by A. Goodwin
S 510 includes passages that would force harmonization with Codex Alimentarius. It is a name most people do not know and one that the media has not exposed though its consequences to human health would be extreme. Codex threatens the lives of millions through limiting access to adequate supplementation.
From an open letter by Dr. Matthias Rath, a renowned cardiologist, sent to Helmut Kohl, the German chancellor and one time pharmaceutical lobbyist who introduced Codex to the world.
This "Codex" Commission is overwhelmingly composed of representatives of German and international pharmaceutical corporations, and its aim is to set world-wide guidelines for vitamins, amino acids, minerals and other dietary supplements. Spearheaded by the German pharmaceutical corporations, this Codex Commission plans to ban, on a world wide scale, any health statements in relation to vitamins, be it preventive or therapeutic. Moreover, the only vitamin formulas which would still be available would have to meet the arbitrary restrictions of the Codex Commission. The nations that do not comply with these restrictions are faced with economic sanctions.
These plans of the pharmaceutical corporations and the Codex Commission are in direct opposition to the overwhelming importance of vitamins and other essential nutrients for human health and, in particular, for preventing cardiovascular disease. ...
With this background, the attack of the Codex Commission is a desperate act by pharmaceutical companies to protect their world-wide drug market against naturally effective and much more affordable vitamins. Particularly disturbing is the spearheading role of the German pharmaceutical corporations within the Codex Commission. Once before in this century, a German pharmaceutical and chemical corporation, I.G. Farben, became responsible for the deaths of millions of people and consequently, was dismantled in 1946 by the Nuremberg Tribunal and split into Bayer, BASF and Hoechst. With the current plans of the German pharmaceutical companies, the predictable dimension of the unnecessary and premature death of millions of people is unavoidable. If the Codex Commission is allowed to obstruct the eradication of heart disease by restricting access to nutritional supplements, more than 12 million people world-wide will continue to die every year from premature heart attacks and strokes. Within the next generation alone, this would result in over 300 million premature deaths, more than in all the wars of mankind together.
Codex for the US began on December 31, 2009. There have been five bills so far this year to remove access to supplements, if one adds S 3767 introduced by Senators Leahy, Klobuchar, and Franken on September 13th.
How dangerous are supplements that they are subject to FDA armed raids?
The Hazardous-Nutritional-Supplements -Target of FDA Police Raids:
Annual Deaths From:
FDA-Approved Drugs (1).......60,000 - 140,000
Food Contamination (2)...........................9,100
All vitamins (4). ............................................ 0
Uncontaminated amino acids (4)..................0
Commercial herbs (4).................................... 0
Why is this happening? The logic is inescapable - illness is worth money and health is worth $0. The FDA would be in charge of whatever agency is set up under S 510 (and S 3767) which would destroy availability of adequate nutrition. The dark history of the FDA's work to cut off knowledge of and access to all treatments for cancer not coming from the pharmaceutical industry is extensive but mostly unknown. The current FDA, pleading it doesn't have enough power to stop food contamination, finds power when it comes to stopping gentle cancer treatments and safe treatments for pain, and loses it again when it comes to drugs causing thousands of heart attacks or deaths and is silent on common pharmaceutical industry pain medications which routinely kill.
The value of supplements is abundantly clear to the pharmaceutical industry. When they were the main support for Germany during WWII, it was "A crime punishable by death to spread information in regard to nutrition in Norway, Belgium, Holland, and all other conquered countries." - D.T. Quigley, MD, Fellow American College of Surgeons, in The National Malnutrition
Today, the FDA is involved in an on-going, unconstitutional effort to stop information about the effectiveness of supplements, especially those which offer alternatives to H1N1 vaccines. The FDA has been and is increasing its removal of freedoms around speech, and health (as relates to food and vaccines/drugs), and now, just as they hope to control vast power over food and remove supplements, has gone so far as to assert in court that there is no fundamental right to one's bodily and physical health. (Is this a necessary legal accompaniment to the devastation that Codex would cause, and to forcing people into exposure to pharmaceutical industry's vaccines which have become increasingly unsafe?)
