40 Infallible Reasons Why You Should Not Vaccinate Infants

By Jagannath Chatterjee

There is no scientific study to determine whether vaccines have really prevented diseases. Rather disease graphs show vaccines have been introduced at the fag end of epidemics when the disease was already in its last stages. In case of Small Pox the vaccine actually caused a great spurt in the incidence of disease killing thousands before public outcry led to its withdrawal.

  1. There are no long-term studies on vaccine safety. Very short-term unscientific tests are carried out where the vaccinated subjects are checked against another group who are given another vaccine. Technically the tests should be carried out against a non-vaccinated group. No one really knows what protocols are followed at such industry-sponsored trials.
  2. There has never been any attempt to compare a vaccinated population against a non vaccinated population to know what vaccines are doing to the children and the society.
  3. The child receives not one but many vaccines. There are no tests to determine the effects of multiple vaccines.
  4. There is no scientific basis for vaccinating infants. As per senior doctors quoted by the Times of India, “Children suffer from less that 2% of vaccine preventable illnesses but 100% of the vaccines are targeted towards them.” The vaccine pioneers who have recommended abundant caution before vaccinating the population have never advocated Mass vaccinations.
  5. Children are vaccinated simply because parents can be frightened to forcefully vaccinate their children. Vaccinating infants is the most profitable business both for the manufacturers as well as the doctors.
  6. The Government of India has come out with a quarter page advertisement in The Hindu warning parents not to vaccinate beyond the Government approved vaccines. Parents have been advised against vaccinating in private clinics and hospitals.
  7. The Orissa Chapter of the Indian Association of Pediatricians has admitted in a letter to the CM, Orissa, that private clinics and hospitals are ill equipped to store vaccines and warned parents not to vaccinate upon the advise of private practitioners and hospitals.
  8. ALL THE VACCINE INGREDIENTS ARE EXTREMELY TOXIC IN NATURE.
  9. Vaccines contain heavy metals, cancer causing substances, toxic chemicals, live and genetically modified viruses, contaminated serum containing animal viruses and foreign genetic material, extremely toxic decontaminants and adjuvants, untested antibiotics, none of which can be injected without causing any harm.
  10. The mercury, aluminum and live viruses in vaccines is behind the huge epidemic of autism (1 in 10 worldwide as per doctors in the USA), a fact that has been admitted by the US Vaccine Court.
  11. The CDC of USA, the vaccine watchdog, has publicly admitted that its much-publicized 2003 study denying any link between vaccines and autism, is flawed. The Chief of CDC Dr Gerberding has confessed to the media (CNN) that vaccines can cause “autism like symptoms”. The Autism epidemic is found only in those countries that have allowed mass vaccinations.
  12. In the year 1999, the US Government instructed vaccine manufacturers to remove mercury from vaccines “with immediate effect”. But mercury still remains a part of many vaccines. The vaccines with mercury were never recalled and were given to children up to the year 2006. “Mercury free” vaccines contain 0.05mcg of mercury, enough to permanently damage a infant.
  13. IN INDIA NO ATTEMPT HAS BEEN MADE TO ENSURE THAT MERCURY AND OTHER HEAVY METALS ARE REMOVED FROM VACCINES SIMPLY BECAUSE IT WOULD MAKE VACCINES COSTLIER.
  14. In a reply to then President Sri Abdul Kalam, the Health Ministry informed, “mercury is required to make the vaccines safe”. To the authors query that “what are these vaccines that it requires the second most dangerous neurotoxin, mercury, to make them safe?”, there was no reply.
  15. Mercury used in vaccines is second in toxicity only to the radioactive substance, Uranium. It is a neurotoxin that can damage the entire nervous system of the infant in no time.
  16. Mercury accumulates in fat. The brain being made entirely of fat cells, most of the mercury accumulates there giving rise to the peculiar symptoms of the autistic children.
  17. The mercury used in vaccines is ethyl mercury. According to Indian doctors this is 1000 times more toxic than the usual methyl mercury.
  18. The aluminum present in vaccines makes the mercury, in any form, 100 times more toxic.
  19. As per an independent study aluminum and formaldehyde present in vaccines can increase the toxicity of mercury, in any form, by 1000 times.
  20. As per a Tehelka article on Autism, children are receiving 250 times more mercury through vaccines than they can possibly tolerate. The same article states that if one considers the WHO limit for mercury in water, they are receiving 50,000 times the limit. The limits set, incidentally, are for adults and not infants.
  21. Autism in India has emerged as the most rapidly growing epidemic amongst children. From 1 in 500 it has steadily climbed to 1 in 37 today. As per Indian doctors, “You can go to any class of any school today and find an autistic child.”
