It is possible to reverse symptoms and
stages with breathing retraining and the Buteyko method by slowing
down one's automatic breathing and, thus, improving oxygen delivery
in the lungs and body cells to prevent development of cystic
fibrosis. Video URL link: treat cystic fibrosis with Buteyko breathing.
In this video, Dr. Artour Rakhimov and
Volker Schmitz discuss the relation of cystic fibrosis and breathing
retraining. Cystic fibrosis is viewed as being genetic, but people
with this health condition are realizing that they can improve their
quality and quantity of life if they apply lifestyle changes.
Historically, it is known that life expectancy was very low for
people with CF. Children would die at a very young age. People with
CF have very salty skin because they are not able to retain the salt.
Previously, this would indicate that children would die.
Recently doctors discovered that people
with CF have a mutation in their body's chemicals. This mutation
does allow the body to effectively transport ions in different
compartments of the body. People with CF have two common
abnormalities that develop. Dr. Artour Rakhimov had students with
CF. They were successfully able to recover from their health
condition and maintained being healthy with breathing retraining.
Breathing retraining increases body-oxygen levels. This allows
people having abnormal genetic factors to function closer to the
medical norm. This
depends on how well people recover.
Two
systems suffer the most for people with CF. They include the
respiratory system because of the transport of ions. People
with CF have their mucus grow and become too thick in their airways.
From this, they are going to be prone to more respiratory
infections. The most common cause of death for people with CF
relates to respiratory failure. This is from accumulating too much
bacteria that comes from the mucus harbouring pathological bacteria.
Many respiratory infections take place for people with CF.
Another type of abnormality that takes
place relates to digestion. It causes an inability to create a mucus
layer in the digestive tract. People with CF have their mucus in the
digestive tract become too thick. This causes an abnormal appearance
of too much bacteria and infections in the digestive tract.
These abnormalities can be solved when
people practice breathing retraining. It is used in addition to
standard medical techniques. 50 years ago the common expectancy of
living for people with CF was 10 to 15 years. While currently, it
has improved to 40 to 45 years of age. It was a huge increase due to
achievements of medicine. Doctors are now able to take out excess
mucus from the lungs. They can provide medication for the lungs and
the digestive system. For the digestion system doctors provide
digestive enzymes. These enzymes allow people with CF to function
better.
Web pages:
- Cystic Fibrosis Symptoms/Stages
Correlate with Cell Oxygen Levels:
http://www.normalbreathing.com/cystic-fibrosis-symptoms.php
.
- Cystic Fibrosis in Lungs Is
Reversible:
http://www.normalbreathing.com/d-cystic-fibrosis-in-lungs.php
.
The YouTube URL of this video from
NormalBreathing Channel by Dr, Artour Rakhimov is:
https://www.youtube.com/watch?v=yZr76yrX6mc /.
The video features Volker Schmitz
(Buteyko practitioner from Hamburg, Germany) and Dr. Artour Rakhimov.
Dr. Artour is an Amazon writer, breathing teacher, and the author of
NormalBreathing.com.
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