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).

Severe ME Day 2026

Access resources and explore our Severe ME Day initiatives, including how to Be Counted, new episodes of the Imagine Podcast and the Faces of PEM.

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.

5 August 2026

The Count ME Campaign

ME/CFS has finally been counted. Refunding Emerge Australia will help ensure that recognition leads to real change

Recognition without infrastructure is just words. The AIHW AIHW Burden of disease study data, the NHMRC Clinical guidelines for ME/CFS, the National strategic framework for chronic conditions, the Parliamentary Friends of ME/CFS committee; all of these create opportunities. None of them, on their own, deliver support to a housebound patient in regional Queensland, or change the mind of a GP who believes these patients are making it up, or help a carer navigate a NDIS application their loved one doesn’t have the capacity to complete.

Emerge Australia converts recognition into action. That is what eight years of service delivery, advocacy, research and relationship-building has produced: an organisation positioned, right now, to be the delivery mechanism for this historic policy moment.

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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Giving a voice to the unseen and unheard.  
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