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
- CoronaVirus
- Freedom of Information Act (FOIA) posts
- General Miscellaneous (US + UK)
- Karina Hansen
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- The "Secret" Files
- The Case of Page v Smith/Humour
- Uncategorized
Valerie Eliot Smith
- @batteredoldbook @BBCBreakfast @ClareGerada @PaulGarnerWoof I’m very sorry to hear of your experiences, James. I ho… twitter.com/i/web/status/1… 1 week ago
- @batteredoldbook @BBCBreakfast @ClareGerada @PaulGarnerWoof It’s well established that the topics you mention are a… twitter.com/i/web/status/1… 1 week ago
- @batteredoldbook @BBCBreakfast @ClareGerada @PaulGarnerWoof Thank you, James. I understand what you’re saying in ge… twitter.com/i/web/status/1… 1 week ago
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