According to the Cystic Fibrosis Foundation Patient Registry, more than 30,000 people are living with cystic fibrosis in the United States with approximately 1,000 new cases diagnosed each year.

What is cystic fibrosis?

Cystic fibrosis (CF) is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time. In order for someone to develop CF, they must inherit two copies of the defective CF gene – one copy from each of their parents. Both parents must have at least one copy of the defective gene in order for their child to develop CF.

Diagnosis

It is a multistep process to diagnose cystic fibrosis. It typically includes a newborn screening, a sweat test, a genetic or carrier test, and a clinical evaluation. More than 75% of people with CF are diagnosed by age 2 but some are diagnosed as adults.

Symptoms

It is a complex disease, and the types and severity of symptoms can vary greatly from person to person. Some symptoms include:

Very salty-tasting skin
Persistent cough, at times with phlegm
Frequent lung infections including pneumonia or bronchitis
Wheezing or shortness of breath
Poor weight gain despite a healthy appetite
Frequent greasy, bulky stools or difficulty with bowel movements
Male infertility

Treatment

Each day, people with CF complete a combination of the following therapies:

Airway clearance to help loosen and get rid of the thick mucus that can build up in the lungs
Inhaled medicines to open the airways or thin the mucus
Pancreatic enzyme supplement capsules to improve the absorption of vital nutrients
Individualized fitness plan to help improve energy, lung function, and overall health
CFTR modulators to target the underlying defect in the CFTR protein

Raising Awareness

Visit the Cystic Fibrosis Foundation website to learn more about how you can help raise awareness and get involved!

What is cystic fibrosis?

Diagnosis

Symptoms

Treatment

Raising Awareness

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