Evie is a 14 year old FULL of life! She is passionate about cooking, loves music, and advocates for those, like herself, living with cystic fibrosis (CF). She continues to need daily medications and vest therapy to maintain her health- much of this has been made possible by caring people like YOU!
Evie was born with Cystic fibrosis, but was diagnosed with cystic fibrosis at the age of 5. Since her diagnosis, YOUR donations have given her access to new medications that directly impact her overall health. This year, our family needed the assistance of Compass (provided by the CFF), to help us navigate her care. Your donation directly helps our family and many other families in need of these important services. THANK YOU!
The Cystic Fibrosis Foundation has teamed up with the medical community to work hard to change the future for those living with CF. It is our mission to help CF stand for Cure Found, but we need YOUR help to make that dream come true! Please join us by making a donation on Evie's behalf and /or joining the Evie's Echoes team!
Love,
The Evie's Echoes Team
Join our team and help add tomorrows!
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers who struggle every day just to breathe. We walk for them. Will you join us? To become a member of our team, just click on the "Join our Team" button. From there you can make a donation and start your fundraising.
By becoming a member and making a donation, you are joining a growing group of people committed to finding a cure for cystic fibrosis. Together, we are adding tomorrows to the lives of people living with CF by supporting the search for a cure.
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
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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.