Jesus said, "Recognize what is in your sight, and that which is hidden from you will become plain to you . For there is nothing hidden which will not become manifest." Gospel of Thomas (5)
Syringes containing a COVID-19 vaccine in Needham, Mass., on June 21, 2022. (Joseph Prezioso/AFP via Getty Images)
Officials across the United States are continuing to spread misinformation about COVID-19 vaccines, The Epoch Times has found.
The claims include unsupported or misleading statements about vaccine effectiveness and safety.
The vast majority of officials responsible for the misinformation were unable or unwilling to provide evidence backing their claims.
The Louisiana Department of Health is among those exaggerating vaccine effectiveness. The agency claims in a promotional message that the vaccines “are 100% effective at preventing serious hospitalizations and deaths.”
The message does not cite any evidence and the department did not respond to a request for comment.
Clinical trials for the Moderna and Pfizer vaccines estimatedeffectiveness against severe illness at 100 percent, but studies since then have shown the protection starts much lower and drops quickly. That’s led to the clearance and recommendation of boosters, which confer a boost that also wanes.
Louisiana’s statement is one of many that rely on data from 2021, before the Omicron virus variant emerged, or even 2020. That data has little connection with the present state of the pandemic.
South Dakota’s health department, meanwhile, says that “Nearly everyone in the United States who is getting severely ill, needing hospitalization, and dying from COVID-19 is unvaccinated.”
Such statements are “directly related” to the drop in public confidence in health authorities during the pandemic, Dr. Jay Bhattacharya, a professor of medicine at Stanford University, told The Epoch Times after reviewing a sample of the claims.
“The public understands when they’re being manipulated,” he added.
Many state health agencies are offering falsehoods about COVID-19 vaccine safety and effectiveness, or downplaying negative information about the shots—a continuation of a trend that dates back to when the vaccines became available in late 2020.
One theme emerged over the summer—hyping vaccine effectiveness for young children after U.S. authorities authorized and recommended the Pfizer and Moderna shots for children aged 6 months to 5 years.
“We welcome having COVID-19 vaccines to help protect our youngest Marylanders against severe illness, hospitalization, or even death from this virus and strongly encourage parents to vaccinate their children,” Maryland Health Secretary Dennis Schrader said in a statement.
“Clinical trials proved that the pediatric vaccine is an effective way to prevent COVID infection and serious illness in young children,” the Massachusetts Department of Public Health says on its website.
But the clinical trials for the age group weren’t able to measure efficacy against severe illness, which has been acknowledged by the U.S. Centers for Disease Control and Prevention (CDC).
“The clinical trials were not powered to detect efficacy against severe disease in this young population,” Dr. Sara Oliver, a CDC medical officer, told a meeting over the summer.
Saying the vaccines protect young children against severe disease “is a leap of faith,” Dr. David McCune, a hematology and oncology doctor in Washington state, told The Epoch Times. “It’s not supported by the research.”
Officials in every state were asked to provide evidence for dubious or false statements. Maryland officials pointed to a CDC page that did not support Schrader’s statement. Massachusetts officials did not respond to an inquiry.
False Statements on New Boosters
The U.S. Food and Drug Administration (FDA) recently authorized updated booster shots from Moderna and Pfizer. The CDC then recommended them for virtually all Americans aged 12 and older, and later enabled children 5 to 11 to get one of the new shots.
Clinical trials for the bivalent boosters, which contain spike protein components targeting the original COVID-19 strain and the BA.4/BA.4 Omicron subvariants, were not done—and have not been completed—on any group of humans as of yet.
Officials relied on data from testing in mice, data from the original vaccines, and a BA.1/Wuhan bivalent that has never been available in the United States.
The testing on that bivalent, done in adults 18 and older (Moderna) and adults 55 and older (Pfizer), showed that the updated boosters triggered higher levels of antibodies than the old boosters. But the trials didn’t provide any efficacy estimates for protection against infection or severe illness.
The dearth of data didn’t stop states from promoting the vaccines as tools that would definitely work.
“Adding a component to the boosters that specifically targets the subvariants currently circulating will help restore protection against COVID-19 infections, including hospitalizations, that has decreased over time,” Dr. Dean Sidelinger, Oregon’s state epidemiologist, said in a statement.
“The updated bivalent COVID-19 booster, along with the flu vaccine, give parents two powerful tools to protect their children from severe illness and hospitalization,” Dr. Sameer Vohra, the director of the Illinois Department of Public Health, said.
Officials in Oregon and Illinois did not respond to requests for comment.
Minimizing Side Effects
Many states emphasize how most side effects are mild. That’s true, according to data from the CDC and studies. But a number of states fail to mention serious side effects, like heart inflammation, that have been linked to the vaccines.
New York, Pennsylvania, and South Carolina, for instance, didn’t mention myocarditis, a form of heart inflammation, or thrombosis with thrombocytopenia syndrome (TTS), a severe blood clotting issue.
Most of the states that did mention myocarditis promoted the idea that the incidence of myocarditis is higher after COVID-19 infection than after COVID-19 vaccination.
“Myocarditis and pericarditis are much more common if you get sick with COVID-19,” the Washington state Department of Health says on its website.
“The risk of developing myocarditis after a COVID-19 infection is much higher than the risk of developing myocarditis after the vaccine,” the Alabama Department of Public Health said in a press release over the summer.
But more papers show a higher rate of myocarditis after vaccination in high-risk groups, especially young men, including one provided by authorities in Alabama.
Asked for evidence for its statement, Alabama officials sent a link to a British study published after its release was issued. But the study detected a higher risk for young males, or men aged younger than 40 years old, after vaccination.
After that was pointed out, Alabama officials stopped responding.
Some states, like Oregon, say no deaths have been linked to myocarditis after COVID-19 vaccination. Researchers around the world, including with the CDC, have determined there’s a causal link between myocarditis and the Pfizer and Moderna vaccines, which both utilize messenger RNA (mRNA) technology. And autopsies and medical records have confirmed deaths from myocarditis among the vaccinated.
Florida and othercountriesrecommend against or don’t advise messenger RNA vaccination, or the Moderna and Pfizer vaccines, for some age groups due to myocarditis.
TTS is an often-fatal form of blood clotting that happens on occasion after receipt of the Johnson & Johnson vaccine, according to federal officials. The FDA restricted the Johnson & Johnson vaccine due to TTS.
Dr. Danice Hertz, who was injured by a vaccine, says that the statements underline her experience with the health care system and top federal officials. That includes the FDA not acknowledging how many Americans have actually been injured by one of the shots.
“I blame the FDA and our federal government for creating this environment where doctors don’t know anything about vaccine injuries,” she said.
Outdated Information
A number of states still cite data from 2021 or even 2020, even though over half a dozen new variants have emerged since COVID-19 first appeared.
“FDA-authorized COVID-19 vaccines protect against Delta and other known variants,” the Oklahoma State Department of Health says on its website.
The Delta variant stopped circulating in the United States in 2021.
Oklahoma also says that so-called breakthrough cases, or post-vaccination infections, “happen in only a small percentage of vaccinated people.”
That hasn’t been true since Omicron displaced Delta in late 2021.
The California Department of Public Health links to a study from the CDC that was published in August 2021 when claiming that unvaccinated people who already had COVID-19 “are more than twice as likely as vaccinated people to get it again.”
Studies from late 2021and2022 show that post-infection protection, known as natural immunity, is superior to vaccination. Natural immunity has also held up better, but also waned against newer variants.
Heavy Reliance on the CDC
Nearly all of the state health agencies rely heavily on the CDC and other federal agencies.
Many repeatedly reference the CDC on their websites. The CDC has promoted misinformation on COVID-19 vaccines during the pandemic, including the unsupported claim that the vaccines protect young children against severe illness and promoting a study that exaggerated the COVID-19 death toll among children.
States that did provide evidence to back claims mostly cited CDC studies and documents.
The CDC publishes a quasi-journal called the Morbidity and Mortality Weekly Report. The CDC has said (pdf) the publication is distinct from “all other health-related publications,” in part because the content “constitutes the official voice” of the CDC and because most articles are not peer-reviewed. Instead, multiple levels of CDC officials review a submission.
“By the time a report appears in MMWR, it reflects, or is consistent with, CDC policy,” the CDC said in one overview of the publication.
The CDC and its partner, the FDA, have aggressively promoted vaccination during the pandemic, even when little evidence supports the vaccines. The agencies have also repeatedly refusedto releaseCOVID-19 vaccinesafety data.
Dr. Todd Porter, a pediatrician in Illinois, said that the effort to get virtually all children vaccinated against COVID-19, despite the small amount of efficacy and safety data, is contributing to parents hesitating over other vaccines.
