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 ...

Parliamentary Friends of ME/CFS event brings together clinicians, policymakers, and patients in Canberra MELBOURNE, ...

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, ...

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 ...

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), ...

‘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 ...