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Tagged as: Bounce Back Give Back

NOW ACCEPTING: Nominations for 2021 Bounce Back Give Back Awards

Nominations are OPEN for our 2021 Bounce Back Give Back Awards! Each year, CKF recognizes two organ transplant recipients who are leading healthy, active lives post-transplant and give back to the transplant community in exceptional ways. Is there someone you’d like to nominate for this year’s Awards? We are accepting

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2020 BOUNCE BACK GIVE BACK AWARD WINNER: TRACY COPELAND

The Chris Klug Foundation (CKF) recently announced the two winners of our Bounce Back Give Back Awards this year! The annual award recognizes two organ transplant recipients who exhibit an outstanding quality of life post-transplant, whether it is through career accomplishments, participation in sports or hobbies, or simply leading fulfilling

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2020 BOUNCE BACK GIVE BACK AWARD WINNER: JOELLE ATKINSON

The Chris Klug Foundation (CKF) recently announced the two winners of our annual Bounce Back Give Back Awards this year. The award recognizes two organ transplant recipients who exhibit an outstanding quality of life post-transplant, whether it is through career accomplishments, participation in sports or hobbies, or simply leading fulfilling

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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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No Greater Love

Written by Kim Hinsley, Brian Hinsley’s wife and caretaker during his lifesaving liver transplant. Brian is one of CKF’s 2018 Bounce Back Award winners. I’m going to share Brian’s journey from my side, the caregiver’s side. Brian and I have been married for 22 years now. On our wedding day,

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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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