The removal of rights is the focus of
this video on Codex: "We Become Silent - The Last Days of Health Freedom" with Dame Judy Dench.
While people may sense that the consequences of the removal of nutritional supplements would be serious, it is possible to see in advance what would result from Codex-compelled vitamin and minerals deficiencies. In viewing the list, however, it is important to realize that those born or already sick with diseases and certain groups such as children, pregnant women and the elderly would be impacted first, given their greatly elevated requirement for nutritional supplementation. And hyper-supplementation to actually treat diseases would be available. Adults who do not fall into those categories would became ill from lack of adequate nutrition, at which point they would join the ranks of the ill and their own nutritional requirements to sustain lives would go up.
"Adequate vitamin D status is necessary and beneficial for health, although deficiency plagues much of the world's population. In addition to reducing the risk for bone disease, vitamin D plays a role in reduction of falls, as well as decreases in pain, autoimmune diseases, cancer, heart disease, mortality, and cognitive function. On the basis of this emerging understanding, improving patients' vitamin D status has become an essential aspect of primary care. Although some have suggested increased sun exposure to increase serum vitamin D levels, this has the potential to induce photoaging and skin cancer, especially in patients at risk for these conditions. Vitamin D deficiency and insufficiency can be both corrected and prevented safely through supplementation."
Vitamin A deficiency
Vitamin A deficiency is a lack of vitamin A in humans. It is common in developing countries but rarely seen in developed countries. Night blindness is one of the first signs of vitamin A deficiency. Xerophthalmia and complete blindness can also occur since Vitamin A has a major role in phototransduction. Approximately 250,000 to 500,000 malnourished children in the developing world go blind each year from a deficiency of vitamin A, approximately half of which die within a year of becoming blind. The United Nations Special Session on Children in 2002 set the elimination of vitamin A deficiency by 2010. The prevalence of night blindness due to vitamin A deficiency is also high among pregnant women in many developing countries. Vitamin A deficiency also contributes to maternal mortality and other poor outcomes in pregnancy and lactation.
Vitamin A deficiency also diminishes the ability to fight infections. In countries where children are not immunized, infectious disease like measles have higher fatality rates. As elucidated by Dr. Alfred Sommer, even mild, subclinical deficiency can also be a problem, as it may increase children's risk of developing respiratory and diarrheal infections, decrease growth rate, slow bone development, and decrease likelihood of survival from serious illness.
Alfred (Al) Sommer's research on vitamin A in the 1970s and 1980s revealed that dosing severely vitamin A deficient children with an inexpensive, large dose vitamin A capsule twice a year reduces child mortality by as much as 34 percent. The World Bank and, recently, the Copenhagen Consensus list vitamin A supplementation as one of the most cost-effective health interventions in the world.
Vitamin B deficiency
Deficiency causes beriberi. Symptoms of this disease of the nervous system include weight loss, emotional disturbances, Wernicke's encephalopathy (impaired sensory perception), weakness and pain in the limbs, periods of irregular heartbeat, and edema (swelling of bodily tissues). Heart failure and death may occur in advanced cases. Chronic thiamine deficiency can also cause Korsakoff's syndrome, an irreversible psychosis characterized by amnesia and confabulation.
Deficiency causes ariboflavinosis. Symptoms may include cheilosis (cracks in the lips), high sensitivity to sunlight, angular cheilitis, glossitis (inflammation of the tongue), seborrheic dermatitis or pseudo-syphilis (particularly affecting the scrotum or labia majora and the mouth), pharyngitis (sore throat), hyperemia, and edema of the pharyngeal and oral mucosa.
Deficiency, along with a deficiency of tryptophan causes pellagra. Symptoms include aggression, dermatitis, insomnia, weakness, mental confusion, and diarrhea. In advanced cases, pellagra may lead to dementia and death (the 3(+1) Ds: dermatitis, diarrhea, dementia, and death).
