Friends and family it is that time of the year again, time to raise funds for research for Cystic Fibrosis, CF. The Cystic Fibrosis Foundation does incredible things and has some very exciting trials in the pipeline that could lead to long, healthy and more normal lives for those living with CF.
Andrew was born with Cystic Fibrosis, a genetic lung disease that causes thick sticky mucus to effect different parts of his body, mainly his lungs and digestive system.
Andrew is now 8 years old and enjoys swimming, riding his bike, playing with his brother, sister and cousins, riding his fourwheeler and mostly snowboarding all winter!! Because of this Andrew has qualified for the USASA Nationals at Copper Mountain, CO this April. We are so thrilled that he is able to do all of the things that he loves and want to ensure he is given every opportunity to live the life he deserves along with all others that have CF. Your donation to the Cystic Fibrosis Foundation (100% Rating from Charity Navigator) will do just that - fund the needed research to keep the cure progressing. THANK YOU!!!!
100% Tax Deductible:
EIN: 13-1930701
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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.