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...
Discuss the article on the Forums.

The Male Pattern Baldness Disease? Chronic Fatigue Syndrome’s Chronic Lack of Research Funding

Discussion in 'General ME/CFS Discussion' started by Dolphin, May 4, 2016.

  1. Dolphin

    Dolphin Senior Member

    Messages:
    10,672
    Likes:
    28,181
  2. alex3619

    alex3619 Senior Member

    Messages:
    12,493
    Likes:
    35,121
    Logan, Queensland, Australia
    I thought this an excellent piece. :thumbsup:
     
    TiredSam, Dolphin and mango like this.
  3. mango

    mango Senior Member

    Messages:
    905
    Likes:
    4,975
    i agree, it's brilliant! well worth a read :)
     
    Dolphin likes this.
  4. Denise

    Denise Senior Member

    Messages:
    1,095
    Likes:
    3,447
    "male-pattern baldness gets more research funds than ME/CFS in the US"
    I have seen/heard Dr. Klimas refer to this in several places but have never seen the source for funding for male-pattern baldness (which has been linked to several diseases).
    If someone knows the source, please share here. @Dolphin, @alex3619 (other)
     
  5. Eeyore

    Eeyore Senior Member

    Messages:
    595
    Likes:
    811
    Last I heard they were cutting the ME budget to 0 at the CDC. No question ME is underfunded.

    Klimas has been clever about it and gets her funding for GWS through the DoD (they have a lot more money - and GWS is taken at least slightly more seriously than ME).
     

See more popular forum discussions.

Share This Page