Category Archives: Articles & Breaking News

Dr. Shiva: Massachusetts Senate Candidate will Back Trump Independent Vaccine Commission

President Trump’s position on vaccines:

We have a Senate candidate who is powerfully with us on the vaccine issue.  See  below.

Attached is our vaccine survey response from Dr. Shiva, midterm candidate for Massachusetts against Pocahontas Elizabeth Warren

https://shiva4senate.com

PRESS RELEASE   TRUMPTAC PressRelease

Powerful Voter Block to Push Trump Aligned Candidates Over the Edge #TrumpTAC (Trump Aligned Candidates video)

———- Forwarded message ———

From: Arvind Kumar <akumar@shiva4senate.com>
Date: Thu, Oct 25, 2018 at 2:27 PM
Subject: Response of Shiva Ayyadurai to Survey
To: <ncowmail@gmail.com>
Not sure if you received this already, but below is the response of Dr. Shiva Ayyadurai who is running for U.S. Senate from MA.
1) Are you aware of President Trump’s position on Vaccines?
Yes. The numbers I have show that it is a recent phenomenon that occurred during our lifetimes. This can be directly linked to GMOs and vaccines.
2) Are you in agreement that there is an Autism Epidemic?
Yes.
3) Are you in agreement with President Trump that Vaccines can and do cause Autism?
We definitely need to have an open mind on this and study this problem. Instead of persecuting Dr. Andrew Wakefield, scientists should have investigated the issue. We also need to look into the link between GMOs and autism. As a person with a PhD in Biological Engineering, I will not put a political or corporate agenda above the safety of our children.
4) Are you in agreement with President Trump that an independent vaccine science and safety commission should be created to investigate the vaccine safety of every government mandated childhood vaccine?
Definitely. We also should not mandate vaccines just to create profits for the pharmaceutical industry. We need to investigate if lobbying led to vaccines being mandated and punish the corporate executives if this was the case.
5) Do you understand the support from Congress needed in order for President Trump to challenge pharmaceutical/medical interests?
I definitely understand the challenges and that is why you need me in the Senate. With four degrees from MIT, I understand this issue and am the person best suited to represent the interests of our safety.
6) Are you aware that a 1986 law gave all manufacturers and vaccine providers complete and full immunity from lawsuits even if their product was contaminated; that they only possible excuse for a lawsuit is “willful misconduct”?
Believe me, their behavior is willful misconduct. They know the dangers of vaccines but put their profits above safety.

7) Will you have President Trump’s back on this issue?

Yes, but my plan goes farther as it will prosecute the criminals in the pharmaceutical and GMO industries who created the epidemic.

FBI/Ford/Kavanaugh

PRESS RELEASE FORD-Kavanaugh 10-3-18

National Coalition of Organized Women Press Release:  Reconciling the disparity between Ford and Kavanaugh

Excerpt: 

Dr. Ford had the unique opportunity to effortlessly “ transpose and substitute” the two victimizers in her adolescent real-life event.  It would be a lie, an alteration to an adolescent event, that could save the melting snowflake nation from a Trump appointed, anti-abortion, Christian, Supreme Court Judge.  After all, who would know the difference, but her! How was her testimony so compelling?  It is simply because Dr. Ford genuinely had had an authentic and personal experience. This enabled her to give details of such an event so convincingly. That is how the disparity can be resolved!

Jeff Sessions Commitment to Religious Freedom (Vaccines?)

Sessions said that the Justice Department and the Trump administration as a whole was now operating under the guidance of 20 fundamental principles pertaining to religious freedom. That, he said, included protecting Americans’ right to worship as they choose and act upon their beliefs without undue government interference.

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Brazil Judge suspends use of Glyphosate

A Brazilian judge has suspended the use of products containing the agrochemical glyphosate, a widely employed herbicide for soy and other crops in the country, according to legal filings.

A federal judge in Brasilia ruled that new products containing the chemical could not be registered in the country and existing registrations would be suspended within the next 30 days, until the government reevaluates their toxicology.

The decision, which could be subject to multiple appeals, also applies to the insecticide abamectin and the fungicide thiram.

The ruling affects companies such as Monsanto Co, which markets a glyphosate-resistant, genetically-modified type of soybean that is planted on a large scale in Brazil. Monsanto is now a unit of Bayer AG, following a $62.5 billion takeover of the U.S. seed major which closed in June.

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Billionaire Vaccine Entrepreneur Buys LA Times & San Diego Tribune

Big Pharma vaccine billionaire just bought the LA Times… yet another example of the media being run by pharma

(Natural News) The latest example of Big Pharma taking over the media is the purchase of the Los Angeles Times and the San Diego Tribune for $500 million by Big Pharma billionaire Dr. Patrick Soon-Shiong. Instead of paying for advertisements, pharma billionaires have decided to just buy the publications outright so they can control the entire publication. All the journalists here are now officially bought; these publications should officially be recognized as propaganda rags from now on.Big Pharma vaccine billionaire just bought the LA Times… yet another example of the media being run by pharma. READ MORE...

 

 

WHO new Vaccine Adverse Reaction Guidelines (2018) Hides ADR’s post vaccination

 

New Delhi  6 July 2018.

