http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/excipient-table-2.pdf

The links are from govt. health agencies, university studies and pharma companies. Vaccine Opponents Do Have Scientific Backing



Science Confirms Vaccines are Dangerous

March 3, 2015

Nothing defines the conspiracy against society better than the vaccine issue.
People who refuse to put their trust in the medical cartel are viciously ridiculed  and told they are ignoring scientific fact.
Here is a list of medical journal abstracts on vaccine hazards.
They prove that science is not on the side of vaccines, and anyone pushing vaccines is an Illuminati stooge.

Compiled by M.P.


Vaccine ingredients list - includes formaldehyde, aluminum, dog, monkey and human fetal tissue, etc. FYI - WI-38, a vaccine ingredient is human female fetal lung tissue. MRC-5 is the male version. Madin-Darby Canine Kidney (MDCK) is kidney cells from an unlucky female cocker spaniel dog.

http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/B/excipient-table-2.pdf?utm_source=wordtwit&utm_medium=social&utm_campaign=wordtwit

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University of Calgary video of brain neuron degeneration. Thimerosal is a mercury compound found in some vaccines.

https://www.youtube.com/watch?v=IHqVDMr9ivo&list=PLYe2wo8dm7xOzXchs-iJnjOnodrCOTsii

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Material safety data sheet for thimerosal

http://www.sciencelab.com/msds.php?msdsId=9925236

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Aluminum adjuvants in vaccines and their toxicity

http://www.ncbi.nlm.nih.gov/pubmed/25428645

antivaxers.jpg----------------------------------------

http://www.ncbi.nlm.nih.gov/pubmed/?term=21568886

Curr Med Chem. 2011;18(17):2630-7.

Aluminum vaccine adjuvants: are they safe?

Tomljenovic L1, Shaw CA.

Abstract

Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. Despite almost 90 years of widespread use of aluminum adjuvants, medical science's understanding about their mechanisms of action is still remarkably poor. There is also a concerning scarcity of data on toxicology and pharmacokinetics of these compounds. In spite of this, the notion that aluminum in vaccines is safe appears to be widely accepted. Experimental research, however, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences. In our opinion, the possibility that vaccine benefits may have been overrated and the risk of potential adverse effects underestimated, has not been rigorously evaluated in the medical and scientific community. We hope that the present paper will provide a framework for a much needed and long overdue assessment of this highly contentious medical issue.

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Simian virus 40 (SV40) a monkey virus found for years in the polio vaccine and is a potent cancer agent.

http://www.ncbi.nlm.nih.gov/pubmed/15258090

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC452549/

Clin Microbiol Rev. 2004 Jul;17(3):495-508, table of contents.

Emergent human pathogen simian virus 40 and its role in cancer.

Vilchez RA1, Butel JS.

Abstract

The polyomavirus simian virus 40 (SV40) is a known oncogenic DNA virus which induces primary brain and bone cancers, malignant mesothelioma, and lymphomas in laboratory animals. Persuasive evidence now indicates that SV40 is causing infections in humans today and represents an emerging pathogen. A meta-analysis of molecular, pathological, and clinical data from 1,793 cancer patients indicates that there is a significant excess risk of SV40 associated with human primary brain cancers, primary bone cancers, malignant mesothelioma, and non-Hodgkin's lymphoma. Experimental data strongly suggest that SV40 may be functionally important in the development of some of those human malignancies. Therefore, the major types of tumors induced by SV40 in laboratory animals are the same as those human malignancies found to contain SV40 markers. The Institute of Medicine recently concluded that "the biological evidence is of moderate strength that SV40 exposure could lead to cancer in humans under natural conditions." This review analyzes the accumulating data that indicate that SV40 is a pathogen which has a possible etiologic role in human malignancies. Future research directions are considered.

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question.jpghttp://www.ncbi.nlm.nih.gov/pubmed/9923853

http://jnci.oxfordjournals.org/content/91/2/119.full.pdf+html

Simian virus 40 (SV40), a polyomavirus of rhesus macaque origin, was discovered in 1960 as a contaminant of polio vaccines that were distributed to millions of people from 1955 through early 1963. SV40 is a potent DNA tumor virus that induces tumors in rodents and transforms many types of cells in culture, including those of human origin.

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http://www.ncbi.nlm.nih.gov/pubmed/25708367

http://www.sciencedirect.com/science/article/pii/S0009898115001023
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Clin Chim Acta. 2015 Feb 21. pii: S0009-8981(15)00102-3. doi: 10.1016/j.cca.2015.02.030. [Epub ahead of print]

Thimerosal: Clinical, epidemiologic and biochemical studies.

Geier DA1, King PG2, Hooker BS3, Dórea JG4, Kern JK5, Sykes LK6, Geier MR7.

Abstract

INTRODUCTION:

Thimerosal (or Thiomersal) is a trade name for an organomercurial compound (sodium ethyl-mercury (Hg) thiosalicylate) that is 49.55% Hg by weight, which rapidly decomposes in aqueous saline solutions into ethyl-Hg hydroxide and ethyl-Hg chloride. Developed in 1927, it has been and is still being used as a preservative in some cosmetics, topical pharmaceuticals, and biological drug products, including vaccines. Concerns have been voiced about its use because it is toxic to human cells. Although it is banned in several countries, it continues to be added to some vaccines in the United States and many vaccines in the developing world.

