When we went in for our 20-week ultrasound, we were filled with excitement and anticipation. But that day brought news we weren’t prepared for. We learned that our baby girl, Emarosa, had a single umbilical artery and would be born with a cleft lip and palate.

In that moment, our joy was overshadowed by fear—fear for the unknown, fear about her health, and especially fear about how she would eat, grow, and thrive in her first precious days of life.

But Emarosa had other plans.

From the moment she arrived, she showed us what true resilience looks like. Thanks to the Dr. Brown’s special bottle and the guidance of our care team, Emarosa was able to feed beautifully. She responded bravely to her NAM treatment and underwent her first surgery to repair her lip with the strength of a fighter.

Now, as we approach her palate repair this July, that early fear has been replaced with awe. Emarosa is growing, thriving, and reminding us every day that she is stronger than we ever imagined.

We are beyond grateful for the incredible care we’ve received through the Stanford Cleft and Craniofacial Center, an ACPA Approved Team. Their kindness, expertise, and support have made all the difference in our journey.

The ACPA has also played an essential role in our story. Their resources helped me stay informed during some of the most overwhelming moments. I’ve been able to share these tools with Emarosa’s daycare and with family members who just want to understand and support us better. That kind of outreach and education is invaluable—and it’s made possible through generous donors like you.

ACPA ensures that families like Emarosa’s never have to walk this path alone. Your donation helps support research, team care, and educational resources that make thriving stories like Emarosa’s possible.

Join us in giving more children the chance to smile, to speak, and to shine.