There are two ways to be fooled. One is to believe what isn’t true; the other is to refuse to believe what is true. —Soren Kierkegaard. "…truth is true even if nobody believes it, and falsehood is false even if everybody believes it. That is why truth does not yield to opinion, fashion, numbers, office, or sincerity–it is simply true and that is the end of it" – Os Guinness, Time for Truth, pg.39. “He that takes truth for his guide, and duty for his end, may safely trust to God’s providence to lead him aright.” – Blaise Pascal. "There is but one straight course, and that is to seek truth and pursue it steadily" – George Washington letter to Edmund Randolph — 1795. We live in a “post-truth” world. According to the dictionary, “post-truth” means, “relating to or denoting circumstances in which objective facts are less influential in shaping public opinion than appeals to emotion and personal belief.” Simply put, we now live in a culture that seems to value experience and emotion more than truth. Truth will never go away no matter how hard one might wish. Going beyond the MSM idealogical opinion/bias and their low information tabloid reality show news with a distractional superficial focus on entertainment, sensationalism, emotionalism and activist reporting – this blogs goal is to, in some small way, put a plug in the broken dam of truth and save as many as possible from the consequences—temporal and eternal. "The further a society drifts from truth, the more it will hate those who speak it." – George Orwell “There are two ways to be fooled. One is to believe what isn’t true; the other is to refuse to believe what is true.” ― Soren Kierkegaard
The FDA announced the removal of the Emergency Use Authorization of the COVID vaccine. The FDA and Pfizer knew of serious safety signals before the Emergency Use Authorization.
Pfizer’s own early safety review, the “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of BNT162b2” dated February 2021, catalogued more than 42,000 adverse event reports with nearly 160,000 individual events in just the first three months.
Pfizer concluded that none of these “were consequential enough” to hold back approval. The FDA went along with it. Now, with independent science repeatedly confirming risks of myocarditis, pericarditis, and waning effectiveness, there is action.
The slogan “safe and effective” became the government’s mantra, repeated endlessly while concerns were dismissed as fringe. Yet large-scale studies now show otherwise.
The Lancet published evidence of elevated myocarditis risk in young men. Nature Communications confirmed that even the dosing interval influenced heart inflammation outcomes.
Multiple NEJM and JAMA reports documented that protection against infection dropped below 20% after just six months.
This is not a profile of safety or effectiveness; it is a failed medical product. To continue marketing it under false pretenses while evidence piles up is a dereliction of duty by both regulators and pharmaceutical executives who cashed in at the expense of public health.
Worse yet, Pfizer and federal agencies had the data in hand. Their confidential February 2021 report detailed tens of thousands of adverse events across multiple organ systems. Yet they waved it away as inconsequential.
Independent researchers, re-analyzing the same trial data, later found a 3.7-fold increase in cardiovascular deaths among the vaccinated compared to placebo. Other peer-reviewed papers have confirmed pregnancy complications, menstrual irregularities, and disproportionate cardiac risks in young males.
These are not side effects “rare enough to ignore.” They are red-flag signals that should have stopped the rollout in its tracks. Instead, Americans became unwitting subjects in a massive, uncontrolled experiment. Even those who earnestly researched before getting the shot were acting off of severely flawed information.
With former skeptics now leading efforts to phase out the vaccine, the writing is on the wall. But why just a partial ban? Every additional day this is allowed means more people exposed to risks that government officials and corporate leaders knew about from the start.
The Pfizer website to this day downplays the side effects of its COVID shot and says that health concerns are rare.
Paul’s warning in Galatians 6:7 comes to mind: “Do not be deceived: God is not mocked, for whatever one sows, that will he also reap.”
We have reaped disastrous results from the sowing of deceptive seeds. It’s time to reap honesty, not deception; transparency, not concealment.
While the FDA move is in the right direction, the COVID vaccine should be banned sooner rather than later. Anything less just prolongs the, say it with me…Stupidocrisy.
Sources
5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of BNT162b2. (Feb 2021) PDF
The U.S. Food and Drug Administration (FDA) under the Trump administration has formally updated the safety labeling on all mRNA COVID-19 vaccines to reflect what many Americans have been warning about for years: a disturbingly high risk of myocarditis—particularly in young men—and the possibility of long-term, irreversible heart damage.
