Dr. Laibow’s presentation on squalene during the second hour of your program last night, 8-24, was impressive. In looking for some verification of the ‘million-times more squalene’ than was in ‘Vaccine A’ that caused the catastrophic Gulf War I Illness (which ruined the lives of hundreds of thousands of troops and killed thousands of others -ed), I came across this article…
What’s The Danger of Swine Flu Vaccinations?
By Dr. Anders Bruun Laursen
“…So, as you see, there is no confusion with regard to swine flu and bird flu viruses. But there is another important consideration: the role of squalene.
The average quantity of squalene injected into the US soldiers abroad and at home in the anthrax vaccine during and after the Gulf War was 34.2 micrograms per billion micrograms of water. According to one study, this was the cause othe Gulf War syndrome in 25% of 697.000 US personnel at home and abroad. (3). You can find this table of FDA analyses from the Gulf War lots on The Military Vaccine Resource Directory website (4)
a.. AVA 020 – 11 ppb squalene (parts per billion)
b.. AVA 030 – 10 ppb squalene
c.. AVA 038 – 27 ppb squalene
d.. AVA 043 – 40 ppb squalene
e.. AVA 047 – 83 ppb squalene
These values were confirmed by Prof. R. F. Garry (5) before the House of Representatives. Prof Garry was the man to discover the connection between the Gulf War syndrome and squalene.
According to his findings, the Gulf War syndrome was caused by squalene, which was banned by a Federal Court Judge in 2004 from the Pentagons use. (6)
As seen on p. 6 of this EMEA document (7), the Pandremix vaccine contains 10,68 mg of squalene per 0,5 ml. This corresponds to 2.136.0000 microgrammes pr. billion microgrammes of water, i.e. one million times more squalene per dose than in (4). There is any reason to believe that this will make people sick to a much higher extent than in 1990/91. This appears murderous to me.”
http://www.globalresearch.ca/index.php?context=va&aid=14851
Then, in looking for some confirmation on Novartis putting gp 120 (an HIV/AIDS protein) in their vaccines, I found the following…
The Vaccine May Be More Dangerous Than Swine Flu
By Dr Russell Blaylock
http://socioecohistory.wordpress.com/2009/07/15/dr-russell-blaylock-
vaccine-may-be-more-dangerous-than-swine-flu/
“…Novartis, the second contender, also has an agreement with WHO for a pandemic vaccine. Novartis appears to have won the contract, since their vaccine is near completion. What is terrifying is that these pandemic vaccines contain ingredients, called immune adjuvants that a number of studies have shown cause devastating autoimmune disorders, including rheumatoid arthritis, multiple sclerosis and lupus.
Animal studies using this adjuvant have found them to be deadly. A study using 14 guinea pigs found that when they were injected with the special adjuvant, only one animal survived. A repeat of the study found the same deadly outcome.
So, what is this deadly ingredient? It is called squalene, a type of oil. The Chiron company, maker of the deadly anthrax vaccine, makes an adjuvant called MF-59 which contains two main ingredients of concern-squalene and gp120. A number of studies have shown that squalene can trigger all of the above-mentioned autoimmune diseases when injected.
The MF-59 adjuvant has been used in several vaccines. These vaccines, including tetanus and diphtheria, are the same vaccines frequently associated with adverse reactions.
I reviewed a number of studies on this adjuvant and found something quite interesting. Several studies done on human test subjects found MF-59 to be a very safe immune adjuvant. But when I checked to see who did these studies, I found-to no surprise-that they were done by the Novartis Pharmaceutical Company and Chiron Pharmaceutical Company, which have merged. They were all published in “prestigious” medical journals. Also, to no surprise, a great number of studies done by independent laboratories and research institutions all found a strong link between MF-59 and autoimmune diseases.
Squalene in vaccines has been strongly linked to the Gulf War Syndrome. On August 1991, Anthony Principi, Secretary of Veterans Affairs admitted that soldiers vaccinated with the anthrax vaccine from 1990 to 1991 had an increased risk of 200 percent in developing the deadly disease amyotrophic lateral sclerosis (ALS), also called Lou Gehrig’s disease. The soldiers also suffered from a number of debilitating and life-shortening diseases, such as polyarteritis nodosa, multiple sclerosis (MS), lupus, transverse myelitis (a neurological disorder caused by inflammation of the spinal cord), endocarditis (inflammation of the heart’s inner lining), optic neuritis with blindness and glomerulonephritis (a type of kidney disease).
