Showing posts with label WHO. Show all posts
Showing posts with label WHO. Show all posts

Friday, October 19, 2018

BILL GATES et al., POLIO VACCINES, DDT, PARALYSIS, MONKEY VIRUSES, CANCER & AIDS...


Bill Gates and his minions have embarked on a global murderous crusade to "vaccinate every child under 5" in the world with the oral polio vaccine (OPV) which has been BANNED in the US since 2000 because it was found & proven to CAUSE poliomyelitis paralysis!

In fact, in 1992 the CDC publicly admitted that every case of poliomyelitis paralysis in the US since the early 1960’s was CAUSED by the oral polio vaccine (OPV) used in the US from the early 1960’s to 2000! And as far back as 1976, Dr Salk publicly admitted under testimony that the OPV used in the US from the early 1960’s to 2000 was “the principal if not the sole cause” of all poliomyelitis paralysis cases in the US since 1961.

So WHY are you Bill Gates and your minions (i.e. GAVI, GPEI, CDC, WHO, UNICEF, ROTARY et al) forcefully vaccinating hundreds of millions/billions of children around the globe with the oral polio vaccine which has been BANNED in the US in 2000 because it was found & proven to CAUSE poliomyelitis paralysis ????????

Read the following paper for details on the criminal, poisonous & murderous oral polio vaccination scam and the global oral polio vaccination campaign funded, spearheaded and literally forcefully shoved down the throats of hundreds of millions/billions of newborns, children and infants worldwide by Bill Gates and his criminal minions:


Arya Vril-ya


Sunday, July 22, 2018

VACCINES CAUSE BRAIN INJURIES, NEUROLOGICAL DISORDERS AND AUTISM



Vaccines trigger a "cytokine storm" of the immune system, leading to severe and permanent neurological disorders, brain injuries and autism.

As vaccinepapers.org writes:

The term “immune activation” describes the activation of the cellular components of the immune system. The developing brain can be injured by immune activation, with life-long consequences (Meyer 2009, Deverman 2009, Estes 2016, neusel 2014, Careaga 2017, Meyer 2014). Immune activation injury is linked to autism, schizophrenia, depression and other mental illnesses or neurodevelopmental disorders. Immune activation effects on the brain are mediated by immune system signaling molecules, especially cytokines (Estes 2016, Meyer 2014, Smith 2007, Choi 2016, Pineda 2013).

Human brain development is controlled by immune-system signals (i.e. “cytokines”). Activation of the immune system during brain development causes disruptions in these signals, resulting in permanent brain injury. The injury manifests as autism, schizophrenia and other mental illnesses. Adverse vaccine reactions are proven to stimulate a cytokine (interleukin-6) proven to cause autism.

In the maternal immune activation experiments, inflammatory signaling and some cytokines (e.g. IL-6) traverse the placenta into the fetus. Consequently, immune activation in the mother causes immune activation and elevated cytokines in the fetus, and in the fetal brain (Oskvig 2012, Ghiani 2011).

Diverse evidence indicates that the brain can be adversely affected by postnatal immune activation. Postnatal immune activation experiments, human case reports, and consideration of brain development timelines suggest that the human brain is vulnerable to immune activation injury for years after birth.

Postnatal immune activation can have adverse neurological effects, including increased seizure susceptibility (Chen 2013,Galic 2008), learning and memory deficits (Harre 2008), and an increase in excitatory synapse formation (Shen 2016). Seizure disorders, learning and memory dysfunction, and elevated excitatory signaling are associated with autism.

The timing of brain development processes in humans supports the idea that the human brain is vulnerable to immune activation and cytokines in the first few years after birth, when vaccines are administered. Disruption of synaptogenesis by vaccine induced immune activation is a particular concern. The accumulating evidence indicates that vaccine-induced immune activation, and aluminum adjuvants in particular, may cause mental illnesses and neurodevelopmental disorders, including autism.

Link to the paper: vaccinepapers.org/review-paper-al-adjuvant-autism-20-pages-97-references/



Wednesday, July 04, 2018

ALUMINIUM & MERCURY (THIMEROSAL) IN CHILDHOOD VACCINES LINKED TO NEUROLOGICAL DISORDERS AND AUTISM


Peer-reviewed studies that found a causal link between aluminium in childhood vaccines and severe neurological disorders including autism: 

Link: http://thinktwice.com/studies_aluminum.htm

Also read the following brief papers on the neurotoxicity of aluminium in vaccines:

Link: http://www.jpands.org/vol21no4/miller.pdf 

Link: http://thinktwice.com/aluminum.pdf

Highest Level of Aluminium Found in Brain of Autistic Children (Study)

The following recently published landmark and highly alarming peer-reviewed study has found the highest levels of aluminium in the brain of 5 autistic children:  

Link: http://info.cmsri.org/aluminum-and-your-health-blog/study-finds-some-of-the-highest-values-for-aluminium-in-human-brain-tissue-yet-recorded-in-brains-of-autistic-patients

CDC childhood vaccine schedule linked to neurological disorders and autism 


The 2017 US CDC (Centre for Disease CREATION and PROMOTION) vaccine schedule requires U.S. children from birth to age 6 to receive 50 doses of 14 vaccines, many of which contain both neurotoxic aluminium and mercury (thimerosal)! Infants in the US are exposed from birth to age 2, to 24 vaccine doses, combining 8-in-1 vaccines to be given to infants 2, 4, and 6 months in a single visit! Babies receive 36 vaccine doses before they are 18 months old! 

THIS IS CRIMINAL INSANITY & STATE-SANCTIONED MEDICAL MURDER OF NEWBORNS, INFANTS AND CHILDREN!

Link to CDC vaccine ingredients: https://www.cdc.gov/vaccines/vac-gen/additives.htm

Link to CDC vaccine schedule: https://www.nvic.org/CMSTemplates/NVIC/pdf/49-Doses-PosterB.pdf

Exponential increase in autism rates in US children linked to CDC vaccine schedule  


In 1985, the autism prevalence rate in the US was 1 in 2,500; in 1995 it was 1 in 500; In 2014 it was 1 in 45! In children aged 3 to 17, the autism prevalence rate increased by 80% from 2011-2013! At this rate, it is predicted that 1 out of 2 children in the US will have autism by 2030!

