When a fetal syndrome diagnosis feels like the end, we have hope for new beginnings.
Dealing with a fetal diagnosis?
We’re here for you.
Advancing Fetal Care
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.
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Your contribution gives hope to families with fetal syndromes.
A Family’s Journey with Rare Disease: Molybdenum Cofactor Deficiency Type A
The Dahab family moved to Ohio to be close to their “second family” at Nationwide Children’s Hospital. Thanks to Nationwide’s excellence in maternal fetal medicine and fetal imaging, a world-class NICU, access to genome sequencing, and rare disease experts, their boys are living longer and better lives.
Saving Luka: From Albania to Ohio to Treat Posterior Urethral Valves
When doctors told the Lame family their son wouldn’t survive his serious diagnosis, they didn’t give up hope. They started to search for answers. Luckily, they found them at Cincinnati Children’s Hospital. With expert, all-encompassing care, baby Luka is thriving.
Deciding to Treat Fetal Renal Failure: Information & Support for Families from Connecticut Children’s
Treating Fetal Renal Failure is a highly personal process with many decisions to be made over the lifetime of the child. Dr. Timothy Crombleholme at Connecticut Children’s details why it’s important to have support, second opinions, and a highly specialized team.