The revised warnings apply to both Pfizer’s Comirnaty and Moderna’s Spikevax vaccines and follow months of mounting pressure over transparency and accountability regarding the true risks of these experimental injections.
The update stems from new studies and data showing persistent cardiac abnormalities months after vaccination—especially among males aged 12 to 24.
During a presentation of the new FDA safety data on Tuesday, Dr. Vinay Prasad, Director, Center for Biologics Evaluation & Research Chief Medical and Scientific Officer, walked the public through the harrowing evidence behind the label change.
Prasad detailed how FDA data reveals a myocarditis rate of 27 per million in young men—a figure that experts say is significantly underreported due to passive surveillance methods and political suppression of adverse event reports.
More troubling, Dr. Prasad cited late gadolinium enhancement (LGE) on cardiac MRIs as proof of sustained, potentially irreversible myocardial injury. According to Prasad, in one FDA-funded study, 60% of patients who suffered post-vaccine myocarditis still showed signs of LGE five months later.
WATCH:
🚨 Dr. Vinay Prasad announces an updated FDA safety label for mRNA COVID vaccines “based on persistent and concerning cardiac MR findings” pic.twitter.com/tRqFeIsuk5
After denying and downplaying the risks for years, the FDA is now requiring both Pfizer and Moderna to update their Prescribing Information, Adverse Reactions sections, and Fact Sheets for patients and caregivers.
FDA has required and approved updates to the Prescribing Information for Comirnaty (COVID-19 Vaccine, mRNA) manufactured by Pfizer Inc. and Spikevax (COVID-19 Vaccine, mRNA) manufactured ModernaTX, Inc. to include new safety information about the risks of myocarditis and pericarditis following administration of mRNA COVID-19 vaccines.
Specifically, FDA has required each manufacturer to update the warning about the risks of myocarditis and pericarditis to include information about
the estimated unadjusted incidence of myocarditis and/or pericarditis following administration of the 2023-2024 Formula of mRNA COVID-19 vaccines and
the results of a study that collected information on cardiac magnetic resonance imaging (cardiac MRI) in people who developed myocarditis after receiving an mRNA COVID-19 vaccine.
FDA also required each manufacturer to describe the new safety information in the Adverse Reactions section of the Prescribing Information and in the Information for Recipients and Caregivers.
The Fact Sheets for Healthcare Providers and for Recipients and Caregivers for Moderna COVID-19 Vaccine and Pfizer-BioNTech COVID-19, which are authorized for emergency use in individuals 6 months through 11 years of age, have also been updated to include the new safety information in alignment with the Comirnaty and Spikevax Prescribing Information and Information for Recipients and Caregivers.
You can watch the full 15-minute presentation below:
One of these grenades was DNA contamination in the mRNAs — a topic that has thus far failed to penetrate the mainstream awareness bubble.
While independent scientists and media have been publishing news of excessive synthetic DNA contamination being detected in the mRNA shots since Boston-based genomics scientist Kevin McKernan first discovered it in early 2023, legacy media has ignored the issue, except for occasional articles brushing aside scientific findings as ‘anti-vax conspiracy theories.’
Most people who took the mRNA shots still have no idea that the vaccines contain plasmid DNA contamination and, in the case of the Pfizer vaccine, that the product they took is not even the same as the one that was tested in the landmark Randomised Controlled Trial (RCT).
Now, millions of listeners worldwide have been introduced to the topic.
The undisputed king of podcasting, Rogan has an audience of a whopping 14.5 million listeners on Spotify, 19.6 million subscribers on YouTube, 19.7 million followers on Instagram and 15.2 million on X.
The Dr Humphries episode had over a million views on YouTube on its first day. So when Dr Humphries told Rogan, “You’re one of the cracks in the matrix here, quite frankly,” she was not wrong.
Dr Suzanne Humphries on the Joe Rogan Experience, episode #2294
Bait and Switch
During a wide-ranging discussion covering everything from polio, to vaccine propaganda, to SV40, to vaccines and autism, to the multitude of risks of the Covid shots, Rogan asked Dr Humphries about the ‘bait and switch’, whereby Pfizer tested one vaccine product in its RCT, then changed its production process for the mass vaccine rollout.
