Angie Sandow: Poland Syndrome, Motorcycles, Music & Living With One Hand

Angie Sandow was born with one hand and Poland syndrome—but that hasn’t stopped her from riding motorcycles, playing guitar, performing onstage, and finding plenty of reasons to laugh along the way.

In this episode of We’re Not Stumped, Mike Bolland reconnects with Angie for a candid and often funny conversation about growing up with a limb difference, dealing with bullying and unwanted attention, and learning to turn difficult experiences into something positive.

Angie shares how music became an important part of her life, including performing with bands and using a custom prosthetic guitar holder. She also talks about becoming a one-handed motorcycle rider and the modifications that allow her to ride, including moving the throttle to the left side.

Mike and Angie also discuss breast cancer, speaking and advocacy, aging with a disability, handling unsolicited help, the importance of supportive communities, and the unique experiences of people born with limb differences compared with those who experience limb loss later in life.

And, of course, there’s plenty of conversation about humor, hockey, the Buffalo Bills, and refusing to let other people’s expectations determine what’s possible.

It’s an entertaining and thoughtful conversation between two people born with one hand who have spent their lives finding their own ways to do things.

🎙️ We’re Not Stumped shares real stories of limb loss, limb difference, disability, recovery, resilience, and the people who prove that life doesn’t end when circumstances change.

https://www.laughswithangie.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 |September 8th, 2026|Congenital Amputee Stories, Upper Limb Amputees|Comments Off on Angie Sandow: Poland Syndrome, Motorcycles, Music & Living With One Hand

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