“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
LETTER TO SEND TO SHOPS TO HIGHLIGHT ISSUE OF SHOPPING PROBLEMS I have an illness known as M.E….
GREAT NEWS regarding my complaint to the GMC about the PACE authors The Information Commissioner’s Office [ICO] has…
The Team at the Royal College of Anaesthetists have kindly done a transcript of the podcast on Anaesthesia…
David Tuller critiques the PACE trial authors for their response to George Monbiot’s column on ME/CFS, accusing them…
Sharon Tiday said on Twitter: For a while now people have told me that I should get this…
Abstract Myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) is a common, poorly understood disease that has no effective…