by Laura Bonnell | Apr 3, 2023 | Blog, Uncategorized
I recently had an amazing opportunity to visit and experience the Vertex Pharmaceuticals campus in San Diego. What an unbelievable opportunity to see and experience many of the people, the labs, the technology, and the beauty of a building that was created with such...
by Laura Bonnell | Apr 3, 2023 | Media/Press, Uncategorized
By Samya Nasr, MD, Director, Cystic Fibrosis Center It was always thought by the Egyptian Medical Society that CF does not exist in Egypt. One major problem has been the lack of the physicians’ awareness of the disease. Addressing that issue began in 1997, first...
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...
