CBS News: Unplugged: H1N1 Vaccine Dangers, plus a few more videos

October 7, 2009Jenny Marie Hatch

Watch CBS News Videos Online
Sharyl Attkisson, CBS News Medical Correspondent Dr. Jennifer Ashton and NVIC’s Barbara Loe Fisher discuss the possible dangers with the H1N1 vaccine

Barbara’s personal blog
National Vaccine Information Centers International Conference
Click on this link to watch the story of a Marine devastated by a shot

What’s in a flu shot?

October 6, 2009Jenny Marie Hatch

My blog entry for the day – What’s in a flu shot?

Video is funny and ironic, the following information is not:
Squalene: Be Afraid, Part I
The following article by Edda West was published in 2005. Given the horrific threat of squalene laced vaccines for a mythical danger concocted in a lab, it is all the more relevant now. Please take time to read and share this post and the one that follows it.
This outstanding article details the mechanism of action, and the enormous dangers, of vaccines which contain squalene in any of its forms. But bare in mind as you read this clear, and enormously important article below, that the adjuvanted vaccine approved by the US Government on September 15, 2009, in the total absence of even a shred of safety testing, will contain 1 million times more squalene than even the deadly Vaccine A.
You may have encountered the squalene story before: how injected squalene, even a few molecules of injected squalene, causes the body to attack itself on a rampage of auto immune destruction like an army gone mad and turned on its country. And that is, in fact, exactly what triggered this onslaught of destruction: the US Department of Defense decided to experiment on its citizens, healthy young men and women who had made the terrible mistake of trusting their country to take care of them while they were willing to give their lives to defend it.
Instead, they were betrayed with unsafe vaccines for (or against, it depends on whom you asked) anthrax. The tragedy was that this was no experimental surprise which was revealed for the first time when the vaccine’s terrible consequences showed up over time. No, this adjuvant, or immune response enhancer molecule was known as “Freund’s Complete Adjuvant” and was used in animal experimentation to produce cataclysmic and lethal auto immune disorders in animals. 100% of the time when they were injected.
Fast forward to today’s news: On September 15, 2009 Health and Human Services Secretary Kathleen Sebelius announced the approval, in the total absence of any safety testing, of 4 new vaccines for the novel A/H1N1 Swine Flu virus which allegedly appeared in Mexico this past April for the very first time in the world’s history.
But wait! Patents for this vaccines “against” this very virus were applied for by Medimmune (parent company to Sanofi Aventis), Novartis and Baxter International. Baxter and Novartis applied for patents using squalene-based adjuvants. Baxter and Novartis’ adjuvant of choice is called MF59, detailed in the article below as a powerful – and highly toxic – squalene compound. GSK’s adjuvant, MLP(AS04) [also identified as AS03 in company statements and, like AS01 and 2, contains MLP, or, in simple terms, squalene] is also a powerful and literally poisonous auto immune stimulant made from squalene.
Baxter knows that, as far as immune enhancement to prevent disease goes, squalene adjuvants do not even work. So we have to wonder if – hard, strong and long, if the introduction of squalene has anything to do, anything at all, with the avowed goal of preventing a pandemic.
Quoting Investigative Report Jane Burgermeister,
“On July 13th, WHO ordered the inclusion of oil-in-water adjuvants in the “swine flu” H1N1 vaccines to be distributed throughout the world this autumn on the recommendation of its vaccine advisory panel, packed with Baxter and pharmaceutical executives, in spite of the fact that clinical studies published by Baxter’s own scientific team that patented the H1N1 vaccine demonstrate that such adjuvants are, at best, useless.
‘SAGE [WHO’s advisory panel on Pandemic Vaccines, on which Baxter and other vaccine manufacturers sit – REL] recommended that promoting production and use of vaccines such as those that are formulated with oil-in-water adjuvants and live attenuated influenza vaccines was important,’ says the WHO pandemic briefing note.
http://www.who.int/csr/disease/swineflu/notes/h1n1_vaccine_20090713/en/index.html
In June 2008, Baxter’s Austrian-based scientists Ehrlich, Kistner and Barret published a clinical trial in the New England Journal of Medicine ((Previous Volume 358:2573-2584 June 12, 2008 Number 24) on the safety of an H5N1 whole-virus vaccine, in which they themselves go on record saying that the use of adjuvants did not improve the antibody response.
http://content.nejm.org/cgi/content/short/358/24/2573
In spite of the evidence that adjuvants are at best useless, vaccine companies such as Baxter and Novartis are rolling out vaccines which contain adjuvants like squalene (MF59), a substance added to the anthrax vaccine given to US soldiers, causing tens of thousands of Iraq Desert Storm soldiers to suffer permanent neurological damage.
Also, WHO is reported to have advised the use of “antigen sparing” protocols which means they are calling for the use of not much virus and lots of adjuvant.
The effects of adjuvants are so destructive to the human body that some people say that adjuvants are part of the next generation of biological or pharmacological warfare.”
http://birdflu666.wordpress.com/2009/07/17/adjuvants-to-be-added-to-h1n1-jab-by-baxter-and-who-programmes-body-for-endless-loop-of-self-destruction/
In Squalene: Be Afraid, Part II we will discuss what the underlying reason for this adjuvant and document why the greatest danger in this Pandemic may not even be the vaccine we all have so much reason to fear.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
http://www.HealthFreedomusa.org
http://www.GlobalHealthFreedom.org
Valley of the Moon (TM) Eco Demonstration Project
http://www.NaturalSolutionsFoundation.org
A Glimpse into the Scary World of Vaccine Adjuvants
By Edda West – Published in VRAN Newsletter – Winter 2005
Adjuvants are formulated compounds, which when combined with vaccine antigens intensify the body’s immune response. They are used to elicit an early, high and long-lasting immune response. “The chemical nature of adjuvants, their mode of action and their reactions (side effect) are highly variable in terms of how they affect the immune system and how serious their adverse effects are due to the resultant hyperactivation of the immune system. While adjuvants enable the use of less *antigen to achieve the desired immune response and reduce vaccine production costs, with few exceptions, adjuvants are foreign to the body and cause adverse reactions”, writes Australian scientist Viera Scheibner Ph.D, (1)
The most common adjuvant for human use is an aluminum salt called alum derived from aluminum hydroxide, or aluminum phosphate. A quick read of the scientific literature reveals that the neurotoxic effects of aluminum were recognized 100 years ago. Aluminum is a neurotoxicant and has been linked to Alzheimer’s disease and other neurological disorders. Prior to 1980, kidney patients undergoing long term dialysis treatments often suffered dialysis encephalopathy syndrome, the result of acute intoxication by the use of an aluminum-containing dialysate. This is now avoided using modern techniques of water purification. In preterm infants, prolonged intravenous feeding with solutions containing aluminum is associated with impaired neurologic development. Scientists speculate that aluminum neurotoxicity may be related to cell damage via free radical production, impairment of glucose metabolism, and effects on nerve signal transduction. (2) Vaccines which contain both aluminum adjuvants and mercury based preservative, greatly magnify the neurotoxic effects. (3)
