One in a million

Meet Owen, he's my 'Tiny Light'.  I recently joined a group of amazing photographers doing wonderful things, The Tiny Light Foundation.  We donate our time to families that have children or babies with life altering diagnosis.  In 2010 little Owen was diagnosed with Kleefstra Syndrome, a deletion of the long arm of one of Owen's 9th chromosomes. I don't want to write about all these things that he cant or wont be able to do because he is such a Delightful, happy boy who has so much love around him.  He will be able to do everything that everyone can do...... just in his own unique way.  It was great to meet the family and would love an update from time to time to hear how Owen is doing :)