 'pure' humans/homo sapiens/Africans with NO Neanderthal admixture. Question: is MS a Neanderthal disease?

  • Or you can fill you body with as much THC and CB's as possible yielding the same results without side effects

  • Northwestern University researchers, led by stem-cell expert Richard Burt, used immunosuppressant drugs to destroy the immune systems of 21 early-stage MS patients and then reconstructed their immune systems with the patient's own cells. To date Jan. Feb. 2011: 75 % of the patients have experienced an improvement in their condition. CHALLENGES: The therapy for early-stage MS makes patients susceptible to infection. Later stages require embryonic stem cells; they face government restrictions.

  • Are we not getting tired of hearing about these new drugs to help or improve symptoms for ms only to find its not good for any type except relapsing remitting ms do not the rest of us count we are in as much discomfort and pain also with just as bleak an outlook as the rest .

    We cant go back and start at the beginning of this problem , we progress at a steady rate.

  • I don't trust these pharmaceutical companies. I have been researching MS treatments for a while now and can never seem to get any real scientific explanation. Every time, the words "thought to believe" are connected to the sentence. Not reassuring enough for me to warrant injecting chemicals into your body everyday (in some cases).

    It made me laugh when they talk about the side effects being "possibly serious" and then went on to say, but don't worry we have more drugs for that.

  • Try Protandim for 30 days and see the difference... :)

  • I was Liberated From MS I don't have it any more look up CCSVI in A World Free of MS, the National MS Society is full of people without a job! like these guys

  • What was the name of that drug?

  • XMRV XMRV XMRV XMRV

  • THE ONLY THING I CARE ABOUT IS THAT YOU CAN GET THIS DONE EVEN IF YOU HAVE NO INSURANCE AND IN THE USA DONT BULL SHIT PEOPLE IF YOU HAVE TO GO SOME WHERE ELSE AND GET THIS AND IT COST LOTS OF MONEY, I LIVE IN OHIO NO INSURANCE SO IF THIS IS WHAT DOES HELP MS THEN GREAT

  • This research looks promising watch?v=-9M5PLhTqjs

  • Do not listen to the alarmists on YouTube telling you this DOESN'T work or WILL make you sick. The two infusions of CAMPATH that I have received have restored my life.

    ZERO relapses in two years, IMPROVED EDSS scores, DECREASING lesion volumes on MRI and there are reams of data via the studies to PROVE it.

    The only concern I have with the Liberation procedure is the lack of that same data, yet. When more of it becomes available, and I believe it will, I'll be first in line.

  • i think this is the drug companies propaganda to steer them away from the Zamboni procedure. i find myself on the brink of disgust for most of these corporate liars.

  • I hope this treatment holds some real promises for MS patients. The diagnosis rate is growing at an alarming rate.. my dad has it, ironically my best friend's dad has it, and it seems like everyone else I know can name off at least a handful of people who they know personally who is stricken with it.

  • @WhiteLionness I share your pain, my dad has it as well and it depresses me, but it makes me try harder in what I do, I feel that my gifted talent in computer programming will someday spark when I'm an adult and I'll help design a program to help find the cure for MS.

  • @TheMMOGameReviews

    I think your computer programing gifts are going to be a tremendous asset in finding a cause and cure for ms - I think this is the only way of correlating all the niche specialized studies and various disciplines and data involved in ms reasearch - only a computer will be able to "imagine" what that fully combined, fully articulated picture of this disease, because it seems to me that it really will require a conception of the big picture to get a sense of what's involved.

  • i know a drug that can also delay the progression of all neurologic diseases. it is called acetyl-l-choline, i was once a medical representative, and in the company where i am working do distribute this kind of drug under the name of LEVOCITILE.

    you can also google it. acetyl-l-carnetine for MS. hope i can help in any way.

  • will this drug imprve the symptoms of Cerberal Palsy??

    

  • This is not the solution to MS. Dr. Zamboni has the treatment MS sufferers need. All the information you need is already here on Youtube. Just search for Paolo Zamboni :)

  • Does this really work?? Anyone please?

  • this drug will really make you sick....

  • I had my first infusion of Campath last year. What a wonderful year I have had! Second infusion in a couple of weeks.

    Thank you to CAMbridge PATHology and my Neurologist for giving me my life back xxx

  • this treatment is like a 2nd chance at life

  • My neighbor had Multiple Sclerosis, went to China and is doing great. The treatments there are much safer than the U.S. because of the zero-antigen UCB. A company called SCC International did an evaluation and made the arrangements. Their number is (407) 610-4248

  • This is NOT a treatment of the MS this is simply another drug that prevent your system to attack your body. Follow what Dr. Zamboni has discoverd. I have ultrasound as a speciality in my medical bacground. My Brother was just diagonsed with MS 3 years ago. And i can tell where the narrowing of the vein is. Yes there are sepcial cases when an Angiogram is nedeed but you still can detect it with ultrasound.

