Bean Corcoran, CT Annual Fund Chair
Please join me in supporting the Cystic Fibrosis Foundation's Partners in Progress Annual Fund
My name is Will Corcoran, I am a 21 year old Cystic Fibrosis patient originally from Weston, Connecticut. I am now in my senior year at the University of Vermont where I major in Environmental Studies with minors in Geography and Writing. I am involved on campus as a chairperson in Student Government, and President of the men’s honor society. I have grown to manage my CF and schoolwork well, I spend about three hours a day doing breathing treatments in addition to exercising consistently, seeing doctors several times a month, and constantly trying new methods to improve my health.
of $0 goal raised
Partners in Progress Annual Fund
Cystic fibrosis is a life-shortening, genetic disease that causes persistent lung infections and progressively limits the ability to breathe. 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.
To carry out its lifesaving mission, the Cystic Fibrosis Foundation depends upon the generosity of people like you. The Foundation’s Partners in Progress Annual Fund enables you to give directly to our mission in support of CF research and specialized care, as well as greater access to assistance and patient engagement initiatives.
Please consider making a contribution – your support at any level is greatly appreciated. Together we can continue to add tomorrows for those living with CF.