Emerge Australia Inc

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

Learn about pacing and PEM - choose from one of three ways that suit you 💛 Three supportive online options: 🌿 Learn, Pac...
11/06/2026

Learn about pacing and PEM - choose from one of three ways that suit you 💛

Three supportive online options:

🌿 Learn, Pace, Connect (workshop series starting in July, limited places)

A structured series of interactive workshops where you enrol in five workshops.
✔ Build and refine your pacing plan
✔ Small group discussions
✔ Option to continue in a peer group supported by a Volunteer Peer Support Champion (a peer, not a pacing expert)

🌼 Pop-Up Live Sessions

A standalone online presentation on a specific topic, followed by Q&A.
✔ Attend a single session only
✔ No ongoing commitment
✔ Camera and mic can stay off
✔ Carers welcome

🦋 Online learning modules

Access to our online education modules.
✔ Log in when you choose
✔ Eight topics to learn from at your own pace
✔ No ongoing commitment
✔ Carers and allies welcome

All three options are free of charge and focus on understanding post-exertional malaise (PEM) and safe pacing - just in different formats.

Find the approach that feels right for you.
Learn more: https://zurl.co/pMHAE

The gap. And the solution.When someone is diagnosed with ME/CFS or long COVID, the hardest part not knowing where to tur...
10/06/2026

The gap. And the solution.

When someone is diagnosed with ME/CFS or long COVID, the hardest part not knowing where to turn.

There is no clear pathway. GPs have not been trained in these conditions. Schools don't know how to help. Families trying to navigate systems that weren't built for invisible illness.

This is the gap Emerge Australia fills.

Telehealth support calls for people too unwell to leave home. Education for GPs. Guidance for carers, schools, and workplaces. Advocacy that reaches Parliament.

This work exists because of people like Henry and you.

Read more about Henry: https://zurl.co/FdVxZ

Please don't miss the chance to provide your feedback 💬 Before 30 June we ask you to provide a rating in response to ou...
09/06/2026

Please don't miss the chance to provide your feedback 💬

Before 30 June we ask you to provide a rating in response to our annual short survey to help Emerge Australia understand how you perceive the work we do on your behalf.

The survey should take around 5 minutes to complete.

Please click here https://zurl.co/g42WZ

Thank you for helping us to continuously improve.

🌟 The GLOW Trial is recruiting! 🌟Do you live with Long COVID and experience fatigue, brain fog, sleep problems, depressi...
09/06/2026

🌟 The GLOW Trial is recruiting! 🌟

Do you live with Long COVID and experience fatigue, brain fog, sleep problems, depression or anxiety?
Researchers at Deakin University are testing whether gut-based therapy (faecal microbiome transplantation, FMT) could improve outcomes for people with Long COVID.

📍 What’s involved:
✔️ 5 visits at University Hospital Geelong
✔️ 3 FMT or placebo enemas
✔️ Blood, urine & stool samples
✔️ Garmin watch to track activity, sleep & heart rate
✔️ Online questionnaires you can complete at home
✔️ Parking costs covered

👉 Eligibility: Adults 18–65 with a long COVID diagnosis and moderate to severe symptoms.

💙 Interested? Learn more by contacting the GLOW team at [email protected] | 📞 (03) 4215 3078

The people behind the people.When someone develops ME/CFS or long COVID, they don’t face it alone.Their family does too....
08/06/2026

The people behind the people.

When someone develops ME/CFS or long COVID, they don’t face it alone.
Their family does too.

Parents become carers.
Partners quietly adjust everything.
Families try to understand an illness that is still too often misunderstood.

More than 650,000 Australians are living with these conditions. Behind many of them is someone doing their best to hold things together.

Too often, those people feel unseen. Unheard.

Emerge Australia exists to change that - supporting patients, carers and families navigating this every day.

This EOFY, your donation helps make sure no one is left unseen or unheard.

Support families navigating this, donate today: https://zurl.co/RXOqv

The Baker Institute/University of Melbourne (VIC) are recruiting for their study.You might be suitable if you are:• Aged...
07/06/2026

The Baker Institute/University of Melbourne (VIC) are recruiting for their study.

You might be suitable if you are:
• Aged 18+ years
• Are living with ME/CFS or orthostatic intolerance
• Able to attend 2 clinic visits at the Baker Institute (Melbourne - parking and time spent reimbursed)

For more information visit:
https://zurl.co/lkfwR

Congratulations to Dr Marie Claire Seeley on a hugely successful POTS Conference in Adelaide. With Drs Seeley and Tavol...
05/06/2026

Congratulations to Dr Marie Claire Seeley on a hugely successful POTS Conference in Adelaide. With Drs Seeley and Tavoletti.

Dr Michelle Tavoletti and Emerge Australia’s CEO Anne Wilson at Emerge Australia’s AusME Poster presentation at the Aust...
05/06/2026

Dr Michelle Tavoletti and Emerge Australia’s CEO Anne Wilson at Emerge Australia’s AusME Poster presentation at the Australian POTS Foundation conference in Adelaide.

The cost no one sees. For people living with ME/CFS and long COVID, the illness is only part of it. There is also the ex...
04/06/2026

The cost no one sees.

For people living with ME/CFS and long COVID, the illness is only part of it.

There is also the exhaustion of not being believed. The isolation of cancelling plans, again. The weight of being misunderstood by the very people and systems meant to help.

Emerge Australia exists so that no one carries that alone.

This work exists because of your support: https://zurl.co/AZlnh

📅 2026 Health Professional Webinar Series: Assessing function in ME/CFSWhen: Thursday the 25 June, 6:30 – 8pm AESTWhere:...
03/06/2026

📅 2026 Health Professional Webinar Series: Assessing function in ME/CFS

When: Thursday the 25 June, 6:30 – 8pm AEST
Where: Live online. Register here https://zurl.co/UfYO0
What: Webinar and question time

Patients with ME/CFS may look “fine” in your consult, but what happens after they leave?

How do you document functional capacity in ME/CFS when it fluctuates and may not be immediately obvious?

Join us as Senior Occupational Therapist Melanie Weeks outlines how to assess and document fluctuating functional capacity in ME/CFS. Learn which assessment tools best capture functional impact in ME/CFS and practical tips to support NDIS, DSP, and service access, even with limited time and resources.

Learning outcomes:

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

*Describe the core features of ME/CFS, including post‑exertional malaise (PEM), severity levels, and their functional consequences
*Assess and document functional capacity in a way that supports access to services and income support
*Adapt modes of communication to support patients experiencing cognitive dysfunction

👉 Register now to strengthen your functional assessments and clinical documentation
📌 Highly relevant for GPs, OTs and physiotherapists needing to understand and document functional capacity in ME/CFS

RACGP CPD approval pending for 1.5 Educational Activity Hours.

A recording will be available after the event on our LMS "https://zurl.co/NEpTs"

Please note: These sessions are for Health Professionals only.

This webinar has been supported by an unrestricted educational grant from Moderna.

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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