by Laura Bonnell | Jul 29, 2022 | Media/Press
Thanks to Marie Osborne, Steve Courtney and Dave Riger at WJR for doing such a wonderful interview with Laura Bonnell. The group talked about Bonnell’s travels to Egypt and all things CF, including the work done by her Foundation.
by Laura Bonnell | Jul 29, 2022 | Media/Press
By Neal Rubin, Detroit Free Press Laura Bonnell had a translator, because the parents in the room were mostly poor, and it’s typically the wealthy in Egypt who are most comfortable with English. When the screen filled with a picture of her daughters, though —...
by Laura Bonnell | May 24, 2022 | Media/Press, Uncategorized
By Amy Lange, FOX 2 Detroit The Bonnell Foundation Founder, Laura Bonnell talks to Fox 2 News reporter/anchor Amy Lange about the importance of raising awareness about cystic fibrosis, fundraising and making people understand that anyone can be born with the disease,...
by Laura Bonnell | May 2, 2022 | Media/Press
Breakthrough cures for cystic fibrosis start by promoting science and innovation....
by Laura Bonnell | Mar 1, 2022 | Media/Press
Laura Bonnell, the founder of a foundation bearing her family’s name, is working to make sure people with rare diseases get representation in Michigan. Read the story here
by Laura Bonnell | Feb 28, 2022 | Media/Press
By Institute for Patient Access The 30 million Americans diagnosed with a rare disease represent a large, underserved patient population. Their complex conditions are often poorly understood, and most have no approved treatment. Nevertheless, rare disease patients and...
