Our sweet Knox is a brave little boy. His journey began at four months old with his first seizure. What started as an occasional occurrence is now a regular reality, with seizures often occurring once or twice a week. Through every emergency and hospital stay, Isac and Maddie have put their trust in the Lord. Even on the hardest days, Knox never stops sharing his sweet smile. We acknowledge this journey is part of his life, but it does not define him. Epilepsy is something he and his amazing parents navigate, but they haven't allowed it to steal their joy or their faith in the One who made Knox perfectly.

Recently, his journey was given a name: Dravet Syndrome. This rare genetic condition makes his path steeper, but it also gives us a roadmap to help him thrive. We aren't just fighting a diagnosis, we're working to give him the most vibrant life possible and help build a flourishing future for Knox and his family.

The Current Hurdle: Knox has started Speech and Occupational Therapy, but insurance will not cover these critical sessions. A specific medication his neurologist believes will best control his seizures has also been denied at this time. Between EMT calls, ambulance transfers, rescue meds, and hospital stays, the costs continue to rise. Through it all, Isac and Maddie have remained calm, convinced God is working, and inspiring us as they care for Knox.

HOW YOU CAN HELP: We believe God will supply all of their needs. This fundraiser is one way for our community to be the hands and feet of Jesus to ease this burden. DONATE: EVERY DOLLAR goes into a Special Needs Trust account specifically for Knox's therapies, medical needs, and specialized care. PRAY: We ask you to pray for healing, peace, and for God to use Knox’s beautiful life in amazing ways. SHARE: Please share this link with your friends, family, and church groups. We know God hears and answers! THANK YOU for walking this journey with us. “I praise You, for [KNOX] is fearfully and wonderfully made; marvelous are Your works.” — Psalm 139:14