Pellagra is a vitamin deficiency disease most commonly caused by a chronic lack of niacin (vitamin B3) in the diet. It can be caused by decreased intake of niacin or tryptophan, and possibly by excessive intake of leucine. It may also result from alterations in protein metabolism in disorders such as carcinoid syndrome. A deficiency of the amino acid lysine can lead to a deficiency of niacin as well, meaning that another potential cause of pellagra is lysine deficiency.
Deficiency may lead to microcytic anemia (because pyridoxyl phosphate is the cofactor for heme synthesis), depression, dermatitis, high blood pressure (hypertension), water retention, and elevated levels of homocysteine.
Deficiency does not typically cause symptoms in adults but may lead to impaired growth and neurological disorders in infants. Multiple carboxylase deficiency, an inborn error of metabolism, can lead to biotin deficiency even when dietary biotin intake is normal.
Initial symptoms of biotin deficiency include:
If left untreated, neurological symptoms can develop, including:
Deficiency results in a macrocytic anemia, and elevated levels of homocysteine. Deficiency in pregnant women can lead to birth defects. Supplementation is often recommended during pregnancy. Researchers have shown that folic acid might also slow the insidious effects of age on the brain.
Deficiency results in a macrocytic anemia, elevated homocysteine, peripheral neuropathy, memory loss and other cognitive deficits. It is most likely to occur among elderly people, as absorption through the gut declines with age; the autoimmune disease pernicious anemia is another common cause. It can also cause symptoms of mania and psychosis. In rare extreme cases, paralysis can result.
Vitamin B12 deficiency is a reduction in vitamin B12 from inadequate dietary intake or impaired absorption. The condition is commonly asymptomatic, but can also present as anemia characterized by enlarged blood corpuscles with characteristic changes in neutrophils, known as megaloblastic anemia.
In serious cases deficiency can potentially cause severe and irreversible damage to the nervous system, including subacute combined degeneration of spinal cord.
The anemia is thought to be due to problems in DNA synthesis, specifically in the synthesis of thymine, which is dependent on products of the MTR reaction. Other blood cell types such as white blood cells and platelets are often also low. Bone marrow examination may show megaloblastic hemopoiesis. The anemia responds completely to vitamin B12; the neurological symptoms (if any) respond partly or completely, depending on prior severity and duration.
Vitamin C deficiency
Symptoms and Signs of Vitamin C Deficiency
It takes several months of low amounts of vitamin C to lead to the symptoms of scurvy. The classic symptoms are bleeding gums, scaly skin, loose teeth, fatigue, increased risk of infection, and poor wound healing. Children and infants with an ascorbic acid deficiency usually have poor bone growth and anemia.
This animation (requires RealVideoPlayer) shows the connection between cardiovascular disease and the sailor's disease scurvy. As opposed to animals, the human body cannot synthesize vitamin C. Ascorbate deficiency results in two distinct morphological changes of the vascular wall: Impaired vascular stability due to decreased collagen synthesis and loss of the endothelial barrier function.
|The sailors of earlier centuries died within a few months from hemorrhagic blood loss due to lack of endogenous ascorbate synthesis combined with a vitamin deficient diet aboard. When the Indians gave those sailors tea from tree barks and other vitamin rich nutrition, blood loss was stopped and the vascular wall healed naturally. |
Today, everyone gets some vitamin C and open scurvy is rare. But almost everyone suffers from chronic vitamin deficiency. Over decades, micro lesions develop in the vascular wall, especially in areas of high mechanical stress such as the coronary arteries.
Vitamin E deficiency
Vitamin E deficiency causes neurological problems due to poor nerve conduction. These include neuromuscular problems such as spinocerebellar ataxia and myopathies. Deficiency can also cause anemia, due to oxidative damage to red blood cells.
Vitamin E deficiency is rare in humans and is almost never caused by a poor diet. Instead, there are three specific situations when a vitamin E deficiency is likely to occur. It is seen in persons who cannot absorb dietary fat, has been found in premature, very low birth weight infants (birth weights less than 1500 grams, or 3.5 pounds), and is seen in individuals with rare disorders of fat metabolism.
