by Sasha Nimmo A charitable trust, the Mason Foundation, is asking researchers to submit proposals for a biobank and patient
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 Senior staff from Australia’s National Disability Insurance Agency (NDIA) met with Emerge Australia and ME Australia to
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 A paper published in Metabolic Brain Disease by Morris, Maes, Burk and Puri suggests Myalgic Encephalomyelitis develops
by Sasha Nimmo Emerge Australia is hosting an international research symposium on the biological basis, diagnosis, treatment and managment of
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.
Prof Don Staines Professor Don Staines is co-director of the National Centre for Neuroimmunology and Emerging Diseases (NCNED) at Australia’s
By Sasha Nimmo Released on the Friday before Christmas, the Australia’s National Health and Medical Research Advisory Commission’s draft report
by Kathy Collett Kathy Collett has lived with Myalgic Encephalomyelitis for more than 30 years. Frustrated by the lack of
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