
Open Letter : Recognition of medical specialty of Myalgic Encephalomyelitis (ME) in Australia
To Whom It May Concern Re: Recognition of medical specialty of Myalgic Encephalomyelitis (ME) in Australia[1] I am writing this
To Whom It May Concern Re: Recognition of medical specialty of Myalgic Encephalomyelitis (ME) in Australia[1] I am writing this
This is my severe ME story. What was your life like before you got sick? I was a full-time practising
By ME Australia Australians with Myalgic Encephalomyelitis and chronic fatigue syndrome are having their disability support pension, NDIS, superannuation and
Andrew gave an impassioned speech at Melbourne’s Millions Missing rally, where 50 people gathered on the steps of the State Library.
by ME Australia member in WA Stunning weather and a brilliant blue sky greeted everyone who gathered in the heart
by Sally Black The original plan went out the window when numbers dwindled, #MillionsMissing T-shirt’s never arrived and I crashed,
by Sasha Nimmo Millions Missing is a global movement calling for action for ME, an underfunded and ignored disease. Australia
By Jac Creedon Since 2015, Adelaide Oval in South Australia has been lit up in blue in recognition of ME
by Sasha Nimmo On Saturday 18 May a federal election will be held in Australia. This is your chance to
by Sasha Nimmo Senior staff from Australia’s National Disability Insurance Agency (NDIA) met with Emerge Australia and ME Australia to
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