Allow me to add a personal note here .Right now I am writing I am recovering from the H5N1 flu,so is my family. It’s not a joy ride i can reassure you,i still feel my muscles stiff and my bones about to crack in pieces. BUT we took NO antibiotics,NO VACCINES- this is a is a must-not-do for my family-,nothing. We had poor luck with all those “lethal” viruses so we got them all,Swine flu in 2009 and again the mutant swine flu last year.WE didn’t die. Of course none of us belongs to the high risk groups. Yet we took a slight taste of pneumonia and other complications like otitis
I can not advise you if you belong to a high risk population group. But if you do not,just take some basic precautions and it will pass. We “survived” of five flu attacks with no harm done . You don’t need any killing Tamiflu or any vaccine that will make you more vulnerable to diseases
A friend of mine,a doctor,he said to me when i asked” you cannot predict a virus when it is bombed with antibiotics,the most possible to happen is to face new,mutant strains,resistant to known drugs”
And when i asked in return,why the Pharma industry doesn’t adapt their antibiotics to the new shown strains,he answered” if they did so,they would never claim a Pandemic“…
the rest is known..
The H5N1 ‘bird flu’ virus could evolve to spread through the air between ferrets by picking up as few as five mutations, according to a long-awaited study from Ron Fouchier from the Erasmus Medical Centre in Rotterdam, the Netherlands1. The paper is published today in Science after months of debate about whether the benefits of publishing the research outweighed the risks.
H5N1 can cause lethal infections in humans but it cannot spread effectively from person to person. Fouchier’s paper is the second of two publications describing how the virus could evolve this ability. The first, from Yoshihiro Kawaoka at the University of Wisconsin–Madison, involved a hybrid virus with genes from both H5N1 and the H1N1 strain behind the 2009 pandemic2 (see ‘Mutant-flu paper published‘). Fouchier’s mutant contains only H5N1 genes.
“Coming after the Kawaoka manuscript, I thought it might be anti-climactic, but it does not fail to deliver,” says Vincent Racaniello, a virologist at Columbia University in New York.
There is only one common mutation in the combinations that Fouchier and Kawaoka identified. “It just means that there are multiple ways to skin a cat,” says Robert Webster, a virologist at St Jude Children’s Research Hospital in Memphis, Tennessee.
Despite their differences, both sets of mutations confer similar properties on H5N1. Some mutations allow the haemagglutinin (HA) protein on the virus’s surface to stick to the kind of receptors found in the human upper airway. Others stabilize the protein, an unexpected property that now seems to be important for transmission among mammals. “Two very different strategies led to common functional changes,” says Malik Peiris, a virologist at the University of Hong Kong, who notes that these changes are “not uncommon in field strains already”.
Fouchier now wants to know whether these traits could make any flu virus go airborne, and whether previous pandemics started in this way. “The virus could evolve in a thousand different ways,” he says. “But if we can show that any receptor-binding mutations, or any that change the stability of HA, can yield airborne viruses, the story becomes completely different. We can then do surveillance for mutations that cause the same phenotype.”
Fouchier’s team began by adding three mutations to an H5N1 strain isolated from Indonesia in 2005. Two of these — Q222L and G224S — changed the HA gene such that its protein preferentially sticks to human-type receptors over those found in bird cells. The third — E627K — changed the PB2 gene, which is involved in copying the virus’ genetic material, so that the virus was able to replicate more easily in the cooler environment of mammalian cells.
The team allowed this mutant virus to evolve naturally by passing it from one ferret to the next, injecting it into the animals’ noses and collecting samples daily for four days. After ten rounds, the virus could spread between ferrets housed in separate cages.
These airborne strains spread less effectively than the 2009 H1N1 virus, and are sensitive to current antiviral treatments and potential vaccines. They are lethal if delivered directly to the ferrets’ airways in high doses, but not if the animals catch the infections naturally through the air.
Fouchier’s airborne viruses carried a diverse array of mutations, with just five mutations shared by them all, including the original three that Fouchier had inserted and two more in the HA gene: T156A, which affects receptor binding, and H103Y, which stabilizes the protein. The five mutations might be enough for H5N1 to spread between ferrets, but it may take nine or even more. “Until the changes are introduced in combinations into H5N1 virus, we won’t know the answer,” says Racaniello.