Macrophagic myofasciitis (MMF) is a muscle disease first identified in 1993, and has been linked to vaccines containing aluminum adjuvants. Muscle pain is the most frequent symptom which can be localized to the limbs or be more diffuse. Other symptoms include joint pain, muscle weakness, fatigue, fever, and muscle tenderness. The disorder is associated with an altered immune system in some, but not all patients. A study published in the journal Brain (2001) revealed that 50 out of 50 patients had received vaccines against hepatitis B virus (86%), hepatitis A virus (19%) or tetanus toxoid (58%), 3-96 months (median 36 months) before biopsy. “We conclude that the MMF lesion is secondary to intramuscular injection of aluminum hydroxide-containing vaccines, shows both long-term persistence of aluminum hydroxide and an ongoing local immune reaction, and is detected in patients with systemic symptoms which appeared subsequently to vaccination”, write the authors of the study. (4)
But aluminum’s neurotoxicity is of less concern to the vaccine industry than the fact that it elicits a lesser antibody response to the so called purer recombinant or synthetic antigens used in modern day vaccines than in older style live or killed whole organism vaccines. “This has created a major need for improved and more powerful adjuvants for use in these vaccines.” (5)
For decades, vaccine developers have been tinkering with various substances to trick the body into heightened immune responses. 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 the1930’s that oil based adjuvants are particularly dangerous, which is why their use has been restricted to experiments with animals.
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, which causes great suffering and is considered by some too inhumane to even inject into animals.
Dr. Jules Freund creator of this oil based adjuvant warned in 1956 that animals injected with his formulation developed terrible, incurable conditions: allergic aspermatogenesis (stoppage of sperm production), experimental allergic encephalomyelitis (the animal version of MS), allergic neuritis (inflammation of the nerves that can lead to paralysis) and other severe autoimmune disorders. (6)
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. Normally, the immune system ignores the constituents of one’s own body. Immunologists call this “tolerance”. But if something happens to break “tolerance”, then the immune system turns relentlessly self-destructive, attacking the body it is supposed to defend. (6)
Scientists theorize that oil based adjuvants have the ability to “hyperactivate” the immune system, and in doing so, create chaos by inducing such an extremely powerful response that the immune system literally goes haywire and starts attacking elements it would normally ignore. (6)
Another theory has to do with “specificity”. One of the great distinguishing characteristics of the immune system is something akin to a highly sensitive innate intelligence that has evolved over eons to be able to respond very precisely to what it deems to be a threat to the body. Because the body contains many types of oily molecules and lipids, it may be that when an 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. A “cross reaction” then happens, sending the immune system into chaos destroying any oils found anywhere in the body that resemble the adjuvant oil. Demyelinating diseases like multiple sclerosis are an example of this destructive autoimmune process. (6)
To deepen one’s understanding of the shadowy world of vaccine development, award winning investigative journalist Gary Matsumoto’s new book is a “must read.” It documents the secret human medical experimentation conducted on American citizens by doctors and scientists working for the U.S. military. It is a book about “betrayal of the most fundamental rules of medical ethics; and betrayal of the basic duty of military and civilian leaders to protect the people they govern.” Vaccine A: The Covert Government Experiment That’s Killing our Soldiers and Why GI’s are Only the First Victims, is a gripping read into the mad science world of the U.S. military’s biowarfare vaccine development program which, since 1987 has injected tens of thousands of U.S. troops with an experimental unlicensed anthrax vaccine containing squalene.
An oil based adjuvant, squalene has been known for decades to cause severe autoimmune diseases in laboratory animals. Writes Matsumoto, “The unethical experiments detailed in this book are ongoing, with little prospect of being self-limiting because they have been shielded from scrutiny and public accountability by national security concerns.” Reading this book, one gets a permanent chill in the spine as we glimpse the “writing on the wall” of what is to come. (6,7)
“When UCLA Medical School’s Michael Whitehouse and Frances Beck injected squalene combined with other materials into rats and guinea pigs back in the 1970’s, few oils were more effective at causing the animal versions of arthritis and multiple sclerosis”, writes Matsumoto. In 1999, Dr. Johnny Lorentzen, an immunologist at Sweden’s Karolinska Institute proved that on injection, “otherwise benign molecules like squalene can stimulate a self-destructive immune response”, even though they occur naturally in the body.
Other research institutes have also shown that the immune system makes antibodies to squalene, but only after it is injected (6) We now know that squalene, added to boost immune response in a formulation known as MF59, is the secret ingredient in certain lots of experimental anthrax vaccine that has caused devastating autoimmune diseases and death in countless Gulf War vets (Canadian, British and Australian troops were also injected with squalene laced vaccine), and continues to be used today.
There is a “close match between the squalene-induced diseases in animals and those observed in humans injected with this oil: rheumatoid arthritis, multiple sclerosis and systemic lupus erythematosus”, writes Matsumoto. These three illnesses have been proven to be caused by this oil, but there is an additional long list of autoimmune diseases associated with squalene injection into humans. (6)
“There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the U.S., Europe, Asia and Australia, documenting that squalene-based adjuvants can induce autoimmune diseases in animals..observed in mice, rats, guinea pigs and rabbits. Sweden’s Karolinska Institute has demonstrated that squalene alone can induce the animal version of rheumatoid arthritis. The Polish Academy of Sciences has shown that in animals, squalene alone can produce catastrophic injury to the nervous system and the brain. The University of Florida Medical School has shown that in animals, squalene alone can induce production of antibodies specifically associated with systemic lupus erythematosus”, writes Matsumoto. (6)
Long List of Side Effects Referring to squalene in her extensive article on adjuvants, Dr. Scheibner writes, “This adjuvant contributed to the cascade of reactions called “Gulf War syndrome”, documented in the soldiers involved in the Gulf War. The symptoms they developed included 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, anemia, 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 diarrhea, night sweats and low-grade fevers. (1)
Matsumoto punctuates his book with poignant interviews of military personnel who suffered many of these extreme and devastating syndromes, all of whom tested positive for anti-squalene antibodies which has become THE definitive marker for people who have been injected with this adjuvant and who have gone on to develop catastrophic diseases.
Immunologist, Dr. Pamela Asa was the first person to recognize that the autoimmune diseases she was seeing in military personnel mirrored those in experimental animals injected with oil formulated adjuvants. When she met a patient with similar autoimmune symptoms who had participated in an experimental herpes vaccine trial, who also knew he had been injected with MF59, a squalene adjuvant being used as a ‘placebo’ in that study, everything began to fall into place.
Pam Asa contacted Dr. Robert Garry, a leading virologist at Tulane University Medical School, whose specialty is developing antibody tests and asked him to develop a test for the detection of anti-squalene antibodies – a test that ultimately became the most important forensic and diagnostic tool identifying patients whose autoimmune diseases followed injection with squalene laced anthrax vaccine. (6)
