Intl Limb Correction Center
A globlal leader providing advanced pediatric care for limb deformities, complex joint reconstruction, limb length discrepancies, and skeletal dysplasia.
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Perthes Chat - Thursday, January 15 @ 8:30 PM ET
Perthes Chat - Thursday, January 15 @ 8:30 PM ET
Our Patients
Care You Can Trust: Alena’s Story
Care You Can Trust: Alena’s Story
At 20 weeks into her pregnancy, Valerie, Alena’s mom, received concerning news during a routine ultrasound: the long bones in Alena’s body weren’t measuring as they should. This unexpected finding led to a series of discussions with medical professionals. Two months after Alena’s birth, the diagnosis of Femoral Hypoplasia with Unusual Facies Syndrome (FHUFS) was confirmed. This rare genetic disorder is characterized by underdeveloped femurs, growth restrictions, and distinctive facial features. Alena’s journey with this syndrome has been a complex one, involving a variety of adaptive tools and treatments. “I use a walker, wheelchair, crutches, leg braces, and have a lift in my left shoe,” Alena explains. In an effort to address her growing needs, Alena and her family sought out orthopedic expertise. Alena’s case was referred to Dr. Shawn Standard, a specialist in pediatric orthopedics, who was based in Baltimore at the time. “We started receiving treatment from Dr. […]
Strength and Comfort: Makyla’s Story
Strength and Comfort: Makyla’s Story
Born with Chondrodysplasia punctata and Conradi-Hunermann, Makyla and her family found the support and care they needed at Nemours Children's.
A New Path Forward: Miguel’s Story
A New Path Forward: Miguel’s Story
Adopted from Colombia two years ago, Miguel’s congenital limb deformity had left him unable to stand or walk, relying on his knees and a wheelchair to navigate the world. “We were aware of his congenital limb deformity, but we weren’t exactly sure what that would mean for him in the course of his life,” his mother, Jennifer, shares. Life before treatment was a series of adaptations and challenges. Miguel had developed his own way of navigating the world. He would “walk” and crawl on his knees, using custom knee pads to cushion his movements. “He was amazingly active,” Jennifer shares, “but he did have frequent pain and skin issues from ‘walking’ on his knees.” His inability to stand or reach things independently made everyday activities a constant challenge. His family’s resolve to find a solution grew stronger with each passing day. “Because he also has shortened arms, we realized that […]
Independence and Confidence: Braulin’s Story
Independence and Confidence: Braulin’s Story
Braulin’s family found out about their son’s diagnosis during Gissette’s pregnancy. Gissette noticed that her local doctor was sending her to do more sonograms and measurements than she had for her previous pregnancies, making Gissette nervous. It was during this time that her care team informed her that Braulin was diagnosed with dwarfism. After receiving the diagnosis, Gissette decided to explore new care options with experts that specialized in dwarfism. “In my country, the Dominican Republic, there wasn’t much information about how to treat or care for a child with dwarfism,” shares Gissette. “I had a lot of questions but no answers. This is when my journey of looking for answers on the internet started.” Through her research, Gissette was able to connect with other parents navigating dwarfism and Little People of America. Once Braulin was born, Gissette took several trips to the United States with Braulin to receive specialized […]
Excellent Care is Out There: Charlotte’s Story
Excellent Care is Out There: Charlotte’s Story
Before she was even born, Charlotte was diagnosed with Congenital Femoral Deficiency and Fibular Hemimelia, a rare condition that would shape her life in ways her family could never have anticipated. Congenital leg length discrepancies are when patients have legs that are different lengths. Femoral deficiency is characterized by a short or missing thighbone and fibular hemimelia by a short or missing fibula. “It was an incredibly emotional and uncertain time for us,” her mother, Melissa, recalls. The news was both a shock and a call to action. As soon as they received the diagnosis, her family was determined to understand the condition and find the best possible care for Charlotte. “We knew this would be a lifelong series of surgeries, rehabilitation, and specialized care,” her father, Brian, recalls. “There was a lot of anxiety and fear about what her future would look like and whether she would be able […]
Limb Differences Awareness Month: Taylor's Story
Limb Differences Awareness Month: Taylor's Story
Limb Differences Awareness Month: Zohan's Story
Limb Differences Awareness Month: Zohan's Story
When Zohan was born, his parents were overjoyed to welcome their little boy into the world. But shortly after his birth, doctors noticed differences in his leg length and foot shape. After further testing, they diagnosed Zohan with fibular hemimelia, a condition where the fibula bone in the lower leg is missing or underdeveloped. From an early age, Zohan adapted to his condition, often running and walking on his toes. But as he grew, he faced challenges—difficulty wearing standard shoes, fatigue, and limitations in certain activities with his peers. His parents, determined to find the best care for him, were introduced to Nemours Children’s Hospital, Florida through their primary care provider. Their own research confirmed Nemours Children’s reputation for advanced limb reconstruction, and they knew they had found the right place. From their first visit, Zohan’s family felt reassured by Dr. Jason Malone, Dr. Shawn Standard, and the entire care […]
Strength and Growth: Elijah’s Story
Strength and Growth: Elijah’s Story
From the day he was born, Elijah has been surrounded by a team of experts at Nemours Children’s Hospital, Florida, who are dedicated to helping him reach his full potential. Born with several medical complexities, Elijah has met each challenge head-on, making remarkable strides every step of the way. “Nemours has always given Elijah a head start with all his goals,” shares his mom, Priscilla. “He’s been with them since day one.” Priscilla first discovered Nemours Children’s when her oldest son, Elias, needed sleep studies for asthma. The exceptional care Elias received made Nemours an easy choice for Elijah’s treatment. Throughout Elijah’s journey, Nemours has remained a constant source of support. Over the years, Elijah’s care has involved many specialists, including neonatologist Dr. Caroline Chua, who cared for him during his early days in the NICU, and plastic surgeon Dr. Brian Kellogg, who has been instrumental in addressing Elijah’s unique […]
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ILCC Patients & Families
ILCC Patients & Families
In the News
#18 in the Nation for Pediatric Orthopedics
#18 in the Nation for Pediatric Orthopedics
Nemours Establishes International Limb Correction Center with World-renowned Orthopedic Surgeon Shawn C. Standard, MD
Nemours Establishes International Limb Correction Center with World-renowned Orthopedic Surgeon Shawn C. Standard, MD
ORLANDO, Florida (Sept. 16, 2025) Nemours Children's Hospital, Florida, announced the creation of the Nemours Children's International Limb Correction Center, and welcomed Shawn C. Standard, MD,...
Correcting Limbs and Expanding Horizons
Correcting Limbs and Expanding Horizons
Top Physicians 2025 : Orlando Family Magazine
Top Physicians 2025 : Orlando Family Magazine
The Unstoppable Zohan
The Unstoppable Zohan
Our Doctors
Dr. Shawn C. Standard, ILCC Medical Director
Dr. Shawn C. Standard, ILCC Medical Director
Dr. Jason B. Malone, ILCC Assistant Director
Dr. Jason B. Malone, ILCC Assistant Director
Jason B. Malone, DO, is an Orthopedics provider affiliated with Nemours Children's Health.
Our PA’s
Nicole Toro-Keister, PA-C
Nicole Toro-Keister, PA-C
Kaitlin Q. Maher, PA-C
Kaitlin Q. Maher, PA-C
Kaitlin Q. Maher, PA-C, is an Orthopedics provider affiliated with Nemours Children's Health.
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