BIDERMAN’S CHART OF COERCION AND MORE…

 

A discussion of Biderman’s Chart of Coercion as applied to COVID, as well as Agenda 21/30, and the implementation of a new broadcast network whose intention is to provide 24/7 information about all of these efforts, so that newbies can tune in and become immediately aware of why the world is crumbling around them. This is a necessity in order for people to wake up and reject this egregious act perpetrated against humanity.

Declaration Against Medical Mandates

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Sign the petition   HERE

If you believe you deserve a choice in what goes in, or on, your body, we ask that you sign the Declaration below. Doing so will help us show it’s a majority viewpoint. A majority public view can begin the change of laws and policy to achieve a fairer, better society for all.

Help us reach one million signatures worldwide in the next six months.

The information you provide below will help establish the validity of this Declaration and will NOT be shared with your employer or anyone else.

We, The Undersigned, Declare:

ONE

We are OPPOSED to medical mandates.  We wish to be fully informed of all facts relevant to our unique circumstances before making health decisions.  We wish to make our decisions freely, without pressure or fear of consequences.  And we hold the same power and responsibility over decisions for our minor children.

TWO

We are OPPOSED to misinformation, disinformation and coercion for medical intervention because these could lead us into decisions we would not otherwise make and/or actions that may be against our wishes.

THREE

There must be NO adverse consequences for those who decline medical intervention, or bodily interfence, for any reason whatsoever. 

ican Chicken Pox Vaccine Update

Since I’m banned from Fakebook and Twitter, I thought I would put these updates in the blog.

 

ICAN sued the FDA in November 2019 in order to obtain copies of the clinical trials relied upon to license the varicella vaccine in 1995.  Over 9 months later, the FDA completed production of the documents, many of which contained numerous unnecessary redactions.  ICAN pushed back on the agency and, except for 12 dates of death, the FDA lifted all of the challenged redactions demonstrating a tendency by the agency to over-redact information that should be available to the public.

 

The CDC vigorously promotes the varicella (chickenpox) vaccine. ICAN, therefore, submitted a FOIA request to the FDA in September 2018 for copies of the clinical trials relied upon to license the varicella vaccine in 1995. ICAN wanted to review and share with the public the clinical trial reports and safety data relied upon when the FDA licensed this vaccine.

 

More than a year later, the FDA had failed to produce the clinical trial reports sought by the FOIA Request and so ICAN brought suit.  The agency’s counsel and ICAN’s attorneys, led by Aaron Siri, then conferred and reached agreement on a schedule by which the FDA would produce all of the responsive clinical trials. On January 9, 2020, FDA made its first production to ICAN and completed its 9-part production on August 31, 2020.  The large production contained many redactions for items including dates of vaccination, dates of adverse events, and date of medical treatment.

 

Given that most of these dates were at least 30 years ago and no identity of any trial participant was disclosed (or requested), ICAN pointed out to the FDA that redactions applied to protect personal information were inappropriate.  It requested that the agency re-review portions of the production and produce the selected pages again without the redactions.  The agency did so last month and the agreement was So Ordered by the Court.

 

The additional unredacted pages further support that, as explained in a prior legal update, this product should never have been licensed.  Indeed, only one trial relied upon to license this vaccine included a placebo control.  Buried deep in the reports, however, it admits that this “placebo” is an injection of lyophilized stabilizer containing approximately 45 mg of neomycin per milliliter.  This is not a placebo! A placebo is an inert substance like saline — it is not another drug!  Worse, this trial only contained 956 children, of which 491 received VARIVAX and 465 received the alleged “placebo.” Compounding its fake placebo and minuscule number of participants, these children were only monitored for clinical complaints for 56 days and then for an additional 14 days thereafter for serious adverse reactions. 

 

Nonetheless, even in this shoddy, underpowered study, four serious adverse events (including seizure and viral enteritis) were reported in the group of children receiving VARIVAX and none were reported in the group receiving the alleged placebo. That differential was deemed acceptable by the FDA because Merck’s paid investigator did not consider these serious adverse events to be related to VARIVAX.  The rest of the trials produced by the FDA were not blinded, not randomized, nor did they include a control group.  These trials could therefore not provide scientifically valid data to support the product’s safety for licensure.

 

The FDA’s basis for licensing VARIVAX is incredible when considering that: (i) states mandate by law that millions of children receive VARIVAX every year; (ii) Merck cannot be sued for most injuries caused by this product under federal law; and (iii)  Merck’s sales of this product, alone or in combination with another of its products, was $2.275 billion in 2019.  But yet, the FDA licensed this product based on one fake “placebo” controlled trial, with only 956 children, and that reviewed safety for only around 2 months!  

