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.
Breakthrough in Hydrocephalus Care: Gene Therapy on the Horizon
A groundbreaking gene therapy developed at UC Davis could change how hydrocephalus is treated in children—offering hope for safer, long-term care.
đź’™ Honoring NICU Families & Their First, Fiercest Journey
Each year, 1 in 10 babies begins life in the NICU. This September, we recognize the strength of NICU families and the care teams who help them thrive.
Facing TTTS: Bridgette and Grace’s Story of Strength and Survival
At 12 weeks, Jackie and Trevor received a frightening diagnosis: their unborn twins had twin-twin transfusion syndrome. With CHOP’s fetal care team, a complex surgery offered new hope—and today, their daughters are thriving.