Showing posts with label Vaccines. Show all posts
Showing posts with label Vaccines. Show all posts

Tuesday, November 10, 2009

Stop the Vax Program


I recently signed a petition at the Australian Vaccination Network to stop the Swine Flu Vaccination Program. If you are a resident of Australia, please consider signing the petition.

After signing, AVN forwarded my protest to the office of a number of politicians including the federal Health Minister and the Treasurer. I received 12 automated “out of office replies” from various ministers. In addition, two office staffers were actually kind enough to hit their keyboards in response.

From the office of Louise Markus:
Thank you for your email regarding the Swine Flu vaccination. As you would appreciate Mrs Louise Markus receives large volumes of correspondence and as the Federal Member for Greenway her priority is that of her constituents. Mrs Louise Markus thanks you for your email and has noted your comments.

Ok, I’m not one of her constituents, fair enough. Now from the office of Kate Ellis of whom I am a constituent, Electorate Officer Pauline Cusack writes:
Thank you for your email concerning the swine flu vaccine.

The Government has no plans for the swine flu vaccine to be mandatory.

Regards

Pauline Cusack

I appreciate the enormous effort and trouble Pauline went to in her reply but I couldn’t help but feel a bit patronized. I sent a reply correspondence as follows:
Dear Pauline

Thank you for your reply.

You assert “the Government has no plans for the swine flu vaccine to be mandatory.” It may surprise you then to learn that it already is mandatory for certain sections of the community.

Since July 2007, every state and territory in Australia has had policies implemented which require all medical staff and allied health students to be fully vaccinated. Students are required to be vaccinated before completing their practical work. Without these vaccines, ten different types including influenza, they are refused a placing in hospitals.

Compliance in these directives is mandatory and supposedly for the protection of patients, but half of those mandated vaccines contain live viruses which can be transmitted to people of contact for up to 90 days.

Panvax H1N1 vaccine also contains live virus portions (subunits). The subunits are produced by “disrupting” the live virus with detergent. It is more than possible that H1N1 vaccinations will inflame H1N1 infection rates among the non-vaccinated.

Panvax H1N1 vaccine was exempted by the government from requiring TGA registration before dispensing, mid September. Only about one week later however it was announced the TGA had approved it (Sept 18th). The time frame from the starting point of the first trials to the date of approval was approx just 7 weeks. That time frame is far from standard practise and very concerning.

If the government has no plans for mandatory vaccinations, why did they rush approval for Panvax H1N1 without due care in the form of the usual safeguards, and why have they (government) ordered 21 million doses of Panvax H1N1 from CSL?

In any event the government doesn’t actually have a say in whether or not vaccinations are ordered mandatory does it?

Pursuant to International Health Regulations (IHR) of 2007, the World Health Organization (WHO) of which Australia is a member has the authority to order forced vaccinations upon all 194 signatory countries to the WHO constitution, in the event of a declared pandemic. H1N1 was declared a pandemic in June.

Please pass this correspondence on to Ms Ellis as I would appreciate my concerns being addressed.


Yours Sincerely

**** ******


I eagerly await more news.


Related post:

Panvax H1N1 monovalent vaccine




Saturday, October 24, 2009

Sid the Pharma Shill Kid





This is the most disgusting abomination I've seen for some minutes. Why oh why is PBS aiming to market poison vaccines to children, who should not be responsible in any way, shape or form for making the decision on whether to vaccinate?










Sunday, October 18, 2009

Truth, Nowhere and everywhere


The world of info wars can be a very murky one indeed, laden with double agents, NWO shills who cloak themselves as info warriors. It’s an absolute mine field, a veritable quagmire of disinformation in the war for your mind.

I was reading an article recently by A. True Ott - The Sound of Silence: The Antithesis of Freedom @ educate-yourself.org I was mildly surprised when in the editor’s forward, he writes:
The second service that this author performs is to "out" two of our more deceptive alleged CIA/Pentagon 'assets' masquerading under the rubric of natural health advocates. Their names are Rima Laibow and her husband, former Major General Albert Stubblebine.
I say mildly surprised because nothing really surprises me anymore, but this was info that I had not seen before.

