Tag: covid-19

Top 7 SCARY TRUTHS the CDC does NOT want you to know about Covid-19 “vaccines” and “boosters”

Some people call it the plandemic. Others call it the scamdemic. Either way, most of the deaths did not come from the “novel” virus, but rather the toxic mRNA spike prions that invaded the vascular system of several billion people across the globe.

Another quiet Holocaust that nobody seemed to recognize, well, except for the natural health enthusiasts, who know better than to trust anything pushed by Big Pharma, especially when it’s created in a criminal-run laboratory, then injected into the sheeple’s “muscle tissue” to “build immunity.”

Then came the wave of “misinformation,” which really meant that all the truth-tellers and the whistleblowers who let everyone else know what the so-called “vaccines” really do, were labeled conspiracy theorists, anti-vaxxers and misinformation terrorists.

Meanwhile, Big Pharma, Big Media and Social Media swung the wrecking balls, destroying popular opinion and spreading ALL the misinformation about how hundreds of millions of people, who all happened to get the Covid jabs, “died suddenly” (from vascular clots, heart attacks, strokes and turbo cancer).

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Doctors Confirm Vaccine Connection after Young Ontario Woman Paralyzed after Moderna Shot – Then Offer Her Euthanasia as Remedy

A young mother’s life has been turned upside down in the wake of receiving her Moderna COVID-19 booster shot, which has left her paralyzed from the neck down, The Canadian Independent reported.

Kayla Pollock, a 37-year-old from Mount Albert, Ontario, has had her vibrant life of motherhood and community involvement brought to a sudden halt due to what doctors have diagnosed as a severe vaccine-related reaction.

Kayla, who suffered an abusive childhood, had overcome her past to find joy in her work as a behavioral trainer for exotic animals and later as an educational assistant. The single mother, known for her active lifestyle, was compelled to get vaccinated to ensure she could continue visiting her father in his long-term care facility.

However, after receiving her booster shot on January 11, 2022, Kayla began experiencing alarming symptoms, culminating in her complete paralysis less than two weeks later. Despite initial skepticism from emergency department staff, an MRI revealed a significant lesion on her spinal cord.

A neurologist, documented on an audio recording, expressed his belief that the vaccine was the likely cause of Kayla’s condition, a view later confirmed with a diagnosis of transverse myelitis – a rare inflammatory disorder caused by damage to the spinal cord.

The once active mother has since spent several months in hospital and rehabilitation centers, even being offered MAID – Medical Assistance in Dying – which she refused.

Medical Assistance in Dying (MAID) in Canada is a legal and voluntary form of euthanasia, allowing eligible adults to request assistance from a medical practitioner to end their lives.

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Vaccinated are susceptible to viral infections and “covid vaccine heart syndrome”

A recent paper examined the mechanisms that cause “covid vaccine heart syndrome.”

It raised the possibility of many mechanisms explaining the broad array of cardiac complications and the varying times from injection to presentation.  While they consider several causative factors, the researchers also speculate the known cardiotoxicity of adjuvants is involved.

Dr. Kevin Stillwagon points out what the researchers failed to mention; adjuvants focus white blood cells, known as T-cells, on what was injected and miss other things which allow them to get through the epithelial barrier.

Epithelial barriers – such as such as the skin, the gastrointestinal mucosal membrane and tissue lining the respiratory tract – are an important line of our bodies’ defence preventing the invasion of microorganisms and their products. Epithelial barriers are essential in protecting the body from the environment, covering internal cells, secretion and excretion, absorption and filtration.

Focusing T-cells to detect constituents of injections while ignoring everything else, means that infections will continue to occur as SARS-CoV-2 naturally mutates and viruses associated with other communicable diseases will get through our bodies’ natural barriers as well.

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The 2024 Santa Monica Film Festival was chock full of red-pilled conspiracy content

The 18th annual Santa Monica Film Festival, which held in-person screenings on Saturday, February 3 and which is running online screenings through February 28, chose to feature and then give awards to some dangerous right-wing conspiracy theories masquerading as “documentary” films.

