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Parent's and child's hands both hold a heart

CHD Patient Stories

Every 15 minutes, a child is born with a congenital heart defect. But that’s only the beginning of their story. Advancements in CHD care mean that these kids can live and thrive with just a little help.

Finding Community

Every year, UVA Health Children’s provides care for many children affected by CHD. Some are first diagnosed here by fetal echo. Some discover their child’s CHD at birth, during a newborn screening. And still others don’t find out until their child is older.

Every family’s path to diagnosis is different. And so are their roads to recovery and healing.

Many families had no idea that CHD affected so many kids. And once their child is diagnosed, it can feel like a whirlwind of information. But in the middle of that, connecting with other CHD families offers community as well as hope.

Sharing Stories & Hope

We love sharing the stories of these families.

As sonographers on the CHD care team say, “We love to be a part of the team and the patient’s overall success story. As patients and families come in for follow-up visits, we get to see these kids overcome CHD, to run around, and thrive like normal kids.”

It’s in these stories that many families are able to find hope through a challenging diagnosis.

We’re honored so many of our patients have come back to share their stories.

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Common Bonds: Mended Little Hearts of Charlottesville Helps Families Affected by Congenital Heart Defects
Kids, Patient Stories 3/22/2012

Recreation therapist Laurie Sewell sits cross-legged on the floor of a UVA hospital conference room. She’s demonstrating infant massage techniques on a doll while 2-year-old Haley Poore watches her and plays with a colorful toddler toy. [caption id="attachment_3742" align="alignright" width="300"] Recreational therapist Laurie Sewell (right) and Mended Little Hearts volunteer…

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