by Laura Bonnell | Feb 6, 2023 | Podcasts, Uncategorized
Almost everyone in the CF community knows who Andy Lipman is and all the contributions he has made. Andy, and his older sister Wendy were born with cystic fibrosis. Wendy died when she was only 16 days old. The Lipman family founded The Wish for Wendy Foundation, in...
by Laura Bonnell | Jan 1, 2023 | Media/Press, Uncategorized
Living with Cystic Fibrosis podcasts are available and are for anyone who wants to learn and be inspired, even those not associated with a diagnosis of Cystic Fibrosis. Read the feature on page 2 of the Michigan Family Connections Newsletter here
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 Guest Author | Feb 15, 2022 | Uncategorized
Meet Rebekah Farley, a CF Mom and advocate. You’ll be able to see Laura Bonnell and Rebekah, “in person” after the introduction. Enjoy the conversation between Laura, who has two adult daughters with CF, is a former news reporter and now runs her...
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 17, 2022 | Blog, Uncategorized
My dear friend Kimberly Bowman, (and friend to so many in the CF community), tells her story with her son Brett Bowman in our Living with cystic fibrosis podcast out today. It will rip your heart out, inspire you and make you laugh. Kim’s been through hell and...
