Multiple Sclerosis: CCSVI and the LIberation procedure; Advocacy for Paolo Zamboni

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Uploaded by on Dec 7, 2009

URGENT:
IF YOU OR SOMEONE YOU LOVE SUFFERS FROM MS, IT IS IMPORTANT TO RESEARCH AND INFORM OTHERS OF THE LIBERATION PROCEDURE AND A DISEASE CALLED CHRONIC CEREBROSPINAL VENOUS INSUFFICIENCY.
THIS DISEASE SHOWS STRONG EMPIRICAL EVIDENCE TO CAUSE THE DESTRUCTIVE DISEASE KNOWN AS MS.
THE MS COMMUNITY MUST GET THE WORD OUT VIA YOUTUBE, FACEBOOK. MYSPACE, GOOGLE, BLOGSPOT, SKYPE WHATEVER FORM OF MULTIMEDIA NETWORKING POSSIBLE.
IF THE MASSES ARE MADE AWARE OF THIS CONDITION AND TREATMENT I BELIEVE MS CAN BE STOPPED. ALTHOUGH PERMANENT DAMAGE CANNOT BE REVERSED AT THIS TIME, MANY PEOPLE CAN BE SPARED A LIFE OF DISABLITY AND MANY OTHERS CAN BE GIVEN BACK FUNCTIONS THAT THEY THOUGHT MAY BE GONE FOREVER.
THIS IS THE MOST IMPORTANT THING ANY MS SUFFERER CAN DO TOWARD ENDING THIS DARK AND HORRIBLE DISEASE.
I find myself thinking of a line from Muse's wonderful song "Apocalypse, Please"- DECLARE THIS AN EMERGENCY. LET'S SPREAD A SENSE OF URGENCY AND PULL US THROUGH

LOVE,
MARK

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Uploader Comments (irishbear76)

  • So what caused the venus issue then? I think the reason some of the veins are closing back up again is because the underlying chronic infection isn't being addressed. Addressed the infection, it eliminates the autoimmune and the vein will stay open after the treatment. thats my take anyway

  • @thane17

    There was a conference of vascular specialists at Georgetown University that concluded CCSVI is present from birth or congenital.

    That was the consensus report from the world's leading vascular studs.

    It makes me think that many of us renarrow simply because the veins do not know any more than being closed because they have been that way our whole lives.

    It has changed my mind about stenting because the Lib Pro is not guaranteed to KEEP THEM OPEN.

    I think efficacy for stents is >

  • I have RR MS and have an appointment in Poland in September for CCSVI examination. I have noticed lately when i take my Betaferon injections that next day MS bad. In Ireland there is a high number of persons with MS.

    A disgrace that i have to travel to another country for CCSVI and 100% agree pharmacutal companies behind any negative press concerning advancements of CCSVI.

    How individuals sleep knowing that they are enchancing suffering.

  • @MACGWEEDORE

    I agree that the bastards should lose sleep for what they are doing to suppress this procedure.

    I am of Scottish and Irish descent (Scott/Crowe) two nations particularly hard hit by MS.

    I am telling you this with the greatest confidence.

    Because you are relapsing-remitting getting this procedure is going to decide how the rest of your life goes. You are doing the best thing possible to make sure that MS doesn't progress to being totally debilitating.

    Slainte,

    Mark

  • where is how much pharmaceut company prpfit per years, please....

  • @milorad173

    8.8 billion dollars on MS drugs alone!!!!!!!

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  • Wish to bring forth this case of young lady in New Delhi having MS syndrome and it is getting worse, unless some proper cure is found. Also praying with hope that some good soul would volunteer and enable for her treatment of MS Syndrome.

  • Other recent MS patients who have had Autologous Stem Cell Transplantation (ASCT), or stem cell therapy have posted videos and comments on YouTube v=jFQr2eqm3Cg. Log on to ccsviclinic. ca for more information.

  • “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.

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