Nicole Kelly: Miss Iowa, Disability Advocate, and Myoelectric Prosthetic Trailblazer

In the first episode of the We’re Not Stumped podcast, I’m very honored to have Nicole Kelly as a guest. Like me, Nicole is an congenital amputee of an upper extremity. Nicole was Miss Iowa 2013 and competed in the Miss America Contest in 2014 and she talks about that experience in this podcast. Nicole was also featured on the The Today Show as well as countless other shows and platforms. She has a masters degree in broadcast journalism from Northwestern University and and has proudly spoken at hundreds of K-12 schools and given educational lectures at universities across the country. Nicole has spoken at corporations including Google, Microsoft, Allstate, and Riot Games. She now works for Coapt, the maker of Complete Control advanced pattern recognition myoelectric control technology for upper limb prosthetics. In this video she will demonstrate her incredible prosthetic made possible by the great team at Coapt. If you are an amputee, a family member of a person with limb loss or a person in the support community, I would love to have you on the show. Please contact mike@mikebolland.com to be considered as a guest.

More Info
Nicole Kelly website: https://www.missnicolegkelly.com
Coapt website: https://coaptengineering.com/

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  • Meegan Winters, CEO and founder of AbleVu

August 19th, 2025|

In this episode of We’re Not Stumped, Mike Bolland sits down with Meegan Winters, CEO and founder of AbleVu, the innovative accessibility search platform making the world easier to navigate for everyone. Meegan shares her inspiring journey—from special education teacher to tech entrepreneur—and how her friendship with Jessica, a power wheelchair user, sparked her mission to improve accessibility for all. Mike and Meegan explore AbleVu’s evolution from virtual tours to a “TripAdvisor for accessibility,” the business model that empowers contributors, and why accessible information benefits both consumers and businesses. Along the way, Meegan opens up about leaving a stable career, overcoming the challenges of building a startup, and the fulfillment that comes from creating real-world impact. Discover how technology and empathy intersect to make the world more inclusive.

  • individuals willing to share their experiences with prosthetists and prosthetic care

August 14th, 2025|

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/

  • Katie Thomas on Parenting, Advocacy, and Living One-Handed

August 12th, 2025|

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.

By |2025-04-09T18:20:15-07:00September 6th, 2022|Congenital Amputee Stories, Podcast, Upper Limb Amputees|0 Comments

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