Dr. Fauci, “There will be a surprise outbreak… the next administration (Trump) will be faced with challenges.”

World Health Organisation Report – Progress Indicators by September 2020 (PAGE 39):
“The United Nations (including WHO) conducts at least two system wide training and simulation exercises, including one covering the deliberate release of a lethal respiratory pathogen.”

The Johns Hopkins Center for Health Security in partnership with the World Economic Forum and the Bill and Melinda Gates Foundation hosted Event 201 (watch the videos)

The Johns Hopkins Center for Health Security: The SPARS Pandemic 2025 – 2028

European Commission Roadmap – Vaccination Passport for EU Citizens (2019)

Bill Gates, ”The world today has 6.8 billion people. That’s headed up to about nine billion. Now, if we do a really great job on new vaccines, health care, reproductive health services, we could lower that by, perhaps, 10 or 15 percent.”

Bill Gates, “We’re taking things that are genetically modified organisms and we’re injecting them in little kids arms, we just shoot them right into the vein.”

Bill Gates, “Eventually what we’ll have to have is certificates of who’s a recovered person, who’s a vaccinated person… so eventually there will be this digital immunity proof that will help facilitate the global reopening up.”

Bill Gates, “The current vaccines are not infection blocking, they’re not broad so new variants come up you lose protection, and they have very short duration, particularly in the people that matter which are old people.”

Bill Gates, “The people like myself and Tony Fauci are saying 18 months. If everything went perfectly we could do slightly better than that but there will be a trade-off. We’ll have less safety testing than we typically would have and so governments will have to decide you know do they indemnify the companies and really say let’s go out with this when we just don’t have the time to do what we normally do.”

Bill Gates, “We’ll have to prepare for the next one… that, I’d say, will get attention this time.”

Bill Gates – Pandemic 2

Big Tech Censors Dissent Over Coronavirus Lockdowns

Kary Mullis – PCR Test Inventor

Kary Mullis – The AIDS Scam

Why We Question the Safety Profile of mRNA COVID-19 Vaccines

How Fauci and Collins Shut Down Covid Debate

COVID-19: politicisation, “corruption,” and suppression of science

Outcome Reporting Bias in COVID-19 mRNA Vaccine Clinical Trials

Facebook CEO Mark Zuckerberg

Facebook partner accused of collusion with vaccine manufacturer J&J

CNN Director Reveals That Network Practices ‘Art of Manipulation’ to ‘Change the World’

Christopher Cole, FDA Executive Officer – Countermeasures Initiative

Dr. David Gortler, Former FDA Director, “I don’t understand how we could consciously still be giving these vaccines”

Dr. Peter Marks, FDA Director of Center for Biologics Evaluation and Research (CBER), “It is important to note that FDA’s authorization and licensure standards for vaccines do not require demonstration of the prevention of infection or transmission.”

Ashley Cheung Honold, FDA Department of Justice lawyer, U.S. Court of Appeals, “FDA is clearly acknowledging that doctors have the authority to prescribe human Ivermectin to treat covid so they are not interfering with the authority of doctors to prescribe drugs or to practice medicine. FDA was not regulating the off-label use of drugs. FDA is merely making information statements, they do have sovereign immunity. These statements are not regulations they have no legal consequences they don’t prohibit doctors from prescribing Ivermectin to treat covid or for any other purpose.”

Sen. Josh Hawley, Senate Homeland Security Committee Hearing, “We now know thanks to the case Missouri versus Biden that that’s exactly what this administration from the White House to the FBI to the state department to the CDC to SISA have all been meeting with the social media companies for years now giving them direct commands about what to censor and take down naming specific accounts and specific speech they want suppressed threatening the social media platforms if they don’t do it and remarkably I’m quoting the court here the Fifth Circuit Court of Appeals and there’s a huge evidentiary record everybody go don’t take my word for it go read the record it’s all on the record.”

Dr. Brad Wenstrup, House Select Committee on the Coronavirus Hearing

Dr. Rich McCormick, House Select Subcommittee on the Coronavirus Hearing

Dr. Scott Jensen: Dr. Tom Shimabukuro, CDC Deputy Director, acknowledges Covid vaccines cause serious health issues

Dr. Tom Shimabukuro, CDC Deputy Director: Preliminary List of Vaers AEs of Special Interest (PAGE 31)

Steven M. Rubin, PhD, Director Vaccine Research Analytics NVIC (Creator of the VAERS Database Search Engine)

Carol Baker, CDC Appointed Chair of Advisory Committee on Immunisation Practices, “We’ll just get rid of all the whites in the United States”

Dr. Peter Doshi, “Does the FDA think these data justify the first full approval of a covid-19 vaccine?“

Federal Judge Orders FDA to Produce Pfizer Covid-19 Data at Rate of 55,000 Pages Per Month. FDA asked the Court for permission to only be required to produce at a rate of 500 pages per month, which would have taken over 75 years to produce all the documents.

Federal Judge Orders CDC to Make Public 7.8 Million V-safe Free-Text Entries Within 12 Months

Pfizer CEO Albert Bourla, “We know that the two doses of the vaccine offer very limited protection, if any. The three doses, with a booster, they offer reasonable protection against hospitalisation and death and less protection against infection.”

Pfizer CEO Albert Bourla, “It was most counterintuitive to go the mRNA route. mRNA was the technology that we had less experience with, only two years working on this. mRNA was a technology that never delivered a single product until that day. Not vaccine, not any other medicine, so it was very counterintuitive.”

Pfizer CEO Albert Bourla, “We believe that there’s very high probability of delivering a solution to an unmet need not because the current vaccines are not effective, but they are don’t have the safety profile that we hope we can achieve with this technology.”

