However, treatments can be used to reduce, if not nearly completely diminish, symptoms and minimize any other complications. Here are the conditional means:
Therapy: People with cystic fibrosis need a way to physically remove thick mucus from their lungs. This is often done by manually clapping with cupped hands on the front and back of the chest -- a procedure that's best performed with the person's head over the edge of the bed so that gravity helps clear the secretions.
Mucus-thinning drugs: make it easier to cough up the mucus; prescriptive or non-prescriptive drugs, which are used to lessen or reduce the stiffness of mucus, ameliorate lung function.
Medications: Antibiotics are prescribed to treat and prevent any lung infections. They may be swallowed in pill form, inhaled in a mist or delivered intravenously.
Bronchodilators: albuterol is applied through an inhaler or a nebulizer; this relaxes the muscles around the bronchial...
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