Multiple Sclerosis: Could Dr. Zamboni's Liberation Procedure for CCSVI cure MS? Part 2

[onehundredvoices100]

Why not ask Dr Zamboni's MS patients, who he treated for venous insufficiency.

The majority of them, some within hours, started walking more normally, with either a complete or major reduction, of their MS symptoms. When neck or chest veins are blocked (stenosis) the blood from the brain, does not drain properly. The pressure pushes iron and white blood cells, into the brain, causing MS symptoms. White blood cells then eat the myelin coating on the brain's nerve cells.

[robert80taylor]

A group of Canadian patients just back from Noble have reported similar results. “I can actually see what I thought were long-dead muscles forming in my feet” said Larry Vermeersch of Kenora, Ontario. “My balance is back and I’m walking without a cane. I’m a pretty hard guy to convince, but getting these two procedures together has made me a believer. I’m looking forward to the physio ahead because I can feel everything coming back.” Log on to ccsviclinic. ca for more information.

[robert80taylor]

“I feel I am completely cured” says Ms. Gianopoulos, “my symptoms have disappeared and I have a recovery of many functions, notably my balance and my muscle strength is all coming (back). Even after six months, I feel like there are good changes happening almost every day. Before, my biggest fear was that the changes wouldn’t (hold). I don’t even worry about having a relapse anymore”. Log on to ccsviclinic. ca for more information.

[mztracyr]

Being 46 and PPMS and in a wheel-chariot, I would try this in a hot second. I see this an amazing 'theory'.

Sadly, the pharmaceuticals do not want to see this or for it to be done. They would lose too much money. Sad...but so very true.

To get this done I would anywhere in the world.

I want to be a good mommy and wife again!!

Blessings!

[AWDESIGNS8]

@mztracyr the cleveland clinic here in cleveland ohio dr fox is doing research on this so maybe you can call down there. love april

[irishbear76]

@AWDESIGNS8

Thank you April.

The CLeveland CLinic is world reknowned for their progressive work with multiiple diseases.

[AWDESIGNS8]

@AWDESIGNS8 they are doing research on that. so at least i got back up mellin center here cleveland clinic i go too thanks i'm glad things are working out for you god is with you and your family love ya

[comeinmykitchen]

Fuck Big Pharma!!!...Fucking Criminal's!!!

[marc9647]

OK I saw the video on the liberation treatement and all. I am a women of 69 and i have MS since 7 years.and I can ardly walk and close to a wheel chair . I am willing to go to anywhre to get the treatment ,but i dont know where to write or phonear what, Can you gave me an e mail adresse that i cen use .thank Margelaine

[irishbear76]

@marc9647

Yes. You can find the contact information for everyone doing the procedure by going to the thisisms website your web address window.

You will be able to choose from any you want.

Dr; Marian Simka in Poland has the most experience doing it.

Please inform yourself about risks and make an informed decision before making any medical decision.

Good luck and God bless.

[omexmc80]

Just watched the video's on CCSVI again.

the grass root videos, without these i would have never known about CCSVI as soon as i did...

Thanx Bro

Omar

[scotia1962]

Well done for this. MS Society UK is doing nothing about this and that pisses me off!

[irishbear76]

There is a CCSVI group in the UK. Check out HKintheUK for details.

The MS Society has been very quite, but they are in cahoots with Big Pharma for funding.

Blessings and warm regards.

Mark

[irishbear76]

Scotia.

That is the ancient name for Ireland, I do believe. It predates Erin?

[scotia1962]

Scotia means Scotland! As in Nova Scotia (New Scotland)

[irishbear76]

@scotia1962

that is right. I get confused because my family is Scots-Irish. The family name is Scott. This is not my last name but was my grandmum's maiden name. She said the family started out in Ireland and then migrated to the border colonies in 900 A.D.

I know the Latin word for the Scots was Scoti which they called the "blue ones"

I also never understood why Scotland was referred to as Caledonia in some poetry either.

