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On the show
From 10 epsHost
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Recent episodes
Belly Cramps, IBS, and the big bad Crohn's Disease
Feb 11, 2026
16m 54s
Chronic Illness Friendships, with a little reiki, herbs, and a lot of honesty, ft. Jess Gardner
Oct 30, 2025
40m 37s
Chronically Yours: ME/CFS Up Close, a personal story of chronic illness and resilience
Oct 3, 2025
9m 31s
ME/CFS is #notjustfatigue, featuring Founder Elizabeth Ansell
Sep 25, 2025
24m 53s
The Price of Inclusion: Chronic Illness, Disability, & Accessibility Fails
Sep 19, 2025
13m 11s
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| Date | Episode | Topics | Guests | Brands | Places | Keywords | Sponsor | Length | |
|---|---|---|---|---|---|---|---|---|---|
| 2/11/26 | ![]() Belly Cramps, IBS, and the big bad Crohn's Disease✨ | chronic illnessbelly pain+3 | — | Crohn's diseaseIBS+4 | — | chronic illnessbelly cramps+3 | — | 16m 54s | |
| 10/30/25 | ![]() Chronic Illness Friendships, with a little reiki, herbs, and a lot of honesty, ft. Jess Gardner✨ | chronic illnessfriendships+4 | Jess Gardner | Muddy Roots | — | chronic illnessreiki+6 | — | 40m 37s | |
| 10/3/25 | ![]() Chronically Yours: ME/CFS Up Close, a personal story of chronic illness and resilience✨ | chronic illnessresilience+4 | JD Fraser | ME/CFSChronically Yours | — | ME/CFSchronic illness+5 | — | 9m 31s | |
| 9/25/25 | ![]() ME/CFS is #notjustfatigue, featuring Founder Elizabeth Ansell✨ | ME/CFSchronic illness+4 | Elizabeth Ansell | notjustfatigue.orgMyalgic Encephalomyelitis+1 | — | ME/CFSchronic fatigue+5 | — | 24m 53s | |
| 9/19/25 | ![]() The Price of Inclusion: Chronic Illness, Disability, & Accessibility Fails✨ | accessibilitychronic illness+4 | — | WNBAADA | — | inclusionaccessibility+5 | — | 13m 11s | |
| 4/2/25 | ![]() Living in the Land of the Undiagnosed: My Chronic Illness Story✨ | chronic illnessundiagnosed+3 | — | — | — | chronic illnessundiagnosed+3 | — | 19m 59s | |
| 3/26/25 | ![]() Navigating Disability, Diagnosis, and Disney Magic with Kim Grant✨ | disabilitychronic illness+4 | Kim Grant | Disney | — | Cerebral PalsyCeliac Disease+6 | — | 22m 11s | |
| 3/19/25 | ![]() Chronically Yours: A New Podcast Segment Sharing Real Stories from the Chronic Illness Community✨ | chronic illnesspersonal stories+3 | Carrie Ferguson | Instagram | — | chronic illnessME/CFS+3 | — | 6m 01s | |
| 3/12/25 | ![]() Body Grief & Chronic Illness: Jayne Mattingly on Healing, Acceptance, and Her New Book✨ | body griefchronic illness+4 | Jayne Mattingly | This is Body Grief | — | body griefchronic illness+6 | — | 30m 42s | |
| 2/26/25 | ![]() From Overwhelmed to Organized: Managing Chronic Illness with Guava Health✨ | chronic illnesssymptom tracking+3 | Isabel | Guava Health | — | chronic illnesssymptom tracking+3 | — | 29m 09s | |
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| 2/21/25 | ![]() Big Three, Little Three, and Chronic Tea: Chatting About Illness Life, ft. Clark from Chronically the Sickest Podcast | In this episode of That Chronic Thing, I chat with Clark from Chronically the Sickest Podcast, and we dive into her "big three" and "little three" diagnoses (yep, there’s a Percy Jackson connection). We talk about managing chronic pain, sorting through overlapping symptoms, and the joys of willow bark tea when you're sick of popping pills. Clark shares how she juggles her conditions, finds support, and makes her social media a sensory delight. There’s humor, there’s validation, and a little y... | 16m 18s | ||||||
| 2/5/25 | ![]() When Support Shows Up: Stories of Unexpected Kindness | This short and sweet solo episode features a few stories from Cathy's Instagram community! I asked, tell me about a time that someone showed up for you unexpectedly and made a difference. Enjoy these stories and remind yourself: there are good, wonderful people in this world, and you are deserving of excellent care and support. Featuring submissions from Instagram friends: → Misty @plantspetsandpics → Liv @chronicpaininyour20s → JD @613jedi 💌 Stay in touch with me at @indoorc... | 8m 25s | ||||||