A. True Ott in his article elaborates with detail on the shadowy background of Major Bert and his wife. There are plenty of comments added to this post and a subsequent follow up - Actionable Disinformation, which lend support to Laibow and Stubblebine having questionable motives. There are also numerous other websites and blogs that make critical examination of their characters, e.g. - THE NATIONAL HEALTH FEDERATION.com, and mind control forums.com

I have personally produced the odd blog post on the topic of vaccines and the “swine flu”. On several occasions, I have made reference to, and linked to the website and publications of Rima E. Laibow, MD. I will not be retracting those references, based on my investigations, I feel what I have quoted from this source is information of value. At the same time, I can not find fault with some of the above character investigations.

So how do I reconcile this position of contradiction? The answer lies within the nature of the info war. The strategies and tactics deployed in this war of dissemination, by those that control the game, are varied and complex.

Disinformation is a predominant weapon of choice. Of course not any old disinformation will do, if it is too silly people just ignore it. Therefore in most cases, disinformation is sophisticated enough as to be largely believable, achieved in most part by in fact reporting the actual truth in a good percentage of the manufactured composition. But then the curved ball is pitched, a small percentage of absurdity or verifiable falsities added and/or vital info omitted.

If no one detects the bullsh*t, all well and good, the agenda of the shill is forwarded by the converted. If it is detected, all well and good because now the information is discredited, all those secret truths revealed can never again be entertained without ridicule. A win win for the puppet masters you may say.

The deception keeps on multiplying from here, disinformation about disinformation disseminates.

Another outing Dr A. True Ott is recently famous for is that of Jane Burgermeister. You may have heard of her and/or her birdflu666 website which has since been updated with a newer site.

The dynamic duo of Dr. Deagle and Dr. Ott have been quite scathing in their attacks on Jane and vice versa. Again Burgermeister is someone that I have found to have spilled important info, but simultaneously I also find some of Dr Ott’s allegations to hold true. One such charge is that she has plagiarised the work of Ott and the team at Nutrimedical.

I could believe this, I read on Jane’s website in a collum discussing thimerosal, mention to Prescott Bush being part of the board of directors at the Eli Lilly Company. This is also something Dr. Ott states in his DVD - The Bird Flu Hoax, as seen here in part 1.

Apart from these two sources, I can find no reference anywhere to this claim. Prescott’s son G.H.W. Bush was an Eli Lilly board director along with many other notable shady characters but as near as I can ascertain, Prescott was not.

There are plenty of detractors for Dr Deagle and Dr Ott also. Let’s look at these two examples.





So now we’re digesting disinformation exposing disinformation agents who exposed disinformation agents.

Again some off the content Dr. Ott has to offer is information of interest but I become sceptical of his character with a visit to the website Mother Earth Minerals Inc. This expensive mineral supplement business appears to be an enterprise of Dr. Ott, the only content at the home page, apart from menus etc, is a sales pitch from Dr. Ott.

A. Ott thanks the Merck pharmaceutical Corporation for their contribution of mineral definitions, odd that he also lobbies against their interests in vaccines no? Something else slightly weird here, check the listed specials, they include “the Horrors of Vaccination” a work published in 1920 (a very good read), but a publication that copyright expired on long ago and is freely available in the public domain. However you can pay Dr. Ott USD $9.95 for this book, if you prefer that to reading it for free.

There are many points of contention that I have found with many content authors of the “truth movement”. I won’t name them all; I’ll let you the reader practice deciphering info, which is what a site like this is for, to ignite some brain activity. Ultimately our puppet masters don’t let us see anything they do not want us to. Sometimes the disclosure is for conditioning us in accepting their sick fantasies, often as previously outlined; it is to throw us off the scent, tell us the truth and have it discredited beyond all reproach.



Saturday, September 26, 2009

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




Saturday, August 22, 2009

This means WAR !!






Operation Fax to Stop the Vax





Click to download, print and distribute this flyer!


Friday, August 21, 2009

Looming Pandemic


There is a world wide pandemic on it’s way, and unlike the swine flu which is complete pish, this one is for real. The US Center for Disease Control (CDC) is predicting a more virulent, extremely dangerous, mutated swine flu to wreak havoc this American Fall. The CDC can be very confident in their prediction, as they will be distributing this lethal virus themselves in mass vaccinations, that is in partnership with the WHO, BARDA and big pharma companies.




