Once a year, I reach out to you about a cause that I support: Cystic Fibrosis. My 14 year-old daughter, Emily, was diagnosed with this terminal disease at birth. We are fighting to give her as many tomorrows as possible by finding a cure with Emily’s Hope.
Over the last 15 years, Emily’s Hope has partnered with the Cystic Fibrosis Foundation, an organization established to find a cure for Cystic Fibrosis. Thanks to your generosity, Emily’s Hope has raised more than a million dollars over the years – an amazing testament to the power of the extended community.
Please know that there is absolutely no obligation to contribute to Emily’s Hope or any other charity. In addition, any contribution you choose to make is anonymous.
Together, we can make a difference in the life of Emily and those with CF!
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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.