Saturday, September 26, 2009

Fcuk the Pittsburgh Police


submitted on reddit by user infernoenigma

Reddit, I had to create an account to post about what just happened on my campus. I go to the University of Pittsburgh. Pittsburgh... G20, you know. President Obama's dinner for the delegates happened just off campus, within eyesight of us -- usually. When people grouped up by the street that would lead to the Phipps Conservatory, they were met with armored police.

For a while the students and locals just stood and talked while the police line faced us. Some people sang and had signs. Others just watched. Slowly, the line of locals began to advance. A police officer with a megaphone stepped out several times and told us to leave the area, but as we weren't doing anything wrong, most people didn't leave.

That's when they shot a canister of gas at us. Reddit, sprinting away from armored police who looked like Storm Troopers from Star Wars, hearing that hissing sound while one of my favorite spots on campus filled with smoke... it was terrifying.

When the smoke cleared the crowd was still there.

This standoff lasted several hours. Around 10:30, the atmosphere had changed. The police had advanced far up the road toward students, who were kept back to a grassy area called Schenley Plaza. Students were singing and dancing. It was very peaceful. Someone said something to a cop.

Suddenly the guy was grabbed and thrown on the ground. The crowd AT ONCE surrounded the cops and started chanting LET HIM GO! LET HIM GO! LET HIM GO!

There was a dumpster lit on fire further up the road, so I went up there to see what I could see, and suddenly there were tons of people sprinting down the sidewalk away from the fire. SWAT vans and six or seven major police cars pulled up to Schenley Plaza.

Reddit, the next two hours were complete chaos. My campus was invaded by armored police officers. They threw actual tear gas into crowds of students. They SHOT students with rubber bullets. They beat slower-moving students with a baton. I saw a group of cyclists being herded down the sidewalk. A cop reached out and pushed a woman on a bike. She turned around and pushed her bike at the cop. Next thing we knew, he grabbed her by the face and slammed her down on the concrete.

They slowly advanced us back down Forbes Avenue, toward the major freshman dorms. Several protesters broke storefront windows. I'd guess 20 protesting, about 1,000 students watching (if that.) The police fired Sound Cannons at us, a new weapon never before used on US citizens, which plays a sonic pulse that gives major headaches. They fired more tear gas at the students.

Then riot squads came running up behind us and forced us into the Litchfield Towers Lobby. People who did not make it into the lobby before the riot squads got to the doors were grabbed, thrown to the ground, beaten, and arrested.

Here is the part where I felt most violated -- The riot cops then ENTERED our dormitory and shouted that students needed to return to their rooms immediately. Anyone arrested, they said, would be expelled from the University of Pittsburgh, no questions asked.

Reddit, is that legal? Would police be able to force someone on the sidewalk back in their home and make them barricade themselves in their basement?

Here's another part that got me -- I saw students try to get in the doors closest to their dorm building (there are 3 towers), and the door was LOCKED. These students did not have time to run around the building. And they were grabbed.

We don't know what to do. We're shocked. BECAUSE THE DEPUTY POLICE CHIEF RELEASED A STATEMENT CLAIMING THEY WERE SECURING THE AREA FROM ANARCHISTS AND THAT "SOME" STUDENTS "PROBABLY GOT CAUGHT UP" IN WHAT HAPPENED.

So, in the news, you'll hear that police secured the campus from anarchists. Not that students were attacked by security forces supposedly there to protect them. PLEASE, help me get the word out.












Global Genocide Part 2


It was reported 15 Sep 2009 by CNBC
The Food and Drug Administration approved the new swine flu vaccine Tuesday, a long-anticipated step as the government works to get vaccinations under way next month.

Studies in children and pregnant women are continuing. The vaccine approved Tuesday is made by CSL of Australia; Switzerland's Novartis; Sanofi-Pasteur of France; and Maryland-based Medimmune, which makes the only nasal-spray flu vaccine.

FDA approved “the vaccine”? Four different vaccine manufacturers are listed and they all make a completely different product, each as different as chalk and cheese, yet they are all reported as “the new swine flu vaccine”

For example the CSL product, we are led to believe has no adjuvants, see Panvax post for details. A report on trials that started also on 15 Sep 2009 in Colorado using Novartis vaccine, detail they do use the adjuvant SQUALENE, it's named in the consent forms for participants, see – Vactruth

It is interesting that the FDA approved the CSL product (Panvax) while the equivalent Australian (TGA) was not so quick to do so, the Australian Government took unusual action to exempt Panvax from regulations requiring approval and registration before it is dispensed.

Many more big pharma companies are all busily concocting their own H1N1 so called vaccinations. Baxter International Inc. filled a patent for a swine flu vaccine in August 2008. To make a vaccine, researchers must first make a recombinant virus. Baxter, some time prior to Aug 2008, produced a H1N1 strain in the kidney cells of African Green Monkeys.

Even after the most stringent filtering and purification procedures, a small portion of this monkey DNA and cell protein remains in the end product vaccine. According to Dr. M Hilleman, the AIDS virus was unleashed upon humans when the Merck pharmaceutical company used African Green Monkey kidneys to make hepatitis B vaccines; the kidney cells contained AIDS which remained present in the finished vaccine product in initial tests.

An interview with Dr. Maurice Hilleman (Merck pharmaceutical company vaccine division chief) by Dr Edward Shorter (medical historian) reveals this abominable truth and another equally disturbing admission that a cancer virus was loose in the 1950’s polio vaccines.

In Lies We Trust Part 14 of 16 by Dr. Leonard G. Horowitz





Extracts from Transcript:

ES: Tell me how you found SV40 in the polio vaccine

MH: I came to Merck and I was going to develop vaccines. We had wild viruses in those days, wild monkey kidney viruses and so forth. I finally after 6 months gave up, I said you can not develop vaccines with these dam monkeys, if I can’t do something about them I quit. So I went to see Bill Mann at Washington DC zoo and I told him, look I got a problem. These lousy monkeys are picking it up (viruses) while being stored at airports in transit. He said it is very simple, get your monkeys out of West Africa, get the African green, bring them into Madrid, unload them there, there are no other traffic through there for animals, fly them into Philadelphia and pick them up. So I brought African greens in. I didn’t know we were importing AIDS virus at the time.

ES: What Merck won’t do to develop a vaccine?

MH: This was the solution because those monkeys didn’t have the wild viruses.

ES: Why didn’t the greens have the wild viruses?

MH: Because they weren’t being infected in these group holding things with all the other 40 different viruses.

ES: But they had the ones they brought from the jungle though?

MH: Yeah they had those but there were relatively few. If you have a gang housing you are going to have an epidemic transmition of infection in a confined space. So anyway the greens came in and we were taking our seed stocks and now I’m discovering new viruses.

I got an invitation from the Sister Kenny Foundation (researched using live viruses), they asked me to come down and give a talk. I though what will I talk about? I know, I’ll talk about the detection of non detectable viruses. So now I got to have something you know that’s going to attract attention, so I thought gee, that dam SV40, I mean that dam vacuolating agent we have, I’m going to pick that particular one. That virus has got to be in the vaccines and it’s got to be in Sabin’s vaccine, so I quickly tested it and sure enough, it was in there.

ES: So you just took stocks of Sabin vaccine of the shelf here at Merck?

MH: No, it was made at Merck.

ES: You were making it for Sabin?

MH: Yeah, it was made before I came.

ES: But at this point Sabin is still doing these massive field trials?

MH: Yes, in Russia and so forth. So I got down and talked about the detection of non detectable viruses. I told Albert (Sabin), look Albert I’m going to talk about a virus that is in your vaccine. You’re going to get rid of it, don’t worry about it.

ES: What did he say?

MH: He said basically that this is just another obfuscation that is going to upset vaccines. I said you are right but we have a new era here of detection and the important thing is to get rid of these viruses.

ES: Why would he call it an obfuscation if it was a virus contaminating the vaccine?

MH: Well because there were 40 different viruses in these vaccines anyway that we were inactivating.

ES: But you weren’t inactivating his though?

MH: No, that’s correct. Yellow fever vaccine had leukemia virus in it; this is in the days of very crude science. So I talked to him about it (Sabin), he said why are you concerned about it? I said well I have a feeling in my bones that this virus is different. I don’t know why, I feel this virus may have some long term effects. He said what? I said cancer. I said Albert you are going to think I’m nuts but I just have that feeling.

In the mean time we had taken this virus and put it into hamsters. So we had this meeting and that was sought of the topic of the day, the jokes that were going around were that “We would win the Olympics because the Russians would all be loaded down with tumours”. This was where the vaccine was made and tested.

But anyway, we know it was in our seed stocks for vaccines. That virus, 1 in 10,000 particles is not inactivated by formaldehyde, it was good science at the time because that was what you did, and you didn’t worry about those wild viruses.

ES: So you discovered it (SV40 cancer virus) wasn’t being inactivated in the Salk (Jonas Salk polio vaccine)?

