VACCINE - FLU VIRUS CURE - DEPOPULATION





The Vaccine Hoax is Over. Documents from UK reveal 30 Years of Coverup
Andrew Baker ( FFN),- Freedom of Information Act in the UK filed by a doctor there has revealed 30 years of secret official documents showing that government experts have
1. Known the vaccines don’t work
2. Known they cause the diseases they are supposed to prevent
3. Known they are a hazard to children
4. Colluded to lie to the public
5. Worked to prevent safety studies
Those are the same vaccines that are mandated to children in the US.
Educated parents can either get their children out of harm’s way or continue living inside one of the largest most evil lies in history, that vaccines – full of heavy metals, viral diseases, mycoplasma, fecal material, DNA fragments from other species, formaldehyde, polysorbate 80 (a sterilizing agent) – are a miracle of modern medicine.
Freedom of Information Act filed in the US with the CDC by a doctor with an autistic son, seeking information on what the CDC knows about the dangers of vaccines, had by law to be responded to in 20 days. Nearly 7 years later, the doctor went to court and the CDC argued it does not have to turn over documents. A judge ordered the CDC to turn over the documents on September 30th, 2011.
On October 26, 2011, a Denver Post editorial expressed shock that the Obama administration, after promising to be especially transparent, was proposing changes to the Freedom of Information Act that would allow it to go beyond declaring some documents secret and to actually allow government agencies (such as the CDC) to declare some document “non-existent.”
Simultaneous to this on-going massive CDC cover up involving its primary “health” not recommendation but MANDATE for American children, the CDC is in deep trouble over its decades of covering up the damaging effects of fluoride and affecting the lives of all Americans, especially children and the immune compromised. Lawsuits are being prepared.  Children are ingesting 3-4 times more fluoride by body weight as adults and “[t]he sheer number of potentially harmed citizens — persons with dental fluorosis, kidney patients tipped into needing dialysis, diabetics, thyroid patients, etc — numbers in the millions.”
The CDC is obviously acting against the health of the American people. But the threat to the lives of the American people posed by the CDC’s behavior does not stop there. It participated in designed pandemic laws that are on the books in every state in the US, which arrange for the government to use military to force unknown, untested vaccines, drugs, chemicals, and “medical” treatments on the entire country if it declares a pandemic emergency.
The CDC’s credibility in declaring such a pandemic emergency is non-existent, again based on Freedom of Information Act. For in 2009, after the CDC had declared the H1N1 “pandemic,” the CDC refused to respond to Freedom of Information Act filed by CBS News and the CDC also attempted to block their investigation.  What the CDC was hiding was its part in one of the largest medical scandals in history, putting out wildly exaggerated data on what it claimed were H1N1 cases, and by doing so, created the false impression of a “pandemic” in the US.
The CDC was also covering up e financial scandal to rival the bailout since the vaccines for the false pandemic cost the US billions. And worse, the CDC put pregnant women first in line for an untested vaccine with a sterilizing agent, polysorbate 80, in it. Thanks to the CDC,  “the number of vaccine-related “fetal demise” reports increased by 2,440 percent in 2009 compared to previous years, which is even more shocking than the miscarriage statistic [700% increase].
The exposure of the vaccine hoax is running neck and neck with the much older hoax of a deadly 1918-19 flu. It was aspirin  that killed people in 1918-19, not a pandemic flu. It was the greatest industrial catastrophe in human history with 20-50 million people dying but it was blamed on a flu. The beginning of the drug industry began with that success (and Monsanto was part of it). The flu myth was used by George Bush to threaten the world with “another pandemic flu that could kill millions” – a terror tactic to get pandemic laws on the books in every state and worldwide. Then the CDC used hoax of the pandemic hoax to create terror over H1N1 and to push deadly vaccines on the public, killing thousands of unborn children and others.  (CDC will not release the data and continues to push the same vaccine.)
The hoax of the vaccine schedule is over, exposed by FOIAs in the UK. 
The hoax of the CDC’s interest in children’s lives has been exposed by its refusal to respond to a doctor’s FOIAs around its knowledge of vaccine dangers.
The 1918-19 pandemic hoax has been exposed by Dr. Karen Starko’s work on aspirin’s role in killing people.
And despite refusing to respond to FOIAS, the CDC’s scandalous hoax of a 2009 flu pandemic and its part in creating it, was exposed by CBS NEWS. 
And the Obama administration, in attempting to salvage the last vestige of secrecy around what is really happening with vaccines, by declaring agency documents non-existent, has made its claim of transparency, non-existent.
But pandemic laws arranging for unknown vaccines to be forced on the entire country are still in place with HHS creating a vaccine mixture that should never be used on anyone and all liability for vaccines having been removed. Meanwhile, a Canadian study has just proven that the flu vaccine containing the H1N1 vaccine which kills babies in utero, actually increases the risk of serious pandemic flu.
Americans who have been duped into submitting their children to the CDC’s deadly vaccines, have a means to respond now. People from every walk of life and every organization, must
1. take the information from the UK FOIAs exposing 30 years of vaccine lies, the refusal of the CDC to provide any information on what it knows about those lies, and the Obama Administration’s efforts to hide the CDC’s awareness of those lies, and go to their state legislatures, demand the immediate nullification of the CDC vaccine schedule and the pandemic laws.
2. inform every vet. active duty military person, law enforcement people, DHS agents and medical personnel they know, of the vaccine hoax, for their families are deeply threatened, too, but they may not be aware of it or that they have been folded into agency structures by the pharmaceutical industry (indistinguishable from the bankers and oil companies) that would make them agents of death for their country with the declaration of a “pandemic” emergency or “bio-terrorist” attack. It is completely clear now that the terrorism/bioterrorism structures are scams so that any actions taken to “protect” this country using those laws would in fact be what threatens the existence of Americans.
It was aspirin that killed millions in 1918-19.  Now it is mandated and unknown, untested vaccines with banned adjuvants in them that threaten the country with millions of deaths.  At the same time, the CDC is holding 500,000 mega-coffins, built to be incinerated, on its property outside Atlanta.  Not to put to fine a point on this, but it’s clear now that the CDC should not be involved in any way with public health.
Thanks to the Freedom of Information Act (FOIA), we know that vaccines are not a miracle of modern medicine.  Any medical or government authority which insists vaccines prevent diseases is either ignorant of government documents (and endless studies) revealing the exact opposite or of the CDC’s attempts to hide the truth about vaccines from the public, or means harm to the public.
Thanks to the Freedom of Information Act (FOIA), we know the vaccine schedule is a hoax.
The health danger to American children and adults are vaccines.
Andrew Baker via Food Freedom News
Related article:
Documentation



Friday, May 3, 2013
Christina England
Activist Post
For many years the medical establishment has denied that the MMR vaccine can cause autism, despite government papers stating that the MMR vaccine can cause an SSPE-like syndrome, which many professionals believe to be autism, the non-fatal form of SSPE. [1] Instead of researching this link further, as one would expect, scientists from the University of Guelph are developing a vaccine believed to alleviate specific symptoms found to be associated with autism.
(SSPE or subacute sclerosing panencephalitis is a degenerative neurological condition which affects a person’s behavior, memory and coordination, leading to fits, blindness and eventually death.)
For years, doctors have been bombarding the systems of autistic children with antibiotics to control the bacteria, clostridium bolteae, reported to be found in abundance in the guts of autistic children. This bacteria causes these children to suffer from constipation, diarrhea and other gastrointestinal related problems.
Just Another Vaccine?
A paper written by Brittany Pequegnat, et al, states:
A paper written by Brittany Pequegnat, et al, states:
Individuals with autistic spectrum disorders (ASDs) are likely to experience chronic gastrointestinal (GI) irritations, such as constipation and diarrhea. GI disorders have a demonstrably high correlation with ASD and current literature suggests that it occurs with rates as high as 91.4% of patients. Of the ASD patients affected, 75.6% suffer from diarrhea. Diarrheal irritations can be extremely uncomfortable for a child and have been noted to have a loose association with regressive autism. [2]
Ms. Pequegna continues by adding:
In a small proof-of-principle intervention trial, vancomycin was orally administered to severely autistic children with chronic, persistent diarrhea, and short-term improvement of symptoms was seen in 8 out of 10 children. However, these improvements were not persistent, and once vancomycin was withdrawn, any behavioral gains in these children were lost; in turn suggesting that microbial dysbiosis was suppressed but not eliminated.
In other words, instead of studying existing papers and eliminating what is believed to be a possible cause of autism, scientists have developed yet another useless vaccine. Surely, it would have been more beneficial for scientists to research what is actually causing autistic children to have the overabundance of clostridium bolteae in their gut, rather than develop yet another vaccine, which by their own admittance does not work?
A Severely Flawed Study
Many parents believe that there are already too many vaccines, putting young children at the potential risk of autism and associated disorders. In a desperate bid to prove them wrong and to carry on the vaccination drive, researchers Dr. Frank DeStefano and his colleagues from the CDC (Centers for Disease Control) and Abt Associates published a fascinating paper in the Journal of Pediatrics in March of this year.
Their paper discussed whether or not a high number of vaccines administered at an early age caused autism. The researchers studied data from 256 children with autism and compared it to the data from 752 children without autism (born from 1994 –1999). All of the children studied came from three managed care facilities. The authors looked at each child’s cumulative exposure to antigens, the substances in vaccines that cause the body’s immune system to produce antibodies to fight disease, and the maximum number of antigens each child received in a single day of vaccination.
The paper states that researchers determined the total antigen numbers by adding the number of different antigens in all vaccines each child received in one day, as well as all vaccines each child received up to two years of age. They found that the total antigens from vaccines received by age two years and the maximum number received on a single day was the same between children with and without ASD (autism spectrum disorder).
The authors recognized that children receive more vaccines today then in the late 1990s and took this fact into consideration. However, they stated that vaccines in the late 1990s contained more antigens than they do today. The authors concluded that:
An infant’s immune system is capable of responding to a large amount of immunologic stimuli and, from time of birth, infants are exposed to hundreds of viruses and countless antigens outside of vaccination … The possibility that immunological stimulation from vaccines during the first 1 or 2 years of life could be related to the development of ASD is not well-supported by what is known about the neurobiology of ASDs. In 2004, a comprehensive review by the Institute of Medicine concluded that there is not a causal relationship between certain vaccine types and autism, and this study supports that conclusion. [3]
Why You Can’t Trust the CDC
I found three major flaws with this study.
1. The number of children in each group is unbalanced.
How can a study of this caliber be fairly examined if the numbers of children taking part in each group are unequal?
2. There was no control group.
All reputable studies need a control group to compare the results with. For this study to be taken seriously researchers would need three groups of participants, the third group being a group of unvaccinated children.
3. There was no mention of genetics or whether any of the children suffered from an underlying condition that may have made them susceptible to adverse reactions.
In recent years researchers have determined that certain genetic disorders have the potential to cause children to react adversely to vaccines. An excellent example of how a genetic condition can affect a child receiving vaccines can be seen in the case of Hannah Polling. [4]
Hannah suffered from a mitochondrial disorder — a dysfunction in basic cell metabolism, which put her at increased risk of injury from vaccines, as determined by the vaccine court. The result of this condition combined with the vast amount of vaccines that Hannah received in one day was autism.
Experts Who Value Science More Than Profit
Professionals like Dr. Rebecca Carley, Dr. Viera Scheibner and psychologist Lisa Blakemore-Brown have been warning parents about the dangers of vaccines and their possible links to autism for many years.
Dr. Viera Scheibner, a retired principal research scientist with a doctorate in natural sciences, has been speaking on the dangers of vaccination since 1985. Dr. Scheibner has published three books and 90 scientific papers in prestigious scientific journals on the subject.
Dr. Rebecca Carley was the first professional to recognize that there was a link between the MMR vaccination and the non-fatal form of SSPE, which she has been classifying as autism for the past fifteen years. Her professional opinions have been backed up scientifically as one hundred percent correct when government documents locked up for thirty years were recently uncovered, revealing that the government had discovered that the MMR vaccine was causing what they referred to as an SSPE like-syndrome.
Psychologist Lisa Blakemore-Brown has been speaking out since 1995 on the link among vaccines, autism and parents being falsely accused of Munchausen Syndrome by Proxy. She began to notice the link after she witnessed the parents of autistic children were being blamed for their children’s illnesses and disabilities as soon as they mentioned that their child/children became ill after they received a vaccine.
Conclusion
Governments are so determined to push vaccinations and reassure mothers that vaccines do not cause autism, they have come up with yet another flawed study to prove it. This effort is followed by a massive vaccination drive and media campaign to scare parents into accepting vaccines. Just to reassure parents further, the government is now encouraging the development of a vaccine to alleviate the symptoms of autism, just in case they are wrong. Really reassuring, isn’t it?
Here we have yet another example of just how desperate governments and the pharmaceutical industries are to protect the vaccination schedule. Instead of admitting that vaccinations are not only damaging the health of our children and that vaccines are totally ineffective at controlling diseases, governments get together with scientists to cash in on children’s suffering and develop yet another useless vaccine to cure the symptoms caused by the original vaccine.
Instead of wasting time developing more vaccinations, scientists, big pharma and governments would be better employed spending more time researching what professionals like Dr. Rebecca Carley, Dr. Viera Scheibner and psychologist Lisa Blakemore-Brown have been saying for years.
A Final Word From the Author
As a mother of two autistic children, I would advise parents against using a vaccine to alleviate debilitating GI (gastrointestinal) disorders, which are often a symptom of autism. Paul Shattock, a leading expert from the Autism Research Unit, Sunderland University, and Dr. Ellowad, an expert in gastroenterology and child allergies, Great Ormond Street, both advise eliminating dairy and wheat from the diets of autistic children to help alleviate their problems. Their dietary advice not only helped me to manage my autistic son’s difficult behavior, but also completely cured the intense pain and chronic diarrhea he suffered as part of his disorder.
This article originally appeared at VacTruth.com 
Christina was born and educated in London, U.K. She left school to work in a children's library, specializing in story telling and book buying. In 1978 Christina changed her career path to dedicate her time to caring for the elderly and was awarded the title of Care Giver of the Year for her work with the elderly in 1980. In1990 she adopted the first of two disabled boys, both with challenging behavior, complex disabilities and medical needs. In 1999 she was accused of Munchausen by Proxy after many failed attempts to get the boys’ complex needs met. Finally, she was cleared of all accusations after the independent psychologist Lisa Blakemore-Brown gave both boys the diagnosis of Autism Spectrum Disorder and ADHD as part of what she described to be a complex tapestry of disorders. During the assessments Ms Blakemore-Brown discovered through the foster care diaries that the eldest boy had reacted adversely to the MMR vaccine. After taking an A Level in Psychology and a BTEC in Learning Disabilities Ms. England spent many years researching vaccines and adverse reactions. She went on to gain a Higher National Diploma in journalism and media and currently writes for the American Chronicle, the Weekly Blitz, VacTruth and Namaste Publishing UK on immunization safety and efficacy whilst continuing to study for a BA Honors degree in English Literature and Humanities. England’s main areas of expertise are researching false allegations of child abuse and adverse reactions to vaccines. Her work is read internationally and has been translated into many languages. Ms England has been a guest on many radio shows and has spoken at seminars worldwide. She is the co author to the book ‘Shaken Baby Syndrome or Vaccine Induced Encephalitis – Are Parents Being Falsely Accused?’ with Dr Harold Buttram.




