It was about 4 years ago now that I really learned about CF for the first time, when I was told that my then two-week old daughter Sadie had been diagnosed with it, and my life was forever altered.
At the time it was so scary. There were so many unknowns, and suddenly I was faced with supporting my child with a disease that I had barely ever heard of.
We've come a long way since then. I have learned so much, not just from the team we are fortunate enough to have for Sadie, but from Sadie herself. She has taught me not to give in to CF, but to fight.
The fight isn't over until there's a cure though. This year we are participating in Great Strides to raise money to help find a cure. I hope you'll consider donating towards this awesome cause!
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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.