I am Bailee Goldman and my youngest sister, Eliana Goldman, lives with cystic fibrosis. Ellie, as we like to call her, was diagnosed with cystic fibrosis at birth. Ever since I remember, I have always been very invested in learning and fundraising for cystic fibrosis. I have gone to Washington DC twice to speak to Congress on CFer's behalves. I have also done much other volunteering and have won the Teen Advocacy Award.
Please consider donating to Ellie’s Army in hopes of finding a cure to make CF stand for Cure Found!
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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.