Sydney (Eskew) Rolle was diagnosed with Cystic Fibrosis before she was 6 months old. She was in and out of the hopsitlal her entire life. 3 years ago she was introduced to new medication that has kept her out of the hospital since she started on it. She is still on all of her other medications and doing her preventative breathing treatments... but this is nothting short of a miracle. Our dream is that all kids with CF live long enough for the CF foundation to help find drugs that extend their lives as well. You can help us reach that goal!
We did the Great Strides walk in California and in Georgia... this will be our first one here in the DC area and we are really excited. We will have TEAM SHIRTS made for everyone that registers on the team.
Our Great Strides Story
Join our team to help make a difference in the lives of all people living with CF. To become a member, click the "Join this team" button. From there, you can donate and start fundraising.
As a member of our team, you are joining a growing community of people committed to finding a cure for cystic fibrosis. Together, we can make CF stand for Cure Found.
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.
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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.