Juxtaposed to heart wrenching testimonies of shattered health and ruined lives is the military’s defiant stonewall and denial that a squalene laced anthrax vaccine was injected into thousands of its people without their informed consent – this despite the fact that the FDA and independent researchers have tested and identified varying amounts of squalene in specific lots of the vaccine.
Even more stunning is the fact that by 1997, hundreds of millions of dollars had already been spent testing vaccines formulated with squalene adjuvants by leading research institutes like NIH (National Institutes of Health) who tested its efficacy in HIV vaccines, the National Cancer Institute who for nearly two decades conducted research with squalene-boosted vaccines, and the National Institutes of Allergy and Infectious Diseases (NIAID) had been testing it in animals since 1988 and began human clinical trials in1991. Nineteen of NIAID’s 23 trials were for prototype HIV vaccines. Writes Matsumoto, ” Squalene adjuvants are a key ingredient in a whole new generation of vaccines intended for mass immunization around the globe.” (6)
Immune System Sees Squalene as an Enemy to Attack Researchers at Tulane Medical School and the Walter Reed Army Institute of Research “have both proven that the immune system responds specifically to the squalene molecule. Squalene’s pathway through the body has been tracked with a radioactive tracer in animals by none other than Chiron, (well known flu vaccine manufacturer) and maker of MF59, the squalene-based adjuvant, now also a component of FLUAD, an Italian influenza vaccine. (6)
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.(6)
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.” (6)
This phenomenon is also known as ‘molecular mimicry’, where the immune system forms antibodies against one of its own structures and will continue to attack the ’self’ molecule in the body that resembles the one in the germ, or as is the case with squalene, an identical substance that is naturally present in the body. Once this self-destructive process begins, it never stops as the body continues to make the molecule the immune system is now trained to attack.
Another example involving autoimmune ‘molecular mimicry’ is when the immune system has been sensitized to attack myelin, the insulating fatty coating around nerve fibers which insures the smooth relay of nerve signals. The body would continue to make myelin in order to replenish and repair the protective sheath around its nerve endings. But says Matsumoto, “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 (myelin) is now the enemy, and the immune system is now programmed to obliterate it in an endless loop of self-destruction” – the process involved in MS (multiple sclerosis), and ALS (Lou Gehrig’s disease).(6)
Tying molecular mimicry to the autism epidemic, many children have regressed into autism spectrum disorders after injection with the triple live virus MMR (measles,mumps,rubella) vaccine. Dr.Vijendra Singh’s research at Utah State University suggests that auto-antibodies are attacking myelin in these children. He has shown that many autistic children have auto-antibodies to brain myelin basic protein (MBP) as well as elevated levels of measles virus antibodies. “Immunoblotting analysis showed the presence of an unusual MMR antibody in 60% (75 of 125) of autistic children, but none of the 92 normal children had this antibody.
In addition, there was a positive correlation (greater than 90%) between MMR antibody and MBP auto-antibody, suggesting a causal association between MMR and brain autoimmunity in autism. This is one of the most important findings in autism to date, which prompted us to link measles virus in the etiology of the disorder”, writes Dr. Singh. (8,9,10)
Immunologist Dr. Bonnie Dunbar has also done extensive research on the mechanisms of injury inflicted by hepatitis B vaccine and has observed similar autoimmune processes involving molecular mimicry in people who developed devastating neuroimmune syndromes after injection with this vaccine. (11)
Molecular Mimicry as a Bio-Weapon Matsumoto reports that Soviet bioweaponeers used the principal of molecular mimicry in the 1980’s to engineer a ‘designer disease’ that would attack myelin. By splicing a fragment of myelin basic protein into legionella bacterium, they created what amounted to a living “nano-bomb”, which they injected into guinea pigs. What they found was that the immune system quickly cleared the legionella bacterium, but the myelin molecule, smuggled in by this microbial “Trojan horse” initiated a second wave of disease which caused experimental allergic encephalomyelitis, the animal version of MS. The Soviets recognized this creation for what it was – a biological time bomb!! (6)
“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,” writes Matsumoto. His assessment is seconded by Dr. Pam Asa – “Oil adjuvants are the most insidious chemical weapon ever devised.” (6)
“Molecular mimicry, seen for its diabolical potential as a weapon by the Soviets as far back as the 1980’s, also applies to squalene. 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,” writes Matsumoto. “So what American scientists conceived as a vaccine booster was another “nano-bomb”, instigating chronic, unpredictable and debilitating disease. When the NIH (National Institutes of Health) 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 ever injected into man!” (6)
Squalene’s natural presence in the body made it one of the most dangerous molecules ever injected into man!” (6)
Squalene’s natural presence in the body made it one of the most dangerous molecules ever injected into man!” (6)
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 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. “By adding squalene to their new anthrax vaccine, they did not make a better vaccine, they made a biological weapon.” (6) .
Why , one would obviously ask, would anyone knowingly inject such a dangerous substance into humans? Certainly in terms of the U.S. military’s decision, they chose to turn a blind eye to the existing science, which for decades had documented the immune destructive properties of squalene. They justified its use because they knew they had a weak and ineffective vaccine which needed a serious boost.
In the face of weaponized biowarfare agents like anthrax already developed by Russia and fear that it was also possessed by Iraq, they were desperate to increase the vaccine’s effectiveness as they launched into the first Gulf War. Additionally, explains Matsumoto, “scientists in the United States are now literally invested in squalene. Army scientists who developed the second generation anthrax vaccine have reputations to protect and licensing fees to reap for the army..[and] .worldwide rights to develop and commercialize the new recombinant vaccine for anthrax.” (6)
He goes on to explain, “the National Institutes of Health (NIH) has been supporting both animal and human research with squalene since the 1980’s. Squalene has become perhaps the most ubiquitous oil adjuvant on the planet, which is something that should concern everyone. Many of the cutting edge vaccines currently in development by the NIH and its corporate partners contain squalene in one formulation or another. There is squalene in the prototype recombinant vaccines for HIV, malaria, herpes, influenza, cytomegalovirus and human papillomavirus. Some of these prototypes like HIV, malaria and influenza are intended for mass immunization around the globe.” (6)
Squalene Adjuvants Enter the Global Market FLUAD, the squalene boosted flu vaccine has been licensed in Italy since 1997. It contains MF59, the squalene adjuvant made by Chiron. Although all the published papers co-authored by Chiron-employed scientists and Italian researchers have reported MF59 to be safe, Gary Matsumoto suggests a flaw in study designs may “prevent researchers from seeing the vaccine’s real risks.” Testing of FLUAD was limited to elderly people in nursing homes – average age was 71.5 which would tend to obscure autoimmune problems that might arise for a number of reasons. If autoimmune symptoms like joint pain and fatigue did occur in geriatric Italians, doctors might not connect these complaints to anything but old age. (6)
