Oliver Barry
Our daughter Quinn was born on June 8, 2024 and diagnosed with Cystic Fibrosis 2 weeks later. The journey that followed has been arduous for our family but through the quantum leaps in treatments for this disease, Quinn has access to medication that has given her hope for a normal future.
After her first hospitalization at 6 weeks from a common cold, we thought that would be her future. But she was able to start Trikafta, a groundbreaking new treatment made possible by the funding from the CF Foundation and the research of Vertex Pharmaceuticals, and has had no hospitalizations or lung issues since.
All this is only possible through the decades of fundraising to bankroll research and the development of new medications by the CF Foundation.
But CF is a progressive disease and treatment is not a cure. Please consider supporting the CF Foundation and our family because with your help the day will come that we are able to put an end to this terrible disease once and for all.
After her first hospitalization at 6 weeks from a common cold, we thought that would be her future. But she was able to start Trikafta, a groundbreaking new treatment made possible by the funding from the CF Foundation and the research of Vertex Pharmaceuticals, and has had no hospitalizations or lung issues since.
All this is only possible through the decades of fundraising to bankroll research and the development of new medications by the CF Foundation.
But CF is a progressive disease and treatment is not a cure. Please consider supporting the CF Foundation and our family because with your help the day will come that we are able to put an end to this terrible disease once and for all.
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