Metal

Vaccine News – Government Issues First Report in 2017 on Vaccine Injuries and Deaths: 275 Injured 4 Dead from Flu Shot

Study – Immunosuppressive and autoimmune effects of thimerosal in mice.

US National Library of Medicine
National Institutes of Health – Apr 2005

Havarinasab S, Häggqvist B, Björn E, Pollard KM, Hultman P.
Author information
Department of Molecular and Clinical Medicine, Molecular and Immunological Pathology (AIR), Linköping University, SE-581 85 Linköping, Sweden.

Abstract
The possible health effects of the organic mercury compound thimerosal (ethylmercurithiosalicylate), which is rapidly metabolized to ethylmercury (EtHg), have recently been much debated and the effect of this compound on the immune system is largely unknown. We therefore studied the effect of thimerosal by treating A.SW (H-2s) mice, susceptible to induction of autoimmunity by heavy metals, with 10 mg thimerosal/L drinking water (internal dose ca 590 microg Hg/kg body weight/day) for up to 30 days. The lymph node expression of IL-2 and IL-15 mRNA was increased after 2 days, and of IL-4 and IFN-gamma mRNA after 6 and 14 days. During the first 14 days treatment, the number of splenocytes, including T and B cells as well as Ig-secreting cells decreased. A strong immunostimulation superseded after 30 days treatment with increase in splenic weight, number of splenocytes including T and B cells and Ig-secreting cells, and Th2- as well as Th-1-dependent serum immunoglobulins. Antinucleolar antibodies (ANoA) targeting the 34-kDa nucleolar protein fibrillarin, and systemic immune-complex deposits developed. The H-2s strains SJL and B10.S also responded to thimerosal treatment with ANoA. The A.TL and B10.TL strain, sharing background genes with the A.SW and B10.S strain, respectively, but with a different H-2 haplotype (t1), did not develop ANoA, linking the susceptibility to H-2. Thimerosal-treated H-2s mice homozygous for the nu mutation (SJL-nu/nu), or lacking the T-cell co-stimulatory molecule CD28 (B10.S-CD28-/-), did not develop ANoA, which showed that the autoimmune response is T-cell dependent. Using H-2s strains with targeted mutations, we found that IFN-gamma and IL-6, but not IL-4, is important for induction of ANoA by thimerosal. The maximum added renal concentration of thimerosal (EtHg) and inorganic mercury occurred after 14 days treatment and was 81 microg Hg/g. EtHg made up 59% and inorganic mercury 41% of the renal mercury. In conclusion, the organic mercury compound thimerosal (EtHg) has initial immunosuppressive effects similar to those of MeHg. However, in contrast to MeHg, thimerosal treatment leads in genetically susceptible mice to a second phase with strong immunostimulation and autoimmunity, which is T-cell dependent, H-2 linked and may at least partly be due to the inorganic mercury derived from the metabolism of ethyl mercury.

Study – Elevated blood histamine caused by vaccinations and Vitamin C deficiency may mimic the shaken baby syndrome.

Clemetson CA. Med Hypotheses. 2004

Clemetson CA
Author information
Department of Obstetrics and Gynecology, Tulane University School of Medicine, New Orleans, LA, USA. megcc2000@yahoo.com

Abstract
The findings of subdural hematoma and retinal hemorrhages in infants, without any documented history of major trauma, do not always indicate child abuse. A combination of ascorbate depletion and the injection of foreign proteins can cause a very high blood histamine level, leading to capillary fragility and venular bleeding. This can be prevented by the administration of vitamin C.

Study – Asymptomatic transmission and the resurgence of Bordetella pertussis

Published: 24 June 2015

Benjamin M. AlthouseEmail author and Samuel V. Scarpino
Affiliated with Santa Fe Institute

Abstract

Background
The recent increase in whooping cough incidence (primarily caused by Bordetella pertussis) presents a challenge to both public health practitioners and scientists trying to understand the mechanisms behind its resurgence. Three main hypotheses have been proposed to explain the resurgence: 1) waning of protective immunity from vaccination or natural infection over time, 2) evolution of B. pertussis to escape protective immunity, and 3) low vaccine coverage. Recent studies have suggested a fourth mechanism: asymptomatic transmission from individuals vaccinated with the currently used acellular B. pertussis vaccines.

Methods
Using wavelet analyses of B. pertussis incidence in the United States (US) and United Kingdom (UK) and a phylodynamic analysis of 36 clinical B. pertussis isolates from the US, we find evidence in support of asymptomatic transmission of B. pertussis. Next, we examine the clinical, public health, and epidemiological consequences of asymptomatic B. pertussis transmission using a mathematical model.

