Our News Articles

$1,200,000 is required over 2 years for the development of national clinical guidelines for ME/CFS to increase safety and quality of care and establish shared care It is a matter of urgency for Australia to update its clinical guidelines for ME/CFS, to ensure Australian ME/CFS patients have access to the best possible care, based on current

Patient Pathways telehealth pilot program Our Patient Pathways telehealth pilot program will be completed on June 30, 2022. Emerge Australia would like to thank the Centre for Community-Driven Research (CC-DR) for including us in this program. Over the next couple of months, we will start to create a new Telehealth Nurse referral process and provide an additional service to

Media Release 11 May 2022 Emerge Australia has urged Political Parties and Candidates standing in the Federal Election to increase their knowledge and understanding of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Anne Wilson, CEO of Emerge Australia, said of the 250,000 Australians who live with ME/CFS, 25 per cent (60,000+ people), have symptoms so severe they

16-22 May 2022 Better together  Emerge Australia was created by volunteers more than 40 years ago. Today, volunteers continue to devote considerable time and expertise to Emerge Australia to ensure that we can continue to provide the high-quality services and programs for people living with ME/CFS. This National Volunteer Week we hope you will join

Update: Feedback from GPCE Sydney shows important education outcomes among GPs  Verbal feedback from Richard’s presentation about, long COVID and ME/CFS: Diagnosis, treatment and management options, in Sydney in late May was overwhelmingly positive. Formal, written feedback, provided to us last week by the organisers of the event, is equally as impressive. 80% of attendees reported that Dr

Release date: 27 April 2022 On ABC’s The Conversation Hour, Richelle Hunt and Jane McNaughton speak with Dr Richard Schloeffel, Emerge Australia’s Medical Director, about how ME/CFS is misunderstood in Australia and if those living with ME/CFS can help those being diagnosed with long COVID. Listen to the interview Published: 6th May, 2022 Share this

Media Release  Existing, 20-year-old Clinical Guides Need Review Enable this content? This content is served by a third party, player.vimeo.com.If enabled, player.vimeo.com may collect information about your activity.Manage preferences to always allow this content. Accept and EnableManage Preferences Read the report – State of the Nation: Because people with ME/CFS matter Emerge Australia has called

Media Release22 April 2022 Political Parties Warned on Major Hit On Health Budgets Enable this content? This content is served by a third party, player.vimeo.com.If enabled, player.vimeo.com may collect information about your activity.Manage preferences to always allow this content. Accept and EnableManage Preferences Read the report: State of the Nation: Because people with ME/CFS matter

Published by ABC News 22/04/2022 Authors: National medical reporter Sophie Scott and the Specialist Reporting Team’s Leonie Thorne Amanda Canzurlo has a career as a singer with a busy touring schedule, performing under the name “Bloom”.  But years ago, that would have been impossible. After a bout of glandular fever when she was 16, she

Emerge Australia’s State of the Nation report includes five priority areas for government to improve the lives of people with ME/CFS. Read: The State of the Nation: Because people with ME/CFS matter In the lead up to the federal election, Emerge Australia is writing to all federal parliamentarians to seek their support for these five

Our International Roundup provides a brief snapshot of some of the ME/CFS research funding, clinical care and advocacy actions around the world in the last few months.  Research The UK ME/CFS Priority Setting Partnership (PSP), facilitated by the James Lind Alliance (JLA), is coming to a conclusion. The aim of the PSP is to provide

Release date: 16 March 2022 On ABC’s Life Matters, Hilary Harper speaks with Emerge Australia’s CEO Anne Wilson and Dr David Putrino, Associate Professor of Rehabilitation and Human Performance, Mount Sinai Health System about how Australia might manage the impact long COVID will have on tens of thousands of Australians and what hints we can take

As part of Emerge Australia’s ongoing specialised education sessions for Allied Health professionals our Nurse Educator, Kate Herbert, presented an education session on Monday March 4th, about the basics of ME/CFS. The group of 11 physiotherapists and exercise physiologists at Merri Health, based in the northern suburbs of Melbourne were particularly interested to know about

Release date: 16 March 2022 The impact of the long term effects of COVID-19 are becoming better understood. It’s estimated that up to 30 per cent of people who get infected with COVID show symptoms months later. ABC NewsRadio’s Cameron Green spoke to Dr Richard Schloeffel, Medical Director of Emerge Australia. He says there are

Media Release: 16 March 2022 One of Australia’s leading medical specialists on complex and chronic disorders today warned the lack of research and treatment information for the medical profession on myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) can lead to inappropriate diagnosis and treatment of patients. Dr Richard Schloeffel OAM, the Medical Director of Emerge Australia, who