Anyway. I am Scottish and Irish so there is my confusion.

Thanks

[MrMarkafisher]

Here's hoping common sense prevails.

[irishbear76]

@MrMarkafisher \

cheers to that. (he drinks and invisible beer)

[trontafrog]

Thank you!! Keeping working. I can't wait till we all get the cure. I will be contacting everyone. Let's get this done!

[irishbear76]

@trontafrog

Keep the faith and feel the love.

That is what the CCSVI in the UK says.

[trontafrog]

I had the same thing happened to be. My doctor says that is not the way she understands the disease. She totally dismissed it. But she doesn't live with MS. I don't care if it's hard for people to change the way they understand MS. Just let us try Dr. Zamboni's treatment! I

[MSconquer]

I went to see an MS specialist today. I discussed with her the Dr. Zamboni's Liberation procedure and she completely dismissed it. She's aware of it but doesn't buy it. I'm not surprised though..Makes me wonder if they actually WANT a cure to this disease.

[irishbear76]

My inner conspiracy theorist is going crazy with this anti-Zamboni nonsense.

This is the biggest breakthrough in MS research and no one will touch it.

YOu see there are no fundraisers when the disease can be dealt with cut and dry.

There are also less need for Big Pharma in complete remission.

[msj4d3]

@MSconquer

Same with my neurologist. I asked her what her thoughts were on this, and of course she gave me the "textbook answer". I myself am on Copaxone..I threw out some numbers to see. I estimated that 250,000 are on it. Every month they charge my insurance $6,500. Do the math. Of course there is "no cure".

[msj4d3]

@MSconquer

They really don't want to. Which medicine are you on? Did you read my last reply to your comment? If you had BILLIONS of dollars deposited into your bank account every month, and the catch was knowing that tons of people in the world suffer/die because of it..I don't think the "average joe/jane" would care eh?..

[MSconquer]

@msj4d3 I'm on Copaxone also My insurance is billed $3,500 monthly. I don't care what they say, I have faith in it. We have to take control of our bodies on not rely on medical opinion. After all, we are the one's suffering from it.

[lynne4cobis]

Good for you Ib! Don't know if I would have been so longsuffering !

[theinsomniac4life]

Not the Nobel "Peace" Prize - that is for Peace. Just the Nobel Prize, for medicine.

[irishbear76]

@theinsomniac4life

I just call it that.

Whether it is in physics, medicine, et al.

It is just what I say and will always continue to say it.

Nobel Peace Prize. Alfred Nobel invented dynamite and felt bad about how it was used in war et set up the foundation.

Not really sure what the point is in correcting me, but okay.

[theinsomniac4life]

The point is that if you want people to take you seriously, being precise in language is important. I'm not knowledgeable enough to judge your comments on MS and this potential treatment, but when I see that you don't seem to understand that there are separate awards for Peace, for Medicine, for Physics, etc., it leaves me skeptical about the other things you are saying. You hurt your credibility by saying "Nobel Peace Prize in Medicine" - no such award exists. It's Peace, or Medicine, not both.

[irishbear76]

It is not my credibility that I am making these videos to establish. And as far as prizes are concerned if this thing works it will be all the prize Dr. Z or anyone else would care about.

The credibility of Dr. Zamboni is really all I care about and making sure that the word gets out that there has been a paradigm shift in the pathogenesis of multiple sclerosis.

I am quite concerned that alot of MS groups are squashing this and neuros are telling their patients not to get tested

take care

M

[rsamberg]

I asked the nurse at my neurologist's office today if they have been following news about the Liberation procedure. She said yes, and that a lot of people have been calling the office about it. She said that the doctor does not believe this has anything to do with MS. Typical neurologist answer. If we find a cure for diseases such as MS, it will put them out of business. I'm fed up!

[irishbear76]

I give them a break. They have just been told that there is a possiblilty that the stand they have had on MS for 20+ years is wrong.

