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Kim Iversen: Biden's SHOTS FOR TOTS Rollout FAILS As Parents Don't Show To Sites
Kim Iversen reviews the success of the Biden administration's campaign to vaccinate babies and toddlers against COVID-19.
According to the CDC the benefits of COVID-19 vaccination outweigh the known and potential risks.
Children who get COVID-19 can get very sick, can require treatment in a hospital, and in rare situations, can even die. After getting COVID-19, children and teens can also experience a wide range of new, returning, or ongoing health problems. Getting eligible children vaccinated can help prevent them from getting really sick even if they do get infected and help prevent serious short- and long-term complications of COVID-19. Vaccinating children can also keep them in school and daycare and safely participating in sports, playdates, and other group activities.
Emerging evidence indicates that people can get added protection by getting vaccinated after having been infected with COVID-19. So, even if a child has had COVID-19, they should still get vaccinated. Serious reactions after COVID-19 vaccination in children and teens are rare. When they are reported, serious reactions most frequently occur the day after vaccination.
Rare cases of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the outer lining of the heart) have been reported after children and teens got a Pfizer-BioNTech COVID-19 vaccine. New studies have shown the rare risk of myocarditis and pericarditis associated with mRNA COVID-19 vaccination—mostly among males between the ages of 12 and 39 years—may be further reduced with a longer time between the first and second dose.
In children ages 5 through 11 years, there were 11 confirmed reports of myocarditis out of 8 million doses given of the Pfizer-BioNTech COVID-19 vaccine between November through December 2021.
In reports of myocarditis following mRNA-based COVID-19 vaccination from December 2020 to August 2021external icon, the risk of myocarditis was highest following the second dose of the Pfizer-BioNTech vaccine in adolescents and young adult males.
Reporting rates were around 70 cases per million doses in males ages 12 through 15 years and 105 cases per million doses in males ages 16 through 17 years.
Everyone ages 12 years and older should get a COVID-19 booster shot. Currently, a booster shot is not recommended for children younger than 12 years of age.
The CDC says Getting a booster enhances or restores protection against COVID-19, which may have decreased over time. People ages 12 years and older who are moderately or severely immunocompromised should receive 4 total doses of COVID-19 vaccine—a primary series of 3 doses, plus, when eligible, 1 booster dose.
In March of 2022, the CDC expanded eligibility for an additional booster dose for certain individuals who may be at higher risk of severe outcomes from COVID-19. Boosters are safe, and people over the age of 50 can now get an additional booster 4 months after their prior dose to increase their protection further. This is especially important for those 65 and older and those 50 and older with underlying medical conditions that increase their risk for severe disease from COVID-19 as they are the most likely to benefit from receiving an additional booster dose at this time.
The CDC says layered prevention strategies — like staying up to date on vaccines and wearing masks — can help prevent severe illness and reduce the potential for strain on the healthcare system. Everyone ages 2 years and older should properly wear a well-fitting mask indoors in public in areas where the COVID-19 Community Level is high, regardless of vaccination status.
According to Pfizer and the CDC, potential side effects from the vaccine include pain, redness, or swelling at the injection site. Other side effects could include tiredness, headache, muscle pain, fever, chills, and nausea. In rare cases, people have experienced serious health events after the COVID-19 vaccination. Any health problem that happens after vaccination is considered an adverse event. According to the CDC: Although the overall risks are low, if you are pregnant or were recently pregnant, you are more likely to get very sick from COVID-19 compared to people who are not pregnant. CDC recommends COVID-19 vaccines for everyone ages 6 months and older, and boosters for everyone ages 5 years and older if eligible.
COVID-19 vaccines available for children include: Pfizer-BioNTech COVID-19 vaccines Moderna COVID-19 vaccines Everyone should continue to follow all current prevention measures recommended by CDC and based on the latest COVID-19 Community Level data.
republished below in full unedited for informational, educational & research purposes:
President Joe Biden addressed the nation on Tuesday to mark the day when children as young as six months old could receive experimental gene therapeutics, aka Covid vaccines, and praised the United States for becoming the first country in the world to offer mRNA shots to babies.
Calling the emergency use authorization of Covid shots from Pfizer-BioNTech and Moderna “a very historic milestone” and a “monumental step forward,” the president said how important it was to offer “lifesaving vaccines” to “nearly every American.”
Biden went on to describe how his administration “has been planning and preparing” to get the littlest ones jabbed and how accessible Covid shots will be for some 20 million of the youngest of Americans thanks to his administration:
My administration, with the help of the CDC, has been planning and preparing [for] this moment — for this moment for a long time. Since I took office, we’ve been committed to making sure every parent has the opportunity to protect their children from COVID-19. We’ve secured enough doses and we’re launching a comprehensive effort with states, local health departments, pediatricians, family doctors, pharmacies, rural health clinics, community health centers, and other trusted messengers and partners to get the word out to get — help to get shots in arms.
(Among other preparations, the White House started ordering Covid vaccines for the youngest children even before they were authorized.)
The president then took a hit at Florida Governor Ron DeSantis, who openly opposes vaccination of children against Covid and who on Monday reaffirmed his decision to not preorder shots or offer them at state health departments for the youngest Americans.
“We are not going to have any programs where we’re trying to jab 6-month-old babies with mRNA,” DeSantis said, according to the Orlando Sentinel. “We still have not ordered it. We’re not going to order it.”
Back in March, the Florida Health Department recommended against Covid vaccines for healthy children, arguing that the risks of vaccinating them “may outweigh the benefits.”
In regard to vaccines for babies, the state’s surgeon general, Dr. Joseph Ladapo, who also serves as the state’s health secretary, expressed his criticism over the federal government allowing for the experimental injections:
Did the COVID-19 vaccine trials for kids <5 show a reduction in severe illness? Did the trials show a benefit for those with a prior COVID-19 infection? Is there a benefit for kids with no pre-existing conditions? Florida puts data over ideology. That’s not going to change.
Biden, apparently, thinks otherwise. He said that the shots were “approved after extensive scientific review” and that “elected officials” should not “make it difficult” for parents to “keep them and those around them safe,” even though it has been a year since the CDC confirmed that the vaccines prevent neither infection nor transmission of Covid.
Speaking with CBS News on Tuesday, White House Chief Covid-19 Response Coordinator Dr. Ashish Jha said that all children should get vaccinated even if they have natural immunity from a previous Covid infection.
Also on Tuesday, the president and First Lady Jill Biden visited a Washington, D.C., vaccine clinic that hosted the first vaccination event for the newly eligible age group.
The CDC’s own data, however, clearly show that Covid poses no “deadly threat” to children and does not justify an emergency authorization of the shoddily tested vaccines. According to CDC data — for what’s it worth — as of June 2, infants younger than one accounted for 299, and children aged one to four for 143, out of 1,005,236 total deaths associated with Covid in the United States. Not a single child has died since March 5.
Further, Pfizer’s and Moderna’s own data submitted to the FDA’s vaccine advisory panel suggest that the shots are useless for children, at best.
In a four-minute video (below), Dr. Clare Craig, co-chair of the HART group, summarized the clinical trial that was used to justify vaccinating our kids. Because of the irregularities of the clinical trial and its results showing an unacceptable lack of efficacy and adequate safety data, the trial should have been recognized as null and void.
Children’s Health Defense, a prominent health nonprofit, has also analyzed the data presented to the FDA and pointed to the numerous shortcomings and irregularities of the trials.
Perhaps the most surprising data point regarding the shots was their negative efficacy, yet not a single FDA vaccine advisory panelist raised the issue of failure to meet the FDA’s required 50% efficacy.
“Pfizer has a serious problem: Its two-dose data reflected the reality [that] the confidence interval for their estimate of the number of cases prevented by three doses of their vaccine points, if anything, to negative efficacy (-369.1 to 99.6),” reads the analysis.
The report’s author predicts “the entire vaccination program is going to drive COVID-19 numbers up across the board routinely and on a regular, ongoing basis due to antibody-dependent enhancement.”
According to Kaiser Family Foundation polling, only about 18 percent of parents of children under the age of five are eager to get their children vaccinated right away, while a larger share (38 percent) plan to wait a while to see how the vaccine is working for others.
republished below in full unedited for informational, educational & research purposes:
(Natural News) One of the faces of America’s Frontline Doctors (AFLDS) has been sentenced to prison after she pleaded guilty back in March to a class A misdemeanor.
Dr. Simone Gold, we reported back in January of 2021, was arrested after she entered the U.S. Capitol building on Jan. 6, 2021, and delivered a speech via megaphone about the dangers and ineffectiveness of Wuhan coronavirus (Covid-19) “vaccines.”
She further discussed viable remedies such as hydroxychloroquine (HCQ) and ivermectin, urging listeners to protect their natural DNA and immune systems rather than take an experimental injection that could – and likely will in the coming years for everyone who took it – kill them.
For the “crime” of entering the People’s building through the neatly positioned velvet ropes that were placed almost as a guide for those herded inside by law enforcement assets, Gold will now have to serve a two-month prison sentence.
Her guilty plea in March of this year admitted to “entering and remaining in a restricted building.” She clearly would have been better off burning down a small business or a target like Black Lives Matter (BLM) terrorists did without penalty.
U.S. District Judge Christopher Cooper in Washington, D.C., also sentenced Gold to 12 months of supervised release following her 60-day prison term and ordered her to pay a $9,500 fine.
Judge called it “unseemly” that AFLDS raised money for Gold’s salary by telling supporters her arrest was unfair prosecution
The judge told Gold that her statements about Fauci Flu shots did not factor into her sentencing. According to him, Gold was not a “casual bystander” on January 6, but rather an “insurrectionist.”
Cooper did accuse AFLDS, Gold’s organization, of “misleading” supporters into believing that her prosecution was politically motivated and that it trampled her First Amendment rights.
Cooper went on to call it “unseemly” that AFLDS is using the Capitol “riot” as a means of raising money, including for Gold’s personal salary.
“I think that is a real disservice to the true victims of that day,” he stated.
Gold traveled to the Capitol on Jan. 5, 2021, to speak at Freedom Plaza. Her intent was simply to deliver a medical speech – and when the gates were opened, so to speak, into the Capitol building, she simply brought her message inside.
Gold never committed any acts of violence, just to be clear. She simply spoke through her megaphone about the scam of the plandemic, and for this she was placed on the FBI’s most wanted release.
“I was paid a visit by the FBI in a Roger Stone kind of takedown moment, which is quite uncalled for,” Gold said about her prosecution.
“You know, if anybody wanted to get a hold of me, they could have picked up the phone and called. I’m very easy to find. But there were literally twenty guys with guns blazing, [and they] broke down my door.”
The FBI essentially raided Gold’s home, all because she spoke her mind about the plandemic and the serious crimes against humanity that were, and still are, being committed in the name of “public health.”
“It was dramatic and what I want to say is that I weep for our country,” Gold added about her mistreatment at the hands of the state.
“If you can pull in a person like me … [and] have the FBI break down your door with 20 guns, shackle you [in] handcuffs [and] drag you off, I mean it was really terrible … I’m telling you, America: this can happen to you.”
More related news about Gold’s arrest and sentencing and other acts of government tyranny can be found at Overlords.news.
republished below in full unedited for informational, educational & research purposes:
COVID-19 is clearly no longer an emergency. The real emergency now is the continued use of the COVID “vaccines,” because they’re creating injuries on a level that is truly alarming and unprecedented. VAERS data reveal the COVID jabs have caused more harm in 18 months than all other vaccines on the market, combined, over the past three decades
Raw data from the Pfizer trial also show the shots were associated with an increased risk for death from the start, and both Pfizer and the FDA knew it
Data also show highly “vaccinated” and boosted nations are now experiencing record case and death rates from COVID compared to countries with low injection rates
We’re now finding the COVID shots have negative efficacy, meaning, if you have received the shot and are exposed to COVID, you are more likely to get sick, not less likely, compared to someone who is unvaccinated
The Frontline COVID-19 Critical Care Alliance (FLCCC) has developed a protocol for those injured by the COVID jabs called I-RECOVER, which you can download from covid19criticalcare.com in several different languages
In the "Tea Time" episode above, Drs. Pierre Kory and Paul Marik review the Frontline COVID-19 Critical Care Alliance (FLCCC) protocol for those injured by the COVID jabs. They also discuss what's in the shots, their lack of safety and efficacy, adverse events, and the controversial issue of "shedding."
Kory and Marik are both part of the FLCCC, which was founded in 2020 to share early treatment protocols for COVID-19. Kory is an ICU specialist, triple board-certified in internal medicine, critical care, and pulmonary medicine. He now runs a private telehealth practice specializing in the treatment of COVID-19, so-called "long-COVID" and vaccine injuries.
Marik is one of the most-published ICU specialists in the world and is best known for his vitamin C protocol for sepsis. The FLCCC's protocol for COVID is known as the MATH+ protocol, which has undergone multiple revisions over the course of the pandemic.
Now, as injuries from the COVID jab are stacking up, they've also added a post-vaccine treatment called I-RECOVER,1 which you can download from covid19criticalcare.com in several different languages.
A Pandemic of Serious Vaccine Injuries
"My heart is so broken, I cannot keep quiet anymore," Marik said, choking back tears during a Children's Health Defense hearing in Ohio where several vaccine-injured patients also shared their tragic journeys. "This is a humanitarian crisis! These people are suffering. This is real disease."
Patients injured by the COVID jab repeatedly report receiving no help when they go to the hospital. There's seemingly no help anywhere. This must change. We have to face the fact that we now have an unrecognized epidemic of vaccine injury.
At present, there are no specialized vaccine injury clinics, but eventually, there probably will be. In the meantime, the FLCCC is sharing their I-RECOVER2 protocol with the world, with the hopes that doctors will begin to take those with COVID jab injuries seriously and treat them appropriately.
As noted by Kory, COVID-19 is no longer an emergency. The real emergency now is the continued use of the COVID "vaccines," because they're creating injuries on a level that is truly alarming and unprecedented.
He also cites life insurance data showing historic rises in excess mortality among young people, and those data are supported by vaccine injuries reported to the U.S. Vaccine Adverse Event Reporting System (VAERS) as well. According to Kory, estimates suggest some 500,000 Americans may have lost their lives to these shots.
Data also show highly "vaccinated" and boosted nations are now experiencing record case and death rates from COVID compared to countries with low injection rates.
What's in the Shots?
The short answer to that question is, "we have no idea," and that puts medical professionals in a very precarious position. Since they do not know what they're giving their patients, they can't even make educated recommendations based on the patient's medical history, allergies, and so on.
While the manufacturers have revealed some of the ingredients — such as mRNA, PEG, and nano lipid particles — investigations have discovered things in the shots that aren't indicated by the manufacturer. One such ingredient is graphene oxide, which can be seen under an electron microscope, but isn't on the list of ingredients. Other unknown contaminants have also been found.
What's more, while we know the shots contain "mRNA," we have no way of knowing exactly what that mRNA is designed to do, or might accidentally do. As noted by Marik, it's been genetically altered, so it's not a direct copy of the mRNA found in the SARS-CoV-2 virus, but aside from that, we cannot be sure about its makeup.
Marik also points out the Pfizer data shows there are distinct differences in side effects depending on the lot you get. So, all lots are not the same. This basically makes it impossible to make definitive assertions about the ingredients, as any given lot may or may not contain them. The amount of any given ingredient may also vary.
Is the COVID Shot Safe and Effective?
When media and health officials say the shots are safe and effective, what does that actually mean? As noted by Kory, "safe and effective" is NOT a statement about a scientific conclusion. They're "neither safe nor effective," he says.
The "safe and effective" claim is simply propaganda and meets the definition of false information because the data "backing" the safe and effective narrative completely ignores the adverse event data.
Kory notes we have documents showing the Department of Health and Human Services paid $1 billion to media companies to advertise the jabs. We also have evidence that first-tier journals are rejecting analyses of injuries. So, they're very selective about what they publish.
Direct-to-consumer prescription drug ads accounted for $6 billion in spending alone in 2016, which amounted to 4.6 million ads, including 663,000 television commercials, mostly for high-cost biologics and cancer immunotherapies.3 It may be close to $10 billion now as that statistic is 6 years old. We know it is at LEAST $7 billion as the government kicked in $1 billion for COVID propaganda.
Public health agencies have also been very selective about the data they publish in order to protect the narrative. Health agencies in Scotland and the U.S., for example, suddenly stopped publishing data when the trend turned against the COVID shots and ineffectiveness and harms were becoming apparent.
Still, VAERS' data reveal these jabs have caused more harm in 18 months than all other vaccines on the market, combined, over the past three decades. Raw data from the Pfizer trial — which were analyzed by experts after Pfizer and the Food and Drug Administration were sued and forced to release them — also show they were unsafe and associated with an increased risk for death from the start, and both Pfizer and the FDA knew it.
