What happens when the limb loss community, prosthetics professionals, nonprofits, and supporters come together for a weekend built around giving back?
In this episode of We’re Not Stumped, Mike Bolland talks with Rob Pittman of Hanger, Chairman of the Hanger Foundation’s Night to Inspire, about the upcoming 2026 Night to Inspire in Nashville, Tennessee.
Now in its third year, Night to Inspire is expanding into a full weekend experience designed to raise funds, build awareness, and support organizations helping people with limb loss, limb difference, and mobility challenges.
Rob shares what attendees can expect, including a Friday evening kickoff at Dolly Parton’s SongTeller Hotel, bourbon experiences, a golf outing, and a Saturday night dinner, reception, and concert at the Country Music Hall of Fame and Museum.
Mike and Rob also discuss:
- How Night to Inspire got started
- The mission of the Hanger Foundation
- Organizations supported through the foundation, including Camp No Limits
- Rob’s lifelong career in orthotics and prosthetics
- The evolution of prosthetic technology
- Why peer support can be so important after limb loss
- Helping new amputees understand what is possible
- Raising awareness and financial support for the limb loss community
- How people can support Night to Inspire even if they can’t attend in person
Rob also reflects on growing up in the orthotics and prosthetics profession and why, after decades in the field, helping people regain mobility and quality of life continues to drive his work.
Night to Inspire 2026 takes place September 19, 2026, in Nashville, Tennessee.
Listen to this episode of We’re Not Stumped to learn more about Night to Inspire, the Hanger Foundation, and the people working to make a difference throughout the limb loss and limb difference community.
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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.