  22. Autism is a permanent disability that affects the child physically, mentally and emotionally. It makes the child loose social contact. It impedes both the physical and mental growth of the child. It destroys the brain causing severe memory and attention problems. According to vaccine researcher Dr Harris Coulter, vaccines cause children to become pervert and criminal. All the school shootings by the children in the USA are by autistic children. Vaccines can cause more harm that even the medical community privately acknowledges.
  23. Autistic children also suffer from severe bowel disorders. As per Dr Andrew Wakefield, this is due to the vaccine strain live measles virus in the MMR vaccine. Nearly all children become fully autistic after the MMR shot.
  24. The DPT also causes children to regress giving rise to fears that multiple live virus vaccines are an important cause behind autism. If three live viruses can cause so much harm we can well imagine what today’s five and seven viruses vaccines will do to children.
  25. Before the autism epidemic, it is already well known that vaccines have caused the cancer epidemic in today’s society. Both the Small Pox and the Oral Polio Vaccine are made from monkey serum. This serum has helped many cancer causing monkey viruses, 60 found so far, to enter the human blood stream.
  26. It is also known that it is the use of green monkey serum in vaccines that has led to the transfer of the Sivian Immune deficiency Virus (SIV) from monkeys into humans. The SIV and the HIV that causes AIDS are very similar.
  27. Not only AIDS, a blood cancer in infants (Acute Lymphoblastic Leukemia) that is affecting children in thousands is also due to the extremely toxic nature of vaccine ingredients.
  28. Infantile jaundice and also infantile diabetes is also scientifically connected to the toxic vaccines.
  29. The live polio viruses used in the Oral Polio Vaccine has caused Vaccine Attributed Paralytic Polio in more than 65,000 children as per doctors of the Indian Medical Association. In the USA this vaccine has caused polio 16 years after administration. The OPV has also let loose a new strain of polio in both India and Africa. The OPV is banned in other countries.
  30. Vaccines contain serum from not only chimpanzees and monkeys but also from cows, pigs, chickens, eggs, horses, and even human serum and tissues extracted from aborted fetuses.
  31. Deaths and permanent disability from vaccines is very common and known by the medical community. They are instructed by the Government to keep quiet and not to associate such cases with vaccines.
  32. Many doctors argue that diseases during childhood are due to the body exercising its immune system. Suppressing these diseases causes the immune system to remain undeveloped causing the various autoimmune disorders like diabetes and arthritis that have become epidemics today.
  33. Vaccines suppress the natural immunity and the body does not have natural antibodies anymore. The mothers milk therefore does not contain natural antibodies and can no longer protect the child against illnesses.
  34. In the USA vaccine adverse effects are recorded and the Government offers compensation of millions of dollars to victims (the most recent case in its Vaccine Court may have received upto $200 million in damages). The Indian Government simply refuses to acknowledge that vaccines can cause deaths and permanent disability.
  35. It has been scientifically proven that vaccines cannot prevent disease. Vaccines try to create humoral (blood related immunity) whereas it has been found that immunity is developed at various levels, humoral as well as cellular. We still do not know enough about the human immune system and therefore should not interfere with it.
  36. In the USA parents are informed about vaccine after effects and their consent has to be taken before vaccinating their children. In India the Government assures the population through massive advertising campaigns that vaccines are extremely safe. Parents refusing to vaccinate are threatened by the administration.
  37. THERE IS NO SYSTEM OF TREATMENT TO TREAT A VACCINE DAMAGED CHILD. The parents have to run from one hospital to another. The Government turns a blind eye and refuses to even acknowledge the vaccine connection.
  38. Medical doctors have challenged even the vaccines recommended by the Government of India. The BCG vaccine for tuberculosis has been extensively tested in India as long back as 1961 and found to be totally ineffective. The OPV is causing polio and other neurological and intestinal disorders in tens of thousands of Indian children. The Hep-B vaccine introduced recently is not meant for children at all, it is a vaccine for a sexually transmitted disease that should be targeted only at promiscuous adults. The tetanus vaccine contains both aluminum and mercury besides the tetanus toxoid.. The doctors themselves avoid the DPT as it is one of the most toxic vaccines ever devised. The measles vaccine is a vaccine that regularly causes severe adverse effects and the health workers want it out.
  39. The pediatricians are introducing dubious vaccines in India, which are being opposed by the doctors, politicians, and public in American and European countries. The Rotavirus vaccine, Hib vaccine, HPV vaccine and the various multi virus vaccines being introduced without any kind of testing is only because the vaccine manufacturers and the doctors administering them want to ensure a good income from them. They care two hoots about medical ethics and the fate of the children who will receive these vaccines. Vaccines containing nano particles and viruses and also plant based genetically modified vaccines are being opposed by honest doctors worldwide.

