EndoTV

Let’s Talk Period is a podcast from EndoTV, hosted by Diana Falzone, bringing real, unfiltered conversations to the forefront of women’s health.

From endometriosis and chronic pain to fertility, mental health, and beyond, this show creates space for the stories, science, and voices that have been overlooked for far too long.

Through candid interviews with patients, doctors, and advocates, Let’s Talk Period breaks stigma, challenges misinformation, and pushes the conversation forward.

Because it’s time we actually talk about it.

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16 episodes
weekly
Avg 31 min
English

Episodes 16

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S1 · E15
September 15 · 39 min
Undiagnosed Endometriosis: A Mother’s Warning After Losing Her Daughter
Undiagnosed endometriosis can change everything. In this deeply moving episode of EndoTV, Diana Falzone speaks with endometriosis advocate Georgia Craig about her daughter Courtney, who was an endometriosis patient, occupational therapist, marathon finisher, beloved daughter, sister, friend, and partner. Georgia shares Courtney’s story with love, grief, and purpose. Courtney was living a full life in Denver, building a career she loved, surrounded by friends, planning her future, and carrying a mantra that defined her determination: “I can do hard things.” But behind that full life was what Georgia calls the hidden enemy of undiagnosed endometriosis. Georgia discusses Courtney’s severe abdominal pain, inflammation, malaise, and the symptoms that were not connected to endometriosis in time. During what was expected to be a routine ovarian cystectomy, doctors discovered advanced endometriosis and frozen pelvis. Georgia shares that Courtney suffered a surgical complication involving her iliac vein and did not survive. Diana and Georgia discuss why endometriosis must be understood as more than painful periods, how advanced disease can involve organs and become dangerous, and why patients need earlier diagnosis, better education, proper surgical training, and a higher standard of care. Georgia also shares how she is honoring Courtney through Team Courtney and Team EndoStrong. Inspired by Courtney’s love of life and her New York City Marathon finish, Courtney’s sister Casey and close friends are running the New York City Marathon in her honor while raising funds for EndoFound. Support Team Courtney here: https://give.endofound.org/fundraiser/7244306 This conversation is about grief, love, medical injustice, advocacy, and the urgent need to make sure patients are heard before endometriosis progresses unnoticed. Guest: Georgia Craig In honor of: Courtney Host: Diana Falzone Presented by: EndoFound & EndoTV
S1 · E15
July 21 · 39 min
How Endometriosis Left One Patient Needing a Blood Transfusion
Heavy bleeding is not something patients should have to prove. In this episode of EndoTV, Diana Falzone speaks with patient advocate Charlie and Dr. Katie Burns about endometriosis, chronic pain, heavy bleeding, anemia, blood transfusions, and the emotional toll of living with an invisible illness. Charlie shares her experience with painful periods, pain with sex, ongoing pelvic pain, severe bleeding, anemia, laparoscopic excision surgery, and needing blood transfusions because of heavy uterine bleeding. She also discusses what it is like to look healthy on the outside while managing symptoms that can be exhausting, painful, and difficult for others to understand. Diana, Charlie, and Dr. Burns discuss what patients should know about heavy bleeding, when to ask about bloodwork such as CBC, hemoglobin, and iron levels, and why patients are so often forced to advocate for themselves in emergency and medical settings. They also discuss pain after excision surgery, possible overlapping conditions such as hypermobility or orthopedic pain, and the importance of accommodating your body when living with chronic illness. This conversation centers Charlie’s story while offering practical takeaways for anyone navigating endometriosis, heavy bleeding, anemia, chronic pain, or the fight to be believed. Guest: Charlie MacKenzie Guest: Dr. Katie Burns Host: Diana Falzone Presented by: EndoFound & EndoTV
S1 · E14
July 14 · 31 min
Endometriosis Surgery & Fertility: What Patients Need to Know
What should endometriosis patients know about surgery, ovarian cysts, fertility, and self-advocacy? In this episode of EndoTV, Diana Falzone speaks with Alexandra Arsenault about her journey with stage 4 deep infiltrating endometriosis, emergency surgery, losing an ovary, and eventually seeking expert excision surgery with Dr. Tamer Seckin in New York. After years of painful periods, repeated ER visits, and symptoms that were dismissed as “normal,” Alexandra learned at 19 that a 12-centimeter endometrioma had completely encapsulated her right ovary. The ovary could not be saved, and she was diagnosed with stage 4 endometriosis. When a cyst later appeared on her remaining ovary, she knew she needed to advocate quickly and seek specialized care. Her story highlights the emotional weight of fertility fears, the importance of medical records and self-advocacy, and the difference between reactive care and proactive treatment. Diana and Alexandra discuss endometriomas, fertility preservation, excision surgery, workplace challenges, medical leave, family history, and why endometriosis education is needed not only for patients, but also for doctors, employers, families, and partners. This conversation is a hopeful reminder that while endometriosis can be devastating, the right care can change the course of a patient’s life. Guest: Alexandra Arsenault Host: Diana Falzone Presented by: EndoFound & EndoTV
