
Insights from recent episode analysis
Audience Interest
Podcast Focus
Publishing Consistency
Platform Reach
Insights are generated by CastFox AI using publicly available data, episode content, and proprietary models.
Most discussed topics
Brands & references
Total monthly reach
Estimated from 3 chart positions in 3 markets.
By chart position
- 🇺🇸US · Non-Profit#5530K to 100K
- 🇨🇦CA · Non-Profit#1675K to 30K
- 🇮🇪IE · Non-Profit#194500 to 3K
- Per-Episode Audience
Est. listeners per new episode within ~30 days
11K to 40K🎙 Daily cadence·43 episodes·Last published 2d ago - Monthly Reach
Unique listeners across all episodes (30 days)
36K to 133K🇺🇸75%🇨🇦23%🇮🇪2% - Active Followers
Loyal subscribers who consistently listen
14K to 53K
Market Insights
Platform Distribution
Reach across major podcast platforms, updated hourly
Total Followers
—
Total Plays
—
Total Reviews
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* Data sourced directly from platform APIs and aggregated hourly across all major podcast directories.
On the show
From 10 epsHost
Recent guests
Recent episodes
The Diagnosis Gap: Culture, Bias & Chronic GI Disease
Jun 24, 2026
Unknown duration
AI Literacy in Healthcare: Patient Advocacy, Medical AI & Navigating Health Tech (Part 1)
Jun 17, 2026
Unknown duration
You’re Not Alone: Living with IBD, Gastroparesis & Chronic Illness Challenges
Jun 10, 2026
Unknown duration
Inside EDS: A Doctor Who Lives It Talks Medicine, Advocacy & Care
Jun 3, 2026
Unknown duration
What It’s Really Like Living With Eosinophilic Esophagitis (EOE)
May 20, 2026
Unknown duration
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| Date | Episode | Topics | Guests | Brands | Places | Keywords | Sponsor | Length | |
|---|---|---|---|---|---|---|---|---|---|
| 6/24/26 | ![]() The Diagnosis Gap: Culture, Bias & Chronic GI Disease | What happens when culture, bias, trauma, and chronic illness intersect?In this episode of Surviving Out of Spite, Sam sits down with patient advocate and non profit leader Tina Aswani-Omprakash to chat about her journey living with Crohn’s disease, gastroparesis, and other GI conditions. Tina shares how cultural expectations, healthcare biases, and how unfortunate medical trauma shaped her experiences as a South Asian woman navigating the healthcare system.Together, they talk about the importance of shared decision-making, culturally sensitive care, and the need to create safe spaces where patients feel seen, heard, and supported. They also talk about the stigma surrounding GI conditions, the role of intergenerational trauma, and why trust between patients and providers is essential for healing.The conversation dives into food and cultural identity, the challenges of restrictive diets, and the importance of finding dietitians and healthcare professionals who understand diverse backgrounds. Sam and Tina highlight the power of community, vulnerability, and advocacy in breaking down stigma and empowering patients living with chronic digestive diseases.Whether you're living with Crohn’s disease, gastroparesis, IBD, or another chronic illness, this episode offers hope, validation, and practical insights on navigating healthcare while honoring your identity and lived experience.Links mentioned in the podcast episode:https://ownyourcrohns.com/https://saia-gi.org/ | — | ||||||
| 6/17/26 | ![]() AI Literacy in Healthcare: Patient Advocacy, Medical AI & Navigating Health Tech (Part 1) | How can patients use artificial intelligence to better understand their health, and should they trust it?In Part 1 of this conversation, Sam chats with Erika Warren, founder of InsightfulMed, to discuss AI literacy in healthcare and how technology can help patients become more informed advocates for their own care.Many patients struggle to understand medical records, test results, research studies, and complex healthcare information. Erika shares how InsightfulMed was designed to help bridge that gap by making health information more accessible, understandable, and actionable for patients navigating chronic illness, rare disease, and complex medical conditions.Together, Sam and Erika talk about the growing role of AI in healthcare, how patients can use technology to ask better questions, and why health literacy is one of the most important tools for improving healthcare outcomes. They also discuss healthcare data privacy, user control, and the importance of transparency when using digital health tools.Whether you're living with a chronic illness, caring for a loved one, or simply interested in the future of healthcare technology, this episode offers practical insights into how AI can empower patients while protecting trust and privacy.More info on Inciteful Med: https://incitefulmed.com/ | — | ||||||
