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OMF ME/CFS Working Group Meeting - September 26 - 28, 2018

Discussion in 'ME/CFS research news' started by Sly Saint, Sep 21, 2018.

  1. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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    "Open Medicine Foundation is sponsoring a three-day focused scientific meeting with a growing group of excellent scientists with diverse expertise prior to the September 29th Community Symposium on the Molecular Basis of ME/CFS at Stanford University.

    Over 50 scientists from all over the world will gather at Stanford from September 26 to September 28 to present their latest findings and ideas. These presentations will be interspersed with in-depth discussions, brainstorming of new ideas and next steps, and developing targeted strategies to find answers. Old collaborations will be intensified; new collaborations launched.

    The working group meeting will emphasize collaboration, open sharing of unpublished data and constructive feedback and critiques in a friendly environment working towards a common goal. The meeting will continue during coffee breaks, lunches, and dinners for three full days.

    OMF is pleased to fund this unique platform for open collaboration and open sharing of data and ideas, unprecedented in ME/CFS research. Our ultimate goal is to accelerate research finding answers and solutions to this dreadful disease.

    We will post the working group agenda daily on our website and social media during these meetings.

    If you haven't already, please register for the free Community Symposium Livestream, click here. "

    eta:
    https://www.omf.ngo/2018/09/19/working-group-meeting/
    note: this webpage is available in several languages
     
    Last edited: Sep 26, 2018
    Creek, Alvin, Webdog and 15 others like this.
  2. Kalliope

    Kalliope Senior Member (Voting Rights)

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  3. Joh

    Joh Senior Member (Voting Rights)

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  4. Joh

    Joh Senior Member (Voting Rights)

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  5. Joh

    Joh Senior Member (Voting Rights)

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  6. Joh

    Joh Senior Member (Voting Rights)

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    Last edited: Sep 27, 2018
    Sasha, Comet, Alvin and 4 others like this.
  7. Joh

    Joh Senior Member (Voting Rights)

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  8. alalush

    alalush Established Member

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    This is al great but when will actual trials and treatments start?
     
    Andy and Perrier like this.
  9. mariovitali

    mariovitali Senior Member (Voting Rights)

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    The problem is that we are currently discovering all the "different faces" of ME/CFS but not their cause.
     
  10. Joh

    Joh Senior Member (Voting Rights)

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  11. JaimeS

    JaimeS Senior Member (Voting Rights)

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  12. Joh

    Joh Senior Member (Voting Rights)

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  13. Joh

    Joh Senior Member (Voting Rights)

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  14. Sasha

    Sasha Senior Member (Voting Rights)

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  15. Sasha

    Sasha Senior Member (Voting Rights)

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    Alvin, ukxmrv, Lisa108 and 4 others like this.
  16. Joh

    Joh Senior Member (Voting Rights)

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    Some more pictures (more in the foto album on the OMF Facebook page):









     
    JaimeS, Cinders66, Alvin and 4 others like this.
  17. mariovitali

    mariovitali Senior Member (Voting Rights)

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    I had a look on the FB Page and was trying to look for "clues" from the presentation slides.

    -The Presentation title slide by Alan Light looks quite interesting. Title : "Mitochondrial, immune and autoimmune gene mutations synergize as risk factors for ME/CFS". Definitely something to look at IMHO.

    -The presentation slide by Rob Phair is "Metabolic TrapS" as opposed to "Metabolic Trap". So we are looking at many traps as opposed to one? (I don't want to suggest that this is necessarily a bad thing)
     
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  18. Sasha

    Sasha Senior Member (Voting Rights)

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    JaimeS, Trish, Lisa108 and 2 others like this.
  19. Roy S

    Roy S Senior Member (Voting Rights)

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  20. Roy S

    Roy S Senior Member (Voting Rights)

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