S1 · E13
July 7 · 32 min
Endometriosis & Infertility: What Patients Need to Know
What should endometriosis patients know about infertility, IVF, fibroids, and surrogacy? In this episode of EndoTV, Diana Falzone speaks with Andrea Syrtash, founder of Pregnantish and the World Fertility Project, about her personal journey with endometriosis, fibroids, infertility, IVF, pregnancy loss, and gestational surrogacy. Andrea was first told she may have endometriosis at age 14 after experiencing debilitating period pain. Years later, as she began trying to build a family, she learned how deeply endometriosis, fibroids, and uterine health could impact fertility and pregnancy. Together, Diana and Andrea discuss the emotional and medical realities of infertility, the financial barriers many patients face, misconceptions around surrogacy, and why fertility education should begin much earlier for people living with endometriosis. They also discuss how Andrea’s experience led her to create Pregnantish, a platform dedicated to breaking stigma and supporting people navigating fertility treatment and nontraditional paths to parenthood. This conversation is for anyone living with endometriosis, facing infertility, supporting a loved one, or looking for hope on the road to parenthood. Guest: Andrea Syrtash Host: Diana Falzone Presented by: EndoFound & EndoTV
S1 · E13
July 1 · 34 min
The Future of Endometriosis Research with Dr. Semir Beyaz
Could understanding the biology of endometriosis change the future of diagnosis and treatment? In this episode of EndoTV, Diana Falzone sits down with Dr. Semir Beyaz of Cold Spring Harbor Laboratory to discuss the groundbreaking research that is reshaping how scientists view endometriosis. Rather than thinking of endometriosis as simply a gynecologic disease, researchers are uncovering evidence that it is a complex, whole body inflammatory condition driven by genetics, the immune system, and cellular changes that extend far beyond the pelvis. Together, they explore: • Why endometriosis may actually represent multiple diseases • The search for the cells of origin of endometriosis • Genetics, inflammation, fibrosis, and immune dysfunction • Why endometriosis shares similarities with cancer biology while remaining a distinct disease • The current research surrounding ovarian cancer risk • Why better molecular classification could transform diagnosis and treatment • The importance of earlier detection and improved access to specialized care • How collaboration across scientific disciplines may accelerate breakthroughs for millions of patients Dr. Beyaz also shares why advancing endometriosis research has implications far beyond this disease and could help scientists better understand chronic inflammation, fibrosis, and even cancer. This conversation offers an inspiring look at where endometriosis research is headed and why there is real reason for hope. Guest: Dr. Semir Beyaz, Cold Spring Harbor Laboratory Host: Diana Falzone Presented by: EndoFound & EndoTV
S1 · E12
June 23 · 7 min
From Pain to Purpose: Building Hope Through Endometriosis Advocacy
After years of surgeries, uncertainty, and watching their daughters fight for answers, the O'Malley family decided they couldn't stand by and do nothing. In Part 2 of this EndoTV conversation, Kara and Krissy O'Malley share how their family's experience with endometriosis inspired the creation of Our Daughters Foundation and their work with the Endo Research Alliance to improve support, increase access to care, and fund the research patients desperately need. They discuss the financial realities of endometriosis treatment, why so many patients struggle to access expert excision surgery, and the hope they have for the future of endometriosis care. Topics include: • Why Our Daughters Foundation was created • The financial burden of endometriosis care • Supporting patients through advocacy • The Endo Research Alliance mission • The importance of research funding • Building partnerships across the endometriosis community • Why every contribution matters • Finding purpose through pain and creating lasting change This episode is a call to action and a reminder that progress happens when patients, families, advocates, researchers, and clinicians come together. Guests: Kara O'Malley and Krissy O'Malley Host: Diana Falzone Presented by: EndoFound & EndoTV
S1 · E11
June 16 · 50 min
Endometriosis Runs in Our Family: Kara & Krissy's Story
