Cystic Fibrosis Book: Triumph With Higher Body O2 (PDF Book)
Here is the PDF version of this book about causes of cystic fibrosis and its successful treatment therapy developed by Soviet and Russian doctors. Info and links to Amazon Kindle and paperback books are provided below.
The therapy is approved by the Russian Ministry of Health. It is based on addressing the key cause of cystic fibrosis: low O2 levels in body cells caused by ineffective breathing patterns that have been found in each medical study that measured breathing parameters in adults and children with cystic fibrosis.
Restoration of normal breathing parameters leads to normal O2 transport and elimination of main symptoms of cystic fibrosis and normal life expectancy.
Any person with the CFTR gene is going to have normal life and normal health, if he or she gets over 50 s for the body-oxygen test 24/7.
You can read first 30 pages of this PDF book here: Cystic Fibrosis. The price of this PDF book is 5.37 USD.
Since this book is enrolled in special KDP Select program on Amazon.com,
it is temporary not available here in PDF form.
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Kindle Book - Cystic Fibrosis Life Expectancy: 30, 50, 70, ...
Thick mucus is the main culprit in cystic fibrosis. It is caused by the abnormal transport of ions (e.g., Na and Cl) and water across the mucosal layers. This thick mucus starts to harbor pathological bacteria and cause GI and respiratory infections.
However, you probably do not know that the transport of ions and the active transport of water is controlled by O2 levels in cells. If O2 is low, then the transport of chemicals is going to be defective. This effect was found in all people. The CFTR gene just makes the whole picture worse.
Therefore, cystic fibrosis develops when tiny pumps that transport chemicals to form mucus have too little oxygen. If you have normal O2 in cells, you will not develop CF symptoms and problems even if you have the CFTR gene.
It makes common sense that oxygen is the key factor in the active transport of ions and water across epithelial layers. Apart from this, low body O2 suppresses the immune system making respiratory and GI infections much worse.
Therefore, the solution to cystic fibrosis is to restore normal body O2 content 24/7.
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February 2017 update. New breathing students with terminal conditions (end-stage disease) are accepted on CureEndStageDisease.com with Dr. Artour's Triple Money-Back Guarantee.
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