980-224-0398 [email protected]
Fetal Health Foundation
  • HOME
  • FETAL SYNDROMES
  • STORIES
  • ABOUT US
    • ABOUT US
    • SOMERS FAMILY STORY
    • OUR MISSION
    • OUR TEAM
    • FINANCIAL DOCUMENTS
    • MEDICAL BOARD OF DIRECTORS
  • MAKE A GIFT
Select Page
CRIB Program at Stanford: Maya’s Care as a Micro-Preemie

CRIB Program at Stanford: Maya’s Care as a Micro-Preemie

by Erika K Wolf | May 20, 2026 | Blogs, Condition, front-page, News, NICU, Story

Maya, a micro-preemie born at 25 weeks, receives highly coordinated, multidisciplinary care through the CRIB Program at Stanford Medicine Children’s Health during a complex, year-long NICU stay.

Evelyn’s Story: A Congenital Heart Defect Diagnosis Before Birth

Evelyn’s Story: A Congenital Heart Defect Diagnosis Before Birth

by Erika K Wolf | May 19, 2026 | Aortic Senosis, Blogs, Condition, Congenital Heart Disease/Defects, Fetal Cardiac Abnormalities, front-page, News, Story

Hannah and Trey were eagerly awaiting the arrival of their first baby when a routine 20-week anatomy scan changed everything. After doctors noticed abnormal heart views, the couple was referred to the Elizabeth J. Ferrell Fetal Health Center at Children’s Mercy Kansas...
Xavier and Bryson’s Story: Hope After a TTTS Diagnosis

Xavier and Bryson’s Story: Hope After a TTTS Diagnosis

by Erika K Wolf | Apr 21, 2026 | Blogs, Condition, front-page, News, Story, Twin-to-Twin Transfusion Syndrome

A twin-twin transfusion syndrome (TTTS) diagnosis marked an unexpected turn in Essence and Eric’s pregnancy journey. At the Connecticut Children’s Fetal Care Center, expert care, precise timing, and resilience shaped the path forward as their story continued to unfold.

Delgado Quadruplets Born at UC Davis Children’s Hospital

Delgado Quadruplets Born at UC Davis Children’s Hospital

by Erika K Wolf | Apr 3, 2026 | Blogs, Condition, front-page, High-risk pregnancy, News, NICU, Story

The Delgado quadruplets were naturally conceived after Kayleen and Zeke Delgado were told they would likely have difficulty conceiving. After two daughters and a miscarriage, the couple’s path to growing their family was uncertain—but not closed. In April 2024,...
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.

« Older Entries

Treatment Centers

Enter an address or zip code and click the find locations button.

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

Privacy Policy