“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
Opposition to Oxford Health NHS Foundation Trust: “Coping with Coronavirus: Fatigue
Opposition to Oxford Health NHS Foundation Trust: “Coping with Coronavirus: Fatigue ”We, the undersigned, request immediate withdrawal of…
Expert reaction to updated NICE guideline on diagnosis and management of ME/CFS
The National Institute for Health and Care Excellence (NICE) has published its updated guideline on the diagnosis and management…
Open letter from Parents and Carers
An open response from parents and carers of people with Severe Myalgic Encephalomyelitis to ‘Management of Nutritional Failure…
NICE Guidelines on ME: Forward-ME statement & Media support
NICE Publishes new Guideline on ME/CFS*, driving major improvements in care Press Statement from Forward-ME, embargoed until publication…
Call for people to take part in a ME research study
The ME Association is funding a study led by Prof Sarah Tyson of University of Manchester (who also…
Myalgic Encephalomyelitis / Chronic Fatigue Syndrome CPD
As an immediately relevant and useful tool for medical professionals and students receiving notice of these updates, it…