MEDIA RELEASE
Parliament Unites in Support of Endometriosis and Pelvic Pain Action
Canberra, ACT – 24 March, 2025
Members from across the political spectrum came together at Parliament House for a special event to reaffirm their ongoing commitment to improving outcomes for people living with endometriosis and pelvic pain in Australia.
This Endometriosis ACTION Month, the Australian Coalition for Endometriosis (ACE) brought together representatives from all levels of government, highlighting the bipartisan support for driving forward change in this critical area of health.
Consumers shared their lived expertise, health professionals talked through the recent progression but persistent barriers, researchers shared their 25+ years work researching a cure. And Australian decision makers listened to understand and take action.
Assistant Minister for Health and Aged Care, Hon Ged Kearney MP, addressed the audience, acknowledging the significant progress made and the tireless work being done by advocates, clinicians, researchers, and people with lived experience. She reiterated the government’s continued focus on improving awareness, early diagnosis, and access to care.
Opposition Leader Peter Dutton also commended the work of ACE, paying tribute to the frontline healthcare workers who are often challenged by systemic gaps when supporting and treating those affected. He applauded the collaborative work of ACE Chair Jess Taylor, noting the “enormous respect and support” the organisation holds across all sides of Parliament.
“The work of the Australian Coalition for Endometriosis is respected across the aisle, across all seats, and in every corner of this country,” said Mr Dutton. “This is a bipartisan issue – and we stand united in our support for continued investment in research, clinical care, and education to improve the lives of people affected by endometriosis and pelvic pain.”
ACE Chair Jess Taylor thanked attendees for their unwavering support and emphasised the importance of continuing to work hand-in-hand with government, clinicians, researchers, and those with lived experience to close the care gaps.
“This is what progress looks like – when Parliamentarians put politics aside and come together to listen, learn, and lead on issues that affect 1 in 7 people across this country,” said Ms Taylor.
The event served as a powerful reminder that lasting change for those affected by endometriosis and pelvic pain is possible – and that it is already underway, with strong support from all sides of government.
Media Contact:
Jess Taylor, Chair, Endometriosis Coalition
Email: info@acendo.com.au
Phone: 0434106341
About the Endometriosis Coalition
The Endometriosis Coalition is Australia’s peak body for endometriosis and pelvic pain, representing patients, healthcare professionals, researchers, and advocacy organisation’s. The Coalition drives national collaboration, policy change, and research investment to improve diagnosis, treatment, and support for the 1 in 7 Australians living with endometriosis and pelvic pain. Through partnerships with health professionals, government, and community organisations, the Endometriosis Coalition empowers those affected and works toward systemic change.