Growing up, I always felt a bit different. But with CF consuming so much of my life, I didn’t have the chance to explore it until Trikafta® stabilized my health. That’s when I was finally able to get ...
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 ...
Through grants, advocacy, and the development of a consensus guideline, the Cystic Fibrosis Foundation continues to advance ...
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 ...
The Georgia Chapter of the Cystic Fibrosis Foundation welcomes you! Volunteers are the key to our success and the lifeblood of our organization. We have many opportunities for you to get involved.
Dear Members of the Maryland Prescription Drug Affordability Board: On behalf of the people living with cystic fibrosis in Maryland, the Cystic Fibrosis Foundation writes to provide comments on the ...
Dear Secretary Yellen and Secretary Becerra: On behalf of the nearly 1,700 people living with cystic fibrosis in New York, the Cystic Fibrosis Foundation appreciates the opportunity to submit comments ...
Although biological fatherhood after a lung transplant is certainly possible, many commonly prescribed anti-rejection medications have been known to cause birth defects. For this reason, some ...
On behalf of the Cystic Fibrosis Foundation, we write to express our concerns about third-party entities that contract with employer-sponsored health plans to import prescription drugs from outside ...
Dear Secretary Becerra and Administrator Brooks-LaSure: The Cystic Fibrosis Foundation thanks the Centers for Medicare and Medicaid Services (CMS) for the opportunity to respond to the Medicare and ...