Hey there, I’m Angie.

I created endokind because I know first-hand how challenging it is to live with endometriosis.

Like many of us, I went undiagnosed and misdiagnosed for 18 years before finally getting my diagnosis via surgery in my mid-30s.

I’ve had several surgeries, some serious post-surgery complications, and have ridden the carousel of symptom management treatments.

Over the years, I’ve needed to withdraw from study, resign from jobs and miss opportunities due to my health.

So I have a deep understanding of the significant impacts that this disease has not only on your physical body and health, but on your quality of life and your mental health and wellbeing.

Having endometriosis can affect all areas of your life, including work, study, travel, diet, finances, dating, relationships, sex, body image, self-esteem, and fertility.

Yep. It’s a lot.

Through my own journey, and hearing from many others, it became clear to me that specialised mental health support for those with endometriosis is desperately needed but almost non-existent.

So here is endokind. A safe space for those in this truly kick-arse community to be seen and heard by someone who gets it.

Where you can process and work towards healing your experiences.

Where you are supported to develop goals and tools to help you feel empowered and better able to take on challenges.

Having endometriosis is hard.

endokind offers you a soft place to land.