  • low dose naltrexone, 3 or 4.5 MG, once a day, is already available, less than a buck a day, needs doc prescription and it Works. minimal side effects, just search for it. I'm on it since 2003 and am stable. works for all auto immune diseases

  • NO Drugs ...... CCSVI Dr zamboni JUST SEARCH AND YOU WILL FIND THE MOST PROMISING TURN AROUND AT LOOKING AND UNDERSTANDING WHY PEOPLE GET MS.

  • I was diagnosed with MS about a year ago but not convinced that i have it. I do not have any symptoms that are common with ms. the diagnosis was made only from a few mri's that were performed. i do however suffer from headaches every day. nothing works except for pain killers (narcotic). ive tried all of the other medications. does anyone else experience headaches from ms? anything else that might work besids taking pain killers?

  • i don't have ms but i take atenelol for for sever migrains ..they have stoped after five years..its a high blood presure / angina pill

  • No more drugs..........

    The answer is CCSVI and the liberation therapy. I will be tested soon.

  • how did you convince your dr. ?

  • Don't be fooled by the Docs pushing drugs when they should encourage ms sufferers for ccsvi testing and then if necessary continue with Dr. Zamboni's 'Liberation Treatment'!!!!

    The truth is out and the pharmaceuticals are worried we have the answer we've been looking for!!! Their billion dollar industry is about to go up in smoke!!

  • Science is our saviour.

  • the comments are more interesting than the Video!

    lets Dr. Zamboni's Liberation Procedure for CCSVI is the cure for MS

  • Do not take the drugs for MS,have an MRI done to see if you have narrowing of the veins in the neck, spine and chest that go and come from the brain.If you do,that's your problem.Look up Dr.Zamboni.....he will win the nobel prize for possibly discovering the cure for MS.

  • yeah i saw that too.. isn't that awesome.. somthing that is so easy to do to change the lives of so many people i can't wait to get that done....

  • Comment removed

  • I have had the ultrasounds. I did not have the blockages. Oh well.. back to the standard treatments I guess.. but I am looking into FP88.

  • the ultrasound will not detect anything.You need the MRI with the dye injection.Your doctor should know this?

  • Hello Kodiak ;

    Could you possibly provide me with Dr. Zamboni's telephone contact .

    I live in canada and here they still don't believe in him and thereffore they won't prescribe MRI in those areas you mentioned .

  • Comment removed

  • @kodiak1966 Dr. Zamboni discovered a separate disease from MS with similar symptoms called CCSVI or Chronic CerebroSpinal Venous Insufficiency.. There are many conditions that mimic MS such as lupus, syphilis, lyme disease, other venous diseases, and more.. The surgical treatment cures ccsvi and not MS.. There are a large number of people who have been diagnosed with MS who have no narrowing or obstruction of the jugular, azygous, or other veins.. I agree with as few drugs as possible though..

  • @lyfeizbutadream you absolute and utter Moron! 

  • @ten10ca2 I can assure you, I am no moron..

  • @lyfeizbutadream then don't talk shit then

  • @ten10ca2 I don't believe I've said anything that can even be misconstrued as "talking shit".. what offended you??

  • If you´re roughly in the 0-5, you can actually be cured. Yes, CURED. If you´re in the 6-10, the progressive nature can be haulted completely and the relapses dramatically decreased, with the very real added possibility of making your way down the 0-10 scale. I´m not trying to induce false hopes here, i´m just letting you lot know that the defficiency can be fough effectively, instead of this symptome treatment. Stop feeding these buzzards capitalizing on symptome treatment.

  • Will it work on the advanced symptoms of MS? My cousin was diagnosed with MS after her daughter was born and it's been hard on our family.

  • What we need would be a Doctor Semmelweiss of today :(

  • Anyone who watches this, may also give some thought to the latest scientific research, as shown in the video by searching on YouTube for CCSVI.

    In Google, you can also search for "CCSVI Multiple Sclerosis" and it will show you many links including various published articles (by Dr Zamboni) in respected scientific magazines. This does NOT appear to be a scam, no one will become rich from it

  • Indeed this is very promising research and marries perfectly with 16 years of research into tilting beds for people with multiple sclerosis.

    Ironically my research began with showing impressive results with chronic venous insufficiency in the legs (varicose veins) during this research people who have vv and ms noted huge improvements with both conditions. I have posted a video atop of this thread, please view it and decide for yourself whether this FREE therapy is of use.

    Andrew K Fletcher

  • CCSVI Chronic Cerebrospinal Venous Insufficiency is the answer to MS.Stenosis in Veins are responsible for MS

  • Can you please email me more details?

  • CCSVI is the answer to MS,are you 100% sure?Big salute to everyone...

  • best treatment is marijuana.

  • Watch

    The Paleo Diet and Multiple Sclerosis (MS) Part 1/7 . Getting through all 7 videos is a bit of a pain.

    Loren Cordain Ph.D. explains very well how your diet effects your MS

    Check his MS page on his site also

  • watch?v=ooeYHGs40Yk

  • who makes this new drug, alemtuzumab, or "campath"

  • Biogen ideac. the vidio before this one in the playlist tells you the name of the pharmaceutical manufacturers. Hope it helps:)

  • nothing for primary progressive something I have asked my MP to do a talk with the government to find a cure instead. I titled my letter to him as cure or benefits? Il be honest I told him get the cure so I can work in a way some people prefer to sit back and get benefits but I don't want to I just want to work according to my qualifications.

