Not Unseen, Not Unheard: Stand with those impacted by ME/CFS

Join us in support for people with ME/CFS

Stand with Emerge Australia – your support can transform lives, bringing hope, understanding, and effective treatment to those living with ME/CFS.

ME/CFS and long COVID Action Forum - online

Join us 1pm – 3pm AEDT, Thursday, 30 October 2025 streamed from Australian Parliament House.
This event calls for action, investment and policy reform to improve the lives of people living with ME/CFS, long COVID and related energy-limiting conditions.

Donate to Power Our Practitioners

Power Our Practitioners is a virtual fundraising challenge. Together, we can ignite a spark of hope, supporting over 600,000 Australians with ME/CFS, long COVID and other energy limiting invisible diseases.

Join the AusME

Your participation only accelerates our progress in advancing knowledge. Join the AusME ME/CFS and long COVID registry today and help us make a difference.

STOP THE PRESS!

An urgent call for action - Parliamentary Friends of ME/CFS Meeting

On Monday 18 November at Australian Parliament House, parliamentarians joined national ME/CFS organisations, clinicians, research and the patient community to spotlight an urgent call for action. The voices of the 250,000 Australians living with ME/CFS can no longer be ignored. It is the right of every Australian living with ME/CFS to equitably access best-practice health care and essential supports.

The Honourable Mark Butler MP, Minister for Health and Aged Care, officially opened the event. Anne Wilson, CEO of Emerge Australia, thanked the Minister for his leadership in enabling Australia’s new ME/CFS Clinical Guidelines through a $1.13 million funding commitment earlier this year.

Mr Alan Singh, Executive Director, Research Quality and Advice at National Health and Medical Research Council, provided an update on the progress of the guidelines. These evidence-based guidelines will make a profound difference in the early diagnosis and safe management of the condition, based on the latest scientific understanding.

This event underscored the pivotal role Parliamentarians can play in championing the needs of the ME/CFS community.

Did You Know?

Creating awareness, driving change

Despite all this, we still struggle to have the impact and severity of ME/CFS acknowledged in our community.

Our Latest ME/CFS News

A laptop, used by someone with ME/CFS, sitting on a desk next to a window.

The CEO Report | October 2025

October 2025 International Research and Advocacy Roundup

The CEO Report | September 2025

The CEO Report | August 2025

Strengthening culturally inclusive care for people with ME/CFS and long COVID

ABC Nightlife: Understanding chronic fatigue, the thriving world of Ethnic Clubs, Thomas Hardy and Limericks

Help us make a difference

Your financial support is vital to enabling us to help those with ME/CFS with Telehealth and Support Services as well as providing key resources to the community.

The voice of
our community

Our Research

Insights & Inspiration

At the heart of our mission lies a deep commitment to unearthing new insights about Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS).

We recognise the urgent need to expand our understanding of this complex and often misunderstood condition. To this end, we tirelessly pursue research initiatives, collaborating with leading experts and institutions.