Inclusive Endometriosis Education for All Australians 

Endometriosis Australia is proud to launch a new initiative aimed at improving access to endometriosis information and support for communities who have historically been underrepresented in health communication. 

Through the establishment of our Priority Populations Working Group, we are working to ensure that every Australian — regardless of language, identity, ability, or geography — has access to accurate, culturally relevant, and empowering information about endometriosis. 

Help Co-Design Resources That Reflect Your Community 

We know that a one-size-fits-all approach to endometriosis awareness doesn’t work. That’s why we’re inviting individuals with lived experience, community leaders, and healthcare advocates to join us in shaping new education and awareness materials — together. 

The working group will help co-design resources that are: 

• Culturally appropriate and language-accessible 

• Disability-inclusive and gender-affirming 

• Reflective of the lived experiences of Aboriginal and Torres Strait Islander peoples, CALD communities, adolescents, rural and regional Australians, and other underserved groups 

Meet Our Chair: Ruhee Meghani 

Ruhee Meghani represents Endometriosis Australia as an Endo Champion, bringing visibility to endometriosis and supporting affected communities

We are honoured to have Ruhee Meghani, founder of Allied Collective, as Chair of the Priority Populations Working Group. Ruhee is one of Australia’s leading voices in health equity and inclusion, and an Endo Champion with lived experience. 

Under Ruhee’s leadership, this group will champion diversity in healthcare communications and work to eliminate the barriers that many people face when trying to understand, manage, or seek care for endometriosis. 

Why Your Voice Matters 

Your lived experience and insight are essential. As a member of the working group, you will: 

• Participate in meaningful conversations around health equity and inclusion 

• Help identify what information your community needs — and in what format 

• Co-create resources that resonate and reflect your culture, language, and experience 

• Collaborate with others who are passionate about reducing health disparities 

How It Works 

• Monthly meetings (via Zoom) for the first three months, then bi-monthly 

• Open to people across Australia, from all backgrounds and identities 

Get Involved 

If you’re passionate about inclusive healthcare and improving endometriosis education, we would love to hear from you. 

Please express your interest by Monday August 4 2025. 

Have questions? Contact us at admin@endoaustralia.org