…bless you all…

New Generation of Vaccine Adjuvants: Worst Ever?

by Heidi Stevenson

A new generation of vaccine adjuvants is being rolled out, literally mass produced. They’re touted as safe, but they share a dirty secret: They’re oil-based, which could make them the most dangerous yet in a product line that is, by definition, toxic.

All vaccine adjuvants are, by definition, toxic. Their function is to stimulate the immune system, that is, to initiate a response to a toxic agent. So, a new generation of adjuvants is being promoted as less toxic than any that have come before, while at the same time doing an even better job of priming the immune system so it will react to weak antigens. This leads to the question of how an adjuvant can be both safer than previous adjuvants and also more capable of agitating the stronger immune system response required to promote antibody creation to weaker antigens.

These new adjuvants are made from outer membrane vesicles (OMVs). A vesicle is a cavity, or sac. In a bacterium, OMVs are sacs that protrude from the exterior—membrane—of its body to protect itself in hostile environments. An OMV’s function is to be toxic.

Recombinant DNA technology is used to engineer bacteria so that they make OMVs to be used as antigens or adjuvants, which are then processed and added to vaccines. All of these products that are grown on the surfaces of microbes have one thing in common: they are proteoliposomes:

A proteoliposome is a liposome with one or more proteins inserted.
A liposome is a minute spherical sac of phospholipid molecules enclosing a water droplet.
A phospholipid is a type of lipid.
A lipid is a fatty acid. That is, a lipid is a fat.

And that makes these new adjuvants, or antigens with adjuvants built in, particularly worrisome. Fats and oils are known to be exceptionally dangerous when injected. Their similarity to normal body tissues is the reason. Fats do not normally enter the body through injections. They are either digested or created by the body, in which case there’s no problem. However, injection is not a normal means for lipids to enter the body.

Therefore, an injected lipid can be seen by the immune system as an invader. Of course, the response to an invader is to create antibodies against it. Since lipids normally exist throughout the body, when the immune system is radicalized into seeing a lipid as the enemy, it’s attacked—wherever it’s found, even when it’s a normal part of the body.

That’s the definition of an autoimmune disorder: the body’s own immune system starts attacking itself.

It’s not a secret that injection of lipids causes autoimmune disorders. In fact, it’s so well known that lipid injection is a standard technique for creating autoimmune disorders in laboratory animals for study. In particular, the active ingredient in Freund’s adjuvant, a lipid, is used to create an analog of human rheumatoid arthritis in lab rats.

