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.
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.
Your contribution gives hope to families with fetal syndromes.
Cincinnati Children’s, a national leader in prenatal myelomeningocele surgery, recently conducted their 100th prenatal surgical repair. Kelly Song’s daughter was diagnosed with spina bifida at 20 weeks. Read more:
Fetal Health Foundation founder and Fetal Care Chat host, Lonnie Somers welcomes esteemed doctors from Cincinnati Children's Fetal Care Center as they discuss bladder outlet obstructions and hear an inspiring story about a miracle little boy, JJ. ...
The morning after I unexpectedly gave birth at 27 weeks, my doctor checked in on me and my baby at the Neonatal Intensive Care Unit (NICU). He said he spent the night in the hospital because we were both in critical condition and he didn’t know if either one of us were going to survive.