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...
by Laura Bonnell | Feb 12, 2022 | Media/Press, Uncategorized
BioMatters – Winter 2022, Patient Advocate Issue by MichBio – Issuu Read the story here
by Laura Bonnell | Jan 26, 2022 | Media/Press
Bonnell was interviewed by Tia Graham and on the Morning Edition show with Pat Batchelor. Listen to the interview:
