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.
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.
Q&A with Dr. Jena Miller: Charting New Frontiers in Fetal Medicine at CHOP
In January 2026, Dr. Jena Miller joined CHOP as Co-Director of the Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment. With over a decade at Johns Hopkins, she brings expertise in minimally invasive fetal procedures, spina bifida, and TTTS. Read her Q&A on advancing fetal medicine and supporting families.