Countess of Mar group condemn NICE plan to do nothing with ME/CFS Guideline review | 28 October 2013
The Countess: leading fight against NICE plan to put ME/CFS Guideline review on static list
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ME Association condemns closure of UK’s only in-patient service for people with ME/CFS
ME Association condemns closure of UK’s only in-patient service for people with ME/CFS Read More »
The UK’s only dedicated hospital-bed service for people with ME
The Search for Long Covid Treatments Takes a Promising Turn
The Search for Long Covid Treatments Takes a Promising Turn Read More »
Scientists believe lasting symptoms following a coronavirus infection are not
Celebrating one year of impact from Doctors with M.E.
Celebrating one year of impact from Doctors with M.E. Read More »
Doctors with M.E. turns one this month on the same
The Times: Scientists trade insults over myalgic encephalomyelitis (ME) study | 01 August 2017
The Times, 01 August 2017. An acrimonious scientific row has
ME affects four times as many women as men. Is that why we’re still disbelieved? | ‘Comment is free’, The Guardian | 27 September 2016
From The Guardian ‘Comment is free’ section, 27 September 2016.
‘Living with chronic fatigue: how I wish my friends would treat me’ | Daily Telegraph | 21 December 2015
From the Daily Telegraph, Lifestyle section, 21 December 2015. By
Nathalie Wright talks about the misery of living with ME |Huddersfield Examiner | 26 November 2015
From the Huddersfield Examiner, 26 November 2015. In this thought
‘The debate over this mysterious disease is suddenly shifting’ | Julie Rehmeyer in ‘Slate’ | 13 November 2015
From Slate, 13 November 2015. Words by Julie Rehmeyer. Last
‘Even my family didn’t believe I have ME’ | Daily Telegraph, Review Section | 31 October 2015
From the Daily Telegraph, 31 October 2015 (Story as told