maanantai 6. toukokuuta 2019

CDC document bombshell reveals list of all vaccine excipients, including “African Green Monkey Kidney Cells” and fibroblast cells from aborted human fetuses

CDC lists all the excipients currently used in vaccines being injected into adults and children

Monday, March 06, 2017 by: 




(Natural News) Almost no one has any real idea what’s found in vaccines. When they allow themselves to be injected with vaccines, they’re oblivious to the fact that they are being injected with aborted human fetus cell lines or African Green Monkey kidney pus cells harvested from infected, disease primates. (See proof from the CDC, below.)
Yet, astonishingly, the CDC openly admits to all this (and more). In a PDF posted on the CDC website entitled “Vaccine Excipient & Media Summary,” the CDC lists all the excipients currently used in vaccines being injected into adults and children across the United States. The CDC’s list, current as of January 6, 2017, was “extracted from manufacturers’ package inserts,” according to the CDC.
The complete list is found in this CDC document (PDF). In case the CDC removes it — because they’ve been known to suddenly “memory hole” documents they don’t want the public to see — we’ve also posted a copy at the Natural News servers (PDF).
The WI-38 cell line is widely known to be “derived from lung tissue of an aborted white (caucasian) female fetus,” as even the pro-vaccine Wikipedia website admits. As the Coriell Institute for Medical Research explains about the MRC-5 cell line / WI-38:
The MRC-5 cell line was developed in September 1966 from lung tissue taken from a 14 week fetus aborted for psychiatric reason from a 27 year old physically healthy woman. The cell morphology is fibroblast-like. The karyotype is 46,XY; normal diploid male. Cumulative population doublings to senescence is 42-48. G6PD isoenzyme is type B.
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The human fetal tissue cells have become such an issue of outrage that even the Vatican has issued a statement concerning their use, in which they address, “vaccines containing live viruses which have been prepared from human cell lines of fetal origin, using tissues from aborted human fetuses as a source of such cells.” You can find the Vatican’s response at this link, in which they discuss the moral and ethical issues of “The principle of licit cooperation in evil.”
Below, you’ll find the complete list published by the CDC, de-duplicated and sorted alphabetically. Notice that these ingredients include toxic metals (aluminum salts), bizarre animal cells from humans, monkeys, cows, pigs and chickens, ingredients derived from GMOs, the radioactive element barium, artificial coloring chemicals, excitotoxins such as glutamate, chemical cleansing agents (Triton X-100), dangerous bacterial strains (E.coli), toxic chemicals such as glutaraldehyde, thimerosal (mercury) and much more.
No one can refute any of this because it’s admitted by the CDC itself. Here’s some of the PROOF:


PROOF that the CDC has approved African Green Monkey kidney cells for use in vaccines

First, a CDC document titled “Vaccine Excipient & Media Summary” lists all the vaccine excipient ingredients found in CDC-approved vaccines. The URL for this document is:
As you can see from the screen shots of the document, below, the list of excipient ingredients is “current as of January 6, 2017,” according to the CDC.

You’ll also see that this document includes a row for a Smallpox vaccine known as “Vaccinia – ACAM2000.” The list of excipients in this vaccine are:
African Green Monkey kidney (Vero) cells, HEPES, human serum albumin, sodium chloride, neomycin, polymyxin B, Glycerin, phenol

Note the inclusion of African Green Monkey kidney cells in the list.
And note carefully that the entire mainstream media is calling Natural News a liar for accurately citing this CDC document.
In addition, this same document also includes an ingredients list for another vaccine calledAdenovirus, which contains the following ingredients, one of which is derived from aborted human fetal cells:
human-diploid fibroblast cell cultures (strain WI-38), Dulbecco’s Modified Eagle’s Medium, fetal bovine serum, sodium bicarbonate, monosodium glutamate, sucrose, D-mannose, D-fructose, dextrose, human serum albumin, potassium phosphate, plasdone C, anhydrous lactose, microcrystalline cellulose, polacrilin potassium, magnesium stearate, microcrystalline cellulose, magnesium stearate, cellulose acetate phthalate, alcohol, acetone, castor oil, FD&C Yellow #6 aluminum lake dye

As you can see form this list, these CDC-approved vaccines are deliberately formulated with all sorts of highly toxic and questionable ingredients, including acetone, a toxic solvent, aluminum, artificial coloring chemicals, human blood components, dextrose (probably from GMO corn), cow blood components and a whole lot more.

FDA confirms these vaccines are licensed and approved for use in the United States

Are these vaccines made with African Green Monkey kidney cells and aborted human fetal cells really used in the United States?
YES.
This page from the FDA lists all the vaccines which are “licensed for use in the United States,” and it includes the vaccines containing African Green Monkey kidney cells and the WI-38 aborted human fetal cells.


LIVE Smallpox viruses grown in monkey kidneys, then harvested to be injected into YOU!

In addition to the CDC confirming Natural News is 100% correct through the documents listed above, the vaccine insert sheet itself also describes the use of African Green Monkey kidney cells.
From the insert sheet for the ACAM2000 smallpox vaccine, approved by the FDA in 2007 and still on the approved list:
Click the following link for a backup copy on Natural News servers.
ACAM2000, Smallpox (Vaccinia) Vaccine, Live, is a live vaccinia virus derived from plaque purification cloning from Dryvax® (Wyeth Laboratories, Marietta, PA, calf lymph vaccine, New York City Board of Health Strain) and grown in African Green Monkey kidney (Vero) cells and tested to be free of adventitious agents. ACAM2000 is provided as a lyophilized preparation of purified live virus containing the following non-active excipients: 6-8 mM HEPES (pH 6.5-7.5), 2% human serum albumin USP, 0.5 – 0.7% sodium chloride USP, 5% mannitol USP, and trace amounts of neomycin and polymyxin B.


Vaccine WARNINGS related to the vaccine using African Green Monkey kidney cells

Not surprisingly, this vaccine is known to cause extremely serious and even deadly side effects at a shockingly high rate. Here’s the WARNING box from the vaccine insert sheet, linked above:
WARNING:
See full prescribing information for complete boxed warning
Myocarditis and pericarditis (suspect cases observed at a rate of 5.7 per 1000 primary vaccinees (95% CI: 1.9-13.3)), encephalitis, encephalomyelitis, encephalopathy, progressive vaccinia, generalized vaccinia, severe vaccinial skin infections, erythema multiforme major (including STEVENS-JOHNSON SYNDROME), eczema vaccinatum resulting in permanent sequelae or death, ocular complications, blindness and fetal death, have occurred following either primary vaccination or revaccination with live vaccinia virus smallpox vaccines. These risks are increased in certain individuals and may result in severe disability, permanent neurological sequelae and/or death [see Warnings and Precautions (5)].
Here’s a screen shot of the warnings section of the vaccine insert:


Note the mention of “death” several times, and the shockingly high rate of serious adverse events at 5.7 per 1000 vaccinees. Notice also that this vaccine can cause permanent blindness, spontaneous abortions and severe neurological damage.
Note also that the entire vaccine pushing mainstream media will deny ever word of this even thought it’s printed right on the vaccine insert sheet. This shows you the extreme dishonesty and medical malpractice of all those who push vaccines while falsely claiming them to be “safe.”
Watch for more analysis of the toxicity of these ingredients will be published atVaccines.news and Natural News.

Here’s what happens to some children when they’re injected with these toxins:

vaxd


The complete list of vaccine excipients published by the CDC, current as of January 6, 2017


  1. betapropiolactone
  2. CTAB (cetyltrimethylammonium bromide)
  3. formalin
  4. L-cystine
  5. 2-phenoxyethanol
  6. a continuous line of monkey kidney cells
  7. acetone
  8. African Green Monkey kidney (Vero) cells
  9. alcohol
  10. aluminum hydroxide
  11. aluminum phosphate
  12. aluminum salts
  13. amino acid supplement
  14. amino acids
  15. amino acids solution
  16. aminoglycoside antibiotic
  17. ammonium sulfate
  18. ammonium sulfate aluminum phosphate
  19. amorphous aluminum hydroxyphosphate sulfate
  20. amphotericin B
  21. anhydrous lactose
  22. anti-foaming agent
  23. arginine
  24. ascorbic acid
  25. asparagine
  26. baculovirus and cellular DNA
  27. baculovirus and Spodoptera frugiperda cell proteins
  28. barium
  29. benzethonium chloride
  30. beta- propriolactone
  31. beta-propiolactone
  32. bovine albumin
  33. bovine calf serum
  34. bovine serum
  35. bovine serum albumin
  36. calcium carbonate
  37. calcium chloride
  38. calf bovine serum
  39. Calf serum
  40. calf serum and lactalbumin hydrolysate
  41. carbohydrates
  42. casamino acids
  43. casamino acids and yeast extract-based medium
  44. casein
  45. castor oil
  46. cell culture media
  47. cellulose acetate phthalate
  48. cetyltrimethlyammonium bromide
  49. chick embryo cell culture
  50. chicken fibroblasts
  51. chlortetracycline
  52. citric acid
  53. citric acid monohydrate
  54. CMRL 1969 medium supplemented with calf serum
  55. complex fermentation media
  56. concentrated vitamin solution
  57. CRM197 carrier protein
  58. CY medium
  59. cystine
  60. D- fructose
  61. D- glucose
  62. defined fermentation growth media
  63. deoxycholate
  64. dextran
  65. dextrose
  66. dibasic potassium phosphate
  67. dibasic sodium phosphate
  68. dimethyl-beta-cyclodextrin
  69. dimethyl-beta-cyclodextrin. glutaraldehyde
  70. disodium phosphate
  71. disodium phosphate dihydrate
  72. D-mannose
  73. DNA
  74. dried lactose
  75. Dulbecco’s Modified Eagle Medium
  76. Dulbecco’s Modified Eagle’s Medium
  77. E. coli
  78. Eagle MEM modified medium
  79. EDTA (Ethylenediaminetetraacetic acid)
  80. egg protein
  81. egg proteins
  82. ethylenediaminetetraacetic acid (EDTA)
  83. FD&C Yellow #6 aluminum lake dye
  84. Fenton medium containing a bovine extract
  85. ferric (III) nitrate
  86. fetal bovine serum
  87. formaldehyde
  88. Franz complete medium
  89. galactose
  90. gelatin
  91. gentamicin sulfate
  92. glutamate
  93. glutaraldehyde
  94. Glycerin
  95. guinea pig cell cultures
  96. HEPES
  97. hexadecyltrimethylammonium bromide
  98. histidine
  99. histidine buffered saline.
  100. host cell DNA
  101. host cell protein
  102. human albumin
  103. human diploid cell cultures (MRC-5)
  104. human diploid cell cultures (WI-38)
  105. human embryonic lung cell cultures
  106. human serum albumin
  107. human-diploid fibroblast cell cultures (strain WI-38)
  108. hydrocortisone
  109. hydrolyzed casein
  110. hydrolyzed gelatin
  111. hydrolyzed porcine gelatin
  112. inorganic salts
  113. iron ammonium citrate
  114. isotonic sodium chloride
  115. kanamycin
  116. L-250 glutamine
  117. lactalbumin hydrolysate
  118. lactose
  119. L-histidine
  120. lipids
  121. L-tyrosine
  122. M-199 without calf bovine serum
  123. Madin Darby Canine Kidney (MDCK) cell protein
  124. magnesium stearate
  125. magnesium stearate. gelatin
  126. magnesium sulfate
  127. maltose
  128. MDCK cell DNA
  129. Medium 199 without calf serum
  130. microcrystalline cellulose
  131. mineral salts
  132. modified culture medium containing hydrolyzed casein
  133. modified Latham medium derived from bovine casein
  134. modified Mueller and Miller medium
  135. modified Mueller and Miller medium (the culture medium contains milk- derived raw materials [casein derivatives])
  136. modified Mueller’s growth medium
  137. modified Mueller-Miller casamino acid medium without beef heart infusion
  138. modified Mueller’s media which contains bovine extracts
  139. modified Stainer-Scholte liquid medium
  140. monobasic potassium phosphate
  141. monobasic sodium phosphate
  142. monosodium glutamate
  143. monosodium L-glutamate
  144. monosodium phosphate
  145. MRC-5 cells
  146. MRC-5 cells (a line of normal human diploid cells)
  147. MRC-5 diploid fibroblasts
  148. MRC-5 human diploid cells
  149. Mueller Hinton casein agar
  150. Mueller’s growth medium
  151. neomycin
  152. neomycin sulfate
  153. non-viral protein
  154. nonylphenol ethoxylate
  155. normal human diploid cells
  156. octoxynol-10 (TRITON X-100)
  157. octylphenol ethoxylate (Triton X-100)
  158. ovalbumin
  159. ovalbumin neomycin
  160. phenol
  161. phenol red
  162. phenol red indicator
  163. phosphate buffer
  164. phosphate-buffered saline solution
  165. plasdone C
  166. polacrilin potassium
  167. polydimethylsiloxane
  168. polygeline (processed bovine gelatin)
  169. polymyxin
  170. polymyxin B
  171. polymyxin B sulfate
  172. polysorbate 20
  173. polysorbate 20 (Tween 20)
  174. polysorbate 80
  175. polysorbate 80 (Tween 80)
  176. potassium aluminum sulfate
  177. potassium chloride
  178. potassium glutamate
  179. potassium phosphate
  180. potassium phosphate dibasic
  181. potassium phosphate monobasic
  182. potassium phosphate potassium chloride
  183. protamine sulfate
  184. protein other than HA
  185. recombinant human albumin
  186. saline
  187. semi-synthetic media
  188. semi-synthetic medium
  189. sodium bicarbonate
  190. sodium borate
  191. sodium carbonate
  192. sodium chloride
  193. sodium citrate
  194. sodium citrate dehydrate
  195. sodium deoxycholate
  196. sodium dihydrogen phosphate dihydrate
  197. sodium EDTA
  198. sodium hydrogenocarbonate
  199. sodium hydroxide
  200. sodium metabisulphite
  201. sodium phosphate
  202. sodium phosphate dibasic
  203. sodium phosphate monobasic monohydrate
  204. sodium phosphate-buffered isotonic sodium chloride
  205. sodium phosphate-buffered isotonic sodium chloride solution
  206. sodium pyruvate
  207. sodium taurodeoxycholate
  208. sorbitan trioleate
  209. sorbitol
  210. soy peptone
  211. soy peptone broth
  212. squalene
  213. Stainer-Scholte medium
  214. sterile water
  215. succinate buffer
  216. sucrose
  217. sugars
  218. synthetic medium
  219. thimerosal
  220. thimerosal (multi- dose vials)
  221. thimerosal (multi-dose vials)
  222. tris (trometamol)-HCl
  223. Triton X-100
  224. uracil
  225. urea
  226. VERO cells
  227. vero cells (a continuous line of monkey kidney cells)
  228. vero cells [DNA from porcine circoviruses (PCV) 1 and 2 has been detected in RotaTeq. PCV-1 and PCV-2 are not known to cause disease in humans.]
  229. vitamins
  230. Watson Scherp casamino acid media
  231. Watson Scherp media containing casamino acid
  232. WI-38 human diploid lung fibroblasts
  233. WI-38 human diploid lung fibroblasts MRC-5 cells
  234. xanthan [Porcine circovirus type 1 (PCV-1) is present in Rotarix. PCV-1 is not known to cause disease in humans.]
  235. yeast extract
  236. yeast protein
  237. α-tocopheryl hydrogen succinate
  238. β-propiolactone


____


A marketing tactic that helps ensure the nearly $60 BILLION vaccine market keeps growing

The facts are clear: infectious disease deaths declined nearly 90% BEFORE vaccines were introduced



“VACCINATION DOES NOT ACCOUNT FOR THE IMPRESSIVE DECLINES IN MORTALITY SEEN IN THE FIRST HALF OF THE CENTURY…NEARLY 90% OF THE DECLINE IN INFECTIOUS DISEASE MORTALITY AMONG US CHILDREN OCCURRED BEFORE 1940, WHEN FEW ANTIBIOTICS OR VACCINES WERE AVAILABLE.



Dr. Lawrence Palevsky, a well-respected pediatrician and fellow of American Academy of Pediatrics, discusses how disease mortality declined well before the introduction of vaccines in this one-minute MUST-WATCH video.


In the United States (and other countries), historical records show that disease mortality declined nearly 90% before the introduction of the vaccine program and routine vaccination programs — as stated in the Trends in the Health of Americans report.



In fact, some of the most prevalent diseases in the early 1900s — including Tuberculosis (TB), Scarlet Fever and Typhoid — followed the same declines WITHOUT ever having a vaccine program (in the US). These diseases were nearly eradicated in the U.S. without the population being vaccinated for them. (See graph)



How is this possible? 
The pharmaceutical/medical industry has spent MILLIONSconvincing us that vaccines saved us all from imminent disease death, but history proves this is more of a marketing tactic than a fact. A marketing tactic that helps ensure the nearly $60 BILLIONvaccine market keeps growing.




Why Did Diseases Decline? 

The 19th-century population shift from country to city that accompanied industrialization and immigration led to overcrowding in newly populated cities that lacked proper sanitation or clean water systems. These conditions resulted in repeated outbreaks of cholera, dysentery, TB, typhoid fever, influenza, yellow fever, and malaria.

By 1900, however, the incidence of many of these diseases had begun to decline because of public health improvements, implementation of which continued into the 20th century.


Sanitation & Hygiene

Local, state, and federal efforts to improve sanitation and hygiene reinforced the concept of collective “public health” action (e.g. to prevent infection by providing clean drinking water). By 1900, 40 of the 45 states had established health departments. The first county health departments were established in 1908 (6).

From the 1930s through the 1950s, state and local health departments made substantial progress in disease prevention activities, including sewage disposal, water treatment, food safety, organized solid waste disposal, and public education about hygienic practices (e.g. food handling and handwashing). Chlorination and other treatments of drinking water began in the early 1900s and became widespread public health practices, further decreasing the incidence of waterborne diseases.


Tuberculosis declines WITHOUT a vaccine

The incidence of Tuberculosis (TB) also declined as improvements in housing reduced crowding and TB-control programs were initiated. In 1900, 194 of every 100,000 U.S. residents died from TB — the second leading cause of death — and most were residents of urban areas.

In 1940 (before the introduction of antibiotic therapy), TB remained a leading cause of death, but the crude death rate had decreased to 46 per 100,000 persons. There was never a vaccine for Tuberculosis in the United States. Yet other countries TB rates also decreased before the TB vaccine was introduced. 









What does the CDC say? It credits clean water, NOT vaccines…

This report from the Center for Disease Control in the US clearly shows that the decline in disease was due to clean water systems and sanitation — NOT vaccines. This report was written before the CDC became grossly intertwined with the pharmaceutical industry.
What does the CDC say? It credits clean water, NOT vaccines…

This report from the Center for Disease Control in the US clearly shows that the decline in disease was due to clean water systems and sanitation — NOT vaccines. This report was written before the CDC became grossly intertwined with the pharmaceutical industry. 





Typhoid & Cholera decline WITHOUT vaccines

Quote from the CDC report (NOTE there was NEVER a vaccine program in the US for typhoid and cholera):

“The occurrence of diseases such as cholera and typhoid dropped dramatically. In 1900, the occurrence of typhoid fever in the United States was approximately 100 cases per 100,000 people. By 1920, it had decreased to 33.8 cases per 100,000 people. In 2006, it had decreased to 0.1 cases per 100,000 people (only 353 cases) with approximately 75% occurring among international travelers.

Typhoid fever decreased rapidly in cities from Baltimore to Chicago as water disinfection and treatment was instituted. This decrease in illness is credited to the implementation of drinking water disinfection and treatment, improving the quality of source water, and improvements in sanitation and hygiene.

It is because of these successes that we can celebrate over a century of public drinking water disinfection and treatment – one of the greatest public health achievements of the 20th century.”


Influenza vaccine was introduced in 1960, Pneumonia vaccine was introduced in 2001, after deaths from both diseases had already declined





Influenza vaccine was introduced in 1960, Pneumonia vaccine was
introduced in 2001,  after deaths from both diseases had already declined








Click here for the CDC report

Studies and reports showing the decline of disease deaths BEFORE vaccinations:




The decline of adult smallpox in eighteenth-century London
This study shows smallpox mortality declined before the vaccine was introduced.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373148



The US Universal Varicella Vaccination Program: CDC Censorship of Adverse Public Health Consequences


The CDC mainly published selective studies and manipulated findings to support universal varicella vaccination and aggressively blocked the Research Analyst’s attempt to publish deleterious trends or outcomes (e.g., declining vaccine efficacy, increasing HZ incidence rates, etc.). His letter of resignation stated, ”When research data concerning a vaccine used in human populations is being suppressed and/or misrepresented, this is very disturbing and goes against all scientific norms and compromises professional ethics.”
https://www.jscimedcentral.com/Pathology/pathology-6-1133.pdf



Annual Summary of Vital Statistics: Trends in the Health of Americans During the 20th Century

“Vaccination does not account for the impressive declines in mortality seen in the first half of the century…Once again nearly 90% of the decline in infectious disease mortality among US children occurred before 1940 when few antibiotics or vaccines were available.”
http://pediatrics.aappublications.org/content/106/6/1307



But what about Polio?

This is the question we always hear. First, it’s important to note that Polio is a very common virus, much like a cold or flu virus. Most Americans had/have the polio virus in our bodies at some point, although we are never tested for it unless we have paralysis. We all have dozens of different viruses in our system at one time because that is how nature keeps our immune systems stimulated.

The paralysis that was blamed on the poliovirus in the 1940s and 50s was actually due to the widespread chemical/pesticide spraying of DDT, a highly toxic (now banned) pesticide.



But the US government and health departments, along with chemical companies, were encouraging the spraying of DDT on the American public. Mass DDT spraying campaigns took place on beaches, aerially over swimming pools and parks — especially during the summer months (aka farming season). Coincidentally most “polio” paralysis cases happened during the summer months and in children. Parents were even encouraged to spray their children directly with the highly toxic chemical as well as put it in baths and other places where children had direct contact with DDT.


As the weather warmed up each year, panic over polio intensified. Late summer was dubbed “polio season.” Public swimming pools were shut down.” — NPR, Chasing Down Polio, October 2012 report.






Polio increased with the introduction of DDT and started declining before the polio vaccine was introduced. Click here for more.


In the mid-1940s, scientists began to alert the government and Congress that DDT spraying was causing a huge increase in paralysis and nervous system damage. But the US government, on the back of World War Two, couldn’t admit their mistake — a mistake that would have cost them MILLIONS in damages through lawsuits from those affected.

Someone then had the brilliant idea to quietly start exporting DDT instead of spraying Americans, slowly ban DDT as not to cause alarm and promote a “solution” in the form of the polio vaccine.

It’s one of the most shocking and most commonly believed medical myths, which is still regularly repeated on television, in history books and by an unaware public that never bothers to look beyond the charade.


Studies showing the benefits of natural diseases

Pharmaceutical companies and the medical system love to vilify viruses, but are they really bad for your body? Science is discovering there are many benefits to common illnesses, particularly in childhood, and theorize that viruses actually help train the immune system in a way that can REDUCE the risk of more serious issues later in life, including cancer.
Yes, you read that right: natural viruses can PROTECT from disease later in life.

For thousands of years, humans have lived synergistically with viruses and bacteria. And now science is discovering that they actually serve a purpose on our journey to transformation and health.

Studies showing the benefits of natural diseases



Why aren’t we afraid of all diseases?

The only diseases we fear are the ones that a vaccine has been developed and marketed for. We never feared measles and mumps in the early 20th century… the media tells us what to fear, so they can then sell you an alleged solution.

There are literally THOUSANDS of diseases. Take Leprosy for instance.

How many parents walk around daily concerned about their child contracting leprosy? But, it still exists – by the thousands in various parts of the world. The United States has roughly 200 cases every year. Did you know that? Probably not…

Because there’s no vaccine for leprosy.
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    WATCH: VIDEO SHOWS WHAT MERCURY DOES TO A BRAIN NEURON IN JUST 20 MINUTES

    April 30, 2019

    WATCH: Video Shows What Mercury Does to a Brain Neuron in Just 20 Minutes
    One of the most serious byproducts of modern living is the inundation of the human body and natural environment with toxic chemicals and substances used in medical and consumer products. Just under our noses are a ton of toxic materials, and when you look at the ingredients of pharmaceuticals and contaminants in foods, you see that people are consuming a ton of dangerous substances.
    Take for instance mercury, a dangerous heavy metal that is commonly used in light bulbs, batteries, and other electronics, is widely used in dental filling and is also an ingredient in many vaccines. As our society attempts to understand the nature and causes of the growing epidemic of autism, which is affecting far too many children and families, many are pointing the finger to mercury poisoning and toxicity as a likely culprit.
    So what exactly does mercury do to healthy brain cells?
    Many scientists and concerned vaccine safety advocates are eager to answer this question. Vaccine awareness advocate Robert F. Kennedy Jr. comments on toxic heavy metals:
    “In nature, toxic metals generally are bound with other elements rather than being present in their pure form. However, with the advent of large-scale industrial processes to extract metals from naturally occurring compounds, humans let the genie out of the bottle, contributing significantly to the distribution of mercury, aluminum and other heavy metals in the environment. When released from nature’s semi-protective hold, these “invariably toxic” metals wreak havoc on living systems, including humans, animals and plants alike.

    Modern-day scientists have been amassing evidence of mercury’s toxicity for decades, with a growing focus in recent years on the metal’s association with neurodevelopmental disorders, including autism spectrum disorder (ASD). A new review article in the multidisciplinary journal Environmental Research pulls together a wide body of literature with the aim of summing up current research and emerging trends in mercury toxicology. Geir Bjørklund, the study’s lead author, is the founder of Norway’s non-profit Council for Nutritional and Environmental Medicineand has published prolifically on topics related to heavy metals, autoimmune disorders and ASD.” ~Robert F Kennedy Jr.
    A study conducted at the University of Calgary looked at the effect that mercury has on brain neurons, photographing the effects and compiling a video of real-time results of mercury vs. your brain. In the study, entitled, How Mercury Causes Brain Degeneration, researchers looked at brain lesions in animals who had inhaled mercury vapor.
    The study recorded actual video of healthy snail brain cells growing, then introduced mercury into the culture, which caused rapid degeneration of the snail brain cells after just 20 minutes of direct exposure. The results are quite startling, especially when you consider the ramifications on human health, most notably children who are receiving doses of vaccines which may contain mercury.

    The results are seen in the video presentation below:

    What do you think? Should we be more cautious about the things we put into our bodies and introduce into our environment?

