posted
Cystic fibrosis is a genetic disease. This means that people inherit it from their parents through genes (or DNA), which also determine a lot of other characteristics including height, hair color and eye color. Genes, found in the nucleus of all the body's cells, control cell function by serving as the blueprint for the production of proteins.
Cystic fibrosis is a life-threatening genetic disease that causes mucus to build up and clog some of the organs in the body, particularly the lungs and pancreas. When mucus clogs the lungs, it can make breathing very difficult. The thick mucus also causes bacteria (or germs) to get stuck in the airways, which causes inflammation (or swelling) and infections that lead to lung damage.
Mucus also can block the digestive tract and pancreas. The mucus stops digestive enzymes from getting to the intestines. The body needs these enzymes to break down food, which provides important nutrients to help people grow and stay healthy. People with cystic fibrosis often need to replace these enzymes with medicine they take with their meals and snacks, which helps them digest food and get proper nutrition.
The severity of cystic fibrosis symptoms is different from person to person. The most common symptoms are:
Very salty-tasting skin Persistent coughing at times producing phlegm Frequent lung infections, like pneumonia or bronchitis Wheezing or shortness of breath Poor growth/weight gain in spite of a good appetite Frequent greasy, bulky stools or difficulty in bowel movements Small, fleshy growths in the nose called nasal polyps
New research shows that the severity of CF symptoms is partly based on the types of CF gene mutations (defects) a person with the disease has. There are more than 1,000 different mutations of the CF gene.
Cystic Fibrosis is a multi-system disorder that causes the body to produce a thick mucus. The mucus accumulates primarily in the lungs and the digestive tract, resulting in chronic lung infections and poor growth. CF does not affect intelligence, howeer other defect may. The carrier rate for CF among all Caucasian individuals is approximately 1 in 25.
The CF carrier test has a detection rate of 97% in the Ashkenazi Jewish population.Posts: 4693 | From: Saturn | Registered: Apr 2012
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posted
This sort of answers the question of, why so few Ashkenazi Jews are able to compete at high level sports. They can't breath, and they are unable to process food adequately.
No wonder they have their daughters (and wives) stalk black athletes.
-------------------- Selenium gives real life and true reality Posts: 4693 | From: Saturn | Registered: Apr 2012
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posted
THIS PIECE OF SHIIT MAKES ONE RIDICULOUS STATEMENT AFTER ANOTHER! AND THE ONLY THING MISSING WITH THIS FOOL IS A BIG RED NOSE AND SOME LONG FLOPPY SHOES! ITS A CAUCASIAN THING! LOL
Nobody listens to you, you filthy degenerate piece of shiit!!! You should have been a brown stain on the sheets between your mothers legs, you reprobate monkey!
""Cystic fibrosis is a common genetic disease within the Caucasian (white) population in the United States. The disease occurs in 1 in 2,500 to 3,500 Caucasian newborns. Cystic fibrosis is less common in other ethnic groups, affecting about 1 in 17,000 African Americans and 1 in 31,000 Asian Americans""
posted
You are far too stupid to make the connection you pink assed stringy haired reprobate! What the data indicates is that Ashkenazi Jews ARE caucasian. Ashkenazi Jews are filthy stringy haired, pink assed culture theives just like YOU are! You are the SAME! Thats what the data indicates you low IQ reprobate!
THIS PIECE OF SHIIT MAKES ONE RIDICULOUS STATEMENT AFTER ANOTHER! AND THE ONLY THING MISSING WITH THIS FOOL IS A BIG RED NOSE AND SOME LONG FLOPPY SHOES! ITS A CAUCASIAN THING! LOL
Nobody listens to you, you filthy degenerate piece of shiit!!! You should have been a brown stain on the sheets between your mothers legs, you reprobate monkey!
""Cystic fibrosis is a common genetic disease within the Caucasian (white) population in the United States. The disease occurs in 1 in 2,500 to 3,500 Caucasian newborns. Cystic fibrosis is less common in other ethnic groups, affecting about 1 in 17,000 African Americans and 1 in 31,000 Asian Americans""
posted
Vansertimavindicated is simply pointing out that Narmertooth is exonerating the larger Caucasian racial class for their responisbility for cystic fibrosis and blaming the condition on the tiny minority within a much larger Caucasian diaspora aka the Jews. Therefore he urges you stop being a reprobate monkey with floppy shoes.
