Posts tagged ‘ME/CFS’
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Recent Posts
- A short post on long Covid media exposure
- Professor Garner, The BMJ and me: an alarming flip-flop on recovery from long Covid
- NICE, the media and the cultural problem of myalgic encephalomyelitis (ME)
- “Ice Cream & Hypothermia” revisited + a chilling NICE consultation process
- “A Demon on My Life”: review of an online play about living with ME (myalgic encephalomyelitis)
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Categories
- Changing the Narrative
- Constitutional & Administrative+Public Law
- CoronaVirus
- Freedom of Information Act (FOIA) posts
- General Miscellaneous (US + UK)
- Karina Hansen
- Media
- National Institute for Health and Care Excellence
- NICE
- Open justice
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- Personal
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- Strategic communications and the media
- The "Secret" Files
- The Case of Page v Smith/Humour
- Uncategorized
Valerie Eliot Smith
- Useful article for those who have an interest in the impact of data protection regulations on health research (thes… twitter.com/i/web/status/1… 3 days ago
- ICYMI: from last week. A short post on the long Covid media blitz and a comparison with #ME media coverage.… twitter.com/i/web/status/1… 2 weeks ago
- "A child may bounce through the system, frequently changing homes and schools, based on decisions influenced by a p… twitter.com/i/web/status/1… 2 weeks ago
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