Cole was diagnosed with Neurofibromatosis Type 1 (NF1) at just 9 months old. From the very beginning, he faced challenges with strength, resilience, and a spirit that inspired everyone around him.

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Cole passed away in May 2024 at 20 months old, but the impact he made in that short time will last forever.

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We used to tell Cole that he was going to do “big, big things” in this world. He showed us every day what that meant through the joy he brought, the connections he created, and the love he shared with everyone around him. Cole taught us what truly matters, and his strength continues to guide everything we do.

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The Cole Constant Foundation is our way of continuing that. Through this work, Cole’s light lives on, helping other children, supporting families, and continuing those “big, big things” in his name every single day.