“Autoimmunity is notorious for taking years to diagnose because the early symptoms (e.g. headaches, joint and muscle pain and fatigue) are so vague; primary care physicians often fail to recognize it…a large Phase lV trial did not even bother to analyze the “common-post immunization reactions” in study participants, recording only those adverse events severe enough to require a doctor’s visit within 7 days of immunization.” In another study patients were observed for 180 days, but only serious events like “admission to hospital or death” qualified as a reaction – nothing else was recorded. Symptoms of adverse reactions listed in the FLUAD package insert are almost identical to the Air Force case-definition for Gulf War Syndrome, and include rashes, malaise, fever, myalgia, arthralgia, weakness, sweating and various autoimmune reactions and neurologic disturbances. (6)
“The question is whether scientists working for pharmaceutical companies are intentionally designing studies so as to miss adverse reactions that inconvenience their marketing strategy?” asks Matsumoto. “Chiron’s conclusion about squalene’s safety are at odds with recent data from studies in both animals and humans.” (6)
Just in from the newslists on February 9, 2005 is an item informing of the European “debut” of a new adjuvant approved for use in a new high-potency hepatitis B vaccine. Fendrix, the new enhanced hepB vaccine is being launched by pharma giant GlaxoSmithKline for use in people with poor immune responses (like dialysis patients) and those at high risk for developing hepatitis B. It is formulated with a new adjuvant that can “significantly improve the effectiveness of immunizations.” AS04, the ‘proprietary’ adjuvant based on MPL, originally developed by U.S. company Corixa, “increases the immune potency of the new vaccine, allowing two dose administration rather than three. It has been shown clinically to be more effective than alum, the most widely used adjuvant in vaccines.” (12)
So what exactly is this new high potency adjuvant? We’re told by the press release that MPL (AS04), is a “derivative of the lipid A molecule found in Gram-negative bacteria, is extracted from bacterial cell walls and is one of the most potent regulators of the immune response, used by the body to alert itself to bacterial infections.”(12) Full name of the lipid is monophosphoryl lipid A (MPL)
This news should put everyone on high alert because guess what? Lipids are oils/fatty acids and according to Matsumoto, MPL is identified in declassified documents as one of two squalene emulsions used in the Army’s new “recombinant protective antigen anthrax vaccine (rPA) which the FDA, the National Institutes of Health (NIH) and the Department of Defense fast-tracked into clinical trials in1998. The other squalene adjuvant they used was Chiron’s MF59. (6)
It appears that Fendrix is only the first of a whole new generation of “enhanced potency” vaccines coming down the pipeline using the new high potency lipid adjuvant, MPL. “The adjuvant is also being used in a number of GSK’s developmental vaccines, including one that could be the first effective vaccine for malaria”, says the article. MPL (AS04) adjuvant is also a component of GSK Bio’s genital herpes vaccine, as well as a component in their cervical cancer vaccine and a new tuberculosis vaccine.” (12)
In the unraveling of the squalene story, we find that a squalene emulsion first known as Triple Mix (based on Freund’s adjuvant) was later given the commercial name “Ribi”. Triple Mix (renamed Ribi) was tested by Dutch scientists on rabbits who found it caused “severe effects the largest number and most severe lesions when compared with the other adjuvants.”(6) Then in June 1999, Ribi ImmunoChem its manufacturer was acquired by Corixa Corporation for $56.3 million, who presumably also own the Ribi formulation. Whether MPL(AS04) is a formula related to Ribi is undoubtedly “proprietary” information, but from Matsumoto’s reseasrch, we know they are all squalene based.
And it doesn’t end there. MPL, Corixa’s multi-million dollar baby, is slated for inclusion not only in the “enhanced potency” vaccines already mentioned, but will also be a strategic component of new allergy and autoimmune vaccines in development. (13)
From their inception, mass vaccinations have acted as a biological weapon, undermining health, manipulating and crippling the immune system, and instigating cycles of new and debilitating diseases.
Monopoly medicine’s solution?
Inject us with more powerful, genetically engineered high potency vaccines. Never mind they are seeding us with “nano-bombs” that will further attack our already compromised immune systems.
The concept of stimulating a hyperactive immune response by using oil-based adjuvants has clearly backfired since we now know that the stronger the antigenic response, the more damaging the adjuvant itself is to the normal functioning of the brain and nervous system.
The precedent for mass medical experimentation via an ever increasing recommended vaccine schedule has been set. We can now predict the grim future of mankind: an epidemic of neurological disorders and autoimmune diseases never before imagined.
Notes & Resources
Adjuvants listed by Scheibner: “Today the most common adjuvants for human use are aluminum hydroxide, aluminum phosphate and calcium phosphate. However, there are a number of other adjuvants based on oil emulsions, products from bacteria (their synthetic derivatives as well as liposomes) or gram-negative bacteria, endotoxins, cholesterol, fatty acids, aliphatic amines, paraffinic and vegetable oils. Recently, monophosphoryl lipid A, ISCOMs with Quil-A, and Syntex adjuvant formulations (SAFs) containing the threonyl derivative or muramyl dipeptide have been under consideration for use in human vaccines
*Definition of Antigen (Scheibner): “Micro-organisms, either bacteria or viruses, thought to be causing certain infectious diseases and which the vaccine is supposed to prevent. These are whole-cell proteins or just the broken-cell protein envelopes, and are called antigens”
1.Viera Scheibner, Ph.D, The Adverse Effects of Adjuvants in Vaccines, Nexus Magazine Dec. 2000 vol.8, No.1
http://www.whale.to/vaccine/adjuvants.html
2. Aluminum Toxicity notes from Dr. Boyd Haley Toxic Test Foundation website: http://www.altcorp.com/DentalInformation/aluminumvaccines.htm
3. Boyd E. Haley, Professor of Chemistry: Thimerosal Containing Vaccines and Neurodevelopment Outcomes: http://64.41.99.118/vran/vaccines/mercury/mer_haley.htm
4. Brain, Vol. 124, No. 9, 1821-1831, September 2001, 2001 Oxford University Press http://brain.oupjournals.org/cgi/content/abstract/124/9/1821
5 Vaccine Adjuvants: current state and future trends, Volume 82: Issue Immunology and Cell Biology http://www.blackwellpublishing.com/abstract.asp ?ref=0818-9641&vid=82&iid=5&aid=5&s=&site=1
6.Gary Matsumoto, Vaccine A-
The Covert Government Experiment That’s Killing our Soldiers and Why GI’s are Only the First Victims
7.Gary Matsumoto Press Release and biography: www.vaccine-a.com
8 Vijendra K Singh, Ph.D, Abnormal Measles Serology and Autoimmunity in Autistic Children – Journal of Allergy & Clinical Immunol, 109 (1): S232, January 2002
9. Vijendra Singh – lecture at ATEDM Conference: http://iquebec.ifrance.com/autismemtl/2002/program_en.html
10. Institute of Medicine Meeting (IOM) on Vaccines and Autism, February 9, 2004
11.. Bonnie Dunbar, Ph.D – articles and research proposal – VRAN website: http://64.41.99.118/vran/vaccines/hepatitis/dunbar_research.htm
12.New adjuvant debuts in new hep B vaccine , February 9, 2005, In-Pharma Technologist.com http://www.in-pharmatechnologist.com/news/news-ng.asp ?n=57959-new-adjuvant-debuts
13. Corixa weblink to MPL press release on allergy & autoimmune applications: http://www.corixa.com/default.asp?pid=auto_capsule&id=22
http://www.vaclib.org/basic/adjuvants.htm#eddawest