“This has created a much different conversation with parents of my patients with respect to benefit/harm and has further eroded parent confidence in public health and has made it harder for me to make recommendations for other more important proven vaccines,” Porter told The Epoch Times in an email. “Most notable has been lack of influenza vaccine uptake in my patients over the past year.”
Steps Forward
Regaining people’s trust is key to moving forward and involves acknowledging information that was conveyed is not correct, experts said.
“When a public health authority or federal official says something that’s incorrect, it has a responsibility to correct it. And when it doesn’t, when it just lets the matter lie, people continue to distrust them even more,” Bhattacharya said.
One example, he said, is how officials repeatedly said—and some are still saying—that the vaccines cut down on transmission, even though a top Pfizer executive recently acknowledged testing on transmission has not been done. The claim that vaccines curb transmission helped lead to vaccine mandates.
“I think it would go a long way if our nation’s public health institutions could demonstrate humility and acknowledge that in the panic of the pandemic they got it wrong where it comes to children,” Porter said.
The urge to get people vaccinated has led to some of the false and misleading claims, according to McCune, who saw the same pattern repeated during the rollout of the new boosters.
“You could have started with the bivalent booster and said, ‘this is what we know. We know some things about antibody levels from basic science studies that were done in animal models and from similar vaccines that were given to humans that we have a reason to believe these antibodies are going to improve,’” he said. “And then to say, ‘the reason we were approving this is we think that this has overall been a safe program, and we don’t anticipate there’ll be future problems. We’re making a leap here to try and get ahead of it, even though there’s some uncertainty.’ That’s an honest statement, but it’s not a very salesy statement.”
McCune foresees it taking years to rebuild trust in public health, and believes it will require changes at both the CDC and FDA.
Zachary Stieber covers U.S. and world news for The Epoch Times. He is based in Maryland.
Eva Fu is a New York-based writer for The Epoch Times focusing on U.S. politics, U.S.-China relations, religious freedom, and human rights. Contact Eva at eva.fu@epochtimes.com
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Spike Protein Disrupting Immunity in Millions After COVID Infection or Vaccination: Here’s How It’s Being Treated
The spike proteins cause inflammation, turn off type 1 interferon response, and reduce autophagy among other things, all of which adds up to a dysregulated immune system MARINA ZHANG Oct 23 2022
The coronavirus spike protein (red) mediates the virus entry into host cells. It binds to the angiotensin converting enzyme 2 (blue) and fuses viral and host membranes. By Juan Gaertner/Shutterstock
Multiple studies have shown that the SARS-CoV-2 spike protein is a highly toxic and inflammatory protein, capable of causing pathologies in its hosts.
The presence of spike protein has been strongly linked with long COVID and post-vaccine symptoms. Studies have shown that spike proteins are often present in symptomatic patients, sometimes even months after infectionsor vaccinations.
The numbers of long COVID and post-vaccine cases have been climbing in the United States, increasingly posing as a healthcare problem.
Data from the Centers for Disease Control and Prevention (CDC) estimates that around 7 percent of Americans are currently experiencing long COVID symptoms, which would be over 15 million people. Some people with long COVID have been so debilitated that they cannot go to work, the same has been reported in people experiencing post-vaccine symptoms.
Over 880,000 adverse events have been reported to the Vaccine Adverse Event Reporting System (VAERS) database for possible post-COVID vaccine symptoms.
However, statisticians argue that the number of people suffering from post-vaccine syndromes is much higher.
Canadian molecular biologist Jessica Rose estimated an underreporting factor of 31, adding up to an estimation that more than 27 million Americans may have suffered from adverse events following vaccination.
“The vaccine-injured are vast,” said Dr. Pierre Kory on Oct. 15 at a Front Line COVID-19 Critical Care Alliance (FLCCC) conference.
“The numbers are massive … they are underserved and their needs are not being met.”
However, many doctors are looking to change this situation. The FLCCC has been at the forefront in treating COVID-19, long COVID, and post-vaccine symptoms.
No large-scale studies have been done on treatment for post-vaccine symptoms. Based on clinical observations, patient feedback, and extensive research, the FLCCC has released its updated treatment recommendations.
The FLCCC co-founder and Chief Scientific Officer Dr. Paul Marik told The Epoch Times that recommendations are always subject to change based on patient feedback, as well as research on a new treatment option.
However, to understand the treatment options, one first needs to understand how the spike protein is causing damage.
Pathology of Spike Proteins
Long COVID and post-vaccine syndrome share a high degree of overlap as the two conditions have both been linked to long-term spike protein presence, and the symptoms are often similar too.
“The core problem in post-vaccine syndrome is chronic ‘immune dysregulation,’” Marik shared at the FLCCC conference.
Spike proteins can cause chronic inflammation. Studies have shown that inflammation can lead to cell stress, damage, and even death. Cells make up tissues, different tissues form organs, and organs are part of our own physiological systems. Therefore spike protein injuries are a systemic syndrome.
Spike proteins trigger chronic inflammation by causing immune dysregulation. Spike proteins enter immune cells, switch off normal immune responses, and trigger pro-inflammatory pathways instead.
The normal immune response for infected immune cells is to release type 1 interferons, this gives signals to other immune cells to enhance defense against viral particles. But spike protein reduces this signaling in infected cells, and uninfected cells will also take in and become damaged by the spike protein as the infection goes out of control.
Marik said that a critical aspect of long-term spike protein damage is that it inhibits autophagy, your body’s way of recycling damaged cells. Usually, when cells have been infected with viral particles, the cells will try to break these particles down and remove them as waste.
However, studies on SARS-CoV-2 viruses have shown that autophagy processes are reduced in infected patients, with spike proteins present many months after the initial exposure.
“The spike protein is a really wicked protein,” said Marik. “It switches off autophagy, that’s why the spike can stay in the cells for such a long time.”
Dr. Paul Marik, co-founder of the Front Line COVID-19 Critical Care Alliance (FLCCC) and former Chief of the Division of Pulmonary and Critical Care Medicine at Eastern Virginia Medical School, at the FLCCC conference “Understanding & Treating Spike Protein-Induced Diseases” in Kissimmee, Fla. on Oct. 14, 2022. (The Epoch Times)
Immune Cell Dysfunction
The immune dysfunction caused by spike protein not only causes inflammation, but also may also contribute to cancer proliferation, and autoimmunity.
Studies have shown that spike proteins can reduce and exhaust the action of T and natural killer cells. These two cell types are responsible for killing infected cells and cancerous cells. Therefore a reduced cellular immunity from T and natural killer cells can contribute to an untimely clearance of spike-infected cells.
Damage from spike proteins can lead to damaged DNA, and studies have shown that spike proteins can also reduce DNA repair. Psychological and environmental stress such as ultraviolet light, pollutants, oxidants, and many other factors, can routinely damage DNA, requiring constant repair.
Damaged DNA puts cells at risk of becoming cancerous, and these cells should be killed to prevent cancer formations. However, with reduced T and natural killer cell activity, this may lead to unchecked proliferation of potentially cancerous cells.
Other dysfunctions that have been reported following vaccinations include autoimmune diseases.
These diseases may be linked to the spike proteins having a high level of molecular mimicry, meaning spike proteins have many regions similar to other proteins in the human body.
So when the immune system attacks the spike protein, due to structural similarities, the antibodies produced against spike protein regions may also react against the body’s own proteins and tissues. Studies have shown that antibodies made against the spike protein can also bind to and attack self tissues.
Spike Protein Causes Fatigue
The spike protein is also linked with dysfunction in the mitochondria. Colloquially known as the powerhouse of the cell, mitochondria are responsible for harnessing energy from the sugar we ingest.
Human neural cells treated with spike protein have been shown to produce more reactive oxygen species, and this is an indication of mitochondrial dysfunction, suggesting possible reduction in energy production.
People with long COVID and post-vaccine syndromes often experience chronic fatigue, brain fog, exercise intolerance, and muscle weakness. These symptoms are also often seen in people with mitochondrial dysfunction, indicating a possible link.
Dr. Paul Marik’s slides presented at the FLCCC Conference in Orlando Florida (Courtesy of the FLCCC)
Spike Protein Damage to Blood Vessels and Organs
Spike proteins have shown to be particularly damaging to cells that line blood vessels. Spike proteins can bind to ACE2 and CD147 receptors and trigger inflammatory pathways.
These receptors are particularly abundant in cells of the blood vessels, heart, immune system, ovaries, and many other areas. Spike protein can therefore trigger inflammation and damage in blood vessels and its related organs, leading to systemic injury.
Marik said that spike protein injury is closer to a systemic syndrome rather than a disease.
“It’s not a disease. It doesn’t fit the traditional model of a disease. This is a syndrome which affects every single organ … the spike goes everywhere … so this is a multi-systems disease and it doesn’t follow the traditional paradigm of a disease which is one symptom, one diagnosis.”
