by Laura Bonnell | Nov 28, 2021 | Media/Press
By Vladislava Sukhanovskaya – Capital News Service About a million Michiganders with rare diseases could receive better treatment if legislators establish a Rare Disease Advisory Council. Read the story here
by Laura Bonnell | Aug 24, 2021 | Media/Press
By Amy Lange and David Komer online producer, FOX 2 Detroit FOX 2 – A local family has made it their mission to help those living with cystic fibrosis and this year — their annual fundraiser will return to in-person for their “Night of Hope.”...
by Laura Bonnell | Mar 9, 2021 | Media/Press
Bonnell Foundation featured in the NY Times “Fighting for a place in line” for the covid vaccine. Thanks to Amy Harmon, a NY Times Pulitzer prize winning journalist for telling not only our story, but the story of so many others with chronic and fatal...
by Laura Bonnell | Jan 31, 2021 | Media/Press
Bonnell Foundation featured in the Arab American News Doctors in Egypt weren’t aware of the prevalence of Cystic Fibrosis (CF) in their country until the efforts of a University of Michigan professor brought the disease to light. CF is genetic disease that causes...
by Laura Bonnell | Dec 16, 2020 | Media/Press
Bonnell Foundation featured in the STAT News When the coronavirus sent cities across the United States into shutdown in March, Laura Bonnell realized that her family’s supply of masks and disinfectant wipes was quickly running out.“We didn’t have any N95 masks and we...
