Let’s begin with a proper introduction, starting with pronunciation. Endometriosis is pronounced...
The word endometriosis was never uttered
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Kayla Itsines’ endo story
Kayla Itsines tells her endo story. When I was 18, I found out that I have endometriosis. It’s an incredibly common...
It takes a village
Endo can be a lonely disease. There are times, particularly during my period, where I feel as if I’m the only one...
7 ways to support someone with endometriosis
Endometriosis can be a difficult disease to manage, both for those who have it and those who love them and watch them...
The cost of endometriosis
This week my rechargeable heat pack, otherwise known as my trusty sidekick, broke. I Immediately rushed out to...
Blood loss, pain and iron deficiency – My endometriosis period reality
My period has never resembled those period product ads that used to be on the TV. You know the ones where the smiling...
EndoWarrior story: Charlotte Dallison
I first felt the symptoms of endometriosis as a young teen, with periods so heavy I was having to change my tampon...
The Gen X endo experience: What it’s like to live for 24 years undiagnosed
The passionate, resilient and endearing Pru Gibson from Kiama NSW, shares her experience of navigating life with a...
Notes from a nurse: How the healthcare system has failed EndoWarriors, and how we can do better
Chloe Timmer is a 31 year old registered nurse who has worked in the field for 5 years. She has experienced...
Why working from home works for me (and my endo)
I was an early adopter of working from home. Almost a year before the government mandated lockdowns, the scramble to...
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About Us
Endometriosis Australia is a nationally accredited charity that endeavours to increase recognition of endometriosis, provide endometriosis education programs, and provide funding for endometriosis research.