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