“Life in Lockdown: What Matters When All Is Lost”
Thoughtful post by Naomi Whittingham who reflects on living through
the lockdown as someone who has effectively had to live through their
own lockdown due to severe ME for decades
Similar Posts
Research on severe ME
“Profile of circulating microRNAs in myalgic encephalomyelitis and their relation to symptom severity, and disease pathophysiology https://www.nature.com/articles/s41598-020-76438-y?fbclid=IwAR3LphYMqzLHxrPpSoxFwYqs15J8x8LSTKvspThsTjiy8v6orYWKmtkgfFw
Personen met ME/CVS ondersteunen in het ziekenhuis
The hospital support pack translated into Dutch Ondersteuning ME-patiënten in het ziekenhuis.ME Centraal
Myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome: diagnosis and management
This guideline covers diagnosing and managing myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome (ME/CFS) in children, young people and…
A life cut short by medical neglect
A life cut short by medical neglect: interview with Sarah Boothby, whose daughter Maeve died at 27 of…
An interview with the sister of Alice Barrett who needed urgent tube feeding
The sister of Alice Barrett has been interview by BBC South West about Alice’s need to be urgently…
Trial By Error
Trial By Error: NICE Squares Off Against Royal College Bullies Over New ME/CFS Guidelines 20 August 2021 By…