“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
Neurovascular dysfunction is a core, increasingly well-supported feature of Myalgic Encephalomyelitis (M.E.)
Neurovascular dysfunction is a core, increasingly well-supported feature of Myalgic Encephalomyelitis (M.E.), especially when M.E. is understood as…
GET and CBT are not safe for ME – summary of survey results
Topline findings A new patient survey of 2274 respondents has confirmed that graded exercise therapy (GET) is harming…
We Live With A Monster A Myalgic Encephalomyelitis (M.E.) Story
Sharon Tiday said on Twitter: For a while now people have told me that I should get this…
ME Question in Parliament
To ask the Secretary of State for Health and Social Care, if he will take steps to expand…
Royal College of Anaesthetists focuses on ME and Anaesthesia.
This podcast from the Royal College of Anaesthetists focuses on ME and Anaesthesia. Dr Anton Kruge, Dr Charles…
Carol Monaghan MP (Chair of the APPG on ME) on the NICE guideline delay
SNP MP Carol Monaghan has slammed the National Institute for HealthCare Excellence (NICE) for delaying its promised guideline on the…
