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.

Jordyn shares her experience with living in a world with endo, from navigating her increasing pelvic pain to being diagnosed with endometriosis just a couple of years ago.

Monique shares her tumultuous journey to be diagnosed with endometriosis, along with Coeliac disease and CRPS, as well as the symptoms and side effects she suffered with.

Bree shares her experiences living with endo, after being misdiagnosed with PCOS first and suffering with symptoms since the age of 11.

In 2020 the COVID-19 pandemic changed the way we lived our lives, it changed the face of medicine for patients and providers. For many with chronic illnesses, it showed the world what it was like to live at the mercy of one’s health. In this piece, Registered Nurse, Dannielle Stewart discusses how we can provide better care for those living with endo as a result of the pandemic.

Jahanna shares her experiences living with endo and pelvic congestion syndrome, as well as ‘growing up’ with the invisible and how she was diagnosed with endo and adeno.

In this piece, Karissa shares her endometriosis story and journey to diagnosis in 2019, after living with symptoms and pain for over 10 years.

She also shares her advice for someone going through the process of getting a diagnosis!

Melissa shares her journey to diagnosis with endometriosis and later, PCOS in this blog. She also discusses why she attempts to remain positive and her goals to advocate for others!

Olivia shares her endo story, having been diagnosed with endometriosis just recently at 18 years old. She shares the relief she felt when endometriosis was confirmed, and her advice for others who are suffering from symptoms.

In this piece Aroha shares about her journey to diagnosis with endo, adeno and PCOS as well as how she manages her chronic illnesses and her biggest lesson she’s learned.

Have you heard of Pelvic Congestion Syndrome? It can be an incredibly painful condition that affects a lot more people than originally thought. This blog chats all about the symptoms, causes, diagnosis and treatment for Pelvic Congestion Syndrome.

Amy is the founder of Making Her Magic, and works with women to go for their aspirations and feel supported and celebrated in ‘the hard stuff’ in life such as building a business, changing jobs, moving cities and setting those BIG, scary goals.

In this piece she shares five ways to boost your confidence and start to love yourself more!