The Treatment of Cystic Fibrosis
Cystic Fibrosis is an incureable disease as of now.  However there are many treatments that improve the quality of life and life span for PWCF.

 
CHEST PHYSIOTHERAPY     
    -helps to loosen lung
     mucus.  
    -stimulates coughing
    -usually done two or more
     times a day.

   
ANTIBIOTICS
 
    -used to treat lung
     infections
    -give through an IV in the
     vein, orally, or in a mist
     that is inhaled.
 
Pulmozyme
   -thins mucus
    -reduces number of lung
     infections.
    -improves lung function

  
TOBI(tobramycin solution for
                inhalation)


    -
improves lung function
    -reduces number of hospital stays
    -can be given in more concentrated
     doses right to the infection.

DIGESTIVE MANAGEMENT

    -eat a well balanced diet high in
     protein and calories.
    -children need to eat 150% of the
     daily amounts of food because of
     their slower growth rate.
    -take multivitamins and fat-soluble
     vitamins like A, D, E, and K.
    -take enzymes before every meal
     and snack to digest food.
    -some PWCF with more severe
     digestive problems may have to be
     fed through a tube in the stomach
     or a vein.
Sections
Home
Introduction
Description
Symptoms
What is CFTR?
The Diagnosis of Cystic Fibrosis
The Cystic Fibrosis Reference Page
Chest Physiotherapy
Proneb nebulizer, the machine used to give the inhaled medicine