Posted on April 27, 2016 by Whitney
Lots going on in the medical part of our journey with Julianne. Sometimes I feel like we’re on the road trip of a lifetime, you know, the kind that takes a lifetime. 😉 Because let’s be real. Road trips aren’t always sunshine… Read More
Category: Epidermolysis Bullosa, Julianne, Uncategorized
Tags: adoption, EB, EB Awareness, Epidermolysis Bullosa, family, kids, medical special needs, speech therapy
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