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).

The Faces of PEM

The Faces of PEM is a growing digital wall of people living with PEM, and the supporters standing beside them. We invite you to upload a photo of your face and become part of a collective presence that cannot be dismissed.

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.

6 July 2026

INTRODUCING

The Count ME Campaign

Coming together for Australians with ME/CFS, long COVID and overlapping energy-limiting conditions

As we conclude a federal government funding cycle and prepare to seek renewed investment, Emerge Australia is proud to launch the Count ME campaign – a powerful movement to highlight the need for continued momentum and growth in support of research, advocacy, clinical education and patient services for Australians living with ME/CFS, long COVID and associated energy limiting conditions.

Over the coming months, Count ME will shine a spotlight on groundbreaking developments surrounding these often misunderstood and stigmatised conditions, and share critical insights to equip decision makers to ensure support to effectively meet the needs of our community. Count ME will feature new patient resources and Severe ME Week activations, along with primary research for Emerge Australia’s burden of disease study.

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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