STORY AT-A-GLANCE
- The rate of COVID-19 associated hospitalization among children aged 5 to 11 is just 0.0008%. In real-world terms, that’s so close to zero you basically cannot lower it any further
- Despite that, the U.S. Food and Drug Administration’s vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — on June 15, 2022, unanimously approved to grant Emergency Use Authorization (EUA) to Pfizer’s and Moderna’s COVID shots for infants and young children
- Pfizer’s EUA is for a three-dose regimen (3-microgram shots) for children 6 months to 5 years old; Moderna’s EUA is for a two-dose regimen (25-microgram shots) for children 6 months to 6 years
- In granting this EUA, the FDA again ignored injury and death data and swept medical ethics aside
- The drug companies need this last remaining age group to be included under the EUA, because once the emergency is finally declared “over,” the next phase of liability shielding requires that the shots receive approval by the CDC’s Advisory Committee on Immunization Practices (ACIP). Once the vaccine is on the childhood vaccination schedule, the vaccine makers are permanently shielded from liability for injuries and deaths that occur in any age group, including adults
Statistics show the rate of COVID-19 associated hospitalization among children aged 5 to 11 is 0.0008%.1 In real-world terms, that’s so close to zero you basically cannot lower it any further. Yet, despite such reassuring data, children in this age group are urged to get two to three doses of the COVID jab, even though side effects of the injection could harm them for life, or kill them.
As noted by the Vaccine Safety Research Foundation in the video below, myocarditis — one of the recognized effects of the COVID jab — “has a mortality rate of 25% to 56% within three to 10 years, owing to progressive heart failure and sudden cardiac death.”
Sudden cardiac death is what the media and public health agencies are now glibly referring to as “sudden adult death syndrome” or SADS. The older and more appropriate description for SADS is “sudden arrhythmic death syndrome,” but they don’t even want to use the word “arrhythmic” anymore, as that tells you what the death is really caused by, and many are now aware that the jab can cause heart inflammation.
By avoiding the word “arrhythmic,” it’s easier for them to pretend as though people are dying for no apparent reason, and certainly not because of the COVID shots. Still, real-world facts tell us that SADS didn’t take off until after the shots were rolled out, and the vast majority of young healthy people who suddenly die for no apparent reason have been jabbed.2
Also, understand that if your child or you are injured by the shot, you cannot sue the drug company for damages and, so far, the U.S. government has rejected all but one of the claims filed with the Countermeasures Injury Compensation Program (CICP).3 At the current pace of about 18 claims a month, it would take 38 years just to get through the current backlog, Reuters has noted.4 Basically, many may die before their case even gets through review.
COVID Jab Authorization Granted for Babies
As if the situation were not bad enough already, June 15, 2022, the U.S. Food and Drug Administration’s vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — unanimously approved (21-0) to grant Emergency Use Authorization (EUA) to both Pfizer’s and Moderna’s COVID shots for infants and young children.5
Pfizer’s EUA is for a three-dose regimen (3-microgram shots) for children 6 months to 5 years old, while Moderna’s EUA is for a two-dose regimen (25-microgram shots) for children 6 months to 6 years.
In the video at the top of the page, Steve Kirsch, president of the Vaccine Safety Research Foundation, interviews reporter Toby Rogers, who endured the entire nine-hour day of the recent VRBPAC meeting.
The day before that meeting, June 14, Rogers published6 a written summary of Pfizer’s trial on young children, which he referred to as “an embarrassment.” “Any VRBPAC member who votes Aye on this junk science application should be removed from his/her job,” he wrote. Apparently, they all need to go.
In the interview, Rogers laments the fact that the VRBPAC members remain “locked in their information bubble” and won’t allow any conflicting data to influence their preconceived biases.
As noted by Rogers, they have a sacred duty to protect public health, and they’re being flippant about it. They’re ignoring data, they’re ignoring the pleas of the vaccine injured, they’re ignoring serious questions, they’re ignoring everything except the flimsiest bits and pieces upon which their narrative is built. Rogers called the experience “heartbreaking.”