In a related paper published in Science3, Derek Smith from the University of Cambridge, UK, and his colleagues has shown that wild H5N1 viruses already have many of the mutations that Fouchier and Kawaoka identified. Some of the viruses are two to four nucleotide substitutions away from the complete sets. However, whether those mutations would allow different strains of H5N1 to spread between ferrets, let alone humans, remains unclear.
Fouchier now wants to work out the number of other individuals who catch the airborne virus for everyone who is infected. This number “needs to be higher than 1 to cause a pandemic”, he says. “We need more quantitative transmission models to start addressing that.”
But Racaniello thinks a different approach would be more effective. “I suggest that we spend research money developing more flu antivirals, and a universal flu vaccine,” he says[Source]
Will Tamiflu save the world from the avian flu?
No one wants to catch the flu! At the very least, it will put you out of commission for a week, and it can also cause life-threatening infections – pneumonia is the most common, although other bacterial diseases like bronchitis are common too. Most people don’t think about problems with secondary infections after catching the flu, but a deadly form of the flu could be just around the corner.
The H5N1 “avian” flu is highly deadly among birds, and it has occurred in humans. Most people who contract the avian flu have had direct contact with infected birds. Fortunately, H5N1 does not appear to spread from human to human, but what if mutations occur in the virus that allow this to happen?
The 2009 H1N1 “swine” flu reminded us of the potential for flu pandemics that cross over to humans from other animals.
Based on its severity in birds and in the humans who have been infected, an H5N1 pandemic could be far more deadly than the H1N1 pandemic; it could kill a significant percentage of the world’s population! For example, in the 1918 flu pandemic, about 5% of the world’s population died. Based on the virulence of H5N1 in birds, it’s predicted that a higher percentage of humans would die as a result of a H5N1 human pandemic, although this is, of course, conjecture. In support of this conjecture, however, is the fact that 63% of the humans who have been infected with H5N1 have died (Hurt et al.).
Fortunately Tamiflu (Oseltamivir) and a related drug, Relenza (Zanamivir), reduce the severity of the flu if they are given when the flu symptoms initially appear. But will the drugs be effective forever?
Seventy years ago, antibiotics such as penicillin seemed like miracle drugs. But now bacteria are evolving to become resistant to antibiotics, in part because the antibiotics have been overprescribed. Could the same thing occur with antivirals as they become used more frequently? It is a possibility.
Mutations, changes in the genetic code of an organism, occur rapidly in the influenza virus. Most mutations are harmful to the virus, but a few are beneficial (and, therefore, potentially harmful to humans). A mutation could occur in an influenza virus that allows it to resist the effects of Tamiflu and Relenza. Such a virus would then grow much more rapidly than a nonresistant form in the presence of the drugs.
To understand how Tamilflu and Relenza function and how the virus might become resistant to them, we need a little background on the life cycle of the flu virus. When an unsuspecting victim inhales a flu virus, a protein on the surface of the virus called hemagglutinin (the ‘H’ in H1N1, for example) binds to a receptor called sialic acid on the surface of cells in the respiratory tract (see structure of sialic acid in picture above).
Influenza life cycle
The cell takes in the virus, which then replicates inside the host cell. The newly formed viruses leave the cell by budding off the surface. The hemagglutinin on the new viruses can then bind to the sialic acid on the surface of other host cells, thus infecting new cells. For this to occur, however, the viruses need to escape the host cells. Another viral surface protein, neuraminidase (the ‘N’ in H1N1, for example), breaks down the sialic acid receptors so the viruses can escape.
Tamiflu and Relenza are structurally similar to sialic acid and will bind to the neuraminidase, but they cannot be broken down. Therefore, neuraminidase cannot bind to sialic acid on the cell surface when it has Tamiflu or Relenza bound to it. Because they prevent neuraminidase from functioning, the two drugs are collectively referred to as neuraminidase inhibitors (NAIs). When NAIs are present, some of the newly produced virus will get stuck to the original host cell and will not be able to infect other cells. Some viruses will still escape, so NAIs don’t cure the flu but rather reduce its severity.