Dr. Pierre Kory’s slides presented at the FLCCC conference in Kissimmee, Fla. (Courtesy of the FLCCC)
FLCCC’s First Line Treatments
Since long COVID and post-vaccine symptoms are both associated with spike protein presence, the first line treatments recommended by the FLCCC therefore focus on two main steps.
The first step is to remove spike protein, the second step is to reduce its toxicity.
The body will then heal itself, and this is “the primary treatment goal,” said Marik.
Most of the first line treatments have focused on clearing out the spike protein by reactivating autophagy—a process that is downregulated by spike protein.
Lifestyle implementations can boost autophagy through intermittent fasting, and photobiomodulation. Photobiomodulation can be done by exposing oneself to the sun, since sunlight contains infrared rays that boost autophagy in cells.
Intermittent fasting can result in multiple health benefits including improved insulin sensitivity, weight loss, reduced inflammation and autoimmunity, and many more.
However it should be noted that intermittent fasting is not recommended for people younger than the age of 18, as it can prevent growth. Pregnant and breastfeeding women are also not recommended to fast intermittently. People with diabetes and kidney disease are also recommended to check with their primary care physicians before considering intermittent fasting.
While intermittent fasting may not be suitable for everyone, there are other treatment options that can boost autophagy and reduce spike protein toxicity.
(Sonis Photography/Shutterstock)
Ivermectin
Ivermectin has been highly recommended by the FLCCC and many doctors treating COVID, long COVID, and post-vaccine syndrome, on the basis that it is inexpensive, highly accessible, has a high safety profile, and a high response rate.
The drug is highly dynamic and has also been documented with a variety of functions: antiviral, anti-parasitic, anti-inflammatory, and also boosts autophagy.
Ivermectin can help with the removal of spike protein. Studies have shown that ivermectin has a higher affinity for the spike protein and will bind to its regions, effectively neutralizing and immobilizing it for destruction.
Ivermectin also directly opposes the pro-inflammatory pathways that are triggered by the spike protein including NF-KB pathway that activates inflammatory cytokines and toll-like receptor 4.
FLCCC doctors reason that ivermectin and intermittent fasting can act “synergistically” to remove the body spike protein, and recommends taking ivermectin with or just after a meal.
Ivermectin is also able to bind to ACE2 and CD147, and therefore blocks spike protein from entering and triggering inflammation in cells that display these receptors. Studies have also shown that ivermectin can maintain the energy produced by mitochondria even under conditions of low oxygen.
Kory said that around 70 to 90 percent of his post-vaccine syndrome patients respond to the drug, generally within 10 days.
“Patients can be classified as ivermectin responders or non-responders … the non-responders—[are] actually a group of patients that are more difficult to treat,” said Marik.
Patients that are non-responsive—typically after four to six weeks of treatment—are recommended to go on a more aggressive treatment.
When overdosed, ivermectin can cause confusion, disorientation, and possibly even death. However, the drug has a high safety profile when used in reasonable doses. There is little literature on its use in pregnant women so the FLCCC cautions against the use of it during pregnancy.
“Ivermectin has continually proved to be astonishingly safe for human use,” wrote Dr. Satoshi Ohmura, the discoverer of ivermectin in his co-authored study.
“Indeed, it is such a safe drug, with minimal side effects, that it can be administered by non-medical staff and even illiterate individuals in remote rural communities, provided that they have had some very basic, appropriate training.”
Screenshot of a photo of naltrexone, a medication approved for opioid and alcohol addiction that is used in low dose to treat long COVID. (innovationcompounding.com/screenshot by The Epoch Times)
Low Dose Naltrexone
Low dose naltrexone (LDN) has recently made the news as an option for long COVID treatment.
“We’ve been using it for many, many months,” said Marik. “Low dose naltrexone is a very potent anti-inflammatory drug. It’s been used in many chronic inflammatory diseases.”
Clinically, FLCCC doctors have seen many of their patients’ symptoms improve following treatment with LDN, though it may take months for the benefits to be clearly visible.
Normal naltrexone is commonly used to prevent overdose in narcotic users. However, when reduced to around a 10th of its normal concentration, to 1 mg to 4.5 mg in LDN, the drug’s mechanism changes dramatically.
LDN has an anti-inflammatory effect; studies show that it is able to block inflammatory toll-like receptors, reduce the production of pro-inflammatory cytokines, and block inflammatory cascades.
Th1 type cytokines tend to produce pro-inflammatory response to kill intracellular parasites and propel autoimmune activities. Th2 type cytokines typically have more of an anti-inflammatory activity and can counteract the activity of Th1 cytokines.
LDN selectively modulates this balance by reducing Th1 activity and increasing Th2 cytokine activities.
Clinically, LDN has been shown to be effective against post-COVID and post-vaccine neurological symptoms. It has been listed by the FLCCC to be effective against neuropathic pain, brain fog, fatigue, bell’s palsy, and facial paresthesia.
This is because LDN also reduces neuroinflammation. It is neuroprotective and is able to cross the blood-brain barrier and reduce inflammatory actions of the microglia, which function as immune cells in the brain.
Blueberries on a wooden table; focus on single blueberry (Shallow DOF)
Resveratrol
Resveratrol is a nutraceutical commonly found in fruits. It can be found in peanuts, pistachios, grapes, red and white wine, blueberries, cranberries, and even cocoa and dark chocolate.
It can also be obtained through vitamins, though there is generally a low bioavailability of resveratrol, and therefore the FLCCC recommends it to be taken with quercetin.
Resveratrol is anti-inflammatory and anti-oxidizing. Studies have shown it to be selective in killing cancer cells. It activates DNA repair pathways and therefore can reduce cellular stress and prevent the formation of cancerous cells.
In stressed cells, resveratrol can reduce reactive oxygen species produced by the mitochondria and promote autophagy. In animal studies on fruit flies and nematodes, the use of resveratrol increased their lifespan, indicating the molecule’s anti-aging and life-extending properties.
An arrangement of aspirin pills in New York. (Patrick Sison/File Photo via AP)
Low Dose Aspirin
Similar to ivermectin, aspirin is another drug that has been found to be multifaceted in its effects on health.
Aspirin is anti-inflammatory and an anticoagulant. The drug therefore reduces the chance of micro-clot formation in the blood vessels. Studies have shown that it can also reduce pro-inflammatory pathways, oxidative stress, and is also neuroprotective.
Neurocognitive impairment has been a major complaint of many people suffering from post-COVID vaccine syndromes. This includes brain fog and peripheral neuropathic pain.
Studies on Alzheimer’s disease patients have shown that taking aspirin was associated with slower cognitive decline, though results have been conflicting across different studies.
Animal studies showed that rats that were given aspirin had lower cognitive decline. Studies in rats with damaged nerves suggested that aspirin may also be neuroprotective due to its anti-inflammatory nature.
The use of aspirin may cause side effects in pregnancy and such as bleeding.
Molecule Of Melatonin. By Sergey Tarasov/Shutterstock
Melatonin
Melatonin is a hormone produced by the pineal gland to promote a restful sleep. It has both anti-inflammatory and anti-oxidizing properties.
In cells, melatonin promotes mitochondrial health by reducing active oxygen species. Because the mitochondria uses a lot of oxygen, when it is stressed through environmental toxins such as radiation or spike protein exposure, it may produce reactive oxygen species.
Melatonin, an antioxidant, can therefore prevent oxidative damage. Studies show that it also prevents leakage of electrons from mitochondria and therefore maximizes energy production.
It also promotes autophagy by unblocking the autophagy pathway, helping the cell to break down spike proteins and boost the removal of these toxic proteins.
Due to its anti-oxidizing property, melatonin repairs DNA damaged by free radicals. Melatonin and its metabolites also activate genes that promote DNA repair, and suppress gene activity that may lead to damaged DNA.
Melatonin also has anti-cancerous properties. Animal studies on melatonin have shown that animals that were administered melatonin had a lower rate of tumor generation.
Melatonin has also been recommended by the FLCCC in treating tinnitus, a symptom of post-vaccine and long COVID. The symptom is a ringing in the ears, and can disturb sleep if severe. Melatonin can help reduce the ringing and help people to get a good night’s sleep.
A bottle is shown reading “Vaccine COVID-19” and a syringe next to the Pfizer and Biontech logo on Nov. 23, 2020. (Joel Saget/AFP via Getty Images)
Differences Between Long COVID and Post-Vaccine Syndrome
Both long COVID and post-vaccine syndrome are driven by spike protein load and damage from spike exposure, and therefore share a high degree of overlap in treatment.
However, doctors notice slight differences in certain clinical presentations between the two conditions, and therefore the FLCCC have prioritized different treatments.
“It seems that with the vaccine injured, the predominant symptom and the predominant organ is neurological,” said Marik. In his observation, roughly “more than 80 percent of patients with vaccine injury have some degree of neurological impairment.”
