Cystic Fibrosis

Cystic fibrosis (CF) is a complex genetic disease that affects the lungs, digestive system, and other organs by causing thick, sticky mucus to build up. Managing CF requires a combination of medications, including inhaled therapies, antibiotics, pancreatic enzyme replacements, and new targeted treatments called CFTR modulators. Pharmacists play a vital role in helping patients navigate these complex regimens by providing education on how and when to take their medications, proper inhaler and nebulizer techniques, and how to store and handle sensitive drugs.

Because cystic fibrosis treatments are often intensive and lifelong, pharmacists work closely with patients to ensure that therapies are as effective and manageable as possible. They monitor for side effects like liver issues, drug interactions, and adherence challenges, offering guidance and encouragement every step of the way. Pharmacists also assist with access to specialty medications, help coordinate refills, and support patients through insurance or assistance programs. By partnering with pharmacists, individuals with cystic fibrosis can better control their symptoms, prevent complications, and live fuller, healthier lives.