1. Patients launch a $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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The Fable known as The PACE Trial
Graham, Janelle and Bob, have once again excelled themselves with their latest take on the 'poisoned apple' that was the PACE Trial...
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VipDx testing for XMRV - in Canada

Discussion in 'XMRV Testing, Treatment and Transmission' started by BRCforME.org, Jun 24, 2010.

  1. Hi. I'm Canadian. Diagnosed in 2001 by Dr. Anil Jain (contributor to Canadian Criteria). In the advent of the Science paper being replicated, I'd like to get tested. However, I find the language from Vipdx to be very confusing.

    Can any other Canadians who have been tested by VipDx please contact me? I need to ask some questions of someone who has been through it.


  2. ixchelkali

    ixchelkali Senior Member

    Long Beach, CA
    I'm not Canadian and I can't help you with your question, but I noticed this is your first post so I want to welcome you to the Phoenix Rising forum. Glad to have you join us, Andrea. Hopefully, one of your fellow Canadians will respond soon.
  3. Thanks for the warm welcome. :) I've been lurking for a long time.
  4. Daffodil

    Daffodil Senior Member

    im canadian and have used VIP many times. u are welcome to message me

  5. Thanks Daffodil. I'll do that. :)

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