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).

600,000 Patients Risk Losing Care Over $220k Grant

Read the Australian article calling attention to the loss of funding to our Support Services

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.

24 September 2026

The Count ME Campaign

The Australian: 600,000 Patients Risk Losing Care Over $220k Grant

Emerge provides direct patient support through telehealth, patient support groups, peer support and evidence-based information services, staffed by experienced nurses and a health system navigator. For many Australians, Emerge Australia is the only outreach, the only evidence-based specialised service of its kind for people who find themselves housebound, if not bedbound, as the public health walls close around them.

Emerge chief executive Anne Wilson speaks of distraught callers, some suicidal on the other end of the line. The nurses who take these calls are highly specialised health professionals who offer support, advice, succour and access to support services.

Federal funding of the patient health service effectively paid for telehealth, information and support service delivery and development. On November 30 that funding ceases and Wilson says there is no certainty of new funding of a service to some of the most vulnerable people in the country.

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.

Join our Newsletter

Giving a voice to the unseen and unheard.  
Sign up to our newsletter today.

Shopping cart0
There are no products in the cart!
Continue shopping
0
Scroll to Top