The Girls Room After Dark

Endo Warriors is a weekly podcast created and hosted by endometriosis experts Callie Greenberg and Jaime Silva. Each episode dives into real stories, unfiltered insights, and what it’s actually like living with chronic pain. Each episode, we spotlight someone’s personal story and have conversations about the things we all think about but no one ever talks about. New episodes every Wednesday.

The Girls Room After Dark is a society podcast hosted by Callie Greenberg & Jamie Silva, with 31 episodes on record and a Required Pod Score of 80. PitchCentric scores this show on Booking Probability, Listen Score, and live audience signals refreshed every 24 hours.

Callie Greenberg & Jamie Silva hosts The Girls Room After Dark, a society show with 31 episodes published.

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  Episode #30

  Painful Sex & Female Pleasure: The Conversation Every Woman Deserves | with Hella Rader

  Jul 29, 202639 min

  For millions of women living with endometriosis, one symptom often remains hidden behind embarrassment and silence: pain during sex. According to research, up to 80% of women with endometriosis experience pain during or after intercourse—yet many are never asked about it by their healthcare providers. In this episode, we change that. Callie Greenberg and Jamie Silva welcome writer, storyteller, somatic coach, and host of Stories That Sparkle, Hella Rader, for one of the most vulnerable conversations we've ever had on The Girls Room After Dark. Hella shares her journey of living with undiagnosed endometriosis, believing for decades that pain was simply part of being a woman, and not experiencing her first orgasm until age 47. Together, we discuss: ✨ Painful sex and endometriosis (dyspareunia) ✨ The shame so many women carry around intimacy ✨ Why doctors rarely ask about sexual pain ✨ Bleeding after intercourse ✨ Pelvic floor dysfunction ✨ Learning pleasure after chronic pain ✨ Masturbation and body acceptance ✨ Vaginal estrogen after hysterectomy and menopause ✨ Medical gaslighting in women's healthcare ✨ Why women deserve better education about their bodies This episode isn't about shock value. It's about removing shame. Because pain should never be normalized—and neither should silence. If this conversation helped you, please share it with someone who may need to hear that they are not broken. Connect with Hella Rader Instagram: @hellarader Website: hellarader.com Somatic Coaching: embodyandcreate.com Follow The Girls Room After Dark & The Girls Room Project Website: thegirlsroomofficial.com Instagram: @thegirlsroomofficial Instagram: @girlsroomafterdark

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  Episode #29

  Peptides, GLP-1s, and the Real Root Causes of Endometriosis | Dr. Joelle Osias | EP29

  Jul 21, 202656 min

  Peptides, microdosed GLP-1s, and why the standard of care in gynecology stops short of actually treating endometriosis: Dr. Joelle Osias, founder of Foreviva Clinic, joins the Girls Room with Callie Greenberg and Jaime Silva for an unusually honest conversation about what she was trained to do and what she does instead. Dr. Osias trained under Dr. Camran Nezhat in minimally invasive gynecologic surgery, then spent twenty years inside the standard of care, birth control pills, estrogen blockers, surgery, before realizing patients kept coming back in pain no matter how many times she operated. She breaks down why the RVU system that determines physician pay makes a real two-hour intake financially impossible, and what she orders and treats instead of staying inside the standard of care: reverse T3, the MTHFR mutation, zonulin and gut permeability, IV iron, microdosed GLP-1s, and peptide therapy most gynecologists have never heard of. They also get into the updated ACOG guidance that now allows endometriosis to be diagnosed by symptoms alone, without surgery, and why Dr. Osias believes real change has to come from patients advocating for themselves, not from the standard of care retraining itself. Show Links and Resources Find Dr. Osias at | Foreviva Medical Clinique Instagram | @Foreviva Girls Room Project @girlsroomafterdark @girlsroomproject Dr. Nezhat Get 10% off your first purchase of Serae Health Hormone and Immune Daily Supplement with code GIRLSROOM at Serae Health Supplement

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  Episode #28

  Creating ENdi | A Life-Changing Endometriosis Tracking App With Co Founder Jemma Bowles | EP28

