It's that time of year again! We are walking to raise money for the CF Foundation. Please join us on Saturday, May 14 at 9am if you are able!
In January 2020 Kaley started taking her "miracle pill", Trikafta. Her health has been steady since then, and this May marks 3 years since her last hospitalization due to a CF exacerbation. This drug has been life-changing for Kaley, but there are others who cannot benefit from this or the other therapies due to specific genetic mutations. We will continue to raise money until all people with CF have their miracle pill.
The CFF is also still doing research on treatments and anti-infectives that help with current lung infections. Kaley has cultured bacteria in her lungs since she was 3 years old. Antibiotic resistant bacteria is a problem for her and many others, so finding other treatments that address this problem continues to be extremely important.
We would love for you to join us before we send Kaley off to college!
To participate, just click on the "Join our Team" button. From there, you can make a donation and start fundraising.
As always, we so appreciate our family and friends who have supported Kaley and our family!
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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.