What happens when you begin losing your vision as a child—and refuse to let it define your future?
In this inspiring episode of We’re Not Stumped, host Mike Bolland welcomes Kathy Nimmer, recipient of the prestigious Helen Keller Achievement Award, author, speaker, and retired high school English teacher who spent nearly three decades educating and inspiring students while living with blindness.
Kathy shares her remarkable journey of progressive vision loss caused by a rare retinal degenerative disease, the challenges she faced along the way, and the resilience that helped her build a life filled with purpose, achievement, and impact.
In this episode, Kathy discusses:
- Growing up with gradual vision loss and adapting to change
- Teaching high school English for nearly 30 years as a blind educator
- Overcoming depression, anorexia, and uncertainty about the future
- The role of advocacy, family support, and disability representation
- Pursuing mountain climbing, writing, public speaking, and teaching
- Employment challenges facing people who are blind or visually impaired
- Practical advice for families navigating vision loss and disability
Kathy also shares insights from her latest book, Two Plus Four Equals One, an anthology celebrating the unique bond between people with disabilities and their assistance dogs.
This powerful conversation is a reminder that while circumstances may change, purpose, passion, and perseverance can help us achieve far more than we ever imagined.
Learn more about Kathy at KathyNimmer.com.
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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.
