Bradley’s journey as a below-the-knee amputee began in September 2014 due to a prolonged battle with osteomyelitis and multiple surgeries. His pivotal moment came three weeks prior to the amputation when he accompanied Jeff Linton, then president of Midwestern Amputee Golf Association (MWAGA) , on a ride. This encounter marked the beginning of Bradley’s deep involvement in adaptive golf.
In 2015, Bradley attended his inaugural MWAGA tournament, followed by joining the MWAGA Board in 2016. Since assuming the presidency in 2017, Bradley has been a driving force in both regional and national adaptive golf circles. He serves as the Midwest Trustee for the National Amputee Golf Association and led the 2022 Phoenix Cup team, representing the USA in England.
Beyond the greens, Bradley cherishes time with his family in McHenry, IL, where he resides with his wife, Heidi, and their children, Brooke and Tyler. Additionally, he plays a pivotal role as the Director of Friends of McHenry Golf, a non-profit dedicated to nurturing junior golf in the community. Professionally, Bradley serves as a Multimedia Instructional Designer in Rolling Meadows, IL. In this capacity, he spearheads the creation of training and eLearning content delivered globally to employees, partners, and end-users.
Links:
Midwestern Amputee Golf Association: http://www.mwaga.org
U.S. Adaptive Golf Alliance: https://www.usaga.org
North American One-Armed Golfer Association: https://www.naoaga.org
The Power of Golf: The Game’s Positive Impact On The Lives Of The Disabled: https://www.amazon.com/Power-Golf-Positive-Impact-Disabled/dp/1952779081
#limbloss #limbdifference #adaptive #adaptive #adaptiveathlete #usaga #adaptivegolf #amputeegolf #golf #golflife #inspiration #prosthetic #prosthetic #mwaga
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.
Leave A Comment