You could be jailed for refusing Swine Flu and regular Flu vaccinations

from Natural Solutions Foundation

The United States Emergency Medical Powers Acts and Federal legislation, including the Patriot Acts I, II and III, BARDA and others provide for mandatory vaccination or drugging. No exemptions (religious or otherwise) are provided. Those who refuse will be classified as felons at the State level, subject to immediate incarceration and quarantine of indefinite length in jails or other facilities reserved for such "vaccine refusers." In a frightening "Big Lie" propaganda move, those who doubt the effectiveness of unproven, uninsurable vaccines are being called “Vaccine Resisters" and being equated to a new form of "terrorism."

Those who refuse at the Federal level will be subject to immediate incarceration and quarantine of indefinite length, probably in FEMA camps set up across the US.



“The Syringe of Death”: Coming Soon to a Police Station near you

Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation

http://www.healthfreedomusa.org/

Published 2005

Senator Richard Burr (R-NC) thinks he owns your body. If he’s right, you will have no say over what gets injected into it and no recourse under the law if it harms or kills you. That is, if Burr gets what he’s after and S. 1873 passes the US Senate. Burr’s bill, "Biodefense and Pandemic Vaccine and Drug Development Act of 2005", establishes the Biomedical Advanced Research and Development Agency (BARDA), a secretive and secret agency exempt from public scrutiny, the Freedom of Information Act and the Federal Advisory Committee Act.

Operating in secret, BARDA will be responsible for the advanced research and development of drugs and vaccines (in partnership with pharmaceutical companies), and, because the contents of those vaccines will remain shrouded in BARDA darkness, any injuries and deaths caused by drugs and vaccines which BARDA labels “countermeasures” to any BARDA-declared threat may never be known.

Even if those contents do become known, S. 1873 cancels any manufacturer liability for the companies that made the vaccines or drugs. Injured parties will have no legal means of securing compensation from either the government or the companies themselves.

Editors Note:

Senate Bill - S. 1873, was never passed by both the House and Senate, but S. 3678 was, which incorporates provisions from S. 1873. Of note are provisions that require the establishment within DHHS of a BARDA as the single point of authority in the Federal Government for civilian medical countermeasure advanced R&D.

In addition, S. 3678 provides clarification of countermeasures covered by Project BioShield, enhanced flexibility for procurement of countermeasures, revitalization of the Commissioned Corps, and enhanced public health and medical preparedness and functions at DHHS. It also facilitates the tracking and distribution of federally purchased influenza vaccine.

Office of Legislative Policy and Analysis

In addition, liability protection protecting swine flu vaccine producers was eventually enacted in April 2009.





“The Syringe of Death”: Coming Soon to a Police Station near you - continued

Can we assume that these vaccines will provide us any protection at all? Perhaps, but it’s not likely. Under BARDA you may be (legally) subjected to experimental drugs – drugs which have no track record at all.

All of us have been carefully conditioned to believe that vaccines are safe. But the truth is ugly and, with BARDA staring us in the face, more than a little frightening. Here are the cold, hard facts:

Cold, Hard Fact # 1: Vaccines are not safe: vaccines are dangerous. The evidence is abundant that the tragic cost of loading babies and children up with toxic brews of mercury, aluminum, formaldehyde, injected foreign protein, stealth viruses and, in the second generation vaccines, the deadly immune enhancer squalene, is unacceptably high.

Autism (occurring in 4 children per 10,000 when I graduated from medical school in 1970) now afflicts a minimum of 1 child in 168 in the US. Children have not changed: the poisons we give them have. Gulf War Syndrome, a pervasive, progressive, deadly auto-immune disease afflicting over half a million US veterans, appears to be a deadly vaccine reaction to an experimental vaccine (Anthrax) which the US used on soldiers without their consent in clear violation of the Helsinki Declaration and the Nuremberg Protocols.

Contaminants make vaccines tremendously dangerous. Swine flu (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.)

