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XMRV studies into CFS put on hold!!! (Government studies accepted for publishing)

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Uploaded by on Jun 30, 2010

Health officials in the USA have put on hold two studies into CFS & the retrovirus XMRV. These studies have already been peer reviewed & accepted for publishing. One from the NIH/FDA has found XMRV in CFS patients, the CDC study has not. WHY THE HOLD?

More information here:
http://online.wsj.com/article/SB10001424052748703374104575337160225739290.htm...
http://news.sciencemag.org/scienceinsider/2010/06/conflicting-papers-on-hold-...
http://oslersweb.com/

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Science & Technology

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Uploader Comments (edittubev)

  • I can't seem to find a place THAT SAYS the symptoms or what XMRV is . I have several Autoimmune issues and had a confirmed ( by a rheumotologist ) diagnosis of Fibromyalgia - Now I can't give blood because they are connecting my Fibro / CFS to this XM thing. I'm O- btw and usually get nagged to death for my blood.

  • @WillExposeYou

    XMRV may cause multiple diseases. Therefore there wont be a specific set of symptoms. This is likely to be down to where the retrovirus integrates into the genome, which they current do not know. Also XMRV is not the only retrovirus of this family that is being found. They are also finding a Polytropic (PMRV) type virus. Again the affects of this may be slightly different than Xentropic (XMRV) variety. Furthermore, in some people they are finding both X & P types.

  • As far as I knwo the studies are public. I have read excert from them. You can find them at the WPI web site and the NIH and FDA sites. Very good reading. What we need if for the CDC to get off there buts and do something. We need meds. I am so sick right now with CFS was dx'd in 95 and I demand answers and meds!!!

  • @Katnet1

    The studies are public now because many people spoke out about the hold. I have left the video up so that no one forgets that the medical authorities tried to control this research.

  • @edittubev thanks for posting. I enjoyed yoru video. Good luck to you and please let me know if u hear anything else. :)

  • @Katnet1

    They are now finding MLV-related viruses in Spain, in 70% of patients tested.

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All Comments (25)

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  • Thanks for this vid

  • @edittubev

    wow...do u have a link to that information?? I wold love to read that.

  • @WillExposeYou I believe the symptoms are the same as what we have with fibro and CFS. I have always felt like I had a virus...you know that flu like feeling.

  • misstree75, I'm not sure what you are trying to say. But so do I

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