This is my daughter Margo. She is 6 years old and is as silly, sweet, and curious as can be. She loves reading, art, dancing, playing dress-up, art, and swimming. Margo is also one of 30,000 Americans living with Cystic Fibrosis. At this point, there is no cure for this disease. But in the six years since Margo was born, tremendous strides have been made in getting us closer to that cure.
Every dollar you donate accelerates the Foundation’s pursuit of new therapies and provides vital support to meet the needs of those with CF, just like Margo.
We are so excited to see what 2024 and beyond will bring for our joyful daughter. Thank you so much for your generosity and continued support for Margo and every person living with Cystic Fibrosis.
xo Meagan
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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.