According to Marik, Moderna and Pfizer also manipulated their efficacy data to make the shots appear far better than they actually were. Recalculations have found the initial efficacy was actually more like 12%, not 95% as claimed, Marik says.
Negative Efficacy Demonstrated
Not only did the shots fail to live up to their initial claims of effectiveness, but we're now finding they even have negative efficacy. As explained by Kory, negative efficacy means that if you have received the shot and are exposed to COVID, you are more likely to get sick, not less likely, compared to someone who is unvaccinated.
According to Kory, negative efficacy is demonstrated in several different data sources, including Walgreens, which created its own COVID tracker database for patients getting their tests and shots at Walgreens. Its data show COVID-jabbed individuals are testing positive for COVID at far higher rates than the unjabbed, and those who got their last shot five months or more ago have the highest risk.
As you can see in the screenshot from Walgreens' COVID-19 tracker4 below, during the week of May 31 through June 6, 2022, 24.4% of unvaccinated individuals who got tested for COVID got a positive result. Of those who had gotten just one COVID shot, the positivity rate was 31.6%.
Of those who received two doses five months or more ago, 34.3% tested positive, and of those who received a third dose five months or more ago, the positive rate was 38.5%. "I'm very, very concerned for those who have been vaccinated and boosted," Kory says.
Data from the U.K. Health Security Agency also shows that the boosted now have three to four times higher COVID case rates, compared to the unvaccinated, and this is true for all age groups except children under 18.5,6 They're also at greater risk of repeated COVID infections.
Do the COVID Shots 'Shed'?
What about "vaccine shedding"? Marik admits to being extremely doubtful about the idea of spike protein shedding when he first heard about it but has since changed his mind. He's now convinced that it does happen, even though we do not yet fully understand the mechanism behind it.
He cites a study that looked at unvaccinated children of parents who had received the injections. The parents all had an antibody against the spike protein in their noses, and surprisingly, a large percentage of the unvaccinated children did as well. "So, somehow, the antibody is getting from the parent to the child," he says.
Another concept that might explain it is that of exosomes. Exosomes are lipid particles that circulate in your blood. They're also found in the nose and lungs. If you've received the COVID jab, you're going to have circulating exosomes with spike protein on them, so it's not inconceivable that you might spread these exosomes via nasal discharge or even just through breathing. "You could exhale these exosomes," Marik says, "which are then inhaled [by others]."
Kory also points out that in the Pfizer trial, they included a "very curious exclusion criteria." Anyone in the same household as someone who had received the shot was excluded from the trial, which suggests they may have been concerned about some sort of transfer or shedding.
Anecdotally, he has also encountered many unvaccinated patients, primarily women, who report severe disruptions to their menstrual cycles after coming into close contact (although not necessarily intimate contact) with someone who had recently received the jab.
Post-Jab Avalanche of Rare Diseases
Regardless of where the spike protein comes from — the virus itself, the shot, or close contact shedding — it's clear it can have wide-ranging adverse effects. The jab itself, however, is the most problematic, as your body is continuously producing this toxic protein, and we still don't know if that production ever shuts off.
As previously predicted, we're now starting to see a rapid rise in a number of conditions, including previously very rare ones. Among them, are hepatitis among young children, appendicitis, and several rare forms of cancer, some of which are extremely aggressive and fast-moving.
In late 2021, Dr. Ryan Cole, a pathologist, reported seeing a 20-fold increase in endometrial cancer, as well as a "massive uptick" in autoimmune diseases.7 (Not surprisingly, he's now accused of misdiagnosing two patients with cancers they never had in order to support a false claim.8)
According to Kory, post-jab cancer proliferation is not all that surprising, as several of the mechanisms of the jabs degrade your immune function, and your immune system is your first line of defense against all diseases, including cancer.
Marik also points out that the spike protein is "profoundly toxic" in and of itself as well, and interferes with cancer-suppressing genes. "So, there's no doubt that the spike protein causes an increase in the risk of cancer," he says. "The problem is, what do you do about it? How do you get rid of the spike?"
Two Strategies to Eliminate Spike Protein
Marik and Kory believe there may be ways to boost the immune system to allow it to degrade and eventually remove the spike from your cells. One of the strategies they recommend for this is TRE (time-restricted easting), which stimulates autophagy, a natural cleaning process that eliminates damaged, misfolded and toxic proteins.
In many ways, Marik is a fairly rigid conventional physician who is simply unaware of many effective therapies natural physicians use. One major omission he is unaware of is sauna therapy. This is especially true when combined with TRE, as it will radically increase autophagy and heat shock proteins which will address the prion-like diseases recently reported with COVID jabs and as predicted last year by MIT research scientist Stephanie Seneff.
Infrared saunas are clearly the best saunas out there as I detail in my epic article on saunas earlier this year. One of the primary reasons is the increase in mitochondrial melatonin.
Ivermectin also binds to the spike protein, thereby facilitating its removal. As noted by Marik, the best advice is to avoid the spike protein in the first place. Don't take the COVID jab, and if you get COVID-19, treat it early and aggressively.
The spike protein is toxic regardless of whether it comes from the natural infection or the injection. Early and aggressive treatment will lower your spike protein load, thereby reducing your risk of long-COVID.
Kory stresses that, at present, they still do not know the exact correct dose for ivermectin. When prescribed for long-COVID and vaccine injury, he monitors the patient and adjusts the dosage based on individual response. That said, he typically starts patients out at a mid-range dose of 0.3 milligrams per kilogram of body weight, daily.
Now, he's noticed that when it comes to ivermectin, there are responders and nonresponders. It works exceptionally well for some, while benefits are negligible in others. That said, a majority of patients do tend to experience a benefit. The length of treatment is also highly variable.
As for safety, it's been used for over 50 years9 and has a remarkably robust safety profile. We now also have a large-scale Brazilian study in which patients received ivermectin for four days every month for six months. Curiously, not only was COVID incidence dramatically reduced but kidney and liver function actually improved with this treatment. Marik also dismisses claims that ivermectin can be harmful to your liver, saying it's actually used to treat fatty liver disease.
So, overall, "we have not seen a safety signal ... with long-term use," Kory says. "Some of that is published data, and some of it is just our experience with treating patients." Marik adds, "It's one of the safest medications ... even when taken in high doses appropriately."
FLCCC Vaccine Injury Protocol: First Line Therapies
The full first-line protocol for vaccine injury is as follows. Keep in mind, however, that the treatment must be individualized to the symptoms of each patient. As explained by Marik, the patient's response will determine future treatment and adjunct therapies. These are not symptom specific but rather listed in order of importance:10
Time-Restricted Eating or periodic daily fasts. Fasting has a profound effect on promoting immune system homeostasis, partly by stimulating the removal of damaged cells and mitochondria and clearing misfolded and foreign proteins. Intermittent fasting likely has an important role in promoting the breakdown and elimination of the spike protein. Fasting is contraindicated in patients under 18 (impairs growth) and during pregnancy and breastfeeding.
Patients with diabetes, as well as those with serious underlying medical conditions, should consult their primary care provider prior to fasting, as changes in their medications may be required and these patients require close monitoring.
Ivermectin — 0.2 to 0.3 mg/kg, daily for up to 4 to 6 weeks. Ivermectin has potent anti-inflammatory properties. It also binds to the spike protein, aiding in the elimination by the host. It is likely that ivermectin and intermittent fasting act synergistically to rid the body of the spike protein.
Ivermectin is best taken with or just following a meal for greater absorption. A trial of ivermectin should be considered as first-line therapy. It appears that patients can be grouped into two categories: i) ivermectin responders and ii) ivermectin nonresponders.
This distinction is important, as the latter are more difficult to treat and require more aggressive therapy. Due to the possible drug interaction between quercetin and ivermectin, these drugs should not be taken simultaneously (i.e., should be staggered morning and night).
Low dose naltrexone (LDN) — Begin with 1 mg/day and increase to 4.5 mg/day, as required. May take 2 to 3 months to see full effect. LDN has been demonstrated to have anti-inflammatory, analgesic, and neuromodulating properties.
Melatonin — 2 to 6 mg slow release/extended-release prior to bedtime. Melatonin has anti-inflammatory and antioxidant properties and is a powerful regulator of mitochondrial function. The dose should be started at 750 mcg (μg) to 1 mg at night and increased as tolerated. Patients who are slow metabolizers may have very unpleasant and vivid dreams with higher doses.
Aspirin — 81 mg/day. (Please note: I do not agree with the routine use of aspirin, and recommend proteolytic enzymes such as lumbrokinase and serrapeptase on an empty stomach instead. Both serve to digest unwanted proteins in your blood, like blood clots.
They also help combat inflammation and rebalance your immune system, facilitating the removal of inflammatory proteins, removing fibrin — a clotting material that restricts blood flow and prolongs inflammation-reducing edema in inflamed regions, and boosting the potency of macrophages and killer cells.)
Vitamin C — 1000 mg orally three to four times a day. Vitamin C has important anti-inflammatory, antioxidant, and immune-enhancing properties, including increased synthesis of type I interferons. Avoid in patients with a history of kidney stones. Oral Vitamin C helps promote the growth of protective bacterial populations in the microbiome.
It is important to note that these high doses are a pharmaceutical application of vitamin C and are NOT recommended for daily use. It is far better to use whole food vitamin C and not ascorbic acid for daily use. I actually will be speaking with Dr. Marik and Korey September 9 and 10 at a vitamin C conference11 in Clearwater, Florida. If you come to the event you will be able to meet me personally there.
Vitamin D and Vitamin K2 — A dose of 4,000 to 5,000 units/day of vitamin D, together with vitamin K2 100 mcg/day is a reasonable starting dose. The dose of Vitamin D should be adjusted according to the baseline vitamin D level.
Quercetin — 250 to 500 mg/day (or mixed flavonoids). Flavonoids have broad-spectrum anti-inflammatory properties, inhibit mast cells, and have been demonstrated to reduce neuroinflammation.
Due to a possible drug interaction between quercetin and ivermectin, these drugs should not be taken simultaneously (i.e., should be staggered morning and night). The use of quercetin has rarely been associated with hypothyroidism.
The clinical impact of this association may be limited to those individuals with preexistent thyroid disease or those with subclinical thyroidism. Quercetin should be used with caution in patients with hypothyroidism and TSH levels should be monitored.
Nigella Sativa — 200 to 500 mg twice daily. It should be noted that thymoquinone (the active ingredient of Nigella sativa) decreases the absorption of cyclosporine and phenytoin. Patients taking these drugs should, therefore, avoid taking Nigella sativa. Furthermore, two cases of serotonin syndrome have been reported in patients taking Nigella sativa who underwent general anesthesia (probable interaction with opiates).
Probiotics/prebiotics — Patients with post-vaccine syndrome classically have a severe dysbiosis with loss of Bifidobacterium. Kefir is a highly recommended nutritional supplement high in probiotics.
Magnesium — 500 mg/day.
Omega-3 fatty acids — DHA/EPA 4 g/day. Omega-3 fatty acids play an important role in the resolution of inflammation by inducing resolvin production.
FLCCC Second Line Therapies for Vaccine Injury
Adjunctive and/or second-line therapies in the FLCCC's vaccine injury protocol are:
Hydroxychloroquine (HCQ) — 200 mg twice daily for 1–2 weeks, then reduce as tolerated to 200 mg/day. HCQ is the preferred second-line agent.
HCQ is a potent immunomodulating agent and is considered the drug of choice for systemic lupus erythematosus (SLE), where it has been demonstrated to reduce mortality from this disease. Thus, in patients with positive autoantibodies or where autoimmunity is suspected to be a prominent underlying mechanism, HCQ should be considered earlier.
Further, it should be noted that SLE and post-vaccine syndrome have many features in common. HCQ is safe in pregnancy; indeed, this drug has been used to treat preeclampsia. With long-term usage, the dose should be reduced (100 or 150 mg/day) in patients weighing less than 61 kg (135 lbs).
Intravenous vitamin C — 25 g weekly, together with oral Vitamin C 1000 mg (1 gram) 2–3 times per day. High-dose IV vitamin C is "caustic" to the veins and should be given slowly over 2–4 hours.
Furthermore, to assess patient tolerability the initial dose should be between 7.5–15 g. Total daily doses of 8–12 g have been well-tolerated, however, chronic high doses have been associated with the development of kidney stones, so the duration of therapy should be limited. Wean IV vitamin C as tolerated.
Non-invasive brain stimulation (NIBS) — NIBS using transcranial direct current stimulation or transcranial magnetic stimulation has been demonstrated to improve cognitive function in patients with long COVID as well as other neurological diseases. NIBS is painless, extremely safe, and easy to administer. It is a recognized therapy offered by many Physical Medicine and Rehabilitation Centers. Patients may also purchase an FDA-approved device for home use.
Fluvoxamine — Start on a low dose of 12.5 mg/day and increase slowly as tolerated.
"Mitochondrial energy optimizer" with pyrroloquinoline quinone (e.g., Life Extension Energy Optimizer or ATP 360®).
N-acetyl cysteine (NAC) — 600–1500 mg/day.
Low dose corticosteroid — 10–15 mg/day prednisone for three weeks. Taper to 10 mg/day and then 5 mg/day, as tolerated.
Behavioral modification, mindfulness therapy, and psychological support — May help improve patient's overall well-being and mental health. Suicide is a real problem in the vaccine-injured patient. Support groups and consultation with mental health professionals are important.
Tai Chi and Yoga — Tai Chi, a health-promoting form of traditional Chinese martial art, has shown to be beneficial for preventing and treating diseases including long COVID. Yoga has immunomodulating properties that may be beneficial in vaccine-injured patients.
It should be noted that long COVID is characterized by severe post-exertional fatigue and/or worsening of symptoms, therefore patients should be counseled to moderate exertion, increasing slowly only as tolerated.
Examples of third-line therapies and other potential remedies include hyperbaric oxygen therapy, whole-body vibration therapy, cold hydrotherapy, nutraceuticals such as dandelion and broccoli sprout powder, and carbon 60 (C60 fullerenes). For the full list, see the I-RECOVER Post-Vaccine Treatment Protocol12 available on covid19criticalcare.com.13
republished below in full unedited for informational, educational & research purposes:
According to a 2011 Health Grades report, the incidence rate of medical harm occurring in the U.S. is estimated to be over 40,000 harmful and/or lethal errors daily
In 2014 10.5% of American doctors admitted they’d made a major medical mistake in the last three months
In 2016, Dr. Marty Makary published a report showing an estimated 250,000 Americans die from medical mistakes each year — about 1 in 10 patients — making it the third leading cause of death, right after cancer and heart disease
The World Health Organization’s Surgical Safety Checklist, developed by Makary, has been proven to reduce adverse event rates and save lives
In 2019, RaDonda Vaught, a registered nurse, was indicted for reckless homicide for administering the wrong drug to an elderly patient who died. She was found guilty and in May 2022, was sentenced to three years probation. It’s the first time a medical professional has been charged over a medical mistake that did not involve fraud or intentional malice. Many now worry this may prevent openness and transparency about unintentional medical mistakes
In July of 2000, I was still receiving a print subscription to JAMA (Journal of the American Medical Association) and I was shocked that they actually published an article1 from Barbara Starfield, who had an MPH (master of public health) from Johns Hopkins.
Why was I shocked? Because I looked at the data in the article (see below) physician mistakes were the third leading cause of death in the United States. My article on it went viral and that meme became very popular in 2000, but I was rarely acknowledged as the person who was responsible for it.
Deaths Per Year (From 2000)
12,000 — unnecessary surgery
7,000 — medication errors in hospitals
20,000 — other errors in hospitals
80,000 — infections in hospitals
106,000 — non-error, negative effects of drugs
These total 225,000 deaths per year from physician or health care mistakes and are only surpassed by heart disease and cancer.
Starfield's Ironic Tragedy — A Victim to What She Chronicled
Ironically, Starfield became a statistic to her own research. She died suddenly in June 2011, a death her husband attributed to the adverse effects of the blood thinner Plavix taken in combination with aspirin. However, her death certificate makes no mention of this possibility. In the August 2012 issue of Archives for Internal Medicine2 her husband, Dr. Neil A. Holtzman, writes, in part:
"Writing in sorrow and anger, I express up front my potential conflict of interest in interpreting the facts surrounding the death of my wife, Dr. Barbara Starfield ... Because she died while swimming alone, an autopsy was required. The immediate cause of death was 'pool drowning,' but the underlying condition, 'cerebral hemorrhage,' stunned me ...
Barbara started taking low-dose aspirin after coronary insufficiency had been diagnosed three years before her death, and clopidogrel bisulfate (Plavix) after her right main coronary artery had been stented six months after the diagnosis.
She reported to the cardiologist that she bruised more easily while taking clopidogrel and bled longer following minor cuts. She had no personal or family history of bleeding tendency or hypertension.
