by Sasha Nimmo National Health and Medical Research Council’s Chief Executive Officer, Prof Anne Kelso, today released her response the
By ME Australia Australians with Myalgic Encephalomyelitis and chronic fatigue syndrome are having their disability support pension, NDIS, superannuation and
by Sasha Nimmo Australia’s Health Minister, Greg Hunt, listened to people with Myalgic Encephalomyelitis (ME), families, scientists and organisations. Minister
By Sasha Nimmo Australia’s government is seeking advice from an advisory committee on current research, gaps in research and whether
By Sasha Nimmo Australian research is underfunded and the government’s clinical guidelines are outdated so the ME and CFS advisory
by Sasha Nimmo Australia’s National Health and Medical Research Council (NHMRC) says it plans to spend $3-5 million dollars over
The Australian federal government is spending the ME and CFS research budget on training medical professionals to use cognitive behavioural therapy and graded exercise therapy on patients in Australia and internationally, despite the fact these therapies show no benefit and may do harm.
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 Up to 240,000 Australians have Myalgic Encephalomyelitis. ME may be mild, moderate or severe. More than 25%
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