The festival awarded “Best Documentary Feature” to The Great Awakening, the third film in anti-vaccine conspiracy theorist Mikki Willis’ Plandemic series. The Santa Monica Film Festival website describes the film:

The Great Awakening is the third installment of the ‘Plandemic’ series. This documentary experience assembles forbidden puzzle pieces to reveal the big picture of what’s really happening in America and beyond. The Great Awakening is intended to be a lighthouse to guide us out of the storm and into a brighter future.

 The Plandemic website also provides a description of the film:

Witness the culmination of truth-seeking as PLANDEMIC 3: The Great Awakening unravels the layers of corruption and unveils a path towards a brighter future. Prepare to be inspired, awakened, and empowered to take a stand for liberty.

After the screening, the audience was treated to a Q&A with Rizza Islam, anti-vaccine conspiracy theorist and member of the Center for Countering Digital Hate’s disinformation dozen.

The first installment of Plandemic was released May 4, 2000, and was largely responsible for the viral spread of COVID-19 conspiracy theories and vaccine disinformation. The New York Times explained in 2020 that nothing in the pandemic had gone as viral as the 26-minute short film, “a slickly produced narration that wrongly claimed a shadowy cabal of elites was using the virus and a potential vaccine to profit and gain power. The video featured a discredited scientist, Judy Mikovits, who said her research about the harm from vaccines had been buried.”

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COVID-19 Tested Our Commitment To Freedom. Three Years Later, We’re Still Failing

“The remedy is worse than the disease.”

– Francis Bacon

The government never cedes power willingly.

Neither should we.

If the COVID-19 debacle taught us one thing it is that, as Justice Neil Gorsuch acknowledged, “Rule by indefinite emergency edict risks leaving all of us with a shell of a democracy and civil liberties just as hollow.”

Unfortunately, we still haven’t learned.

We’re still allowing ourselves to be fully distracted by circus politics and a constant barrage of bad news screaming for attention.

Three years after the onset of the COVID-19 pandemic, which gave world governments (including our own) a convenient excuse for expanding their powers, abusing their authority, and further oppressing their constituents, there’s something being concocted in the dens of power.

The danger of martial law persists.

Any government so willing to weaponize one national crisis after another in order to expand its powers and justify all manner of government tyranny in the so-called name of national security will not hesitate to override the Constitution and lockdown the nation again.

You’d better get ready, because that so-called crisis could be anything: civil unrest, national emergencies, “unforeseen economic collapse, loss of functioning political and legal order, purposeful domestic resistance or insurgency, pervasive public health emergencies, and catastrophic natural and human disasters.”

COVID-19 was a test to see how quickly the populace would march in lockstep with the government’s dictates, no questions asked, and how little resistance the citizenry would offer up to the government’s power grabs when made in the name of national security.

“We the people” failed that test spectacularly.

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Caught Red Handed: Fauci, Gates & Moderna are responsible for the COVID Pandemic – U.S. D.O.D issued a ‘COVID-19 Research’ contract 3 Months before COVID was known to exist – & Fauci & Moderna had a Vaccine ready in Dec. 2019

The discovery of a contract awarded by the U.S. Department of Defense to Labyrinth Global Health for “COVID-19 Research” in November 2019 has raised questions about the permanent U.S. Government’s knowledge of the novel coronavirus.

The contract was part of a larger project for a “Biological threat reduction program in Ukraine,” suggesting the permanent U.S. Government was at the very least aware of the alleged virus before it spread through Wuhan, China in December 2019.

But the findings also suggest the permanent U.S. Government may have had a hand in the creation of this alleged virus in Biolabs through Gain of Function Research overseen by Dr Anthony Fauci.

This would explain why they knew the name of the novel coronavirus disease three months prior to the World Health Organization officially naming it Covid-19 in February 2020.

And it may also explain why Moderna and Fauci’s National Institute of Allergy and Infectious Diseases (NIAID) had a confidentiality agreement for an mRNA Coronavirus vaccine candidate in early December 2019, which was developed and jointly owned by Moderna and Fauci’s NIAID.

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Study of Nearly 100 Million COVID-19 Vaccine Recipients Reveals a Host of Adverse Events

A multinational study of over 99 million vaccinated people has identified higher incidences of neurological, cardiovascular, and blood disorder complications than what the researchers expected.

