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In this episode of Endo Warriors, host Callie Greenberg and Jamie Silva talk with Carly Turner, a PhD student and endometriosis advocate, about her decades-long struggle with pelvic pain, misdiagnoses, and the limits of common treatments.

Carly shares her experience with confusing imaging, risky surgery by an underqualified provider, and the difficult decisions around hormonal drugs and their side effects. The conversation highlights the importance of finding experienced specialists and seeking second opinions.

The episode also explores less-visible options—nerve blocks, pelvic floor therapies, suppositories, and community support—and encourages patients to research treatments, trust their bodies, and find allies in their care journey.

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Emma's story reveals how endometriosis can silently take over a young woman's life. At just 19, she endured years of misdiagnoses, dismissive providers, and invasive surgeries, all while fighting to be heard. Emma's journey from stubborn pain and ignorance to empowerment and advocacy is a powerful reminder: no one should accept "normal" pain when it's a sign of something more serious.

In this episode, Emma shares how her early symptoms escalated unnoticed—pain so intense she was crying on the floor, irregular cycles, GI issues—and how she confidently challenged the medical system that failed to listen. You'll discover the critical importance of patient advocacy, the pitfalls of relying solely on hormonal treatments, and the value of finding a compassionate, knowledgeable specialist. Emma also dives into her college experiences navigating her health, her decision to start an awareness movement on social media, and her vision for transforming women's health through policy and education.

We break down the often-overlooked systemic issues: medical complacency, gaps in healthcare provider training, and the urgent need for comprehensive women's health curricula. Emma's story highlights the missed opportunities for early detection and the life-changing possibilities of timely, specialized care. Her perspective offers hope and a call to action for anyone feeling dismissed or overwhelmed by their symptoms.

This episode is perfect for young women, students, parents, and healthcare professionals alike.

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Hosts share candid experiences using low‑dose GLP‑1 medications for endometriosis, describing improvements in inflammation, brain fog, digestion, and energy.

The episode covers dosing strategies, injection tips, differences between drugs, insurance and compounding options, interactions (birth control, surgery, alcohol), and how to discuss GLP‑1s with clinicians.

Listeners get practical, patient‑focused advice and real‑world insights to help advocate for care and consider GLP‑1 as a management tool.

Host Callie Greenberg and guest Arianna Jacono discuss the emotional and medical realities of living with endometriosis, including diagnostic delays, medical gaslighting, and the limits of traditional therapy and medication management.

They explore the healing power of peer-led support, the role of trauma-aware care, the fact that surgery is not a cure, and practical steps for finding better, more empathetic providers and community resources.

Find Arianna Jacono on instagram and tiktok @endojustice

In this episode, host Callie Greenberg interviews co- host Jamie Silva about her long, painful journey with endometriosis and adenomyosis — from early misdiagnoses and traumatic treatments to finding relief through excision surgery and better care. Jamie shares candid stories about heavy bleeding, medical dismissal, mental health impacts, and the challenges of navigating the healthcare system.

The conversation highlights the need for earlier education, improved provider training, patient-centered care, and new solutions like telemedicine and care navigation to help women advocate for themselves and access appropriate treatment.

Hosts Callie and Jamie sit down with endometriosis advocate Savannah Regensberger to hear her decade-long health journey from concussion recovery to an eventual endometriosis diagnosis. They discuss how she built her community, her clinical practice, and a toolbox of lifestyle and medical strategies.

The episode covers micro-dosing GLP-1 medications like tirzepatide and semaglutide for inflammation and symptom management, the role of nutrition and supplements, navigating medical gaslighting, and the importance of validation, mental health care, and research for women’s health.

https://www.iamendometriosis.com/?utm_source=ig&utm_medium=social&utm_content=link_in_bio&fbclid=PAZXh0bgNhZW0CMTEAc3J0YwZhcHBfaWQMMjU2MjgxMDQwNTU4AAGneHMKXLowuvOzUy5ELQaIwCLBr0ownjZX_c8E0HNOBngbA2Y2wac9J1LTtBE_aem_2hb7IgaRDG4YOmuukyq1yg

https://www.instagram.com/savannahregensburger/?hl=en

The shared journey of Tamika Smith and her mother, Rita Smith, as they navigate endometriosis, lupus, and racial bias. Their experiences getting a diagnosis were different, but they share the same feelings of being medically gaslit and bullied due to the color of their skin.

Courtney Gately made the brave decision to pursue a hysterectomy at the age of 18. Despite pushback from her doctors, who deemed her too young to make such a significant decision, Courtney stood her ground.

For the entire month of March, Courtney's business, Pembroke Bakery, is donating 10% of all proceeds to the non-profit Endo Excision For All to support Endometriosis Awareness Month

https://www.pembrokebakery.com/faqs