PRIORITY SETTING ROUNDTABLE FOR ENDOMETRIOSIS

The Australian Coalition for Endometriosis invites all Tasmanian’s with an interest in endometriosis attend “An evening for action on Endometriosis in Tasmania“. 

This is not just another awareness raising event, the Australian Coalition for Endometriosis is currently leading a national roundtable consultation to identify key priorities for endometriosis in every state and territory in Australia. Insights from these consultations will inform its report to the Australian Government, due in June 2025. 

What you can expect: 

• Enjoy champagne and charcuterie boards on arrival
• Dinner with local Tasmanian wines (ALL GLUTEN FREE)
• Hear from those working in the endometriosis sector in Tasmania told alongside patients who will share their experiences of diagnosis and treatment of Endometriosis in Tasmania. (Further details to follow)
• All participants add their views and vote on the priorities for Endometriosis in Tasmania

These sessions are an opportunity to:

✅ Share your lived experience
✅ Contribute to national priority-setting
✅ Connect with advocates, clinicians, and community groups
✅ Shape the future of care, policy, and research

Who should attend? These roundtables are open to: – People living with endometriosis, adenomyosis, and/or pelvic pain (diagnosed or suspected) – Parents, partners, carers, and support people – Health professionals working in women’s health, chronic pain, primary care, allied health, and fertility – Researchers, students, and academics in relevant fields – Representatives from community groups, peak bodies, and advocacy organisations – Policymakers, government representatives, and service providers – Anyone passionate about improving care and outcomes for people affected by these conditions

All from Tasmania who work in endometriosis and pelvic pain and those impacted by endometriosis are invited to tell their stories. 

• What’s working? 
• What’s not working ?
• What needs to change? 

Please register to share your experiences and expertise and raise your voice to the callout for better support for endometriosis and pelvic pain in Australia. 

The Australian Coalition for Endometriosis (ACE) is Australia’s peak body for endometriosis and pelvic pain, uniting patients, healthcare professionals, researchers, and advocacy organisations. We drive national collaboration, influence policy, and promote research investment to improve diagnosis, treatment, and support for the 1 in 7 Australians affected by endometriosis and pelvic pain.

Through strong partnerships with health professionals, government, and community organisations, ACE empowers those affected and advocates for meaningful, systemic change. In collaboration with our members, ACE led the development of the world’s first National Action Plan for Endometriosis.

Membership as an Individual Supporter of the Australian Coalition for Endometriosis in FREE in 2025. Please join here.