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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Upvote this question to someone on the Gates Foundation

Discussion in 'General ME/CFS Discussion' started by Bradford, Oct 9, 2014.

  1. Bradford

    Bradford

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    Little Bluestem, WillowJ and ahmo like this.
  2. Snow Leopard

    Snow Leopard Hibernating

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    Specifically, the gates foundation does not fund interventions or research into health conditions in western countries. To make a case, you have to suggest that research on CFS (particularly epidemiology) is sorely neglected in developing countries. Otherwise the Gates foundation will explicitly ignore such requests.
     
  3. WillowJ

    WillowJ คภภเє ɠรค๓թєl

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    That's true, too, that it's present there and neglected there.

    However, I thought they did include domestic research for populations considered disadvantaged, which would basically include patients of nearly any disease which affects more women than men. (not counting breast cancer, which I think has caught up to everything else, via advocacy).

    Though we're at the bottom even of this list. Someone (you?) made a chart showing ME/CFS is the worst underfunded (of diseases in general) by far, and migraines pretty bad also. Not sure you included fibro and IBS but they are not tons better than us, though they get about 2-3x the funding (US-NIH).

    Don't they have women, children, and minorities on their list, even in Western countries?
     
  4. WillowJ

    WillowJ คภภเє ɠรค๓թєl

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    However, reddit's Rule #2:

     

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