“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 are extremely concerned that some medical/care professionals and sports/exercise specialists are still recommending exercise programmes and/or graded…
Useful medical information when treating COVID-19 in patients with underlyingmyalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and severe fibromyalgia (FM)…
Introduction As a doctor, and perhaps especially as a junior doctor, there will no doubt be occasions when…
The hospital support pack translated into Dutch Ondersteuning ME-patiënten in het ziekenhuis.ME Centraal
Alice Barrett who is an inpatient at Royal Devon and Exeter Hospital was unable to lie at 30…
Trial By Error: A Letter Urging NICE to Publish ME/CFS Guideline Without Delay 1 September 2021 by David…