Welcome.

This is the story of our daughter Emma. Her story begins with a rare birth defect called Gastroschisis. This space is dedicated to the days before her birth and the many that are sure to follow.

Surgery #1

Dr. Rice informed us that Emma's condition is more severe than they had anticipated. She's in surgery and will be for the next 2 hours. I sat with Emma in the NICU while singing her lullabyes and stroking her hair. Mom was still too weak to visit. After an hour or so we went across the hospital to the OR. The doctors tried to assure me that she's in capable hands, but there aren't any words for this. Now we wait and pray.

1 comments:

kandi said...

i am praying for emma. please keep updating if you have time.

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