The US government have been stating for the past 2 decades that it’s only a question of when a pandemic will come, not if it will come. Influenza A pandemics come every 30 years or so, severe ones every hundred years or so. The last pandemic, the Hong Kong flu, occurred in 1968 - killing 34,000 Americans. In 1918, the Great Flu Epidemic killed more than 500,000 Americans. So many millions died in other countries, they couldn’t bury the bodies. Young healthy adults, in the prime of their lives in the morning, drowning in their own inflammation by noon, grossly discolored by sunset, were dead at midnight. Their body’s own broad-spectrum natural antibiotics, called antimicrobial peptides, seemed nowhere to be found. An overwhelming immune response triggered by the over the counter drug Aspirin caused the white blood cells to release large amounts of inflammatory agents called cytokines and chemokines into the lungs of the doomed - resulting in millions of unnecessary deaths in 1918.

Today we now have another Influenza A pandemic, or so the US government has declared. The distinctions from this outbreak and past outbreaks is that this H1N1 influenza A viral outbreak was man made and intentionally released by the US government. The virus was created in the biological weapons research labs at Fort Detrick Maryland. It was created as a biological weapon for a political agenda. It was created to target a specific group of people in the US public. It is not contagious and because of this the US government had to declare a medical state of emergency in order to trick people into being infected with the H1N1 virus. The only way for anyone to be infected with the virus is to have the virus injected directly into the blood stream - via a syringe (a vaccine). Millions of people became infected with the H1N1 virus after they received the live virus laced vaccine or H1N1 drug treatment that also contained the live virus. Those who the government claimed were infected by the H1N1 virus by coming into contact with another person with the virus, were actually sick with regular flu virus (the CDC maintains that seasonal flu kills 36000 Americans each year compared to just 3,198 H1N1 death for all of North America). Seasonal flu kills between 4,000 to 8,000 Canadians and between 250,000 and 500,000 people worldwide each year. Yet as of late last week, seven months into this outbreak, H1N1 has killed a little as 161 Canadians and an estimated 6,260 people around the globe. The US government distorted the facts in order to launch a nation wide vaccination program. Millions are now infected with the H1N1 virus as a direct result of being vaccinated - the vaccine is the pandemic.

All those who have been infected with the US government made and dispersed H1N1 virus can be cured - naturally, safely and in most cases free of charge. The WHO and the CDC have both stated that there is no cure for the H1N1 virus. There are many cures. A group of scientists from UCLA published a remarkable paper in the prestigious journal, Nature. In the article, the UCLA group confirmed two other recent studies, showing that a naturally occurring steroid hormone - a hormone most of us take for granted - was, in effect, a potent antibiotic. Instead of directly killing bacteria and viruses, the steroid hormone under question increases the body’s production of a remarkable class of proteins, called antimicrobial peptides. The 200 known antimicrobial peptides directly and rapidly destroy the cell walls of bacteria, fungi, and viruses, including the influenza virus, and play a key role in keeping the lungs free of infection. The steroid hormone that showed these remarkable antibiotic properties was plain old vitamin D - 2,000 units of vitamin D every day for the duration of the influenza season.

Vitamin D is unique in the vitamin world by virtue of three facts.

First, it’s the only known precursor of a potent steroid hormone, calcitriol, or activated vitamin D. Most other vitamins are antioxidants or co-factors in enzyme reactions. Activated vitamin D - like all steroid hormones - damasks the genome, turning protein production on and off, as your body requires. That is, vitamin D regulates genetic expression in hundreds of tissues throughout your body. This means it has as many potential mechanisms of action as genes it damasks.

Second, vitamin D does not exist in appreciable quantities in normal human diets. True, you can get several thousand units in a day if you feast on sardines for breakfast, herring for lunch and salmon for dinner. The only people who ever regularly consumed that much fish are peoples, like the Inuit, who live at the extremes of latitude. The milk Americans depend on for their vitamin D contains no naturally occurring vitamin D; instead, the U.S. government requires fortified milk to be supplemented with vitamin D, but only with what we now know to be a paltry 100 units per eight-ounce glass.

The vitamin D steroid hormone system has always had its origins in the skin, not in the mouth. Until quite recently, when dermatologists and governments began warning us about the dangers of sunlight, humans made enormous quantities of vitamin D where humans have always made it, where naked skin meets the ultraviolet B radiation of sunlight. We just cannot get adequate amounts of vitamin D from our diet. If we don’t expose ourselves to ultraviolet light, we must get vitamin D from dietary supplements.

