Team TYLER

Team TYLER Raising NF awareness & building a community of support — inspired by Tyler’s strength and resilience. No one fights alone.

When Tyler was just a few months old, we noticed unusual marks on his body. After a visit to the doctor, we were referred to a children’s hospital—where we first heard the word “Neurofibromatosis.” Tyler was officially diagnosed just before his first birthday, after an MRI revealed an optic glioma. Since then, Tyler has faced multiple rounds of chemotherapy, surgeries, and the discovery of a secon

d tumor on his brainstem. He’s been life-flighted, endured hospital stays, and knows more medical terms than any child should—but through it all, he continues to smile, inspire, and fight with unmatched courage. Today, Tyler is a healthy, spunky 14-year-old with a true passion for cars and trucks. This July, he’ll celebrate 10 years chemo-free—a milestone he’s incredibly proud of. He continues to light up every room with his smile, charm, and sense of humor. Though he still has annual checkups and scans, he is currently symptom-free. Team Tyler was created not only to share his journey but to raise awareness and support others affected by NF. Neurofibromatosis will not define Tyler—Tyler will define Tyler.

🚨 Something BIG is Coming... 🚨Get ready to sweat, laugh, compete, and have an amazing time—all while supporting an incre...
08/07/2026

🚨 Something BIG is Coming... 🚨

Get ready to sweat, laugh, compete, and have an amazing time—all while supporting an incredible cause! 💙💚

Whether you're tackling the challenge with a team of 2, a team of 4, or taking it on solo, this event is for YOU!

🏋️ Fun fitness challenges
🏆 Prizes
💪 All fitness levels welcome
💙 Supporting Team Tyler's mission

📅 September 27, 2026
Registration opens soon... and trust us, you won't want to miss this one!

May is Neurofibromatosis Awareness Month 💙Every day, I watch Tyler face something most people have never even heard of. ...
05/01/2026

May is Neurofibromatosis Awareness Month 💙

Every day, I watch Tyler face something most people have never even heard of. Neurofibromatosis isn’t just a diagnosis — it’s uncertainty, strength, courage, and a fight that never takes a day off.

As his mom, I will always be his voice when he needs one, his strength when days are hard, and his biggest advocate in the fight for awareness and a cure.

This month, I’m asking you to stand with us.
Learn about NF.
Share Tyler’s story.
Help us spread awareness.

Because my son — and every person living with NF — deserves more answers, more support, and a future without limits.

We fight for Tyler. Always. 💙

Address

Windber, PA

Website

Alerts

Be the first to know and let us send you an email when Team TYLER posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Organization

Send a message to Team TYLER:

Shortcuts

Share