Sicilee is a fun-loving 8 year old who was diagnosed at just 2 days old with Cystic Fibrosis. She's had 4 sinus surgeries due to CF sinus disease, which has proven to be her toughest battle so far. This year our girl started 2nd grade and has excelled despite numerous absences due to her CF. Sicilee also participates in allstar cheerleading to help keep her active, and recently learned her back handspring.
It takes a lot of work, medications and dedication to keep our girl healthy! The CF community has made huge advancements in CF care, but we still need a cure. That's where you come in! Please consider donating to the CF foundation. If you can't donate, then please share and ask others to donate. And keep spreading awareness!
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.