Dr. Hodkinson: “It’s Not a Time to Say ‘I’m Sorry’ – It’s a Time to Put These Bastards in Jail”
“Should we forgive and forget?” “Absolutely not!” roared Dr. Roger Hodkinson.
“How can you look into the eyes of a pregnant woman and tell her that this experimental product is safe? How can you do that as a physician? No! Any physician that has done that should be in jail.”
“This crime, according to Mr. Berkovich, is reckless endangerment and other similar crimes. And I say similar crimes because state legal codes vary right state by state,” explained Dr. Wolf.
“But basically, these people are criminals, and they hurt people by concealing the evidence that this was a dangerous injection.”
Teryn Gregson & Ed Dowd Say COVID Started a Great Awakening Drawing People to God
“This is a spiritual battle between light and dark”
Perhaps it is time to consider the universe is attempting to get our attention and in the broader since, it is humanity’s wakeup call. Since the plandemic, we have been masked, vaccinated, misinformed, censored and the list goes on. In all the chaos and confusion, we generate positive and negative emotions from fear, worry, anger, judgmental to love, compassion and wanting to help others. All those emotions generates positive and negative energy that goes in to our world and the universe.
Our connection to the Universe, God, Infinite Intelligence, and many other descriptive names, is something most strive to understand and define through religions that have been established by man. No religion has all the truth but all religions have some truth.
Perhaps it is time to consider God is pure divine energy, love being the dominant source of vibration, the vibration that we are here to learn and balance with wisdom. Consider that each of us have a spark of pure divine energy within. As we learn how our thoughts, emotions and actions are part of our grand spiritual evolution, we are creating the world around us. Within each of us, exist a higher power waiting to be awakened. We all have the divine gift of discernment, the act or process of exhibiting keen insight and good judgment. In its broadest sense, discernment is closely related to wisdom as an expression of God. Discernment alone can bring about a sense of balance between the physical and metaphysical worlds.
If only the world lived by one simple message our teachers were trying to tell us, we could change our world. Jesus told us to “Love your neighbor as yourself.” The Buddha said, ” the only way you can become free is to love those who hate you”. Krishna said, “to me, all beings are the same. I hate none, and no one is more dear to me than another, and The Taoist Sage Lao Tzu said, “Nothing but good comes to him who loves others as he loves himself”. By honoring and respecting others’ beliefs and religions, not only will it bring us closer together, but closer to our Creator in our spiritual battle between light and dark.
Attorney Edward A. Berkovich Urges 13 AGs to Investigate & Prosecute the CDC for Criminal Charges
“This crime, according to Mr. Berkovich, is reckless endangerment and other similar crimes. And I say similar crimes because state legal codes vary right state by state,” explained Dr. Wolf.
“But basically, these people are criminals, and they hurt people by concealing the evidence that this was a dangerous injection.”
The Simpsons made this episode in 2010
Psychiatric Treatment? The Unvaccinated Are the Envy of the World Right Now
“I’ve been following the news story out of Canada where it’s been proposed that people who declined the vaccine should receive psychiatric treatment,” shared Dr. McCullough (http://t.me/c19expertchannel).
“[The] people [who] are declining the vaccine are the ones that have the most critical thinking, the most discernment — the strongest minds and bodies around us. They’re the last people that need psychiatric medication.”
Dr. Peter A. McCullough (http://t.me/c19expertchannel) is a world-renowned MD — fighting against censorship and reprisal. He has partnered with The Wellness Company (http://t.me/thewellnesscompany), a parallel structure to pharma-dominated medicine, where he serves as Chief Scientific Officer.
Debilitated, Demoralized, and On Their Own: The Federal Government Has Abandoned the Vaccine-Injured
“I am not alone,” attested Brianne Dressen after being diagnosed with a severe form of neuropathy after participating in the AstraZeneca trials.
“There is one word that summarizes what’s happening to the COVID vaccine-injured. There is one word to describe us — and it is ghost.
