Halotherapy and Cystic Fibrosis

Cystic fibrosis, also known as mucoviscidosis, is an incurable, hereditary condition. Individuals with cystic fibrosis have glands in their bodies that secrete mucus that is thicker than normal. The role of this mucus is to eliminate waste products such as inhaled particles and bacteria. However, the mucus in patients with cystic fibrosis is thick.

Additionally, the mucus accumulates, leading to inflammation in the lungs. Breathing becomes more difficult as a result. Symptoms commonly associated with cystic fibrosis include breathlessness, shortness of breath, and coughing up thick, sticky mucus.