Amazing New Treatment For (MS) Multiple Sclerosis!

[maciejwrotek]

why they dont say what is the drug name ?

[globalpreparation]

@maciejwrotek Glad to know I'm not the only one that noticed that!

[maciejwrotek]

@globalpreparation hmmm yes that is wierd....check out hydration therapy by foreydoon batmangelidj :P for multiple sclerosis, if u intrested

[louispaitson]

The drugs probably killing the undiagnosed virus/nanobacteria thats the likely real cause of MS, and then the body is healing. But using toxic chemicals will just create further problems in the longterm. There are other ways.

[0302isis]

@btilaro- would love to know more. I have just returned from Chicago and preparing to go back in Jan. To do the transplant.

[MsLucky443]

Watch out. Some of this stuff is EUGENIC MEDICATION!!!!!!!!!! It may effect not just reproductive organs but heart and liver, ect!!!!!!!!!!!

[qualisarx]

CCSVI is a proceedure that boorrows . A real all natural treatment for all types of MS is Hemp oil. Watch run from the cure to heal thy self.

[TheKatieb1991]

I'll take it!!! lol

[TheBbinca]

Um, the brain grew by 5%?? Wouldn't that hurt, like swelling?

[mcoolle]

if this is cladribine its not treatment for ms its calling for cancer

[perryhtc]

Also, too many vaccine using Thimerosal (A Mercury compound) as a preservative.

[perryhtc]

How many people know that chronic Mercury poisoning cause many disease including Multiple Sclerosis? Do you know Dental Amalgam have 50% Mercury and non-stop leaking Mercury vapor? Do you know Sweden have banned the use of Dental Amalgam in their country already.

[joofoodani]

I've had MS for 13 years and it is yet to progress to any seriously limiting degree. My personal recommendation is to try whatever you believe is worth trying, but place highest priority on nutrition & lifestyle. Eat unprocessed, real-food, vegetarian diet (with seafood). Lots of gentle exercise. Relax - meditation, music, art, whatever will lower yr stress. Lots of scientific backing 4 the simple things. Doctors only know what they've been taught, and this is not it. Best wishes my friends x

[kawah420]

hi dear, where do you get this drug?

[mooseasaurusrex]

Big Pharma has close ties to 'government'.

They just don't care.

[N6NZE]

Richard Burt rebuilds the immune system of multiple-sclerosis patients using their own stem cells. Northwestern University researchers, led by Richard Burt, used immunosuppressant drugs to destroy the immune systems of 21 early-stage MS patients and then reconstructed their immune systems with the patients own stem cells. To date Jan. Feb. 2011: 75 % of the patients have experienced an improvement in their condition. They face government restrictions and lack of funds.

[btilaro]

@N6NZE

I had the procedure at Northwestern University in July of 2007. Dr. Burt was my doctor. My EDSS score was 3.5 and progressing rapidly. Since the procedure, my EDSS scores have steadily declined to 0.5 in Sept. of 2010. I still feel some neurological effects, but it is a tremendous improvement from 2007. Unfortunately, you are correct about restrictions and funding. Big Pharma won't fund it, because there is no new drug to market.

[btilaro]

@N6NZE

-cont'd... The same type of procedure has been done for leukemia, and certain other cancers. It's the application of this type of procedure to treat Autoimmune diseases that has gotten little support, despite the impressive success rate. In the marketplace, there is no return on investment. It is an expensive procedure requiring two months of treatment. So many health insurance companies will not pay, as they consider it to be "experimental".

[seekirk]

Omega 3s, low saturated-fat diet (<10g/day), vitamin D (5000IU/day), and a multivitamin. Takes time to regenerate the brain with the right fat (15 weeks to 2 years), but it will help build myelin and reduce inflammation in the long run.

[seekirk]

High Saturated Fat diet -> young age (active thymus) -> exposure to herpesviridea or other neurovirus -> high permeability of BBB caused by poor, brittle structure from high saturated fat diet, low levels of vitamin D -> T cells in CNS -> sensitization of T Cells -> later onset of MS -> recovery -> anything that can cause a proper situation for episodes (stress, Epstein Barr, etc.) -> disability

[deepan66]

What about the many MS sufferers that do not have blockages or stenosis in their veins. I think Zamboni's deal is good for some, but if one has MS and no CCSVI ALL THE BLIND FAITH IN THE WORLD WONT HELP.