Pfizer Regional President of Pfizer Vaccines in International Developed Markets testifying before the European Union Parliament – Was the Pfizer Covid vaccine tested on stopping the transmission of the virus before it entered the market?

Pfizer Exposed For Exploring “Mutating” COVID-19 Virus For New Vaccines Via ‘Directed Evolution’

AstraZeneca CEO Pascal Soriot, “There are millions of people in the world that will need a protection that cannot be coming from a vaccine”

Moderna CEO Stéphane Bancel, ”There’s a Pandemic Coming Next Year”

Fauci vs Fauci

Dr. Fauci: Covid Vaccine Ineffective

Dr. Fauci: Truth About Hospital Cases

Dr. Birx, “I knew these vaccines were not going to protect against infection and I think we overplayed the vaccines”

Dr. Leana Wen: Pandemic Of The Unvaccinated

US Senator Ron Johnson – Vaccine Mandates Expert Panel Highlights

Biden’s Bounty on Your Life: Hospitals’ Incentive Payments for COVID-19

British MP Andrew Bridgen Leads An Adjournment Debate On The Efficacy Of The mRNA Covid-19 Booster

British MP Christopher Chope: Covid Jab Caused More Damage Than Any Other Vaccine In History

Christine Anderson – European Parliament: COVID Had Nothing to Do With Public Health

Rob Roos MEP (Member European Parliament)

WHO Forging Ahead With Plans To Implement A Global Digital Health Certificate

COVID vaccine questions that no one will answer

Right on cue, just for you

Nobody is Safe!

Lies, Lies and More Lies

Nuremberg Code Violations

Pathologized Totalitarianism 101

As of 19 March 2020, COVID-19 is no longer considered to be a high consequence infectious disease (HCID) in the UK.

Coronavirus Advice for care home residents on ‘Do Not Attempt Resuscitation’ forms

Evidence Not Fear

The COVID Coup

Powerful summary of tyranny we endured for last three years

Laura Aboli, ”The Final Goal is to Eradicate Humanity as We Know It”


Dr. Peter Doshi: Vaccine Mandates

Dr. Bret Weinstein: ‘Perverse Incentives’ in the Vaccine Rollout and the Censorship of Science

Dr. Robert Malone, Inventor of mRNA Vaccine warns about the risks of the experimental vaccines

Dr. Aseem Malhotra, “Covid-19 vaccines rollout must stop immediately until raw data has been released for fully independent scrutiny”

Dr. Mark Trozzi: When will health regulators follow the science?

Dr. James Thorp: Increased Risk of Menstrual Abnormalities & Miscarriages After Vaccine

Dr. Stephanie Seneff: mRNA Vaccines and the Risk of Prion Disease

Dr. William Makis: Testimony to National Citizens Inquiry (NCI)

Dr. Ben Edwards’s Testimony to Texas Senate Health and Human Services Committee

Dr. Scott Youngblood: Efficacy of COVID Vaccines

Dr. Ryan Cole: Covid-19 Vaccine & ADE

Dr. Vladimir Zelenko: Covid-19 Vaccine

Dr. Geert Vanden Bossche: Mass Vaccination in a Pandemic – Benefits versus Risks (McMillan Research)

Dr. Peter McCullough: COVID Vaccine Agenda & The Rush To Suppress Alternative Treatments

Dr. Mike Yeadon, Former CSO & VP Allergy Respiratory Research Pfizer Global

Dr. Roger Hodkinson: How governments responded to COVID

Dr. Richard Fleming: Covid-19 Vaccine

Dr. Harvey Risch: Covid Taboos

Dr. Jenny Harries, Deputy CMO for England: Children are at greater risk from flu or road accidents than COVID-19

Dr. Meryl Nass: Myocarditis – The one they couldn’t hide

Dr. Charles Hoffe: Children and COVID Vaccines

Dr. Paul Marik: Covid Exposed A Corrupt Medical System

Dr. Tess Laurie, “These are not vaccines and the studies were not done”

Dr. Rochagné Kilian: Covid-19 Vaccines and D-Dimer Levels

Dr. Scott Jensen, “You’re Being Played”

Dr. Scott Atlas: They killed people with their lies

Dr. Suneel Dhand: Completely SAFE and 98 Percent EFFECTIVE

Dr. Jayanta Bhattacharya: There Was Never a Scientific Consensus on Lockdowns, Masks, or the Vaccine.

Dr. Chris Martenson: Midazolam Murders – When a Common Sedative Becomes an Execution Drug

Dr. Julie Ponesse: ETHICS 101

Prof. Fukushima Condemns mRNA Vaccines as ‘Evil Practices of Science’

Prof. Masayasu Inoue: A Message from Japan to the World

Prof. Luc Montagnier, “It is the vaccination that is creating the variants”

Prof. Sucharit Bhakdi: Perspectives on the Pandemic

Prof. Retsef Levi, MIT Professor & expert on drug safety, calls for an immediate suspension of all Covid mRNA vaccines

Prof. Michael Levitt: Does the data support the lockdown policy?

Prof. Carl Heneghan: Can we trust Covid-19 death numbers?

Prof. Norman Fenton: How flawed statistics have manipulated the Covid narrative

Prof. Denis Rancourt, The Elephant in the Room: C-19 Vaccines All-Cause Mortality

Prof. Mattias Desmet: Mass Formation Psychosis

Children Have 0.00% Chance of Dying from COVID but are Harmed for Life by Social Distancing

Why are we vaccinating children against COVID-19?
“The bulk of the official COVID-19-attributed deaths per capita occur in the elderly with high comorbidities, and the COVID-19 attributed deaths per capita are negligible in children. A novel best-case scenario cost-benefit analysis showed very conservatively that there are five times the number of deaths attributable to each inoculation vs those attributable to COVID-19 in the most vulnerable 65+ demographic. The risk of death from COVID-19 decreases drastically as age decreases, and the longer-term effects of the inoculations on lower age groups will increase their risk-benefit ratio.”

