Hannah Williams was twelve years old when what everyone assumed was dandruff turned out to be psoriasis — and by sixteen, it had covered nearly 95% of her body. For years, she wore long sleeves in summer and avoided mirrors. Then, slowly, in small steps, something shifted: a kids' camp in America, a cross-country trip, a decision to start an Instagram — and eventually, tattoos as acts of deliberate, joyful self-decoration on the skin she'd spent a decade trying to hide. In this episode, Hannah talks about what it actually takes to stop hiding, what it means to build community around visibility, and what she wants every newly diagnosed twelve-year-old to know. Plus, Holly traces the word "stigma" all the way back to its ancient Greek roots — where it literally meant a mark burned into skin — and follows the long, complicated history of how tattooing traveled from punishment, to shame, to one of the most powerful forms of self-reclamation we have. Including what happens when psoriasis decides to have its own opinion about the process.

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When Dayna Pham was diagnosed with severe psoriasis at 21, the hardest part wasn't the plaques. It was the staring, the dating she stopped doing, and the version of herself she had to grieve. A few years later, on her first day of medical school, psoriatic arthritis arrived too. Now a University of Chicago med student, NPF advocate, and mentor for chronically ill students, Dayna talks candidly about the internal stigma that follows you even when no one's watching, the full-time job of managing a chronic illness on top of everything else, and what kind of doctor she's determined to become. Plus, Holly tells the story of a 12th-century Persian physician who linked a patient's psoriasis to emotional conflict — and why it took Western medicine until practically yesterday to admit that the mind and body are linked.

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Alisha Bridges was seven years old when a bout of chicken pox triggered psoriasis across 90% of her body — and she spent the next decade hiding it, until a beauty pageant, a department-store makeup counter, and a grandmother who refused to let her quit changed everything. In this episode, Alisha talks about turning shame into a platform, taking her story to Capitol Hill, and why mental health and diversity in research sit at the heart of her advocacy work. Plus, Holly digs into the surprisingly recent legal history that made it illegal to fire someone for having psoriasis — from an outrageous 1989 termination letter in the UK to the courtroom fight that finally forced American law to recognize chronic illness as the disability it actually is.

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If you've ever felt like no one in the room really gets what you're going through — this season is for you. Holly Frey of Stuff You Missed in History Class returns with Season 3 of Our Skin, expanding the conversation to include psoriasis, hidradenitis suppurativa (HS), and the full, complicated reality of living in a body that others don't always see clearly.

Each episode, we pull up a seat for people who've been there — through the appointments, the flare-ups, and everything in between. Honest, practical conversations about how to advocate for yourself, leave a doctor's office feeling heard, and navigate the hard parts without figuring it all out alone.
Then we zoom out — into the wild, weird history of how we've treated our skin, from ancient remedies to modern breakthroughs still being written.

Because when we share our stories with people who understand them, we create something bigger than awareness. We create community. A place where you're never the only one in the room.

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Model, actress, and stunt driver Ivy Smith first noticed psoriasis after the birth of her second child, but it took years, another pregnancy, and mounting pain before she finally got a diagnosis. In this episode, she opens up about battling stigma on set, the slow journey to show her skin with pride, and how adrenaline-fueled stunt driving became a surprising outlet. Plus, we rewind to the 1960s to uncover how a single classified ad led to the creation of the National Psoriasis Foundation–and forever changed the landscape of patient advocacy

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Victoria Voos was in college when her psoriasis “went full rampage,” setting off a cascade of diagnoses—from psoriatic arthritis to insulin resistance—that could have been overwhelming. Instead, she built online communities, mastered the art of the clap back, and became a fierce advocate for herself and others. In this episode, she shares how clinical trials gave her both hope and hard data, the boundaries that keep her online space safe, and why humor is one of her best defenses. Plus, the surprising story of the science behind monoclonal antibodies—and how they’re changing treatment for psoriasis.

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Diagnosed with psoriasis at age five, Lianne Hunter grew up learning to explain, defend, and sometimes hide her skin. Today, she’s built an online community, FixMyPsoriasis, and co-leads the Get Your Skin Out campaign, turning personal vulnerability into collective strength. Lianne opens up about raising her son with honesty and empathy, navigating tough moments in public, and why community is the key to living openly with psoriasis. And in our skin history segment, we uncover the story of Josh White—the groundbreaking blues guitarist whose psoriasis shaped both his career and a one-of-a-kind partnership with Ovation Guitars.

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When Allison Sowle showed up to a model casting with oozing eczema and no makeup, she didn’t expect to be chosen out of 30,000 people. But her message was clear: “I’m proud to be myself.” In this episode, Allison talks about claiming space in the modeling world, surviving without insurance, and the beauty of showing up as you are. Plus, we look back at some of the most bizarre and misguided psoriasis treatments in history.

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Jess Tran was 24, thriving in her career, and training as a powerlifter when a mysterious rash changed everything. It turned out to be guttate psoriasis—and it forced her to rethink everything from ambition to self-image. In this episode, Jess shares how she learned to listen to her body, why visibility can be both empowering and exhausting, and what she wants to change about the wellness industry. Plus, a scientific journey into the immune system—and the breakthrough that changed how we treat psoriasis today.

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India Bolton was first diagnosed with guttate psoriasis in college. Years later, that diagnosis expanded—through two pregnancies, psoriatic arthritis, and months-long flare-ups that covered her body. In this episode, India opens up about parenting through chronic illness, how she found strength in community, and why her children are part of her motivation to keep showing up. Plus, we dive into the science and history behind one of the world’s most effective natural treatments for psoriasis: the Dead Sea.

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