The third way vitamin D is different from other vitamins is the dramatic difference between natural vitamin D nutrition and the modern one. Today, most humans only make about a thousand units of vitamin D a day from sun exposure; many people, such as the elderly or African Americans, make much less than that. How much did humans normally make? A single, twenty-minute, full body exposure to summer sun will trigger the delivery of 20,000 units of vitamin D into the circulation of most people within 48 hours. Twenty thousand units, that’s the single most important fact about vitamin D. Compare that to the 100 units you get from a glass of milk, or the several hundred daily units the U.S. government recommend as “Adequate Intake.” It’s what we call an “order of magnitude” difference.

Humans evolved naked in sub-equatorial Africa, where the sun shines directly overhead much of the year and where our species must have obtained tens of thousands of units of vitamin D every day, in spite of our skin developing heavy melanin concentrations (racial pigmentation) for protecting the deeper layers of the skin. Even after humans migrated to temperate latitudes, where our skin rapidly lightened to allow for more rapid vitamin D production, humans worked outdoors. However, in the last three hundred years, we began to work indoors; in the last one hundred years, we began to travel inside cars; in the last several decades, we began to lather on sunblock and consciously avoid sunlight. All of these things lower vitamin D blood levels. The inescapable conclusion is that vitamin D levels in modern humans are not just low - they are aberrantly low.

In the last several years, dozens of medical studies have called attention to worldwide vitamin D deficiency, especially among African Americans and the elderly, the two groups most likely to die from influenza. Cancer, heart disease, stroke, autoimmune disease, depression, chronic pain, depression, gum disease, diabetes, hypertension, and a number of other diseases have recently been associated with vitamin D deficiency. Was it possible that influenza was as well?

There exists 3 medical mysteries: (1) although the influenza virus exists in the population year-round, influenza is a wintertime illnesses; (2) children with vitamin D deficient rickets are much more likely to suffer from respiratory infections; (3) the elderly in most countries are much more likely to die in the winter than the summer (excess wintertime mortality), and most of that excess mortality, although listed as cardiac, is, in fact, due to influenza.

Vitamin D, specifically Vitamin D deficiency explain these three mysteries, mysteries that account for hundreds of thousands of deaths every year? Studies have found the influenza virus is present in the population year-around; why is it a wintertime illness? Even the common cold got its name because it is common in cold weather and rare in the summer. Vitamin D blood levels are at their highest in the summer but reach their lowest levels during the flu and cold season. Could such a simple explanation explain these mysteries?

The British researcher, Dr. R. Edgar Hope-Simpson, was the first to document the most mysterious feature of epidemic influenza, its wintertime surfeit and summertime scarcity. He theorized that an unknown “seasonal factor” was at work, a factor that might be affecting innate human immunity. Hope-Simpson was a general practitioner who became famous in the late 1960’s after he discovered the cause of shingles. British authorities bestowed every prize they had on him, not only because of the importance of his discovery, but because he made the discovery own his own, without the benefit of a university appointment, and without any formal training in epidemiology (the detective branch of medicine that methodically searches for clues about the cause of disease).

After his work on shingles, Hope-Simpson spent the rest of his working life studying influenza. He concluded a “seasonal factor” was at work, something that was regularly and predictably impairing human immunity in the winter and restoring it in the summer. He discovered that communities widely separated by longitude, but which shared similar latitude, would simultaneously develop influenza. He discovered that influenza epidemics in Great Britain in the 17th and 18th century occurred simultaneously in widely separated communities, before modern transportation could possibly explain its rapid dissemination. Hope-Simpson concluded a “seasonal factor” was triggering these epidemics. Whatever it was, he was certain that the deadly “crop” of influenza that sprouts around the winter solstice was intimately involved with solar radiation. Hope-Simpson predicted that, once discovered, the “seasonal factor” would “provide the key to understanding most of the influenza problems confronting us.”

Hope-Simpson had no way of knowing that vitamin D has profound effects on human immunity, no way of knowing that it increases production of broad-spectrum antimicrobial peptides, peptides that quickly destroy the influenza virus. We have only recently learned how vitamin D increases production of antimicrobial peptides while simultaneously preventing the immune system from releasing too many inflammatory cells, called chemokines and cytokines, into infected lung tissue.

In 1918, when medical scientists did autopsies on some of the fifty million people who died during the 1918 flu pandemic, they were amazed to find destroyed respiratory tracts; sometimes these inflammatory cytokines had triggered the complete destruction of the normal epithelial cells lining the respiratory tract. It was as if the flu victims had been attacked and killed by their own immune systems. This is the severe inflammatory reaction that vitamin D has recently been found to prevent.

Clinical research has shown that annual fluctuations in vitamin D levels explain the seasonality of influenza. The periodic seasonal fluctuations in 25-hydroxy-vitamin D levels, which cause recurrent and predictable wintertime vitamin D deficiency, predispose human populations to influenza epidemics. That influenza is a symptom of vitamin D deficiency in the same way that an unusual form of pneumonia (pneumocystis carinii) is a symptom of AIDS. George Bernard Shaw was right when he said, “the characteristic microbe of a disease might be a symptom instead of a cause.”

