Israeli agency told to quit operations in Russia as ties hit new low
Press TV – July 6, 2022
The Russian Justice Ministry has asked an Israeli agency to wind down its operations in Russia as the two sides’ ties hit a remarkable new low.
The Jerusalem Post reported the development on Tuesday, citing the “Jewish Agency,” which purportedly handles the affairs of the Jewish people on the Russian soil.
“The order was given in a letter received from the Russian Justice Ministry earlier this week. Officials in the Jewish Agency confirmed that the letter was received,” the report said.
The agency, it added, was trying to coordinate a response in consultation with the Israeli regime’s foreign ministry and Israeli Prime Minister Naftali Bennet’s office.
‘Dramatic order’
The paper described the order handed to the agency as “dramatic.”
It cited a “senior diplomatic official” as making the following remarks concerning the order and Tel Aviv’s potential response to the move.
“Russia is saying the Jewish Agency illegally collected info about Russian citizens… We will bring up the Jewish Agency [with Russian authorities] and address it in an organized way. It will be taken care of at the embassy level.”
“We don’t totally understand the reasoning,” the source claimed.
The daily also said cessation of the agency’s operations in Russia would mean that the Jews would no longer be able to “escape” the country and make their way to the occupied territories.
Relations between Russia and the Israeli regime have gone through dire straits on several occasions since 2018.
The ties were hit with what observers rate as a major crisis in September 2018, when a Russian Il-20 military plane was mistakenly shot down by Syrian air defenses when it was preparing to land in Russia’s Hmeimim airbase in Latakia Province in northwestern Syria. The Syrian S-200 missile defense system was responding to a wave of strikes by four Israeli warplanes.
Moscow blames Tel Aviv for the incident, which killed all the 15 people on board the plane, saying the Israeli warplanes had deliberately “created a dangerous situation” that led to the crash. The Russian military also said the ill-fated plane was used as a cover by the Israeli air force, and that Moscow reserved the right to give a due response.
Tensions flared again between the two sides over the Israeli regime’s recurrent airstrikes against Syria last month after the regime targeted the Damascus International Airport. Russia subsequently summoned the Israeli ambassador to the country, expressing “serious concern” over the strikes that targeted the civilian facility.
And in May, Russian Foreign Minister Sergei Lavrov suggested that Nazi dictator Adolf Hitler had Jewish origins, triggering strong reactions from Tel Aviv. The Israeli foreign ministry said Lavrov’s comments were “ghastly,” and stated that it had summoned Russian Ambassador to Tel Aviv Anatoly Viktorov for “a tough talk” over the statements.
The Russo-Israeli ties have also been suffering as a result of Tel Aviv’s siding with the West over Ukraine, where Russia has been engaged in a special military operation since February, as well as the occupying regime’s agreement with the European Union to supply natural gas as an alternative to Russian energy imports.
Russia responds to reports Turkey detained its ship
Samizdat | July 6, 2022
Moscow has denied reports of Turkish customs seizing or arresting a Russian dry-cargo ship carrying grain near Karasu Port, as Ukrainian officials have claimed.
During a briefing on Wednesday, the deputy director of the Information and Press Department of the Russian Foreign Ministry, Aleksey Zaitsev, stated that the vessel, the Zhibek Zholy, was merely going through all the standard procedures before entering a port.
“According to Russia’s embassy in Turkey, the ship is currently in the roadstead of the port of Karasu and is undergoing standard procedures, including sanitary control,” Zaitsev stated. He further explained that based on the results of these inspections, the Turkish authorities will make a decision on whether or not to let the ship enter the port. Zaitsev noted that no matter the decision, there is absolutely no talk about detention or arrest of the vessel.
The ship’s crew members have also denied being arrested or detained by Turkish officials. Speaking to TASS on Tuesday, one member stated that none of the standard detention procedures have been carried out against the vessel, adding that it is at anchor due to bad weather.
“During a detention procedure, the ship is usually brought into the port under guard, meaning that it should specifically be done under the jurisdiction of Turkey’s guards if something really did happen. No arrest was made. The ship is simply at anchor due to weather conditions. A surveyor arrived on the ship, checked the cargo. This always happens,” the crew member explained.
Ukraine’s ambassador to Turkey, Vasily Bodnar, claimed on July 3 that Turkish customs, at the behest of Kiev, had arrested a Russian cargo ship allegedly carrying “stolen” Ukrainian grain.
According to Reuters, which cited unnamed Ukrainian officials, the Zhibek Zholy, which was traveling to the Turkish port of Karasu from the Russian-held Azov Sea port of Berdiansk, was allegedly loaded with around 4,500 tons of grain.
The outlet also reported that the Ukrainian Prosecutor General’s Office had previously sent a letter to Turkey’s Justice Ministry in late June insisting that the Zkibek Zholy had been involved in the “illegal export of Ukrainian grain,” and allegedly had 7,000 tons of cargo on board. Ukraine reportedly asked Turkey to inspect the vessel and seize samples of grain for forensic examination to determine its origin.
Neither Turkish customs officials nor the authorities in Ankara have given any official comments on the situation regarding the ship so far.
Grain exports by sea from Ukraine, a major producer, were undermined by the ongoing conflict in the country. Kiev has previously accused Russia of “stealing” its grain – which Moscow has denied.
Western nations have accused Russia of blocking the ports. Moscow has repeatedly stated it would guarantee safe passage for the grain shipments if Kiev clears its ports of mines. Ukraine has accused Russian forces of mining the Black Sea ports. Russia suggested exporting the grain through the Russian-controlled ports of Berdiansk and Mariupol.