| 6/10/26 | ![]() You’re Not Alone: Living with IBD, Gastroparesis & Chronic Illness Challenges | In this episode of Surviving Out of Spite, Sam chats with Amber Tresca of AboutIBD to discuss the realities of living with inflammatory bowel disease (IBD), gastroparesis, and other chronic health challenges. Amber shares her personal journey with J-pouch surgery, navigating life after major medical interventions, and learning how to balance work, health, and personal growth.Sam and Amber talk about the emotional and practical aspects of chronic illness, including managing unpredictability, building supportive communities, protecting mental health, and finding resilience during difficult seasons. They discuss the importance of flexibility, radical acceptance, and creating a life that works with your condition rather than constantly fighting against it.Whether you're living with IBD, gastroparesis, a chronic illness, or supporting someone who is, this conversation offers honest insights, encouragement, and practical wisdom for navigating the ups and downs of long-term health challenges.Where to find more from Amber? IG: @aboutIBDYT: @aboutIBDWeb: www.aboutIBD.comEmail: amber@aboutibd.com | — | ||||||
| 6/3/26 | ![]() Inside EDS: A Doctor Who Lives It Talks Medicine, Advocacy & Care | In this episode of Surviving Out of Spite, Sam sits down with Dr. Sarah Cohen Solomon for a deeply honest conversation about chronic illness, Ehlers-Danlos Syndrome (EDS), and what it really takes to build a more humane healthcare system.Dr. Solomon brings a unique dual perspective as both a physician and a patient, offering insight into the lived reality of navigating chronic illness while practicing medicine. They talk about the complexities of individualized care, the importance of listening to patient concerns, and why curiosity, not assumptions, should guide clinical decision-making.This episode is about shifting healthcare toward collaboration, where patients are not dismissed, but believed, supported, and involved in their own care decisions. It’s a call for a more compassionate, responsive, and patient-centered medical system.If you’re living with chronic illness, supporting someone who is, or working in healthcare, this conversation offers grounded insight into how care can be improved through empathy, advocacy, and listening. | — | ||||||
| 5/20/26 | ![]() What It’s Really Like Living With Eosinophilic Esophagitis (EOE) | In this episode of Surviving Out of Spite, Sam sits down with Maddie, the voice behind Eosinophilic Chick, to talk about what it’s really like living with Eosinophilic Esophagitis (EOE).Maddie shares her personal journey; from early symptoms and diagnosis to navigating strict dietary restrictions and the reality of starting medication injections. This conversation dives into the physical challenges of managing EOE, as well as the emotional and mental toll that comes with chronic illness.Together, Sam and Maddie also open up about the fear and frustration surrounding food, and what it looks like to slowly reintroduce foods after periods of restriction. They discuss how these moments can be both physically and emotionally overwhelming, and incredibly meaningful.Beyond EOE, this episode highlights the importance of advocacy, community, and connection when living with chronic conditions like EOE and gastroparesis. Because no one should have to navigate this alone.Want to connect with Maddie? Follow her on IG @eosinophilic.chick | — | ||||||
