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  • Fundraise
  1. Get involved
  2. Fundraisers

Fundraise

Welcome to the fundraisers page,

Would you like to run, cook, knit, craft or come up with your own great fundraising idea to help improve the lives of people living with ME/CFS?

The ME/CFS community (aka ‘MEEPS’ / Jarmy Army) is amazing. In both words and actions, supporters of our cause demonstrate incredible compassion for fellow sufferers, people more severely impacted than themselves, people who might be isolated by the condition and especially people who are just beginning their journey. 

From persuading friends and family to run marathons, to organising sausage sizzles, to knitting or crafting – supporters across Australia find ways to raise critical funds for people affected by ME/CFS in Australia.

Simply click through below to create your own fundraising campaign.



Set up your own fundraiser page
Looking for a fundraiser?
Tom’s buzz for ME/CFS

Tom’s buzz for ME/CFS

Tom Nicoll

I'm fundraising to give hope and help to the 250,000 people living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) across Australia, including my older brother Zach.

Published: 21st March, 2023

Blue Sunday 2023 for Emerge Australia

Blue Sunday 2023 for Emerge Australia

Anna Redshaw

Fundraising for Emerge Australia to help them continue to advocate and support people living with M.E. in Australia

Published: 10th February, 2023

Item.Title

Shine a Light On ME/CFS

Sue Price

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

Published: 9th August, 2022

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Showing 3 of 3

Latest

  • Research Digest 30/3/23

    Research Digest 30/3/23

    Welcome to the Research Digest’s 93rd edition. This month's edition summarises research that investigates factors that influence the prognosis of ME/CFS and demonstrates that high muscle sodium content, maybe a contributing factor to the pathophysiology of ME/CFS. A review is also highlighted that conveys what is presently known about Long COVID and finally, a local study sheds light on brain structure changes that are common to Long COVID and ME/CFS.

  • Run Melbourne 2023

    Run Melbourne 2023

    We're participating in Run Melbourne 2023. Join now to help reach our goal by running, walking or performing your own activity with us!

  • Tom’s buzz for ME/CFS

    Tom’s buzz for ME/CFS

    I'm fundraising to give hope and help to the 250,000 people living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) across Australia, including my older brother Zach.

  • GP Education at GPCE in 2023

    GP Education at GPCE in 2023

    We know how difficult it is to find a GP with knowledge of ME/CFS. One of the main aims for our GP education program is to grow the GP workforce confident to take on people with complex presentations.

Most read

  • Contact Us

    Contact Us

    Emerge Australia provides an information line where you can find out about the latest news and information about ME/CFS.

  • What we do

    What we do

    Who we are and what we do

  • What is ME/CFS?

    What is ME/CFS?

    Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex and disabling disease that affects many parts of the body, including the brain and muscles, as well as the digestive, immune and cardiac systems, among others.

  • Post-Exertional Malaise (PEM)

    Post-Exertional Malaise (PEM)

    The central feature of ME/CFS, and a common symptom of Long COVID, is post-exertional malaise (PEM). PEM is when symptoms get worse after physical or mental activity.

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  • Coronavirus and ME - Simplified facts

    Coronavirus and ME - Simplified facts

    Many people with ME/CFS and other vulnerable communities in Australia are concerned about the impacts of the spreading coronavirus disease COVID-19. This is an easy-read resource with the latest information and advice.

  • What is ME/CFS?

    What is ME/CFS?

    Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex and disabling disease that affects many parts of the body, including the brain and muscles, digestive, immune and cardiac systems. ME is classified as a neurological disorder by the World Health Organization.

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    Patient Advisory Group

    The Patient Advisory Group provides Emerge Australia with ongoing advice about the needs of the community, as well as invaluable input into projects

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Emerge Australia
Level 7, 276 Flinders Street
Melbourne VIC 3000
1800 865 321
03 9529 1344
[email protected]

Media enquiries contact Claire Heaney
Mobile: 0421 612 507
Email: [email protected]

Emerge Australia is registered as a charity with the Australian Charities and Not-for-profits Commission (ACNC). We are authorised by the Australian Tax Office as a deductible gift recipient (DGR). 

ABN/DGR: 22 385 438 041

Donations of $2 or more are tax-deductible. 

Emerge Australia acknowledges Aboriginal and Torres Strait Islander people as the Traditional Custodians of the land and pays respect to their Elders past and present.

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