Emerge Australia, the national patient organisation providing services and evidence-based education about myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) today issued an alert on a potential major hit to the Federal Budget and health services facing both major parties. Read more
Emerge Australia’s State of the Nation report includes five priority areas for government to improve the lives of people with ME/CFS. In the lead up to the federal election, Emerge Australia is writing to all federal parliamentarians to seek their support for these five priority areas. Read more
ABC NewsRadio's Cameron Green spoke to Dr Richard Schloeffel, Medical Director of Emerge Australia about the similarities between ME/CFS and Long COVID. Read more
“Australia has dropped the ball on myalgic encephalomyelitis/chronic fatigue syndrome research and funding which dramatically impacts 250,000 patients across the country." Read more
Emerge Australia has urged Political Parties and Candidates standing in the Federal Election to increase their knowledge and understanding of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Read more
Thank you to our amazing volunteers who contribute their support to the ME/CFS community through our services and programs. Read more
This article explains more about our participation at the General Practice Conference & Exhibition (GPCE) conference series in 2022, and our broader strategy to improve GP education about ME/CFS. Read more
On ABC's The Conversation Hour, Richelle Hunt and Jane McNaughton speak with Dr Richard Schloeffel, Emerge Australia's Medical Director, about how ME/CFS is misunderstood in Australia and if those living with ME/CFS can help those being diagnosed with Long COVID. Read more
Emerge Australia has called for an urgent, major overhaul of the current, 20 year old clinical guidelines for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) to provide the medical profession, especially general practitioners, with the most update information to assist the 250,000 Australians living with the disease. Read more
Amanda Canzurlo has a career as a singer with a busy touring schedule, performing under the name "Bloom". But years ago, that would have been impossible. After a bout of glandular fever when she was 16, she was bed-bound for about 10 weeks. Read more
Our International Roundup provides a brief snapshot of some of the ME/CFS research funding, clinical care and advocacy actions around the world in the last few months. Read more