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Read the latest in Emerge Australia news for ME/CFS and long COVID.

Laura Kool

NDIS: Pricing Changes Affect Our Community

Published: 13 June 2025 Our Call To The NDIA  We call on the NDIA to:  Reverse the decision to cap travel at 50% of the hourly rate; Price all allied health practitioners the same;   Prioritise equity and complexity in future pricing reform.  People with ME/CFS are forced to advocate persistently for recognition of their disability

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A laptop, used by someone with ME/CFS, sitting on a desk next to a window.
Laura Kool

The CEO Report | June 2025

Read the full June Newsletter Hello to all our supporters and readers of the Emerge Australia newsletter! It is hard to believe we are only weeks away from the end of the financial year which means we are already half-way through 2025. I don’t know about you but that is a scary thought – I

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Peter McCluskey, carer for his wife Jenny, sitting up in bed. Peter wearing an "ME/CFS Sucks" t-shirt.
Indiara Wake

The Guardian: SBS’s Insight accused of betraying people living with chronic fatigue syndrome who appeared on program

Read Emerge Australia’s response to the episode Published: 9 June 2025 Media correspondent Amanda Meade reports on the backlash following an SBS Insight episode about myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Participants and advocacy groups, including Emerge Australia, have criticized the program for presenting a potentially harmful and unscientific narrative. The episode prominently featured an individual

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A laptop, used by someone with ME/CFS, sitting on a desk next to a window.
Laura Kool

A message from the CEO

SBS Insight program “Invisible Illness” Emerge Australia would like to express its concern, deep frustration and disappointment about the harmful narrative presented on Insight’s program that aired on SBS on Tuesday evening (20/5/2025) about Invisible Illnesses. Based on Insight’s positive reputation as well-researched, serious journalism, we promoted the episode to our community. We were pleased

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A laptop, used by someone with ME/CFS, sitting on a desk next to a window.
Laura Kool

The CEO Report | May 2025

Read the full May Newsletter Hello to all our supporters and readers of the Emerge Australia newsletter! What a month it has been culminating on 3 May with the Federal Election and a historic win for the Australia Labor Party. We congratulate the Albanese government on being re-elected for another term and look forward to

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Indiara Wake

Emerge Australia & Bateman Horne Centre Collaboration

Published: 1 May 2025 📣 Exciting Collaboration Announcement 🌏 Emerge Australia and Bateman Horne Center (BHC) are partnering to strengthen international efforts in patient-centered care for ME/CFS, long COVID, and other energy limiting conditions. Together, we’re building on Emerge Australia’s exceptional library of self-paced education modules — designed by and for people with ME/CFS —

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Indiara Wake

Zoom: ME/CFS Meet the Gilmore Election Candidates 2025!

Zoom Webinar: April 23, 2025 05:00 PM AEST Meet the federal election candidates in Gilmore in a virtual meeting about ME/CFS, long COVID, fibromyalgia and associated conditions. Fiona Phillips ALP Andrew Constance Liberal Kate Dezarnaulds Independent In the context of the five organisation’s federal election priorities, Emerge Australia is supporting Tracey Collins, a Gilmore resident

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A laptop, used by someone with ME/CFS, sitting on a desk next to a window.
Indiara Wake

The CEO Report | April 2025

Read the full April Newsletter Hello to all our supporters and readers of the Emerge Australia newsletter! As I write, Australia is gearing up for a federal election on 3 May. In our previous newsletter we outlined to you our election strategy designed in collaboration with our colleagues in Bridges & Pathways; ME/CFS Australia; MEANA

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Indiara Wake

ABC News: When illness forced Sarah out of work, she thought she’d be off for six months. It turned into eight years

Published: 7 April 2025 Journalist Hayley Gleeson, winner of Emerge Australia’s Media Awards for Excellence in Journalism 2025 (Long COVID), shares the story of Sarah Williams, after chronic illness forced Sarah to leave her university job, a planned six-month break turned into eight years. Battling ME/CFS, she returned to her childhood home in Tasmania’s Meander

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A laptop, used by someone with ME/CFS, sitting on a desk next to a window.
Laura Kool

A message from the CEO

I want to briefly address feedback from a few regarding quotes attributed to me in a recent article published in The Age and SMH about a machine-learning tool developed by researchers at University of Melbourne that can predict ME/CFS. I was reported as commenting that people with long COVID will largely recover over a period of

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