MH: Right, so then the next thing you know is 3 or 4 weeks after that, we found that there were tumours popping out of these hamsters.


See also:

sciencedirect.com
Hilleman determined that poliovirus replicated well in AGMK cells. As a test to determine that the poliovirus was inactivated by this treatment, he placed the formalin inactivated poliovirus vaccine, which did not grow in rhesus cells and was inactivated, onto these AGMK cells. Surprisingly he saw the cytopathic effects of a virus in the vaccine extract that had been made in rhesus cells. The rhesus cells themselves harbored a virus that had no cytopathic effects in rhesus and that failed to be inactivated by the formalin treatment that killed the polio virus, and this new virus, which was named Simian Vacuolating Virus 40 or SV40, replicated and killed AGMK cells.

As Hilleman stated in his publication about this surprising result; “The discovery of this new virus, the vacuolating agent, represents the detection for the first time of a hither-to “nondetectable” simian virus of monkey renal cultures and raises the important question of the existence of other such viruses” Antibodies directed against SV40 could be detected in five of seven children who received the Salk vaccine.

Extracts from Baxter H1N1 patent

United States Patent Application

Method for producing viral vaccines

Assignees: Baxter International Inc.

Filed: Aug 28, 2008

The present invention provides a method for the manufacture of a preparation comprising virus antigens comprising:
  • inoculation of cells with infectious virus in a fluid
  • propagation of said virus in said cells
  • collecting said propagated virus
  • inactivating said collected virus, and
  • treating said inactivated virus with a detergent, resulting in a preparation comprising viral antigens
In another aspect the present invention provides the method of increasing the resistance to a viral infection in a subject comprising manufacturing a preparation comprising viral antigens and administering said preparation to a subject.


Invention details a Monovalent Virus Harvest. Monovalent - one antigen only, for vaccinating against one specific pandemic only.

Apart from the actual details of the invention, Baxter details general industry info of note in this patent, eg. –

An essential step in the production of viral vaccines is the inactivation of the infectious viruses. Formalin is the most frequently used inactivating agent, usually around 37% formaldehyde. Ultraviolet (UV) irradiation has been considered for integration into the manufacturing process. By combining formalin and UV, scientists tried to overcome the limitations of one isolated method when inactivating particularly resilient virus families.

Alternatively many manufacturers use detergent to inactivate or modify the live virus. This process disrupts the lipid envelope of influenza viruses to yield either split (partially disrupted) or sub-unit (fully disrupted) vaccine antigen.

Extracts from the Detailed Description of Invention
[0029] e) treating said inactivated virus with a detergent, resulting in a preparation comprising antigens. Central to this procedure is that it is possible to reduce the number of steps performed on an active virus and thus the virus is inactivated after collection of the primary harvest prior to the detergent treatment and/or optional purification steps.

[0041] in a further embodiment of the present invention, the cells use for cell culture and viral propagation may be primary cells or any cultured cell line. Examples of cells which may be used include mammalian (e.g., CHO, BHK, VERO, HELA, or perC6), avian and insect.

  • CHO - derived from the ovary Chinese hamster

  • VERO – derived from the kidney of African Green Monkeys

  • BHK - Syrian hamster

  • HELA - a cancerous cell belonging to a strain continuously cultured since its isolation in 1951 from a patient who died from cervical cancer. Also an immortal cell line (ability to proliferate indefinitely).

  • perC6 - derived from human embryonic retinal cells

[0044] in embodiments of the invention, the virus is modified by detergent treatment to produce a modified whole virus or split virus vaccine. Suitable detergents include Tween 80 and Triton X100.

[0056] in further embodiments a vaccine composition is provided which comprises one or more viral antigens. Such a composition can further comprise a pharmaceutical carrier and/or an adjuvant. A further aspect of the present invention is a pharmaceutical composition or preparation as vaccine comprising an antigen.

[0057] suitable adjuvants can be selected from mineral gels, aluminium hydroxide, lysolecithin, or oil emulsions.

[0062] three different influenza strains, two A-strains Hiroshima (HR, H3N2), a New Caledonia (NC, H1N1) and a B-strain, Malaysia (MA), were produced in Vero cell cultures.

[0079] Benzonase, a recombinant nuclease produced in E. coli, is added to the virus suspension at a final concentration of 3 U/ml to degrade cell derived DNA.

[0085] for virus splitting, Triton X100 is added to a final concentration of 0.5% (w/w) and incubated over night at room temperature.

[0089] formalin is added into the Ultra/Diaretentate to a final concentration of 0.025% for antigen stabilization. Formalin is a saturated acqueous solution of 36-37% formaldehyde gas.

[0104] for the New Caledonia strain at the end of purification, total Vero protein could be reduced from 8mg to 2mg from the Peak Pool to the Monovalent Bulk (MVB). Vero DNA content in the MVB was 0.27 µg. Total protein was reduced from 382mg to 162mg.

It is very interesting indeed what can be learned from reading pharmaceutical patents. Here is another made jointly by MedImmune Vaccines Inc. and the US Gov. NIH (National Institutes of Health). The patent is for Influenza Hemagglutinin and Neuraminidase Variants, filled Aug 2007.

Background info:

Hemagglutinin - rcsb.org
A spike-shaped protein that extends from the surface of the virus, the name to the ability of influenza to agglutinate red blood cells: the virus is covered with many hemagglutinin molecules, which together can glue many red blood cells together into a visible clump.
Neuraminidase - enzyme that removes sialic acid from mucoproteins and is found chiefly in microorganisms of the respiratory and intestinal tracts.

wikipedia
Human flu viruses have a neuraminidase enzyme, signified in the name "H#N#", where the H refers to an isoform of hemagglutinin and N refers to an isoform of neuraminidase.
Another pretext, the patent is concerned with producing peptides –

patentstorm.us
US Patent 5200320 - Method for identifying useful polypeptide vaccines

In order to immunize an animal (including humans) against a particular infectious agent, it is necessary to activate T-cells specific for a protein (antigen) derived from the agent. It has previously been suggested that the final step in this activation of T helper cells is the creation of a trimolecular complex consisting of major histocompatibility complex (MHC) II molecules (Ia molecules), `processed` antigenic protein (both on antigen presenting cells -APC), and the T-cell receptor. As a necessary step in the formation of the foregoing complex, the processed antigen must bind to Ia molecules of the APC of the individual animal to be immunized. For a number of reasons, synthetic peptides derived from infectious agents may be useful as vaccines.

Extracts from MedImmune/NIH patent

United States Patent Application

Influenza Hemagglutinin and Neuraminidase Variants

Assignees: MedImmune Vaccines Inc., the Government of the United States of America National Institutes of Health

Filed: Aug 9, 2007

Abstract
Polypeptides, polynucleotides, methods, compositions and vaccines comprising (avian pandemic) influenza hemagglutinin and neuraminidase variants are provided.

[0003] live attenuated virus vaccines have the advantage of being able to stimulate local mucosal immunity in the respiratory tract. Considerable work in the production of influenza viruses, and the fragments thereof, for production of vaccines has been done by the present inventors and co-workers.

[0004] because of the continual emergence (or re-emergence) of different influenza strains, new vaccines are continually desired. Such vaccines are created using antigenic moieties of the newly emergent virus strains, thus, polypeptides and polynucleotides of novel, newly emergent, or newly re-emergent virus strains (especially sequences of antigenic genes) are highly desirable.

[0005] the present invention provides new and/or newly isolated influenza hemagglutinin and neuraminidase variants that are capable of use in production of numerous types of vaccines.

[0009] Methods for stimulating the immune system of an individual to produce a protective immune response against influenza virus, through administering an immunologically effective amount of such recombinant influenza virus in a physiologically acceptable carrier are also part of the invention.

[0069] The term “host cell” means a cell that contains a heterologous nucleic acid, such as a vector, and supports the replication and/or expression of the nucleic acid. Host cells can be prokaryotic cells such as E. coli, or eukaryotic cells such as yeast, insect, amphibian, avian or mammalian cells, including human cells. Exemplary host cells can include, eg., Vero (African Green Monkey kidney) cells, BHK (baby hamster kidney) cells, primary chick kidney (PCK) cells, Madin-Darby Canine Kidney (MDCK) cells, Madin-Darby Bovine Kidney (MDBK) cells, 293 cells (eg., 293T cells), and COS cells (eg., COS1, COS7 cells), etc.

* 293T - Human Embryonic Kidney cells, also often referred to as HEK 293.

* COS cells - obtained by immortalizing (ability to proliferate indefinitely) a CV-1 cell line derived from African green monkey kidney cells with a version of the SV40 monkey virus genome.

[0076] various embodiments of the invention utilize A/Ann Arbor (AA)/6/60 influenza strain as a “backbone” upon which to add HA and/or NA genes to create desired reassortant viruses.