Fauci lied, people died – Musk
“My pronouns are Prosecute/Fauci,” the new Twitter boss has announced
Tesla and Twitter CEO Elon Musk triggered a social media firestorm on Sunday after suggesting that US Covid-19 czar Dr. Anthony Fauci should be investigated and prosecuted for allegedly lying under oath about the funding of research at a Wuhan lab in China.
In what initially appeared to simply be a humorous dig, Musk also posted a meme showing the retiring White House chief medical adviser whispering “Just one more lockdown, my king” in President Joe Biden’s ear.
However, after Fauci’s name was propelled to the top of Twitter’s trends with over 600,000 mentions, Musk apparently felt the need to elaborate why he thought the controversial face of America’s response to the pandemic should be investigated.
“As for Fauci, he lied to Congress and funded gain-of-function research that killed millions of people,” Musk said in response to one critic, adding “not awesome imo.”
“Fauci’s resignation should not prevent a full-throated investigation into the origins of the pandemic. He must be required to testify under oath regarding any discussions he participated in concerning the Wuhan lab leak. His policies destroyed lives,” Paul tweeted.
The senator previously accused Fauci of directing public funding to gain-of-function research at the Wuhan lab and lying about it under oath in congressional testimony, as the two sparred repeatedly in Senate hearings.
Gain-of-function is the modification of pathogens to enhance them in various potential ways, including transmissibility. The rationale is that scientists can study new strains and find ways to stop them before similar adaptations emerge naturally.
The ‘lab leak’ theory – that the coronavirus leaked from a Chinese lab – was popularized by former US President Donald Trump, who made the allegation amid a trade war with China. Major US media organizations and tech platforms initially labeled it as ‘disinformation’ and tried to suppress the theory from public discourse. However, after Musk took over Twitter, the company stopped enforcing its Covid-19 “misleading information policy.”
Human Bodies Scanned At Airports for Luciferase Proof of Vaccination
“Religious groups want more souls on the planet” “I want Less Souls On The Planet”
Officials Across United States Spread Misinformation on COVID-19 Vaccines
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 estimated effectiveness 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.”
That’s not true, and hasn’t been for months.
South Dakota officials did not return an inquiry.
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.
Hyping Vaccines for Children
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.
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.
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 2021 and 2022 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 refused to release COVID-19 vaccine safety 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.”
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.
Megyn Kelly Reveals Her 58-Year-Old Sister Died Suddenly Over the Weekend of a Heart Attack
John Young from Apollo 12 was asked to put his hand on the Bible and swear if he was really on the moon.
See for yourself how he reacted.
This is how ELITE is vaccinated in front of the cameras
Spike Protein Disrupting Immunity in Millions After COVID Infection or Vaccination: Here’s How It’s Being Treated
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 infections or 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.”
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.
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.”
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.
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.”
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.
LDN works to balance the activity between Th1 and Th2 type cytokines.
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.
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.
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.
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.
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.”
We’ve Had 25 Million Covid Jab Deaths So Far: Analyst
“Peter Halligan, whom Dr. Roger Hodkinson says in the video above (https://rumble.com/v1o5csw-october-15-2022.html) ‘is a most-experienced analyst in the financial industry and is very skilled at looking at and translating statistics into a summary statement,’ estimated global deaths related to Covid vaccines at (https://peterhalligan.substack.com/p/20-million-saved-or-20-million-killed) 20 million and vaccine injuries at 2.2 billion through August 2022.
Criminals at Work as the CDC Advisers Recommend Adding COVID-19 Vaccines to Childhood Immunization Schedule
Advisers to the U.S. Centers for Disease Control and Prevention (CDC) on Oct. 20 recommended adding COVID-19 vaccines to the child and adolescent immunization schedules, despite the vaccines still being under emergency authorization for some children.
The Advisory Committee on Immunization Practices (ACIP) cast the vote during a meeting on updating the schedules for youth and adults.