Individuals who cannot absorb fat may require a vitamin E supplement because some dietary fat is needed for the absorption of vitamin E from the gastrointestinal tract. Anyone diagnosed with cystic fibrosis, individuals who have had part or all of their stomach removed, and individuals with malabsorptive problems such as Crohn's disease, liver disease or pancreatic insufficiency may not absorb fat and should discuss the need for supplemental vitamin E with their physician. People who cannot absorb fat often pass greasy stools or have chronic diarrhea and bloating.
Abetalipoproteinemia is a rare inherited disorder of fat metabolism that results in poor absorption of dietary fat and vitamin E. The vitamin E deficiency associated with this disease causes problems such as poor transmission of nerve impulses, muscle weakness, and degeneration of the retina that can cause blindness. Individuals with abetalipoproteinemia may be prescribed special vitamin E supplements by a physician to treat this disorder. In addition, there is a rare genetic condition termed isolated vitamin E deficiency or ataxia with isolated with vitamin E deficiency, caused by mutations in the gene for the tocopherol transfer protein. These individuals have an extremely poor capacity to absorb vitamin E and develop neurological complications that are reversed by high doses of vitamin E.
Vitamin K deficiency
Vitamin K is a group of lipophilic, hydrophobic vitamins that are needed for the posttranslational modification of certain proteins, mostly required for blood coagulation but also involved in metabolism pathways in bone and other tissue.
Symptoms of Vitamin K Deficiencies
Vitamin K is known to be needed to coagulate blood and to maintain proper bone density. It plays a key role in proper development of the fetus. Deficiencies of vitamin K have been linked to:
Heavy menstrual bleeding*
The following birth defects have been linked to anticonvulsant drugs, which block vitamin K:
Iron deficiency (sideropenia or hypoferremia) is one of the most commonly known forms of nutritional deficiencies. In the human body, iron is present in all cells and has several vital functions—as a carrier of oxygen to the tissues from the lungs in the form of hemoglobin, as a transport medium for electrons within the cells in the form of cytochromes, and as an integral part of enzyme reactions in various tissues. Too little iron can interfere with these vital functions and lead to morbidity and death.
Boron deficiency is a pathology which may occur in animals due to a lack of boron. A report given by E. Wayne Johnson et al. at the 2005 Alan D. Leman Swine Conference suggests that boron deficiency produces osteochondrosis in swine that is correctable by addition of 50 ppm of boron to the diet. The amount of boron required by animals and humans is not yet well established.
According to some natural therapy researchers, topsoil used over long periods of time for agriculture become boron-deficient to some extent, and humans eating produce from boron-rich soils have reduced incidence of arthritis and osteoporosis.
Information on boron deficiency in humans is minimal; however, it appears a deficiency in boron impacts mineral metabolism, cognitive function, steroid hormone and vitamin levels, and bone integrity. (20) Boron-deficient diets have resulted in embryological defects in some but not all animals (e.g., not in rodents), pointing to a possible role in reproduction and/or development. Limited growth is also commonly noted in boron-depleted animals, (17,21) while boron-deficient chicks present increased insulin secretion. (19,22)
Clinical Applications Anemia
Boron supplementation to subjects who had previously followed a dietary regimen deficient in boron resulted in increases in blood hemoglobin concentrations, mean corpuscular hemoglobin, and mean corpuscular hemoglobin concentration, and decreases in hematocrit, red cell count and platelet count. (23)
Osteo- and Rheumatoid Arthritis
In a double-blind, placebo-controlled trial of 20 subjects with osteoarthritis, half of the subjects receiving a daily supplement containing 6 mg boron noted subjective improvement in their condition. (24)
Clinical commentary suggests children with juvenile arthritis (Still's disease) improve with boron supplementation (6-9 mg daily). (25)
Individuals with rheumatoid arthritis might experience an aggravation of symptoms (Herxheimer response) for 1-3 weeks, but generally notice improvement within four weeks of beginning boron supplementation (6-9 mg daily). (25)
Collectively, data indicate that boron might play a role in human brain function, alertness, and cognitive performance. In humans, low boron intake compared to high boron intake was associated with poor short- and long-term memory, eye-hand coordination, and manual dexterity. (26) Boron deficiency has also been associated with decreased brain electrical activity similar to brainwave patterns observed in nonspecific malnutrition. (27)
Selenium deficiency is thought to contribute to autoimmune disease by making the body more susceptible to nutritional and biochemical stresses as well as infectious diseases. Three diseases caused directly by selenium deficiency include Keshan Disease, which causes an enlarged heart, Kashin-Beck Disease, which causes osteoarthropathy, and Myxedematous Endemic Cretinism, a form of hypothyroidism which results in mental retardation.