Marik said post-vaccine symptoms can also be harder to treat than long COVID, and are more persistent, with some patients presenting with debilitating symptoms for almost two years.
Therefore treatment for people with post-vaccine symptoms are “more aggressive and more brain targeted,” said Marik.
“It seems like long COVID gets better with time. While some patients persist, it seems to be somewhat self resolving to a degree,” said Marik. “The problem with the vaccine-injured is that it can persist. We have patients who were vaccinated in December of 2020 … [who] are still severely, severely injured.”
“The two are similar, but we’ve put much more emphasis on the vaccine-injury because it’s a much more difficult disease to treat.”
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Dr. Ryan Cole: “Instead of like a wildfire, where we see people pass away quickly … we’re seeing more of a smoldering wildfire until the burden of disease … finally adds up to incompatibility of life.”
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“Dr. Francis Boyle is an international lawyer and biowarfare expert of over 30 years.
He confirms both Australian and United States legislation and documentation proving planned gain-of-function bioweapon releases that work hand-in-hand with what the globalists are doing through the WHO Treaty takeover.
Boyle says this will land dissidents in prison if the globalists are successful with their plans.”
The account behind the pro-Western meme also denied the Holocaust
The Polish Twitter user behind the ‘NAFO’ phenomenon locked his account on Saturday after critics discovered his lengthy record of posts praising Nazi Germany, insulting Jews and denying the Holocaust. The troll-in-chief insists he posted the controversial material “to fit in.”
Kamil Dyszewski has received glowingpraise in Western media for posting a crudely-edited Shiba Inu avatar to Twitter earlier this summer. The cartoon dog soon caught on, and pro-Ukrainian accounts began to display their own Shiba avatars and refer to themselves as ‘NAFO’, or the ‘North Atlantic Fellas Organization.’
Since then, the ‘Fellas’ can be found spreading Kiev’s talking points, ganging up to swarm polls and report pro-Moscow accounts, and soliciting donations for the Ukrainian military.
Before his work was lauded by American weapons manufacturers and their sponsored think tanks, Dyszewski used online platforms to post racialist propaganda about Jews, dispute the Holocaust, and praise Adolf Hitler and other top Nazis. Among the posts are cartoons denying the existence of gas chambers at concentration camps and a meme describing a comparison to Hitler as “nice,” as well as additional photos of the Nazi leader and his propagandist, Joseph Goebbels.
Questioned by some within his own ranks, Dyszewski locked his Twitter account on Saturday, but not before posting an explanation. Describing the controversial posts as “overly edgy and incredibly inappropriate ‘jokes,’” Dyszewski said that he made them “to fit in,” without explaining with whom he was attempting to fit in. He added that these posts, all made around 2020, “do not represent me as a person.”
While NAFO may have started with an offhand internet post by a Polish gamer, it has since grown into a internet-wide phenomenon, counting US Congressman Adam Kinzinger, Ukrainian Defense Minister Aleksey Reznikov, and a host of Western analysts, spies, and othermembers of the intelligence community as ‘Fellas.’
This member roll has led some critics to argue that NAFO is a creation of Western intelligence agencies. Similar pro-Ukrainian social media campaigns have previously been identified as relying on masses of ‘bot’ accounts.
For thousands of years, mystics have alluded to the presence of a biologically generated energy field, or aura, surrounding humans. Now scientific investigation indicates this may be more than mere mysticism and folklore. Biochemist John Norman Hansen, Ph.D., at the University of Maryland has found evidence that such an energy field could be real, lending credence to what spiritual practitioners have pointed to for eons.
Dr. Hansen conducted hundreds of experiments with dozens of subjects, and his results are consistently replicable. Other scientists have also reproduced his results, including Willem H. van den Berg of the department of biochemistry and biophysics at the University of Pennsylvania, and physicist William van der Sluys at Gettysburg College, who published their study in the Journal of Scientific Exploration on March 15.
Previous investigation of human bioenergy fields has used photon sensors. Dr. Hansen took a different approach. He wondered whether a bioenergy field, if it exists, would have enough force to push a torsion pendulum—a device sensitive enough to be moved by a subtle force. He hung the pendulum above the subject’s head and saw a clear change in the pendulum’s momentum.
He hung the pendulum above the subject’s head and saw a clear change in the pendulum’s momentum.
“After conducting control experiments to rule out effects of air currents and other artifacts, it is concluded that the effects are exerted by some kind of force field that is generated by the subject seated under the pendulum,” he explained in his 2013 study, titled “Use of a Torsion Pendulum Balance to Detect and Characterize What May Be a Human Bioenergy Field,” also published in the Journal of Scientific Exploration. “We know of no force, such as one within the electromagnetic spectrum that can account for these results. It may be that a conventional explanation for these surprising results will be discovered, but it is possible that we have observed a phenomenon that will require the development of new theoretical concepts.”
One of the outstanding observations was that the effect of the human presence continued for some 30 to 60 minutes after the human subject had already left. With other forces, such as air currents, the pendulum would immediately return to its classic, non-driven motion.
The mental state of a subject can strongly affect the behavior of the pendulum.
Every subject had roughly the same power to influence the pendulum “indicating that the effects on the pendulum require neither unique talent nor practice,” wrote Hansen in a synopsis of a talk he gave at the 34th annual Society for Scientific Exploration conference at the end of May 2015. “However, it has been observed that some subjects, especially ones that have pursued a meditative practice for many years, exert very different effects during a meditative state compared to a non-meditative state … which shows that the mental state of a subject can strongly affect the behavior of the pendulum.”
Is There a Conventional Explanation?
Van den Berg and van der Sluys used the same pendulum device—as Hansen has made the design public, encouraging others to replicate his results—and observed the same change in its movement when in proximity to a human head. They wondered, however, if this change may have been due to a change in air temperature from the heat emanated by a human head. The change in air temperature could cause convection currents, they said.
They wondered, however, if this change may have been due to a change in air temperature from the heat emanated by a human head.
They placed a layer of plastic between the head and the pendulum and found the effect on the pendulum disappeared. They suggested the plastic either cut the pendulum off from the mysterious bioenergy field, or it simply cut off the heat source.
Hansen published a reply to this study, however, noting what he sees as flaws in the theory that body heat caused the pendulum movement.
For starters, Hansen said, “If you were to place a thick plastic shield between the subject and the pendulum, the pushing force [of the bioenergy field] would initially be against the shield, and the pendulum would only respond to whatever pushing force remained after pushing against the shield. For the pushing force to survive passage through the shield and then push against the pendulum would violate fundamental principles of physics; i.e. you can only use a force once, and if it is utilized to push against the shield it cannot subsequently push against the pendulum.”
Another factor Hansen said that van den Berg failed to take into account is the persistent aftereffects. Hansen wrote: “A fundamental principle of pendulum physics is that if the pendulum is driven by an outside force and the force is removed, then the pendulum will immediately return to classic non-driven motion.”
Any accumulation of heated convection currents would quickly dissipate after the subject left. So convection currents could not explain these aftereffects. Hansen described the effects of the subject’s bioenergy field as being somehow “imprinted” on the pendulum.
He said the van den Berg study also failed to acknowledge the varied frequencies with which the pendulum oscillates in the presence of a human subject. The pendulum oscillates with a single frequency when the subject is absent. It oscillates with many new frequencies when the subject is present, and for some half an hour or more after the subject has left—something not explained away by convection currents caused by air temperature variations.
What does meditation really means? Dr. Joe Dispenza explains.
“There is no such thing as a bad meditation.”
I like that POV. As long as you attempt to control the immature ego, it’s better than not attempting at all.
In a COVID hearing, #Pfizer director admits: #vaccine was never tested on preventing transmission.
“Get vaccinated for others” was always a lie.
The only purpose of the #COVID passport: forcing people to get vaccinated.
The world needs to know. Share this video!
Pfizer Exec Concedes COVID-19 Vaccine Was Not Tested on Preventing Transmission Before Release
By Jack Phillips
October 11, 2022Updated: October 11, 2022
A Pfizer executive said Monday that neither she nor other Pfizer officials knew whether its COVID-19 vaccine would stop transmission before entering the market last year.
Member of the European Parliament, Rob Roos, asked during a session: “Was the Pfizer COVID vaccine tested on stopping the transmission of the virus before it entered the market? Did we know about stopping immunization before it entered the market?”
Pfizer’s Janine Small, president of international developed markets, said in response: “No … You know, we had to … really move at the speed of science to know what is taking place in the market.”
Roos, of the Netherlands, argued in a Twitter video Monday that following Small’s comments to him, millions of people around the world were duped by pharmaceutical companies and governments.