The peer-reviewed observational cohort study, published in the Vaccine journal on Feb. 12, aimed to evaluate the risk of 13 adverse events of special interest (AESI) following COVID-19 vaccination. The AESIs spanned three categories—neurological, hematologic (blood), and cardiovascular.

It reviewed data collected from more than 99 million vaccinated people from eight nations—Argentina, Australia, Canada, Denmark, Finland, France, New Zealand, and Scotland—looking at risks up to 42 days after getting the shots.

The study looked at three vaccines—Pfizer and Moderna’s mRNA vaccines as well as AstraZeneca’s viral vector jab.

Researchers found higher than expected cases that they deemed met the threshold to be potential safety signals for multiple AESIs, including for Guillain-Barre syndrome (GBS), cerebral venous sinus thrombosis (CVST), myocarditis, and pericarditis. A safety signal refers to information that could suggest a potential risk or harm that may be associated with a medical product.

  • GBS is a disorder in which a body’s immune system attacks the nerves, and can eventually paralyze the whole body. Most people with the condition require hospitalization. A “statistically significant increase” in GBS cases was observed after the first AstraZeneca shot. The researchers had expected 76 GBS events in the observational cohort study but ended up identifying 190.
  • Acute disseminated encephalomyelitis (ADEM) is a condition that typically occurs after a bacterial or viral infection. It causes inflammation of the central nervous system. Two cases were expected. However, the study identified seven events after the first Moderna jab.
  • Bell’s palsy is a weakness or paralysis of facial muscles. Higher than expected Bell’s palsy cases were identified after the first dose of the Pfizer and Moderna vaccines.
  • CVST is a condition in which blood clots form in the brain, blocking the blood from draining out. This can end up causing a hemorrhage. While 21 events were expected, researchers identified over three times the number of cases at 69 following the first dose of AstraZeneca vaccine. CVST cases were also higher than expected after the first and second Pfizer shots.
  • Myocarditis is inflammation of the heart muscle. Higher than expected cases of myocarditis that met the threshold for “prioritized safety signals” for the condition were “consistently identified following a first, second, and third dose of mRNA vaccines,” both Pfizer and Moderna, according to the study.
  • Pericarditis is an inflammation of the outer lining of the heart. The number of pericarditis cases exceeded expectations following “all doses of all the three vaccines,” researchers wrote.

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US Officials Concede No Active Surveillance On Long-Term Effects Of COVID-19 Vaccines

In a Feb. 15 hearing by the Select Subcommittee on the Coronavirus Pandemic, U.S. health officials side-stepped a question when asked whether the U.S. Food and Drug Administration (FDA) is actively conducting extended safety surveillance on those who received early COVID-19 vaccines.

Rep. Nicole Malliotakis (R-N.Y.) asked Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, whether the FDA is conducting active surveillance and if there are any specific health markers they’re studying that may signal trends requiring further inquiry.

“Every time we go through and do the safety surveillance, we start back, and it goes back to 2020. In some cases where we’re looking for certain things, we might use a different window, but indeed, we have to look from the beginning of the period of surveillance. I can turn it over to Dr. Jernigan because he can speak for CDC [Centers for Disease Control and Prevention] in that regard,” Dr. Marks said.

“So with regard to myocarditis, we certainly have been monitoring the issue with various different data systems. I think the most recent data really demonstrates that you’re about eight times less likely to get myocarditis if you’re vaccinated compared to those that are unvaccinated,” Dr. Daniel Jernigan, director of the National Center for Emerging and Zoonotic Infectious Diseases at the CDC responded.

Rep. Malliotakis told Jernigan she wanted to know about “everything,” not just myocarditis.

Dr. Jerrigan asked her to repeat the question, and she asked again whether the FDA was conducting extended safety surveillance on early recipients of COVID-19 vaccines.

“Most of the reports that we get of adverse events are in the few weeks following the vaccination,” Jernigan said. In terms of monitoring these over time, Jernigan said the agency has “vaccine effectiveness” systems in place at the CDC.

