Milly’s Journey: Building Abilities Through Collaboration

 

When Tessa and David Williamson learned their daughter Milly had Down syndrome and duodenal atresia, they knew her first months would be challenging. Milly required IV nutrition for several weeks and faced feeding difficulties and developmental delays due to hypotonia. That’s when the Williamson family turned to Capper Foundation for support.

“Milly was having difficulty just sitting up and pushing up on her hands,” recalls Cris Teter, Milly’s physical therapist at Capper Foundation. “Her strength and endurance were low, and that impacts everything—eating, speech, and overall development.”

Capper’s unique approach to pediatric therapy focuses on collaboration. Milly’s care team includes physical therapy, occupational therapy, and speech therapy specialists working together to address her needs. Chris helped Milly build core strength for sitting and standing, while Deborah focused on oral motor skills, and sensory strategies supported feeding progress.

What stands out most is Milly’s transformation. Once a quiet observer, she now explores her environment with confidence—grabbing toys, standing on tiptoes, and even crawling into her parents’ laps. Her communication skills have blossomed, giving her independence and control. “She’s taking the spoon herself now,” says Tessa. “Seeing that independence increase has been incredible.”

The Williamson family credits Capper Foundation—and its donors—for making this progress possible. “I don’t think Milly would have made as much progress without Capper,” says David. “We’re so grateful to the therapists and everyone who supports this mission.”

Capper Foundation’s impact is profound, but the need continues to grow. Last year, the gap between unreimbursed costs and service delivery exceeded $5.2 million—the largest in our 105-year history. Every dollar donated helps ensure children like Milly receive life-changing therapy.

As David puts it, “Milly runs on smiles.” Thanks to Capper Foundation and its supporters, those smiles—and her abilities—keep growing every day.

Milly’s story was also featured at our 2025 Donor Dinner Celebration and can be watched here.