Category Archives: Big Pharma

Golden Dawn Immigrants-Fake NeoNazi’s

All those links were sent to me on Twitter and I am more than glad to post them,I do beleive I will find more on those people due time.No threats allowed according to the WP policy or the HR declaration. So please stay vigilant of what you are going to post :)I checked all blog categories so that the post can get the most views possible. Regards!

“##Spiros Macrozonaris## IMMIGRANT Golden Dawn Deputy leader in Montreal, Canada” :

Facebook profile :

INTERESTING FACEBOOK POST MR. MACROZONARIS, HE CANNOT EVEN WRITE GREEK! BAD NAZI BAD! :

His NON 100% PURE GREEK son’s Facebook : https://www.facebook.com/macrozonaris?ref=ts&fref=ts

1. Greek Immigrant who married a “foreigner” >>>>>French-Canadian Doris Morrissette, they bore a son, Nicolas Macrozonaris (World-Class Sprinter – CANADIAN Olympian 🙂 ..who unfortunately is not 100% Pure Greek…

2. Conversations with Nicolas on Twitter, lead to nothing, he is ‘pretending’ that he has NO knowledge of what Golden Dawn supports and believes YET he states that he does not condone his fathers “actions”

Twitter @Macrozonaris TWEETER CONVERSATIONS with Nicolas –>

###### MUST WATCH #####
Video from CBC Montreal, from week of Oct 12th – INTERVIEW with Spiros Macrozonaris – next to him sits LOOSER Ilias Hondronicolas : http://www.youtube.com/watch?v=v-3rbLI4K78

#Ilias Hondronicolas ———> on PHOTO second guy from the left :

#MORE HONDRONICOLAS:

(FRIENDS WITH ELENI ZAROULIA SHARING HER PHOTOS!)
( MUST SEE )

#MORE PAPAGEORGIOU:

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Mutant Avian flu: Expanding global vaccine production

 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[2011].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..
21 June 2012

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.).

antiviral compounds

Antiviral compounds

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

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

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.)

Neti Pot

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.

References:

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
7-7-9

Bioweapons, Dangerous Vaccines,
And Threats Of A Global Pandemic
By Stephen Lendman
7-7-9

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.

Laibow adds:

“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 lendmanstephen@sbcglobal.net.

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.

http://rense.com/general86/bio.htm


Big pharma takes aim at deadly counterfeits

 

By Katie McQue [Source]

GATEWAY TO AFRICA | In Africa the cost of all medications, including generic drugs, exceeds the means of most and many people are faced with a grim choice: purchase counterfeit medications, ingredients unknown, or go without treatment.

With 30% of the total available pharmaceuticals in Uganda believed to be counterfeit, the country, like many others, is struggling to keep control of a business that is both deadly and lucrative.

“A lot of deaths occur. But nobody reports these and nobody is going to investigate,” said Suraj Ali, a partner at the Ugandan legal firm Muwema & Mugerwa.

The situation in Uganda is typical in much of sub-Saharan Africa, and the reasons are economic. In regions of high prevalence of poverty the cost of all medications, including generic drugs, exceeds the means of most. Few people have medical insurance, and they are faced with a grim choice: purchase counterfeit medications – ingredients unknown – or simply go without treatment.

The big pharmaceutical firms are worried. “When you visit a market in Tanzania, you see that they are being sold everywhere,” Ed Wheatley, AstraZeneca’s investigations director for the region, said at June’s Visiongain Pharmaceutical Anti-Counterfeiting conference, in which representatives from major drug makers gathered to deliberate the problem.

This big problem is also a big business – it is widely estimated that counterfeit drugs have an annual turnover of US$75 billion worldwide, with a profit margin of about 70%. This means that the global share of counterfeit medications is 10% of the pharmaceutical market. Around the world 200,000 people die annually due to counterfeits.

Most of the fakes hail from factories in China, India and Pakistan, and counterfeiters are more concerned with matching the packaging than the ingredients of the original. Criminals steal hospital vials with branded labels, print their own hologrammed boxes – even buy tablet-making presses on eBay.

The World Health Organisation estimates that 32.1% of these drugs do not contain any active ingredients; 20.2% have incorrect quantities of active ingredients; 21.4% include wrong ingredients and 8.5% have high levels of impurities or contaminates.

The loss of sales and reputation is significant, as users of the fake drugs may still associate their illness with the genuine article. In some countries, drug makers can also be liable for harm caused by fakes.

In Germany, for example, a company can be called to account if it can be proven that it did not utilise all the possibilities provided by state-of-the-art technology to prevent counterfeiting. In most US states, any part of the manufacturing and sales chain can be liable for damages to the consumer arising from faults in a product’s construction, manufacturing or labelling.

Given this risk it is understandable why pharmaceutical companies are keen to intervene in the African counterfeit market. Some assist local governments with on-the-ground intelligence, leading to raids and prosecutions. This assistance is necessary in countries where awareness is low, resources devoted to the problem are scarce and corruption is high.

“There is a lot of corruption,” Ali said. “A lot of the magistrates are underpaid and they get bribed.

“We have a national drug authority that is supposed to prevent counterfeiting, but it is underfunded,” he added. “There are very few inspectors; they don’t have the equipment to check drugs properly… Things find their way into the country – the borders are very porous.”

