Fetoscopic MMC (Spina Bifida) Repair: One Family’s Journey
When Katarina’s unborn baby was diagnosed with myelomeningocele (MMC), “It was kind of a shock, but my doctor said the best bet was fetal surgery. He referred me to Colorado right away, and he said we needed to do it as soon as possible,” she says. “That just kind of threw me for a whirlwind, and I have other kids to take care of too. It was a lot to process.”
Cecelia: Expert Care for Fetal Heart Block Before and After Birth
When Brittany and Nicholas’ unborn baby, Cecelia, was diagnosed with fetal heart block at 24 weeks gestation, their lives changed immediately — in the most literal sense of the word. They lived in Montana and when their doctor first suspected the heart issue, he told...
Charlotte: Surviving a Fetal Omphalocele and Finding Silver Linings
When Charlotte first received an omphalocele diagnosis, her parents didn’t know it’s severity. After one of the longest months of their lives, they got some good news. Maternal fetal medicine specialists at the Colorado Fetal Care Center diagnosed Charlotte with an isolated omphalocele, meaning a small part of her intestine was growing outside her abdomen but it wasn’t affecting other organs.
Fetal Surgery for Spina Bifida: Jaxyn’s Story
Fetal surgery for spina bifida is improving outcomes. The fetal surgeons at Cincinnati Children’s Fetal Care Center, who have extensive experience and innovative intervention therapies to help treat spina bifida in utero, recently shared this story of hope with...
Fetomaternal Alloimmunization: Alexandra’s Story
I was diagnosed with fetomaternal alloimmunization, a condition in which a mother’s body creates antibodies against a fetus’ blood antigens. This diagnosis crushed us. My husband and I wanted a lot of children, and now we were left wondering whether we could even have a second.