by Laura Bonnell | Nov 10, 2020 | Videos
Laura Bonnell, Founder of the Bonnell Foundation talks about the need and scarcity of PPE in the CF community. Bonnell was asked to speak in the National Organization for Rare Disease Disorders (NORD). You can see her at about 25:45 in this video.
by Laura Bonnell | Oct 23, 2020 | Videos
The Bonnell Foundation held their 2nd annual Night of Hope Celebration 2020 virtually to help raise money for families in need of medical assistance, lung transplant grants and college...
by cromano | Oct 2, 2020 | Videos
When the pandemic hit our country and Michigan most people were not stocked up on disinfectant wipes and other PPE. The cystic fibrosis community was scared because they regularly required N95 masks and PPE. We didn’t realize there would be a shortage, and panic set...
by cromano | Nov 26, 2019 | Videos
This is the video of Emily getting the newly approved medication Trikafta that they have waited 24 years for. Emily’s Mom surprised her at an MSU tailgate with the new drug. Emily had no idea when it would arrive and she said she wouldn’t believe it until...
by cromano | Nov 25, 2019 | Videos
Emily and Laura Bonnell are supporting the Exocrine Pancreatic Insufficiency Coalition. See their commercials. Emily Bonnell tells the story of her life with Cystic Fibrosis (CF) and Exocrine Pancreatic Insufficiency (EPI). Laura Bonnell shares her story of being the...
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....