Vitamin D explains the following 14 observations:

1. Why the flu predictably occurs in the months following the winter solstice, when vitamin D levels are at their lowest,

2. Why the flu disappears in the months following the summer solstice,

3. Why influenza is more common in the tropics during the rainy season,

4. Why the cold and rainy weather associated with El Nino Southern Oscillation (ENSO), which drives people indoors and lowers vitamin D blood levels, is associated with influenza,

5. Why the incidence of influenza is inversely correlated with outdoor temperatures,

6. Why children exposed to sunlight are less likely to get colds,

7. Why cod liver oil (which contains vitamin D) reduces the incidence of viral respiratory infections,

8. Why scientists found that vitamin D-producing UVB lamps reduced colds and flu in schoolchildren and factory workers,

9. Why scientists found that volunteers, deliberately infected with a weakened flu virus - first in the summer and then again in the winter - show significantly different clinical courses in the different seasons,

10. Why the elderly who live in countries with high vitamin D consumption, like Norway, are less likely to die in the winter,

11. Why children with vitamin D deficiency and rickets suffer from frequent respiratory infections,

12. Why an observant physician (Rehman), who gave high doses of vitamin D to children who were constantly sick from colds and the flu, found the treated children were suddenly free from infection,

13. Why the elderly are so much more likely to die from heart attacks in the winter rather than in the summer,

14. Why African Americans, with their low vitamin D blood levels, are more likely to die from influenza and pneumonia than Whites are.

High doses of Vitamin D kills the flu. The governments keep natural medicine very quiet because there is no money in it. Vitamin D increases the immune system by 3-5 times and is BETTER than any vaccine at helping the immune system beat both the h5n1 (bird flu) virus and the H1N1 (Swine Flu) virus.

Research from PubMed: In 1981, R. Edgar Hope-Simpson proposed that a ’seasonal stimulus’ intimately associated with solar radiation explained the remarkable seasonality of epidemic influenza. Solar radiation triggers robust seasonal vitamin D production in the skin; vitamin D deficiency is common in the winter, and activated vitamin D, 1,25(OH)2D, a steroid hormone, has profound effects on human immunity. 1,25(OH)2D acts as an immune system modulator, preventing excessive expression of inflammatory cytokines and increasing the ‘oxidative burst’ potential of macrophages. Perhaps most importantly, it dramatically stimulates the expression of potent anti-microbial peptides, which exist in neutrophils, monocytes, natural killer cells, and in epithelial cells lining the respiratory tract where they play a major role in protecting the lung from infection. Volunteers inoculated with live attenuated influenza virus are more likely to develop fever and serological evidence of an immune response in the winter. Vitamin D deficiency predisposes children to respiratory infections. Ultraviolet radiation (either from artificial sources or from sunlight) reduces the incidence of viral respiratory infections, as does cod liver oil (which contains vitamin D). An interventional study showed that vitamin D reduces the incidence of respiratory infections in children.

One reason why the flu may be more contagious in the winter time is because of the lack of sunlight. During the winter months people spend most of the time indoors. During the summer months people spend most of the time outdoors. The lack of sunlight, when we find shelter from the cold, prevents our skin from producing sufficient levels of vitamin D. There is now documented evidence about the roles of solar ultraviolet-B radiation and vitamin D in reducing case-fatality rates from the 1918-1918 influenza Pandemic in EU. “There are two mechanisms whereby vitamin D can reduce the risk of death once the pandemic influenza virus infection took hold: reduced production of pro-inflammatory cytokines and reduced risk of bacterial pneumonia. The type of vitamin D which can fight viruses can ONLY be made from natural sunlight. It is known as D3, which is made from sunlight when 7-dehydrocholesterol in our skin reacts with UV light. It is then twice activated in the liver and kidney to make 1,25-dihydroxyvitamin D. This attaches to receptors on genes that control their expression, which turn protein production on or off. Vitamin D regulates the expression of more than 1,000 genes throughout the body. They include genes in macrophages, cells in the immune system that, among other things, ATTACK AND DESTROY VIRUSES.”

Definition of Cure - To heal, to make well, to restore to good health. Vitamin D is therefore a cure for the H1N1 virus


Hundreds of thousands of swine flu shots for children have been recalled because tests indicate the vaccine doses lost some strength, government health officials said Tuesday.

The shots, made by Sanofi Pasteur, were distributed across the country last month and most have already been used, according to the Centers for Disease Control and Prevention.

The issue is the vaccine’s strength. Tests done before the shots were shipped showed that the vaccines were strong enough. But tests done weeks later indicated the strength had fallen slightly below required levels.