 

ICAN will continue to put the power of scientifically researched health information in your hands, with full transparency, even when it means suing and challenging public health authorities.  When it comes to our children, we will chase down even the smallest details in order to provide complete information to parents in order to empower them to make educated decisions.

 

Share this Legal Update via this link: https://www.icandecide.org/ican_press/further-evidence-chicken-pox-vaccine-should-never-have-been-licensed/

 . . . 

 

PLEASE SIGN THE MOST CRITICAL PETITION THERE COULD EVER BE FOR THE RESTORATION OF LIBERTY AND THE REPUBLIC

  SIGN PETITION TO CONGRESS DEMANDING ADHERENCE TO THE CONSTITUTION

THE NEW NUREMBERG TRIALS – 2021

FACEBOOK IMMEDIATELY SUSPENDED MY ACCOUNT FOR 30 DAYS AS I POSTED A LINK TO INFORMATION ON THE MASSIVE COURT CASE FORMING AGAINST THE MEDICAL ESTABLISHMENT AND GOVERNMENT FOR CRIMES AGAINST HUMANITY…

NUREMBERG 21

The New Nuremberg Trials 2021

A team of over 1,000 lawyers and over 10,000 medical experts led by Dr. Reiner Fuellmich have begun legal proceedings against the CDC, WHO & the Davos Group for crimes against humanity. Fuellmich and his team present the faulty PCR test and the order for doctors to label any comorbidity death as a Covid death as fraud. The PCR test was never designed to detect pathogens and is 100% faulty at 35 cycles. All the PCR tests overseen by the CDC are set at 37 to 45 cycles. The CDC admits that any tests over 28 cycles are not admissible for a positive reliable result. This alone invalidates over 90% of the alleged covid cases / ”infections” tracked by the use of this faulty test.

In addition to the flawed tests and fraudulent death certificates, the “experimental” vaccine itself is in violation of Article 32 of the Geneva Convention. Under Article 32 of the 1949 Geneva Convention IV, “mutilation and medical or scientific experiments not necessitated by the medical treatment of a protected person” are prohibited. According to Article 147, conducting biological experiments on protected persons is a grave breach of the Convention.

The “experimental” vaccine is in violation of all 10 of the Nuremberg Codes which carry the death penalty for those who seek to violate these International Laws.

The “vaccine” fails to meet the following five requirements to be considered a vaccine and is by definition a medical “experiment” and trial:

Provides immunity to the virus
This is a “leaky” gene therapy that does not provide immunity to Covid and claims to reduce symptoms yet double-vaccinated are now 60% of the patients requiring ER or ICU with covid infections.

Protects recipients from getting the virus
This gene-therapy does not provide immunity and double-vaccinated can still catch and spread the virus.

Reduces deaths from the virus infection
This gene-therapy does not reduce deaths from the infection. Double-Vaccinated infected with Covid have also died.

Reduces circulation of the virus
This gene-therapy still permits the spread of the virus as it offers zero immunity to the virus.

Reduces transmission of the virus
This gene-therapy still permits the transmission of the virus as it offers zero immunity to the virus.

The following violations of the Nuremberg Code are as follows:

Nuremberg Code #1: Voluntary Consent is Essential

No person should be forced to take a medical experiment without informed consent. Many media, political and non-medical persons are telling people to take the shot. They offer no information as to the adverse effects or dangers of this gene-therapy. All you hear from them is – “ safe and effective” and “ benefits outweigh the risks.” Countries are using lockdowns, duress and threats to force people to take this vaccine or be prohibited to participate in free society under the mandate of a Vaccine Passport or Green Pass. During the Nuremberg trials, even the media was prosecuted and members were put to death for lying to the public, along with many of the doctors and Nazis found guilty of Crimes Against Humanity.

Nuremberg Code #2: Yield Fruitful Results Unprocurable By Other Means

As listed above, the gene-therapy does not meet the criteria of a vaccine and does not offer immunity to the virus. There are other medical treatments that yield fruitful results against Covid such as Ivermectin, Vitamin D, Vitamin C, Zinc and boosted immune systems for flu and colds.

Nuremberg Code #3: Base Experiments on Results of Animal Experimentation and Natural History of Disease

This gene therapy skipped animal testing and went straight to human trials. In mRNA research that Pfizer used – a candidate study on mRNA with rhesus macaques monkeys using BNT162b2 mRNA and in that study all the monkeys developed pulmonary inflammation but the researchers considered the risk low as these were young healthy monkeys from the age of 2-4. Israel has used Pfizer and the International Court of Law has accepted a claim for 80% of the recipients having pulmonary inflammation from being injected with this gene-therapy. Despite this alarming development Pfizer proceeded to develop their mRNA for Covid without animal testing.

