Michaela and Nic were excited to welcome their first baby, Xander. The pregnancy was going smoothly until a growth scan at 32 weeks. Only a week before Christmas, Michaela was told her baby was in heart failure and she needed to get to a hospital that provided expert fetal and neonatal he needed.
Baby Ellie spent 21 days recovering in the neonatal intensive care unit (NICU) at Children's Minnesota after she was born with a rare condition that required immediate surgery. She's now home and all smiles.
Grant and Brittany have been married for more than eight years. But at their 20-week ultrasound, their lives changed forever. Grant and Brittany were told that further testing may confirm a more severe and potentially fatal form of dwarfism.
We take great pride in every newborn who graduates from the NICU, but that’s truly just the beginning of their journey. Unfortunately, many premature babies face a range of challenges, including staying on track with growth milestones, delays in speech and fine motor development, and learning differences and disabilities, just to name a few. That’s where Children’s Minnesota’s NICU Follow-up Clinic comes in.
Mycaela Scalzo and Donovan Martin, parents of one with another on the way, were going to their 20-week ultrasound appointment with the typical feelings of anxiousness and excitement parents have. During this appointment, the baby’s size, organs and overall health are checked. But Mycaela and Donovan’s excitement soon turned to fear. During the check-up, an unknown mass was found on their baby’s face. The provider suspected it was oral teratoma – a noncancerous but still potentially dangerous tumor that could block the baby’s airway, create feeding issues and more.
Mycaela Scalzo and Donovan Martin, parents of one with another on the way, were going to their 20-week ultrasound appointment with the typical feelings of anxiousness and excitement parents have. During this appointment, the baby’s size, organs and overall health are checked. But Mycaela and Donovan’s excitement soon turned to fear. During the check-up, an unknown mass was found on their baby’s face. The provider suspected it was oral teratoma – a noncancerous but still potentially dangerous tumor that could block the baby’s airway, create feeding issues and more.
Mindy Torres has dedicated three years to working at Children’s Minnesota. When Mindy was just 22.6 weeks pregnant, her water broke due to a pregnancy complication and her baby Javier was then born at just 24.3 weeks, which meant that he was nearly four months premature! Javier was immediately brought to the NICU where he spent 133 days slowly getting stronger and stronger every day.
When Darby, and her husband Brad, went in for a routine check-up at their family care provider in Fort Dodge, Iowa, the doctors diagnosed baby Muller with spina bifida, a birth defect that occurs when a section of the baby’s spinal column does not form properly and a gap appears.
Recently, Elliot, diagnosed with spina bifida before he was born, set one very important goal for himself: he wanted to ride the bus to school. But there was one thing in his way. He needed to learn to climb the bus stairs by himself.
When Darby and Brad went in for a routine check-up at their family care provider in Fort Dodge, Iowa, the doctors diagnosed baby Muller with spina bifida.