In May 2025, our family’s world changed when Myles was diagnosed with neuroblastoma. What started as a terrifying unknown quickly became a new daily reality—filled with doctor visits, lab work, imaging scans, and conversations no parent is ever prepared to have. We learned how fast life can shift, and how much strength it takes to keep moving forward when your heart is trying to catch up.

As Myles began chemotherapy, our days revolved around treatment schedules, follow-up testing, and frequent appointments to monitor how his body was responding. Some days were steady, and others were incredibly hard—days where he didn’t feel well, had little energy, or just wanted the comfort of home and normal routines. Watching him go through side effects and long medical days was heartbreaking, but Myles continued to show a courage that amazes us.

From October through December, we faced one of the most challenging stretches of all, spending extended time away from home with long hospital stays. It was a season that tested our endurance as a family—missing home, missing normal moments, and learning to find comfort in small wins. And still, through every test, every long night, and every tough day, Myles remained mighty—brave, resilient, and full of heart.