It will take alot of proof to turn them away from what they have been taught.

[lynne4cobis]

Just read on Facebook that the results for the deblocking surgery were not so good for PPMS andSPMS after 18 months or so and the cost seems pretty prohibitive for those on Disability allowance. We in Scotland have just placed petitions before the British and Scottish governments to get LDN on the NHS. I pay privately to get it to strengthen my immune system but lots of folks cant afford that either. What about poor folk. They deserve to be well!

[irishbear76]

I know. It just isn't fair.

[lynne4cobis]

Hey Ib you're doing great work. There's lots on Facebook now, but this seems less angry more helpful and especially about what we can do now. I was told to take or massage in extract of horse- chestnut when I had very sore varicose veins when I was pregnant with my fourth baby! It worked and my legs have no bumps now and only ache when I wear tight high socks. Is this the same horse/ chestnut I need for my MSy venous probs?

[irishbear76]

In theory, I DO BELIEVE it can give our poor jugulars and azygous veins a break.

Yes, it is the very same horse chestnut.

[trithers]

Hi Mark,

And thank you for making these videos to raise awareness. I learned about CCSVI mid-September and, like most MS'ers, I was elated. It was hard early on because I was so excited, and not many would pay attention because of all the false MS claims out there.

Thanks for the information about iron chelators. I had no idea about the horse chestnut. I've already inclined my bed and spend hours searching for more information each day. Keep up the great work!

Jen

[irishbear76]

Thanks Jen.

Keep watching the vids I will keep looking into things.

I have been swamped at work, but once I pay the bills I can talk about the ills.LOL

[mudman38104]

I'm kinda wowed right now. Is this making too much to me?

[lameshe24]

I am totally feeling the same way as you. I'm 21 and both myself and my mom have been diagnosed just this year. It's been a tough ride, but this is soooo exciting! I know those exact tears of joy. It's overwhelming. Noone can understand the feeling unless you have MS. I live up in Canada and I hope to God they figure this out and start doing this procedure. For now, I'm interested to see what my veins look like in my neck...so curious

[Chirinium]

I haven't read all the comments, so I don't know if the question has been asked already but:

With the jugular veins clogged or tight, would one feel local symptoms such as tension around the neck area or dizziness if the head is raised backwards?

And would there be you think some kind of massage or stretching that could help relax or release the vein?

[marykaygwinn]

Wonderful video! You are right we have to put pressure on... the ms society in Canada has been overwhelmed with comments from ms patients wanting funding for more research.

Power in numbers!!!

[irishbear76]

Power in numbers, indeed.

It is great to see so many MS'ers fighting back.

A little fire in the old belly, AYE!!!

[2011ruby]

Great Man!!!

I hope that all this can conduct to the final solution for everybody of us who's soffering for this disease!!!

[irishbear76]

Amen to that!!!

[rocketav8r]

Your research is like mine. I'm just as excited, haven't slept, ect. Check out my video. Thats me on wcny interview talking about my MS. Thanks for sharing your excitement. Take care!

[irishbear76]

You take care.

I loved the interview.

Please see my video there is an MJ one or two in there.

Take care, man

Mark

[trithers]

Great interview Joe... it's people like you that will elicit change in laws that need SERIOUS overhaul. Thanks for standing up and doing what's right!

[akfhome27]

Oh I almost forgot, thank you for mentioning the horse chestnuts! That was going to be my next step today what can I take in the meantime. Also I'm happy I am subscribing to you. I've watched a couple of your vids and I'm so glad to meet a proactive positive person who has MS. Thank you.

[irishbear76]

You are welcome.

I guess I should have read this first YOU SUBBED.

[akfhome27]

I found out about this yesterday, I have done nothing but research. I am as giddy as can be like you. I'm trying to stay grounded but everything, everything is pointing to this as the reason of MS. I can't stop smiling. I am so glad you admitted to crying, because literally I sat here today and burst into tears. For the 1st time I felt hope. I felt like maybe just maybe one day I can play with my daughter. WE MUST demand them to acknowledge this treatment!

