The Fetal Health Foundation marks its 20th anniversary, celebrating two decades of progress in fetal care, family support, and global awareness for fetal health conditions.
20 Years of Advancing Fetal Health
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News
White Paper – Recommendations for Facility Design Guidelines – Fetal Care Center
Fetal Health Foundation's Fetal Therapy Think Tank has authored a new white paper establishing environmental and spatial guidelines for the design of fetal care centers. “Recommendations for Facility Design Guidelines – Fetal Care Center” is available through FGI, the...
Mozarc Medical Partners with FHF in Shared Commitment to Pediatric Renal Care
Mozarc Medical, a leader in pediatric dialysis innovation, has partnered with Fetal Health Foundation. FHF supports Mozarc’s advanced renal technologies and is proud to help expand awareness of their impact in fetal and pediatric care.
What Mental Health Really Means for NICU Families | Inside the NICU Part 3 | More than Nine Podcast and Transcript
At the NICU, these providers are medically supporting the babies, but they are also seeing the emotional strain on families. They don’t have the capacity or skillset to really support them in the way that they always need- that’s where this program comes in.
Farrah’s Story: When a Rare Mediastinal Teratoma Met Perfect Timing
Farrah’s mediastinal teratoma fetal care story is about timing—how the right care, in the right place, at the right moment changed everything for her and her family at Children’s Mercy.
6 Ways the Fetal Health Foundation Supports Families and the Fetal Health Community
Families facing a fetal health diagnosis often find themselves navigating unfamiliar medical terms, urgent decisions, and intense emotional stress, all at once. The Fetal Health Foundation strives to make that journey more informed, connected, and supported. Guided by...
2025 Impact Report: Advancing Fetal Health Through Partnership and Community
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.
Facing an Omphalocele Diagnosis: One Family’s Journey to CHOP’s Specialized Care
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.
Caring for Complex Fetal and Pregnancy Conditions: Expert Insights from Stanford Children’s Health
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.
Shining a Light on Birth Defects Awareness
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.
Q&A with Dr. Jena Miller: Charting New Frontiers in Fetal Medicine at CHOP
In January 2026, Dr. Jena Miller joined CHOP as Co-Director of the Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment. With over a decade at Johns Hopkins, she brings expertise in minimally invasive fetal procedures, spina bifida, and TTTS. Read her Q&A on advancing fetal medicine and supporting families.
Rose’s Story: Prenatal Spina Bifida Diagnosis
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.