Jaxen's Journey 7th Annual Golf Tournament

Jaxen's Journey started in June 2016 by Andy and Kim Kettler when their son, 2-year-old Jaxen, was diagnosed with pediatric pineoblastoma. He fought very hard for 5 weeks before passing away. Since then, the Kettler family has dedicated their lives to helping others going through this horrific process. Childhood cancer research receives a tiny portion of federal funding. Children, who have their whole lives ahead of them, deserve more. Because of this, the Kettler family honors Jaxen's life through Jaxen's Journey, an approved 501c3 Foundation they started that raises funds strictly for pineoblastoma research.

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Pediatric Brain Tumor Foundation
Questions? Please contact Emily Clark

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