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
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.
Leave A Comment