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Post by crystalriver on Mar 22, 2009 13:28:12 GMT -5
Here is a doozy--albeit it is from a religious perspective--I still think I can post it here without offending.
Here is the deal ---been looking for answers about blood there is not much---this article posts a twist of what I thought (with this subject) I have had many questions and think it could hold the answer for healing, health and cure. Hopefully others will pitch in and help with this line of thought.
Poisoning of Mankind: Blood Types, Copper Deficiency, Evolution Theory, Global Warming, Shroud of Turin & Illuminati
The abomination that causes desolation (depopulation) spoken of through the prophet Daniel
The Blood Typing Farce: Nearly 95% of the population, who have blood type ‘O’ and ‘A’ which are the thinnest blood and lowest blood volume, and blood type ‘B’, have copper deficiency, due to slow poisoning from blood thinners, alkalizing chemicals, copper binders, and copper antagonists, that they have completely and thoroughly saturated the food and food chain with, in addition to wireless radiation poison which is the quickest and most effective method for depleting copper, and is one of the primary methods for expediting our death. These poisons have altered and damaged the proteins/DNA of the blood and other tissues of the body, with the damage (and deficiency) passing down through the generations. Starting in 1996, the copper depletion rate was significantly increased and coincides with the onslaught of GMO foods, chemtrails, wireless technology, increase of diseases and debilitating symptoms, and decreasing lifespan. Copper is essential in the formation of normal healthy proteins, that is, normal amino acid sequences, in that it provides a balanced pH state for the blood and tissues, maintaining the proper concentration of hydrogen for forming the bonds in normal protein synthesis. Copper is acidic at a pH of 5.5 and is important in providing a balance of the numerous alkaline and acidic nutrient minerals. A balanced pH of 7.00 is present in blood type AB, which is the only normal blood type, while the pH of the alkaline blood types (A/O) was set up to 7.54 by 31 March/1 April 2005 and the pH of the acidic blood type B decreased further by the same date. Deaths increase as blood pH moves further away from 7.00. The desired death rate was set up by increasing the pH level of the alkaline blood types to 7.54, while decreasing the pH of the acidic blood type. Consequently, due to unbalanced pH levels, the vast majority of the population has malformed proteins and is missing normal proteins, as can be evidenced just in the blood properties as noted in different “blood types”. The blood types of A, B, and O are missing the normal (clotting) proteins; type A is missing B, B is missing A, and O is missing both A and B proteins. The “Rhesus Factor” (D-protein) is a probable malformed or variant A or B protein, resulting from insufficient copper levels. The blood type AB is balanced and therefore does not carry the malformed “Rhesus Factor” protein as found in the other blood types, thus, only AB negative blood is possible.
“The life of a creature is its blood.”
Population Closer to 200 Million: Reporting shows increase of deaths in the age groups of 45-54 and 55-64 years of age and decreases in the ages 65 years and older. More interesting, a huge discrepancy is noted in raw death number totals (one state in 2008) versus the “official” death numbers coming from the national level. The raw data is consistently 65-70%, or about two thirds of the “official” numbers. These are indicators that not only is the population not increasing in numbers as we have been led to believe, but is in fact now decreasing. True population numbers and current average lifespan are being concealed.
Blood pH Levels Background: The A-protein is alkaline as it is made up of more of the alkaline amino acids. The B-protein is acidic with more of the acidic amino acids. Although no specific range was found for type B blood, a person with diabetes is known to have a pH of 6.8, and some references document a pH range of human blood of 6.8 – 7.7, which would encompass the type B blood at the acidic end. When the A and B proteins are present together, as in Type AB blood, the pH of the blood is in a balanced state or approximate pH of 7.00. A balanced pH is also indicative of the nutrient minerals being in balance. Individuals with blood types A and O have a propensity to carry a blood mineral/metal imbalance toward the alkaline, while those with blood type B have a propensity to carry a blood imbalance toward acidic minerals/metals, all cases due to copper deficiency.
With type O blood, the alkaline level is so high that even the normal alkaline A-protein cannot be formed, and thus, is missing. According to numerous references and texts, at least up to about the mid 1970’s, the pH range for blood in the US was 7.35 – 7.45, with an average pH of 7.40. (Some reference books document a pH above 7.45 is indicative of severe alkalosis and is fatal.) Assuming Type B is acidic and Type AB is at or near 7.00, this range apparently included type A’s and O’s, which comprised 86% of the US population. The same dated texts and references document the percentages of type O as 45 % and type A as 41%, in the US population. It is interesting to note that a clinic in the US recently measured blood pH samples of 259 clients, from January 2004 to June 2005, and found the average pH to be significantly higher at 7.54, as of December 2004 – March 31, 2005. (Ref 12) If assuming only Type A’s and O’s were recorded in the samples, and O’s are the higher pH, this data may indicate that type O blood in the US could be currently near the 7.60 pH level. Additionally, many individuals with type A blood may change over to type O blood if the pH has increased to a point or range at which the A protein disappears.