Rogan: “All the things you said about the Covid vaccine I’m sure are correct and true, but isn’t it also different to the one they used in the test?”
Dr Humphries: “Yes. The vaccine that was produced for the general public, at least when it comes to Pfizer, they used magnetic beads for purification which was totally different to what they did for the one they gave to us.
“And they produced it using… they didn’t use plasmids and they didn’t use all these different components that were given to us.
“There were two aspects of the test vaccine that were very different — it was the production, and how they purified it.”
This is exactly right.
As highlighted by Dr Josh Guetzkow and Professor Retsef Levi in a rapid response in the British Medical Journal (BMJ) in July 2022, Pfizer used one method (Process 1) to manufacture its RCT vaccine, but switched to a different method (Process 2) to scale-up production for the mass rollout.
As Dr Guetzkow has since explained, when dealing with highly complex biological medical products, “the process is the product.”
Almost all of the 43,448 participants in Pfizer’s RCT received the Process 1 vaccine, while only 252 participants in the trial received the Process 2 vaccine, meaning that the vaccine doses administered to billions of people around the world were never tested at scale before being approved for use. No further safety data on the Process 2 product was ever provided to regulators.
“The differences include changes to the DNA template used to transcribe the RNA and the purification phase, as well as the manufacturing process of the lipid nanoparticles,” wrote Dr Guetzkow and Prof Levi.
Process 1 used In Vitro Transcription of synthetic DNA to make the spike-producing mRNA and a ‘clean,’ high-quality filtration process, as described by Dr Humphries.
Process 2, however, involves growing DNA plasmids in E. coli bacteria, from which the vaccine mRNA is then produced. The filtration is done with an enzyme that chops the leftover plasmids into tiny pieces, which are then supposed to be filtered out.
It is this manufacturing process, used by both Pfizer and Moderna, that has resulted in DNA contamination at levels far above the regulatory limit being found in an increasing number of mRNA vaccine vials around the world, including in an FDA lab, and most recently reported for vials from Ireland and from Slovakia (the full formal write up for both studies has yet to be released).
Verifications of mRNA vaccine DNA contamination to the end of 2024. Source.
In the Pfizer vaccine (but not Moderna), a genetic sequence called the SV40 enhancer-promoter has been detected, also there as a result of the switch to Process 2. This gene therapy sequence is known for its ability to drag material into the nucleus of cells, something that Covid vaccine components are not supposed to be able to do.
The potential implications of the DNA contamination arising from Process 2 are risks of genomic instability, cancers, immune system disruption, and adverse hereditary effects, warn leading scientists, doctors and academics.
Dr Humphries went on to add that the lipid nanoparticles (LNPs) encasing the DNA contamination effectively deliver this material straight into recipient cells, contrary to the promise that it would “never get past the deltoid and will be disintegrated in there.” [Note: Dr Humphries used the term lipopolysaccharide at first to refer to E. coli endotoxin resulting from Process 2, but I believe, based on the context, when she moved on to describing materials shuttling into cells, she muddled the terms and actually meant LNPs.]
Revelations
During the episode, Kevin McKernan (Anandamide) also got a mention for his discovery of the SV40 enhancer-promoter sequence in the Pfizer vaccine, which the pharma giant did not disclose to drug regulators during the approvals process.
Regulators have since confirmed that the Pfizer vaccine does indeed contain the SV40 sequence, but maintain that it is non-functional, despite admissions made in internal emails between staff of Australia’s Therapeutic Goods Administration (TGA) that it can, in fact, “promote nuclear transport of DNA,” which could give rise to genomic integration (which can in turn give rise to cancer).
Hopefully, the prospect of millions of Rogan’s followers hearing about DNA contamination in the mRNAs and that the Process 2 vaccine wasn’t even tested before being given to them will afford the opportunity for sober reflection and future informed consent.
The intent is not to scare the bejesus out of people, but to provide them with the information that they have a right to know. As McKernan likes to say, the stress hormone cortisol is not good for your health either.
The ‘crack in the matrix’ on this issue is welcome after long-held media silence on DNA contamination in the mRNAs and its implications for those who have taken (or are still taking) them.
