A new package of measures to improve support for people affected by myalgic encephalitis/chronic fatigue syndrome (ME/CFS) has been announced by the Government and welcomed by ME charities. The ...

People who are severely ill with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) are often too sick to leave home, but clinicians can still support them in many ways, experts say. Speaking ...

The Solve ME/CFS Catalyst Award-winning studies will fast-track clinical and immunological studies aimed at delivering new treatment strategies and diagnostic insights for ME/CFS and Long Covid, ...

Myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) is a chronic illness that severely limits the quality of life of many people affected. Symptoms include fatigue (i.e. severe exhaustion), ...

Change in medicine is never easy, especially when practitioners are asked to dispense with long-held beliefs about an illness. It is this challenge—of steering an entire community to collectively ...

A new Stanford study has identified biomarkers linked to the severity of chronic fatigue syndrome, offering evidence that inflammation is a powerful driver of this mysterious disease, long dismissed ...

Two more MPs have pledged their backing to a charity supporting people with a chronic illness. Mid Sussex MP Alison Bennett and Horsham's John Milne have joined the Sussex ME/CFS Society. The Brighton ...

People with ME/CFS have significant differences in their blood compared with healthy individuals, a new study reveals, suggesting a path towards more reliable diagnosis of the long-term debilitating ...

‘Lives We Cannot Live’, a new photographic exhibition by documentary film-maker and photographer Jeremy Jeffs, and presented by The ME Association, reflects the stark realities of daily life for ...