Norway-Russia Tensions Escalate Over Sanctions Impacting Arctic Islands
By Kyle Anzalone | The Libertarian Institute | July 6, 2022
The latest point of confrontation between NATO and Russia is the Svalbard archipelago, located midway between Norway and the North Pole. Moscow claims Oslo is restricting trade with the island’s hundreds of Russian residents. A top member of the Russian legislature is now calling for Moscow to leave its agreement with Oslo that resolved the territorial dispute over the far-northern archipelago.
During a discussion about Norway restricting trade to the islands in the Russian Duma, the body’s speaker, Vyacheslav Volodin, requested the head of the chamber’s international affairs committee to look into “denouncing” the treaty. The agreement was signed in 2010.
In June, a shipment of goods to a Russian-operated mining colony on Svalbard was turned back. Moscow claimed the move by Oslo deprived the miners of needed food and medicine. “Norwegian authorities are trying to leave Russian miners without food, which is inherently immoral. This violates human rights and the principles of humanism,” said Russian Senator Konstantin Kosachev.
Konstantin went on to claim that Norway’s blocking of shipments violated international agreements. Oslo disputed the accusations saying it had not broken treaties and was legally enforcing sanctions. The shipment was “stopped on the basis of the sanctions that prohibit Russian road transport companies from transporting goods on Norwegian territory,” Norway’s Foreign Minister Anniken Huitfeldt said.
Huitfeldt noted there were potential options to allow the Kremlin to supply the miners without violating sanctions. The Russian Foreign Ministry promised Moscow would take “retaliatory measures” in response, though did not elaborate on what that might entail.
Ukraine suffers appropriation of Western humanitarian and military aid
Samizdat | July 6, 2022
Ukraine’s Financial Investigations Service says it has uncovered numerous cases where humanitarian and even military aid provided by the West has been appropriated and sold at a profit inside the country.
Appearing on the TV news channel Ukraina 24 on Tuesday, the head of the investigative body, Vadim Melnik, lamented that “even goods destined for the military are being realized for money,” adding that his subordinates had “ascertained such facts.”
The official went on to reveal that the service had launched around ten criminal probes in connection with the sale of humanitarian or military aid.
According to Melnik, the true number of such cases is likely higher, as other Ukrainian law enforcement branches are also uncovering such crimes.
“We need to set clear control algorithms of both arrival, distribution as well as the use of aid, which our international partners are giving us today,” the head of the Financial Investigations Service argued.
Previously, Ukraine’s Prosecutor General’s office had reported multiple cases of misuse of Western humanitarian and military aid.
Last month, RT spoke with an American volunteer, Andy Huynh, who had fought for Ukraine before surrendering to Russian forces.
He claimed, among other things, that the “commanders were very corrupt and troops were very ill-prepared and supplied” in the ‘International Legion’ he had served in.
Another US volunteer told journalists back in May that corruption was rampant in units made up of foreign fighters, “with basic equipment going missing.”
“There’ll be weapons with no ammo, or no body armor or medical kit,” he explained.
Brazilian mercenaries die in Ukraine
By Lucas Leiroz | July 6, 2022
Two Brazilians were killed in Ukraine in the first week of July after a Russian drone operation in Kharkiv. In all, three Brazilian mercenaries have died in Ukraine since the beginning of the Russian special military operation on February 24th. In the South American country, the mainstrem media has a strong pro-Western ideological orientation, which is why it encourages “volunteers” to go to Eastern Europe. In their speech, the media outlets claim that it is “easy” to fight against Russians because Kiev is supposedly “winning” the conflict. However, upon arriving in Ukraine, the foreign mercenaries are faced with a different and much harsher reality.
Between the night of July 1 and the morning of July 2 Brazilian mercenaries Douglas Rodrigues Búrigo and Thalita do Valle died after a Russian attack in Khakiv. Douglas was a former soldier of the Brazilian Army and had been fighting in Ukraine since May. Thalita was a model, lawyer, and professional sniper, who had previously worked as a military volunteer and propaganda agent for the Kurdish women’s battalions in the Middle East. Apparently, she died of asphyxiation while trying to flee her accommodation in the face of a drone attack, while Douglas was reportedly hit by shrapnel from mortar shells on the outside.
In June, another Brazilian had already died in Ukraine. André Hack Bahi was fatally shot during Russian bombing raids in Severodonetsk. Bahi was a former fighter in the French Legion and had already participated in some missions in Africa, but he was not able to survive the intense reality of the fighting in Ukraine. It is also necessary to mention that not all the dead have been properly identified yet, which leads one to believe that there may be more Brazilians among the dead in Ukraine, since there is ample participation of mercenaries from the South American country in the region.
There is still no official report by the authorities indicating the precise number of Brazilian citizens who are fighting for Kiev’s side in the conflict, but the number is certainly greater than what was expected from a neutral country with good relations with Russia. Even Brazilian parliamentarians fought in favor of Kiev, such as former deputy Artur do Val, who had a quick and scandalous performance in Ukraine, where he committed acts of sexual harassment against Ukrainian women. It is also known that over the last eight years several Brazilians have tried to join the Ukrainian neo-Nazi paramilitary troops to fight in Donbass, having been rejected due to the anti-Latin racism of these groups. Now these same militants are finding their way into the Ukrainian positions due to Kiev’s policy of accepting all foreign volunteers.