Discussing the media blackout on a swathe of vaccine-safety concerns, Dr Humphries raised a 1984 publication by the US Food and Drug Administration (FDA) on the federal register relating to standards for polio vaccines, which states that:
“… any possible doubts, whether or not well founded, about the safety of the vaccine cannot be allowed to exist in view of the need to assure that the vaccine will continue to be used to the maximum extent consistent with the nation’s public health objectives.”
Indeed, the idea that suppression of “well-founded” doubts about vaccine safety in the interest of maintaining public confidence in public health programs appears to be the prevailing sentiment among regulators and their media henchmen to this day (with the exception of a handful of limited hangouts).
Interested readers can find out more about efforts to raise awareness of the DNA contamination in Covid mRNA vaccines in this recent press release sent to over 2,000 media contacts across the US, Europe, the UK, and Australia calling attention to a citizen petition filed with the FDA to revoke the mRNAs.
Note: I have not fact-checked every claim made by Dr Humphries over the course of the two-and-a-half-hour interview. On the topics I am well-versed in, I found her to be broadly accurate.
Historical records estimate that the atomic bombing of Hiroshima in 1945 killed at least 140,000 people. This catastrophic event changed the way the world viewed war and its consequences.
During the Covid-19 pandemic, physical bombs were not dropped, but the death toll from the vaccines has far surpassed that of Hiroshima, the city that bore the brunt of widespread nuclear devastation.
Dr. Nicolas Hulscher, an epidemiologist for the McCullough Foundation, made the association between nuclear bombs and Covid-19 vaccines for one simple reason–“the substantial data linking them to a catastrophic number of deaths.”
Hulscher has cited many research studies and databases which document the evidence that the Covid-19 injections have caused significant death and injuries worldwide. The list can be found here.
The Evidence is Overwhelming
He stresses, “There’s already enough evidence, there is now thousands upon thousands of peer reviewed manuscripts indexed in the National Library of Medicine that demonstrate harms from these injections. There are three facets that have been fulfilled and these include, number one excess mortality. There are 12 studies now and the Vaccine Adverse Events Reporting System (VAERS) that demonstrate these injections do in fact increase your risk of death, reduce life expectancy, and contribute to excess mortality among populations worldwide. We also have DNA contamination– this is confirmed worldwide across multiple manufacturers, multiple batches, and all these researchers use different methods, so it strengthens these findings even more. And then we have this negative efficacy–the vaccines don’t work, they increase your risk of infection. Clearly these shots have been demonstrated to be dangerous, ineffective and they need to be removed off the market.”
Hulscher writes, “COVID-19 vaccine death acknowledgment by federal agencies may mirror the same path as finally declaring smoking harmful in 1964 after years of claiming cigarettes to be healthy.”
Even though clear safety signals have been seen in the VAERS system, as well as the CDC’S V-Safe data, these agencies continue to hide the truth from the public. Just recently, after two years of FOIA (Freedom of Information Act) requests and lawsuits from ICAN (Informed Consent Action Network), the FDA finally released data that reveals “a long list of adverse events that far surpassed FDA’s standard alert threshold.”
World’s Largest Covid-19 Vaccine Safety Study Shows Safety Signals
In early 2024, the largest Covid-19 vaccine safety study ever conducted was published in the journal Vaccine. Results confirmed that Pfizer and Moderna’s mRNA injections and AstraZeneca’s adenoviral vector shots, are not safe. The study, involving up to 99 million vaccinated people, was led by researchers from the Global Covid Vaccine Safety Project based out of New Zealand and received funding from the Centers for Disease Control (CDC) and the U.S. Department of Health and Human Services (HHS).
Scientists in the study “calculated post-vaccination rates of neurological, cardiovascular and other outcomes occurring up to 42 days after the shots and compared them to background rates before the pandemic.” Data was collected and analyzed from Covid vaccinations given December 2020 through August 2023 across ten sites in Denmark, France, Canada, Argentina, Australia, Finland, Scotland and New Zealand.
