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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