The autopsy findings and the official lack of feedback prompted me to call attention to deficiencies in medical care and clinical research in the United States reified by Barbara's death and how the deficiencies can be rectified. Ironically, Barbara had written about all of them."
2022 Updated Medical Mistakes Stats
The video above features an interview between Dr. Peter Attia and Dr. Marty Makary, a professor of surgery at Johns Hopkins, in which they discuss the prevalence of medical mistakes in conventional medicine and advancements in patient safety.
Makary is also a public health researcher, a member of the National Academy of Medicine, the editor-in-chief of MedPage Today (the second-largest trade publication in medicine), and the author of two best-selling books.
As a busy surgeon, Makary has worked in many of the best hospitals in the country and can testify to the power of modern medicine. But he’s also witnessed a medical culture that leaves surgical sponges inside patients, amputates the wrong limb, overdoses patients because of sloppy handwriting, or enters prescriptions into the wrong patient chart.
Medical Mistakes Are Commonplace
According to a 2011 Health Grades report,3 the incidence rate of medical harm occurring in the U.S. was estimated to be over 40,000 harmful and/or lethal errors daily. Makary cites a 2014 Mayo Clinic survey of 6,500 American doctors, 10.5% of whom admitted they’d made a major medical mistake in the last three months.
He also cites a 2015 study by researchers at Massachusetts General Hospital that showed about half of all operations involved some kind of medication error. That study and corresponding press release have since been removed and are no longer available online, Makary says. Possibly because the hospital was embarrassed by the results.
In 2016, Makary and his research team published a report showing an estimated 250,000 Americans die from medical mistakes each year4 — about 1 in 10 patients — which (at that time) made it the third leading cause of death, right after cancer and heart disease.
According to Makary, that number may be higher, because the Centers for Disease Control and Prevention does not collect vital statistics on medical errors. Death cannot be recorded as a medical error as there’s no code for it.
Of course, since they didn’t do autopsies on every death, that number could also be lower, so the final estimate they came up with was between 125,000 and 350,000 deaths per year.
Another widely-cited study5 published in 2013 estimated the annual death toll for medical mistakes in the U.S. at 400,000 a year,6 Makary says. But whatever the true number, and whether it’s the third cause of death or the ninth, medical mistakes are clearly a serious and too-frequent problem.
An estimated 30% of all medical procedures, tests, and medications may also be completely unnecessary,7, and each of these unnecessary interventions opens the door for a medical mistake that didn’t need to happen.
Many doctors have long been concerned about the frequency of medical mistakes, unnecessary testing, and overtreatment, but the culture was such that it dissuaded open discussion and transparency.
It’s really only in the past decade or so that doctors and hospital administrators have started being more honest about these problems. Now, a case (discussed below) in which a nurse was charged and found guilty of negligent homicide after accidentally administering the wrong medication threatens to undo much of that progress.
Milestones in Patient Safety
In medical jargon, a “near-miss” refers to a medical mistake that could have resulted in patient harm but didn’t, and a “preventable adverse event” refers to a medical mistake that does result in harm to the patient.
A “never event” is one that should never happen, regardless of circumstance. One example of a “never event” would be leaving a surgical instrument or sponge inside the patient.
In 2008, Medicare decided it would no longer pay for “never events,” in an effort to de-incentivize sloppiness. Shortly thereafter, private insurance companies followed suit. The following year, in 2009, the World Health Organization organized a committee to address patient safety, as, worldwide, it was becoming apparent that many patients were dying from the care and not just from disease.
At the time, Makary had just published a surgery checklist for Johns Hopkins, and the WHO invited him to present it to the newly formed committee on patient safety. This checklist eventually became known as the WHO Surgical Safety Checklist.8 To this day, it hangs on operating room walls across the world.
Later investigations have revealed this pre-op checklist does in fact reduce adverse event rates and save lives. If a loved one is in the hospital, print it out, bring it with you and confirm that each of the 19 items has been done.
This can help you protect your family member or friend from preventable errors in care. It’s available in several languages, including Arabic, Chinese, English, French, Russian, Spanish, Portuguese, Farsi, German, Italian, Norwegian, and Swedish.
Opioid Overdose Is a Leading Death Among Young Adults
As of 2017, opioid overdoses have been the leading cause of death among Americans under the age of 50.9 The most common drugs involved in prescription opioid overdose deaths are methadone, oxycodone (such as OxyContin®), and hydrocodone (such as Vicodin®).10
Lawsuits that have made their way through the judicial system in recent years have shown opioid makers such as Purdue Pharma, owned by the Sackler family, knew they were lying when they claimed opioids — which are chemically very similar to heroin — have an exceptionally low addiction rate when taken by people with pain.
As a result of their lies, doctors handed out opioids for pain as if they were candy. Even Makary admits to being fooled by the fraudulent PR. “That is a form of a medical mistake,” he says, adding “I’m guilty of it myself. I gave opioids out like candy, and I feel terrible about it.”
In recent years, the medical industry has cracked down on prescription opioids, making them harder to obtain, but many patients still struggle with addiction, and fentanyl-laced products obtained illegally are still causing many unnecessary deaths.
The RaDonda Vaught Case
In this interview, Makary also reviews the RaDonda Vaught case which, as mentioned earlier might reverse much of the progress achieved with regard to openness and transparency about medical mistakes.
Vaught was hired as a nurse at Vanderbilt hospital in 2015. Two years later, on Christmas eve in 2017, she was taking care of a patient named Charlene Murphy, a 75-year-old woman admitted for a subdural hematoma (a brain bleed). Murphy made a rapid recovery and after two days she was ready to go home.
The doctor ordered one last scan while she was in the hospital, so Vaught brought her to the scanner and ordered Versed (midazolam), a sedative commonly used to help the patient lay still. The hospital had installed an automated drug dispensary system, the alerts of which often had to be overridden due to poor coordination between the electronic health records and the pharmacy.
On this fateful day, Vaught typed “ve” into the system to pull up Versed, but by default, the system populated the search with “vecuronium,” a potent paralyzing agent. Vaught didn’t realize the mistake and overrode the alert. Now, vecuronium is a powder, and most experienced nurses would know that Versed is a liquid.
Vaught, however, didn’t catch the discrepancy and suspended the powder with saline as indicated and gave it to Murphy, who subsequently died inside the scanner.
“The nurse [Vaught] immediately feels horrible; says exactly what she did, recognized her mistake as the patient was deteriorating, and felt ‘I may have caused this,’” Makary says. “[She] admitted [and] reported this whole thing; was 100% honest. I mean, [she] even said, subsequently, that her life will never be the same, that she feels that a piece of her has died.”
In 2019, Vaught was indicted for reckless homicide.11,12 She was found guilty and in May 2022, was sentenced to three years probation with judicial diversion,13 which means her criminal record can be expunged if she serves her probationary period with good behavior. Her nursing license was also revoked.
Should Medical Mistakes Be Prosecuted?
Now, while Vaught immediately admitted her mistake, Vanderbilt hospital, for its part, appears to have been trying to cover it up.
“Vanderbilt had documentation where two neurologists listed the cause of death as the brain bleed. It was deemed, essentially, a natural cause of death. This was reported to the medical examiner,” Makary says.
An investigation by the Tennessean revealed Vanderbilt did not report the death to state or federal officials as a preventable adverse event, as is required by law. Instead, they fired Vaught and immediately negotiated an out-of-court settlement with the family, which included a gag order.
So, it wasn’t the family that brought charges against Vaught but rather a team of district attorneys in Davidson county. Vaught’s case is the first of its kind and has triggered emotional reactions across the country among doctors and nurses alike, as everyone knows how easily and frequently medical mistakes occur.
According to the Tennessean, “The case has put a spotlight on how nurses should be held accountable for medical mistakes.” But should they? Never before has a medical professional been criminally charged for a medical mistake that didn’t involve intentional fraud or malice. As noted by Makary:
“One of the principles of patient safety that we have been advocating throughout the entire 23 years of the patient safety movement in America has been the concept ‘just culture’ — a doctrine which says that honest mistakes should not be penalized ... That is a doctrine that has enabled people to speak up about this epidemic of medical mistakes in the United States ...
In my opinion, we have had decades of progress in patient safety, about 23 healthy years of significant improvements in the culture of safety and the way we approach safety, undone with a single group of assistant young district attorneys that decided to go after one individual at the exclusion of doing anything about a hospital that, unlike the nurse, did not admit to anything initially and broke the law.
There's a preliminary statistic that 1 in 5 nurses are quitting during the pandemic. Now, some of that is pandemic burnout, some of it's a number of [other] factors, but a lot of nurses are leaving the profession and there's this feeling that they don't feel valued, and this [case] has been a bit of a smack in their face.
So, hospitals around the country that are dealing with critical nursing staffing shortages are trying to pay attention to the concerns that nurses have about this case. I have talked to lawmakers at the state level in different states who are thinking about passing protections for nurses. It’s delicate, but this is now a conversation that has surfaced.”
The U.S. Is an Unmitigated Failure at Treating Chronic Illness
The U.S. has the most expensive health care in the world, spending more on health care than the next 10 biggest spenders combined (Japan, Germany, France, China, the U.K., Italy, Canada, Brazil, Spain, and Australia). If the U.S. health care system were a country, it would be the sixth-largest economy on the entire planet.
Despite that, the U.S. ranks last in health and mortality when compared with 17 other developed nations. We may have one of the best systems for treating acute surgical emergencies, but the American medical system is clearly an unmitigated failure when it comes to treating chronic illness.
The fact that properly prescribed and administered drugs kill well over 100,000 every year in the U.S. should really be food for some serious thought. For starters, drug safety needs to become a priority, not an afterthought.
Indeed, one of Starfield's points of contention was the lack of systematic recording and studying of adverse events, and her own death highlights this problem. It was the Plavix-aspirin combination that actually killed her, yet if it hadn't been for an autopsy and her husband insisting on an adverse event report, no one would ever have been the wiser about such a connection.
Only a tiny fraction of all adverse drug reactions are ever reported to the FDA; according to some estimates, as few as 1%. In order to truly alert the FDA to a problem with a product they've approved, they must be notified by as many people as possible who believe they have experienced a side effect.
By filing a report, you help make medicine safer for everyone. So, if you believe you've experienced a side effect from a drug, please report it. Simply go to the FDA Consumer Complaint Coordinator page, find the phone number listed for your state, and report your adverse reaction.
In all, preventable medical mistakes may account for one-sixth of all deaths that occur in the U.S. annually.14 To put these numbers into even further perspective, medical mistakes in American hospitals kill four jumbo jets' worth of people each week.15
According to statistics published in a 2011 Health Grades report,16 the incidence rate of medical harm occurring in the U.S. may be as high as 40,000 harmful and/or lethal errors DAILY. According to co-author John T. James, Ph.D.:17
"Perhaps it is time for a national patient bill of rights for hospitalized patients. All evidence points to the need for much more patient involvement in identifying harmful events and participating in rigorous follow-up investigations to identify root causes."
Many Tests and Treatments Do More Harm Than Good
Overtesting and overtreatment are also part of the problem. Instead of dissuading patients from unnecessary or questionable interventions, the system rewards waste and incentivizes disease over health.
According to a report by the Institute of Medicine, an estimated 30% of all medical procedures, tests and medications may in fact be unnecessary, at a cost of at least $750 billion a year.18 To learn which tests and interventions may do more harm than good, browse through the Choosing Wisely website.
It's also important to be aware that many novel medical treatments gain popularity over older standards of care due mostly to clever marketing, as opposed to solid science. An investigation by the Mayo Clinic published in 2013 proved this point. To determine the overall effectiveness of our medical care, researchers tracked the frequency of medical reversals over the past decade.
They found that reversals are common across all classes of medical practice, and a significant proportion of medical treatments offer no patient benefit at all.
In fact, they found 146 reversals of previously established practices,19 treatments, and procedures over the previous 10 years. The most telling data in the report show just how many common medical treatments are doing more harm than good. Of the studies that tested an existing standard of care, 40.2% reversed the practice, compared to only 38% reaffirming it.
The remaining 22% were inconclusive. This means that anywhere between 40 and 78% of the medical testing, treatments, and procedures you receive are of NO benefit to you — or are actually harmful — as determined by clinical studies.
Safeguarding Your Care While Hospitalized
Knowing that medical errors can and do frequently occur, what can you do to ensure your safety, or the safety of a loved one, who has to go to the hospital? Makary offers the following suggestions:
“Every hospital has a patient relations department and if things just don't seem right, if you feel that you're not communicating effectively with your care team, if you feel care is not coordinated, if you have a concern or there was an error, you can call the patient relations department. They’ve got somebody on call 24/7. That's basically a standard thing in the hospitals now.
It’s important to have an advocate with you anytime you get medical care or you've got a loved one in the hospital. It's amazing how it seems that the care is just overall much better, holistic, comprehensive and coordinated when there's a family member or loved one there, taking notes, asking questions ...
Ask about the medication that's being given to you. You should know what it is and what it's for, and you should ask your doctor or whoever walks in the room if they've washed their hands ...
This is the sort of new dialogue that we are trying to promote to make the patient a participant in their care and not just a bystander. When you do it, what I’ve noticed the more educated they are, or their surrogate is, the better the care is. You are in the middle of a very complicated system of care when you're in the hospital. The more you can be aware of what's happening, the safer the care.”
Once you're hospitalized, you're immediately at risk for medical errors, so one of the best safeguards is to have someone there with you. Dr. Andrew Saul has written an entire book20 on the issue of safeguarding your health while hospitalized.
Frequently, you're going to be relatively debilitated, especially post-op when you're under the influence of anesthesia, and you won't have the opportunity to see the types of processes that are going on. This is particularly important for pediatric patients and the elderly.
It's important to have a personal advocate present to ask questions and take notes. For every medication given in the hospital, ask questions such as: "What is this medication? What is it for? What's the dose?" Most people, doctors, and nurses included, are more apt to go through that extra step of due diligence to make sure they're getting it right if they know they'll be questioned about it.
If someone you know is scheduled for surgery, you can print out the WHO surgical safety checklist and implementation manual, which is part of the campaign "Safe Surgery Saves Lives." The checklist can be downloaded free of charge here. If a loved one is in the hospital, print it out and bring it with you, as this can help you protect your family member or friend from preventable errors in care.
(Natural News) EXCLUSIVE: Today we are publishing a series of lab microscopy photos of bizarre clots which are now being routinely found in adults who “suddenly died,” usually in a number of months following covid vaccinations.
These clots are often referred to as “blood clots” but they are nothing at all like normal clots, and they consist of far more than mere blood cells. Unlike normal clots which are gelatinous, almost jelly-like, these so-called “clots” contain extremely large, complex, repeating structural elements (all shown below) that are clearly being constructed in the blood of the victims who died from these clots.
All of these clots were extracted from patients within a few hours of their death. These are not the result of post-mortem blood stasis. These are structures found in blood vessels and arteries. They are not congealed blood.
We wish to publicly thank Dr. Jane Ruby for connecting us to the embalmer (Richard Hirschman) who provided these clots. (Telegram channel T.ME/DRJANERUBY) Without the persistence of Dr. Ruby, you would not be seeing this report. Dr. Ruby is frequently featured on the Stew Peters Show (StewPeters.TV) and will also be my featured guest Monday on the Infowars.com broadcast.
Here’s a vial of these raw clots, washed of blood and preserved, before staining:
republished below in full unedited for informational, educational & research purposes:
(Natural News) The latest drop of pages from the secret Pfizer documents reveals that the pharmaceutical giant is fully aware that its Wuhan coronavirus (Covid-19) “vaccine” will soon result in mass depopulation of the world.
The June 1 dump contains a document called “reissue_5.3.6 postmarketing experience.pdf,” page 12 of which includes disturbing data on getting Pfizer’s Fauci Flu injection during pregnancy and lactation.
It turns out that 90 percent of pregnant women who took the shot ended up losing their babies. This is a shocking figure that the U.S. Food and Drug Administration (FDA) apparently did not think twice about when granting Emergency Use Authorization (EUA) to the jab.
“Pfizer states in the document that by 28th February 2021 there were 270 known cases of exposure to the mRNA injection during pregnancy,” reports Exposé News. “Forty-six percent of the mothers (124) exposed to the Pfizer Covid-19 injection suffered an adverse reaction.”
“Of those 124 mothers suffering an adverse reaction, 49 were considered non-serious adverse reactions, whereas 75 were considered serious. This means 58% of the mothers who reported suffering adverse reactions suffered a serious adverse event ranging from uterine contraction to fetal death.”
Of 270 tracked pregnancies, Pfizer lost track of 238 of them
The latest batch of released Pfizer documents also contains a concerning revelation about pregnancies of which the company somehow lost track. Of the 270 pregnancies Pfizer was tracking, a shocking 238 of them just disappeared from the dataset.