Fraudulent History & Evolution Theory: “In 1900, Karl Landsteiner, a physician in Vienna, Austria, noted that the sera of some individuals led to the ‘discovery’ of ABO blood types.” (Ref 1) Essentially, he noted a distinct difference in viscosity/pH level or the clotting factors of blood. Later on his students “discovered” the AB blood type. Then, in 1940, the “Rhesus Factor” (D-Protein) was detected. In truth, there is only one blood type among humans, and that is type AB. Anything else is a mutation due to copper deficiency. As each generation has been deprived and depleted of copper, the mutated genes/proteins have become weaker. These mutations of the blood and other structures that have manifested over the generations, is used as supporting evidence for the fraudulent “Evolution Theory”. The mutated blood types of A, B, and O and the presence of the “Rhesus Factor” are used to establish a lineage/correlation of the vast majority of the human population to the man-apes. This correlation does not exist, since humans are created solely with blood type AB, and the man-apes do not carry this blood type.
Blood types and DNA are used to establish fraudulent migratory patterns of different populations around the world. The higher the percentage of type B blood in a given population correlates to a more severe copper deficiency in that population. This is because the type B blood has a longer lifespan on average than the alkaline blood types of A and O. In other words the alkaline blood types are dying off much more quickly than the blood type B, and in fact are in the process of moving toward extinction, followed closely by blood type B, all because of copper deficiency. It should be mentioned here that according to Ref 2, in 1959 20% of Black Americans had type B blood and Caucasians had 10% type B, different severity levels of copper deficiency, indicating that Blacks may have been copper deficient (poisoned) before being brought over on slave ships. (One last note is, there were a small number of populations that contain only alkaline blood types, but these populations may have been manipulated by intentional extraction of the type B blood.)
We were all created with type AB blood, with normal viscosity/balanced pH level with normal protein structures. Through a misinformation campaign the “official” history is that blood type AB is the newest and rarest, emerging 500-1000 years ago, while blood type O is the oldest. It is interesting to note that the Shroud of Turin, the suspected burial cloth of Jesus, has blood type AB. The cloth has been dated to about the first century AD, and as of yet has not been disproved.
Copper Functions: Copper maintains mineral balance, thus a balanced pH with normal blood viscosity, by functioning as the primary antioxidant in the body. When the blood is of normal viscosity with optimal blood flow, the blood is able to rid the body of toxic metals, chemicals, and any overload of other minerals, (and harmful bacteria and viruses), thereby retaining and balancing out the nutrient minerals. It has been documented that a “decrease in antioxidant protection caused by copper deficiency goes beyond a decrease in the activity of copper-dependent enzymes by inducing a wide range of disturbances in the other enzyme systems.” (Ref 4) This is because copper provides a balanced neutral pH of 7.00 that is required by these enzyme systems in order to activate and function at normal levels. Enzymes are made up of proteins and if any are missing or malformed due to copper deficiency, they do not activate and function at normal levels. These other enzyme systems are involved in the formation of bone and connective tissue, immune system, cardiovascular and heart, brain, liver, blood vessels, pigmentation, collagen and elastin, blood clotting factors, all the glandular systems, and many others. (Ref 4) Thus, it can be stated with certainty that copper is the single most important nutrient in the body. This is why copper is the target for deprivation and depletion.
Restated, copper deficiency causes a complete breakdown of the blood’s ability to eliminate toxins/poisons from the body. These toxins then deposit and accumulate in various locations of the body, which then acidify those locations causing serious life threatening disease states such as cancer, cardiovascular disease, diabetes, obesity, immune deficiencies, neurological dysfunction, and many other diseases and symptoms. Alkalizing the blood and body does not solve the problem, and will only deplete more copper and move the pH further away from 7.00. The solution is neutralizing the pH (7.00) by balancing the nutrient minerals. The mineral that performs this function is copper. Thus, the solution is to replenish copper and remove all copper depleting poisons from the food chain and the environment.
