Trans & Gender Diverse People

A Resource Series for Trans and Gender Diverse Folks

These resources have been co-designed by and for trans and gender diverse people with endometriosis.

They centre lived experience and aim to provide you with up-to-date information, share collective knowledge, and help you to find community and relevant resources.

What does co-designed mean? This means that we recruited trans and gender diverse folk with endometriosis and facilitated an online space where they were actively involved in making decisions about the contents and wording of these resources.

This project involved researchers from Western Sydney University, Monash University and was generously funded by Endometriosis Australia.

This series includes three co-designed resources:

An introduction to pelvic pain and endometriosis
A guide to signs and symptoms of endometriosis
Management strategies for pelvic pain and endometriosis
A note on language

This resource uses non-gendered, accessible, and medically accurate language to describe bodies and experiences. This includes terms like uterus, menstruation or period.

We recognise that language is deeply personal and is always growing and changing. If these terms don’t feel right for you, we encourage you to use – and ask others to use – words that feel more comfortable and affirm your gender.

An intro to pelvic pain
& endometriosis

An intro to pelvic pain & endometriosis

A guide to signs and symptoms
of endometriosis

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Management strategies used for pelvic pain and endometriosis

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