Thursday, May 02, 2013


See more at: HERE
By Dave Mihalovic
How many babies have to die for Doctors to get it? Synergistic toxicity is a well-known phenomenon where the combination of toxic substances can be greater than the sum of its parts. Therefore, mixing two non-lethal levels of chemicals inside a vaccine can lead to an extremely toxic mixture. The medical community appears to gloss over this very pertinent fact that appears to be progressively killing more infants every year. 
“Synergistic toxicity” refers to the effect that when exposed to two toxins, the toxicity level is far greater than the additive toxicity levels of the two toxins. A good example demonstrating ‘synergistic toxicity’ is a 1978 study on mice (Shubert et al. Combined Effects in Toxicology — A Rapid systematic Testing Procedure: Cadmium, Mercury & Lead. J. of Toxicology & Environmental Health 4:763, 1978). The study took the amount of mercury salt that kills 1 in 100 mice and 1/20th of the amount of lead salt that kills 1 in 100 mice. When these amounts of mercury salt and lead salt were administered, the synergistic toxicity of these two toxins killed 100 in 100 mice. 
It is important to understand the concept of ‘synergistic toxicity’, as research is increasingly showing that different toxins are typically synergistic rather than additive in the human body. However when testing is performed on a toxicity of a substance, the ‘level of harm’ is set based on an assumption that the substance is the only toxin to which he body is being exposed. 
A study published in the Human and Experimental Toxicology journal has found a direct statistical correlation between higher vaccine doses and infant mortality rates. It is a confirmation that many anti-vaccine advocates have long awaited and further establishes and adds to preliminary evidence that vaccinations are toxic poisons having no place in the human body. The study, Infant mortality rates regressed against number of vaccine doses routinely given: Isthere a biochemical or synergistic toxicity?, was conducted by Gary S. Goldman and Neil Z. Miller who has been studying the dangers of vaccines for 25 years. 
The infant mortality rate (IMR) is one of the most important indicators of the socio-economic well-being and public health conditions of a country. The US childhood immunization schedule specifies 26 vaccine doses for infants aged less than 1 year–the most in the world–yet 33 nations have lower IMRs. Australia and Canada are a close 2nd and 3rd respectively with 24 vaccine doses. 
Some countries have IMRs that are less than half the US rate: Singapore, Sweden, and Japan are examples. According to the Centers for Disease Control and Prevention (CDC), “The relative position of the United States in comparison to countries with the lowest infant mortality rates appears to be worsening. ” 
Many nations adhere to an agreed upon International Classification of Diseases (ICD) for grouping infant deaths into 130 categories. Among the 34 nations analyzed, those that require the most vaccines tend to have the worst IMRs. Thus, we must ask important questions: 
  1. Is it possible that some nations are requiring too many vaccines for their infants and the additional vaccines are a toxic burden on their health? 
  2. Are some deaths that are listed within the 130 infant mortality death categories really deaths that are associated with over-vaccination? 
  3. Are some vaccine-related deaths hidden within the death tables? 
“A single vaccine given to a six-pound newborn is the equivalent of giving a 180-pound adult 30 vaccinations on the same day. Include in this the toxic effects of high levels of aluminum and formaldehyde contained in some vaccines, and the synergist toxicity could be increased to unknown levels. Further, it is very well known that infants do not produce significant levels of bile or have adult renal capacity for several months after birth. Bilary transport is the major biochemical route by which mercury is removed from the body, and infants cannot do this very well. They also do not possess the renal (kidney) capacity to remove aluminum. Additionally, mercury is a well-known inhibitor of kidney function. “–Boyd Haley Ph.D.  
How Many Deaths Are Necessary?
The end of 2011 was masked with sadness for Belgium parents Raphael Sirjacobs & Beatrice Dupont, as their nine week old daughter Stacy Sirjacobs lost her fight for life. Stacy died just one week after her first vaccinations and left her twin sister Lesly behind. The twins received Prevenar, a vaccine against meningitis and pneumonia, Infanrix Hexa, a six in one vaccination for diphtheria, tetanus, polio, pertussis, hepatitis B and Haemophilus type B, and finally the Rotarix, a preventive vaccine for gastroenteritis. This means that these tiny vulnerable babies received a staggering nine vaccines in one day, vaccines that may have caused one of them to die.
A government inquiry was launched in 2011 has found that polio vaccines for infants funded by the Global Alliance for Vaccination and Immunisation are causing deaths and disabilities in regional countries including Pakistan. The report on The Express Tribune also suggested suspending the mass polio campaign, including the administration of pentavalent vaccines — a mixture of five vaccines until an inquiry finds these vaccines safe for children. There is now evidence that polio paralysis has also been a very common yet discreetly hidden side effect associated with polio vaccines.
When the first, injectable, polio vaccine was tested on 1.8 million American children, within a few days they had a huge epidemic of paralytic polio: in the vaccinated, their parents and other contacts. 
On February 21, 2013, a one month-old baby girl died after receiving 5 vaccinations. Baby Ayushi Gupta died at the Maltibai Hospital, Thane, West Mumbai in India just hours after receiving her vaccinations for Hepatitis B, DPT (diptheria, pertussis and tetanus) and oral pulse polio drops.  
Vaccine Composition
This analysis calculated the total number of vaccine doses received by children but did not differentiate between the substances, or quantities of those sub-stances, in each dose. 
Common vaccine substances include 
  • antigens (attenuated viruses, bacteria, toxoids), preservatives (thimerosal, benzethonium chloride,2-phenoxyethanol, phenol), 
  • adjuvants (aluminum salts), 
  • additives (ammonium sulfate, glycerin, sodium borate, polysorbate 80, hydrochloric acid, sodium hydroxide, potassium chloride), 
  • stabilizers (fetal bovine serum, monosodium glutamate, human serumal bumin, porcine gelatin), 
  • antibiotics (neomycin, strep-tomycin, polymyxin B), 
  • and inactivating chemicals (formalin, glutaraldehyde, polyoxyethylene). 
For the purposes of this study, all vaccine doses were equally weighted. 
Using linear regression, the immunization schedules of these 34 nations were examined and a correlation coefficient of 0.70 was found between IMRs and the number of vaccine doses routinely given to infants. When nations were grouped into five different vaccine dose ranges, 98.3% of the total variance in IMR was explained by the unweighted linear regression model. These findings demonstrate a counter-intuitive relationship: nations that require more vaccine doses tend to have higher infant mortality rate. 
Mercury Still In 50 Percent of All Flu Vaccines
In 2009, eight out of ten H1N1 vaccines had thimerosal. For 2011/2012 flu vaccine season, three out of five FDA approved vaccines has thimerosal. This past year, the 2012/2013 season offered three out of six flu vaccines which contained thimerosal and were FDA approved. 
If you have any doubts on the neurotoxic potential of thimerosal, please review the following scientific publications which document the adverse effects of mercury, merthiolate and ethyl mercury
“One publication showed that combining mercury and lead both at LD1 levels caused the killing rate to go to 100% or to an LD100 level (12). An LD1 level is where, due to the low concentrations, the mercury or the lead alone was not very toxic alone (i.e. , killed less than 1% of rats exposed when metal were used alone). The 100% killing, when addition of 1% plus 1% we would expect 2%, represents synergistic toxicity. Therefore, mixing to non-lethal levels of mercury plus lead gave an extremely toxic mixture! What this proves is that one cannot define a “safe level of mercury” unless you absolutely know what others toxicants the individual is being exposed to. The combined toxicity of various materials, such as mercury, Thimerosal, lead, aluminum, formaldehyde, etc. , is unknown. The effects various combinations of these toxicants would have is also not defined except that we know they would be much worse than any one of the toxicants alone. So how could the ADA take any exception, based on intellectual considerations, to my contention that combinations of Thimerosal and mercury could exacerbate the neurological conditions identified with autism and AD? Autism and AD have clinical and biological markers that correspond to those observed in patients with toxic mercury exposure. 
Why would the ADA take this position? I personally feel like I have been in a ten-year argument with the town drunk on this issue. Facts don’t count and data is only valid if it meets the pro-amalgam agenda. The synergistic effects of mercury with many of the toxicants commonly found in our environment make the danger unpredictable and possibly quite severe, especially any mixture containing elemental mercury, organic mercury and other heavy metal toxicants such as aluminum. ” ~ Boyd Haley



Monday, April 01, 2013  - H1N1 VACCINE


Flu vaccine causes 1,400 percent increased risk of narcolepsy
(NaturalNews) Speculation that an emergency vaccine widely administered for H1N1 (swine flu) may have caused a sharp uptick in cases of narcolepsy has been confirmed following the release of a new study out of the U.K. As reported in the British Medical Journal (BMJ), individuals given the Pandemrix vaccine for influenza during the 2009/2010 swine flu "pandemic" had a 1,400 percent increased risk of developing the neurological disorder compared to those not vaccinated. 
Drawing from data collected in the aftermath of the vaccine's release, researchers found that the use of Pandemrix, particularly among young people between the ages of four and 18, increased the risk of narcolepsy by a factor of about 14 compared to those who did not get the jab. And the ingredient believed to be primarily responsible for this increase is an adjuvant known as AS03, a squalene-based component used in a number of vaccines produced by Glaxo Smith Kline (GSK). 

"This study shows a significantly increased risk of narcolepsy in children who received the AS03 adjuvanted pandemic strain vaccine in England," explains the study. "Our case coverage method gave an odds ration of 14.4 (4.3 to 48.5) for the primary analysis and is consistent with the relative risk of 13 reported from Finland in a retrospective study.
Many health authorities knew about the dangers associated with squalene-based adjuvants like AS03, which are used to significantly boost immunogenicity, or the overall immune response prompted by a vaccine, but they have done little or nothing to stop their use. Such dangers include conditions like severe autoimmune disease, neurological damage, rheumatoid arthritis, multiple sclerosis and systemic lupus erythematosus, as well as many others. 
"(Squalene) contributed to the cascade of reactions called Gulf War syndrome," says Dr. Viera Scheibner, a micropaleontologist who has long studied the adverse effects associated with vaccines and vaccine adjuvants.
"(GIs developed) 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, Raynaud's phenomenon, Sjorgren's syndrome, chronic diarrhea, night sweats and low-grade fever."
Squalene-based adjuvants like AS03 definitively linked to causing neurological damage 
This is quite the laundry list of health conditions associated with squalene-based adjuvants, and yet these chemical toxins were indiscriminately injected into millions of children across the globe, many of whom are now permanently injured. And according to the study, the results speak for themselves -- the AS03 squalene-based adjuvant used by GSK in Pandemrix is causally-associated with an increased risk of narcolepsy
"It is now abundantly clear that throughout the world, Pandemrix has caused thousands of children to develop narcolepsy during only a couple of years," explains Gaia-Health.com. "There is now no evading the reality of the devastation caused by this vaccine that was pushed through a campaign of fear mongering about a mild disease." 
Beyond this, the AS03 adjuvant itself has been fully indicted as a dangerous toxin. It and many other squalene-based adjuvants like it simply have no legitimate place in vaccines administered to humans. And the many dangers associated with squalene-based adjuvants have been known for decades, which means there is no excuse as to why health authorities allowed it to be used in a rushed-to-market pandemic flu vaccine that was targeted towards young, developing children.
"These children with narcolepsy are condemned to lives constrained by the effects of both narcolepsy and the drugs they may take," adds Gaia-Health.com. "When you consider that the disease they were supposedly being protected from, swine flu, proved to be a rather mild type of influenza, the tragedy of what has happened is inexcusable." 
Sources for this article include:
HERE,HERE and HERE
Learn more: HERE

20 February , 2008  08:24:00 - H5N1




US involved in bird flu conspiracy: Indonesia
Reporter: Geoff Thompson
PETER CAVE: Indonesia’s Health Minister has suggested that the United States may be involved in a conspiracy to use the bird flu virus to develop biological weapons. The extraordinary allegation is included in a new book, endorsed by President Susilo Bambang Yudhoyono, which describes Indonesia’s fight to assert its ownership of its virulent strains of avian influenza.Concerns over that issue prompted Indonesia last year to stop sharing virus samples with the World Health Organization as Jakarta correspondent Geoff Thompson reports.


GEOFF THOMPSON: No country in the world has been hit by bird flu like Indonesia. Already this year 11 people have died and ten of those were from Jakarta or surrounding areas. Indonesia’s uniquely virulent strain of H5N1 gave the country "bargaining power" according to Indonesia’s Health Minister Dr Siti Fadilah Supari, in her new book called "It’s Time for the World to Change" and strangely subtitled "The Divine Hand Behind Avian Influenza". It’s this bargaining power which led Dr Supari in late 2006 to stop sharing Indonesia’s strains of bird flu with World Health Organization laboratories because of fears that any vaccines developed would then be sold for profit to developing countries with no benefit to Indonesia. In essence, Indonesia sought to retain the "virus rights" and any profits to be made from its bird flu problem. Back then on AM, Dr Supari effectively accused Australia of stealing Indonesia’s strain of H5N1 to make bird flu vaccines.


SITI FADILAH SUPARI: I never, I never give permission to send sample to the, send a specimen of the virus to Australia.


GEOFF THOMPSON: Now in her book Dr Supari has revealed, the full scope of the conspiracy she believes she is up against. "Developed countries become richer", she writes, "because they have the capability to develop the vaccine and control the world". Dr Supari expresses alarm at WHO laboratories sharing bird flu virus data with the United States national laboratory in Los Alamos, New Mexico, where nuclear weapons are developed.


"Whether they use is it to make vaccine or develop chemical weapons, would depend on the need and interest of the US Government. It is indeed a very dangerous situation for the destiny of humanity", she writes and goes on to say ".. it is a matter of choice whether to use the material for vaccines or biological weapon development". Despite the clear implication contained in her book, last night Dr Supari told the ABC, she didn’t intend to accuse the United States of being interested in turning H5N1 into a biological weapon.


SITI FADILAH SUPARI: I didn’t know whether our virus will be develop into a vaccine or will be develop into a biological weapon. So just a question - I didn’t blame United States, I didn’t blame any country.


PETER CAVE: Indonesia’s Health Minister, Dr Siti Fadilah Supari, speaking there to Indonesia correspondent Geoff Thompson. 


The Vaccination Myth [ HERE ]
The government requires us to get various vaccinations either before entering primary school, employment, or as a first-time citizen. These vaccinations purport to protect citizens from a variety of maladies, from Polio to Rubella. While the medical viability of these vaccinations may not be an issue, the ethical usage of these vaccinations are. In other words, although the government may require all citizens to obtain vaccinations for medical reasons, there may be other purposes the government may have, particularly for tracking and experimental weapon purposes. With respect to the tracking issue, the government places miniscule tracking devices in these vaccinations. These tracking devices act as beacons for various satellites. In this way, similar to the technology found in controlling airplane traffic, the government knows where we are at all times. Indeed, it is unclear how much information is provided in these beacon devices. These beacons may, for example, provide rudimentary data, such as age, heart rate, blood pressure, or speed. They may also provide more detailed information, such as what we are saying at any given time.  As new technology has developed over the years, the need to vaccinate each and every one of us has become more creative, particularly with older citizens. Enter the Flu Vaccination. The flu vaccination has provided a perfect way for the government to implant updated beacon devices, particularly for those individuals who recieved vaccinations fourty or more years ago, whose beacons may not have had the benefit of various technological advances.These vaccinations are also used for experimental weapon purposes as well. The government not only implants various forms of biological and chemical warfare within the citzenry for experimental purposes, but also for mind control techniques, such as implanting specific types of criminal or anti-social behavior -- also for warfare experimental purposes
In conclusion, the vaccination process has provided the government with a convenient way not only to plant beacon devices within the entire citizenry, but also to test experimental warfare and mind-control techniques . 

The Swine Flu Conspiracy: A Plan to Commit Mass Murder 
by The Underground Health Reporter™

"A chilling tale of conspiracy to commit mass murder by those who are responsible for protecting human lives. The Swine Flu Conspiracy:  A Plan to Commit Mass Murder -- coming to a town near you." 
The above reads like a suspenseful trailer for a blockbuster Hollywood movie like "The Manchurian Candidate" or "Enemy of the State."
     But it's not a movie at all.
     It's a TRUE STORY that's happening right now.
     The World Health Organization, which has been predicting a massive swine flu pandemic that will infect one-third of the entire world's population, has every reason to be 100% certain of its prediction.  It's because...
     ...the swine flu virus is about to be deliberately unleashed upon the unsuspecting public.

