Cystic Fibrosis Treatment: Medical Success with More O2 in Cells
Each and every person with cystic fibrosis can eliminate all major symptoms of
the disease, if he or she gets up to 50 s for the body-oxygen test using cystic fibrosis treatment
methods outlined on this site.
mainstream treatments for cystic fibrosis have had dramatic improvement, one
treatment (the most important one) remains unknown to people with cystic
fibrosis and their care providers.
The crucial difference and advantage of this treatment is that it addresses the cause of
cystic fibrosis: low oxygen levels in body cells. Other therapies are mainly
targeted to address the effects of the CFTR gene in the lungs, GI tract and
other parts of the body. However, the smart approach is to prevent abnormal
expression of the CFTR protein.
Treatments of cystic fibrosis: Breathing Devices and Buteyko Lifestyle
official medical strategy that allows better survival of cystic fibrosis
patients is lung transplantation. However, most
patients are able to restore their lungs and health without transplantation.
The alternative medical therapy for cystic fibrosis is to restore normal
O2 in cells due to correct breathing parameters 24/7. Increased CO2 levels in lungs alveoli promotes
their repair. Improved work of the sweat glands and normalization of
chloride and water transport on mucosal surfaces makes mucus less thick
reversing the pathological effects discussed above.
Breathing normalization requires correction of all risk lifestyle factors
that intensify breathing. For patients with
cystic fibrosis, due to chronic
inflammation, sleep-related lifestyle factors are particularly important and
their morning CP (body-oxygen test results) is the main criteria of the health state achieved.
More details can be found in
Cystic fibrosis books.
In relation to
breathing exercises, the reduced breathing exercise of the
Buteyko method does gradually reduce their overbreathing and improve their
body-oxygen test results. However, the better options include the Frolov device,
Amazing DIY breathing device and Oxygen Remedy
therapy coupled with the Buteyko lifestyle program.
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.
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
You can click on the book image to visit the Amazon Kindle store and get this
The main features of this book: - over 160 relevant medical studies
- cutting-edge research articles about the cellular causes of cystic fibrosis
(low O2 pressure in cells of the body leading to the malfunction of ionic pumps that
transport ions and water across epithelial layers)
- causes of low body oxygenation (ineffective breathing patterns) confirmed by numerous studies
- crucial lifestyle factors that lead to ineffective breathing
- the outline of the program to restore normal breathing and normal body oxygenation