[irishbear76]

I must say that I am right where you are.

Giddy. Excited and hopeful to the point of tears yet cautious with my optimism.

This is the breakthrough I have waited for.

I can reconcile ALL OF MY PERSONAL research with this.

I have made 4 videos on this subject alone so please subscribe to get them.

Mark

[Xenderdrax]

From memory Viagra was intended for the heart before they found Other uses for it. I realize this is simplistic, please excuse my ignorance. Maybe high but safe doses of prescribed caffeine medications may also be beneficial. I suffered from 19 severe migraines in 20 days, my physician prescribed heart plus high dose caffeine medications to help with this and it may also work with MS.

[irishbear76]

It is funny that you should mention Viagra.

It was initially used for pulmonary hypertension. The stenosis of these veins in CCVSI would be very similar to that process.

Interesting.

[Xenderdrax]

This maybe the break through that suffers have been looking for. Thinking on Zambonis research, If the blood flow is restricted, wouldnt a heart medication to expand the blood vessels be beneficial.

[irishbear76]

In a nutshell, certain medications would work.

HOWEVER.

it is just a mild treatment.

This procedure is offering complete relief.

An analogy, you can have a rotten tooth and take vicodin and it will give you relief for awhile.

The tooth has got to go!!!!!!

I want this procedure because it will give real relief from symptoms.

Take care.

Mark

[omexmc80]

Hey, first thank you for that amazing news.. wow u got me very happy and excited.. i have forwarded your link to all my friends with MS and also my MS nurse as i havn't heard anyone mention anything about this in the UK, even though i went to see my neuro a few days ago. i had tears of joy watching the vid... well again, thanx Mark and happy thanx giving..

[irishbear76]

Yes this is exciting news!!!

This procedure needs to get out to the people.

Happy thanksgiving to you!!!!

Mark

[gekiryudojo]

I have just been in contact on Phone to a News team member

from the BBC I asked them Why is this Story not being reported! I said it is going like wild fare on the net! 2000,000 suffer from this and they have a breakthrough! I told them about CCSVI and about Dr Zamboni they are checking the story out and they are getting back to me.

they were curious but tentative a but they sounded more interested when I told them the MS Society had posted info on it! more later!

[irishbear76]

Keep informing!!!!!!!

People will not be able to NOT hear about this.

I want CCSVI as one of the most popular searches on yahoo and Google!!!!!!!

Mark

[woodphoto21]

Any news from the news team?

[eddysacat]

I've had some time to think about this. There is no way that the drug companies will get behind this. ZERO chance. I'm on welfare and there is no way that they will pay for any of this....My MS isn't bad right now so hopefully I'll be able to get this treatment one day. Dr. Zamboni better watch out. I wouldn't be surprised if Teva Neuroscience send a hit squad to knock him off. It's all about money. Everything!

[irishbear76]

I know.

They cannot silence the millions of MS sufferers who we are going to make sure hear about this.

THe research is published. The cat is out of the bag.

It is only a matter of time.

The only problem I have, is how many people have to sufferer, progress in illness, and succumb to illness in the meantime.

Mark

[gekiryudojo]

The MS society in the UK has posted their findings on this and

are very serious about it the balloon is going up folks!

[irishbear76]

LOOK WHAT YOU DID, MATE!!!!!!!

THey just needed to hear about it!!!!

I am convinced that this procedure is the beginning of the END OF MS!!!

Dr. Zamboni's findings are more important than words can convey.

Take good care, brother.

Mark

[notapplicable66]

Something tells me we are born with this. As we get older it gets worse. And of course all of us are on a different time frame of when it decides to fully raise it's ugly head. What causes it? Maybe it's simply a lack of vitamin D throughout childhood.

