In this powerful episode of We’re Not Stumped, Mike Bolland sits down with Kelvin Crosby , a remarkable individual whose journey from hearing loss and blindness to becoming an inventor, artist, and advocate will leave you inspired. Diagnosed with hearing loss as a child, Kelvin later lost his vision due to Usher Syndrome Type 2. He opens up about the emotional toll this took on him, including thoughts of suicide, and the turning point when he chose to embrace his deafblindness instead of letting it define him.
Kelvin shares how this decision sparked a new purpose in life—one rooted in helping others. His invention, the See Me Cane, is a game-changer for people with visual impairments. Designed to enhance safety and awareness, the cane features a light that gives users control over their environment while maintaining their ability to hear. Kelvin explains how this tool has not only improved his own life but also empowered others with confidence and mobility.
The conversation also explores Kelvin’s unexpected journey into pottery. Losing his vision at 32, he found healing through clay, eventually becoming the Deaf Blind Potter. What began as a side project blossomed into a thriving business and popular TikTok channel. Kelvin also shares his goal of funding 1,000 See Me Canes and his collaboration with an engineer to bring his invention to market.
Mike and Kelvin discuss his three podcasts—Perseverance Podcast, See Me Cane Podcast, and Investing in Accessibility—each focused on uplifting stories, product development, and accessibility innovation. They even touch on goalball, a thrilling Paralympic sport played by blind athletes.
Kelvin’s story is one of grit, creativity, and choosing joy. Whether you’re facing your own challenges or seeking inspiration, this episode reminds us that adversity can lead to purpose.
Links:
Personal Website: https://kelvincrosby.com/
DeafBlindPotter: https://www.deafblindpotter.com/
SeeMeCane: https://www.seemecane.com/
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Listen on Spotify
Podcast host Mike Bolland is looking to connect with individuals willing to share their experiences with prosthetists and prosthetic care. If you’ve ever faced challenges with a prosthetist, received a prosthetic that didn’t meet your needs, or discovered a provider who went above and beyond, your story can make a difference. On his show, We’re Not Stumped, Mike engages in open, honest conversations about life with limb loss, prosthetics, and advocacy. His mission is to give a voice to the limb loss community, spotlight real experiences — both the good and the bad — and work toward improving the system for everyone. Mike invites you to be part of this important dialogue, knowing that your insights could help others navigate their own prosthetic journeys with greater confidence and support. 📩 Interested in being a guest? Visit: https://werenotstumped.com/were-not-stumped-limb-loss-podcast-guest-guide/
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.
Jeanette Jones returns to the We’re Not Stumped podcast with host Mike Bolland for a powerful conversation that goes beyond music. She shares a shocking and emotional story about the accessibility barriers she and her partner Frank encountered at a Def Leppard concert at the Bethel Woods Center for the Arts. From steep hills to discriminatory treatment by staff, their experience sheds light on how accessibility still falls short—even in 2025. But that’s just the beginning. Jeanette also opens up about her own journey—surviving childhood cancer, transitioning from prosthetics to a wheelchair, and the incredible resilience of her partner Frank after his life-changing accident. This episode is about more than one bad night—it’s a call to action for accessibility, empathy, and real change.