“Millions of people worldwide felt forced to get vaccinated because of the myth that ‘you do it for others,’” Roos said. “Now, this turned out to be a cheap lie” and “should be exposed,” he added.
The Epoch Times has contacted Pfizer for comment.
What Was Said
The Food and Drug Administration wrote in late 2020 that there was no data available to determine whether the vaccine would prevent transmission and for how long it would protect against transmission of the SARS-CoV-2 virus that causes COVID-19.
“At this time, data are not available to make a determination about how long the vaccine will provide protection, nor is there evidence that the vaccine prevents transmission of SARS-CoV-2 from person to person,” the agency specifically noted.
Meanwhile, Pfizer CEO Albert Bourla, around the same time, said his firm was “not certain” if those who receive its mRNA vaccine will be able to transmit COVID-19 to other people.
”I think this is something that needs to be examined. We are not certain about that right now,” Bourla told NBC News in December 2020 in response to a question about transmissibility.
Former White House medical adviser Dr. Deborah Birx in June revealed that there was evidence in December 2020 that individuals who received COVID-19 vaccines, including Pfizer’s, could still transmit the virus.
“We knew early on in January of 2021, in late December of 2020, that reinfection was occurring after natural infection,” Birx, the White House COVID-19 response coordinator during the Trump administration, told members of Congress this year.
‘Not Going to Get COVID’
A number of officials in the United States and around the world had claimed COVID-19 vaccines could prevent transmission. Among them, President Joe Biden in July 2021 remarked that “you’re not going to get COVID if you have these vaccinations.”
President Joe Biden speaks, flanked by White House Chief Medical Adviser on COVID-19 Dr. Anthony Fauci, during a visit to the National Institutes of Health in Bethesda, Md., on Feb. 11, 2021. (Saul Loeb/AFP via Getty Images)
Chief Biden administration medical adviser Anthony Fauci in May 2021 said in a CBS interview that vaccinated people are “dead ends” for COVID-19, suggesting they cannot transmit the virus. “When you get vaccinated, you not only protect your own health and that of the family but also you contribute to the community health by preventing the spread of the virus throughout the community,” Fauci said.
Two months later, in late July of that year, Fauci said that vaccinated people are capable of transmitting the virus.
In the coming months, Fauci, Biden, CDC Director Dr. Rochelle Walensky, and others pivoted to say the vaccine prevents severe disease, hospitalization, and death from COVID-19.
One of the world’s largest open-access journal publishers is retracting more than 500 papers, based on the discovery of unethical actions.
London-based Hindawi, which publishes more than 200 peer-reviewed journals across multiple disciplines, stated that its research team identified in June “irregularities” in the peer review process in some of the journals.
“All Hindawi journals employ a series of substantial integrity checks before articles are accepted for publication. Following thorough investigation, we identified that these irregularities in the peer review process were the result of suspicious and unethical activities. Since identifying this unethical activity and breach of our processes, we began proactively adding further checks and improving our processes and continue to do so,” Liz Ferguson, a senior vice president for John Wiley & Sons, Hindawi’s U.S.-based parent company, said in a Sept. 28 statement.
As a result of the investigation, 511 papers will be retracted.
The papers have all been published since August 2020.
Sixteen journals published the papers that are being retracted.
Some of the authors and editors who contributed to the articles may have been “unwitting participants” in the unethical scheme, according to Ferguson. She said the scheme involved “manipulation of the peer review process and the infrastructure that supports it.”
Richard Bennett, vice president of researcher and publishing services for Hindawi, told the Retraction Watch blog that the review uncovered “coordinated peer review rings,” which featured reviewers and editors coordinating to get papers through peer review.
Neither Ferguson nor Bennett identified any of the suspects.
Bennett said the investigation started after an editor flagged some suspicious papers. He also said the individuals identified by the review as “compromised” will be banned from Hindawi journals. Other people were described as “potentially compromised.”
“These efforts, and the individuals who participate in them, impede scientific discovery and impact the validity of scholarly research and will not be tolerated,” Ferguson said.
She also said the company has been in touch with other publishers and industry bodies.
Further retractions are expected as the investigation proceeds.
Hindawi journals include Advances in Agriculture, the Canadian Journal of Infectious Diseases and Medical Microbiology, and the Journal of Nanotechnology.
More Studies Confirm the COVID Jab Does More Harm Than Good
Cardiologist calls for the immediate suspension of all COVID shots as real-world data show they cause more harm than good.
STORY AT-A-GLANCE
A peer-reviewed scientific review in the Journal of Insulin Resistance, written by cardiologist Dr. Aseem Malhotra, calls for the immediate suspension of all COVID shots as real-world data show they cause more harm than good
Data from Israel shows myocarditis post-jab is occurring at a rate of 1 in 6,000. Hong Kong data from male children and teens found a rate of 1 in 2,700
Data from the British Yellow Card system shows 1 in 120 people who have received at least one mRNA injection suffer an adverse event “that is beyond mild.” In Norway, the rate of serious adverse events post-jab is 1 in 1,000 after two doses of Pfizer
Researchers looking at data from the FDA, Health Canada and the Pfizer and Moderna trials concluded the absolute risk of a serious adverse event from the mRNA shots was 1 in 800, which massively exceeds the risk of COVID-19 hospitalization found in randomized controlled trials
Leaked audio from a June 2022 meeting between Israeli researchers and the Israeli Ministry of Healthy reveals the Pfizer jab causes long-term adverse effects and is associated with more severe side effects upon rechallenge (i.e., with repeated doses). While the researchers wanted to warn the public, the Ministry altered their final report to say that adverse effects are mild and short-lived. The government then canceled any further research into adverse effects
The COVID jabs are an absolute disaster, with injuries and deaths piling up by the day. Yet so-called health authorities, doctors, media, drug makers and many of the jabbed themselves claim there’s nothing to see here. Ever since their release, brave medical professionals have spoken out against them, calling for a more cautious approach.
Now, a peer-reviewed scientific review,1 2 3 published in two parts4 5 in the Journal of Insulin Resistance calls for the immediate suspension of all COVID shots as real-world data show they cause more harm than good.
According to this paper, “Curing the Pandemic of Misinformation on COVID-19 mRNA Vaccines Through Real Evidence-Based Medicine,” authored by cardiologist Dr. Aseem Malhotra:
“In the non-elderly population the ‘number needed to treat’ to prevent a single death runs into the thousands. Re-analysis of randomized controlled trials using the messenger ribonucleic acid (mRNA) technology suggests a greater risk of serious adverse events from the vaccines than being hospitalized from COVID-19.
Pharmacovigilance systems and real-world safety data, coupled with plausible mechanisms of harm, are deeply concerning, especially in relation to cardiovascular safety.
Mirroring a potential signal from the Pfizer Phase 3 trial, a significant rise in cardiac arrest calls to ambulances in England was seen in 2021, with similar data emerging from Israel in the 16–39-year-old age group.
Conclusion: It cannot be said that the consent to receive these agents was fully informed, as is required ethically and legally. A pause and reappraisal of global vaccination policies for COVID-19 is long overdue.”
COVID Jab Boomerang
In recent months, disability, excess mortality and live birth statistics all point in the same direction. Something horrific started happening around April 2021, and continues to get worse. Something is killing an extraordinary number of people in the prime of their life, who should have decades left to live. Something is causing people to file for permanent disability in numbers we’ve not seen before.
What changed in the world, in 2021? That is the question. The answer is ridiculously simple to answer, yet many choose to drive their heads deeper into the sand than face plain facts. The COVID shots, using mRNA technology to trigger antibody production in a way that had never been used before, were rolled out in 2021 under emergency use authorization. That’s what changed.
At the time of their rollout, human trials were far from finished, and much of their value had already been destroyed by unblinding the trials and offering the real injection to everyone in the placebo groups.6
This year, we’ve also come to realize that Pfizer, the U.S. Food and Drug Administration and the Centers for Disease Control and Prevention have all repeatedly lied about the safety and effectiveness of the shots, as Pfizer’s own trial data show they’re about as dangerous as they come.
The only reason we now know this is because the FDA was sued and forced by a judge to release the trial data they initially wanted to keep hidden for 75 years. Pfizer data is now being released at a pace of 55,000 pages per month,7 and these batches have proven to be a treasure trove of bad and worse news.
Pfizer hid serious injuries, falsely categorizing almost all of them as unrelated to the shot without investigation, and misrepresented data showing massive risks as being of no concern. Participants who suffered serious injuries were often simply withdrawn from the trial, and their data excluded from the results.8
Real-world data now conclusively show these risks are extremely real. For example, Pfizer’s Phase 3 clinical trial showed an increased risk for cardiac problems, and during 2021, U.K. ambulance services recorded an extra 27,800 cardiac arrest calls above the national average in previous years, or about 500 per day9 10 — and disproportionally among the young.11 Importantly, COVID-19 cannot account for this rise, as the relevant increase began in the spring of 2021.
