Posts tagged ‘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
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- Freedom of Information Act (FOIA) posts
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- Karina Hansen
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- The Case of Page v Smith/Humour
- Uncategorized
Valerie Eliot Smith
- "The business of running the state is a shared constitutional endeavour with built-in checks and balances, and thos… twitter.com/i/web/status/1… 1 month ago
- Very helpful video from @Rivkatweets for @NewsHour about living with #ME (myalgic encephalomyelitis). The brain-fo… twitter.com/i/web/status/1… 1 month ago
- @CGATist @AJansen118 @OwenJones84 @davidtuller1 @keithgeraghty @b_m_hughes @GeorgeMonbiot @TomKindlon… twitter.com/i/web/status/1… 2 months ago
- Follow valerieeliotsmith on WordPress.com
