When You’re the “Limb Loss Friend” Everyone Texts

What happens when a story about limb loss hits the news—and suddenly everyone you know is texting you about it?

If you’re part of the limb loss community, you already know.

In this solo episode of We’re Not Stumped, host Mike Bolland dives into the experience of being “the limb loss friend”—the person others turn to when they don’t fully understand what they’re seeing but want to connect.


What This Episode Covers

Mike shares insights on:

  • What it feels like when everyone sends you the same limb loss story
  • Why people reach out—and why it usually comes from a good place

Why Enable Review Was Created

This episode also talks about Enable Review, a community-powered platform designed specifically for the limb loss community.

Enable Review allows amputees to share real, experience-based feedback about:

  • Prosthetists
  • Orthotists
  • Clinics and rehabilitation care

Because when someone is new to limb loss, they shouldn’t have to rely on headlines, guesswork, or generic online reviews.

They should be able to learn from people who have actually lived it.

👉 Learn more or share your experience: https://enablereview.com/

Listen on Apple Podcasts

Watch on YouTube

Listen on Spotify

  • Meegan Winters, CEO and founder of AbleVu

August 19th, 2025|

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.

  • individuals willing to share their experiences with prosthetists and prosthetic care

August 14th, 2025|

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/

  • Katie Thomas on Parenting, Advocacy, and Living One-Handed

August 12th, 2025|

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.

By |March 26th, 2026|General Disability Related Resources and News|Comments Off on When You’re the “Limb Loss Friend” Everyone Texts

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