Join us for the 100th episode of We’re Not Stumped! Host Mike Bolland reflects on the incredible journey so far, and the lessons learned from celebrating resilience and overcoming challenges. In this special milestone episode, Mike also walks listeners through the process of becoming a guest on the podcast, offering insight into how stories of triumph and inclusivity are selected and shared. Whether you’re a longtime listener or new to the podcast, this episode is filled with gratitude, inspiration, and exciting updates for the future. Thank you for being part of our journey—here’s to the next 100!
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In this episode, host Mike Bolland shares the inspiring story of Carter Henning, a high school freshman from Calamus-Wheatland in Iowa who returned to lead his varsity golf team just two months after losing his leg in a snowmobile accident. Carter’s determination and passion for the game showcase what’s possible with resilience and heart. Mike also highlights the Dallas Amputee Network (DAN), a nonprofit offering vital support and peer mentorship to amputees and their families across North Texas. Founded by Ellen Winchell in 2002, DAN empowers individuals through monthly meetings, the Certified Peer Visitor program, and a strong community of encouragement.
In this episode, we sit down with Vanessa Abraham, a certified Speech-Language Pathologist whose life took an unexpected turn when she became the patient. After a sudden illness left her paralyzed and unable to speak, Vanessa faced the daunting task of reclaiming her voice and identity. Vanessa shares her harrowing experience of battling Post-Intensive Care Syndrome (PICS), the emotional toll of being unable to communicate, and her path to recovery. Her story is not just one of survival but of transformation, leading her to become an advocate for ICU survivors and author of the memoir Speechless: How a Speech Therapist Lost Her Ability to Speak and Her Silent Struggle to Reclaim Her Voice and Life.
In this inspiring episode of We’re Not Stumped, we spotlight adaptive athlete Tracy LaMarche as she takes on the Ride to End ALZ South Carolina—a three-day cycling journey across the state with deep personal meaning. After losing her leg, Tracy found freedom and strength through cycling. Now, she rides to honor her late mother-in-law, who battled dementia, and to support vital Alzheimer’s research. Riding alongside her husband Blair, Tracy embodies resilience and hope, pedaling toward a future where no family has to face this disease alone.