Gabriel and Dianely's journey together began in 2003, and since then, they have built a life full of love, resilience, and growth. They married in 2012, and soon after, their family began to take shape with the arrival of their son, Max, in 2014. For a while, life felt complete. But on January 5, 2015, everything changed when they learned that Max was suffering from infantile spasms. Four months later, doctors diagnosed him with a rare genetic mutation known as SCN8A.

Being first-time parents was challenging enough, but becoming parents to a medically vulnerable child with special needs brought an entirely new set of responsibilities. Through it all, Gabriel and Dianely have grown stronger, united in their love for Max and their determination to provide him with the best life possible.

The arrival of Zac in 2016 brought new light and joy into their home. Zac, ever the compassionate little brother, quickly became Max’s greatest ally. At just one year old, Zac instinctively found ways to comfort Max during difficult moments, like the first time he acknowledged one of Max’s severe seizures. In that moment, Zac waddled over, gently patted his brother’s leg, and soothingly repeated “ya… ya… ya…”—a tender, familiar expression meant to calm. By age 4, Zac was advocating for others with disabilities, telling his classmates about the importance of being a hero to those who need help. At 6, he dreamed of inventing a time machine that would transport him into the future, where he could find a cure for Max and his friends. Every day, Zac seeks ways to connect with and support his brother.

The Cabrera family’s journey has been one of perseverance and love. Whether navigating family trips to Disney World, visiting loved ones, or simply spending time at the park, they face countless challenges. But through it all, they choose to create lasting memories, embracing each moment of their unique and beautiful adventure together.