Results
We find that: 1) the timing of changes in age-specific attack rates observed in the US and UK are consistent with asymptomatic transmission; 2) the phylodynamic analysis of the US sequences indicates more genetic diversity in the overall bacterial population than would be suggested by the observed number of infections, a pattern expected with asymptomatic transmission; 3) asymptomatic infections can bias assessments of vaccine efficacy based on observations of B. pertussis-free weeks; 4) asymptomatic transmission can account for the observed increase in B. pertussis incidence; and 5) vaccinating individuals in close contact with infants too young to receive the vaccine (“cocooning” unvaccinated children) may be ineffective.

Conclusions
Although a clear role for the previously suggested mechanisms still exists, asymptomatic transmission is the most parsimonious explanation for many of the observations surrounding the resurgence of B. pertussis in the US and UK. These results have important implications for B. pertussis vaccination policy and present a complicated scenario for achieving herd immunity and B. pertussis eradication.

Government Issues First Report in 2017 on Vaccine Injuries and Deaths: 275 Injured 4 Dead from Flu Shot

These quarterly meetings include a report from the Department of Justice (DOJ) on cases settled for vaccine injuries and deaths as mandated by the National Vaccine Injury Compensation Program (NVICP).
The NVICP was started as a result of a law passed in 1986 that gave pharmaceutical companies total legal immunity from being sued due to injuries and deaths resulting from vaccines.
Drug manufacturers in the vaccine market can now create as many new vaccines as they desire, with no risk of being sued if their product causes injury or death.
This has resulted in a huge increase of vaccines entering the market, and the U.S. government, through the Centers for Disease Control (CDC), is the largest purchaser of these vaccines, spending in excess of $4 billion taxpayer dollars each year to purchase these vaccines.
If you or a family member is injured or dies from vaccines, you must sue the federal government in this special vaccine court. Many cases are litigated for years before a settlement is reached.

James Chestnut, DC – Dubious Method Used By CDC & Big Pharma to “Prove” Flu Vaccine Efficacy
Is the CDC a defacto pharmaceutical company with an over $4 billion incentive to protect Merck and its other Big Pharma suppliers of vaccines? Is there proof of collusion and fraud at the highest levels of the CDC administration, and top-down influence on the allied health practitioners who administer the flu vaccine in blind faith to an unwitting public? What follows is an interview conducted by Toni Bark, MD of “Vaccines Revealed” with James Chestnut, DC an Evidence-Based Wellness and Prevention Lifestyle Clinician. Register for free for the entire 9-part docu-series “Vaccines Revealed” at their website by the same name.

VAXXED TV – Vaccines injured my children #vaxxed #DidYouKnow #Praybig

My son has autism from vaccines #vaxxed #DidYouKnow #Praybig

Vaccines gave my son autism #vaxxed #Didyouknow #Praybig

I didn’t know vaccines could hurt my children #vaxxed #DidYouKnow #Praybig

I’m done vaccinating my children #Vaxxed #PrayBig #DidYouKnow

I now know the truth about vaccines #DidYouKnow #vaxxed #Praybig

My son has autism from vaccines #Vaxxed #PrayBig #DidYouKnow

I will never vaccinate again. #Vaxxed #PrayBig #DidYouKnow

Heavy Metal Toxicity

Anu says goodbye
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How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:

Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.

Vaccine News – Stephen recalls the decline of his health and symptoms as a result of vaccine injury – VAXXED TV

VAXXED TV – I Had an Adverse Reaction
Stephen recalls the decline of his health and symptoms as a result of vaccine injury.
Interview recorded on April 26th, 2017 in The United Kingdom

My son has autism from vaccines #Vaxxed #PrayBig #DidYouKnow

I will never vaccinate again. #Vaxxed #PrayBig #DidYouKnow

Heavy Metal Toxicity

Anu says goodbye

I Carried On Being Bullied
Mother recalls accounts of her son’s reaction to vaccines.
Interview recorded on April 26th, 2017 in The United Kingdom

45 Minutes Later He Was DEAD!
Mother reveals accounts of her son’s death after the MMR Vaccine.
Interview recorded on April 26th, 2017 in The United Kingdom

I Trusted My GPs
Paula explains the account details of her children’s reactions to vaccinations
Interview recorded on April 26th, 2017 in The United Kingdom

He Kept Banging His Head
Diana recalls events with her children as a result of the vaccinations that were administered to them.

