Emmy's 3 month check-up...
But Emmy’s pain didn’t stop there. We started to notice that something seemed “different” when we would look into her beautiful dark blue eyes. She wouldn’t look back at us, and her eyes would wander or bounce, but we kept hoping for the best for our beautiful little blessing.
At Emmy's 3 month pediatric check-up that her doctor made a comment about her eyes and recommended she see a pediatric ophthalmologist.
It was at that appointment that we heard the most devastating words we have ever heard, “Your baby has Optic Nerve Hypoplasia (ONH), we can’t be sure what she sees or if she can see anything at all, and there is no treatment”.
The doctor’s file went on to state:
10 week old showing no visual attention; severe, bilateral optic nerve hypoplasia--very likely to have lifelong, severe visual handicap
How do you respond as parents when you get news like that? We were numb. We did the only thing we knew to do…. we cried together, and then we prayed together.
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The day finally came! Like children waiting for Christmas morning, we had waited anxiously wanting to see our beautiful baby’s face, fingers, toes and EYES! We knew we were having a girl, so we prayerfully chose the name Emmalyn Kae. .jpg)
Hi, we are Kristen and Elmer Latchford and we have an amazing story we would like to share with you about a precious little beautiful life and the impact she has already made in her short little life so far on this earth.