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 myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).

Living with ME/CFS or long COVID?

Edith Cowan University and Emerge Australia invite Australians with ME/CFS or long COVID to take part in a confidential online survey, "Living with ME/CFS or long COVID in Australia: A National Burden of Disease Study

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.

22 July 2026

The Count ME Campaign

In a condition defined by ‘dismissal’, trust is not a given. It is earned.

Building trust with a community that has been systematically let down by the health system is not a marketing exercise. It requires years of doing what you say you will do: providing information that is safe, evidence-based and honest; advocating in rooms where it matters. Emerge Australia has done that, consistently, for eight years, building on the knowledge and experience gained over forty years serving this community.

The result is an organisation that is trusted by patients who have nowhere else to turn, by clinicians who need a credible source, by researchers who need community infrastructure, and by policy makers who need a reliable partner at the table. That trust took years to build. Without ongoing funding assurances, it would take only moments to lose.

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.

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.

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