[AWDESIGNS8]

@deepan66 mind body and soul . you have to take god in your life . if its mind over matter thats ok to . check out dr nemeh he is a healer he is a man of god. love april

[ajm180561]

Thing is that every study that has been done shows that "liberation" doesn't work. Campath is the most effective treatment. Liberation is the emperors new clothes.

[DINGLEtheBERRY]

drugs...how sad. lies ...how sad. Dr. Zamboni is the man.

[omv08]

XMRV XMRV XMRV XMRV

[AWDESIGNS8]

WELL I WATCHED THIS WHAT IS TH E NAME OF THE DRUG

[bockydo]

@AWDESIGNS8 Marijuana , dont trust this bull shit .

[AWDESIGNS8]

@bockydo what ever works for you do i'm not knocking it i just know it cost alot of money like stem cell 30.000 just dont give hope people dont have insurance

[AmTickProductions]

beware of ccsvi. placebo...  trust me!

[guitarobsessed85]

@AmTickProductions I don't think it's placebo. What I think is that it helps the body to clear immune cells from the brain in people who have the issue. Not all MS patients have CCSVI. I don't think it's a cure by any means but I you can't argue with the statistics. It helps some, but not all ms patients.

[AmTickProductions]

@guitarobsessed85 i travelled all over the US with dake as my guide. after a faulty mrv, i became an absolute believer in zambonis theory. found a neurorad to do the lib treatment and during the venogram found out that my mrv was not accurate. withthe catheter in my head, the doc says, "_____, theres really no need to balloon anything. you look like a normal patient to me..."

so, having riden the emotional roller coaster of ccsvi, and getting negative results, i am a bit jaded with ccsvi...

[AmTickProductions]

@AmTickProductions BUT, i was great to feel HOPE for the 5 months that i was wrapped up in the ccsvi thing. it was nice to not feel like dying...

[guitarobsessed85]

@AmTickProductions Well I don't believe every patient with MS has CCSVI to be honest. I'm not an MS patient, but I am someone interested in curing this disease. I am a biologist and I am trying to get back into school to complete a doctoral program so I can help search for a cure. I have done a lot of research on this disease. I hope that you ask your doctor about simvastatin.

[armysandy]

My wife and my son have MS - it disgusts me that they cannot get the Zamboni treatment if they want it. We do not have the finances to go across the ocean for help.

[guitarobsessed85]

@armysandy Look up the effects of simvastatin on ms.

[suicide871]

name of the druG?:S

[MIGsCT]

marijuana.

[Mnkv1]

thats God's Help

[salonwithapeal]

is this low dose naltrexone?

[nominnaw]

What is the name of the drug??

[GreatAuntCayce]

Will The Liberation Treatment be available in America any time soon? My cousin Lynn was diagnosed with MS when her 6 year old daughter Chloe was 6 weeks old. Lynn's taken a turn for the worst. She's in the Hospital and they're going to put her in Rehab because she can't feed herself anymore.

[search4acure]

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

[gphx]

This drug is promising with a 71% improvement. However, studies have shown supplementation with vitamin D can reduce relapses by up to 50%. Whatever therapy you do or do not use please consider checking and supplementing vitamin D. Cheap, easy, may will likely improve upon what is already working for you.

[TheWholesailor]

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?

[lshandikful]

@TheWholesailor Have you tried low power laser therapy?Have you been tested for possibility of chronic viral infection?My close co- worker has been diagnosed with MS and live with headaches.Some options has been taken to improve her quality of life.

[gekiryudojo]

CCSVI  is the CURE because it is the cause

[gphx]

@gekiryudojo Further tests need to be done and recurrence of venous insufficiency after treatment needs to be explained.

[gekiryudojo]

I shall Explain it for you then! they have done loads of work, and we know that the Veins need to be opened twice sometimes, that is because they are used to being in that collapse state, if you are going to be a neh sayer just don't get it done, I'm sure someone would take your place!

