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Supporting Patients with Cystic Fibrosis

Cystic fibrosis is a genetic condition that affects multiple organ systems, but has greatest impact on the lungs and the digestive system. It is Canada’s most common fatal genetic disease affecting young children and adults.

Approximately one in every 3,600 children in Canada is born with cystic fibrosis. 

Cystic fibrosis does not have a cure but medical advances have radically changed and extended the lives of people with cystic fibrosis. In the 1960s, the median (average) age of survival for people with cystic fibrosis in Canada was 4 years of age. In 2019, the median age of survival was 57 years and there are now far more adults with cystic fibrosis than children.  

The severity of cystic fibrosis differs between individuals. Most cystic fibrosis patients experience persistent and ongoing lung infections, which result in progressive destruction and loss of lung function that threaten their lives. 

Cystic fibrosis is no longer just a childhood disorder. It is very much an expanding complex adult disease with more adult cystic fibrosis patients than pediatric in B.C. We expect the adult cystic fibrosis population to continue growing as management becomes more patient specific.

Screening newborns for cystic fibrosis

Cystic fibrosis newborn screening and early introduction of care in a child's life help manage the condition and prevent or reduce later complications. Advances in management of the disease have led to better patient outcomes and increased life expectancy. These advances include some patients receiving lung transplants later in their lives.

Newborn screening is done on day two of life for all babies born in B.C. and the Yukon. This screening has dramatically reduced the age of diagnosis from 3 - 4 years of age to within the first month of life. As a result, care has shifted from being reactive and dealing with active disease to being proactive and preventing disease progression.

Screening process

The screening process for cystic fibrosis involves three steps:

  1. Measure the level of a protein in the baby's blood
  2. Perform a DNA test that looks for changes (variants) in one of the baby's genes
  3. Perform a sweat test to confirm if the baby has cystic fibrosis by measuring how much salt is in the baby's sweat. A large amount of salt in sweat indicates cystic fibrosis.

For more information about screening and testing, visit Perinatal Services BC: Newborn Blood Spot Card Screening

Mental well-being

Keeping healthy while living with cystic fibrosis means taking care of yourself emotionally as well as physically. Attention to your mental health is a part of cystic fibrosis care in British Columbia. Your cystic fibrosis teams are there to listen to you and help find the best supports and resources available to promote your mental well-being.

Feelings of sadness, anger and frustration are common, and there are options to help you with them. Do not hesitate to connect with your cystic fibrosis team about emotional challenges and for assistance. See the list of clinics below for contact information.

Clinics providing specialized care services

Care that is focused on people with cystic fibrosis is available at four B.C. cystic fibrosis clinics.

BC Children's Hospital - Cystic Fibrosis Clinic
K3-189, 4480 Oak Street
Vancouver, BC V6H 3V4 (Map)

Phone: 604-875-2146

Toll Free: 1-888-300-308 (Local 2146)


Victoria General Hospital - Pediatric Clinic
1 Hospital Way
Victoria, BC V8Z 6R5 (Map)
Phone: 250 727 4450

St. Paul's HospitalAdult Cystic Fibrosis Clinic
8B Providence Wing - 1081 Burrard Street
Vancouver, BC V6Z 1Y6 (Map)
Phone: 604-806-8522


Royal Jubilee Hospital – Adult Cystic Fibrosis Clinic
Royal Block - RB 4351952 Bay Street
Victoria, BC V8R 1J8 (Map)
Phone: 250-370-8111 extension 13395

SOURCE: Supporting Patients with Cystic Fibrosis ( )
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