- Lack of mental dexterity
However, there are diseases that can be caused by this deficiency as well and they include Keshan disease and Kashin-Beck disease.
Keshan disease is viral disease and mostly affects children. It is caused by a deficient amount of selenium present in the body. The main symptom of this condition is myocardial necrosis, which leads to the weakening of the heart and a general weakness of the heart muscle. Keshan disease can also make a person much more susceptible to developing other illnesses.
Kashin-Beck disease occurs when the body is deficient of both selenium and iodine. The symptoms this can then present include the degeneration of cartilage.
So, what exactly causes a selenium deficiency in the first place? Eating food that is grown in soil lacking this nutrient is thought to be the primary cause. Also, people suffering from intestinal disorders that make the absorption of selenium next to impossible are at an elevated risk for developing this deficiency.
Treatment usually consists of taking selenium supplements until the body's levels have returned to normal. However, supplements may always be necessary if absorption is a problem.
Adults with insomnia have been shown to have lower melatonin levels.4 Frequent travelers and shift workers are also likely to benefit from melatonin for the resynchronization of their sleep schedules,5 though a melatonin "deficiency" as such does not exist for these people. Patients with heart disease have been reported to have low melatonin levels, but whether this abnormality increases the risk of heart disease or whether heart disease leads to the low melatonin level is not yet known.6 People with schizophrenia were found to have low melatonin output and experienced significantly improved sleep following melatonin replacement supplementation.7
Adeficient production of melatonin can result in anxiety and mood disorders, lowered basal body temperature insomnia, elevated estrogen/progesterone ratio, and immune suppression associated with cancer.
The diets of all Americans are likely to be deficient........Even a mild deficiency causes sensitiveness to noise, nervousness, irritability, mental depression, confusion, twitching, trembling, apprehension, insomnia, muscle weakness and cramps in the toes, feet, legs, or fingers.
Magnesium (Mg) is a trace mineral that is known to be required for several hundred different functions in the body. A significant portion of the symptoms of many chronic disorders are identical to symptoms of magnesium deficiency. Studies show many people in the U.S. today do not consume the daily recommended amounts of Mg. A lack of this important nutrient may be a major factor in many common health problems in industrialized countries. Common conditions such as mitral valve prolapse, migraines, attention deficit disorder, fibromyalgia, asthma and allergies have all been linked to a Mg deficiency. Perhaps not coincidentally, these conditions also tend to occur in clusters together within the same individual. A magnesium deficiency as a root cause would provide a logical explanation of why some people suffer from a constellation of these types of problems. Many of the following conditions commonly occur in conjunction with each other and all have been linked to a Mg deficiency. Contents: What is the percentage of Americans with inadequate intakes of Mg from food based on estimated average requirements? 56%
Magnesium - Part Two - Covers the links between magnesium deficiency and diverse conditions such as fibromyalgia, hearing loss, migraines, menstrual cramps (dysmenorrhea), mitral valve prolapse, muscle cramps, nystagmus, osteoporosis, pectus excavatum, TMJ and more.