What happens when endometriosis affects an entire family? In this deeply personal episode of EndoTV, Diana Falzone sits down with Kara and Krissy O'Malley to discuss the realities of living with endometriosis and adenomyosis across generations. Kara reflects on decades of unexplained symptoms, infertility, abnormal bleeding, and discovering years later that adenomyosis had been documented in her medical records without ever being discussed. Krissy shares how painful periods progressed into debilitating daily pain that ultimately ended her Division I volleyball career and led to multiple surgeries. Together, they explore what it means to navigate a disease that is often misunderstood, dismissed, and minimized. They discuss: • Growing up with symptoms that weren't recognized • Medical gaslighting and delayed diagnosis • Endometriosis and adenomyosis across generations • Infertility and reproductive health challenges • Multiple surgeries and organ involvement • The emotional toll of invisible illness • Learning to trust your instincts and advocate for yourself • Finding hope through community and shared experiences Whether you're newly diagnosed, supporting someone you love, or have been living with endometriosis for years, this conversation is a reminder that you are not alone. Guests: Kara O'Malley and Krissy O'Malley Host: Diana Falzone Presented by: EndoFound & EndoTV
S1 · E10
June 9 · 35 min
Validation, Advocacy & Endometriosis: Folake’s Story
What happens when years of pain are finally validated? In this emotional and powerful EndoTV conversation, advocate and Blossom Ball honoree Folake joins Diana Falzone and Dr. Tamer Seckin to discuss diagnosis, dismissal, advocacy, and the impact of The Doctor Will See You Now: Endometriosis. For many patients, years of pain, medical gaslighting, and misdiagnosis create emotional scars long before treatment begins. This conversation explores why validation matters and how patient voices continue changing the future of endometriosis care. Together they discuss: • Medical dismissal and diagnostic delay • The history of women’s pain being ignored • Why validation matters • Patient advocacy and education • Genetics and future research • Hope for better care and treatment Learn more about Dr. Seckin’s updated book: The Doctor Will See You Now: Endometriosis https://www.amazon.com/Doctor-Will-See-You-Endometriosis/dp/B0FJ55H8PR Guests: Dr. Tamer Seckin & Folake Host: Diana Falzone Presented by: EndoFound & EndoTV
S1 · E8
June 2 · 22 min
The New Science of Endometriosis with Dr. Tamer Seckin
How has our understanding of endometriosis changed over the last decade? In this special EndoTV conversation, Diana Falzone sits down with renowned endometriosis surgeon, researcher, and EndoFound co-founder Dr. Tamer Seckin to discuss the updated release of The Doctor Will See You Now: Endometriosis and the growing understanding of endometriosis as a systemic disease. From fibrosis and inflammation to fertility, thoracic and sciatic endometriosis, and advances in excision surgery, Dr. Seckin explains why endometriosis is far more than pelvic pain and why patient voices continue reshaping the field. Together they discuss: • Systemic inflammation and fibrosis • Peritoneal endometriosis • Surgical advances and excision • Fertility and IVF concerns • Thoracic and sciatic endometriosis • Why early diagnosis matters • The future of endometriosis care Learn more about Dr. Seckin’s updated book: The Doctor Will See You Now: Endometriosis https://www.amazon.com/Doctor-Will-See-You-Endometriosis/dp/B0FJ55H8PR Guest: Dr. Tamer Seckin Host: Diana Falzone Presented by: EndoFound & EndoTV
S1 · E7
May 19 · 24 min
The Gut, Brain & Inflammation Connection in Endometriosis | Savannah Regensburger, MS, MBA, CNS
“Endometriosis is not just a reproductive disease. It affects the entire body.” -- Savannah Regensburger, MS, MBA, CNS What if your digestive issues, fatigue, brain fog, and chronic pain weren’t separate problems — but all connected to endometriosis? In this episode of EndoTV, Diana Falzone speaks with Savannah Regensburger, MS, MBA, CNS, clinical nutritionist and endometriosis advocate, about the realities of living with chronic illness, navigating a 12-year diagnostic delay, and learning how inflammation, gut health, hormones, and nutrition all play a role in endometriosis management. They discuss anti-inflammatory nutrition, fertility, iron deficiency, flares, and the emotional toll of feeling dismissed for years. This is an honest and empowering conversation for anyone living with endometriosis or supporting someone who is.
S1 · E5
May 12 · 37 min
The Missing Piece in Endometriosis Care After Surgery
What happens after endometriosis surgery? In this episode of EndoTV, Diana Falzone speaks with Nicoletta and Jessica about the overlooked reality many patients face after excision surgery: persistent inflammation, fatigue, hormone imbalance, pain flares, and nervous system dysfunction. Together, they discuss the neuroimmune component of endometriosis, MTHFR genetic variants, nutrient therapy, hormone support, low-dose naltrexone, and why multidisciplinary long-term care matters. This conversation sheds light on the growing understanding that endometriosis is far more than a reproductive disease — and why surgery alone is not always enough for lasting symptom relief.
S1 · E4
May 5 · 24 min
Alexis Roderick Joel on Endometriosis Misdiagnosis, Pain, and Hope