Children’s Health Defense reported, “Myocarditis and pericarditis risks were significantly elevated after both mRNA vaccines and were seen across the first three doses. The highest risks were after the second Moderna vaccine dose—a 6.1 times increase in risk — and for pericarditis after the third dose of AstraZeneca—a 6.91 times increased risk…acute disseminated encephalomyelitis, or swelling in the brain, was 3.78 times more likely after the first Moderna dose. Researchers found a 2.49 times higher-than-expected occurrence of Guillain-Barré syndrome following the initial dose of the AstraZeneca vaccine. Cases of CVST (cerebral venous sinus thrombosis), which can lead to strokes, increased by 3.23 times after the first AstraZeneca dose.”
Though the results showed clear safety signals, it stands to reason that all possible adverse events could not have been documented because the cut-off date of 42 days post-injection is “unrealistic for all of the adverse events considered, especially cardiac conditions which appear primarily after physical exertion.”
Safety Signals are a Big Deal
Researchers in the study, funded by the CDC and HHS, maintain that adverse events are rare and pose a small risk, but cardiologist and epidemiologist Peter McCullough states, “As an epidemiologist, I can tell you these are not ‘small’ risks with COVID-19 vaccination. Adverse events were diluted over all age groups and were truncated at 42 days. For large populations, relative risks of 1.2 or greater are important, greater than 2 or 3 are frankly alarming.” McCollough added that under-reporting of adverse events to safety databases must be taken into consideration as well. Oftentimes, doctors, nurses, or people who are injured, fail to fill out a report in the databases that monitor vaccines.
McCullough stresses that the study’s data “fully support” the global withdrawal of all Covid 19 vaccines and boosters. He says, “They are not safe for human use.”
It should be noted that this particular study did not analyze or report on deaths following COVID-19 vaccination. Additionally, data from the United States Vaccine Adverse Events Reporting System (VAERS) was not included, which documented some of the worst Covid-19 outcomes.
Let the Evidence Speak
The evidence of harm from Covid-19 vaccines cannot be ignored. Public hearings in Washington D.C. have taken place, hosted by Senator Ron Johnson, that clearly document safety issues and devastating injuries. Doctors and whistleblowers continue sharing their stories, hoping that Covid-19 vaccines will no longer be offered, and that the CDC and FDA will be held accountable.
The Brownstone Institute posted an article on January 7, 2025 titled The Trump Administration Must Bring Moderna to Heel, which reported that Moderna withheld vital safety information about adverse events experienced during its trials. One such example included a preschool-aged child who died of “cardio-respiratory arrest” after receiving Moderna’s Covid mRNA vaccine during its clinical trials. “The death of the child only became known because of an obscure European report released last year, which revealed Moderna has known about the death for over two years while it continues to advertise Covid shots to children as young as six months old.”
It’s clear that the Covid-19 vaccines have caused worldwide devastation. There must be a global moratorium on these injections. Many organizations, physicians, and health freedom groups have been working tirelessly to make this a reality.
Accountability Must Happen
Intercessors, we must keep praying that the CDC, the FDA and other health agencies/authorities around the world are made accountable for the deaths and injuries the Covid vaccines have caused. We must also pray that further attempts at creating mRNA vaccines, such as the novel mRNA Bird Flu vaccines, would be halted in their tracks.
Lord Jesus, you are aware of every injury and death that the Covid-19 vaccines have caused. We cry out for justice for those who have been harmed. Please have mercy and help us win this difficult battle.
How are you praying about the mountain of evidence showing injuries and deaths from the Covid vaccines?
Angela Rodriguez is an author, blogger and former teacher who studies the historical and biblical connections between Israel and the United States. You can visit her blogs at 67owls.com and 100trumpets.com. She is also the author of Psalm 91: Under the Wings of Jesus and Hallelujah’sGreatRide. Photo Credit: Elen Sher on Unsplash.
President Trump’s “Stargate” project has come under fire, as many right-wingers are wary of its connection to mRNA vaccines. Should we be worried, or is this fear being blown out of proportion?