Are NAI-resistant viral mutants forming? Studies have identified a few flu viruses that are resistant to these drugs. A very dedicated (and patient) group of scientists (Monto et al.) grew up a whopping 2287 samples of flu virus that were collected from all over the world during the first three years (1999-2002) the drugs were prescribed. They grew these samples in the presence of each of the two NAIs. While the vast majority of the viruses were not resistant to the drugs, a few samples were. Resistance was determined by measuring the concentration of the drug needed to inactivate each virus. These results were concerning; however, another team of scientists (Yen et al.) studied two NAI-resistant flu mutants and found that they were not as contagious nor as fit as the non-resistant strains.
Ferrets used in nasal washes
Yen et al. (2005) also showed that the virus didn’t grow as well in vitro, and they measured how well the virus grew in an in vivo model. In those studies, three ferrets were infected with the virus: two with the mutant strains and one with a wild type (not mutated) virus.
After two days, each ferret was put into close contact with two other ferrets. Each day after exposure, the researchers took nasal washes of each ferret and quantified the amount of virus in the wash. (I wonder if there is a neti pot for ferrets.)
Net pot for sinus infection
The washes showed that less virus was produced by the two resistant mutants. In fact, one of the ferrets exposed to a mutant virus was less contagious. Other studies have found this to be the case with the most resistant flu virus mutants. That is, the more resistant the flu virus is to an NAI, the less virulent is the virus.
However, exceptions were found in a further study by Yen et al. in 2006, where they found two mutants that were resistant to the drugs but still grew relatively well, which is more concerning. While these mutants did not appear naturally (they were designed by the lab) they could, in principle, occur in nature.
None of these studies looked at the H5N1 avian flu directly, but because the drug-resistant viruses were found over a wide variety of strains, there is potential for an H5N1 mutant that is resistant to Tamiflu and Relenza. Fortunately the drug-resistant mutants are usually less fit, so an H5N1 NAI-resistant mutant might not be as deadly. It appears that Tamiflu and Relenza would help reduce the impact of an H5N1 pandemic. However, we must monitor the virus for resistant mutants.
Silver, G. (2003) The treatment of influenza with antiviral drugs. Canadian Medical Association Journal 168 (1), 49–57.
Monto, A., McKimm-Breschkin, J., Macken, C., Hampson, A., Hay, A., Klimov, A., Tashiro, M., Webster, R., Aymard, M., Hayden, F., & Zambon, M. (2006). Detection of Influenza Viruses Resistant to Neuraminidase Inhibitors in Global Surveillance during the First 3 Years of Their Use Antimicrobial Agents and Chemotherapy, 50 (7), 2395-2402 DOI: 10.1128/AAC.01339-05
Yen, H., Herlocher, L., Hoffmann, E., Matrosovich, M., Monto, A., Webster, R., & Govorkova, E. (2005). Neuraminidase Inhibitor-Resistant Influenza Viruses May Differ Substantially in Fitness and Transmissibility Antimicrobial Agents and Chemotherapy, 49 (10), 4075-4084 DOI: 10.1128/AAC.49.10.4075-4084.2005
Hurt, A., Holien, J., & Barr, I. (2009). In Vitro Generation of Neuraminidase Inhibitor Resistance in A(H5N1) Influenza Viruses Antimicrobial Agents and Chemotherapy, 53 (10), 4433-4440 DOI: 10.1128/AAC.00334-09
Yen, H., Hoffmann, E., Taylor, G., Scholtissek, C., Monto, A., Webster, R., & Govorkova, E. (2006). Importance of Neuraminidase Active-Site Residues to the Neuraminidase Inhibitor Resistance of Influenza Viruses Journal of Virology, 80 (17), 8787-8795 DOI: 10.1128/jvi.00477-06
- Bioweapons, Dangerous Vaccines,
And Threats Of A Global Pandemic
By Stephen Lendman
Bioweapons, Dangerous Vaccines,
And Threats Of A Global Pandemic
By Stephen Lendman
Although international law prohibits the use of chemical and bacteriological weapons, America has had an active biological warfare program since at least the 1940s. In 1941, it began secret developmental efforts using controversial testing methods. During WW II, mustard gas was tested on about 4000 servicemen. Biological weapons research was also conducted. Human subjects were used as guinea pigs in various other experiments, and numerous illegal practices continued to the present, including secretly releasing toxic biological agents in US cities to test the effects of germ warfare.