Yet, lipids, in the form of recombinantly-created OMVs, are being added to vaccines for injection into humans!

Why Move to OMV Adjuvants?

The push for OMV adjuvants is happening because vaccine antigens—the part of a vaccine that’s supposed to trigger an autoimmune response that results in antibodies—need to create a strong immune response. But that’s not an easy task unless the antigen is a live microbe, which could cause a full-fledged disease. That’s why weakened or killed microbes have traditionally been used.

However, such weakened and killed microbes are not easy to produce, nor can the process be hurried. It is, therefore, expensive and, in the case of influenza, can take too long to respond to an ongoing outbreak. So, the modern approach is to utilize bits of microbes, or better yet, to grow those bits through recombinant DNA, such as in tobacco plants. The problem with this method is that these protein bits don’t create much of an immune response. Therefore, since the old standard, aluminum, doesn’t accomplish the job well enough, stronger adjuvants are required to initiate that response.

That’s why there’s a rush to implement OMV antigens and adjuvants. Once the process for a particular antigen or adjuvant is worked out, it becomes a relatively inexpensive process to grow it on a large scale for vaccines.

At this point, there is one vaccine with an OMV adjuvant on the market, Cervarix. Its adjuvant is marketed as AS04. It contains aluminum and OMV-derived 3-O-desacyl-4’-monophosphoryl lipid A (MPL). You can see from the chemical name that MPL is a lipid.

OMV Adjuvant Safety?

Adjuvants were discovered by accident when it was noted that dirty—literally dirty, contaminated—vaccine containers produced better results in terms of a vaccine’s ability to create antibodies. It was literally the dirty secret of vaccinology, and led to the intentional contamination of vaccines. The contaminants were relabeled as adjuvants.

Of course, there are side effects to adjuvants. The one that became standard, aluminum, is a known toxin. But, as long as it made the vaccine more effective at producing antibodies, the toxic properties of aluminum were—and still are—swept under the rug.

Other adjuvants had been tried, but all were even more toxic. Among the very worst were ones based on oils, Freund’s adjuvants. These were quickly determined to be far too toxic for use in vaccines, though they did find another marketable use. Freund’s adjuvants are now routinely used in medical research because they create the equivalent of human autoimmune disorders, such as rheumatoid arthritis, in laboratory animals, which are then studied to find treatments for the human disorders.

Now they have found OMV adjuvants, which are being promoted as the safest yet. A recent report in Proceedings of the National Academy of Sciences (PNAS), discusses “a less toxic mixture of monophosphorylated lipid A species (MPL)” made through the OMV methodology. Notice that the emphasis is on “less toxic”.

The fallacious claim that OMV lipids are safe is based on their being natural. It’s that very fact, that they’re natural—literally analogs of normal body chemistry—that makes them so dangerous. Their injection can cause them to be seen as toxins—which, of course, in this context they are—which can result in antibodies being developed against chemicals that are naturally found in the body. An autoimmune disease is the body’s immune system turning on itself.

There is, though, a great deal of emphasis on OMV lipids’ ability to elicit a strong immune system response to create antibodies. Just how something can be less toxic, yet cause a stronger response to toxicity is not explored.

Apparently, it’s to be taken on faith that these lipids are safe, when all other lipids are too dangerous for use in humans. But where are the trials to prove it?

Slipping Around the Approval Process

The FDA has made clear that they don’t approve adjuvants. Their logic is that adjuvants are not produced for end users. They’re produced for use in products that go to end users. The FDA doesn’t focus on individual ingredients in medical products. So they approve vaccines that include adjuvants, thus evading the issue of adjuvants’ toxicity.

Obviously, you cannot run tests of products that are intended to do harm, which is the case with all vaccine adjuvants, and hope to demonstrate safety. So, you won’t see safety trials of them. It would, of course, be considered unethical.

But apparently not so unethical that there’s any reason to stop their use in vaccines.

OMV adjuvants are now being promoted as “designer bacteria”. They’re being touted as safe, yet better able to elicit a response from weak antigens—a process that, by definition, requires more toxic adjuvants, not less toxic ones.

