By Sasha Nimmo Australia’s University of New South Wales (UNSW) is trialling an education module for health professionals. The trial
by Sasha Nimmo In September 2016, Queen Mary University of London (QMUL) was compelled to release the data from the
Parliament was told that 75% of Australians with ME and CFS recover. The real figure is closer to 5%.
Why would the government allocate funding for medical research and treatment if it is told that most patients recover without it?
ME patients, family, friends, health practitioners and researchers are joining together to bring ME to the attention of government. Melbourne’s MillionsMissing will be on the steps of Parliament House, Spring St, Melbourne, from 1pm to 2pm on Wednesday 12 October 2016.
by Sasha Nimmo Myalgic Encephalomyelitis is estimated to affect between 0.4% and 1% of the population, according to the International Consensus
by Sasha Nimmo Online public consultation on the second draft National Strategic Framework for Chronic Conditions is now open. This
by Sasha Nimmo Update 3 September: In June I asked South Australia’s ME/CFS Australia (SA) if they were recruiting patients (as indicated by
by Sasha Nimmo #MillionsMissing is a global day of protest for the millions missing from work, life, school, and families because
by Sasha Nimmo Up to 240,000 Australians have Myalgic Encephalomyelitis. ME may be mild, moderate or severe. More than 25%
by Sasha Nimmo Australia’s Myalgic Encephalomyelitis (ME) and chronic fatigue syndrome (CFS) Awareness Week is 11-17 May. The Week coincides
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