Cold, Hard Fact # 2: Vaccines have not eradicated diseases: vaccines spread diseases. Attenuated viruses (infective, weakened versions of the dangerous ones) are commonly used in vaccines so that your body will develop an immune ‘memory’ for that virus. The next time your immune system meets that specific virus, it rapidly combats it by producing large numbers of antibodies.

This practice and theory derive from the dawn of vaccination: Edward Jenner’s pioneering use of cowpox pus inoculations to eliminate smallpox. This innovative and surprising medical treatment is touted as one of the triumphs of modern medicine. 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, especially babies (who have immature immune systems).

In spite of the documented associated dangers of leprosy, syphilis, smallpox, death and blindness, England provided free vaccination in 1840, made it compulsory in 1853, and punished lack of vaccination with seizure of property and imprisonment in 1857 (which should sound familiar). It took a British Royal Commission some 41 years more to put a stop to the deaths and disease that Jenner’s unproven technique caused. Finally, in 1898, England’s compulsory smallpox vaccination laws were overturned.

In 1854, the first year of British compulsory vaccination, deaths from syphilis in infants under 1 year increased by 50% and continued to rise steadily after that. In 1802 Jenner was paid 10,000 pounds by the House of Commons. Shortly afterwards, it became clear that vaccines did not work. Rather than lose face, the House of Commons granted Jenner another 20,000 pounds in 1807 and 3,000 pounds a year thereafter.

Jenner knew that milk maids who milked with active pus-filled sores on their hands transmitted pox to their cows. Local superstition held that the cow’s pus was a preventive against small pox. Jennings learned from a local farmer, Benjamin Jestey that he had inoculated his wife and 3 children with cowpox pus by jabbing them with a darning needle and they did not contract small pox. Jenner assumed that this meant they were protected against smallpox.

Although immunity fails to develop more than 80% of the time, serious side effects are distressingly common from the modern small pox vaccines: At least 52 people out of every million will have life threatening events and 1-2 will die.

The Center for Disease Control (CDC) notes that serious side effects and dangers probably occur much more often since many people can be harmed by live virus vaccines: immune compromised people (on steroids, with eczema or psoriasis, nursing babies, pregnant women and their fetuses, people with HIV/AIDs, transplant patients, chemotherapy and radiation patients, people with auto-immune diseases, young children, asthmatics, etc.) are at serious risk for contracting the same disease that the inoculation is designed to prevent or worse.

In the US, the CDC classifies more than 60 million people as immune compromised. People who are re-inoculated after many years are particularly susceptible to severe and life threatening reactions. Those who are ill are likely to develop sever effects as well. In fact, Tommy Thompson, former Health and Human Services boss, said that he would not take the vaccine although the US is stock piling “a dose of smallpox vaccine with every American’s name on it”.

Dr. Mike Lane, former director of the CDC’s so-called “smallpox eradication program” in the 1970’s, is a proponent of mass vaccination with no exemptions saying, “Medical contraindications would not apply…there would be NO exceptions.

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 A. R. 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.

Cold, Hard Fact # 3: Flu vaccines do not protect people from flu-related deaths. The CDC claims that an astonishing 36,000 people die from flu in an average year. But according to the former Secretary of Health and Human Services, Tommy Thompson, 68 people under 65 die from flu each year in the US. The truth is that in 4 years, a total 4,440 people, mostly elderly, died from flu, no where near the CDC’s touted 144,000 deaths. While that figure is great for flu vaccine sales, it derivers not from reality but from the CDC’s industry-friendly statistical trick of classifying all pneumonia-related deaths, despite any lack of evidence, as flu deaths.





Thursday, August 13, 2009

Mandatory chemical weapon assult


Refraining from blogging about flying pigs (swine flu) for some time now because lets face it, there has been no shortage of media coverage; I will interrupt this reprieve for some important updates, as people of Earth are facing an immanent catastrophe. And it’s not a viral menace that threatens our existence; it’s the planned mandatory mass poisonation programs of injections.

On July 12, 2009 the timesonline.co.uk reported:

The path of a popular medicine from the laboratory to the chemist or doctor’s surgery can involve years of clinical trials on a select group of patients.

