“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
Myalgic Encephalomyelitis / Chronic Fatigue Syndrome Announcements
Statement My Rt Hon Friend the Secretary of State for Health and Social Care (Sajid Javid) has made…
Forward ME: upcoming NICE round table
Update from Forward-ME on the upcoming round table event, hosted by the National Institute for Health and Care…
Trial By Error: Guardian Publishes Response to Boothby O’Neill Inquest
By David Tuller, DrPH My heart sinks every time I see another ridiculous article from a member of…
An interview with the sister of Alice Barrett who needed urgent tube feeding
The sister of Alice Barrett has been interview by BBC South West about Alice’s need to be urgently…
Treating COVID-19 in patients with underlying ME
Useful medical information when treating COVID-19 in patients with underlyingmyalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and severe fibromyalgia (FM)…
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…