[MSVlogSupport]

The thing that has us here in the US is the FDA and big drug companies.

They stand to loose a lot of money if this works and that is the problem, they have so much control.

We don't CURE ANYTHING we manage it. keep you alive by pushing more and more drugs and they make more and more money.

Hate to be the downer but this the battle I see coming and lobbist for the drug companies are going to be all over this.

[haiqin]

I had the same thought myself; that it might be a battle to make this protocol if it turns out to work. On the other hand, if it works, people will find a way to get access to it. Hopefully the global nature of travel will require the US to compete with the rest of the world, once a cure exists.

[irishbear76]

Excellent point!

[MSconquer]

You took the words right out of my mouth. I agree with you totally.

[irishbear76]

Thanks man!

[notapplicable66]

They can say whatever they want evidence doesn't lie. If everyone with MS has this wrong with them. They will not be able to deny that there is a connection!! And if other people who are healthy don't have this, then it's pretty clear that we need to get operated on to get this fixed.

[eddysacat]

Damn,

I'm getting excited and I'm only into the 1st minute of the 2nd video.

My name's Andy and I live in Phoenix, Arizona. I grew up in Southern California though and spent a lot of time on the beach (no vitamen D deficiency for me). I had Herpes simplex 6 as a child though (rubiollla). Jeez, you're a smart guy. I'd love the opportunity to correspond with you.

[gekiryudojo]

I Slept very well last night :) At the moment I have 22 windows up on my browser! I have this morning contacted my neurologist, made an appointment with my Doctor and spread this with my 1350 subscribers and more on the net I'm this job man!

[gekiryudojo]

I'm on this job I meant! and very excited

[irishbear76]

You are a beast of information distribution!!!!!!!!!!!!!!

Dude, I thank you so very much

Now on to YOUR VIDEO

I CAN"T WAIT!!!!!

Mark

[haiqin]

Thanks so much for this video! I am always wary of cures, but it seems that you have done the research, and this is something I can ask my doctor about. I am very excited, too, listening to your video. Excited, and impatient! :)

[irishbear76]

I am wary as well.

I actually made a video about witchdoctors.

The only way this is not real is if the information has been fabricated as a hoax, but they would have implicated academia because they are using the very same research.

I do not agree with surgery and I would have this done TOMORROW!!!!!

[haiqin]

I feel the same way. I know I have to wait and research more about it, but I'm saving up my money just in case it works, and it's possible. :)

I should look up your video about witch doctors.

[irishbear76]

Please research this information.

It is always smart to save some dough. LOL.

Hopefully, it will be a covered procedure.

(It will probably be marketed under a trade name so the drug companies get a kick back.

Haha

Mark

[ThePennygirl]

MY DOC, was on this info last visit, she knew of this stuff!

[irishbear76]

IT will be difficult. They were trained by pharmaceutical companies.

This will meet resistance I am sure, but MS'ers will unite to make this available.

Mark

[ThePennygirl]

Thought I Was crazy thinking of this! thank you Mark!

[irishbear76]

CRAZY LIKE A FOX!!!!!

This seems to be the real deal sweetheart and I have never had more hope.

Mark

[bluejaysification]

We have to get the message out there. Spread the word. This is amazing.

[irishbear76]

YOU ARE RIGHT!!!

Big Pharma will fight it but the truth will set us free.

I need to see this paper.

The preliminary reports are staggering.

WE ARE THE RESISTANCE to the current way of handling MS. The time has come to do what is right. This has been hidden in plain sight and finally the masses are getting this info., It is always the simplest thing you know.

[tazscott14]

Hi Mark, Thank you for the videos. You have me so very excited! I appreciate people like you!

Thanks, Bill

[irishbear76]

Bill,

Thank you for your kind words!!

Do not forget to push your doctors to look into this.

