Two year old Gavin, was born with Leber’s Congenital Amaurosis (LCA). There is no cure, but we are helping to try to change that. This blog was started within 48 hours of receiving his diagnosis, at 4 months of age. It documents the triumphs, struggles and joys of raising a child, who happens to be blind.
Tuesday, May 25, 2010
CRUNCH TIME -- 13 days and counting!
Vision Walk '10
9am @ Cal State Fullerton on June 6
Gavin's Groupies in Full Force!
Will you be there?
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