Mucoviscidosis or Cystic Fibrosis is a hereditary disease that affects mainly the exocrine glands of the lungs, liver, pancreas, and intestines, causing progressive disability due to multisystem failure.

Glutathione decrease in Cystic Fibrosis is noticeable in the fluid lining of the lungs, and also in the blood serum, red cells and elsewhere. This points to whole-body depletion as a result of oxidative stress. Inflammation is central to Cystic Fibrosis. It always precedes lung infection and lung infection almost always follows inflammation. Continued inflammation depletes antioxidants and Glutathione even more. The vicious circle goes on and on.


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