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Tagged as: Cystic Fibrosis

Ain’t No Party Like a West Coast Party…with CKF!

CC Cunningham is the Program Coordinator for the Chris Klug Foundation. …’cause a West Coast [CKF] party don’t stop! And what a party it was! On September 19th, as part of our Patient Ambassador Program, sponsored by Astellas, the Chris Klug Foundation traveled to sunny San Diego, California to visit

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Living and Breathing a Love for Life

Samantha Rick is one of CKF’s 2018 Bounce Back Award winners. Samantha Rick was diagnosed with cystic fibrosis (CF), a fatal genetic lung disease, when she was just three years old. Sam’s lung capacity slowly deteriorated as she got older and, at the age of 27, she was put on

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I have been given another chance!

CF (short for Cystic Fibrosis) has no cure yet, and so having crumby lung function and frequent infections leads to needing a double lung transplant. That is the stage that I’m at. I have now received my life-saving transplant at 27 years old. Thank you to my beautiful donor and

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