[0078] Live attenuated influenza A virus vaccines against human influenza viruses were recently licensed in the US. Such vaccines are reassortant H1N1 and H3N2 viruses. Classical genetic reassortment and plasmid-based reverse genetics techniques have been applied to generate reassortant viruses that contain the Hemagglutinin and Neuraminidase genes from avian influenza A viruses. The generation and evaluation of these reassortant viruses as seed viruses for vaccines are important steps in pandemic preparedness.

[0080] The term “cold adapted” (ca) indicates that the virus exhibits growth at 25˚ C. within 100 fold of its growth at 33˚ C., while the term “attenuated” (att) indicates that the virus replicates in the upper airways of ferrets but is not detectable in their lung tissues.

[0088] A related aspect of the invention provides methods for stimulating the immune system of an individual to produce a protective immune response against influenza virus. In the methods, an immunologically effective amount of a recombinant influenza virus (eg., comprising an HA and/or NA molecule of the invention), an immunologically effective amount of a polypeptide of the invention, and/or an immunologically effective amount of a nucleic acid of the invention is administered to the individual in a physiologically acceptable carrier.

[0089] Generally, the influenza viruses of the invention are administered in a quantity sufficient to stimulate an immune response specific for one or more strains of influenza virus (i.e., against the HA and/or NA strains of the invention).

[0090] Typically, the attenuated recombinant influenza of this invention as used in a vaccine is sufficiently attenuated such that symptoms of infection, or at least symptoms of serious infection, will not occur in most individuals immunized (or otherwise infected) with the attenuated influenza virus. In some instances, the attenuated influenza virus can still be capable of producing symptoms of mild illness and/or dissemination to unvaccinated individuals.

[0093] Optionally, the formulation for prophylactic administration of the influenza viruses also contains one or more adjuvants for enhancing the immune response to the influenza antigens. Suitable adjuvants include: complete Freund’s adjuvant, aluminium hydroxide, oil or hydrocarbon emulsions, Bacille Calmette-Guérin (BCG) and Corynebacterium parvum.

[0125] The present invention also relates to host cells that are introduced (transduced, transformed or transfected) with vectors of the invention, and the production of polypeptides of the invention by recombinant techniques. Host cells are genetically engineered (i.e., transduced, transformed or transfected) with a vector, of this invention.

[0126] Most commonly, mammalian cells are used to culture the HA and NA molecules of the invention. Suitable host cells for the replication of influenza virus include, e.g., Vero cells, BHK cells, MDCK cells, 293 cells and COS cells. Commonly, co-cultures including two of the above cell lines, e.g., MDCK cells and either 293T or COS cells are employed at a ratio, e.g., of 1:1, to improve replication efficiency.

These two patents paint a horrific picture from the world of mad science vaccine production. The MedImmune/NIH patent is just mind boggling in the way it casually advocates for example that; suitable adjuvants include complete Freund’s adjuvant.

See post – mandatory chemical weapon assault
The classic oil-based adjuvant called Freund’s Complete Adjuvant can cause permanent organ damage and irreversible disease – specifically autoimmune diseases. When scientists want to induce autoimmune disease in a lab animal, they inject it with Freund’s Complete Adjuvant.
And the “suitable and/or exemplary host cells” for propagating the viruses that go into the vaccines, unbelievable! Chinese hamster, African Green Monkeys crossed with monkey virus genome, cancerous cells, human embryonic cells, dogs, and the icing on the cake, splicing dog and human embryonic cells together to “improve replication efficiency”.

The later patent is also most revealing in the disclosure that “In some instances, the attenuated influenza virus can still be capable of producing symptoms of mild illness and/or dissemination to unvaccinated individuals.”

Doctors have long known this to be true. Rima E. Laibow, MD writes in the publication “The Syringe of Death”
Vaccines have not eradicated diseases: vaccines spread diseases. Attenuated viruses (infective, weakened versions of the dangerous ones) are commonly used in vaccines.

This practice derives from the dawn of vaccination: Edward Jenner’s pioneering use of cowpox pus inoculations to eliminate smallpox. It makes a wonderful story but, in fact, inoculation not only spread smallpox, it caused well-documented epidemics of syphilis and leprosy in inoculated people.

When a live virus is used in the vaccine, infective virus is shed for anywhere from 4 to 21 days (or more) and, during that time, inoculated persons can give the disease, or the side effects of the inoculation, to any vulnerable person they come into contact with.

Neither Jenner’s cowpox inoculation nor modern smallpox inoculation did anything to eliminate smallpox (quite the contrary). The fact is Dr. Charles Campbell discovered that smallpox is transmitted by the flying bedbug, Cimex lectularius, and that eliminating this parasitic insect from human habitation eliminates smallpox too. Personal hygiene and better housekeeping eliminated the deadly scourge. (Dr. Campbell also discovered that the disfiguring pocks of the disease could be prevented by a diet high in Vitamin C.)

When the World Health Organization (WHO) declared the planet “smallpox free” in 1980, they did so administratively, not medically: small pox incidence was reduced, but not gone, despite nearly universal vaccination. What to do? WHO solved the problem cleverly: they renamed the disease “cowpox” and “monkey pox”. Shazam: a smallpox free planet, quicker than you can say, “Junk Science!”

Despite the considerable hype, in fact, there is no unbiased evidence which connects disease prevention with inoculation.

The “Horrors of Vaccination Exposed and Illustrated” published in 1920 by Chas Higgins, Higgins writes of the 1918 Spanish H1N1 flu pandemic.
In a previous letter to the Secretary of War, dated October 14, 1918, I have pointed out the dangerous nature of vaccination, particularly during epidemics, and the hygienic importance of suspending all vaccination during our recent epidemic of influenza and pneumonia.

I also then called attention to the probability that the repeated and multiple vaccinations of millions of men, in this country and Europe, with various septicemic infections for the last two years, may have had some relation to this epidemic, which seems to have been more severe among the vaccinated men in the military camps and hospitals than among the rest of the population.

From the rapidity, severity and mortality of this disease, it would seem not to be a true influenza as its worst cases are characterized by septic pneumonia, with abscesses in the lungs. This suspicion is strengthened by the fact that the chief germ found in the fatal cases is the “streptococcus,” which is found in the worst forms of blood poisoning or “septicemia.” The act of ordinary vaccination is in itself, an act of blood poisoning, pure and simple. It is also classed in medical and statistical works as a form of “septicemia” and one disease germ commonly found in vaccine virus is the streptococcus, which is the chief germ found in all bad pus infections and abscess formations.

Therefore, as the act of vaccination is simply the impregnation of the body and blood with a pus infection identical with “septicemia”, and this process has been repeated in tens of thousands of men closely massed in camps, should it be any wonder if an epidemic of some sort of “septicemia” should crop out at some time under such conditions?

Is it physically or medically possible to go on sowing and spreading some known and unknown septic diseases at wholesale, within human bodies, without reaping some big harvest of deadly septic diseases as a necessary consequence?



Friday, September 25, 2009

Global Genocide Part 1


Dr. Leonard G. Horowitz, and Sherri Kane, an investigative journalist, have made legal affidavits exposing a drug cartel accused of creating, releasing, injecting, infecting, and depopulating planet with Pandemic H1N1 Swine Flu Viruses and Vaccines. Their documents have been sent through attorneys to the FBI for investigation.

Extracts from the AFFIDAVIT of LEONARD G. HOROWITZ, published at fluscam.com
I have reviewed the records and files cited herein and attest to the following facts that evidence of fraud, official malfeasance, organized crime, and the administration of genocide operating under the guise of “public health” within a trust organization established by David Rockefeller called “Partnership for New York City” involving the US Federal Government, and New York State Government, pertaining to the 2009 H1N1 Swine Flu “outbreak,” “pandemic,” and advancing vaccination campaign.

It is a well-established fact that “outbreaks” have been caused by laboratory “accidents.” For instance, the 1977 Influenza A outbreak of human “swine flu” H1N1 that went extinct for twenty years between 1957 and 1977 suddenly re-emerged immediately following:
  • The suspicious unexplained 1976 military outbreak at Fort Dix, New Jersey of this strain that was most likely a covert military experiment; and
  • The subsequent swine flu deadly vaccination program that followed the Fort Dix outbreak.
The 1977 re-emergence of this Influenza A H1N1 strain in the former Soviet Union is best explained by the National Cancer Institute’s 1978 publication titled: Special Virus Cancer Program. This report revealed a June 15, 1976 contract with the American Type Culture Collection, to supply “virus materials . . . to investigators throughout the world” via a “US-USSR Agreement”

Virus materials cited in this document included numerous infectious agents including influenza, parainfluenza and even laboratory recombinations of influenza with acute lymphocytic leukaemia viruses that might spread quick acting lymphatic cancers by sneezing.