The second ingredient, and one that greatly concerns me, is called gp120, a glycoprotein. Researchers found when it was mixed with squalene, the glycoprotein became strongly antigenic – that is, it produced a powerful and prolonged immune response to the vaccination. In fact, their studies show that with each dose, the intense immune reaction lasts over a year.
Now for the shocker-the glycoprotein-gp120, a major component of MF-59 vaccine adjuvant, is the same protein fragment isolated from HIV – the virus that is responsible for the rapid dementia seen in AIDS patients.
Studies have shown that when gp120 is taken up by the microglia cells in the brain, it causes intense inflammation and makes the brain subject to excitotoxic damage-a process called immunoexcitotoxicity. This is also the cause of the MS and optic neuritis associated with vaccines that contain MF-59.
So, how would the gp120 get into the brain? Studies of other immune adjuvants using careful tracer techniques have shown that they routinely enter the brain following vaccination. What most people do not know, even the doctors who recommend the vaccines, is that most such studies by pharmaceutical companies observe the patients for only one to two weeks following vaccination-these types of reactions may take months or even years to manifest.
It is obvious that the vaccine manufacturers stand to make billions of dollars in profits from this WHO/government-promoted pandemic. Novartis, the maker of the new pandemic vaccine, recently announced that they would not give free vaccines to impoverished nations-everybody pays.
One must keep in mind that once the vaccine is injected, there is little you can do to protect yourself-at least by conventional medicine. It will mean a lifetime of crippling illness and early death.
There are much safer ways to protect oneself from this flu virus, such as higher doses of vitamin D3, selective immune enhancement using supplements, and a good diet.” End of excerpt by Dr. Blaylock.
- Gary Jacobucci
Get the book “Vaccine-A” and learn what this devil’s potion is made of. I read it years ago and still people do not know what is going on with this stuff. Scripture says 7 vials will be poured out upon mankind in those days and the last of which was worse that the one before. So, what is next? I tell you this, they will do anything using the whore media to make you unaware of the death they are planning for us. Wake up now and get mad a hell over this or you will see your children and family members will die before your eyes. Don’t take this poison.
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Mary from Illinois, USA Reply:
September 10th, 2009 at 10:20 am
I wonder if they will add something to the water……good idea to get that berkey water purifier or buy bottled water now
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vueflix Reply:
September 10th, 2009 at 9:11 pm
Just say NO to the Vaccine.
Alternative media has its own YouTube
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maybe he took the vaccine and is now with his god lucifer
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B. A Reply:
September 10th, 2009 at 7:19 pm
we can only hope.
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PLEASE be aware that even if the adjuvants were removed from the vaccine IT IS STILL UNSAFE to take….this reminds me of the mercury argument regarding autism and vaccines….people were demanding that the mercury be removed from the vaccine thinking the autism problem would go away……..the MMR vaccine NEVER contained mercury yet children were exhibiting s&s of autism following this vaccine administration……….vaccines do not provide immunity (why do you think they recommend ‘boosters’?)…….this ‘flu’ vaccine will CAUSE the pandemic to take hold……SAY NO!!!!!!!
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I think it would be quite educational (and revealing) to the general public, if a good writer with a bio-medical background were to describe the body’s reaction to puncture damage or intestinal perforations… VERSUS what transpires when a syringe needle introduces scores or (more realistically) hundreds of foreign biological and potentially toxic substances rapidly and directly into the circulatory system.
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Come on everybody…I mean if Obama says its safe then it must be safe right? I mean he wouldn’t lie to us now would he?
These people are demons!
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Defend US Flag Reply:
September 10th, 2009 at 1:45 pm
Call Congressman Joe Wilson and
thank him for calling Barry/Barack a
“liar” . The CongressmaN DESERVES support call 202-225-2452.
