by Childrens Hospital Boston staff on September 11, 2009

This story was written by Sarah Doyle, mother of Aidan.
I’m sure that I’m one of many parents who credit Children’s Hospital Boston with having saved their child’s life. But I don’t think many parents have had an experience quite like ours. Aidan was born in April of 2007, with a giant omphalocele, a defect in which the abdominal organs develop within the umbilical cord, outside of the abdomen. This only occurs in an estimated 1 in 2,500 pregnancies. The defect was detected during a routine ultrasound at 20 weeks gestation. It’s pretty hard news to take when you are told your unborn child has a life threatening defect, and that the defect may be associated to chromosomal abnormalities or that other anomalies may be present. We thought ourselves lucky; the omphalocele appeared to be isolated, and his chances of survival seemed pretty good. Full story »
by Childrens Hospital Boston staff on August 19, 2009
By Tricia Garcia-Dergay
Riley arrived on July 6, 2007, via c-section at a hefty 9 pounds and 10 ounces. She was gorgeous, plump and hairy. The doctors mentioned she had a heart murmur, but probably nothing we needed to worry about.
Fast-forward two weeks. Riley is home but has been fussy for a few days and not eating. She’s grunting and her color is off. Her dad and mom (who is herself dealing with a bout of Bell’s Palsy) take her to her pediatrician. He takes one look and goes into full “I’m more heroic and ‘take charge’ than Dr. Green from ER!” mode and rides with Riley (now in respiratory distress) in an ambulance to New England Medical Center (NEMC).
Riley spent the new two weeks at NEMC. While there, she underwent a cardiac catheterization to better diagnose the underlying problem. We knew she had pulmonary hypertension and mitral valve regurgitation. But we were still uncertain about the underlying cause. Full story »