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Prematurity Awareness Month: Supporting Families, Advancing Healthy Pregnancies

Prematurity Awareness Month: Supporting Families, Advancing Healthy Pregnancies

by Erika K Wolf | Nov 7, 2025 | Blogs, Condition, front-page, News, NICU, Story

November is Prematurity Awareness Month, a time to raise awareness about preterm birth, honor the resilience of premature infants, and support families with educational resources for healthy pregnancies.

UC Davis Surgeon Dr. Diana Farmer Honored for Groundbreaking Spina Bifida Research

UC Davis Surgeon Dr. Diana Farmer Honored for Groundbreaking Spina Bifida Research

by Erika K Wolf | Oct 9, 2025 | Blogs, Condition, front-page, Myelomeningocele/Spina Bifida, News, Spina Bifida, Story

Dr. Diana Farmer of UC Davis is pioneering new spina bifida treatments by combining fetal surgery with stem cell therapy in the groundbreaking CuRe Trial. Her work is transforming patient care and offering hope.

Help Shape the Future of Fetal Care Centers: We Need Your Feedback

Help Shape the Future of Fetal Care Centers: We Need Your Feedback

by Erika K Wolf | Oct 7, 2025 | Blogs, front-page, News, Story

Have you or your partner received care at a fetal care center? The Fetal Therapy Think Tank is developing national recommendations for how these spaces are designed — and your feedback can help. Take a short, 8-question survey by Oct. 28 to share your insights and help improve fetal care center design for future families.

Honor Your Baby This Pregnancy & Infant Loss Awareness Month

Honor Your Baby This Pregnancy & Infant Loss Awareness Month

by Erika K Wolf | Sep 30, 2025 | Blogs, Condition, front-page, News, Story

October marks a special time to honor the babies we carry in our hearts. Contributing writer Faith Dulany from CarryMe Health shares heartfelt insights from her personal journey, offering hope and healing through meaningful rituals.

🍭 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.

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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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