But it is absolutely impossible to analyze the situation without criticizing the destabilizing role that the Brazilian local media has played in its coverage of the events in Ukraine. Pro-Western media outlets report the conflict fallaciously, pointing to a non-existent “Ukrainian victory” and “ease” in fighting Moscow’s forces, portraying voluntary combat as a kind of “hunting safari” against Russians. Obviously, when the “volunteers” (almost all of them being paid private soldiers linked to mercenary companies) arrive on the battlefield, they are faced with situations very different from those reported by the journalists who encourage volunteering.
Agencies also have tried to publicize an image of “heroism” when talking about Brazilians fighting in Ukraine, ignoring important issues, such as the fact that they are cooperating with neo-Nazi militants and supporting a government that practices genocidal policies against the Russian population. Since the beginning of the Russian operation, Brazilian media agencies and Brazilian branches of foreign agencies have praised the “heroism” of the mercenaries who would be “helping to fight the invasion”, which also serves as propaganda and incentive for volunteering.
Brazilian media is not acting alone, but following the agenda imposed by the great world media agencies, which have increasingly bet on the narrative of “Ukrainian victory” as a way to raise the morale of the troops and justify the irresponsible military aid that the Western countries are sending to Kiev.
Private security companies hired to help Kiev are the ones that profit most from the propagation of this fallacious narrative among the public opinion, as they manage to convince an increasing number of volunteers to go and fight in Ukraine. In fact, some of these volunteers are not designated for direct combat but remain in safe places taking photos and videos to publish on the internet, reproducing propaganda to encourage more men to go – always trying to convince that combats are “easy” and “safe”, so that more people enlist in the mercenary companies. The result is that of the deluded enlisted men only a few are directed to propaganda, while others die on the battlefield.
Obviously, for Western countries and for private companies, investing in this type of propaganda is strategic and profitable, but not for Brazil. As a member of the BRICS, not participating in anti-Russia sanctions and being Moscow’s partner in several areas, the Brazilian government should act more incisively to monitor the destabilizing role that its media agencies are playing, seeking to prevent foreign narratives from taking Brazilians to die on the battlefield. Furthermore, it is not at all beneficial to Brasilia’s international image that the country is known for having a large number of citizens volunteering to fight alongside neo-Nazi battalions.
It is important to remember that mercenaries and “volunteers are not considered prisoners of war, but common criminals, which means that Brazilian citizens can be tried by courts in the liberated parts of Ukraine if they are captured. This type of situation will certainly generate diplomatic discomfort and, as Brazil and Russia are members of the BRICS, this is not a favorable condition for either side.
The best thing for the Brazilian government to do is to ban its citizens from volunteering in wars that do not concern the national interest of Brazil.
Lucas Leiroz is a researcher in Social Sciences at the Rural Federal University of Rio de Janeiro; geopolitical consultant.
Russia says it destroyed US HIMARS rocket launchers dubbed ‘powerful tools’ by Kiev
Samizdat | July 6, 2022
Russian forces destroyed two US-made rocket launchers in Donbass, the defense ministry said on Wednesday.
The US provided Kiev with eight High Mobility Artillery Rocket Systems (HIMARS) and ammunition since the beginning of the Russian military offensive in Ukraine, according to a Pentagon fact sheet published on Tuesday.
“In the area of the settlement of Malotaranovka in the Donetsk People’s Republic, high-precision air-launched missiles destroyed two US-made HIMARS multiple launch rocket systems and two ammunition depots for them,” the Russian military said in a statement.
At the end of June, the Lugansk People’s Republic (LPR) said that an М142 HIMARS had been used by Ukrainian forces in Donbass, the first time that local authorities reported the US-supplied systems had been used in combat.
Prior to that, the chief of Ukraine’s General Staff, Valery Zaluzhny, posted a video, purporting to show pro-Kiev forces operating the long-range rocket system.
On June 23, Ukrainian Defense Minister Alexey Reznikov welcomed the arrival of HIMARS and expressed gratitude to his “American colleague and friend Lloyd Austin (the Pentagon chief) for these powerful tools.”
“Summer will be hot for Russian occupiers. And the last one for some of them,” he wrote on Twitter.
Russia has constantly warned the US and its allies against providing Ukraine with weapons saying that it would only lead to the prolongation of the conflict and the creation of long-term problems.
Russian Defense Minister Sergey Shoigu said on Tuesday that some of the foreign weapons intended for Ukraine were spreading throughout the Middle East and are turning up on the black market.
Two and 3-year-old kids with seizures is “the new normal”
I’m getting multiple reports from nurse friends about 2 and 3 year-olds having seizures. It is only happening to vaccinated kids, and symptoms start 2 to 5 days after the COVID jab.
By Steve Kirsch | July 4, 2022
Doctors are mystified by a rash of seizures, rashes, etc. happening to 2 and 3-year-old kids.
The only thing these kids have in common is that they were given the COVID vaccine just days earlier (two to five days earlier).
The doctors cannot figure out what is causing the seizures (since it couldn’t be the vaccine since those are safe and effective). The medical staff is not permitted to talk about the cases to the press or on social media or they will be fired.
One nurse posted something to the effect of “how is this legal????” I had to paraphrase to protect the poster.
This is why you are hearing these reports from me. They can’t fire me.
There is nothing on the mainstream media about this since the nurses and doctors aren’t allowed to talk about it.
This will all come out some day, but for now, everyone is keeping quiet about it and the doctors are instructed to convince the parents that it isn’t vaccine related and that they are the only ones having the problem.
