by Bonnell Foundation | Feb 28, 2020 | Media/Press
Laura Bonnell is the mother of two children with Cystic Fibrosis and is the founder of The Bonnell Foundation. Laura joins the 1 Girl Revolution podcast to share her own life story; what cystic fibrosis is and more about her own family’s journey with CF; she talks...
by Bonnell Foundation | Oct 29, 2019 | Videos
The Bonnell Foundation held their first Night of Hope Celebration in 2019 to help raise money for families in need of medical assistance, lung transplant grants and college scholarships. Melissa Yaeger speaks at the Bonnell Foundation Night of Hope Celebration 2019....
by Bonnell Foundation | May 3, 2019 | Advocating for CF
National Cystic Fibrosis Awareness Month in May encourages education in the battle against a lung disease affecting more than 30,000 people in the United States. Cystic Fibrosis (CF) affects more than just the lungs. This genetic disease causes constant lung...
by Bonnell Foundation | Apr 24, 2019 | Advocating for CF
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...
by Bonnell Foundation | Mar 30, 2019 | Inspirational Stories
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...
