Emerge Australia Inc

Emerge Australia Inc Providing hope & help for people living with myalgic encephalomyelitis/chronic fatigue syndrome and long COVID

Are you caring for someone with ME/CFS or long COVID who is predominantly bedbound?Caring for a loved one who is predomi...
02/09/2026

Are you caring for someone with ME/CFS or long COVID who is predominantly bedbound?

Caring for a loved one who is predominantly bedbound can be incredibly rewarding, but it can also be isolating. Connecting with others who truly understand can make a real difference.

We're launching a new virtual support group, Carers Connect, starting soon. It's a welcoming space where carers can share experiences, gain support, and connect with others who understand the unique challenges of caring for someone with severe ME/CFS or long COVID.

đź—“ 5 fortnightly sessions
đź“… Mondays at 1:00pm (Melbourne time), starting 28 September
đź’» Online via Microsoft Teams
👥 Small group (up to 12 participants)
đź’™ Professionally facilitated

At the end of the program, participants will have the opportunity to explore continuing the group as an ongoing peer-led support group.

If you're looking for understanding, connection, and support from people who truly "get it", we'd love to welcome you.

Find out more and register here: https://zurl.co/jJ4fv

/CFS

Donate a blood sample to the AusME Biobank!  You hold the key to advancing medical research outcomes for ME/CFS and long...
01/09/2026

Donate a blood sample to the AusME Biobank!
You hold the key to advancing medical research outcomes for ME/CFS and long COVID.

If you reside in VIC, NSW or QLD and have ME/CFS, long COVID, or are willing to donate blood as a healthy volunteer, find out how you can become an AusME Biobank blood donor by visiting:
https://zurl.co/5zvq2
https://zurl.co/GWa2P

Emerge Australia has lodged a submission about the Australian Government’s new Inclusive Communities Fund.We support mak...
01/09/2026

Emerge Australia has lodged a submission about the Australian Government’s new Inclusive Communities Fund.

We support making community organisations more inclusive, however this cannot replace individual NDIS funding, especially with NDIS funding for Social, Community and Civic Participation (SCCP) being cut by half from 1 October 2026.

Feedback from our community shows that NDIS participants with ME/CFS and long COVID use this funding to:
• attend medical appointments
• obtain groceries
• connect with other people.

Making venues more accessible will not help people who cannot safely leave home.

We seek support from Government to:
• protect funding for essential support
• prioritise housebound and bedbound people
• fund online, flexible and home-based participation
• recognise PEM and fluctuating capacity.

Read our full submission: https://zurl.co/oHrm4

🌍 Free Learning Opportunity 🌿  Emerge Australia and Bateman Horne Center have partnered to launch a free, self-paced Lea...
31/08/2026

🌍 Free Learning Opportunity 🌿
Emerge Australia and Bateman Horne Center have partnered to launch a free, self-paced Learning & Education Centre designed for people living with ME/CFS, long COVID, and other energy-limiting chronic conditions.

đź§  These modules bridge expertise from Australia and the U.S., offering:
✔️ Practical tools for managing PEM, pacing & orthostatic intolerance
✔️ Supportive strategies for daily life
✔️ Insight for caregivers & nonclinical professionals into the lived experience
✔️ Resources to build better care, together

đź’ˇ What to expect:
✔️ Gentle, flexible guidance tailored to your energy limits
✔️ Tools to create a personalised pacing plan
✔️ Realistic strategies for adapting everyday tasks
✔️ A supportive, no-pressure learning space—pause and return anytime

✨ Respecting your experience. Supporting your journey.

đź”— Start exploring today: https://zurl.co/gsfhI

📅 2026 Health Professional Webinar Series: Redefining sleep success in ME/CFSWhen: Thursday 17 September, 6:30pm – 8:00p...
31/08/2026

đź“… 2026 Health Professional Webinar Series: Redefining sleep success in ME/CFS

When: Thursday 17 September, 6:30pm – 8:00pm AEST

Where: Live online. Register here https://zurl.co/M14K3

What: Webinar and question time. You can also submit your questions prior to the event.

Sleep problems are common in ME/CFS, but is "normal" sleep always achievable or even the right goal?

Join David Cunnington, specialist sleep physician and author of Australia's national insomnia guidelines, as he explores what clinicians need to know about sleep dysfunction in ME/CFS and when sleep disorders should be treated.

Learning outcomes:

By the end of this webinar you will be able to:

*Explain why disrupted sleep is an expected part of ME/CFS - sleep as an auto-regulated process affected by the illness, like dysautonomia, temperature or gut symptoms, rather than a sign of treatment failure.

*Recognise the harm in expecting "normal" sleep - how rigid sleep rules and a "fixable sleep" message add burden and hopelessness for patients.

*Identify the sleep problems worth treating - distinguish intrinsic sleep dysregulation from comorbid disorders (sleep apnoea, restless legs, circadian rhythm problems) that warrant assessment and management in their own right.

*Set realistic, functional sleep goals - practical strategies within the patient's energy envelope, sensible use of medication, and removing counterproductive rules.