The Hague Convention of 1907 banned chemical weapons usage, and the 1928 Geneval Protocol prohibited gas and bacteriological warfare. The 1972 Biological Weapons Convention (BWC) “Prohibit(ed) the Development, Production and Stockpiling of Bacteriological (Biological) and Toxin Weapons and Their Destruction.” The 1989 Biological Weapons Anti-Terrorism Act “implement(ed the) Prohibition of the Development, Production, and Stockpiling of Bacteriological (Biological) and Toxin Weapons and Their Destruction….”
In 2001, the Bush administration rejected the 1972 BWC, took advantage of a loophole allowing “prophylactic, protective or other peaceful uses,” continued a secret Clinton administration bioweapons initiative, and asserted its right to spend multi-billions illegally to develop, test and stockpile “first-strike” chemical and biological weapons that potentially can kill millions.
In his August 14, 2008 article titled, “The Pentagon’s alarming project: Avian Flu Biowar Vaccine,” F. William Engdahl cited:
“alarming evidence accumulated by serious scientific sources that the US Government is about to or already has ‘weaponized’ Avian Flu. If reports are accurate, this could unleash a new pandemic on the planet that could be more devastating than the 1918 Spanish Flu epidemic which killed an estimated 30 million people worldwide before it eventually died out. Pentagon and NIH experiments with remains in frozen state of the 1918 virus are the height of scientific folly” unless something more nefarious is afoot in collaboration with Big Pharma to produce weaponized viruses and/or dangerous mandatory vaccines that, at the least, can cause serious autoimmune diseases or, as some allege, a Swine Flu or other viral pandemic.
Alarming News about Baxter International
On February 27, 2009, various news agencies including Helen Branswell in the Canadian Press, reported:
Baxter International that “released contaminated flu virus material from a plant in Austria confirmed (today) that the experimental product contained live H5N1 avian flu viruses.” The WHO said the incident occurred at the company’s research facility in Orth-Donau, Austria, but claimed “that public health and occupational risk is minimal” thus far. What’s not known, however, “are the circumstances” behind the incident that, according to some, raise suspicions while others call it a willful criminal act. More on that below.
The contaminated product, “a mix of H3N2 seasonal flu viruses and unlabelled H5N1 (Avian Flu) viruses, was supplied to an Austrian research company….Avir Green Hills Biotechnology.” It then “sent portions of it to sub-contractors in the Czech Republic, Slovenia and Germany.”
The problem was discovered when The Czech Republic company discovered that ferrets innoculated with the product died. “Ferrets shouldn’t die from exposure to human H3N2 flu viruses.” Public health authorities called it a “serious error” that showed “the H5N1 virus in the product was live.” But Baxter “has been parsimonious about the amount of information it has released about the event.” Christopher Bona, the company’s global bioscience communications director, did confirm that the material was a “live….experimental virus” made at the Orth-Donau research laboratory.
Security experts expressed alarm that something this serious could happen, calling the co-mingling (or reassortment) of human H3N2 with H5N1 avian viruses a dangerous practice that should never occur because of the potentially devastating effects to human health. “If someone exposed to a mixture of the two had been simultaneously infected with both strains, he or she could have served as an incubator for a hybrid virus able to transmit easily to and among people,” who, in turn, could transmit it to enough others to potentially cause a pandemic. So far, nothing this extreme has happened, but a future threat remains.
As Medical Director of the Natural Solutions Foundation, Dr. Rima Laibow warns about dangerous, toxic drugs and vaccines. On March 6, 2009, she posted a “Pandemic Flu Emergency Action eAlert on her healthfreedomusa.org web site stating:
“World media (outside America) are reporting that Baxter Pharmaceuticals has admitted that it ‘accidently’ contaminated various vaccine batches with Avian Flu viruses. These batches were shipped to 18 countries. Clearly, either 1. stupidity and incompetence (are to blame) or 2. intentional contamination of flu vaccine lots was at work.”
Many Avian Flu vaccines compete with each other, yet they’re “profitable ONLY if used in huge numbers.” Although “Avian Flu has been slow to be become pandemic by ‘jumping the species barrier’ to humans in large numbers,” might Baxter’s “accident” be a way to do it? If so, Big Pharma will score “One of the biggest wins in history.”