Age-stratified infection fatality rate of COVID-19 in the non-elderly population:
“At a global level, pre-vaccination IFR may have been as low as 0.03% and 0.07% for 0–59 and 0–69 year old people, respectively.”

COVID vaccination and age-stratified all-cause mortality risk:
“The risks of COVID vaccines and boosters outweigh the benefits in children, young adults and older adults with low occupational risk or previous coronavirus exposure.”

CDC Admits Crushing Rights of Naturally Immune Without Proof They Transmit the Virus

Children develop robust and sustained cross-reactive spike-specific immune responses to SARS-CoV-2 infection

Persistent immune memory of COVID-19 found in recovered patient T cells

Longitudinal analysis shows durable and broad immune memory after SARS-CoV-2 infection with persisting antibody responses and memory B and T cells

COVID-19 Natural Immunity

Comparing SARS-CoV-2 Natural Immunity to Vaccine-Induced Immunity: Reinfections Versus Breakthrough Infections

COVID-19 vaccines and adverse events of special interest: A multinational Global Vaccine Data Network (GVDN) cohort study of 99 million vaccinated individuals
“This multi-country analysis confirmed pre-established safety signals for myocarditis, pericarditis, Guillain-Barré syndrome, and cerebral venous sinus thrombosis.”

Serious adverse events of special interest following mRNA COVID-19 vaccination in randomized trials in adults

Risk of Myopericarditis following COVID-19 mRNA vaccination in a Large Integrated Health System: A Comparison of Completeness and Timeliness of Two Methods

SARS-CoV-2 mRNA Vaccination-Associated Myocarditis in Children Ages 12-17: A Stratified National Database Analysis

BNT162b2 Vaccine-Associated Myo/Pericarditis in Adolescents: A Stratified Risk-Benefit Analysis
“Male patients ages 12-17 years have an elevated risk of mRNA vaccination-associated myo/pericarditis. A risk-benefit analysis of first and second doses of mRNA vaccination in adolescent boys by health status and history of SARS-CoV-2 infection has not been performed.”

Covid-19 Vaccine Adverse Reactions – Strong Association With Cardiovascular Death

MRNA COVID Vaccines Dramatically Increase Endothelial Inflammatory Markers and ACS Risk as Measured by the PULS Cardiac Test: a Warning

Pfizer Amends U.S. Government Paxlovid Supply Agreement and Updates Full-Year 2023 Guidance:
PAXLOVID includes ritonavir, a strong CYP3A inhibitor, which may lead to greater exposure of certain concomitant medications, resulting in potentially severe, life-threatening, or fatal events. Severe, life-threatening, and/or fatal adverse reactions due to drug interactions have been reported in patients treated with PAXLOVID. Hepatic transaminase elevations, clinical hepatitis, and jaundice have occurred in patients receiving ritonavir. Because nirmatrelvir is coadministered with ritonavir, there may be a risk of HIV-1 developing resistance to HIV protease inhibitors in individuals with uncontrolled or undiagnosed HIV-1 infection. Systemic exposure of nirmatrelvir increases in renally impaired patients with increase in the severity of renal impairment. Available data on the use of nirmatrelvir during pregnancy are insufficient to evaluate for a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. There are no available data on the presence of nirmatrelvir in human or animal milk, the effects on the breastfed infant, or the effects on milk production. Authorized or approved mRNA COVID-19 vaccines show increased risks of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining outside the heart), particularly within the first week following vaccination. For COMIRNATY, the observed risk is highest in males 12 through 17 years of age.

“There is limited experience with use of COVID-19 mRNA vaccine in pregnant women. The safety profile of the vaccine is not yet fully known in pregnant or breastfeeding women due to their initial exclusion from the pivotal clinical study. It is unknown whether COVID-19 mRNA vaccine is excreted in human milk. The safety profile of the vaccine is not known in immunocompromised individuals due to their exclusion from the pivotal clinical study. There is limited information on the safety of the vaccine in individuals with autoimmune or inflammatory disorders and a theoretical concern that the vaccine may exacerbate their underlying disease. There is limited information on the safety of the vaccine in frail patients with co-morbidities who are potentially at higher risk of severe COVID-19. Events of Myocarditis and Pericarditis have been reported. Post-authorization reports have been reported more frequently in adolescent and young adult male patients following the second dose of vaccine; however, reports have been received for adult males and females of broader age range and following the first vaccination also. The long-term safety of COVID-19 mRNA vaccine is unknown at present.”

“Two novel excipients are included in the finished product, the cationic lipid ALC-0315 and the PEGylated lipid ALC-0159. ALC-0315 and ALC-0159 are novel excipients, not previously used in an approved finished product within EU. Some uncertainties remain regarding the ALC-0315 long half-life. Lipid related impurities have been observed in some recently manufactured finished product batches. Data demonstrate the presence of significant amounts of truncated/modified forms of mRNA at somewhat higher levels in the batches manufactured with the commercial process as compared to material used in clinical trials. No traditional pharmacokinetic or biodistribution studies have been performed with the vaccine candidate BNT162b2. No genotoxicity nor carcinogenicity studies have been provided. Several literature reports indicate that LNP-formulated RNAs can distribute rather non-specifically to several organs such as spleen, heart, kidney, lung and brain.”

“There is an increased risk of myocarditis and pericarditis following vaccination with Comirnaty. These conditions can develop within just a few days after vaccination and have primarily occurred within 14 days. They have been observed more often after the second vaccination, and more often in younger males. Some cases required intensive care support and fatal cases have been observed. No Comirnaty data are available on vaccine placental transfer or excretion in milk. Neither genotoxicity nor carcinogenicity studies were performed.”

