Welcome back to the “We’re Not Stumped” podcast! Host Mike Bolland introduces an exceptionally inspiring guest, Jonathan Cowley. Jonathan’s story is a profound example of resilience and determination in the face of formidable challenges.
Jonathan’s journey began in early 2013 when he discovered a small lump on his right hand. With a young child at home, bumps and scrapes were commonplace, so initially, neither Jonathan nor his doctor thought it was a cause for concern. However, a few months later, while on a family cruise, the lump became a significant issue. What started as minor discomfort evolved into severe pain, and the lump turned discolored, clearly signaling something was wrong.
Following this alarming development, Jonathan went through numerous doctor visits and medical tests. The results were unexpected and devastating: Jonathan was diagnosed with a rare form of cancer, with only about 20 cases reported annually in the United States. This diagnosis led to a series of surgeries, but despite the efforts, the only feasible option was to amputate his right hand above the wrist, just five months after returning from the cruise.
Undeterred by this life-changing event, Jonathan immersed himself in rehabilitation and was soon fitted with a prosthetic hand. Unfortunately, the prosthetic was uncomfortable and did not fit well. Jonathan faced the difficult choice of whether to persevere with the prosthetic or adapt to life without it.
Today, Jonathan joins the podcast to share more about his journey, the challenges he overcame, and how he transformed his story into one of triumph. The conversation will explore his experiences with prosthetics, his recovery, and how he navigates life post-amputation.
Jonathan, welcome to the show!
Listen on Apple Podcasts
Watch on YouTube
Listen on Spotify
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.
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.
Leave A Comment