A tiny superhero pays it forward (10 Photos)
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I remember the day I met Zoe Lush. Brian Mercedes and I had driven to a park in southern California for “Wishbone Day.” Zoe’s parents were there to educate anybody who walked by about osteogenesis imperfecta, a.k.a. brittle bone syndrome, and they were determined to get the word out about her rare disorder, one person at a time.