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Cystic Fibrosis

Cystic Fibrosis (CF) is a hereditary disease affecting the mucus glands of
the lungs and other organs such as the pancreas and the liver.  Related
symptoms include excessively  thick and sticky mucus production which
clogs up the airways and makes it difficult to breathe which then creates a
place where bacteria can easily grow, causing serious damage to the
lungs.  Cystic fibrosis is one of the most common life-shortening
childhood-onset diseases.

Our
Soup A and Soup B and LC Balancer treatment is able to help CF
patients improve their breathing and reduce related symptoms.  With a
2-4 weeks treatment, patients should notice less phlegm and improved
breathing.  A minimum of 3 months of treatment is required to achieve
significant improvement in their condition  Based on limited case
observations, the improvement results can last approximately one year.