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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.

Cord Blood Awareness: Stem Cells at Birth—A Powerful Choice for the Future!

Cord Blood Awareness: Stem Cells at Birth—A Powerful Choice for the Future!

by Erika K Wolf | Jul 3, 2025 | Blogs, Condition, Cord Blood Awareness, front-page, News, Story

Cord Blood Awareness Month is a time to spotlight the powerful, life-saving potential of stem cells found in cord blood—and why expectant parents should understand their options.

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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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