 


Gates Foundation Funds Surveillance of Anti-Vaccine Groups

[SOURCE]
The Bill & Melinda Gates foundation launched the Grand Challenges in Global Health (GCGH) in partnership with the National Institutes of Health in 2003 which, according to the GCGH website, is aimed at “creating new tools that can radically improve health in the developing world.” So far, 45 grants totaling $458 million were awarded for research projects involving scientists in over 30 countries.

But where has all the money actually gone? Towards developing and implementing water purification and sanitation systems? Or basic nutritional support aimed at optimizing immune function? How about providing shelter and medical facilities for the homeless? Not even close.

For example, a $100K grant was recently disbursed to Seth C. Kalichman, professor at the Department of Psychology, University of Connecticut, for “Establishing an Anti-Vaccine Surveillance and Alert System,” which intends to “establish an internet-based global monitoring and rapid alert system for finding, analyzing, and counteracting misinformation communication campaigns regarding vaccines to support global immunization efforts.”

We can only wonder what organizations might be labeled as “misinformation communication campaigns” considering the fact that Bill Gates, in a Feb. 4th, 2011 interview on CNN with Sanjay Gupta said that “anti-vaccine groups “kill children.”” Here is the full quote:

“So it’s an absolute lie that has killed thousands of kids. Because the mothers who heard that lie, many of them didn’t have their kids take either pertussis or measles vaccine, and their children are dead today. And so the people who go and engage in those anti-vaccine efforts — you know, they, they kill children. It’s a very sad thing, because these vaccines are important.”

It is quite possible that any dissenting voice not in support of universal vaccination campaigns may be included in this type of “surveillance and alert system” as a potentially endangering the lives of others, i.e. “killing children.” What is so ironic about the situation is that the Gates Foundation supported Polio Global Eradication Initiative may have resulted in over 47,500 cases of vaccine-induced paralysis in Indian children in 2011 alone, and which is twice as deadly as the wild-type polio it claimed to have put an end to officially on Jan. 11 2012. Who here then, is truly concerned about the health of children?

Moreover, it is exceedingly difficult to view Bill & Melinda Gates foundation’s GCGH as a strictly humanitarian foundation considering many of the projects it chooses to fund. Here are a few listed on their website which have already received funding.

Synthetic Lymph Nodes: Steven Meshnick and Carla Hand of the University of North Carolina in the U.S. will develop a bio-compatible, biodegradable polymer device that can be placed under the skin to introduce vaccines and antigens to the immune system. The device will attract immune cells and trigger their proliferation as well asact as an adjuvant at the site of injection. If successful, the device could help boost immune response to new and existing vaccines. [see our article on transhumanistic technologies].

Needle Free Vaccination Via Nanoparticle Aerosols: Vaccine delivery systems that target specific areas of the body have the potential to be especially effective against some types of infection. For example, inhaled vaccines may better guard against respiratory diseases, such as tuberculosis, and those that commonly infect the tissues of the nose and throat, such as diphtheria. Dr. Edwards is leading a multidisciplinary team using materials science technologies combined with infectious disease, device, and toxicology expertise to reformulate tuberculosis and diphtheria vaccines into aerosol sprays that can be inhaled. The team’s ultimate objective is to develop a cell-based BCG vaccine for tuberculosis and a protein antigen CRM 197 vaccine for diphtheria in the form of novel porous nanoparticle aggregate (PNAP) aerosols.

Plant-Produced Synthetic RNA Vaccines: Alison McCormick of Touro University, California in the U.S. will test the ability of a low-cost plant-based synthetic biology method to produce a combined viral protein epitope with an antigen RNA expression system for use in an RNA malaria vaccine. Using plants for this viral transfection system could make RNA vaccine production scalable and cost effective.

Profitable Vaccine Distribution In Emerging Markets: Lisa Ganley-Leal and Pauline Mwinzi of Epsilon Therapeutics, Inc. in the U.S. will test the hypothesis that selling vaccines through medicine shops in emerging markets can lead to profits for both vaccine developers and the small business owners. Demonstrating profitability may lead pharmaceutical companies to invest greater resources in vaccine development and distribution and develop local partnerships for profitability strategies.

Genetically Programmed Pathogen Sense and Destroy: Saurabh Gupta and Ron Weiss of Massachusetts Institute of Technology in the U.S. proposed creating sentinel cells that can detect the presence of a pathogen, report its identity with a biological signal, and secrete molecules to destroy it. This project’s Phase I research demonstrated that commensal bacteria can be engineered to detect and specifically kill the model bacterial pathogen Pseudomonas aeruginosa. In Phase II, Gupta and Weiss will engineer the human microbiota to specifically detect and destroy the gut pathogen Shigella flexneri, which is responsible for high mortality rates in children.

Vaccine in a Salt Shaker: A New, Safe, Low-Cost Approach: Shiladitya DasSarma will lead a team at the University of Maryland, Baltimore in the U.S. to develop an inexpensive, safe, and effective oral vaccine against invasive Salmonella disease using gas-filled bacterial vesicles. The project seeks to produce a salt-encased, shelf-stable vaccine requiring no refrigeration for distribution worldwide.

