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.
Thaddeus’s Story: Beyond Open Fetal Surgery, A Spina Bifida Success
5-minute read
Ester and Samuel traveled across country and stayed away from home for months to ensure the health of their baby boy. His serious spina bifida diagnosis and mom’s cervical complications were challenges that Dr. Timothy Crombleholme accepted and triumphed over.
The McGrew Family Story: When Your Baby Has FNAIT
3-minute read
Parents aren’t the only ones who may not be aware of the dire consequences of FNAIT. Many doctors and other medical professionals aren’t familiar with the blood disorder until there’s a serious problem. Raising awareness allows for better disease management and prevention. See how the McGrew family dealt with four FNAIT pregnancies.
What is FNAIT?
2-minute read
When a baby experiences FNAIT or NAIT it’s often not discovered until symptoms appear. That’s why it’s important to know the signs and understand if you and your pregnancy are at risk. The consequences of this condition that involves a low blood platelet count can be alleviated through awareness and prompt action.