From Newsweek. A number of Donald Trump supporters and vaccine skeptics have criticized the president after he talked up multibillion-dollar artificial intelligence infrastructure project, which, it was suggested, could help develop vaccines for cancer. …
When it comes to vaccines, Trump has appeared to find himself between a rock and a hard place. He has faced frequent backlash from his own supporters for expressing support for the COVID-19 vaccine, especially when he praised the Operation Warp Speed initiative he launched during the pandemic, which accelerated vaccine development. …
What To Know
Trump announced a joint venture between OpenAI, Oracle, and SoftBank, which will be called Stargate, during a press conference on Tuesday. The project, which could cost up to $500 billion, was described by Trump as the “largest AI infrastructure project in history.” …
Stargate will start building data centers and the electricity generation needed for AI development in Texas, according to the White House.
Oracle Chairman Larry Ellison highlighted the potential medical benefits of the investment, stating that AI could be used to detect cancers and customize mRNA vaccines to treat them within 48 hours. …
The AI project has faced backlash from some Trump supporters and vaccine skeptics on social media.
In December 2021, Trump was booed by a section of the crowd after revealing he had received a COVID-19 booster shot while on stage at a speaking event with former Fox News host Bill O’Reilly. …
… Some have been skeptical about mRNA vaccines, which were used for COVID-19 …
What People Are Saying
Trump supporter @sovereignbrah posted on X, formerly Twitter: “Donald Trump will lose his base if he supports more mRNA vaccines. Mark my words.” …
Right-wing political commentator Evan Kilgore posted on X: “The ‘mRNA cancer vaccines’ discussed at Donald Trump’s first press conference tonight were a BIG turn off for a lot of Right-Wingers. The Trump Administration must learn that his base largely DESPISES him for Operation Warp Speed and how heavily experimental vaccines were pushed.” …
What do YOU think of Stargate? Share your thoughts and prayers below.
Experts warn that genetic fragments in inoculations might overstimulate the immune system, potentially leading to cancer
Pfizer’s mRNA Covid-19 vaccines contain residual DNA levels exceeding regulatory safety limits, according to a peer-reviewed study published this week in the Journal of High School Science.
The research was conducted by student scientists at the US Food and Drug Administration’s (FDA) White Oak Campus lab in Maryland.
Residual DNA refers to small pieces of genetic material that may remain in vaccines or medicines after manufacturing. These fragments come from the cells or processes used to make the products.
World Health Organization (WHO) guidelines state that a single vaccine dose should not contain more than 10 nanograms of residual DNA. The study, however, found levels in Pfizer’s vaccines exceeding this limit by six to 470 times.
Researchers analyzed vaccines obtained from BEI Resources, a supplier linked to the National Institute of Allergy and Infectious Diseases. They used NanoDrop and Qubit methods to measure DNA levels. Both methods showed contamination above acceptable thresholds. Residual DNA was found in six vials from two different vaccine lots.
While the study stated that health risks posed by the DNA fragments are “currently unknown,” researchers warned that, in theory, they could integrate into human DNA and increase the risk of gene mutations. They also raised concerns that the fragments may contain oncogenes, which could lead to cancer. The authors recommended further testing to assess the potential risks.
The FDA has not yet commented on the findings. While reports of DNA contamination in Covid-19 vaccines have been circulating for years, US regulatory authorities have repeatedly brushed them off, stating that they pose no health risks.
Kevin McKernan, founder of Medicinal Genomics, described the findings as a “bombshell,” and warned that DNA fragments might overstimulate the immune system, potentially “fueling cancer growth.”
“Repeated exposure to foreign DNA through Covid-19 boosters may amplify this risk over time, creating conditions conducive to cancer development,” McKernan said in an interview with Maryanne Demasi, an Australia-based investigative journalist who first drew public attention to the study.
Nikolai Petrovsky, professor of immunology and head of Vaxine, an Australian biotechnology company, said the findings were a “smoking gun” and needed urgent attention from regulators. Petrovsky also accused the FDA of withholding information from the public, saying that the study “clearly shows the FDA was aware of these data,” given that it was conducted in its own lab under the supervision of its own scientists.
The 2024 election is over, and many prayer warriors are breathing a sigh of relief. However, as members of the Biden Administration prepare to hand the reins to President Trump, some wonder how many eleventh-hour plans they can accomplish before exiting the White House.