Magnesium (Mg) is a trace mineral that is known to be required for several hundred different functions in the body. A significant portion of the symptoms of many chronic disorders are identical to symptoms of magnesium deficiency. Studies show many people in the U.S. today do not consume the daily recommended amounts of Mg. A lack of this important nutrient may be a major factor in many common health problems in industrialized countries. Common conditions such as mitral valve prolapse, migraines, attention deficit disorder, fibromyalgia, asthma and allergies have all been linked to a Mg deficiency. Perhaps not coincidentally, these conditions also tend to occur in clusters together within the same individual. A magnesium deficiency as a root cause would provide a logical explanation of why some people suffer from a constellation of these types of problems.
Many of the following conditions commonly occur in conjunction with each other and all have been linked to a Mg deficiency.
What is the percentage of Americans with inadequate intakes of Mg from food based on estimated average requirements?
Symptoms of Calcium deficiency
- Muscle cramps
- Muscle aches
- Muscle pain
- Muscle twitching
- Muscle spasms
- Tooth decay
- Weak bones
- Reduced bone density
- Rickets in children
- Poor growth in children
- Maldeveloped bones in children
- Delayed puberty in teens
- Menstrual problems in teens
- Premenstrual cramps
- Increased blood pressure
- Pale skin
- Dry scaly skin
- Coarse hair
- Brittle nails
- Convulsions - in extreme cases
- Easily fatigued
- more information...»
Symptoms of Hypocalcaemia
▪ Petechia which appear as one-off spots, then later become rashes.
- Perioral tingling and paraesthesia, 'pins and needles' sensation over the extremities of hands and feet. This is the earliest symptom of hypocalcaemia.
- Tetany, carpopedal spasm are seen.
- Latent tetany
- Trousseau sign of latent tetany (eliciting carpal spasm by inflating the blood pressure cuff and maintaining the cuff pressure above systolic)
- Chvostek's sign (tapping of the inferior portion of the zygoma will produce facial spasms)
- Tendon reflexes are hyperactive
- Life threatening complications
- ECG changes include:
- Prolonged QTc
- Prolonged ST interval
Both sea salt and rock salt were well known to the ancient Greeks who noted that eating salty food affected basic body functions such as digestion and excretion (urine and stools). This led to salt being used medically. The healing methods of Hippocrates (460 BC) especially made frequent use of salt. Hippocrates mentions inhalation of steam from salt-water. We know today that the antiinflammatory effects of inhaled salt provide relief from respiratory symptoms (c). Thus, 2000 years ago, Greek medicine had already discovered topical use of salt for skin lesions, drinking salty or mineralized waters for digestive troubles and inhaling salt for respiratory diseases.
Symptoms of hyponatremia [salt deficiency] include nausea and vomiting, headache, confusion, lethargy, fatigue, appetite loss, restlessness and irritability, muscle weakness, spasms, or cramps, seizures, and decreased consciousness or coma. The presence and severity of symptoms are associated with the level of serum sodium, with the lowest levels of serum sodium associated with the more prominent and serious symptoms. However, emerging data suggests that mild hyponatremia (serum sodium levels at 131 mEq/L or above) was associated with numerous complications and undiagnosed symptoms.
Many medical illnesses, such as congestive heart failure, liver failure, renal failure, or pneumonia may be associated with hyponatremia. These patients frequently present because of primary disease symptomatology and are diagnosed after presenting due to manifestations of other medical issues.
Neurological symptoms often show for extremely low levels of sodium. When sodium levels in blood become too low, excess water enters cells and causes the cells to swell. Swelling in the brain is especially dangerous because the brain is confined by the skull and is unable to expand. Neurological symptoms most often are due to very low serum sodium levels (usually <115 mEq/L), resulting in intracerebral osmotic fluid shifts and brain edema. This neurological symptom complex can lead to tentorial herniation with subsequent brain stem compression and respiratory arrest, resulting in death in the most severe cases. The severity of neurological symptoms correlates with the rapidity and severity of the drop in serum sodium. A gradual drop, even to very low levels, may be tolerated well if it occurs over several days or weeks, because of neuronal adaptation. The presence of underlying neurological disease, like a seizure disorder, or non-neurological metabolic abnormalities, also affects the severity of neurologic symptoms.