Contact Us
Donate
  • Fetal Syndromes
  • Fetal Treatment Centers
  • Pregnancy Journey
  • Supporting Families
  • Medical Experts
  • About Us
Turning a Frightening Pregnancy Diagnosis into a Lifeline for Families: Our Founders’ Story

Turning a Frightening Pregnancy Diagnosis into a Lifeline for Families: Our Founders’ Story

by Fetal Health Foundation | Nov 5, 2025 | Blogs, front-page, Story, Twin-to-Twin Transfusion Syndrome

A Joyful Beginning When Lonnie and Michelle Somers learned they were expecting twins, they were overjoyed — and full of hopes for their future as parents. But that excitement was…

The Happiest Little Baby: Chase’s CDH Survivor Story

The Happiest Little Baby: Chase’s CDH Survivor Story

by Fetal Health Foundation | Apr 11, 2019 | Congenital Diaphragmatic Hernia, front-page, News

Chase Juergens came out blue. His mother, Alicia, had a caesarean section, and the nurses said that wasn’t unusual. Sometimes c-section babies take a little longer to catch their breath….

Lucy’s sacrococcygeal teratoma (SCT) story

Lucy’s sacrococcygeal teratoma (SCT) story

by Fetal Health Foundation | Feb 11, 2020 | Blogs, front-page, News, Sacrococcygeal Teratoma, Story

Article and photos courtesy of Katherine Stahl, patient’s mom. Shared with the permission of our partners at Texas Children’s Fetal Center. Chicago residents Kat and Justin were eager to get…

Home at Last: Parker Overcomes a Life-Threatening CDH Diagnosis

Home at Last: Parker Overcomes a Life-Threatening CDH Diagnosis

by Fetal Health Foundation | Apr 29, 2021 | Blogs, Congenital Diaphragmatic Hernia, front-page, News

We love a follow up CDH story with a happy ending! Our Friends Steward Partner, Children’s Hospital of Philadelphia, graciously agreed to let us share the story of Parker, a…

Advocacy from Anguish: Bethany Weathersby’s Story

Advocacy from Anguish: Bethany Weathersby’s Story

by Fetal Health Foundation | Dec 14, 2021 | Blogs, fetomaternal alloimmunization, front-page, HDFN, News, Story

How a mother’s struggle with a rare condition, fetomaternal alloimmunization, drove her to advocate for proper care in her future pregnancies and for other mothers in need. Bethany Weathersby had…

« Older Entries
Next 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