In this heartfelt and uplifting episode of We’re Not Stumped, host Mike Bolland welcomes Katie Thomas for a conversation filled with honesty, humor, and hard-earned wisdom. Born without her right arm below the elbow, Katie began receiving care at Shriners Hospital in Tampa at age 3 and experimented with various prosthetics throughout her childhood. Over time, she discovered that prosthetics were a helpful tool—but not essential for her to live a full, capable life.
Now a devoted parent, Katie opens up about raising her son, who has Witteveen Colk syndrome, a rare genetic disorder. She shares her journey through early intervention services, advocating for genetic testing, and ensuring her child receives the support he needs. Her advice to parents? Trust your instincts, push for answers, and never hesitate to speak up for your child.
Katie and Mike also trade stories about life with one hand, from adapting daily tasks to navigating public perceptions and occasional misconceptions. Their conversation touches on sports, school, prosthetic “show-and-tell,” and their shared mission to be seen as capable—not simply inspirational for living their lives.
This episode is a mix of candid storytelling, practical insight, and lighthearted connection that will leave you informed and inspired.
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Post-amputation pain can be debilitating, but a new treatment called hydrodissection is showing promise in providing relief. In this episode of We're Not Stumped, we explore this groundbreaking therapy and its potential to improve the lives of amputees. Hydrodissection is a relatively new and promising treatment for post-amputation pain, particularly for neuroma-related pain and phantom limb pain. Here’s how it compares to other common pain treatments for amputees. Mike Bolland also shines a spotlight on Infinite Dance Flow, an inclusive dance company that is redefining what it means to move, featuring dancers of all abilities.
In this episode of the We're Not Stumped podcast, host Mike Bolland welcomes Allison Sweet Grant, author of I Am The Cage, a powerful novel inspired by her own medical experiences. Allison shares her journey of undergoing the Lizarov limb-lengthening procedure as a teenager and how those experiences shaped her writing. Like her protagonist Elisabeth, Allison grappled with feelings of isolation, a lack of agency, and the struggle to be heard in a confusing healthcare system. She opens up about translating her personal trauma into fiction, creating a character who faces her own battles with bodily autonomy and self-forgiveness.
In this episode of We’re Not Stumped, we highlight two incredible stories of resilience and empowerment. First, we celebrate Forreston High School wrestler Lucas Nelson, who recently reached his 100th career win—an impressive feat made even more inspiring by the fact that he competes with a limb difference. His journey is a testament to the power of perseverance, proving that hard work and determination can overcome any challenge. We also spotlight Penta Prosthetics, a nonprofit organization dedicated to making prosthetic devices more accessible to those in need. With millions of people worldwide unable to afford proper prosthetic care, Penta Prosthetics works to bridge the gap by recycling, refurbishing, and redistributing prosthetic limbs to individuals who need them most. Their mission is transforming lives, giving people the mobility and independence they deserve.
