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.
Facing an Omphalocele Diagnosis: One Family’s Journey to CHOP’s Specialized Care
When Addie and Ryan received a prenatal diagnosis of omphalocele, they were referred to CHOP for specialized fetal and neonatal care. From a highly coordinated birth to weeks in the NICU, their journey reflects the complexity of this rare birth defect.
Caring for Complex Fetal and Pregnancy Conditions: Expert Insights from Stanford Children’s Health
Stanford Children’s Health offers expert, coordinated care for complex fetal and pregnancy conditions. Discover how multidisciplinary teams support families from diagnosis through delivery and beyond.
Shining a Light on Birth Defects Awareness
January is Birth Defects Awareness and Prevention Month—a time to raise awareness, support families navigating unexpected fetal health challenges, and highlight the importance of early care, prevention, and compassionate resources. Learn how knowledge and community can make a difference for families.