  Jul 14, 202647 minS1

  Jemma Bowles spent two decades bouncing between doctors before anyone said the word endometriosis. She was hospitalized for suspected appendicitis more than once. She was told to take a bath. Nobody put it together until her dad saw an article and asked if it sounded familiar. In this episode, Jemma joins Callie Greenberg and Jaime Silva to talk about what it actually took to get diagnosed, why she chose to wait on surgery and how she and her co-founder Will Nixon built ENdi, an app designed specifically for endometriosis patients after every period tracker on the market failed her. They get into the difference between NHS and private care in the UK, the ring binder folder she used to carry to every appointment, and the emergency feature in the app built for the moments she collapses without warning. This episode covers a lot of ground: diagnosis delays, healthcare access, chronic pain, and what it looks like to build something because nothing else did the job. This episode reflects Jemma's personal experience and the app is not medical advice. It is for educational use and support only. Please talk to a doctor about your own symptoms and treatment options. Show Resources and Links Jemma Bowles | Jemma struggled to manage her appointments, medications, and medical history. Recognizing the need for a better solution, she teamed up with co-founder, Will, and together, they created ENdi, a much-needed app designed to simplify these tasks and help others facing similar challenges. Find ENdi: ENdi App Website Instagram | @endi.app The Girls Room Instagram | @girlsroomafterdark | @girlsroomproject Receive 10% off your first purchase of Serae Immune & Hormonal Supplement by using code GIRLSROOM Serae Health Supplement

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  Episode #27

  Useless Things Doctors Tell Women in Pain | Bonnie Gross Writer of Lady Parts Film | EP27

  Jun 30, 202640 min

  Bonnie Gross is the writer and executive producer of Lady Parts, an award-winning indie comedy based on her own true story of living with chronic vulvar pain and eventually moving home with her parents to undergo a vestibulectomy — surgery to remove excess nerve endings in the vulvar vestibule. The film has screened across the country and won multiple awards, but before any of that, Bonnie spent years being told to relax, drink wine, try lube, and just "breathe." Callie and Jaime sit down with Bonnie to go deep on what it's really like to have a condition called neuroproliferative vestibulodynia — where too many nerve endings in the vulvar vestibule cause severe, chronic pain. Bonnie describes what it felt like from the time she was a teenager: tampons that felt like burning, sex that felt like a hot knife, everyday activities like wearing pants or riding a bike that most people don't think twice about. She walks through the years of medical gaslighting she experienced, including doctors who blamed anxiety, suggested she stop being "so promiscuous" (ironic, since pain was the actual problem), and prescribed Xanax instead of investigating her symptoms. The conversation gets into the real details that nobody talks about: what dilator therapy actually involves after surgery, how long it took (about a year to get to dilator number four), and the mental work required to retrain a body that had spent years in protective guarding mode. They also talk about pelvic floor dysfunction, what "hypertonic" actually means, and why pelvic PT is one of the most under-recommended tools in women's healthcare. Bonnie shares the moment her insurance company called her surgery cosmetic, denying coverage for the removal of nerve tissue causing her daily pain. She also opens up about her traumatic first pap smear at 18 — a doctor who held her down and told her to stop squirming — and how that experience kept her away from life-saving screenings for years, even knowing cervical cancer runs in her family. The group digs into a bigger systemic issue: right now, there is nothing in OBGYN residency curriculum requiring that doctors learn about conditions like vestibulodynia or lichen sclerosus. Endometriosis was only recently added to training guidelines. Bonnie volunteers with an organization called Tightlips, which is currently pushing to change that. LINKS AND RESOURCES Lady Parts | IG Lady Parts Website Watch Lady Parts Film Serae Health Supplement | use code GIRLSROOM for 10% off Girls Room Project Girls Room After Dark | IG Girls Room Project | IG

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  Episode #27

  Useless Things Doctors Tell Women in Pain | Bonnie Gross Writer of Lady Parts Film | EP27

  Jun 30, 202640 minS0

  <p >Bonnie Gross is the writer and executive producer of Lady Parts, an award-winning indie comedy based on her own true story of living with chronic vulvar pain and eventually moving home with her parents to undergo a vestibulectomy — surgery to remove excess nerve endings in the vulvar vestibule. The film has screened across the country and won multiple awards, but before any of that, Bonnie spent years being told to relax, drink wine, try lube, and just "breathe."</p> <p >Callie and Jaime sit down with Bonnie to go deep on what it's really like to have a condition ca...

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