Ep. 123 The Healing Power of Podcasts for Invisible Illness Warriors

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Have you ever wondered how podcasts could be a lifeline for those with invisible illnesses? Come and be part of an enriching dialogue with our esteemed guests, Professor Melanie Finney and the brains behind a startling study, Kate Pederson. Kate was inspired to do the study because her sister is living with POTS, one of the invisible illnesses that falls under the umbrella of fibromyalgia. We'll unravel the layers of isolation experienced by the invisible illness community and the surprising solace they find in podcasts. According to Kate's study, a staggering 97% felt less isolated, and an alarming number expressed a lack of empathy from their healthcare providers. 

As we move forward, we discuss fibromyalgia, an invisible illness with its unique set of challenges, and the pivotal role podcasts play here. The majority, 94%, found the information shared by podcast hosts invaluable, and three-quarters could trust the host they tuned into. We also tackle the conundrum of making podcasts more interactive, considering it's often a one-way communication. But, we also celebrate the power of storytelling and the platform podcasts offer for these unsung heroes to share their narratives. Join us as we shed light on these invisible battles being fought every day.

Click here for the Fibromyalgia 101 link.

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When I started this podcast—and the book that came before it—I had my patients in mind. Office visits are short, but understanding complex, often misunderstood conditions like fibromyalgia takes time. That’s why I created this space: to offer education, validation, and hope. If you’ve been told fibromyalgia “isn’t real” or that it’s “all in your head,” know this—I see you. I believe you. You’re not alone. This podcast aims to affirm your experience and explain the science behind it. Whether you live with fibromyalgia, care for someone who does, or are a healthcare professional looking to better support patients, you’ll find trusted, evidence-based insights here, drawn from my 28+ years as an MD.

Please remember to talk with your doctor about your symptoms and care. This content doesn’t replace personal medical advice.*