When Nolan was diagnosed with cardiomyopathy at five months old, his family faced an uncertain future. For families facing pediatric cardiomyopathy, they need trusted information, connections to specialized care, and a community that understands.
Your year-end gift helps CCF provide that support, from the first questions to the next steps. Help more families feel informed, supported, and less alone.
When Nolan was diagnosed with cardiomyopathy at just five months old, his parents faced an unfamiliar diagnosis and an uncertain future. As they learned that he would need a heart transplant, they also needed clear information, guidance, and reassurance from families who understood what they were facing. This is where the Children's Cardiomyopathy Foundation (CCF) makes a meaningful difference. CCF helps families feel informed and supported through some of the most difficult moments.
Today, Nolan is 13. He loves music, talks to everyone he meets, and is embracing the start of seventh grade. Thanks to his heart transplant and specialized care, he and his family can enjoy the everyday moments his parents once feared they might never experience.
There is so much more to Nolan’s story than his diagnosis. And there is so much more we can do for children and families like his.
For families facing pediatric cardiomyopathy, a diagnosis is often just the beginning of a long and complex journey. Along with medical care, families need trusted information, connections to specialized care, and a community that understands. CCF is there for them.
Your year-end gift helps us provide families with the resources and support they need from diagnosis through treatment and ongoing care.
There’s so much more to do. More families to support. More connections to make. More research to advance.
Please consider making a year-end gift today. Your generosity helps families understand their child’s diagnosis, navigate the next steps, and find support along the way.
Thank you for standing with us and with families like Nolan’s.