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CF Task Force Raises Awareness

The Bonnell Foundation: Living with Cystic Fibrosis and Rock CF organized the CF Task Force in January of 2017 to make certain that we were raising awareness as a CF community. Our hope since then has been that lawmakers will use us as a resource when making decisions...

Charity’s Story

Living with CF for 19 years has been a struggle:  school, homework, treatments and my job. My name is Charity, I was diagnosed with CF when I was 3 months old. I am the third of four sisters. I believe it was hard on my parents and my siblings to watch me...

Hayley’s Story

My daughter Graysen was diagnosed “late” at 10 months old after an intense beginning of life. She was a preemie born at 34 weeks old and was in the NICU for 17 days and even with the NICU stay, she was not diagnosed with CF until after 2 inconclusive...