VRBPAC Refuses to Answer Lawmakers’ Questions
The VRBPAC members aren’t even swayed by concerns from lawmakers. They simply ignore their questions too. As reported by The Defender:7
“The Vaccines and Related Biological Products Advisory Committee (VRBPAC) ignored pleas from experts, the vaccine injured and a congressman representing 17 other lawmakers to halt authorization until questions about the safety and efficacy of COVID-19 vaccines for the nation’s youngest children could be properly addressed …
Rep. Louie Gohmert (R-Texas) said there are many unanswered questions … ‘I’m deeply concerned that the push to vaccinate these children is nothing more than a dystopian experiment with unknown consequences,’ Gohmert told the committee. ‘Some of us have outlined these questions in a letter8 to VRBPAC but have not received any answers, and I pose some of them here.’ Gohmert said:
‘Number 1, why has the FDA refused to release the hundreds of thousands of pages of data from preapproval manufacturer studies, post-approval adverse events data and other post-approval manufacturer data?
Number 2, what is the cardiac risk factor in administrating these COVID vaccines to children?
Number 3, world-renowned immunologists have raised concerns about potential antibody-dependent enhancement, or ADE, resulting from COVID vaccines, and since ADE was a problem in prior unrelated respiratory vaccine trials, we need to know what studies, if any, the FDA has that it’s used regarding ADE from COVID vaccines in children 5 and under or any age group. Can the FDA affirm there’s no risk of ADE for vaccinated children?
Number 4, if widely approved among children 5 and under, how many lives, if any, does FDA estimate will be saved next year? Given the injuries reported in the FDA’s VAERS [Vaccine Adverse Event Reporting System] system, how will FDA evaluate serious vaccine injuries versus serious COVID outcomes?
Number 5, is it possible the proposed COVID vaccines in young children could create increased risk in future novel COVID variants?
Number 6, why has the FDA recently lowered the efficacy bar for COVID vaccines for youngest children? This change significantly lowers the expected benefits from any COVID vaccination for young children and it’s of particular concern given that over 70% of that age cohort already is seropositive.’
Gohmert said these questions and 13 other questions posed by lawmakers are critical and deserve answers from the FDA and VRBPAC prior to any EUA with the ‘accompanied protection for liability for all harm done.'”
Trial Showed COVID Jab Increases Infection Risk in Babies
In this video, you can see Centers for Disease Control and Prevention director Dr. Rochelle Walensky, with a forced grin on her face, claiming “rigorous scientific review” has proven the shots to be safe and effective in infants and young children.
The video also features excerpts from a video in which Dr. Clare Craig, a diagnostic pathologist and “lover of data,”9 reviews what this “rigorous scientific review” actually found and what the FDA and CDC aren’t telling you. To hear Craig’s full summary of how Pfizer twisted its clinical data for young children, check out the video below.
Craig points out that of the 4,526 children, aged 6 months to 4 years, who participated in Pfizer’s trial, 3,000 didn’t make it to the end of the trial. Why did two-thirds of the children drop out? Oftentimes, this happens when side effects are too severe for the participant to continue. Here, we don’t know why two-thirds of the participants were eliminated, and “on that basis alone, this trial should be deemed null and void,” Craig says. Moreover:
•Six of the children, aged 2 to 4 years, in the vaccinated group were diagnosed with “severe COVID,” compared to just one in the placebo group. So, what this actually shows is that the likelihood the shot is causing severe COVID is higher than the likelihood that it’s preventing it.
•The only child who required hospitalization for COVID was also in the “vaccinated” group.
•In the three weeks following the first dose, 34 of the children in the vaccinated group and 13 of the unvaccinated children were diagnosed with COVID. That means the children’s risk of developing symptoms of COVID within the first three weeks of the first dose actually increased by 30%. These data were ignored.