All members voted to add the Moderna, Pfizer, and Novavax vaccines to the 2023 schedules, asserting that the vaccines, despite waning effectiveness, can still prevent severe disease.
“We view this as COVID is here to stay,” said Dr. Matthew Daley, one of the advisers. “When I think about the routine immunization schedule as a pediatrician, I think of it as an opportunity to prevent serious disease and death. And if something is added to the schedule, it’s because I feel like the benefits continue to strongly outweigh the risks.”
The Pfizer and Moderna bivalent boosters will also be added if ACIP’s advice is taken.
The CDC and partner groups review schedule recommendations from the ACIP. The American Academy of Family Physicians, one of the groups, said that it would review the ACIP’s recommendation.
The COVID-19 vaccines have proven increasingly ineffective against both infection and severe illness from newer virus variants. In addition, there is no evidence the vaccines protect against severe disease for children under 5. The clinical trials for that population weren’t powered to measure such efficacy. Further, the new bivalent boosters haven’t been tested in humans at all.
“I suppose we should not be surprised that the ACIP has voted to add it to the CDC’s recommended childhood vaccine schedule, even though it has not been fully licensed by FDA for use in children. The past three years has [sic] taught us that federal health officials have politicized the COVID vaccine development, licensing, and policymaking process and rubber-stamped the questionable science provided by pharmaceutical companies,” Barbara Loe Fisher, president and co-founder of the National Vaccine Information Center, told The Epoch Times in an email.
“Now it is up to parents to let their state legislators know they want vaccine informed consent protections in public health laws and are opposed being forced to give their children the COVID vaccine as a condition of attending school, receiving medical care or for any other reason.”
Advisers stressed before the vote that adding the vaccines to the schedules doesn’t in itself mean the vaccines will be mandated for school children. But laws in 31 states and the District of Columbia require the vaccines on the schedules to be taken by children for school attendance, according to the Policy, Practice, and Prevention Research Center at the University of Illinois Chicago’s School of Public Health. Some other states impose requirements that largely align with the schedules.
The COVID-19 vaccines are still under emergency use authorization for children aged 6 months to 11 years. No vaccines are available to children under 6 months of age. Lynn Bahta, a CDC adviser, asked whether it was allowed to add such a vaccine to the schedules.
“Before we brought this to the workgroup, we had a conversation about this with the Office of General Counsel and we’re told it’s OK to add it to the schedule,” Dr. Patricia Wodi, a CDC official, responded.
The Department of Health and Human Services’ Office of General Counsel and the Department of Justice Office of Legal Counsel didn’t respond to requests for comment. The Epoch Times has submitted Freedom of Information Act requests for communications between the offices and the CDC on the matter.
Biden Promises Ukraine’s Zelenskyy Advanced Air Defense Systems After Russian Missile Attacks
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.
“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.
‘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.
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.
George Webb Investigative Reporter on Russian and Ukraine
Jefferson Earl, political candidate for the Federal 2022 election sends a message to Vladimir Putin from Melbourne.
Directors of CDC, NIH, and FDA Commissioner will have no place to hide
The Plandemic was intentional and The Psychologic Operations Revealed
EXCLUSIVE: FDA Refuses to Provide Key COVID-19 Vaccine Safety Analyses
U.S. drug regulators are refusing to provide key analyses of a COVID-19 vaccine safety database, claiming that the factual findings cannot be separated by internal discussions protected by law.
The Epoch Times asked the Food and Drug Administration (FDA) in July for all analyses performed by the agency for the COVID-19 vaccines using a method called Empirical Bayesian data mining, which involves comparing the adverse events recorded after a specific COVID-19 vaccine with those recorded after vaccination with non-COVID-19 vaccines.
According to operating procedures laid out by the agency and its partner in January 2021 and February 2022, the FDA would perform data mining “at least biweekly” to identify adverse events “reported more frequently than expected following vaccination with COVID-19 vaccines.” The agency would perform the mining on data from the Vaccine Adverse Event Reporting System (VAERS).
