Table of Contents


Cystic Fibrosis (CF)

What is CF?

Cystic fibrosis (CF) is a genetic condition that causes progressive respiratory and digestive system damage. Someone with CF has thick, sticky mucus, versus “healthy” slippery mucus, which builds up in their system. That build-up can clog airways, trapping bacteria, leading to breathing problems, frequent infections, lung damage and respiratory failure. Additionally, the thick mucus prevents the release of digestive enzymes, making it difficult for patients to absorb necessary nutrients. Cystic fibrosis typically occurs in one in 2,500- 3,500 Caucasian newborns in the US. In other ethnicities, it is even more rare, occurring in one in 17,000 and one in 31,000 African Americans and Asian Americans respectively.

What are the symptoms of CF?

Cystic fibrosis symptoms typically manifest in the respiratory and digestive systems. Those symptoms include:
  • Persistent coughing and wheezing
  • Shortness of breath
  • Difficulty exercising
  • Frequent lung infections
  • Stuffy nose
  • Difficulty gaining weight
  • Constipation
  • Salty-tasting skin
  • Male infertility
  • Exercise intolerance

What causes CF?

Cystic fibrosis is a recessive, genetic disorder, meaning both parents have to carry at least one copy of the defective gene for the child to inherit it. The genetic mutation affects the protein that regulates salt movement. This results in respiratory, digestive and reproductive issues. The genetic mutation also varies in severity.

How is CF diagnosed?

Cystic fibrosis is usually diagnosed at birth as newborn screening in the US is standard. Screening newborns for CF includes the following tests:
  • Blood sampling for high levels of immunoreactive trypsinogen (IRT)
  • Genetic testing for specific defects in the gene that causes CF
  • Sweat tests, conducted at two weeks old, for saltier than normal sweat

What are the treatments for CF?

Cystic fibrosis treatment aims to prevent or control infections, removing mucus from the lungs, preventing intestinal blockage and providing nutrition. CF treatment includes:
  • Antibiotics
  • Anti-inflammatory medications
  • Meds that help cough up mucus
  • Bronchodilators
  • Pancreatic enzymes and devices to help add these back in
  • Exercise therapy
  • Chest physical therapy
  • Vest therapy
  • Vertex’s “triple combo treatment” option, coming soon!
  • Surgery to:
    • Remove bowel blockages
    • Remove nasal polyps
    • Replace lungs (lung transplant)
    • Place a feeding tube

Where can I find out more about CF?

Cystic Fibrosis (CF) Articles

We believe rare disease patients are people, not a diagnosis. Through education, awareness and some humor, we help patients, caregivers and support persons by providing relevant and often inspirational news and stories.
Our goals are to share stories, cultivate strong community, provide the latest medical findings, connect people and pioneer production of patient worthy information. Help us attain these goals by telling us a little bit about yourself!

© Copyright Patient Worthy

Close Menu