Between doses two and three, there was an eight-week gap, and the vaccinated arm again experienced higher rates of COVID. This too was ignored. After the third dose, incidence of COVID was again raised in the vaccine group, and this was ignored as well.
In the end, they only counted three cases of COVID in the vaccine arm and seven cases in the placebo group. They literally ignored 97% of all the COVID cases that occurred during the trial to conclude that the shots were “effective” in preventing COVID.
•While they claim the triple-dose regimen reduced COVID, 12 of the children actually caught COVID twice in the two-month follow-up, and 11 of them were vaccinated.
•The confidence interval for Pfizer’s jab is -370% at the lower end of the 95%, which suggests children who get the jab are nearly four times more likely of getting sick with COVID than their unvaccinated peers.10
Unscientific and Unethical Behavior
As reported by The Defender:11
“Combining all ages together, Pfizer said its three-dose regimen for children 6 months to 5 years old was 80% effective at preventing illness from the Omicron variant based on preliminary data from its clinical trial.
The 80% number was calculated 30 days after the third dose. As noted by committee members, the efficacy number is likely to go down after 30 days and post-approval monitoring was suggested.
Moderna said its two-shot vaccine was about 51% effective against infection from Omicron in children under 2, and about 37% among kids 2 to 5 years old, citing different efficacy numbers than what was reported by the company in March.
In a March 23 press release, Moderna said its vaccine in the 6-month to 2-year age group was only 43.7% effective. In the older age group, the company said its vaccine was 37.5% effective. A top official at Moderna has already said a booster will be necessary.”
As noted by the Vaccine Safety Research Foundation, vaccinating infants and children who have no need for the shots and don’t benefit from them, just to “protect” adults, violates medical ethics. And since those who are jabbed still readily transmit the virus, the children are actually put at risk for no reason at all.
It’s All About Securing Indemnification
🧐So I’m guessing everyone is wondering why the FDA voted unanimously to give not one — but THREE shots of the C@ViD 💉to the youngest of children when there’s N🚫 emergency.
It is IMPERATIVE they have this approval.
R. obert K. ennedy Jr. tells us why: pic.twitter.com/denjlTchMF— NANCY (@9_News_Nancy_) June 15, 2022
So, how can we explain the irrational behavior of the FDA and CDC? Why don’t any of the data matter? Why doesn’t the science matter? Why don’t any of the red flags matter? And why are they handing out EUAs when the criteria for EUA are satisfied? Products must satisfy four criteria in order to get EUA:
- There must be an emergency
- A vaccine must be at least 30% to 50% effective
- The known and potential benefits of the product must outweigh the known and potential risks of the product
- There can be no adequate, approved and available alternative treatments (drugs or vaccines)
Unless all four criteria are met, EUA cannot be granted or maintained, yet here we are. COVID, by any reasonable measurement, is no longer an emergency, there are plenty of adequate alternative treatments, and the potential benefits in no way, shape or form outweigh the potential risks — especially not in infants and children under 5. That’s three out of four criteria that, clearly, are not met.
The short answer to the question, “Why are the CDC and FDA acting so irrationally?” is that both agencies are corrupt to the core and are no longer in the business of protecting public health. They are securing profits for the drug industry, and getting EUA for infants and young children is a crucial step toward securing permanent legal indemnity for the drugmakers.
As explained by Robert F. Kennedy Jr., in the short video clip above, they need this last remaining age group to be included under the EUA, because once the emergency is finally declared “over,” the next phase of liability shielding requires that the shots receive approval by the CDC’s Advisory Committee on Immunization Practices (ACIP).
This is the group that decides which vaccines are to be added to the childhood vaccination schedule. Once the vaccine is on the childhood vaccination schedule, the vaccine makers are permanently shielded from liability for injuries and deaths that occur in ANY age group, including adults.
