Luke Teat

At 3 days old we found out Luke had PKU, phenylketonuria. We knew he was special since birth as his apgars were dangerously low, he was put on a heart monitor and he had myoclonic jerks that we have never seen before.
Its now the beginning of 2017 and Luke has had over 100 fractures due to his ehlers danlos syndrome, he was dx with Chiari, osteoporosis and asthma. He has had a very long ten years with many rough roads but he is the happiest child I have ever known. we are so lucky God chose us to be his family.

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