📌 Target audience and CPD: The session will best suit all healthcare professionals. All are welcome, whether you are new to the topic or seeking to advance your skills.

All participants will be issued with a certificate of attendance for your CPD records.

RACGP CPD approval pending for 1.5 Educational Activity Hours.

If you would like more information about our speaker, please sign into https://zurl.co/YlEr5

Please note: This session is for healthcare professionals only, including students.

Access to COVID-19 vaccines is changing. From 1 October 2026, access to free COVID-19 vaccines will only be available to...
30/08/2026

Access to COVID-19 vaccines is changing.

From 1 October 2026, access to free COVID-19 vaccines will only be available to specific groups at higher risk of severe illness.

If you have been thinking about getting a COVID-19 vaccine or booster, now is a good time to speak with your GP, pharmacist or healthcare provider about your options before the changes take effect.

Visit our website for more information about this change: https://zurl.co/UIkFG

We’re looking for local or Australia-wide community-led support groups focused on ME/CFS, long COVID, or related conditi...
27/08/2026

We’re looking for local or Australia-wide community-led support groups focused on ME/CFS, long COVID, or related conditions to include on our website. The groups listed operate independently from Emerge Australia, but we list them to build connections within our community.

If you run a group, we would love to hear from you. Please share your details with us so we can help others connect and feel supported.

Together, we can strengthen our community.

đź”—https://zurl.co/3l5yp

Emerge Australia remains concerned about what some of these changes could mean for people with ME/CFS and long COVID, pa...
27/08/2026

Emerge Australia remains concerned about what some of these changes could mean for people with ME/CFS and long COVID, particularly changes affecting access to the NDIS, treatment requirements and how functional capacity is assessed.

We thank everyone in our community who contributed their experiences and perspectives to our advocacy on the Bill, including members of Emerge Australia’s Community Advisory Panel. Your input helped us clearly communicate to decision-makers where the proposed changes could create particular risks for people living with ME/CFS and long COVID.

With the Bill now passed, our focus turns to implementation. Emerge Australia will continue advocating with government, parliamentarians, the NDIA and the broader disability sector to ensure the needs and experiences of people with ME/CFS and long COVID are understood as the new arrangements are developed.

Our key priorities include:
* Ensuring permanence is assessed appropriately for conditions such as ME/CFS and long COVID, where there are currently no evidence-based curative or reliably restorative treatments.
* Ensuring people are not required to undertake treatments that are inappropriate, inaccessible or risk worsening their health, including through post-exertional malaise (PEM).
* Making sure functional capacity assessments recognise PEM, delayed symptom exacerbation and fluctuating capacity, including that being able to do something once does not necessarily mean it can be done safely, reliably or repeatedly.
* Ensuring assessment and NDIS processes are accessible for people who are housebound, bedbound or unable to participate in standard processes without significant health consequences.
* Protecting access to appropriate supports for people with substantial functional impairment, including where support needs are complex.

We know some people in our community may be wondering what these changes mean if they are considering applying for the NDIS. Changes to access and eligibility criteria do not occur until January 2028. Existing participants will be reassessed progressively over 3 years from January 2028.

Eligibility will continue to depend on each person’s individual circumstances and whether they meet the NDIS access requirements. Emerge Australia has developed resources about applying to the NDIS which are available here: https://zurl.co/5m5SJ

The passage of the Bill is not the end of this process. Many important details will be determined through implementation, and Emerge Australia will continue working to ensure the voices and experiences of people with ME/CFS and long COVID are heard.

Huge thanks to Dr. Carina Garland Member for Chisholm for meeting with us and speaking about Count ME in Parliament on A...
27/08/2026

Huge thanks to Dr. Carina Garland Member for Chisholm for meeting with us and speaking about Count ME in Parliament on August 11! 🙏

Dr Garland spoke powerfully about why being counted matters: the difference between a condition the health system plans for and one it overlooks, and between research that gets funded and research that doesn't happen.

Grateful for her time, her support, and for helping make sure the 600,000+ Australians living with ME/CFS, long COVID and energy-limiting conditions are seen and counted. đź’™

Share and tag your MP. Being counted matters.

👉 View the speech here:
https://www.aph.gov.au/News_and_Events/Watch_Read_Listen/ParlView/video/4838628?startTime=16605

Dr Mike Freelander MP Mark Butler MP MillionsMissing Australia

Introducing Emerge Australia’s latest edition of the Research Digest, curated with most recent findings in ME/CFS and lo...
26/08/2026

Introducing Emerge Australia’s latest edition of the Research Digest, curated with most recent findings in ME/CFS and long COVID. Stay up-to-date with groundbreaking discoveries and advancements in the field.
• Summarised
• Easy to read
• Convenient
• Accessible

For delivery into your inbox each month, subscribe now for exclusive access

Browse previous editions or listen along with the audio versions on our website: https://zurl.co/fJZAC

Address

Level 7, 276 Flinders Street
Melbourne, VIC
3000

Opening Hours

Monday 9am - 4:30pm
Tuesday 9am - 4:30pm
Wednesday 9am - 4:30pm
Thursday 9am - 4:30pm
Friday 9am - 4:30pm

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