The only way to break that indemnity is by proving the vaccine maker knew about the safety issues and withheld that information. You can learn more about this indemnification process in “The Real Reason They Want to Give COVID Jabs to Kids.”
So, the end goal is permanent immunity against liability for injury and death from the COVID shots in all age groups, and to get there, they first need the EUA to cover all children. After that, the ACIP approval becomes more or less a matter of rubber stamping. This is why they’re playing Russian roulette with the health of infants and young children.
Murder Has No Statute of Limitation
That said, if fraud can be proven, all indemnity falls by the wayside, and there’s no statute of limitation when it comes to murder, which some insist is what’s happening here.
The video above features “To The Lifeboats” podcaster Sam Dodson’s comments to the FDA VRBPAC during its open public hearing session to approve the COVID jabs for children between the ages of 6 months and 5 years. In a rapid-fire manner, he reviews several data points that ought to have put a halt to these injections, but didn’t; several instances where the FDA knew harm was occurring from these shots, or would occur, and they did nothing.
Another public comment was submitted by an as-yet unidentified individual. The submitted comment was provided to and reposted on Coquin de Chien’s Substack. Here are some select pieces:12
“This comment is NOTICE of possible criminal liability to Lauren K. Roth and members of the Vaccines and Related Biological Products Advisory Committee who owe duties of care, diligence, good faith, and loyalty in recommending ‘for’ or ‘against’ the EUA amendment for COVID-19 mRNA vaccine in children 6 months through 4 years of age.
Only two deaths are listed herein to establish knowledge. If the amendment is approved, it will have been done by committee members ‘knowing’ of felony crimes in context. Your investigation of these deaths should include death certificates, autopsy records, witness interviews, and immunization records.
Massachusetts Death Certificate 2022 SFN 5980 is a 7yo girl died January 18, 2022 listed as died from U071 ‘COVID-19,’ B49 ‘unspecified mycosis,’ J450 ‘predominantly allergic asthma,’ and R091 ‘pleurisy.’
VAERS_ID 2038120 is a 7yo girl in Massachusetts, who received her 2nd dose 1/13/2022 and was reported to VAERS 1/15/2022. PRIOR_VAX states, ‘Severe nausea and vomiting from 5 min post vaccination and for the next 8-10 hours.’
SYMPTOM_TEXT states, ‘Spiked a 103 fever, severe stomachache, has not had a bowel movement since the day before vaccination, which makes today 3 days without one. First vaccine caused severe nausea and vomiting from 5 minutes post injection and for the next 8-10 hours.’ This little girl suffered immeasurably 4 to 5 days as her intestines shut down due likely to impeded blood vessels servicing intestines.
Massachusetts Death Certificate 2021 SFN 56611 is a 48yo man died 11/16/2021 listed as died from U071 ‘COVID-19’ and E669 ‘OBESITY.’ SFN 56611 is known to have died less than 24 hours after inoculation.
In both cases, the Medical Examiners listed the cause of death as ‘COVID-19,’ when it was clearly not COVID-19. And in both cases, the Medical Examiners omitted listing causes Y590 ‘Viral vaccines’ and T881 ‘Other complications following immunization, not elsewhere classified,’ when these clearly were proximate and actual causes.
Death certificates from the state of Massachusetts are sent to the CDC, a federal entity. Thus, fraud on a state death certificate is a federal crime as it affects federal death records. Several federal felony crimes apply in this instance and are listed below.
If you dismiss this NOTICE and recommend the EUA amendment without first investigating these two deaths, you become liable for inchoate crimes and the felony crime of ‘misprision of felony.’ If a single person subsequently dies as a result of the amendment, all the elements will have been satisfied for you to face felony murder charges or involuntary manslaughter. Qualified immunity is not a valid defense …
There were found sixty likely C19 vaccine deaths in a 25-minute perusal of the 2021 and 2022 death certificates, which extrapolates to hundreds, probably thousands of C19 vaccine deaths in Massachusetts.