Why the potency dropped isn’t clear. “That’s the $64,000 question,” said Len Lavenda, a Sanofi Pasteur spokesman.

The answer to the mystery is simple. The H1N1 virus cannot survive past 7 days. Biological weapons expert Marc S Griswold, who travelled to Mexico with President Obama on April 16, 2009 is the first documented and confirmed A-H1N1 swine flu infection case. The agent is patient zero. Patient zero infected several members of his family in Anne Arundel County, prompting assurances from the White House that the president was safe.

Marc S. Griswold, a former Secret Service agent who was serving as the lead advance special agent for Energy Secretary Steven Chu on president Obama’s April trip to Mexico, said in an interview that the minor cough he developed in Mexico grew into swine flu. Although he has recovered and is back to work, he and his family have watched in shock as his illness has sparked national security concerns, severely strained his relationship with his brother (Griswold probably infected his nephew) and put his family at the center of rumors and panic in his Severna Park neighborhood. Griswold said in frustration on the front steps of his house. “We’ve been told we’re not contagious. We’re already past the seven-day mark for that.”

How did the H1N1 virus spread globally?

Biological weapons expert Marc S. Griswold returned from Mexico on April 18, officials said, on United Flight 822 to Dulles International Airport. Washington Dulles International Airport is a public airport located 25 miles (40 km) west of the central business district of Washington, D.C., in Dulles, Virginia. Dulles is served by nearly a dozen U.S.-flagged carriers and nearly two dozen international carriers. Airlines serving Dulles provide non-stop service to over 80 domestic destinations and to over 40 international destinations. On a typical day, Dulles sees 1,000 to 1,200 flight operations.

When word got out that Agent Marc S. Griswold was infected with the H1N1 virus the government was only concerned about the health of president Obama. No one sought to contact everyone on the same flight as Griswold. If you have a confirmed case of an influenza outbreak the immediate response is for the government to immediately track down everyone who came in contact with Patient Zero and initiate a quarantine. No one, not even Obama, bothered to spring into to action to prevent the spread of the H1N1 virus that the WHO has declared a pandemic. Obama, the WHO and the CDC failed to do their job to protect the people from this influenza outbreak. It is as if they wanted it to happen. Instead of quarantining Griswold, his family, and everyone who came in contact with Griswold on United Airlines Flight 822 they allowed the H1N1 influenza virus to spread. Dulles international airport was the hub for the H1N1 virus to spread globally.

Obama has a responsibility to the people. As president he failed as miserably as George W Bush’s handling of Hurricane Katrina. Obama’s complete inaction shows complacency. Inaction could also imply conspiracy. Perhaps the rumours are true. Did Obama order a biological attack against Mexico and his own country? What was Obama’s motive to unleash a biological weapons grade influenza strain? What was the means? What opportunity did he have? Motive could be the Tax Day Tea Party which millions of ordinary US citizens participated in as a nation wide protest against Obama’s government policies and out of control spending that occurred on April 15, 2009 - the day before Obama landed in Mexico. Not even in office 100 days the people were angrily protesting and petitioning Obama and his government for change. Did Obama fear they would ask for his resignation? Did he react out of anger because the US people no longer saw him as their saviour and out of anger ordered the H1N1 virus released? He surely had the means. Fort Detrick where this new viral infection was created is just outside Washington DC. He did have Air Force One at his disposal as a means to transport the virus from Fort Detrick to Mexico. Air Force one is considered US soil no matter where it lands and as such no country can board it or inspect it. He did have an excuse to go to Mexico right away. Mexico had a very violent and deadly drug war going on until the first case of H1N1 virus was reported in Mexico. Before the H1N1 virus outbreak the news was reporting daily about the battle between the Mexican government and the drug lords. Bodies were being discovered by US border guards on a daily bases. That has all but stop as a result of the H1N1 flu.

Bioterrorism is terrorism by intentional release or dissemination of biological agents (bacteria, viruses, or toxins); these may be in a naturally-occurring or in a human-modified form.

According to the US-based Centers for Disease Control and Prevention (CDC): A bioterrorism attack is the deliberate release of viruses, bacteria, or other germs (agents) used to cause illness or death in people, animals, or plants. These agents are typically found in nature, but it is possible that they could be changed to increase their ability to cause disease, make them resistant to current medicines, or to increase their ability to be spread into the environment.

The very definition of bioterrorism (deliberate release of viruses, bacteria, or other germs (agents) used to cause illness or death in people, animals, or plants.) makes the H1N1 vaccine a bioweapon because it contains an adjuvant (additive) designed to weaken the immune system, and replicated RNA from the virus responsible for the 1918 pandemic Spanish flu, causing global sickness and mass death.