When the new vaccine for swine flu arrives in Britain, regulators said this weekend, it could be approved for use in just five days.

The UK government has ordered enough vaccine to cover the entire population. GPs are being told to prepare for one of the biggest vaccination campaigns in almost 50 years.

The article received hundreds of comments from readers, overwhelmingly (probably 99.9% from what I saw), the input was anti vaccination. Many even accused authorities of a deliberate culling of the population with a planned poisoning by syringe. In what the Times UK has assured us was coincidence, they upgraded their website shortly afterward and all those comments were erased.

Also on this day, July 12, cidrap website reported that the United States ordered another $1 billion worth of bulk ingredients for H1N1 influenza vaccine. That is, additional to the first $1 billion of spending announced on May 22, to buy vaccine antigen and adjuvant and fund clinical studies.

On the 13th of July 2009, the WHO accepted recommendations for mandatory H1N1 vaccinations of the entire population of nations. The recommendation was made by the Strategic Advisory Group of Experts (SAGE) on Immunization, and in a time of pandemic, as is declared, it is apparently legally binding on all 194 signatory countries to the International Health Regulations act of 2005 and the WHO pandemic plan of April 2009.

From birdflu666.wordpress.com

SAGE is composed of executives from Baxter, Sanofi, Novartis and other vaccine manufacturers. To clarify: WHO has given lucrative contracts, worth billions in the USA alone, to Baxter, Novartis, Sanofi and others for the H1N1 vaccination programme mandated by WHO on the advice of Baxter, Novartis and Sanofi.

In Australia, ABC News reported on 15th July that pharmaceutical company CSL has made a vaccine for swine flu and will test it out on 240 healthy adults in Adelaide next week.

It was reported on May 29 by smh.com.au, that:
The Australian Government had sealed a deal with CSL to develop a vaccine and that;

"For its part CSL was all set to go. It had already taken delivery of the seed strains from California and will now produce small batches to test on ferrets and ultimately on humans".

Interestingly before CSL imported H1N1 into the country, “took delivery of the seed strains”, with a couple of exceptions from people who had arrived from overseas by air travel, Australia had no confirmed cases of swine flu.

Surely it is merely coincidental that infections in Australia ignited in the population within days of H1N1 arriving in the CSL laboratories. It is also no doubt completely coincidental that initially, from 1266 confirmed cases of swine flu in Australia on June 10th, 1011 of those cases were affecting residents in and around the city of Melbourne, the location of CSL’s laboratories.


US vaccine trials

First reported July 21 - Reposted on Fighting for Liberty blog

The H1N1 vaccine is going to be tested at the beginning of August in Rochester, New York, on those people who belong to sections of the community that have been hit especially hard by the economic downturn. The clinic conducting the trials has asked specifically for elderly people, black people or children. In return for participating, people will get $50 - $100 or the children will get a toy.

Novartis appears to have paid people in Poland 3 Euros to get them to participate in clinical trials of their lethal bird flu drug last summer, which caused death and injury to hundreds of people.


July 23rd – By DEBORAH FELDMAN, KING 5 News

Seattle will be one of the cities where a swine flu vaccine will be tested. Several thousand people living in eight different U.S. cities will participate in the testing.

WTF? When experimental vaccines are trialled, standard protocol is to evaluate in a strictly controlled and confined area. Dispersing unknown, potentially dangerous vaccine product upon populations over eight different cities is unheard of and simply astounding.


July 31, 2009 – Planned US Military deployment in support of Nationwide Vaccination

by Michel Chossudovsky, Global Research

The Pentagon is "to establish regional teams of military personnel to assist civilian authorities in the event of a significant outbreak of the H1N1 virus this fall, according to Defense Department officials."

"The proposal is awaiting final approval from Defense Secretary Robert Gates.

The plan calls for military task forces to work in conjunction with the Federal Emergency Management Agency.

As a first step, Gates is being asked to sign a so-called "execution order" that would authorize the military to begin to conduct the detailed planning to execute the proposed plan.”

The decision points towards the militarization of civilian institutions, including law enforcement and public health.

A nationwide vaccination program is already planned for the Fall.