Refusal to investigate these fraudulent records is a crime that, because of the felony murder aspect, has no statute of limitations. Five, ten, or twenty years from now, if a federal prosecutor were to learn of this NOTICE, he or she would have significant evidence to bring charges for felony murder.
In summary, this NOTICE places you in a position requiring you to investigate these deaths prior to recommending the amendment. If you dismiss this NOTICE, you may be criminally liable for involuntary manslaughter, felony murder, and a list of federal crimes and inchoate crimes … Comment Tracking Number l4d-m52d-ge4m.”
Florida Bucks the Trend
My home state of Florida now stands out as the only U.S. state that is recommending AGAINST the COVID jab for 6-month-olds to 5-year-olds. Parents can still get their infants jabbed if they want, but the official state recommendation is not to do it, as there’s simply no scientific or logical rationale for doing so.
Florida also did not preorder any extra doses for this age group.13 In a June 18, 2022, Substack article, Dr. Robert Malone addressed the latest EUA authorization for infants and young children, and applauded Florida Gov. Ron DeSantis’ decision to buck the trend. It’s hard to believe he is the only governor in the U.S. who resisted this murderous threat to the children:14
“Have you looked at the VAERS data lately? The CDC apparently has not. In the USA alone, there have been 831,801 adverse events, of which 12,776 are life threatening. There have been 63,978 hospitalizations. There have been 13,293 deaths and 14,232 permanent disabilities from these vaccines.
True, these are ‘unverified’ — but previous research has shown that the VAERS system under-reported adverse events associated with vaccines, not over-reported … Then there are the international post-vaccine adverse event summaries.15
The CDC, under Freedom of Information Act Request (FOIA) has now admitted16 that even though they had promised to analyze the VAERS data before advising about these vaccines for children, they did not.
The VAERS data were NOT taken into consideration before the authorization of these genetic agents for babies and young children. Frankly, this is shocking. So shocking, it is hard for me to even write about it.
Now, approximately 430 children with other severe illnesses have died with COVID in the last 2.5 years (that would be 172 per year). Plus there have been 2,600 hospitalizations of children, most with underlying conditions — over that 2.5 year period. These numbers show that even before Omicron, in the case of children, COVID is less severe than flu …
Omicron in children is much less severe. We know this. The scientific evidence is clear. Yet the FDA goes back to data from the DELTA variant when discussing the effects of this virus … Governor DeSantis again has it right. It is time to stop. Parents must stop. The time is now to just say no.”
Last but not least, if you’re still unsure whether the COVID shot is the “right” choice for your child, please read through Dr. Byram Bridle’s “COVID-19 Vaccines and Children: A Scientist’s Guide for Parents,”17 published by the Canadian Covid Care Alliance. It goes through how the shots work, what the known side effects are, results from the clinical trial, the effects of the spike protein and much more.
- 1 Rumble Vaccine Safety Research Foundation June 9, 2022
- 2 Steve Kirsch Substack June 21, 2022
- 3, 4 Reuters June 16, 2022
- 5, 7, 11 The Defender June 15, 2022
- 6 uTobian Substack June 14, 2022
- 8 Letter to VRBPAC June 7, 2022
- 9 Twitter Clare Craig
- 10 Twitter Ben@USMortality June 16, 2022
- 12 Coquin de Chien Substack June 13, 2022
- 13 New York Times June 16, 2022
- 14 Robert Malone Substack June 18, 2022
- 15 World Council for Health June 17, 2022
- 16 Jackanapes Junction Substack June 16, 2022
- 17 Canadian Covid Care Alliance, COVID-19 Vaccines and Children: A Scientist’s Guide for Parents
d
Two Storms, One Harvest
Every food crisis in living memory has been a one-shock event. The 2008 price spike was a commodity bubble. The 2020 shortages were a logistics failure. The 2022 grain scare was a war on one exporter’s ports. Each time, the system bent, adjusted, and recovered, and each time the experts assured us afterward that global markets are simply too big and too diversified to fail.
