MEDIA RELEASE
Endometriosis Coalition Welcomes New Medicare Item Number for Endometriosis Ultrasound in Federal Budget
The Endometriosis Coalition (ACE), Australia’s peak body for endometriosis and pelvic pain, proudly welcomes the Federal Government’s announcement of a new Medicare Benefits Schedule (MBS) item number for advanced ultrasounds for people with severe endometriosis, set to commence on 1 November 2025.
This announcement, included in tonight’s Federal Budget, follows years of sustained advocacy by the Endometriosis Coalition and our dedicated members, researchers, ultrasonologists, sonographers, gynaecologists, and community advocates across Australia.
These specialised ultrasounds are essential in diagnosing and managing complex cases of endometriosis, particularly deep infiltrating disease affecting the bowel, bladder, ovaries, and other pelvic structures. Historically, access to these scans has been limited due to high out-of-pocket costs — placing a significant burden on patients and delaying vital diagnosis and care.
“This is a monumental step forward. We know that access to the right diagnostic tools — including expert ultrasound — can significantly reduce the diagnostic delay, improve treatment planning, and change the lives of those living with this debilitating disease,” said Ms Jess Taylor, Chair, Endometriosis Coalition.
One in nine Australian women and people assigned female at birth are affected by endometriosis, yet the average time to diagnosis is seven years. The annual cost of the disease is estimated at $30,900 per person, including medical expenses, lost productivity, and associated care.
This new Medicare item number is part of a broader Federal Budget investment in endometriosis and pelvic pain, which also includes:
Eleven new Endometriosis and Pelvic Pain Clinics to increase access to timely, multidisciplinary care
Expansion of all 33 federally funded clinics to include support for people navigating menopause and perimenopause
Ongoing commitment to reducing diagnostic delays and improving access to specialised treatment
“This outcome is the result of true collaboration between the community, clinicians, researchers, and advocates. It is a powerful reminder that when people with lived experience lead the way — and are backed by evidence and clinical expertise — real change is possible,” said Ms Jess Taylor, Chair, Endometriosis Coalition.
The Endometriosis Coalition extends its gratitude to all members, experts, and supporters who have tirelessly advocated for this change. We also acknowledge the Federal Government for recognising the critical role of accessible imaging in the effective management of endometriosis.
We remain committed to continuing this work — until every person living with endometriosis and pelvic pain has access to the care, support, and recognition they deserve.
Media Contact:
Jessica Taylor
0434106341
info@acendo.com.au
www.endometriosiscoalition.org.au
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.