| 5/13/26 | ![]() Poop Talk, But Make It Helpful | Gut Health & Symptom Tracking | In this episode, Sam sat down with Ruth O’Driscoll to have the kind of conversation most people avoid, but absolutely shouldn’t.They dive into the reality of living with digestive issues, why we need to normalize talking about gut health (yes, even the awkward parts), and how self-tracking can be a powerful tool for understanding your body.Ruthie shares her personal journey with digestive health challenges and how it led her to develop an innovative app, Tuut, designed to make symptom and bowel movement tracking easier, more intuitive, and far less overwhelming than traditional methods. Together, they explore how removing shame and simplifying tracking can help people feel more in control of their health.This conversation also goes deeper, touching on the importance of sleep, self-care, and building a supportive community when navigating chronic digestive conditions. Because managing your health isn’t just about data, it’s about feeling seen, supported, and understood.Meet tuut: the first digestive health app that fits lifestyle tracking into your busy life while providing actionable insights. Log data in seconds and let clinically-informed AI algorithms uncover patterns so you can finally identify triggers and feel better. https://www.tuutapp.net/ | — | ||||||
| 5/6/26 | ![]() Surviving Celiac Disease: Hidden Gluten, Hard Lessons & Learning to Live Anyway | In this episode, Casey shares her personal journey living with celiac disease, from diagnosis to the ongoing realities of managing a strict gluten-free diet. She opens up about the challenges of navigating hidden gluten in unexpected foods, the learning curve that comes with dietary restrictions, and the emotional impact that can follow a life-changing diagnosis.Together, Sam and Casey explore what it really means to live with celiac disease in everyday life; highlighting coping strategies, symptom management, and the importance of self-compassion along the way. They also discuss the emotional weight of food-related guilt, the evolving landscape of gluten-free options, and how access to better products has helped improve quality of life for many in the gluten-free community.This conversation also emphasizes the power of community support, strong relationships, and self-advocacy when navigating chronic dietary restrictions. Whether you’re newly diagnosed, supporting someone with celiac disease, or simply wanting to better understand gluten-free living, this episode offers validation, education, and hope.Instagram & TikTok: @collegeceliackc https://www.glutenfreewithcasey.com | — | ||||||
| 4/22/26 | ![]() She Refused to Let Gastroparesis Define Her | A Powerful Patient Story✨ | gastroparesischronic illness+3 | Sarah | — | — | chronic digestive conditiondiagnosis+2 | — | 1h 03m 14s | |
| 4/15/26 | ![]() Ehlers-Danlos Syndrome (EDS): The Fight for Diagnosis, Care & Advocacy✨ | Ehlers-Danlos Syndromehealthcare advocacy+2 | Lara Bloom | Ehlers-Danlos Societythe EDS Society+1 | — | diagnosiscare+2 | — | 32m 02s | |
| 4/8/26 | ![]() He Survived Multiple Organ Transplants, and Chose Hope Anyway✨ | resiliencechronic illness+3 | Ty Gipson | — | — | growthtransplant recovery+2 | — | 41m 00s | |
Want analysis for the episodes below?Free for Pro Submit a request, we'll have your selected episodes analyzed within an hour. Free, at no cost to you, for Pro users. | |||||||||
| 4/1/26 | ![]() It’s Not in Your Head—It’s Your Gut (And Here’s Why)✨ | chronic illnessgastroparesis+4 | Dr Ali Navidi | Surviving Out of Spite | — | mental healthemotional well-being+2 | — | 55m 10s | |
| 3/25/26 | ![]() Fighting to Be Heard: The Reality of Chronic Illness in Healthcare✨ | chronic illnesshealthcare advocacy+3 | Meredith Mangold | Surviving Out of Spite | — | ulcerative colitismedical gaslighting+2 | — | 48m 49s | |
| 3/20/26 | ![]() Living with Gastroparesis & Building a Podcast✨ | gastroparesispodcasting+3 | — | Living with GastroparesisSurviving Out of Spite | — | journeylessons learned+1 | — | 4m 22s | |
| 3/18/26 | ![]() Gastroparesis, Gut Health & Everything in between✨ | gastroparesisgut health+8 | Liz Roman | labs decoded seriesfitmom.co+1 | — | chronic illnessdigestion+2 | — | 59m 50s | |
| 3/17/26 | ![]() What a Panic Attack Feels Like | Anxiety & Chronic Illness✨ | panic attackanxiety+3 | — | Surviving Out of Spite | — | grounding techniquesnervous system+1 | — | 21m 11s | |
| 3/11/26 | ![]() Chronic Illness Might Be Your Superpower✨ | chronic illnessstrengths+3 | Lilly Stairs | chronicboss.com | — | secret sauceadaptability+3 | — | 34m 36s | |
| 2/25/26 | ![]() Resilient Body, Fragile System: Living a Full Life on TPN✨ | chronic illnesshealthcare+3 | Vincent | gymbodybuilding competition | — | TPNcentral lines+3 | — | 44m 33s | |