Because that’s how science works.
Financial Times Censors Criticism of Vaccine Article
BY TOBY YOUNG | THE DAILY SCEPTIC | JULY 5, 2022
Earlier today, the Financial Times removed a comment from a reader calling himself ‘Mykonos Mike’ underneath an article about why COVID-19 infection and vaccination are only partially effective – and, in some cases, completely ineffective after a certain period of time has passed – when it comes to reducing a person’s likelihood of becoming re-infected, infecting others, and ending up with a severe bout of the disease. The reason given for removing the comment, in spite of the fact that it was the most liked and commented on, was “violating our community guidelines”, although, needless to say, no more detail was provided.
In light of this, we thought it was only right to republish Mykonos Mike’s comment in full.
Is this the long winded drivel to explain how people who have taken four doses of a 95% effective vaccine can get infected multiple times? The science in the pandemic has been so wrong it entered fairy tale wonderland story telling level, almost from the beginning. This is volume 15 of series four of the story. I’ll provide a spoiler – nobody cares anymore. And the decisions made in relation to this virus were ineffective and have created massive social and economic problems that will last decades. Time to start calling it as it is FT, the media are hugely complicit in this nonsense. Governments, scientists, health authorities and pharmaceutical companies need to answer very direct questions.
You can read the FT article Mike is commenting on here. Here’s an excerpt.
A surge in COVID-19 hospital admissions driven by the BA.5 subvariant of Omicron, accompanied by the inability of vaccines to prevent reinfection, has prompted health policymakers to rethink their approach to boosters.
U.S. regulators last week recommended changing the design of vaccines to produce a new booster targeting Omicron — the first change to the make-up of shots since their introduction in late 2020. Research into immune imprinting, whereby exposure to the virus via either infection or vaccination determines an individual’s level of protection, is now driving the debate over the make-up of COVID-19 vaccines.
Immunologists say that, more than two years into the coronavirus pandemic, people have acquired very different types of immunity to the SARS-CoV-2 virus, depending on which strain or combination of strains they have been exposed to — leading to big differences in COVID-19 outcomes between individuals and countries.
“The effect is more nuanced than ‘more times you have it, less protection you get’,” said Professor Danny Altmann of Imperial College London, who is investigating the phenomenon with colleagues. “It’s more helpful to consider it as progressive fine-tuning of a huge repertoire. Sometimes this will be beneficial for the next wave, sometimes not.” …
A study of 700 U.K. healthcare workers by the Imperial team, published last month in the journal Science, found that Omicron infection had little or no beneficial effect of boosting any part of the immune system — antibodies, B-cells or T-cells — among people who had been imprinted with earlier SARS-CoV-2 variants.
The Daily Sceptic has addressed the claims being made about this study and the supposed loss of natural immunity with Omicron here.
Will Pfizer Be Charged for Mislabeling Vaccine Side Effects?
By Dr. Joseph Mercola | July 5, 2022
As the U.S. Food and Drug Administration continues to release Pfizer’s clinical trial documentation,1 we’re finding more and more evidence that very little has been done on the up-and-up, and the COVID jab trials may be among the most fraudulent in medical history.
Can All Serious Adverse Effects Be Written Off?
Importantly, Pfizer classified almost all severe adverse events that occurred during its Phase 3 trials as unrelated to the injection. As reported by The Defender, June 21, 2022:2
“The latest release by the U.S. Food and Drug Administration (FDA) of Pfizer-BioNTech COVID-19 vaccine documents reveals numerous instances of participants who sustained severe adverse events during Phase 3 trials. Some of these participants withdrew from the trials, some were dropped and some died.
The 80,000-page document cache includes an extensive set of Case Report Forms (CRFs) from Pfizer Phase 3 trials conducted at various locations in the U.S., in addition to other documentation pertaining to participants in Pfizer-BioNTech vaccine trials in the U.S. and worldwide …
The CRFs included in this month’s documents contain often vague explanations of the specific symptoms experienced by the trial participants. They also reveal a trend of classifying almost all adverse events — and in particular severe adverse events (SAEs) — as being ‘not related’ to the vaccine.”
The Defender article includes 11 examples3 of trial participants who experienced severe adverse effects that were classified as “unrelated” to the experimental gene transfer technology they’d received just days or weeks earlier.
A 2,566-page document4 catalogues the serious adverse events and six deaths that occurred during the trial. These events were all classified as “toxicity level 4,” which is the most serious, yet none of them were deemed related to the injection.
This simply isn’t believable. It’s completely unrealistic, especially when serious events occur in multiple participants. A handful of examples of Level 4 adverse events listed in this document — all of which were written off as “not related” to the mRNA injection — include:5
- Acute respiratory failure
- Cardiac arrest
- Brain abscess
- Adrenal carcinoma (adrenal cancer)
- Chronic myeloid leukemia (blood and bone marrow cancer)
The six deaths reported were listed as being caused by arteriosclerosis, cardiac arrest, hemorrhagic stroke and myocardial infarction.6 Many participants also dropped out or were excluded from the trial due to serious side effects involving the heart, cardiovascular system, cancer, stroke, hemorrhage and neurological impacts.
