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Hope Begins With You

Support CCF’s 2025 Holiday Appeal

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The Children's Cardiomyopathy Foundation is a 501(c)3 tax-exempt organization, and your donation is tax deductible within the guidelines of U.S. law.

EVERY DOLLAR MATCHED

AskBio will match every donation $1 for $1 up to $20,000!

MEET BENNETT

When Bennett was just 10, her dream was to make the school cheer squad. But a routine physical changed everything. After discovering a heart murmur, doctors diagnosed her with dilated and hypertrophic cardiomyopathy, a serious heart condition. The months that followed were filled with fear, medical tests, and anxiety as Bennett adjusted to life with a defibrillator vest and later an implanted device. The alarms, hospital visits, and isolation from friends took a toll until her family found the Children’s Cardiomyopathy Foundation (CCF). Through CCF, they found guidance, community, and hope.

Today, Bennett is dancing again, and her mom, Cara, is giving back as a parent ambassador and advisory board member for CCF’s patient registry.

With your support, more families like Bennett’s can find the strength, resources, and hope they need. Hope begins with you.

DOLLARS AT WORK

Through your support, we are making
great strides to end pediatric cardiomyopathy.

Provide Resources

Fund critical family services to provide information and emotional support through CCF Connect, our family online community. Help connect families for peer-to-peer support so families no longer feel alone.
$
50
USD
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Advance Research

Help fund ground breaking research that advances the understanding of pediatric cardiomyopathy. Your donation supports scientific discoveries that could improve treatment and save young lives.
$
25
USD
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Promote Education

Support the development of educational materials to empower families to better manage their child's care and to further our outreach to recognized Cardiomyopathy Centers of Care.
$
10
USD
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Creating a future of hope for children with cardiomyopathy

The Children's Cardiomyopathy Foundation was founded in 2002 by Lisa Yue and Eddie Yu in memory of their sons, Bryan and Kevin, who tragically died of hypertrophic cardiomyopathy. They transformed their pain into passion to help other parents and children with this rare and often progressive heart disease. Twenty two years later, CCF has grown into an international community of families and physicians, committed to advancing treatments, outcomes, and the quality of life for children with cardiomyopathy.

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