In episode 4 of season 2, I get the pleasure of speaking to Wafa Lavelle.
Wafa was born in the Middle East in the country of Jordan. While her mother was pregnant with her, she became sick and had to take medication. Nothing was known at the time about the medication’s side effects on pregnancy, and this led to Wafa being born with birth defects. These included two club feet, legs that were bent to her thighs and hip dysplasia. Because of these birth defects, she was unable to walk and was only able to crawl until seven years of age.
At seventeen Wafa stepped on a nail, and this led to the amputation of one of her feet. With over sixty surgeries behind her and an unpleasant experience with a prosthetist, Wafa is now better than ever. She is a Certified Peer Visitor for the Amputee Coalition and was recently profiled on WCVB TV in Boston for all of the goodwill she offers to others.
Wafa talks about those experiences and more – including funny stories from her life – in this episode of the We’re not Stumped podcast.
Helpful links from this episode:
Hanger Clinic: https://hangerclinic.com/
Wafa in InMotion Magazine: https://www.amputee-coalition.org/inmotion_online/inmotion-29-06-web/10/
Wafa on WCVB TV: https://www.wcvb.com/article/5-for-good-quincy-woman-offers-peer-support-to-others-with-limb-loss-differences/43215101
Amputee Coalition: https://www.amputee-coalition.org/
Amputee Coalition Certified Peer Visitors: https://www.amputee-coalition.org/support-groups-peer-support/certified-peer-visitor-program/
Wafa on Instagram: https://www.instagram.com/wafahaddadlavelle/
#amputee #amputeestrong #Limbloss #prosthetics #prosthetic #staypositive
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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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