Examples of Level 3 Adverse Events
Most Level 3 adverse events were also dismissed as unrelated to the shot. As reported by The Defender, only a “small number” were listed as being related to the injection. Examples of Level 3 side effects include:7
- Deafness/hearing loss
- Tachycardia (disruption of the normal electrical impulses that control your heart rate — the very problem that underlies most cases of “sudden adult death syndrome” or SADS)
- Ventricular arrhythmia (abnormal heart rhythm that makes the lower chambers twitch rather than pump — another underlying cause of SADS)
- Neutropenia (low neutrophil level in your blood; neutrophils are a type of white blood cell made by your bone marrow that fight infections by destroying viruses and bacteria)
- Vertigo
45% Experienced One or More Adverse Events
Another document8 that raises suspicions of bias is one admitting that “40% to 45% of participants who received BNT162b1 and BNT162b2 across age groups and across dose levels reported one or more AEs [adverse events] from Dose 1 through 28 days (i.e., 1 month) after Dose 2.”
BNT162b2 was the candidate injection that went on to receive Emergency Use Authorization (EUA) from the FDA. Among those who got the highest dose (30 micrograms) of BNT162b2, 50% of younger participants 25% in the older age group reported one or more adverse events.
The most common adverse events were nervous system disorders, followed by musculoskeletal and connective tissue disorders. Yet despite high rates of side effects across dose levels, this document also insists that “most AEs were considered by the investigator as not related to study intervention.”
During the open-label period of the study, 12,006 participants were followed for a minimum of six months, and among those, 28.8% reported at least one adverse event at some point during that follow-up, and 2.1% reported one or more severe adverse events.
Incidence Rate in Treatment Group FAR Higher Than Placebo
As reported by The Defender :9
“The review provides data for participants from dose 3 … to the data cutoff date. The severe adverse event incidence rate (IR) was 6.0 per 100 PY (patient-years), with specific conditions reported including pulmonary embolisms, thrombosis, urticaria, a cerebrovascular accident and COVID-19 pneumonia.
Here, the review adds that the IR for original placebo participants who had at least 1 life-threatening AE from Dose 3 to the data cutoff date was 0.5 per 100 PY.
Only one such life-threatening event, an instance of anaphylactoid reaction, was considered to be related to the vaccination. Other life-threatening, serious adverse events included cardio-respiratory arrest, gastrointestinal necrosis, deep vein thrombosis and pulmonary embolism …
Notably, according to the review, ‘all … events of facial paralysis were considered by the investigator as related to study intervention.” [Editor’s note: these specifically refer to events that occurred during the open-label follow-up period when BNT162b2 Dose 3 or Dose 4 was offered to both placebo and initial treatment groups.]
Young Children Have Extremely Low Risk of Death From COVID
In the end, we all know what happened. Despite all the evidence to the contrary, Pfizer concluded the shot was safe and effective for everyone and the FDA went along with it. The vaccine manufacturers and the FDA have decided it isn’t even worth invoking the precautionary principle for the very youngest of children, which is nothing short of reprehensible, criminal maleficence.
In mid-June 2022, against strong objections from physicians, scientists and researchers, the FDA’s vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — unanimously agreed to grant EUA to both Pfizer’s and Moderna’s COVID shots for infants and young children.10,11
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.
According to the U.S. Centers for Disease Control and Prevention,12 an estimated 75% of American children ages birth to 11 already have some level of immunity, having been exposed to one of the several variants that have come into circulation over the past two-plus years.
This immunity level alone makes EUA for COVID shots questionable. CDC data also prove young children have a very low risk of hospitalization and death from COVID, which makes the EUAs even more questionable.
Data13 published in mid-March 2022 suggest babies and young children under the age of 4 have had a peak hospitalization rate for COVID of 14.5 per 100,000. That peak occurred after Omicron became predominant. The hospitalization rate for the Delta variant in this age group was 2.9 per 100,000.
In all, since March 2020, a total of 2,562 infants and young children (6 months to 4 years) have been hospitalized WITH COVID. Of those, 2,068 had COVID listed as the primary reason for admission (84.7% of the total), and only 624 required ICU admission.
The median length of hospital stay was 1.5 days (range: one to three days). Of the 2,562 children with suspected COVID infection, 16 of them (0.6%) died in the hospital. Death certificate data push that number a bit higher. The Vaccine Reaction notes,14 “According to death certificate data,15 202 deaths have been attributed to COVID-19 among children 6 months to 4 years of age through May 11, 2022.”
While any death is tragic, it’s worth noting that 923 (35.8%) of the children hospitalized with suspected COVID also had one or more underlying medical conditions.16 We don’t know for sure, but it’s quite possible that those who died with a COVID diagnosis actually died from whatever underlying condition was present or had brought them to the hospital in the first place.
What I’m trying to say is that 16 to 202 deaths over two-plus years aren’t cause for panic, and that’s true even if COVID was the primary cause of those deaths. The likelihood of your child getting injured by the mRNA shot is undoubtedly significantly greater than their risk of dying from COVID.
Jab More Likely to Put You in the Hospital Than Keep You Out
The same is true for adults, by the way. A June 2022 analysis17,18 of Pfizer and Moderna trial data found the shots are more likely to put you in the hospital than keep you out of it. As reported by The Daily Sceptic :19
“A new paper20 by BMJ Editor Dr. Peter Doshi and colleagues has analyzed data from the Pfizer and Moderna COVID vaccine trials and found that the vaccines are more likely to put you in hospital with a serious adverse event than keep you out by protecting you from COVID.
