Cystic fibrosis

• What is cystic fibrosis primarily associated with?

  Genetic disease affecting mucus production
• How does cystic fibrosis affect the body?

  It affects cells producing mucus, sweat, and digestive juices
• What are the consequences of cystic fibrosis on breathing?

  It can cause breathing problems and digestive issues
• What symptoms are associated with cystic fibrosis?

  Constant cough, wheezing, and shortness of breath
• What digestive issues can arise from cystic fibrosis?

  Constipation, stomach pain, and bloating
• What treatments are available for cystic fibrosis?

  • CFTR modulators to improve lung function
  • Antibiotics for infections
  • Steroid medications
  • Physiotherapy for mucus clearance
  • Nutritional support and dietary management
• What role do CFTR modulators play in cystic fibrosis treatment?

  They help the lungs work better
• Why are antibiotics used in cystic fibrosis treatment?

  To treat lung infections caused by bacteria
• How does physiotherapy assist cystic fibrosis patients?

  It helps clear mucus from the lungs
• What is the purpose of dietary management in cystic fibrosis?

  To provide nutritional support for better health
• What diagnostic test is commonly used for cystic fibrosis?

  Blood testing for carrier status
• What does carrier testing for cystic fibrosis involve?

  Testing blood to identify genetic mutations
• How does blood testing help in diagnosing cystic fibrosis?

  It identifies mutations in the CFTR gene