Global Warming: with the alkaline blood types in particular, the body uses compensation or buffer measure to bring down the blood pH and that mechanism is to retain carbon dioxide (CO2). It is not the fraudulent “Global Warming”, an “increase of carbon dioxide in the environment” that is causing humans to die off.
from this link (more there as well):
Poisoning of Mankind: Blood Types, Copper Deficiency, Evolution Theory, Global Warming, Shroud of Turin & Illuminati
The abomination that causes desolation (depopulation) spoken of through the prophet Daniel
The Blood Typing Farce: Nearly 95% of the population, who have blood type ‘O’ and ‘A’ which are the thinnest blood and lowest blood volume, and blood type ‘B’, have copper deficiency, due to slow poisoning from blood thinners, alkalizing chemicals, copper binders, and copper antagonists, that they have completely and thoroughly saturated the food and food chain with, in addition to wireless radiation poison which is the quickest and most effective method for depleting copper, and is one of the primary methods for expediting our death. These poisons have altered and damaged the proteins/DNA of the blood and other tissues of the body, with the damage (and deficiency) passing down through the generations. Starting in 1996, the copper depletion rate was significantly increased and coincides with the onslaught of GMO foods, chemtrails, wireless technology, increase of diseases and debilitating symptoms, and decreasing lifespan. Copper is essential in the formation of normal healthy proteins, that is, normal amino acid sequences, in that it provides a balanced pH state for the blood and tissues, maintaining the proper concentration of hydrogen for forming the bonds in normal protein synthesis. Copper is acidic at a pH of 5.5 and is important in providing a balance of the numerous alkaline and acidic nutrient minerals. A balanced pH of 7.00 is present in blood type AB, which is the only normal blood type, while the pH of the alkaline blood types (A/O) was set up to 7.54 by 31 March/1 April 2005 and the pH of the acidic blood type B decreased further by the same date. Deaths increase as blood pH moves further away from 7.00. The desired death rate was set up by increasing the pH level of the alkaline blood types to 7.54, while decreasing the pH of the acidic blood type. Consequently, due to unbalanced pH levels, the vast majority of the population has malformed proteins and is missing normal proteins, as can be evidenced just in the blood properties as noted in different “blood types”. The blood types of A, B, and O are missing the normal (clotting) proteins; type A is missing B, B is missing A, and O is missing both A and B proteins. The “Rhesus Factor” (D-protein) is a probable malformed or variant A or B protein, resulting from insufficient copper levels. The blood type AB is balanced and therefore does not carry the malformed “Rhesus Factor” protein as found in the other blood types, thus, only AB negative blood is possible.
“The life of a creature is its blood.”
Population Closer to 200 Million: Reporting shows increase of deaths in the age groups of 45-54 and 55-64 years of age and decreases in the ages 65 years and older. More interesting, a huge discrepancy is noted in raw death number totals (one state in 2008) versus the “official” death numbers coming from the national level. The raw data is consistently 65-70%, or about two thirds of the “official” numbers. These are indicators that not only is the population not increasing in numbers as we have been led to believe, but is in fact now decreasing. True population numbers and current average lifespan are being concealed.
Blood pH Levels Background: The A-protein is alkaline as it is made up of more of the alkaline amino acids. The B-protein is acidic with more of the acidic amino acids. Although no specific range was found for type B blood, a person with diabetes is known to have a pH of 6.8, and some references document a pH range of human blood of 6.8 – 7.7, which would encompass the type B blood at the acidic end. When the A and B proteins are present together, as in Type AB blood, the pH of the blood is in a balanced state or approximate pH of 7.00. A balanced pH is also indicative of the nutrient minerals being in balance. Individuals with blood types A and O have a propensity to carry a blood mineral/metal imbalance toward the alkaline, while those with blood type B have a propensity to carry a blood imbalance toward acidic minerals/metals, all cases due to copper deficiency.
With type O blood, the alkaline level is so high that even the normal alkaline A-protein cannot be formed, and thus, is missing. According to numerous references and texts, at least up to about the mid 1970’s, the pH range for blood in the US was 7.35 – 7.45, with an average pH of 7.40. (Some reference books document a pH above 7.45 is indicative of severe alkalosis and is fatal.) Assuming Type B is acidic and Type AB is at or near 7.00, this range apparently included type A’s and O’s, which comprised 86% of the US population. The same dated texts and references document the percentages of type O as 45 % and type A as 41%, in the US population. It is interesting to note that a clinic in the US recently measured blood pH samples of 259 clients, from January 2004 to June 2005, and found the average pH to be significantly higher at 7.54, as of December 2004 – March 31, 2005. (Ref 12) If assuming only Type A’s and O’s were recorded in the samples, and O’s are the higher pH, this data may indicate that type O blood in the US could be currently near the 7.60 pH level. Additionally, many individuals with type A blood may change over to type O blood if the pH has increased to a point or range at which the A protein disappears.
