independent

  1. E

    Muscle abnormalities worsen after post-exertional malaise in long COVID, 2023/4, Wüst, van Vugt, Appelman et al

    Muscle Abnormalities Contribute to Post-Exertional Malaise in Long COVID A poster presentation of the very soon to be published work by Rob Wüsts team has been uploaded to Twitter. Paper now published, see post #8
  2. Hutan

    2012 Letter to the Independent on harassment of researchers

    IoS letters, emails & online postings (2 December 2012) https://www.independent.co.uk/voices/letters/ios-letters-emails-online-postings-2-december-2012-8373777.html Chronic Fatigue Syndrome/ME is a debilitating condition affecting some 1 per cent of the UK population (“ME: bitterest row yet in...
  3. Trish

    UK Independent: 'The NHS is underprepared for a no-deal Brexit – and I am one of the thousands that might die as a result', 2019

    https://www.independent.co.uk/voices/brexit-no-deal-nhs-epilepsy-bipolar-medicine-stockpiling-a8855131.html?amp See link for the rest of the article.
  4. Sly Saint

    The Independent - What are the symptoms of ME and how is it treated? May 2019

    Pretty awful article imo. Includes quotes from SC AfME, and the MEA making the psych vs physical point. Also links to MERUK and the CDC. Very muddled mish mash. Not the best kind of 'awareness raising'...
  5. Sly Saint

    Independent - ME is a nasty, insidious disease... it thieves from every element of your life

    Long piece (from last year but republished) "Myalgic encephalomyelitis sufferer Anne Brennan writes about her long, painful, frustrating battle with the disease that has stolen her once full and vibrant life Five years ago, I was flying high: I was a partner in my Dublin law firm, a zealous...
  6. Alvin

    Jen Brea's comments on the article Time for Unrest: Why patients with ME are demanding justice (image heavy)

    @_NathalieWright's withering @Independent piece lays bear the gaps in how #mecfs is viewed on either side of the pond and the vested interests that have contributed to the disability and death of millions...
  7. MsUnderstood

    "Time for Unrest": ME article by Nathalie Wright

    Here's an excellent article published at independent.co.uk, plus on a number of other news sites: "Time for Unrest: Why patients with ME are demanding justice A new film sheds light on a condition that is largely ignored. Nathalie Wright reports on the struggles patients face to be taken...
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