Cystic Fibrosis Foundation4d
Copay Accumulators, Maximizers, and Alternative Funding Programs
In response to rising drug costs, some insurance plans are using strategies to contain costs that shift financial and administrative burdens to enrollees. These strategies, known as copay accumulator ...
Cystic Fibrosis Foundation3d
A New Era of CF Care: Possible Future Changes
New clinical guidance was created to help cystic fibrosis care centers care for people with CF as they face a widening range of health needs. The guidance covers how and when routine CF care is ...
Cystic Fibrosis Foundation5d
Cystic Fibrosis Foundation Position Paper: Redefining the Cystic Fibrosis Care Team
The Cystic Fibrosis Foundation assembled a panel to summarize available evidence, synthesize expert opinion, and provide clinical guidance for the composition of the care team at an accredited CF ...
Cystic Fibrosis Foundation5d
Cystic Fibrosis Foundation Position Paper: Redefining the Care Model
The Cystic Fibrosis Foundation organized a multidisciplinary committee to reevaluate key aspects of the current care model and considered potential modifications based on a widening range of health ...
Cystic Fibrosis Foundation12d
National Resource Center Award
With advances in cystic fibrosis care and the changing needs of the CF clinical research community, the Cystic Fibrosis Foundation intends to support National Resource Centers that will address and ...
Cystic Fibrosis Foundation15d
Cystic Fibrosis Foundation Leads the Way in Improving CF Newborn Screening Across the U.S.
Through grants, advocacy, and the development of a consensus guideline, the Cystic Fibrosis Foundation continues to advance ...
Cystic Fibrosis Foundation23d
How I’m Advocating for the CF Community as Miss Alabama
Becoming friends with Maddie, who has cystic fibrosis, inspired me to begin raising CF awareness and fundraising from a young age. Now I’m eager to make a larger impact with the platform I have since ...
Cystic Fibrosis Foundation21d
Why We Chose Not to Have Children
I imagine most people have vivid memories of the first date they went on with their spouse. Emily took me on a hike through Will Rogers State Park in Los Angeles. It was a perfect, blue-sky, Southern ...
Cystic Fibrosis Foundation16d
How We Found Strength and Support in the CF Community
This site contains general information about cystic fibrosis, as well as personal insight from the CF community. Opinions and experiences shared by members of our community, including but not limited ...
Cystic Fibrosis Foundation17d
My Journey to an Autism and ADHD Diagnosis
Have you ever wondered if there was something else going on with you? Something else affecting you that you were not aware of? Well, I felt that way. Ever since I was young, I have always struggled ...
Cystic Fibrosis Foundation1mon
Works by the CF Community 2024
Air of Optimism is a six-episode collection of interviews with my incredible friend Bernadette. Bern was born with cystic fibrosis in 1967, when very little was known about the disease. I have been ...