Posts: 42920 | From: , | Registered: Jan 2010
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Hey Van, you're supposed to be a Black radical, what do you care?
I mean, it sounds like you are a "Pink Boy" defending your race.
What gives?????
Someone's panties are in a bunch.
Mike, if you haven't figured it out yet, this Van character is one of the site employees. He's probably the one responsible for the recent ads and Google ad words updates.
Of course, he is an Ashkenazi Jew. There is no way Jews will allow this site to not be under their direction and control.
Isn't that incident rate of 97% of Ashkenazi Jews being CF carriers a fantastic figure!? Unbelievable!
Posts: 4693 | From: Saturn | Registered: Apr 2012
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posted
^ You are the employee. You tell me, but if your lips or fingers move, I'll know you're lying.
Ashkenazi Jewish Genetic Diseases Victor Center for Jewish Genetic Diseases, Philadelphia, PA
A number of genetic disorders occur more frequently in certain ethnic populations.In the Ashkenazi Jewish population (those of Eastern European descent), it has been estimated that one in four (25%!!!) individuals is a carrier of one of several genetic conditions.
These diseases include Tay-Sachs Disease, Canavan, Niemann-Pick, Gaucher, Familial Dysautonomia, Bloom Syndrome, Fanconi anemia, Cystic Fibrosis and Mucolipidosis IV.S ome of these diseases may be severe and may result in the early death of a child.
What are the diseases?
Tay-Sachs Disease is a condition where children develop normally until about four to six months of age. It is at this time that the central nervous system begins to degenerate. Individuals with Tay-Sachs Disease lack an enzyme called hexosaminidase (Hex A). The child loses all motor skills and becomes blind, deaf and unresponsive. Death usually occurs by the age of four. The carrier rate in the Ashkenazi Jewish population is approximately 1 in 25.
Canavan Disease is very similar to Tay-Sachs Disease, with normal development until age two to four months, followed by progressive loss of previously attained skills. Most individuals with Canavan Disease die by the age of five. An estimated 1 in 40 Ashkenazi Jews is a carrier for this disease.
Niemann-Pick Disease Type A is a disease in which a harmful amount of a fatty substance accumulates in different parts of the body. Failure to thrive and a progressive neurodegenerative course lead to death by three years of age. The carrier rate in the Ashkenazi Jewish population is approximately 1 in 90.
Gaucher Disease Type 1 (pronounced go-shay) is a variable condition, both in age of onset and in progression of symptoms. A painful, enlarged and overactive spleen, with anemia and low white blood cell count are usually the initial features of Gaucher Disease. Bone deterioration is a major cause of discomfort and disability. Approximately 1 in 14 Ashkenazi Jews is a carrier of this condition.
Familial Dysautonomia (FD) is a disease that causes the autonomic and sensory nervous systems to malfunction. This affects the regulation of body temperature, blood pressure, stress response, normal swallowing and digestion. An estimated 1 in 30 Ashkenazi Jews is a carrier of FD.
Bloom Syndrome is characterized by short stature, sun-sensitive facial skin lesions, an increased susceptibility to infections and a higher incidence of leukemia and certain cancers. The carrier rate is about 1 in 100 in the Ashkenazi Jewish population.
Fanconi anemia Type C is a disease associated with short stature, bone marrow failure and a predisposition to leukemia and other cancers. Some children may have learning difficulties or mental retardation. Approximately 1 in 89 Ashkenazi Jews is a carrier for this condition.
Mucolipidosis IV (ML IV) is caused by the accumulation of certain harmful substances throughout the body. Individuals with ML IV experience a range of levels of motor and mental retardation, with developmental delays often manifesting themselves as early as the first year of life. Other symptoms can be related to the eyes, such as corneal clouding, pseudostrabismus and retinal degeneration.
Cystic Fibrosis (CF) is a multi-system disorder that causes the body to produce a thick mucus. The mucus accumulates primarily in the lungs and the digestive tract, resulting in chronic lung infections and poor growth. CF does not affect intelligence. The carrier rate for CF among all Caucasian individuals is approximately 1 in 25. The CF carrier test has a detection rate of 97% in the Ashkenazi Jewish population.
posted
Dr. Mengele to you propose an ethnic cleansing program for the genetically defective?