    Does anybody else think the same too?

  • People stop being so angry and aggressive!

    Whether it is Rebif, Copaxone, Tysabri...blabla what you have to always remember is that your MS is directly related to your attitude.

    And by the way 7mumfred7, Tysabri is for people with more progressive prognoses and has tremendous side effects.

    Just be positive and look after yourself, then your MS will leave you alone.

    Good luck to us all

  • You write as if it's all s simple: "your MS will leave you alone." Ha! I wish! I have had MS for 20 years and have the most positive attitude the entire time. But now I can't walk my dog and do much physically with my kids. I've had a positive attitude for 20 years.......now I want a CURE!!

  • And I pray for all you MS sufferers that that cure is just around the corner with Dr. Paulo Zamboni's new treatment" The Liberation Treatment".

  • Im glad tysabri works for you. My comment about avonex was made because no one brought it up...

  • I'm very hopeful. I will continue to keep my eyes open for more information as this clinical trial goes further along. I would love to be able to eventually not have to do a shot 3 times a week.

  • Why dont ppl take Avonex? I have had MS since '96 and started on Avonex in 2002 and have had only 1 relapse since 2002.

  • Because you have the understand rule one in any any medication, luv. What may work for you, in this case: Avonex, may not work for others.

    I tried Avonex, turned out i was allergic to it, hence, I can not take it, and honestly, I don't want to take it when the flu-like side effects.

    I'm currently on Tysabri and have been Flare free since I started it.

    Not all people can take any one specific drug just because it works like a dream for people you can, like you.

  • I also have MS. I play football at the University of Minnesota Crookston. I started a documentary about my battle. Search Playing With MS

  • Reversing it is not a cure.The potential for it coming back still exists.Cure means gone away never coming back.This just halts it before it does to much irreversible nerve damage.And the side effects Hemophilia and Thyroid problems can be easily treated.The next stage of these drugs will be even better.

  • WHATS THE DRUG CALLED, MY DOC NEEDS TO GET ME ON DIS ASAP, im on rebif right know is it the same shit ?

  • No. It's Alemtuzumab or "Campath" and it's 70% more effective than rebif. But it is not yet licensed for general use, it is in the 3rd round of clinical trials. Don't expect to be offered it by your doctor for about another 4 years.

  • where have you heard these statistics from? im just curious because i have MS and am taking rebif, so im trying to do some research here. thanks,

  • Never mind the media hype. Do a Youtube search for "Tysabri", it is far stronger than Rebif, and is just a monthly infusion.  And Tysabri should be available for MS now in Canada.

    GOOD LUCK.

  • upcspine , find an upper cervical specific doctor. Dont take those drugs.

    Some techniques, light toggle recoil, Palmer upper cervical specific, atlas orthogonal. Also known as AIO, .and atlas orthogonality, Knee chest, Grostic, HIO, known as, Hole in one, techniques that can untwist, untilt and position atlas in a neutral position under the counterpoint of the skull. Adjustment is painless. Keep appointments. Begin exercises slowly. Sleep on back.

    No full spine or diversified

  • I suggest reading the article on this that has been publishes in the New England Journal of Medicine. The results are indeed incredible. The caution, however is that over 25% of the people on it do get thyroid disease. This can be treated with drugs also. It is the individual's choice to weigh out the risks and benefits. Personally, the risk is too high for me, but I do believe we are going in the right direction and congratulate all involved in this 'breakthrough'!

  • Amen!!!!

  • That's great, I hope it works!

    And after that, please, somebody, remember us who are not in "early stages", we want medicine too!

  • Hi - do you have SPMS with Relapses or without Relapses ?

    Somewhere I saw that Tysabri is approved for SPMS with Relapses, both in USA and UK.

    Good Luck & God Bless.

  • look, i have MS, first attack from around 7 years, Ive took by chance the black seed oil. it had done miracles in letting me get away of the permanent symptoms. Brain MRI test after 3 years of taking Black Seed Oil proves the stop of lesion growth.

    It is a natural ingredient and itll not cause any side effects.

  • great!

  • i was diagnosed with MS in january this year .. myuy mum told me about the break through last week

  • Already there is Tysabri available, it is just as good, and it stops and even reverses MS progression.

    Just search for Tysabri here on YouTube, there are plenty of MS patients who have had mirace results.

  • I highly doubt MS can be reversed. That would be considered a cure. There is no cure for MS.

  • The most serious evidence is here on YouTube or in the "Tysabri User Diaries" on the MSRC site which you can find with a google.

    Actually I see you are from Australia and I can guarentee you that you will quickly find other Australians with great benefit from Tysabri - search for it here (at least 2 on UTube that I know) or in the MSRC User Diaries.

    Good Luck in the days/months ahead.

  • They are talking about reversal of some of the damage from MS, not the disease itself.

    I've been diagnosed since '95 and started a hormone treatment last year. Since then some of my disability has reversed, so it IS possible. The body will heal given the chance.

  • What is the name of the drug?:

  • 71% is worth looking at.

  • This is amazing information.

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