Two brothers and two friends take on and wi, an 80-mile Atlantic paddleboard challenge in an effort to provide support for ...

Most children with CF treated at a San Francisco CF clinic did not receive CF liver disease screening in accordance with current guidelines.

Dr Uta Hill discusses the advancing clinical landscape of cystic fibrosis, with insight into the game-changing CFTR modulator ...

Metro Cystic Fibrosis Foundation grants Cleveland Clinic $5M for lung transplant research Published: May. 29, 2025, 10:31 a.m.

Discover how cystic fibrosis genetics affect inheritance patterns and symptom. Learn about CFTR mutations, testing options, and emerging genetic therapies.

But despite decades of life-changing breakthroughs, treatment for cystic fibrosis still has a long way to go. CFTR modulators only work for those with specific mutations. For the remaining 10% to 15% ...

Cystic fibrosis is the most common inherited life-threatening condition in the UK. It affects the ability of cells to transport salt and water which can cause sticky mucous to build up.

Cystic fibrosis might sound intimidating, but tremendous advances in treatment have transformed what it means to live with this diagnosis. Children born with CF today face a very different future ...

Newly uncovered mechanism could drive next-gen cystic fibrosis treatments Date: March 13, 2025 Source: The Hospital for Sick Children Summary: Protein clustering mechanism on the cell membrane ...

Cystic fibrosis (CF) is a progressive genetic disease that adversely affects a person's lungs, pancreas and other vital organs, says Dr. Michael Boyle, president and CEO of the Cystic Fibrosis ...

Today, cystic fibrosis — a genetic disorder that causes a buildup of thick, sticky mucus that can damage organs, especially the lungs — has become a centerpiece of my family’s lives, sending ...

From a young age, Emily Naismith watched her peers die from cystic fibrosis. The drug Trikafta gave her a future but she says forming a new identity has been complex.