Fraudulent History & Evolution Theory: “In 1900, Karl Landsteiner, a physician in Vienna, Austria, noted that the sera of some individuals led to the ‘discovery’ of ABO blood types.” (Ref 1) Essentially, he noted a distinct difference in viscosity/pH level or the clotting factors of blood. Later on his students “discovered” the AB blood type. Then, in 1940, the “Rhesus Factor” (D-Protein) was detected. In truth, there is only one blood type among humans, and that is type AB. Anything else is a mutation due to copper deficiency. As each generation has been deprived and depleted of copper, the mutated genes/proteins have become weaker. These mutations of the blood and other structures that have manifested over the generations, is used as supporting evidence for the fraudulent “Evolution Theory”. The mutated blood types of A, B, and O and the presence of the “Rhesus Factor” are used to establish a lineage/correlation of the vast majority of the human population to the man-apes. This correlation does not exist, since humans are created solely with blood type AB, and the man-apes do not carry this blood type.
Blood types and DNA are used to establish fraudulent migratory patterns of different populations around the world. The higher the percentage of type B blood in a given population correlates to a more severe copper deficiency in that population. This is because the type B blood has a longer lifespan on average than the alkaline blood types of A and O. In other words the alkaline blood types are dying off much more quickly than the blood type B, and in fact are in the process of moving toward extinction, followed closely by blood type B, all because of copper deficiency. It should be mentioned here that according to Ref 2, in 1959 20% of Black Americans had type B blood and Caucasians had 10% type B, different severity levels of copper deficiency, indicating that Blacks may have been copper deficient (poisoned) before being brought over on slave ships. (One last note is, there were a small number of populations that contain only alkaline blood types, but these populations may have been manipulated by intentional extraction of the type B blood.)
We were all created with type AB blood, with normal viscosity/balanced pH level with normal protein structures. Through a misinformation campaign the “official” history is that blood type AB is the newest and rarest, emerging 500-1000 years ago, while blood type O is the oldest. It is interesting to note that the Shroud of Turin, the suspected burial cloth of Jesus, has blood type AB. The cloth has been dated to about the first century AD, and as of yet has not been disproved.
Copper Functions: Copper maintains mineral balance, thus a balanced pH with normal blood viscosity, by functioning as the primary antioxidant in the body. When the blood is of normal viscosity with optimal blood flow, the blood is able to rid the body of toxic metals, chemicals, and any overload of other minerals, (and harmful bacteria and viruses), thereby retaining and balancing out the nutrient minerals. It has been documented that a “decrease in antioxidant protection caused by copper deficiency goes beyond a decrease in the activity of copper-dependent enzymes by inducing a wide range of disturbances in the other enzyme systems.” (Ref 4) This is because copper provides a balanced neutral pH of 7.00 that is required by these enzyme systems in order to activate and function at normal levels. Enzymes are made up of proteins and if any are missing or malformed due to copper deficiency, they do not activate and function at normal levels. These other enzyme systems are involved in the formation of bone and connective tissue, immune system, cardiovascular and heart, brain, liver, blood vessels, pigmentation, collagen and elastin, blood clotting factors, all the glandular systems, and many others. (Ref 4) Thus, it can be stated with certainty that copper is the single most important nutrient in the body. This is why copper is the target for deprivation and depletion.
Restated, copper deficiency causes a complete breakdown of the blood’s ability to eliminate toxins/poisons from the body. These toxins then deposit and accumulate in various locations of the body, which then acidify those locations causing serious life threatening disease states such as cancer, cardiovascular disease, diabetes, obesity, immune deficiencies, neurological dysfunction, and many other diseases and symptoms. Alkalizing the blood and body does not solve the problem, and will only deplete more copper and move the pH further away from 7.00. The solution is neutralizing the pH (7.00) by balancing the nutrient minerals. The mineral that performs this function is copper. Thus, the solution is to replenish copper and remove all copper depleting poisons from the food chain and the environment.
Global Warming: with the alkaline blood types in particular, the body uses compensation or buffer measure to bring down the blood pH and that mechanism is to retain carbon dioxide (CO2). It is not the fraudulent “Global Warming”, an “increase of carbon dioxide in the environment” that is causing humans to die off.
