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Join us as Breath of Life Foundation spokeswoman Lily Arkens shares her personal experience with Cystic Fibrosis. Lily is the daughter of Lauren Arkens who was born in 1984 with Cystic Fibrosis. Lily shares how the disease and her mother’s experience shaped her life prior to and after her passing from complications of a double lung transplant in 2019.This event is FREE and open to the public. Join us as Lily opens the audiences eyes to the life of families living with Cystic Fibrosis.
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Event Venue & Nearby Stays
Mulva Library, St. Norbert College, 406 S 3rd St, De Pere, WI 54115, United States
