It took visits to more than 10 doctors over six years for Tasha Ross to finally get a diagnosis. The 23-year-old swimwear model had battled intense pain, bloating and hormonal acne from the age of 15, only to be told by one specialist that it was ‘all in her head’.
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Endometriosis Australia partnered with CHARLI app to launch the first Australian hybrid technology and real-world...
Endometriosis Australia is grateful to have received generous media support for our first-ever brand campaign, both...
I've known endo from a young age. Watching my mum and older sister crippled in pain every month, with limited answers...
By Tania Forlano I’ve supported Endometriosis Australia for a long time. As someone who was very familiar with effects...
SCA today announced a two-year partnership with Endometriosis Australia and Cancer Council as part of its charity...
Gold Coast 18th January 2024: Endometriosis Australia, the country’s leading patient advocacy group for those living...
Endometriosis affects 10 per cent of women around the world, but it's rarely spoken about. Many women live with...
Season’s Greetings and best wishes for the holiday season - wherever you are across Australia - stay safe, healthy and...
By Dr Eliza Colgrave I am an aggressive optimist, and my experience of living with endometriosis has played a big part...
Christie Whelan Browne has been announced as Endometriosis Australia’s newest ambassador. The musical theatre star...
