
Episode #20
Mobility Impairment - Day in the Life with Kelly & Avery
Disability is not one simple story, and neither is congenital muscular dystrophy. In this episode, Kelly and Avery share what daily life with an ultra-rare form of CMD actually looks like, from care coordination, mobility access, advocacy, and community to friendship, travel, dance, media representation, and the work of building a more inclusive world. This conversation is warm, honest, and grounded in lived experience. Kelly and Avery talk about the complexity of disability without reducing it to struggle or inspiration, and they remind listeners that access, respect, representation, and community are not extras. They are what make full participation possible. Wheel Talk With Kelly & Avery Podcast: http://ladieslivingrare.com/wheel-talk-podcast https://www.facebook.com/TheWheelTalkPodcast/ https://www.instagram.com/thewheeltalkpodcast https://www.youtube.com/@TheWheelTalkPodcast https://www.tiktok.com/@thewheeltalkpod creators.spotify.com/pod/show/the-wheel-talk-podcast https://podcasts.apple.com/us/podcast/wheel-talk-with-kelly-and-avery-podcast/id1836473324 Connect with Kelly Berger: https://www.instagram.com/thekellyberger/ https://www.facebook.com/thekellyberger/ https://www.linkedin.com/in/thekellyberger/ Connect with Avery Roberts: https://www.instagram.com/avery.nicole916/ https://www.facebook.com/averyroberts916 https://www.linkedin.com/in/averyroberts916/ Podcast Feedback Form: https://docs.google.com/forms/d/e/1FAIpQLSdxpoPFCLF_XINFGDQ3DApxri0PmCo708zse20o2ky94RQEhg/viewform?usp=sharing&ouid=118209669073480259176