“Postmarketing data with authorized or approved mRNA COVID-19 vaccines demonstrate increased risks of myocarditis and pericarditis, particularly within the first week following vaccination. For COMIRNATY, the observed risk is highest in males 12 through 17 years of age. COMIRNATY has not been evaluated for the potential to cause carcinogenicity, genotoxicity, or impairment of male fertility. Available data on COMIRNATY administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy. It is not known whether COMIRNATY is excreted in human milk. Data are not available to assess the effects of COMIRNATY on the breastfed infant or on milk production/excretion.”

“Causal association between Spikevax and myocarditis is considered of at least a reasonable possibility. The majority of the cases have been reported in young males, and shortly after the second dose of the vaccine. Available data suggest that the course of myocarditis and pericarditis following vaccination is not different from myocarditis or pericarditis in general.”

“The review of the data received during the reporting review showed that the events of myocarditis and pericarditis continue to primarily occur in young adult males, shortly after the second dose of the vaccine with a TTO less than 7 days. The same pattern was observed for cases reported after receiving a booster dose of Spikevax.”

“There is an increased risk for myocarditis and pericarditis following vaccination with Spikevax. These conditions can develop within just a few days after vaccination, and have primarily occurred within 14 days. They have been observed more often in younger males, and more often after the second dose compared to the first dose. Some cases required intensive care support and fatal cases have been observed. No data are available of Spikevax vaccine placental transfer or excretion in milk. Carcinogenicity studies were not performed.”

Moderna SPIKEVAX (COVID-19 Vaccine, mRNA):
“Postmarketing data with authorized or approved mRNA COVID-19 vaccines demonstrate increased risks of myocarditis and pericarditis, particularly within the first week following vaccination. For SPIKEVAX, the observed risk is highest in males 18 years through 24 years of age. Information is not yet available about potential long-term sequelae. SPIKEVAX has not been evaluated for carcinogenic, mutagenic potential, or impairment of male fertility. Available data on SPIKEVAX administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy. It is not known whether SPIKEVAX is excreted in human milk. Data are not available to assess the effects of SPIKEVAX on the breastfed infant or on milk production/excretion.”

Moderna mRNA Platform ‘The Software of Life’:
“mRNA drug development has substantial clinical development and regulatory risks due to the novel and unprecedented nature of this new category of medicines. Gene therapies and mRNA based medicines may activate one or more immune responses against any and all components of the drug product (e.g. the mRNA or the delivery vehicle, such as a lipid nanoparticle) as well as against the encoded protein, giving rise to potential immune reaction related adverse events. Most of our investigational medicines are formulated and administered in an LNP which may lead to systemic side effects related to the components of the LNP which may not have ever been tested in humans.”

Informed consent disclosure to vaccine trial subjects of risk of COVID-19 vaccines worsening clinical disease:
“The specific and significant COVID-19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.”

Comprehensive investigations revealed consistent pathophysiological alterations after vaccination with COVID-19 vaccines:
“Historically, vaccine research has been focused on whether or not vaccination could generate neutralizing antibodies to protect against viral infections, whereas short-term and long-term influences of the various newly developed vaccines to human pathophysiology and other perspectives of the human immune system have not been fully investigated.”
IgG4 Antibodies Induced by Repeated Vaccination May Generate Immune Tolerance to the SARS-CoV-2 Spike Protein:
“Recent investigations have found abnormally high levels of IgG4 in people who were administered two or more injections of the mRNA vaccines. Emerging evidence suggests that the reported increase in IgG4 levels detected after repeated vaccination with the mRNA vaccines may not be a protective mechanism; rather, it constitutes an immune tolerance mechanism to the spike protein that could promote unopposed SARS-CoV2 infection and replication by suppressing natural antiviral responses. Increased IgG4 synthesis due to repeated mRNA vaccination with high antigen concentrations may also cause autoimmune diseases, and promote cancer growth and autoimmune myocarditis in susceptible individuals.”

The mRNA-LNP platform’s lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory:
“In summary, here we show that the LNPs used for many preclinical studies are highly inflammatory. Thus, their potent adjuvant activity and reported superiority comparing to other adjuvants in supporting the induction of adaptive immune responses likely stem from their inflammatory nature. Furthermore, the preclinical LNPs are similar to the ones used for human vaccines, which could also explain the observed side effects in humans using this platform.”

Spikeopathy: COVID-19 Spike Protein Is Pathogenic, from Both Virus and Vaccine mRNA
“The inflammatory properties of the nanoparticles used to ferry mRNA; N1-methylpseudouridine employed to prolong synthetic mRNA function; the widespread biodistribution of the mRNA and DNA codes and translated spike proteins, and autoimmunity via human production of foreign proteins, contribute to harmful effects.”

SARS–CoV–2 Spike Protein Impairs DNA Damage Repair:
“Our findings reveal a potential molecular mechanism by which the spike protein might impede adaptive immunity and underscore the potential side effects of full-length spike-based vaccines.”

Pfizer-BioNTech COVID-19 Vaccine (PAGE 25):
“BNT162 vaccines have not been administered to humans before and thus there are no previous clinical data with these specific vaccines.”

