Holiday Appeal is Now Underway

Dear CCF Friends,

For more than 17 years, the Children's Cardiomyopathy Foundation (CCF) has connected families to medical professionals, educational resources, and research studies with one goal in mind – to improve health outcomes and quality of life for children with cardiomyopathy.

CCF has also made it a priority to connect families to one another during difficult and unpredictable times. Until cures are found, we will continue to serve families around the world who turn to us for answers and assistance.

In the coming weeks, we'll share stories of how CCF has connected families through the years. You will meet Myesha Bruce and the Cosby family who became involved with CCF after they lost their child to cardiomyopathy. You'll also hear about Gilberto and Tara Piña and how they are living with their son's diagnosis.

You can help us to continue supporting families like these and many others that come to CCF for information, guidance, and comfort.

Please consider giving to our 2019 Spring Appeal so that we can reach our goal of raising $10,000 to fund support services and educational resources for families affected by pediatric cardiomyopathy.

In gratitude,


Lisa Yue
Founding Executive Director

Stay Informed
Keep current on PCM research and CCF happenings in our Heart to Heart newsletter.
Unite and Fight
Connect with hundreds of other families struggling with this disease through our online member community.
Shop for a Cure
Shop for CCF merchandise to support our research and education efforts.
The Children's Cardiomyopathy Foundation is a 501 (c)(3) non-profit recognized by the U.S. Internal Revenue Service.
© 2019 Children's Cardiomyopathy Foundation. All rights reserved.