President Trump will not take office until January 20, 2025, and this gives the Biden Administration a window of opportunity to sign executive orders and implement policies in what’s been dubbed a “sprint to the finish.” A recent CNN article reported that Biden “will direct his Cabinet to get as much work done as possible–whether that’s moving funding out the door, announcing new programs and policies, or delivering on programs and policies we have already announced.”
Vaccine Passports and Digital ID
While the list of damaging policies is long, Liberty Counsel, a law and policy organization that advocates Christian principles, warns that the Biden Administration’s plan to cede power to the World Health Organization before the end of the year is one of the most daunting. A recent email alert stated, “On December 1, the WHO will launch a Vaccine Passport. This is part of the new amendments to the International Health Regulations (IHR) that were ‘agreed’ upon in May of this year. Joe Biden and Kamala Harris are racing to position the WHO over America.”
For several months, media sources have reported that the White House is working on a cybersecurity executive order that would focus on identity management and artificial intelligence. A recent article in Biometric Update reveals, “A draft executive order yet to be signed by U.S. President Joe Biden will “strongly encourage the use of digital identity documents.” This order would piggyback off Biden’s 2021 Executive Order to tackle “unfinished business in the cybersecurity policy landscape.”
Liberty Counsel explains that this executive order is supposed to “strongly encourage the use of digital identity documents” and that the digital ID could be required to use “biometric authentication.”
Currently, there are 13 states that have launched a digital ID based on driver licenses, and at least 11 others are looking into it. Liberty Counsel stresses, “when this is digitized for a mobile device, government surveillance, tracking and tracing create a digital prison. This digital ID has the capacity to consolidate your health and financial data–in addition to all the information the government has on you.”
Big Pharma is Moving Forward
In April 2024, an international meeting called the World Vaccine Congress was held in Washington D.C., bringing together key players in the vaccine industry, such as Pfizer and Moderna, as well as representatives from the Rockefeller Foundation. The World Vaccine Congress will convene again in April 2025, where large numbers of vaccine developers, regulators, and investors will gather to discuss how to tackle the WHO’s “priority pathogens,” which include diseases such as COVID-19, RSV, and influenza. Even though the COVID mRNA vaccine caused record injuries and deaths worldwide, the pharma train keeps pushing “novel technology” before safety.
Vaccine Patch Technology
In tandem with the push for vaccine passports and digital IDs, new technologies such as vaccine patches are being developed at break-neck speed. In October 2024, University of Connecticut associate Professor Thanh Nguyen received “significant” funding from the Bill and Melinda Gates Foundation to develop vaccine microneedle patches. So far, the Gates Foundation has awarded a series of grants equaling $6.6 million to pursue this technology, which is supported by the National Institutes of Health and the US Department of Agriculture. Because of its affordability, patch enthusiasts believe the new technology will have a global health impact on human and animal vaccination.
Covid Restrictions Could’ve Been Worse!
The possibility of vaccine passports does not sit well in a post-Covid world. A recent article by the Brownstone Institute reminds the public how these digital or paper documents can infringe upon personal freedoms. “Consider the vaccine passports alone. Six cities were locked down to include only the vaccinated in public indoor places. They were New York City, Boston, Chicago, New Orleans, Washington D.C., and Seattle. The plan was to enforce this with a vaccine passport. It broke. Once the news leaked that the shot didn’t stop infection or transmission, the planners lost public support and the scheme collapsed.”
The article reveals that even though these Covid policies were bad, they were “intended to be worse.” The vaccine passport was meant to be permanent, nationwide, and possibly worldwide.
The Brownstone article highlights a plan that the CDC posted to its website on July 26, 2020, describing nationwide quarantine camps. The CDC titled this plan Interim Operational Considerations for Implementing the Shielding Approach to Prevent COVID-19 Infections in Humanitarian Settings. The framework prioritized isolating “high-risk individuals” and banning (shielding) them from interacting with the rest of the population.
The original document read, “High-risk individuals would be temporarily relocated to safe or ‘green zones’ established at the household, neighborhood, camp/sector or community level depending on the context and setting. They would have minimal contact with family members and other low-risk residents.” Another detail noted within the plan says, “One entry point is used for exchange of food, supplies, etc. A meeting area is used for residents and visitors to interact while practicing physical distancing (2 meters). No movement into or outside the green zone.”