A Humanized Mouse Model to Evaluate Live Attenuated Vaccine Candidates: To develop new vaccines against some of the world’s biggest killers, including HIV, malaria, and tuberculosis, scientists must be able to evaluate promising candidates. Some of the most promising potential vaccines, are made from weakened live versions of the infectious agent. As a result, they cannot be studied in human trials unless researchers can be confident that the weakened vaccines will be safe. Dr. Flavell and his colleagues are working to genetically engineer laboratory mice whose immune systems are similar enough to humans to permit testing of vaccines against diseases that disproportionately affect people in the developing world.

Alternative Delivery of Human Milk Proteins to Infants: Qiang Chen of Arizona State University in the U.S. proposes to engineer edible plants, such as lettuce and rice, to express beneficial proteins found in human milk. The protein bodies in these plants allow for the stable, high accumulation of these human milk proteins, and the plants can either be eaten directly by infants or formulated into baby food to provide essential nutrients and antibacterial benefits.

Non-Hormonal Female Contraceptive Targeting Egg-Specific Metalloprotease: John Herr of the University of Virginia in the U.S. will research the egg-specific membrane enzyme metalloprotease as a target for a non-hormonal female contraceptive. After determining the nature of the enzyme’s catalytic pocket, a family of peptidomimetic compounds will be tested for their ability to bind to the enzyme and block its key role in egg fertilization.

Bacillus-Fermented Natto as Edible Vaccines for the Developing World: Michael Chan of the Ohio State Research Foundation in the U.S. will develop an engineered strain of bacteria used to ferment beans in traditional Asian and African diets, to display an antigen from the Tuberculosis bacterium. The engineered bacillus will then be used to make the traditional Asian dish natto, which can serve as a kind of oral vaccine to elicit a strong immune response. If successful, this strategy can be used to introduce a variety of disease antigens through culturally accepted foods.

Nanotechnology-Based Contraception: David Clapham of Children’s Hospital Boston in the U.S. will develop and test a nanoparticle contraceptive that releases sperm tail inhibitors in response to vaginal pH changes or exposure to prostatic fluid. If successful, the nanoparticles could be incorporated into a vaginal gel to block sperm motility required for fertilization. Circumcision tool For Traditional Ceremonies In Africa: Kathleen Sienko of the University of Michigan in the U.S. has developed a prototype circumcision tool for use in traditional ceremonies in Africa, and seeks to demonstrate the functionality, cultural suitability, and potential for low-cost mass production of the device. Such a tool could increase the circumcision rates leading to lower rates of HIV transmission in the region.

Discovery of Chemosensory Molecules as Novel Contraceptives: John Ngai and Scott Laughlin of the University of California, Berkeley in the U.S. seek to identify chemical compounds in the female reproductive system that guide sperm cells to the egg. By characterizing these “odorants,” synthetic versions can be produced and administered to disrupt this navigation system thus inhibiting fertilization.

Transgenic Cow Milk Containing Human Antimicrobial Protein: Hironori Matsushima of the University of Toledo in the U.S. will test the hypothesis that adding an antimicrobial peptide to powdered milk products can confer protection against enteric diseases. Research will focus on testing the peptide for its ability to kill pathogens in stomach conditions, and on its ability to maintain integrity through the milk pasteurization and drying processes.

Ultrasound as a Long-Term, Reversible Male Contraceptive: James Tsuruta and Paul Dayton of the University of North Carolina, Chapel Hill will study the ability of therapeutic ultrasound to deplete testicular sperm counts. Characterizing the most beneficial timing and dosage could lead to the development of a low-cost, non-hormonal and reversible method of contraception for men.

You will notice from the examples listed above that all of these funded projects involve the development of proprietary (read: potentially profitable) and as-of-yet unproven technologies, and which will require the transformation and/or alteration of a natural process or substance. Also, many of the grant disbursements have gone towards contraception. This appears to diverge from the GCGH’s mission statement of “improving health in the developing world,” insofar as it is focused on reducing population in the developed world, rather than supporting the health of those already living, in need of help.[read the article]

 


DARPA Continues Human Experiments to Create Military Super Soldiers

 

Susanne Posel
Occupy Corporatism
September 25, 2012

The Defense Advanced Research Projects Agency (DARPA) has a $2 billion yearly budget for research into creating a super solider as well as developing a synthetic police force. Working with the human genome, DARPA hopes to manipulate certain gene expressions. In experimentation, DARPA and the military industrial pharmaceutical complex are using natural abilities that are enhanced through genetic engineering.

Some of the medical feats DARPA would like to enhance are the ability of military soldiers to regrow limbs destroyed in battle.

By eliminating empathy, the Department of Defense (DoD) hopes to “enhance” a soldier’s ability to “kill without care or remorse, shows no fear, can fight battle after battle without fatigue and generally behave more like a machine than a man.”

Scientists are researching the construction of soldiers that feel no pain, terror and do not suffer from fatigue as tests on the wiring of the human brain are furthered by Jonathan Moreno, professor of bioethics at Pennsylvania State University. Moreno is working with the DoD in understanding neuroscience. The Pentagon allocated $400 million to this research.