Of the 33 pregnancies that Pfizer still tracked, a shocking 23 of them resulted in spontaneous abortion. Two resulted in premature baby death; two resulted in
intrauterine death; one resulted in neonatal death; one is listed as “outcome pending;” and only one resulted in a “normal outcome.”
What this means is that almost every pregnant woman who takes Pfizer’s mRNA (messenger RNA) injections for covid will lose her baby. Conversely, only a tiny fraction of fully jabbed women will successfully deliver to term.
Keep in mind that some governments, including that of the United Kingdom, had quietly dissuaded pregnant women from taking Pfizer’s injections – at least up until recently.
“There are no or limited amount of data from the use of COVID-19 mRNA Vaccine BNT162b2,” reads a now-altered U.K. government guidance entitled “REG 174 INFORMATION FOR UK HEALTHCARE PROFESSIONALS.”
“COVID-19 mRNA Vaccine BNT162b2 is not recommended during pregnancy. For women of childbearing age, pregnancy should be excluded before vaccination. In addition, women of childbearing age should be advised to avoid pregnancy for at least 2 months after their second dose.”
The new version of the same guidance claims that pregnant women can take Pfizer’s injections, but only “when the potential benefits outweigh any potential risks for the mother and fetus.”
As of this writing, the UK government guidance is recommending that pregnant women take the Pfizer shots just so long as they have evaluated the risks involved. At the same time, these same authorities continue to tell pregnant women to avoid soft cheese, herbal tea, and vitamin supplements because they could be dangerous.
All of this just goes to show once again that governments cannot be trusted. They routinely dispense advice in the form of guidance that, if followed, will probably lead to injury or death. This is true both for vaccines and the covid plandemic itself.
“Covid is a cult and ‘Stay Safe’ is a mantra,” wrote a regular commenter at Natural News. “I personally saw through the delusion in the same way most churches are tools for keeping God as far away as possible from your life.”
“I would rather have the virus than the lockdown and that is a fact.”
To keep up with the latest news about Fauci Flu shot injuries and deaths, visit ChemicalViolence.com.
republished below in full unedited for informational, educational & research purposes:
(Natural News) The murderous medical regime knows that covid vaccines are killing healthy young people at an alarming rate, so they’ve suddenly assigned a medical label for the phenomenon in order to distract people from the truth. Now, healthy young people who suddenly die without any medical explanation are said to have died from Sudden Adult Death Syndrome (SADS) rather than from vaccines.
While SADS has existed in medical terminology long before covid, doctors and the media are now using this syndrome label in a new way: To try to explain away vaccine deaths. From what we can tell so far, there are no such “sudden deaths” in unvaccinated young adults. So far, this seems to be happening solely among those who have been vaccinated.
The UK Daily Mail has published an article detailing this new so-called “syndrome” which is of course just a convenient label to mask the true underlying cause of these sudden deaths. The title of their article is, “Healthy young people are dying suddenly and unexpectedly from a mysterious syndrome – as doctors seek answers through a new national register,” and it says that everyone under the age of 40, “…may potentially be at risk of having Sudden Adult Death Syndrome (SADS).”
All people under the age of 40 are now supposed to “get their hearts checked,” while oblivious doctors claim to be searching for the “genetic cause” behind SADS.
Never before in the history of medicine have doctors and the media urged young people to “get their hearts checked.” This is only happening after the global push for covid vaccines which hijack the body’s cells and force them to create spike protein particles that cause blood clots.
Murderous doctors are killing young people en masse with “clot shots”
You can’t make this up. The medical negligence, incompetence, and even maliciousness behind all this are mind-boggling. Medical doctors who function as Big Pharma shills inject young people with gene therapy cocktails containing
experimental mRNA sequences that produce spike proteins in the blood, contributing the artificial clotting. In some people, the clots build slowly over time, meaning many people are walking around with partially-formed blood clots in their circulatory system.
At some point, one or more of the clots in the body completely shuts off the blood circulation necessary to maintain consciousness. At this point, the person loses consciousness and dies. Often this happens when they are driving, flying an airplane, or even sleeping at night. This is why so many pilots are dying on the flight deck, for example, which is a major cause contributing to the current nationwide shortage of commercial airline pilots.
A doctor named Dr. Elizabeth Paratz — who claims to be wondering “what genes cause this” syndrome — says that 90 percent of these spontaneous deaths occur outside the hospital. (Source: UK Daily Mail)
Australia is now launching a “SADS registry” to try to solve the mystery of why seemingly healthy adults are spontaneously dying. They are doing this while pushing more mRNA injections onto those very people, apparently oblivious to the fact that mRNA injections are “clot shots.”
It is widely known in the biosciences that viral genetic code is readily and automatically incorporated into human DNA
mRNA injections aren’t even technically vaccines. They are “gene therapy” experimental medicines that alter not just cellular protein synthesis but are even incorporated into human DNA via reverse transcription. It turns out that a significant percentage of human DNA was acquired via this very process over many thousands of generations, where genetic material circulating in the environment is incorporated into human chromosomes. This phenomenon is widely known even in the conventional scientific community.
“Non-retroviral RNA virus sequences have been detected in the genomes of many vertebrate species, including humans,” said biomedical researcher Liguo Zhang from MIT’s Whitehead Institute. (Source: MIT.edu)
Zhang even ran an experiment to test if SATS-CoV-2 viral fragments might incorporate themselves into human DNA:
With this in mind, Zhang and Jaenisch began to design experiments to test whether this viral integration could be happening with the novel coronavirus. With the help of Jaenisch lab postdoc Alexsia Richards, the researchers infected human cells with coronavirus in the lab and then sequenced the DNA from infected cells two days later to see whether it contained traces of the virus’ genetic material.
In all samples, they found fragments of viral genetic material…
In other words, parts of the SARS-CoV-2 were incorporated into the DNA of human cells. Another researcher explains:
“There’s a very clear footprint for LINE1 integration,” Jaenisch says. “At the junction of the viral sequence to the cellular DNA, it makes a 20 base pair duplication.
Anyone claiming spike protein genetic code can’t be incorporated into DNA is flatly ignorant of the state of modern genetic science.
Spike protein mRNA becomes human DNA which turns the body into a clotting factory
As the above experiment shows, when the body is injected with genetic material, some of that material can be incorporated into the chromosomes of living cells. Although this is an oversimplification of the mechanisms in play, the overall result is the same: The body becomes a factory for spike proteins, producing them far beyond the intended time window during which an mRNA vaccine might be expected to function.
In other words, the vaccinated person becomes a walking spike protein factory that can never be turned off. From that point, they become a spike protein shedding machine while increasingly dumping self-synthesized spike proteins into their own circulating blood.
Over time, this forms blood clots. When those clots complete their blockage of large arteries, blood can no longer reach the brain. When the brain has no blood supply, brain death occurs, and the death of the body quickly follows.
This is now being called “Sudden Adult Death Syndrome” even though it’s clearly caused by vaccine-induced blood clots.
Here’s a photo of a blood clot taken from a covid patient. It shows the clotting power of the spike protein, which is also present in covid vaccines:
Billions of people on our planet are now at risk of blood clot-induced sudden death, all by design: Vaccine Depopulation Syndrome
In summary, the murderous medical regime first injects billions of people with a biological weapon that might kill them, then they pretend to be shocked and surprised when so many healthy young adults start dying for no apparent medical reason. Do these medical monsters have no humanity (or scientific credibility) remaining at all?
Although this syndrome is called SADS, what’s really sad is that it was all done on purpose in order to achieve global depopulation. If anything, these deaths should be labeled, “Vaccine Depopulation Syndrome” deaths. But of course, the media and the medical tyrants are working triple time to cover all this up, and they know that dead vaccine victims don’t talk, so they can’t tell the living humans to save themselves by avoiding these deadly jabs.
Get full details on this story and much more in today’s Situation Update podcast, which also covers economic survival strategies for surviving the total collapse of fiat currencies around the world:
republished below in full unedited for informational, educational & research purposes:
Three physicians have filed a lawsuit against the U.S. Food and Drug Administration (FDA) this month for the agency’s “crusade” against ivermectin as a treatment for Covid-19. The lawsuit contends the FDA “unlawfully interfered” with the doctors’ ability to practice medicine by directing the public, health professionals, and patients not to use ivermectin.
The Epoch Timesreports that Drs. Robert L. Apter, Mary Talley Bowden, and Paul E. Marik filed the lawsuit with the U.S. District Court, Southern District of Texas, Galveston Division. In addition to the FDA, the suit names the U.S. Department of Health and Human Services (HHS), HHS Secretary Xavier Becerra, and Acting FDA Commissioner Robert Califf. The physicians are represented by Boyden, Gray & Associates, a Washington, D.C.-based law firm.
According to the lawsuit, the FDA acted outside of its authority, which is limited to approving drugs and drug labeling.
“The FDA generally cannot ban particular use of human drugs once they are otherwise approved and admitted to the market, even if such use differs from the labeling — commonly referred to as “off-label” use,” the lawsuit reads. “The FDA also cannot advise whether a patient should take an approved drug for a particular purpose. Those decisions fall within the scope of the doctor-patient relationship. Attempts by the FDA to influence or intervene in the doctor-patient relationship amount to interference with the practice of medicine, the regulation of which is — and always has been — reserved to states.”
The lawsuit specifically cites an FDA publication titled, “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19” and several tweets from the FDA discouraging the use of ivermectin as examples of FDA interference.
One such tweet includes a photo of a doctor with a horse beside an image of a doctor with a patient. The tweet reads, “You are not a horse. You are not a cow. Seriously, y’all. Stop it.”
The tweet is intentionally misleading, as ivermectin has, in fact, been approved by the FDA for human use. Newsmax reported that though ivermectin was developed in the 1970s as a treatment for parasitic diseases in livestock, it became hailed as a “wonder drug” and received approval for human use against diseases such as river blindness. The Epoch Times observed it has been used widely since 1987, even earning William Campbell and Satoshi Omura the 2015 Nobel Prize in Physiology or Medicine for their research on the drug.
The plaintiffs contend that the FDA’s unlawful interference in the practice of medicine creates a dangerous precedent that will “metastasize to other circumstances, destroying the carefully constructed statutory wall between federal and state regulatory powers, and between the FDA and the professional judgment of health professionals.”
The plaintiffs have seen first-hand the dangers that this interference can create.
“Doctors are increasingly employees of entities that look to the FDA for guidance and enforce standards accordingly,” the lawsuit argues.
As such, despite the plaintiffs’ extensive academic and professional credentials, all of which are outlined in the lawsuit, they all faced disciplinary action for treating their patients with ivermectin.
Dr. Apter, despite his 99.8-percent success rate in treating Covid-19 patients, was referred to the Washington Medical Commission and Arizona Medical Board for disciplinary proceedings for prescribing ivermectin as part of his Covid treatment, The Epoch Times report.
Apter asserted in a press release that the FDA’s treatment of ivermectin has resulted in disciplinary actions against doctors and inhibited physician freedom to treat patients according to their best judgment, resulting in more deaths and serious disabilities. He adds the FDA’s interference has been so overreaching that even pharmacies have refused to fill ivermectin prescriptions.
Like Apter, plaintiff Dr. Mary Bowden also successfully treated Covid-19 patients with ivermectin before being forced to resign by her employer, Houston Methodist Hospital.
Bowden told The Defender that she initially supported the widespread vaccines for Covid until she noticed the prevalence of breakthrough cases and adverse reactions to the vaccine.
“If I hadn’t seen that firsthand,” she said, referring to the adverse reactions, “I would still think the vaccine was the way to go.”
Prompted by the realization that the vaccines were not the answer to the pandemic, Bowden created her own Covid protocol, which includes ivermectin, vitamins C and D, quercetin, zinc, and black seed oil. She said the results were excellent.
Similarly, Dr. Paul Marik developed a Covid-19 Management Protocol for the Eastern Virginia Medical School (EVMS) in Norfolk, Virginia, where he worked from 2009 to 2021. Dr. Marik also served as director of the intensive care unit at Sentara Norfolk General Hospital until he was forced out of both positions for promoting the use of ivermectin to treat Covid-19.
Marik contends that the FDA’s attempt to stop the use of ivermectin for Covid has “led to innumerable hospitalizations and deaths, and caused extreme distress for patients, their families, and health professionals.”
The plaintiffs’ successes in treating Covid-19 with ivermectin are not unique to them. Studies continue to show the drug is associated with lower Covid-19 death rates, but ivermectin continues to be demonized by the FDA and the mainstream media.
Despite the evidence that ivermectin is a viable treatment for Covid-19, the plaintiffs contend the lawsuit is not about the drug’s effectiveness, but about “who determines the appropriate treatment for each unique patient and whether the FDA can interfere with that process.”
The lawsuit argues the FDA acted in violation of the Federal Food, Drug, and Cosmetic Act (FDCA), which expressly states that nothing in the FDCA “shall be construed to limit or interfere with the authority of a health care practitioner to prescribe or administer any legally marketed device for any condition or disease within a legitimate health care practitioner-patient relationship.”
The plaintiffs are asking the court to hold the FDA’s actions unlawful, issue declaratory relief declaring the Defendants’ actions unlawful, and issue declaratory relief declaring that the FDA cannot interfere with the practice of medicine. The lawsuit also asks for injunctive relief enjoining all defendants from engaging in such actions as to interfere with the practice of medicine and issue statements or directives dictating the off-label use of ivermectin. Plaintiffs are also seeking attorney fees and allowable costs, and any further relief “to which they are justly entitled at law and in equity.”
JUNE 2020 - Bill Gates announced a startup called BIOMILQ. It’s backed by some of the richest investors in the world, like Zuckerburg. It raised $3.5 million in Series A funding from Breakthrough Energy Ventures. Breakthrough Energy Ventures is Bill Gates's investment firm focused on climate change.
SEPTEMBER 2020 - Remember that $3.5 million in BIOMILQ money? Well, according to a receipt from the Gates Foundation, it paid The Guardian $3.5 million in September 2020. This was an initial offering from the Gates Foundation. Of course, right after on September 27, the Guardian published an article entitled “Antibodies in breast milk remain for 10 months after Covid infection – study.”
February 2022 - Customs and Border Patrol officers said that they inspected 17 separate shipments of formulas that came from Europe. Border patrol consulted with the FDA. Of course, the FDA said it had safety concerns about non-compliant baby formula. The same month, the FDA announces it is looking into bacterial contamination at the Abbott formula production plant in Michigan that's supposedly behind the baby formula shortage.
MAY 2022 - The Gates Foundation paid the Guardian again as part of annual funding. The very next day, The Guardian wasted no time and published a hit piece on breastfeeding. It’s called “Turns out breastfeeding really does hurt - why does no one tell you?”
republished below in full unedited for informational, educational & research purposes:
Bill Gates appears to be behind the push to stop breastfeeding and encourage uptake of BIOMILQ, a cell-cultured “human milk” made in a lab, along with other varieties of fake food
Nearly every large meat and dairy processor/manufacturer has also acquired or developed plant-based meat and dairy substitutes
This “protein” industry convergence is jeopardizing the resilience of the food system and reducing the genetic diversity of livestock and crops
When you factor in soy production as well as the use of conventional energy sources, lab-grown meat may be worse for the environment than conventionally produced chicken and pork
There are signs that the fake meat industry may be failing before it ever gets off the ground; shares of Beyond Meat lost $6 billion since March 2020 due to weak sales growth
To save the planet and support your health, skip all the fake meat alternatives and opt for real food that’s being raised using regenerative, grass-fed methods
Fake food is being poised as a panacea to end world hunger and food shortages, but there’s nothing miraculous about synthetic, lab-made food. It can’t compare to food that comes from nature in terms of nutrition or environmental protection, and as we’re seeing with the mysterious infant formula shortages, when you’re dependent on fake food, your very survival is also dependent on the handful of companies that manufacture them.
With parents getting desperate in the search for infant formula, it’s eye-opening that campaigns haven’t been started to encourage new mothers to breastfeed — the best food for infants and one that also happens to be free and readily available in most cases. If you haven’t read my article on the best workaround for infant formula for those that are unable to breastfeed, it is on Substack.
In the video above, you can watch a concerning timeline about why this may be, as Bill Gates appears to be behind the push to stop breastfeeding and encourage uptake of BIOMILQ, a cell-cultured “human milk” made in a lab,1 along with other varieties of fake food.