Pfizer Documents the FDA Tried to Hide Shows LNPs from COVID-19 Vaccine Travel Everywhere in the Body

Urgent Expert Hearing on Reports of DNA Contamination in mRNA Vaccines

Worse than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19

COVID-19 RNA Based Vaccines and the Risk of Prion Disease

New Quality-Control Investigations on Vaccines: Micro and Nanocontamination
“We verified the presence of saline and Aluminum salts, but further presence of micro, sub-micro and nanosized, inorganic, foreign bodies (ranging from 100nm to about ten microns) was identified in all cases, whose presence was not declared in the leaflets delivered in the package of the product.”–and-nanocontamination.html

Cause of Death After COVID-19 Vaccination: Undeclared Components of the COVID-19 Vaccines

Autopsy-based histopathological characterization of myocarditis after anti-SARS-CoV-2-vaccination

AAPS Statement: Mask Mandates Do Not Prevent Spread of Respiratory Viruses, They Cause Harm, and Violate the Right to Informed Consent


Inclusive Digital ID for a Resilient Recovery from COVID-19–6owU2NA

Digital Documentation of COVID-19 Certificates: Vaccination Status

World COVID-19 Strategic Preparedness and Response Project:
“Available evidence now shows that COVID-19 is causing mild and self-limiting disease in most people who are infected, with severe disease more likely among older people or those with comorbidities, such as pulmonary disease, and other chronic health conditions. Data from China indicates, unsurprisingly, that tobacco smoking is playing a large part in the gender distribution and severity of COVID-19.”

World Economic Forum and UN Sign Strategic Partnership Framework

World Economic Forum – Now Is The Time For A ‘Great Reset’

World Economic Forum – The Great Reset

World Economic Forum – The Fourth Industrial Revolution

The Rockefeller Foundation – Lock Step

The Rockefeller Foundation – Reset the Table

World Health Organization, “The pandemic has given new impetus to the need to accelerate efforts to respond to climate change.”

Immunization Agenda 2030: A Global Strategy to Leave No One Behind

John Hopkins (CDC):
“Self-spreading vaccines are genetically engineered to move through populations like communicable diseases, but rather than causing disease, they confer protection. The vision is that a small number of individuals in a target population could be vaccinated, and the vaccine strain would then circulate in the population much like a pathogenic virus, resulting in rapid, widespread immunity.”

ID2020 – Digital Identity

Accenture, Microsoft Create Blockchain Solution to Support ID2020.

ID2020 Alliance launches digital ID program with Government of Bangladesh and Gavi, announces new partners at annual summit.

ID2020 and Partners launch program to provide Digital ID with Vaccines

ID2020 COVID-19 Immunity Passports

The Role of Pandemics, Vaccines and Genetics in the UN’s Plan to Halt Population Growth.’s_Plan_to_Halt_Population_Growth

Implications of Worldwide Population Growth For U.S. Security and Overseas Interests (THE KISSINGER REPORT)

The United Nations hosted the world’s first regional COVID-19 concert. The concert closed with a performance of a song, “A New World Order Behind Closed Doors”.

Operation Warp Speed (OWS)

U.S. President Donald Trump, September 2019, Executive Order 13887 — Modernizing Influenza Vaccines in the United States To Promote National Security and Public Health

U.S. President Donald Trump, “When we have the vaccine, we have the military all lined up and the military is going to be doing it in a very powerful manner.”

In quest for vaccine, US make ‘big bet’ on company with unproven technology

Moderna mRNA Operating System Platform

COVID-19 Vaccination Program Interim Playbook for Jurisdiction Operations

Government consultation on changes to the Human Medicines Regulations to support the rollout of COVID-19 and flu vaccines

Dr. Meryl Nass: Why Are Legislatures Now Imposing Vaccine Mandates?

Nanotechnology, Blockchain for COVID-19 Immunity Passports

Hydrogel Nanoparticles and Nanocomposites for Nasal Vaccine Delivery

Quantum-Dot Vaccination Record

World Economic Forum – Covid Action Platform

The Rockefeller Foundation – National Covid-19 Testing Action Plan

H.R.6666 – COVID-19 Testing, Reaching, And Contacting Everyone (TRACE) Act.

The Coronavirus (Retention of Fingerprints and DNA Profiles in the Interests of National Security) Regulations 2020

CommonPass – Travelling The World In The Covid Era


National Childhood Vaccine Injury Act of 1986:
“No vaccine manufacturer shall be liable in a civil action for damages arising from a vaccine-related injury or death: (1) resulting from unavoidable side effects; or (2) solely due to the manufacturer’s failure to provide direct warnings.”

PREP Act Immunity from Liability for COVID-19 Vaccinators:
“The PREP Act authorizes the Secretary of the Department of Health and Human Services (Secretary) (HHS) to issue a PREP Act Declaration (“Declaration”) that provides immunity from liability for any loss caused, arising out of, relating to, or resulting from administration or use of countermeasures to diseases, threats and conditions determined in the Declaration to constitute a present or credible risk of a future public health emergency.”

Human Rights Violations in Healthcare Provision in Developing Countries and the Effectiveness of Current Measures:
“Since the early 2000s, the Global Alliance for Vaccines and Immunizations (Gavi), Global Health Innovative Technology Fund and PATH, all heavily funded by the Gates
Foundation, have been distributing vaccines and drugs to vulnerable populations in Africa and India. In 2010, the Gates Foundation funded experimental malaria and meningitis vaccine trials across Africa and HPV vaccine programs in India. All of these programs resulted in numerous deaths and injuries, with accounts of forced vaccinations and uninformed consent. Ultimately, these health campaigns, under the guise of saving lives, have relocated large scale clinical trials of untested or unapproved drugs to developing markets where administering drugs is less regulated and cheaper.”

Lessons learnt in Japan from adverse reactions to the HPV vaccine:
“The adverse reactions following human papilloma virus (HPV) vaccination in Japan, and the measures taken by the Ministry of Health, Labour and Welfare (MHLW) to withdraw active recommendation of the vaccine.”

U.S. District Judge Orders Merck to Produce Entire Database of Adverse Event Reporting and Review System (MARRS):
“Plaintiffs’ attorneys and experts will now have access to Merck’s Gardasil HPV vaccine adverse event database under a protective order.”

