| 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. |
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| Sections | ||||||||||||||||||||||||||
| Home | ||||||||||||||||||||||||||
| Introduction | ||||||||||||||||||||||||||
| Description | ||||||||||||||||||||||||||
| Symptoms | ||||||||||||||||||||||||||
| What is CFTR? | ||||||||||||||||||||||||||
| The Diagnosis of Cystic Fibrosis | ||||||||||||||||||||||||||
| The Cystic Fibrosis Reference Page | ||||||||||||||||||||||||||
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| Chest Physiotherapy | ||||||||||||||||||||||||||
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| Proneb nebulizer, the machine used to give the inhaled medicine | ||||||||||||||||||||||||||
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