     If you find this hard to believe, here's proof: 
     A medical journalist named Jane Burgermeister has recently filed criminal charges with the FBI against theWorld Health Organization (WHO), the United Nations (UN), and several of the highest ranking government and corporate officials concerning their attempts to commit mass murder via the swine flu. [Source:  NaturalNews]
     This comes in the wake of charges filed last April against US-based pharmaceutical company, Baxter AG, and Avir Green Hills Biotechnology.  Baxter was recently connected to the disturbing scandal involving  flu vaccines.  Several sources, including the Times of India, reported that last December, Baxter inserted deadly live avian flu viruses into vaccines that were distributed to 18 countries around the world to be injected into patients as "flu shots" -- allegedly as a deliberate act to trigger a pandemic and profit from the sale of vaccines.  
     However, a batch of the tainted vaccines was first tested on ferrets in the Czech Republic before being shipped out for injection into humans.  Every one of the ferrets died -- and the SHOCKING discovery was made. 
     Since the contamination of the vaccination couldn't be blamed on an "honest mistake," newspapers immediately questioned whether the events were part of a conspiracy to deliberately provoke a pandemic, following up on accusations already made by health officials in other countries.
     Jane Burgermeister contends that the WHO, the UN and high-ranking corporate government officials conspired with each other (and others) in a covert international program involving the pharmaceutical companies Baxter and Novartis.  
     The conspiracy entailed the bioengineering and then releasing of lethal biological agents -- specifically the “bird flu” virus and the “swine flu virus” in order to accelerate the pandemic by making the virus ever morevirulent (with the addition of the Avian flu).  This would then make an otherwise mild swine flu outbreak disastrous enough to justify forced mass vaccinations. 
     Such a forced mass vaccination program would rake in billions of dollars in vaccine revenues -- while the hoards of people who are vaccinated run the risk of suffering serious injury or even death in massive numbers!  
Can you REALLY be forced to take the swine flu vaccine?
     Most people have never heard of the international health regulations and the national pandemic plansthat ALLOW mandatory flu vaccinations.  Most people think that no one can be FORCED to take the swine flu vaccine.  Wrong! 
     Did you know ... that in the event of a Pandemic Level 6 emergency declaration, you would be required to follow the orders of the World Health Organization?  
In such an emergency, the WHO has the authority to force anyone (and that includes you) to be vaccinated and also to be quarantined. Under such circumstances, it would be a CRIMINAL OFFENSE if you refuse to be vaccinated.
So what's the worst thing that could happen if you were to be vaccinated?
     For starters, if the vaccine you receive happens to be laced with live avian flu viruses, which Baxter has demonstrated itself capable of doing without being penalized -- the vaccine would be virulent enough to kill you. This is the basis for Burgermeister's charges against the WHO and UN for conspiracy to commit mass murder. Furthermore, if the swine flu vaccine doesn't kill you, you may have an increased CANCER RISK. According to German lung specialist Wolfgang Wodarg (who is also the chairman of the health committee in the German parliament and European Council), the swine flu vaccine's nutrient solution contains CANCEROUS cells from animals.  It therefore stands to reason that injection of the vaccine might also cause cancer in humans. 
     The swine flu vaccine contains shockingly higher concentrations of squalene than was used in the anthrax vaccines, which caused hundreds of thousands of troops to suffer the catastrophic effects of Gulf War Syndrome
     Furthermore, the swine flu vaccine, which is being rushed to market without the appropriate testing and evaluation, may cause a repeat of the swine flu vaccine catastrophe of 1976, in which people died or developed crippling Guillain-Barré Syndrome or paralysis as a result of the experimental vaccine.

In the event that forced vaccinations are implemented, what can YOU do?
     You can just say "No!" 
     Would it make you a criminal offender -- and possibly land you in jail -- if you refused the vaccine?
     If large numbers of people refuse the vaccination, the government would NOT have the resources to enforce a mandatory vaccination -- nor have the capacity to imprison hundreds of thousands (or millions) of people.
     That's why it's necessary to urge as many people as possible to refuse the swine flu vaccine. 
     Should you refuse the vaccine, you definitely WON'T be alone.  According to research reported in the August 25 issue of the British Medical Journal...
     ... more than 50% of doctors and nurses in public hospitals would refuse the swine flu vaccinebecause they're concerned about its side effects, and have doubts about its efficacy.
     And according to a Fox News poll conducted in August, the MAJORITY of Americans now believe that the swine flu vaccine may be DEADLIER than the swine flu virus itself.
Without a vaccine, what can YOU do to protect yourself from the swine flu virus?
     There's a natural, scientifically proven method for creating an environment in the body which is uninhabitable by the swine flu virus, as well as other disease micro-organisms, germs and bacteria.  It involves a natural oxygenating substance that makes your body immune to swine flu and virtually all diseases. 
     I urge you to watch the 7-minute video titled 
at HERE
     
This is the video the pharmaceutical industry does NOT want you to watch.  
Why?  
Because it threatens the billions of dollars they could potentially make from the swine flu vaccine. Don't forget to forward this article to everyone you know because no one can escape exposure to the swine flu virus this flu season.  It's that important.  You might even end up saving someone's life. 
Go watch the video now by going to the following webpage:  HERE
01 April 2012 - H7N9 - AT TAIWAN AND HONGKONG




TAIWAN DAN HONGKONG SIAGA, VIRUS BARU FLU BURUNG DITEMUKAN DI SHANGHAI 
Menyusul tewasnya dua pria setelah meninggalkan Shanghai, pemerintah Taiwan meningkatkan kewaspadaan. Otoritas di Taiwan Senin (1/4) memerintahkan agar pengunjung daratan Cina diperiksa saat masuk wilayah tersebut. Komisi Kesehatan Nasional dan Keluarga Berencana Cina mengatakan bahwa kedua pria yang meninggal awal Maret itu, akibat terkena virus H7N9, jenis baru dari fu burung. Tidak hanya dua pria itu, seorang wanita berusia 35 tahun dikabarkan juga berada dalam kondisi kritis akibat virus tersebut. 
Akibat peristiwa tersebut, otoritas kesehatan di Shanghai telah memerintahkan rumah sakit yang ada di wilayah tersebut untuk memeriksa secara khusus, pasien yang mengalami gangguan pernafasan. Harian Shanghai juga melaporkan bahwa petugas kesehatan yang menangani kasus meninggalnya dua pria tersebut belum mendapat kepastian penyebab mereka terpapar virus tersebut, selain masalah kesehatan yang kronis. Sementara perempuan yang masih kritis diduga terkena virus secara langsung, karena ia memang dikenal sering menangani unggas. 
Atas peristiwa itu, tidak hanya Taiwan yang siaga, Hongkong juga meningkatkan kewaspadaan. Semua pendatang yang masuk lewat Macau wajib menjalani pemeriksaan. Seorang ahli 
kesehatan Hongkong, Jiang Qingwu, dari Universitas Fudan mengatakan bahwa H7N9 pada dasarnya adalah virus yang menyerang binatang. Bukan virus yang menyerang manusia. Tidak diketahui bagaimana virus tersebut bisa menyebar pada manusia. 
(KF-EDU/Mrg/ Deutsche Welle/Foto Virus H7N9: bbs68.meiwasuisan) 
April 2, 2013



A group of leading scientists has urged President Obama’s advisers to investigate the ethical issues raised by a decision to create a highly infectious strain of bird-flu virus that could be transmitted easily between people. 
The scientists, who include a former UK Government chief scientist and a Nobel laureate, said that it is “morally and ethically wrong” to create a new type of influenza virus in the laboratory that is more lethal and transmissible than what actually exists in nature. 
Two teams of flu researchers – led by Ron Fouchier of the Erasmus Medical Centre in Rotterdam and Yoshihiro Kawaoka of the University of Wisconsin-Madison – announced in 2011 that they had succeeded in mutating the H5N1 avian virus so that it could in theory be transmitted through the air between people. 
They stopped the research last year as part of a wider voluntary moratorium following public outrage over the work. But they announced an end to the moratorium earlier this year, and even an expansion into new areas involving other viruses and diseases. 
In a strongly-worded letter sent to the US Presidential Commission for the Study of Bioethical Issues, opponents of the research warned that there has not been enough debate over the threats posed by lifting the moratorium on increasing the transmissibility of highly lethal viruses such as the H5N1 strain of bird-flu. 
They said that the 60 per cent mortality rate of the H5N1 virus – on the relatively rare occasions that it has infected humans – puts it in a “class of its own” and that attempting to make it more transmissible through laboratory experiments is tantamount to risking a devastatingly deadly flu pandemic. 
“The accidental release of an artificial, laboratory-generated, human-transmissible H5N1 virus into the community has the potential to cause a global pandemic of epic proportions that would dwarf the 1918 Spanish flu pandemic that killed over 50 million people,” the scientists said.“A majority [of life scientists] considers the creation in the laboratory of a pathogen more lethal than exists in nature is morally and ethically wrong. Indeed, a majority are of the opinion that there is no scientific justification that outweighs the moral and ethical problems,” they said. 
The letter, sent at the end of last week, was organised by the Foundation for Vaccine Research, a private organisation based in Washington campaigning for better vaccines. It was sent to the Presidential Commission in order to bypass the powerful US National Institutes of Health, which has funded both research projects into H5N1 transmissibility and has controlled much of the debate over the issue. 
Among the 17 signatories of the letter are Professor Lord May, a former chief scientist to the Prime Minister and an expert on disease transmission, Professor Marc Lipsitch, a communicable disease expert at Harvard University, and Sir Richard Roberts, who won the 1993 Nobel Prize in Physiology or Medicine for his pioneering work in genetics. 
Other signatories include Professor Robin Weiss, a distinguished British virologist working on HIV, Professor Michael Lederman of Case Western Reserve University in Cleveland, Ohio, and Joshua Plotkin of the University of Pennsylvania. 
The scientists are particularly concerned that attempts of create more lethal forms of H5N1 in an attempt to study the threat posed to humans are just the start of further work on other potentially lethal viruses in what they term “gain of function” studies – where more lethal viral mutations are actively encouraged. 
“The H5N1 studies represent the first of no doubt many such studies involving other potential pandemic pathogens. Gain-of-function studies with H5N1 virus are being conducted in China, and a team in The Netherlands is expanding their H5N1 studies to include studies with the H7N7 virus, and has announced plans to conduct similar gain-of-function studies with the SARS coronavirus,” the scientists said. 
“Just ten days ago we learned that a team in Germany has conducted experiments to see what it would take for canine distemper virus to be transmitted from dogs to humans,” they said. Professor Simon Wain-Hobson, an eminent virologist at the Pasteur Institute in Paris who was first to sign the letter, said that the WHO has essentially failed to take the lead by widening the ethical debate over an area of contentious research that has been controlled by vested interests. 
“The recent calling off of the moratorium by 40 flu researchers alone – not funders, governments or international bodies – says it all. The flu community simply hasn’t understood that this is a hot-button issue that will not go away,” Professor Wain-Hobson said. 
Flu researchers have argued that the laboratory work is necessary in order to study the kind of lethal mutations that could arise in nature, but Professor Wain-Hobson said that the artificial selection of dangerous viruses could result in mutants that would be very unlikely to ever exist in nature. He cites the example of the artificial selection of canine genes by dog breeders over the centuries. “Would nature have come up with the dachshund,” he asks?






April 02, 2013 11:38
A group of leading scientists – including a Nobel Prize winner - has proclaimed that it is “ethically and morally” wrong to alter the deadly H5N1 virus to make it more contagious for research purposes, and have asked President Obama to ban it. 
“The accidental release of an artificial, laboratory-generated, human-transmissible H5N1 virus into the community has the potential to cause a global pandemic of epic proportions that would dwarf the 1918 Spanish flu pandemic that killed over 50 million people,” read a letter to the Presidential Commission for the Study of Bioethical Issues. 
The petition was drafted by the Foundation for Vaccine Research (FVR), a scientific advocacy group, and numbered world-leading biologists among the 17 signatories, including Lord May, the former chief science advisor to the UK government, and Sir Richard Roberts, the recipient of the 1993 Nobel Prize for Medicine, for genetics research. 
Late in 2011, two groups of scientists courted controversy, when they prepared to publish studies showing a modified version of the avian flu virus that could be passed through the air between mammals. In its current form, the virus, which has killed 60 percent of those it infects, is not easily caught by people from birds, and is even more difficult to transmit from one human to another 
Ron Fouchier, author of the original study.
But, Ron Fouchier, of Erasmus Medical Center in the Netherlands, and Yoshihiro Kawaoka, from the University of Wisconsin, the scientists behind the purposeful mutations, known as gain-of-function studies, say the virus will itself change without lab research, and foreseeing its progression might enable a vaccine or cure to be developed sooner. 
They had voluntarily placed a moratorium on gain-of-function research after their initial research created concern that details about how these modifications to a virus that has killed more than 350 people since its discovery in 2003, were achieved would fall in the hands of careless scientists or worse, terrorists and hostile governments. 
The moratorium was lifted earlier this year.
“The recent calling off of the moratorium by 40 flu researchers alone – not funders, governments or international bodies – says it all. The flu community simply hasn’t understood that this is a hot-button issue that will not go away,” Professor Simon Wain- Hobson, one of the signatories, told UK’s Independent newspaper.
FVR hopes the further gain-of-function experiments – most of which are funded by the government - will be postponed, pending a more thorough scientific debate on the ethics. 
The US government is currently making tentative steps to regulate the research. The White House has published a draft paper that would require government agencies to evaluate the potential risk of any study involving 15 most dangerous cultures, but it has no plans to curb gain-of-function studies altogether. 
And even if the petitioners manage to persuade Barack Obama, their plea is unlikely to stem the tide of similar new manipulations around the world. 
“The H5N1 studies represent the first of no doubt many such studies involving other potential pandemic pathogens. Gain-of-function studies with H5N1 virus are being conducted in China, and a team in The Netherlands is expanding their H5N1 studies to include studies with the H7N7 virus, and has announced plans to conduct similar gain-of-function studies with the SARS coronavirus,” admits the petition.
 TOP SCIENTISTS TO OBAMA: Ban Bird Flu Mutation Experiments - 4/4/2013