Neither Jernigan nor Marks referenced any active surveillance initiatives being undertaken by their agencies to monitor people who received the original COVID-19 vaccines for long-term health effects.

“There is no system in place for long-term vaccine safety surveillance in this country,” Ms. Liz Willner, founder of OpenVAERS, told The Epoch Times.

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BREAKING: FIRST LOOK AT THE “FREE-TEXT” COVID VACCINE SAFETY DATA THE CDC WANTED TO HIDE

When the CDC created V-Safe as a way to track individuals who received the experimental COVID-19 “vaccines,” the agency vowed to be completely transparent. Remember—despite forcing millions of frightened human beings to take the jab—there were subpar clinical trials. One recipient shared, “The only reason I took this b******* vaccination is because my job gave me two choices. Sign a waiver or get the shot. I [got] the shot in fear of losing any benefits.” So it makes sense, and seems mandatory, that the CDC create a system for individuals to share how they feel after receiving the experimental, mRNA-driven “vaccines.” To build trust in that system, the CDC touted V-Safe as “the most intensive safety monitoring effort in U.S. history.” Yet, as severe adverse events, including death, rapidly ascended following the EUA-pushed jabs, the CDC failed to be transparent with the data, releasing, when ordered by the Court in 2022, only superficial details. But persistence paid off. Last month, a federal judge ordered the CDC to release all 7.8 million detailed “free-text” data entries over the next 12 months. The “free-text” section is the only place in V-Safe for participants to potentially report serious adverse events. Yesterday, the CDC released the initial batch of data containing symptoms reported after being injected. The eye-opening entries are telling.

The free-text entries are critical because, shockingly, despite having an index of “adverse events of special interest” listed in its protocol, V-Safe entirely omitted those same adverse events from being tracked. As explained by ICAN, instead of asking V-safe participants about whether, for example, they experienced things such as anaphylaxis, myocarditis, or coagulopathy after taking an entirely experimental “vaccine” based on technology never before used, the CDC carelessly only asked about minor and generalized reactions, such as “chills,” “headache,” “fatigue or tiredness,” and “vomiting.” Thus, for users who may have wanted to report more serious adverse events, they must use the “free-text” field, which allows up to 250 characters. This data is crucial to understanding the safety profile of the COVID-19 “vaccines.” The fact the CDC had not thus far voluntarily released this critical data is indicative of the overall failure of the federal government’s responsibility to protect the health of Americans.

ICAN’s initial win in two previous lawsuits opened the door to obtaining V-Safe data. However, the taxpayer-funded CDC argued that producing the “free-text” entries was too burdensome an endeavor for them to be responsible for. Nevertheless, the Court strongly disagreed, noting that the “Production of the free-text data will permit independent researchers to put the government agencies to their proof by considering all of the available data.” Reporting on this outstanding victory  brought by the lawyers that regularly represent ICAN on behalf of the Freedom Coalition of Doctors for Choice, ICAN explained the Court recognized that:

“The development and distribution of the COVID-19 vaccine was one of the greatest endeavors in recent history. Predictably, the American public now seeks access to COVID-related papers to ensure that relevant government policies were — and still are — supported and justified by the available data. That is precisely what FOIA contemplates and facilitates.”

Indeed, District Court Judge Matthew Kacsmaryk’s ruling is a huge win for transparency, and yesterday’s first production of at 390,000 entries outlining what users experienced in the first two days of receiving the “vaccine” is telling. And unfortunately, it’s indicative of what’s to follow. Indeed, the “free-text” data, which is available here, has an overall theme of uneasiness. Users reported “anaphylaxis”—a severe, potentially life-threatening allergic reaction—numerous times, detailing experiences such as, “Emergency room visit for anaphylaxis … went to the ER … I had repeat facial swelling.” One user wrote, “Anaphylaxis within 10 min. of being vaccinated. Throat swollen almost shut.” Another user wrote:

“After receiving the shot (within 15 mins) I had an allergic reaction (tightening of the throat, dizziness, confusion, elevated heart rate) and was taken to the ER. Received steroid shot, Benadryl shot, and ephephrine shot. Was released to go home.” The user later wrote, “Feeling of mild allergic reaction in the throat. Elevated heart rate.”

