Magnesium Inhalation and Cystic Fibrosis

Cystic fibrosis, also known as mucoviscidosis, is an incurable, hereditary condition. In people affected by cystic fibrosis, the glands in the body produce mucus that is thicker than normal. The mucus secreted by these glands is intended to expel waste products such as inhaled particles and bacteria. However, in patients with cystic fibrosis, the mucus is thick.

Furthermore, the mucus accumulates, leading to inflammations in the lungs. Breathing also becomes more difficult. Wheezing, shortness of breath, and coughing up thick, sticky mucus are the most common symptoms of cystic fibrosis.