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).
Join us from 11-17 May as we launch a range of initiatives, including our annual online Symposium.
Inclusive fundraising built around safety and pacing supporting care for our community. Participate solo, as a team or by donating towards pledges.
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.
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.
First meeting of 2026 – March 10 at 11am, Australia Parliament House. Read the wrap up below.
ME/CFS Alliance Australia members – Bridges & Pathways, Emerge Australia, ME Advocacy Network, ME/CFS Australia, Myalgic Encephalomyelitis Group Australia.
Despite all this, we still struggle to have the impact and severity of ME/CFS acknowledged in our community.
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.
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.
Giving a voice to the unseen and unheard.
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