A report by EPA scientists Timing of Increased Autism Disorder Cumulative Incidence analyzed the cumulative incidence of autistic disorder during a 10-year period (1987–1996) pinpointed a sharp “changepoint” year (1988) when the incidence of autism sharply increased. The “changepoint” year is concomitant with the year childhood vaccination schedules expanded.  
Source: http://ahrp.org/disconnect-between-evidence-cdc-claims-re-childhood-vaccination-schedule/


Causal link between mercury (thimerosal) contained in vaccines, neurological disorders and autism

Scientific research and CDC internal documents on the toxicity of mercury (thimerosal) in vaccines reveal exposure to thimerosal during the first month of life increased the relative risk of autism by 7.6 (760%), 1.8 (180%) increased relative risk for a neurodevelopmental disorder; 2.1 (210%) relative risk for speech disorder; and 5-fold (500%) increased relative risk for a nonorganic sleep disorder. CDC also suppressed the original findings of another of its own studies that found a 340% (3.6) relative increased risk of autism for African American male babies following MMR vaccination in accordance with the CDC-recommended Childhood Vaccination Schedule.

The alarming and damning scientific evidence documents that infants exposed to vaccines laced with thimerosal during the first month of life are at alarmingly high increased the relative risk of serious harm. “The data on its toxicity (shows) it can cause neurologic and renal toxicity, including death," writes Dr. Richard Johnston, M.D., an immunologist and pediatrician from the University of Colorado.

Dr. Verstraeten also said: “what I will present to you is the study that nobody thought we should do.” The study categorized the cumulative effect of thimerosal-containing vaccines administered to infants after one month of life and assessed the subsequent risk of degenerative and developmental neurologic disorders, and renal disorders before the age of six. Dr. Verstraeten stated that ALL of these relative risks were statistically significant.
Source: http://ahrp.org/betrayal-of-public-trust-institutional-corruption-vaccine-safety-ratings-vaccine-science-falsified/


Additional published peer-reviewed studies that found a causal link between childhood vaccines containing mercury (Thimerosal) and neurological disorders including autism: 

Link: http://thinktwice.com/studies_autism.htm

Synergistic Toxicity of Aluminium & Thimerosal in Vaccines

Dr. Boyd Haley, former professor of medicinal chemistry and chairman of the chemistry department at the University of Kentucky, published a study in which he investigated the effect of combining aluminum hydroxide with thimerosal. In this study, cultured neurons showed no significant cell death six hours after they were exposed to just aluminum; more than 90% survived. Thimerosal alone also caused few neurons to die after six hours of exposure. Again, more than 90% survived. However, when cultured neurons were exposed to aluminum and thimerosal, only about 40% survived after six hours, clearly demonstrating synergistic toxicity (Figure 3). Source: http://www.jpands.org/vol21no4/miller.pdf

As Neil Miller writes:

" Millions of children every year are injected with vaccines containing mercury and aluminum despite well-established experimental evidence of the potential for additive or synergistic toxicity when an organism is exposed to two or more toxic metals. Dr. Haley’s study in which cultured neurons died at an accelerated rate following concurrent exposure to aluminum and thimerosal provides evidence of an enhanced detrimental effect. In addition, aluminum toxicity levels published by FDA indicate that two-month-old babies who are vaccinated according to CDC guidelines may be receiving quantities of aluminum that are significantly higher than safety levels."

Statements from Prominent & Eminent Medical Doctors & Scientists on the Toxicity of Aluminium in Childhood Vaccines:


Conclusion:

Both neurotoxic aluminium and mercury (thimerosal) contained in multiple doses of childhood vaccines as well as the CDC vaccine schedule cause severe and permanent neurological disorders including autism in newborns, infants and children!

When will the US sanctioned Vaccine Holocaust of newborns, infants and children end ???????????????

Arya Vrilya








Monday, May 14, 2018

EPA (Flawed) Draft Human Health and Ecological Risk Assessments for Glyphosate.


The US EPA has finally completed its (pseudo) Draft Human Health and Ecological Risk Assessments for Glyphosate. Tragically but unsurprisingly, the EPA (Every Poison Allowed) concludes that glyphosate is not likely to be carcinogenic to humans; the EPA writes:

"The Agency’s assessment found no other meaningful risks to human health when the product is used according to the pesticide label. The Agency’s scientific findings are consistent with the conclusions of science reviews by a number of other countries as well as the 2017 National Institute of Health Agricultural Health Survey.

EPA’s human health review evaluated dietary, residential/non-occupational, aggregate, and occupational exposures. Additionally, the Agency performed an in-depth review of the glyphosate cancer database, including data from epidemiological, animal carcinogenicity, and genotoxicity studies.

The ecological risk assessment indicates that there is potential for effects on birds, mammals, and terrestrial and aquatic plants. EPA used the most current risk assessment methods, including an evaluation of the potential effects of glyphosate exposure on animals and plants. Full details on these potential effects as well as the EPA’s methods for estimating them, can be found within the ecological risk assessment."

However, Beyond Pesticides has written a damning letter to the EPA highlighting and explaining the numerous and blatant scientific flaws that plague the EPA's pseudo risk assessment of glyphosate. As Beyond Pesticides write in their concluding remarks:

" However, the EPA has taken a myopic approach to its risk assessment. As debate surrounds glyphosate’s cancer classification and overall safety, the agency fails to consider actual product formulations that present exposures to the public. People are questioning whether the Roundup products they buy at the local garden store and sprayed on their food can increase their risk of cancer. EPA’s human health assessment does NOT answer this question. 

EPA chose to ignore the wealth of evidence that show glyphosate-formulated products are more toxic then glyphosate alone. This evidence shows formulated products lead to cell death, potential endocrine disruption, liver damage, and cancer. On the contrary, EPA’s ecological assessment does find it relevant to include glyphosate formulations in assessing exposures to non-target organisms, which affirms the higher toxicity of formulated products.

We urge the agency to hasten its collaboration with the US National Toxicology Program (NTP) to evaluate glyphosate formulations and their impacts on human health. Until such assessments are completed, this human health assessment should be interpreted with caution as its findings are misleading and incomplete. Given glyphosate’s association with increased weed resistance, making it harder and more expensive for farmers to farm, habitat loss, and water contamination, uses of glyphosate must be restricted." 

NTP Research Plan

" NTP is currently pursuing glyphosate and glyphosate formulations research. Human exposure to glyphosate usually occurs in the form of glyphosate-based formulations. Few studies have made side-by-side comparisons of the toxicity of glyphosate and glyphosate-based formulations using the same experimental protocols and endpoints. Also, there have been few direct comparisons of the toxicity of different glyphosate products.

Many existing studies of glyphosate and glyphosate-based formulations have focused on whether they induce DNA damage (genetic toxicity) and/or oxidative stress, as both are mechanisms that contribute to carcinogenesis (Smith et al., 2016).

As part of the research plan, NTP will use in vitro and in vitro approaches to further investigate whether glyphosate and glyphosate-based formulations can induce genetic toxicity and/or oxidative stress. Furthermore, NTP will use a transcriptomics (changes in gene expression) approach in vitro to examine whether any other biological perturbations are caused by the test articles. This research effort to interrogate key outcomes will aid interpretation of the existing literature on glyphosate and glyphosate-based formulations. " Link: https://ntp.niehs.nih.gov/resul…/areas/glyphosate/index.html

Mike DeVito, acting chief of the National Toxicology Program Laboratory, told the Guardian the agency’s work is ongoing but its early findings are clear on one key point. “We see the formulations are much more toxic. The formulations were killing the cells. The glyphosate really didn’t do it,” DeVito said. A summary of the NTP work stated that glyphosate formulations decreased human cell “viability”, disrupting cell membranes. Cell viability was “significantly altered” by the formulations, it stated.

Monsanto has never tested the toxicity of its Roundup "secret" formulation

Internal emails from Monsanto reveal that Monsanto never tested the toxicity of Roundup; In a 2003 internal Monsanto email, Monsanto's lead toxicologist Donna Farmer wrote: “You cannot say that Roundup is not a carcinogen … we have not done the necessary testing on the formulation to make that statement. The testing on the formulations are not anywhere near the level of the active ingredient.” Another Monsanto internal email written in 2010 stated: “With regards to the carcinogenicity of our formulations we don’t have such testing on them directly.” And an internal Monsanto email from 2002 stated: “Glyphosate is OK but the formulated product … does the damage.” Source: https://www.theguardian.com/…/weedkiller-tests-monsanto-hea…

The EPA's final decision for the re-approval of glyphosate/Roundup/GBH in the US is due in 2019.

 The battle continues...

Arya Vrilya

Sunday, February 25, 2018

POISONOUS CHILDHOOD VACCINES = MEDICAL MURDER!


 VACCINE INGREDIENTS:

Aborted human fetal DNA (human-diploid fibroblast cell cultures strain WI-38, MRC-5 human diploid cells), animal DNA (swine, bovine, chicken, etc.), fetal bovine and calf serum (cow/calf blood), human serum albumin (human blood), dog & monkey kidney cells, VERO cells (a continuous line of monkey kidney cells), African Green Monkey kidney (Vero) cells, Gelatine (bovine or porcine derived), Formaldehyde (cancer-causing chemical), Aluminium phosphate, aluminium hydroxyde, aluminium sulfate (brain damaging neurotoxins), Mercury (Thimerosal - neurotoxin linked to autism and neurological damage in children), SV40 (a cancer-causing monkey virus found in oral polio vaccines and human tumors; also linked to the HIV-AIDS virus), polysorbate 80 (used in pharmacology to open the brain-blood barrier; also used to embalm dead corpses), alcohols, anti-foaming agent, 2-phenoxyethanol (antifreeze), etc. (list not exhaustive) ☠️☠️☠️☠️
See following CDC link for a complete list of vaccine ingredients: https://www.cdc.gov/vaccines/vac-gen/additives.htm
Does any SANE person believe that injecting multiple doses of poisonous cocktails of highly toxic chemical poisons, brain-damaging neurotoxins, cancer-causing viruses and chemicals, animal viruses, bacteria, blood, DNA, filth, etc. into fetuses, newborns, infants and children are required to purportedly protect them against infectious diseases (+50 doses of 14 vaccines by the age 6 in the US!) ??????? 🤔
The 2017 CDC (Centre for Disease CREATION and PROMOTION) vaccine schedule requires U.S. children from birth to age 6 to receive 50 doses of 14 vaccines! Infants in the US are exposed from birth to age 2, to 24 vaccine doses, combining 8-in-1 vaccines to be given to infants 2, 4, and 6 months in a single visit! Babies receive 36 vaccine doses before they are 18 months old! www.nvic.org/CMSTemplates/NVIC/pdf/49-Doses-PosterB.pdf
Injecting fetuses, newborns, infants and children with multiples doses of highly toxic and poisonous vaccine cocktails that contain both live and "inactivated" viruses, bacteria, animal DNA, blood and filth, brain-damaging neurotoxic aluminium and autism-causing ethyl mercury (thimerosal), cancer-causing formaldehyde and other poisons and filth to purportedly prevent infectious diseases - caused largely if not solely by environmental factors such as poor nutrition, unclean water, toxic environments, poor sanitation, poor hygiene, etc. - is INSANE and MEDICAL MURDER!!!!  

And vaccines undermine and destroy the immune system of fetuses, newborns, infants and children opening the floodgates to infectious and chronic diseases, leading to an endless vicious murderous cycle of vaccinations and infectious diseases...

Moreover, the immune system of fetuses, newborns, infants and children is too immature to fight off the cocktail of poisons and filth contained in vaccines; to use an analogy, it's like sending fetuses, newborns, infants and children to fight a real war on the battlefield with trained adult soldiers and weapons of war to train and prepare them to become soldiers!

When will the CRIMINAL MADNESS, MASS MURDER and VACCINE HOLOCAUST of fetuses,  newborns, infants and children end ??????????????????????????????????????????
Arya Vrilya :-(


#vaccines #CDC #VaccineHolocaust #NAZI #GAVI

DEL BIG TREE & ROBERT F. KENNEDY: CONTROLLED OPPOSITION


Robert F. Kennedy and Del BigTree's "vaccine safety" campaign is a Trojan horse

All those who blindly follow and trust Del Bigtree and Robert F. Kennedy in the anti-vaccine movement are being led to the slaughterhouse; they can all thank Bigtree and Kennedy the day the HHS/Alex Azar rubber stamps all vaccines as "safe" and the US govt mandates and forcefully injects hundreds of millions of pregnant women, fetuses, newborns, infants, children and adults alike with hundreds of "safe" vaccines waiting in the pipeline (+250 as of 2017)...

Read details below at the following links:

DEL BIGTREE'S LEGAL NOTICE TO THE SECRETARY OF THE HHS FOR "SAFE" VACCINES (AN OXYMORON): http://yajnacentre.blogspot.ca/2017/12/del-bigtree-is-threatening-to-sue-us.html


ROBERT F. KENNEDY LOBBYING FOR "VACCINE SAFETY" (AN OXYMORON):
http://yajnacentre.blogspot.ca/2017/12/robert-f-kennedy-lobbying-for-vaccine.html

As Lenin stated: "The best way to control the opposition is to lead it ourselves." (Modus Operandi for Big Pharma)

Arya Vrilya

 

#DelBigTree #RobertFKennedy #HHS #AlexAzar #Vaccines #CDC #ICAN #NCVIA #Congress #VaccineSafety #VaccineHolocaust

CDC VACCINE SCHEDULE & VACCINES LACED WITH MERCURY (Thimerosal) LINKED TO SPIKE IN AUTISM



Exponential increase in autism rates in US children linked to CDC vaccine schedule 

In 1985, the autism prevalence rate in the US was 1 in 2,500; in 1995 it was 1 in 500; In 2014 it was 1 in 45! In children aged 3 to 17, the autism prevalence rate increased by 80% from 2011-2013! At this rate, it is predicted that 1 out of 2 children in the US will have autism by 2030!

A report by EPA scientists Timing of Increased Autism Disorder Cumulative Incidence analyzed the cumulative incidence of autistic disorder during a 10-year period (1987–1996) pinpointed a sharp “changepoint” year (1988) when the incidence of autism sharply increased. The “changepoint” year is concomitant with the year childhood vaccination schedules expanded.  
Source: http://ahrp.org/disconnect-between-evidence-cdc-claims-re-childhood-vaccination-schedule/


Mercury (thimerosal) contained in childhood vaccines has also been proven to cause autism. 

Scientific research and CDC internal documents on the toxicity of mercury (thimerosal) in vaccines reveal exposure to thimerosal during the first month of life increased the relative risk of autism by 7.6 (760%), 1.8 (180%) increased relative risk for a neurodevelopmental disorder; 2.1 (210%) relative risk for speech disorder; and 5-fold (500%) increased relative risk for a nonorganic sleep disorder. CDC also suppressed the original findings of another of its own studies that found a 340% (3.6) relative increased risk of autism for African American male babies following MMR vaccination in accordance with the CDC-recommended Childhood Vaccination Schedule.

The alarming and damning scientific evidence documents that infants exposed to vaccines laced with thimerosal during the first month of life are at alarmingly high increased the relative risk of serious harm. “The data on its toxicity (shows) it can cause neurologic and renal toxicity, including death," writes Dr. Richard Johnston, M.D., an immunologist and pediatrician from the University of Colorado.

Dr. Verstraeten also said: “what I will present to you is the study that nobody thought we should do.” The study categorized the cumulative effect of thimerosal-containing vaccines administered to infants after one month of life and assessed the subsequent risk of degenerative and developmental neurologic disorders, and renal disorders before the age of six. Dr. Verstraeten stated that ALL of these relative risks were statistically significant.
Source: http://ahrp.org/betrayal-of-public-trust-institutional-corruption-vaccine-safety-ratings-vaccine-science-falsified/

The alarming and damning evidence presented in this paper should be used to sue the industry and their criminal minions i.e., CDC, World Health Organization (WHO), UNICEF, Gavi, the Vaccine Alliance, Bill & Melinda Gates Foundation, Bill Gates, Melinda Gates et al. for Crimes Against Humanity and Genocide.

Arya Vrilya





Saturday, November 25, 2017

NO, THE ZIKA VIRUS DOES NOT CAUSE MICROCEPHALY!


There is not an iota of evidence in the scientific and medical literature of a causal relationship between the Zika virus and microcephaly, contrary to the deceitful and fraudulent claims made by both Tom Frieden/CDC and Margaret Chan/WHO. Furthermore, out of the 404 diagnosed cases of microcephaly in Brazil, the virus has purportedly been found in the tissues of less than 15 babies (0.034%), which does not prove causality let alone correlation.

According to the medical literature, microcephaly is caused by:

- Craniosynostosis: The premature fusing of the joints (sutures) between the bony plates that form an infant's skull keeps the brain from growing.

- Chromosomal abnormalities. Down syndrome and other conditions may result in microcephaly.

- Decreased oxygen to the fetal brain (cerebral anoxia). Certain complications of pregnancy or delivery can impair oxygen delivery to the fetal brain.

- Infections of the fetus during pregnancy. These include toxoplasmosis, cytomegalovirus, German measles (rubella) and chickenpox (varicella).

- Exposure to drugs, alcohol or certain toxic chemicals in the womb. Any of these put your baby at risk of brain abnormalities.

- Severe malnutrition. Not getting adequate nutrition during pregnancy can affect your baby's development.

- Uncontrolled phenylketonuria, also known as PKU, in the mother. PKU is a birth defect that hampers the body's ability to break down the amino acid phenylalanine.
Source: http://www.mayoclinic.org/…/micr…/basics/causes/con-20034823

In fact, in the US there are on average 25,000 diagnosed cases of microcephaly every year (in the absence of the Zika virus). Moreover, although the virus has been widely diagnosed in neighboring Colombia and in both French polynesia and Micronesia, there has been no diagnosed cases of microcephaly in those countries. This further proves that microcephaly is not caused by the Zika virus.

Many independent researchers have linked the “spike” of microcephaly in Brazil (from 147 diagnosed cases in 2014 to 404 in 2015) to a number of plausible factors such as the GM mosquitoes released in the region, the Tdap vaccine administered to pregnant women in late 2014, larvicides (pyriproxyfen) added to the public drinking water supply, and birth-causing pesticides such as glyphosate/Roundup, atrazine, 2,4-D, etc. copiously sprayed in GM soy/crop plantations in Brazil (note: Brazil is the largest consumer of pesticides in the world).

Although it is highly plausible that a synergistic combination of the above factors could be responsible for the “spike” of microcephaly in Brazil, there is to my knowledge no evidence in the scientific and medical literature of any causal relationship between the GM mosquitoes, the Tdap vaccines, the larvicide pyriproxyfen and microcephaly. Further epidemiological studies and research is clearly needed to confirm the causal relationship between the above plausible factors and microcephaly.

Pesticides, birth-defects and microcephaly

On the other hand, there is ample documented evidence in the scientific and medical literature of a causal relationship between pesticides such as glyphosate/Roundup, atrazine, 2,4-D, etc. and various birth defects, including microcephaly: http://www.beyondpesticides.org/…/pesticide-i…/birth-defects

In fact, birth defects and microcephaly are ubiquitous in regions and villages surrounding GM soy plantations in both Brazil and Argentina. In 2010, Dr. Andre Carrasco from Argentina published an alarming paper on the causal relationship between glyphosate based herbicides (GBH) and birth defects.

Dr Carrasco alarmingly found and wrote: “The direct effect of glyphosate [on the embryos]… opens concerns about the clinical findings from human offspring in populations exposed to GBH [glyphosate-based herbicides] in agricultural fields. There is growing evidence raising concerns about the effects of GBH on people living in areas where herbicides are intensely used. Women exposed during pregnancy to herbicides delivered offspring with congenital malformations, including microcephaly, anencephaly [missing major parts of brain and skull in embryos], and cranial malformations.” Link to the paper: http://www.gmwatch.org/imag…/pdf/Carrasco_research_paper.pdf

Unsurprisingly, however, neither the WHO/Margaret Chan, the CDC/Tom Frieden nor the Brazilian and global so-called public health authorities ever mention the causal relationship between GBH and microcephaly. It is blatantly obvious that the WHO/CDC deceitful and fraudulent Zika-microcephaly propaganda is manufactured for the sole purpose of promoting and selling the soon-coming concocted (toxic) Zika vaccine and to further mass poison both the Brazilian and the global population with the ongoing massive spraying of poisonous insecticides/pesticides under the guise and pretext of eradicating the WHO/CDC/industry invented Zika-microcephaly causing mosquitoes while enriching Big Pharma, the biotech/pesticide industry and their minions.

Arya Vrilya
Founder & Executive Director
Yajna Centre

Wednesday, October 04, 2017

THE ZIKA-MICROCEPHALY HOAX IS A REPLAY OF THE MURDEROUS DDT-POLIO SHAM


DDT-POLIO


1946-1955: Mass DDT spraying campaigns across the US to purportedly kill mosquitoes (fraudulently) blamed for carrying the polio virus and causing poliomyelitis paralysis. Mass DDT spraying campaign ended up CAUSING the poliomyelitis paralysis epidemic in the US in the 1950's.

In response, Big Pharma developed and administered over 100 million doses of the polio vaccine to children and pregnant women in the US, which CAUSED millions of cases of poliomyelitis paralysis in the US!

In 1992, the CDC publicly admitted that every case of poliomyelitis paralysis in the US since the early 1960's was CAUSED by the oral polio vaccine (OPV) used in the US from the early 1960's to 2000! Moreover, as far back as 1976, Dr Salk publicly admitted under testimony that the OPV used in the US from the early 1960's to 2000 was "the principal if not the sole cause" of all poliomyelitis paralysis cases in the US since 1961.

Read this paper for details about the murderous DDT-POLIO hoax: https://www.academia.edu/34215258/BILL_GATES_et_al._POLIO_VACCINES_DDT_PARALYSIS_MONKEY_VIRUSES_and_CANCER

ZIKA-MICROCEPHALY HOAX (2015)


70 years later, Big Pharma and their criminal political minions i.e. CDC, WHO et al. are using the EXACT same murderous script with the ZIKA-MICROCEPHALY hoax.

- Mosquitoes (fraudulently) blamed for carrying the zika virus.

- Zika virus (fraudulently) blamed for causing microcephaly.

- Mass land and aerial spraying campaigns conducted in the US and worldwide by the US govt to purportedly kill zika-carrying mosquitoes using neurotoxic chemicals (i.e. NALED, a neurotoxic nerve gas developed and used by the NAZI's during WW2 for chemical warfare) that have been proven to CAUSE neurological brain damage in fetuses, newborns and children including MICROCEPHALY!

Jennifer Sass PhD, senior scientist with Natural Resources Defense Council warned that Naled is a neurotoxin and “among the class of the most toxic pesticides.” According to Dr. Sass, pregnant women are the most at risk because Naled “would damage the neurological development of fetuses.” Moreover, Dr. Elvia Melendez-Ackerman, environmental biologist at the University of Puerto Rico’s Rio Piedras says: "Studies have shown that exposure of pregnant animals for just three days during brain development resulted in 15% smaller brains in their babies."

Naled is 20 times more toxic when exposure occurs through inhalation versus ingestion. Alarmingly, the CDC has mandated and carried out aerial sprayings of Naled over Miami in 2016 to purportedly kill mosquitoes carrying the zika virus. Naled is banned in the European Union due to its extreme toxicity for both human health and the environment. 

Big Pharma is now developing a zika vaccine (using $ BILLIONS from the public purse) which will likely CAUSE a spike in microcephaly and other neurological brain damage in fetuses, newborns and children, which will then conveniently but fraudulently be blamed on the mosquitoes, further poisoning fetuses, newborns, children, pregnant women and the global population with global mandatory zika vaccination campaigns, leading to an endless and murderous cycle of global zika vaccination campaigns and a global epidemic of microcephaly and other neurological brain damage in children worldwide.

You can read this paper for more details about the Zika-Microcephaly hoax: https://www.academia.edu/34216411/NO_THE_ZIKA_VIRUS_DOES_NOT_CAUSE_MICROCEPHALY

Arya Vrilya

Saturday, August 12, 2017

BILL GATES et al., POLIO VACCINES, DDT, PARALYSIS, MONKEY VIRUSES AND CANCER



Summary
Polio vaccines contaminated with cancer-causing monkey virus (SV40)
In 2007, the US Centre for Disease Control and Prevention (CDC) alarmingly admitted that between 1955–1963 over 98 million American children and pregnant women received one or more doses of a polio vaccine which was found to be contaminated with a cancer-causing monkey virus called Simian Vacuolating 40 (SV40).
SV40 found in several human cancers.

In 1961, the virus was found to cause tumors in rodents (Eddy et al., 1961) The SV40 virus was also found in several types of tumors in humans, for instance mesotheliomas (rare tumors located in the lungs), brain, and bone tumors (Carbone et al., 1994; Jasani et al., 2001). More recently, SV40 has also been found to be associated with some types of non-Hodgkin's lymphoma (Shivapurkar et al., 2002; Vilchez et al., 2002).

SV40 was linked with mesothelioma after tumors developed in hamsters that were injected with SV40 into the lungs, heart and abdomen (Cicala et al., 1993). Mesotheliomas are rare cancers usually located in the lining of the lungs in humans and are believed to be associated with asbestos exposure. SV40 has been found in 47% to 83% of human mesothelioma tumors (Carbone, 1999). In addition, reports have documented an association between SV40 and brain and bone tumors (Jasani, 2001). Two recent studies also found an association between SV40 and non-Hodgkin's lymphoma (Shivapurkar et al., 2002; Vilchez et al., 2002). These studies identified the virus in 42 to 43 percent of non-Hodgkin's tumors, while finding no SV40 in tissue from healthy study volunteers.

The CDC and the industry claim that the SV40 virus was removed from all polio vaccines after 1963. However, recent published studies as well as legal documents from a court case filed against the manufacturer of the vaccine (Lederle) reveal that SV40 was not removed from the oral polio vaccines after 1963. Over 600 million doses of the oral polio vaccines were manufactured and sold by Lederle in the US and around the globe between 1963-2000.
Oral Polio Vaccine found to CAUSE polio and poliomyelitis paralysis!
Moreover, In 2000 the CDC discontinued and banned the sale and the use of the OPV in the US because it was found to cause both vaccine-derived polio viruses (VDPVs) and vaccine-associated paralytic poliomyelitis (VAPP).
A paper published in 2004 by prominent and eminent vaccine researcher and author Neil Z. Miller [11] reveals that: “In 1992, the US Center for Disease Control and Prevention (CDC) published an admission that the live polio virus vaccine (OPV) had become the dominant cause of polio in the United States. In fact, according to CDC figures, every case of polio in the U.S. since 1979 was caused by the oral polio vaccine. As far back as 1976, "Dr. Jonas Salk, creator of the killed-virus polio vaccine (IPV) used in the 1950s, testified that the live-virus polio vaccine (used almost exclusively in the U.S. from the early 1960s to 2000) was the ‘principal if not sole cause’ of all reported polio cases in the U.S. Since 1961.”
DDT caused poliomyelitis paralysis in the US
Historical and recent scientific evidence alarmingly reveals a causal link between the mass DDT spraying campaigns launched in the US from 1946-1955 to purportedly combat the polio virus before the polio vaccines were developed and the epidemic of poliomyelitis paralysis that followed.
In light of the alarming and damning historical and scientific evidence presented in this paper on the extreme toxicity, human health hazards and inefficacy of the polio vaccines (both the IPV and the OPV), why are you Bill GatesMelinda Gates, the Bill & Melinda Gates FoundationUNICEF, the World Health Organization (WHO), the Global Polio Eradication InitiativeRotary International and the CDC forcefully vaccinating hundreds of millions/billions of children and their mothers around the globe without their informed consent and often under military escort and at gun point with the SV40-contaminated and cancer-causing oral polio vaccine (OPV) which has been discontinued and banned in the US since 2000 because it was found and proven to cause both vaccine-associated paralytic poliomyelitis (VAPP) and vaccine-derived polioviruses (VDPVs) ?
Link to my paper: https://www.academia.edu/34215258/BILL_GATES_et_al._POLIO_VACCINES_DDT_PARALYSIS_MONKEY_VIRUSES_and_CANCER