Apr. 5, 2013, 6:36 PM | Jennifer Welsh 

A new bird flu is infecting patients across China, currently 16 patients have tested positive for the virus and six have died. But some flu watchers are convinced that the test that doctors are using to detect the H9N7 virus are faulty — that they aren't sensitive enough. 
Even patients on their death beds are only "weakly positive" Laurie Garrett, senior editor for the Council on Foreign Relations and flu-outbreak-follower notes on twitter: 
This could mean that the test is missing vital cases before they get to the seriously ill stage, so we won't know who is infected until it gets really bad. It could also mean the virus is more widespread than tests are showing us. 
This is especially important for the 520 people that the WHO is monitoring for infection. These people were in close contact with people who died or became seriously ill. Reports yesterday said that one of these people showed flu-like symptoms but tests later confirmed to show negative results. 
If that test was faulty.... that person could still have the virus. And it would be a sign that the virus can spread between humans — a very dangerous omen. 
There are also reports that animals are falling ill with the disease, even birds falling out of the sky. These animals test negative for the virus, but if the tests are faulty, that could be a big problem. Read more: HERE
Freedom of Information Act in the UK filed by a doctor there has revealed 30 years of secret official documents showing that government experts have
1. Known the vaccines don’t work
2. Known they cause the diseases they are supposed to prevent
3. Known they are a hazard to children
4. Colluded to lie to the public
5. Worked to prevent safety studies
Those are the same vaccines that are mandated to children in the US.
Educated parents can either get their children out of harm’s way or continue living inside one of the largest most evil lies in history, that vaccines – full of heavy metals, viral diseases, mycoplasma, fecal material, DNA fragments from other species, formaldehyde, polysorbate 80 (a sterilizing agent) – are a miracle of modern medicine.  
Freedom of Information Act filed in the US with the CDC by a doctor with an autistic son, seeking information on what the CDC knows about the dangers of vaccines, had by law to be responded to in 20 days. Nearly 7 years later, the doctor went to court and the CDC argued it does not have to turn over documents. A judge ordered the CDC to turn over the documents on September 30th, 2011. 
On October 26, 2011, a Denver Post editorial expressed shock that the Obama administration, after promising to be especially transparent, was proposing changes to the Freedom of Information Act that would allow it to go beyond declaring some documents secret and to actually allow government agencies (such as the CDC) to declare some document “non-existent.” 
Simultaneous to this on-going massive CDC cover up involving its primary “health” not recommendation but MANDATE for American children, the CDC is in deep trouble over its decades of covering up the damaging effects of fluoride and affecting the lives of all Americans, especially children and the immune compromised. Lawsuits are being prepared.  Children are ingesting 3-4 times more fluoride by body weight as adults and “[t]he sheer number of potentially harmed citizens — persons with dental fluorosis, kidney patients tipped into needing dialysis, diabetics, thyroid patients, etc — numbers in the millions.” 
The CDC is obviously acting against the health of the American people. But the threat to the lives of the American people posed by the CDC’s behavior does not stop there. It participated in designed pandemic laws that are on the books in every state in the US, which arrange for the government to use military to force unknown, untested vaccines, drugs, chemicals, and “medical” treatments on the entire country if it declares a pandemic emergency. 
The CDC’s credibility in declaring such a pandemic emergency is non-existent, again based on Freedom of Information Act. For in 2009, after the CDC had declared the H1N1 “pandemic,” the CDC refused to respond to Freedom of Information Act filed by CBS News and the CDC also attempted to block their investigation.  What the CDC was hiding was its part in one of the largest medical scandals in history, putting out wildly exaggerated data on what it claimed were H1N1 cases, and by doing so, created the false impression of a “pandemic” in the US. 
The CDC was also covering up e financial scandal to rival the bailout since the vaccines for the false pandemic cost the US billions. And worse, the CDC put pregnant women first in line for an untested vaccine with a sterilizing agent, polysorbate 80, in it. Thanks to the CDC,  “the number of vaccine-related “fetal demise” reports increased by 2,440 percent in 2009 compared to previous years, which is even more shocking than the miscarriage statistic [700% increase]. 
The exposure of the vaccine hoax is running neck and neck with the much older hoax of a deadly 1918-19 flu. It was aspirin  that killed people in 1918-19, not a pandemic flu. It was the greatest industrial catastrophe in human history with 20-50 million people dying but it was blamed on a flu. The beginning of the drug industry began with that success (and Monsanto was part of it). The flu myth was used by George Bush to threaten the world with “another pandemic flu that could kill millions” – a terror tactic to get pandemic laws on the books in every state and worldwide. Then the CDC used hoax of the pandemic hoax to create terror over H1N1 and to push deadly vaccines on the public, killing thousands of unborn children and others.  (CDC will not release the data and continues to push the same vaccine.) 
The hoax of the vaccine schedule is over, exposed by FOIAs in the UK.
The hoax of the CDC’s interest in children’s lives has been exposed by its refusal to respond to a doctor’s FOIAs around its knowledge of vaccine dangers. 
The 1918-19 pandemic hoax has been exposed by Dr. Karen Starko’s work on aspirin’s role in killing people. 
And despite refusing to respond to FOIAS, the CDC’s scandalous hoax of a 2009 flu pandemic and its part in creating it, was exposed by CBS NEWS.  
And the Obama administration, in attempting to salvage the last vestige of secrecy around what is really happening with vaccines, by declaring agency documents non-existent, has made its claim of transparency, non-existent. 
But pandemic laws arranging for unknown vaccines to be forced on the entire country are still in place with HHS creating a vaccine mixture that should never be used on anyone and all liability for vaccines having been removed. Meanwhile, a Canadian study has just proven that the flu vaccine containing the H1N1 vaccine which kills babies in utero, actually increases the risk of serious pandemic flu.
Americans who have been duped into submitting their children to the CDC’s deadly vaccines, have a means to respond now. People from every walk of life and every organization, must:
1. take the information from the UK FOIAs exposing 30 years of vaccine lies, the refusal of the CDC to provide any information on what it knows about those lies, and the Obama Administration’s efforts to hide the CDC’s awareness of those lies, and go to their state legislatures, demand the immediate nullification of the CDC vaccine schedule and the pandemic laws.
2. inform every vet. active duty military person, law enforcement people, DHS agents and medical personnel they know, of the vaccine hoax, for their families are deeply threatened, too, but they may not be aware of it or that they have been folded into agency structures by the pharmaceutical industry (indistinguishable from the bankers and oil companies) that would make them agents of death for their country with the declaration of a “pandemic” emergency or “bio-terrorist” attack. It is completely clear now that the terrorism/bioterrorism structures are scams so that any actions taken to “protect” this country using those laws would in fact be what threatens the existence of Americans.
It was aspirin that killed millions in 1918-19.  Now it is mandated and unknown, untested vaccines with banned adjuvants in them that threaten the country with millions of deaths.  At the same time, the CDC is holding 500,000 mega-coffins, built to be incinerated, on its property outside Atlanta.  Not to put to fine a point on this, but it’s clear now that the CDC should not be involved in any way with public health.
Thanks to the Freedom of Information Act (FOIA), we know that vaccines are not a miracle of modern medicine.  Any medical or government authority which insists vaccines prevent diseases is either ignorant of government documents (and endless studies) revealing the exact opposite or of the CDC’s attempts to hide the truth about vaccines from the public, or means harm to the public.
Thanks to the Freedom of Information Act (FOIA), we know the vaccine schedule is a hoax.
The health danger to American children and adults are vaccines.
“The greatest lie ever told is that vaccines are safe and effective”
-Dr. Len Horowitz
Source
Sunday, April 7, 2013
Petroleum forms the basis of one of the most devastating adjuvants in existence. Historically, it was considered too dangerous for use in vaccines, but it's making a comeback in this new age of recombinant DNA vaccine development. Of course, the public relations mantra is that it's safe—so why is it kept quiet?
The current hype in a new vaccine against foot-and-mouth disease is all about how the new ones are safer. But are they? The clue is in what isn't discussed: the adjuvants. PLoS reports that a UK government and Big Pharma funded study has found a new approach, usingrecombinant DNA technology, to create empty capsids, that is, empty virus protein shells, to use as antigens against foot-and-mouth disease.[1] The hollow antigens would be grown inside insects.
Antigens and Adjuvants
Only the surface of an antigen is required to show the immune system how to create antibodies. This method of vaccine development makes it impossible to spread the infection, since none of the active part of a virus is included. It also means that vaccine antigens can be made both rapidly and relatively cheaply.
There's one big disadvantage, though. The immune system isn't all that dumb. It does appear to be capable of distinguishing between genuine and fake threats. So, something is needed to trick it.
These synthetic antigens aren't able to trigger much of an immune response when injected. Therefore, an adjuvant is required, and it must be particularly strong for the vaccine to trigger a strong enough immune response to result in antibodies to the antigen.
The problem is that all adjuvants are, by definition, toxic. Their function is to fire up the body's immune system. Try this analogy:
Picture a tiger in a cage, one that's well-fed, content, and has spent his entire life in it. The audience wants a show and the zookeepers want to give it. So they toss some chicken skins in his cage, hoping he'll get excited, and start growling and shredding the skins.
But they fail to interest him. He's used to a certain amount of aggravation. Kids hooting don't faze him at all. People tossing odds and ends of things into his cage ... oh well, he's gotten used to it. So, the zookeepers—having no moral sense about the animals under their care—spray the tiger with pepper spray.
Now, that gets him riled up! He roars and looks for something to attack. And what does he find? Those chicken skins. So he puts on a great show, fussing and fuming and shredding those skins to bits.
The pepper spray is equivalent to a vaccine adjuvant. Had the zookeepers tossed live chickens into the cage, that tiger would have gone after them and put on a great show. But chicken skins just weren't interesting enough.
Empty capsids are to the immune system much like chicken skins are to that tiger. You can inject and inject them, but the immune system won't care. So, you need to toss something really aggravating into the mix. That something is a strong adjuvant.
And that's exactly what this vaccine will require. According to the PLoS study, the adjuvant proposed for use is called Seppic 206B.
The manufacturer's website defines it as:
Ready-to-use oily vaccine adjuvant for water-in-oil-in-water (W/O/W) emulsion
Based on high-grade injectable mineral oil[2]
Mineral oil is made from petroleum. It is the same oil that's the basis of Freund's adjuvant, which is used to create autoimmune disorders in laboratory animals by injection. Shortly after discovery, they were banned from use in humans because they were recognized as too dangerous.
And this is what is now being praised as safe. The publicity gives the impression that the vaccine itself is safe, but careful reading shows that the safety element is associated only with the manufacturing process—the fact that no live virus is used, so there's no chance of accidental infection or escape. It has nothing to do with the safety of injecting it.
Animal Abuse
The initial goal of this new technology is to produce a new vaccine against hoof-and-mouth disease so that it can be used on a mass scale in livestock. The plan, obviously, is to use the same kind of adjuvant that's sold to science labs around the world for the purpose of creating severe autoimmune disorders like rheumatoid arthritis in lab animals.
As long as their pain from these horrible diseases isn't obvious, who's going to know how the animals suffer? You know that no one's going to be watching to see if they're harmed. One of the most difficult things to deal with in an autoimmune disorder is that they often don't show on the outside. Sufferers of myalgic encephalitis (chronic fatigue syndrome) have routinely been accused of malingering simply because their misery showed only on their faces.
In the case of animals raised for food ... well, these won't be healthy beasts, and it isn't healthy to eat meat from sick animals. In the case of animals raised for dairy, their milk would likely contain the inflammatory agents that result from an autoimmune disorder. You have to wonder at that. Will they redefine the "safe" levels of inflammation markers in milk, since they usually won't find pathogens associated with it? Or just pasteurize it more? That process already exists in long shelf life milk that doesn't require refrigeration.
The Real Goal
The study's authors state:
... the approach we have demonstrated here may be applicable across a wide range of human and animal picornaviruses, including polioviruses and coxsackieviruses.[1][Emphasis mine.]
It is not the intention to use this technology only on animals. The goal is to develop vaccines for humans. These vaccines, by their very nature, will require very strong adjuvants.
The nature of any adjuvant is to be toxic. That's what makes them work. The weaker the antigen, the stronger the adjuvant must be. The new technology utilizes an adjuvant that's known to be extremely toxic, so much so that it's used to produce autoimmune disorders in lab animals.
This mineral oil adjuvant is already in use on farm animals. Aside from the incredible abuse that factory farming heaps on those poor beasts, how many of them live in constant pain simply because of the vaccinations given? But these animals are kept out of sight—and out of sight does tend to mean out of mind. After all, most people still buy their meat in supermarkets, which are the mainstay of these industrialized farms.
The real goal is to bring these mineral oil based adjuvants to humans. These, and others like squalene, which is responsible for the recent mass outbreak of debilitating narcolepsy from the swine flu vaccine, will be used so that Big Pharma can produce vaccines quickly and cheaply.
We're living in an era of mass vaccination. The results are showing up in our children. The average child is now sick. The countries with the highest vaccination rates have the highest child mortalityrates. Rather than do legitimate studies to identify the reasons for it, we see junk study after pseudo study trying to convince us that vaccines are just fine. Meanwhile, even with strong evidence of vaccination harm, the push is on to produce more and more, faster and faster.
And the lives that are devastated? Oh well, that's too bad ... and anyway, it's mere coincidence when a child gets autism or arthritis or asthma or bullous pemphigoid or cancer or diabetes or eczema or ...
Note: Study funders were the Wellcome Trust, a foundation started by the company now called GlaxoSmithKline; DEFRA, UK agency that controls animal vaccination and promotes it; Medical Research Council, an agency funded by the taxpayers.
Five of the nine researchers have deep ties to the vaccine industry, including a lead researcher who's a Jenner Investigator, two students supported by the Wellcome Trust, and two supported by the Medical Research Council.
Resources:
October 24, 2012 

Scientist that discovered GMO health hazards immediately fired, team dismantled
 by: Jonathan Benson 
(NaturalNews) Though it barely received any media attention at the time, a renowned British biochemist who back in 1998 exposed the shocking truth about how genetically-modified organisms (GMOs) cause organ damage, reproductive failure, digestive dysfunction, impaired immunity, and cancer, among many other conditions, was immediately fired from his job, and the team of researchers who assisted him dismissed from their post within 24 hours from the time when the findings went public.
Arpad Pusztai, who is considered to be one of the world's most respected and well-learned biochemists, had for three years led a team of researchers from Scotland's prestigious Rowett Research Institute (RRI) in studying the health effects of a novel GM potato with built-in Bt toxin. Much to the surprise of many, the team discovered that, contrary to industry rhetoric, Bt potato was responsible for causing severe health damage in test rats, a fact that was quickly relayed to the media out of concern for public health.
But rather than be praised for their honest assessment into this genetically-tampered potato, Pusztai and his colleagues were chastised by industry-backed government authorities, including British Prime Minister Tony Blair, whose office was discovered to have secretly contacted RRI just hours after Pusztai and his team announced the results of their study on television. For speaking the truth, Pusztai was immediately fired from his position, and his team dismissed from their positions at the school.

Research out of Egypt finds similar results - GMOs cause severe, long-term health damage
As reported recently in Egypt Independent, similar research by Hussein Kaoud from Cairo University's Faculty of Veterinary Hygiene also made some fascinating, though politically incorrect, discoveries about the effects of GMOs on the body. After feeding nine groups of rats varying combinations of GM soy, corn, wheat, and canola, Kaoud and his team observed that these genetic poisons clearly obstructed the normal function of the animals, affirming Pusztai's research.
"I recorded the alteration of different organs, shrinkage of kidneys, change in the liver and spleen, appearance of malignant parts in the tissues, (and) kidney failure and hemorrhages in the intestine," said Kaoud about the effects of GMOs as observed in the test rats. "The brain functions were touched as well, and the rats' learning and memory abilities were seriously altered."
In Kaoud's case, his groundbreaking findings will soon be published in the respected journals Neurotoxicology and Ecotoxicology. But it remains to be seen whether or not the scientific community at large, which is heavily influenced by biotechnology interests, and the political structures that control it will accept the results as valid, or pull a similar character assassination on Kaoud and his team as punishment for defying the status quo.
What all this clearly illustrates, of course, is that modern science can hardly be considered the independent, truth-seeking, "gold standard" of interpreting and understanding reality that many people mistakenly think it is. The truth about GMOs, as uncovered by mounds of independent research, is that they are inadequately safety tested, at best, and deadly at worst. But this fact remains shrouded in deception, thanks to the corporatized, pro-GMO culture of mainstream science.
Sources for this article include:
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Apr 8, 2013 12:32pm

H7N9 Bird Flu Update: 21 Infected, 6 Dead




A health worker prepares to take swab samples from ducks at Meijiang poultry wholesale market, April 8, 2013, in Changde, China. 
Three new cases of the new bird flu strain, H7N9, have been reported in China, bringing the total number of cases to 21, according to the World Health Organization. Six of those who were infected have died, but no new deaths have been reported since Friday. 
The new patients include a 59-syear-old Shanghai man who is in critical condition, and a 55-year-old Anhui man who is in stable condition. Another new patient, a 67-year-old Shanghai man, has a mild case, according to the WHO. 
“They’ve already seen some changes that allow it to survive in people, 
” ABC News chief health and medical editor Dr. Richard Besser told  “Good Morning America.”  
“The big concern is could this become the next pandemic strain?” 
More than 530 close contacts of the H7N9 patients  have been monitored, according to the WHO. The U.S. Centers for Disease Control and Prevention is already working on a vaccine, using the virus’s genetic code  rather than the virus itself — a first for the agency, according to Nancy Cox, head of the CDC’s influenza division. 
Although H7N9 is more easily transmittable from birds to humans than the original bird flu strain, H1N1, Cox said she expects to see limited human-to-human transmission. 
Since H7N9 is not as deadly to birds as it is to humans, it will be harder to track because there won’t be large bird kill-offs, Cox said. 
“That’s very concerning because you can’t tell where it is without testing the birds directly,” Besser said. 
On Friday, a Shanghai market where the virus was detected in pigeons halted live bird sales and slaughtered all poultry, amounting to more than 20,500 chickens, ducks, geese and pigeons, according to China’s  Xinhua News Agency
“The key to controlling the number of H7N9 patients depends on whether the virus can spread among human beings,” said Wu Fan, director of the Shanghai Municipal Center for Disease Control and  Prevention, at a news conference last Friday, according to Xinhua. “So far we haven’t found any cases that show this kind of virus can spread from people to people.”

Posted: 04 Spetember 2004
The Truth About The Vaccine Cover-Up 
Dr Russell Blaylock MD



