For nearly 15 years years I have worked for an incredible organization - the Cystic Fibrosis Foundation - that is pioneering healthcare and medicine for the rare disease community. Real progress has been, but the lives of people with CF are still cut far too short.
I am raising money this year for the many moms, dads, sisters, brothers, daughters, sons, spouses, and friends who struggle every day just to breathe. Who spend birthdays in hospitals, require feeding tubes to enjoy a meal, or who are on their first or second lung transplant. I hope you will support me in my efforts.
Will you join me? Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting life-saving research and medical progress.
Connect With Us
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.