When a fetal syndrome diagnosis feels like the end, we offer support & hope.
November is Prematurity Awareness Month. Learn how to support families, honor premature infants, and promote healthy pregnancies—read the full blog post here. 💛
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.
Prematurity Awareness Month: Supporting Families, Advancing Healthy Pregnancies
November is Prematurity Awareness Month, a time to raise awareness about preterm birth, honor the resilience of premature infants, and support families with educational resources for healthy pregnancies.
Turning a Frightening Pregnancy Diagnosis into a Lifeline for Families: Our Founders’ Story
A Joyful Beginning When Lonnie and Michelle Somers learned they were expecting twins, they were overjoyed — and full of hopes for their future as parents. But that excitement was soon overshadowed by a diagnosis of twin-to-twin transfusion syndrome (TTTS), a rare and...
UC Davis Surgeon Dr. Diana Farmer Honored for Groundbreaking Spina Bifida Research
Dr. Diana Farmer of UC Davis is pioneering new spina bifida treatments by combining fetal surgery with stem cell therapy in the groundbreaking CuRe Trial. Her work is transforming patient care and offering hope.