Further study could be passed onto the general public in order to maximize profits as well as enhance the drug’s effectiveness. According to Joel Garreau, professor at Arizona University, DARPA is learning how to genetically modify human fat into pure energy by rewiring the metabolic switch which would create soldiers that require less food. By using gene therapy and combining enhancements to alter the color of the human eye is a blending of mutations that have no basis in the natural world.

In 2011, the British Academy of Medical Sciences published a paper explaining the necessity for “new rules to avoid ethical missteps.” Specifying the injection of human brain cells into animals that may give animals human memories or thought consciousness as the goal should be dealt with differently than a non-modified animal.

Human embryos can strengthen or deteriorate the animal test subject which prompted Senator Sam Brownback to push the Human Chimera Prohibition Act of 2005. Brownback expressed need for prevention of closed-door experiments that “blur the lines between human and animal, male and female, parent and child, and one individual and another individual.” The ethical aspect could be defined by two mandates of consideration:

1. They could target the hypothetical scientists creating monsters in petri dishes.
2. They could take a close look at the science that’s really happening in labs around the world.

In addition to genetically modifying the human genome, global Elite are obsessed with the merging man and machine, transhumanism and immortality. Basing advancements on scientific research, the 2045 Program will create “a new vision of human development that meets global challenges humanity faces today, realization of the possibility of a radical extension of human life by means of cybernetic technology, as well as the formation of a new culture associated with these technologies.”

The globalists at the 2045 Program assert that humanity “is in need of a new evolutionary strategy” consisting of a balance between the complexity of technological advances and the acceleration of informational processes to expand the “limited, primitive human” into a “highly self-organized” and technologically “higher intelligence”.

The Project for the New American Century (PNAC) published a document entitled Rebuilding America’s Defenses in 2000 which frameworks a strategy for American hegemony in the near future, identifying “problem areas” of the world and advising regime change of unfavorable governments so that in the end the nations of the world will be unified under the banner of American democracy.

The revelation of former US President George Bush’s “axis of evil” defined American policy under the guidelines of the PNAC with the identification of Iran, Iraq and North Korea which is literally mentioned in the PNAC as governments that require a regime change.

In the PNAC, the globalists have described the use of scientific enhancement and clinical trials turning the US armed forces into gueinia pigs for the advancement of a super solider.

While Roger Pitman , professor of psychiatry at Harvard University is experimenting with propranolol which is a beta blocker that is believed to erase “terrifying memories”, soldiers are subjected to more research while serving to alleviate the psychological effects of war. Moreno explains: “The problem is: what else are they blocking when they do this? Do we want a generation of veterans who return without guilt?”

Allan Snyder, professor of neuroscience in Australia, has been working to understand how transcranial magnetic stimulation (TMS) can effect higher mental processing with the use of magnetic fields to promote unfettered reasoning.

The US Academy of Sciences reported in 2009 that they expected to be successful in using TMS against soldiers to “enhance [their] fighting capabilities.” Moreno reveals that TMS helmets could be used in battlefields to expand a soldier’s technical expertise and become a more proficient marksman and master electronics used in training exercises.

[….]

[source]
I never thought I would be talking about genetically modified people outside of pitching some new science fiction movie to the predictive programming industry called Hollywood. Instead I find the government admitting to secret tests being conducted on soldiers in order to genetically modify their abilities. The agency in charge of this Island of doctor Moreau research just happens to be the same department responsible for making drones and surveillance robots that will be used to gather up dissidents during the coming conflagration.
Human Hunters?

The Defense Advanced Research Projects Agency (DARPA) is an agency of the United States Department of Defense that receive over 2 billion dollars annually to conduct secret experimentation’s on soldiers and to create an Orwellian programmed robotic police force that will be used domestically as well as abroad. The manipulation of the human genome is perhaps the most disturbing demonstration of human arrogance this century has yet begun to exploit. DARPA has recently released some of the details to the genes they are manipulating and their expected expression and possible application. Here is a list of the current experimentation’s that have been conducted in secrecy on soldiers in the United States military or at least some of the recent confession from the military industrial pharmaceutical complex:

  • Do you want a soldier that can run faster than an Olympic Athlete?
  • Do you want a soldier that won’t need food or sleep for days?
  • Do you want a soldier that can regrow lost limbs?
  • Do you want a soldier that can out lift Olympic weightlifters?
  • Do you want a soldier that can communicate telepathically?

Genetically Modified Soldiers?

All of these manipulations to the human genome will eventually be pushed into the public sector to cash in on all the money that would be made from pills that will enhance your appearance and abilities. Just imagine how much revenue would be generated by a pill that could convert fat into energy or keep you awake for days on end with no need to worry about exercise or your dietary intake. Professor Joel Garreau of Arizona University confirmed that DARPA was experimenting with turning fat into energy. He recently disclosed this information to thedailymail stating, ‘Finding that metabolic switch would wipe out the £40billion diet industry in a heartbeat’. This is a covert way of saying it could create a monopoly that would destroy all its competitors which is the chosen model for the eugenicists natural selection propagandist. Gene therapy will be hitting the market in the next decade offering enhancements that at first will seem innocuous like changing the color of your eyes but in the end this blending of the human genome will only lead to mutations Mother Nature will create from our own arrogance.

