Review: 'Through the Shadowlands’ describes Julie Rehmeyer's ME/CFS Odyssey
I should note at the outset that this review is based on an audio version of the galleys and the epilogue from the finished work. Julie Rehmeyer sent me the final version as a PDF, but for some reason my text to voice software (Kurzweil) had issues with it. I understand that it is...
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Patient database for those of us who are willing to participate in Research?

Discussion in 'Action Alerts and Advocacy' started by Wasbeer, Jul 16, 2010.

  1. Wasbeer

    Wasbeer

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    Amersfoort, Netherlands
    Hello everybody,

    I'm just throwing up a ball here, but when I listened to yesterday's webinar and heard people say that finding cohorts with well-defined patients was a problem, and that there was need of multi-city, multi-continent research for XMRV, I thought of Phoenix Rising. Maybe we could find a way to create a database here with people who are, under their own conditions ofcourse, willing to participate in research programmes. Ofcourse we would have to think about a way to deal with privacy-issues, and there are other practical issues to consider before organising this.

    On the other hand: we are a multi-city and multi-continent community and most of us here probably have a pretty good idea if they would meet the Canadian Consensus Criteria, or if they 'only' meet the Fukuda Criteria (no disrespect in any way intended). Couldn't that be very useful to the scientific community trying to solve this puzzle? Or is my plan incredibly naive because of things i cannot oversee right now?

    :D Tell me what you think!
     
  2. Sean

    Sean Senior Member

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    The membership of this forum is not randomly selected from among patients. Or at least, we don't know if it is or not.

    Proper studies need a degree of randomness in the patient selection.
     
  3. Mala

    Mala

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    Sweden
  4. Wasbeer

    Wasbeer

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    Amersfoort, Netherlands
    Done! Didn't know it existed, thanks.
     
  5. jspotila

    jspotila Senior Member

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    You can also sign up for the SolveCFS BioBank. Your clinical information will be collected and securely stored. When a study opens that needs patients like yourself, you receive a blood collection kit in the mail. Most labs will do the blood draw for free, so there is no cost to you.

    More information, including consent materials, are available at http://www.solvecfs.org

    And we need healthy controls, too! Family members, friends, neighbors, etc. are all eligible.
     
  6. taniaaust1

    taniaaust1

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    Sth Australia

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