Skylar’s Story: Strength, Courage & a New Beginning 

Some journeys begin before a child can even walk. For Skylar, hers started at just 5 months old, when she broke her left leg. It would be the first of many chapters in a story defined not by hardship, but by an extraordinary spirit that refused to be held back. 

A week after that initial break, doctors diagnosed Skylar with Congenital Pseudarthrosis of the left tibia and fibula, a rare condition in which the bone takes on a “joint-like” appearance, causing it to bow, become fragile, fracture easily, and struggle to heal on its own. By 15 months old, she received a second diagnosis: Neurofibromatosis Type 1, or NF1. 

Skylar, full of smiles, even with her purple cast and her matching doll in a wheelchair by her side. 

Understanding Pseudarthrosis in NF1 

Bone abnormalities can occur in people with NF1, but pseudarthrosis is considered rare, affecting only about 5% of NF1 patients. When it does occur, it presents an enormous challenge: the affected bone lacks the ability to heal properly, making fractures a recurring reality and surgical intervention a constant companion. 

For Skylar and her family, this meant years of navigating that reality head-on. Over the course of 12 years, she underwent approximately 12 surgeries on her leg and ankle, each one a renewed attempt to give her leg a chance to heal. 

X-rays from Skylar’s surgical journey (December 2020 and April 2021), showing the hardware used in her leg and ankle to support healing. 

A Brave Decision at Age 11 

After years of painful surgeries and continued setbacks, Skylar, at just 11 years old, made one of the bravest decisions a child could face. She chose to have a below-the-knee amputation. 

It wasn’t a decision born of defeat. It was a decision born of wisdom, self-knowledge, and a fierce desire to live fully. The ongoing pain had become too much, and surgery after surgery had not brought the relief she deserved. Skylar and her family chose a different path forward. 

Today: Pain-Free and Unstoppable 

Today, Skylar is 12½ years old, and she is thriving. It has been a year since her amputation, and she is completely pain-free. With her prosthetic leg, she is living the life she always deserved — a normal, joyful, busy one. 

She is in 6th grade. She loves dance and theatre. If you look closely, you’ll notice her prosthetic is actually Taylor Swift inspired, using a patterned fabric. Her favorite singer and one that brought a lot of comfort to her during procedures. 

Skylar today. Striking a power pose in her dance costume, her custom Taylor Swift inspired prosthetic on full display. She is radiant. 

Why Skylar’s Story Matters 

NF1 affects approximately 1 in 2,500 people worldwide, and while pseudarthrosis is one of its rarer complications, its impact on those who live with it is profound. Stories like Skylar’s give voice to what families navigate, the diagnoses, the surgeries, the heartbreak, and ultimately, the resilience.

While Skylar will live with NF1 for the rest of her life, she moves forward with confidence. She is proof that the path forward isn’t always the one you expected, and it can be more beautiful for it. 

💜 Share Skylar’s story this NF Awareness Month. 💜 

Recent Posts

  • Meet the 2026 NF Midwest Scholarship Recipients 

    The NF Midwest Scholarship Program is proud to celebrate another year of supporting students with neurofibromatosis as they work toward their educational dreams.  Each year, NF Midwest awards scholarships to students across our six-state region. These students are pursuing their goals while also navigating life with NF, and we are honored to play a small... Read More
  • Why Clinical Trials Matter, and Why They Matter Especially for NF

    Every treatment that exists today: every medication, every therapy, every breakthrough, started somewhere. It started with a question, a hypothesis, and eventually, a clinical trial. May 20 is National Clinical Trials Day, a moment to recognize the remarkable system that turns scientific ideas into real-world answers. For the NF community (patients, families, caregivers, and advocates)... Read More

Responses

Respond

Your email address will not be published. Required fields are marked *