 


Criminal Big Pharma: They Paid Off Your Doc To Poison You

New UK data finds prescription drugs 62,000 times more likely to kill than supplements

Wednesday, August 15, 2012 by: Tony Isaacs [source]

 

(NaturalNews) According to data just released by the UK-based Alliance for Natural Health International(ANH-Intl), pharmaceutical drugs are 62,000 times more likely to kill you than supplements. In fact, the data collected by ANH-Intl demonstrates that food supplements are the safest substances regularly consumed by UK citizens even though they are the target of increasingly restrictive European legislation aimed at ‘protecting consumers.’

The newly released data found that pharmaceutical drugs were also 7,750 times more likely to result in death than herbal remedies. Both food supplements and herbal remedies were placed in the ‘supersafe’ category of individual risk – with a less than one in ten million risk of death.

The stark contrast between the safety of supplements and mainstream medicine

By contrast, being admitted to a UK hospital or taking prescription drugs exposes a person to one of the greatest preventable risks in society. Overall, preventable medical injuries in UK hospitals expose patients to the same risk of death as being deployed on military service to Afghanistan – both of which are around 300,000 times greater than the risk of death from taking natural health products.

ANH-Intl executive and scientific director, Dr. Robert Verkerk, PhD, hailed the figures as shedding new light on the question of natural healthcare’s safety. “These figures tell us not only what activities an individual is most or least likely to die from, but also what the relative risks of various activities are to society as a whole. It puts some real perspective on the actual risk of death posed by food supplements and herbal remedies at a time when governments are clamping down because they tell us they’re dangerous.”

Verkerk added, “When compared with the risk of taking food supplements, an individual is around 900 times more likely to die from food poisoning and nearly 300,000 times more likely to die from a preventable medical injury during a spell in a UK hospital. The latter is on a par with the risk of death from active military service in Iraq or Afghanistan.”

According to Dr. Verkerk, the new figures should put pressure on UK and European authorities to reduce regulatory burdens on natural health products. “Governments justify the increasingly elaborate and restrictive new laws affecting natural health products on grounds of public safety,” said Verkerk. “They argue that reducing consumer access to food supplements and herbal remedies, with the consequent negative impacts on small businesses manufacturing, distributing and selling such products, is in society’s interest. But the evidence is simply not there – where are the bodies?”

Among other key points presented in the data were:

* Pharmaceutical drugs pose nearly double the risk of death than motorcycle accidents on UK roads

* While herbal medicines can both be regarded as ‘supersafe,’ preventable medical injuries in UK hospitals are in the ‘Dangerous’ category, with a risk of death greater than 1 in 1,000.

About that bone scan and the meds that follow…

Wednesday, August 15, 2012 by: Craig Stellpflug

(NaturalNews) Bone scans can be useful to find out bone density status, but most MD’s use bone scans to sell more bone scans and bone meds. Oh sure, they can tell you that your bones are thin with their technology, but what happens after the diagnosis is a real problem: prescriptions, procedures, worsening bone brittleness and more cancer. If we just assume that we need to be concerned about bone health and treat our bones naturally, there would be no need for bone scans.

The scoop on bone meds

Long-term use of bone meds like Actonel, Boniva, Fosamax and Reclast have been linked to femur fractures. One study found bones on these meds turning brittle at four years. Two studies found an increased risk of fracture at five years on these meds in healthy, active women. These bad drugs are linked to esophageal cancer, necrosis of the jaw, heartburn, abdominal pain, fever, bone and muscle pain, low energy and low levels of calcium in the blood.

The treatment with the drug Infuse for bone growth, causes the overall cancer risk (including pancreatic) to shoot up by more than 250 percent in one year and 500 percent by three years. Infuse also gives about 50 percent of patients the “side effects” of infection, male sterility, pain, bone loss, and unwanted bone growth.

The most damning vaccination study not publically disclosed to date

Wednesday, August 15, 2012 by: Paul Fassa

(NaturalNews) There have been reports from epidemiological studies confirming suspicions that those who are vaccinated often don’t do as well with long-term health as those who are vaccination free.Those epidemiological studies (statistical surveys) have shown that bad health is more common among the vaccinated who survive without serious injury than children not vaccinated.But how and why has not come under controlled animal lab studies until Japan’s Kobe Universityanimal lab study of 2009.This study was reported and peer reviewed in the PLOS One Open Journalat the end of 2009, but has not received much if any public attention. It was brought to public’s attention very recently by homoeopathist and health writer Heidi Stevenson’s article on her Gaia Health blog. (Source below)

Japanese study summary

Here’s the conclusion quoted from the Kobe University study’s journal report:

“Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s immune ‘system’ by repeated immunization with antigen, to the levels that surpass system’s self-organize criticality.” (Emphasis added.)

The initial purpose of this independently funded study was to understand how autoimmune diseases develop from autoimmunity. It was not an effort to prove vaccination safety or danger.

The researchers used mice that were bred to avoid autoimmune diseases and injected them with solutions that contain antigens. Antigens generate antibodies to protect against invading disease pathogens. Antibodies can turn against the host if they become self generated, causing autoimmune diseases.

