When a fetal syndrome diagnosis feels like the end, we offer support & hope.
💖 February is Heart Month! 💖
Heart disease is the leading cause of death for women, yet many don’t realize the risks or symptoms. February is a reminder to take care of your heart, know the signs, and make heart-healthy choices every day.
Learn about protecting your heart and join the movement to save lives at Go Red for Women.
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.
DONATE NOW
Your contribution gives hope to families with fetal syndromes.
Rose’s Story: Prenatal Spina Bifida Diagnosis
When Taylor and James learned their baby, Rose, had spina bifida, their world shifted overnight. From high-risk pregnancy care to in-utero surgery at Children’s Mercy, their story of hope, resilience, and the power of compassionate medical support unfolded.
Inés’ Journey: Life After TRAP Sequence and the Loss of Her Twin
Diagnosed with TRAP sequence, Inés’ survival came after her twin’s loss, meticulous fetal monitoring, and the expert care at CHOP. Explore the pivotal moments and life-saving decisions that shaped her remarkable beginning.
A Fragile Start, a Fierce Future: Nora and Hattie’s sIUGR Story
Hattie and Nora faced sIUGR in the womb, a rare condition that threatened their lives. Years later, they continue to thrive, a testament to expert care at CHOP, resilience, and their extraordinary early journey.