Dialogues for a neglected illness – or Dialogues for ME/CFS
Dialogues for a neglected illness – or Dialogues for ME/CFS is a new project being made with an award from the…
Kara Jane Spencer: Severely ill singer seeks help finishing album
A singer seriously ill with a severe form of ME has asked musicians and studio technicians to help…
Australian ME/CFS advocacy award honours Alem Matthees
Last year on his birthday, we presented Alem Matthees with an award and framed certificate on behalf of…
ME sufferers demand end to exercise treatment
More than 21,000 Scots suffer from ME which is also known as chronic fatigue syndrome Scottish ministers are…
ME Awareness Day May 2020
WHAT IS ME AWARENESS DAY? May 12th is a well known date in the ME world as it…
European Parliament resolution on additional funding for biomedical research on Myalgic Encephalomyelitis
A. whereas the Committee on Petitions has received several petitions raising concerns over the absence of treatments and…
‘I want to go out on a high’: Meet Parliament’s last Countess
The Countess of Mar, Britain’s only female hereditary peer, is stepping down from the House of Lords after…
Underfunding of biomedical research into Myalgic Encephalomyelitis is unjustified, say MEPs
Press Releases PETI Today An estimate of 2 million Europeans affected by the disease EU research remains fragmented…
Don’t Leave Disabled People Behind
Why is this important? The Government has chosen to ‘focus on new claimants’ by providing an extra £20…
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…