In this deeply moving episode of We’re Not Stumped, host Mike Bolland welcomes Scott Martin, a bilateral hand amputee, soccer coach, and author of the upcoming memoir Play From Your Heart. Scott opens up about the life-altering infection in 1993 that led to the loss of both hands and parts of his feet, and the emotional aftermath that followed. He speaks honestly about denial, detachment, and the five-year struggle with depression that tested his identity, confidence, and purpose.
Despite unimaginable challenges, Scott refused to step away from the game he loved. He continued coaching soccer using adaptive equipment, determination, humor, and grit—doing everything he could to show up for his players while still processing his trauma internally. Eventually, his journey intersected with advanced prosthetics research, leading him to Johns Hopkins to test cutting-edge myoelectric prosthetic technology. Scott offers powerful insight into what works, what doesn’t, and why technology must always stay grounded in real human needs.
Scott also shares the emotional turning points that helped him heal, including his mother’s unwavering encouragement and the mindset shift that allowed him to rebuild his life. His story eventually led him back to the soccer field, where he coached a youth team to a state championship and rediscovered purpose, leadership, and community. That experience inspired his book, Play From Your Heart, which speaks to the disability community, the soccer world, and anyone who has ever had to rebuild life after loss.
This conversation is about resilience, identity, mental health, disability advocacy, and what it truly means to adapt and keep moving forward. Scott reminds us that healing takes time, purpose can look different than we imagined, and strength often shows up when we need it most.
If you’re part of the amputee or limb difference community, a caregiver, an athlete, or someone navigating your own life challenges, Scott Martin’s story will stay with you long after you listen.
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What does it mean to truly be heard when you can’t speak? Jessica Frew, a nonverbal actress, model, and passionate disability advocate, joins We’re Not Stumped to share her powerful story of living with cerebral palsy and using an eye gaze device to communicate—a technology she began using at just nine years old. While Jess initially limited the device to school and close friends, she opens up about the emotional weight of using it publicly and the deeply personal regret of not speaking to her father through it before he passed away. Over time, Jess found strength in her voice and now uses it to educate, advocate, and challenge misconceptions about nonverbal individuals. She speaks with host Mike Bolland about the common experience of being talked down to or ignored—and how she responds with patience, courage, and relentless advocacy.
What do you do when life is going perfectly—until it’s not? In this powerful episode of We’re Not Stumped, host Mike Bolland talks with Kijuan Amey—a U.S. Air Force veteran, entrepreneur, and traumatic brain injury survivor whose life changed in an instant. At just 25, Kijuan was thriving: one year from earning his degree, running his own business (Kiwi Enterprise LLC), and proudly serving his country. Then, a sudden motorcycle accident nearly took it all away. But instead of asking, “Why me?”, Kijuan chose a different question: “What now?” Through faith, grit, and a desire to help others, he turned unimaginable trauma into purpose—and a message of hope.
In this episode, host Mike Bolland shares the inspiring story of Carter Henning, a high school freshman from Calamus-Wheatland in Iowa who returned to lead his varsity golf team just two months after losing his leg in a snowmobile accident. Carter’s determination and passion for the game showcase what’s possible with resilience and heart. Mike also highlights the Dallas Amputee Network (DAN), a nonprofit offering vital support and peer mentorship to amputees and their families across North Texas. Founded by Ellen Winchell in 2002, DAN empowers individuals through monthly meetings, the Certified Peer Visitor program, and a strong community of encouragement.