Wednesday, May 25, 2016

HUMAN HEALTH RISKS RESULTING FROM ROUNDUP RESIDUES IN OUR FOOD AND WATER



HUMAN HEALTH RISKS RESULTING FROM ROUNDUP RESIDUES IN OUR FOOD AND WATER
The WHO-FAO Joint Meeting on Pesticide Residues (JMPR) - the arm of the WHO that determines and sets the so-called "safe" level of pesticide residues allowed on our food, water, etc. - has declared that glyphosate/Roundup is unlikely to cause cancer through pesticide residues in our food. The summary report from the JMPR is available at this link:http://www.who.int/foodsafety/jmprsummary2016.pdf?ua=1
Source: http://www.reuters.com/…/us-health-who-glyphosate-idUSKCN0Y…
Monsanto and regulatory agencies in the US (EPA), EU (EFSA) and in Canada (Health Canada) are attempting to discredit and to dismiss the recent WHO/International Agency for Research on Cancer (IARC) credible and alarming classification of glyphosate as a "probable human carcinogen” by arguing that a health hazard is not a health risk, because - they erroneously argue - a health risk is based on the level of human exposure to glyphosate/Roundup.
However, both glyphosate, Roundup and each one of its "secret" co-formulants have alarmingly been found to be endocrine disrupting chemicals (EDCs) which are extremely toxic to human health at low doses.
As the following paper explains:
" The endocrine disrupting effect of glyphosate and its commercial formulations (i.e. Roundup) is their most insidious and worrying toxic effect. This is because EDC's do not function like normal poisons, where a higher dose gives greater toxicity. Often, endocrine disruptive effects are seen at lower doses but not at higher doses. The studies conducted by industry for regulatory purposes use relatively high doses and are not able to detect these effects.
Endocrine disruption in humans is thought to contribute to some cancers, birth defects, reproductive problems such as infertility, and developmental problems in foetuses, babies, and children.
Under European law, pesticides that disrupt hormones (“endocrine disrupting chemicals” or EDCs) are not allowed to be marketed. Governments recognize the threat posed by endocrine disruption, which are believed to be implicated in serious diseases, such as cancer, reproductive and developmental problems, and birth defects. These effects are thought to result from very low doses over a long period of exposure or from exposures in critical windows of development, such as foetal development in the womb.
Alarmingly, professor Gilles-Éric Séralini and his team of researchers have recently found both glyphosate, Roundup as well as their "secret" co-formulants to be Endocrine Disrupting Chemicals (EDC).
Excerpts:
" A new study shows that the acceptable daily intake (ADI), the supposedly safe level, for glyphosate is unreliable in terms of assessing the risks of the complete commercial formulations that we are actually exposed to. The co-formulants were shown in the new study to have a far more powerful endocrine-disrupting effect at lower doses than the isolated active ingredient, glyphosate. The complete formulations (i.e Roundup) were also found to have much greater endocrine disrupting effects at lower doses than glyphosate alone.
The research shows that the ADI should be calculated from toxicity tests on the commercial formulations as sold and used. The new study is the first ever demonstration that the endocrine disrupting effects of glyphosate based herbicides (GBH) are not only attributable to glyphosate, the declared active ingredient, but above all to the co-formulants."
Link to the study: http://www.gmoseralini.org/new-research-shows-regulatory-s…/
As the following paper further explains:
" The so-called safe levels of glyphosate exposure have never been tested directly to determine if indeed they are really safe to consume over the long term. Instead the “safe” levels are extrapolated from higher doses tested in industry studies.
Industry toxicity study protocols are out of date. All toxicity tests conducted by industry for regulatory purposes are based on the old adage: “The dose makes the poison” – that is, the higher the dose, the greater the degree of toxicity. However, in some cases, low doses corresponding to human exposures can be more toxic than the higher doses tested in laboratory animals in industry studies.
This is especially true for chemicals that disrupt the hormonal system (endocrine disruptors). Safe levels of these chemicals cannot be extrapolated from effects at higher doses. Evidence from in vitro and animal experiments shows that glyphosate may be an endocrine disruptor at levels permitted in tap water in the EU.
Findings that glyphosate and its commercial formulations may be endocrine disruptors imply that the standard industry long-term animal studies are inadequate. These studies are conducted on adult animals, and fail to test the effects of exposure during important windows of development, such as foetal development.
Yet hormones are vital regulators of development. A subtle hormonal effect during early life can modify organ morphology and function for the rest of the life, as well as potentially leading to chronic diseases such as cancer and reproductive dysfunction in adults.
The complete glyphosate herbicide formulations as sold and used contain additives (adjuvants), which are toxic in their own right and/or increase the toxicity of glyphosate. Safety limits are set for the isolated ingredient glyphosate, but the whole formulations, which are generally more toxic, are never tested to determine long-term toxic effects.
This limitation of the regulatory process applies to all pesticides in all countries worldwide. Studies in rats confirm that the complete glyphosate herbicide formulations are toxic at levels deemed safe by regulators for the isolated ingredient glyphosate. Other feeding studies in pigs and rats directly comparing the toxicity of formulations with glyphosate alone found that the formulations were far more toxic.
Even glyphosate alone may not be as safe as claimed. Industry tests on glyphosate alone revealed toxic effects, notably birth defects, below the levels that regulators claimed showed no toxic effect – but these results were ignored or dismissed by regulators in setting the supposedly safe ADI
Independent studies have found toxic effects of glyphosate and its commercial formulations at environmentally realistic levels, which have never been tested by regulators. Effects include oxidative stress on liver and kidneys and endocrine disrupting effects.
These findings, taken as a whole, suggest that the levels of Roundup we are exposed to may not be safe over the long term."
Several other studies have also found both glyphosate and Roundup to be EDCs:
http://www.endocrinedisruption.org/…/tedx-l…/chemicalsearch…
Moreover, a Scientific Consensus Statement recently published by a number of prominent and eminent scientists states:
Abstract:
" Our Statement of Concern considers current published literature describing glyphosate based herbicides (GBH) uses, mechanisms of action, toxicity in laboratory animals, and epidemiological studies. It also examines the derivation of current human safety standards.
We conclude that: (1) GBHs are the most heavily applied herbicide in the world and usage continues to rise; (2) Worldwide, GBHs often contaminate drinking water sources, precipitation, and air, especially in agricultural regions; (3) The half-life of glyphosate in water and soil is longer than previously recognized; (4) Glyphosate and its metabolites are widely present in the global soybean supply; (5) Human exposures to GBHs are rising; (6) Glyphosate is now authoritatively classified as a probable human carcinogen; (7) Regulatory estimates of tolerable daily intakes for glyphosate in the United States and European Union are based on outdated science. (emphasis is mine)
We offer a series of recommendations related to the need for new investments in epidemiological studies, biomonitoring, and toxicology studies that draw on the principles of endocrinology to determine whether the effects of GBHs are due to endocrine disrupting activities.