The pre-print (not yet peer-reviewed) focuses on serious adverse events highlighted in a WHO-endorsed ‘priority list21 of potential adverse events relevant to COVID-19 vaccines.’ The authors evaluated these serious adverse events of special interest as observed in ‘phase III randomized trials of mRNA COVID-19 vaccines’ …
Dr. Doshi and colleagues found that the Pfizer and Moderna mRNA COVID-19 vaccines were associated with an increased risk of serious adverse events of special interest of 10.1 events per 10,000 vaccinated for Pfizer and 15.1 events per 10,000 vaccinated for Moderna …
When combined, the mRNA vaccines were associated with a risk increase of serious adverse events of special interest of 12.5 per 10,000 vaccinated … The authors note that this level of increased risk post-vaccine is greater than the risk reduction for COVID-19 hospitalization in both Pfizer and Moderna trials, which was 2.3 per 10,000 participants for Pfizer and 6.4 per 10,000 for Moderna.
This means that on this measure, the Pfizer vaccine results in a net increase in serious adverse events of 7.8 per 10,000 vaccinated and the Moderna vaccine of 8.7 per 10,000 vaccinated.”
Doshi’s team wasn’t the first to reanalyze Pfizer’s trial data. The Canadian COVID Care Alliance has also published a clear and easy-to-read summary22 of the Pfizer trial results, and the many questions raised by it. As noted by Dr. Robert Malone:23
“The bottom line is that the Pfizer Phase 3 trial which was used by NIAID [the National Institutes of Allergy and Infectious Diseases], FDA and CDC to justify the emergency use authorization is pretty much a junk clinical trial which was inappropriately halted long before it even got close to meeting the intended follow up period, did not provide a sufficiently long follow up analysis of vaccination-associated adverse events, and in which the control group was intentionally eliminated.
This resulted in basically erasing any opportunity to ever get to the bottom of what the major true risks of the Pfizer mRNA inoculations were. In terms of more minor risks, the study was not powered (not big enough) to evaluate those.”
FDA and CDC Have Neglected Important Duties
Doshi and his coauthors also note the FDA also watered down results by including “thousands of additional participants with very little follow-up, of which the large majority had only received one dose.”
They then further diluted the appearance of risk by counting only the number of people affected rather than counting the total number of individual adverse events. This makes a big difference, as twice as many people in the treatment group reported multiple serious adverse events, as compared to the placebo group.
The FDA and CDC have both also failed to produce promised follow-up investigations. In July 2021, now a full year ago, the FDA said it would investigate four “potential adverse events of interest following Pfizer vaccination,” namely pulmonary embolism, acute myocardial infarction, immune thrombocytopenia and disseminated intravascular coagulation, but to date, no update has been issued.
Similarly, in early 2021, the CDC published a protocol on how to use proportional reporting ratios to detect signals in the U.S. Vaccine Adverse Event Reporting System (VAERS), but no study or report showing what that protocol might have found has ever been published.
As it turns out, the CDC hasn’t been looking for safety signals in VAERS — not with the proportional ratios protocol or any other. So, while they’ve publicly claimed they haven’t seen any signals of concern, the reason they haven’t seen any signals is very simple: They never looked at the data!24
That’s how ridiculous things are now. When a drug company or health agency claims they haven’t found a problem, you actually have to ask them, “where, when, how and how often did you look?” But of course, virtually no one would ever ask such questions because they would assume these agencies are competent, which of course is a false assumption.
Their Fraudulent Behavior Could Be Their Undoing
As you probably know, the makers of the COVID shots are indemnified against legal liability for any injuries and all deaths stemming from their products. No one is able to sue them for damages.
The only way to hold them responsible is to prove they’ve committed fraud. This would remove their liability immunity. As detailed at the beginning of the article, their consciously choosing to miscategorize adverse events during the initial trials and concealing the harms should be a slam dunk to convict them of fraud.
But there is also another fact they concealed: There’s evidence showing they knew the mRNA doesn’t stay in the injection site but, rather, distributes throughout the body,25 and this too could be a smoking gun that proves fraud. If convicted of fraud, Pfizer, Moderna and Janssen would likely face liabilities in the trillions of dollars in damages.
When I exposed Merck’s Vioxx scandal in 1999 in this newsletter, before they even released their drug on the market, I thought that was huge. Their drug killed more than 60,000 people, and they could have been liable for $25 billion in damages, but their clever lawyers reduced it to $5 billion.
Well, that catastrophe is a drop in the bucket compared to the COVID scam, which has likely killed between 600,000 and 750,000 Americans, disabled as many as 5 million, and injured an estimated 30 million Americans in one way or another.26,27 That’s just the estimated toll in the U.S., so you can imagine what the global numbers might be. It’s a catastrophe of unprecedented proportions. A June 2022 survey by Steve Kirsch also found:28
- 6.6% of COVID jabbed respondents suffered heart injury (about 10 million Americans, based on the national vaccination rate)
- 6.3% had to be hospitalized for their side effects (another 10 million Americans)
- 9.2% of those who took the jab had to seek medical help for their injury, which translated over the whole country would be about 18 million doctor’s visits
- People who got the shot were more likely to die from COVID than the unvaccinated
- 2.63% of the responders had lost someone in their household to COVID infection, and 2.03% had lost someone in their household to the COVID jab
Expect Depopulation
Whether intentional or not, mounting evidence now indicates the COVID-19 injections will result in depopulation through premature death and adverse effects on fertility in women and men alike. I’ve previously discussed the risk of pregnancy loss and infertility in women who get the shot, as the mRNA has an affinity for accumulating in the ovaries29 (as well as the adrenals, liver and bone marrow).
