For the past 26 years, our family has supported the Cystic Fibrosis Foundation - and we haven't done it alone! So many of you have been on this journey with us, and we are so thankful for your support!
Decades ago, the CF Foundation was founded by families whose children were not living past elementary school. It is because of their grassroot advocacy and fundraising efforts that today, children with CF are living into adulthood, and why families like ours continue to fight for the cure.
When Andrew was born, we had only dreamt of the medical advancements that have improved outcomes for people with CF. The CFF has proven itself time and time again to be an organization that uses their resources efficiently; funding science that delivers! Because of their research, we know our dream of a one-time cure for this disease will become a reality. And because of your continued support, we know this reality will happen for Andrew and the many others born with this disease.
We thank you for sharing in our fight to end this disease.
Tom, Tonya, Andrew, Becca, and Sparty
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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.