The pharmaceutical industry is slated to deliver 160 million vaccine doses by the Fall, enough doses to vaccinate more than half of America's population.

The Pentagon is already planning on the number of troops to be deployed, with a view to supporting a mass vaccination program.

Much of the groundwork for the intervention of the military has already been established. There are indications that these "regional teams" have already been established under USNORTHCOM, which has been involved in preparedness training and planning in the case of a flu pandemic.

From July 27th – 31st 2009, FEMA and the US Military conducted a National Level Exercise (NLE 09). This type of exercise is conducted annually, however NLE 09 seems to have been comprehensively expanded upon and even included foreign military powers operating inside the United States.

FEMA website

NLE 09 is a White House directed, Congressionally - mandated exercise that includes the participation of all appropriate federal department and agency senior officials, their deputies, staff and key operational elements. In addition, broad regional participation of state, tribal, local, and private sector is anticipated. This year the United States welcomes the participation of Australia, Canada, Mexico and the United Kingdom in NLE 09.

Related Article: Massachusetts!! You Have A Problem!! - National Guard takes over school in Swine Flu "Vaccine Riot" Drill


A special events organisation company, New Fields Exhibitions Inc, is hosting an International Swine Flu Conference in Washington DC from August 19 – 21, 2009.

Conference Brochure

"Top leaders and key decision-makers of major companies representing a broad range of industries will meet with distinguished scientists, public health officials, law enforcers, first responders, and other experts to discuss pandemic prevention, preparedness, response and recovery at the 1st International Swine Flu Summit."


The agenda topics include:

Mass Fatality Management Planning
  • Activate fatality management operations
  • Conduct morgue operations
  • Manage ante-mortem data

Psychological Issues

  • Public’s distress of exposure and safety
  • Breakdown of public services, utilities
  • Medical supplies shortage
  • Unwillingness to follow government orders

Business Continuity Planning

Continuity of Operations (COOP) and Continuity of Government Planning

Emergency Management Services

  • Manage panic caused by sudden disruption of services & interruptions in essential goods & services

Law Enforcement Agencies

  • Protect the delivery of vaccines & essential goods & services.
  • Manage a surge in crime & meet routine requests at the same time
  • Control & diffuse social unrest & public disorder
  • Isolate prisons & other facilities

First Responders: Fire Department

  • Effectively transition into All-Hazards Incident Management Responders
  • Effectively undertake mass vaccinations
  • Enforce quarantines

First Responders: Public Works

911 Call Center Services

Hospital and Emergency Medical Services

Workplace Planning

School / University Pandemic Planning

Airlines, Travel, Airport, Quarantine and Border Health Services

  • Apprehension, examination and release
  • Aviation & Transportation Security Act, 2002 (49 U.S.C. 114)

Infectious Medical Waste

Swine Flu: Agriculture Perspective & Interventions




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So what is in these vaccines that governments of the world seem so determine to administer upon their populations with the use of military force? To date it would appear that there are no published ingredient details from any of the pharmaceutical companies named in producing the trial products.

That glaring absence of detail is most conspicuous indeed. From what can be ascertained from general research, it would seem highly probable that we are looking at a new breed of vaccines here that will be utilizing the adjuvant known as Squalene.

Traditionally Aluminum and Mercury have been used as vaccine adjuvants. Aluminum has been linked to Alzheimer’s disease and other neurological disorders. There is now widespread medical opinion that Mercury contained within vaccinations has significantly attributed to instances of Autism.

Those were the days; we could probably all consider ourselves lucky now if becoming autistic was the least of side effects to be concerned about.

Posted by Jeff on the 12.160Mhz blog

Fish oil vaccine adjuvant programs bodies for "endless loop of self-destruction"

It’s a race — will we all be injected with substances that program our own bodies to attack us before or after we realize that the newest weapon in the New World arsenal is our own immune system?

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" that will prevent the injected person from contracting the disease against which he had been vaccinated.

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.

Most people understand that both aluminum and mercury are toxic. It is our body’s reaction to toxic exposure that vaccine advocates measure to determine vaccine efficacy. That elevated levels of mercury and aluminum can cause side-effects worse than the disease is not a consideration for most pro-vaccinators.

