Overview

The cystic fibrosis program at Children’s Minnesota ranks among the top 10 programs nationally in key outcome measures by the Cystic Fibrosis Foundation Patient Registry.

Services offered

• 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

Refer a patient

• Patient Name
• DOB
• Referring provider
• Primary care provider
• Insurance information
• Diagnosis and isolation requirements
• Special needs requirements

Related specialty

• Genetics/Genomics