“We’re all going through different battles,” said 15-year-old Kely from Laredo, Texas.
“You never know what someone else is feeling, so I just try to be kind.”
And kind is exactly how those around Kely describe her. Encouraging, friendly and full of joy, Kely is a typical 10th-grader in many ways. She loves singing along to Doja Cat, spending time with friends, eating tacos al pastor and watching movies like The Princess Diaries and Clueless. She adores her two dogs and especially enjoys science class at school. But unlike most teenagers, Kely has spent much of her life navigating complex orthopedic care.
She was born with proximal femoral focal deficiency (PFFD), a congenital condition that affects the development of the femur and hip. “My femur was smaller, I only had the tibia, and my foot pointed downward, like a Barbie foot,” Kely said.
As a young child, frequent falls were common. Still, they never stopped her from trying new things like riding a bike or roller skating.
“Honestly, I always did whatever I wanted, even though I would fall all the time,” she said.
When she was 7, Kely began specialized orthopedic treatment with Shriners Children’s Texas. She received an extension prosthesis commonly used for patients with PFFD, and began physical therapy. As part of her care, she also worked with the behavioral health team, including psychologist Laura Rosenberg, Ph.D., who helped Kely navigate the emotional challenges that came with her condition, especially conversations surrounding amputation.
“I always knew I was different, and I wouldn’t care,” Kely said. “But then when I was like 10 or 12, I started to care.”
As she entered her teenage years, Kely found herself wanting a prosthesis that offered more flexibility and mobility. She wanted to sit comfortably in a car or on a bus without removing her prosthesis and hoped for a limb that felt like a true part of her body. Through her care at Shriners Children’s Texas, she had the opportunity to meet another patient who was also born with PFFD. Seeing what was possible helped Kely envision a new future for herself. After thoughtful consideration, she made the brave decision to undergo amputation of her left foot in May 2025.
“This was a process,” Kely said. “I needed time to understand myself and accept myself. I wouldn’t have made this decision when I was younger. But I knew I was in the best hands with Dr. Sanderson. He is brilliant, and I admire him so much.”