In fact, it already has after the Center for Infectious Disease Research & Policy (CIDRAP) reported that Congress (in mid-June) “approved $7.65 billion for battling pandemic influenza, more than three times what the House and Senate had earlier proposed.” Unsurprisingly, it was part of “a $106 billion (Iraq and Afghanistan war) supplemental appropriation bill” to open a new front at home in the form of dangerous vaccines – perhaps to be mandated for everyone.
Laibow sees a “manipulated disaster of unprecedented magnitude precipitated by unprecedented avarice and greed,” and adds that “Baxter International Inc. is no stranger to recalls and lethal contaminations.” Its record includes producing faulty infusion and volumetric pumps, HIV-2 tainted Albumin Buminate 5 percent, faulty dialysis machine tubing and blood-cleaning filters, and various other products that should make everyone leery of its soon-to-be-released Swine Flu vaccine. Along with similar ones from other pharmaceutical companies, these drugs cause serious autoimmune diseases and absolutely should be avoided, even if mandated.
Laibow expresses great alarm in stating:
“Baxter mixed a virus which has a hard time infecting people (H5N1 Avian flu) with one that infects them easily (“Seasonal Flu”) in a medium which can promote mutations of the H5N1 virus into a type which can infect us easily. What will be in the vaccine you are forced/coerced/threatened into allowing into your body? Who knows?”
What is known are our constitutional and Nuremberg Code rights. The Fifth Amendment protects against abusive government authority in stating that “No person shall….be deprived of life, liberty, or property, without due process of law….” The Eight Amendment prohibits “cruel and unusual punishments.” Depriving someone of health is tantamount to the latter as well as life by harming and potentially shortening it.
The Nuremberg Code requires voluntary consent of human subjects without coercion, fraud, deceit, and with full disclosure of known risks. It also affirms that experiments should avoid “all unnecessary physical and mental suffering and injury,” and should never be conducted if there’s “an a priori reason to believe death or disabling injury will occur” or harm to human health.
The FDA as an Industry Front Group
As stated on its web site, the FDA is mandated to protect human health and well-being.
As an agency in the Department of Health and Human Services (HHS), “The FDA is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation.”
Run by officials of the industries it “regulates,” it fails on all counts. Byron J. Richards is a clinical nutritionist and founder of Wellness Resources. In his book “Fight for Your Health: Exposing the FDA’s Betrayal of America,” he discusses FDA complicity with Big Pharma, dangerous drugs worth billions of dollars to the industry, and the serious risks to people who use them. He states:
“The FDA has put into mothballs its federal mandate to protect the public. In order to foster drug sales, the FDA hides important medical data from the public and from doctors, including the risks of heart attacks, suicide, seizures, and serious mental-health debility. Even worse, the FDA has changed sides. They are actively undermining the rights of citizens to claim damages if injured by drugs. And they are seeking to remove safety barriers to drug testing. They are planning to expose many individuals to unproven drugs, a new form of human experiment” that may rise to a higher level if HHS mandates dangerous Swine Flu vaccines for all Americans despite no forensic evidence of an outbreak or even a single proved death attributable to H1N1.
Yet, in advance of what looks to be coming, on June 11, the WHO declared that “The world is now at the start of the 2009 influenza pandemic (in) decid(ing) to raise (its) influenza pandemic alert from phase 5 to (its highest) phase 6” level.
Dr. Laibow advises that everyone has a “right to say “NO!” to vaccinations and other treatments that (they) do not want. The Police Power of the State ENDS at my skin and yours!” If a pandemic erupts, as a longtime natural health practitioner, she advises what she’ll use herself – Nano Silver as well as vitamins, minerals, and herbs like echinacea that boost the immune system, unlike dangerous vaccines that destroy it. For more information, she directs individuals to the web site: <http://www.nutronix.com/naturalsolutions>www.nutronix.com/naturalsolutions.
WHO, CDC, and Canada’s Public Health Agency (PHAC) Fearmongering Misinformation
Besides declaring its highest Level 6 influenza pandemic alert on June 11, the BBC reported on July 3 that WHO’s Director-General, Dr. Margaret Chan, warned that the spread of swine flu is “unstoppable” while admitting that most cases are mild and many people recover unaided.