| 1/29/25 | ![]() Embracing Imperfection while Coping with Chronic Illness, ft. Dr. Talia | In this episode of That Chronic Thing, host Cathy chats with Dr. Talia, an inspiring digital creator who shares her journey of coping with multiple chronic illnesses. Dr. Talia discusses her experiences with perfectionism, the impact of chronic illness on mental health, and the importance of self-acceptance. Recently achieving her Ph.D. in clinical psychology, Dr. Talia offers insights into how to balance striving for health and finding joy in the present. She also delves into her creative pr... | 30m 24s | ||||||
| 1/22/25 | ![]() Inside the world of "Being (Sick) Enough," ft. Jessica Graham | In this episode of That Chronic Thing, we welcome Jessica Graham, a trauma resolution guide, meditation teacher, author, and filmmaker. Celebrating the release of their latest book, Being (Sick) Enough, Jessica explores themes of invisible illness, chronic pain, childhood trauma, and resilience. They share their personal experiences with chronic illnesses and how it has influenced their life and work. ➡️ Get Being (Sick) Enough 📚 Episode topics include: → the impact of COVID and chroni... | 37m 50s | ||||||
| 1/15/25 | ![]() The Chronic Chronicles: Turning Endometriosis Pain to Purpose, ft. Lexy Halloran | In this episode, we feature Lexy from the Chronic Chronicles podcast! 🎧 We chat about-- Lexy's personal journey with endometriosis and the challenges she faced in getting diagnosed and treated. The difficulties of managing chronic illness while pursuing a demanding career path The moment Lexy eventually accepting her condition.Experiences that led Lexy to start her podcast, focusing on community and valuable info for others in similar situations. Lexy's work in science, h... | 46m 44s | ||||||
| 1/8/25 | ![]() Chicken Glimmers, Wheelchair Freedom, and Finding the Joy in Aging despite Illness | In this episode, I’m talking with my friend Nic, all the way from New Zealand. We dive into the ups and downs of life with chronic illness, from finding freedom in her wheelchair to the small joys her animals bring. It’s a conversation full of real talk, relatable moments, and the kind of stories that stick with you. What’s in this episode: → 🐔 A chicken named Lola, heartbreak, and the glimmer of hope that followed. → 🦽 How using a wheelchair became a symbol of freedom—and the... | 23m 24s | ||||||
| 12/18/24 | ![]() Spreading Joy: Bringing Light to Others While Navigating Chronic Illness, ft. Casey Taton | In this episode, we sit down with Casey, a chronic illness warrior whose journey with MALS and comorbidities began in 2016. Despite facing her own health struggles, Casey found purpose and healing through helping others. From hospital celebrations to community support, Casey shares how she balances her passion for creating joy with the realities of chronic illness. → Casey shares how her health journey led her to create hospital celebrations that bring joy and comfort to kids and families fi... | 17m 23s | ||||||
| 12/4/24 | ![]() Cathy’s Chronic Illness Journey with ME/CFS, Cannabis, and Connection, ft. Julie Jo Hughes | In this special episode, Cathy is interviewed by her longtime friend, Julie Jo, for an honest and entertaining discussion about life, chronic illness, and the importance of connection. → WHOOPS: I say that EBV was linked to MS in the past 5-10 years. I’m completely wrong. It was as early as the 1970s. → Early Signs of Chronic Illness: Cathy shares her struggles with undiagnosed IBS during college and how a severe case of mono in junior year set the stage for her ME/CFS and MS diagnoses. →... | 43m 09s | ||||||