Mark

[kezzcass]

:-D Good work friend! If this is really it... it has got to be fast! I will be contacting MS Australia. Every month MS progresses in me and if it is just some pesky vein interfering I want to know today! Now I am feeling impatient! I hope, pray that this works and can lead to preventing people from ever suffering the symptoms of MS. Bless you mate, Kerri xo

[irishbear76]

I sure hope this treatment gets made available for Aussies and Americans alike.

Prevention, Treatment, DIagnosis.

This research will help in all these areas.

We just have to override greater than 15 years of conditioning that a virus causes this autoimmunity.

Take care.

Mark

[thebackporchman]

Great video! I saw Dr. Zamboni on the news, and it totally blew my mind... you just can't argue with the evidence! I'm with you. It may, unfortunately, take a while to catch on, but I believe that this is a cure.

[irishbear76]

Yup.

It is the best answer for what happens to cause MS. It is very cool!!!!!!!!!

The evidence and logic is irrefutable.

Take care,

Mark

[gekiryudojo]

thanks for this Mate, I has not heard of this and I will start looking into it tomorrow Thank You and good health :)

p.s. I have had MS since 1995 and Have been lucky so far

see me in a video with my kid (latest vid)

[notapplicable66]

Let's hope that this is it!!! And we're about to bitch slap MS once and for all!!! Then we can all say, "Now we are free!"

[irishbear76]

Ding dong. The witch is DEAD!!!!!

[notapplicable66]

Did you spell that right? lol!!!!

[irishbear76]

I implore you to forgive me.

THE BITCH IS DEAD!!!!LOL

[notapplicable66]

next time use spell check! LOL!!!!!

[notapplicable66]

Inflammation interferes with the electrical signals. Take the inflammation away then the electrical signals can get through again. If the cause of the inflammation is T-cells attacking the iron, then this will stop once you open up a narrowed or clogged artery. Ms societies and Pharmaceutical companies are against all this because they stand to lose Billions of dollars.

[irishbear76]

YOu are correct.

The resistance will come from Big Pharma.

No money in cures only in treatments.

MS patients will make this procedure available. We will not shut up or lay down.

Mark

[angelusa73]

Dear Mark,

I would like to repeat and say to everyone that the MS Society in Canada is supporting Zamboni's research and he is going to support scientists that will want to study this. I am not sure how long it will take before the US and the MS Society will open up to this idea and you are right when you say that we should push our doctors believe this and help support this.

Thanks, Mark! Greato job! :)

Hugs,

Angela

[irishbear76]

Absolutely.

We must remember that pharmaceutical compaines are pivotal in a lot of training for young doctors and they make sure their interests are taken care of.

This is no fault of the doctors. Just the system.

God bless.

Mark

[lovingfatalist]

Vern Beachy said it the best:

Great researching - I'm impressed!

I'll follow this with interest,

And ask my neurologist.

T x

[irishbear76]

Stay with it if you meet resistance.

It is hard to learn that DOWN is the new UP (sorry I had to steal a Radiohead title at some point)LOL

Take care and keep playing your instruments!!!

mark

[vbeachy]

Way to go Mark;

I do quite a bit of research on MS myself, but, clearly not as extensive as you. I totally and completely agree with you that this may be the step and discovery that results in a cure for MS.

It all fits as you so eloquently stated in these two videos. I will continue to do research on my own, as willothers for themselves too, but I know I will see more informative videos from Irishbear76. You are a great MS reporter and researcher, Mark. Keep up the great work!

[irishbear76]

Thanks man.

you are a great writer and a friend.

your MS videos are great to watch you have that "radio voice" which makes your vids very easy to watch.

I could use some of your skill to get this stuff out of my head without confusing the hell out of people LOL.

Take care buddy

God bless,

Mark

[vbeachy]

Thanks Mark. You are a great friend too. You seem to be very skillful in doing your videos, especially the last two about CCSVI. In fact I linked to them on my MS page on my website. Take care and have a Happy Thanksgiving! God bless.

Vern