The April, 2009 “outbreak” of the H1N1 “swine flu” is, like the 1976 Fort Dix and 1977 general “outbreaks,” highly suspicious according to genetic analysts and leading virologists. The rapid mutation rates of the novel agent circulating and feared as the 2009 “swine flu” strongly suggests a laboratory source, either intentionally or accidentally released.

To make it more difficult for the public to comprehend what is ongoing in flu labs, World Health Organization (WHO) officials developed new terminology to describe viruses used in vaccinations, gene therapies, and advancing biotechnologies. The new terms “reference materials,” “biosimilars,” “data packages,” and “mock-up files,” each designate viruses and/or viral materials including gene sequences that cause disease and immune system reactions.

It is certain that when the Mexican Swine Flu 2009 “outbreak” occurred in mid April, 2009, first in the United States in two unrelated children living approximately 100 miles apart in southern California, then soon after in Mexico among people who had not been exposed to these two children, that foul play is a most reasonable explanation, especially since this unique virus held genes from avian, swine, Spanish, and regular flu strains—unprecedented in the history of “natural selection”

Accountable US Federal officials overseeing America’s “biopreparedness” response against this mutant H1N1 flu, including vaccinations and predicted quarantines, offer no definitive explanation for the initial outbreak of this laboratory sourced recombinant; nor does the mainstream media. So called “experts” accept and regurgitate the lame explanation of “somehow” and “somewhere” bird, pig, and 1918 Spanish flu viruses mated curiously synchronously with the first availability of biotechnology to produce vaccines alleged to be safe and effective against this precise new H1N1 and H5N1 genetic recombinant.

Thomas H. Glocer is the Chief Executive Officer of the Thomson Reuters Corporation (TRC) and Director of the TRC that partnered in David Rockefeller’s biotechnology trust called “Partnership for New York City,” (PNYC). Thomas H. Glocer is also a Merck [pharmaceutical company] Director since 2007.

Two additional “partners” are the New York State Government, and the US Federal Government, likewise advancing vaccine research in partnership with private companies in this PNYC. Both governments then purchase vaccines from other partners in the PNYC.

Rupert Murdoch is Co-Chairman with Honorary Co-Chairman David Rockefeller in the PNYC.

Rupert Murdoch’s mother, Elisabeth Murdock is Dame Commander of the Order of the British Empire, a Companion of the Order of Australia (AC), which is an order established by Elizabeth II, Queen of Australia. Elisabeth Murdock administers the Royal Woman’s Hospital in Victoria, Australia, a vaccine research center and heavy promoter of the swine flu vaccines and drugs for pregnant women.

Jerry I Speyer, owner of the Rockefeller Center, is chair emeritus of the PNYC and on their board of directors. He is Chairman and Co-Chief Executive Officer of Tishman Speyer, Chairman of the Museum of Modern Art, former Chairman of the Board of Directors, the Federal Reserve Bank of New York; chairman emeritus of Columbia University; chairman emeritus of the Real Estate Board of New York; and a member of the David Rockefeller-directed Council on Foreign Relations.

Nelson Rockefeller’s protégé, Dr. Henry Kissinger, is a highly influential member of The Council on Foreign Relations, composed of the most influential business leaders in America, and his Kissinger Associates, Inc. is Merck and Company, Inc.’s leading management consulting firm.

Merck and Company, Inc. is the world’s largest vaccine maker. The company not only profits from flu frights and pandemics by sales of Pneumovax, but also is credited for having spread the AIDS virus, HIV, through contaminated hepatitis B vaccines.

Further evidencing an Anglo-American conspiracy to commit genocide using vaccines, a CSL Biotherapies report explains:

“The first step in making the influenza vaccine is preparing a ‘seed’ virus. This is a safe form of the influenza virus, which can be grown in hens’ eggs to produce the vaccine. Preparation of the seed takes around 3-4 weeks following receipt of a potential candidate virus from international health bodies such as the World Health Organization (WHO) or the US Centers for Disease Control and Prevention (CDC).”

CSL’s primary H1N1 swine flu vaccine testing site is closely linked to Rupert Murdock. Murdock funds the Murdock Children’s Research Institute (MCRI) of Victoria, Australia. His daughter-in-law, Sarah Murdock, is an Ambassador for the MCRI and a member of its development board. Murdock’s mother’s, Royal Woman’s Hospital is testing the H1N1 vaccines, at the time of this writing, on children and pregnant women.

The Associate Director of Clinical Development for vaccines at CSL is Dr. Michael Greenberg. CSL is conducting H1N1 vaccine studies on babies at the Murdock Children’s Research Institute, according to the MCRI website. Dr. Greenberg joined GlaxoSmithKline in 2005 and CSL in 2009.

The MCRI is the largest child health research and vaccine testing institute in Australia. It researches childhood diseases, including many that are vaccine-induced autoimmune diseases associated with antigenic complex formation from geneto-protein recombinations and blood intoxications.

In September 2009, babies and children were being recruited by the MCRI, for “a pandemic H1N1 swine flu vaccine trial” in Melbourne wherein “about 100 Victorian children aged between 6 months to eight years” were selected for study in collaboration with the University of Melbourne and Federal Government of Australia.

White House Environmental Advisor for Barack Obama, Van Jones, resigned for signing a petition in 2004 asking for an investigation of high level Bush administration officials implicated by foreknowledge in the September 11, 2001 World Trade Center “terrorist” attacks.

This infamous New York site is now home to the PNYC—the world’s most powerful biotechnology trust established by David Rockefeller in 1979 with co-partner and co-chairman Ruppert Murdock.

In the United States, the NIH, PHS, and the American Academy of Pediatricians (AAP) have incestuous relationships with “BigPharma” and its ring of organized PNYC criminals.

The reach and impact of the defendants’ trust, the PNYC, obviously taints geopolitics, economics, and vaccine science globally. For example, according to recent Biomedical Research Alliance promotions, and PNYC promotions, Kathryn S. Wylde, the President and CEO of the PNYC since 1982, was appointed to the Board of Directors of the Federal Reserve Bank of New York in 2009. She describes Asian financial influence on the PNYC thusly:
“The announcement of the China Center is a step toward economic recovery for New York. The Vantone Group's commitment to helping New York become the western headquarters location for the increasing number of global businesses coming out of China is extremely important to our city’s future as a global capital of business and finance.”
The “China Center” lease is being administered by Silverstein Properties, Inc. a “partner company” in the PNYC.

Vantone Group director Feng Lun, according to Mr. Silverstein’s press announcement, is “a pioneer of China's booming real estate market, so influential that some of the biggest names in American real estate, like Jerry Speyer, Mortimer Zuckerman and Sam Zell, have expressed an interest in forming a partnership with him.”

The Mortimer B. Zuckerman Research Center (MBZRC) is the namesake created by the chairman and co-founder of the publicly traded Boston Properties, also a partner company in PNYC. Zuckerman is also a member of the Council on Foreign Relations largely directed by honorary PNYC chairman, David Rockefeller.

Mr. Zuckerman, a candidate for US Ambassador to Israel, is also a leading financier of the American Lyme Disease Foundation that heavily promoted Smith Kline Company’s disastrous Lymerix vaccine. This vaccine was pulled from the market following hundreds-of-thousands of reported cases of recipients suffering post-vaccination symptoms of Lyme disease.

Another major promoter and Federal Government endorser of SmithKlein’s toxic and terminated Lyme disease vaccine is the US Federal Government’s, National Institute of Health, National Institute for Allergies and Infectious Diseases (NIAID) Director, Anthony S. Fauci, upon whom Mr. Zuckerman bestowed an “America’s Best Leaders” award on November 24, 2008.

At this same meeting Mr. Zuckerman provided the same award to David Baltimore, the senior pioneer of retroviral research associated with HIV/AIDS-like immunodeficiency bioengineering during the Special Virus Cancer Program (SVCP).

The SVCP is undoubtedly linked to the origin of HIV/AIDS as evidenced by its documentation revealing HIV co-discoverer, Dr. Robert Gallo, and his employment with the National Cancer Institute overseeing Litton Bionetics’s contract “Investigation of Viral Carcinogenesis in Primates,” as “Project Officer.” This document relates to the Merck company SVCP contract “Oncogenic Virus Research and Vaccine Development,” directed by Dr. Maurice Hilleman.

Before his death, Dr. Hilleman, Merck’s vaccine division chief, stated that he brought the AIDS virus into North America in contaminated monkeys destined for vaccine research at Merck.

Litton Bionetics also exclusively administered the NCI’s facilities at Fort Detrick, Maryland at the time Litton supplied chimpanzees were used by the CDC, FDA, NIAID, and the Merck drug company to produce four subtypes of hepatitis B virus vaccines for testing on at least three known populations: 1. homosexual men in New York City, 2. African villagers in Zaire/Congo/Uganda, and 3. Willowbrook State School for mentally retarded children on Staten Island in New York. The latter studies were conducted under U.S Army contract with the New York University Medical Center’s Dr. Saul Krugman.