Research30,31 from Israel now also reveals the shot deteriorates sperm count and sperm motility in men for about three months. Considering the multidose mRNA shots are recommended at three-month intervals, you can see how this can really decimate a man’s prospects of fathering a child.
Fertility has been on a steady decline for decades in most parts of the world,32 but the worldwide COVID jab campaign may massively speed that up. Germany recently released data showing a 10% decline in birth rate during the first quarter of 2022.33
Other countries are also seeing a drop in birth rate, nine months after the start of the mass vaccination campaign against COVID. Between January and April 2022, Switzerland’s birth rate was 15% lower than expected, the U.K.’s was down by 10% and Taiwan’s was down 20%.34
What punishment could possibly be appropriate for company heads and health agency leaders responsible for causing massive depopulation worldwide through products that were based on fraudulent science and fictional claims? I doubt if there’s enough money in the world to set that right.
Future Trials To Be Skipped Altogether
As if matters weren’t already beyond horrible, the FDA is considering allowing manufacturers to reformulate their COVID injections in perpetuity without conducting any additional clinical trials!35 In other words, they’d allow drug companies to change the mRNA and/or other ingredients without any safety or efficacy testing whatsoever. As reported by Toby Rogers, Ph.D., in a June 27, 2022, article in The Defender :36
“FDA released a briefing document37 in connection with this scheme to end science as we know it in connection with future COVID-19 shots … The briefing document is 18 pages of text, 1.5 line spacing, with just 19 references — 9 of which are pre-prints or from the CDC’s in-house newsletter Morbidity and Mortality Weekly Report (MMWR) which means they are not peer-reviewed.
Any true believer in The Narrative(TM) could have written this in a few hours. To base the entire future of COVID-19 shots on this glorified undergrad term paper is madness …
The core argument of the briefing document is hilarious (or rather, it would be hilarious if it was not a plan to permanently institutionalize genocide and hide the evidence). In several places the FDA argues (colloquialisms mine):
1. These COVID-19 shots work great … Boosters too, total home run, the Israelis even have 10-weeks of data showing that they might help old people. What more evidence could you want?
2. Okay, well, it depends on what you mean by ‘work.’ These shots do not stop infection, transmission, hospitalization, or death, even though that’s why we licensed them. Any protection wears off fairly quickly, but It’s Not Our Fault(TM) because This Wily Virus(TM) mutates too fast and no one told us that it would ever mutate.
3. So these shots must be reformulated but we cannot possibly ask Lord Pharma to do proper clinical trials ever again because we already know that these shots work great (see point #1)!”
In short, the FDA argues that since there are time constraints, evaluation of effectiveness must rely on “measures other than actual health outcomes.” In other words, whether the shots actually lower your risk of severe illness, hospitalization and death will have no bearing.
The only measure they’ll take into account is whether or not the jab triggers a rise in antibody levels, which has never been proven to be beneficial. If anything, the increase in COVID antibodies actually increases your risk of infection. This also means that as long as antibody levels are through the roof, the death rate could be just about anything, because it’s not part of the safety equation.
Faith in Magic Has Officially Replaced Science
As noted by Rogers,38 “The ‘Future Framework’ is a plan to base the entire COVID-19 vaccine program on magical thinking rather than science.” Indeed, Dr. Deborah Birx recently confirmed that the whole vaccine push has been based in faith in magic.39
June 23, 2022, Birx answered questions from the House Select Subcommittee on the Coronavirus Crisis. Rep. Jim Jordan, R-Ohio, asked whether the government was lying or guessing when they stated that vaccinated individuals couldn’t catch or spread COVID. At first, she claimed she didn’t know, but when pressed, she replied, “I think it was hope that the vaccine would work in that way.”40
So, the government issued mandates and made unequivocal, absolute statements that were not allowed to be questioned because they HOPED the shots would work a certain way — all while insisting they were the ones following and trusting the science and anyone who questioned their logic was a dangerous nut job. Let that sink in. Hope is literally the diametrical opposite of science.
It’s an Insiders’ Plot
As explained by Rogers, the same old players are behind this brazen attempt to eliminate the need for clinical trials: CDC staffers, academics who are in the pockets of Bill Gates and the NIAID, the drug companies themselves and the World Health Organization. Rogers writes:41
“I did not understand until just yesterday (as I started to write this article) that this entire ‘Future Framework’ is actually coming from the WHO. The Bill & Melinda Gates Foundation is the biggest voluntary contributor to the WHO. So Gates is likely directing the play.
Gates requires that WHO use the McKinsey consulting firm so this is probably a McKinsey operation (and McKinsey also works for Pharma so this is a huge conflict of interest). As Naomi Wolf points out, the involvement of the WHO also raises troubling questions about the influence of the Chinese Communist Party over this process.
As far back as January, the WHO/Gates/McKinsey junta realized that these shots were terrible and so they decided to use that as an opportunity to seize even more power and control.
The WHO set up a Technical Advisory Group on COVID-19 Vaccine Composition (TAG-CO-VAC) to implement these Orwellian ‘Future Frameworks’ across the developed world to lower manufacturing costs for Pharma and avoid bothersome health data that might hurt profits. All the messaging we have seen from the FDA and leaked to the press was initially developed and released by TAG-CO-VAC.”
No doubt, we live in unprecedented, precarious times. Logic, reason, science and sanity itself has been tossed aside by those who claim the right to make decisions for all mankind. If the FDA goes forward with this “Future Framework” scheme, the only safe assumption is that COVID shots will become more and more dangerous.
