Cystic Fibrosis (CF), Mucoviscidosis

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Cystic Fibrosis (CF), also known as Mucoviscidosis, is an autosomal recessive genetic disorder affecting most critically the lungs, and also the pancreas, liver, and intestine. It is characterized by abnormal transport of chloride and sodium across an epithelium, leading to thick, viscous secretions.

The name cystic fibrosis refers to the characteristic scarring (fibrosis) and cyst formation within the pancreas, first recognized in the 1930s. Difficulty breathing is the most serious symptom and results from frequent lung infections that are treated with antibiotics and other medications. Other symptoms, including sinus infections, poor growth, and infertility affect other parts of the body.

CF is caused by a mutation in the gene for the protein cystic fibrosis transmembrane conductance regulator (CFTR). This protein is required to regulate the components of sweat, digestive juices, and mucus. CFTR regulates the movement of chloride and sodium ions across epithelial membranes, such as the alveolar epithelia located in the lungs. Although most people without CF have two working copies of the CFTR gene, only one is needed to prevent cystic fibrosis due to the disorder's recessive nature. CF develops when neither gene works normally (as a result of mutation) and therefore has autosomal recessive inheritance.

CF is most common among Caucasians; one in 25 people of European descent carries one allele for CF. The World Health Organization states that "In the European Union, 1 in 2000-3000 newborns is found to be affected by CF".
Individuals with cystic fibrosis can be diagnosed before birth by genetic testing, or by a sweat test in early childhood. Ultimately, lung transplantation is often necessary as CF worsens.

Please have a look at the following:

For all illnesses that are in any way linked to the (quick) degradation of cells the first and foremost TEST should be in the right direction of the (actual) underlying causes.
As long as the body is exposed to EMF/EMR and/or geopathic zones, it will respond to by degrading - and even serious problems like genetic breaks of the double helix of the DNA/RNA.

You will find that when the person is moved out of the affected zone, the body can cope with the problems much better and finally get enough chance to start repairing the problems, as the body has an effective self-healing mechanism, as the said radiation is no longer affecting it. This is the time when medication can be adjusted and reduces as well as the treatments and therapy adjusted accordingly.
- Please do not adjust the medication yourself !!

This website is not a Self Help Guide, but for training and as guideline for professionals working in the Environmental and/or Health Fields !
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Cystic Fibrosis
Cystic Fibrosis & Geopathic Stress
Cystic Fibrosis & Electro Stress
Cystic Fibrosis & EMF
Cystic Fibrosis & EMR
Cystic Fibrosis & EHS
Cystic Fibrosis & Electro Sensitivity
Cystic Fibrosis & Electromagnetic Hypersensitivity
Cystic Fibrosis & Aspartame
Cystic Fibrosis & Fluoride
Cystic Fibrosis & Prozac
Cystic Fibrosis & Ritalin
Cystic Fibrosis & Video Games
Spastic Colon & Geopathic Stress
Spastic Colon & Electro Stress
Spastic Colon & EMF
Spastic Colon & EMR
Spastic Colon & EHS
Spastic Colon & Electro Sensitivity
Spastic Colon & Electromagnetic Hypersensitivity


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