In a recent response, the FDA records office told The Epoch Times that it would not provide any of the analyses, even in redacted form.
The agency cited an exemption to the Freedom of Information Act that lets the government withhold inter-agency and intra-agency memorandums and letters “that would not be available by law to a party other than an agency in litigation with the agency.”
The agency also pointed to the Code of Federal Regulations, which says that “all communications within the Executive Branch of the Federal government which are in written form or which are subsequently reduced to writing may be withheld from public disclosure except that factual information which is reasonably segregable in accordance with the rule established in § 20.22 is available for public disclosure.”
It’s not clear why the FDA could not produce copies of the analyses with non-factual information redacted. The Epoch Times has appealed the determination by the records office. The FDA declined to comment, citing the appeal.
Kim Witczak, co-founder of Woodymatters, a nonprofit that advocates for a stronger FDA and drug safety system, said the agency’s refusal to provide the analyses was not acceptable.
“The secrecy is unacceptable for an agency that said it is transparent with the public about vaccine safety,” Witczak, who sits on one of the FDA’s outside advisory panels, told The Epoch Times.
“What’s the point of having VAERS if you’re not releasing it to the public?” she added.
Witczak said her concerns about vaccine safety were heightened by a recent paper from Dr. Joseph Fraiman and others that found a higher incidence of serious adverse events in vaccinated participants in the original Pfizer and Moderna vaccine trials than in placebo recipients. She noted that the FDA’s 2004 warning for antidepressants that the drugs could increase the risk of suicidal thoughts and behavior came over 10 years after the trials on which it was based.
“If this data is available, shame on you for not making it known to the public,” Witczak said. “It’s as if they don’t trust the people to make their own best decision for what’s good for them and their families.”
The Centers for Disease Control and Prevention (CDC), according to the documents outlining operating procedures, was going to perform a different type of data mining analyses, called Proportional Reporting Ratio (PRR) mining.
The CDC has also refused, so far, to provide the results for those analyses.
It has also twice provided false information when responding to questions.
The agency initially said that no PRR analyses were done and that data mining is “outside of th[e] agency’s purview.” The agency then said that it did perform PRRs, starting in February 2021.
Later, the agency acknowledged that wasn’t true. The agency did not begin performing PRRs until March 2022, a spokesperson told The Epoch Times.
Roger Andoh, a records officer, gave the initial response, citing the CDC’s Immunization and Safety Office. Dr. John Su, a CDC official, gave the second response. It remains unclear with whom the information originated.
The Epoch Times has submitted Freedom of Information Act requests for internal emails that may provide answers.
Data Mining Reports
The Empirical Bayesian (EB) is focused on identifying disproportional numbers of adverse events, CDC scientist Dr. Tom Shimabukuro said in January 2021. It identifies “with a high degree of confidence, adverse event-vaccine pairs reported at least twice as frequently as expected for a COVID-19 vaccine compared to the VAERS database,” he said, or a comparison between the incidence of a specific event such as kidney disease after COVID-19 vaccine compared to the incidence of the same event after all other U.S.-licensed vaccines.
The FDA and CDC have provided periodic updates on the EB data mining effort.
“Importantly, there were no Empirical Bayesian data mining alerts detected for any adverse event COVID-19 vaccine pairs as of the last data mining run that the FDA performed on February 18th,” Shimabukuro told members of the FDA’s vaccine advisory panel on Feb. 26, 2021.
In a review memorandum (pdf) for an expansion of the emergency authorization granted to Pfizer’s vaccine, FDA researchers said that data through April 16, 2021, showed only a possible signal for body temperature.
In the journal Vaccine in June 2021, FDA researchers said an analysis of cases of blood clotting after the Pfizer and Moderna vaccines did not suggest a safety concern. The FDA and CDC paused the Johnson & Johnson vaccine in April 2021 over cases of blood clotting, some fatal, but lifted the pause just 10 days afterward. The FDA later restricted use of the Johnson & Johnson shot.
