In this special episode of The Endo Edit, Katie and Ragan are joined by their first guest — Chief Meteorologist Danielle Breezy.

Danielle opens up about her endometriosis journey, from her initial diagnosis in 2020 to navigating different doctors, advocating for herself, and ultimately undergoing surgery this year (2026). She shares what it’s been like balancing a demanding career as Chief Meteorologist while managing chronic pain — and the importance of trusting your instincts when something doesn’t feel right.

This conversation is honest, empowering, and a reminder that you know your body better than anyone else.

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In this special Q&A episode of The Endo Edit, Katie and Ragan answer your questions — getting more personal than ever before.

From their individual endometriosis journeys to how the condition has impacted their relationships, they open up about the realities of navigating life with endo. They also share how they met, what inspired them to start The Endo Edit, and what it’s really like building a platform centered around women’s health.

This episode is honest, unfiltered, and feels more like a conversation than anything else.

If you’ve been following along, this is your chance to get to know the voices behind the mic.

In Part 2 of Living Well with Endo, Katie and Ragan take you inside their daily routines, and the small, intentional changes that have helped them better support their bodies.

From morning and evening habits to creating a lower-tox lifestyle, they share the products they use, the swaps they’ve made, and the routines that help them feel more balanced day to day.

This episode covers everything from non-toxic beauty and skincare to home essentials like candles and fragrance — along with the mindset behind making these changes without feeling overwhelmed.

Because living well with endometriosis isn’t about perfection, it’s about creating a lifestyle that works for you.

Living with endometriosis isn’t easy — but there are ways to better support your body along the way.

In Episode 4 of The Endo Edit, Katie and Ragan share what’s actually helped them manage symptoms and feel more like themselves again. From supplements and nutrition to movement, pelvic floor therapy, and simple daily habits, this episode focuses on realistic, supportive tools — not quick fixes.

They also touch on the importance of nervous system support, including things like morning sunlight, grounding, and slowing down in a world that often encourages the opposite.

This is not a one-size-fits-all approach — but a starting point for exploring what might work for you.

✨ Part 2 coming next, where they dive deeper into daily routines and non-toxic lifestyle swaps.

When it comes to endometriosis, misinformation isn’t just frustrating — it’s harmful.

In Episode 3 of The Endo Edit, Katie and Ragan break down the most common myths surrounding endometriosis — and why they continue to delay diagnosis, dismiss pain, and impact treatment.

From “it’s just bad cramps” to “pregnancy will cure it,” they unpack where these misconceptions come from, how they affect real women, and what the truth actually looks like.

Because the more we normalize these myths, the longer women go without answers.

If you’ve ever been told your symptoms are “normal,” this episode will hit home.

Getting diagnosed with endometriosis shouldn’t take years—but for many women, it does.

In Episode 2 of The Endo Edit, Katie and Ragan unpack why endometriosis is so often missed, misdiagnosed, or dismissed altogether. From being told symptoms are “normal” to navigating a healthcare system that isn’t built to catch it early, this episode sheds light on the real reasons behind the delay.

They share personal experiences, break down common barriers to diagnosis, and talk about what needs to change—so more women can get answers sooner.

If you’ve ever questioned your symptoms or felt unheard, this episode is for you.

In the very first episode of The Endo Edit, hosts Katie Turner and Ragan Hubbard share their personal journeys with Endometriosis — from the early symptoms and long road to diagnosis, to how the disease has shaped their health, careers, and advocacy. Through honest conversation, they open up about the challenges, the lessons, and the motivation behind creating a space for real talk about women’s health.