What we do

Emerge Australia is a national organisation providing information, support and advocacy for people living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Our work gives hope and help to more than 250,000 Australians living with ME/CFS.

The impacts of ME/CFS can be devastating, leaving 25% of patients housebound or bedbound, with many people unable to work or participate in community life. People living with ME/CFS often feel invisible due to the unknown cause of the condition, lack of effective treatment options and limited community awareness, leading many to 'go missing' from their own lives.

In order to continue our essential work, Emerge Australia relies on generous support from the community as we continue to lobby for increased public awareness and funding for biomedical research.

Our mission

To support, provide information and advocacy for people associated with myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS).

Our vision

Universal awareness and acknowledgement of ME/CFS as a medical condition.

Our values

To serve the best interests of people affected by ME/CFS with integrity, compassion and empathy.

Our work

We provide expertise on issues to do with ME/CFS at a national level
We host a range of community, national and international events that aim to increase awareness of ME/CFS as a biomedical illness
We provide a variety of resources, as well as news and updates, for people living with ME/CFS
We provide a telehealth nurse service to help meet the needs of people living with ME/CFS
We advocate for systemic reform to improve access to financial and social supports, and to improve access to better healthcare for people living with ME/CFS
We lobby for increases in community support for people with the disease and to drive more biomedical research into ME/CFS

Latest

Research Digest 10/01/20

Welcome to the 38th edition, featuring a Nature paper examining blood lactate levels in ME/CFS patients whilst at rest and a paper investigating the effect of pharmaceutical intervention on NK cell cytotoxicity in ME/CFS patients compared to healthy individuals.
Meg's 50th Birthday Fundraiser

I'm fundraising to give hope and help to the 250,000 people living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) across Australia. ME/CFS sorely lacks funding for advocacy, patient support and research, so anything you can contribute would be welcome.
Siobhan's 30th Birthday Fundraiser

I'm fundraising to give hope and help to the 250,000 people living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) across Australia.
Bunnings Sausage Sizzle Raises Money for Emerge Australia

'We just wanted to do something for our daughter who was diagnosed about five years ago with sudden onset ME/CFS,' Peter and Bronwyn said. '...after considering a few different options for raising money, we thought about a Bunnings BBQ.'

Accessibility
Siobhan's 30th Birthday Fundraiser

I'm fundraising to give hope and help to the 250,000 people living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) across Australia.
Bunnings Sausage Sizzle Raises Money for Emerge Australia

'We just wanted to do something for our daughter who was diagnosed about five years ago with sudden onset ME/CFS,' Peter and Bronwyn said. '...after considering a few different options for raising money, we thought about a Bunnings BBQ.'
Health and Wellbeing Survey

Emerge Australia published results from its first ME/CFS Health and Wellbeing Survey in 2018 and launched another survey in 2019. We plan to stay current and informed about the needs of the ME/CFS community by running an updated version of this Health and Wellbeing Survey every three years.
Disability Support Pension

The Disability Support Pension (DSP) is a Centrelink payment providing financial support if you have a physical, intellectual or psychiatric condition that stops you from working. Click here to access resources developed to assist people with ME/CFS to understand DSP and what is required to apply.
National Disability Insurance Scheme

The National Disability Insurance Scheme (NDIS) is designed to help support people with disability. Click here to access resources developed to assist people with ME/CFS to understand the NDIS and what is required to apply.
Research Digest 10/01/20

Welcome to the 38th edition, featuring a Nature paper examining blood lactate levels in ME/CFS patients whilst at rest and a paper investigating the effect of pharmaceutical intervention on NK cell cytotoxicity in ME/CFS patients compared to healthy individuals.
Research Digest 17/05/19

Welcome to the 23rd edition, featuring articles on the validation of impaired transient receptor potential melastatin 3 ion channel activity in natural killer cells from ME/CFS patients, and markers of non-coeliac wheat sensitivity in patients with ME/CFS.
Research Digest 13/12/19

Welcome to the 37th edition, featuring a retrospective study on the effectiveness of using low-dose naltrexone on ME/CFS patients, and a meta-analysis comparing protein biomarkers of inflammation between ME/CFS patients and non-affected controls.
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