by Sasha Nimmo Australia’s Health Minister, Greg Hunt, announced $3 million in medical research funding. In 2018-19 the government will
By Sasha Nimmo and ME Australia Australia’s National Health and Medical Research Council (NHMRC) called for feedback on their advisory
by Sasha Nimmo Australia’s Health Minister, Greg Hunt, listened to people with Myalgic Encephalomyelitis (ME), families, scientists and organisations. Minister
By Sasha Nimmo Australians are having their concerns dismissed by GPs, receiving harmful medical advice, refused insurance claims, refused access
Macquarie University are recruiting people with chronic fatigue syndrome, fibromyalgia, gastrointestinal disorders and multiple chemical sensitivity for a study measuring somatic symptoms, hypochondria, anxiety and depression, catastophising and co-morbid diseases.
by Sasha Nimmo Emerge Australia has been given $370,000 by the federal government in a grant for a research symposium,
by Sasha Nimmo Three senators have formed a Parliamentary Friends of Myalgic Encephalomyelitis (ME) and chronic fatigue syndrome (CFS) group
by Sasha Nimmo The petition against the ‘increasing exercise’ trial using Xbox video gaming at the University of South Australia
By Sasha Nimmo Australia’s National Health and Medical Research Council (NHMRC) answered questions from Greens, Centre Alliance and Labor senators
by Mary Macrae Sydney ME community members marked #MillionsMissing with a screening of the film ‘Unrest’ in Newtown, hosted by
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