This entry was posted on Sunday, September 27th, 2009 at 6:34 pm and is filed under Activism, Compulsory Drugging, Disinformation, Genocide, Legislation to Oppose, Medical Hazards, Miscellaneous, Pandemic Threats, Self Quarantine, Self-Shield, Vaccination, Valley of the Moon, Weaponized Avian Flu . You can follow any responses to this entry through the RSS 2.0 feed. Responses are currently closed, but you can trackback from your own site.

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Dr. Carley interviews Jane Burgermeister

October 5, 2009Jenny Marie Hatch

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Jenny Hatch with Benjamin – three hours after his unassisted lotus birth at home! No SHOTS! No Poison, No Pressure! Just Natural, Family Centered Birth! Ben has never had a vaccine shot into his bloodstream and he is extremely healthy.
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Just get your damn vaccine…

October 4, 2009Jenny Marie Hatch

A couple of videos to help educate my readers. The title of this blog entry was a quote from Dr. Nancy Snyderman.

Here is the link to the National Vaccine Information Center
Jenny Hatch

Benjamin Johnson Hatch – 2 hours old after being born at home into his Fathers hands. I did my own prenatal care, birthed him after a six hour labor of love, and he was born Lotus style (we did not cut the cord) and let it fall off naturally six days after his birth. October 25th, 2002
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URGENT PREPARE FOR INFERTILITY PROBLEMS WITH THE FLU VACCINE – Please warn the military and their families!!!

September 26, 2009Jenny Marie Hatch Leave a comment

UPDATE October 1st, 2009

*URGENT* PREPARE FOR INFERTILITY PROBLEMS WITH THE FLU VACCINE ( SPREAD LIKE WILD FIRE )

Too bad the elites in our world think they can use the Military and their families as the “test subjects” for the efficacy of the swine flu vaccine. I suppose the Obama administration just looks at this as an efficient way to prevent a whole generation of conservative american voters from being born. I have been ill all day thinking about this scam…
Jen
More videos on Janes site

Stop the Shot: “Swine Flu” Vaccine: Untested, Uninsurable, Unproven
Dr. Rima E Laibow MD – Natural Solutions Medical Director continues her discussion of the Swine Flu Vaccine in this Part 2 of her recent series. In this part she discusses the situation in the States and urges several Action Items to Stop the Shot.

Alex Jones Tv:6 Nurses”Fired!”For NOT Taking The H1N1 Vaccine & Navy Pandemic Exercise
Nurses fired in New York
Free Republic post on the article
Military to get mandatory swine flu shots soon
WASHINGTON —

“U.S. military troops will begin getting required swine flu shots in the next week to 10 days, with active duty forces deploying to war zones and other critical areas going to the front of the vaccine line, a top military commander said Tuesday.

Air Force Gen. Gene Renuart also told The Associated Press that as many as 400 troops are ready to go to five regional headquarters around the country to assist federal health and emergency management officials if needed as the flu season heats up.

The Pentagon has bought 2.7 million vaccines, and 1.4 million of those will go to active duty military. National Guard troops on active duty are also required to receive the vaccine, as are civilian Defense Department employees who are in critical jobs.

As a result, the military is expected to provide health officials with an early assessment of the vaccine.”

These are the last people on the planet who should be providing lab rat results on this untested vaccine!
Maddening!!!

