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.

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.

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

Fetal Care Chat: Women in Fetal Medicine

Fetal Care Chat: Women in Fetal Medicine

Fetal Health Foundation founder and Fetal Care Chat host, Lonnie Somers welcomes three amazing pioneering women in fetal medicine. Dr. Jenan Miller, Dr. Courtney Stephenson, and Dr. Diana Farmer.

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Home at Last: Parker Overcomes a Life-Threatening CDH Diagnosis

Home at Last: Parker Overcomes a Life-Threatening CDH Diagnosis

CDH affects 1,600 babies in the U.S. each year. In CDH, a hole in the diaphragm allows abdominal organs to move upwards into the chest during development, crowding the lungs and inhibiting their proper growth. Underdeveloped lungs and blood vessels that supply the lungs can cause high blood pressure in the lungs, asthma, gastrointestinal reflux, feeding disorders and developmental delays in childhood survivors of CDH.

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