On June 25, Daniel DeNoon in WebMD Health News reported that CDC’s influenza surveillance chief, Dr. Lyn Finelli, said: “Right now, we are estimating over 1 million (Swine Flu) cases in the US” in 2009 affecting about 6% of households in major cities. She, too, admitted that the vast majority of cases have been mild but avoided the fundamental issue – that no forensic evidence attributes a single death globally to Swine Flu and all or most known instances may be ordinary viral influenza or common colds, bad enough to cause fever (at times high) and discomfort, last several days and then pass for most people.
With no proof, Finelli cited 3065 Swine Flu hospitalizations and 127 deaths. In a June 26 telebriefing, Dr. Anne Schachat, CDC’s National Center for Immunization and Respiratory Diseases director, cited no verifiable forensic documentation in saying:
“The novel H1N1 (Swine Flu) influenza is continuing to spread here in the United States and around the globe. The key point is that this new infectious disease is not going away. In the US, we’re still experiencing a steady increase in the number of reported cases (and they’re just) the tip of the iceberg.” She added that vaccines are being hurriedly produced. No decisions have been made about “which populations” will need them, but “it’s very important for states and communities to begin intensifying their efforts on planning to administer a vaccine should such be necessary in the fall,” especially for “young people including school children, pregnant women, babies, and adults, particularly younger adults with those underlying conditions….” That said, it “doesn’t mean we’ve finalized any vaccine recommendations.”
On June 21, Canada’s National Post published Sharon Kirkey’s Canwest News Service report headlined, “Vaccinate Canadians under 40 and (aboriginal) natives first: experts.” She added that “Under Canada’s official pandemic plan, the entire population would ultimately be immunized against H1N1 swine flu,” but not at once as vaccines will only be available in batches.
Canada’s Public Health Agency (PHAC) “is working on a priority list,” effective for all provinces and territories. Gymnasiums will be used for mass vaccinations of school children, but no final decisions have been made.
In a June 26 news release, PHAC reported that “The Government of Canada today launched a three-year public education campaign to encourage parents to have their children immunized against certain diseases before the age of two. The Honorable Leona Aglukkaq, Minister of Health, made the announcement at the annual meeting of the Canadian Paediatric Society” saying that “Immunization is one of the best tools we have to protect the health of our children.”
In fact, all vaccines are dangerous and should be avoided. They contain squalene-based adjuvants that cause a menu of autoimmune diseases in test subjects. In humans they include chronic fatigue, various type rashes, chronic headaches, anemia, aphthous ulcers, seizures, weakness, neuropsychiatric problems, ALS, Raynaud’s phenomenon, and multiple sclerosis, among other illnesses and diseases, some causing death.
It’s why Dr. Laibow says “No insurance company in the world will insure against” their risks. In America, a special fund “has paid out over 2 billion dollars to parents of children killed or maimed by vaccinations.” However, the vast majority of those harmed are never compensated, and US law ‘immunizes’ drug companies from lawsuits.
“In fact, vaccines are explicitly acknowledged NOT to protect against diseases they supposedly are designed to prevent (read the Package Inserts for vaccines, available on line and in your doctors’ offices if you doubt that) and often” cause them.
Yet they continue in use because they’re so “immensely, enormously and hideously profitable,” and Big Pharma has enough clout to proliferate products that “in a rational society (should) be banned forever.”
Bioterrorism Criminal Charges Filed
On June 10, Austrian journalist Jane Burgermeister filed sweeping criminal charges with the FBI in addition to earlier ones on April 8 with the Vienna State Prosecutor’s Office against Baxter AG, Baxter International and Avir Green Hill Biotechnology AG, “for manufacturing, disseminating, and releasing a biological weapon of mass destruction on Austrian soil between December 2008 and February 2009 with the intention of causing a global bird flu pandemic virus and of intending to profit from that same pandemic in an act that violates laws on international organised crime and genocide.”
Baxter operates Biosafety Level 3 (BLS-3) labs that take strict precautions to assure no possibility of accidental H3N2 and H5N1 co-mingling contamination unless something more nefarious is afoot.
BLS-3 personnel are trained in handling pathogenic and potentially lethal agents and are supervised by competent scientists with extensive experience with them. In addition, these labs have specially engineered design features for added safety.
On its web site, CDC lists four biosafety levels:
— BLS-1 labs are “suitable for work involving well-characterized agents not known to consistently cause disease in healthy adult humans, and (pose) minimal potential hazard to laboratory personnel and the environment.”