A Change of Heart
In his paper, Malhotra details his personal journey from staunch COVID jab proponent to concerned questioner. He got Pfizer’s two-dose regimen at the end of January 2021. You can see more of Maholtra’s efforts in the lecture he recently gave captured in the video above.
A few months later, his father, who also got the shot, suffered cardiac arrest six months after his second dose. The post-mortem findings were “shocking and inexplicable,” Malhotra writes, and got him to take another look at the data.
“After six months of critically appraising the data myself, speaking to eminent scientists involved in COVID-19 research, vaccine safety and development, and two investigative medical journalists, I have slowly and reluctantly concluded that contrary to my own initial dogmatic beliefs, Pfizer’s mRNA vaccine is far from being as safe and effective as we first thought,” Malhotra writes.12
He goes on to review how post-mortem examination revealed his father, who was extremely active and fit, had severe blockages in two of the three major arteries. His left anterior descending artery was 90% blocked and his right coronary was 75% blocked. The last scan, “a few years earlier,” according to Malhotra, had revealed perfect blood flow and no obstructions. He continues:13
“I couldn’t explain his post-mortem findings, especially as there was no evidence of an actual heart attack … This was precisely my own special area of research. That is, how to delay progression of heart disease and even potentially reverse it … Then, in November 2021, I was made aware of a peer-reviewed abstract published in Circulation, with concerning findings.
In over 500 middle-aged patients under regular follow up, using a predictive score model based on inflammatory markers that are strongly correlated with risk of heart attack, the mRNA vaccine was associated with significantly increasing the risk of a coronary event within five years from 11% pre-mRNA vaccine to 25% 2–10 weeks post mRNA vaccine.
An early and relevant criticism of the validity of the findings was that there was no control group, but nevertheless, even if partially correct, that would mean that there would be a large acceleration in progression of coronary artery disease, and more importantly heart attack risk, within months of taking the jab.
I wondered whether my father’s Pfizer vaccination, which he received six months earlier, could have contributed to his unexplained premature death and so I began to critically appraise the data.”
Data Points to Consider
Malhotra reviews a number of data points in the paper, including:14
Pfizer data showing there were four cardiac arrests in the injection group and only one in the placebo group.
The misleading use of relative risk reduction (95%) when speaking of effectiveness, rather than absolute risk reduction, which was only 0.84%.
119 people would have to be injected to prevent one positive test, which may or may not be indicative of infection.
Pfizer’s trial found no statistically significant reduction in serious illness or COVID mortality from the injection over the course of six months (the length of the trial). Moreover, the risk of serious COVID-19 infection in the placebo group was only 0.04%, showing just how low the risk of serious illness was in the first place, and this despite the fact that the regions chosen for the trial were chosen for their perceived high prevalence of infection.
While there were two deaths from COVID in the placebo group and only one COVID death in the injection group, all-cause mortality over a longer period revealed 19 deaths in the injection group and 17 deaths in the placebo group.
The pediatric trial used a surrogate measure of antibody levels rather than reduction in symptomatic infection, even though there was no known correlation between antibody levels and protection from infection. The FDA even warns that: “[R]esults from currently authorized SARS-COV-2 antibody tests should not be used to evaluate a person’s level of immunity or protection from COVID-19 at any time, and especially after the person received a COVID-19 vaccination.”
Extrapolating Data to Determine Protection Against Death
Malhotra goes on to describe how he extrapolated data to determine the level of protection these mRNA shots provide against COVID-related death:15
“Now that we know what the published trial did and did not show in terms of the vaccine efficacy, we can attempt to extrapolate what the effect of the vaccine would be in reducing mortality or any other adverse outcome from the virus.
If there is a 1 in 119 chance the vaccine protects you from getting symptomatic infection from ancestral variants, then to find the protection against death, this figure (n = 119) must be multiplied by the number of infections that lead to a single death for each age group.
This would give (for up to two months after the inoculation) the absolute risk reduction (for death) from the vaccine. For example, if my risk at age 44 from dying from Delta (should I get infected with it) is 1 in 3,000, then the absolute risk reduction from the vaccine protecting me from death is 1 over 3,000 multiplied by 119, that is, 1 per 357,000 …
From observational data it is possible to calculate the number who would need to be vaccinated to prevent a COVID-19 death. For example, comparing the population death rates during the Delta wave gives 230 for people over 80s needing to be vaccinated to prevent a single death in that period with that number rising to 520 for people in their 70s and 10,000 for people in their 40s …
Depending on your age, several hundreds or thousands of people like you would need to be injected in order to prevent one person from dying from the Delta variant of COVID-19 over a period of around three months.
For the over 80s, this figure is at least 230, but it rises the younger you are, reaching at least 2,600 for people in their 50s, 10,000 for those in their 40s, and 93,000 for those between 18 and 29 years. For omicron, which has been shown to be 30% – 50% less lethal, meaning significantly more people would need to be vaccinated to prevent one death.”
What Are the Harms?
Next, Malhotra reviews the hams, noting that one of the most common side effects reported is myocarditis, or inflammation of the heart, especially among young men. He rejects health authorities’ claim that myocarditis is far more prevalent in those who suffer serious COVID infection, stating:16
“Incidence of myocarditis rocketed from spring 2021 when vaccines were rolled out to the younger cohorts having remained within normal levels for the full year prior, despite COVID-19.
With the most up-to-date evidence, a paper from Israel found that the infection itself, prior to roll- out of the vaccine, conferred no increase in the risks of either myocarditis or pericarditis from COVID-19, strongly suggesting that the increases observed in earlier studies were because of the mRNA vaccines, with or without COVID-19 infections as an additional risk in the vaccinated …
Although vaccine-induced myocarditis is not often fatal in young adults, MRI scans reveal that, of the ones admitted to hospital, approximately 80% have some degree of myocardial damage. It is like suffering a small heart attack and sustaining some — likely permanent — heart muscle injury.”
Data from Israel shows myocarditis post-jab is occurring at a rate of 1 in 6,000. Hong Kong data from male children and teens found a rate of 1 in 2,700. Data from the British Yellow Card system shows 1 in 120 people who have received at least one mRNA injection suffer an adverse event “that is beyond mild.”
In Norway, Malhotra notes, the rate of serious adverse events post-jab is 1 in 1,000 after two doses of Pfizer. These are injuries that are life changing for the worse.
In all, nearly 500,000 adverse events had been reported to the Yellow Card system when Malhotra wrote this paper, which he points out is “unprecedented in the modern medical era and equals the total number of reports received in the first 40 years of the Yellow Card reporting system (for all medicines — not just vaccines) up to 2020.”
What VAERS Data Tell Us
The same trend is seen in the U.S., where the Vaccine Adverse Event Reporting System (VAERS) has received more adverse event reports for the COVID jabs than all other vaccines over the last 30 years combined. Malhotra writes:
“As with the UK’s system, the level of reports — including serious ones — associated with COVID-19 vaccines is completely unprecedented. For example, over 24,000 deaths have now been recorded in VAERS as of March 2, 2022; 29% of these occurred within 48 h of injection, and half within two weeks.
The average reporting rate prior to 2020 was less than 300 deaths per annum. One explanation often given for this is that the COVID-19 vaccine roll-out is unprecedented in scope; however, this is not valid, since (for the last decade at any rate) the United States has administered 150 million – 200 million vaccinations annually.”
Another criticism of VAERS is that ‘anyone can make an entry,’ yet, in fact, an analysis of a sample of 250 early deaths suggested that the vast majority are hospital or physician entries, and knowingly filing a false VAERS report is a violation of Federal law punishable by fine and imprisonment.
Given that VAERS was set up to generate early signals of potential harm for new vaccines, and was instrumental in doing so for several products, it seems perverse to only now criticize it as unreliable when there seem to have been no changes in the way it operates.”
It has been estimated that serious adverse effects that are officially reported are actually a gross underestimate, and this should be borne in mind … For example, a paper by David Kessler (a former FDA Commissioner) cites data suggesting that as few as 1% of serious adverse events are reported to the FDA. Similarly, in relation to the Yellow Card scheme in the United Kingdom, it has been estimated that only 10% of serious adverse effects are reported.”
1 in 800 Absolute Risk of Serious Side Effect
Malhotra also cites a recent study17 “coauthored by some of the most trusted medical scientists in the world in relation to data transparency,” which looked at data from the FDA, Health Canada and the Pfizer and Moderna trials.
Researchers looking at data from the FDA, Health Canada and the Pfizer and Moderna trials concluded the absolute risk of a serious adverse event from the mRNA shots was 1 in 800, which massively exceeds the risk of COVID-19 hospitalization found in randomized controlled trials.
