When a baby was born in South Africa, he had to undergo major surgery just moments after his birth as his entire small intestine was developed outside his tiny body instead of inside due to a rare birth defect.
Juan-Luc Language was born on July 28 to parents Melize, 26, a teacher, and Juan, 31, a technician at 34 weeks’ gestation. The little boy was born via a cesarean section and weighed 4.1 pounds (approx. 2 kg).
The couple was informed that Juan-Luc suffered from gastroschisis in their third month of pregnancy, but they weren’t aware of what form it would really take until he was born.
For Juan-Luc, this meant that he needed to undergo surgery almost immediately after he entered the world. The parents, who hail from Jeffreys Bay, were forced to relocate to Cape Town so that pediatric surgeon Professor Brown, who specializes in neonatal surgery and pediatric gastroenterology, could perform the operation.
This so-called mesh sack is called the “silo.” Gradually, in a few weeks, the intestine returns to the baby’s abdominal cavity and the defect is closed. However, throughout the recovery, the baby is extremely vulnerable to infection and has a very hard time processing its mother’s milk.
Luckily, according to Caters News, Juan-Luc’s aunt, Michelle, who resides in Wimbledon, southwest London, said the operation was successful. She said: “Thankfully according to the doctors, the operation was a big success but recovery is very slow and the costs are astronomical.”
“Juan and Melize knew there would be additional medical costs and tried to make provision for this,” she explained, “but after receiving the first bill it’s clear that the scope of the charges is much more than they could have ever imagined.”
Alluding to the effort, Michelle said: “The next couple of weeks and months are critical for his recovery and I just want to do anything I can to help.” So far, the campaign has raised 1,185 pounds (US$1,582) of the total goal of 5,000 pounds (US$6,675).
As of September, Juan-Luc has been at the hospital for 38 days. He might have to stay for up to three months depending on how quickly his digestive system can start functioning on its own.
His family is relieved and delighted to see how well he is progressing. The silver lining for the Language family is that most babies with gastroschisis go on to make a full recovery. Given how far Juan-Luc has already come, there’s every reason to hope for the best.
