In this episode of We’re Not Stumped, host Mike Bolland sits down with Brooke Brown—a passionate advocate, spiritual wellness guide, and founder of Brooke’s Butterfly Touch. Brooke, who lives with cerebral palsy and uses a wheelchair, shares how her journey led her to discover Reiki, energy healing, and the power of self-connection.
As an Ambassador for United Cerebral Palsy of Central Arizona and host of the Rolling in Grace podcast, Brooke empowers others to live with purpose, embrace their uniqueness, and become their own biggest advocates. She shares her message of accessibility, inclusion, and disability visibility, along with the importance of assuming competence in every interaction.
💜 Brooke’s mission is simple but powerful: help others reconnect with their spirit, lead fulfilling lives, and see disability through a lens of strength, not limitation.
🎧 In this episode:
- Brooke’s journey with cerebral palsy
- Discovering Reiki and spiritual healing
- The story behind Brooke’s Butterfly Touch
- Her role as a UCP Ambassador
- The Rolling in Grace podcast and disability advocacy
- Why we must always assume competence and bless our differences
📹 Watch Brooke speak at Life Recovery Church:
Always Assume Competence – Blessing Our Differences
🦋 Learn more about Brooke:
https://brookesbutterflytouch.com/
👩🦼 UCP Ambassador Profile:
https://ucpofcentralaz.org/ambassadors/brooke-brown/
🎧 Listen to Rolling in Grace:
https://podcasts.apple.com/us/podcast/rolling-in-grace-podcast/id1674482810
If you’re passionate about disability advocacy, spiritual growth, or building a more inclusive world, this episode will uplift and inspire.
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.
