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Lessons from implementing the Australian National Action Plan for Endometriosis.

Michael ArmourJodie AveryMathew LeonardiLeesa Van NiekerkMarilla L DruittMelissa A ParkerJane E GirlingBrett McKinnonAntonina Mikocka-WalusCecilia H M NgRebecca O'HaraDonna CicciaKatherine StanleySubhadra Evans
Published in: Reproduction & fertility (2022)
Endometriosis is a chronic disease where tissue like the lining of the uterus is found in other locations around the body. For the 830,000 people living with endometriosis in Australia, this often results in an immense burden on all aspects of daily life. In 2018, Australia was the first country to introduce a roadmap and blueprint to tackle endometriosis in a nationwide coordinated manner with the National Action Plan for Endometriosis. This plan was created as a partnership between government, endometriosis experts and advocacy groups. There are several other countries who are now considering similar plans to address the burden of endometriosis. As researchers and clinicians are working to improve the lives of those with endometriosis, we share our experiences and discuss areas that should be considered when developing these national plans, including diagnostic pathways without the need for surgery, and building new centres of expertise in Endometriosis and Pelvic Pain.
Keyphrases
  • quality improvement
  • chronic pain
  • coronary artery disease
  • pain management
  • health insurance
  • neuropathic pain