Dr. Darrell Salk Testimony to Senate Committee (PAGE 174)
“Live poliovirus vaccine now causes more disease than the virus against which it is used. The occurrence of vaccine-associated poliomyelitis is a result of instability inherent in the live poliovirus vaccine; such cases will continue to occur as long as the vaccine is used.”

Thiomersal in Vaccines (C9H9HgNaO2S):
“The culmination of the research that examines the effects of Thimerosal in humans indicates that it is a poison at minute levels with a plethora of deleterious consequences, and there is a clear cause for concern. To date, there are over 150 studies that show harm from Thimerosal including increased risk of neurodevelopmental disorders, such as autism, attention-deficit/hyperactivity disorder, and language and speech delay. The cost-effectiveness of adding Thimerosal to multidose vaccines still overrides safety concerns. Clearly, Thimerosal should be banned and eliminated as a vaccine preservative throughout the world.”

Methodological Issues and Evidence of Malfeasance in Research Purporting to Show Thimerosal in Vaccines Is Safe:
“There are over 165 studies that have focused on Thimerosal, an organic-mercury (Hg) based compound, used as a preservative in many childhood vaccines, and found it to be harmful. Of these, 16 were conducted to specifically examine the effects of Thimerosal on human infants or children with reported outcomes of death; acrodynia; poisoning; allergic reaction; malformations; auto-immune reaction; Well’s syndrome; developmental delay; and neurodevelopmental disorders, including tics, speech delay, language delay, attention deficit disorder, and autism.”

A comparative evaluation of the effects of MMR immunization and mercury doses from thimerosal-containing childhood vaccines on the population prevalence of autism:
“The results of this study agree with a number of previously published studies. These studies have shown that there is biological plausibility and epidemiological evidence showing a direct relationship between increasing doses of mercury from thimerosal-containing vaccines and neurodevelopmental disorders, and measles-containing vaccines and serious neurological disorders. It is recommended that thimerosal be removed from all vaccines, and additional research be undertaken to produce a MMR vaccine with an improved safety profile.”

Increased risk for an atypical autism diagnosis following Thimerosal-containing vaccine exposure in the United States: A prospective longitudinal case-control study in the Vaccine Safety Datalink
“The present study provides important epidemiological evidence significantly associating increasing Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of atypical autism diagnosis, and suggests that Thimerosal should be eliminated from vaccines.”

Aluminum vaccine adjuvants: are they safe?

Congressman Dan Burton House Hearings on Autism: Thimerosal (Mercury) still being used in Vaccines

Congressman Bill Posey calling for an Investigation of the CDC’s MMR Research Fraud

NIH Director Dr. Bernadine Healy speaks about Autism Susceptibility

Aaron Siri, Civil Litigation Attorney – Clinical Trials Fail To Support Claim ‘Vaccines Do Not Cause Autism’

Aaron Siri, Civil Litigation Attorney – Testimony To Arizona State Senate

Dr. James Neuenschwander: Coalition For Informed Consent

Dr. James Lyons-Weiler: Medical Freedom Press Conference

Dr. Lawrence Palevsky: Legislative Informational Forum on Public School Immunizations

Dr. Peter Doshi: Why was the public not told of early warning signs?

Dr, Peter Gøtzsche, Director of Nordic Cochrane Center, Exposes Big Pharma as Organized Crime

European Medicines Agency – Adverse Drug Reactions



Pfizer $2.3 Billion Fraudulent Marketing

GlaxoSmithKline Plead Guilty and Pay $3 Billion for Fraudulent Marketing and Failure to Report Safety Data

Johnson & Johnson Pay More Than $2.2 Billion in Criminal and Civil Investigations for Fraudulent Marketing and Kickbacks to Doctors and Pharmacists

Committee on Oversight and Reform Report on Emergent BioSolutions Uncovers Extensive Vaccine Manufacturing Failures and Deliberate Efforts to Hide Deficiencies

Merck Gardasil Clinical Trials: Gardasil Vaccine Lawsuit

Blood Money: Bayer’s Inventory of HIV Contaminated Blood Products and Third World Hemophilias

In Bed With Big Pharma: Corruption Fears As Report Finds US Doctors Received Record $12Bn In Pharma Payments In Past Decade

Parliamentary Assembly of the Council of Europe (PACE) Investigation of the World Health Organisation Motives for Declaring H1N1 a Pandemic (2010):
“On 11 June 2009, the World Health Organization (WHO) officially declared “Pandemic (H1N1) 2009”. The way in which the H1N1 influenza pandemic has been handled, not only by WHO, but also by the competent health authorities at the level of the European Union and at national level, gives rise to alarm. Some of the consequences of decisions taken and advice given are particularly troubling, as they led to distortion of priorities of public health services across Europe, waste of large sums of public money and also unjustified scares and fears about health risks faced by the European public at large.”

Pfizer-BioNTech Annual Report (PAGE 6):
“Our revenue depends heavily on sales of our COVID-19 vaccine, and our future revenues from our COVID-19 vaccine are uncertain. We may not be able to demonstrate sufficient efficacy or safety of our COVID-19 vaccine and/or variant-specific formulations to obtain permanent regulatory approval in the United States, the United Kingdom, the European Union, or other countries where it has been authorized for emergency use or granted conditional marketing approval. Significant adverse events may occur during our clinical trials or even after receiving regulatory approval, which could delay or terminate clinical trials, delay or prevent regulatory approval or market acceptance of any of our product candidates.”

Pfizer-BioNTech EU Contract:
“The Participating Member State further acknowledges that the long-term effects and efficacy of the Vaccine are not currently known and that there may be adverse effects of the Vaccine that are not currently known. Each Participating Member State shall indemnify and hold harmless the Contractor, their Affiliates, sub-contractors, licensors and sub-licensees, and officers, directors, employees and other agents and representatives of each (together, the “Indemnified Persons”) from and against any and all liabilities incurred.”

