The wait times in our emergency departments are longer than usual due to illnesses like RSV and the flu. View our estimated ED wait times and learn more about where to get care for your sick child.

Overview

The cystic fibrosis program at Children’s Minnesota ranks among the top programs nationally in key outcome measures by the Cystic Fibrosis Foundation Patient Registry.

  • Comprehensive diagnosis, treatment and management of cystic fibrosis
  • Nutritional status evaluation and education.
  • Genetic counseling and newborn screening interpretation
  • Sweat chloride testing
  • Pulmonary function testing
  • Supportive counseling for patients and families adjusting to new diagnosis or chronic illness
  • Information and referral to hospital and community resources
  • Education from multidisciplinary team that includes: respiratory therapists, dietitians, a social worker, genetic counselors and physical therapists
  • Referral and collaboration with multidisciplinary care clinics including:
    • Endocrinology
    • ENT
    • Genomics
  • Opportunities to participate in research studies
  • Parent-lead support group
  • CF Family Advisory Council
  • Patient Name
  • DOB
  • Referring provider
  • Primary care provider
  • Insurance information
  • Diagnosis and isolation requirements
  • Special needs requirements
  • Patient’s city and state

24/7 access to referrals, consults and admissions. Learn more.
Intended only for health care providers. Patients, please contact your doctor directly.