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Brianna Worden has faced unimaginable challenges since being diagnosed with NF as an infant; these obstacles have not stopped her from becoming a cheerleader, a photographer and Miss Teen New York International.

NF Forward

Brianna

Jada Smoot is a lively, sweet 11-year-old just starting middle school who likes to swim, bike and spend time with her friends; her mother, Teaqua, is starting a new job with United Airlines and enjoys reading.

Teaqua & Jada

Identical twins, Adam and Neil Pearson, are navigating life in South London with a rare genetic disorder, neurofibromatosis; despite their identical DNA, the twins are affected in vastly different ways.

The Pearson Twins

From his diagnosis of neurofibromatosis in a country with few medical resources to treat his disfiguring tumor, to his miraculous new life in America, Victor's story touches to the core.

Victor

Kylie suffers from a rare genetic disease called neurofibromatosis, which from birth affected her left eye; she has never been able to see from it, as she got older the plexiform tumors caused her eye to be removed.

Being Kylie Earl

Renie and Philip Moss are on top of the world; they have fulfilling careers, a loving circle of family and friends, a strong faith, and two beautiful children, Philip Jr. and Helen.

The Moss Family

Maddox Gibson is a fun-loving 5th grader with a big smile who loves Legos and wants to be a chef; in 2017, Maddox was a 10 year-old in China who had been living in an orphanage his entire life.

Maddox

Travis has lived in the fear of breaking his bones most of his life; from the age of two, a tumor caused by a rare disease called neurofibromatosis, has been growing from his spine down his leg.

Off the Breaks

Aidan Fraser has undergone 20 major surgeries and been on five different chemotherapies in 17 years due to NF; despite the magnitude of this challenges, Aidan is a video blogger, YouTube channel host and CTF staff member.

Aiden

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