A vaccination injects cultured vaccine antigens of weakened or dead viruses to create an immune response of antibodies to that antigen, supposedly for creating immunity to that particular disease.

It’s not very unusual for cytokine storms (immune system overreactions) to overwhelm one who has been vaccinated. Vaccine adverse reactions have caused injuries of permanent disability, autism spectrum disorders, or death more often than publicly disclosed.

The Kobe researchers injected the mice that were bred to not develop autoimmune diseases repeatedly with antigens, much like vaccinations are administered to infants and children, to study how an immune system could turn on itself to create autoimmune diseases.

They were pushing the mice’s immune systems to see if and when they would no longer bend, but break. They used Staphylococcus entertoxin B (SEB) as their injected antigens.

The study report did not mention including any toxic adjuvants or preservatives such as mercury, aluminum, or formaldehyde used in vaccines. Antigens were used without the toxic additives normally used in vaccinations.

After seven injections the mice recovered each time with their immune systems intact. But after the eighth injection, problems with key immunity cells began arising.

Damaged cells were observed microscopically and showed signs of early autoimmunity. Their immune systems had started to self generate antibodies for autoimmune reactions after repeated antigen inoculations. (Source below)

FDA drug reviewer: ‘one manager threatened my children’

Wednesday, August 15, 2012 by: Jon Rappoport

(NaturalNews) In a stunning interview with Truthout’s Martha Rosenberg, former FDA drug reviewer, Ronald Cavanaugh, exposes the FDA as a relentless criminal mafia protecting its client, Big Pharma, with a host of mob strategies.http://truth-out.orgCavanaugh: “…widespread racketeering, including witness tampering and witness retaliation.””I was threatened with prison.””One [FDA] manager threatened my children… I was afraid that I could be killed for talking to Congress and criminal investigators.”Cavanaugh reviewed new drug applications made to the FDA by pharmaceutical companies. He was one of the holdouts at the Agency who insisted that the drugs had to be safe and effective before being released to the public.

But honest appraisal wasn’t part of the FDA culture, and Cavanaugh swam against the tide, until he realized his life and the life of his children was on the line.

What was his secret task at the FDA? “Drug reviewers were clearly told not to question drug companies and that our job was to approve drugs.” In other words, rubber stamp them. Say the drugs were safe and effective when they were not.

Cavanaugh’s revelations are astonishing. He recalls a meeting where a drug-company representative flat-out stated that his company had paid the FDA for a new-drug approval. Paid for it. As in bribe.

He remarks that the drug pyridostigmine, given to US troops to prevent the later effects of nerve gas, “actually increased the lethality” of certain nerve agents.

Cavanaugh recalls being given records of safety data on a drug—and then his bosses told him which sections not to read. Obviously, they knew the drug was dangerous and they knew exactly where, in the reports, that fact would be revealed.

Read the entire landmark interview for yourself and see what the FDA really is. We are not dealing with isolated incidents of cheating and lying. We are not dealing with a few isolated bought-off FDA employees. The situation at the FDA isn’t correctable with a few firings. This is an ongoing criminal enterprise, and any government official, serving in any capacity, who has become aware of it and has not taken action, is an accessory to mass poisoning of the population.

Twelve years ago, the cat was let out of the bag. Dr. Barbara Starfield, writing in the Journal of the American Medical Association, on July 26, 2000, in a review titled, “Is US health really the best in the world,” exposed the fact that FDA-approved medical drugs kill 106,000 Americans per year.

Eli Lilly admits to more than $200 million dollars worth of doctor payoffs

Wednesday, August 15, 2012 by: Willow Tohi

(NaturalNews) Prozac. Cialis. Cymbalta. If you have a television or read magazines, you’ve heard of their drugs. Eli Lilly, out of Indiana, makes billions of dollars every year off the sale of their patented chemicals, which are used to suppress the symptoms of disease in the human body. Founded by a chemist in the late 19th century; today the pharmaceutical giant has offices in 18 countries, and its products are sold in 125 countries, with revenues exceeding $20 billion annually.Most of their arsenal is available in other countries for much less money than it is here in the United States, as is the case with most prescription medication. The reason, the pharmaceutical industry claims, is that the health care systems of other countries demands affordable medication, and they need somebody somewhere to foot the research bill, so they can get the next patents lined up before others expire, allowing generic versions of their drugs to become available on the market. That leaves us Americans, with our broken healthcare system, footing the bill of their continued financial success.We’re not only footing the bill, we have to deal with how the pharmaceutical machine warps the medical system. While historically a trade secret, it is standard operating procedure for pharmaceutical giants to pay doctors and other healthcare professionals to promote their drugs. Seducing doctors into becoming mouthpieces for a share of their bottom line is where it begins, but it ends up dictating your options.

A history of questionable ethics

Beginning in 2012, all drug and medical device companies will be required to report their promotional expenditure numbers to the federal government, but several companies started disclosing their information in 2009. According to the disclosed information, last year Eli Lilly paid out more than $200 million in payments to doctors and healthcare providers for promoting their drugs. ProPublica.org’s Dollars for Docs database is tracking 11 other companies’ disclosures as well.

