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Summary:

Every CHD parent remembers the moment the world stopped. The diagnosis. The surgery date. The waiting room. But what happens to the family holding it all together while their child is in the OR?

In this episode, Katelyn sits down with Conner Hill, co-founder of Stronger Hearts Foundation, to talk about his son Dawson's diagnosis of Hypoplastic Left Heart Syndrome (HLHS) at 20 weeks, the 100+ inpatient days that followed, and how one family's experience navigating the gaps in the CHD support system became a foundation that is already changing lives.

From emergency housing assistance and day-of-surgery care packages to a community built on the belief that no CHD family should walk this road alone, Stronger Hearts Foundation is filling a critical gap that too many families don't know exists until they're already in crisis.

Katelyn also shares exciting news: she and her husband Stephen have joined Stronger Hearts Foundation as Managing Directors, leading West Coast expansion efforts — and 10% of all Tiny Little Hearts listener support goes directly to Stronger Hearts Foundation.

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Keywords: CHD financial assistance, congenital heart disease support, HLHS family resources, CHD housing help, day of surgery care packages, Stronger Hearts Foundation, hypoplastic left heart syndrome, CHD nonprofit, cardiac surgery family support, CHD community, interstage monitoring, Fontan surgery, CHD advocacy

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