Caleb

Caleb was enjoying simple family life, time outdoors, little getaways, and fun with neighborhood friends not knowing the difficulty that was ahead. Caleb is undergoing experimental treatment to fight his disease. He loves superheroes. He plays in his “hospy-tal” room. His feeding tube is a normal part of his life, and he no longer says “no pokey” when the nurses come into his room. His smile still lights up the room, and he still smiles often. He has lost a little hearing (high frequency), but other than that, he has emerged relatively unscathed. And Caleb’s family still maintains the most important thing of all: hope.

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