New York health care workers protest Swine flu vaccine mandate
I’m pleased to report that I have become a writer at Blog Critics Magazine.
My first article is found here.
Jane Burgermeister – Whistleblower Extraordinaire
For the past few months I had been hearing through the alternative healing grapevine that a Medical Reporter in Austria had filed criminal charges against Swine Flu Vaccine Manufacturers. Curious but skeptical, I have quietly followed the story on the internet for the past few months.
From Janes Web Site:

“I have filed criminal charges in Austria against Baxter and Avir Green Hills Biotechnology for producing and distributing contaminated bird flu vaccine material this winter, alleging that this was a deliberate act to cause a pandemic, and also to profit from that pandemic.”

A few months after learning about her, I read an article at Natural News where it was claimed that she also had the World Health Organization and the United Nations in her sightlines. Amazing!!!

“As the anticipated July release date for Baxter’s A/H1N1 flu pandemic vaccine approaches, an Austrian investigative journalist is warning the world that the greatest crime in the history of humanity is underway. Jane Burgermeister has recently filed criminal charges with the FBI against the World Health Organization (WHO), the United Nations (UN), and several of the highest ranking government and corporate officials concerning bioterrorism and attempts to commit mass murder. She has also prepared an injunction against forced vaccination which is being filed in America. These actions follow her charges filed in April against Baxter AG and Avir Green Hills Biotechnology of Austria for producing contaminated bird flu vaccine, alleging this was a deliberate act to cause and profit from a pandemic.”

Who was this woman?
I’m ashamed now to admit that I did not believe it at first. It was just too much to accept. A worldwide conspiracy to gin up a pandemic and then poison people with the vaccine? To depopulate the world? To make people intentionally sick?
Yes as I thought it all out, and then watched Jane herself on You Tube a few nights ago, I had to admit that it fit all of the various bits and pieces of research I had conducted for myself over the past twenty years. I also appreciated her confidence, clarity, and spirit as she was interviewed. My final confirmation that she was speaking truth to power came when she explained how she had been fired from her job and personally attacked in a most vicious manner. If she was a nothing, no one would have bothered to attack her.
Difficult Choices
We made the emotionally wrenching and difficult choice not to vaccinate our five children when they were little. I was a vaccine damaged child, suffering from lifelong asthma and deadly allergies. I guess something deep in my own heart was telling me not to vaccinate the children despite intense pressure from family members to do so back in the early 90’s.
The research that I have conducted over the past five years has vallidated all of my instincts as I considered that the very years when my children would have been getting the shots were the worst in terms of how much thimerisol was in the vaccines. Drug manufacturers have claimed that all mercury is now out of the vaccines, but the flu vaccine still has toxic levels of mercury in it as a preservative.
I’m glad we did not poison our children with those chemicals. But I had to wonder about these claims of depopulation and intent to cause a pandemic. Was it possible that these were the end game goals of the drug makers?
United Nations Population Goals
Everyone watching the world scene understands that we have some elites who believe population control is a priority one goal for the new millenium. Members of the Obama Administration have made it clear through past writings that they do not apologize or hide from these goals. They certainly have not disavowed those beliefs, and some of us believe they are working overtime to control population in the future through government healthcare mandates.
I believe it is only a matter of time before parents in America and the world at large are told how many children they can give birth to. And if it is true that the rush to American health care reform is an attempt to push through legislation that would give elites the green light to move ahead with these goals, is it so hard to accept that the money mongers at the Big Pharma companies would come up with a plan to not only skim the taxpayers by pushing vaccines, but also stand waiting in the wings for those who are “vaccine damaged” to come to them for help with the many side effects from the vaccine itself?
It is certainly true that they have written into the health care pandemic rules that no company can be sued for damages, and I read the other day that the UK quietly and quickly wrote a law that says if you refuse the vaccine, health care workers have the green light to use it as evidence of being clinically insane, with coercive powers to hospitalize in mental hospitals and then force medications and vaccines on said patients. Refusal of drugs equals insanity? Maybe some psychiatrists like the idea of being able to use refusal of drugs as a “symptom” of insanity, but for normal people, this smacks of big brother bullying and monopolistic control of the marketplace to force consumers to use one form of so called healing over another…
How much money?
When I think about the amount of money I have personally spent on allergy medication, asthma medication, the many runs to the ER for help with breathing and anaphalaxis that resulted from ingesting a pathogen that triggered an immune response, the cortisone creams and skin care that I needed for horrifying skin outbreaks and rashes, thousands and thousands of dollars out of pocket and from insurance… it is just mind boggling to consider that a few MMR shots could trigger and explode that sort of lifelong immune reaction in my body.
And when I think of the time, energy, and money spent reading and researching to learn how to heal myself naturally.. also in the tens of thousands of dollars, almost all out of pocket (as my insurance did not cover most of those expenses)…. then, yeah, I can accept a big, fat, noxious medical conspiracy.
In a few weeks we will all get to witness if whistleblower Jane was spot on in her analysis of the short and long term goals of the medical elites over We the People of the world. As for me? I’m not getting the shot…