Thus, the leading HIV/AIDS institute in the US, the NIAID, directed by the leading American infectious disease official, HIV/AIDS czar, and leading swine flu vaccination proponent, Dr. Anthony Fauci, has grossly and criminally neglected compelling documents and solid science that indicts Merck, the FDA, CDC, and his own NIAID. The suppressed and neglected evidence proves the origin of the world’s deadliest plague, AIDS, was triggered by hepatitis B vaccinations advanced by this alliance between these defendants’ public and private enterprises.

Related to current swine flu propaganda, the NIAID director, Dr. Fauci, has been heavily promoting swine flu vaccinations by way of the defendants’ media properties as he did previously with the Lyme vaccine.

The NIAID and Dr. Fauci operate subject to Central Intelligence Agency (CIA) review and direction according to CIA documentation and the Washington Post.

Dr. Fauci is also co-patent holder on “Immunologic enhancement with intermittent interleukin-2 therapy” described as being central to gene therapies and the future of “geneto-pharmaceuticals.” The Assignee on this patent is: The United States of America as represented by the Department of Health (Washington, DC).

The Associated Press reported that the government owns the patents and the scientists are listed as inventors so they can share in licensing deals struck with private manufacturers. The government licensed the treatment they invented to drug maker Chiron Corp.

Thus, Dr. Fauci’s co-patent filing evidences entrepreneurship of the US Federal Government, through its Department of Health, at the expense of taxpayers, in this valuable biotechnology now licensed to CHIRON Corporation, makers of the swine flu vaccine adjuvant additive MF59 with squalene.
I am aware of substantial scientific evidence, some of which was attended by the United States Congress during its investigation into Gulf War Syndrome, that squalene adjuvant is implicated in poisoning masses of military personnel who received the anthrax vaccine.

Regarding the history of IL-2, now in vaccine adjuvant, on Monday, Oct. 6, 2008, Dr. John Niederhuber, the director of the NCI, told Lawrence K. Altman of the New York Times that Dr. Gallo "was instrumental in every major aspect of the discovery of the AIDS virus." He added: "Dr. Gallo discovered interleukein-2 (Il-2), an immune system signaling molecule, which was necessary for the discovery of the AIDS virus, serving as a co-culture factor that allowed the virus to grow.”

I am also aware that IL-2 is the “common denominator” among immune system functions, and can cause severe side effects. IL-2 has been recommended for adjuvants.

Regarding the other principle ingredient in adjuvants, according to Dr. Andrus Brun Laursen, the amount of squalene in the Pandremix vaccine made by GlaxoSmithKlein is far more concentrated in the swine flu vaccine than in anthrax vaccine implicated in producing Gulf War Syndrome.

CHIRON’s MF59 adjuvant used in the 2009 swine flu vaccines by GlaxoSmithKline and Novartis, and Merck’s Lymerix vaccines, contain squalene along with Dr. Fauci’s co-patented Interleuken-2, preferred by the drug trade due to its toxic side effects as this makes money for shareholders in BigPharma.

Humanity is being seduced by persuasive media to be physically poisoned by misplaced faith in the CDC, FDA, AAP, NIAID, PHS, NCI; and in Novartis, Novavax, SmithKlein, Merck, CSL, and Baxter Corporation’s vaccines.

Thus, the constitutionally guaranteed religious freedom from “mandated” blood intoxications are being attacked and suppressed by Anglo-American agents for David Rockefellers PNYC trust.

Among the trust’s deceptive, coercive, unethical, and fraudulent media machinations is their promoted myth that vaccinations are “mandatory” when, by Constitutional law, they shall be voluntary.

Another second key deception is the notion that “immunization” means “vaccination” or visa versa; when, in fact, “immunization” traditionally referred to a natural exposure to antigens and innate immune response associated with acquiring lasting natural immunity. The word “vaccination,” alternatively, refers to a medical procedure that typically triggers hyper-sensitization reactions within the lymphatic system.

Another fraudulent myth is that the FDA tests products and/or assures safety and efficacy of vaccines. This myth persists due to continuous reinforcement by the news media controlled by the trust, and brainwashed or blindly-biased health officials that repeat this seductive mantra--”vaccines are safe and effective.”

These intentional obfuscations by the media and institutionalized medicine and public health, manipulated and misdirected by the trust, illustrate the social engineering and cross-cultural suppression of native and traditional beliefs in natural healing, sustaining wellness, and spontaneous recovery.

And unless We the People diagnose and treat the root causes of this genocidal imposition - a psycho-social, geopolitical, economically debilitating, physically-enslaving pathology, humanity may literally go extinct from genetic mutations and chemical intoxications.




Thursday, September 17, 2009

Panvax H1N1 monovalent Vaccine


While the name Panvax conjures an image for some sort of urination collection retrieval system, eg – vacuum assisted bedpan, it is in fact the new vaccine produced by Australia’s Commonwealth Serum Laboratories (CSL), for combating the scourge of flying pigs (swine flu).

The first glimpses of the details for this product come from the Western Australian Government in a published Public Health Training PowerPoint presentation.(PDF file)

Lets start with the good news first. Panvax H1N1 is not to be confused with CSL’s previous Panvax product which was designed for Avian Influenza. Panvax H1N1 is a monovalent vaccine, indicating the use of one antigen only, for immunizing against (allegedly), one specific pandemic only. At this current time it is an unregistered (unapproved) vaccine in Australia. See slide 51 – Panvax Training

To repeat, the Australian Government in its infinite wisdom has granted an exemption allowing the dispensing of this vaccine, without it being approved by the Therapeutic Goods Administration (TGA). That’s the good news, for the moment, because what that means is that consent from the victim to be assaulted by vaccine, must be obtained and recorded in detail on special Commonwealth consent forms. So for the time being, there will be no mandatory, forced vaccinations in Australia.

It’s a novel concept (consent) when in reference to Government and H1N1 vaccinations. It appears that US citizens will have no such freedoms, documents that order incarceration at a quarantine detention facility in the event of vaccination non-compliance; from several US states including Florida have now been cited. To date only China has actually issued warrants for mass inoculations.

The second bit of good news for Australians is that this CSL H1N1 vaccine appears to have far less potential for crippling, maiming and killing the host body after injection. According to slide 17 – Panvax Training, Panvax H1N1 is "unadjuvanted".

According to Jeffry John Aufderheide of VacTRUTH, trials just underway (Sept 15, 09) in Colorado for an experimental H1N1 vaccine contain the adjuvant Squalene (MF59).

Squalene (fish oil) is readily digestible if taken orally. However when injected, the immune system responds to it with intensity because it resembles so closely the natural oils found in the body. The result is that the immune system becomes a deadly weapon of aggressive destruction against its own host body. More squalene info, see post Mandatory chemical weapon assault

The theory that vaccines prevent the spread of infectious disease is based upon the belief that, by injecting a small amount of a disease into the body, it will develop "antibodies".

The theory is complicated by the fact that attenuated doses of pathogens alone will not initiate an "antigenic response." So, vaccines contain compounds known as "adjuvants" to intensify the body’s immune response.

Attenuation - reducing the virulence of a pathogen, so that it becomes harmless or less virulent, but still keeping it viable (or 'live').

So how can the CSL Panvax be an effective vaccination without the adjuvant? The answer (if there was such a thing as an effective vaccination) may be that Panvax is not attenuated. It is claimed that Panvax is not a “live” vaccine. Technically it is true that it contains no complete live virus, just live virus portions. Note ingredients named include Haemagglutinin (influenza surface proteins) and subunits of H1N1, the live virus is disrupted by detergent to produce the subunits.


Panvax Formulation:

  • Monovalent vaccine
  • 15ug of antigen per 0.5mls
  • Unadjuvanted
  • 10ml Multi Dose Vials (containing thiomersal – compound partly composed of mercury and ethylmercury.


Each 0.5mls contains

  • Sub units of A/California/7/2009 (H1N1) v-like virus
  • 15ug haemagglutinin
  • 0.01%w/v Thiomersal
  • Sodium Chloride 4.1mg
  • Sodium phosphate – dibasic anhydrous 0.3mg
  • Sodium phosphate- monobasic 80ug
  • Potassium chloride 20 ug
  • Potassium phosphate – monobasic 20 ug
  • Calcium chloride 1.5ug
  • Taurodeoxycholate ≤ 5ug (Bile salt-related, anionic detergent) (can give red eyes, blurred vision etc)
  • Ovalbumin ≤ 1.0ug
  • Sucrose <10ug>
  • Neomycin ≤ 0.7ug – check for allergies to this antibiotic
  • Polymyxin B sulfate ≤0.11ng – check for allergies to this antibiotic
  • Beta-propiolactone ≤1.4ng

It is interesting to note that the two antibiotics within Panvax, Neomycin and Polymyxin B Sulfate, are both used for the treatment of serious bacterial infection and are not effective against viral infection. Neomycin and Polymyxin B Sulfate are also both noted for serious side effects, predominantly kidney failure. Also interesting, or just wrong would be a better way to put it, it is warned both these antibiotics not be used by pregnant women. Neomycin is in the FDA pregnancy category D. This means that it is known to be harmful to an unborn baby. The problem is that in the “first tier” of candidates to receive this unregistered, unapproved vaccine, pregnant women are on top of the list.

