Did you know that nearly 40,000 children and adults live with Cystic Fibrosis in the United States alone? Given its cyclical nature, life with CF can be difficult to manage, especially for children, as it limits them from going about their normal lives.
The Cystic Fibrosis Foundation (CFF) is a non-profit organization dedicated to finding a cure for CF, a genetic disease that affects the respiratory and digestive systems. In addition to its research and care efforts, CFF engages in advocacy and awareness activities to raise public awareness of CF and promote policies supporting the CF community. As community members, it is our responsibility to support organizations that work hard to cure those on this difficult journey. To better advocate for them, we’ve decided to join hands with CFF in their mission to provide care and resources CF patients need to live healthy and fulfilling lives.
We hope to change many lives, and you can help us achieve this goal! Just recommend your friends, family, and co-workers to receive a no-obligation insurance quote from us, and we’ll donate $10 for each one! So, how many names can you give us of people who care about our community’s youth and future?