Fetal Health Foundation: Hope for Families Experiencing Fetal Syndromes

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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COVID-19 RESOURCES

OUR FAMILY IS GROWING

The Fetal Health Foundation now includes the Fetal Therapy Think Tank, bringing the expertise of 100’s of fetal therapy and medical industry experts to create a bright future for more young families through fetal medicine.

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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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NICHD Recognizes Hydrops Research Funded by FHF and the Brianna Marie Foundation as a Top Advancement of 2020

We're happy to share exciting news from recipients of our two-time research grant winner! In 2018 and 2019, the Fetal Health Foundation teamed up with the Brianna Marie Foundation to support Dr. Teresa Sparks and her team at the University of California, San...

Foundation and Fetal Therapy Think Tank Join Forces with 3 Bold New Initiatives

Dr. Timothy Crombleholme, Director Fetal Care Center of Dallas, and Lonnie Somers, Chair and Founder of the Fetal Health Foundation announce the joining of the Fetal Therapy Think Tank and the Fetal Health Foundation as one organization with the mission of improving...

One step closer to treating spina bifida with stem cells

With the CIRM funding, the UC Davis team will be able to launch their one-of-a-kind treatment in the coming months. It will be delivered while the baby is still in the mother’s womb (in utero). The complex procedure, with its unique use of a stem cell “patch,” could improve outcomes for children who are born with the severe form of spina bifida known as myelomeningocele.