More info about Neomycin and Polymyxin B Sulfate:

http://www.drugs.com/mtm/neomycin.html

http://www.rxlist.com/neomycin-sulfate-drug.htm

http://www.nlm.nih.gov/medlineplus/druginfo/meds/a682274.html

http://www.drugs.com/cdi/polymyxin-b-sulfate.html


Probably the least dangerous possible side effect of Panvax is anaphylactic, egg allergy reaction. This is another difference between Panvax and the experimental vaccines being produced for the USA, where early reports detailed manufacturers utilizing stem cell technology to culture the vaccines. Panvax has used good old fashioned chick embryos (Ovalbumin).

More on the deadly side is the ingredient Beta-Propiolactone.
Ranked as one of the most hazardous compounds (worst 10%) to humans and "reasonably expected to be a human carcinogen" (International Agency for Research on Cancer - IARC, 1999). Once widely used in the manufacture of acrylic acid, its use has been mostly phased out in favor of safer alternatives. Βeta-Propiolactone is a disinfectant and has been used to sterilize blood plasma, vaccines, tissue grafts, surgical instruments, and enzymes.

http://en.wikipedia.org/wiki/Beta-propiolactone


Listed as a possible Panvax side effect in slide 66 – Panvax Training is Guillian-Barre Syndrome (nervous system disorder featuring paralysis).
Contaminants make vaccines tremendously dangerous. Swine flu vaccine (for a pandemic which never materialized) was contaminated with polio virus in 1976. Over 45 million Americans were vaccinated in just 77 days and although there were only 6 cases of Swine flu in the entire country the vaccine reportedly caused at least 565 cases of polio paralysis (renamed “Guillain-Barre Syndrome” for the occasion), 60 deaths and other serious problems, including blindness and impotence. (There is no reason to feel reassured because this particular disaster occurred in the past: every flu vaccine is capable of passing along Guillain-Barre (polio) and other unsuspected viral diseases.)

"The Syringe of Death": Coming Soon to a Police Station near you
Rima E. Laibow, MD


Last but not least in the Panvax list of toxic ingredients is Thiomersal (by weight, 50% mercury). In slide 20 –Panvax Training, we are informed that:
According to the Commonwealth

"There is no evidence that thiomersal has caused any developmental or neurological abnormalities, such as ADHD or Autism."

Yet for something that has no relation to “neurological abnormalities”, in slide 28 –Panvax Training, It is recommended that all children under 10 years of age wait for the thiomersal free vaccine.

However slide 28 then continues:

Yes the vaccine is available to those ≥ 6 months of age and so if clients request the vaccine and are aware of the vaccine content they may receive the thiomersal vaccine with out waiting for the thiomersal free vaccine.

Ok, that’s great news, if you would like to poison your children, and you are aware that you are poisoning your children, feel free, vaccine dispensaries will oblige.

http://www.naturalnews.com/011764.html

Studies on thimerosal poisoning describe tubular necrosis and nervous system injury, including obtundation, coma and death. As a result of these findings, Russia banned thimerosal from children's vaccines in 1980. Denmark, Austria, Japan, Great Britain and all the Scandinavian countries have also banned the preservative.

Some scientists say the estimated number of cases of autism has increased 1,500 percent – since 1991, when the number of childhood vaccinations doubled. Whereas one in every 2,500 children was diagnosed with autism before 1991, one in 166 children now have the disease.

Editors Note – according to statistics from the Center for Disease Control (CDC), the number is as high as 1 in 152.

According to Tom Verstraeten, an epidemiologist who had analyzed the data on the CDC's database, thimerosal appeared to be responsible for a dramatic increase in autism and other neurological disorders.

However, given no causal relationship, the CDC and industry representatives were quick to discredit the evidence.

Consequently, the CDC paid the Institute of Medicine (IOM) to conduct another study on thimerosal. According to Robert F. Kennedy Jr., this study was fixed in order to "whitewash" previous findings. In its 2001 report, the IOM's Immunization Safety Review Committee did conclude that the link between thimerosal and neuro-developmental disorders was biologically plausible.


MMR Causes Autism – Another Win In US Federal Court

Julia a three year old US citizen has just won substantial compensation in the US Federal Court for autism caused by MMR (measles, mumps, reubella, chicken pox) vaccine – says her mother.
They kept the “autism” word out of the case. Many parents in other US cases have been advised to do this:

"CBS News has found that since 1988, the vaccine court has awarded money judgments, often in the millions of dollars, to thirteen hundred and twenty two families whose children suffered brain damage from vaccines. In many cases, the government paid out awards following a judicial finding that vaccine injury lead to the child’s autism spectrum disorder. In each of these cases, the plaintiffs’ attorneys made the tactical decision to opt out of the highly charged Omnibus Autism Proceedings and argue their autism cases in the regular vaccine court. In many other successful cases, attorneys elected to steer clear of the hot button autism issue altogether and seek recovery instead for the underlying brain damage that caused their client’s autism."


http://en.wikipedia.org/wiki/Vaccine_court

Vaccine court is the popular term which refers to the Office of Special Masters of the U.S. Court of Federal Claims, which administers a no-fault system for litigating vaccine injury claims. These claims against vaccine manufacturers cannot normally be filed in state or federal civil courts, but instead must be heard in the Court of Claims, sitting without a jury.



See also:

http://www.whale.to/vaccine/king.html

Autism myth #1: Autism is a disorder whose cause is unknown.

Autism myth #2: Those having a diagnosis of autism or a diagnosis of mercury poisoning do not have the same symptoms.

Autism myth #3: Evidence is accumulating that autism is largely a genetic disorder (Szatmari 2008).

Autism myth #4: The families that have children who regressed into autism have always been anti-vaccine.

Autism myth #5: The autism “epidemic” does not represent a true increase in the disorder, but rather is an artifact of expanding the diagnosis (now referred to as autism spectrum disorder, ASD) and increased surveillance (Taylor 2006).

Autism myth #6: The science involving vaccines and autism is complex, making it difficult for the average person to sift through all the misdirection and misinformation.

Autism myth #7: Currently, the evidence leads to the firm conclusion that vaccines do not cause autism.

Vaccine myth #1: Vaccines are one of the most successful programs in modern health care, reducing, and in some cases even eliminating, serious infectious diseases.

Vaccine myth #2: Public support for the vaccination program remains strong, especially in the United States where vaccination rates are currently at an all-time high of greater than 95% (CDC 2004).

Vaccine myth #3: Despite a long history of safety and effectiveness, vaccines have always had their critics: some parents and a tiny fringe of doctors question whether vaccinating children is worth what they perceive as the risks.

Vaccine myth #4: Vaccines, like most medical interventions, are not without risk; however, the benefits far outweigh those risks.

Vaccine myth #5: There are multiple independent lines of evidence that indicate vaccines do not cause autism.

Vaccine myth #6: The findings in the epidemiological studies relied upon by the 2004 IOM have been proven to be scientifically sound.

Vaccine myth #7: Robert Kennedy Jr. and others point to dubious evidence, such as the myth that the Amish do not vaccinate and do not get autism. Both of these claims are not true, and the data RFK Jr. refers to is nothing more than a very unscientific phone survey (Leitch 2007).

Vaccine myth #8: A victory for the anti-vaccination activists would undermine public confidence in what is arguably the single most effective public health measure devised by modern science.

Vaccine myth #9: There is an anti-vaccination movement that threatens the effectiveness of public health programs.

Vaccine myth #10: The decrease in public confidence in the current U.S. national vaccination programs from the disclosure of the factual risks and harms inherent in each vaccine will lead, as it has before, to declining vaccination compliance and an increase in infectious disease.

Vaccine myth #11: The anti-vaccination movement is largely based on poor science; and fear mongering has become more vocal and even hostile (Hughes 2007)



Related blog posts:

Mandatory chemical weapon assault

Looming Pandemic

The horrors of vaccinations




Friday, September 11, 2009

The Pharma Reich


For anyone who has ever wanted to see just how deep the rabbit-hole goes, nothing unearths the big picture like investigating pharmaceutical companies.

The same usual suspects keep appearing time and time again, joining the dots to the matrix of deceit which enslaves and poisons humanity. A majority of modern day big pharma companies all derive from one source.

Financed by Wall St, in 1925 a super corporation was created in Germany from six already giant chemical companies: BASF, Bayer, Agfa, Hoechst, Weiler-ter-Meer, and Griesheim-Elektron. These six companies were merged into Interessens-Gemeinschaft Farbenindustrie AG, or IG Farben for short.