Worse, we can expect other vaccines and drugs to be allowed on the market without clinical trials as well. It truly could change the science of medicine as we know it.
Of course the WHO also wants to seize control over health care worldwide, which would eliminate medical rights everywhere. It’s a nightmare scenario with no end in sight as of yet. All we can do is continue to push back, to inform ourselves, to speak out, share facts and data, and refuse to comply with unscientific recommendations based on little more than hope in fabricated conclusions.
Sources and References
- 1 PHMPT.org Pfizer Documents Released by FDA
- 2, 3, 5, 6, 7, 9 The Defender June 21, 2022
- 4 PHMPT.org 16.2.7.1 Adverse Events Legend
- 8 PHMPT.org 2.5 Clinical Overview for BNT162b2
- 10 The Defender June 15, 2022
- 11, 14 The Vaccine Reaction June 21, 2022
- 12 CDC MMWR April 29, 2022; 71(17): 606-608
- 13, 16 CDC MMWR March 18, 2022; 71(11): 429-436
- 15 FDA. Briefing Document on EUA amendment request for Pfizer-BioNTech COVID-19 vaccine for use in children 6 months […]. VRBPAC Meeting June 15, 2022
- 17, 20 SSRN June 23, 2022
- 18, 23 Robert Malone Substack June 22, 2022
- 19 The Daily Sceptic June 22, 2022
- 21 SPEAC October 26, 2021
- 22 Canadian COVID Care Alliance, More Harm Than Good
- 24 Jackanapes Substack June 16, 2022
- 25, 29 Paul Alexander Substack June 27, 2022
- 26 the New American June 27, 2022
- 27, 28 Steve Kirsch Substack June 25, 2022
- 30 Andrology June 17, 2022 DOI: 10.111/andr.13209
- 31 Expose June 26, 2022
- 32 Bloomberg June 21, 2022
- 33 Twitter Jikkyleaks June 26, 2022
- 34 SWPRS June 2022
- 35, 36, 38, 41 The Defender June 27, 2022
- 37 FDA Briefing Document June 28, 2022
- 39, 40 Daily Caller June 23, 2022
Internet Searches for “death after vaccine” Increased After Covid Injection Roll-out
By Ryan Matters | New Brave World | July 3, 2022
Google is the largest and most used search engine in the world with a desktop market share of over 85%!
Data from Google Trends shows a marked increase in people searching for “death after vaccine” immediately after Covid-19 injections were rolled out around the world.
Google Trends provides insights into the popularity of certain search terms within a given timeframe and locality. According to Google:
Google Trends provides access to a largely unfiltered sample of actual search requests made to Google. It’s anonymized (no one is personally identified), categorized (determining the topic for a search query) and aggregated (grouped together). This allows us to display interest in a particular topic from around the globe or down to city-level geography.
The Covid-19 injection roll out began in January 2021 (with trials being run for months before). Data from Google Trends suggests that searches for terms such as “death after vaccine”, “vaccine chest pains”, “vaccine side effects”, “vaccine pain” and “vaccine vomiting” increased at almost the exact same time.
An increase in searches for the term “death after vaccine” could be interpreted as being due to people looking specifically for that kind of data. However, it could also be due to people knowing someone who died shortly after getting injected and looking for more information.
VAERS (the Vaccine Adverse Events Reporting System) provides further corroboration for this hypothesis. The reporting system has received almost 30,000 reports of death following Covid injections since December 14, 2020. (And it is important to keep in mind that vaccine adverse events are not required to be reported. In fact, they are criminally underreported, and many physicians are uneducated on how to use the platform).
According to a recent article on Children’s Health Defense:
VAERS data released Friday by the Centers for Disease Control and Prevention show 1,314,594 reports of adverse events from all age groups following COVID-19 vaccines, including 29,162 deaths and 241,226 serious injuries between Dec. 14, 2020, and June 24, 2022.
Noteworthy is that “death after vaccine” wasn’t the only term that saw an increase in searches. So did “vaccine chest pains”, “vaccine side effects”, “vaccine pain” and “vaccine vomiting”.
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From the Archives
Britain’s secret role in the brutal US war in Vietnam
By Mark Curtis | MintPress News | November 16, 2022
There is a myth the UK did not support Washington’s war against Vietnam in the 1960s and 1970s. In fact, Labour and Conservative governments backed every phase of US military escalation and played secret roles in the conflict, declassified files show.
- UK sent SAS team to Vietnam in 1962, flew secret RAF missions to deliver arms, and provided intelligence to US
- UK governments lied to parliament they were not providing military advice to South Vietnam’s brutal regime
- Labour government secretly gave arms to US for use in Vietnam, stressing need for “no publicity”
- It also connived with Washington to deceive UK public over its support for US
- UK governments knew of atrocities against civilians but backed US war aims
- Whitehall only started to advocate a peaceful solution, on US terms, once the war became unwinnable
During its war in Vietnam in the 1960s and 1970s the US dropped more bombs than in the whole of World War Two, in a conflict that killed over two million people. The wholesale destruction of villages and killing of innocent people was a permanent feature of the US war from the beginning, along with widespread indiscriminate bombing.
Britain’s role in the war has been largely buried and must be almost completely unknown to the public. When the UK media mentions the war now, reports often simply reference the refusal by Harold Wilson’s government to agree to US requests to openly deploy British troops.
Although this was certainly a public rebuff to Washington, Britain did virtually everything else to back the US war over more than a decade, the declassified documents show. … continue
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