The 2025 Impact Report tells the story of what’s possible when families, providers, and supporters move forward together—advancing fetal care through connection, collaboration, and shared purpose.
When Addie and Ryan received a prenatal diagnosis of omphalocele, they were referred to CHOP for specialized fetal and neonatal care. From a highly coordinated birth to weeks in the NICU, their journey reflects the complexity of this rare birth defect.
Stanford Children’s Health offers expert, coordinated care for complex fetal and pregnancy conditions. Discover how multidisciplinary teams support families from diagnosis through delivery and beyond.
January is Birth Defects Awareness and Prevention Month—a time to raise awareness, support families navigating unexpected fetal health challenges, and highlight the importance of early care, prevention, and compassionate resources. Learn how knowledge and community can make a difference for families.
When Taylor and James learned their baby, Rose, had spina bifida, their world shifted overnight. From high-risk pregnancy care to in-utero surgery at Children’s Mercy, their story of hope, resilience, and the power of compassionate medical support unfolded.
Diagnosed with TRAP sequence, Inés’ survival came after her twin’s loss, meticulous fetal monitoring, and the expert care at CHOP. Explore the pivotal moments and life-saving decisions that shaped her remarkable beginning.