welcome to body of evidence

Honest, informed conversations about endometriosis and adenomyosis.

Endometriosis affects millions of people, yet it remains widely misunderstood, dismissed, and underrepresented — in healthcare, in media, and in everyday conversation. Body of Evidence exists because I want to help change that.

This is a space where lived experience meets evidence-based conversation. Through podcast interviews, long-form writing, and research translation, I want to explore endometriosis not just as a medical condition, but as something cultural, social, and deeply human — shaping identity, relationships, work, and how we experience our own bodies.

I talk to people living with endometriosis, researchers and clinicians working to understand it, athletes navigating chronic illness in sport, and journalists examining how it’s portrayed in the media. The goal isn’t to simplify or sensationalise. It’s to bring depth, nuance, and honesty to a discussion that’s long, long overdue.

Long-form writing on endometriosis, adenomyosis, and the world around them.

It’s not to say that coverage of diseases like endometriosis doesn’t exist. It absolutely does, but how much of it is accurate? How much of it is helpful?

Articles on this site will explore endometriosis and adenomyosis through different lenses such as media, identity, healthcare, sport, and culture. Not enough time has been spent connecting personal experience to the bigger picture of how these conditions are understood, discussed, and represented.

You’ll find pieces that translate research into accessible language, examine how women’s pain is portrayed (or ignored), and reflect on what it means to live with chronic illness in everyday life.

I am not here to provide quick wellness tips or surface-level explainers. Body of Evidence aims to produce well-thought-out stories written to educate, challenge, and start conversations.

A unique podcast exploring endometriosis and adenomyosis through the art of the interview.

Each episode of The Endo Show brings together people with endo and adeno, researchers, clinicians, athletes, and journalists to talk openly about pain, diagnosis, identity, and the systems that shape the understanding of these conditions.

Again, this isn’t a wellness podcast, nor is it a clinical lecture. It’s a space for thoughtful conversations and interviews that take women’s pain seriously.

Whether you’re navigating your own diagnosis, working in healthcare or research, or simply want to understand these conditions better, The Endo Show offers conversations that are intelligent, accessible, and real.