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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Sometimes, the biggest changes don't happen in a lab—they happen with a few carefully chosen words. In this episode of the We're Not Stumped podcast, I want to personally thank the LN-4 Hand Project (https://ln4handproject.org/) for updating its mission statement to better reflect the entire upper limb limb loss community. For many years, organizations have understandably focused on a specific group of individuals. But recognizing and including everyone living with upper limb loss and limb difference sends a powerful message: you belong, your story matters, and you are seen. As someone born without a right hand, this change means a great deal to me personally, and I believe it represents an important step toward greater inclusion across our community.
What happens when disability advocates from across the country come together to shape the future of independent living and accessibility? In this solo episode of We're Not Stumped, I share my personal reflections after attending the National Council on Independent Living (NCIL) Annual Conference in Washington, D.C., where I represented Ability360 as a member of its Board of Directors. From celebrating ADA36: We Won't Go Back to hearing powerful stories from advocates, policymakers, and leaders in the disability community, the conference reinforced why protecting and advancing disability rights remains so important.
In this episode of We're Not Stumped, Mike Bolland sits down with Karen Morales, a wheelchair user and leader of Fora Travel's Accessibility Initiative, to discuss how the travel industry can become more inclusive for everyone. After becoming a wheelchair user in 2020, Karen quickly discovered that planning an accessible trip often meant endless phone calls, unanswered questions, and uncertainty about whether hotels, transportation, and attractions would truly meet her needs. Rather than accepting those challenges, she helped create an initiative that's training hundreds of travel advisors to better serve travelers with disabilities and other accessibility needs.
