Affordable Care Act Anniversary News Conference
The Bonnell Foundations Laura Bonnell participated in a news conference that was red on WWJ celebrating the anniversary of the Affordable Care Act. Thanks to Rep. Elissa Slotkin and Protect Our Care of Michigan for organizing. Thanks to WLNS, MIRS, WOOD TV, WWJ, and...
Payer Programs – All Sides Speak Up (Including our Laura Bonnell)
ViewPoints: Patients with cystic fibrosis not alone in grappling with payer copay adjustment programmes by Jessica D'Amico Like so many others among the 40,000 Americans living with cystic fibrosis (CF), Molly and Emily Bonnell were waiting for a cure. While the...
WJR community interview with Vanessa Denha
“It’s Your Community” | Sundays 6 to 6:30 a.m. Each Week, WJR‘s “It’s Your Community” focuses on the names, faces, and happenings that are affecting our community. Join your host Vanessa Denha Garmo as she meets with community leaders, experts, and insiders to ask the...
Living with Cystic Fibrosis podcasts featured in Michigan Family Connections Newsletter
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
WJR community interview with Vanessa Denha
“It’s Your Community” | Sundays 6 to 6:30 a.m. Each Week, WJR‘s “It’s Your Community” focuses on the names, faces, and happenings that are affecting our community. Join your host Vanessa Denha Garmo as she meets with community leaders, experts, and insiders to ask the...
WJR Interview with Laura Bonnell
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.
Former Detroit radio voice takes cystic fibrosis fight to Egypt
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 — her...
Cystic Fibrosis Awareness Month: Foundation raises money to help those with rare disease
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,...
Innovation – A Mother’s Story
Breakthrough cures for cystic fibrosis start by promoting science and innovation. https://www.youtube.com/watch?v=X9W4LLQrzBo
Michigan mom fighting for daughters with cystic fibrosis
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