Cystic Fibrosis Reversal: Increase Body O2
While medical authorities
continue to deny that symptoms of cystic fibrosis
can be eliminated with those methods and techniques that increase body-O2 levels
up to the norms, hundreds of people with cystic fibrosis have been trained by Soviet and
Russian Buteyko breathing doctors and Western breathing practitioners to achieve
complete clinical remission and normal life: no lung or digestive symptoms with
normal life expectancy.
YouTube video: Trailer of the Amazon Kindle Book "Cystic Fibrosis Life Expectancy: 30, 50, 70"
Cystic Fibrosis Web Pages:
- As epigenetics (the modified and proven version of
genetics) teaches us, it is not genes, and not even environmental factors that
cause expression of genes. Genes are controlled by physiological factors within the
person. The CFTR mutation gene is triggered by cell
hypoxia. This page reviews medical studies that discovered
something that makes common sense: tiny pumps that transport
ions across mucosal layers in the respiratory and GI tracts require oxygen for
their normal work. Therefore, low body oxygen levels is the key factor that
allows the CFTR gene to be expressed leading to symptoms of cystic fibrosis.
- These cystic fibrosis symptoms, therefore,
correlate with parameters of automatic breathing in the dose-dependent manner.
Those who have faster and deeper breathing have less oxygen and worse symptoms. With approaching death or during last stages of CF, people have very high respiratory rates, critically low CO2 levels in the lungs and O2 in body cells (tissue hypoxia).
- Cystic fibrosis cause: Each and
every study that measured the breathing in people with CF found that they have
ineffective breathing, which reduces body O2
- Cystic fibrosis in lungs develops
according to laws of physiology and due to effects of hyperventilation. There
are documented injurious effects of hypocapnia (low CO2 levels) in the lungs. This casues damage to lung tissue and progression of respiratory symptoms.
- Cystic fibrosis prognosis
depends on one key factor: how heavy the person with CF breathes 24/7. More
breathing means less oxygen in body cells, suppressed immune system and development
of respiratory (cough, infetcions, more mucus, etc.) and digestive (smelly stool,
burping, belching, nausea, and so forth) symptoms.
- Cystic fibrosis life expectancy
can be normal if a person maintains normal body oxygenation 24/7. This requires breathing retraining with the goal to achieve normal automatic breathing day and night.
- Therapy for cystic fibrosis: treatment
with breathing retraining that includes breathing exercises, physical exercise with
nose breathing (all the time: in and out) and lifestyle changes described in other
sections of this site.
- The suggested cystic
fibrosis treatment is 100% natural since breathing is the central and
fundamental function of the human body. Modern treatment methods for cystic fibrosis
are currently missing the most important part: techniques that lead to breathing
normalization and improved O2 concentrations in body cells.
Cystic Fibrosis Defeated (PDF Book)
If you are interested in the PDF version of my Amazon book about CF, it can be
found here: Cystic Fibrosis book. There are also
Amazon Kindle and paperback versions of this book.
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