I am the mama of a beautiful little girl named Macy. She is 1 of the 30,000 Americans living with cystic fibrosis. She is a daughter, sister, grand daughter, niece, cousin and friend of many. She, along with thousands of others, struggles every day just to breathe. 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 my Macy, and ALL those with cystic fibrosis have a cure.
Will you please join me and support my fundraising goal? Your gift will help add tomorrows to my girl and everyone living with CF.
Thank you!
-Mama of Macy
(Visit the Team Page for Macy’s story)
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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.