DISCUSSION:

This critical review focuses on the clinical, epidemiological, and biochemical studies of adverse effects from Thimerosal in developing humans. This review will include research that examines fetal, infant, and childhood death; birth defects; neurodevelopmental testing deficits in children; and neurodevelopmental disorders (attention deficit/hyperactivity disorder, autism spectrum disorder, tic disorder, and specific developmental delays). The review will also look at the research that examined the outcomes of acute accidental ethyl-Hg poisoning in humans. The studies that examine the underlying biochemical insights into the neuronal cellular damage will also be explored.

CONCLUSION:

The culmination of the research that examines the effects of Thimerosal in humans indicates that it is a poison at minute levels with a plethora of deleterious consequences, even at the levels currently administered in vaccines.


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http://www.ncbi.nlm.nih.gov/pubmed/?term=20628439

Acta Neurobiol Exp (Wars). 2010;70(2):147-64.

Influence of pediatric vaccines on amygdala growth and opioid ligand binding in rhesus macaque infants: A pilot study.

Hewitson L1, Lopresti BJ, Stott C, Mason NS, Tomko J.

Abstract

This longitudinal, case-control pilot study examined amygdala growth in rhesus macaque infants receiving the complete US childhood vaccine schedule (1994-1999). Longitudinal structural and functional neuroimaging was undertaken to examine central effects of the vaccine regimen on the developing brain. Vaccine-exposed and saline-injected control infants underwent MRI and PET imaging at approximately 4 and 6 months of age, representing two specific timeframes within the vaccination schedule. Volumetric analyses showed that exposed animals did not undergo the maturational changes over time in amygdala volume that was observed in unexposed animals. After controlling for left amygdala volume, the binding of the opioid antagonist [(11)C]diprenorphine (DPN) in exposed animals remained relatively constant over time, compared with unexposed animals, in which a significant decrease in [(11)C]DPN binding occurred. These results suggest that maturational changes in amygdala volume and the binding capacity of [(11)C]DPN in the amygdala was significantly altered in infant macaques receiving the vaccine schedule. The macaque infant is a relevant animal model in which to investigate specific environmental exposures and structural/functional neuroimaging during neurodevelopment.
-------------------------------

http://www.ncbi.nlm.nih.gov/pubmed/22235057

Lupus. 2012 Feb;21(2):223-30. doi: 10.1177/0961203311430221.

Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations.

Tomljenovic L1, Shaw CA.

Abstract

Immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune function. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants can overcome genetic resistance to autoimmunity. In some developed countries, by the time children are 4 to 6 years old, they will have received a total of 126 antigenic compounds along with high amounts of aluminum (Al) adjuvants through routine vaccinations. According to the US Food and Drug Administration, safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic. Taken together, these observations raise plausible concerns about the overall safety of current childhood vaccination programs. When assessing adjuvant toxicity in children, several key points ought to be considered: (i) infants and children should not be viewed as "small adults" with regard to toxicological risk as their unique physiology makes them much more vulnerable to toxic insults; (ii) in adult humans Al vaccine adjuvants have been linked to a variety of serious autoimmune and inflammatory conditions (i.e., "ASIA"), yet children are regularly exposed to much higher amounts of Al from vaccines than adults; (iii) it is often assumed that peripheral immune responses do not affect brain function. However, it is now clearly established that there is a bidirectional neuro-immune cross-talk that plays crucial roles in immunoregulation as well as brain function. In turn, perturbations of the neuro-immune axis have been demonstrated in many autoimmune diseases encompassed in "ASIA" and are thought to be driven by a hyperactive immune response; and (iv) the same components of the neuro-immune axis that play key roles in brain development and immune function are heavily targeted by Al adjuvants. In summary, research evidence shows that increasing concerns about current vaccination practices may indeed be warranted. Because children may be most at risk of vaccine-induced complications, a rigorous evaluation of the vaccine-related adverse health impacts in the pediatric population is urgently needed.

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Merck MMR vaccine information insert.

http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf


The following adverse reactions are listed in decreasing order of severity, without regard to causality,
within each body system category and have been reported during clinical trials, with use of the marketed
vaccine, or with use of monovalent or bivalent vaccine containing measles, mumps, or rubella:
Body as a Whole
Panniculitis; atypical measles; fever; syncope; headache; dizziness; malaise; irritability.
Cardiovascular System
Vasculitis.
Digestive System
Pancreatitis; diarrhea; vomiting; parotitis; nausea.
Endocrine System
Diabetes mellitus.
Hemic and Lymphatic System
Thrombocytopenia (see WARNINGS, Thrombocytopenia); purpura; regional lymphadenopathy;
leukocytosis.
Immune System
Anaphylaxis and anaphylactoid reactions have been reported as well as related phenomena such as
angioneurotic edema (including peripheral or facial edema) and bronchial spasm in individuals with or
without an allergic history.
Musculoskeletal System
Arthritis; arthralgia; myalgi

Nervous System
Encephalitis; encephalopathy; measles inclusion body encephalitis (MIBE) (see
CONTRAINDICATIONS); subacute sclerosing panencephalitis (SSPE); Guillain-Barré Syndrome (GBS);
acute disseminated encephalomyelitis (ADEM); transverse myelitis; febrile convulsions; afebrile
convulsions or seizures; ataxia; polyneuritis; polyneuropathy; ocular palsies; paresthesia.