— BLS-2 labs are “similar to Biosafety Level 1 and (are) suitable for work involving agents of moderate potential hazard to personnel and the environment. It differs from BLS-1 in that (lab personnel) have specific training in handling pathogenic agents,” and are “directed by competent scientists.” In addition, access to the labs are limited, and “extreme precautions are taken with contaminated sharp items….”
— BLS-3 labs work with “indigenous or exotic agents which may cause serious or potentially lethal disease as a result of exposure by the inhalation route. Laboratory personnel have specific training in handling pathogenic and potentially lethal agents, and are supervised by competent scientists who are experienced in working with these agents.” Labs also have “special engineering and design features,” and follow strict procedures. In addition, protective clothing, equipment, and other extreme precautions are taken.
— BLS-4 labs are for the most highly toxic and dangerous agents – ones “that pose a high individual risk of aerosol-transmitted laboratory infections and life-threatening disease.” As a result, the strictest possible procedures and precautions are always taken.
By combining human influenza H3N2 with bird flu H5N1 virus in its BLS-3 lab, “Baxter produced a highly dangerous biological weapon with a 63 per cent mortality rate. The H5N1 virus is restricted in its human-to-human transmissibility, especially because it is less airborne.”
“However when….combined with seasonal flu viruses (easily transmitted by air), a new flu virus is created which is unknown to the human immune system and which will have a severe impact on an unprotected population. A deadly virus of this kind could spread around the world in a short time and (potentially) infect millions and even billions of people.”
Baxter (via Avir) “distributed (72 kilos of) contaminated (live bird flu) vaccines using false concealment and a false labels to 16 laboratories in Austria and….other countries at the end of January/beginning of February, potentially infecting at least 36-37 laboratory staff, who (were) treated preventively for bird flu and ordinary flu.” On the same day, 18 Avir employees were as well at Vienna’s Otto Wagner Hospital.
Burgermeister cited a Baxter-Avir 2006 contract with Austria’s Health Ministry for 16 million vaccine doses in case a bird flu pandemic was declared. She maintains that this “laboratory incident shows that national and international authorities are not able to fulfill their obligations to ensure the safety of the Austrian people” and claims that authorities were engaged in a cover-up.
“If a pharmaceutical company can breach laws – and almost trigger a bird flu pandemic, which (potentially could spread worldwide) – without being made accountable for it….then there is, de facto, no rule of law on Austrian territory.”
She also contends that Baxter’s production system, “namely, the use of 1200 liter bioreactors and vero cell technology,” meets “the technical criteria to be classified as a secret dual purpose large-scale bioweapon production facility (able to produce) a huge amount of contaminated vaccine material….rapidly.”
“If (this) material were added to the 1200 liter bioreactors, it would replicate and infect the entire batch of vaccine material in (it). Contaminated material could (then) be distributed among sections of the population using false labels and secretly marked batches (able to) infect millions of people.”
Burgermeister accused high-level Austrian Health and other Ministry officials of knowledge and support of this practice. Otherwise, controls would have been in place to prevent it. In June, she named drug producers Baxter, Novartis and Sanofi Aventis, world agencies, including the WHO, UN, and CDC, and high-level officials in Austria, other European countries, and America.
Whether or not there’s enough evidence to substantiate her charges, her case is vital to alert people globally to the potential health threat they face because inadequate controls are in place if the worst occurs.
It highlights the importance of being alert to this and other potential health hazards given lax government regulations and public complicity with powerful corporate interests, that in alliance show a disturbing indifference to public safety and well-being – worse still because dominant print and broadcast media stoke fear by reporting misinformation to convince people to use dangerous drugs and vaccines they should avoid.
As they say, forewarned is forearmed. Better be safe than sorry. Something nefarious may or may not be afoot, but it’s vital to learn the truth, know the risks, and assert your legal right to refuse all dangerous vaccines and other medications, even if mandated.
Stephen Lendman is a Research Associate of the Centre of Research on Globalization. He lives in Chicago and can be reached at firstname.lastname@example.org.
Also visit his blog site at sjlendman.blogspot.com and listen to The Global Research News Hour on RepublicBroadcasting.org Monday – Friday at 10AM US Central time for cutting-edge discussions with distinguished guests on world and national issues. All programs are archived for easy listing.