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.

29 July 2026

The Count ME Campaign

The system wasn’t designed for people with ME/CFS. Emerge Australia is.

Consider what it takes to access support if you are housebound with ME/CFS. You need a GP who understands your condition well enough to complete NDIS or DSP paperwork correctly. You need to know which supports you’re eligible for, which you’re not, and how to appeal a decision you don’t have the cognitive or physical energy to contest. You need someone who understands that your capacity fluctuates, that you may be well enough to speak on Tuesday but not on Wednesday, and who can plan around that rather than penalise you for it.

No single government service joins these dots for people with energy-limiting conditions. Emerge Australia does; helping patients understand what they’re entitled to, where to go, and how to ask the right questions.

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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