I was asked to write a paper on some of the newer mechanisms of vaccine damage to the nervous system, but in the interim I came across an incredible document that should blow the lid off the cover-up being engineered by the pharmaceutical companies in conjunction with powerful governmental agencies.
It all started when a friend of mind sent me a copy of a letter from Congressman David Weldon, M.D. to the director of the CDC, Dr Julie L. Gerberding, in which he alludes to a study by a Doctor Thomas Verstraeten, then representing the CDC, on the connection between infant exposure to thimerosal-containing vaccines and neurodevelopmental injury. In this shocking letter Congressman Weldon referrers to Dr. Verstraeten's study which looked at the data from the Vaccine Safety Datalink and found a significant correlation between thimerosal exposure via vaccines and several neurodevelopmental disorders including tics, speech and language delays, and possibly to ADD.
Congressman Weldon questions the CDC director as to why, following this meeting, Dr. Verstraeten published his results, almost four years later, in the journal Pediatrics to show just the opposite, that is, that there was no correlation to any neurodevelopmental problems related to thimerosal exposure in infants. In this letter, Congressman Weldon refers to a report of the minutes of this meeting held in Georgia, which exposes some incredible statements by the "experts" making up this study group. The group's purpose was to evaluate and discuss Dr. Verstraeten's results and data and make recommendation that would eventually lead to possible alterations in the existing vaccine policy.
I contacted Congressman Weldon's legislative assistant and he kindly sent me a complete copy of this report. Now, as usual in these cases, the government did not give up this report willingly, it required a Freedom of Information Act lawsuit to pry it loose. Having read the report twice and having carefully analyzed it; I can see why they did not want any outsiders to see it. It is a bombshell, as you shall see. In this analysis, I will not only describe and discuss this report, but also will frequently quote their words directly and supply the exact page number so others can see for themselves.
The official title of the meeting was the "Scientific Review of Vaccine Safety Datalink Information." This conference, held on June 7-8, 2000 at Simpsonwood Retreat Center, Norcross, Georgia, assembled 51 scientists and physicians of which five represented vaccine manufacturers. These included Smith Kline Beecham, Merck, Wyeth, North American Vaccine and Aventis Pasteur.
During this conference, these scientists focused on the study of the Datalink material, whose main author was Dr. Thomas Verstraesten who identified himself as working at the National Immunization Program of the CDC. It was discovered by Congressman Weldon that Dr. Verstraeten left the CDC shortly after this conference to work for GlaxoSmithKline in Belgium which manufacturers vaccines, a recurring pattern that has been given the name a "revolving door" It is also interesting to note that GlaxoSmithKline was involved in several lawsuits over complications secondary to their vaccines.
To start off the meeting, Dr. Roger Bernier, Associate Director for Science in the National Immunization Program (CDC), related some pertinent history. He stated that Congressional action in 1997 required that the FDA review mercury being used in drugs and biologics (vaccines). In meeting this order, the FDA called for information from the manufacturers of vaccines and drugs. He notes that a group of European regulators and manufacturers met on April 1999 and noted the situation but made no recommendations or changes. In other words it was all for show.
At this point Dr. Bernier made an incredible statement (page 12). He said, "In the United States there was a growing recognition that cumulative exposure may exceed some of the guidelines." By guidelines, he is referring to guidelines for mercury exposure safety levels set by several regulatory agencies. The three guidelines were set by the ATSDR, the FDA and the EPA. The most consistently violated safety guideline was that set by the EPA. He further explains that he is referring to children being exposed to thimerosal in vaccines.
Based on this realization that they were violating safety guidelines he says, this then "resulted in a joint statement of the Public Health Service (PHS) and the American Academy of Pediatrics (AAP) in July of last year (1999), which stated that as a long term goal, it was desirable to remove mercury from vaccines because it was a potentially preventable source of exposure."(Page 12)
As an aside, one has to wonder, where was the Public Health Service and American Academy of Pediatrics during all the years of mercury use in vaccines and why didn't they know that, number one, they were exceeding regulatory safety levels and second, why weren't they aware of the extensive literature showing deleterious effects on the developing nervous system of babies? As we shall see even these "experts" seem to be cloudy on the mercury literature.
Dr. Bernier notes that in August 1999 a public workshop was held at Bethesda in the Lister Auditorium by the National Vaccine Advisory Group and the Interagency Working Group on Vaccines to consider thimerosal risk in vaccine use. And based on what was discussed in that conference, thimerosal was removed from the hepatitis B vaccine (HepB). It is interesting to note that the media took very little interest in what was learned at that meeting and it may have been a secret meeting as well. As we shall see, there is a reason why they struggle to keep the contents of all these meetings secret from the public.
He then notes on page 13 that on October 1999 the Advisory Committee on Immunization Practices (ACIP) "looked this situation over again and did not express a preference for any of the vaccines that were thimerosal free." In this discussion he further notes that the ACIP concluded that the thimerosal-containing vaccines could be used but the "long-term goal" is to try to remove thimerosal as soon as possible. Now, we need to stop and think about what has transpired here. We have an important group here; the ACIP that essential plays a role in vaccine policy that affects tens of millions of children every year. And, we have evidence from the Thimerosal meeting in 1999 that the potential for serious injury to the infant's brain is so serious that a recommendation for removal becomes policy. In addition, they are all fully aware that tiny babies are receiving mercury doses that exceed even EPA safety limits, yet all they can say is that we must "try to remove thimerosal as soon as possible." Do they not worry about the tens of millions of babies that will continue receiving thimerosal-containing vaccines until they can get around to stopping the use of thimerosal?
It should also be noted that it is a misnomer to say "removal of thimerosal" since they are not removing anything. They just plan to stop adding it to future vaccines once they use up existing stocks, which entails millions of doses. And, incredibly, the government allows them to do it. Even more incredibly, the American Academy of Pediatrics and the American Academy of Family Practice similarly endorse this insane policy. In fact, they specifically state that children should continue to receive the thimerosal-containing vaccines until new thimerosal-free vaccine can be manufactured at the will of the manufacturers. Are they afraid that there will be a sudden diphtheria epidemic in America or tetanus epidemic?
The most obvious solution was to use only single-dose vials, which requires no preservative. So, why don't they use them? Oh, they exclaim, it would add to the cost of the vaccine. Of course, we are only talking about a few dollars per vaccine at most, certainly worth the health of your child's brain and future. They could use some of the hundreds of millions of dollars they waste on vaccine promotion every year to cover these cost for the poor. Yet, that would cut into some fat-cat's budget and we can't have that.
It was disclosed that thimerosal was in all influenza vaccines, DPT (and most DtaP) vaccines and all HepB vaccines.
As they begin to concentrate on the problem at hand we first begin to learn that the greatest problem with the meeting is that, they know virtually nothing about what they are doing. On page 15, for example, they admit that there is very little pharmacokinetic data on ethylmercury, the form of mercury in thimerosal. In fact they say there is no data on excretion, the data on toxicity is sparse, yet it is recognized to cause hypersensitivity, it can cause neurological problems and even death, and it is known to easily pass the blood-brain barrier and the placental barrier.
Therefore, what they are admitting is that we have a form of mercury that has been used in vaccines since the 1930s and no one has bothered to study the effects on biological systems, especially the brains of infants. Their defense throughout this conference is "we just don't know the effects of ethylmercury." As a solution, they resort to studies on methylmercury, because there are thousands of studies on this form of mercury. The major source of this form is seafood consumption.
It takes them awhile to get the two forms of mercury straight, since for several pages of the report they say methylmercury is in thimerosal rather than ethylmercury. They can be forgiven for this. On page 16, Dr. Johnson, an immunologist and pediatrician at the University of Colorado School of Medicine and the National Jewish Center for Immunology and Respiratory Medicine, notes that he would like to see the incorporation of wide margins of safety, that is 3 to 10-fold margins of safetyto "account for data uncertainties." What he means is that there are so many things we do not know about this toxin that we had better use very wide margins of safety. For most substances the FDA uses a 100-fold margin of safety.
The reason for this, which they do not mention, is that in a society of hundreds of millions of people there are groups of people who are much more sensitive to the toxin than others. For instance, the elderly, the chronically ill, the nutritionally deficient, small babies, premature babies, those on certain medications and inborn defects in detoxification, just to name a few. In fact, in this study they excluded premature babies and low birth weight babies from the main study, some of which had the highest mercury levels, because they would be hard to study and because they had the most developmental problems, possibly related to the mercury.
On page 16 as well, Dr. Johnson makes an incredible statement, one that defines the problem we have in this country with the promoters of these vaccines. He states, "As an aside, we found a cultural difference between vaccinologist and environmental health people in that many of us in the vaccine arena have never thought about uncertainty factors before. We tend to be relatively concrete in our thinking." Then he says, "One of the big cultural events in that meeting ---was when Dr. Clarkson repetitively pointed out to us that we just didn't get it about uncertainty, and he was actually quite right."
This is an incredible admission. First, what is a vaccinologist? Do you go to school to learn to be one? How many years of residency training are required to be a vaccinologist? Are there board exams? It's a stupid term used to describe people who are obsessed with vaccines, not that they actually study the effects of the vaccines, as we shall see throughout this meeting. Most important is the admission by Dr. Johnson that he and his fellow "vaccinologist" are so blinded by their obsession with forcing vaccines on society that they never even considered that there might be factors involved that could greatly affect human health, the so-called "uncertainties." Further, that he and his fellow "vaccinologists" like to think in concrete terms-that is, they are very narrow in their thinking and wear blinders that prevent them from seeing the numerous problems occurring with large numbers of vaccinations in infants and children. Their goal in life is to vaccinate as many people as possible with an ever-growing number of vaccines. On page 17 his "concrete thinking" once again takes over. He refers to the Bethesda meeting on Thimerosal safety issues and says, "there was no evidence of a problem, only a theoretical concern that young infants' developing brains were being exposed to an organomercurial." Of course, as I shall point out later, it is a lot more than a "theoretical concern". He then continues by saying, "We agree that while there was no evidence of a problem the increasing number of vaccine injections given to infants was increasing the theoretical mercury exposure risk."
It's hard to conceive of a true scientist not seeing the incredible irony of these statements. The medical literature is abound with studies on the deleterious effects of mercury on numerous enzymes, mitochondrial energy production, synaptic function, dendritic retraction, neurotubule dissolution and excitotoxicity, yet, he sees only a "theoretical risk" associated with an ever increasing addition of thimerosal-containing vaccines. It is also important to note that these geniuses never even saw a problem in the first place, it was pressure from outside scientists, parents of affected children and groups representing them that pointed out the problem. They were, in essence, reacting to pressure from outside the "vaccinologist club" and not discovering internally that a problem "might" exist.
In fact, if these outside groups had not become involved these "vaccinologists" would have continued to add more and more mercury-containing vaccines to the list of required vaccines. Only when the problem became so obvious, that is of epidemic proportion (close to that now) and the legal profession became involved would they have even noticed there was a problem. This is a recurring theme in the government's regulatory agencies, as witnessed with fluoride, aspartame, MSG, dioxin and pesticides issues.
It is also interesting that Dr. Johnson did admit that the greatest risk was among low birth weight infants and premature infants. Now why would that be if there existed such a large margin of safety with mercury used in vaccines? Could just a few pounds of body weight make such a dramatic difference? In fact, it does but it also means that normal birth weight children, especially those near the low range of normal birth weight, are also in greater danger. It also would mean that children receiving doses of mercury higher than the 75 ug in this study would be at high risk as well because their dose, based on body weight, would be comparable to that of the low birth weight child receiving the lower dose. This is never even considered by these "vaccinologist experts" who decide policy for your children.
Now this next statement should shock everyone, but especially the poor who in any way think that these "vaccinologists" experts have their best interest in mind. Dr. Johnson says on page 17, "We agree that it would be desirable to remove mercury from U.S. licensed vaccines, but we did not agree that this was a universal recommendation that we would make because of the issue concerning preservatives for delivering vaccines to other countries, particularly developing countries, in the absence of hard data that implied that there was in fact a problem."
So, here you have it. The data is convincing enough that the American Academy of Pediatrics and the American Academy of Family Practice, as well as the regulatory agencies and the CDC along with these organizations all recommend its removal as quickly as possible because of concerns of adverse effects of mercury on brain development, but not for the children in the developing countries. I thought the whole idea of child health programs in the United States directed toward the developing world was to give poor children a better chance in an increasingly competitive world. This policy being advocated would increase the neurodevelopmental problems seen in poor children (also in this country) of developing countries, impairing their ability to learn and develop competitive minds. Remember, there was a representative of the World Health Organization (WHO), Dr. John Clements, serving on this panel of "experts". He never challenged this statement made by Dr. Johnson.
It also needs to be appreciated that children in developing countries are at a much greater risk of complications from vaccinations and from mercury toxicity than children in developed countries. This is because of poor nutrition, concomitant parasitic and bacterial infections and a high incidence of low birth weight in these children. We are now witnessing a disaster in African countries caused by the use of older live virus polio vaccines that has now produced an epidemic of vaccine related polio, that is, polio caused by the vaccine itself. In, fact, in some African countries, polio was not seen until the vaccine was introduced.
The WHO and the "vaccinologist experts" from this country now justify a continued polio vaccination program with this dangerous vaccine on the basis that now that they have created the epidemic of polio, they cannot stop the program. In a recent article it was pointed out that this is the most deranged reasoning, since more vaccines will mean more vaccine-related cases of polio. But then, "vaccinologist" have difficulty with these "uncertainties". (Jacob JT. A developing country perspective on vaccine-associated paralytic poliomyelitis. Bulletin WHO 2004; 82: 53-58. See commentary by D.M. Salisbury at the end of the article.)
Then he again emphasizes the philosophy that the health of children is secondary to "the program" when he says, "We saw some compelling data that delaying the birth dose of HepB vaccine would lead to significant disease burden as a consequence of missed opportunity to immunize." This implies that our children would be endangered from the risk of hepatitis B should the vaccine program stop vaccinating newborns with the HepB vaccine.
In fact, this statement is not based on any risk to U.S. children at all and he makes that plain when he states, "that the potential impact on countries that have 10% to 15% newborn hepatitis B exposure risk was very distressing to consider." (page 18) In other words the risk is not to normal U.S. children but to children in developing countries. In fact, hepatitis B is not a risk until the teenage years and after in this country. The only at-risk group among children is with children born to drug using parents; mothers infected with hepatitis B or HIV infected parents. The reason for vaccinating the newborns is to capture them before they can escape the "vaccinologist's" vaccine program. This is a tactic often used to scare mothers into having their children vaccinated. For example, they say that if children are not vaccinated against measles millions of children could die during a measles epidemic. They know this is nonsense. What they are using is examples taken from developing countries with poor nutrition and poor immune function in which such epidemic death can occur. In the United States we would not see this because of better nutrition, better health facilities and better sanitation. In fact, most deaths seen when measles outbreaks occur in the United States occur either in children in which vaccination was contraindicated, the vaccine did not work or in children with chronic, immune-suppressing diseases.
In fact, in most studies these children catching the measles or other childhood diseases have been either fully immunized or partially immunized. The big secret among "vaccinologists" is that anywhere from 20 to 50% of children are not resistant to the diseases for which they have been immunized.
Also on page 18, Dr. Johnson tells the committee that it was Dr. Walt Orenstein who "asked the most provocative question which introduced a great deal of discussion. That was, should we try to seek neurodevelopmental outcomes from children exposed to varying doses of mercury by utilizing the Vaccine Safety Datalink data from one or more sites." (page 18)
I take from this no one had ever even thought of looking at the data that had just been sitting there all these years un-reviewed. Children could have been dropping like flies or suffering from terrible neurodevelopmental defects caused by the vaccine program and no one in the government would have known. In fact, that is exactly what the data suggested was happening, at least as regards neurodevelopmental delays.
We should also appreciate that the government sponsored two conferences on the possible role of metals, aluminum and mercury, being use in vaccines without any change in vaccine policy occurring after the meetings. These meetings were held a year before this meeting and before any examination of the data which was being held tightly by the CDC, (which was denied to other independent, highly qualified researchers). I will talk more about what was discussed in the aluminum conference later. It is very important and is only briefly referred to in this conference for a very good reason. If the public knew what was discussed at the aluminum meeting no one would ever get a vaccination using the presently manufactured types of vaccines again.
Despite what was discussed in the aluminum meeting and the scientific literature on the neurotoxicity of aluminum, Dr. Johnson makes the following remark; "Aluminum salts have a very wide margin of safety. Aluminum and mercury are often simultaneously administered to infants, both at the same site and at different sites." Also on page 20, he states, "However, we also learned that there is absolutely no data, including animal data, about the potential for synergy, additively or antagonism, all of which can occur in binary metal mixtures..."
It is important her to appreciate a frequently used deception by those who are trying to defend an indefensible practice. They use the very same language just quoted, that is, that there is no data to show, etc, etc. They intend it to convey the idea that the issue has been looked at and studied thoroughly and no toxicity was found. In truth, it means that no one has looked at this possibility and there have been no studies that would give us an answer one way or the other.