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dba Reply:
September 10th, 2009 at 4:13 pm
ALREADY CALLED HIM
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underbull Reply:
September 11th, 2009 at 1:50 pm
Suppose you have the water heater in your house start leaking and shut down leaving you with no hot water and leaking water making a mess. Would you call a plumber who will “GUARANTEE” his work and the materials needed to fix the problem or would you call some “jack leg” joker of a handy man who happens to have a good used water in the back of his truck and maybe, just maybe, it’ll work but it will not have a “GUARANTEE” and no warranty on the job. Since there are no guarantees or warrantees on any vaccines you have the possibilities of being harmed from a defective product which in the case of the H1N1 vaccine, you will have no recoarse except to bend yourself all the way over far enough to kiss your ass goodby. You cannot truly trust the most dangerous animal on the face of this old world. No “GUARANTEE”.
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Yes, what a man, this Joe Wilson. He looked somewhat apprensive about what he had just done. They probably threatened him if he did not give a retraction. The atmosphere in Washington District of Criminals is of course not new. They are so comfortable with the status quo that nothing except exposure will ever stop these creeps. Knoxville among other places will have 911 ceremonies today and reveal even more about that fateful day. I say again, nothing but nothing will ever move forward without ful disclosure about who really planned and carried out the murder of our beloved fellow Americans in the Towers. George Bush, Dick Cheney, and all those who are guilty of this must be prosecuted and sentenced accordingly or this country is doomed. Call and write as I have and then we will set a date to haunt the White House lawn. Remember, the perpetrators are mocking God all the while they remain free from prosecution. Time seemed to mask the act of Pearl Harbor, but, absolutely nothing including time will ever make 911 go away. Justice serves Liberty and Freedom. Freedom will be defended!!!
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http://www.vaclib.org/index.htm
http://www.sweetliberty.org/issues/health/index.html
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Anyone looking for an eye-catching ANTI VACCINE demonstration symbol or graphic image (B/W skull & bones with syringe eyes), please checkout the following URL:
http://darethefuture.com/
This site should also have a song called “Anti Vaccine Anthem” (although I did not immediately spot it on my initial viewing)
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Androgynus Reply:
September 13th, 2009 at 8:21 pm
On this site there’s three down-loadable mp3 song files (hip-hop style)… One is anti-Swine Flu vaccination… Another is anti psychotropic drugging…and the third deals with the Wall Street banker bail-out obscenity… By Micheal Adams–The Health Ranger
http://www.naturalnews.com/Dont_Inject_Me_The_Swine_Flu_Vaccine_Song.html
Don’t know how police would react to boom boxes blaring away anti vaccination, psycho-drugging (or anti-Wall Street bailout) music…but perhaps “legally” safer than megaphones…and, way better then getting hoarse from street shouting.
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The people in this country need to organize massively to stop this. Strike in a massive scale. Stop going to work for 3 days or whatever. STOP giving them money! Stop paying taxes! But they won’t. There are too busy watching football, baseball, basketball, planning parties, watching Tel- lie- vision to be concerned about their own country going up in flames! They still think left and right. God help us and this world!
http://www.youtube.com/watch?v=PbSpPs05YAc&feature=PlayList&p=A6B66867E18D26F1&playnext=1&playnext_from=PL&index=45
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They were intent on creating something Mother Nature had not. “Designer disease,” they would later call it.
Dr. Sergei Popov was one of the Soviet Union’s best germ warriors, and running highly classified field research projects at The State Research Center of Applied Microbiology at Obolensk, and another laboratory in Siberia, specializing in viruses called VECTOR. While at Obolensk, Popov supervised a program codenamed “FACTOR”—as in “pathogenic factors” or “virulence factors”—where he helped engineer designer germs resistant to antibiotics. That is when he got interested in U.S. research with myelin basic protein.