What nobody in Washington seems eager to discuss is that 2026 is shaping up to be something the modern food system has never actually faced. Two independent shocks, one climatic and one geopolitical, are converging on the same harvest cycle at the same time. Not sequentially. Simultaneously.
Start with the weather. The Pacific Ocean is currently building toward what forecasters now openly call a record event. NOAA’s Climate Prediction Center puts the odds of at least a strong El Niño near 88 percent, with roughly two in three odds it reaches “very strong” status, the tier reserved for perhaps three or four events in the entire satellite era. Every major global model now projects a median peak in Super El Niño territory, and most of them project it exceeding the 2015-16 event, which until now held the modern record. Sea surface anomalies were already brushing the super threshold in mid-July, months before these events normally peak. The atmosphere has already shifted into El Niño mode, and the event is forecast to crest in late fall and early winter.
This is not about “climate change.” It’s about the standard cycles of weather, and the cycle we’re currently in is one that has likely devastated societies in the past. We’re better prepared as a society today, but not all Americans are equally prepared.
Serious households have started doing the quiet math on their own. Grocery bills tell part of the story, and the forecast maps tell the rest, which is why long-term food storage has moved from fringe hobby to mainstream line item in the family budget, with established suppliers like Heaven’s Harvest seeing demand from people who five years ago would have rolled their eyes at the idea. That instinct is not paranoia. It is pattern recognition, and the pattern is worth walking through carefully.
Editor’s Note: Heaven’s Harvest IS a sponsor, but the warnings of this article are real and would be written even if we didn’t have a survival food sponsor. With that said, those who take advantage of what they offer can use promo code “Patriot” for 15% off.
The Fertilizer Clock Is Already Running
While the Pacific warms, the second shock has been unfolding in the Strait of Hormuz. The conflict with Iran turned the world’s most important energy chokepoint into a contested waterway, and the consequences reach far beyond the gas pump. Roughly a third of global fertilizer trade moves through Hormuz, and the disruption sent urea prices up 86 percent year over year by March, with a 53 percent jump in a single month.
The World Bank projects energy prices rising about 24 percent in 2026 and fertilizer about 31 percent. By its own accounting, fertilizer prices ran 35 percent higher in the first five months of this year than the same period last year.
Here is the mechanism the nightly news will not explain. Fertilizer is not a grocery item. It is a time-delayed input. The nitrogen a farmer in Iowa or Punjab could not afford to apply this spring does not show up as a problem this spring. It shows up as a thinner harvest six to twelve months later.
The World Bank’s own food security brief concedes that the effects of reduced applications earlier this season “are likely to become visible only later in harvest outcomes.” Translate that from institutional language into plain English and it means this. The damage is already done, it is already in the ground, and we are simply waiting for it to arrive on the shelf.
Now check the calendar. Six to twelve months from the spring planting season lands us squarely in late 2026 and early 2027. Which is precisely when the strongest El Niño in the instrumental record is forecast to peak, bringing its signature droughts to Southeast Asia, Australia, southern Africa, northern Brazil, and South Asia, the very regions that grow the world’s rice, sugar, and oilseeds.
The World Bank warns openly that a strong El Niño “could disrupt multiple crop belts simultaneously” on top of the conflict-driven input costs. Their baseline projection assumes the Middle East disruptions ease by autumn. What in the last two years of Middle East history suggests that assumption is safe?
The System Has No Slack Left
The comfortable answer is that global markets always adjust. But adjustment requires slack, and the slack is gone. Global cereal production is expected to decline from last year’s records even before El Niño does its work. The UN World Food Programme, hardly a den of right-wing preppers, is calling this the most significant disruption to its supply chains since Covid and the invasion of Ukraine, and its supply chain director put the stakes bluntly.
Today’s supply chain challenges are tomorrow’s hunger crisis.