In a paper in the CDC’s quasi-journal in August 2021, FDA and CDC researchers said that the FDA used EB mining to monitor events in children aged 12 to 17 after vaccination. The results indicated a lack of a safety signal for post-vaccination heart inflammation, or myocarditis, though other surveillance systems had detected the issue as an adverse event.
And in a preprint in May 2022, scientists, including Su, said that EB mining analyzing data through Nov. 12, 2021, revealed only one signal for VAERS death reports, for “vaccination failure” after receipt of the AstraZeneca vaccine, which is not authorized in the United States.
More Reports of COVID Vaccine-Linked Heart Inflammation in Young Males Submitted to CDC
Reports submitted to the U.S. Centers for Disease Control and Prevention (CDC)’s vaccine surveillance system suggest that cases of post-COVID-19 vaccine-linked heart inflammation among young males have risen.
Recent figures published in the CDC’s Vaccine Safety Datalink surveillance system show that within a week of getting the two-dose Pfizer-BioNTech vaccine, there were 14 cases of myocarditis or pericarditis among 102,091 males between the ages of 16 and 17. And of the 206,000 12- to 15-year-old males who got the same two-dose vaccine series, there were 31 cases within a week, according to the CDC (pdf).
Those reports were presented to the CDC’s Advisory Committee on Immunization Practices on Sept. 1 show that the incident rate for the 12- to 15-year-old group is 150.5 per million—or about 1 in 6,600—and 137.1 per million for the 16- to the 17-year-old group—or about 1 in 7,262.
Following the first booster dose, CDC-presented figures show that it jumps to 188 per million among the 16- to 17-year-old group. But for the 12- to 15-year-old males, 61.3 per million developed heart inflammation after the booster dose, according to the figures.
In August 2021, the figures submitted to the CDC system (pdf) show that of 42.6 myocarditis and pericarditis cases per million and 71.5 per million for 12- to 15-year-old males and 16- to 17-year-old males, respectively. That breaks down to about one in 23,500 for the younger group and around one in 14,000 for the older group.
The agency noted that “myocarditis is a rare event following mRNA COVID-19 booster vaccination” and that it has “verified 131 myocarditis case reports to VAERS in people ages [5 years and older] after 123,362,627 million mRNA COVID-19 booster vaccinations.”
In analyses of the data, “myocarditis [and] pericarditis incidence following first booster dose and dose 2 of the primary series are similar, though case counts are small and confidence intervals around point estimates are wide,” said the CDC.
The Vaccine Safety Datalink is described by the agency as “a collaborative project between CDC’s Immunization Safety Office and nine health care organizations” and is designed to “monitor [the] safety of vaccines and conduct studies about rare and serious adverse events following immunization.”
In May, the CDC said reports of heart inflammation linked to the Pfizer vaccine were much lower in 5- to 11-year-old boys than in adolescents and young males. Among that group, the rate of heart inflammation stood at 2.7 cases per million.
After the figures were presented, the Advisory Committee on Immunization Practices recommended updated boosters, which was, in turn, endorsed by CDC Director Rochelle Walensky, the CDC’s director.
Walensky said that “updated COVID-19 boosters are formulated to better protect against the most recently circulating COVID-19 variant,” adding, “They can help restore protection that has waned since previous vaccination and were designed to provide broader protection against newer variants.”
“This recommendation followed a comprehensive scientific evaluation and robust scientific discussion. If you are eligible, there is no bad time to get your COVID-19 booster and I strongly encourage you to receive it,” she added on Sept. 1.
A study that was led by Dr. Tracy Hoeg, with the Florida Department of Health, and released in mid-2021 showed figures similar to the ones submitted to the CDC’s advisory committee on Sept. 1.
Hoeg said she and others published a preprint study last year showing a rate of 94 instances of myocarditis per million in 16- to 17-year-old males—or 1 in 10,6000—and 162 per one million in 12- to 15-year-old males—or 1 in 6,200—she wrote on Sept. 1.
