When a fetal syndrome diagnosis feels like the end, we offer support & hope.
April is Multiple Birth Awareness Month 💜
In April 2024, Kayleen Delgado and her husband Zeke received life-changing news: they were expecting. At a routine ultrasound, that news became even bigger…they were having quadruplets.
Read about the Delgado Quadruplets and their incredible journey!
Dealing with a fetal diagnosis?
We’re here for you.
Celebrating 20 Years
Advancing Fetal Health
Over the last two decades, we have helped turn hope into possibilities for babies.
- Fetal care has become more personalized and predictive, and less invasive
- Diagnoses once considered untreatable before birth now have treatment options
- Whole-family support across the perinatal journey has expanded
We honor these milestones and look ahead, staying committed to raising awareness, championing better outcomes, and connecting communities worldwide.
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.
Xavier and Bryson’s Story: Hope After a TTTS Diagnosis
A twin-twin transfusion syndrome (TTTS) diagnosis marked an unexpected turn in Essence and Eric’s pregnancy journey. At the Connecticut Children’s Fetal Care Center, expert care, precise timing, and resilience shaped the path forward as their story continued to unfold.
Delgado Quadruplets Born at UC Davis Children’s Hospital
The Delgado quadruplets were naturally conceived after Kayleen and Zeke Delgado were told they would likely have difficulty conceiving. After two daughters and a miscarriage, the couple’s path to growing their family was uncertain—but not closed. In April 2024,...
20 Years of Advancing Fetal Health
The Fetal Health Foundation marks its 20th anniversary, celebrating two decades of progress in fetal care, family support, and global awareness for fetal health conditions.