American molecular biologist had mapped out the entire amino acid sequence for myelin—one of the chief components of the insulation surrounding nerve endings. Now they were hard at work trying to identify the epitopes on viruses that would cross-react with a special site on the myelin molecule to which an antibody might react and, cause experimental allergic encephalomyelitis—the animal version of multiple sclerosis. As the California-based scientists Robert Fujinami and Michael Oldstone explained in a landmark paper in Science: “during the cross-reacting immune response, virus may be cleared, but the components of the immune attack continues to assault self elements. The autoimmune response leads to tissue injury that, in turn, releases more self antigen, and the cycle continues.” Fujinami and Oldstone called the initial infection a “hit and run event.” By this they meant the virus attacked, and though it didn’t stick around, it left behind lasting damage. That is because the immune system continues to attack the molecule in the body that resembles the one in the germ, long after the immune system has gotten rid of the germ. Once this self-destructive process begins, it never stops; our bodies continue making the molecule the immune system is now trained to attack. If this new target for the immune system happened to be myelin, for example, the body would continue making this protein in order to replenish and repair the sheath around it’s nerve endings. But in the act of doing so, the body immunizes itself against itself, administering over and over again what amounts to a booster dose of something that the immune system now wants to get rid of. This vital constituent of your own body is now the enemy, and the immune system is now programmed to obliterate it in an endless loop of self-destruction [italics mine]. Dr. Sergei Popov saw real potential here.
He would not bother looking for a naturally occurring molecule that could trigger this process. He would make one. Popov spliced a fragment of myelin basic protein into legionella—the bacterium that causes Legionnaire’s Disease—creating a “chimera,” named for the mythical creature with a lion’s head, goat’s body and serpent’s tail. Inside Popov’s new constructed chimera was what amounted to a living “nano-bomb”—molecular contraband that could theoretically cause MS. When Popov infected guinea pigs with his chimera, the immune system cleared the legionella, and, just as he predicted, the myelin molecule smuggled into the guinea pigs inside of his microbial Trojan horse germ initiated a second wave of disease. This stealth germ caused experimental allergic encephalomyelitis, the animal version of MS. Popov felt as proud as a new parent. He could not wait to show “the client.”
“The client” is what VECTOR scientists called the Soviet Army officers who commissioned their biological warfare research projects. “Their initial response was rather discouraging,” says Popov, “because they did not see the fast onset of symptoms.” What the generals were accustomed to seeing was a germ with an immediate and catastrophic effect, but when they came back a few weeks later and saw the guinea pigs crippled MS, they recognized Popov’s creation for what it was—a biological time bomb. Soviet scientists then constructed another one of these time bombs with a virus. They chose vaccinia, the non-lethal cousin of smallpox. Popov, who is now living in America, believes the “final construct” for this viral time bomb was not vaccinia, but smallpox itself. In any case, it worked. “The client” had seen enough. The generals were sold on the idea. “The Russian Ministry of Defense wanted us to construct these designer germs, using myelin basic protein from monkeys and humans,” says Popov. “That would create a human version of the disease.”
Molecular mimicry, seen for its diabolical potential as a weapon by the Soviets as far back as the 1980s, also applies to SQUALENE [caps mine]. But the real problem with using squalene, of course, is not that it mimics a molecule found in the body; it is the same molecule. So what American scientists conceived as a vaccine booster was another “nano-bomb,” instigating chronic, unpredictable and debilitating disease [italics mine]. When the National Institutes of Health (NIH), argued that squalene would be safe because it is native to the body, just the opposite was true. Squalene’s natural presence in the body made it one of the most dangerous molecules injected into human beings [italics mine]. When UCLA Medical School’s Michael Whitehouse and Frances Beck injected squalene combined with other materials into rats and guinea pigs back in the 1970s, few oils were more effective at causing the animal versions of ARTHRITIS, and MULTIPLE SCLEROSIS [caps mine]. By the late 1990s, Sweden’s Karolinska Institute proved that injecting squalene all by itself could cause arthritis. The Polish Academy of Sciences proved that squalene alone could severe neurological damage. Now Tulane University Medical School and its ardent intellectual adversary—the Army’s Col. Carl Alving—have both shown that the immune system makes antibodies to squalene, but only after it is injected [italics mine].
For Squalene’s proponents in the U.S. Army and the NIH, this has been a relentless march towards an unpalatable truth. By adding squalene to their new anthrax vaccine, they did not make a better vaccine; they made a biological weapon [italics mine]. The anti-squalene antibodies in sick U.S. and British military personnel are evidence that military experiments may have caused more casualties with its new anthrax vaccine than have been caused by anthrax weapons since they were first used by the Japanese Army in the 1940s.
