A recent discovery by Dr. Zamboni in Italy has intrigued researchers at the University of Buffalo, NY, McMaster University in Hamilton, Ont., and the University of British Columbia. There is a section of an article discussing UBC’s involvement in CCSVI research below, as well as a few donation links. “A medical centre in British Columbia says it wants to become the first in the country to test the controversial theory that multiple sclerosis patients have blocked veins, preventing proper blood flow from the brain. ‘There’s a large demand for us to look into this,’ Dr. Anthony Traboulsee told CTV News. ‘Patients are very excited. We are very interested ourselves, and we want to meet the demand of our patients.’ A group of researchers at the University of British Columbia MS Clinic, part of the Vancouver Coastal Health Authority, are planning to study the theory, using a variety of imaging techniques. If it gets approval and funding, it appears to be the most comprehensive examination of this novel theory in the world. They will be studying the findings of Italian researcher Dr. Paolo Zamboni, who believes that blocked veins in the neck and chest of MS patients lead to blood drainage problems and triggers the immune responses that mark the disease. Zamboni contends that angioplasty surgery on these blocked veins, a procedure he calls the Liberation Treatment, can then open them. A preliminary study of the treatment in 65 patients showed it improved the quality of life for …
Tag: Byrne, ccsvi, disease, Kara, MS, Multiple, Research, sclerosisDottor T. Il divulgatore scientifico
Thank you for making this video, Kara. You inspire me… there is hope…we will keep fighting the battle.
All the best,
Nicole
Absolutely Brilliant!
Great video Kara. Obviously, you’re a brave and smart woman, a self-thinker as well. CCSVI is a new and marvelous discovery. Hopeful for some and scary for others as all new creations can often be. Your idea of raising funds to support that effort is an awesome way to stand up for what you believe in. I think it will get others motivated in many ways. Keep positive and strong.
Many blessings,
Nicole’s Mom
The most amazing and touch video I have ever seen.. i can just watch it over and over again..
brings tears to my eyes..
we will fight for the liberation, we will fight for each other and we will fight together as ONE!
I love the MS family… I love you all..
Omar
Amazing video, truly inspiring.
Thank you!
Benissimo! Credo che CCSVI e LDN sono bene tutte le due e insieme. Come va con LDN?
bene, ho recuperato la sensibilità sotto i piedi quindi posso stare in piedi senza appoggiarmi al muro per qualche secondo in equilibrio.
Thank you Kara!
To much money for MS ends up contraproductive making it a too juicy business for parasites.
What MS-patients now need is political activism.
Don’t donate money but be very LOUD and never give up if you don’t want to be keept ill a lifetime long!
bravo.
you are most welcome girl.
and seing this video made me feel so related you wouldn’t believe. the “if i was a girl with ms i would be her” kind of thing…
Hang in there. There is true hope for us all k?
One more thing: Mykonos should be the first place you visit when you get “liberated”
If each of us with MS, who is able to participate in an MS walk, should wear advertisements about CCSVI to bring awareness to people all over. I’m in a walk in Monticello, NY on 4/17 & I will be handing out flyers with websites that tell all about it. I’m going to look online for buttons I can have made up to advertise CCSVI so my team & I can wear them. We’ve got to band together on this!
Cara, since your vid made me cry when i first watched it i thought i d share here my satisfaction that both my jugs seem to be severely stenosed. I dont know if you have already had a doppler or whatever but if not please give it a chance to any radiologist available. It may be to obvious even for an untrained eye to miss.This goes for everyone else of course.
Good luck to all of us.
Great Video Kara, it brought tears to my eyes the first time I saw it!
I can help you Kara. Google inclined bed therapy about tilting beds for ms.
Check out my video abut Inclined bed Therapy
Also visit thisisms and read about experiences of people with ms using IBT.
No surgery required and therapy is free.
@kara98222 . This video was TRUELY inspiring. Well done. I am part of a team that is raising awareness of CCSVI (FB CCSVI Australia) and have recently had a win with the MS Society giving us space in a tent at the upcoming MS walk to promote CCSVI. Im curious as to the vid that you refer to in your post, as we need something like that going forward to help raise awareness. There was sooo much impact in that vid. Well done.
Saw my family doctor whom I deeply respect last week. I Told him about my trip to Poland with my sister for her CCSVI treatment. He was very interested and supportive. He won’t however be making any radical efforts to change the status quo.
I don’t think that my efforts were wasted though. I think that GP physicians have a certain amount of influence over medical policy. They want their patients to have improved quality of life.
OMG Kare you have, and had me in tears as I am writing this to you. This was very touching and great work. I hope that people understand what we go through and help to put an end to all of his. Best of luck.
Beautiful. Thank you. I’m doing everything I can, believe me. But thank you for the additional inspiration…
Nice video Kara. CCSVI liberation works. I’ve seen it. My sister is completely without symptoms 3 months after the liberation. She was diagnosed less than 2 years ago and was not very far progressed with MS, but she did have many symptoms.
Hang in there.
this is the most heartfelt video ive ever seen,
and now im crying like a baby.. my mother has MS, and had had it for 27 years, and i just picture her, first getting it, still being able to walk and explore like you….
i want her to walk again, i want to walk with her… and i cant.
im so glad theres help for you at this early stage, help that she didnt have when she was diagnosed.
i really hope this new treatment helps, and fast.
ive love to walk with my mother again
Thank you so much for this video! AMAZING!! We will get there!
Call CCSVI Clinic; (404)461-9560 to schedule your screening today in Fargo, ND or email us at apply@ccsviclinic.ca. Yes, get screened within the US. No waiting….find out more at ccsviclinic.ca
I wanted to say another quick thank you to everyone for their comments. They mean a lot to me and I am truly grateful for such a positive response.
Thank you for mentioning IBT
Andrew