Saturday, December 22, 2018

"The most vital issue of the age is whether the future progress of humanity is to be governed by the modern economic and materialistic mind of the West or by a nobler pragmatism guided, uplifted and enlightened by spiritual culture and knowledge...

We must return and seek the sources of life and strength within ourselves. It is the spiritual revolution we foresee and the material is only its shadow and reflex. The world is in continuous evolution and there is a need to bring down a higher truth with each age.
The present evolutionary crisis comes from a disparity between the limited faculties of Man - mental, ethical and spiritual - and the technical and economic means at his disposal. 
Without an inner change, Man can no longer cope with the gigantic development of outer life. If humanity is to survive, a radical transformation of human nature is indispensable. Only spiritual realization and experience can achieve the change of the mental being into a spiritual being."
 Sri Aurobindo

A Tale of European Missionaries in Kenya...

"When the European missionaries came to Kenya, they had the Bible in their hands and we had our fertile lands.

When the European missionaries left Kenya, we had the bible in our hands and they had our fertile lands."
Jomo Kenyatta, Former PM & first President of the republic of Kenya



Wednesday, December 05, 2018

Les Gilets Jaunes et la Révolution française de 1789: L'Histoire se répète...



Un cahier de doléances 1789:
« Sire, nous sommes accablés d’impôts de toutes sortes ; nous vous avons donné jusqu’à présent une partie de notre pain, et il va bientôt nous manquer si cela continue. Si vous voyiez les pauvres chaumières que nous habitons, la pauvre nourriture que nous prenons, vous en seriez touché. Cela vous dirait mieux que nos paroles que nous n’en pouvons plus et qu’il faut nous diminuer nos impôts. Ce qui nous fait bien de la peine, c’est que ceux qui ont le plus de bien paient le moins. Nous payons la taille, et le clergé et la noblesse rien de tout cela. Pourquoi donc est-ce que ce sont les riches qui paient le moins et les pauvres qui paient le plus ? Est-ce que chacun ne doit pas payer selon son pouvoir ? Sire, nous vous demandons que cela soit ainsi, parce que cela est juste. »
Il faut décrypter cette révolte populaire charnière dans un contexte historique en remontant à la Révolution Française de 1789. Je ne suis pas historien de profession, mais ma lecture sur le sujet révèle que ce sont les franc-maçons français instrumentalisés et financés par les banquiers juifs (Rothchilds, etc.) qui ont planifié et financé clandestinement la Révolution française pour se débarasser de la monarchie en France dans le but de la remplacer, comme l'explique ce livre sur le sujet.

Le peuple s'est ensuite gréffé à la Révolution pour protester contre leurs conditions de vie misérables y compris la hausse du prix du pain. Hélas, la Révolution et l'abolition de la monarchie n'a pas profité au peuple français mais aux banquiers et à la cRasse politique et dirigeante française qui à ce jour exploitent la France et les Français à travers leurs fidèles marionnettes politiques comme Macron (ex-banquier des Rothchilds).

En effet, la révolte populaire des "gilets jaunes" est dans son essence une révolte populaire contre la cRasse politique et dirigeante française qui exploitent et appauvrissent sans cesse les Français et vivent dans l'opulence aux dépends de la classe moyenne laborieuse et ouvrière française...

L'Histoire se répète...

Révolution à suivre...

Arya Vril-ya






Tuesday, October 23, 2018

"MYSTERIOUS" PARALYZING ILLNESS CAUSED BY ENTEROVIRUSES OR BY NEUROTOXIC VACCINES ?

Photo: Geneviève Blais at the Montreal Children's Hospital diagnosed with AFM

A new “unknown” and “mysterious” paralyzing neurological illness named Acute Flaccid Myelitis (AFM) has been paralyzing young children across the US and Canada since 2014. According to the US CDC, there have been 368 registered cases of AFM since 2014; 149 cases were registered in 2016 alone (the highest number of cases in any single year) and 68 cases have been reported so far in 2018. 
 “AFM is a rare, but serious condition that affects the nervous system. It specifically affects the area of spinal cord called gray matter and causes muscles and reflexes to become weak. In most cases, the patient’s arms or legs become weak, similar to the results of infection with polio. In some cases, patients recover quickly. In other cases, patients remain paralyzed. There is a lot we don’t know about AFM, and I am frustrated that despite all of our efforts, we haven’t been able to identify the cause of this mystery illness," said Dr. Nancy Messonnier, director of the CDC’s National Center for Immunization and Respiratory Diseases.

According to the Public Health Agency of Canada, there were fewer than five cases reported in Canada between January and August 2018. However, over the last few weeks, more than 20 additional cases were alarmingly reported in Canada including 6 in Montréal, Québec.

In Septembre 2018, a four-year old Canadian girl from Québec (Geneviève Blais, pictured above) was diagnosed with AFM in Québec. Her treating physician Dr. Christos Karatzios, a Pediatric Infectious Diseases Specialist at Montréal Children's Hospital briefly explained the "mysterious" illness of his patient in the following television interviews: 

TV interview in French

TV interview in English 

In response to a question on his FB page about this “mysterious” paralyzing neurological illness, Dr. Karatzios wrote: 

" We are actually uncertain what exactly is causing it, but we suspect it to be an enterovirus - similar to polio virus (that is also an enterovirus but has been pretty much eradicated because of vaccination) We suspect enterovirus D68 or 71. We have not been able to easily isolate it from the spinal fluid and so we can only make an association when we isolate it in saliva or stool. Very similar clinical symptoms to polio but can be caught like a cold." 

In other words, there is no conclusive scientific evidence to confirm a causal relationship between the “suspected” enterovirus D68 or 71 and the “mysterious” crippling neurological illness (AFM) that is causing myelitis paralysis in young children. 

Enteroviruses or Neurotoxic Vaccines Causing Myelitis Paralysis ? 

I, in turn, asked Dr. Christos Karatzios whether this new “mysterious” paralyzing neurological illness could be caused by a long list of mandatory or recommended vaccines administered to newborns, infants and children that contain neurotoxic mercury (thimerosal) and/or aluminium which are extremely neurotoxic for the central nervous system and the developing brain of newborns, infants and children ?

In fact, several published scientific studies have found a causal relationship between vaccines that contain mercury and/or aluminium and neurological disorders in children and more specifically between vaccines and transverse myelitis. Moreover, the vaccines inserts CLEARLY list transverse myelitis as an adverse “side effect” of vaccines, as the following insightful paper and articles reveal:

Transverse myelitis and vaccines: a multi-analysis

https://www.learntherisk.org/news/paralysis-vaccines/?fbclid=IwAR2xLo7QS9GzotrQQEbh82GO5OHh8TR1wR7iEtK8BuoOgPHoHeqW5Yexpac

https://www.learntherisk.org/news/myelitis/

Polio Vaccines and Acute Flaccid Myelitis (AFM) 

Acute Flaccid Myelitis (AFM) is also an adverse "side effect" of the polio vaccine. In fact, over 47,500 children in India were paralyzed after being injected with the polio vaccine a few years ago. AFM, also known as Acute Flaccid Paralysis (AFP) or non-polio AFP (NPAFP), has been reported since 2014 as a “mysterious polio-like illness”.

In a paper published in the Indian Journal of Medical Ethics in 2012, Neetu Vashisht, MD and Jacob Puliya, MD wrote: “Clinically indistinguishable from polio paralysis but twice as deadly, the incidence of NPAFP was directly proportional to doses of oral polio vaccine received.”

Moreover, 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. 

Dr Karatzios, however, categorically denies that vaccines could be causing transverse myelitis in children by arguing that patients that he diagnosed with AFM had not been vaccinated 2 months prior to contracting the "mysterious" paralyzing illness.

In response, I argued that most neurological vaccine injuries often manifest several months or years after the administration of the vaccine; moreover, several published studies cited in the linked articles above have found a causal link between vaccine and transverse myelitis, including AFM. And last but not least, the vaccines inserts CLEARLY list transverse myelitis as an adverse “side effect” of several vaccines administered to children and adults alike.

Note: Dr. Karatzios has deleted both his FB post and our correspondence exchanged on his FB page.

Affaire à suivre... 

Arya Vril-ya

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


O CANADA: POISONED BREAD, BEER, CIRCUS AND POT...


Pot Minister Justin Trudeau célèbre et justifie la légalisation du cannabis au Canada pour (je cite) "protéger nos enfants..." 🤔
C'est tout le contraire! En effet, de nombreuses études scientifiques démontrent et prouvent que la consommation de cannabis est néfaste pour la santé et plus particulièrement pour le cerveau (en croissance) des jeunes enfants et des adolescents!
De plus, la légalisation du cannabis permettra à des millions de NOS enfants de s'en acheter légalement et d'en consommer facilement, ce qui aura pour effet d'augmenter exponentiellement la consommation de cannabis chez NOS jeunes enfants et adolescents! Et, Pot Minister Trudeau offrira bientôt des bonbons, des chocolats, des muffins, etc. au cannabis à NOS enfants et jeunes adolescents!
Et l'age légal de 18 ans n'empêchera pas les mineurs de s'en procurer; en effet, les ados de +18 ans pourront acheter et ensuite revendre le cannabis aux mineurs, faisant d'eux des 'dealers"...
Et la légalisation ne fera pas disparaître le marché noir, contrairement aux arguments stupides et trompeurs de Pot Minister Justin Trudeau (ils vendront tout simplement moins cher que le prix légal) et à la mission sociale de la SQDC dont le mandat est « d’aller chercher les parts du marché noir, sans faire croître le marché »
« La raison pour laquelle on fait la légalisation, c'est parce que, actuellement, dans l'ancien système, les enfants ont trop facilement accès au cannabis. On n’est pas en train de contrôler le cannabis parce qu’on pense que c’est bon pour la santé. Au contraire, on est en train de contrôler le cannabis parce qu’on sait que c’est pas bon pour nos enfants, c’est un produit qui n’est pas recommandé. Mais on sait que nous devons faire une meilleure job pour protéger nos enfants et éliminer ou réduire massivement les profits qui vont au crime organisé » explique Justin Trudeau 😵
Et bientôt Pot Minister Justin Trudeau offrira des céréales au cannabis pour le petit déjeuner matinal de NOS enfants, aspergées de Roundup cancérogènes (aussi légal au Canada) et accompagnées de lait américain bourré d' hormones de croissance de Monsanto...(interdites au Canada depuis 1999)😬
Pot Minister Justin Trudeau a vendu et sacrifié la santé, le bien-être et l'avenir de NOS enfants ainsi que le bien-être, la sécurité et l'avenir de la société dans son ensemble pour remplir les caisses de l'Etat et celles des entreprises privées...(entre autres)😠
O Canada: Poisoned bread, beer, circus and pot...
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





Betrayal of Public Trust & Institutional Corruption: Vaccine Safety Ratings & Vaccine Science Falsified


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 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 (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.

The alarming evidence contained in this landmark investigative work on the extreme toxicity of vaccines proves beyond the shadow of a doubt that vaccines are indeed maiming and prematurely killing newborns, children and adults alike!

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.


Link to the paper:  http://ahrp.org/betrayal-of-public-trust-institutional-corruption-vaccine-safety-ratings-vaccine-science-falsified/

Arya Vrilya

Saturday, February 10, 2018

OPEN LETTER TO PRIME MINISTER JUSTIN TRUDEAU REGARDING THE UNCONSTITUTIONAL AND FRAUDULENT BANKING POLICIES AND PRACTICES OF THE BANK OF CANADA.



“ Until the control and the issue of currency and credit is restored to government and recognized as its most conspicuous and sacred responsibility, all talk of sovereignty of Parliament and democracy is idle and futile. Once a nation parts with the control of its currency and credit, it matters not who makes the nation's laws. Usury, once in control, will wreck any nation.”  
~ William Lyon Mackenzie King, longest serving Prime Minister of Canada.

03 November, 2016

OFFICE OF THE PRIME MINISTER

Prime Minister Justin Trudeau
80 Wellington Street
Ottawa, Ontario K1A OA2
 

cc:  

Bill Morneau
Canadian Finance Minister
Ottawa, Canada

Stephen Poloz
Governor of the Bank of Canada
Ottawa, Canada

Prime Minister Justin Trudeau,

I am writing to you with reference to a landmark lawsuit filed against the government of Canada, The Bank of Canada, the Minister of Finance, the Attorney General of Canada, the Minister of National Revenue and the Queen by COMER – a Canadian economic think thank represented by constitutional lawyer Rocco Galati for "abdicating their statutory and constitutional duties with respect to article ss. 18 (i) and (j) of the Bank of Canada Act which stipulates that the Minister of Finance and the Government of Canada are required to request and the Bank of Canada is statutorily required to make interest-free loans for the purpose of human capital expenditures, infrastructure expenditures and federal, provincial and municipal expenditures." Details about the lawsuit can be found at www.comer.org

Both the COMER lawsuit as well as my personal research into the subject reveals that the Bank of Canada was constitutionally created as a public bank in 1938 and constitutionally mandated with the exclusive power and right to issue and loan the federal, provincial and municipal governments interest-free money for budgetary support, public infrastructure development and “human capital” expenditures such as education, health and other social programs.

Prior to 1938, Canada did not have a public bank. As a result, the government had to borrow money for government expenditures from private commercial banks at interest. The country's largest private commercial bank – the Bank of Montreal – was the government's de facto bank. However, on the eve of the Great Depression (1929), the interest on the government debt had reached an alarming one third of government expenditure. As a result, a Royal Commission was set up in 1933 to study the setting up of a Canadian public Central Bank to issue and loan interest-free money to the government for budgetary support and public expenditure.

In 1974 (under your late father Prime Minister Pierre E. Trudeau) the Bank of Canada became a member of the Bank for International Settlements (BIS)( an apex private central banking organization regrouping all private Central Banks around the world) which started dictating monetary, financial, fiscal, economic and budgetary policy in Canada. Furthermore, under the BIS, the Bank of Canada was forbidden to provide interest-free loans to the government, contrary to the Bank Act of 1938. 


Instead, the Canadian government started borrowing fiat money created ex nihilo (out of nothing) from private commercial banks at exorbitant compounded interest rates. As a direct result, the Canadian so-called "public debt" has since exponentially increased from $24 billion in 1974 (before the Bank of Canada joined the BIS) to over $600 billion in 2014. 
Source: www.qualicuminstitute.ca/federal-debt/

Furthermore, according to official statistics published by the Canadian Ministry of Finance, Canadian taxpayers paid $28.2 billion in compounded interest on the so-called "public debt" in 2014 alone, representing 10% of total government expenditure for 2014 ($271.7 billion), exceeding health and other social expenditures, employment insurance, children's benefits, Public Safety and National Defense. Source: http://www.fin.gc.ca/taxdollar/index-eng.asp

 
Public debt, budget deficits and austerity policies and measures
 

It is truly alarming and incomprehensible that you Prime Minister Justin Trudeau and your government are spending over $30 billion annually to pay the compounded interest on the “public debt,” while imposing deadly austerity measures on the Canadian public, slashing federal, provincial and municipal budgets and borrowing additional billions of dollars from private banks at compounded interest to fund infrastructure development and “human capital” expenditures such as education, health care and other public and social services!

Moreover, according to Paul Hellyer (the former Canadian Defense Minister and author of The Money Mafia: http://www.paulhellyerweb.com), Canadian taxpayers have paid over $ 1,100 billion ($1.1 TRILLION) in compounded interest payments on the “public debt” over the last 30 years from 1974-2004 (twice the current “public debt”!) With the current level of government debt ($ 611.9 billion/2014), Canadian taxpayers will pay another TRILLION dollars in compounded interest only over the next 20-25 years, ad infinitum...

Why should the government borrow fiat money created ex nihilo at exorbitant compounded interest rates from private commercial banks when it can create and issue its own currency interest-free...?

The obvious question that any sane and thinking person would ask you as Prime Minister of Canada and that I hereby ask you Justin Trudeau is why does the government have to borrow fiat money created ex nihilo from chartered private commercial banks at exorbitant compounded interest rates which hard-working Canadian taxpayers are coerced to repay through taxation, when the Bank of Canada Act of 1938 gives the Bank of Canada the constitutional mandate and the exclusive right, power and obligation to issue and loan money to the government for public infrastructure, human capital expenditures and budgetary support ?

In 1939, Mr Graham Towers – the first Governor General of the Bank of Canada from 1934 to 1954 - testified in front of the Canadian Government's Standing Committee on Banking and Commerce, during which he provided factual evidence and openly revealed much about the modus operandi of the private banking system in Canada.

In one question he was asked by the Committee:"Will you tell me why a government with power to create money, should give that power away to a private monopoly, and then borrow that which parliament can create itself, back at interest, to the point of national bankruptcy?" To which Mr Towers replied:"If parliament wants to change the form of operating the banking system, then certainly that is within the power of parliament" 

Source: http://www.michaeljournal.org/appenE.htm

I hereby ask you the same question as Prime Minister of Canada Justin Trudeau.

Last but not least, I wish to share with you a quote by the late Honourable Prime Minister William Lyon Mackenzie King on the dangers of surrendering and granting a monopoly of the Canadian money supply to private international central bankers:

“Until the control and the issue of currency and credit is restored to government and recognized as its most conspicuous and sacred responsibility, all talk of sovereignty of Parliament and democracy is idle and futile. Once a nation parts with the control of its currency and credit, it matters not who makes the nation's laws. Usury, once in control, will wreck any nation.”

I await your response.

Arya Vrilya
A very concerned Canadian citizen.