The above is an excerpt from Gary Matsumoto’s book (with modifications):
VACCINE.A
The Covert Government Experiment
That’s Killing Our Soldiers
and Why GI’s Are Only the First Victims
http://books.google.com/books?id=Irw82Iv5nyoC&printsec=frontcover&source=gbs_navlinks_s#v=onepage&q=&f=false
MP has H1N1 concerns.
CBC News – September 14, 2009
An NDP MP from Winnipeg: Judy Wasylycia-Leis wants to know what measures Elections Canada has in place to safeguard voters from the spread of swine flu, considering an election poses significant health risks with large public events and many people coming into contact during canvassing…hmmm
(hmmm-mine).
$400M contract goes to GlaxoSmithKline factory in Quebec City.
August 6, 2009 – CBC News.
Canada to order 50.4 million H1N1 (SWINE FLU) vaccine doses – One dose should be enough, because: GlaxoSmithKline is using an additive (AS03 – SQUALENE based) known as ADJUVANT. Adjuvants are used to boost immune response from vaccines [italics, caps and info on AS03 mine].
THE WORLD HEALTH ORGANIZATION (WHO) recommends countries should use SWINE FLU vaccines with ADJUVANTS [caps mine] – to stretch the global supply of the vaccines.
August 4, 2009 – THE CANADIAN PRESS
Flu vaccines in Europe often contain adjuvants [italics and underline mine].
The European Medicines Agency has previously said swine flu vaccines based on a pre-approved bird flu vaccine could be licensed within five days, even without extensive testing in humans.
In the United States, there are no licensed flu vaccines with adjuvants – The U.S. has ordered $979 million worth of bulk vaccine and Novartis’ adjuvant (MF59®) [italics and underline mine].
MF59; is a sub-micron oil-in-water emulsion of a squalene, polyoxyethylene sorbitan monooleate (TweenTM 80) and sorbitan trioleate. SQUALENE is a natural organic compound originally obtained from shark liver oil and a biochemical precursor to steroids. The “MF59” adjuvant was developed by Chiron Corp., a company acquired by Novartis. MF59 is approved in Europe and is found in several vaccines; such as an influenza vaccine manufactured by Novartis. It has also been licensed to other companies and is being actively tested in vaccine trials.
http://www.whale.to/vaccines/mf59_h.html
Information compiled and provided by Christopher-Peter: Maingot; without prejudice, malice aforethought, ill will, vexation, or frivolity.
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Received 11 February 2003;
revised 12 April 2003;
accepted 2 May 2003. ;
Available online 11 June 2003.
Abstract
Exposure to the hydrocarbon oil pristane induces lupus specific autoantibodies in non-autoimmune mice. We investigated whether the capacity to induce lupus-like autoimmunity is a unique property of pristane or is shared by other adjuvant oils. Seven groups of 3-month-old female BALB/cJ mice received a single intraperitoneal injection of pristane, squalene (used in the adjuvant MF59), incomplete Freund’s adjuvant (IFA), three different medicinal mineral oils, or saline, respectively. Serum autoantibodies and peritoneal cytokine production were measured. In addition to pristane, the mineral oil Bayol F (IFA) and the endogenous hydrocarbon squalene both induced anti-nRNP/Sm and -Su autoantibodies (20% and 25% of mice, respectively). All of these hydrocarbons had prolonged effects on cytokine production by peritoneal APCs. However, high levels of IL-6, IL-12, and TNFα production 2–3 months after intraperitoneal injection appeared to be associated with the ability to induce lupus autoantibodies.
The ability to induce lupus autoantibodies is shared by several hydrocarbons and is not unique to pristane. It correlates with stimulation of the production of IL-12 and other cytokines, suggesting a relationship with a hydrocarbon’s adjuvanticity. The potential to induce autoimmunity may complicate the use of oil adjuvants in human and veterinary vaccines.
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WHC-48TMCJ6-3&_user=10&_rdoc=1&_fmt=&_orig=search&_sort=d&_docanchor=&view=c&_searchStrId=1018959749&_rerunOrigin=google&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=1265afaf82232cd896af7e8b4b1e928f
Information compiled and provided by Christopher-Peter: Maingot; without prejudice, malice aforethought, ill will, vexation, or frivolity.
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