From just 13 Jacqui was experiencing the excruciating symptoms associated with endometriosis, however it would take 22 years for her to be diagnosed and get answers for her pain. In this piece Jacqui shares about her experiences, as well as her advice for anyone navigating a similar path.

Scarlet CEO Jo Barry never asked for endometriosis, but it changed everything. In this honest reflection, she shares how chronic pain reshaped her relationship with her body, her people, and her purpose.

Tarsh shares the importance of knowing and advocating for yourself, through her endo, PCOS and fertility story.

Tiff shares her experiences being diagnosed with endometriosis and living with the condition.

What is Pelvic Organ Prolapse? What are the causes and symptoms? How can it be diagnosed and treated? All these questions and more are answered in our latest blog!

Sammii shares her experience of living with endometriosis and how she is supported within the workplace. She also calls on employers to do more when it comes to assisting those living with endometriosis.

Izzy shares her endo story and experience getting diagnosed.

Jess shares her story of beigng diagnosed with endometriosis and adenomyosis after struggling to conceive.

Chantelle shares her story being diagnosed with endometriosis

Morgan shares her experience being diagnosed with endo, as well as post op complications she experienced.

The team from See Red Australia share their favourite mentions of periods on Australian TV!

Aimee shares her experience with endometriosis

Lara shares the heartbreak and emotional toll of living with endometriosis.

From being told she was miscarrying, to having STIs and her partner was being unfaithful, Holly shares her extensive journey to diagnosis with both endometriosis and adenomyosis. She also talks about her fears now she is a mum to a beautiful little girl.

Eloise from @endowithel details her long journey to being diagnosed with endometriosis. She talks on facing misdiagnosis, increasing pain and symptoms, and having to be her own advocate.

In this piece, Zara shares her journey to diagnosis with endometriosis and PCOS and the validation that comes with knowing she is not alone.

Leah details what it’s like living with vaginismus, how she was diagnosed and how she’s turned her pain into her passion through launching the GINA app last year!

Vonn shares shares the symptoms she experienced, the tests, scans and theories as to what could be wrong with her, before it was finally identified, she had endo and adeno.

Phoebe details her experience from rupturing her fallopian tube as a teen during a dance performance, to being diagnosed with PCOS, and eventually adenomyosis as well. She also shares how she now works with people on the daily who live with pelvic pain as a pelvic physiotherapist

Peta shares her experiences living with endo and adeno, as well as undergoing the process of creating embryos and undergoing a hysterectomy at just 30 years old.