Article "A Look into the Scary World of Vaccine Adjuvants”, explains that modern, synthetic or recombinant vaccines are "purer" and less toxic to the body than their live and dead virus predecessors and, therefore, require more potent adjuvants to illicit an immune response.

Under this line of logic, alum is scheduled to be phased out and replaced with oil-based adjuvants such as squalene—an essential fatty acid derived from fish.

The most effective adjuvants are formulated with oils but have long been considered too reactive for use in humans. Immunologists have known for decades that a microscopic dose of even a few molecules of adjuvant injected into the body can cause disturbances in the immune system and have known since the 1930s that oil-based adjuvants are particularly dangerous.

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.

Adjuvants can break ‘tolerance,’ meaning they can disable the immune system to the degree that it loses its ability to distinguish what is ‘self’ from what is foreign. The immune system then turns relentlessly self-destructive, attacking the body it is supposed to defend.

When oil is injected, the immune system responds to it not only specifically, but with heightened intensity because the oil adjuvant resembles so closely the natural oils found in the body.

Journalist Gary Matsumoto authored a book "Vaccine A - The Covert Government Experiment That’s Killing our Soldiers and Why GI’s are Only the First Victims”. Matsumoto who was the first journalist to break the story of squalene-containing anthrax vaccine’s link to Gulf War Illness, documented decades of secret medical experimentation on Americans without their knowledge or consent.

Squalene is an oil that is readily digestible if taken orally. However, it behaves much differently when injected. Regardless of the known toxic effects on animals and the toxic effects on humans as experienced with squalene-containing vaccines given to Desert Storm personnel, Matsumoto claims, "Squalene adjuvants are a key ingredient in a whole new generation of vaccines intended for mass immunization around the globe."

In her article, "The Adverse Effects of Adjuvants in Vaccines" (Nexus Magazine Dec. 2000), Australian vaccine researcher Viera Scheibner, Ph.D., lists the autoimmune diseases that have been linked to squalene injections in humans—arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS (amyotrophic lateral sclerosis) also known as Lou Gehrig’s disease, Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhoea, night sweats and low-grade fevers.

But that, believe it or not, is the good news because its merely describes squalene’s experimental contribution to global epidemics of chronic autoimmune dysfunction. Once it becomes a common ingredient in vaccines (already, the squalene-based adjuvant MF59 is a component of the Italian flu vaccine FLAUD), it will be best described as a biological time bomb.

From Edda West: "The immune system does in fact ‘see’ squalene and recognizes it as an oil molecule native to the body. The key is ‘route of administration.’ As Gary Matsumoto says, ‘Squalene is not just a molecule found in a knee or elbow – it is found throughout the nervous system and the brain.’ When it is injected into the body, the immune system sees it as an enemy to be attacked and eliminated."

"As any immunologist will tell you, the way an antigen encounters the immune system makes all the difference. You can eat squalene – no problem as it is an oil the body can easily digest. But studies in animals and humans show that injecting squalene will galvanize the immune system into attacking it, which can produce a self-destructive cross reaction against the same molecule in the places where it occurs naturally in the body – and where it is critical to the health of the nervous system.”

"Squalene is a kind of trigger for the real biological weapon: The immune system. When the immune system’s full repertoire of cells and antibodies start attacking the tissues they are supposed to protect, the results can be catastrophic," wrote Matsumoto. Dr. Pam Asa concurs with Matsumoto when she stated," Oil adjuvants are the most insidious chemical weapon ever devised."

West continues, "The main proponents for the use of squalene in vaccines have been the U.S Department of Defense and the NIH. The anti - squalene antibodies found in sick American and British military personnel are evidence that military experimentation has caused an unprecedented health catastrophe in tens of thousands of people onto whom the vaccine was forced and who were denied the right to make an informed decision based on existing scientific knowledge of the dangers of injecting squalene."

Based upon decades of research in animals and humans, once oil-based adjuvants become the most common adjuvant contained in vaccines, there will be no way the pharmaceutical industry will be able to claim mass vaccination is necessary to prevent the spread of infectious diseases—it will be an open declaration of war on mankind.