Senator Rand Paul Questions Moderna CEO Stéphane Bancel Over COVID-19 Vaccine Side Effects, “Mr. Bancel, Moderna recently paid NIH $400 million. Do you believe it creates a conflict of interest for the government employees who are making money now off of the vaccine to also be dictating the policy about how many times we have to take the vaccine?”

UK Parliament Select Committee on Health:
“The evidence to this inquiry indicated that, in recent years, large pharmaceutical companies have become ever more focused on a marketing-based approach. In our view, this is the source of many of the problems we have identified. Our over-riding concerns are about the volume, extent and intensity of the industry’s influence, not only on clinical medicine and research but also on patients, regulators, the media, civil servants and politicians. The regulatory system, the medical profession and Government have all failed to ensure that industry’s activities are more clearly allied to the interests of patients and the NHS.”

Pandemic Response and Recovery All-Party Parliamentary Group – Failings of the Yellow Card System (MHRA):
Prof. Carl Heneghan, Director of Centre for Evidence Based Medicine, “Under-reporting of adverse drug reactions to the Yellow Card system could be as high as 98%, meaning the ability to detect signals and assign causation is substantially hindered. Should the MHRA, our regulatory body, be primarily funded by fees derived from services to the pharmaceutical industry?”

MHRA awarded over £980,000 for collaboration with the Bill and Melinda Gates Foundation and the World Health Organisation

Dr. Maryanne Demasi, “Patients and doctors expect drug regulators to provide an unbiased, rigorous assessment of investigational medicines before they hit the market. But do they have sufficient independence from the companies they are meant to regulate?”

Medical royal colleges receive millions from drug and medical devices companies

UK 10 Year Partnership with Moderna

Revisiting financial conflicts of interest in FDA advisory committees:
“The Food and Drug Administration (FDA) Safety and Innovation Act has recently relaxed conflict-of-interest rules for FDA advisory committee members, but concerns remain about the influence of members’ financial relationships on the FDA’s drug approval process.”

FDA’s Revolving Door

Aaron Siri, Civil Litigation Attorney: Why Are Vaccine Manufacturers the Most Protected Companies in America?
Aaron Siri, Civil Litigation Attorney: How the Vaccine Paradigm Has Led to Medical Coercion and Conflicted Health Agencies

Dr. Peter Doshi – Marketing Vaccine By Marketing Disease:
“The cleverest aspect of the influenza marketing strategy surrounds the claim that “flu” and “influenza” are the same. All influenza is “flu,” but only one in six “flus” might be influenza. It’s no wonder so many people feel that “flu shots” don’t work: for most flus, they can’t.”

Dr. Lee D. Merritt: The Treatment of Viral Diseases – Has the Truth Been Suppressed for Decades?

Africa to Become Testing Ground for “Trust Stamp” Vaccine Record and Biometric Digital Payment System:
“The program, which was first launched in late 2018, will see Trust Stamp’s digital identity platform integrated into the GAVI-Mastercard “Wellness Pass,” a digital vaccination record and identity system that is also linked to Mastercard’s click-to-play system that powered by its AI and machine learning technology called NuData.”

CDC 2019 Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel (PAGE 40):
“Since no quantified virus isolates of the 2019-nCoV were available for CDC use at the time the test was developed and this study conducted, assays designed for detection of the 2019-nCoV RNA were tested with characterized stocks of in vitro transcribed full length RNA.”

Changes to CDC RT-PCR for SARS-CoV-2 Testing:
“After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only.”

COVID-19 Vaccine Efficacy and Effectiveness – The Elephant (NOT) in the Room:
“These considerations on efficacy and effectiveness are based on studies measuring prevention of mild to moderate COVID-19 infection; they were not designed to conclude on prevention of hospitalisation, severe disease, or death, or on prevention of infection and transmission potential. Assessing the suitability of vaccines must consider all indicators, and involve safety, deployability, availability, and costs.”

Guidance for the Prevention of COVID-19 Infections Among High-Risk Individuals in Urban Settings (Green Zones):
“The main feature of this approach is to create ‘green zones’–dedicated areas at either the household, extended family or neighbourhood level, in which high-risk individuals (the elderly and those with chronic, underlying conditions) are relocated temporarily, and have minimal contact with family members and other community members at lower risk of severe disease.”

Scientific Advisory Group for Emergencies (SAGE) – Options for Increasing Adherence to Social Distancing Measures:
“The perceived level of personal threat needs to be increased among those who are complacent, using hard-hitting emotional messaging.”

MINDSPACE – Influencing Behaviour Through Public Policy:
“This means that citizens may not fully realise that their behaviour is being changed or, at least, how it is being changed. Clearly, this opens government up to charges of manipulation.”

Belgian Flu Commissioner on Public Engagement – How to Work With Media to Mislead the Public

Dr. Peter Doshi, “Will covid-19 vaccines save lives? Current trials aren’t designed to tell us.”
Dr. David Bauer: Pfizer vaccine produces fewer key antibodies
Dr. Peter Hotez: Testimony regarding development of coronavirus vaccine and unique safety challenges
Dr. Reiner Fuellmich: German Corona Committee – Dr. David Martin
Dr. David Martin: Covid-19 was deliberately released on the populations by entities with intent

Dr. David Martin: The Fauci COVID-19 Dossier

Gain-of-Function Hall of Shame

FOI Documents on Origins of Covid-19 Gain-Of-Function Research and Biolabs

Dr. Wu Zunyou: They Didn’t Isolate The Virus (Chinese Center for Disease Control)
Congressman Matt Gaetz Exposes Taxpayer-Funded Wuhan Lab Experiments

In December 2002, after President George W. Bush appointed Dr. Anthony Fauci to lead the US bioweapons program, Fauci discussed acquiring knowledge about bioweapons from “Soviet Union defectors who had vast experience in the ways of biowarfare.”

