Stories about: necrotizing enterocolitis

Persevering after the unimaginable: Jacob’s journey with short bowel syndrome

little boy after treatment for short bowel syndrome

Yankees or Red Sox? Giants or Patriots? Rangers or Bruins? Seven-year-old Jacob Hersko and his physician, Dr. Christopher Duggan, may playfully debate whose hometown is better, but in one area, it’s clear that Boston comes out on top: “Jacob loves coming to Boston Children’s Hospital,” says his mother, Rachel. “He says it’s like going to Disney World.”

When she was pregnant with Jacob, Rachel and her husband, Geoff, never anticipated that they would be traveling to Boston every few months. The little boy was born at full-term, with no apparent complications. But when he was just a week old, the unimaginable happened: He was diagnosed with necrotizing enterocolitis (NEC), a serious intestinal illness in babies that results in the death of intestinal tissues.

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Isaac’s story: A ‘new normal’ with short bowel syndrome

Isaac stays active with short bowel syndrome

It was the morning after their baby son Isaac had come home from the hospital, and Jennifer and Brian Campbell were performing the same sweet act of bonding as many new parents: giving him a bath in the sink. But as they maneuvered around the room, they suddenly realized something was very wrong. “I fell to the floor and started screaming and crying as formula shot out of his stomach,” remembers Jennifer. “I thought we’d broken him.”

The reality, of course, was that the Campbells were simply adjusting to their new “normal” — something any parent of a medically complex child can understand. Isaac wasn’t a newborn. He had finally been discharged from the hospital after nine months. And his parents hadn’t hurt him. They’d just accidentally pulled out his gastrostomy (G-tube), which provided his body with nutritional support.

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