Here is some more information about the fertility side of the whole swine flu vaccine scam:
Squalene: Be Very Afraid Part II
OK. Now for the tough stuff
The article below details the horrific reality that I wish were not true. The Natural Solutions Foundation has been saying for quite some time that we see clear evidence of a genocidal intention in the overblown, clearly intentional Swine Flu “Pandemic”.
When WHO moved the “Pandemic” from Level 4 to Level 5 the disease was so mild and inconsequential that they literally had to change the definition of a Pandemic at Level 5, leaving out the words “with the ability to cause serious illness and death” from the definition because it did not and could not.
We believe that this must have been a great disappointment to the folks at the WHO who have been both predicting and involved with genetically engineering one failed pandemic after another. But WHO, you will remember, believes in a “sustainable planet” and that sustainability (favor them, not us, of course) means that they believe, too, that 90% of the world’s population needs to die.
Die
They do not much care how we die as long as we do it on demand and they manage to squeeze out a good dollop of profit as we do so.
Some of us, however, will die because we are never born. That, too, is part of the genocidal plan. You may recall that we reported some time back that we had seen official WHO documents from 1985 stating that the real purpose of the current vaccination program taking place in Africa at that time was not disease control (they know perfectly well that vaccines are hokum, without a shred of valid scientific evidence behind them) or prevention, but the dissemination of materials which cause infertility in the women into whom it is injected.
At that time, they were using vaccines with strong response patterns laced with Human Chorionic Gonadotrophin (HCG), a reproductive hormone (a glycoprotein, by the way – that figures into this true horror story a little later on). When you train the immune system through injecting it with adjuvants to “break tolerance” or attack the molecules as “not me” that it normally recognizes as “me”, if you prime it properly, you can create an immune intolerance to the hormones or other molecules of your own body.
In this case, and the same system has been used against untold millions (billions?) of women in many third world countries all over the world, the body attacks every molecule of HCG it encounters after that.
The problem is that without HCG, the uterus cannot retain the embryo, or the fetus and it will expel the future baby if she were pregnant at the time of the injection. If she were not pregnant, she will never again become a mother. Her body now destroys the very hormone without which she cannot sustain a pregnancy.
This damage is irreversible.
But not universal. Apparently, that is the problem: there are still a few people whose immune response is not sufficient to destroy all of their fertility. So now we move, in the march of mad science, propelled by forces of such deep inhumanity that it is difficulty to confront them with clear, calm eyes, to another infertility system.
In 1998 a Patent Application was made for a system which uses a person’s own immune system to render them permanently infertile, sterile, unable to have children.
The system is irreversible, once injected.
Knowing that:
– Both Novartis and GSK vaccines “against” the trivial Swine Flu both contain 1 million times more squalene than the devastatingly dangerous Vaccine A which crippled and killed so many Gulf War I military personnel (See Squalene: Be Very Afraid Part I )
– Even a few molecules of squalene injected into the body causes it to “break tolerance” and attack the body’s own molecules to which it is now trained for attack, including the body’s own squalene, a vital component of the Central Nervous System (which accounts for the profound and cataclysmic neurological symptoms of squalene injection)
– The WHO, UN and US governments agree on the “need” to reduce population to only 10% of its current levels
– When the WHO declared a Level 6 Pandemic on June 11, offical control of the political and health functions of all 194 countries in the WHO passed to that body, per an agreement signed in 2005 which took effect in 2007
– The haste with which this Level 6 Pandemic was declared makes it clear that the agenda was agreed to whether or not the genetically engineered virus did its job
– FDA/CDC has said that the $1/2 billion stock pile of injectable squalene adjuvant which the US Government admitted it was stock piling will be used to add the squalene to the bodies of people receiving the vaccines which do NOT have adjuvants in them at the time of injection
– The patents for a glycoprotein-containing, squalene adjuvanted H1N1 vaccine were filed in 2007 and 2008 by Novartis, Baxter International and GSK despite the fact that the virus did not yet officially exist, there had never been approval of a squalene adjuvanted vaccine and use of squalene in mass vaccines was illegal through the permanent restraining order of Judge Emmett Sullivan and through the fact that squalene was forbidden to even be tested in the US.
The investment of billions of dollars into the development of these vaccines for a virus that did not yet exist, using substances which had never been approved for use in vaccines by 3 separate companies, allegedly competitors in the vaccine industry, is worthy of note all by itself
– The most vulnerable members of society, children and pregnant women, will be vaccinated first.
Now you know what the game is. Since the goal is infertility, what better target population could you choose?
With one fell swoop of a needle, a whole generation of “useless eaters” is wiped off the map – the next one while this one is too sick to make much trouble and you clean up like the bandit that you are, if, of course, you are Big Pharma and the global genocidalists!
So now we have mandates for “Influenza vaccines” which are designed to roll the “Swine Flu” up under them. Understand clearly that although your State may offer you exemptions for philosophical, religious or medical reasons, there is every liklihood that there will be NO pandemic vaccination exemptions. The way the federal and state regulations are reading right now, that is the situation.
The confusers really do want you to feel:
– All vaccinations will be voluntary for the pandemic flu. This is true if by voluntary you really mean “under duress and pain of incarceration, fine and imprisonment.”
– Conventional exemptions will hold for the pandemic flu. This is not true. The pandemic vaccine is governed by separate regulations and laws which do not allow for exemptions.
– Parents will be given the choice of whether to vaccinate their children and themselves or not. This is utterly false unless we take back our freedom to make these decisions for ourselves and our children. Experimental medical procedures are never carried out on the most vulnerable and defenseless first, not until now, that is.
As an aside, do you suppose that President Obama’s children will get the same vaccine that yours and mine will? How would we know?
How about the President himself, who bravely agreed to wait until near the bottom of the list.
How courageous and public spirited. I will be happy to join him below the bottom of the list and, if all of us have any sense at all, we will all do so by making it abundantly clear to our legislators that this WILL not happen.
That is the purpose of the action item.
So far more than 2,222,940 of your emails have reached the legislative and decision making desks of this country.
These people need to hear that the deception is broken, like immune tolerance when adjuvants are injected.
We want the right to determine what happens to our bodies. We will not be sickened and die for the depopulationists. We will not be made infertile for the neo-aristocrats. We will not be brought into slavery through a diabolical brew in a syringe of illness, infertility and death..
Now, please read the following article and share it widely while you take the time and effort to mobilize every single person you can reach to help mobilize the groundswell to make it impossible for the vaccine effort to go forward as intended.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
“Swine flu” vaccine has adjuvants that impair fertility
Daniel Solis from the Czech Republic has researched the side-effects of the adjuvant, squalene, and discovered it is known to destroy fertility as well as causing other forms of damage.
A patent for a vaccine to impair fertility in animals contains squalene.
The plan to use this fertility-impairing adjuvant in the “swine flu” vaccine against a flu that has so far been far less irksome than the ordinary seasonal flu underscores concerns that this H1N1 mass vaccination programme mandated by WHO with the support of pharma companies such as Baxter is designed primarily to cause death and injury, and so significantly reduce the global population.
Is it any wonder that these “vaccines” are classified as bioweapons by the regulators?
For expert information on the dangers of vaccines, check out Dr Rebecca Carley’s website.
http://www.drcarley.com/
Daniel Solis has also made a formal complaint against the head of the Czech Republic’s FDA and the Deputy Health Minister for awarding a contract to Baxter worth 1,5 billion CZK without an open tender. More legal action in the Czech Republic is planned with the aim of getting Baxter’s licence to manufacture the “swine flu” vaccine at Bohumil suspended and to make Baxter accountable for the incident at the BioTest lab, which detected the live bird flu virus in vaccine material from Baxter on February 6th. Members of the lab had to be treated preventatively for bird flu and were put in quarantine.
Also, a Czech translation of “Evidence-of-the-Use-of-Pandemic-Flu-to-Depopulate-USA” can be found here: http://www.outsidermedia.cz/Obvinuji-Vas-z-masove-vrazdy-1.aspx
http://www.outsidermedia.cz/Obvinuji-Vas-z-pripravy-masove-vrazdy-II-1.aspx
“I have focused on the adjuvants made of monophosforyl lipid A (MPL) MF59TM (containing a polysorpate TweenTM 80) or AS03, AS04 also known as squalene in the proposed vaccines, which are immunosterilant or an immunocontraceptive,” Daniel Solis writes.
“The patent of the veterinary FERTILITY IMPAIRING VACCINE can be found on-line. It mentions both, the lipoid adjuvans squalene and the polysorbate TM80.
Here are the qotes from the patent and further some clinical studies about the toxicity of both.
(WO/1999/034825) FERTILITY IMPAIRING VACCINE AND METHOD OF USE
This application claims the benefit of U. S. Provisional Application No. 60/070,375, filed January 2,1998, U. S. Provisional Application No. 60/071,406, filed January 15,1998

