Thank you for considering a donation!
The Cystic Fibrosis Foundation continues to make great headway towards a cure for cystic fibrosis! CF is a rare, genetic disease that makes breathing difficult, among other issues as it affects multiple organs. Amazing advancements are being made in the fight against CF and we need your support to keep the momentum going! With supporters like you by our side, the CFF continues to lead the way in fueling extraordinary medical and scientific progress. The life expectancy of someone born with CF has doubled in the last 30 years! What was once identified as a childhood disease, now has more adults living with CF than children! Despite this progress, many people with CF do not benefit from existing therapies because their disease is too advanced or their specific genetic mutations do not respond, resulting in the need for continued research. By donating to our team, you will be part of a tenacious and passionate group of people committed to ending CF!
I am excited to share that my health remains stable! This is a direct result of ongoing research leading to new medications! In late 2019, I started a new modulator drug that works to correct the defective CFTR gene. Since then, my lung function has stabilized, and even improved, my cough and congestion are nearly nonexistent, and my sinus issues have mostly resolved! I am unbelievably grateful for my improved health! My family and I are very appreciative of the CFF and supporters like you for giving us continued hope for a bright future!
Your donation is making a positive impact on the lives of people with CF!
Together, we can make CF stand for Cure Found!
THANK YOU ~ Katie and Her KureFinders
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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.