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Vaccine court decisions.

http://www.uscfc.uscourts.gov/sites/default/files/opinions/CAMPBELL-SMITH.MOJABI-PROFFER.12.13.2012.pdf

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http://www.ncbi.nlm.nih.gov/pubmed/12145534

J Biomed Sci. 2002 Jul-Aug;9(4):359-64.

Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism.

Singh VK1, Lin SX, Newell E, Nelson C.

Abstract

Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies. Using serum samples of 125 autistic children and 92 control children, antibodies were assayed by ELISA or immunoblotting methods. ELISA analysis showed a significant increase in the level of MMR antibodies in autistic children. Immunoblotting analysis revealed the presence of an unusual MMR antibody in 75 of 125 (60%) autistic sera but not in control sera. This antibody specifically detected a protein of 73-75 kD of MMR. This protein band, as analyzed with monoclonal antibodies, was immunopositive for measles hemagglutinin (HA) protein but not for measles nucleoprotein and rubella or mumps viral proteins. Thus the MMR antibody in autistic sera detected measles HA protein, which is unique to the measles subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism

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From Penn State Center for Infectious Disease Dynamics , pertussis vaccine responsible for whooping cough increase. 40 fold increase of B. parpertussis in lungs after vaccination.

http://www.cidd.psu.edu/research/synopses/acellular-vaccine-enhancement-b.-parapertussis

Acellular pertussis vaccination enhances B. parapertussis colonization

 An acellular whooping cough vaccine actually enhances the colonization of Bordetella parapertussis in mice; pointing towards a rise in B. parapertussis incidence resulting from acellular vaccination, which may have contributed to the observed increase in whooping cough over the last decade.

Despite widespread vaccination, whooping cough incidence is on the rise worldwide, making it the only vaccine-preventable disease associated with increasing deaths in the United States. Although this disease is most often attributed to Bordetella pertussis infection, it is also caused by the closely related pathogen, B. parapertussis. However, B. pertussis has remained the center of attention, whereas B. parapertussis has been greatly overlooked in the development of whooping cough vaccines.

In this study, former CIDD post-doctoral researcher Grainne Long, CIDD graduate student Alexia Karanikas, and professors Eric Harvill, Andrew Read, and Peter Hudson evaluated a commonly used acellular pertussis vaccine for its efficacy against both of these causative agents of whooping cough during single infection and co-infection.

Their data showed no within-host competition between B. pertussis and B. parapertussis, as well as a strong acellular vaccine-induced protection against infection with B. pertussis in both singly and co-infected mice. In contrast, vaccination led to a 40-fold enhancement of B. parapertussis colonization in the lungs of mice. Though the mechanism behind this increased colonization was not specifically elucidated, it is speculated to involve specific immune responses skewed or dampened by the acellular vaccine, including cytokine and antibody production during infection. Despite this vaccine being hugely effective against B. pertussis, which was once the primary childhood killer, these data suggest that the vaccine may be contributing to the observed rise in whooping cough incidence over the last decade by promoting B. parapertussis infection. Highlighting the extreme consideration that should be exercised in future vaccine development, this work supports the use of vaccines that also target B. parapertussis as a potentially more efficient way to battle whooping cough.

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Vaccine adjuvants cause myalgia, myositis, muscle weakness, arthralgia, arthritis, chronic fatigue, sleep disturbances, cognitive impairment and memory loss, also known as ASIA (autoimmune/inflammatory syndrome induced by adjuvants) ., plus Human papilloma virus (HPV) vaccine and primary ovarian failure medical journal abstract.

http://www.ncbi.nlm.nih.gov/pubmed/24774584


J Autoimmun. 2014 Jun;51:10-6. doi: 10.1016/j.jaut.2014.03.003. Epub 2014 Apr 26.

Sjögren's syndrome: another facet of the autoimmune/inflammatory syndrome induced by adjuvants (ASIA).

Colafrancesco S1, Perricone C1, Priori R2, Valesini G2, Shoenfeld Y3.

Abstract

Recently, a new syndrome, namely the "Autoimmune/inflammatory syndrome induced by adjuvants" (ASIA) has been defined. In this syndrome different conditions characterized by common signs and symptoms and induced by the presence of an adjuvant are included. The adjuvant is a substance capable of boosting the immune response and of acting as a trigger in the development of autoimmune diseases. Post-vaccination autoimmune phenomena represent a major issue of ASIA. Indeed, despite vaccines represent a mainstay in the improvement of human health, several of these have been implicated as a potential trigger for autoimmune diseases. Sjogren's Syndrome (SjS) is a systemic chronic autoimmune inflammatory disease characterized by the presence of an inflammatory involvement of exocrine glands accompanied by systemic manifestations. Own to the straight association between infectious agents exposure (mainly viruses) and sicca syndrome development, the possible link between vaccine and SjS is not surprising. Indeed, a few cases of SjS following vaccine delivery have been reported. At the same extent, the induction of SjS following silicone exposure has been described too. Thus, the aim of this review was to focus on SjS and its possible development following vaccine or silicone exposure in order to define another possible facet of the ASIA syndrome
--------------------------------------

http://www.ncbi.nlm.nih.gov/pubmed/24620624

Rom J Intern Med. 2013 Jul-Dec;51(3-4):131-4.

ASIA or Shoenfeld's syndrome--an autoimmune syndrome induced by adjuvants.

Cojocaru M, Chicoş B.

Abstract

Recently, reports have suggested grouping different autoimmune conditions that are triggered by external stimuli as a single syndrome called autoimmune syndrome induced by adjuvants (ASIA). This syndrome is characterized by the appearance of myalgia, myositis, muscle weakness, arthralgia, arthritis, chronic fatigue, sleep disturbances, cognitive impairment and memory loss, and the possible emergence of a demyelinating autoimmune disease caused by systemic exposure after vaccines and adjuvants. As there are no markers for ASIA, the authors intend to present ASIA, or Shoenfeld's syndrome, as an autoimmune syndrome induced by adjuvants.
--------------------------------------

http://www.ncbi.nlm.nih.gov/pubmed/23902317


Am J Reprod Immunol. 2013 Oct;70(4):309-16. doi: 10.1111/aji.12151. Epub 2013 Jul 31.

Human papilloma virus vaccine and primary ovarian failure: another facet of the autoimmune/inflammatory syndrome induced by adjuvants.

Colafrancesco S1, Perricone C, Tomljenovic L, Shoenfeld Y.

Abstract

PROBLEM:

Post-vaccination autoimmune phenomena are a major facet of the autoimmune/inflammatory syndrome induced by adjuvants (ASIA) and different vaccines, including HPV, have been identified as possible causes.

METHOD OF STUDY:

The medical history of three young women who presented with secondary amenorrhea following HPV vaccination was collected. Data regarding type of vaccine, number of vaccination, personal, clinical and serological features, as well as response to treatments were analyzed.

RESULTS:

All three patients developed secondary amenorrhea following HPV vaccinations, which did not resolve upon treatment with hormone replacement therapies. In all three cases sexual development was normal and genetic screen revealed no pertinent abnormalities (i.e., Turner's syndrome, Fragile X test were all negative). Serological evaluations showed low levels of estradiol and increased FSH and LH and in two cases, specific auto-antibodies were detected (antiovarian and anti thyroid), suggesting that the HPV vaccine triggered an autoimmune response. Pelvic ultrasound did not reveal any abnormalities in any of the three cases. All three patients experienced a range of common non-specific post-vaccine symptoms including nausea, headache, sleep disturbances, arthralgia and a range of cognitive and psychiatric disturbances. According to these clinical features, a diagnosis of primary ovarian failure (POF) was determined which also fulfilled the required criteria for the ASIA syndrome.

CONCLUSION:

We documented here the evidence of the potential of the HPV vaccine to trigger a life-disabling autoimmune condition. The increasing number of similar reports of post HPV vaccine-linked autoimmunity and the uncertainty of long-term clinical benefits of HPV vaccination are a matter of public health that warrants further rigorous inquiry.



- See more at: http://henrymakow.com/#sthash.KY1nbXey.dpuf

Major US news media have presented a grossly distorted and misleading interpretation of vaccines and their relationship to public health since early January. These journalistic organs have suggested the recent measles outbreak in the Western US has been a crisis of monumental proportions.

This flagrant and cynical sensationalism has become a foundation for intense advocacy on behalf of the pharmaceutical corporate and regulatory cartel targeting patient informed consent—a founding principal of modern medical practice and personal freedom. Keeping in mind the close to 300 vaccine products now in the pharmaceutical industry’s pipeline,[1] closer analysis of “measles outbreak” press coverage suggests a conscious effort by corporate news media to virtually banish such notions and practices from the public mind. A news media dependent on over $1 billion in advertising dollars from big pharma must almost by necessity indulge their clients’ broader agenda. 

David Dees (right)

An impartial journalistic approach to the question of vaccination and personal choice would provide equal and unprejudiced airing of “both sides,” in addition to the varied grey areas in the debate, from the corporate and statist entities flying the banner of mandatory vaccination to cautious segments of the citizenry voicing reservations toward such technology alongside the foremost prerogative of personal choice.

A LexisNexis search of US newspaper and wire service articles from December 28, 2015—the official start date of the California measles outbreak—to February 8, 2015 [2] using the search terms “measles” and “vaccination” yields 799 press releases or wire stories and 746 newspaper articles and opinion pieces. Much of this coverage predictably emphasizes the array of vaccine-friendly assumptions and pronouncements from entities abetting the pharmaceutical industry’s long-term profit-specific objectives.

For example, the Centers for Disease Control and Prevention is, alongside the Food and Drug Administration, the most powerful bureaucratic arm utilized by the global pharmaceutical cartel to elicit compliance with the federal vaccine schedule for children from the medical profession and broader population. Of the article sample referenced above, close to one-third (517) reference the “Centers for Disease Control” or “CDC” in their text, suggesting citation of the agency and its policies to persuasively instruct readers on vaccine efficacy and safety.

In contrast, the same body of over 1,500 press releases, news stories and editorials reference “informed consent” only three times—and when the term is used it is done so either in passing or to disparage the practice itself. For example, Arthur Caplan, a professor of medicine at New York University, warns against doctors even considering the practice of informed consent in regard to vaccines. “The science is unimpeachable,” Caplan proclaims. ” Vaccines do not cause autism; measles is dangerous and contagious; inoculating against the disease is neither pointless nor riskier than abstention.” The physician then amazingly suggests that genuine informed consent–explaining how a vaccine such as Measles, Mumps, Rubella, which can severely injure, incapacitate, or kill the child patient–must be categorically replaced by the dissemination of pharmaceutical industry propaganda and half-truths. “Those doctors who counsel otherwise – who distort what patients need to know to preserve their health or that of their children – have crossed a bright red line. They have violated a patient’s right to informed consent, which depends on accurate information.”[3]

The foremost US organization advocating the fundamental doctrine of informed consent, the National Vaccine Information Center, is referenced a paltry 22 times in the sizable article sample. And while the NVIC routinely emphasizes that it is not “anti-vaccine” and merely advocates that patients or their parents fully understand the risks associated with the industrialized, “one size fits all” immunization process, it is nevertheless framed as the official voice of “anti-vaccination.” A recent New York Times article from the data set is exemplary of this practice. “Members of the anti-vaccine movement said the public backlash had terrified many parents. ’People are now afraid they’re going to be jailed,’ said Barbara Loe Fisher, the president of the National Vaccine Information Center, a clearinghouse for resisters.”[4]

Of the 746 articles published in newspapers, 143 are editorial and opinion pieces. Almost without exception each vigorously supports wide-scale vaccination, even proposing punitive measures for those clinging to informed consent and personal choice. Such uniform opinion among newsroom management provides a clear indication of exactly how warped the overall news coverage of the “measles outbreak” has been.

“If we’re not willing to permanently exile anti-vaxxers from the public square,” one opinion in the Philadelphia Daily News remarks, “we should at least make emergency provisions to do so. Anti-vaxxers should be made to understand that when there is a public-health emergency – such as a measles outbreak – they’ll be quarantined for the duration.”[5] “Those who refuse to vaccinate are wrong,” the Salt Lake Tribune argues. “They endanger themselves and those around them.”[6] “The growing anti-vaccination movement is one of the most frustrating developments of this decade,” the San Jose Mercury News similarly contends. “Some of the parents who mistrust vaccine are uneducated and have no access to pediatric counsel, but there’s no excuse for the irresponsible parents who have access to the latest science yet irrationally fear that vaccines are not safe for their children.”[7]

In an effort to console parents concerned about the very real possibility of vaccines causing autism, US government press releases and US news outlets alike reference a 1998 study authored by British physician and medical scientist Andrew Wakefield linking vaccination to Crohn’s disease and autism. “Public health officials blame a decline in parents having their kids vaccinated that began after a now-thoroughly discredited 1998 British report alleged that common early childhood vaccinations triggered autism,” the San Diego Union Tribune grouses. “Unfortunately, that discredited report continues to be cited by know-nothing celebrities and vapid New Age authors who broadly reject modern medicine. They do so even as life expectancy hits all-time highs and medical researchers make steady progress on many fronts.”[8]

The US government’s own public relations service—US Official News—likewise chimes in on Wakefield’s alleged deceit. “A 1998 article in the medical journal The Lancet caused a firestorm of controversy when it was published and helped create the anti-vaccine movement that continues today,” one US government press release reads. “There’s only one problem–the article was later retracted by the publisher for being ‘utterly false,’ and the author, Andrew Wakefield, was found to have been paid big bucks by plaintiffs’ lawyers.”[9]

The fact that Wakefield’s 1998 findings have been upheld in 19 peer-reviewed papers he has contributed to the literature between 1998 and 2010, in addition to 28 studies from other scientists around the world [10] has been consciously overlooked by US newspaper editors and other drug industry propagandists. That this key piece of disinformation–soundly rebutted in the published research–continues to be repeated by journalists and government publicists alike suggests the hardcore disinformation tactics deployed to perpetuate the misunderstanding and unwarranted faith the majority of US families continue to place in big pharma’s immensely profitable vaccine agenda.

As direct result of this well-coordinated publicity campaign and resulting hysteria the legal right by which families may exercise informed consent is now under intense legal assault across the US. “Hearings to remove philosophical/conscientious exemptions to vaccine mandates have already taken place in Washington and Oregon,” NVIC reports.

California, Maine, Minnesota, Pennsylvania, Texas, and Vermont all have bills already filed or press announcements of bills about to be filed to remove philosophical/conscientious exemptions. Maine, Minnesota and Texas have bills to substantially restrict philosophical/conscientious exemptions. Religious exemptions are also under attack. Maryland, New Jersey, Texas and Vermont have bills filed or announced to eliminate religious exemptions, and Illinois, New Mexico and Texas have bills filed or announced to unconstitutionally restrict religious exemptions.

In addition, Connecticut, Florida, Indiana, Maine, Maryland, Montana, Nebraska, Nevada, New York, Pennsylvania, Tennessee, Texas, Vermont, Virginia, and West Virginia all have legislation underway to expand vaccine mandates.[11]

In light of the above one should be unsurprised at the mob-like antipathy toward “anti-vaxxers,” and how the notions of personal liberty and informed consent have been made to appear increasingly bizarre by being effectively stricken from public discourse. The population has been expertly propagandized on the issue by medical practitioners, their professional associations, and regulatory agencies tethered to the pharmaceutical industry’s agenda vis-a-vis a news media reliant on drug advertising revenue. With these observations in mind one must seriously ask themselves, In what meaningful way would a wholly scientific authoritarianism differ from what is witnessed in America today?

I heard you could say that it is against your religious belief to avoid vaccination, is that true?
What are some of the ways to avoid vaccines where it is otherwise mandatory like in schools, colleges, hospital workers, people immigration or traveling the west, etc.

AUTISM BREAKTHROUGH FOR THE TRUTH MOVEMENT:

02 Mar 2015

http://www.jimstonefreelance.com/

Virtually all vaccines since 1985 have been cultured in stem cells from babies aborted in 1985!

How’s that for a shell shocker? And as it turns out, it is absolutely true. If you want to know how they have produced brain destroying vaccines from DAY ONE (and it has not been any different since 1985, which is a real awakening for me) it is because they have used fetal stem cells to produce practically all the childhood shots.
What is wrong with this? Well, the answer is obvious. You are not supposed to create a vaccine based on the tissues of whatever species receives them. Prior to 1985, the world had enough morals to not use aborted babies to create vaccines. Instead, compatible species were used to culture the pathogens which were then extracted and used to create the vaccines. This might end up making people allergic to dogs, cats, or whatever else after a vaccine, but their immune system would not be fooled into making people allergic to their own existence. This is why, prior to the mid 80’s vaccines were not horrible like they are now

Use of fetal tissue to grow cultures which are then extracted and put into a shot is not only immoral, it is dangerous and intentional wilful sabotage of the immune system. All the auto immune disorders (where the immune system attacks the body and starts wrecking organs) that we never heard of before only came into huge prominence after 1985. Prior to that, I never heard of them, and in a nation and world that is now running scamming medical systems, it fits PERFECT into creating profits with a corrupted medical system.

The immune system is brainless. It just operates (basically) via a series of chemical reactions. If an enemy protein (or any other material that is flagged as an enemy) is detected by the immune system, the immune system will then proceed to brainlessly remove it from the body. Absent sabotage, this system works great.

However, by producing a majority of vaccines in human cells, a huge disaster is invited and caused, because when these substances are injected in the presence of a pathogen which is a recognized enemy, the immune system also sees the additional fetal materials as the enemy. Since these materials are identical to what is in the body naturally, the immune system, tricked by the pathogen into believing human tissue is the enemy, then proceeds to destroy those tissues in the body. And brain tissue is one of the types used to make vaccines. THERE IS YOUR DUMBING DOWN AND AUTISM CAUSING PROCESS IN A CUTE LITTLE PACKAGE NO DOCTOR CAN HONESTLY DENY.

This is the direct answer for why vaccines are killing babies with sudden infant death syndrome, and why the shaken baby scam was needed to blame parents for vaccine induced deaths. They knew they were going to kill a lot of babies with these vaccines, and since there never was a reason to use human stem cells to produce vaccines before 1985, it is fairly obvious the decision to do so was made by a satanic cult. Have you ever heard of the grove? Probably. Ode to Molech!

I now have a totally new take on vaccines and autism, and it goes like this:

The luciferian sects of (mainly) the Jewish community, and a few others (luciferian is the key here) made the decision to unwittingly make all of mankind complicit in their oath to Satan by putting aborted fetal tissue in something everyone gets – vaccines, so the sins of the elite few would be sent into the blood of every man woman and child they could possibly get it into, all under the disguise of “health” and helping mankind.

Because they are Satanists, it is easily concluded that they hate mankind, which God created, and have actively sought to corrupt everyone without any consent from them whatsoever. As a bonus, they could formulate their abortion derived vaccines to cause a whole new line of illnesses that they could cash in on via a totally corrupt medical system. Additionally, they could intellectually sculpt all of the children down to a level the “elite” believed they could not be challenged by.

It all fits now, FULL CIRCLE. Parents, if you want to opt out of vaccines, USE FETAL TISSUE “DERIVED” AS THE REASON, it would be damn hard for a doctor to say no to THAT!

Take a look through the following search result. In these results, you will see every excuse given, from No, there is no fetal materials in the vaccines to Rabbis saying Oh, don’t worry, all the stem cells are from 1985 so by now the sin has worn off to outright admissions even through MSM channels that it is all true, and practically all vaccines have this now. And this provides PERFECT grounds to refuse all vaccines for time immortal, If I ever get another shot, it will be after at least three people were killed trying to get me to submit. Knowing the truth really anchors convictions, eh? Take a look at THIS: https://duckduckgo.com/?q=fetal+stem+cell+vaccines

Here is another articles which I believe our sajha experts will avoid to read and provide their own opinion.

Attacking Ourselves: Top Doctors Reveal Vaccines Turn Our Immune System Against Us

The research is hard to ignore, vaccines can trigger autoimmunity with a laundry list of diseases to follow. With harmful and toxic metals as some vaccine ingredients, who is susceptible and which individuals are more at risk?

No one would accuse Yehuda Shoenfeld of being a quack. The Israeli clinician has spent more than three decades studying the human immune system and is at the pinnacle of his profession. You might say he is more foundation than fringe in his specialty; he wrote the textbooks. The Mosaic of Autoimmunity, Autoantibodies, Diagnostic Criteria in Autoimmune Diseases, Infection and Autoimmunity, Cancer and Autoimmunity – the list is 25 titles long and some of them are cornerstones of clinical practice. Hardly surprising that Shoenfeld has been called the "Godfather of Autoimmunology" – the study of the immune system turned on itself in a wide array of diseases from type 1 diabetes to ulcerative colitis and multiple sclerosis.  

But something strange is happening in the world of immunology lately and a small evidence of it is that the Godfather of Autoimmunology is pointing to vaccines – specifically, some of their ingredients including the toxic metal aluminum – as a significant contributor to the growing global epidemic of autoimmune diseases. The bigger evidence is a huge body of research that's poured in in the past 15 years, and particularly in the past five years. Take for example, a recent article published in the journal Pharmacological Research in which Shoenfeld and colleagues issue unprecedented guidelines naming four categories of people who are most at risk for vaccine-induced autoimmunity.

"On one hand," vaccines prevent infections which can trigger autoimmunity, say the paper's authors, Alessandra Soriano, of the Department of Clinical Medicine and Rheumatology at the Campus Bio-Medico University in Rome, Gideon Nesher, of the Hebrew University Medical School in Jerusalem and Shoenfeld, founder and head of the Zabludowicz Center of Autoimmune Diseases in the Sheba Medical Center at Tel Hashomer. He is also editor of three medical journals and author of more than 1,500 research papers across the spectrum of medical journalism and founder of the International Congress on Autoimmunology. "On the other hand, many reports that describe post-vaccination autoimmunity strongly suggest that vaccines can indeed trigger autoimmunity. Defined autoimmune diseases that may occur following vaccinations include arthritis, lupus (systemic lupus erythematosus, SLE) diabetes mellitus, thrombocytopenia, vasculitis, dermatomyosiositis, Guillain-Barre syndrome and demyelinating disorders. Almost all types of vaccines have been reported to be associated with the onset of ASIA."

ASIA – or Autoimmune/inflammatory Syndrome Induced by Adjuvants (also known as Shoenfeld's syndrome) -- first appeared in the Journal of Autoimmunology four years ago. It is an umbrella term for a collection of similar symptoms, including Chronic Fatigue Syndrome, that result after exposure to an adjuvant – an environmental agent including common vaccine ingredients that stimulate the immune system. Since then an enormous body of research, using ASIA as a paradigm, has begun to unravel the mystery of how environmental toxins, particularly the metal aluminum used in vaccines, can trigger an immune system chain reaction in susceptible individuals and may lead to overt autoimmune disease.

Autoimmune disease results when the body's system meant to attack foreign invaders turns instead to attack part of the body it belongs to (auto is Greek for self). If the immune system is like a national defence system, antibodies are like drones programmed to recognize a certain type of invader (a bacteria say) and to destroy them or mark them for destruction by other special forces. Autoantibodies are like drones that are misidentifying a component of the human body and have launched a sustained attack on it. If they mistakenly target a component of the conductive sheath around neurons, for example, nerve impulses stop conducting properly, muscles go into spasm and coordination fails; multiple sclerosis results. If autoantibodies erroneously focus on joint tissue; rheumatoid arthritis results. If they target the islets of Langerhans in the pancreas, Type 1 diabetes, and so on

"Throughout our lifetime the normal immune system walks a fine line between preserving normal immune reactions and developing autoimmune diseases," says the paper. "The healthy immune system is tolerant to self-antigens. When self-tolerance is disturbed, dysregulation of the immune system follows, resulting in emergence of an autoimmune disease. Vaccination is one of the conditions that may disturb this homeostasis in susceptible individuals, resulting in autoimmune phenomena and ASIA."

Who is "susceptible" is the subject of the paper entitled, "Predicting post-vaccination autoimmunity: Who might be at risk?" It lists four categories of people: 1) those who have had a previous autoimmune reaction to a vaccine, 2) anyone with a medical history of autoimmunity, 3) patients with a history of allergic reactions, 4) anyone at high risk of developing autoimmune disease including anyone with a family history of autoimmunity, presence of autoantibodies which are detectable by blood tests and other factors including low vitamin D and smoking.

PREVIOUS REACTION

Regarding those who have had a previous adverse reaction to vaccines, the paper cites five relevant studies including the case of a death of a teenage girl six months following her third Gardasil injection against HPV virus.  She had experienced a range of symptoms shortly after her first dose, including dizziness, numbness and tingling in her hands, and memory lapses. After her second injection, she developed "intermittent arm weakness, frequent tiredness requiring daytime naps," worse tingling, night sweats, chest pain and palpitations. A full autopsy was unrevealing but blood and spleen tissue analysis revealed HPV-16 L1 gene DNA fragments – matching the DNA found in vials of the Gardasil vaccine against cervical cancer – "thus implicating the vaccine as a causal factor." The DNA fragments had also been found to be "complexed with the aluminum adjuvant" which, according to the report, have been shown to persist for up to 8 to 10 years causing chronic immune system stimulation.

"Although data is limited," Shoenfeld and his colleagues concluded, "it seems preferable that individuals with prior autoimmune or autoimmune-like reactions to vaccinations, should not be immunized, at least not with the same type of vaccine."

ESTABLISHED AUTOIMMUNE CONDITION

The second group which the paper cites for vaccine exemption is patients with "established autoimmune conditions." Vaccines don't work so well in them, say Shoenfeld and his colleagues, and they are at "risk for flares following vaccination." Inoculations that contain live viruses including chickenpox, yellow fever and the measles, mumps and rubella triple vaccine (MMR) are "generally contraindicated" for people with autoimmune conditions because of  the risk of "uncontrolled viral replication." But inactivated vaccines are not such a good idea either because they usually contain the added ingredient aluminum, linked to autoimmunity.

The immunologists describe recent studies in which patients with autoimmune rheumatic disease given the influenza vaccine (without aluminum) suffered more joint pain and fever than controls and whose levels of autoantibodies (the drones that attack self)  increased after receiving the flu vaccine. What's more, they developed new types of autoantibodies that weren't present before the vaccines, and those persisted. As the presence of autoantibodies can be predictive of developing autoimmune disease in patients without symptoms, even years ahead of disease onset, this is troubling to those who understand immunology.

 A number of studies claim vaccines are safe for the "overwhelming majority of patients with established autoimmune diseases," the study allows, but they only looked at rheumatoid arthritis and lupus and not at severe and active cases so "the potential benefit of vaccination should be weighed against its potential risk," they cautioned.

PATIENTS WITH A HISTORY OF ALLERGY

Vaccine trials have usually excluded "vulnerable" individuals -- only extremely healthy individuals with no allergies are recruited. It's a "selection bias," say Soriano and Shoenfeld, and has likely resulted in serious adverse events being "considerably underestimated" in "real life where vaccines are mandated to all individuals regardless of their susceptibility." The true incidence of allergic reactions to vaccines, normally estimated at between one in 50,000 to one in a million doses, is probably much higher and particularly where gelatin or egg proteins are on the ingredients list, they say.

There's a long list of vaccine ingredients that are potential allergens: besides the infectious agents themselves, there are those from hen's egg, horse serum, baker's yeast, numerous antibiotics, formaldehyde and lactose, as well "inadvertent" ingredients such as latex. People's allergic histories have to be taken before vaccination say the researchers. But some signs of reaction don't show up until after the shot.

The public health nurse or GP might tell patients that a long-lasting swelling around the injection site after a vaccine is a normal reaction, for example. But that is not what the immunologists say. "[A]luminum sensitization manifests as nodules [hard lumps] at the injection site that often regress after weeks or months, but may persist for years." In such cases, they say, a patch test can be done to confirm sensitivity and to avoid vaccination.

According to a growing body of research, though, allergy may be only the beginning of many dangerous aluminum-induced phenomena.

THE TROUBLE WITH ALUMINUM

Aluminum has been added to vaccines since about 1926 when Alexander Glenny and colleagues noticed it would produce better antibody responses in vaccines than the antigen alone. Glenny figured the alum was inducing what he called a "depot effect" – slowing the release of the antigen and heightening the immune response. For 60 years his theory was accepted dogma. And over the same time, the vaccine schedule grew decade on decade, but few ever questioned the effects of injecting aluminum into the body, which is strange considering its known toxicity.

A PubMed search on aluminum and "toxicity" turns up 4,258 entries. Its neurotoxicity is well documented. It affects memory, cognition, psychomotor control; it damages the blood brain barrier, activates brain inflammation, depresses mitochondrial function and plenty of research suggests it is a key player in the formation of the amyloid "plaques" and tangles in the brains of Alzheimer's patients. It's been implicated in Amyotrophic Lateral Sclerosis and autism and demonstrated to induce allergy.

When kidney dialysis patients were accidentally infused with aluminum, the "dialysis-induced encephalopathy" (DAE) they developed neurological symptoms: speech abnormalities, tremors, memory loss, impaired concentration and behavioural changes. Many of the patients eventually went into comas and died. The lucky ones survived: when the source of toxicity, aluminum, was removed from their dialysis they recovered rapidly.

With these new observations, researchers began investigating the adjuvant effects of aluminum and in the past decade there has been a flurry of research. Far from being a sandbag that holds the antigen for a while and then gets excreted, it turns out that aluminum salts trigger a storm of defence action. Within hours of injection of the same aluminum oxyhydroxide in vaccines into mice, for example, armies of specialized immune cells are on the move, calling in grid coordinates for more specialist assault forces. Within a day, a whole host of immune system commandos are in play -- neutrophils, eosinophils, inflammatory monocytes, myeloid and dendritic cells, activating lymphocytes and secreting proteins called cytokines. The cytokines themselves cause collateral damage but they send out signals, directing cell-to-cell communication and recruiting other cells into action. If the next phase of the attack is launched: fibroblast growth factor, interferons, interleukins, platelet derived growth factor, transforming growth factor and tumour necrosis factor might all be engaged. There's evidence that poorly understood and pesky inflammasomes, (currently a topic of cutting- edge cancer causation research) such as the Nod-like receptor 3( NLRP) are activated too, but it's all still too early to say exactly what they're doing.

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Rid,
Your thread will benefit if you let other side to speak too. If you just delete what others are writing, how would it be a discussion?

some postings were deleted cause they didnt bother to back their argument with proof or rather post from mainstream media sources(which act as the voice of the pharmaceutical industry). I have provided Facts not opinions

@rid

i hope you have done a through research on this topic if you say u r correct.. i totally go against you you are simply wrong my friend. I just hope your research is not based on documentaries and commercial videos. Vaccines are important to humans.. very important. heard of measles polio hepatitis outbreak? yes they were real and millions of people had to suffer from that just because they didn't had this vaccines. Yes vaccines used diff chemicals like Hg and animal product like pigs intestine duodenum but remember human body in itself is chemically formed. i would not be able to give u all the vast details on the topic but if i would def urge u to give ur children all the vaccines when they r born. i don't want any parent to regret because of it in future.