So, are the new generation of OMV adjuvants the worst ever? Is there any reason to assume otherwise?

Of one thing we can be certain: We’ll find out on the bodies of our children. These adjuvants are now being rolled out in a big way. They’re the basis of the enormous number of vaccines in the pipeline.

Sources:

  1. Modulating the innate immune response by combinatorial engineering of endotoxinPNAS, Brittany D. Needham, Sean M. Carroll, David K. Giles, George Georgiou, Marvin Whiteley, andM. Stephen Trent
  2. Bacterial outer membrane vesicles and the host–pathogen interactionGenes and Development, Meta J. Kuehn and Nicole C. Kesty
  3. Outer Membrane Vesicles Derived from Escherichia coli Induce Systemic Inflammatory Response Syndrome, PLoS One, Kyong-Su Park, Kyoung-Ho Choi, You-Sun Kim, Bok Sil Hong, Oh Youn Kim, Ji Hyun Kim, Chang Min Yoon, Gou-Young Koh, Yoon-Keun Kim, Yong Song Gho, doi:10.1371/journal.pone.0011334
  4. Outer membrane vesicle of Neisseria meningitidis serogroup B as an adjuvant in immunization of rabbit against Neisseria meningitidis serogroup AAfrican Journal of Microbiology Research, Seyed Davar Siadat, Saied Reza Naddaf, Mehrangiz Zangeneh, Arfa Moshiri, Seyed Mehdi Sadat, Mehdi Shafiee Ardestani, Mohammad Hassan Pouriayevali, Safieh Amini, and Mohammad Reza Aghasadeghi. DOI: 10.5897/AJMR11.361
  5. Briefing Materials for the Meeting of the Vaccines and Related Biological Products Advisory Committee, 7th April, 2011
  6. Immunogenicity and Tolerability of Recombinant Serogroup B Meningococcal Vaccine Administered With or Without Routine Infant Vaccinations According to Different Immunization SchedulesA Randomized Controlled Trial, doi:10.1001/jama.2012.85
  7. Delivery of foreign antigens by engineered outer membrane vesicle vaccinesPNAS, David J. Chen, Nikolaus Osterrieder, Stephan M. Metzger, Elizabeth Buckles, Anne M. Doody, Matthew P. DeLisa, and David Putnam
  8. Outer membrane vesicle of Neisseria meningitidisserogroup B as an adjuvant to induce specific antibody response against the lipopolysaccharide of Brucella abortus S99
  9. Contribution of bacterial outer membrane vesicles to innate bacterial defense, doi:10.1186/1471-2180-11-258
  10. Analysis of outer membrane vesicle associated proteins isolated from the plant pathogenic bacterium Xanthomonas campestris pv. campestris, doi:10.1186/1471-2180-8-87
  11. PorA Variable Regions of Neisseria meningitidisEmerging Infectious Diseases
  12. Restored functional immunogenicity of purified meningococcal PorA by incorporation into liposomes
  13. Liposomal meningococcal B vaccination: role of dendritic cell targeting in the development of a protective immune response. Infection and Immunity, doi:  10.1128/IAI.71.9.5210-5218.2003
  14. Immunogenicity and tolerability of a multicomponent meningococcal serogroup B (4CMenB) vaccine in healthy adolescents in Chile: a phase 2b/3 randomised, observer-blind, placebo-controlled studyThe Lancet, doi:10.1016/S0140-6736(11)61713-3
  15. Use of an investigational multicomponent meningococcal serogroup B vaccine (4CMenB) in a clinical trial in 3630 infants
  16. Adjuvant Activity of Emulsan, a Secreted Lipopolysaccharide fromAcinetobacter calcoaceticus, doi:  10.1128/CDLI.9.6.1240-1247.2002
  17. Lipopolysaccharide Vaccine Adjuvant
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  20. Routine 4CMenB immunizations effective against meningococcal strains in infants
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…bless you all…