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Tagged as: Cystic Fibrosis

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

Written by CC Cunningham, blog writer and 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,

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Living and Breathing a Love for Life

Written by Samantha Rick, lung transplant recipient and one of CKF’s 2018 Bounce Back Award winners. Edited by CC Cunningham, CKF Program Coordinator. 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

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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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