In this episode of the We’re Not Stumped, we sit down with Kelly J. Mendenhall—an accomplished author, speaker, and advocate—to explore her transformative journey from a thriving career in nonprofit fundraising to becoming a disabled entrepreneur and patient advocate. Diagnosed with rare spinal cord conditions in 2017, Kelly faced a medical mystery that led her to redefine her life and purpose.
Kelly shares her experiences navigating the healthcare system, the challenges of living with invisible disabilities, and how she channeled her struggles into writing and advocacy. Her memoir, “Skin in the Game: The Stories My Tattoos Tell,” delves into her personal narrative, offering insights into resilience and self-discovery.
Kelly’s dedication to empowering others is evident in her efforts to raise awareness about chronic pain, mental health, and the importance of patient-centered care.
Join us for an inspiring conversation that highlights the power of storytelling, the importance of self-advocacy, and the resilience of the human spirit. Whether you’re interested in personal development, healthcare advocacy, or the art of memoir writing, this episode offers valuable insights and motivation.
Key Topics:
- Kelly’s transition from nonprofit fundraising to becoming a disabled entrepreneur
- Navigating the complexities of rare spinal cord conditions and chronic pain
- The inspiration behind her memoir, “Skin in the Game: The Stories My Tattoos Tell”
- Strategies for self-advocacy within the healthcare system
Don’t miss this episode filled with wisdom, courage, and actionable advice for anyone facing life’s unexpected challenges.
Connect with Kelly J. Mendenhall:
Website: kellyjmendenhall.com
Subscribe to Our Podcast: https://werenotstumped.com/were-not-stumped-amputee-podcast-mailing-list/
Stay updated with our latest episodes by subscribing and hitting the notification bell. If you enjoyed this conversation, please leave a review and share it with your network. Your support helps us bring more inspiring stories to light.
Disclaimer:
The content of this podcast is for informational purposes only and should not be considered medical advice. Consult with a healthcare professional for medical concerns.
Listen on Apple Podcasts
Watch on YouTube
Listen on Spotify
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.
Jeanette Jones returns to the We’re Not Stumped podcast with host Mike Bolland for a powerful conversation that goes beyond music. She shares a shocking and emotional story about the accessibility barriers she and her partner Frank encountered at a Def Leppard concert at the Bethel Woods Center for the Arts. From steep hills to discriminatory treatment by staff, their experience sheds light on how accessibility still falls short—even in 2025. But that’s just the beginning. Jeanette also opens up about her own journey—surviving childhood cancer, transitioning from prosthetics to a wheelchair, and the incredible resilience of her partner Frank after his life-changing accident. This episode is about more than one bad night—it’s a call to action for accessibility, empathy, and real change.