Hello everyone!
This will be my 10th Great Strides walk since getting involved with the CF Foundation, and I am excited to walk again this year! My wife and brother-in-law both live with cystic fibrosis, so I have been in the unique position to see how all of the fundraising and awareness and advocacy efforts have directly impacted their lives. My wife Jackie has been fortunate to be eligible to take Trikafta and benefit from the modulator - her lung function has improved and held steady, she no longer needs to do vest therapy, and she has been able to live an active and healthy lifestyle while raising our 5 month old daughter! I continue to fight for additional modulators that will benefit ALL people living with CF and ultimately find a cure. Together we can and will cure this thing.
Please support me and my family by donating to my page or registering to walk with us at Great Strides this May!
Thanks,
Luke
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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!
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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.