We suggest that common commercial formulations of GBHs should be prioritized for inclusion in government-led toxicology testing programs such as the U.S. National Toxicology Program, as well as for biomonitoring as conducted by the U.S. Centers for Disease Control and Prevention."
Link to the Scientific Consensus Statement:http://ehjournal.biomedcentral.com/…/10.1…/s12940-016-0117-0
The Endocrine Society has also recently published an alarming (2nd) Scientific Statement on the toxicity of EDC's:
Excerpts:
This Executive Summary to the Endocrine Society's second Scientific Statement on environmental endocrine-disrupting chemicals (EDCs) provides a synthesis of the key points of the complete statement. The full Scientific Statement represents a comprehensive review of the literature (1300 studies) on seven topics for which there is strong mechanistic, experimental, animal, and epidemiological evidence for endocrine disruption, namely: obesity and diabetes, female reproduction, male reproduction, hormone-sensitive cancers in females, prostate cancer, thyroid, and neurodevelopment and neuroendocrine systems.
Scientific advances over the past 5 years (encompassing 1300 studies) reveal numerous EDC effects on obesity, diabetes, male and female reproduction (including cancer), the prostate and thyroid glands, and neurodevelopment. The past 5 years represent a leap forward in our understanding of EDC actions on endocrine health and disease."
Link to the complete Scientific Statement:http://www.healthandenvironment.org/partnership_calls/18015
Glyphosate Risk Assessment: Health Hazard vs Health Risk
Furthermore, the risk assessment of glyphosate/Roundup carried out by regulatory agencies is scientifically flawed for the reasons briefly explained below.
1) “The dose makes the poison”
The health hazards vs health risks assessment used by all regulatory agencies is scientifically flawed and invalid because regulators erroneously believe and argue that the “dose makes the poison.” However, toxicology peer-reviewed and published scientific research has shown that this belief is in many cases inaccurate and quite often the opposite is true (i.e. linear vs nonmonotonic dose-response curves) Study link:http://www.ncbi.nlm.nih.gov/pubmed/22419778
2) Active Principle (glyphosate) vs Formulation/product (Roundup)
Regulatory agencies only review the toxicity of the Active Principle alone (i.e. glyphosate) and not the whole product formulation (i.e Roundup) which contains other highly toxic and synergistic “secret” adjuvants. However, a recent landmark peer-reviewed and published study has alarmingly found Roundup and other pesticide formulations to be 125-1000 times more toxic than their declared Active Principle. The authors of the study alarmingly found and write:
“We tested the toxicity of 9 pesticides, comparing active principles and their formulations, on three human cell lines[...] Despite its relatively benign reputation, Roundup was among the most toxic herbicides and insecticides tested. Most importantly, 8 formulations out of 9 were up to one thousand times more toxic than their active principles. Our results challenge the relevance of the acceptable daily intake for pesticides because this norm is calculated from the toxicity of the active principle alone. Chronic tests on pesticides may not reflect relevant environmental exposures if only one ingredient of these mixtures is tested alone.”
Study Link: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955666/
EPA and EFSA recognize the toxicity of GBH formulations
Both the US Environmental Protection Agency (EPA) and the European Food Safety Authority (EFSA) have publicly recognized the toxicity of glyphosate based herbicides (GBH) formulations.
In its own risk assessment, the EPA publicly admits and states that it evaluated only the "human carcinogenic potential for the active ingredient," not that of "glyphosate-based pesticide formulations." The EPA acknowledges that the formulations may be more toxic than glyphosate and expresses the need to evaluate the toxicity of the entire formulation i.e. Roundup. The EPA is developing a “research plan” with the National Institute of Environmental Health Sciences to “evaluate the role of glyphosate in product formulations and the differences in formulation toxicity.”
Similarly, EFSA's risk assessment was based purely on the toxicity of glyphosate alone, not on the complete formulation; although EFSA acknowledged that one common ingredient in glyphosate based herbicides - POE-tallowamine - is more toxic than glyphosate itself, EFSA publicly admits and writes that the carcinogenic potential of GBH formulations "should be further considered and addressed."
3) Acceptable Daily Intake (ADI)
The WHO-FAO/JMPR and regulatory agencies worldwide determine and set the Acceptable Daily Intake (ADI) based exclusively on the Active Principle alone (AP) (i.e. glyphosate) and not on the product formulation (i.e. Roundup).
However, the actual product that is approved by regulatory agencies and copiously sprayed on our food crops, soil, water, air and environment is not only glyphosate (AP) but the whole product formulation (i.e. Roundup). This constitutes a flagrant flaw in the risk assessment of glyphosate/Roundup and a serious hazard to public health .
Roundup residues in food and water
Roundup residues have alarmingly been found in various common food items i.e. flour, bread, cereals, dairy, eggs, fruits, vegetables, wine, beers, etc., as well as in human urine, blood and breastmilk!
http://beyondpesticides.org/…/glyphosate-residues-found-in…/
Roundup is truly ubiquitous in our daily food supply, as the following recent investigative articles alarmingly reveal: http://www.truth-out.org/…/35919-not-just-for-corn-and-soy-…
http://www.huffingtonpost.com/…/fda-tests-confirm-oatmeal_b…
In fact, Roundup is not only used on GMO crops; it is also widely used as a dessicant to dry and kill non-GMO grain crops such as wheat, oats, barley, flax, etc. a few weeks before harvest; it is also copiously sprayed on nuts, lentils, peas, beans, potatoes, fruits and vegetables.
A preharvest weed control application is an excellent management strategy to not only control perennial weeds, but to facilitate harvest management and get a head start on next year’s crop,” according to a Monsanto “pre-harvest staging guide.” https://usrtk.org/…/Monsanto-application-guide-for-preharve…
Roundup is also present in our daily drinking water supply. A recently published study also found ultra-low dose exposure to Roundup in drinking water to adverse impacts on rat livers and kidneys:http://ehjournal.biomedcentral.com/…/10.1…/s12940-015-0056-1
Monsanto of course denies that glyphosate/Roundup residues in our food and water supply are dangerous to our health. "According to physicians and other food safety experts, the mere presence of a chemical itself is not a human health hazard. It is the amount, or dose, that matters," Monsanto senior toxicologist Kimberly Hodge-Bell said in the Monsanto blog; "trace amounts are not unsafe".
Source: http://www.reuters.com/…/us-food-agriculture-glyphosate-idU…
This statement by Kimberly Hodge-Bell and Monsanto is not supported by scientific evidence and is contradicted by the science of toxicology and endocrinology, as I have argued and demonstrated in this paper.
Therefore, it is fair to conclude that both the Risk Assessment and the ADI for glyphosate based herbicides (GBH) such as Monsanto's Roundup - as well as Monsanto's Xtend which combines both glyphosate and dicamba and Dow's Enlist Duo which combines both glyphosate and 2,4-D - are scientifically flawed and extremely hazardous to both our health and our lives since they expose us to high doses of endocrine disrupting chemicals (EDC) and other "secret" toxic chemical formulations present in the form of high pesticide residues in our food, water, soil, air, environment and bodies which seriously endangers both our health and our lives.
Toxic Food For Thought.
Arya Vrilya
National Health Federation (NHF)
Canada Representative

‪#‎Roundup‬ ‪#‎Glyphosate‬ ‪#‎Monsanto‬ ‪#‎GMO‬ ‪#‎FAO‬ ‪#‎WHO‬ ‪#‎JMPR‬‪#‎pesticides‬ ‪#‎EPA‬ ‪#‎EFSA‬ ‪#‎HealthCanada‬ ‪#‎Dow‬ ‪#‎Syngenta‬ ‪#‎BASF‬‪#‎BAYER‬