"Alexis Roderick Joel opens up about her long, painful journey with endometriosis—and how years of misdiagnoses, frustration, and self-advocacy finally led her to answers. In this episode of EndoTV, Alexis talks with host Diana Falzone about the stigma, silence, and suffering that so many with endo experience—and the importance of research, self-education, and hope.Read Alexis's full endo story here:https://www.endofound.org/fashion-designer-entrepreneur-and-social-media-influencer-making-endometriosis-awareness-a-priority-Presented by: EndoFound & EndoTV
S1 · E3
May 5 · 36 min
How Elsie Hewitt Finally Got Answers About Her Pain
Elsie Hewitt @ElsieEats opens up to EndoTV host Diana Falzone about her years of being misdiagnosed, the internal struggle of owning her pain, and the turning point that led to answers. From misunderstood symptoms to finding the right doctor, Elsie shares what it took to get a proper diagnosis and the courage it took to speak out—especially now, as she prepares to welcome her first child with Pete Davidson. In this candid interview, Elsie talks about:Her battle with severe symptoms since her teensWhy it took so long to be taken seriouslyHer decision to finally advocate for herselfThe emotional toll of having her pain minimizedPregnancy cravings (including a lot of pickles!)Why sharing her story was never a questionRead her full story: https://www.endofound.org/model-and-actress-elsie-hewitt-talks-to-endotv-about-her-endometriosis-journey-and-pregnancy Presented by: EndoFound & EndoTV
S1 · E2
May 5 · 24 min
Dr. Danielle Luciano: Why Endometriosis Must Be Redefined as a Systemic Disease
In this powerful episode of EndoTV, Dr. Danielle Luciano returns to share groundbreaking updates from Connecticut—where state funding for the EndoRise biorepository and awareness initiatives is being renewed. This crucial support is helping drive research, education, and hope for those with endometriosis.Dr. Luciano discusses:The molecular complexity of endometriosisWhy it should no longer be classified as a “benign gynecologic disease”Challenges of recurrence even after excision surgeryThe psychological toll and importance of mental health supportThe need to end patient-blaming and embrace interdisciplinary careThe impact of systemic inflammation, comorbidities, and misunderstood symptomsHer personal mission to help redefine how we treat and understand endoPresented by: EndoFound & EndoTV
S1 · E1
May 5 · 32 min
Leslie Mosier, Doug the Pug’s Mom: You Can Still Have a Beautiful Life with Endometriosis
"You can still have a beautiful life when you're in pain."In this deeply moving episode of EndoTV, Leslie shares her journey with endometriosis—from her first symptoms at age thirteen, to years of misdiagnoses, ablation surgery, and finally the life-changing relief of excision surgery. She opens up about the darkest days of her pain, the medical gaslighting she endured, and how community support gave her strength to keep going."I had to learn that advocating for myself was the only way forward. I want people to know you are not crazy, you are not alone."Leslie’s story is a reminder that living with chronic illness does not erase joy, hope, or love. By giving her endo “a seat at the table,” she has found resilience, gratitude, and the ability to live fully—even in the face of pain.Her words will inspire anyone navigating endometriosis, chronic illness, or supporting a loved one: you can still create a beautiful, meaningful life.Together, we are stronger. Together, we bring light to endometriosis.Presented by: EndoFound & EndoTV
S1 · E1
Jan 19, 2021 · 22 min
Doctor shares harrowing experience on the frontlines of Covid
Dr. Haydee Brown talks with Diana Falzone about treating Covid patients, the new vaccine, and what she predicts will happen within the next six months of the pandemic. Connect with Dr. Brown online! Connect with Dr. Brown: Instagram: https://www.instagram.com/drhaydeebro... Black Women Orthopaedic Surgeons: https://www.instagram.com/bwos2020/?h... » Subscribe to EndoTv: https://www.youtube.com/c/EndoTV?sub_confirmation=1 » Watch more EndoTv video: https://www.youtube.com/c/EndoTV Connect with EndoTv online! Diana Falzone: Instagram: https://www.instagram.com/dianafalzone/?hl=en Facebook: https://www.facebook.com/DianaFalzone1/ Twitter:https://twitter.com/dianafalzone?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor Endofound: Instagram: https://www.instagram.com/endofound/?hl=en Facebook: https://www.facebook.com/endofound/ Twitter: https://twitter.com/Endofound?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor Shop Endofound: https://shop.endofound.org/ DONATE: https://www.endofound.org/donation With every gift, YOU advance cutting-edge endometriosis research, educate adolescents, advocate for endometriosis legislation, and promote widespread disease recognition and awareness. Welcome to EndoTV, where we talk about the latest research, policy, diagnosis, and treatment for endometriosis and other issues related to menstrual health. Join us as we speak with some of todays most respected health clinicians and researchers, authors, advocates, patients, and lawmakers changing the future for endometriosis care. #endofound #endotv #askthedoctors EndoTv Lets Talk Period… – January 19, 2021

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