The CDC “is now finally catching up & reporting similar,” Hoeg wrote on Twitter earlier this month.
“If we hadn’t been villified as ‘anti-vaxxers’ spreading ‘mis’ & ‘disinformation,’ how would the conversation around minimizing the chance of this adverse event have changed & how many cases of myo/pericarditis in young males would have been prevented over the last year?” she asked.
Hoeg also questioned recent statements made by CDC officials in recommending boosters to anyone aged 12 and older.
“Now today the CDC is recommending with no human data on benefits or risks that everyone 12 and up get a bivalent booster. ‘There is no bad time to get your COVID-19 booster.’ Really?” she asked. “Why are nuance & individualized recs so difficult for @CDCgov?”
Murder by Vaccines Documentary
In CDC Survey of Over 13,000 Children, More Than Half Had ‘Systemic Reaction’ After COVID-19 Vaccine
In a CDC survey of over 13,000 children, more than 55 percent of the subjects between the ages of 6 months and two years had a “systemic reaction” in response to their first dose of the Pfizer-BioNTech or Moderna COVID-19 vaccines, the CDC said on Sept. 1.
A systemic reaction is a response beyond the injection site. The CDC said almost 60 percent had a systemic reaction to the second dose of the Moderna vaccine.
While the most common systemic reactions were fatigue, fever, irritability, and crying, parents of more than 6 percent of the children in the study said their child was unable to perform normal activities after the second dose of either the Pfizer-BioNTech or Moderna vaccine.
The CDC collected the data through a program called V-Safe—a smartphone-based monitoring system that operates through an app that parents download to their phones.
Between June 18 and Aug. 21, parents of more than 10,000 young children reported reactions to the CDC through V-Safe in the seven days after their child received a COVID-19 vaccination.
Parents of 8,338 children ages six months to 2 years who received the Moderna vaccine reported information through V-Safe, with 55.7 percent reporting a systemic reaction after the first dose and about 58 percent after the second dose. For the Pfizer vaccine, parents of 4,749 children ages six months to 2 years submitted reports showing that 55.8 percent had a systemic reaction after the first dose and about 47 percent after the second dose of the vaccine.
The most frequently reported reactions for children six months to 2 years were irritability or crying, sleepiness, and fever. The most common reactions for children aged 3-5 years were injection site pain, fatigue, and fever.
The data also showed a more serious reaction category labeled “any health impact.”
About 10 percent of all children six months to 2 years were reported to have a “health impact” after getting their first dose of either the Moderna or Pfizer vaccine. For the Moderna vaccine, slightly more children had a health impact after the second dose; for the Pfizer vaccine, it was slightly less.
The information was presented to the CDC’s Advisory Committee on Immunization Practices (ACIP) on Sept. 1 as part of an overview of all data related to the safety of COVID-19 vaccines.
In addition to V-Safe, data was presented summarizing reports from the Vaccine Adverse Event Reporting System (VAERS) and the Vaccine Safety Data Link (VSD), which includes data from several large health maintenance organizations in the United States.
All three systems look at the safety of vaccines after they’ve already gone to market and have been administered to large numbers of people.
Tom Shimabukuro, the head of the CDC’s vaccine safety team, headed the presentation and told committee members that no “statistical signals” of COVID-19 vaccine reactions were found for young children in the VSD data.
Shimabukuro also said that systemic reactions were “commonly reported” following vaccines.
However, other medical professionals like Dr. Meryl Nass from Children’s Health Defense have expressed caution over the reported reactions, pointing to the high number of systemic reaction reports among very young children.
She told The Epoch Times on Sept. 2 that she was questioning why the government doesn’t collect and present more information on these cases.