Bill Gates’ Formula for Disaster
In June 2020, Bill Gates announced the startup company BIOMILQ, which is using biotechnology to create lab-made human milk for babies. Using mammary epithelial cells placed in flasks with cell culture media, the cells grow and are placed in a bioreactor that the company says “recreates conditions similar to in the breast.”2
This synthetic lab-made breast milk replacement raised $3.5 million in funding from Gates’ investment firm Breakthrough Energy Ventures.3 Gates has also contributed at least $319 million to the media,4 including The Guardian, allowing him to control and dictate what they print. The day after the Gates Foundation paid The Guardian its annual funding in May 2022, it released a hit piece on breastfeeding titled, “Turns out breastfeeding really does hurt — why does no one tell you?”5
U.S. Customs and Border Protection (CBP) offers also seized 588 cases of infant formula from Europe in April 2021 because it lacked appropriate nutritional labeling. In February 2021, CBP officers said they inspected 17 separate shipments of infant formula from Germany and The Netherlands, leading to a warning against buying infant formula online from overseas.
At the time, Keith Fleming, CBP’s acting director of field operations in Baltimore, Maryland, said in a news release:6
“Consumers should be very careful when contemplating the purchase of items over the internet from an international source, because they may not get what they expect. People expect that the products they purchase comply with existing U.S. health and safety laws and regulations and they’ll be safe for them or their family. That’s not always the case.”
While warning Americans against purchasing infant formula from overseas, in February 2022 the U.S. Food and Drug Administration announced bacterial contamination at the Abbott Nutrition’s Sturgis, Michigan facility,7 which is behind the current infant formula shortages. While Gates is clearly behind the push to stop breastfeeding and encourage BIOMILQ in lieu of breastmilk or formula, the formula shortages highlight the risks of consolidated food production.
Abbott Enriched Shareholders While Formula Sickened Babies
Corporate consolidation is rampant in the U.S. baby formula market, of which 90% is controlled by four companies. Abbot is among them, responsible for 43% of baby formula production in the U.S.8 Yet, according to a whistleblower filing from October 2021, equipment at the company’s Sturgis facility was “failing and in need of repair.”
Pitting and pinholes reportedly existed in a number of pipes, allowing bacterial contamination. Leadership was aware of the failing equipment for up to seven years before the February 2022 outbreak, according to the whistleblower’s report.9
With equipment in need of repair, and a bacteria outbreak in their formula sickening babies, Abbott used its massive profits from 2019 to 2021 to announce a lucrative stock buyback program.10 According to The Guardian:11
“Abbott detected bacteria eight times as its net profits soared by 94% between 2019 and 2021. And just as its tainted formula allegedly began sickening a number of babies, with two deaths reported, the company increased dividends to shareholders by over 25% while announcing a stock buyback program worth $5bn.”
Speaking with The Guardian, Rakeen Mabud, chief economist for the Groundwork Collaborative, added, “Abbott chose to prioritize shareholders by issuing billions of dollars in stock buybacks instead of making productive investments.”12
Big Meat and Dairy Companies Dominate Fake Meat Industry
The increasing number of plant-based fake foods and lab-grown meat companies give the illusion that consumers are getting more choices and the food industry is becoming less consolidated. However, there are still relatively few firms that are controlling the global grab for “protein” markets.
In a research article published in Frontiers in Sustainable Food Systems, Philip Howard, a faculty member in the department of community sustainability at Michigan State University, and colleagues explain how this “protein” industry convergence is further jeopardizing the resilience of the food system and reducing the genetic diversity of livestock and crops:13
“Recent years have seen the convergence of industries that focus on higher protein foods, such as meat processing firms expanding into plant-based substitutes and/or cellular meat production, and fisheries firms expanding into aquaculture. A driving force behind these changes is dominant firms seeking to increase their power relative to close competitors, including by extending beyond boundaries that pose constraints to growth.
The broad banner of “protein” offers a promising space to achieve this goal, despite its nutritionally reductionist focus on a single macronutrient. Protein firm strategies to increase their dominance are likely to further diminish equity in food systems by exacerbating power asymmetries.”
Tyson and Cargill, two of the largest meat processors in the world, for instance, have invested in fake meat company Memphis Meats, which also has backing from Bill Gates and Richard Branson. Other billionaires who invested in fake foods include Sergey Brin (Mosa Meat), Peter Thiel (Modern Meadow), and Marc Benioff (Eat Just).
“These companies wouldn’t be making these investments if they didn’t expect that the intellectual properties held by these start-ups will lead to monopoly profits,” Howard notes.14 In “The Politics of Protein,” a report from the International Panel of Experts on Sustainable Food Systems (IPES-Food), Howard explains:15
“Nearly every large meat and dairy processor/manufacturer has also acquired or developed plant-based meat and dairy substitutes, establishing footholds in a market that is growing approximately 20% per year.
More than a dozen of these firms have also invested in start-ups that are attempting to commercialize lab-grown meat and fish. Meanwhile, Vanguard and BlackRock — two of the world’s biggest asset management firms — have investments in almost all the largest meat, dairy, and animal feed companies.”
It is important to understand why all of these fake meat products are an absolute metabolic disaster relates to the fact that they are using vegetable fats to replace animal fats. Not only are they devoid of important vitamins like vitamin A and vitamin K2, but they are loaded with the dangerous omega-6 fat linoleic acid LA.
In some cases, they contain up to 10 to 20 times the amount found in meats, which will radically contribute to diseases like diabetes, obesity, cancer, and heart disease.
Lab-Grown Food Is an Environmental Catastrophe
The push for fake food is being made on the platform that it will somehow save the environment from the ravages of factory farming, which has devastated the environment with its concentrated animal feeding operations and monocultures. But this, too, is misleading.
In February 2021, the Good Food Institute (GFI), a nonprofit group behind the alternative protein industry, released a techno-economic analysis of cultivated meat, which was prepared by consulting firm CE Delft.16 In it, they developed a model to reduce the current costs of cultured meat production down to a point that would make it economically feasible in full-scale plants by 2030, a model they said is “feasible.”
In attempting to create cultured meat on the scale that would be necessary to feed the world, logistical problems are numerous and, possibly, insurmountable. There are waste products — catabolites — to deal with, as even cultured cells excrete waste that is toxic.
And, the oxygen and nutrients available must be adequately distributed to all the cells — something that’s difficult in a large reactor. Stirring the cells faster or adding more oxygen may help, but this can cause fatal stress to the cells.17
The environmental “benefits” are also on shaky ground when you factor in soy products as well as the use of conventional energy sources. When this is factored in, GFI’s life-cycle analysis found that cultured meat may be worse for the environment than conventionally produced chicken and pork.18,19
Farmer and historian John Lewis-Stempel also points out that the world’s farmers already produce enough food for the global population: “[A]ny discussion of global food policy needs to begin with one plain fact: there is … no actual food shortage. Already, the planet’s farmers produce enough food to cater for the projected 10 billion humans of 2050. The problem is waste and distribution.”20
Yet, the push for the creation of fake protein sources continues. In the foreword to Navdanya International’s report “False Solutions That Endanger Our Health and Damage the Planet,” Vandana Shiva also details how lab-grown foods are catastrophic for human health and the environment, as they are repeating the mistakes already made with industrial agriculture:21
“In response to the crises in our food system, we are witnessing the rise of technological solutions that aim to replace animal products and other food staples with lab-grown alternatives. Artificial food advocates are reiterating the old and failed rhetoric that industrial agriculture is essential to feed the world.
Real, nutrient-rich food is gradually disappearing, while the dominant industrial agricultural model is causing an increase in chronic diseases and exacerbating climate change. The notion that high-tech, “farm free” lab food is a viable solution to the food crisis is simply a continuation of the same mechanistic mindset which has brought us to where we are today — the idea that we are separate from and outside of nature.
Industrial food systems have reduced food to a commodity, to “stuff” that can then be constituted in the lab. In the process, both the planet’s health and our health have been nearly destroyed.”
Signs the Fake Meat Industry Is Stalling
For all of its fanfare, there are signs that the fake meat industry may be failing before it ever gets off the ground. Shares of Beyond Meat, for one example, lost $6 billion since March 2020 due to weak sales growth and has resorted to partnering with PepsiCo to release a plant-based jerky product.
“My analysis is the launch will do very little to increase the company’s fortunes,” writes business development consultant Victor Martino in Just Food.22 He argues that the “plant-based meat revolution” is just a PR stunt, a narrative that’s set to implode:23
“The fact is, despite increased product availability in terms of brand choices and added retail outlets, plant-based meat sales stalled in 2021, recording zero growth, according to recent research from SPINS, data commissioned and released by The Plant-Based Foods Association and The Good Food Institute.
According to the research, the total annual sales of plant-based meat in the US remained stable at $1.4 billion. That’s a continuation of the 1.4% share of total meat category sales.”
Shares of Beyond Meat and Oatly, a plant-based milk substitute, have lost more than half their value in 2022,24 but this isn’t to say that their executives are suffering. Beyond Meat’s former chief growth officer Chuck Muth sold shares valued at more than $62 million from 2019 to 2021, while Biz Stone, a current board member, and Twitter co-founder, has made millions on Beyond Meat stock.25
The fact remains that when private companies control the food supply, they will also ultimately control countries and entire populations. Biotech will eventually push farmers and ranchers out of the equation and will threaten food security and human health. In other words, the work being done in the name of sustainability and saving the planet will give greater control to private corporations while weakening the population.
To save the planet and support your health, skip all the fake meat alternatives and opt for real food that’s being raised the right way instead. When you shop for food, know your farmer and look for regenerative, biodynamic, and/or grass-fed farming methods, which are bringing you truly sustainable food for a healthy population and planet.
In light of the Tulsa medical center shooting this week, a lot of attention is being placed on violence in hospitals. Any act of mass violence against innocent people is abhorrent, yet we must not forget the systematic, daily medical violence committed against patients by doctors and surgeons in America and around the world.
republished below in full unedited for informational, educational & research purposes:
(Natural News) In light of the Tulsa medical center shooting this week, a lot of attention is being placed on violence in hospitals. Any act of mass violence against innocent people is abhorrent, yet we must not forget the systematic, daily medical violence committed against patients by doctors and surgeons in America and around the world.
For the record, there are many surgeons and doctors who are wonderful people and who save lives rather than end them. ER doctors, for example, save many lives each day. Trauma surgeons bring people back from the brink of death following industrial accidents, car wrecks, accidents, and other causes. Not all doctors and surgeons are bad people. But a surprising number of them truly are.
Doctors and surgeons carry out medical violence against innocent patients every day in America and around the world:
Some surgeons mutilate children for profit as part of “transgenderism” surgeries that cause permanent disfiguration.
Nearly all doctors kill patients with deadly vaccines, violating their Hippocratic Oath to “first do no harm.” They don’t even do basic research on vaccine safety or vaccine ingredients. They blindly inject countless patients and condemn many of them to die.
Most practicing doctors obediently withheld life-saving treatments from covid patients when ordered to do so by “authorities” such as HHS and the CDC. They withheld ivermectin, hydroxychloroquine, and other beneficial therapeutics that could have saved lives. Withholding life-saving treatments is a form of medical violence.
Many doctors in America took part in the ventilator homicide of covid patients, often combining ventilator suffocation with remdesivir damage (to kidneys and lungs), resulting in unnecessary fatalities. Even when warned to stop these failed practices, they continued to carry them out and needlessly killed countless victims.
All sorts of doctors routinely take part in the mass murder of human babies as they’re being born via abortion procedures that end a human life and silence a beating human heart. This is all celebrated by the political Left, who openly advocate the murder of human babies and the grooming of young children who
aren’t murdered via abortion.
Nearly all doctors prescribe deadly medications to children, teens, and adults, killing 100,000+ Americans each year from FDA-approved medications such as statin drugs, blood pressure drugs, and even psychiatric medications that lead to acts of violence and suicide.
Some surgeons in America, China, and other nations openly engage in harvesting organs from living patients because the organ transplant business is so lucrative. Just this week, a Wall Street Journal article revealed that the Journal of Transplantation has documented hundreds of cases of Chinese surgeons harvesting organs from living patients (i.e. those not yet declared dead). Worse yet, surgeons extracted the beating heart of living patients as part of their organ harvesting operations. As the WSJ writes, “…[R]ather than wait until the judicial authorities had executed the prisoner, the doctors carried out the execution themselves—by heart extraction.”
This means that in many cases, surgeons are murderers. They are the executioners. This is beyond medical malpractice… this is medical murder.
Organ harvesting, blood farming, and child trafficking in America
Author Scott Carney has documented just a few of the horrors of the U.S. medical system in his book, “The Red Market: On the Trail of the World’s Organ Brokers, Bone Thieves, Blood Farmers, and Child Traffickers.” That book, available on Amazon.com, is described as follows:
Award-winning investigative journalist and contributing Wired editor Scott Carney
leads readers on a breathtaking journey through the macabre underworld of the global body bazaar, where organs, bones, and even live people are bought and sold on The Red Market. As gripping as CSI and as eye-opening as Mary Roach’s Stiff, Carney’s The Red Market sheds a blazing new light on the disturbing, billion-dollar business of trading in human body parts, bodies, and child trafficking, raising issues and exposing corruptions almost too bizarre and shocking to imagine.
I have also interviewed Mitchell Nicholas Gerber, who documents communist China’s organ harvesting operations targeting the Falun Gong. This interview reveals yet more crimes against humanity carried out by surgeons and doctors:
In my Situation Update podcast today, I go into far more detail about violence in hospitals, mass shootings, medical murder, hospital homicide, transgender mutilations, organ harvesting, and more. It’s a messy, ugly topic but somebody needs to expose the truth:
Isn’t it amazing how the anti-gun Left goes totally insane over one shooting in a hospital that kills 4 people, but they completely ignore 1,000 abortions a day and over a million Americans now killed by covid vaccines? Yes, there is violence in hospitals, and nearly all that violence is committed by doctors themselves.
republished below in full unedited for informational, educational & research purposes:
(Natural News) A Canadian researcher and ER doctor recently put the Pfizer and Moderna covid-19 vaccines under the microscope to see what they are made of. The electron microscope images show no sign of biological material, not DNA nor the glorified mRNA that the experimental injection was supposed to deliver.
Lead researcher, Dr. Daniel Nagase is a former ER doctor who was persecuted for using ivermectin to treat covid-19 patients in Canada. On involuntary leave since 2021, Dr. Nagase has been traveling through Alberta and British Columbia to educate others on the treatment options for covid-19.
Canadian researcher claims to find non-biological aluminum and carbon nano-particles in Moderna vaccines
When the contents of the vaccine were put under an electron microscope, Dr. Nagase was able to identify basic elements like carbon and oxygen. “You would expect to see carbon, oxygen, nitrogen, and phosphorus – all the things you would normally see in a protein,” Nagase said. However, none of the samples contained nitrogen or phosphorous, not in the X-ray spectroscopy or the electron microscope images.
“X-ray spectroscopy didn’t detect any nitrogen or phosphorus. So, if those complex shapes – that rectangle with all the dots arranged in a grid – were the result of some kind of biological process … then there should be nitrogen and phosphorus there in addition to carbon and oxygen. Because every living thing, whether it’s a virus, plant, or animal, is made up of proteins that contain nitrogen, carbon, oxygen, and phosphorus,” he said.
Dr. Nagase found some very interesting shapes inside the contents of the so-called vaccines. One of the non-biological life forms (in the Moderna vaccine) contained neurotoxic aluminum and looked like a “ball with the legs growing out of it.” The object was not a biological contaminant because it did not contain nitrogen or phosphorous. “So, this thing that’s growing is non-biological,” Nagase concluded.
He found no mRNA in the samples, either. The mRNA is the principal ingredient of the vaccine that is intended to interfere with the biological process of protein transcription in human cells. The mRNA is the vehicle by which toxic, lab-made spike proteins are encoded. According to this discovery, it’s safe to say that not all covid-19 vaccine lots are the same, and some may have no mRNA at all because it degrades easily and may not be preserved properly. Nagase cautioned that there is no way of ensuring that this vaccine lot was properly refrigerated to preserve the mRNA.
Pfizer vaccine appears to contain rare-Earth metal, thulium
The Pfizer sample contained an unusual fiber-like structure that contained a rare-Earth element called thulium, says the researcher. Thulium is one of the highly-reactive elements in the lanthanides series of the periodic table. This rare metal is easy to work with and is used as a source of radiation in portable X-ray devices. Under the electron microscope, these thulium samples were found in various polymorphic forms, including crystals, chips, strands, bulbs, spheres, fibers, and balls with legs growing out of them.
Polish biologist Dr. Franc Zalewksi previously discovered these one-headed, three-legged objects in 2021. He found bromine, carbon, and aluminum in the peculiar structures, and he named them “nano-octopus.” Pathologists have also found unknown objects in the blood of vaccinated Germans.
“I don’t even know if this carbon technology is in every batch or is it just in the batches they sent to Canada?” Dr. Nagase questioned. “Is Canada one half of an experiment and certain States in the US are getting a slightly different batch without the carbon nanotech?” As post-vaccine deaths pile up, more doctors are asking questions.
