Fetal Health Foundation

WHEN A FETAL SYNDROME DIAGNOSIS FEELS LIKE THE END, WE HAVE RESOURCES AND HOPE FOR NEW BEGINNINGS.

YOU'LL NEVER FORGET THE MOMENT YOU HEAR YOUR BABY MAY NOT SURVIVE. WE REMEMBER.

LIFE CHANGES THE INSTANT YOU LEARN YOUR UNBORN BABY HAS A FETAL SYNDROME. WE HAVE RESOURCES TO HELP.

OVERWHELMED BY A FETAL DIAGNOSIS? WE’RE HERE FOR YOU.

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Fetal Syndrome Month

As a parent-founded non-profit, we are grateful for the support of our Stewardship Circle member institutions.

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YOU’RE NOT ALONE.

This is a scary and lonely moment. We have a network of people to stand with you. Read their stories.

4,000 PARENTS HEAR A FETAL CONDITION DIAGNOSIS EVERY DAY.

The first step? Understand the diagnosis. Learn more here.

HOPE FOR A FETAL SYNDROME DIAGNOSIS

Connect with medical specialists around the globe. Find a treatment center.

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Your contribution gives hope to families with fetal syndromes.

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New Fetal Surgery Treatment for Congenital Diaphragmatic Hernia

Fetal Health Foundation Medical Advisory Board member Dr. Ahmet Baschat and 2015 Recipient of the Brianna Marie Memorial Research grant Dr. Jena Miller are co-authors of a new Johns Hopkins Center for Fetal Therapy study that gives hope to families experiencing a diagnosis of fetal congenital diaphragmatic hernia.

Lucy’s sacrococcygeal teratoma (SCT) story

Lucy’s tumor was Type 3, both internal and external, and much larger than her doctors considered operable. It was also mostly solid, which meant it required a blood supply, causing the heart to work harder to supply blood to both the baby and the tumor.

2019 Fetal Health Foundation Impact Report

Your support made a real difference to young families facing a fetal syndrome diagnosis. Read about the impact that the Fetal Health Foundation made in 2019. Download the report PDF and share!