Dr. Fauci Backed Controversial Wuhan Lab with U.S. Dollars for Risky Coronavirus Research

Dr. Fauci worked behind the scenes to cast doubt on Wuhan lab leak hypothesis

Dr. Fauci Head of Creation and Development for Bill Gates Vaccine Research Center

Dr. Fauci Leadership Council for Bill Gates Decade of Vaccines Collaboration

Research on Highly Pathogenic H5N1 Influenza Virus: The Way Forward
Dr. Fauci, “The voluntary moratorium on gain-of-function research related to the transmissibility of highly pathogenic H5N1 influenza virus should continue, pending the resolution of critical policy questions concerning the rationale for performing such experiments and how best to report their results.”

Dr. Francis Collins, Director National Institutes of Health – Statement on Funding Pause on Certain Types of Gain-of-Function Research:
“NIH has funded such studies because they help define the fundamental nature of human-pathogen interactions, enable the assessment of the pandemic potential of emerging infectious agents, and inform public health and preparedness efforts. These studies, however, also entail biosafety and biosecurity risks, which need to be understood better.”

Dr. Peter Daszak, President of EcoHealth Alliance, “To sustain the funding base beyond the crisis, we need to increase public understanding of the need for MCMs such as a pan-influenza or pan-coronavirus vaccine. A key driver is the media, and the economics follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of process.”

Senate Committee on Health Education, Labor and Pensions Minority Oversight Staff: An Analysis of the Origins of the COVID-19 Pandemic
“The EcoHealth Alliance NIH grants and DARPA grant proposals, in partnership with the WIV, sought to collect and conduct genetic recombination experiments on SARS-related coronaviruses with specific traits that made those viruses a “high-risk” for zoonotic spillover into animals and humans. SARS-CoV-2 shares many of the traits these researchers were interested in finding in SARS-related coronaviruses or interested in engineering such traits if they were not found naturally. Based on the analysis of the publicly available information, it appears reasonable to conclude that the COVID-19 pandemic was, more likely than not, the result of a research-related incident.”

A Proposed Oversight and Decision Mechanism for Creating and/or Researching Potential Pandemic Pathogens:
“The viruses that are the subject of the White House order include highly pathogenic Asian influenza viruses that can transmit disease from mammal to mammal by the respiratory route (airborne transmission). Such viruses have already been created in the laboratory, in particular but not limited to the laboratories of Ron Fouchier and Yoshihiro Kawaoka. If one of these viruses escaped a laboratory, it could seed a pandemic with thousands to millions of human fatalities. These are called GOF studies of concern by the National Science Advisory Board forBiosecurity (NSABB), or simply studies of concern.”

Methods for producing recombinant coronavirus (PATENT: US7279327B2)
“This invention was made possible with government support under grant numbers AI23946 and GM63228 from the National Institutes of Health. The United States government has certain rights to this invention. The present invention relates to methods of producing recombinant nidovirus vectors, particularly coronavirus vectors, and expressing heterologous genes from said vectors.”

Nano coronavirus recombinant vaccine taking graphene oxide as carrier (PATENT: CN112220919A)
“The invention discloses a brand-new vaccine development method based on a graphene oxide material serving as a framework for loading CpG molecules and recombinant proteins. Based on the technical platform, a new nano new crown vaccine is prepared by combining the recombinant protein of the RBD region of the Spike protein of the SAR-CoV-2.”

Forensic examination of Wuhan Institute of Virology COVID-19 patient specimens from December 2019 reveals gross contamination of the laboratory, including undisclosed research on a lethal BSL-4 pathogen.

A Bayesian analysis concludes beyond a reasonable doubt that SARS-CoV-2 is not a natural zoonosis but instead is laboratory derived

Leaked Grant Proposal Details High-Risk Coronavirus Research

NIH Documents Provide New Evidence U.S. Funded Gain-of-Function Research in Wuhan

U.S. Department of Defense issued a contract for ‘COVID-19 Research’ in Ukraine 3 months before Covid was known to even exist
U.S. Government Gain-of-Function Deliberative Process and Research Funding Pause on Selected Gain-of-Function Research Involving Influenza, MERS, and SARS Viruses
U.S. Department of Health and Human Services – Framework for Guiding Funding Decisions about Proposed Research Involving Enhanced Potential Pandemic Pathogens
Gain-of-Function Deliberative Process

Gain of Function Research

Project DEFUSE: Defusing the Threat of Bat-borne Coronaviruses

Global Pandemics: Gain-of-Function Research of Concern

EcoHealth Alliance: Understanding the Risk of Bat Coronavirus Emergence

Dr. Andrew Huff, Former Vice President of EcoHealth Alliance: The Truth About Wuhan

A New Approach to Evaluating the Risk–Benefit Equation for Dual-Use and Gain-of-Function Research of Concern
Methods and compositions for chimeric coronavirus spike proteins
A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence
Baric to lead $10 million NIH grant
NIAID renews 5 year grant for research on emerging viruses
DECEMBER 12, 2019 an agreement was signed (PAGE 105) that Dr. Ralph Baric of the University of North Carolina would receive “mRNA corona virus vaccine candidates developed and jointly-owned by NIAID and Moderna”

WUHAN Institute of Virology Lab press release about partnership with Department for International Development and Bill & Melinda Gates Foundation
Meet the world’s most powerful doctor: Bill Gates
Bill Gates and his coronavirus conflicts of interest
Journalism’s Gates keepers

Who Funds The WHO?

U.S. Philanthrocapitalism and the Global Health Agenda: The Rockefeller and Gates Foundations, Past and Present

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