Informed consent has been vanquished from medicine over the past three years, so Dr. Nagase asks, “Are countries around the world being given different injections, and we’re being observed to see, ‘well, who dies the fastest, who gets the sickest or what kind of illnesses result’ from experimental ingredients being indiscriminately and without disclosure being given to people?”
republished below in full unedited for informational, educational & research purposes:
(Natural News) It is undeniable, based on mounting evidence, that the new monkeypox scare is another contrived “outbreak” that has been deployed for the purpose of committing “domestic terror” against the public – which should know better by now that we are once again being scammed and terrorized.
Appearing on the “Man in America” program, Dr. David Martin told his host that the modus operandi behind this operation is nothing new. The world got a heavy dose of it all throughout the Wuhan coronavirus (Covid-19), for which monkeypox appears to be round two.
“When you want to terrorize a population, what do you do? Turn to the experts!” Martin explained.
It turns out that monkeypox was planned, just like covid was, to be released at just this point on the timeline. And many of the same players who profited from covid are once again slated to rake in the cash from monkeypox.
“I love to point out (that) a lot of people have been really upset about this monkeypox scheduled release on May of 2022 coming from a March 21 publication,” Martin added.
“And people sit there and go, ‘oh my gosh – how on earth could they have ever been so prescient to find out that they were going to have a monkeypox release three days away from the stated date for the alleged outbreak to occur?'”
A full 15 months before now back in March of 2021, the global architects had scheduled a later monkeypox release that landed right on schedule “plus or minus three days,” Martin notes.
“Listen, this is a willful continuation of a campaign of domestic terror, and it is done to make sure the public remains in fear and in cognitive dissonance and in the disbelief of what Plato described in The Republic,” he says.
“You know Plato in The Republic made reference to the fact that sometimes crimes are so audacious that the mere statement of their audacity paralyzes the population.”
We the People must say NO to another round of plandemic tyranny
Millions of people already have covid burnout and are unlikely to be fearful about monkeypox, recognizing that many of the same tactics are being used to spread fear and paranoia about testing “positive” for it.
On the other hand, millions of other people also bought all in to the covid plandemic and still believe that there is some invisible threat out there just waiting to kill them and their grandmas – hence why some people are still wearing a face mask while out in public.
Which side wins out in the next wave of health wars remains to be seen. Hopefully, there are enough people wide awake to what is really going on that another scheduled plandemic fails to gain traction.
The government and the media can fearmonger all they want about monkeypox, but their power ends where and when the public refuses to listen to or comply with any of it.
We the People hold far more power than we realize, after all. All it takes is for a few good men and women to take a stand against these attempted crimes against humanity, inspiring others to do the same until a snowball of resistance is formed.
“We can be glad that the CCP-Davos axis chose the comparatively benign monkey-pox over Marburg, smallpox, and bird flu, for their next global pandemic hoax, justifying world depopulation through starvation and lethal injections,” commented someone at Natural News about the situation.
“I have read that shingles is a known adverse effect of the jab,” wrote another. “I searched for images on the net. Shingles and monkeypox look the same. How do doctors identify one from the other?”
republished below in full unedited for informational, educational & research purposes:
Just as hysteria about COVID-19 is winding down, another “pandemic” is poised to take its place. This time, it’s monkeypox, a typically mild infection that often resolves in three to four weeks without treatment
The first European case of monkeypox was confirmed on May 7, 2022, in the U.K. Then, seemingly overnight, cases were being reported across the world. On May 20, 2022, the World Health Organization held an emergency meeting to discuss reports of more than 100 suspected or confirmed cases in at least nine countries
A tabletop simulation exercise of a monkeypox outbreak took place in March 2021, and in this fictional scenario, the first European case of monkeypox was also identified on May 7, 2022
The first case in the U.S. was reported on May 18, 2022. By May 23, suspected monkeypox cases were reported in three additional states: New York, Florida, and Utah
President Joe Biden has stated that strict quarantine protocols are not likely to be implemented in the U.S. He has, however, already placed a $119 million order for a monkeypox vaccine. Belgium, meanwhile, has introduced a 21-day quarantine for anyone who tests positive, and the U.K. is urging anyone who has had direct contact with a confirmed case to voluntarily isolate for 21 days
As predicted, just as hysteria about COVID-19 is winding down, another “pandemic” is poised to take its place. This time, it’s monkeypox, an infection that just so happens to mimic many of the symptoms of COVID jab-induced shingles — so much so, the Department of Health in Queensland, Australia, used the same photo to illustrate both infections (the photos have since been removed or updated1).
The first European case of monkeypox was confirmed on May 7, 2022, in the U.K.2 Then, seemingly overnight, cases were being reported across the world.3 May 20, 2022, the World Health Organization held an emergency meeting to discuss reports of more than 100 suspected or confirmed cases in at least nine countries, including Belgium, France, Germany, Italy, the Netherlands, Portugal, Spain, Sweden, the U.K., the U.S., Canada and Australia.4
By the time this article goes to print, the number of countries affected and the caseload totals are likely going to be significantly higher. The first case in the U.S. was reported on May 18, 2022.5
By May 23, suspected monkeypox cases were reported in three additional states: New York, Florida, and Utah.6 All of the patients were said to be in good condition and state health departments were in agreement that the cases posed no serious risk to the public.
President Joe Biden has stated that strict quarantine protocols are not likely to be implemented in the U.S. He has, however, already placed a $119 million order for a monkeypox vaccine.7,8
Belgium, meanwhile, has introduced a 21-day quarantine for anyone who tests positive, and the U.K. is urging anyone who has had direct contact with a confirmed case to voluntarily isolate for 21 days.9
As noted by Jimmy Dore in the video above, the worldwide monkeypox outbreak seems perfectly timed to pressure countries to relinquish health care authority to the WHO.
The World Health Assembly was voting on amendments to the International Health Regulations (IHR)10 as the first cases were being identified. I discussed the implications of these amendments in a recent article. As noted by Dore, a pandemic rehearsal conducted just last year also featured monkeypox specifically. I’ll review that further below.
What Is Monkeypox?
Monkeypox, a relative of the smallpox virus, is a typically mild viral illness, characterized by fever, headache, muscle aches, exhaustion, swollen lymph nodes, and a bumpy rash that tends to start on the face before spreading to other parts of the body.
The pus-filled lesions are known as “pox.” The lesions eventually scab over and fall off after three to four weeks. The infection is not readily transmissible, as it requires direct contact with bodily fluids.
While there’s no known effective treatment, most patients recover without any treatment whatsoever. Historically, the infection has primarily plagued the African continent, where a few thousand cases are reported each year. However, many of the current cases are not linked to travel, making the outbreak in so many different areas a rare oddity. As noted by Nature magazine:11
“On 19 May, researchers in Portugal uploaded the first draft genome12 of the monkeypox virus that was detected there, but Gustavo Palacios, a virologist at the Icahn School of Medicine at Mount Sinai in New York City, emphasizes that it’s still a very early draft, and more work needs to be done before any definitive conclusions can be drawn.
What researchers can tell from this preliminary genetic data is that the strain of the monkeypox virus found in Portugal is related to a viral strain predominantly found in West Africa. This strain causes milder disease and has a lower death rate — about 1% in poor rural populations — compared with the one that circulates in Central Africa.
But exactly how much the strain causing the current outbreaks differs from the one in West Africa — and whether the cases popping up in various countries are linked to one another — remains unknown.”
Outbreaks Blamed on Gay Sex
Several of the Spanish cases were linked to a “superspreader event at an adult sauna” in Madrid, at least three Belgian cases were linked to a gay fetish festival in Antwerp,13 and cases in Italy and Tenerife have been linked to a gay pride festival on the Canary Islands.14 Health officials also claim a “notable proportion” of British cases are in the gay and bisexual community.15,16
Is the singling out of gays another ploy in the totalitarian takeover plan? Totalitarian regimes always need an enemy onto which the fear and irrational aggression of the hypnotized masses can be directed, and since the hatred against those refusing the COVID jab has significantly abated, they clearly need a new scapegoat.
It would not surprise me if, after two years of promoting the gay and trans community, the far Left will now begin to incite anger and fear against it. Why? Because it causes confusion and uncertainty. People who once showed allegiance to this group will now be splintered against them. At the end of the day, it’s all about psychological splintering and pitting various groups against each other.
Making the monkeypox outbreaks all the more suspicious is the fact that a tabletop simulation exercise of a monkeypox outbreak took place in March 2021,18 and the start date of this fictional scenario was mid-May 2022. Coincidence?
In the video above, AmazingPolly reviews the details of this simulation. She also reminds us how Event 201 ended up “predicting” the COVID pandemic to a tee and shows how we’re now seeing a replay of “coincidences” between the monkeypox simulation and real-world events.
The monkeypox exercise was held by the Nuclear Threat Initiative (NTI), which is funded by Bill Gates. NTI was founded to assess and reduce threats associated with the proliferation of nuclear weapons,19 but they’ve since expanded to include biological threats.20 Gates has not only funded NTI pandemic simulations but has also given grants to the NTI for vaccine development in relation to biological threats.21
The final report22,23 from this event was funded by the Open Philanthropy Project, which in turn is funded by Facebook co-founder Dustin Moscowitz. As reported by The Defender:24
“This ‘fictional exercise scenario’ involved the simulation of ‘a deadly, global pandemic involving an unusual strain of monkeypox virus that first emerged in the fictional nation of Brinia and spread globally over 18 months’ ...
The outcome of this ‘exercise scenario’ found the fictional pandemic, ‘caused by a terrorist attack using a pathogen engineered in a laboratory with inadequate biosafety and biosecurity provisions and weak oversight,’ led to ‘more than three billion cases and 270 million fatalities worldwide.’
The fictional start date of the monkeypox pandemic in this exercise was May 15, 2022. The first European case of monkeypox was identified on May 7, 2022.”
As mentioned, the first European case of monkeypox was in fact confirmed on May 7, 2022, in the U.K.25 Not only is the date identical to that in this supposedly fictional scenario, but the country of emergence, “Brinia,” even sounds very much like “Britannica,” or “Great Britain.” Coincidence?
Key Recommendations From the Pandemic Exercise
As reported by The Defender, among the key recommendations from this monkeypox simulation were recommendations that clearly support the WHO’s takeover of pandemic preparedness and response, and the implementation of Gates’ "Global Epidemic Response & Mobilization" (GERM26) Team:27
Bolstering international systems “for pandemic risk assessment, warning, and investigating outbreak origins,” calling upon the WHO to “establish a graded, transparent, international public health alert system” and the United Nations system to “establish a new mechanism for investigating high-consequence biological events of unknown origin.”
The development and implementation of “national-level triggers for an early, proactive pandemic response,” including the adaptation of the “no-regrets” approach to responding to pandemics via “anticipatory action” based on “triggers” that would automatically generate a response to “high-consequence biological events.”
The establishment of “an international entity dedicated to reducing emerging biological risks associated with rapid technological advances,” that would “support interventions throughout the bioscience and biotechnology research and development life cycle — from funding, through execution, and on to publication or commercialization.”
Anticipatory action based on triggers includes everything we’ve seen during the COVID pandemic, such as mask mandates, the banning of mass gatherings, travel health screening, and vaccine passports. This despite overwhelming evidence showing these strategies are ineffective at best, while being devastating to public health and economies.
Why Does Fiction so Often Turn Into Reality?
As noted by The Defender,28 Michael P. Sanger29 and Tim Hinchliffe,30 among others, fictional tabletop exercises have had an uncanny ability to predict details of near-future events. Event 201 accurately “predicted” the COVID pandemic and its focus on censorship and lockdowns.
In June 2001, Operation Dark Winter examined “the national security, intergovernmental, and information challenges of a biological attack on the American homeland,” and less than three months later, the 9/11 attacks and subsequent anthrax scare occurred. In January 2005, Operation Atlantic Storm involved the fictional scenario of a transatlantic bioterrorist attack, and that same month we had the bird flu pandemic. The Defender continues:31
“Predictions for the future don’t end there, however. For instance, in September 2017, NTI and the WEF organized a roundtable discussion on the current state of biological risks presented by technology advancement in light of the Fourth Industrial Revolution.
And in January 2020, NTI and the WEF again joined forces, issuing a report titled ‘Biosecurity Innovation and Risk Reduction: A Global Framework for Accessible, Safe and Secure DNA Synthesis.’ According to the report:
‘Rapid advancements in commercially available DNA synthesis technologies — used for example to artificially create gene sequences for clinical diagnosis and treatment — pose growing risks, with the potential to cause a catastrophic biological security threat if accidentally or deliberately misused.’
Merck, whose head of corporate affairs participated in the monkeypox simulation, was the subject of an FBI and CDC investigation in November 2021 regarding 15 suspicious vials labeled “smallpox” at a Merck facility in Philadelphia.”
In a National Pulse exclusive,32 Natalie Winters also summarizes research by the Wuhan Institute of Virology (WIV), in which they “assembled monkeypox strains using methods flagged for creating ‘contagious pathogens.’”
“Are we here because of China’s experiments again?” she asks, referring to the apparent monkeypox outbreaks. The research paper33 in question was published at the end of February 2022, just a few months before the first cases suddenly appeared outside of Africa.
What Do We Know About the Monkeypox Vaccine?
The monkeypox vaccine currently being stockpiled by the U.S. and Europe is not specific to the monkeypox. It’s actually a smallpox vaccine, claimed to be 85% effective at stopping monkeypox. In the U.K., close contacts of those infected with monkeypox have reportedly already been given the smallpox vaccine — a strategy known as “ring vaccination.”34 In the U.S., there are currently two smallpox vaccines available:
• ACAM2000 was approved by the U.S. Food and Drug Administration in 2007 and has primarily been restricted to use in military personnel due to its safety risks, which include infection with the vaccine strain, vaccine shedding, and death.
Package insert warnings include myocarditis and pericarditis at a rate of 5.7 per 1,000 vaccinated, encephalitis, severe skin infection, blindness, fetal death, and more. Household contacts face the same risks as the vaccinated individual due to shedding.
• Jynneos (known as Imvamune in Canada or Imvanex in Europe35) was approved by the FDA in 2019. It’s an attenuated live vaccine, indicated for the prevention of smallpox and monkeypox in adults aged 18 and older, and those who cannot be vaccinated with ACAM2000 due to contraindications such as atopic dermatitis, immunocompromising conditions, breastfeeding, or pregnancy. It’s the only FDA-approved monkeypox vaccine for non-military use.
The U.S. Biomedical Advanced Research and Development Authority (BARDA) has also signed a contract with Bavarian Nordic for a freeze-dried version of the Jynneos smallpox vaccine, which will give it a longer shelf-life.36 Moderna already has a monkeypox vaccine in pre-clinical trials.37 It’s unclear when those trials began.
As noted by independent journalist Whitney Webb, Emergent BioSolutions and SIGA Technologies — both of which have been struggling recently — will be cashing in on the monkeypox scare:38
“Regardless of how the monkeypox situation plays out, two companies are already cashing in. As concern over monkeypox has risen, so too have the shares of Emergent BioSolutions and SIGA Technologies.
Both companies essentially have monopolies in the U.S. market, and other markets as well, on smallpox vaccines and treatments. Their main smallpox-focused products are, conveniently, also used to protect against or treat monkeypox as well. As a result, the shares of Emergent BioSolutions climbed 12% on Thursday, while those of SIGA soared 17.1%.
For these companies, the monkeypox fears are a godsend, specifically for SIGA, which produces a smallpox treatment, known by its brand name TPOXX. It is SIGA’s only product.
While some outlets have noted that the rise in the valuation of SIGA Technologies has coincided with recent concerns about monkeypox, essentially no attention has been given to the fact that the company is apparently the only piece of a powerful billionaire’s empire that isn’t currently crumbling.
That billionaire, ‘corporate raider’ Ron Perelman, has deep and controversial ties to the Clinton family and the Democratic party as well as troubling ties to Jeffery Epstein. Aside from his controlling stake in SIGA, Perelman has recently made headlines for rapidly liquidating many of his assets in a desperate bid for cash.
Similarly, Emergent BioSolutions has also been in hot water. The company, which has troubling ties to the 2001 Anthrax attacks, came under fire just under two weeks ago for engaging in a ‘cover-up’ over quality control issues relating to their production of COVID-19 vaccines.
A Congressional investigation found that quality control concerns at an Emergent-run facility led to more than 400 million doses of COVID-19 vaccines being discarded.
The Emergent factory in question had been shut down by the U.S. Food and Drug Administration (FDA) in April 2021. They were allowed to reopen last August before the government terminated the contract.”
What’s the Truth of the Matter?
In addition to Webb’s article above, which dissects the sordid histories of Emergent and SIGA, another early analysis of the new monkeypox scare that is well worth reading is Dr. Robert Malone’s Substack article,39 “Monkey Pox — Truth Versus Fearporn.” In it, he reviews what monkeypox actually is, where it came from, how it’s related to smallpox, its signs and symptoms, how disease spread is effectively controlled, and much more.
