The staff at the hospital where Natalia Rodriguez Sabala was born hadn’t seen a patient like her in seven years. She was born with cloacal exstrophy, also known as OEIS syndrome: Her bladder and portions of her large intestine were on the outside of her belly, and her bladder was split open into two halves. She didn’t have a vaginal opening, anus or belly button.
“It was intimidating,” says mom Stephany. “I remember thinking, How are we going to take care of her? How can we make her life better?”
Stephany and husband Miguel knew that for their daughter to have a healthy, full life, she needed the right experts by her side. So after surgery in Florida failed to keep Natalia’s bladder inside her body, they decided to do whatever it took. They picked up and moved from Florida to Connecticut, close to Connecticut Children’s — the only health system in the state 100% dedicated to children, with an entire program for Natalia’s condition.
From the first visit, says Stephany, “I knew it would be okay.”