IGF was described as “a state within a state”, and it was said by Anthony C. Sutton that: “Without the capital supplies by Wall Street, there would have been no I.G. Farben, and almost certainly no Adolph Hitler and World War II.”

In 1928 American interests in Farben were organised into a Swiss holding company – I.G. Chemie, control of which rested in Germany. In 1929 the American firms that comprised I.G. Chemie merged to become American IG Chemical Corporation, or American IG, later renamed General Aniline & Film.

William Dodd, U.S. ambassador to Germany, 1937: “A clique of U.S. industrialists is hell-bent to bring a fascist state to supplant our democratic government and is working closely with the fascist regime in Germany. I have had plenty of opportunity in Berlin to witness how close some of our American ruling families are to the Nazi regime. . .They extended aid to help Fascism occupy the seat of power, and they are helping to keep it there.”

Three board members of American IG were tried and convicted as German 'war criminals' at the Nuremberg Trials.

I.G. Farben’s contributions to the world include Zyklon B (cyanide-based pesticide), and the more deadly Sarin nerve gas. Sarin is such a speedy and efficient exterminator due to it being a fluorinated gas (Isopropyl methylphosphonofluoidate).

I.G. Farben had developed plans during the war to fluoridate the occupied countries, because it had been found that fluoridation caused slight damage to a specific part of the brain. This damage had a very particular effect. It made it more difficult for the person affected to defend his freedom, he became more docile towards authority.

Both the Germans and the Russians added sodium fluoride to the drinking water of prisoners of war to make them stupid and docile.

Dr. Phyllis Mullenix established conclusively that fluoride crosses the blood/brain barrier. (Very few substances can cross this barrier, whose job it is to protect the brain from toxic exposure.)

Dr. George Waldbott:
"Another well-substantiated case, severe brain damage, convulsions form drinking Saginaw (Washington) water. Through investigation including exploratory brain surgery, patient continued to eliminate 4 mgs daily of retained fluorine two months after fluoridation discontinued."
When Mrs Marsh the Colgate lady said “It really does get in”, she wasn’t f*cking around.

The Mellon family were the founders of the original Mellon Institute whence came the "amazing (but totally fallacious) sodium fluoride/dental caries prevention discovery" - the discovery that literally turned 'garbage into gold'.

The Mellon family also founded the American Aluminium Company (Alcoa), the largest producer of the waste toxin, sodium fluoride, which up to this point of 'caries discovery' had a relatively little known commercial or industrial value, was an environmental hazard of great public concern, and was very costly in terms of safe disposal.

It is also interesting to note that Alcoa’s Andrew Mellon became Treasury Secretary under President Woodrow Wilson in 1928. Conveniently, Mellon now headed the agency that funded the Public Health Service (PHS).

In 1939 Alcoa transferred its technology to Germany; the Dow Chemical Company transmitted its experience and technology in that same period. At this time the US itself, was in search of incapacitating agents to put in the enemy's water supply. LSD was one such “agent” tested; the program went on for many decades and included the infamous MK-ULTRA experiments.

The "Rockefeller Report" to the United States President on CIA activities said: "The drug program was part of a much larger CIA program to study possible means of controlling human behaviour".

An adviser to the US Government on hypnotism or psychological behaviour control, Dr. George Estabrooks, later became Chairman, Department of Psychology at Colgate University. Colgate was and remains the most ardent producer and advocate for the fluoridation of a domestic product - fluoridated toothpaste.

Incidentally, I.G. Farben not only controlled subsidiaries that are today’s big pharma companies, they also commanded cartel agreements with companies such as General Mills, M.W. Kellogg Co., Nestle and Colgate.

Included in I.G.'s business plan for the last half of the twentieth century was the successful rise of the "Forth Reich." Their records record this as the "neuordnung," that is "New Order."

The DuPont family also had their allies in Germany, aiding armament businesses. To digress a little, Lammont DuPont, his banker Andrew Mellon (ALCOA founder) and one William Randolph Hearst were the co-conspirators who also brought us “Reefer Madness”, the campaign for convincing Americans that marijuana was the devils weed.

Mellon appointed his nephew-in-law, Harry J. Anslinger, to Commissioner of the newly created Federal Bureau of Narcotics in order to successfully stamp out the threat of hemp production.

Swiss based Hoffman-La-Roche is another pharma company linked to I. G. Farben. Roche are the marketers of Rohypnol (fluoridated Valium), and they also produced BZ (3-quinuclidinyl benzilate) – one of the more potent substances utilized in the fore mentioned MK-ULTRA experiments.

Sandoz, now Novartis (Swiss pharma), was the original provider of LSD to the CIA in those experiments. In 1953 the CIA provided Eli Lilly with funding to attempt synthesis of LSD as the reagents required by Sandoz for production were expensive and scarce. Lilly chemists succeeded in their quest, and subsequent supplies were from Eli Lilly.

Eli Lilly of course are the makers of Fluoxetine (Prozac), a fluoride based SSRI antidepressant which reportedly, Lilly knew increased violent and suicidal behavior in patients, as far back as 1988, but instructed employees to hide that information.

The Lilly company in 2005 paid out $690 million to settle an estimated 8,000 pending lawsuits in the US, concerning their alleged failure to warn about the risk of their antipsychotic drug Zyprexa causing diabetes.

In the early 1920’s, the Eli Lilly Co. was given the sole and only monopoly for the manufacture and sale of insulin. It is said that Lilly, in order to do the manufacturing, had to steal the procedures and technique for production from the creator of insulin, Dr Scott.

In 2009, Eli Lilly was fined $1.5 billion for marketing Zyprexa for uses not approved by the FDA, namely a treatment for dementia, including Alzheimer's.

Mercury in vaccines is yet another thing we can thank Eli Lilly for. The addition of thimerosal (ethyl mercury) to vaccines was an initiative undertaken by Lilly in 1929. It is now widely accepted that thimerosal is a significant contributing factor in autism, afflicting 1 child in 168 in the US.

In a congressional hearing examining the use of thimerosal, Congressman Dan Burton said: “You mean to tell me that since 1929, we've been using Thimerosal, and the only test that you know of is from 1929, and every one of those people had meningitis, and they all died?”

Depression is caused by brain inflammation which depletes the body of serotonin. Brain inflammation is one of the side effects of vaccines. In the United States, 37% of autistic children are given SSRI's like Prozac.

Mitch Daniels, once vice president of Eli Lilly, was appointed to the Office of Management and Budget under G. W. Bush in 2001. The Director of the OMB is also a member of the National Security Counsel and Homeland Security Division.

In Nov 2002, an insertion of a "provision" in the "appendix" of the Homeland Security Act was made for exempting Eli Lilly from liability for all damages resulting from thimerosal poisoning. In June 2002, President George W. Bush had also appointed Eli Lilly’s CEO, Sidney Taurel, to a seat on his Homeland Security Advisory Council.

GW wasn’t the first Bush to pimp Eli Lilly. After father George Herbert Walker Bush left his CIA director post in 1977 and before becoming vice president in 1980, he was on Eli Lilly’s board of directors. As vice president, Bush failed to disclose his Lilly stock and lobbied hard on behalf of Big Pharma, especially Eli Lilly.

In 1981, GHW placed this stock ($145,000.00 worth) into a blind trust, meaning that Bush allegedly had no way of knowing whether his trust still owned shares in the firm or not.

GHWB loves a blind trust, just one year prior, 1980; he had also placed his father’s Nazi inheritance into a blind trust. One can only guess how much that inheritance was worth in 1980, but when Prescott Bush was reimbursed in 1951 for his “one share” of Union Banking Corporation, it paid $1.5 million.

Prescott managed UBC directly. His father in law, George Herbert Walker, along with German industrialist Fritz Thyssen, financed Hitler before and during WWII. Near the end of WWI, August Thyssen had opened the Bank voor Handel en Scheepvaart in Rotterdam.

W.A. Harriman & Co., managed by G.H. Walker, set up a Berlin branch in 1922. The managing director of Bank voor Handel en Scheepvaart met with Walker and the Harriman brothers in New York, 1924 to establish UBC.

Through the mid to late 1920s, UBC sold over $50,000,000 worth of German bonds to American investors. UBC managed banking transactions for the Third Reich until being seized under the trading with the enemy act in 1942.

Walker hired Bush to help him supervise Thyssen/ Flick United Steel Works. Consolidated Silesian Steel Corp was one portion of United Steel Works.

The Auschwitz concentration camp was named after the town of Oswiecim, one of Poland’s richest mineral regions, with Silesian Steel Corp. nearby, utilizing the slave labourers from the camp (an IG Farben factory). Thyssen sold Consolidated Steel to UBC. Under the complete control of Harriman and the management of Bush, the company became the Silesian American Corp.

Another interesting fact about Prescott Bush is that he was integral to the success of the Manhattan Project as US liaison with the UK. Appointed by Eisenhower, his primary duties were to assist the US in acquisition of Uranium and fission technology from the British.

