Cystic Fibrosis

Cystic Fibrosis (CF) is an inherited disease characterized by abnormalities in the body’s salt, water, and mucus-producing cells. While CF is a chronic and progressive condition, advancements in treatment have significantly extended life expectancy.

Many children are now diagnosed with cystic fibrosis (CF) through newborn screening programs before symptoms appear. Common symptoms of CF include:

Salty-tasting skin
Chronic respiratory symptoms such as wheezing, cough, and colored sputum
Lung infections
Poor growth
Constipation
Greasy and bulky stools
Respiratory symptoms, including cough, wheezing, and breathing difficulties

Specific treatment for cystic fibrosis (CF) is tailored to your child’s health condition and may include:

Exercise
Medications such as bronchodilators and anti-inflammatories
Antibiotics
Chest physical therapy

Management of digestive problems associated with CF may involve:

A suitable diet
Pancreatic enzymes to aid digestion
Vitamin supplements
Treatments for intestinal obstructions

Each child’s treatment plan is individualized based on their specific needs to manage the disease effectively and improve their quality of life.

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