Interestingly, thousands of users reported an odd “metallic taste” in their mouth, often accompanied by a tingling feeling in their tongue, lasting anywhere from a few minutes to hours or longer. Equally as many people—in the thousands—experienced rapid and concerning heart rates. Likewise, in addition to ongoing feelings of intense anxiety, numbness, dizziness, stiffness, fatigue, and diarrhea, thousands went to the emergency room within 24 to 48 hours of receiving the “vaccine.” One user described their experience at the ER, stating, “3 to 5 days after my shot, I experienced a rash around my eye that was painful and burning. I reported to the emergency room on Thursday, 12/24, diagnosed with shingles/herpes zoster, which I’ve never had before, so I’m just suspicious if that could have been a result of my first dose of the COVID vaccine.” Sadly, over 600 users specifically noted they were pregnant when they received the shot. Did the CDC monitor them more closely? They should have. Twenty-two users reported having a miscarriage that coincided with receiving the “vaccine.” One such user wrote:

“I had a miscarriage. I should’ve been 8 weeks pregnant but the baby stopped  growing at 6 weeks which would’ve been very close to when I received my vaccine.”

It will take weeks to sift through the disturbing “free-text” entries detailing the myriad of troubling symptoms users experienced within the first couple of days after getting the “vaccine.” The 390,000 initial entries emphasize the potential for more serious adverse event symptoms like myocarditis that may be revealed as more “free-text” data files are released. Despite the unsettling entries, given the disaster that has been the COVID-19 “vaccine” campaign, reviewing the data is a massive step in the right direction. ICAN remarked, “This ruling sends a clear message to our federal agencies: we are not moving on and forgetting about the pandemic or the actions they took. ICAN will not stop until ALL the data is released to the public and there is true transparency and accountability around COVID-19.”

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Conspiracy Theory Debunker Finds Real Conspiracies

The 2023 book Misbelief by Dan Ariely belongs to a genre I would label “debunking Covid conspiracy theories.” The book is meant to explore the thought process of people who subscribe to conspiracy theories, especially about Covid and the Covid vaccines. 

Thus I was surprised to encounter in the book two stories in which the author uncovered real conspiracies to hide information about Covid from the public. 

Ariely, a professor of psychology at Duke University, played a bit part in promoting Covid lockdowns around the world. By his own description, he worked 

…on projects related to Covid-19 with the Israeli government and a bit with the British, Dutch, and Brazilian governments as well…I was mostly working to try to get the police to use rewards to incentivize good mask-wearing behavior and observance of social distancing instead of using fines… (p. 4) 

The first genuine conspiracy he describes involved the US Food and Drug Administration (FDA) manipulating data in the Vaccine Adverse Events Reporting System (VAERS).

The second involved a newspaper editor-in-chief refusing to report about vaccine side effects observed by a hospital. The author reports these situations matter-of-factly, and even gives the conspirators the benefit of the doubt, saying maybe they did the right thing! 

Let’s look at the VAERS conspiracy (recounted on pp. 274-276). Ariely says he got this information directly from a person who works “in the information technology department of the FDA.” The agency, according to the story, determined that: 

…foreign powers, mostly Russian and Iranian, had found a way to spread disinformation using VAERS. So when the FDA identified cases that had clearly come from such sources, it removed them from the system…

Not only did it delete this data, but it did so silently. Ariely only found out by accident: Parents of vaccine-injured children maintained their own copy of the VAERS data, downloaded from the FDA site. They noticed that cases appearing in their downloaded data later disappeared from the government copy of the database, and they told Ariely about this. 

Supposedly the FDA tried to keep these actions secret because it “did not want to announce to the foreign powers that it was onto them,” the FDA employee told him. But to anyone reasonably well-versed in information technology, keeping such acts secret is an obvious mistake. The bad guys will figure out what is going on; the folks we are trying to protect are left in the dark about possible mischief affecting data they rely on. And that’s the most charitable assessment of their actions. It could be worse: the FDA might have removed valid information inadvertently (putting aside possible nefarious intentions at this point). How might that come about? 

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