Welcome to Iconically Ill, I'm your host Laura Lyons, where I interview other disabled and chronically ill people with humor and heart over the clinical part.
We talk Conradi-Hünermann Syndrome with Cassidy Huff.
Cassidy is a disability rights activist, content creator, and performer dedicated to amplifying disabled voices and challenging ableism. As a hard-of-hearing creator with a background in the performing arts, she uses her platform to educate, advocate, and share authentic experiences of disability. Cassidy has built a community of over 400,000 followers across social media, where she creates content focused on accessibility, identity, and social change. She is also the owner of Little & Loud Music, where she teaches creative arts and helps students build confidence through self-expression.
Follow Cassidy at cass_huff on Instagram
Show transcript bit.ly/3UKUymI
2 Jun 2026
We Talk Friedreich's Ataxia
We talk Friedreich's Ataxia with Jennifer Gasner.
Jennifer is a member of the International Memoir Writers Association, where she was member of the month in September 2023. Her writing has been published in Shaking the Tree, volumes 3 and 4, and in Six Feet Apart...In the Time of Corona. Her debut memoir, My Unexpected Life: Finding Balance Beyond My Diagnosis, was published on September 7, 2023, and won a Red Ribbon from The Wishing Shelf Book Awards. The book was a Finalist for the National Indie Excellence Awards, the Reader's Favorite Book Awards, and the Eric Hoffer Awards in 2024. She was Author of the Month for April 2024 at San Diego Library and won several awards from The Chrysalis BREW Project, including Nonfiction Book of the Year in 2024.
You can follow Jennifer at @jennygwriter on Instagram
Show transcript bit.ly/3UKUymI
26 May 2026
We Talk Congenital Muscular Dystrophy
We talk Congenital Muscular Dystrophy with Kelly Berger and Avery Roberts
Kelly and Avery are dynamic, empowered, rare disease warriors and disability champions who share their stories, spark conversations, and build a world that listens and activates real change. Their spirited advocacy is bold, personal, and impossible to ignore. They both live with the ultra-rare form of congenital muscular dystrophy (CMD), Collagen 6. They've turned their lived experiences into powerful platforms for global change. The fierce changemakers are driving visibility, authentic representation, and access, championing the next generation for a brighter, more inclusive future.
Their podcast, Wheel Talk gives a front row seat to bold conversations about the thriving disability community. The show amplifies voices, breaks down barriers, and celebrates the power of disability identity. It's where wit, wisdom, and wheels are all part of the party.
Follow Kelly at @thekellyberger and Avery at @Avery.nicole916 and their podcast at @thewheeltalkpodcast on Instagram
Show transcript bit.ly/3UKUymI
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Dustin D'Addato
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Madelein Murphy
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