- Updated on August 31, 2023
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.
But you can get a Kindle version of this book from Amazon (see the text and image below);
or contact me (see the link at the bottom of the page) if you want to get the PDF book
(learn when and how you can get this PDF book).
How to pay for and open your books
You can find details on this page: How to pay and open your books. Short summary: use your credit card and open the book with your email address as the password.
If you are interested in this or other books that I wrote, but cannot afford it (e.g., you are unemployed, low-income, from non-western country, etc.), visit this page. It provides details of exchange that we can make: you promote health- or breathing-related content and get a book in exchange for that. I can help you to get nearly any of my books (with a few exceptions) for only 1 USD or even for free.
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.
You can click on the book image to visit the Amazon Kindle store and get this book now.
The main features of this book: