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
Meet the Scientists: Rhiannon Morris is from Melbourne’s The Walter and Eliza Hall Institute of Medical Research (WEHI) which is the oldest research institute in Australia.
by Sasha Nimmo Around 38% of Australians diagnosed with chronic fatigue syndrome (CFS) and Myalgic Encephalomyelitis (ME) do not meet
Three recently published Australian studies took a look at the blood, brains and bodies of patients with Myalgic Encephalomyelitis (ICC) and chronic fatigue syndrome (Fukuda).
by Sasha Nimmo Up to 240,000 Australians have Myalgic Encephalomyelitis. ME may be mild, moderate or severe. More than 25%
March 2015 has been a busy month for biomarker discoveries for patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: two new papers published and one patent registered.
Australia needs to leave behind ME/CFS and CFS/ME. Why is it important to use ME and CFS?
Dr Brett Lidbury Meet Dr Brett Lidbury, biometrics researcher at the Australian National University in Canberra. He shares with us
Ask the medical research council to fund research into ME and CFS, here’s a letter template to send to the NHMRC.
© 2021 ME Australia. All Rights Reserved.