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.
That video is AWESOME! I like the laugh and play part too.
ReplyDeleteaw!! sooooo sweet!! -jodi (milo's mom, lca)
ReplyDeleteHe DEFINETELY made me smile! Love it
ReplyDelete