In fact, we know that aluminum is a significant neurotoxin and that it shares many common mechanisms with mercury as a neurotoxin. For example, they are both toxic to neuronal neurotubules, interfere with antioxidant enzymes, poison DNA repair enzymes, interfere with mitochondrial energy production, block the glutamate reuptake proteins (GLT-1 and GLAST), bind to DNA, and interfere with neuronal membrane function. Toxins that share toxic mechanisms are almost always additive and frequently synergistic in their toxicity. So, Dr. Johnson's statement is sheer nonsense.
A significant number of studies have shown that both of these metals play a significant role in all of the neurodegenerative disorders. It is also important to remember, both of these metals accumulate in the brain and spinal cord. This makes them accumulative toxins and therefore much more dangerous than rapidly excreted toxins.
To jump ahead, on page 23 Dr, Tom Sinks, Associate Director for Science at the National Center for Environmental Health at the CDC and the Acting Division Director for Division of Birth Defects, Developmental Disabilities and Health, ask, "I wonder is there a particular health outcome that is related to aluminum salts that may have anything that we are looking at today?" Dr. Martin Meyers, Acting Director of the National Vaccine Program Office, answers, "No, I don't believe there are any particular health concerns that was raised." This is after an aluminum conference held the previous year that did indeed find significant health concerns and an extensive scientific literature showing aluminum to be of great concern.
On page 24 Dr. William Weil, a pediatrician representing the Committee on Environmental Health of the American Academy of Pediatrics, brings some sense to the discussion by reminding them that, "there are just a host of neurodevelopmental data that would suggest that we've got a serious problem. The earlier we go, the more serious the problem." Here he means that the further back you go during the child's brain development, the more likely the damage to the infant. I must give him credit; at least he briefly recognized that a significant amount of brain development does take place later. He also reminds his collogues that aluminum produced severe dementia and death in dialysis cases. He concludes by saying, "To think there isn't some possible problem here is unreal." (page 25)
Not to let it end there, Dr. Meyers adds, "We held the aluminum meeting in conjunction with the metal ions in biology and medicine meeting, we were quick to point out that in the absence of data we didn't know about additive or inhibitory activities." Once again we see the "no data" ploy. There is abundant data on the deleterious effects of aluminum on the brain, a significant portion of which came out in that very meeting.
Dr. Johnson also quotes Dr. Thomas Clarkson, who identifies himself as associated with the mercury program at the University of Rochester, as saying that delaying the HepB vaccine for 6 months or so would not affect the mercury burden. (page 20). He makes the correct conclusion when he says, "I would have thought that the difference was in the timing. That is you are protecting the first six months of the developing central nervous system."
Hallelujah, for a brief moment I thought that they had stumbled on one of the most basic concepts in neurotoxicology. Then Dr. Meyers dashed my hopes by saying that single, separated doses would not affect blood levels at all. At this juncture, we need a little enlightenment. It is important to appreciate that mercury is a fat soluble metal. That is, it is stored in the body's fat. The brain contains 60% fat and therefore is a common site for mercury storage. Now, they establish in this discussion that about half of methylmercury is excreted over several months when ingested. A recent study found that ethylmercury has a half-life of 7 days.
Even so, a significant proportion of the mercury will enter the brain (it has been shown to easily pass through the blood-brain barrier) where it is stored in the phospholipids (fats). With each new dose, and remember these children are receiving as many as 22 doses of these vaccines, another increment is added to the brain storage depot. This is why we call mercury an accumulative poison. They never once, not once, mention this vital fact throughout the entire conference. Not once. Moreover, they do so for a good reason, it gives the unwary, those not trained in neuroscience, assurance that all that matters here is blood levels.
In fact, on page 163, Dr. Robert Brent, A developmental biologist and pediatrician at the Thomas Jefferson University and Dupont Hospital for Children, says that we don't have data showing accumulation and "that with the multiple exposures you get an increasing level, and we don't know whether that is true or not." He redeems himself somewhat by pointing out that some of the damage is irreversible and with each dose more irreversible damage occurs and in that way it is accumulative.
On page 21 Dr. Thomas Clarkson makes the incredible statement implying that he knows of no studies that shows exposure to mercury after birth or at six months would have deleterious effects. Dr. Isabelle Rapin, a neurologist for children at Albert Einstein College of Medicine, follows up by saying that "I am not an expert on mercury in infancy" but she knows it can affect the nerves (peripheral nervous system). So, here is one of our experts admitting that she knows little about the effects of mercury on the infant. My question is-Why is she here? Dr. Rapin is a neurologist for children at Albert Einstein College of Medicine who stated that she has a keen interest in developmental disorders, in particular those involving language and autism, yet she knows little about the effects of mercury on the infant brain.
This conference is concerned with the effects of mercury in the form of thimerosal on infant brain development, yet throughout this conference our experts, especially the "vaccinologists" seem to know little about mercury except limited literature that shows no toxic effects except at very high levels. None of the well known experts were invited, such as Dr. Aschner from Bowman Grey School of Medicine or Dr. Haley Boyd, who has done extensive work on the toxic effects of low concentrations on the CNS. They were not invited because they would be harmful to the true objective of this meeting, and that was to exonerate mercury in vaccines.
Several times throughout this conference, Dr. Brent reminds everyone that the most sensitive period for the developing brain is during the early stages of pregnancy. In fact, he pinpoints the 8th to 18th week as the period of neuromaturation. In fact, the most rapid period of brain maturation, synaptic development and brain pathway development is during the last three months of pregnancy continuing until two years after birth. This is often referred to as the "brain growth spurt." This is also not mentioned once in this conference, again because if mothers knew that their child's brain was busy developing for up to two years after birth they would be less likely to accept this safety of mercury nonsense these "vaccinologists" proclaim.
The brain develops over 100 trillion synaptic connections and tens of trillions of dendritic connections during this highly sensitive period. Both dendrites and synapses are very sensitive, even to very low doses of mercury and other toxins. It has also been shown that subtoxic doses of mercury can block the glutamate transport proteins that play such a vital role in protecting the brain against excitotoxicity. Compelling studies indicate that damage to this protective system plays a major role in most of the neurodegenerative diseases and abnormal brain development as well.
Recent studies have shown that glutamate accumulates in the brains of autistic children, yet these experts seem to be unconcerned about a substance (mercury) that is very powerful in triggering brain excitotoxicity.
It is also interesting to see how many times Dr. Brent emphasizes that we do not know the threshold for mercury toxicity for the developing brain. Again, that is not true-we do know and the Journal of Neurotoxicology states that anything above 10ug is neurotoxic. The WHO in fact states that there is no safe level of mercury.
On page 164 Dr. Robert Davis, Associate Professor of Pediatrics and Epidemiology at the University of Washington, makes a very important observation. He points out that in a population like the United States you have individuals with varying levels of mercury from other causes (diet, living near coal burning facilities, etc.) and by vaccinating everyone you raise those with the highest levels even higher and bring those with median levels into a category of higher levels. The "vaccinologists" with their problem of "concrete thinking" cannot seem to appreciate the fact that not everyone is the same. That is, they fail to see these "uncertainties."
To further emphasize this point lets take a farming family who lives within three miles of a coal-burning electrical plant. Since they also live near the ocean they eat seafood daily. The fertilizers, pesticides and herbicides used on the crops contain appreciable levels of mercury. The coal-burning electrical plant emits high levels of mercury in the air they breathe daily and the seafood they consume has levels of mercury higher than EPA safety standards. This means that any babies born to these people will have very high mercury levels.
Once born, they are given numerous vaccines containing even more mercury, thereby adding significantly to their already high mercury burden. Are these "vaccinologists" trying to convince us that these children don't matter and that they are to be sacrificed at the alter of the "vaccine policy?"
Recent studies by neurotoxicologists have observed that as our ability to detect subtle toxic effects improves, especially on behavior and other neurological functions, we lower the level of acceptable exposure. In fact, Dr, Sinks brings up that exact point, using lead as an example. He notes that as our neurobehavioral testing improved, we lowered the acceptable dose considerably and continue to do so. Dr. Johnson had the audacity to add, "The smarter we get, the lower the threshold." Yet, neither he, nor the other participants seem to be getting any smarter concerning this issue.
Dr. Robert Chen, Chief of Vaccine Safety and Development at the National Immunization Program at the CDC, then reveals why they refuse to act on this issue, he says, "the issue is that it is impossible, unethical to leave kids unimmunized, so you will never, ever resolve that issue. So then we have to refer back from that." (page 169) In essence, immunization of the kids takes precedence over safety concerns with the vaccines themselves. If the problem of vaccine toxicity cannot be solved, he seems to be saying, then we must accept that some kids will be harmed by the vaccines.
Dr. Brent makes the statement that he knows of no known genetic susceptibility data on mercury and therefore assumes there is a fixed threshold of toxicity. That is, that everyone is susceptible to the same dose of mercury and there are no genetically hypersensitive groups of people. In fact, a recent study found just such a genetic susceptibility in mice. In this study they found that mice susceptible to autoimmunity developed neurotoxic effects to their hippocampus, including excitotoxicity, not seen in other strains of mice. They even hypothesize that the same may be true in humans, since familial autoimmunity increases the likelihood of autism in offspring. (Hornig M, Chian D, Lipkin WI. Neurotoxic effects of postnatal thimerosal are mouse strain dependent. Mol Psychiatry 2004; (in press).
For the next quotation you need a little discussion to be able to appreciate the meaning. They are discussing the fact that in Dr. Verstraeten study frightening correlations were found between the higher doses of thimerosal and problems with neurodevelopment, including ADD and autism. The problem with the study was that there were so few children who had received no thimerosal-containing vaccines that a true control group could not be used. Instead they had to use children getting 12.5ug of mercury as the control and some even wanted to use the control dose as 37.5ug. So the controls had mercury levels that could indeed cause neurodevelopmental problems. Even with this basic flaw, a strong positive correlation was found between the dose of mercury given and these neurodevelopmental problems.
It was proposed that they compare a group of children receiving non-thimerosal vaccines to those who had. In fact, we later learn that they had a large group of children who could have been used as a thimerosal-free control. It seems that for two years before this conference the Bethesda Naval Hospital had been using only thimerosal-free vaccines to immunize the children. They knew this and I would assume someone would have told Dr. Verstraeten of this important fact before he did his study.
So, now to the quote. Dr. Braun responds to the idea of starting a new study using such thimerosal-free controls by saying, "Sure we will have the answer in five years. The question is what can we do now with the data we have?" (page 170). Well, we have the answer to that, they simply covered this study up, declare that thimerosal is of no concern and continued the unaltered policy. That is, they can suggest the pharmaceutical manufacturers of vaccines remove the thimerosal but not make it mandatory or examining the vaccine to make sure they have removed it.
Lets us take a small peak at just how much we can trust the pharmaceutical manufacturers to do the right thing. Several reports of major violations of vaccine manufacturing policy have been cited by the regulatory agencies. This includes obtaining plasma donations without taking adequate histories on donors as to disease exposures and previous health problems, poor record keeping on these donors, improper procedures and improper handing of specimens.
That these are not minor violations is emphasized by the discovery that a woman with variant Mad Cow Disease was allowed to given plasma to be used in vaccines in England. In fact, it was learned only after the contaminated plasma was pooled and used to make millions of doses of vaccines that her disease was discovered. British health officials told the millions of vaccinated not to worry, since we have no idea if it will really spread the disease.
Contamination of vaccines is a major concern in this country as well, as these regulatory violations make plain. It is also important to note that no fines were given, just warnings.
Conclusions by the study group
At the end of the conference, a poll was taken asking two questions. One was, Do you think that there is sufficient data to make a causal connection between the use of thimerosal-containing vaccines and neurodevelopmental delays? Second, do you think further study is called for based on this study?
First, let us see some of the comments on the question of doing further studies. Dr. Paul Stehr-Green, Associate Professor of Epidemiology at the University of Washington School of Public Health and Community Medicine, who voted yes, gave as his reason, "The implications are so profound these should be examined further." (page 180) Meanwhile, Dr. Brent interjects his concern that the lawyers will get hold of this information and begin filing lawsuits. He says, "They want business and this could potentially be a lot of business." (Page 191)
Dr. Loren Koller, Pathologist and Immunotoxicologist at the College of Veterinary Medicine, Oregon State University, is to be congratulated in that he recognized that more is involved in the vaccine effects than just ethylmercury. (page 192). He mentions aluminum and even the viral agents beings used as other possibilities. This is especially important in the face of Dr. RK Gherardi's identification of macrophagic myofascitis, a condition causing profound weakness and multiple neurological syndromes, one of which closely resembled multiple sclerosis. Both human studies and animal studies have shown a strong causal relationship to the aluminum hydroxide or aluminum phosphate used as a vaccine adjuvants. More than 200 cases have been identified in European countries and the United States and has been described as an "emerging condition."
Here are some of the neurological problems seen with the use of aluminum hydroxide and aluminum phosphate in vaccines. In two children aged 3 and 5, doctors at the All Children's Hospital in St. Petersburg, Florida described chronic intestinal pseudo-obstruction, urinary retention and other findings indicative of a generalized loss of autonomic nervous system function (diffuse dysautonomia). The 3-year old had developmental delay and hypotonia (loss of muscle tone). A biopsy of the children's vaccine injection site disclosed elevated aluminum levels.
In a study of some 92 patients suffering from this emerging syndrome, eight developed a full-blown demyelinating CNS disorder (multiple sclerosis). [Authier FJ, Cherin P, et al. Central nervous system disease in patients with macrophagic myofasciitis. Brain 2001; 124: 974-983. ] This included sensory and motor symptoms, visual loss, bladder dysfunction, cerebellar signs (loss of balance and coordination) and cognitive (thinking) and behavioral disorders.
Dr. Gherardi, the French physician who first described the condition in 1998, has collected over 200 proven cases, One third of these developed an autoimmune disease, such as multiple sclerosis. Of critical importance is his finding that even in the absence of obvious autoimmune disease there is evidence of chronic immune stimulation caused by the injected aluminum, known to be a very powerful immune adjuvant.
The reason this is so important is that there is overwhelming evidence that chronic immune activation in the brain (activation of microglial cells in the brain) is a major cause of damage in numerous degenerative brain disorders, from multiple sclerosis to the classic neurodegenerative diseases (Alzheimer's disease, Parkinson's and ALS). In fact, I have presented evidence that chronic immune activation of CNS microglia is a major cause of autism, attention deficit disorder and Gulf War Syndrome.
Dr. Gherardi emphasizes that once the aluminum is injected into the muscle, the immune activation persists for years. In addition, we must consider the effect of the aluminum that travels to the brain itself. Numerous studies have shown harmful effects when aluminum accumulates in the brain. A growing amount of evidence points to high brain aluminum levels as a major contributor to Alzheimer's disease and possibly Parkinson's disease and ALS (Lou Geherig's disease). This may also explain the 10X increase in Alzheimer's disease in those receiving the flu vaccine 5 years in a row. (Dr. Hugh Fudenberg, in press, Journal of Clinical Investigation). It is also interesting to note that a recent study found that aluminum phosphate produced 3X the blood level of aluminum, as did aluminum hydroxide. (Flarend RE, hem SL, et al. In vivo absorption of aluminum-containing vaccine adjuvants using 26 Al. Vaccine 1997; 15: 1314-1318.)
Of course, in this conference, our illustrious experts tell us that there is "no data showing an additive or synergistic effect between mercury and aluminum."
Dr. Rapin expressed her concern over public opinion when this information eventually gets out. She says (page 197), they are going to be captured by the public and we had better make sure that a) "We council them carefully and b) that we pursue this because of the very important public health and public implications of the data." Dr. Johnson adds. "the stakes are very high..." From this, how can one conclude anything than the fact that at least these scientists were extremely concerned by what was discovered by this study examining the vaccine safety datalink material? They were obviously terrified that the information would leak out to the public. Stamped in bold letters at the top of each page of the study was the words-"DO NOT COPY OR RELEASE" and "CONFIDENTIAL."
This is not the wording one would expect on a clinical study of vaccine safety; rather you would expect it on top-secret NSA or CIA files. Why was this information being secreted? The answer is obvious-it might endanger the vaccine program and indict the federal regulatory agencies for ignoring this danger for so many years. Our society is littered with millions of children who have been harmed in one degree or another by this vaccine policy. In addition, let us not forget the millions of parents who have had to watch helplessly as their children have been destroyed by this devastating vaccine program.
Dr. Bernier on page 198 says, "the negative findings need to be pinned down and published." Why was he so insistent that the "negative findings" be published? Because he said, "other less responsible parties will treat this as a signal." By that he means, a signal of a problem with thimerosal-containing vaccines. From this, I assume he wants a paper that says only that nothing was found by the study. As we shall see, he gets his wish.
In addition, on page 198, Dr. Rapin notes that a study in California found a 300X increase in autism following the introduction of certain vaccines. She quickly attributes this to better physician recognition. Two things are critical to note at this point. She makes this assertion on better physician recognition without any data at all, just her wishful thinking. If someone pointing out the dangers of vaccines were to do that, she would scream "junk science"
Second, Dr. Weil on page 207, attacks this reasoning when he says, "the number of dose related relationships are linear and statistically significant. You can play with this all you want. They are linear. They are statistically significant." In other words, how can you argue with results that show a strong dose/response relationship between the dose of mercury and neurodevelopmental outcomes? The higher the mercury levels in the children the greater the number of neurological problems.
