Posts tagged ‘ME/CFS’
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Recent Posts
- “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)
- COVID-19, NICE and ME: towards litigation?
- Life in the Time of CoronaVirus #2: the Rule of Law, a Shifting Political Landscape and a “Clash of Arms”
- Life in the time of CoronaVirus #1: Democracy, Data and Saving Lives
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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 Case of Page v Smith/Humour
- Uncategorized
Valerie Eliot Smith
- @twocitiesnickie Pls take up this issue on behalf of your affected constituents (I am one). Misinformation & vilifi… twitter.com/i/web/status/1… 4 days ago
- @MEawareness Tks for the question, Heath. The answer is too long & complicated for tweeting but is partially addres… twitter.com/i/web/status/1… 1 week ago
- New medium-length post. Brief personal update and a short take on the ongoing NICE guideline update process on ME (… twitter.com/i/web/status/1… 1 week ago
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