Posts: 42920 | From: , | Registered: Jan 2010
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quote:Originally posted by Narmerthoth: ^ You are the employee. You tell me, but if your lips or fingers move, I'll know you're lying.
Ashkenazi Jewish Genetic Diseases Victor Center for Jewish Genetic Diseases, Philadelphia, PA
A number of genetic disorders occur more frequently in certain ethnic populations.In the Ashkenazi Jewish population (those of Eastern European descent), it has been estimated that one in four (25%!!!) individuals is a carrier of one of several genetic conditions.
These diseases include Tay-Sachs Disease, Canavan, Niemann-Pick, Gaucher, Familial Dysautonomia, Bloom Syndrome, Fanconi anemia, Cystic Fibrosis and Mucolipidosis IV.S ome of these diseases may be severe and may result in the early death of a child.
What are the diseases?
Tay-Sachs Disease is a condition where children develop normally until about four to six months of age. It is at this time that the central nervous system begins to degenerate. Individuals with Tay-Sachs Disease lack an enzyme called hexosaminidase (Hex A). The child loses all motor skills and becomes blind, deaf and unresponsive. Death usually occurs by the age of four. The carrier rate in the Ashkenazi Jewish population is approximately 1 in 25.
Canavan Disease is very similar to Tay-Sachs Disease, with normal development until age two to four months, followed by progressive loss of previously attained skills. Most individuals with Canavan Disease die by the age of five. An estimated 1 in 40 Ashkenazi Jews is a carrier for this disease.
Niemann-Pick Disease Type A is a disease in which a harmful amount of a fatty substance accumulates in different parts of the body. Failure to thrive and a progressive neurodegenerative course lead to death by three years of age. The carrier rate in the Ashkenazi Jewish population is approximately 1 in 90.
Gaucher Disease Type 1 (pronounced go-shay) is a variable condition, both in age of onset and in progression of symptoms. A painful, enlarged and overactive spleen, with anemia and low white blood cell count are usually the initial features of Gaucher Disease. Bone deterioration is a major cause of discomfort and disability. Approximately 1 in 14 Ashkenazi Jews is a carrier of this condition.
Familial Dysautonomia (FD) is a disease that causes the autonomic and sensory nervous systems to malfunction. This affects the regulation of body temperature, blood pressure, stress response, normal swallowing and digestion. An estimated 1 in 30 Ashkenazi Jews is a carrier of FD.
Bloom Syndrome is characterized by short stature, sun-sensitive facial skin lesions, an increased susceptibility to infections and a higher incidence of leukemia and certain cancers. The carrier rate is about 1 in 100 in the Ashkenazi Jewish population.
Fanconi anemia Type C is a disease associated with short stature, bone marrow failure and a predisposition to leukemia and other cancers. Some children may have learning difficulties or mental retardation. Approximately 1 in 89 Ashkenazi Jews is a carrier for this condition.
Mucolipidosis IV (ML IV) is caused by the accumulation of certain harmful substances throughout the body. Individuals with ML IV experience a range of levels of motor and mental retardation, with developmental delays often manifesting themselves as early as the first year of life. Other symptoms can be related to the eyes, such as corneal clouding, pseudostrabismus and retinal degeneration.
Cystic Fibrosis (CF) is a multi-system disorder that causes the body to produce a thick mucus. The mucus accumulates primarily in the lungs and the digestive tract, resulting in chronic lung infections and poor growth. CF does not affect intelligence. The carrier rate for CF among all Caucasian individuals is approximately 1 in 25. The CF carrier test has a detection rate of 97% in the Ashkenazi Jewish population.
That's the genetic price the Chosenites/Ice People pay for thousands of years of deliberate inbreeding. Not to mention the numerous mental health issues-paranoia,malignant narcissism and schizophrenia are quite common.
Posts: 433 | From: nairobi | Registered: Oct 2011
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posted
^ Yes. Would you want to breed with this? Would you wish your son to bring home a good diseased Jewish girl? With their goal of Integration, wide spread realization of their genetic defectiveness would cause serious opposition from those they wish (NEED) to integrate with.
Notice that all of the written collateral for these sites are written by Jewish editors. They neglect (deceive) into believing an illness such as CF is wide spread when it is in fact confined and distributed by Ashkenazi Jews.
No wonder New York Jews want to ban Internet access. Their secrets are getting out, and they have no way to stop it.
Posts: 4693 | From: Saturn | Registered: Apr 2012
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