This is our 19th year participating in Great Strides!
Chase continues to thrive since starting Trikafta. His lung function has remained consistent and he continues to feel well and energetic! He did have 1 scare this spring when he got bronchitis and was home from school for 3 days with a bad cough. Whereas before Trikafta this episode would have most likely landed him in the hospital, he was able to treat it at home with oral medications and returned to baseline within 2 weeks. It was definitely a reminder of what life was like pre-Trikafta though.
Your donations and support over the past 19 years have made all this possible, but we aren't done yet. We won't stop raising money until we find a cure for CF. While life is easier than it used to be, there are still struggles and hurdles that people with CF have to face daily.
We won't stop until a cure is found for everyone with CF. Will you please consider donating again this year in support of Chase and all those living with CF?
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. Will you join me and support my fundraising goal?
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We’ve come so far, but there’s still so much work to do. I will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.
Please support me!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!
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.