In the latest episode of the “We’re Not Stumped” podcast, the spotlight is on Dave Gibson, an inspiring individual living in Arizona who shares his powerful story of resilience and humor in the face of life’s daunting challenges. Dave was born and raised in Southern California and moved to Arizona in the spring of 2004. He loves riding motorcycles, playing hockey, and being introduced to anything new. Dave’s journey is marked by a series of life-altering events, beginning with a severe motorcycle accident that led to the loss of his left leg. This traumatic incident could have easily defined his life, but Dave chose a different path.
Despite the physical and emotional hurdles of limb loss, Dave’s indomitable spirit shines through. He continues to ride his motorcycle, a testament to his determination and love for life on the road. Riding isn’t just a hobby for Dave; it’s a symbol of his refusal to be confined by his circumstances.
However, Dave’s journey doesn’t end there. He also candidly discusses surviving two strokes, which added another layer of complexity to his life. These strokes left him with a speech quality that he humorously likens to sounding “like I’ve had a bit to drink.” Yet, this change hasn’t dimmed his zest for life or his ability to bring joy to those around him. Instead, Dave embraces his unique voice and continues to engage with the world around him, often bringing laughter to his friends and family.
Throughout the podcast, Dave opens up about the challenges he has faced, offering an honest and heartfelt look at his journey. From the initial shock of his accident and strokes to the daily struggles and triumphs of living as an amputee, he provides valuable insights and encouragement for others facing similar obstacles.
Listeners of “We’re Not Stumped” will find Dave’s story both moving and uplifting. His experiences highlight not only the physical and mental battles that come with severe medical issues but also the incredible resilience of the human spirit. Dave Gibson’s journey is a testament to the power of perseverance and the importance of maintaining a sense of humor, even in the toughest times.
To hear Dave’s full story and learn more about his inspiring outlook on life, check out the latest episode of the “We’re Not Stumped” podcast.
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In this impactful episode of We’re Not Stumped, host Mike Bolland speaks out about a disturbing incident from the UK, where a woman without limb loss took to social media to mock individuals with visible limb differences—specifically targeting those with “nubs.” Mike calls out the cruelty and ignorance behind her actions, while emphasizing an important point: don’t give bullies the attention they crave. Sharing her posts only gives her more exposure and power. Instead, Mike encourages the limb loss community to rise above the hate—and to support one another with confidence and pride. “You are strong. You are resilient. And your difference is nothing to be ashamed of.” This episode is both a call for accountability and a reminder that dignity, not mockery, deserves the spotlight.
In this episode, we welcome Adrienne Hill, a certified prosthetist orthotist (CPO) and Program Director of the Master’s of Science in Prosthetics and Orthotics at Kennesaw State University. With a background in physics, mathematics, and health administration, Adrienne brings a unique perspective to the field. Her passion for prosthetics and orthotics is deeply personal—both her great-grandfather and father were amputees, inspiring her commitment to improving patient care. Adrienne has extensive experience as a former area clinic manager, where she provided clinical care, advocated for patients, and mentored future professionals. Now, she is dedicated to shaping the next generation of POP (Prosthetist-Orthotist-Prosthetist) professionals, ensuring they blend traditional care with cutting-edge technology.
In this episode of We’re Not Stumped, host Mike Bolland shares his candid thoughts on Limb Loss and Limb Difference Awareness Month — and why he believes awareness shouldn't be limited to just one month a year. Born without a right hand, Mike reflects on his lived experiences and how, for decades, many didn’t pay attention to people like him until they themselves became part of the limb loss community. He challenges listeners to think beyond temporary awareness campaigns and to embrace year-round inclusion, visibility, and support — not just when it becomes personal.
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