Martin from MS-CCSVI-UK.org on Sky News talking about CCSVI

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Uploaded by on Feb 10, 2010

www.ms-ccsvi-uk.org
committed to raising awareness of CCSVI in the UK

please sign our petition to bring CCSVI research into the UK:
http://petitions.number10.gov.uk/ccsvinow

thank you

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Top Comments

  • The evidence really ISN'T there?!? That piece of $h!t mother fu(ker..

  • Good job for uploading this very COOL and VERY BRITISH TV spot about CCSVI.

    I am proud of you buddy.

    Mark

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All Comments (22)

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  • Dr,Doug Brown is obviously being paid off by drug companies to shoot down Dr.Zamboni's great discovery.

  • I was Liberated in Serbia in Oct 2010 I was born in England ! my left Jugular was 2mm wide and my right 25% narrowed After 15 years of MS it is now GONE!! GET your bloody fingers out and start screening people!!!!!! for CCSVI

  • 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

  • 2 points. Point one - people with MS have too much iron in their brains. Healthy people without MS do not. Point two - people with MS have Killer T-cells in their brains. Healthy people without MS do not. The two go hand in hand. Doctors don't think that this is related or not important??!!!!!! It all supports the theory of CCSVI being the cause of MS.

  • thanks for the post.if we can just get them moving faster insted of the deer in the head light look.LETS GO MOVE IT MOVE IT !!!!! thanks mike

  • I am glad Martin got liberated and feels better. Some doctors want to wait for more evidence !!!! Because they need to do "more research".

  • I can't believe some one would actually document himself for the world and the future to see as he makes comments against a new research that is so successful already. Someday you might end up in court Mr./Ms. MS society.

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