invisible illness

  1. Andy

    Sunday Times readers comments: "The ‘invisible illness’: what it feels like to live with chronic fatigue syndrome or ME"

    Sunday Times publishes three readers accounts of their personal experiences of ME. https://www.thetimes.co.uk/magazine/style/readers-stories-myalgic-encephalomyelitis-me-chronic-fatigue-syndrome-7ghbwdkbj And at the bottom Shame they don't tackle their own ignorance..
  2. Dolphin

    Invisible disabilities: perceptions and barriers to reasonable accommodations in the workplace

    https://www.emeraldinsight.com/doi/pdfplus/10.1108/LM-10-2017-0101
  3. Sly Saint

    ME sufferers speak out about their battle with the 'invisible illness'

    " THIS week marks ME Awareness Week, culminating in a campaign day called ‘Millions Missing’ in cities across the world. Leamington and Stratford Observer deputy editor Laura Kearns is using this as a chance to speak out about her battle with the illness and talk to others with the condition...
  4. A

    'But you don’t look sick': What it's like to live with a 'silent' disease

    Not specific to ME or CFS, but sharing here as saw it tweeted by ME/CFS biomedical researcher Maureen Hanson. "Paige Wyant and Joy Brandys, along with the writer Jade Lennox, share the challenges of having a disease that isn’t obvious."...
  5. Andy

    BBC Newsbeat: " Stansted Airport staff told me I 'don't look ill enough' to be disabled "

    http://www.bbc.co.uk/newsbeat/article/42556222/stansted-airport-staff-told-me-i-dont-look-ill-enough-to-be-disabled
  6. Cheshire

    Toni Bernhard - The Burdens Posed by Invisible Physical and Mental Illnesses

    https://www.psychologytoday.com/blog/turning-straw-gold/201712/the-burdens-posed-invisible-physical-and-mental-illnesses
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