“The vaccine of the invention preferably additionally includes an immunological adjuvant to enhance the immunological response of the subject to the glycoprotein antigen. Examples of adjuvants include Freund’s Complete Adjuvant, Freund’s Incomplete Adjuvant, and an adjuvant comprising an immunostimulant such as synthetic trehalose dicorynomycolate (STDCM) and an oil such as squalene oil (see P. Willis et al., J. Equine Vet. Sci., 14,364-370 (1994)). An adjuvant comprising synthetic trehalose dicorynemycolate, squalene oil, and a surfactant such as lecithin is preferred. Lecithin typically includes phosphatidyl choline. In a preferred embodiment the vaccine comprises oil, preferably a biodegradable oil such as squalene oil. Typically, the vaccine is prepared using an adjuvant concentrate which contains lecithin in squalene oil. The aqueous solution glycoprotein is typically a phosphate-buffered saline (PBS) solution, and additionally preferably contains Tween 80.”

Abstract:
A vaccine comprising an antigen derived from a zona pellucida glycoprotein is effective to impair fertility in animals, preferably carnivores. The vaccine can be used as an immunosterilant or an immunocontraceptive.
http://www.wipo.int/pctdb/en/wo.jsp?wo=1999034825
Description:
http://www.wipo.int/pctdb/en/wo.jsp?IA=US1998027658&wo=1999034825&DISPLAY=DESC
__________________________________________________________
Annals of Allergy, Asthma and Immunology, Volume 95, Number 6, December 2005 , pp. 593-599(7)
“Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. Conclusions: Polysorbate 80 is a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.”
Gajdova M, Jakubovsky J, Valky J.
Institute of Preventive and Clinical Medicine, Limbová, Bratislava.
Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats. Food Chem Toxicol. 1993 Mar;31(3):183-90. PMID: 8473002.
“Baby female rats were injected with polysorbate 80 at days 4-7 after birth. It accelerated the maturing of the rats and caused changes to the vagina and womb lining, hormonal changes, ovary deformities and degenerative follicles.”
http://www.ncbi.nlm.nih.gov/pubmed/8473002
The Endogenous Adjuvant Squalene Can Induce a Chronic T-Cell-Mediated Arthritis in Rats
Barbro C. Carlson*, Åsa M. Jansson*, Anders Larsson, Anders Bucht and Johnny C. Lorentzen*
http://ajp.amjpathol.org/cgi/content/abstract/156/6/2057
__________________________________________________________
Now, how can WHO claim the adjuvans is harmless:
http://www.who.int/vaccine_safety/topics/adjuvants/squalene/questions_and_answers/en/index.html
when there is clear evidence of its effects provoking AI deseases:
ANTI-SQUALENE ANTIBODIES LINK GULF WAR SYNDROME TO ANTHRAX VACCINE
http://www.autoimmune.com/GWSGen.html
or
“Dr. Jules Freund creator of this oil-based adjuvant warned in 1956 that animals injected with his formulation developed terrible, incurable conditions: allergic aspermatogenesis (stoppage of sperm production), experimental allergic encephalomyelitis (the animal version of MS), allergic neuritis (inflammation of the nerves that can lead to paralysis) and other severe autoimmune disorders.
Source: : Gary Matsumoto, Vaccine A-The Covert Government Experiment That’s Killing our
Soldiers and Why GI’s are Only the First Victims, Kapitola 3. “The Greatest Story Never Told” http://www.vaccine-a.com/excerpt.html”
Daniel Solis, Prague, Czech Republic
http://www.denikpolitika.cz/politici/daniel-solis/blog#31
http://www.czechfp.cz/site/?p=8009
Source: Jane Burgermeister
More Information here:
Vaccine Damnation: Retired Vaccine Researcher Speaks Out on Vaccine Dangers
“The Greatest Crime in the History of Humanity”: President Obama Named as a Defendant
Austrian Journalist Files Charges Against WHO, U.N. and Several Highest Ranking Government and Corporate Officials for Bioterrorism and Attempts to Commit Mass Murder
My Comment replys from the Blog Critics Magazine Web Site:
Baritone,
You said: “I’m curious to see your source for the British insanity gobbledigook.”
I found the story here: Swine flu prompts changes to Mental Health Act
Here is the text from the article:

“The government plans to rush through measures allowing people with suspected mental health issues to be quickly detained because of fears over staff shortages in any forthcoming swine flu outbreak, it has been revealed.

The temporary changes to the Mental Health Act, as laid out in an unusually short consultation lasting just one month, would mean it would only take one doctor, rather than two, to have a person sectioned and put on medication without their consent.

The measures could have a serious effect on the thousands of patients with psychiatric issues who currently live outside state care, meaning many could be detained against their will on the word of just one health professional.

With very little information on the proposed changes published, many mental health experts have warned the government that they risk side-lining an already vulnerable community and have called on it to spell-out the full raft of changes proposed in the consultation.”

And the text from Janes site where I found the link:

“The change in the law opens the door to allowing people who refuse the “swine flu” vaccine to be declared paranoid and summarily sectioned (and thus forcibly drugged) under government guidelines.”

The new law “Opens the door” to a change in the mental health situation which could easily be manipulated by those planning to force the vaccine.
As for the “conspiracy”, the difference between Jane and the other whistleblowers is that she has taken it upon herself to fight these monsters in the courts.

Jenny Hatch with Andrew in 1996 – ready for church on his blessing day
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