We’ve Stopped Questioning Anything
Anna explains her symptom after receiving vaccinations in her adult life.
Interview recorded on April 26th, 2017 in The United Kingdom

How to accept Jesus Christ as your personal Saviour

Mercury In Vaccines Was Replaced With Something Even MORE Toxic

Mercury In Vaccines Was Replaced With Something Even MORE Toxic
January 27, 2009
Dr. Mercola’s Comments:
When mercury was removed from many vaccines (except the flu vaccine) years ago, it was under the false guise that finally vaccines were now safe. What health agencies did not want you to know is that there are many other toxic additives still in vaccines, and one of them is aluminum.
Aluminum has not received the widespread media attention that mercury has, therefore many people don’t realize it’s a health risk.
“Aluminum is not perceived, I believe, by the public as a dangerous metal. Therefore, we are in a much more comfortable wicket in terms of defending its presence in vaccines,” said Dr. John Clements, WHO vaccine advisor.
Notice he said that aluminum is “not perceived” by the public as a dangerous metal … he couldn’t say simply that aluminum is safe, because this would be a lie.
Why is Aluminum Added to Vaccines?
Most vaccines have at least two components, the agent that you’re seeking to elicit an immune response to, such as a measles virus, and an immune adjuvant, which enhances the immune response and is typically made from a variety of highly toxic compounds including aluminum compounds, MSG, and mercury. The purpose of immune adjuvants is to boost your immune system, or to make it react as intensely as possible for as long as possible.
Unlike a natural immune boost that would come from, say, eating healthy and exercising, artificial immune adjuvants can be dangerous in and of themselves. Says Dr. Russell Blaylock, M.D., a board-certified neurosurgeon and author:
“Studies have shown that these adjuvants, from a single vaccine, can cause immune overactivation for as long as two years. This means that the brain microglia remain active as well, continuously pouring out destructive chemicals.
In fact, one study found that a single injection of an immune activating substance could cause brain immune overactivation for over a year. This is very destructive.”

Aluminium DOES cause Alzheimer’s: Expert says new findings confirm the metal plays a role in the devastating brain disease
Chris Exley is a professor in bioinorganic chemistry based at Keele University
A link between between aluminium and Alzheimer’s has existed for many years
But a lack of evidence has caused the scientific community to remain unsure
However, his new research confirms the metal plays a role in cognitive decline
By Professor Chris Exley For The Hippocratic Post
Published: 09:58 GMT, 19 December 2016
A link between aluminium and Alzheimer’s disease has long existed.
But many scientists says there is not enough evidence to blame the metal, used by thousands for everyday purposes to cook and store food.
However, Professor Chris Exley, from Keele University, says his latest research confirms it does indeed play a role in cognitive decline.
Here, in a piece for medical-blogging website The Hippocratic Post, he reveals the findings from his latest study.

Can A Toxic Metal Found in Vaccines Cause Heart Disease?

Aluminum is a metal found in many childhood vaccines. The stated role of aluminum as an adjuvant in vaccines is to enhance the immune response to the main ingredient in the vaccine. This would be either a virus or bacterial component.

Vaccines which currently contain aluminum are: hepatitis A, hepatitis B, diphtheria-tetanus-pertussis (DTaP, Tdap), Haemophilusinfluenzae type b (Hib), human papillomavirus (HPV) and pneumococcal.

Aluminum Stops Cellular Cleaning
Lysosomes are organelles inside of most cells in the body. These are the garbage cans of the cell that digest proteins and other molecules, spitting out their parts to be recycled into other cell components.

The interior of the lysosome is very acidic. This is necessary to break down the garbage. The acidity comes from an energy consuming process that pumps hydrogen ions into the lysosome.

Guess what blocks that hydrogen pump? You guessed it (by the title of the article), aluminum (1).

Yes, aluminum blocks the ability of the lysosome to get acidic. If not acidic, it doesn’t work, and cellular garbage starts to collect.

You can imagine the consequences of excess cellular garbage? How would your house look if you didn’t take out the garbage? It reminds me of the TV show, Hoarders.

Could Aluminum Link to Autoimmune Disease
The lysosome clears out the garbage. This includes dead cells, old cellular debris, and just about everything else.

If the lysosomes are working, the useless debris floats around the body. The debris is sensed by the immune system as foreign material. The immune system goes into attack mode and this process is linked to subsequent autoimmune conditions. Please read an excellent review by Drs. Shaw and Tomljenovic (2).

Aluminum Leads to Arterial Blockages
Lysosomes breakdown lipid particles that contain cholesterol. As LDL returns to the liver, it is taken up by LDL receptors. These receptors are like little catchers’ mitts that trap the LDL and bring it into the liver cell. The LDL particle, along with the receptor travel into the lysosome inside the cell.

But because of aluminum, the lysosome is not acidic enough, and this LDL particle/receptor complex is not broken down. So now, the cell becomes full of cholesterol. In a form of negative feedback, the cell no longer puts out receptors to trap LDL particles.

Without uptake into the liver for breakdown and reprocessing, the LDL particles keep circulating around the body, become damaged by inflammation and oxidation, and are TAKEN UP into plaque.

Get Thrashed: The Story Of Thrash Metal (Full)

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