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20 Years of Advancing Fetal Health

20 Years of Advancing Fetal Health

by Erika K Wolf | Mar 6, 2026 | Blogs, front-page, News, Story, Twin-to-Twin Transfusion Syndrome

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.

White Paper – Recommendations for Facility Design Guidelines – Fetal Care Center

White Paper – Recommendations for Facility Design Guidelines – Fetal Care Center

by Erika K Wolf | Mar 3, 2026 | Blogs, Fetal medicine, front-page, High-risk pregnancy, News, Resource News, Story

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...
Mozarc Medical  Partners with FHF in Shared Commitment to Pediatric Renal Care

Mozarc Medical Partners with FHF in Shared Commitment to Pediatric Renal Care

by Erika K Wolf | Mar 2, 2026 | Blogs, Condition, Fetal Renal Failure, front-page, Kidney, Bladder, and Genital Abnormalities, News, Story

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.

Farrah’s Story: When a Rare Mediastinal Teratoma Met Perfect Timing

Farrah’s Story: When a Rare Mediastinal Teratoma Met Perfect Timing

by Erika K Wolf | Feb 18, 2026 | Blogs, Condition, front-page, Mediastinal Teratoma, News, Story

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.

2025 Impact Report: Advancing Fetal Health Through Partnership and Community

2025 Impact Report: Advancing Fetal Health Through Partnership and Community

by Erika K Wolf | Feb 4, 2026 | Blogs, Condition, front-page, News, Story

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

Facing an Omphalocele Diagnosis: One Family’s Journey to CHOP’s Specialized Care

by Erika K Wolf | Jan 27, 2026 | Blogs, Condition, front-page, News, Omphalocele, Story

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.

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Treatment Centers

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What It Was Like For Our Family

Stories of Fetal Diagnosis and Treatment

Fetomaternal Alloimmunization: Alexandra’s Story

Fetoscopic MMC (Spina Bifida) Repair: One Family’s Journey

Spina Bifida Stories

TTTS Stories

Maternal Fetal Medicine and Fetal Syndromes: The Basics for Expectant Parents

Rose’s Prenatal Spina Bifida Story

Make a Donation

Expert Voices

Insight from Professionals

Gastroschisis and the search for better, earlier interventions with Dr. Geoanna Bautista

Q & A with a Trailblazer: Dr. Scott Adzick at CHOP

Dr. Chmait Performs Minimally-Invasive Fetoscopic Surgery for Spina Bifida

Our Medical Board of Directors

 

Who We Are

A Parent-Founded Nonprofit

What We Do: Our Annual Impact Report

Renny and Benny’s Story

Our Founders Story: The Somers Family

Learn about our Flagship Fundraiser, The Great Candy Run

Contact Our Staff

 

980-224-0398
9786 South Holland St.

Littleton, CO 80127

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