Key take-homes are that monkeypox is not a particularly deadly disease and one that can be readily controlled without reverting back to COVID restrictions. To quote Malone:40
“So, is the biothreat real? Is it imminent? Does it justify the global media hype? As I was waiting in an airport lounge to travel from USA to the UK two days ago, I saw a newsreel from CNN which was breathlessly reporting on this ‘threat’ while displaying historic images of patients suffering from Smallpox disease.
This provides a classical example of public health fearporn, in my opinion, and CNN should be reprimanded for broadcasting irresponsible propaganda — misinformation and disinformation — under the guise of journalism.
In my opinion, based on currently available information, Monkeypox is a virus and disease which is endemic in Africa, emerges sporadically after transmission into humans from animal hosts, and is typically spread by close human contact. It is readily controlled by classical public health measures.
It does not have a high mortality rate. Unless there has been some genetic alteration, either through evolution or intentional genetic manipulation, it is not a significant biothreat, and has never been considered a high threat pathogen in the past. So, stop the fear mongering, misinformation and disinformation.”
The way it looks right now, it appears the monkeypox outbreaks are intended to rile the public into another fear-fueled frenzy in order to justify the WHO’s takeover of public health globally, usher in those reviled health passports, and everything else that goes along with The Great Reset. As noted by Hinchliffe in a 2020 Sociable article:41
“If you are World Economic Forum (WEF) Founder Klaus Schwab, you attempt to sell your vision of a global Utopia via a great reset of the world order in three simple steps:
1. Announce your intention to revamp every aspect of society with global governance, and keep repeating that message
2. When your message isn’t getting through, simulate fake pandemic scenarios that show why the world needs a great reset
3. If the fake pandemic scenarios aren’t persuasive enough, wait a couple of months for a real global crisis to occur, and repeat step one ...
The so-called ‘great reset’ promises to build ‘a more secure, more equal, and more stable world’ if everyone on the planet agrees to ‘act jointly and swiftly to revamp all aspects of our societies and economies, from education to social contracts and working conditions.’
But it wouldn’t have been possible to contemplate materializing such an all-encompassing plan for a new world order without a global crisis, be it manufactured or of unfortunate happenstance, that shocked society to its core.”
COVID simply didn’t take the globalist cabal far enough. So, here comes global pandemic No. 2 — be it real or mostly fabricated — which will be rapidly followed by renewed calls for a New World Order and a Great Reset. Essentially, we can expect a repeat of the insanity we just lived through, which means we must also repeat our response, and reject the fearmongering and the global power grab.
NextNewsNetwork.com reports, During a fundraiser for Scott Kaspar, a candidate for Illinois’ 6th congressional district, Former Trump attorney and New York Mayor, Rudy Giuliani got up and spoke and ripped into Hunter Biden and the Democrats during his 30-minute speech.
Just like Bill Gates’ Event 201 pandemic simulation exercise announced the novel coronavirus just months before it appeared, this simulation exercise in Munich predictively programmed monkeypox a few months before it started appearing in the media.
Attendees at the conference were told that by May 15, 2022, monkeypox would appear out of nowhere and begin spreading. At first, the fallout would be minimal, but by January 10, 2023, the death toll is scheduled to reach 1.3 million people. And by the end of 2023, hundreds of millions of people will be dead from monkeypox.
By the end of 2022, it is to be revealed that the unusual monkeypox strain in circulation is resistant to all vaccines. This is to add more fear and paranoia surrounding the virus, allowing “national responses” that likely include even more medical tyranny than what was seen throughout the covid plandemic.
The supply chain will continue to degrade throughout this time, only to culminate in mass chaos and destruction that will be blamed on a “terror group,” the simulation revealed. “Infiltration of a civilian bio lab” will be dubbed the cause of the new global monkeypox plandemic.
“Monkeypox was first identified in 1958, but there’s never been a global Monkeypox outbreak outside of Africa until now – in the exact week of the exact month predicted by the biosecurity folks in their pandemic simulation,” writes Michael P. Senger on his Substack blog. “Take these guys to Vegas!”
American government just ordered 13 million monkeypox “vaccines” from Bavarian Nordic
Corporate media fearmongers like The Atlantic‘s Ed Yong, who previously wrote numerous hysterical pieces about covid, is already drumming up a fresh firestorm of fear over monkeypox. His latest exposé claims that monkeypox is especially scary because it is being unleashed “in the third year of a pandemic,” referring of course to covid.
Dr. Eric Feigl-Ding, a Ph.D. at the Soros Fellowship for New Americans, is also spreading fear all over Twitter about how monkeypox is supposedly spreading across the United States and Canada.
“Twitter epidemiologists Jennifer Nuzzo and Bill Hanage are on the scene – but still no word from them as to whether they see anything strange about the first-ever global Monkeypox outbreak occurring in mid-May 2022, a year after they acted as advisers on an international biosecurity simulation of a global Monkeypox outbreak occurring in mid-May 2022,” Senger further writes with joking wit.
The World Health Organization (WHO), which just so happens to be convening this week to demand that all member nations, including the United States, hand over their sovereignty and allow the United Nations arm to make everyone’s medical decisions from here on out, also convened an “emergency meeting” to deal with this new “crisis.”
And the United States, of course, is hot on the scene as well with a new Big Pharma partnership that will bring 13 million monkeypox “vaccines” into the country from manufacturer Bavarian Nordic.
“The global Monkeypox outbreak – occurring on the exact timeline predicted by a biosecurity simulation of a global Monkeypox outbreak a year prior – bears a striking resemblance to the outbreak of COVID-19 just months after Event 201, a simulation of a coronavirus pandemic almost exactly like COVID-19,” Senger writes.
“Event 201 was hosted in October 2019 – just two months before the coronavirus was first revealed in Wuhan – by the Gates Foundation, the World Economic Forum, Bloomberg, and Johns Hopkins. As with Event 201, the participants at the Monkeypox simulation have thus far been stone silent as to their having participated
in a pandemic simulation the facts of which happened to come true in real life just months later.”
More news coverage about monkeypox can be found at Outbreak.news.
republished below in full unedited for informational, educational & research purposes:
The Wuhan Institute of Virology used a method research flagged for potentially creating a “contagious pathogen” to assemble a monkeypox virus genome that allowed the virus to be identified through PCR tests. This research came mere months before the current outbreak of monkeypox that has global health authorities raising alarm.
The monkeypox study in question was first published in February of 2022. Authored by nine Wuhan Institute of Virology researchers and published in the lab’s quarterly scientific journal Virologica Sinica, the paper follows the wide-scale use of Polymerase Chain Reaction (PCR) tests to identify Covid-19-positive individuals.
The study showed that researchers appeared to identify a portion of the monkeypox genome, which enabled PCR tests to identify the virus.
The paper is titled “Efficient Assembly of a Large Fragment of Monkeypox Virus Genome as a qPCR Template Using Dual-Selection Based Transformation-Associated Recombination.”
Within its pages, monkeypox viruses, referred to as “MPXVs,” are described as having strains that are “more pathogenic and [have] been reported to infect humans in various parts of the world.”
“Quantitative polymerase chain reaction (qPCR) is the gold standard for the detection of orthopoxvirus (including MPXV). For pan-orthopoxviruses detection, the E9L (DNA polymerase) gene has been shown to be an excellent target for qPCR assays. For MPXV detection, Li et al. reported that the C3L (complement-binding protein) gene could be used as the qPCR target for the MPXV Congo Basin strain,” explained the paper, before noting that China lacked sufficient genetic information on the virus for PCR detection.
“Since MPXV infection has never been associated with an outbreak in China, the viral genomic material required for qPCR detection is unavailable,” the study adds. “In this report, we employed dual-selective TAR to assemble a 55-kb MPXV genomic fragment that encompasses E9L and C3L, two valuable qPCR targets for detecting MPXV or other orthopoxviruses.”
“The primary purpose of assembling a fragment of the MPXV genome is to provide a nucleotide template for MPXV detection,” the study noted.
“As an efficient tool for assembling large DNA fragments up to 592 kb in length, TAR assembly has become essential for preparing infectious clones of large DNA/RNA viruses,” they explain.
The paper acknowledged that TAR “applied in virological research could also raise potential security concerns, especially when the assembled product contains a full set of genetic material that can be recovered into a contagious pathogen.”
“In this study, although a full-length viral genome would be the ideal reference template for detecting MPXV by qPCR, we only sought to assemble a 55-kb viral fragment, less than one-third of the MPXV genome. This assembly product is fail-safe by virtually eliminating any risk of recovering into an infectious virus while providing multiple qPCR targets for detecting MPXV or other Orthopoxviruses,” the researchers wrote.
Notably, the Wuhan Institute of Virology performed similar research into strains of bat coronaviruses that could infect humans. This took place prior to the outbreak of the Covid-19 pandemic.
Similarly, the unearthed study reveals that the Wuhan Institute had likewise been working with monkeypox not long before the outbreak that has health authorities and governments alarmed at the possibility of another pandemic.
The Biden White House last week ordered 13 million doses of the monkeypox vaccine after a Massachusetts man contracted the disease.
The U.S. Biomedical Advanced Research and Development Authority (BARDA), a daughter-agency of the U.S. Department of Health and Human Services (HHS), spent $119 million on the acquisition of the vaccine for the monkeypox virus from the Denmark-based biotechnology company Bavarian Nordic A/S. The federal government has an additional $180 million in options if it chooses to exercise them.
It recently came to light that James LeDuc, an Anthony Fauci-funded lab director, gave a heads-up to Wuhan Institute of Virology researchers ahead of a potential U.S. investigation into the lab for its involvement in the Covid-19 outbreak.
As seen in new emails obtained via a Freedom of Information Act (FOIA) request filed by Judicial Watch, there was a close relationship between the Wuhan lab and LeDuc, who heads the Galveston National Laboratory — which describes itself as “constructed under grants awarded by [Fauci’s] National Institute of Allergy and Infectious Diseases (NIAID).”
republished below in full unedited for informational, educational & research purposes:
(Natural News) Most people do not believe that their government, especially the US government, is interested in drastically reducing the population of their country or nation using insidious methodologies, including medical “interventions.” Why in the world would the government want fewer people to be healthy, and more people dying, and what goals would be accomplished in that process?
Most consumers live their shortened lives in the dark because they don’t understand what’s happening to them, how, or why. Nearly everything from medicine to vaccines, from food to personal care products, and from cleaning products to food packaging, is manufactured with toxins that lead to chronic, expensive health issues, diseases, and disorders.
Nicotine is like a deadly undertow, dragging its victims into deep water as they slowly ‘drown’ in an oxygen-and-nutrient-deprived existence
We start this off with nicotine, the world’s third-most addictive drug, used by every sixth person in the world, daily. Most people begin using nicotine in their early teen years (25 percent of teens try it), thinking it’s cool and they can quit whenever they want to, only to find out they can’t. Big Tobacco and the US government (think regulatory agencies) have colluded and conspired to get as many people addicted to nicotine as possible, dating all the way back to the 1930s.
Doctors literally recommended their favorite brand of cancer sticks for good digestion, good health, and great flavor! Doctors even recommended cigarettes for pregnant women, even though the science had already proven the smoke caused lung cancer. This went on until the 1960s when the public caught wind of the science and the FDA and CDC had to start pretending to help people quit.
Nicotine use constricts blood vessels, limiting oxygen and nutrient supply to vital organs, including the brain, liver, pancreas, lungs, and kidneys. Nearly all nicotine users shorten their lifespan by at least a decade if they don’t quit before age fifty,
including people who smoke, vape, dip, or chew.
If you shop “in the dark,” the odds are your life will be shortened by several decades and your journey to that end may be very miserable
Did you know that “shopping in the dark” includes going to the medical doctors and hospitals and taking any medications and vaccines they recommend? Without doing your own research, consulting nutritionists or naturopath physicians, you’ll never find out what most prescription medications and vaccinations do to the human systems that cause MORE disease and disorder than you initially were having addressed.
People who take prescription medications become and remain the sickest people on the planet. Some overdose on those meds, even when taken as directed, as we’ve all witnessed with the opioid epidemic. The same goes for blood thinners (rat poison), deadly statin drugs, and other cholesterol medications that feature side effects that are worse than the condition being treated.
Toxic food packaging, inside and out, is a leading cause of disease and disorder in America
Wait, you thought cancer, diabetes, and heart disease are mainly genetic problems with no cure or possible prevention, didn’t you? Have you been listening to those drug dealers (MDs) and disease spreaders (Centers for Disease Continuation – CDC) again? Most processed foods are packaged in plastic, paper, cardboard, bags, wrappers, and cans using additives and preservatives that cause disease and disorder, and also packaging that leaches toxins into the food.
Dangerous PFAS (per-and-poly-fluoroalkyl substances), also known as “forever chemicals,” are in many food packages manufactured by large corporations who are more concerned about prolonging the “shelf life” of the food, all while compromising and shortening the life expectancy of the consumers of those food products. These chronic, serious health issues include immune system suppression and increased risk for cancers.
Many foods are bleached white to look “clean,” even though the food manufacturers know good and well that bleach causes cancer of the pancreas, bladder, and prostate. Most white foods are bleached, including fish, rice, pasta, flour, bread, and sugar. Even tap water contains deadly fluoride that leaches calcium from the bone marrow and leads to bone cancer and dementia.
Now the COVID-19 vaccines are designed using nano-parasites to deliver (J&J) or create (mRNA) billions of toxic spike proteins that travel THROUGHOUT the entire vascular system, polluting your cleansing organs, the brain, and the heart, while causing deadly blood clots, myocarditis, nervous system disorders, and severe allergies. They haven’t even been proven to help fight Wuhan Coronavirus at all, so why even risk getting them? Get smart, and do lots of research before engaging deadly “delivery devices” that insert toxins into the human body.
Top 10 delivery devices used for population reduction and genocide
#1. Cigarettes, patches, gum, and vape gadgets deliver nicotine and chemicals.
#2. Vaccines deliver spike protein toxins, heavy metal toxins, and genetically modified viruses and bacteria.
#3. Pain pills deliver diluted heroin (opioids).
#4. Genetically modified foods and processed foods deliver GMOs, pesticides, insecticides, and chemical herbicides.
#5. Chemotherapy and radiation treatments spread and create new cancers.
#6. Pharmaceutical prescription medications deliver deadly venoms from snakes, frogs, snails, and other deadly animals.
#7. Water is used to deliver deadly fluoride, lead, and other toxins.
#8. Food packaging and plastics used as hormone (endocrine) disrupters (PFA and
Back in 2018, Bourla appeared at the World Economic Forum (WEF) in Davos where he openly fantasized about feeding people below him on the economic food chain microchip-laced pharmaceutical pills capable of communicating with the government.
Bourla explained that each tablet would contain a “biological chip” for tracking and surveillance purposes. Once consumed, dissolved, and digested, the chip would tell the “authorities” that the drug was taken, ensuring compliance.
“So imagine the applications of that, the compliance,” Bourla said with a maniacal grin. “The insurance companies know that the medicines patients should take, they take them.”
You can watch Bourla giving his 2018 speech in the video below:
Pfizer CEO Albert Bourla explains Pfizer’s new tech to Davos crowd: “ingestible pills” – a pill with a tiny chip that send a wireless signal to relevant authorities when the pharmaceutical has been digested. “Imagine the compliance,” he says pic.twitter.com/uYapKJGDJx
Bourla did not exactly receive positive feedback for these statements from anyone other than his fellow one-percenters. To this, Bourla responded that microchip-laced drugs are for the benefit of humanity, and could be used to treat “specific” conditions such as “schizophrenia and cancers.”
“‘Compliance’ he says – consumers are clearly not his customers; government bodies are,” tweeted someone in response to the video clip.
“And Pfizer is fully aligned with ‘compliance’ because it means more and more sales volume to their government customers.”
Israeli professor wants “total biometric surveillance” of the human herd in order “to monitor what’s happening under their skin”
It turns out that Bourla is hardly the only WEF globalist pushing for biometric tracking and surveillance. Yuval Noah Harari, a professor from The Hebrew University of Jerusalem‘s Department of History had this to say about the topic: “COVID is critical because this is what convinces people to accept and legitimize total biometric surveillance. We need to not just monitor people; we need to monitor what’s happening under their skin.”
A video clip of Harari can be viewed below:
World Economic Forum shill, Yuval Noah Harari:
“Covid is critical because this is what convinces people to accept to legitimize total biometric surveillance. We need to not just monitor people, we need to monitor what’s happening under their skin” pic.twitter.com/qoPKVGxR7d
In other words, the human cattle of the world need to be monitored, tracked, surveilled, and controlled at all times by people like Bourla and Harari who believe that they exist above and beyond everyone else in the world who is not part of their little club.
