We are so excited to be walking again after Covid and Dylan’s fight against the bacteria in her lungs. We are beyond thrilled that treatment for the M. Abscessus was successful and Dylan is doing great. It’s because of these walks and other fundraising efforts that made this possible! The advancements in care and treatment for people living with CF continues to improve and we can’t wait for CF to stand for “Cure Found”!
I know Dylan will love to see all her friends and family and school mates at the walk this year supporting her!
Mark your calendars for May 13th in OKC and register today! Even if you can’t attend in person you can still sign up on her team as a virtual walker.
We will be designing and selling team shirts this year too!!! Yay!
With supporters like you by our side, the Cystic Fibrosis Foundation continues to lead the way in the fight against CF, fueling extraordinary medical and scientific progress. The life expectancy of someone born with CF has doubled in the last 30 years. Despite this progress, many people with CF do not benefit from existing therapies either because their disease is too advanced or because their specific genetic mutations will not respond. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers who struggle every day in the face of this devasting disease.
We walk in Great Strides for them.
Will you join us?
Great Strides is a fun event that provides a fantastic opportunity for family, friends, students, and colleagues to come together to make a difference in the lives of people with CF.
To participate, just click on the "Join our Team" button. From there, you can make a donation and start fundraising.
By joining our Great Strides team and making a donation, you will be part of a tenacious and passionate group of people committed to ending this disease. Together, let’s 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.