Will There Be Another Pandemic?
Future pandemics are always on the minds of the World Health Organization and the CDC. Currently, the newsfeeds are abuzz with bird flu fears. Since January 2024, bird flu outbreaks among birds and cows have caused health authorities to sound the alarm that the H5N1 virus (bird flu) could spread all over the United States. Thus far, it’s suspected that bird flu has infected over 100 million birds and almost 500 dairy cattle herds across 15 states. The CDC reports that there have been 46 “confirmed” human cases of bird flu in the United States since the outbreak began, and those cases were mainly among dairy or poultry workers who had very close contact with infected animals.
Even though illness is mild in humans and there’s no evidence that the virus spreads from person to person, the U.S. government awarded Moderna $176 million in July 2024 to produce an mRNA bird flu vaccine against pandemic influenza. That same month, the WHO announced it had “launched an initiative to help accelerate the development of a human bird flu vaccine using mRNA technology.” The initiative is part of the WHO’s mRNA Technology Transfer Program, which will allow for a more “equitable response” when the next pandemic arrives. The Bill and Melinda Gates Foundation has also funded clinical trials for a self-amplifying mRNA vaccine targeting the bird flu virus.
While the Covid pandemic seems to have come and gone, there are still plans in the works that must be stopped in their tracks. There is a continual push for digital ID, both nationally and globally. Additionally, the pharmaceutical industry is producing a never-ending supply of vaccines for the WHO’s projected disease threats.
It’s Time to Take Action
Liberty Counsel states, “The WHO launched ‘voluntary’ international vaccine passports in March 2022, and instantly, two continents and the European Union jumped on board. Now the WHO wants these digital health records to be mandatory around the world. We have a very short window to stop the WHO Pandemic Agreement/Treaty and the IHR amendments!”
Liberty Counsel warns that Biden’s impending cybersecurity executive order and the last-minute plan to push the expanded International Health Regulations onto the American public pose a real danger to our freedoms. The World Health Organization continues to meet in a last-ditch effort to finalize its Pandemic Agreement/Treaty.
The White House plans to cede power to the WHO before President Trump takes office. Liberty Counsel stresses, “Once America signs on to this WHO Pandemic Agreement/Treaty, the global damage will be done…even if President Trump opts the U.S. out of the WHO, it will take 18 months to undo this entanglement. In the meantime, many other nations will be wrapped up in the international web. And this will directly impact America far beyond the 18-month window.”
Liberty Counsel has provided this link where you can fax members of Congress and let them know that you are against this globalist plan. The Sovereignty Coalition, an organization dedicated to stopping the WHO’s international takeover, has also provided resources and links where intercessors can take action.
Intercessory prayer is critical in addressing the looming threats of digital ID/vaccine passports and the release of “novel” vaccines.
Pray that any last-minute plans of the Biden Administration to launch digital ID and/or vaccine passports are stopped immediately. Pray that the executive order in process will fall to pieces.
Pray that Big Pharma projects, such as new mRNA vaccines or vaccine patches, would be halted.
Pray that the WHO’s Pandemic Treaty and IHR amendments would be scattered to the four winds as countries and their citizens rise up and speak out against schemes of global control.
Pray that the United States will exit the WHO and sever ties with the United Nations. (President Trump began the process to exit the WHO when he was in office, so pray that he is successful in securing a full withdrawal when he is back in the White House.)
Pray that people will not be overcome by a spirit of fear when it comes to pandemics and that God will protect our medical freedoms, as well as our national sovereignty.
Lord Jesus, the globalists want to control our country and our lives. Please protect us from these dangers and infuse our leaders and citizens with the courage to fight for our freedoms.
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Angela Rodriguez is an author, blogger and former teacher who studies the historical and biblical connections between Israel and the United States. You can visit her blogs at 67owls.com and 100trumpets.com. She is also the author of Psalm 91: Under the Wings of Jesus, and her first children’s book, Hallelujah’s Great Ride, was releasedin September 2023. Photo Credit: Gage Skidmore from Peoria, AZ, United States of America – Joe Biden, CC BY-SA 2.0, https://commons.wikimedia.org/w/index.php?curid=81734758.
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