They concluded the absolute risk of a serious adverse event from the mRNA shots was 1 in 800, which massively exceeds the risk of COVID-19 hospitalization found in randomized controlled trials.
“Given these observations, and reappraisal of the randomized controlled trial data of mRNA products, it seems difficult to argue that the vaccine roll-out has been net beneficial in all age groups … and when the possible short-, medium- and unknown longer-term harms are considered (especially for multiple injections, robust safety data for which simply does not exist), the roll-out into the entire population seems, at best, a reckless gamble,” Malhotra writes.18
“It’s important to acknowledge that the risks of adverse events from the vaccine remain constant, whereas the benefits reduce over time, as new variants are (1) less virulent and (2) not targeted by an outdated product.
Having appraised the data, it remains a real possibility that my father’s sudden cardiac death was related to the vaccine. A pause and reappraisal of vaccination Policies for COVID-19 is long overdue.”
The Israeli Cover-Up
In related news, leaked audio from a June 2022 meeting between Israeli researchers and the Ministry of Healthy reveals the researchers knew the COVID shots were associated with serious risks and wanted to alert the public.
However, whereas the researchers pointed out evidence showing the Pfizer jabs cause long-term adverse effects and are associated with more severe side effects upon rechallenge (i.e., with repeated doses), the Ministry altered the researcher’s final report to say that adverse effects are mild and short-lived. The government then canceled any further research into adverse effects.
At the end of September 2022, GB News interviewed Dr. Yaffa Shir Raz, who broke the story internationally19 (see video above for leaked audio and GB’s report).20 21 Importantly, the researchers noted the phenomenon of rechallenge is very strong evidence of causality, meaning the shots are definitely causing the problems reported.
However, they also warned the Ministry of Health that they’d have to be careful with the wording and think “medical-legal,” as the evidence would expose the government to liability, since they’d not been upfront with the risks and had endorsed the shots. The Ministry, apparently, decided to simply alter the conclusions of the study and close down further investigation rather than risk liability.
COVID Jab Makers Seek Authorization for Child Boosters
At the same time as more and more damning data are coming to light, Pfizer and Moderna are both seeking emergency use authorization for their bivalent COVID boosters for children. Moderna is seeking authorization for children ages 6 through 17, while Pfizer’s shot is for children aged 5 through 11.22 As reported by Reuters September 23, 2022:23
“… the U.S. Centers for Disease Control and Prevention said it expects COVID-19 vaccine boosters targeting circulating variants of the virus to be available for children aged 5-11 years by mid-October.
Moderna’s mRNA-1273.222, a bivalent booster shot, contains the dominant BA.4/BA.5 variants along with the original coronavirus strain. The updated vaccine is already authorized for adults, while rival Pfizer’s bivalent vaccine is authorized as a booster dose for children over 12 years of age.”
Follow the Data and Think for Yourself
Considering how reckless the FDA and CDC have been so far, there’s little doubt they’ll authorize these reformulated boosters for children, even though they’ve only been tested for antibody levels in mice. Meanwhile, in the real world, the injuries and deaths continue to pile up.
Were there any sanity and humanity left inside the walls of our health agencies, these shots would be pulled from the market without delay. Unfortunately, that doesn’t appear to be the case, which means We the People are the ones who must put a stop to the carnage by educating each other and simply saying “NO” to these and all future mRNA shots.
Biden Promises Ukraine’s Zelenskyy Advanced Air Defense Systems After Russian Missile Attacks
By Katabella Roberts
October 11, 2022Updated: October 11, 2022
President Joe Biden on Monday promised President Volodymyr Zelenskyy that Washington will supply Ukraine with advanced air defense systems amid Russia’s ongoing invasion.
The two leaders spoke on the phone shortly after Russia launched its largest air strike yet on Ukraine following the destruction of a bridge linking Russia to the annexed Crimean peninsula over the weekend. Russian President Vladimir Putin accused Ukraine’s security services of perpetuating the attack.
Russia’s strikes killed at least 11 civilians, Ukrainian officials said, and knocked out Ukraine’s power grid, leaving parts of the country with no electricity, water, or heat.
Thousands of residents were forced to shelter in bomb shelters throughout the day as missiles rained down on multiple cities, with explosions reported in Kyiv, Lviv, Ternopil, and Zhytomyr in western Ukraine, Dnipro, and Kremenchuk in the center, Zaporizhzhia in the south and Kharkiv in the east.
During Monday’s call, Biden “expressed his condemnation of Russia’s missile strikes across Ukraine, including in Kyiv, and conveyed his condolences to the loved ones of those killed and injured in these senseless attacks” according to a White House readout of the call.
“President Biden pledged to continue providing Ukraine with the support needed to defend itself, including advanced air defense systems,” the readout said.
Smoke rises over the city after a Russian missile strike, in Kyiv, Ukraine, on Oct. 10, 2022. (Oleksandr Klymenko/Reuters)
“He also underscored his ongoing engagement with allies and partners to continue imposing costs on Russia, holding Russia accountable for its war crimes and atrocities, and providing Ukraine with security, economic, and humanitarian assistance,” the statement added.
The White House did not state exactly which air defense systems Biden said he will supply to Zelenskyy during their call but earlier this year, Washington committed to provide Ukraine with National Advanced Surface-to-Air Missile Systems (NASAMS)
Those anti-aircraft systems are manufactured by the Norwegian company Kongsberg Defence & Aerospace and used to protect the airspace around the White House and Capitol in Washington. They can be used to strike Russian cruise missiles.
Ukrainian President Volodymyr Zelensky in Kyiv on Sept. 8, 2022. (Genya Savilov/POOL/AFP via Getty Images)
‘Sign’ of Russian Weakness
Zelenskyy’s office also issued a statement on Monday detailing his phone call with Biden which stated that the Ukrainian president informed Washington about the “consequences of the massive missile strikes against civilian infrastructure perpetrated today by the Russian aggressor.”
Zelenskyy said the “strikes against civilian targets throughout Ukraine are a sign of weakness of the Russian army which is losing on the battlefield. It is pure terror” but that Ukraine “will not succumb to the Russian missile blackmail,” according to the statement.
Biden and Zelenskyy also discussed the “importance of air defense, and continued U.S. contributions to increase this capability” the statement adds.
Cars are seen on fire after Russian missile strikes in Kyiv, Ukraine, on Oct. 10, 2022. (Valentyn Ogirenko/Reuters)
Russia-Ukraine Conflict Escalates
The two leaders also discussed the “upcoming extraordinary meeting of the Group of Seven Leaders (G7) dedicated to Ukraine and most pressing measures of support for Ukraine which can be adopted by the international community,” according to Zelenskyy’s office.
In total, the Biden administration has committed a total of $15.8 billion in military aid to Ukraine since Russia invaded Ukraine on Feb. 24.
The latest promise of advanced air defense systems to Ukraine comes as its conflict with Russia continues to escalate.
On Monday, Belarusian President Alexander Lukashenko, one of Vladimir Putin’s closest allies, said that some of his country’s 60,000-strong army will deploy with Russian forces near Ukraine.
Lukashenko said the decision was made because Ukraine had been preparing to attack Belarus with help from allies Poland and Lithuania, although he did not provide any evidence relating to such claims.
“Strikes on the territory of Belarus are not just being discussed in Ukraine today, but are also being planned,” Lukashenko said at a meeting on security. “Their owners are pushing them to start a war against Belarus to drag us there.”
Following Lukashenko’s announcement, Polish citizens in Belarus were being advised by the government to leave the country as relations between the two countries increasingly turned sour.
Reuters contributed to this report.
Katabella Roberts is a news writer for The Epoch Times, focusing primarily on the United States, world, and business news.
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The Plandemic was intentional and The Psychologic Operations Revealed
When he was 19 years old, Jeffrey C. attempted suicide after finding out his girlfriend was cheating on him with his best friend. After he swallowed a lot of pills, his mother realized what had happened and called an ambulance.
Jeffrey hadn’t been a model citizen, but his experience of nearly dying was pivotal in mending his ways.
He recalled seeing the afterlife.
Seeming to exit his body, Jeffrey saw a doctor standing over him, he stated in an article on the Near-Death Experience Research Foundation’s website. He found he was able to enter the doctor’s body and could read his mind.
“I went into him and saw images of his wife, kids, and his car. I felt the panic in him,” Jeffrey recalled.
A spirit being took his hand and pulled him away. He could see his own body and a doctor and nurse working to revive him. The being took him into a “column of light.” At first, he was in a place that he thought was heaven, with cloud-like walls. There he saw his grandmother.
Then suddenly, he was in a foul-smelling field with people who had jackal faces. A demonic creature grabbed him and brought him to a place with a bunch of cubes stacked up.
The demonic creature told him that each person gets a custom-made hell.
