“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
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
We call on the National Institute for Health and Care Excellence (NICE) to publish the finalised ME/CFS guideline…
The Countess of Mar, Britain’s only female hereditary peer, is stepping down from the House of Lords after…
This is the inpatient experience of a patient with very severe ME, whose father Michael Gordon gave an…
“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
#DecodeME Matters As many of you are aware our advocacy worker, Helen Baxter, has been assisting people with…
August 01, 2018 The latest update to the electronic health records system used by GPs in England was…