Media Release  Emerge Australia today revealed that approximately 75% of an estimated 250,000 Australians living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) are women. Speaking on the eve of International Women’s Day, Anne Wilson, CEO of Emerge Australia said, myalgic encephalomyelitis (ME/CFS) is a complex and disabling neurological disease that affects many parts of the body, including

Emerge Australia is pleased to announce the appointment of our new Medical & Scientific Advisory Committee (MSAC).  The MSAC combines the knowledge of ME/CFS clinicians and researchers, as well as Emerge Australia staff, to pool the collective knowledge to set in motion objectives which will improve the outcomes for Australians impacted by ME/CFS.  Members of MSAC

Recently the Board of Emerge Australia unanimously voted to appoint Dr. Richard Schloeffel OAM to the position of Medical Director.  This is a significant appointment that will result in Dr. Schloeffel having oversight of direction regarding clinical programs and our work on ME/CFS Clinical Guidelines among other areas. Dr. Schloeffel will provide a link between

After an initial delay, it was announced on October 29th, that the new National Institute of Health and Care Excellence (NICE) guideline (UK) for ME/CFS have finally been published.  The new guidelines represent a significant shift in the medical treatment of ME/CFS in the UK. In particular acknowledging that exercise programs can make ME/CFS worse and that cognitive behavioural therapy (CBT) is not a curative

During National Carers Week, Emerge Australia would like to acknowledge and thank all those who extend care and support to the 250,000 Australians impacted by ME/CFS. Nationally, 2.65 million Australians provide care for others, making you part of a large community. The theme for this year’s celebration is Millions of Reasons to Care. Most people who provide care don’t see themselves as carers, they instead see themselves as parents, partners,

7 October 2021 An important part of improving outcomes for people living with ME/CFS is educating healthcare professionals about the condition and what they can to do help. Last week, our Nurse Educator Kate Herbert delivered a “Back to Basics” presentation to nurses and social workers at Echuca Regional Health for their recent professional development day.   Only two of the participants who responded to the pre-presentation survey had received any formal training about ME/CFS. So, Kate covered the basics including both outdated and

Did you know that carers make up nearly 11% of Australia’s population? Meaning that there are approximately 2.65 million carers across Australia. Carers and family members of those living with ME/CFS can benefit from joining our online peer support groups, to connect with others who undertake caring roles for their loved ones.   As part of

Emerge Australia is very disappointed to learn that the UK’s National Institute of Health and Care Excellence (NICE) has announced that it has paused the publication of its new ME/CFS clinical guidelines, which had been due to be released on August 18. This is a devastating development for ME/CFS patients around the world, especially those in the UK who have waited years for these new guidelines.   The draft of the new guidelines, released late last

Funded by the National Health and Medical Research Council Deakin University and Barwon Health, the CHROMIC study aims to improve the understanding of the disorder as well as to look for new treatments for ME/CFS. To take part in the study, only one appointment is required of the participants. This appointment includes the collection of

Recruitment has commenced for the ANCHOR Study. This landmark ME/CFS research is funded by the Medical Research Future Fund to investigate the quality of life, social, educational and economic impacts of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) on people living with the condition and their carers. This project is a collaboration of researchers from the University

In May, the US Centers for Disease Control and Prevention (CDC) released a draft of its evidence review on the diagnosis and treatment of ME/CFS for public comment. This review has been in development since 2018, and was to be the CDC’s first step in the development of new US clinical guidelines for ME/CFS. Emerge

Ricky Buchanan worked with Emerge to write this in 2021 and was too ill to update or add to it in 2022, as her severe ME/CFS has worsened since 2021 What is Severe ME day?  Severe ME Day is recognised globally as a day to acknowledge the strength and spirit of the estimated 25% of

We would like to introduce to you the ME/CFS Pacing App created by our generous contributor, Mathew Blake. The app is designed to help people with mild to moderate ME/CFS better manage their daily energy use and adjust their pacing habits as needed. The app is not designed to manage all symptoms that ME/CFS can

Information about COVID-19 vaccination is rapidly changing. This can be confusing, especially when each state may have different eligibility criteria. That’s why we have created a hub to help the ME/CFS community find the information appropriate for each state and territory, all in one spot. The links provided below lead directly to both Federal and

By Jason Murphy Meet Mike Musker.  A former mental health nurse who took the path less traveled. Musker is now a scientist with some excellent research underway.  He works with the South Australian Health and Medical Research Institute, and his research – including one major project near completion and another about to start – is