We’re Not Stumped Amputee Podcast Season 2 Episode 10 with Kayla Inman

In 2017 Kayla Inman slid on ice while leaving her workplace, and this event changed the course of her life. That slide caused her to feel constant pain in her foot, a pain that doctors failed to diagnose until December 2020, when she discovered she was developing complex regional pain syndrome (CRPS). After numerous consultations with medical experts and many conversations with her family, Kayla came to terms with the fact that the only solution to her pain and inability to walk was amputation.

On Sept. 30, 2021, orthopedic surgeon David Hahn successfully amputated Kayla’s leg below the knee. When she awoke from her anesthesia- induced nap, she quickly shot upright in her hospital bed to look at where her right leg once was. She would need to learn how to walk again with the prosthetic, but she was overcome with joy that, finally, the pain was gone.

Since then, Kayla has moved forward in amazing ways. She has given a TEXx Talk and also founded an amputee support group in Grand Junction, Colorado. We talk about all of this and more in this episode of the We’re not Stumped podcast.

Links:
Kayla Inman TEDx Talk: https://www.youtube.com/watch?v=QhOQMW2sMlk

Grand Valley Amputee Support Group: https://www.facebook.com/groups/1107576273319053/

Kayla Inman Instagram: https://www.instagram.com/thehappyamputee/

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Want to be considered as a guest? Fill out the form here: https://werenotstumped.com/contact-amputee-podcast/
Want to learn more about our host Mike Bolland? See his website https://mikebolland.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 |2024-01-10T12:01:32-07:00May 17th, 2023|Lower Limb Amputees, Podcast|0 Comments

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