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Family Celebrates One-in-a-Million Odds

Family Celebrates One-in-a-Million Odds

by Fetal Health Foundation | Jul 11, 2019 | Pericardial Teratoma, Story

…and internationally in supporting families and medical treatment centers dealing with intrauterine fetal syndromes. The 501c3 nonprofit organization connects families diagnosed with a fetal condition to top-rated medical specialists, provides…

New Technology for TRAP Syndrome Treatment

New Technology for TRAP Syndrome Treatment

by Lonnie Somers | Dec 1, 2017 | front-page, News, Twin Reversed Arterial Perfusion Sequence

…Parents come to us to help find the newest treatment options, and hope for their unborn babies. When progress is made, we are all the more pleased to be able…

New Fetal Surgery Treatment for Congenital Diaphragmatic Hernia

New Fetal Surgery Treatment for Congenital Diaphragmatic Hernia

by Fetal Health Foundation | Feb 20, 2020 | Blogs, Congenital Diaphragmatic Hernia, front-page, News, Story

…be serious. The team is seeing success with a new treatment method “FETO — fetoscopic tracheal balloon occlusion — is a minimally invasive procedure in which a fetoscope is inserted…

Spina Bifida Research at UC Davis Provides Hope

Spina Bifida Research at UC Davis Provides Hope

by Fetal Health Foundation | Aug 6, 2019 | front-page, Myelomeningocele/Spina Bifida, News, Spina Bifida

…enable the UC Davis team to do the final testing and preparations needed to apply to the FDA for an Investigational New Drug Application for the new treatment. This treatment…

Twin Anemia Polycythemia Sequence: The Slow Change That Alters Everything

Twin Anemia Polycythemia Sequence: The Slow Change That Alters Everything

by Fetal Health Foundation | Sep 23, 2020 | Blogs, front-page, News, Story

…need to worry about TAPS Right now, the biggest problem is that TAPS remains under-diagnosed. There is no current “best treatment,” but treatment options do exist. However, because there’s no…

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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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