This is their plan for the future, by the way: to control the human herd with ingestible and injectable tracking chips. It will probably start with the former and morph into the latter once the herd gets used to the idea of technocratic elitists monitoring what’s happening under their skin at all times.
Amazingly, the Hill‘s Kim Iverson, a former disbeliever in “conspiracy theories,” is now convinced that there might just be a secret cabal of evil ones who want to enslave the entire world under a bio-surveillance matrix of total slavery.
“I shall never scoff at so-called conspiracy theorists again,” Iverson tweeted. “I will listen and remain open-minded that perhaps what they’re saying is actually happening.”
In the comment section at Zero Hedge, many stated that they will never, ever comply with such schemes, no matter what the “authorities” demand of them.
“I wouldn’t be surprised if Pfizer first tested its tablet chip in its Ukraine biolabs on the Ukrainian people,” one of them added.
More related news stories about Albert Bourla and others like him can be found at Evil.news.
republished below in full unedited for informational, educational & research purposes:
The World Health Organization is attempting to seize control over global pandemic monitoring and response and, ultimately, all health care decisions
Bill Gates intends to play a key part in this takeover. He’s building a pandemic response team for the WHO, dubbed the "Global Epidemic Response & Mobilization" or GERM Team, which will have the authority to monitor nations and make pandemic response decisions, such as when to suspend civil liberties to prevent the spread of an illness
The globalist cabal plans to seize control through biosecurity governance, and they’re attempting to do this using two different avenues. If we fail to fight off both attacks, we’ll end up under totalitarian governance
The first attack comes in the form of amendments to the International Health Regulations (IHR), which are currently being voted on by the World Health Assembly. These amendments will strip member nations of their sovereignty and give the WHO unprecedented power to restrict your medical freedoms and civil liberties in the name of biosecurity. Get involved and urge your nation’s leaders to reject the amendments if passed. Unless rejected, they will become binding law in November 2022
The second attack comes through a new international pandemic treaty with the WHO. They intend to eliminate individualized medicine and provide blanket rulings for how a given threat is to be addressed, and this can only result in needless suffering — not to mention the loss of individual freedom
In “The Corbett Report” above,1 independent journalist James Corbett reviews the contents of Bill Gates’ book, “How to Prevent the Next Pandemic.”
“It’s every bit as infuriating, nauseating, ridiculous, laughable and risible as you would expect,” he says. “This is a ridiculous book ... There’s certainly nothing of medical or scientific value in here ... It’s a baffling book even from a propagandistic perspective ...
Gates’ goal in writing the book is to disarm the public and prepare us to accept the agenda that Gates and his allies would like to impose on the world. Ultimately, what this is about is drumming up general public support — or at least general public understanding — of the unfolding biosecurity agenda.”
Another reviewer of Gates’ book, economist Jeffrey Tucker, offered similarly negative feedback:2
“Imagine yourself sidled up to a bar. A talkative guy sits down on the stool next to you. He has decided that there is one thing wrong with the world. It can be literally anything. Regardless, he has the solution.
It’s interesting and weird for a few minutes. But you gradually come to realize that he is actually crazy. His main point is wrong and so his solutions are wrong too. But the drinks are good, and he is buying. So you put up with it. In any case, you will forget the whole thing in the morning.
In the morning, however, you realize that he is one of the world’s richest men and he is pulling the strings of many of the world’s most powerful people. Now you are alarmed. In a nutshell, that’s what it’s like to read Bill Gates’s new book ‘How to Prevent the Next Pandemic.’”
Gates’ Book Chapter by Chapter
Corbett goes through Gates’ book chapter by chapter, so if you’re short on time, you can review the ones that interest you the most:
Chapter 1: Learn from COVID (timestamp: 12:58)
Chapter 2: Create a pandemic prevention team (timestamp: 18:23)
Chapter 3: Get better at detecting outbreaks early (timestamp: 26:21)
Chapter 4: Help people protect themselves right away (timestamp: 31:01)
Chapter 5: Find new treatments fast (timestamp: 37:26)
Chapter 6: Get ready to make vaccines (timestamp: 39:46)
Chapter 7: Practice, practice, practice (timestamp: 47:06)
Chapter 8: Close the health gap between rich and poor countries (timestamp: 50:49)
Chapter 9: Make — and fund — a plan for preventing pandemics (timestamp: 57:40)
Afterword: How COVID changed the course of our digital future (timestamp: 1:03:00)
As Gates explains in a video at the beginning of Corbett’s report, he’s building a pandemic response team for the WHO, dubbed the "Global Epidemic Response & Mobilization" or GERM Team. This team will be made up of thousands of disease experts under WHO’s purview and will monitor nations and make decisions about when to suspend civil liberties to prevent the spread of an illness.3
Alas, as noted by “Rising” host Kim Iversen in the video compilation above, if COVID-19 has taught us anything, it’s that stopping the spread of a virus is more or less impossible, no matter how draconian the rules. Meanwhile, the side effects of lockdowns and business shutdowns are manifold.
People’s health has suffered from a lack of health care. Depression and suicide have skyrocketed. Economies have gone bust. Violent crime has risen. Tucker also points out the false premise behind Gates’ pandemic prevention plan, stating:4
“This theory of virus control — the notion that muscling the population makes a prevalent virus shrink into submission and disappear — is a completely new invention, the mechanization of a primitive instinct.
Smallpox occupies a unique position among infectious diseases as the only one affecting humans that has been eradicated. There are reasons for that: a stable pathogen, a great vaccine, and a hundred years of focused public health work. This happened not due to lockdowns but from the careful and patient application of traditional public-health principles.
[T]he attempt to crush a respiratory virus through universal avoidance could be worse than allowing endemicity to it to develop throughout the population.”
Gates’ Destructive Greed
During COVID, we basically traded false protection against one thing for a multitude of other ills that are far worse in the long run. Now, Gates and the WHO want to make this disastrous strategy the norm.
Once again, we see Gates is basically paying the WHO to dictate what the world must do to make him a ton of money because he’s always heavily invested in the very “solutions” he presents to the world. While he’s built a reputation as a philanthropist, his actions are self-serving, and more often than not, the recipients of his “generosity” end up worse than they were before.
Case in point: After 15 years, Gates’ Green Revolution in Africa (AGRA) project has now been proven an epic fail.5 Gates promised the project would “double yields and incomes for 30 million farming households by 2020.”
That false prognosis was deleted from the AGRA website in June 2020, after a Tuft University assessment revealed hunger had actually increased by 31%. February 28, 2022, the first-ever evaluation report6 confirmed the failure of AGRA.
The Globalists’ Double-Prong Attack on National Sovereignty
But getting back to the globalists’ plan to seize global control through biosecurity governance, they are attempting to do this using two different avenues. If we fail to fight off both attacks, we’ll end up under totalitarian governance.
The first attack comes in the form of amendments7 to the International Health Regulations (IHR). The second attack comes through a new international pandemic treaty with the WHO.
Starting with the first takeover strategy, as you read this, countries around the world are in the process of voting on amendments to the IHR.8 By May 28, 2022, the World Health Assembly will have concluded their vote on these amendments and, if passed, they will be enacted into international law in November 2022.
The IHR, adopted in 2005, is what empowers the WHO to declare a Public Health Emergency of International Concern (PHEIC).9 This is a special legal category that allows the WHO to initiate certain contracts and procedures, including drug and vaccine contracts. While the IHR grants the WHO exceptional power over global health policy already, under the current rules, member states must consent to the WHO’s recommendations.
This is one key feature that is up for revision. Under the new amendments, the WHO would be able to declare a PHEIC in a member state over the objection of that state. The amendments also include ceding control to WHO regional directors authorized to declare a Public Health Emergency of Regional Concern (PHERC).
In summary, the IHR amendments establish “a globalist architecture of worldwide health surveillance, reporting and management,” Robert Malone, Ph.D., warns,10 and we the public have no say in the matter.
We have no official avenue for providing feedback to the World Health Assembly, even though the amendments will give the WHO unprecedented power to restrict our rights and freedoms in the name of biosecurity. There’s not even a publicly available list of who the delegates are or who will vote on the amendments.
Summary of Proposed IHR Amendments
A summary of the proposed changes to the IHR was recently provided by Malone.11 In all, the WHO wants to amend 13 different IHR articles (articles 5, 6, 9, 10, 11, 12, 13, 15, 18, 48, 49, 53, and 59), the end result of which is the following:12
1. “Increased surveillance — Under Article 5, the WHO will develop early warning criteria that will allow it to establish a risk assessment for a member state, which means that it can use the type of modeling, simulation, and predictions that exaggerated the risk from COVID-19 over two years ago. Once the WHO creates its assessment, it will communicate it to inter-governmental organizations and other member states.
2. 48-hour deadline — Under Articles 6, 10, 11, and 13, a member state is given 48 hours to respond to a WHO risk assessment and accept or reject on-site assistance. However, in practice, this timeline can be reduced to hours, forcing it to comply or face international disapproval led by the WHO and potentially unfriendly member states.
3. Secret sources — Under Article 9, the WHO can rely on undisclosed sources for information leading it to declare a public health emergency. Those sources could include Big Pharma, WHO funders such as the Gates Foundation and the Gates-founded-and-funded GAVI Alliance, as well as others seeking to monopolize power.
4. Weakened sovereignty — Under Article 12, when the WHO receives undisclosed information concerning a purported public health threat in a member state, the Director-General may (not must) consult with the WHO Emergency Committee and the member state. However, s/he can unilaterally declare a potential or actual public health emergency of international concern.
The Director General’s authority replaces national sovereign authority. This can later be used to enforce sanctions on nations.”
Once the amendments are adopted by the World Health Assembly, nations will have only a limited time — six months — to reject them. That would put us into November 2022. Any nation which hasn’t officially rejected the amendments will then be legally bound by them, and any attempt to reject them after the six-month grace period will be null and void.
Attack No. 2: The WHO Pandemic Treaty
The second attempt to gain global control is through an international pandemic treaty with the WHO. An intergovernmental negotiating body (INB) was established as a subdivision of the World Health Assembly in December 2021,13 for the purpose of drafting and negotiating this new pandemic treaty.
In summary, the WHO wants to make its pandemic leadership permanent. It can then extend its power into the healthcare systems of every nation, and eventually implement a universal or “socialist-like” healthcare system as part of The Great Reset.
While a WHO-based universal health care system is not currently being discussed, there’s every reason to suspect that this is part of the plan. WHO Director-General Tedros Adhanom Ghebreyesus has previously stated that his “central priority” as director-general is to push the world toward universal health coverage.14
And, considering the WHO changed its definition of “pandemic” to “a worldwide epidemic of a disease,”15 without the original specificity of severe illness that causes high morbidity,16,17 just about anything could be made to fit the pandemic criterion.
The problem with this treaty is that it simply cannot work. The whole premise behind this pandemic treaty is that “shared threat requires shared response.” But a given threat is almost never equally shared across regions.
Take COVID-19 for example. Not only is the risk of COVID not the same for people in New York City and the outback of Australia, but it’s also not even the same for all the people in those areas, as COVID is highly dependent on age and underlying health conditions.
The WHO insists that the remedy is the same for everyone everywhere, yet the risks vary widely from nation to nation, region to region, and person to person. They intend to eliminate individualized medicine and provide blanket rulings for how a given threat is to be addressed, and this can only result in needless suffering — not to mention the loss of individual freedom.
Are You Ready to Cede All Authority to Gates-Led Group?
In closing, Gates’ GERM team would be the ones with the authority to declare pandemics and coordinate global response.18 Are you ready to cede all authority over your life, health, and livelihood to the likes of Gates? I hope not.
In the video above, Del Bigtree with “The Highwire” provides poignant examples where Gates is now admitting what “The Highwire,” I and many others have been saying since the earliest days of the COVID pandemic, and getting censored and de-platformed for it.
Gates is two years behind everyone else, yet despite his apparent inability to interpret the readily available data, he now wants power to dictate health rules to the whole world. We can’t let that happen.
Join the Global #StopTheWHO Campaign
It’s going to require a global response to prevent these two power grabs, starting with the IHR amendments under vote by the World Health Assembly. To that end, the World Council for Health has launched a global #StopTheWHO campaign. Here’s how you can get involved:19
Speak — Raise awareness on the ground and online. Use articles, posters, videos
Act — Campaign through rallies, political mobilization, legal notices and cases and similar campaigns
Collaborate with health freedom coalitions such as the World Council for Health
Explore activist toolboxes such as: www.dontyoudare.info and stopthewho.com
Engage global indigenous leadership to take a united stand against the WHO’s IHR
Notify World Health Assembly country delegates to oppose the IHR amendments
Activate people’s parliaments, legislatures or referendums to oppose power grabs
Dr. Richard Fleming ofhttps://flemingmethod.com joins The Alex Jones Show in-studio to break down the case currently being examined by multiple state attorneys general to indict Fauci, Gates, and those involved in engineering a pandemic.
Monkeypox, a Misdirection Play: Dr. Malone Provides Insight to the Latest Developments
Monkeypox, a Misdirection Play: Dr. Malone Provides Insight to the Latest Developments
Bannon: "What is Monkeypox?"
Dr. Malone: "Misdirection play."
"... they already have stockpiled vaccines for smallpox. What they bought is more smallpox vaccines... The name of the product is called JYNNEOS... It is marketed by Bavarian Nordic in you all you have to do is search for package insert JYNNEOS and you'll pull up the package insert for the product and they will find that this is absolutely not a benign product just as with the old Dr. X product, which is somewhat safer than that I had experienced with that and this product when I was working for DOD. This has as one of the leading rare serious adverse events. Wait for it. cardiotoxicity myocarditis."
Economic Collapse is a Real Threat, Monkeypox is Not
Ed Dowd gives a warning of economic collapse and I cover information that exposes the Monkeypox scam. Don't let the media, which lies about everything, win this information battle.
republished below in full unedited for informational, educational & research purposes:
(Natural News) Monkeypox, a very mild contagious disease that deserves no panic whatsoever, is reportedly spreading across the world among attendees of a gay pride gathering of 80,000 people in Gran Canaria.
As The Sun (UK) reports, “The Canaria Pride festival, held in the town of Maspalomas between May 5 and 15, has become a hotspot for the monkeypox outbreak, reports El País.”
Note that there isn’t a single corporate media outlet in the world that will admit such a fact. They cover up the filthy sexual habits and pretend that anal intercourse among multiple sex partners is perfectly normal, perhaps even preferred.
“Many known patients are gay men who were tested after going to STI clinics, the WHO said. Health chiefs warned gay and bisexual men to be on the lookout for new unexplained rashes,” adds The Sun. “Cases have now been detected in Israel, Norway, Australia, Portugal, Spain, Belgium, Germany, France, Netherlands, Sweden, Switzerland, the United States, and Canada.”
But monkeypox presents virtually zero risk to the world. The media hysteria surrounding the topic is just the latest effort to try to spread fear and panic in order to push — you guessed it — the inevitable monkeypox vaccine that will be forced onto everyone if they can conjure up enough panic.
Anyone dumb enough to fall for this latest “outbreak” hysteria is dumber than a monkey, of course. Among primates on planet Earth, human beings are the only species dumb enough to poison their food supply with pesticides, mass murder their own offspring with widespread abortions, and inject themselves with genetically altering experimental “vaccines” that cause infertility and death. Even rats aren’t stupid enough to engage in those practices… it takes an obedient human progressive to be that stupid.
Only 10 weeks of wheat supply left in the world
As Insider.com reports, a food expert named Sara Menker, testifying before the United Nations, warned that there are only 10 weeks of wheat supply remaining in the world. Importantly, she also recognizes that it’s not merely “Putin’s fault.” From that story:
Sara Menker, the CEO of agriculture analytics firm Gro Intelligence, told the UN Security Council that the Russia-Ukraine war was not the cause of a food security crisis but “simply added fuel to a fire that was long burning.”
“It is important to note that the lowest grain inventory levels the world has ever seen are now occurring while access to fertilizers is highly constrained,” she said. “And drought in wheat-growing regions around the world is the most extreme it’s been in over 20 years. Similar inventory concerns also apply to corn and other grains.”
So what happens after the “wheat wars” hit a critical point of collapse? Food riots, of course. Upheaval, civil unrest, and revolution around the world. The lack of affordable food will push every nation across the world toward the boiling point. Some of those nations will see violent revolts. Others will see their governments fall (as is happening right now in Sri Lanka).
Understand that the oblivious masses still have no clue the food supply is collapsing. They think that grocery stores in November and December will be fully stocked. Oblivious Europeans think heating energy will be widely available, too. (They are wrong.) The expectations of supply currently held by the oblivious masses are catastrophically inaccurate and subject to radical, painful corrections as reality kicks in.
The situation isn’t going to be pretty.
Listen to more details on all this — including my “Shock the Monkey Pox” song intro — in today’s Situation Update podcast: