Studien, die von den US-Behörden und pharmahörigen Medien unterdrückt werden:
– Zusammenhänge zwischen Impfungen und Autismus
– Quecksilber als Verdummungsprogramm zur IQ-Absenkung
– absichtliche Vergiftung unserer Kinder seit Jahrzehnten zur Profiterhöhung [der Pharma-Aktionäre als Premium-Regelsatz für die Elite]
Das zeigt: Ein Arzt, der impft, ist kein Arzt mehr, sondern nur noch Mediziner, Pharma-Außenstelle!
50 Studien, die die AAP vergessen hat zu erwähnen!
Die AAP (American Academy of Pediatrics – Kinderärzte) schrieben am 07.02.2017 einen Protestbrief an Präsident Trump, der dabei ist, mit Robert F. Kennedy Jr. eine Untersuchungskommission über Impfstoff-Sicherheit einzurichten.
In dem Brief heißt es, daß die Impfstoffe sicher seien und die Behauptungen der Impfkritiker durch Studien widerlegt worden seien.
Offenbar ist der Brief der AAP leicht als unbegründet und leichtfertig zu widerlegen, denn hier sind 50 Studien, die die AAP vergessen hat dem Brief beizulegen und die belegen, daß Impfstoffe NICHT sicher sind:
200 evidenzbasierte peer-reviewed-Studien beweisen, daß die Impfstoffe nicht wie behauptet, sicher und wirksam sind. Warum werden diese Studien von RKI und CDC ignoriert?
Alles in einer 351-Seiten-pdf-Datei zum kostenlosen Download!
Einführung:
http://www.greenmedinfo.com/blog/200-evidence-based-reasons-not-vaccinate-free-research-pdf-download
Download:
https://impfen-nein-danke.de/u/gmipub_58635_anti_therapeutic_action_vaccination_all.pdf
Studie belegt: SSPE-Gehirnentzündung (Enzephalitis) durch Masernimpfung!
Hier Studien, die den Zusammenhang zwischen Impfungen und Alzheimer-Erkrankung belegen!
Abstracts of 90 studies compiled by Sandy Gottstein confirming the dangers of thimerosal!
Yale-Studie belegt Zusammenhang zwischen Impfungen und Hirnerkrankungen! Besprechung von RFK Jr.!
Miller’s Review of Critical Vaccine Studies 400 Important Scientific Papers Summarized for Parents and Researchers
———————–
Millers Übersichtsarbeit kritischer Impfstudien. 400 wichtige wissenschaftliche Arbeiten, zusammengefaßt für Eltern und Forscher
Foto: Miller, New Atlantean Press, fair use.
Kommentar von Dr. Joseph Mercola vom 02.07.2017.
Neil z. Miller in US-Ärztezeitschrift: Es gab nie klinische Studein zur Sicherheit von Impfstoffen und keien Daten über synergistische Toxizität, die öffentlichen Impfempfehlungen beruhen nicht wissenschaftlichen Beweisen:
“Conclusion: The safety of CDC’s childhood vaccination schedule was never affirmed in clinical studies. Vaccines are administered to millions of infants every year, yet health authorities have no scientific data from synergistic toxicity studies on all combinations of vaccines that infants are likely to receive. National vaccination campaigns must be supported by scientific evidence. No child should be subjected to a health policy that is not based on sound scientific principles and, in fact, has been shown to be potentially dangerous.”
– zit. nach: Journal of American Physicians and Surgeons (JPANS), Volume 21, Number 2, Summer 2016, pp. 47-49, Hervorh. von uns.
Narkolepsie (Dauerschläfrigkeit) durch Schweinegrippe-Impfstoff Pandemrix
[in Schweden als Impfschaden anerkannt]
Narcolepsy Associated with Pandemrix Vaccine
Affiliations
PMID: 29855798 DOI: 10.1007/s11910-018-0851-5
2013: Studiensammlung von Educate4theInjured
“There are unanswered questions about vaccine safety, no one should be threatened by the pursuit of this knowledge.”
– Bernadine Healy, former director National Insitutes of Health (NIH), and current health editor US News and World Report
Educate others in honor of the ones Injured by vaccines. WE can make a difference! Knowledge is Power! I made this page for mothers like me, who want the facts, and nothing but. Researching takes HOURS and HOURS and no other site had them compiled for me without paying. So please help our mission out and DONATE TODAY!!! But even if you cant, remember I will always provide this info for the sake of the CHILDREN!
We MUST be the voice for the children! ALL VACCINES ARE CONTAMINATED.
The only variable is the EXTENT of Damage! STOP accepting allergies (skin, food, environmental), asthma, adhd, and SIDS as coincidence or normal.
Dissect the literature> ignore the studies funded by companies who have financial gain in vaccines!
“Repeated immunization with antigen causes systemic autoimmunity in mice otherwise not prone to spontaneous autoimmune diseases. Overstimulation of CD4+ T cells led to the development of autoantibody-inducing CD4+ T (aiCD4+ T) cell which had undergone T cell receptor (TCR) revision and was capable of inducing autoantibodies.” “Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s immune ‘system’ by repeated immunization with antigen, to the levels that surpass system’s self-organized criticality.”
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795160/
“Vaccine-type rotavirus was detected in all 50 antigen-positive specimens and 8 of 8 antigen-negative specimens. Nine (75%) of 12 EIA-positive and 1 EIA-negative samples tested culture-positive for vaccine-type rotavirus. Fecal shedding of rotavirus vaccine virus after the first dose of RV5 occurred over a wide range of post-vaccination days not previously studied.”
http://www.ncbi.nlm.nih.gov/pubmed/21477676
• Effectiveness of trivalent inactivated influenza vaccine in influenza-related hospitalization in children: a case-control study.
“Using the Cochran-Mantel-Haenszel test for asthma status stratification, there was a significant association between hospitalization in asthmatic subjects and TIV (p = 0.001). TIV did not provide any protection against hospitalization in pediatric subjects, especially children with asthma. On the contrary, we found a threefold increased risk of hospitalization in subjects who did get the TIV vaccine. This may be a reflection not only of vaccine effectiveness but also the population of children who are more likely to get the vaccine.” Allergy Asthma Proc. 2012 Mar-Apr;33(2):e23-7.
http://www.ncbi.nlm.nih.gov/pubmed/22525386
• “The odds of having a history of asthma was twice as great among vaccinated subjects than among unvaccinated subjects The odds of having had any allergy-related respiratory symptom in the past 12 months was 63% greater among vaccinated subjects than unvaccinated subjects”
http://www.ncbi.nlm.nih.gov/pubmed/10714532
• “Conclusions (THE ONLY THING THAT SHOULD MATTER) There are significantly elevated risks of primarily emergency room visits approximately one to two weeks following 12 and 18 month vaccination. Future studies should examine whether these events could be predicted or prevented.”
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236196/
• Administration of thimerosal to infant rats increases overflow of glutamate and aspartate in the prefrontal cortex: protective role of dehydroepiandrosterone sulfate. http://www.ncbi.nlm.nih.gov/pubmed/22015977
• Lasting neuropathological changes in rat brain after intermittent neonatal administration of thimerosal. “These findings document neurotoxic effects of thimerosal, at doses equivalent to those used in infant vaccines or higher, in developing rat brain, suggesting likely involvement of this mercurial in neurodevelopmental disorders” http://www.ncbi.nlm.nih.gov/pubmed/21225508
• FEDERAL COURT CASE – BAILEYS PERVASIVE DEVELOPMENTAL DISORDER/ASD
“the MMR vaccine at issue actually caused the condition(s) from which Bailey suffered and continues to suffer”
http://www.generationrescue.org/resources/vaccination/vaccine-related-court-cases/bailey-banks/
• “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”.
http://www.cidd.psu.edu/research/synopses/acellular-vaccine-enhancement-b.-parapertussis
• “Our data suggests that the current schedule of acellular pertussis vaccine doses is insufficient to prevent outbreaks of pertussis.” http://cid.oxfordjournals.org/content/early/2012/03/13/cid.cis287.short
• “Our unvaccinated and under-vaccinated population did not appear to contribute significantly to the increased rate of clinical pertussis. Surprisingly, the highest incidence of disease was among previously vaccinated children in the eight to twelve year age group.” http://www.ncbi.nlm.nih.gov/pubmed/22423127
• HIGH PITCHED SCREAMING AFTER VACCINATION {VERY COMMON}
http://boards.babyzone.com/high-pitched-screaming-after-vaccines-t8348610.html
THERE ARE OTHER UNINTENDED VIRUSES IN VACCINES AND WE HAVE SEEN THIS OVER AND OVER
• Investigations of porcine circovirus type 1 (PCV1) in vaccine-related and other cell lines. “Porcine circovirus type 1 (PCV1) is highly prevalent in swine and was recently reported in some rotavirus vaccines.” 011 Oct 26;29(46):8429-37. Epub 2011 Aug 9. http://www.ncbi.nlm.nih.gov/pubmed/21835219?dopt=Abstract
• ABORTED FETAL CELLS- “In some cases the cell lines (aborted fetal cells) that are used might be tumorigenic, that is, they form tumors when injected into rodents. Some of these tumor-forming cell lines may contain cancer-causing viruses that are not actively reproducing. Such viruses are hard to detect using standard methods. These latent, or “quiet,” viruses pose a potential threat, since they might become active under vaccine manufacturing conditions.” WOULD YOU RISK THIS ON YOUR CHILD????
http://www.fda.gov/biologicsbloodvaccines/scienceresearch/biologicsresearchareas/ucm127327.htm
• ‘Xenotropic murine leukemia virus-related virus (XMRV) is a recently discovered human retrovirus that has been found in both chronic fatigue syndrome & prostate cancer patients. There is a potential safety concern regarding XMRV in cell substrates used in vaccines…’ http://www.fda.gov/biologicsbloodvaccines/scienceresearch/biologicsresearchareas/ucm127327.htm
NO aborted fetal DNA IS SAFE TO INJECT!!!!
23 vaccines today contain them.
• “It is known from gene therapy studies that injected naked DNA can be transported to the brain (Wang et al. 2001); that improperly integrated therapeutic DNA has caused cancer in young children (Hacein-Bey-Abina et al. 2008); and that shorter DNA fragments have a higher probability of entering the nucleus [of the cells] (Lechardeur et al. 2002)”, noted Dr Theresa whose company recently received a $500,000 grant from the Murdock foundation for their research.
• “Changepoint analysis of autism disorder demonstrates a temporal correlation with events associated with human DNA residuals in vaccines. The levels of residual DNA are well over FDA-recommended limits”, stated Dr Deisher.
“Meruvax-II contains >140ng/vial ssDNA and >30ng/vial dsDNA, with average lengths of 215bp. Havrix contains >270ng/vial ssDNA and >30ng/vial dsDNA. The FDA-recommended amounts are 10ng/dose.”
http://www.cogforlife.org/scpiautismstudypress.htm
• “Unvaccinated children tended to be white, to have a mother who was married and had a college degree, to live in a household with an annual income exceeding $75,000 dollars, and to have parents who expressed concerns regarding the safety of vaccines and indicated that medical doctors have little influence over vaccination decisions for their children.”
http://www.ncbi.nlm.nih.gov/pubmed/15231927
• “Although persons often use vaccination and immunization interchangeably in reference to active immunization (VACCINES), the terms are not synonomous because the administration of an immunobiologic cannot be automatically equated with the development of adequate immunity.”
http://www.cdc.gov/mmwr/PDF/rr/rr4301.pdf
• “Hib immunization contributed to an increased risk for H. influenzae type a meningitis through selection of circulating H. influenzae type a clones.” ” the incidence for H. influenzae type a meningitis increased 8-fold”
http://jid.oxfordjournals.org/content/187/1/109.full.pdf+html
• “Virus-induced autoimmunity may play a causal role in autism. To examine the etiologic link of viruses in this brain disorder, we conducted a serologic study of measles virus, mumps virus, and rubella virus. Viral antibodies were measured by enzyme-linked immunosorbent assay in the serum of autistic children, normal children, and siblings of autistic children. The level of measles antibody, but not mumps or rubella antibodies, was significantly higher in autistic children as compared with normal children (P = 0.003) or siblings of autistic children (P <or= 0.0001).
Furthermore, immunoblotting of measles vaccine virus revealed that the antibody was directed against a protein of approximately 74 kd molecular weight. The antibody to this antigen was found in 83% of autistic children but not in normal children or siblings of autistic children. Thus autistic children have a hyperimmune response to measles virus, which in the absence of a wild type of measles infection might be a sign of an abnormal immune reaction to the vaccine strain or virus reactivation.“
http://www.ncbi.nlm.nih.gov/pubmed/12849883
• “Thus vaccination DOES NOT account for the impressive declines in mortality seen in the first half of the century”
http://pediatrics.aappublications.org/content/106/6/1307.abstract
Annual Summary of Vital Statistics: Trends in the Health of Americans During the 20th Century Guyer, et al. American Academy of Pediatrics 2000; 106:6 1307-1317
“However, in 2001, the vaccine was found to cause a serious, frequently fatal, multisystemic illness, called yellow fever vaccine–associated viscerotropic disease (YEL-AVD), which resembles the illness it was designed to prevent (1–3). “
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3310656/
“Our findings show a positive correlation between the number of vaccine doses administered and the percentage of hospitalizations and deaths. Since vaccines are given to millions of infants annually, it is imperative that health authorities have scientific data from synergistic toxicity studies on all combinations of vaccines that infants might receive. “
Maternal transfer of mercury to the developing embryo/fetus: is there a safe level?
“This study focused on standardized embryonic and fetal Hg exposures via primary exposure to the pregnant mother of two common Hg sources (dietary fish and parenteral vaccines). Data demonstrated that Hg exposures, particularly during the first trimester of pregnancy, at well-established dose/weight ratios produced severe damage to humans including death. ” Toxicological & Environmental Chemistry Vol 94 2012
http://www.tandfonline.com/doi/full/10.1080/02772248.2012.724574
“reporting bias was too low to explain the magnitude increase in fetal-demise reporting rates in the VAERS database relative to the reported annual trends. Thus, a synergistic fetal toxicity likely resulted from the administration of both the pandemic (A-H1N1) and seasonal influenza vaccines during the 2009/2010 season.”
http://www.ncbi.nlm.nih.gov/pubmed/23023030
“Hepatitis B vaccine might be followed by various rheumatic conditions and might trigger the onset of underlying inflammatory or autoimmune rheumatic diseases. “
http://www.ncbi.nlm.nih.gov/pubmed/10534549
“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 anti bodies, 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.”
http://www.ncbi.nlm.nih.gov/pubmed/12145534
Myocarditis, Pericarditis, and Dilated Cardiomyopathy after Smallpox Vaccination among Civilians in the United States, January–October 2003
“We describe an association between smallpox vaccination, using the US vaccinia strain, and myo/pericarditis among civilians.”
“Most civilian vaccine recipients (75%) and case patients with myo/pericarditis (86%) were revaccinees. In contrast, Arness et al. found a 7.46 unadjusted risk among primary vaccinees in the US military and suggest that their findings support a causal relationship between smallpox vaccination and myo/pericarditis only among primary vaccinees.”
“Given the now-documented association between smallpox vaccine and myo/pericarditis, it is biologically plausible that the 3 case patients who we identified may have been the result of the progression of vaccinia-induced myocarditis to DCM.”
http://cid.oxfordjournals.org/content/46/Supplement_3/S242.abstract
FULL TEXT HERE
• “According to Hippocratic tradition, the safety level of a preventive medicine must be very high, as it is aimed at protecting people against diseases that they may not contract. This paper points out that information on the safety of hepatitis B vaccine (HBV) is biased as compared to classical requirements of evidence-based medicine (EBM), as exemplified by a documented selectivity in the presentation or even publication of available clinical or epidemiological data. Then, a review is made of data suggesting that HBV is remarkable by the frequency, the severity and the variety of its complications, some of them probablyrelated to a mechanism of molecular mimicry leading to demyelinating diseases, and the others reproducing the spectrum of non-hepatic manifestations of natural hepatitis B. To be explained, this unusual spectrum of toxicity requires additional investigations based upon complete release of available data.”
http://www.ncbi.nlm.nih.gov/pubmed/15722255
FULL TEXT http://www.educate4theinjured.org/#/pdf-full-text-studies/4568262801
• “Although there is no information regarding the duration of acceptable observation period, 1–3 months may not be long enough for the purpose, considering that it takes 2–6 months for adjuvant oils to induce lupus autoantibodies in mice [8,9,34] and that the oil-induced granulomatous inflammation can last for years.”
“An important factor to consider in vaccine-induced autoimmunity is the fact that vaccines contain a microbial component (or other type of antigens) and adjuvant [75]. Differentiating adverse reactions caused by these two factors is often difficult, or it can even be a result of the combination of both. Nevertheless, the microbial components are generally considered responsible for adverse reactions and minimum attention has been paid to the potential effects of the adjuvant component. Molecular mimicry of a microbial antigen in a vaccine and a host tissue self-antigen is often considered important [61]. Immune complexes also may be formed following vaccination [61,76], deposit in vascular endothelium and induce vasculitis. Induction of cytokines or shifting cytokine balance may also play an important role.”
http://www.ncbi.nlm.nih.gov/pubmed/15194169
FULL TEXT http://www.educate4theinjured.org/#/pdf-full-text-studies/4568262801
• “We find that ethylmercury not only inhibits mitochondrial respiration leading to a drop in the steady state membrane potential, but also concurrent with these phenomena increases the formation of superoxide, hydrogen peroxide, and Fenton/Haber-Weiss generated hydroxyl radical. These oxidants increase the levels of cellular aldehyde/ketones. Additionally, we find a five-fold increase in the levels of oxidant damaged mitochondrial DNA bases and increases in the levels of mtDNA nicks and blunt-ended breaks. Highly damaged mitochondria are characterized by having very low membrane potentials, increased superoxide/hydrogen peroxide production, and extensively damaged mtDNA and proteins. These mitochondria appear to have undergone a permeability transition, an observation supported by the five-fold increase in Caspase-3 activity observed after Thimerosal treatment.”
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395253/
FULL TEXT http://www.educate4theinjured.org/#/pdf-full-text-studies/4568262801
NOW THE FAMOUS LINE PROVAXXERS USE “MERCURY ISN’T IN VACCINES ANYMORE” EVEN THOUGH IT IS IN SOME (flu shots especially) WHO CARES ABOUT MERCURY LETS FOCUS ON THE ALUMINUM ADJUVANT.
• “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” http://www.ncbi.nlm.nih.gov/pubmed/21568886
Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration.
“Possible causes of GWS include several of the adjuvants in the anthrax vaccine and others. The most likely culprit appears to be aluminum hydroxide. In an initial series of experiments, we examined the potential toxicity of aluminum hydroxide in male, outbred CD-1 mice injected subcutaneously in two equivalent-to-human doses. After sacrifice, spinal cord and motor cortex samples were examined by immunohistochemistry. Aluminum-treated mice showed significantly increased apoptosis of motor neurons and increases in reactive astrocytes and microglial proliferation within the spinal cord and cortex. Morin stain detected the presence of aluminum in the cytoplasm of motor neurons with some neurons also testing positive for the presence of hyper-phosphorylated tau protein, a pathological hallmark of various neurological diseases, including Alzheimer’s disease and frontotemporal dementia. A second series of experiments was conducted on mice injected with six doses of aluminum hydroxide. Behavioural analyses in these mice revealed significant impairments in a number of motor functions as well as diminished spatial memory capacity. The demonstrated neurotoxicity of aluminum hydroxide and its relative ubiquity as an adjuvant suggest that greater scrutiny by the scientific community is warranted.”
http://www.ncbi.nlm.nih.gov/pubmed/19740540
Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations
“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 Aluminum 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.”
http://www.ncbi.nlm.nih.gov/pubmed/22235057
• Influence of pediatric vaccines on amygdala growth and opioid ligand binding in rhesus macaque infants: A pilot study
“In this pilot study, infant macaques receiving the recommended pediatric vaccine regimen from the 1990’s displayed a different pattern of maturational changes in amygdala volume and differences in amygdala-binding of [11C]DPN following the MMR/DTaP/Hib vaccinations between T1 and T2 compared with non-exposed animals. There was also evidence of greater total brain volume in the exposed group prior to these vaccinations suggesting a possible effect of previous vaccinations to which these animals had been exposed. Because primate testing is an important aspect of pre-clinical vaccine safety assessment prior to approval for human use (Kennedy et al. 1997), the results of this pilot study warrant additional research into the potential impact of an interaction between the MMR and thimerosal-containing vaccines on brain structure and function.”
http://www.ane.pl/pdf/7020.pdf
Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure- Entropy 2012, 14(11), 2227-2253; doi:10.3390/e14112227
“Autism is a condition characterized by impaired cognitive and social skills, associated with compromised immune function. The incidence is alarmingly on the rise, and environmental factors are increasingly suspected to play a role. This paper investigates word frequency patterns in the U.S. CDC Vaccine Adverse Events Reporting System (VAERS) database. Our results provide strong evidence supporting a link between autism and the aluminum in vaccines.
A literature review showing toxicity of aluminum in human physiology offers further support. Mentions of autism in VAERS increased steadily at the end of the last century, during a period when mercury was being phased out, while aluminum adjuvant burden was being increased. Using standard log-likelihood ratio techniques, we identify several signs and symptoms that are significantly more prevalent in vaccine reports after 2000, including cellulitis, seizure, depression, fatigue, pain and death, which are also significantly associated with aluminum-containing vaccines. We propose that children with the autism diagnosis are especially vulnerable to toxic metals such as aluminum and mercury due to insufficient serum sulfate and glutathione. A strong correlation between autism and the MMR (Measles, Mumps, Rubella) vaccine is also observed, which may be partially explained via an increased sensitivity to acetaminophen administered to control fever.”
http://www.mdpi.com/1099-4300/14/11/2227
FULL TEXT http://www.educate4theinjured.org/#/pdf-full-text-studies/4568262801
“These findings are consistent with the hypothesis that immunization with the recombinant hepatitis B vaccine is associated with an increased risk of MS, and challenge the idea that the relation between hepatitis B vaccination and risk of MS is well understood. “
http://www.neurology.org/content/63/5/838.abstract
“Hepatitis B vaccination does not “generally” increase the risk of CNS inflammatory demyelination in childhood. However, the Engerix B vaccine appears to increase this risk, particularly for confirmed multiple sclerosis, in the longer term.”
http://www.ncbi.nlm.nih.gov/pubmed/18843097
Vaccinations create more powerful and virulent strains of bacteria and viruses. The reason for the current whooping cough outbreak. Read more here from the CDC
“Vaccination against 2 avian viruses, the Marek disease virus, and the infectious bursal disease virus, were associated with the emergence of more virulent strains (33). An important role of host immunity in selecting for virulence is also suggested by the co-evolution of the myxomatosis virus and rabbits (34). Furthermore, immune pressure was shown to select for more virulent Plasmodium chabaudi parasites in mice (35). Based on mathematical modeling, vaccines designed to reduce pathogen growth rate and/or toxicity may result in the evolution of pathogens with higher levels of virulence (36).”
http://wwwnc.cdc.gov/eid/article/15/8/08-1511_article.htm
“A majority of the ophthalmological complications seen following hepatitis B vaccination consist of vision loss, optic neuritis, papillary edema, uveitis, acute placoid pigment epitheliopathy and central vein occlusion. We present a 9-year-old girl who was referred to our hospital with decrease in vision and pain in the left eye a week after hepatitis B vaccination. A diagnosis of vaccine induced optic neuritis was made.”
http://www.ncbi.nlm.nih.gov/pubmed/19948437
FULL TEXT http://www.educate4theinjured.org/#/pdf-full-text-studies/4568262801
WHAT DOES THIS SAY ABOUT THE VACCINATED POPULATIONS HEALTH?
“Most high-risk medical conditions that were measured were more prevalent among vaccinated than among unvaccinated persons.”
http://www.nejm.org/doi/pdf/10.1056/NEJMoa070844
