We hope you will join our team, A Cure 4 Chris, and help us get one step closer to a CURE for Cystic Fibrosis – a rare, genetic disease that affects the lungs, digestive system, and liver for Chris. When Chris was born in 2007, there were 30,000 cfers in the US, and 70,000 worldwide. Thanks to donations like yours and the advancement of better medications, like Trikafta, it is now 40,000 in the US and 105,000 worldwide!! Why?? Because Trikafta, the miracle drug, is helping cfers live longer, healthier, happier lives!! Chris has been on Trikafta for over 4.5 years and he is finally consistently hitting over 100 on his PFT, pulmonary function test, AND NO MORE VEST AND NEB EVERYDAY!!! I never thought I'd see the day!! But it's not a cure. We will not stop until a CURE is found. Please join us in raising the MUCH needed funds to help Chris and the other 105,000 like him who are so deserving of a normal life. Click to join our team and help raise money, or click to donate to our team. Thank you in advance, and special thank you to those who support us year after year. We are forever grateful!!
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.