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
Watch on YouTube
Listen on Spotify
What happens when you survive COVID… but wake up to a completely different life? In this powerful episode of We’re Not Stumped, host Mike Bolland sits down with Brianna Heitzman, a certified employment specialist with Down Syndrome of Louisville, whose life was forever changed after a severe battle with COVID-19. After being placed on a ventilator and ECMO, Brianna faced an unimaginable outcome—the loss of her legs. But her story doesn’t end there. This is a conversation about resilience, identity, and rebuilding a life with purpose. Brianna’s journey is raw, real, and deeply inspiring—a reminder that even after life-changing trauma, there is still a path forward.
What happens when a story about limb loss hits the news—and suddenly everyone you know is texting you about it? If you’re part of the limb loss community, you already know. In this solo episode of We’re Not Stumped, host Mike Bolland dives into the experience of being “the limb loss friend”—the person others turn to when they don’t fully understand what they’re seeing but want to connect.
Stacy and Courtney Walker are proving that teamwork knows no limits. As the only known mother-daughter duo in wheelchair power soccer, they proudly represent Arizona Heat Power Soccer—competing, training, and pushing boundaries together on and off the court. Their journey is about more than just the game. It’s about resilience, family, and the power of adaptive sports to change lives. On this episode of We’re Not Stumped, host Mike Bolland sits down with Stacy and Courtney to share their story—how they got involved in power soccer, what it’s like competing side by side, and what being part of Arizona Heat Power Soccer truly means. Now, they’re working toward their next big goal: competing at Power Soccer Nationals.




Leave A Comment