jennie spotila

  1. Andy

    Blog: "The Death Threat Myth Exposed", Jennie Spotila

    Last week, an old story was recounted to a new audience. During the March 30, 2021 NIH telebriefing with the ME/CFS community, Dr. Vicky Whittemore said that there had been death threats against grant reviewers in the past, and that this was one reason why NIH is now withholding the names of...
    • Andy
    • Thread
    • activism blog harassment jennie spotila militancy myths nih violent patient myth
    • Replies: 45
    • Forum: General ME/CFS news
  2. Cheshire

    Who Reviews ME/CFS Applications for NIH? Jennie Spotila

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  3. John Mac

    STAT: 'The NIH is thwarting research on a poorly understood yet serious condition', 2019, Jennifer Spotila

    Opinion piece in STAT by Jennifer Spotila https://www.statnews.com/2019/01/10/nih-obstacles-thwart-myalgic-encephalomyelitis-research/
  4. Cheshire

    Shining a light on chronic fatigue syndrome, a little understood disease among doctors - The Inquirer Jennie Spotila

    http://www2.philly.com/philly/health/chronic-fatigue-syndrome-myalgic-encephalomyelitis-unrest-20181109.html
  5. D

    Blog: Occupy ME: 2018 NIH funding estimate

    Jennie Spotila has an important post on 2018 NIH funding. http://occupyme.net/2018/07/30/how-much-will-nih-spend-in-2018/
  6. Sasha

    16 July 2018 - Jennie Spotila blog - 'How to represent'

  7. Indigophoton

    Blog: All The Time and None At All, Jenny Spotila

    http://occupyme.net/2018/04/25/all-the-time-and-none-at-all/
  8. Sasha

    2017 NIH spending on ME/CFS research (Jennie Spotila blog, 20 March 2018)

    Read the rest at: http://occupyme.net/2018/03/20/2017-nih-spending-on-mecfs-research/ I haven't read it yet but Jennie is always good value. :)
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