When a fetal syndrome diagnosis feels like the end, we offer support & hope.
January is Birth Defects Awareness & Prevention Month 💛
We recognize the importance of early care, informed choices, and meaningful support for families facing unexpected fetal health challenges—while raising awareness that helps create healthier beginnings.
Learn more about birth defects now. 🌱
Dealing with a fetal diagnosis?
We’re here for you.
Everyone can be a part of our Sweetest Foundation Fundraiser
Our parent-founded non-profit is supported by family fun.
Register now to donate sponsor or run in
Denver’s Great Candy Run November 9
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.