The reason this information has been disclosed in Eli Lilly’s case is because Eli Lilly was involved in a criminal settlement, and was ordered to disclose these payments, since 2009. They agreed to pay $1.4 billion to settle criminal and civil allegations of promoting drugs for unapproved uses. An official from the FDA testified in a court of law that Eli Lilly concealed the risks of its schizophrenia drug Zyprexa from U.S. officials, knowing the serious health risks it caused. They defrauded Medicare/Medicaid and blatantly put profit over the concern of the consumer.

The disclosure documents say the payments were for speaking, consulting, and research, as well as travel and meal reimbursement. You can look up the breakdown of the payments; how much was paid into your state, if your doctor was among those paid. The data provides insights into how firms adapt their strategies over time, even though complete analysis has proved challenging. So few companies report their data, and the data that is reported is inconsistent in both content and format. Its unclear exactly how much money is being spent where, and by whom. Needless to say, there will be more on this story in the future.

The transparency of the newly required disclosures has some companies reevaluating the current strategy. Most of the pharmaceutical giants have begun to reduce their promotional expenditures, since they started disclosing the figures. Most of them offer explanations such as, “normal year-to-year fluctuations.” Experts predict physicians will begin backing away from these arrangements as well, as the increased scrutiny of the pharmaceutical sales practices also exposes their names and pay. Some doctors are raking in a quarter of a million dollars, but actually claim they “wouldn’t want the appearance of being influenced by anything the company gave” them. Interesting choice of words, huh? [read more]

 


Barack Obama,the Killer Companies and the Temple of Doom

 

By Amy Goodman with Denis Moynihan [source]

If a volcano kills civilians in Indonesia, it’s news. When the government does the killing, sadly, it’s just business as usual, especially if an American president tacitly endorses the killing, as President Barack Obama just did with his visit to Indonesia.

As the people around Mount Merapi dig out of the ash following a series of eruptions that have left more than 150 dead, a darker cloud now hangs over Indonesia in the form of renewed U.S. support for the country’s notorious Kopassus, the military’s special forces commando group. Journalist Allan Nairn released several secret Kopassus documents as the Obamas landed in Jakarta, showing the level of violent political repression administered by the Kopassus—now, for the first time in more than a decade, with United States support.

Last March, Nairn revealed details of a Kopassus assassination program in the Indonesian province of Aceh. These new Kopassus documents shed remarkable detail on the province of West Papua. As Nairn wrote in his piece accompanying the documents, West Papua is “where tens of thousands of civilians have been murdered and where Kopassus is most active. … When the U.S. restored Kopassus aid last July the rationale was fighting terrorism, but the documents show that Kopassus in fact systematically targets civilians.” In the Kopassus’ own words, the civilians are “much more dangerous than any armed opposition.”

One document names 15 leaders of the Papuan civil society, all “civilians, starting with the head of the Baptist Synod of Papua. The others include evangelical ministers, activists, traditional leaders, legislators, students and intellectuals as well as local establishment figures and the head of the Papua Muslim Youth organization.”

President Obama lived in Indonesia from the ages of 6 through 10, after his mother married an Indonesian man. Obama said in Jakarta this week: “[M]uch has been made of the fact that this marks my return to where I lived as a young boy. … But today, as president, I’m here to focus not on the past, but on the future—the Comprehensive Partnership that we’re building between the United States and Indonesia.” Part of that relationship involves the renewed support of Kopassus, which has been denied since the armed forces burned then-Indonesian-occupied East Timor to the ground in 1999, killing more than 1,400 Timorese.

A series of cell-phone videos have come out of Papua showing torture being inflicted on men there at the hands of what appear to be members of the military. In one video that surfaced just two weeks ago, soldiers burn a man’s genitals with a burning stick, cover his head with a plastic bag to suffocate him, and threaten him with a rifle. Another video shows a Papuan man slowly dying from a gunshot wound as the soldier with the cell-phone camera taunts him, calling him a savage.

I spoke with Suciwati Munir, the widow of the renowned Indonesian human-rights activist Munir Said Thalib, at the Bonn, Germany, reunion of Right Livelihood Award laureates. Her husband, an unflinching critic of the Indonesian military, received the award shortly before his death. In 2004, as he traveled to the Netherlands for a law fellowship, on board the Indonesian national airline Garuda, he was given an upgrade to business class. There, he was served tea laced with arsenic. He was dead before the plane landed. Suciwati has a message for Obama:

“If Obama has a commitment to human rights in the world … he has to pay attention to the human-rights situation in Indonesia. And the first thing that he should ask to President Susilo Bambang Yudhoyono is to resolve the Munir case.” I asked her if she wanted to meet President Obama when he came to Indonesia. She replied: “Maybe yes, because I want to remind him about the human-rights situation in Indonesia. Maybe not, because of his wrong decision, he has perpetuated the impunity in Indonesia.”

This was the third attempt by President Obama to visit Indonesia. His first delay was to allow him to push through health-care reform. The second was canceled in the wake of the BP oil disaster. This time he made it, although the Mount Merapi eruption forced him to leave a few hours early. Speaking from Jakarta, journalist Nairn reflected: “It’s nice to be able to go back to where you grew up, but you shouldn’t bring weapons as a gift. You shouldn’t bring training for the people who are torturing your old neighbors.”

