Parker and Presley Collins. 3 years old. NICU graduates.
Mile Sponsor: Dr. Brian Barkemeyer and Michelle Barkemeyer
At only 24 weeks and 6 days gestation, Presley was born 1 pound, 7 ounces, and one minute later, her sister Parker entered the world at 1 pound, 5 ounces. Both Parker and Presley had reduced lung capacity, but it was clear from the beginning that Parker would need additional care to survive. Parker’s condition was declining. She went on a ventilator and developed Necrotizing Enterocolitis (NEC). It is the most common and serious intestinal disease among premature babies and happens when tissue in the small or large intestine is injured or inflamed. Doctors started putting her on antibiotics, but she wasn’t getting any better. On August 25, Parker was transferred to Manning Family Children’s for more specialized care.
Doctors believed a heart defect was likely a reason for her declining condition. Parker had Patent Ductus Arteriosus (PDA), a blood vessel which every infant is born with and necessary for normal development. After birth, the PDA should naturally close. When it does not, it is a form of congenital heart defect that can cause serious problems in premature infants. On September 1, doctors successfully performed surgery to close the PDA.
Sister, Presley continued to grow and did not experience the same health issues as Parker. Both babies made it home after a few months of specialized care and growth. It was a long road, parents Katie and Ryan say they are grateful to have had the doctors and nursing staff at Children’s helping them along the way.
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“One day, the mountain that is in front of you will be so far behind, it will barely be visible in the distance. But the person you become in learning to get over it… that will stay with you forever. And that is the point of the mountain.” – Brianna Wiest