He continues by saying that the increase in neurobehavioral problems is probably real. He tells them that he works in a school system with special education programs and "I have to say the number of kids getting help in special education is growing nationally and state by state at a rate not seen before. So there is some kind of increase. We can argue about what it is due to." (page 207)
Dr. Johnson seems to be impressed by the findings as well. He says on page 199, "This association leads me to favor a recommendation that infants up to two years old not be immunized with thimerosal containing vaccines if suitable alternative preparations are available." In credibly, he quickly adds "I do not believe the diagnosis justified compensation in the Vaccine Compensation Program at this point." It is interesting to note that one of our experts in attendance is Dr. Vito Caserta, the Chief Officer for the Vaccine Injury Compensation Program.
At this point Dr. Johnson tells the group of his concerns for his own grandchild. He says, (page 200) "Forgive this personal comment, but I got called out at eight o'clock for an emergency call and my daughter-in-law delivered a son by c-section. Our first male in the line of the next generation and I do not want that grandson to get a Thimerosal containing vaccine until we know better what is going on. It will probably take a long time. In the meantime, and I know there are probably implications for this internationally, but in the meanwhile I think I want that grandson to only be given Thimerosal-free vaccines."
So, we have a scientist sitting on this panel which will eventually make policy concerning all of the children in this country, as well as other countries, who is terrified about his new grandson getting a thimerosal-containing vaccine but he is not concerned enough about your child to speak out and try to stop this insanity. He allows a cover-up to take place after this meeting adjourns and remains silent.
It is also interesting to note that he feels the answers will be a long time coming, but in the mean time, his grandson will be protected. The American Academy of Pediatrics, The American Academy of Family Practice, the AMA, CDC and every other organization will endorse these vaccines and proclaim them to be safe as spring water, but Dr, Johnson and some of the others will keep their silence.
It is only during the last day of the conference that we learn that most of the objections concerning the positive relationship between thimerosal-containing vaccines and ADD and ADHA were bogus. For example, Dr. Rapin on page 200 notes that all children in the study were below age 6 and that ADD and ADHD are very difficult to diagnose in pre-schoolers. She also notes that some children were followed for only a short period.
Dr. Stein adds that in fact the average age for diagnosis of ADHD was 4 years and 1 month. A very difficult diagnosis to make and that the guidelines published by the American Academy of Pediatrics limits diagnosis to 6 to 12 year olds. Of course, he was implying that too many were diagnosed as ADHD. Yet, a recent study found that the famous Denmark study that led to the announcement by the Institute of Medicine that there was no relationship between autism and the MMR vaccine, used the same tactic. They cut off the age of follow-up at age six.
It is known that many cases appear after this age group, especially with ADD and ADHD. In fact, most learning problems appear as the child is called on to handle more involved intellectual material. Therefore, the chances are they failed to diagnose a number of cases by stopping the study too early.
Several of the participants tried to imply that autism was a genetic disorder and therefore could have nothing to do with vaccines. Dr. Weil put that to rest with this comment, "We don't see that kind of genetic change in 30 years." In other words, how can we suddenly see a 300% increase in a genetically related disorder over such a short period? It is also known that there are two forms of autism, one that is apparent at birth and one that develops later in childhood. The former has not changed in incidence since statistics have been kept; the other is epidemic.
In one interesting exchange, which ends up being their justification for the view that mercury is of no danger in children vaccinated with vaccines containing thimerosal, involves two studies in children born to mothers consuming high intakes of mercury contaminated fish. One study reported in the journal Neurotoxicology, examined children living in the Republic of Seychelles. In this study, they examined the effect of prenatal exposure to mercury through the mother's consumption of fish high in methylmercury.
A battery of developmental milestone tests were done and no adverse effects were reported in the study reported by Dr. Clarkson and co-workers, the very same person in this conference. He never mentions that a follow-up study of these same children did find a positive correlation between methylmercury exposure and poor performance on a memory test. In a subsequent study of children living on the Faroe Islands exposed to methylmercury, researchers did find impairments of neurodevelopment. This experiment was done by scientists from Japan.
Throughout the remainder of this discussion, Dr. Clarkson and others refer to these two studies. When they are reminded that the Faroe study did find neurological injury to the children, they counter by saying that this was prenatal exposure to mercury and not after birth as would be seen with vaccination. The idea being that prenatally the brain is undergoing neural formation and development making it more vulnerable. As I have mentioned this rapid brain growth and development continues for two years after birth and even at age 6 years the brain is only 80% formed.
Dr. Clarkson keeps referring to the Seychelles study, which demonstrated that the children reached normal neurodevelopmental milestones as shown by a number of tests. Dr Weil points out on page 216 that this tells us little about these children's future brain function. He says, "I have taken a lot of histories of kids who are in trouble in school. The history is that developmental milestones were normal or advanced and they can't read at second grade, they can't write at third grade, they can't do math in the fourth grade and it has no relationship as far as I can tell to the history we get of the developmental milestones. So I think this is a very crude measure of neurodevelopment."
In other words, both of these studies tell us nothing about the actual development of these children's brain function except that they reached the most basic of milestones. To put this another way, your child may be able to stack blocks, recognize shapes and have basic language skills but later in life they could be significantly impaired when it came to higher math, more advanced language skills (comprehension) and ability to compete in a very competitive intellectual environment, like college or advanced schooling. Their future would be limited to the more mundane and intellectually limited jobs.
Post-natal brain development, that is from birth to age six or seven, involves the fine tuning of synaptic connections, dendritic development and pathway refinement, all of which prepare the brain for more complex thinking. These brain elements are very sensitive to toxins and excessive immune stimulation during this period. This is never mentioned in this conference.
In addition, it must be remembered that the children in these two studies were exposed only to methylmercury and not the combined neurotoxic effect of mercury, aluminum and excessive and chronic activation of the brain's immune system (microgia). This is what makes it so incredible, that several of these "vaccinologists" and so-called experts would express doubt about the "biological plausibility" of thimerosal or any vaccine component causing neurodevelopmental problems. The medical literature is exploding with such studies. The biological plausibility is very powerful.
Mercury, for example, even in low concentrations, is known to impair energy production by mitochondrial enzymes. The brain has one of the highest metabolic rates of any organ and impairment of its energy supply, especially during development, can have devastating consequences. In addition, mercury, even in lower concentrations, is known to damage DNA and impair DNA repair enzymes, which again, plays a vital role in brain development. Mercury is known to impair neurotubule stability, even in very low concentrations. Neurotubules are absolutely essential to normal brain cell function. Mercury activates microglial cells, which increases excitotoxicity and brain free radical production as well as lipid peroxidation, central mechanisms in brain injury. In addition, even in doses below that which can cause obvious cell injury, mercury impairs the glutamate transport system, which in turn triggers excitotoxicity, a central mechanism in autism and other neurological disorders. Ironically, aluminum also paralyzes this system.
On page 228, we see another admission that the government has had no interest in demonstrating the safety of thimerosal-containing vaccines despite over 2000 articles showing harmful effects of mercury. Here we see a reference to the fact that the FDA "has a wonderful facility in Arkansas with hundreds of thousands of animals" available for any study needed to supply these answers on safety. The big question to be asked is -So, why has the government ignored the need for research to answer these questions concerning thimerosal safety? You will recall in the beginning the participants of this conference complained that there were just so few studies or no studies concerning this "problem."
Again, on page 229 Dr, Brent rails about the lawsuit problem. He tells the others that he has been involved in three lawsuits related to vaccine injuries leading to birth defects and concluded "If you want to see junk science, look at those cases..." He then complains about the type of scientists testifying in these cases. He adds, "But the fact is those scientist are out there in the United States." In essence, he labels anyone who opposes the "official policy" on vaccines as a junk scientist. We have seen in the discussion who the "junk scientists" really are.
Knowing that what they have found can cause them a great deal of problems he adds, "The medical/legal findings in this study, causal or not, are horrendous... If an allegation was made that a child's neurobehavioral findings were caused by thimerosal-containing vaccines, you could readily find a junk scientist who will support the claim with 'a reasonable degree of certainty." On page 229 he then admits that they are in a bad position because they have no data for their defense. Now, who are the junk scientists?
Is a "real scientist" one who has no data, just wishful thinking and a "feeling" that everything will be all right? Are real scientists the ones who omit recognized experts on the problem in question during a conference because it might endanger the "program?" Or are they the ones who make statements that they don't want their grandson to get thimerosal-containing vaccines until the problem is worked out, but then tell millions of parents that the vaccines are perfectly safe for their children and grandchildren?
Dr. Meyers on page 231 put it this way, "My own concern, and a couple of you said it, there is an association between vaccines and outcomes that worries both parents and pediatricians." He sites other possible connections to vaccine-related neurobehavioral and neurodevelopmental problems including the number of vaccines being given, the types of antigens being used and other vaccine additives.
Dr. Caserta tells the group that he attended the aluminum conference the previous year and learned that often metals could act differently in biological systems than as an ion. This is interesting in the face of the finding that fluoride when combined to aluminum forms a compound that can destroy numerous hippocampal neurons at a concentration of 0.5 ppm in drinking water. It seems that aluminum readily combines with fluoride to form this toxic compound. With over 60% of communities having fluoridated drinking water this becomes a major concern.
It has also been learned that fluoroaluminum compounds mimic the phosphate and can activate G-proteins. G-proteins play a major role in numerous biological systems, including endocrine, neurotransmitters, and as cellular second messengers. Some of the glutamate receptors are operated by a G-protein mechanism.
Over the next ten to fifteen pages, they discuss how to control this information so that it will not get out and if it does how to control the damage. On page 248 Dr. Clements has this to say:
"But there is now the point at which the research results have to be handled, and even if this committee decides that there is no association and that information gets out, the work has been done and through the freedom of information that will be taken by others and will be used in other ways beyond the control of this group. And I am very concerned about that as I suspect that it is already too late to do anything regardless of any professional body and what they say."
In other words, he wants this information kept not only from the public but also from other scientists and pediatricians until they can be properly counseled. In the next statement he spills the beans as to why he is determined that no outsider get hold of this damaging information. He says,
"My mandate as I sit here in this group is to make sure at the end of the day that 100,000,000 are immunized with DTP, Hepatitis B and if possible Hib, this year, next year and for many years to come, and that will have to be with thimerosal containing vaccines unless a miracle occurs and an alternative is found quickly and is tried and found to be safe."
This is one of the most shocking statements I have ever heard. In essence, he is saying, I don't care if the vaccines are found to be harmful and destroying the development of children's brains, these vaccines will be given now and forever. His only concern by his own admission is to protect the vaccine program even if it is not safe. Dr. Brent refers to this as an "eloquent statement."
On page 253, we again see that these scientists have a double standard when it comes to their children and grandchildren. Dr. Rapin raises the point about a loss of an IQ point caused by thimerosal exposure. She says,"an we measure the IQ that accurately, that this one little point is relevant? Then she answers her own question by saying, "Even in my grandchildren, one IQ point I am going to fight about." Yet, they are saying in unison, in essence-TO HELL WITH YOUR CHILDREN- to the rest of America.
It is also interesting that they bring up the history of lead as a neurobehavioral toxin. Dr. Weil noted that the neurotoxicologists and regulatory agencies have lowered the acceptable level from 10 to 5 ug. In fact, some feel that even lower levels are neurotoxic to the developing brain. Before the toxicologists began to look at lead as a brain toxin in children most "experts" assumed it was not toxic even at very high levels. Again, it shows that "experts" can be wrong and it is the public who pays the price.
Dr. Chen on page 256 expresses his concern about this information reaching the public. He remarks, "We have been privileged so far that given the sensitivity of information, we have been able to manage to keep it out of, lets say, less responsible hands..." Dr. Bernier agrees and notes, "This information has been held fairly tightly." Later he calls it "embargoed information" and "very highly protected information."
That they knew the implications of what they had discovered was illustrated by Dr. Chen's statement on page 258. He says, "I think overall there was this aura that we were engaged in something as important as anything else we have ever done. So I think that this was another element to this that made this a special meeting." You may remember, Dr. Weil emphasized that the data analysis left no doubt that there was a strong correlation between neurodevelopmental problems and exposure to thimerosal-containing vaccines. So if they understood the importance of this finding and this was the most important thing they have ever dealt with-why was this being kept from the public? In fact, it gets even worse.
Just so you will not doubt my statement that this audience of experts was not objective, I give you the words of Dr. Walter Orenstein, Director of the National Immunization Program at the CDC, on page 259. He tells the group, "I have seen him (Verstraeten) in audience after audience deal with exceedingly skeptical individuals..." "Exceedingly skeptical individuals" does that sound like objective scientists who wanted to look at the data with a clear mind or were they scientists who were convinced before the meeting was held that there was no danger to children from thimerosal or any other vaccine component?
In one of the closing remarks by Dr. Bernier (page 257) he says, "the other thing I was struck by was the science," meaning the science expressed by the attendees of the meeting. Then Dr, Orenstein adds, "I would also like to thank Roger Bernier who pulled off this meeting in rather short notice..." Here is a meeting that has been called one of the most important they have ever dealt with and we learn that it was pulled off on short notice. In addition, we were told that the results of this meeting would lead to eventual vaccine policy.
He then has the nerve to add:
"In a sense this meeting addresses some of the concerns we had last summer when we were trying to make policy in the absence of a careful scientific review. I think this time we have gotten it straight."
Well, I hate to be the one to break the news, but he didn't get it straight. There was little or no science in this meeting; rather it was composed of a lot of haggling and nit picking over epidemiological methodology and statistical minutia in an effort to discredit the data without success. In fact, the so-called mercury experts admitted they had to do some quick homework to refresh their memories and learn something about the subject.
Conclusions
This top secret meeting was held to discuss a study done by Dr. Thomas Verstraeten and his co-workers using Vaccine Safety Datalink data as a project collaboration between the CDC's National Immunization Program (NIP) and four HMOs. The study examined the records of 110,000 children. Within the limits of the data, they did a very through study and found the following:
Exposure to thimerosal-containing vaccines at one month was associated significantly with the misery and unhappiness disorder that was dose related. That is, the higher the child's exposure to thimerosal the higher the incidence of the disorder. This disorder is characterized by a baby that cries uncontrollably and is fretful more so than that see in normal babies.
Found a nearly significant increased risk of ADD with 12.5ug exposure at one month.
With exposure at 3 months, they found an increasing risk of neurodevelopmental disorders with increasing exposure to thimerosal. This was statistically significant. This included speech disorders.
It is important to remember that the control group was not children without thimerosal exposure, but rather those at 12.5ug exposure. This means that there is a significant likelihood that even more neurodevelopmental problems would have been seen had they used a real control population. No one disagreed that these findings were significant and troubling. Yet when the final study was published in the journal Pediatrics Dr. Verstraeten and co-workers reported no consistent associations were found between thimerosal-containing vaccine exposure and neurodevelopmental problems. In addition, he list himself as an employee of the CDC, not disclosing the fact that at the time the article was accepted, he worked for GlaxoSmithKline, a vaccine manufacturing company.
So how did they do this bit of prestidigitation? They simply added another HMO to the data, the Harvard Pilgrimage. Congressman Dave Weldon noted in his letter to the CDC Director that this HMO had been in receivership by the state of Massachusetts because its records were in shambles. Yet, this study was able to make the embarrassing data from his previous study disappear. Attempts by Congressman Weldon to force the CDC to release the data to an independent researcher, Dr. Mark Geier, a researcher with impeccable credentials and widely published in peer-reviewed journals, have failed repeatedly.
It is obvious that a massive cover-up is in progress, as we have seen with so many other scandals-fluoride, food-based excitotoxins, pesticides, aluminum and now vaccines. I would caution those critical of the present vaccine policy not to put all their eggs in one basket, that is, with thimerosal as being the main culprit. There is no question that it plays a major role, but there are other factors that are also critical, including aluminum, fluoroaluminum complexes, and chronic immune activation of brain microglia.
In fact, excessive, chronic microglial activation can explain many of the effects of excessive vaccine exposure as I point out in two recently published articles. One property of both aluminum and mercury is microglial activation. With chronic microglial activation large concentrations of excitotoxins are released as well as neurotoxic cytokines. These have been shown to destroy synaptic connections, dendrites and cause abnormal pathway development in the developing brain as well as adult brain.
In essence, too many vaccines are being given to children during the brain's most rapid growth period. Known toxic metals are beings used in the vaccines that interfere with brain metabolism, antioxidant enzymes, damage DNA and DNA repair enzymes and trigger excitotoxicity. Removing the mercury will help but will not solve the problem because overactivation of the brain's immune system will cause varying degrees of neurological damage to the highly-vulnerable developing brain.

