In this episode of We’re Not Stumped, host Mike Bolland sits down with Christopher Rodriguez, CEO of Ability360, to discuss the organization’s powerful role in promoting independence for individuals with disabilities. Learn about the wide range of programs and resources Ability360 offers, from adaptive sports to advocacy, and how they are transforming lives by empowering people to live fully and independently. Tune in for an inspiring conversation about inclusion, accessibility, and the future of disability support.
Website: https://ability360.org/
Ability360 is a 501 (c)(3) non-profit corporation. Through its comprehensive programs, Ability360 touches the lives of individuals with disabilities and addresses the disability concerns of their family members, co-workers and employers.
Ability360 began in 1977 as the Arizona Congress for Action (ACA), a group of people with diverse physical disabilities who launched a grassroots effort to educate the community about disability-related issues in Central Arizona. In 1978, Congress enacted Independent Living Center legislation as part of the amended Rehabilitation Act of 1973. In 1981, Ability360 received funding and began services.
With more than 130 staff members and volunteers, more than 1,500 personal care attendants and hundreds of volunteers, Ability360 has offices in Phoenix, Gilbert/Mesa, Glendale, Tucson, along with Coolidge, and provides services throughout Maricopa, Pima, Pinal, and Gila Counties. Ability360 programs are made possible through grants, fee-for-service contracts, and individual and corporate contributions.
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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.
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