Andrew gave an impassioned speech at Melbourne’s Millions Missing rally, where 50 people gathered on the steps of the State Library.
by Helen Donovan May 12 is Alem Matthee’s birthday. Around the world, people with ME, their friends, families and scientists
by Anthony Clarke Anthony Clarke of BLOXAS, an architecture practice for empathic and experimental architecture, was contacted by a South
by Sasha Nimmo Senator Jordon Steele-John this week announced the Australian Greens’ policy on Myalgic Encephalomyelitis (ME) and Chronic Fatigue Syndrome
By Sasha Nimmo and ME Australia Australia’s National Health and Medical Research Council (NHMRC) called for feedback on their advisory
by Sasha Nimmo A paper published in Metabolic Brain Disease by Morris, Maes, Burk and Puri suggests Myalgic Encephalomyelitis develops
Meet the Scientists: Dr Christopher Armstrong is an Australian scientist researching Myalgic Encephalomyelitis (ME). He moved to California late last year to take up a position at the Open Medicine Foundation.
By Sasha Nimmo Australians are having their concerns dismissed by GPs, receiving harmful medical advice, refused insurance claims, refused access
Andrew talks about his experience on SBS Insight: how the show focussed on recovered sports stars and exercise clinics while he was told to ‘let others speak’ when he tried to talk.
by Sasha Nimmo Emerge Australia has been given $370,000 by the federal government in a grant for a research symposium,
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