In this powerful episode of the We’re Not Stumped podcast, host Mike Bolland welcomes Susan Fumagalli Mahoney, a true inspiration and advocate for amputees around the world. Susan opens up about her personal journey through limb loss and her experience with osseointegration—a groundbreaking technology that has changed her life and could reshape the future of prosthetics for countless individuals. Susan shares her story, from the physical and emotional challenges of losing a limb to the hope and transformation that osseointegration has brought to her life.
As someone who’s experienced the unique struggles and triumphs of the limb-loss community, Susan offers a candid perspective on overcoming adversity, adapting to new advancements, and living life with confidence and independence. Osseointegration has not only given her improved mobility but also empowered her to pursue her dreams and inspire others facing similar challenges.
Join us for this heartfelt conversation as Susan and Mike discuss the impact of medical innovations like osseointegration, the power of resilience, and the importance of advocating for accessible and effective solutions for amputees. From overcoming challenges to pushing for improved care, this episode highlights the inspiring journey of thriving beyond limb loss. Whether you’re in the limb-loss community, know someone who is, or simply want to be inspired, Susan’s story is a reminder of what’s possible with courage, innovation, and support in transforming lives.
Topics Covered:
Susan’s limb-loss journey and challenges
Understanding osseointegration and its benefits for amputees
The importance of resilience and advocacy in the disability community
How medical advancements can change lives
Tune in to learn more about how Susan and others in the amputee community are pushing the boundaries of what’s possible and why stories like hers matter in the movement for greater accessibility, inclusion, and technological advancement.
Link: https://integrum.se/
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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.
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