| 11/27/24 | ![]() Slushy Gratitude and Holiday Hacks: Surviving the Season with Chronic Illness | The holidays are here, bringing cinnamon scents, cozy vibes—and a whole lot of challenges when chronic illness is in the mix. In this episode, we unpack the messy feelings around holiday gratitude, share real-life stories from our listeners, and explore how to celebrate without overextending. Plus, get inspired with simple, low-energy gift ideas to show your love without draining your spoons. Let’s navigate the season together—slush and all! 💌 Stay in touch with me at&nbs... | 16m 07s | ||||||
| 11/22/24 | ![]() A Light in the Darkness: Remembering Sammy Lincroft | In this deeply heartfelt episode, we celebrate the life and legacy of Sammy Lincroft, a cherished member of the ME/CFS community whose advocacy, knowledge, and friendship impacted thousands. Sammy was a beacon of hope, sharing invaluable resources, navigating the complexities of chronic illness, and connecting with others in a way that made everyone feel seen and valued. I’ll begin by sharing my personal journey with Sammy—how her posts and friendship changed my life during some of my hardes... | 28m 50s | ||||||
| 11/20/24 | ![]() How to Be Seen and Heard After Illness: Lessons from Keeley Shantz | In this moving episode, I sit down with Keeley Shantz, a vibrant actor and storyteller who survived multiple strokes and turned her pain into a powerful mission. Keeley shares her journey from dancing in Iowa to pursuing acting in New York City, and how her life changed forever when she experienced a stroke while home alone. We talk about the raw, emotional details of that day—what it felt like to lose control of her body, her struggle to call for help, and her unexpected transformation into... | 34m 14s | ||||||
| 11/13/24 | ![]() Crummy Days, Cozy Reads, and My Cannabis Lifeline: Chronic Illness Real Talk | Hello my little ducklings! In this solo episode, I’m back after a few tough weeks, here to catch up and chat about life with ME/CFS, post-exertional malaise, and the ways I’ve been coping. From audiobooks (and my new “brain fog ratings” for each one) to podcasts that are giving me life, I’m sharing my latest finds and recommendations, including some great listens from Christina Applegate, Jamie Lynn Sigler, and Nora McInerney. On a more serious note, I’m navigating a big healthcare switch fo... | 15m 31s | ||||||
| 10/23/24 | ![]() Love & Care: Strong Partnerships with Chronic Illness, ft. Whitney Fox | In this episode, Whitney Fox returns to discuss relationships with chronic illness and disability. Key takeaways include: → Whitney’s story: How she and her husband, Andrew, create shared experiences despite the challenges of chronic illness. → Partnership tips: Whitney provides insights on how couples can nurture connection, even when one partner is mostly homebound. → Caretaking dynamics: Andrew’s approach to balancing the role of a partner and caretaker, both at home and when he’s away. →... | 25m 41s | ||||||
| 10/16/24 | ![]() (Fixed) Long-Covid & ME/CFS: when post-viral meets post-viral - a conversation with Whitney | Audio problem? What audio problem? A replay of an interview with Whitney Fox from May 2023. Sadly, as relevant as-ever! We talk about our fear of COVID, with the context that we’re already ill. We chat about… → Whitney’s arrest story?! → What happens when you get COVID plus ME/CFS? → Going out in a COVID world when you have ME/CFS… → and more! 💌 Stay in touch with me at @indoorcathy on Instagram. Make sure you leave a rating and a review! Thanks a bunch. <... | 19m 59s | ||||||
| 10/9/24 | ![]() Battery Alert: Surviving Festivals, Flare Ups, and Post Exertional Malaise | Hello my chickadees! In this episode of That Chronic Thing, we dive into the internal battery metaphor, a common way to explain energy depletion in ME/CFS. I share my experience attending a festival with my faulty battery and the onset of post-exertional malaise (PEM) that followed. We’ll discuss what PEM is, strategies to avoid it, and how to manage when it hits. Plus, I’ll provide practical tips from personal experience and the Open Medicine Foundation’s PEM Avoidance Toolkit to help naviga... | 12m 44s | ||||||
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