In the days after their son was born, the news kept getting worse.
Baby Cole suffered HIE at birth after getting stuck in the birth canal and aspirating meconium. He was having seizures, he needed emergency cooling treatment hours away from home and tests of his brain activity weren’t looking good.
Sara Ames Saltzman felt alone and terrified. She didn’t know how to tell her friends and family the devastating news she was receiving in the hospital from her baby’s many doctors.
Throughout our lives, we form communities.
Our hometown, our cliques of friends in school, our co-workers, our couples friends and then the families we want our kids to grow up with.
I have been a part of some amazing communities in my life. And when my daughter suffered a birth injury, hypoxic ischemic encephalopathy or HIE, I needed another one in my life.
By Andy Chrestman
I remember standing in our son’s bedroom the day after he was born and bracing myself for the real possibility that we would lose our first and only child.
Kohler Henson Chrestman was born the previous day and, because of an abrupt lack of blood and oxygen to his brain, he was born with severe, global brain damage.
For one HIE mom, hope has taken her across the country this year.
Betsy Pilon, president of the Hope for HIE foundation, has traveled from her home state of Michigan to Texas, New York and New Orleans so far this year, making her slogan for 2016 “Have hope, will travel.”