Harper DeWare is a precious little girl born March 25, 2016 to parents Amanda & Crawford DeWare. Harper was diagnosed with cystic fibrosis through her newborn screenings and Amanda and Crawford began the process of doing everything they can to give Harper a full, healthy and long life. “Harper’s Heroes” was created as a way to create support for the DeWare family and to raise money with the aim of finding a cure for cystic fibrosis. Join us in the fight FOR A CURE, FOR HARPER and all those fighting cystic fibrosis. A cure is within reach and WE NEED YOU to get us there! Let’s give Harper MORE TOMORROWS!
WHAT IS CYSTIC FIBROSIS?
Cystic fibrosis is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time. In people with CF, a defective gene causes a thick, buildup of mucus in the lungs, pancreas and other organs. In the lungs, the mucus clogs the airways and traps bacteria leading to infections, extensive lung damage and eventually, respiratory failure. In the pancreas, the mucus prevents the release of digestive enzymes that allow the body to break down food and absorb vital nutrients.
ABOUT THE CYSTIC FIBROSIS FOUNDATION
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.
The CF Foundation is the world’s leader in the search for a cure for cystic fibrosis, and nearly every CF-specific drug available today was made possible with their financial support. They are a donor-funded, 501(c)(3) nonprofit that is fully accredited by the Better Business Bureau’s (BBB) Wise Giving Alliance program.
To learn more about CF and the Cystic Fibrosis Foundation, please visit www.CFF.org.
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