| 2/18/26 | ![]() Why Chronic Pain Patients feel Ignored by Doctors (and what needs to change) | Chronic pain isn’t just physical; it affects your mental health, emotions, and daily life. In this powerful conversation, Sam and Alec break down what chronic pain management really looks like when empathy, trust, and communication are at the center of care.Alec, a primary care provider, shares the personal experience that led him into medicine and shaped his approach to patient-centered care. Sam brings the lived patient perspective, opening up about the frustration and harm that can happen when pain is dismissed or misunderstood by healthcare providers.Together, they explore why communication breakdowns are so common in healthcare, how validation impacts patient outcomes, and what both patients and providers can do to build stronger, more compassionate relationships, especially when navigating chronic illness and chronic pain.Whether you’re living with chronic pain, supporting someone who is, or working in healthcare, this conversation offers insight, validation, and practical takeaways. | — | ||||||
| 2/13/26 | ![]() ‘Complicated’ and Chronic Illness: Patient Advocacy, Mental Health, and Healthcare Awareness | In this powerful conversation, Donna and Sam explore what it really means to live with chronic illness while navigating a complex and often broken medical system. Through personal stories and lived experience, they discuss patient advocacy, the emotional toll of being dismissed or misunderstood, and why awareness and systemic change in healthcare are so urgently needed.The episode also reflects on the emotional impact of the film Complicated, using it as a starting point to unpack how chronic illness affects not just the body, but mental health, identity, and everyday life. They highlight the critical role of patient voices, the intersection of physical and mental health, and the collective responsibility; patients, providers, and communities alike to push for better care.This conversation is for patients, caregivers, advocates, and healthcare professionals who want to better understand the realities of chronic illness, the importance of listening to patient experiences, and how advocacy can drive meaningful change in the healthcare system.The virtual screening is Sun, Feb 15, 2026 at 2:00 PM ESTInfo on where to watch at the link below:https://gathr.com/events/60654f28/complicated-worldwide-screening-panel-discussion | — | ||||||
| 2/11/26 | ![]() What Doctors Miss: HCM, Women’s Health, and Patient Voices | What does it mean to be diagnosed with a serious heart condition at a young age, and then have to fight to be believed?In this powerful conversation, Hannah shares her journey as a heart patient diagnosed with HCM and the realities of navigating a healthcare system that often overlooks young patients. She opens up about misdiagnosis, self-advocacy, and the emotional toll of living with a heart condition that doesn’t “look” sick.Hannah also dives into the mission behind the nonprofit, HeartCharged, which is working to raise awareness about heart conditions in young people and push for better education within the medical community. Together, the conversation explores how social media has become a lifeline for patient connection, why advocacy matters, and what it will take for patient organizations to collaborate more effectively.This conversation is for patients, advocates, caregivers, healthcare professionals, and anyone passionate about improving care for young people with chronic illnesses. https://www.getheartcharged.org/IG: @heartcharged | — | ||||||
| 1/28/26 | ![]() Gut-Immune Connection Explained | #ChronicIllness #GutHealth #DigestiveHealth #gastroparesis In this week’s episode, Sam sits down with Dahlia and James Marin, co-founders of Married to Health, where they unpack the gut-immune connection and why food is so much more than fuel when you live with chronic digestive illness.Together, they explore the concept of “gut debt,” the emotional and psychological weight we carry around eating, and why traditional nutrition advice often falls flat for people whose bodies don’t follow the rules. From pre-digestion techniques and mindful eating to building the right care team and repairing your relationship with food, this conversation offers real-world strategies that meet you where you actually are — not where wellness culture thinks you should be.Because healing your gut isn’t about perfection. It’s about listening, adjusting, and choosing yourself — even on the days your stomach is louder than your dreams. | — | ||||||
