The Cystic Fibrosis Foundation is a nonprofit organization dedicated to improving the lives of individuals with cystic fibrosis, a genetic disorder that affects the lungs and digestive system. Founded in 1964, the foundation focuses on funding research, providing access to care, and supporting patients and families affected by the disease. Through its efforts, the foundation has played a significant role in advancing treatments and therapies for cystic fibrosis. It also offers educational resources and advocacy to raise awareness about the condition, aiming to enhance the quality of life for those living with it.