The respiratory and digestive systems are the two systems in the body most affected by cystic fibrosis, and are the most likely to require medication. These can be taken by mouth, given by IV (intravenously), or inhaled using a nebulizer.
Cystic fibrosis patients who are well-nourished grow better, have better lung function, and live longer than patients with poor nutrition.
- Special Programs
- COPD Clinic
- Cystic Fibrosis
- Interventional Pulmonology
- Neuromuscular Clinic
- Pulmonary Function Testing Lab (PFT)
- Pulmonary Rehabilitation Program (DHMC)
- Clinical Trials
- Our Team
- More Appointment Information