“He told me this was hell, and in every cube was a custom-made hell for every soul,” Jeffrey said. “He explained that people adapt to every kind of hell, and some people are more tolerant of some things than others, so hell is ever changing. He took great joy out of watching people suffer.”
Jeffrey was sucked into one of the cubes, where people fed him rank food and laughed. Then he was shown flashes of all the bad things he had ever done.
“I was being put into other people’s shoes as I was doing bad things to them,” he said.
“I could see how insensitive I was to people and didn’t even know it. It was excruciating and overwhelming to relive things that I had forgotten about, or just didn’t care about. I was made to feel the way I made others feel.”
Then he was kneeling in a cave, with other people around him also kneeling.
“I saw a girl kneeling with her wrists cut, a man with a rope around his neck, and another with the back of his head blown out,” Jeffrey said. “I could hear screaming from the cave ahead, and I was trying to get one of these people to talk to me and tell me where I was. One of them told me to be quiet or I would be next. Then a huge, ugly demon reached out of the cave, grabbed them, and dragged them into the cave.”
When he closed his eyes, he was suddenly overwhelmed again by the visions of the bad things he had done. He realized that’s why everyone there was wide-eyed, because they would also experience these visions if they closed their eyes.
“You cannot close your eyes. You cannot talk to the others,” Jeffrey said. “You cannot stand up. You cannot sit down. You can only kneel there on the tips of your toes and the points of your knees. All you could do was stare at the hole of fire, listen to the screams, and hope you are not next.”
But there was still hope.
“After a long time, my eyes began to burn so badly, I finally decided that it was worth it to put up with the bad flashes if I could just close my eyes for a while,” he said. “I began to sob quietly as the flashes of my evil ways rushed in, and I heard a voice. It said, ‘If you ask him, maybe he will save you.’”
Jeffrey pleaded again and again for salvation.
He was brought before a spiritual being who asked what brought him there. Jeffrey replied that the world is not fair and he didn’t want to be a part of it anymore.
He realized his life has meaning.
The being explained that Jeffrey had begged to be born into the material world, and had even chosen when and to whom he would be born.
He revealed also that Jeffrey had been saved when he asked for it, because he still had a spark of belief.
“My belief means way more than I had ever realized,” Jeffrey said. “He saw something in me that even I did not see. I began to weep so badly that I was frozen there on the floor with my head in my hands and crying uncontrollably.”
He was then shown future events, including how he would break his back and how that would impact him. These things later came true.
He was told that he had chosen these things for a reason before he was born, aware of the consequences, and he must return to finish them. He didn’t want to go back, but as he returned to his body he felt comfort and peace from God.
Jeffrey’s Life After Death
He remained in a coma for three days, though his mind was aware. He thought over all the details of his experience while he lay there incapacitated. When he came out of the coma, a nurse disclosed that he had died and been revived.
“I was an alcoholic drug dealer who had become a thug,” he said. But he turned his life around. He no longer fears death—even after his hellish experience—because of his overarching, peaceful connection to the divine.
The future events he’d foreseen during his near-death experience (NDE) came to pass, like puzzle pieces falling into place.
“I knew it was real because it was more vivid than any dream,” he said. “No dream or illusion could have given me such a puzzle that puts itself together with each year that goes by and still form such a perfect picture.
“You see the picture had to be formed before the puzzle was cut into pieces. Each piece of it was designed to be found and placed right, when it was needed and relevant. That is significant.”
He shared what he had learned about life’s challenges: “[They] are what give us experience and sometimes things are thrown in our way to change the timing of events. A flat tire on the freeway may seem like a problem but may have helped you avoid an accident down the road.”
Other NDEers have reported seeing scenes not unlike what Jeffrey had seen.
Many aspects of Jeffrey’s NDE are common among NDEers. NDE researcher Dr. Jan Holden, while giving a lecture to present her book “The Handbook of Near-Death Experiences,” told the story of another man who’d attempted suicide.
The man reported that he found himself free-falling through space, landing on a clay-like surface. When he landed, he shattered into several versions of himself.
He, like Jeffrey, found himself on the receiving end of all the bad things he had done to others.
One of him was wailing in distress. Two others were encountering people in his past, reviewing his life. The man experienced being on the receiving end of his actions. It wasn’t necessarily about the important people in his life either. One of them was a stranger he had been nasty to in a grocery store one day.
Others of him were experiencing the near future, such as seeing his mother getting the call about his suicide. He saw also the distant future. His daughter was an infant at the time of this suicide attempt. He saw her on her graduation day crying because her father wasn’t there.
Another of him was crying out for salvation. A hand picked that one up, and all the other versions of him rose with it. A spiritual being told him he had to go back, that he still had things to do. Now he is the CEO of a nonprofit to prevent suicide.
The average person who finds out they have cancer is faced with a frightening number of decisions. Those of us who have been there, understand that standing at the precipice of a cliff is not only scary, it’s mind-numbing.
But don’t let the fear paralyze you. The first thing to do is to take a deep breath. Understand you’re likely in a state of shock. Recognize that while you’ll not want to put off treatment indefinitely, you do have time to learn about your options. Cancer is something that often takes years to develop, and it’s not likely to kill you next week.
I recently interviewed Dr. Michael Karlfeldt, ND, PhD, a brilliant naturopath who has successfully treated thousands of patients and guided them through the process of healing. He uses the analogy of a firefighter who is dealing with a burning building.
What Is Causing the Building to Burn?
A naturopath like Dr. Karlfeldt will look for the fires first. What is causing the building to burn, i.e., what is driving the cancer? There are often many answers to this question. Are you exposed to a parasite, pathogen, or other toxin? Are certain foods you’re eating negatively impacting your immune system? What are the causes of the inflammatory markers and what are the numbers they show?
In other words, what is the root cause of your disease? Cancer didn’t just happen in a vacuum, there’s always an underlying cause.
What tests does a naturopath perform? It depends on the individual. Do you live in an old house with present mold? What kind of diet do you have? What other health issues do you have? What is your emotional state? Tests might include:
An antibody test with 3 different panels for food, heavy metals, and pathogens such as Lyme, mold, viruses, and bacteria.
Urine test (chronic inflammation test) to determine the level of inflammation we’re dealing with.
Nutritional or mineral tests to determine deficiencies or excess overload (lead, copper, fluoride, etc.).
Bring In The Construction Crew to Rebuild the Body
Much like firefighters, a naturopath will assist you in using the body’s natural ability to CLEAR the cause. Then he’ll bring in the construction crew to rebuild the body with basics like nutrition, vitamins, and supplements.
He’ll also utilize some of the most cutting-edge treatments available today. Some of the treatments Dr. Karlfeldt recommends include:
Photodynamic Therapy (PDT) – a treatment that uses the power of light to destroy cancer cells. It involves using light-sensitive medicine and a light source to destroy abnormal cells and utilizes a photosensitizer that can be injected into or around the therapy location to pull light to itself as a stronger concentration. By matching the frequency of a laser with the photosensitizer so that it triggers oxidation within the cancer cells, it kills them in a very targeted manner.
Oxygen Therapies – these types of therapies are designed to create an oxygen-rich environment within the tumors. Research like a study by the University Georgia shows that “low oxygen levels in cells may be a primary cause of uncontrollable tumor growth in some cancers.” Oxygen therapies are highly effective when combined with other therapies. For example, a lot of time chemotherapy is not effective because it isn’t combined with oxygen therapy.
High-dose vitamin C IV, mistletoe IV, and other therapies can also be highly effective in treating cancer. Learn more about Dr. Karlfeldt’s recommended therapies, including the innovative platelet derived nanoparticle delivery system of substances, in the video interview below.
Putting the Fire Out
It has been proven that people who feel in control of their own health experience better outcomes than those who don’t. Being in charge of your own journey is not only your right, but it is to your advantage. When you’re dealing with something as important as cancer, a can-do attitude is paramount. Choosing a health coach or a team of professionals you trust is critical to your success in many ways. Working with someone you trust and are comfortable with helps to reduce your stress, a very important factor in fighting any disease. Just having someone in your corner can confirm the success you’re making and put to rest any doubts you have.
and observed the same change in its movement when in proximity to a human head. They wondered, however, if this change may have been due to a change in air temperature from the heat emanated by a human head. The change in air temperature could cause convection currents, they said.
between the subject and the pendulum, the pushing force [of the bioenergy field] would initially be against the shield, and the pendulum would only respond to whatever pushing force remained after pushing against the shield. For the pushing force to survive passage through the shield and then push against the pendulum would violate fundamental principles of physics; i.e. you can only use a force once, and if it is utilized to push against the shield it cannot subsequently push against the pendulum.”
Any accumulation of heated convection currents would quickly dissipate after the subject left. So convection currents could not explain these aftereffects. Hansen described the effects of the subject’s bioenergy field as being somehow “imprinted” on the pendulum.
