National Action Plan for Endometriosis

Painaustralia is Australia’s leading pain advocacy body working to improve the quality of life of people living with pain, their families and carers, and to minimise the social and economic burden of pain on individuals and the community

The Australian Coalition for Endometriosis (ACE) is a peak consumer and advocacy body representing the needs of girls and women with Endometriosis in Australia. ACE aims to provide strategic direction and leadership to improve the outcome, treatment and support for women with endometriosis.

The purpose of the Pelvic Pain Foundation of Australia (Foundation) is to build a healthier and more productive community by improving the quality of life of people with pelvic pain and to minimise the suffering and burden of pelvic pain on individuals, their families and the community through awareness, education, funding, support, research and improving access to treatment and services.

Australia & NZ

Raising awareness and providing information and advocacy for thousands of women

Australian Women's health organisation. Providing resources for women with Endometriosis.

Beyondblue provides information and support to help everyone in Australia achieve their best possible mental health, whatever their age and wherever they live.

Free counselling 24/7

A national not for profit organisation with a focus on education. Free webinars available.

The Endometriosis Association (Qld) Inc.

Support hotline available.

National Action Plan for Endometriosis

Painaustralia is Australia’s leading pain advocacy body working to improve the quality of life of people living with pain, their families and carers, and to minimise the social and economic burden of pain on individuals and the community

The Australian Coalition for Endometriosis (ACE) is a peak consumer and advocacy body representing the needs of girls and women with Endometriosis in Australia. ACE aims to provide strategic direction and leadership to improve the outcome, treatment and support for women with endometriosis.

The purpose of the Pelvic Pain Foundation of Australia (Foundation) is to build a healthier and more productive community by improving the quality of life of people with pelvic pain and to minimise the suffering and burden of pelvic pain on individuals, their families and the community through awareness, education, funding, support, research and improving access to treatment and services.

Australia & NZ

Raising awareness and providing information and advocacy for thousands of women

Australian Women's health organisation. Providing resources for women with Endometriosis.

Beyondblue provides information and support to help everyone in Australia achieve their best possible mental health, whatever their age and wherever they live.

Free counselling 24/7

A national not for profit organisation with a focus on education. Free webinars available.

The Endometriosis Association (Qld) Inc.

Support hotline available.

The World Endometriosis Society (WES) advances evidence-based standards and innovations for education, advocacy, clinical care, and research in endometriosis, adenomyosis, and related disorders, in collaboration with its stakeholders and global partners to improve the lives of all affected women and their families.

A Portrait of Infertility

Endo What is a groundbreaking, bi-partisan movement dedicated to educating and empowering people with endometriosis while informing health care providers and policymakers and holding decision makers accountable.

EndoMetropolis* is a community for patients with endometriosis and their loved ones, and those who are involved in the endometriosis community (physicians, researchers, advocates…).

EWG's Skin Deep® cosmetic database gives people practical solutions to protect themselves and their families from everyday exposures to potentially toxic chemicals in personal care and beauty products. Skin Deep®, launched in 2004, lists easy-to-navigate hazard ratings for nearly 70,000 products and 9,000 ingredients on the market.

The World Endometriosis Society (WES) advances evidence-based standards and innovations for education, advocacy, clinical care, and research in endometriosis, adenomyosis, and related disorders, in collaboration with its stakeholders and global partners to improve the lives of all affected women and their families.

A Portrait of Infertility

Endo What is a groundbreaking, bi-partisan movement dedicated to educating and empowering people with endometriosis while informing health care providers and policymakers and holding decision makers accountable.

EndoMetropolis* is a community for patients with endometriosis and their loved ones, and those who are involved in the endometriosis community (physicians, researchers, advocates…).

EWG's Skin Deep® cosmetic database gives people practical solutions to protect themselves and their families from everyday exposures to potentially toxic chemicals in personal care and beauty products. Skin Deep®, launched in 2004, lists easy-to-navigate hazard ratings for nearly 70,000 products and 9,000 ingredients on the market.

Dr. Stephanie Davies Dr Nicholas Cooke and Julia Sutton

Pain and Prejudice: A Call to Arms for Women and Their Bodies
by Gabrielle Jackson

This free, informative and easy to understand, downloadable Pelvic Pain Booklet aims to provide preliminary information for those suffering with pelvic pain whilst they await further medical assistance.

Dr Susan Evans

The Doctor Will See You Now: Recognizing and Treating Endometriosis

Dr. Cook’s Endometriosis Books

Dr. Stephanie Davies Dr Nicholas Cooke and Julia Sutton

Pain and Prejudice: A Call to Arms for Women and Their Bodies
by Gabrielle Jackson

This free, informative and easy to understand, downloadable Pelvic Pain Booklet aims to provide preliminary information for those suffering with pelvic pain whilst they await further medical assistance.

Dr Susan Evans

The Doctor Will See You Now: Recognizing and Treating Endometriosis

Dr. Cook’s Endometriosis Books