Daily Life with Cystic Fibrosis: Treatments

Despite the very fact that there's presently no cure for Cystic Fibrosis, there are treatments that improve patients’ quality of life and expectancy. In fact, children with CF tend to stay healthy once medicated till adulthood, however as lung function declines, the patient usually becomes disabled. 

Totally different therapies address the varied symptoms, and not all patients would like every type of medication, however, the common feature remains that every patient needs daily and demanding treatments.

Advancements created in recent years have to be compelled to result in a rise in patients’ life expectancy from 10 years to 37.5 years, on average. Some live to be much older.

Lung therapies include antibiotics for prevention and treatment of lung and sinus infections like inhalers, DNAse enzyme therapy, inhaling mists of high salt concentrations, contagious diseases like flu and bacterial vaccines, Oxygen therapy, percussion vests, and in some cases lung transplant.


Bowel therapies are also necessary to extend the absorption of nutrients. Patients usually place their full confidence in exocrine gland enzymes to assist in digestion and absorption of fats and proteins; vitamin supplements like A, D, E and K; and anti-constipation drug.


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