| 1/21/26 | ![]() Episode 30: Still Hot, Still Sick: Dating When Your Body Doesn’t Cooperate | Dating is hard. Dating with chronic illness or disability? That’s a whole different battlefield.In this episode, Sam sits down with the founders of Dateability, the first dating app built specifically for people with chronic illnesses and disabilities. Together, they unpack the emotional reality of navigating dating in bodies that don’t always cooperate, the isolation so many experience on mainstream apps, and the power of creating spaces where disability is normalized — not hidden.The founders share their personal journeys, the inspiration behind Dateability, and how community, inclusivity, and empowerment are at the heart of everything they’re creating. They also reveal what’s next for the app and why fostering real, supportive connections isn’t just a feature, it’s the mission.https://info.dateabilityapp.com/ | — | ||||||
| 1/14/26 | ![]() Episode 29: Hope in a Broken Digestive System | Gastroparesis isn’t just about digestion — it’s about identity, grief, resilience, and learning how to fight for yourself. In this episode, Sam and Dr. Eva Alsheik unpack the science behind gastroparesis, the mental health piece that’s often ignored, and what real treatment looks like beyond a prescription pad. They explore options like G-POEM, gastric stimulators from Enterra therapy, and emerging research; while reminding patients that knowledge is power, and reminding us how community can be everything.See here for more information on the medical device from Enterra Medical: http://www.enterramedical.com/important-safety-information/ | — | ||||||
| 12/31/25 | ![]() Episode 28: When Voices Become a Movement | In this final episode of the year, Sam pulls back the curtain on what it really takes to grow a chronic illness community. From the early days of G-PACT to the powerful network it’s become today, she reflects on the wins, the setbacks, and the moments that nearly broke her, and the people who helped her keep going.This episode is a love letter to every person who has ever felt isolated by illness, unheard by the system, or invisible in their own body. Sam shares why authenticity in advocacy isn’t optional, how real connection changes everything, and why sharing our stories is one of the most radical acts of healing we have.As we head into 2026, she also gives a glimpse into what’s next for G-PACT and the continued mission to make sure no one has to navigate chronic illness alone.Because this journey is hard — but it’s a hell of a lot lighter when we carry it together. | — | ||||||
| 12/24/25 | ![]() Episode 27: The Missing Piece in GI Treatment | In this week's episode, Megan Riehl joins the show to break down the brain–gut connection and why it’s a physiological process, not a dismissal. We explore how stress and nervous system dysregulation directly affect GI function, shaping symptoms that too often get misunderstood or minimized.Megan explains how psychological therapies, including gut-directed hypnotherapy, can be powerful, evidence-based tools for managing GI disorders, and why truly effective care has to be holistic and patient-centered. We also talk about the complicated relationship many patients develop with food, and how chronic digestive illness changes the way people relate to their bodies.Along the way, Megan shares practical insights and trusted resources for navigating GI care, advocating for yourself, and finding support that treats you as a whole person—not just a set of symptoms.This episode is for anyone who’s felt dismissed, stuck, or gaslit by the system and wants to understand what’s really been missing in GI treatment.Resources mentioned in the episode:Megan's Website: https://www.drriehl.com/ Mind Your Gut Book: https://www.drriehl.com/general-8 telehealth clinic: www.gipsychology.com The Gut Health Podcast: https://www.drriehl.com/podcast Additional Resources: https://www.drriehl.com/shop | — | ||||||
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Chart Positions
3 placements across 3 markets.
Chart Positions
3 placements across 3 markets.