Recently declassified US Military documents show how Fluoride is the key chemical in atomic bomb production and millions of tons of it were needed for the manufacture of bomb-grade uranium and plutonium.

The Manhattan Project was a joint venture between two of the world’s largest and oldest commercial powerhouses of the "Electrical/Energy" industry, Westinghouse and General Electric who have been the primary nuclear contractors for the Pentagon, ever since.

International General Electric was the largest shareholder (30%) of German General Electric (A. E. G.), another big contributor to Hitler. Several of AEG's Directors were also on the board of I. G. Farben. IGF and International General Electric also had the same shareholders.

Polycarbonate, the plastic that leaches Bisphenol A, was developed in Germany and the United States at the same time, in 1955, by Bayer in Germany and General Electric in the United States respectively.

Bisphenol A has been well documented for having hormonal effects on the human body. Scientists have discovered that women who have had three or more consecutive miscarriages had 3 times higher levels of Bisphenol A in their blood than women who had successfully given birth. Bisphenol A is also known to cause Polycystic Ovary Syndrome, a growing epidemic.

There are hundreds of types of plastic, many of them having no effect on the endocrine system, but the industry insists on using Bisphenol A.

Just as Bayer and General Electric had conspired to came up with this product at exactly the same time, financed by Wall St and international bankers, so it is that business continues in the present time.

Today the world’s largest pharmaceutical company is Pfizer Inc. after acquiring rival giant Wyeth for $68 billion in January 2009. The sum included $22.5 billion loaned by five major Wall St Banks.

Pfizer merged with Warner-Lambert in 2000. Warner-Lambert previously acquired Parke-Davis (formerly of the I.G. Farben cartel). In 2002 Pfizer merged with Pharmacia, a conglomerate from the merging of Pharmacia & Upjohn with Monsanto. Monsanto had previously bought G.D. Searle.

Incidentally, General Electric Healthcare ended up buying a biotech division of Pharmacia & Upjohn in 2004, that is after it had undergone mergers in between.

Also in Jan 09, Pfizer pleaded guilty to the largest health care fraud in U.S. history and agreed to pay $2.3 billion to settle a federal investigation into its alleged off-label marketing of the now-withdrawn painkiller Bextra.

This was Pfizer's fourth such settlement with the U.S. Department of Justice in the last ten years.

The pact follows Pfizer's October accord to pay $894 million to settle most of the personal-injury suits filed against it by patients who took Bextra or Celebrex. The FDA had recommended the withdrawal citing an increased risk of heart attack and stroke.

Bextra was originally marketed by G.D. Searle & Company, the kind folk who delivered to us Aspartame, well known as NutraSweet. Developed as an ulcer treatment, a Searle scientist discovered its sweet taste in 1965 while licking it from his fingers and thought, hello, we can sell this to hundreds of millions instead of just a few ulcer sufferers.

In early tests by Searle, the substance showed it produced microscopic holes and tumours in the brains of experimental mice, epileptic seizures in monkeys, and was converted by animals into dangerous substances, including formaldehyde.

To their credit, Searle didn’t let these pesky little details interfere with their aspirations (world domination). Despite the FDA refusing to approve aspartame for 16 years, still they remained undeterred. Searle knew one day, for the right price, someone in government with the necessary authority, would be their whore.

Enter Donald Rumsfeld; he had the toxic sweetener approved by an FDA Commissioner that he had personally installed, even before the swearing in of the government elect (Reagan’s transition team).

Rumsfeld was of course, CEO of Searle at the time. Today aspartame is found in over 5000 products under the names: NutraSweet/Equal/Spoonful, E951, Canderel and more. Having no calories, it is marketed in all its forms as a diet product. The great irony is that it has been noted for precipitating the obesity epidemic in the US as it induces a craving for carbohydrates.

Aspartic acid (40% of aspartame), is an excitotoxin that stimulates the neurons of the brain to death causing brain damage. Aspartame is 50% phenylalanine, neurotoxic and goes directly into the brain lowering the seizure threshold and depleting serotonin. Lowered serotonin triggers manic depression or bipolar, suicidal tendencies, mood swings, panic attacks and other types of behavioural and psychiatric problems.

This is all very good news indeed for Novartis, the makers of Ritalin, an amphetamine derivative. Before the approval of aspartame, there was no epidemic of ADHD and no epidemic of Ritalin prescriptions. Rember Novartis formerly Sandoz, were the CIA’s original source of LSD.

From this outstanding contribution to humanity, Mr Rumsfeld never looked back; he continued to excel himself, with each new enterprise being more putrid than the last. During the mid eighties as Ronald Reagan’s special envoy to the Middle East, he supervised the relationship with Saddam Hussein, in which the US supplied to Iraq intelligence, military technology and the necessary ingredients to make weapons of mass destruction.

Those ingredients included the ones for Sarin gas (the I.G. Farben developed, fluorinated nerve gas), which Iraq deployed against Iran. It is reported that the LaFarge Company in America supplied many of the chemicals; Vice President GHW Bush was a sizeable stockholder in this French owned firm. A noted director of American LaFarge was one Hillary Rodham Clinton.

The good will to Iraq wasn’t limited to a bit of fluoride, tributes also included bio weaponry. Senator Riegle’s Congressional Report of 1994 documented that American Type Culture Collection, shipped biological materials to Iraqi government agencies, 1985 – 1986, under license by the U.S. Commerce Department.

Between governments, Donny mainly filled his time selling more weapons, he was CEO of General Instruments and had a board position with Gulfstream Aerospace, later acquired by General Dynamics in 1999, where upon Donny was returned $11 million for his stock shares. He was also on the board of Swiss-based engineering company ABB who happened to sell two nuclear reactors to North Korea for a cool US$200 million.

When Rumsfeld returned to office as Secretary of Defense for G.W. Bush, and made great fanfare over Iraq possessing WMDs, he was right, he had the receipts. However, he also knew full well that junior’s father GHW, had destroyed most of them in operation Dessert Storm, and that the remaining weapons were eradicated by UN inspectors in 1993.

During the hiatus in government for Rumsfeld, he also became Chairman of Gilead Sciences in 1997, another pharmaceutical company; he loves his pharma nearly as much as his weapons, often they are the same thing though.

Gilead owns the intellectual property rights to the anti-viral Tamiflu which is marketed by Hoffman-La Roche (Swiss I.G. Farben). Rumsfeld stood down from the board when he was appointed Secretary of Defense, but it goes without saying that he managed to keep hold of his Gilead stock shares.

Those shares went up and up when in 2005, nothing to do with Donald I’m sure but solely for the good of the nation, G.W. Bush approved an order for 20 million courses of Tamiflu. Bush claimed that 2 million Americans were about to die from an avian flu pandemic.

Tamiflu side effects include: delirium, hallucinations, convulsions, disturbed consciousness, abnormal behaviour and death. As a treatment for influenza, it’s completely f*cking useless, more favourable side effects include all the symptoms of flu: nausea, vomiting, diarrhoea, headache, dizziness, fatigue and coughing. Taken as directed, Tamiflu can reduce the duration of flu symptoms by up to a whole day, but of course, that day you will be experiencing its side effects.

Rumsfeld’s stock shares in Gilead were estimated at between $25-$50 million long before pigs started flying (swine flu) and an absolute sh*t load of Tamiflu has been sold since then.

Nice work if you can get it, selling products to treat the symptoms of the products sold.

Pharma companies make billions producing vaccines. Vaccines do nothing to reduce disease; on the contrary, they are nothing less than injected illness. They make billions pedaling the likes of aspartame. Next they profit in the billions from psychiatric drugs.

Then at this point, if for some reason the consumer still has a functioning heart, liver and kidneys, but obviously is emotionally FUBAR, they will sell even better psych drugs, if not, the billion dollar finale is with selling insulin, other diabetic treatments and heart medications. And when all else fails, their chemical creations will always be in high demand as weapons of war.


Related Stink pages:

Wall Street and the Rise of Hitler

Truth Decay - the history of Fluoride

Bitter Sweet - the Aspartame story

Reefer Madness


Related Stink blogs:

Sheeple of Australia

The horrors of vaccinations

Looming Pandemic


References:

http://www.sourcewatch.org/index.php?title=Martin_Faga

http://www.gulfweb.org/bigdoc/report/r_1_2.html#exports

http://en.wikipedia.org/wiki/American_IG

http://www.hbs.edu/bhr/archives/bookreviews/78/phayes.pdf

http://www.whale.to/b/lsd_lilly.html

http://www.healthfreedomusa.org/docs/Syringe_of_death.pdf

http://www.corbettreport.com/articles/20090816_biochemical_manipulation.htm

http://www.redrat.net/gorebush/dictator.htm

http://www.healthcarealternatives.net/fluoride.html

http://www.sweetliberty.org/issues/health/flouride.html