On October 7th, 2025, Erin and I experienced a parent's worst nightmare. Our sweet 2-year-old, Juliana Elizabeth was diagnosed with a terminal, neurodegenerative, genetic condition called Infantile Neuroaxonal Dystrophy (INAD). Over the next months/years, Juliana's disease will slowly steal each of her physical, cognitive, and emotional capabilities - and ultimately her life. Through the grief and suffering, Erin and I are beginning to discern the logistics of navigating this next chapter. As we do so, one thing is certain - we know we can't do this alone. Through the encouragement of friends and family, we have decided to start this GoFundMe as an avenue to raise funds to cover large medical expenses, adaptive equipment needs, experiences for Juliana, and the many other unforeseen costs likely to come. If you’d like to contribute by means of Venmo, our profile name is: @Jacob-erin_falbo

For frequent updates and more on Juliana's journey, please visit our Caring Bridge.

In your mercy, please continue to pray for us and for our dear Juliana.

Jesus, we trust in you.

With sincere gratitude,

Jacob Falbo