Liz was diagnosed with cystic fibrosis at just four months old. By her sophomore year of college, her health began to decline, and she had to move back home with her parents. She knew that a lung transplant was in her future. By February 2018, her illness became much more severe. Her doctors decided that […]
Power Player – Lara
Written by Lara G Have faith in God. All that’s required is that you really believe and do not doubt in your heart. You can pray for anything, and if you believe, you will have it. Mark 11:22-24. I’ve lived by this since March 2017 and have often referred to it as my lifeline because […]
Power Player – Caleigh
Caleigh was diagnosed at birth with Cystic Fibrosis. Despite her diagnosis, Caleigh lived a normal childhood and participated in sports and social activities. At the age of 19, Caleigh moved to San Francisco to attend culinary school. Unfortunately, during this time, she found herself in end-stage lung disease. At just 23 years old, she was […]
Power Player – Lauren
I am a 28-year-old female who has lived with Cystic Fibrosis her whole life. If you don’t know, Cystic Fibrosis causes thick mucus build-ups in lungs, which become nearly impossible for medicine to cure, thus resulting in a lung transplant. For the last six years, my doctor has causally mentioned lung transplant at various appointments. […]
Power Player – Brigette
Written by: Brigette McKern At the age of four, I was diagnosed with Cystic Fibrosis – a disease that affected my lungs and digestive systems. Even with receiving quality care, my parents were told I would most likely not survive past school age. My parents kept me compliant with treatments, medications, and appointments, and as a […]
Power Player – Paul
Paul is avid about working out and staying healthy. He never misses an opportunity to go to the gym and improve himself. He is also the recipient of two double lung transplants. When Paul was born, he was diagnosed with Cystic Fibrosis. Despite his illness, he played sports and remained active growing up. He believes […]
Power Player – Alice
By Alice Vogt I am South African and was born with Cystic Fibrosis, a genetic disease affecting the lungs and digestive system. I was diagnosed at age two, and my parents were told that there is about a 20% chance of me reaching the age of 20. However, I had a fairly normal childhood, apart […]
Power Player – Rima
Rima has spent most of her life in and out of hospitals due to Cystic Fibrosis. She knew she would eventually need a double lung transplant, but for so long, she was told that she wasn’t sick enough. She was so used to being told it wasn’t time, that when she was finally told that […]