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Post by crystalriver on Mar 24, 2009 14:06:51 GMT -5
Ah yes, I have asked myself the same thing--if it is only about genes than why are animals affected I am of the present opinion (could change) but this has seemed to be holding for the last year and with morgs that is saying something, that those of a certain genetic group show morgellons symptoms, i.e. including but not limited to black specks, leisons, fibers, black oil--and as this gene is lessoned less is shown. For instance, hubby has the black flecks and had one itchy spot but most of what he has had is going on unnoitced inside; but enough to cause havoc personally. Those of us with a certain genetic group has a DNA rememberance of this not being a good thing. It is like Cliff Carnicom's tests that show most people have it in their blood but only some present certain symptoms. It could be considered that those that are presenting have a strained immunue system--hence the response. However; I really think after speaking with so many folks that our immune system recognized this as an invader and reacted to it. Kicking it out through the skin which results in lesions. No we are not possessed by demons--if ones bodies natural response is looked at as an evil thing; than one must question the person or group saying such things. Hence it is the group that is not presenting symptoms that could be more at risk if this is what I think it is. (Morgellons is most likely put upon us by some dark source--but that doesn't make humanity evil) This is like the murderer blaming the person he murdered; go figure. Dead and ill people do have a hard time fighting back don't they? Does that make sense? I saw an article today about Wellcome Trust making artificial blood O negative to be exact: www.redicecreations.com/article.php?id=6101A major research project is to be announced this week that will culminate in three years with the first transfusions into human volunteers of "synthetic" blood made from the stem cells of spare IVF embryos. It could help to save the lives of anyone from victims of traffic accidents to soldiers on a battlefield by revolutionising the vital blood transfusion services, which have to rely on a network of human donors to provide a constant supply of fresh blood. The multimillion-pound deal involving NHS Blood and Transplant, the Scottish National Blood Transfusion Service and the Wellcome Trust, the world's biggest medical research charity, means Britain will take centre stage in the global race to develop blood made from embryonic stem cells. The researchers will test human embryos left over from IVF treatment to find those that are genetically programmed to develop into the "O-negative" blood group, which is the universal donor group whose blood can be transfused into anyone without fear of tissue rejection. This blood group is relatively rare, applicable to about 7 per cent of the population, but it could be produced in unlimited quantities from embryonic stem cells because of their ability to multiply indefinitely in the laboratory. The aim is to stimulate embryonic stem cells to develop into mature, oxygen-carrying red blood cells for emergency transfusions. Such blood would have the benefit of not being at risk of being infected with viruses such as HIV and hepatitis, or the human form of "mad cow" disease. The military in particular needs a constant supply of fresh, universal donor blood for battlefield situations when normal supplies from donors can quickly run out. But developing blood made from the cells of spare IVF embryos will raise difficult ethical issues for people not happy with the idea of destroying embryos to create stem cells. It also raises the intriguing philosophical question of whether the synthetic blood will have come from someone who never existed. In theory, just one embryo could meet the nation's needs. The Wellcome Trust is believed to have promised £3m towards the cost of the project, with further funding coming from the blood transfusion services of Scotland, and England and Wales. The Irish government is also understood to be involved. A spokesman for the Wellcome Trust said complicated legal issues were still being ironed out between all the parties involved but that an announcement is likely to be made in the coming week. The project will be led by Professor Marc Turner, of Edinburgh University, the director of the Scottish National Blood Transfusion Service. Professor Turner has been involved in studies investigating how to ensure donated blood is free of the infectious agent behind variant CJD, the human form of "mad cow" disease. Several vCJD patients are thought to have contracted the disease by blood transfusions. Professor Turner was unavailable for comment but a spokeswoman for the National Blood Service for England and North Wales confirmed that negotiations on the joint research project were at an advanced stage and that legal, rather than scientific, issues were holding up the announcement. The multi-centre collaboration is also understood to involve scientists at the Medical Research Council's Centre for Regenerative Medicine at the University of Edinburgh, and Roslin Cells, a spin-off company that has emerged out of the Roslin Institute, where Dolly the sheep was cloned in 1996. Scientists in other countries, notably Sweden, France and Australia, are also known to be working on the development of synthetic blood from embryonic stem cells. And last year, a team from a US biotechnology company, Advanced Cell Technology, announced that it has been able to produce billions of functioning red blood cells from embryonic stem cells. But the US work had been held up because of funding problems dating back to the ban on embryonic stem cell work under the Bush administration. President Barack Obama has since reversed that policy. In Britain, the project was held up because of the difficulty of finding funding for "translational" research that attempts to take scientific studies in the laboratory into the earliest stages of commercial development. This problem has now been overcome. -------------------------------------------------------------------------------- CR
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