The rate of gastroschisis, an abdominal wall defect that is often discovered in utero, has been on the rise in the US. Thanks to Dr. Geoanna Baustista and the Baby Intestines Group at UC Davis Health, research is being done to find potential fetal interventions and improve babies’ outcomes.
The Dahab family moved to Ohio to be close to their “second family” at Nationwide Children’s Hospital. Thanks to Nationwide’s excellence in maternal fetal medicine and fetal imaging, a world-class NICU, access to genome sequencing, and rare disease experts, their boys are living longer and better lives.
When doctors told the Lame family their son wouldn’t survive his serious diagnosis, they didn’t give up hope. They started to search for answers. Luckily, they found them at Cincinnati Children’s Hospital. With expert, all-encompassing care, baby Luka is thriving.
Treating Fetal Renal Failure is a highly personal process with many decisions to be made over the lifetime of the child. Dr. Timothy Crombleholme at Connecticut Children’s details why it’s important to have support, second opinions, and a highly specialized team.
Fetal care pioneer Dr. Timothy Crombleholme at Connecticut Children’s Fetal Care Center explains what families need to understand about their deeply personal options for treating Fetal Renal Failure.
Children’s Hospital of Philadelphia is specially equipped with technology and expertise to deliver babies with birth defects. In fact they lead the nation in these deliveries. See what a “delivery room of the future” looks like.