Two leading pediatricians  in India have urged the   World Health Organization (WHO)  to urgently revise its manual on classification of “Adverse Events Following Immunization (AEFI),” warning that the new guidelines put children’s life at risk.

 This needs to be done “urgently in the interest of child safety,”  doctors Jacob Puliyel at St Stephen’s Hospital in Delhi, and Pathik Naik of  Children Hospital in Surat, say in a report published in the prestigious journal ‘F1000Research’

 Under  WHO’s revised   manual on AEFI,  only those adverse  reactions observed during  clinical trials of a vaccine,    should be  classified as   vaccine related.     All new serious adverse reactions including deaths  seen during post-marketing of the vaccine   should be considered  as ‘coincidental’  or ‘unclassifiable’, and the vaccine should not be blamed.

READ SOURCE ABSTRACT

 The WHO has also changed the  definition of  “causal association,” the authors say. Under the revised guidelines,  if there is an alternate explanation for the adverse event, or another factor is involved, causative association with vaccine should not be made.   “In other words,  if after vaccination,  a child with an underlying congenital heart disease  develops    cardiac failure, it would not be considered causally related to the vaccine.”

 The revised classification by WHO  “is a major step backward for patient safety,” the authors say.  “This could embolden vaccine manufacturers to be more reckless with regard to adverse reactions,” they warn.

 Puliyel and Naik note that the Global Advisory Committee on Vaccine Safety has documented many deaths in children with pre-existing heart disease after they were administered the pentavalent vaccine (combined diphtheria, tetanus, pertussis, Hib, and hepatitis-B vaccine).    “Under  WHO’s  new definition of causal association, these deaths would not be acknowledged as related to  vaccination.” 

 Both Sri Lanka and Vietnam governments withdrew  the pentavalent vaccine following the deaths of  five children in Sri Lanka and 12 in Vietnam soon  after vaccination.  But  WHO investigating teams declared that the deaths were ‘unlikely’ to be related to vaccination, the report says.   The authors point out that  a new study in India,    showed that the switch from DPT (diphtheria, tetanus, pertussis)  to pentavalent vaccine almost doubled the deaths following vaccination. “A large number of these deaths could have been avoided had the AEFI manual not been revised.”

 According to their  report, the consequence of India adopting WHO’s new classification   can be seen from the causality assessment of 132 serious AEFI cases uploaded on the website of the Ministry of Health and Family Welfare.  Of the total AEFI cases,  54   babies died and 78 survived,   “but not even one death was classified as vaccine-related. Nearly all the deaths were simply classified as unclassifiable or coincidental.”  

 Vaccines are drugs used as a preventive measure, given to   healthy persons.  . Adverse events following immunization   must be monitored more carefully than other drugs, the authors note. “A credible immunization safety evaluation and monitoring system is essential for the success of immunization programmes.”   

 Adverse reaction and deaths may not show up as significantly increased in small safety studies. However, records of all deaths and serious adverse events following vaccinations should be maintained and periodically reviewed for safety signals.     

According to the authors,  WHO’s  new AEFI classification scheme “that allows for an outright denial of any new causative association with vaccination” could fall foul of Article 2 of the  European Convention on Human Rights. Adverse reaction and deaths may not show up as significantly increased in small safety studies. However, records of all deaths and serious adverse events following vaccinations should be maintained and periodically reviewed for safety signals.     

 “Paradoxically, the AEFI algorithm is said to be for vaccine safety,” says Puliyel. “Perhaps we need a scheme for public safety rather than vaccine safety.” (END)

 Jacob Puliyel MD MRCP M Phil

puliyel@gmail.com

Phone 0091 9868035091

REVISED Revised World Health Organization (WHO)’s causality assessment of adverse events following immunization—a critique [version 2; referees: 2 approved]

OPEN PEER REVIEWREFEREE STATUS

The World Health Organisation (WHO) has recently revised how adverse events after immunization (AEFI) are classified. Only reactions that have previously been acknowledged in epidemiological studies to be caused by the vaccine are classified as a vaccine-product–related-reaction. Deaths observed during post-marketing surveillance are not considered as ‘consistent with causal association with vaccine’, if there was no statistically significant increase in deaths recorded during the small Phase 3 trials that preceded it. Of course, vaccines  noted to have caused a significant increase in deaths in the control-trials stage would probably not be licensed. After licensure, deaths and all new serious adverse reactions are labelled as ‘coincidental deaths/events’ or ‘unclassifiable’, and the association with vaccine is not acknowledged. The resulting paradox is evident. VLA Comment: INTERESTING POINT IN PINK
The definition of causal association has also been changed. It is now used only if there is ‘no other factor intervening in the processes’. Therefore, if a child with an underlying congenital heart disease (other factor), develops fever and cardiac decompensation after vaccination, the cardiac failure would not be considered causally related to the vaccine. The Global Advisory Committee on Vaccine Safety has documented many deaths in children with pre-existing heart disease after they were administered the pentavalent vaccine. The WHO now advises precautions when vaccinating such children. This has reduced the risk of death. Using the new definition of causal association, this relationship would not be acknowledged and lives would be put at risk. In view of the above, it is necessary that the AEFI manual be revaluated and revised urgently. AEFI reporting is said to be for vaccine safety. Child safety (safety of children) rather than vaccine safety (safety for vaccines) needs to be the emphasis.

 

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