Nuremberg Code #4: Avoid All Unnecessary Suffering and Injury

Since the rollout of the experiment and listed under the CDC VAERS reporting system over 4,000 deaths and 50,000 vaccine injuries have been reported in America. In the EU over 7,000 deaths and 365,000 vaccine injuries have been reported. This is a grievous violation of this code.

Nuremberg Code #5: No Experiment to be Conducted if There’s Reason to Think Injury or Death Will Occur

See #4, based on fact-based medical data this gene-therapy is causing death and injury. Past research on mRNA also shows several risks that have been ignored for this current trial gene-experiment. A 2002 study on SARS-CoV-1 spike proteins showed they cause inflammation, immunopathology, blood clots, and impede Angiotensin 2 expression. This experiment forces the body to produce this spike-protein inheriting all these risks.

Nuremberg Code #6: Risk Should Never Exceed the Benefit

Covid-19 has a 98-99% recovery rate. The vaccine injuries, deaths and adverse side-effects of mRNA gene-therapy far exceed this risk. The use of “leaky” vaccines was banned for agriculture use by the US and EU due to the Marek Chicken study that shows ‘hot-viruses’ and variants emerge… making the disease even more deadly. Yet, this has been ignored for human use by the CDC knowing fully the risk of new deadlier variants emerge from leaky vaccinations. The CDC is fully aware that the use of leaky vaccines facilitates the emergence of hot (deadlier)strains. Yet they’ve ignored this when it comes to human

Nuremberg Code #7: Preparation Must Be Made Against Even Remote Possibility of Injury, Disability or Death

There were no preparations made. This gene therapy skipped animal trials. The pharmaceutical companies’ own Phase 3 human clinical trials will not conclude until 2022 /2023. These vaccines were approved under an Emergency Use only act and forced on a misinformed public. They are NOT FDA-approved.

Nuremberg Code #8: Experiment Must Be Conducted by Scientifically Qualified Persons

Politicians, media and actors claiming that this is a safe and effective vaccine are not qualified. Propaganda is not medical science. Many retail outlets such as Walmart & drive-through vaccine centers are not qualified to administer experimental medical gene-therapies to the uninformed public.

Nuremberg Code #9: Anyone Must Have the Freedom to Bring the Experiment to an End At Any Time

Despite the outcry of over 85,000 doctors, nurses, virologists and epidemiologists – the experiment is not being ended. In fact, there are currently many attempts to change laws in order to force vaccine compliance. This includes mandatory and forced vaccinations. Experimental ‘update’ shots are planned for every 6 months without any recourse to the growing number of deaths and injuries already caused by this experiment. These ‘update’ shots will be administered without any clinical trials. Hopefully this new Nuremberg Trial will put an end to this crime against humanity.

Nuremberg Code #10: The Scientist Must Bring the Experiment to an End At Any Time if There’s Probable Cause of it Resulting in Injury or Death

It is clear in the statistical reporting data that this experiment is resulting in death and injury yet all the politicians, drug companies and so-called experts are not making any attempt to stop this gene-therapy experiment from inflicting harm on a misinformed public.

What can you do to help put an end to this crime against humanity? Share this information. Hold your politicians, media, doctors and nurses accountable – that if they are complicit in this crime against humanity they too are subject to the laws set forth in the Geneva Convention and Nuremberg Code and can be tried, found guilty and put to death. Legal proceedings are moving forward, evidence has been collected and a large growing body of experts are sounding the alarm.

Visit the Covid Committee website at: https://corona-ausschuss.de/ and if you have been affected by this crime, report the event, persons involved, and as much detail to the following website: https://www.securewhistleblower.com/

 

Crimes against humanity affect us all. They are a crime against you, your children, your parents, your grandparents, your community and your country and your future.


HELP US DISSEMINATE INFORMATION AND TAKE ACTION WITH PETITIONS AND ORGANIZING AND MOBILIZING ACTION.





SPEAKING OF PETITIONS

 

PLEASE SIGN THE MOST CRITICAL PETITION THERE COULD EVER BE FOR THE RESTORATION OF LIBERTY AND THE REPUBLIC

  SIGN PETITION TO CONGRESS DEMANDING ADHERENCE TO THE CONSTITUTION

ELIMINATION AND PREVENTION OF UNCONSTITUTIONAL LAW

 

Sign the petition   HERE

This petition is for the purpose of demanding that Congress repeal all unconstitutional laws.  And, further, to put them on notice that they will be charged with treason if they do not actively review and eliminate unconstitutional laws and actively reject all currently introduced legislation. 

Share with everyone and implore those with whom you share it to keep it going.

This is the most critical moment in our lifetime. If we do not act now to reverse the current trend, we will soon be passing totalitarian on to our children.