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).

Parliamentary Friends of ME/CFS

Join us virtually for the first meeting of 2026. Bringing together lived experience, parliamentarians and experts.
March 10, 11am-1pm (AEDT)

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.

STOP PRESS!

9 December 2025

Parliamentary Friends of ME/CFS launched for the 48th Parliament

The Parliamentary Friends of ME/CFS for the 48th Parliament is co-chaired by Dr Mike Freelander MP and Senator Jordon Steele-John, along with 18 other members of Parliament, ME/CFS advocacy groups and community members.

Attend the first meeting of 2026 virtually on March 10 at 11am. Register via the link

ME/CFS Alliance Australia members – Bridges & Pathways, Emerge Australia, ME Advocacy Network, ME/CFS Australia, Myalgic Encephalomyelitis Group Australia.

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.

Our Latest ME/CFS News

NDIS New Framework Planning

A laptop, used by someone with ME/CFS, sitting on a desk next to a window.

The CEO Report | February 2026

The CEO Report | December 2025

The CEO Report | November 2025

Making the Invisible Visible: Safer Shared Air for All

The CEO Report | October 2025

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.