“That stuff is not considered by the CDC to be very important … It’s assumed that all those side effects go away after a few days and leave the people perfectly well,” she said, mentioning the fevers and fatigue. “Those reactions may in fact may be harbingers of more serious reactions, but nobody to my knowledge has published anything looking at whether these acute local or systemic reactions are indicators of a later problem.”
The FDA approved the emergency-use authorization of COVID-19 vaccines for children aged six months to 5 years on June 17. According to the CDC, about 599,460 children in this age group have received the Pfizer-BioNTech vaccine, and about 440,770 have received the Moderna vaccine.
From June 18 through Aug. 31, approximately 1 million doses of the Moderna and Pfizer vaccines were administered to children in this age group.
In a review of the VAERS data on young children from June 18 to Aug. 31, the CDC had 496 reports of adverse events for children aged six months to 4 years who received the Pfizer vaccine and 521 for children aged six months to 5 years who received the Moderna shot, with an adverse event defined as a possible side effect.
Over 98 percent of reports were for what the CDC considers non-serious events.
There are 220 reports of persons aged six months to 5 years of age being taken to the emergency room following a COVID-19 vaccine. In one case involving a 2-year-old boy in Arizona, the VAERS report says he was given the Pfizer vaccine on July 29 and on July 30 had a “life threatening episode.”
The report lists his symptoms as “clammy skin and vomiting leading (8 minutes) to difficulty breathing.” The boy “turned blue,” was “limp” and “non-responsive,” and “fully stopped breathing for two minutes,” according to the report.
He was revived after chest compressions.
Never Forget What They Did
Judge Grants Trump Motion for Special Master to Review Records FBI Seized
CDC Admits Dramatic Mistakes in COVID Response
Sen. Ron Johnson: Pandemic Politics & America’s COVID Cartel
How Doctors Detect COVID
Fauci Announces He’s Stepping Down as NIAID Director, Medical Adviser to Biden
Dr. Anthony Fauci is stepping down from three government positions he holds, he announced on Aug. 22.
Fauci is resigning as director of the National Institute of Allergy and Infectious Diseases (NIAID), chief of the NIAID Laboratory of Immunoregulation, and chief medical adviser to President Joe Biden.
The moves will take effect in December, Fauci said.
He indicated that he will leave the government, but not retire.
“While I am moving on from my current positions, I am not retiring,” Fauci said. “After more than 50 years of government service, I plan to pursue the next phase of my career while I still have so much energy and passion for my field. I want to use what I have learned as NIAID Director to continue to advance science and public health and to inspire and mentor the next generation of scientific leaders as they help prepare the world to face future infectious disease threats.”
Fauci, 81, has repeatedly hinted he would step down from his positions, but has not committed before to a specific time for resigning.
Republicans have vowed to investigate Fauci and other architects of U.S. pandemic policy if they gain control of either or both congressional chambers in the upcoming midterm elections.
“Dr. Fauci is conveniently resigning from his position in December before House Republicans have an opportunity to hold him accountable for destroying our country over these past three years,” Rep. Andy Biggs (R-Ariz.) said in a statement.
Longtime Government Official
Fauci has directed the NIAID since 1984. He has advised Biden since he took office in 2021, and was one of President Donald Trump’s chief advisers on the COVID-19 pandemic.
Fauci has drawn ire for recommending lockdowns as a bid to slow the spread of the virus that causes COVID-19, acknowledging he deliberately misled the American public on mask-wearing, and defending NIAID funding for the laboratory in Wuhan, China, that is located near where the first COVID-19 cases occurred.
Supporters say Fauci has been a voice of reason during the pandemic and that his positions have evolved as the science has developed.
NIAID is part of the National Institutes of Health (NIH).
Dr. Lawrence Tabak, the acting director of the NIH, said in a statement that Fauci is “the model public servant” and “is always guided by the science.
“It’s been an extraordinary privilege and honor to have worked by his side and to have learned so much from him—I will miss him greatly. But I also look forward to seeing what Tony will do next. I have no doubt that he will continue to have an enormous impact on the world,” Tabak said.