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, February 17, 2009
Flyer
Update for all friends and family who have asked if I have a flyer. I am in the middle of creating one (finally). If you would like a flyer to print and distribute, please email me.
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