There is also a political dimension that markets cannot price. When food gets scarce, governments do not behave like economists. They behave like politicians. Export bans, hoarding mandates, and panic buying at the national level turned the modest rice shortfall of 2008 into a global crisis, and analysts are already warning that import-dependent nations are the first dominoes.
The 2015-16 Super El Niño, a far weaker event than what is now forecast, threw tens of millions into food stress across Africa and Asia. This one is projected to be stronger, and it arrives with fertilizer already rationed by price and shipping lanes already contested by missiles.
What Joseph Knew
Scripture does not treat preparation for lean years as faithlessness. It treats it as wisdom delivered in advance to those willing to act on it.
Behold, there come seven years of great plenty throughout all the land of Egypt: And there shall arise after them seven years of famine; and all the plenty shall be forgotten in the land of Egypt.
Joseph did not respond to that warning with a hashtag or a committee. He stored grain during the years of abundance, and when the famine came, Egypt stood while its neighbors begged. The lesson is not that famine is certain. It is that the time to prepare is precisely when preparation still looks optional.
Nobody who filled a pantry in a year of plenty has ever regretted it, and nobody standing in an empty aisle has ever been glad he waited for certainty.
None of this calls for panic, and panic is the enemy of sound judgment anyway. It calls for the same unglamorous prudence our grandparents considered ordinary. Keep some cash margin, know your local growers, and put real food in deep storage while it is cheap and available, because the entire arc of this story is that cheap and available is a closing window.
Families looking for a straightforward place to start can visit Heaven’s Harvest and use promo code Patriot for 15 percent off long-term storable food. The forecasts may yet soften, the strait may yet reopen, and we should pray they do. But hope is a fine thing to hold and a foolish thing to eat.
Wow…a whole page when just a sentence or 2 will easily do. Let’s see…
“Why Big Pharma Is Desperate to Get Covid Jabs Into Babies”
Because Jews created them to kill white and black people.
And yes, I can prove it. Here’s an excerpt from the .pdf –
We found that the distribution of deleterious variants
in ACE2 differs among 9 populations in gnomAD (v3).
Specifically, 39% (24/61) and 54% (33/61) of deleterious
variants in ACE2 occur in African/African-American
(AFR) and Non-Finnish European (EUR) populations,
respectively (Fig. 1b). Prevalence of deleterious variants
among Latino/Admixed American (AMR), East Asian
(EAS), Finnish (FIN), and South Asian (SAS) populations
is 2–10%, while Amish (AMI) and Ashkenazi Jewish
(ASJ) populations do not appear to carry such variants
in ACE2 coding regions
while Amish (AMI) and Ashkenazi Jewish
(ASJ) populations do not appear to carry such variants
in ACE2 coding regions – read that part again.
Everything I say, 100% provable and factual. And don’t have to take 10 minutes to read it.
And by the way, “Dr. Mercola”, Dr’s Kauffman and Cowan are correct. There is NO SUCH THING as “COVID 19”.
PROVABLE IN A COURT OF LAW.
Jab for thee, but not me. I still have and will retain my original DNA.
Good Luck suckers.
sO exactly how many Jews were working in the Wuhan Lab again?
Look at John Walters, banking wholeheartedly on what he was told in the Jew-controlled media as being correct. Hoping desperately that Wuhan being the rollout center for 5g in China is un-related. Because unlike big pharma, big telecom is full of saints and angels, right?
Oh, btw, did you know Lebron James got cancer in his face from using his cell phone? And that to keep him quiet, he got a nice lucrative T-mobile spokesman contract?
No Jews in big telecom, either, I bet.
Who do you work for, John?
By the way, John, are you aware the China is controlled by a Jew-owned Rothschild central bank…just like us?
This is called a “drive by”, this likely isn’t even a real person but one of many accounts ran by someone in a “comment farm” where Jews in the military work someplace called “Unite 8200”, where soldiers sit and spin Jew propaganda all day long.
Don’t you, Jews?