a child smiling in an examination room

Finding Her Footing: Emily's Path to Confidence

Meet Emily.

For most 13-year-old girls, the biggest worries in eighth grade involve homework or social dynamics.

But for Emily, a bright and eclectic teen with a love for vintage culture, the challenge was physical. While her friends were worrying about what to wear, Emily was worrying about how she would walk.

Emily has a lot of varied interests for a modern teenager. She plays golf, is learning guitar and has a love for 80s music: The Smiths, Stevie Nicks and Selena are in her regular rotation. She’s a Toronto Maple Leafs fan, prefers The Karate Kid over most modern movies, and will never say no to homemade enchiladas. She also has big dreams: to become an actor, FBI agent or maybe even a nutritionist. But alongside all of that, Emily has been living with a rare orthopedic condition called macrodactyly.

Macrodactyly is a congenital condition, meaning children are born with it, where one or more fingers or toes grow abnormally large. It happens because of overgrowth of bone, fat, nerves and other soft tissues. It’s not typically inherited, and it often affects just one hand or foot. In some children, the affected area grows at a normal rate, while in others it grows faster than the rest of the body. In Emily’s case, the condition affected her right foot. Over time, it became significantly wider and larger than the other. Before treatment, she couldn’t wear the same size shoe on both feet and was limited in the types of shoes she could choose.

Emily invested in herself and chose a path that will allow her to move through life more comfortably. I’m glad I was able to partner with her and be a part of her journey.
Janay McKie, M.D., chief of staff of orthopedics, Shriners Children's Texas

“Macrodactyly is rare, and treatment isn’t just about appearance, it’s about function,” explained Janay McKie, M.D., chief of staff of orthopedics at Shriners Children’s Texas. “Our goal for Emily was to create a foot that worked better for her long term. That meant carefully reducing the enlarged bone and soft tissue and, ultimately, removing the most affected toe so she could walk more comfortably and confidently.”

The decision wasn’t rushed. Emily and her family worked closely with her care team, including psychology services, to ensure she felt supported and empowered throughout the process.

“Emily invested in herself and chose a path that will allow her to move through life more comfortably. I’m glad I was able to partner with her and be a part of her journey,” said Dr. McKie.

Emily is now in a cast for six weeks and will begin physical therapy soon. Recovery takes patience, but if you ask her, she’s already planning her comeback on the golf course.

For parents navigating similar orthopedic journeys, Emily’s story is a reminder that with the right care and support, kids can get back to doing what they love – whether that’s sinking a putt, strumming a favorite song on the guitar, or simply walking confidently into the future.

Emily Takes the Next Step

After her surgery, she had her cast removed so she could get back to doing what she loves.

a provider removes the cast of a smiling teenager

Janay McKie, M.D., removes the cast from Emily's foot.

an adult woman next to a child holding a teddy bear

Dr. McKie and Emily share a smile in the cast room.

a woman in pink hospital scrubs smiling next to a teenage girl

Emily receives comfort and support from psychologist Catherine Tallant, Psy.D.

a child playing an acoustic guitar in a hospital bed

Emily plays her guitar in her hospital bed after her surgery.

a teenager reading in a large library

Emily enjoys a quiet moment reading books.

Next Steps

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