Endometriosis Australia: Our Impact
How we help those living with endometriosis
Endometriosis Australia advocates for people affected by endometriosis, a chronic condition impacting millions worldwide.
We’re dedicated to improving lives through comprehensive support programs, patient education, research funding, policy advocacy and support services designed to make a real difference.
Our services are designed to help with endometriosis access to better care. Read more about how we help below.
Spotlight: EndoAcademy - Regional Nurses Scholarship Program
Living with Endo Podcast
Videos
Find Specialist Pain Clinics
Connect with others
Workplace support
Participate in research
Past and Present Campaigns
Where do my donations go?
- Endometriosis patients wait on average 6.5 years to receive a diagnosis, which is one of the most significant barriers to receiving adequate medical treatment and improving their quality of life.
- It is crucial that individuals living with endometriosis can access the medical and fertility care information they need.
- Donations raised with Endometriosis Australia go towards helping individuals affected by endometriosis through our key pillars.
- All funds raised through community donors and the gift of philanthropy are directed to our research grants, production costs for digital and other resources, information, and education.
Raising awareness for the nearly 1 million people living with endometriosis to reduce the stigma and lessen the isolation.
- State and Federal Government advocacy including the National Action Plan for Endometriosis
- Advocating for more specialised endometriosis and pelvic pain clinics
- Creating resources providing evidence-based information
- Educating about endometriosis to reduce the time between symptoms and diagnosis
- Delivering our EndoAcademy Nurses Scholarship program to support regional areas
- Funding for endometriosis research















