“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
The Team at the Royal College of Anaesthetists have kindly done a transcript of the podcast on Anaesthesia…
LETTER TO SEND TO SHOPS TO HIGHLIGHT ISSUE OF SHOPPING PROBLEMS I have an illness known as M.E….
An open response from parents and carers of people with Severe Myalgic Encephalomyelitis to ‘Management of Nutritional Failure…
Over a hundred academics, patient groups, lawyers, and politicians have now signed an open letter to the Lancet calling on…
A. whereas the Committee on Petitions has received several petitions raising concerns over the absence of treatments and…
EMBARGOED UNTIL: 00:01, 29 October 2021 PRESS RELEASE NICE ME/CFS guideline outlines steps for better diagnosis and management…