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  • Liang YX, Sun RK, Sun Y, Chen ZQ, Li LH Psychological effects of low exposure to mercury vapor: application of a computer-administered neurobehavioral evaluation system. Environ Res 1993 Feb;60(2):320-7.
  • Sundberg J, Jonsson S, Karlsson MO, Oskarsson A Lactational exposure and neonatal kinetics of methylmercury and inorganic mercury in mice. Toxicol Appl Pharmacol 1999 Jan 15;154(2):160-9.
  • Inouye M., Murao K., Kajiwara Y., Behavorial and neuropathological effects of prenatal methyl Mercury exposure in mice.. Neurobehav.Toxicol Teratol. ,1985:7;227-232.
  • Koos et al., Mercury toxicity in pregnant women, fetus and newborn infant. Am J Obstet And Gynecol., 1976:126;390-409.
  • Khera et al., Teratogenic and genetic effects of Mercury toxicity. The biochemistry of Mercury in the environment. Nriagu, J.O.Ed Amsterdam Elsevier, 503-18,1979.
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  • Yuan,Y; Atchison,WD. Comparative effects of inorganic divalent mercury, methylmercury and phenylmercury on membrance excitability and synaptic transmission of CA1 neurons in hippocampal slices of the rat Neurotoxicology. 14(2):403-411, 1994.
  • Desi I, Nagymajtenyi L, Schulz H Effect of subchronic mercury exposure on electrocorticogram of rats. Neurotoxicology 1996 Fall-Winter;17(3-4):719-23.
  • Bucio L, Garcia C, Souza V, Hernandez E, Gonzalez C, Betancourt M, Gutierrez-Ruiz MC Uptake, cellular distribution and DNA damage produced by mercuric chloride. Mutat Res 1999 Jan 25;423(1-2):65-72.
  • Hua MS, Huang CC, Yang YJ Chronic elemental mercury intoxication: neuropsychological follow-up case study. Brain Inj 1996 May;10(5):377-84.
  • Grandjean P, Weihe P, White RF, Debes F Cognitive performance of children prenatally exposed to "safe" levels of methylmercury. Environ Res 1998 May;77(2):165-72.
  • Hock C, Drasch G, Golombowski S, Muller-Spahn F, Willershausen-Zonnchen B, Schwarz P, Hock U, Growdon JH, Nitsch RM Increased blood mercury levels in patients with Alzheimer's disease. J Neural Transm 1998;105(1):59-68.
  • Oskarsson A, Palminger Hallen I & Sundberg J. Exposure to toxic elements via breast milk. Analyst 120(3):765-770 (1995).
  • Hock C, Drasch G, Golombowski S, Muller-Spahn F, Willershausen-Zonnchen B, Schwarz P, Hock U, Growdon JH, Nitsch RM Increased blood mercury levels in patients with Alzheimer's disease. J Neural Transm 1998;105(1):59-68.
  • Wenstrup D, Ehmann WD, Markesbery WR Trace element imbalances in isolated subcellular fractions of Alzheimer's disease brains. Brain Res 1990 Nov 12;533(1):125-31
  • Basun H, Forssell LG, Wetterberg L, Winblad B Metals and trace elements in plasma and cerebrospinal fluid in normal aging and Alzheimer's disease. J Neural Transm Park Dis Dement Sect 1991;3(4):231-58.
  • Hock C, Drasch G, Golombowski S, Muller-Spahn F, Willershausen-Zonnchen B, Schwarz P, Hock U, Growdon JH, Nitsch RM Increased blood mercury levels in patients with Alzheimer's disease. J Neural Transm 1998;105(1):59-68.
  • Pendergrass JC, Haley BE, Vimy MJ, Winfield SA, Lorscheider FL Mercury vapor inhalation inhibits binding of GTP to tubulin in rat brain: similarity to a molecular lesion in Alzheimer diseased brain. Neurotoxicology 1997;18(2):315-24.
  • Opitz H, Schweinsberg F, Grossmann T, Wendt-Gallitelli MF, Meyermann R Demonstration of mercury in the human brain and other organs 17 years after metallic mercury exposure. Clin Neuropathol 1996 May-Jun;15(3):139-44.
  • Sanfeliu C, Sebastia J, Cristofol R, Rodriguez-Farre E. Neurotoxicity of organomercurial compounds. Neurotox Res. 2003;5(4):283-305.
  • el-Fawal HA, Gong Z, Little AR, Evans HL Exposure to methylmercury results in serum autoantibodies to neurotypic and gliotypic proteins.Neurotoxicology 1996 Summer;17(2):531-9.
  • Faustman EM, Ponce RA, Ou YC, Mendoza MA, Lewandowski T, Kavanagh T. Investigations of methylmercury-induced alterations in neurogenesis. Environ Health Perspect. 2002 Oct;110 Suppl 5:859-64.
  • Reading R. Thimerosal and the occurrence of autism: negative ecological evidence from Danish population-based data. Child Care Health Dev. 2004 Jan;30(1):90-1.
  • Qvarnstrom J, Lambertsson L, Havarinasab S, Hultman P, Frech W. Determination of methylmercury, ethylmercury, and inorganic mercury in mouse tissues, following administration of thimerosal, by species-specific isotope dilution GC-inductively coupled plasma-MS. Anal Chem. 2003 Aug 15;75(16):4120-4.
  • Shanker G, Syversen T, Aschner M. Astrocyte-mediated methylmercury neurotoxicity. Biol Trace Elem Res. 2003 Oct;95(1):1-10.
  • Zheng W, Aschner M, Ghersi-Egea JF. Brain barrier systems: a new frontier in metal neurotoxicological research. Toxicol Appl Pharmacol. 2003 Oct 1;192(1):1-11.
  • Kawase T, Ishikawa I, Orikasa M, Suzuki A. An assessment of the impact of thimerosal on childhood neurodevelopmental disorders. Geier DA, Geier MR. J Biochem (Tokyo). 1989 Jul; 106(1): 8-10. Aluminum enhances the stimulatory effect of NaF on prostaglandin E2 synthesis in a clonal osteoblast-like cell line, MOB 3-4, in vitro. Pediatr Rehabil. 2003 Apr-Jun;6(2):97-102.
  • Geier MR, Geier DA. Thimerosal in childhood vaccines, neurodevelopmental disorders, and heart disease in the United States. J Amer Physc Surg 8: 6-11, 2003.
  • Allen JW, Shanker G, Tan KH, Aschner M. The consequences of methylmercury exposure on interactive functions between astrocytes and neurons. Neurotoxicology 23: 755-759, 2002.
  • Hansen JC, Reske-Nielsen E, et al. Distribution of dietary mercury in a dog. Quantitation and localization of total mercury in organs and central nervous system. Sci Total Environ 78: 23-43, 1989.
  • Zanoli P, Cannazza G, Baraldi M. Prenatal exposure to methyl mercury in rats: focus on changes in kyrenine pathway. Brain Res Bull 55: 235-238, 2001.
  • Olivieri G, Brack C, et al. Mercury induces cell cytotoxicity and oxidative stress and increases beta-amyloid secretion and tau phosphorylation in SHY5Y neuroblastoma cells. J Neurochem 74: 231-236, 2000.
  • Juarez BI, Mattinez M, et al. Methylmercury increases glutamate extracellular levels in frontal cortex of awake rats. Neurotoxicology and Teratology 24: 767-771, 2002.
  • Geier DA, Geier MR. An assessment of the impact of thimerosal on childhood neurodevelopmental disorders. Pediatric Rehabil 6: 97-102, 2003.
  • Geier DA, Geier MR. A comparative evaluation of the effects of MMR immunization and mercury doses from thimerosal-containing childhood vaccines on the population prevalence of autism. Med Sci Monit 10: P133-139, 2004.
  • Baskin DS, Ngo H, Didenko VV. Thimerosal indices DNA breaks, caspase-3 activation, membrane damage, and cell death in cultured human neurons and fibroblast. Toxicol Sci 74: 361-368, 2003.
  • Pichichero ME, et al. Mercury concentrations and metabolism in infants receiving vaccines containing thimerosal: a descriptive study. Lancet 360: 1737-1741, 2002.
  • Murata K, Dakeishi M. Impact of prenatal methylmercury exposure on child neurodevelopment in the Faroe Islands. Nippon Eiseigaku Zasshi 57: 564-570, 2002.
  • Davidson PW, Myers GJ, et al (Clarkson TW-member of panel) Effects of prenatal and postnatal exposure from fish consumption on neurodevelopment: outcomes at 66 months of age in the Seychelles Child Development Study. JAMA 280: 701-707, 1998.
  • Palumbo DR, Cox C, et al. (ClarksonTW) Association between prenatal exposure to methylmercury and cognitive functioning in Seychellois children: a reanalysis of the McCarthy Scales of Children's Ability from the main cohort study. Environ Res 84: 81-88, 2000.
  • Hornig M, Chian D, Lipkin WI. Neurotoxic effects of postnatal thimerosal are mouse strain dependent. Mol Psychiatry (In press).
  • Ueha-Ishibashi T, et al. Property of thimerosal-induced decrease in cellular content of gluatathione in rat thymocytes: a flow cytometric study with 5-chloromethylfluorescein. Toxicol in Vitro 18: 563-569, 2004.
  • Ueha-Ishibaschi T, et al. Effect of thimerosal, a preservative in vaccines, on intracellular Ca+2 concentration of ra cerebellar neurons. Toxicology 195: 77-84, 2004.
  • Havarinasab S, Lambertsson L, et al. Dose-response study of thimerosal-induced murine systemic autoimmunity. Toxicol Appl Pharmacol 194: 169-179, 2004.
  • Verstraeten T, Davis RL, DeStefano F, et al. Safety of thimerosal-containing vaccines: a two-phase study of computerized health maintenance organization databases. Pediatrics 112: 1039-1048, 2003. (This is the published study that was discussed in the conference. Here the damaging data is erased and the public is told the thimerosal-containing vaccines are perfectly safe. In this paper Dr. Verstraeten identified himself as working for the CDC, but in fact he is working for GlaxoSmithKline. The editors of the journal Pediatrics should have been willing to disclose this information once it was brought to their attention but they would not.).
Aluminum References
  • Murayama H, Shin RW, Higuchi J, Shibuya S, Muramoto T, Kitamoto T. Interaction of aluminum with PHFtau in Alzheimer's disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method.Am J Pathol. 1999 Sep;155(3):877-85.
  • Shin RW, Kruck TP, Murayama H, Kitamoto T. A novel trivalent cation chelator Feralex dissociates binding of aluminum and iron associated with hyperphosphorylated tau of Alzheimer's disease. Brain Res. 2003 Jan 24;961(1):139-46.
  • Li W, Ma KK, Sun W, Paudel HK. Phosphorylation sensitizes microtubule-associated protein tau to Al(3+)-induced aggregation. Neurochem Res. 1998 Dec;23(12):1467-76.
  • Singer SM, Chambers CB, Newfry GA, Norlund MA, Muma NA. Tau in aluminum-induced neurofibrillary tangles. Neurotoxicology. 1997;18(1):63-76.
  • Toda S, Yase Y. Effect of aluminum on iron-induced lipid peroxidation and protein oxidative modification of mouse brain homogenate. Biol Trace Elem Res. 1998 Feb;61(2):207-17.
  • Sayre LM, Perry G, Harris PL, Liu Y, Schubert KA, Smith MA. In situ oxidative catalysis by neurofibrillary tangles and senile plaques in Alzheimer's disease: a central role for bound transition metals. J Neurochem. 2000 Jan;74(1):270-9.
  • Xie CX, Yokel RA. Aluminum facilitation of iron-mediated lipid peroxidation is dependent on substrate, pH and aluminum and iron concentrations. Arch Biochem Biophys. 1996 Mar 15;327(2):222-6.
  • Kawase T, Ishikawa I, Orikasa M, Suzuki A. Aluminum enhances the stimulatory effect of NaF on prostaglandin E2 synthesis in a clonal osteoblast-like cell line, MOB 3-4, in vitro. J Biochem (Tokyo). 1989 Jul; 106(1): 8-10.
  • Jope RS. Modulation of phosphoinositide hydrolysis by NaF and aluminum in rat cortical slices. J Neurochem. 1988 Dec; 51(6): 1731-6.
  • Blair HC, Finch JL, Avioli R, Crouch EC, Slatopolsky E, Teitelbaum SL. Micromolar aluminum levels reduce 3H-thymidine incorporation by cell line UMR 106-01. Kidney Int. 1989 May; 35(5): 1119-25.
  • Shainkin-Kestenbaum R, Adler AJ, Berlyne GM, Caruso C. Effect of aluminium on superoxide dismutase. Clin Sci (Lond). 1989 Nov; 77(5): 463-6.
  • Kawase T, Orikasa M, Suzuki A. Aluminofluoride- and epidermal growth factor-stimulated DNA synthesis in MOB 3-4-F2 cells. Pharmacol Toxicol. 1991 Nov; 69(5): 330-7.
  • Gomes MG, Moreira CA, Mill JG, Massaroni L, Oliveira EM, Stefanon I, Vassallo DV. Effects of aluminum on the mechanical and electrical activity of the Langendorff-perfused rat heart. Braz J Med Biol Res. 1994 Jan; 27(1): 95-100.
  • Jope RS. Modulation of phosphoinositide hydrolysis by NaF and aluminum in rat cortical slices. J Neurochem. 1988 Dec; 51(6): 1731-6.
  • Husaini Y, Rai LC, Mallick N. Impact of aluminium, fluoride and fluoroaluminate complex on ATPase activity of Nostoc linckia and Chlorella vulgaris. Biometals. 1996 Jul; 9(3): 277-83.
  • Blair HC, Finch JL, Avioli R, Crouch EC, Slatopolsky E, Teitelbaum SL. Micromolar aluminum levels reduce 3H-thymidine incorporation by cell line UMR 106-01. Kidney Int. 1989 May; 35(5): 1119-25.
  • Lai JC, Lim L, Davison AN. Effects of Cd2+, Mn2+, and Al3+ on rat brain synaptosomal uptake of noradrenaline and serotonin. J Inorg Biochem. 1982 Nov; 17(3): 215-25.
  • Shainkin-Kestenbaum R, Adler AJ, Berlyne GM, Caruso C. Effect of aluminium on superoxide dismutase. Clin Sci (Lond). 1989 Nov; 77(5): 463-6.
  • Department of Health and Human Services National Vaccine Program Office Presents: Workshop on Aluminum in Vaccines. Caribe Hilton International Hotel, San Juan, Puerto Rico: Jointly sponsored by: task Force for Child Survival and Development. May 12, 200.
  • Varner JA, Jenson KF, Harvath W, Isaacson RL. Chronic administration of aliminum-fluoride or sodium-fluoride to rats in drinking water: alterations in neuronal and cerebrovascular integrity. Brain Res 784: 284-298, 1998.
  • Strunecka A, Pataocka J. Aluminofluoride complexes: new phosphate analogues for laboratory investigations and potential danger for living organisms. | HERE
  • Candura SM, Castildi AF, et al. Interaction of aluminum ions with phosphoinositide metabolism in rat cerebral cortical membranes. Life Sci 49: 1245-1252, 1991.
  • Publicover SJ. Brief exposure to the G-protein activator NaF/ AlCl3 induces prolonged enhancement of synaptic transmission in area of rat hippocampal slices. Expl Brain Res 84: 680-684, 1991.
  • Brenner A. Macrophagic myofascitiitis: a summery of Dr. Gherardi's presentations. Vaccine 20LSupp 3): S5-6, 2002.
  • Lacson AG, D'Cruz CA, et al. Aluminum phagocytosis in quadriceps muscle following vaccination in children: relationship to macrophagic myofasciitis. Pediatr Dev Pathol 5: 151-158, 2002.
  • Flarend RE, Hem SL, et al. In vivo absorption of aluminum-containing vaccine adjuvants using 26 Al. Vaccine 15: 131401318, 1997.
  • Authier FJ Cherin P, et al. Central nervous system disease in patients with macrophagic myofasciitis. Brain 124: 974-983, 2001.
  • Gherardi RK. Lessons from macrophagic myofasciitis: towards definition of a vaccine adjuvant-related syndrome. Rev Neurol (Paris) 159: 162-164, 2003.
  • Bergfors E, Trollfors B, Inerot A. Unexpectantly high incidence of persistent itching and delayed hypersensitivity to aluminum in children after the used of absorbed vaccines from a single manufacturer. Vaccine 22: 64-69, 2003.
  • Deloncle R, Fauconneau B, et al. Aluminum L-glutamate complexes in rat brain cortex: in vivo prevention of aluminum deposit by magnesium D-aspartate. Brain Res 946: 247-252, 2002.
  • Mundy WR, Freudenrich TM, Kodavanti PR. Aluminum potentates glutamate-induced calcium accumulation and iron-induced oxygen free radical formation in primary neuronal cultures. Mol Chem Neuropathol 32: 41-57, 1997.
References Concerning Lead
  • Naatala JT, Loikkanen JJ, et al. Lead amplifies glutamate-induced oxidative stress. Free Radical Biology Medicine 19: 689-693, 1995.
  • Morgan RE, Garavan H, et al. Early lead exposure produces lasting changes in sustained attention, response initiation, and reactivity to errors. Neurotoxicology and Teratology 23: 519-531, 2001.
  • Needleman HL, McFarland C, et al. Bone lead levels in adjudicated delinquents: A case control study. Neurotoxicology and Teratology 24: 711-717, 2002.
  • Dietrich KN, Ris MD, et al. Early exposure to lead and juvenile delinquency. Neurotoxicology and Teratology 23: 511-518, 2001.
My References
  • Blaylock R. Interaction of cytokines, excitotoxins, and reactive nitrogen and oxygen species in autism spectrum disorders. J. Amer Nutr Assoc 6: 21-35, 2003.
  • Blaylock RL. The central role of excitotoxicity in autism spectrum disorders. J Amer Nutra Assoc 6: 7-19, 2003.
  • Blaylock RL. Chronic microglial activation and excitotoxicity secondary to excessive immune stimulation: possible factors in Gulf War Syndrome and autism. J Amer Phys Surg 9: 46-51, 2004.

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Vaccines and Brain Development  | Dr Russell Blaylock MD  | HERE
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About Octa Dandy Saiyar

Kelahiran Jakarta keturunan asli Bukittinggi, Sumatera Barat .
07 Oktober 1983.



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