Joanne Hunt
NHS Digital refuse to place clear caveats on inaccurate ME/CFS webpages
Back in December, I (again) emailed NHS Digital to ask them to remove inaccurate and potentially harmful information from their ME/CFS...
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Joanne Hunt
Jan 30, 2021
Health politics in action? Professor Garner’s change of heart on Long Covid (and ME/CFS)
Trigger warning: gaslighting, ableism, death, coercive control, cult psychology Note: this a long blogpost, take it easy! Politics...
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Joanne Hunt
Dec 21, 2020
Reflections on NICE draft for diagnosis and management of ME/CFS
On 10 November, NICE released its long-awaited draft of the guidelines on diagnosis and management of myalgic encephalomyelitis...
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Joanne Hunt
Oct 26, 2020
Are ‘medically unexplained symptoms’ really unexplained? My experience as a patient
ME/CFS is discussed in this post within the context of 'medically unexplained symptoms' (MUS); I do *not* believe ME/CFS should be...
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