[gphx]

All I'm saying is any therapy needs to go through extensive double blind trials to become an accepted therapy. I'm not saying CCSVI will or will not, just that it needs to be done. Anything else is emotion not medicine. There is nothing in the way of being a 'neh sayer' in mentioning accepted protocols. If people want CCSVI to be accepted then that should be the goal.

[gekiryudojo]

say what you want Angioplasty is done every day around the world as for emotions If I had the Kit I would do it Myself as for double Blind where are enough Blind people around thanks,

Im going to get it done as it wont kill you but MS will so good luck waiting for everyone else to get their Ass in gear :)

[SagDec15]

no it's not

[TheSpankymonkey]

@gekiryudojo - Not true at all. Shouting nonsense like that just helps perpetuate it.

[gekiryudojo]

@TheSpankymonkey You retard you have no idea what you are blabbing on about. Mr stupid name

[TheSpankymonkey]

@gekiryudojo - "You retard you have no idea what you are blabbing on about. Mr stupid name" - Indeed, family of consultant surgeons, pathologists, brain surgeons, neurologists, physiotherapists. Did i forget to mention that i suffer from type 2 MS and my father with type 1, neither of which are treatable with this method of treatment. Care to tell me what the cause of MS is again without sounding like a fucking idiot? Much irony to be found in your last comment calling me a retard.

[angelusa73]

I knew about this medicine and I have good hopes for this one too!

[denabach]

@angelusa73 Don't waste your time on drugs, Look up Dr. Paulo Zamboni's treatment, His theory is based on blocked blood vessels to the brain. Please look up the " The Liberation Treatment " of Dr. Zamboni. You won't be disappointed.

[angelusa73]

Dear friend,

I am aware about this too. In fact, if you go on my page, I posted a video that I did yesterday where I talk about this!

I am from Italy and I trust and respect anyone that will prove that we don't need drugs to get better every time!

Thank you for writing me back! I am very excited about this!

Hugs,

Angela

[kodiak1966]

@denabach I wish the liberation treatment was available to all,sadly,health care will not cover the teasts..The drug companies know they will lose billions in MS drug revenues if this proves to be true.They are already paying off doctors to say zamboni is a quack.

[rooflee]

@kodiak1966 God I hope you're right. I really do. I hope Zambonis findings are correct.

[jerseygrl5]

@denabach The pharmaceutical companies have the power and they don't want a cure. They are raking in the cash on MS. If CCSVI was approved as a cure, big pharma would lose billions.

[vinny5389]

@jerseygrl5 100% agree with you!

[jerseygrl5]

@vinny5389 Thanks Vinny, time for more people to wake up!

[AWDESIGNS8]

@jerseygrl5 iagree with you but i would hope they have a heart and dont think that . i want a cure for ms . to many people have this ms or kids too with immune disorders

[561400]

@jerseygrl5 its an amazing surgery yes but this is coming from an MS patient who has had the surgery & knows other who did to this IS NOT a cure, so everyone please stop posting this as a cure.

[AWDESIGNS8]

@denabach hey that sounds good but i dont have insurance maybe they dont have it in the usa he sounds like a great doctor come to cleveland ohio i have ms i'll try what he thinks is a cure. i'm sure any one with ms would if it wasnr so expence.

[globalpreparation]

@denabach I was totally anti-drug until my symptoms, especially my pain and function in life became unbearable. I hate taking them, but my improvement in life has increased so much, I now worship pharma science. Life w/0 so much pain is more bearable!

There is NO CURE for MS, no diet or herb regimen will cure you, believe me, I've tried! I'm tired of people saying they cured themselves of MS, you're just not in a relapse people, you're not CURED!

[parttygnome]

Why is this treatment not recommended for advanced MS patients?

FMartin

[cujojila01]

you know during my relapse i will just be sitting up an fall asleep is one of the things that will happen i did not put it with ms until you brougt it up in the vido when you said it happend when you said it was one of your sideeffect when you were beging ms thanks

[Venom7707]

i would go for stem cells not this crap with side effects

[kobidobidog]

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

[Entropy56]

alemtuzumaboughington

[dmplaura]

The name of the drug is Alemtuzmab.

[lunalas]

what is the name of this medicine? is it available in the us? my best friend has ms. thanks.