    Read more articles by Alex Pietrowski

    About the Author

    Alex Pietrowski is an artist and writer concerned with preserving good health and the basic freedom to enjoy a healthy lifestyle. He is a staff writer for WakingTimes.com. Alex is an avid student of Yoga and life.
    This article (WATCH: Video Shows What Mercury Does to a Brain Neuron in Just 20 Minutes) originally created and published by Waking Times and is published here under a Creative Commons license with attribution to Alex Pietrowski and WakingTimes.com. 
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    THE TALMUD UNMASKED

    Chapter II. Christians are to be Exterminated.  Art. 2. Christians to be Harmed Directly

    THE TALMUD UNMASKED

    THE SECRET RABBINICAL TEACHINGS CONCERNING CHRISTIANS

    By
    Rev. I. B. Pranaitis
    (Roman Catholic Priest)

    With Ecclesiastical Imprimatur

    The Talmud Unmasked, with Ecclesiastical Imprimatur 
    "Forsaken by His own."

    Father I.B. Pranaitis[Author, Father I. B. Pranaitis]- Roman Catholic Priest; Master of Theology and Professor of the Hebrew Language at the Imperial Ecclesiastical Academy of the Roman Catholic Church in Old St. Petersburg.
    St. Petersburg, Printing office of the Imperial Academy of Sciences, 1892
    *IMPRIMATUR:
    St. Petersburg, April 13, 1892
    KOZLOWSKY ARCHBISHOP METROPOLITAN OF MOGHILEFF
    C. Propolanis, S.Th.C, Secretary
    All Rights Reserved Printed at the Imperial Academy of Sciences (Vas. Ostr., 9 Line, No. 12)
    Copyright 1939 by E. N. SANCTUARY, 156 Fifth Avenue - New York
    INTERNATIONAL COPYRIGHT - ALL RIGHTS RESERVED


    Picture of Book/Imprimatur

    Scanned copy of the inside of Fr. Pranaitis book:
    The Talmud Unmasked (The Secret Rabbinical Teachings Concerning Christians) showing Ecclesiastical Imprimatur 



    Table of Contents:

    Epilogue
    Editor's Note
    Author's Dedication
    Antiphone
    Prologue
    Description of the Talmud
    List of Talmudic Books
    Sources

    Part I - Teaching of the Talmud Concerning Christians

    Chapter I. Jesus Christ in the Talmud
    Art. 1. The Names of Christ
    Art. 2. The Life of Christ/The Christian Cross
    Art. 3. The Teachings of Christ
    Chapter II. Christians in the Talmud
    Art. 1 The Names of Christians
    Art. 2. What the Talmud teaches about Christians
    Art. 3. Christian Worship
    Part II - Precepts of the Talmud Concerning Christians

    Chapter I. Christians are to be Avoided
    Art. 1. Christians Unworthy to Associate with Jews
    Art. 2. Christians are Unclean
    Art. 3. Christians are Idolaters
    Art. 4. Christians are Evil
    Chapter II. Christians are to be Exterminated
    Art. 1. Christians to be Harmed Indirectly
    1. By not helping them
    2. By interfering in their work
    3. By deceit in legal matters
    4. By harming them in things necessary for life
    Art. 2. Christians to be Harmed Directly
    1. Renegades to be killed
    2. Apostates
    3. Princes especially the Prince of Rome (the Pope) to be exterminated
    4. All Christians to be killed
    5. Killing a Christian is an acceptable sacrifice to God
    6. Heaven promised to those who kill Christians
    7. A Christian may be beheaded on the most solemn festivals
    8. The Messiah expected will be revengeful
    9. Jewish prayers against Christians
    10. Christian prayers for the Jews

    Appendix - How the Popes Treated the Jews

    Note from the Webmaster: This unchanged, online version of Fr. Pranaitis scholarly book, The Talmud Unmasked, is dedicated to the Holy Infant Martyr St. Simon of Trent, who was mercilessly slayed by the Jews in Trent, Italy on the 21st March, 1475 A.D.

    Learn more:
    https://graviolateam.blogspot.com/p/the-talmud-unmasked.html
    ___


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