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  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?
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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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  • Shine a Light On ME/CFS

    Shine a Light On 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.

  • RMIT Journal Article: Dismissal of debilitating disease is dangerous as Long Covid cases rise

    RMIT Journal Article: Dismissal of debilitating disease is dangerous as Long Covid cases rise

    One of our volunteers, Jenny, Dr Richard Schloeffel and CEO Anne Wilson were recently interviewed for the RMIT Journal by Rebecca Kazmierczak.

  • July International Research and Advocacy Roundup

    July International Research and Advocacy Roundup

    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.

  • Educating over 100 physios about ME/CFS

    Educating over 100 physios about ME/CFS

    One cold evening in late July, Emerge Australia’s Nurse Educator, Kate Herbert, presented to the Australian Physiotherapy Association pain special interest group about ME/CFS. With over 100 participants, including attendees also from other special interest groups, this was the most well attended presentation Kate has delivered to date.

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    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.

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  • 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.

  • 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.

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Emerge Australia
Level 7, 276 Flinders Street
Melbourne VIC 3000
1800 865 321
03 9529 1344
Media enquiries: Ron Smith [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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