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
Everett’s Update: Flourishing After Fetoscopic Surgery

Everett’s Update: Flourishing After Fetoscopic Surgery

by Fetal Health Foundation | May 30, 2019 | Blogs, front-page, Myelomeningocele/Spina Bifida, News, Story

Most mothers would probably tell their child to sit down and stop standing on the chair in the middle of their family photography session. But when you’re told your son will never walk and he mischievously climbs onto a chair with no help and stands there, posing for the camera … well, you let him do it.

What a Difference a Year Can Make

What a Difference a Year Can Make

by Fetal Health Foundation | May 13, 2019 | front-page, Myelomeningocele/Spina Bifida, News, Story

This time last year, I was taking a pregnancy test. Today, I’m the mother of a healthy four month-old little boy who loves to smile and kick his legs like crazy.

My Son’s First Surgery for Spina Bifida

My Son’s First Surgery for Spina Bifida

by Fetal Health Foundation | May 13, 2019 | front-page, Myelomeningocele/Spina Bifida, News, Story

Johnna Kerres tells her story of the surgery she and her son underwent before he was born. The fetoscopic surgery contributed to medical research.

Preeclampsia and How It Snuck Into My Pregnancy

Preeclampsia and How It Snuck Into My Pregnancy

by Fetal Health Foundation | May 6, 2019 | front-page, News, Story

After a dangerous experience, mom Paula Yost Schupp encourages all pregnant women to be familiar with the signs of preeclampsia, even if they, like her, seem to have no initial risk factors. She tells her story of how she was diagnosed, and what happened as a result.

The Worst News Becomes A Beautiful, Life-Changing Moment

The Worst News Becomes A Beautiful, Life-Changing Moment

by Fetal Health Foundation | Apr 29, 2019 | front-page, Hydrocephalus/ Ventriculomegaly, Story, Ventriculomegaly

Logan’s story is so much bigger than his diagnosis. To fully understand you have to know I had a stillborn baby named Andrew 12 years before I had Logan. Andrew had the same diagnosis as Logan. I can never forget the day I knew something was wrong with Logan. We went...
Research Grant Awardee: Understanding the Underlying Causes of Hydrops

Research Grant Awardee: Understanding the Underlying Causes of Hydrops

by Fetal Health Foundation | Apr 29, 2019 | Blogs, Fetal Hydrops, front-page, Grant Winner, Marie Grant Winner, News

The Fetal Health Foundation Awarded the 2018 Research grant to Dr. Teresa Sparks and team at the University of California, San Francisco. They are working to understand the underlying causes of Hydrops.

« 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