“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
Opposition to Oxford Health NHS Foundation Trust: “Coping with Coronavirus: Fatigue ”We, the undersigned, request immediate withdrawal of…
The Scottish Govermnet have provided an email update on implementing undertakings given by the Cabinet Secretary to the…
An open response from parents and carers of people with Severe Myalgic Encephalomyelitis to ‘Management of Nutritional Failure…
Look after your mental wellbeing It’s always important to look after your mental health, but even more so…
The ME/CFS Priority Setting Partnership (PSP) is giving you the opportunity to define your top ten priorities for…
Why is this important? The Government has chosen to ‘focus on new claimants’ by providing an extra £20…