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  1. Kalliope

    Blog Africa Clockwise: M.E. Too or Why I am No Longer NOT Speaking to Doctors about Chronic Illness

    Africa Clockwise: M.E. Too or Why I am No Longer NOT Speaking to Doctors about Chronic Illness
  2. Andy

    Blog: Spoonseeker: Probing the Holes in MUS

    https://spoonseeker.com/2018/07/29/probing-the-holes-in-mus/
  3. Andy

    Blog: Occupy ME: NIH 2017 Funding Fact-Check

    http://occupyme.net/2018/07/23/nih-2017-funding-fact-check/
  4. Andy

    Blog: Let's Do It for Myalgic Encephalomyelitis: Dear MP...

    http://ldifme.org/2018/06/28/dear-mp/
  5. Andy

    Blog: Neuroskeptic: Psychology, Neuroscience: Lacking in Individuality?

    http://blogs.discovermagazine.com/neuroskeptic/2018/06/23/psychology-neuroscience-individuality/#.Wy5jCKkh0i9
  6. Andy

    Blog: Occupy ME: NIH Forms New Working Group on ME/CFS

    http://occupyme.net/2018/06/22/nih-forms-new-working-group-on-mecfs/
  7. Andy

    Blog: Occupy ME: Public Comment on Engaging People with ME

    http://occupyme.net/2018/06/20/public-comment-on-engaging-people-with-me/
  8. Andy

    Blog: Spoonseeker: A Morass of MUS

    https://spoonseeker.com/2018/06/20/a-morass-of-mus/
  9. Indigophoton

    The Canary: Esther McVey and her department are now totally out of control

    Another article by Steve Topple using ME and PACE as illustrative of current government policy, https://www.thecanary.co/opinion/2018/06/18/esther-mcvey-and-her-department-are-now-totally-out-of-control/
  10. Indigophoton

    The Stories We Tell Ourselves: Prisons or Paths to Freedom

    From the blog "A Chronic Voice", https://www.achronicvoice.com/2018/06/03/stories-freedom/
  11. Andy

    Occupy ME blog post: NIH Time Warp

    http://occupyme.net/2018/06/07/nih-time-warp/
  12. Sly Saint

    Personality as a risk factor for ME/CFS and similar diseases

    Merged thread Why Attributing 'Type A' Personalities to Myalgic Encephalomyelitis Needs to Stop "I recently had an experience with a relative that caught me off guard. In passing, she mentioned reading somewhere that it’s mostly “type A” individuals who develop ME (myalgic encephalomyelitis)...
  13. Andy

    David Tuller: Trial By Error: More on the CDC; Reader’s Digest; and BBC’s Newsbeat

    http://www.virology.ws/2018/05/23/trial-by-error-more-on-the-cdc-readers-digest-and-bbcs-newsbeat/
  14. Andy

    Blog: Spoonseeker, "How Many Times Must a Story Be Told…?"

    https://spoonseeker.com/2018/05/12/how-many-times-must-a-story-be-told/
  15. Andy

    UK - The Young ME Sufferers (TYMES) Trust

    TIME FOR A PROFESSIONAL RETHINK ON ME : Your heart is as important as your head - blog by Jane Colby https://uttingwolffspouts.com/2018/05/12/when-children-dont-get-well/
  16. Indigophoton

    Blog: Don't Call The Doctor!

    https://runninonemptee.blogspot.co.uk/2018/05/dont-call-doctor.html
  17. Andy

    Tips for ME blog: Waxing lyrical: ME Awareness

    https://tipsforme.wordpress.com/2018/05/07/waxing-lyrical-me-awareness/
  18. Simon M

    There’s a yawning gap in ME/CFS research funding. Take action. (Simon McGrath blog, May 8)

    One for ME Awareness week There’s a yawning gap in ME/CFS research funding. Take action. When I got ME more than 20 years ago, I thought that science would soon provide the answers to my illness. Instead, I saw little good research going on, and there’s been a spectacular lack of progress...
  19. Andy

    Blog: Ill versus disabled – is there a distinction between the two?

    http://inclusionproject.org.uk/social-model/ill-versus-disabled-is-there-a-distinction-between-the-two/
  20. Andy

    Blog: Department for Snakes and Ladders?

    http://inclusionproject.org.uk/guest-post/department-for-snakes-and-ladders/
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