Amy Goodman is the host of “Democracy Now!,” an independent, daily global TV/radio news hour airing on more than 950 stations in the United States and around the world. She is the author of “Breaking the Sound Barrier,” recently released in paperback and now a New York Times best-seller.

© 2011 Amy Goodman

“Three years ago, President Obama cut a secret deal with pharmaceutical company lobbyists to secure the industry’s support for his national health care law. Despite Obama’s promises during his campaign to run a transparent administration, the deal has been shrouded in mystery ever since. But internal emails obtained by House Republicans now provide evidence that a deal was struck and GOP investigators are promising to release more details in the coming weeks.

“What the hell?” White House Deputy Chief of Staff Jim Messina, who is now Obama’s campaign manager, complained to a lobbyist for the Pharmaceutical Research and Manufacturers of America (PhRMA) in January 15, 2010 email. “This wasn’t part of our deal.”

This reference to “our deal” came two months before the final passage of Obamacare in an email with the subject line, “FW: TAUZIN EMAIL.” At the time, Billy Tauzin was president and CEO of PhRMA.

The email was uncovered as part of investigation into Obama’s closed-door health care negotiations launched by the House Energy and Commerce committee’s oversight panel.

“In the coming weeks the Committee intends to show what the White House agreed to do as part of its deal with the pharmaceutical industry and how the full details of this agreement were kept from both the public and the House of Representatives,” the committee’s Republican members wrote in a memo today.

On June 20, 2009, Obama released a terse 296-word statement announcing a deal between pharmaceutical companies and the Senate that didn’t mention any involvement by the White House.

“The investigation has determined that the White House, primarily through Office of Health Reform Director Nancy Ann DeParle and Messina, with involvement from Chief of Staff Rahm Emmanuel, was actively engaged in these negotiations while the role of Congress was limited,” the committee members wrote. “For example, three days before the June 20 statement, the head of PhRMA promised Messina, ‘we will deliver a final yes to you by morning.’ Meanwhile, Ms. DeParle all but confirmed that half of the Legislative Branch was shut out in an email to a PhRMA representative: ‘I think we should have included the House in the discussions, but maybe we never would have gotten anywhere if we had.’”
[read more]

Obama’s Half-Billion-Dollar Crony Drug Deal

“Here comes Siga-Gate.

This latest Chicago-style payoff on your dime involves a dubious smallpox drug backed by a liberal billionaire investor, along with a former union boss who was one of the White House’s most frequent visitors. They’re the “1 percent” with 100 percent immunity from the selectively outraged Occupier mobs that purport to oppose partisan government bailouts and handouts to privileged corporations.

Ronald Perelman is the New York City-based leveraged buyout wheeler-dealer who controls Siga Technologies. He has donated nearly $130,000 mostly to Democrats over the past two election cycles alone (history here), and he forked over $50,000 to pay for the president’s lavish inaugural parties. A Siga affiliate (MacAndrews and Forbes) pitched in nearly half a million more in contributions — 65 percent of which went to Democrats — and the firms have spent millions on lobbying.

Perelman’s pharma company makes an experimental antiviral pill used by smallpox patients who received diagnoses too late to be treated with the existing smallpox vaccine. Smallpox experts cast doubt on the need for the drug given ample vaccine stockpiles, the remoteness of a mass attack and questions about its efficacy. But over the objections of federal contract negotiators, competitors and scientists, the Obama administration approved a lucrative $433 million no-bid deal for Siga in May. No other manufacturers were able to compete for the “sole source” procurement, according to the Los Angeles Times.”[read more]

Exxon Makes $104 Million In Profit Per Day So Far In 2012, While Americans Are Stuck With A Higher Gas Bill

By Rebecca Leber on Apr 26, 2012 at 10:08 am

Last year, ExxonMobil, one of the world’s most profitable companies, earned $1,300 in profits per second. As consumers paid record-high springtime gas prices, Exxon posted first quarter profits of $9.45 billion.

This is down slightly from the first quarter of 2011, when Exxon posted $10.65 billion in profits. Exxon benefited from the high price of oil, but analysts expected slightly lower profits due in part to the cheap price of natural gas, which the company is heavily invested in.

A by-the-numbers look shows how Exxon’s executives and Big Oil’s allies are rewarded generously for the company’s billions, while Americans are stuck with rising gas bills:

$9.45 billion profits, or almost $104 million per day in the first three months of the year.

13 percent: The tax rate Exxon paid last year, lower than the average American family.

60 percent of its first quarter earnings, or $5.7 billion, on buying back stock. Became world’s largest dividend payer by increasing dividends 21 percent.

$1,091,000: Political contributions sent to federal politicians for the 2012 election cycle, making it the largest oil and gas spender.

91% of these contributions went to Republicans.

More than $52,000,000: Lobbying for the first three years of the Obama presidency, 50 percent more than in the Bush Administration.

$34.9 million: Exxon CEO Rex Tillerson’s salary for 2011, a 20 percent raise.

$52,300: Political contributions from Exxon CEO Rex Tillerson in the 2012 cycle, alone.

No. 2: Fortune 500 list of richest companies and for highest-paid CEO.[read more]

 


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