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.

Severe ME Awareness 2025

Join us for a 1-hour symposium on 8 August, read lived experiences from the community and access resources around severe ME.

Donate to Emerge Australia

As a not-for-profit organisation Emerge Australia relies on the generosity of the community to ensure critical services and programs can continue to run. Help us to improve the lives of people living with ME/CFS and long COVID across Australia.

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.

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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.