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🍭 Why The Great Candy Run Is So Much More Than a Race

🍭 Why The Great Candy Run Is So Much More Than a Race

by Erika K Wolf | Sep 17, 2025 | Blogs, Condition, front-page, News, Story

The Great Candy Run is a sweet, family-friendly 5K that brings people together for fun, lasting memories—and most importantly, to support families facing fetal syndrome diagnoses.

Breakthrough in Hydrocephalus Care: Gene Therapy on the Horizon

Breakthrough in Hydrocephalus Care: Gene Therapy on the Horizon

by Erika K Wolf | Sep 8, 2025 | Blogs, Condition, front-page, Hydrocephalus/ Ventriculomegaly, News, Story

A groundbreaking gene therapy developed at UC Davis could change how hydrocephalus is treated in children—offering hope for safer, long-term care.

💙 Honoring NICU Families & Their First, Fiercest Journey

💙 Honoring NICU Families & Their First, Fiercest Journey

by Erika K Wolf | Sep 4, 2025 | Blogs, Condition, front-page, News, NICU, Story

Each year, 1 in 10 babies begins life in the NICU. This September, we recognize the strength of NICU families and the care teams who help them thrive.

Facing TTTS: Bridgette and Grace’s Story of Strength and Survival

Facing TTTS: Bridgette and Grace’s Story of Strength and Survival

by Erika K Wolf | Jul 21, 2025 | Blogs, Condition, front-page, News, Story, Twin-to-Twin Transfusion Syndrome

At 12 weeks, Jackie and Trevor received a frightening diagnosis: their unborn twins had twin-twin transfusion syndrome. With CHOP’s fetal care team, a complex surgery offered new hope—and today, their daughters are thriving.

Children’s Mercy Joins the FHF Partner Network

Children’s Mercy Joins the FHF Partner Network

by Erika K Wolf | Jul 8, 2025 | Blogs, Condition, front-page, News, Story

We’re proud to welcome Children’s Mercy Kansas City to the Fetal Health Foundation Partner Network. Their expert fetal care team is helping improve outcomes for babies diagnosed before birth.

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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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