At thirty weeks pregnant Matt Mooney and his wife Ginny were informed that their child had a genetic disease Trisomy 18. They were told that birth was unlikely. That life was not viable. That a bleak future awaited. They were not told that they would get 99 days with this child and these precious days would change them forever. Through the sleepless nights, an unrelenting desire for answers, and the frightening reality that slides in where optimism once resided, Matt and Ginny walked with family and friends through the life and death of their first born son.
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