Kiev blasts calls for oversight of US military aid to Ukraine
Samizdat | July 9, 2022
Kiev has reacted angrily to a call voiced by US Congresswoman Victoria Spartz (R-Ind) to “establish proper oversight” over weapons and aid deliveries to Ukraine. The idea amounts to an attempt to “undermine” existing mechanisms of delivering aid to Ukraine amid the ongoing conflict with Russia, Ukraine’s Foreign Ministry spokesman Oleg Nikolenko said Saturday.
Spartz’s stance is particularly cynical given the Ukrainian origins of the congresswoman, Nikolenko noted in a Facebook post.
“The Congresswoman should stop undermining the existing mechanisms of US military assistance to Ukraine. The Ukrainian side is interacting with American partners with maximum openness, providing them full information about the use of technology,” the spokesman said, claiming that “further bureaucratization” of the process would only help Moscow.
Rep. Spartz sent a stern message to both the US President Joe Biden and his Ukrainian counterpart Volodymyr Zelensky earlier this week, telling them to take at least “three urgent action items” she believes would help “get the situation under control.” According to Spartz, Biden must “stop playing politics, have a clear strategy and align security assistance with our strategy.” Zelensky should “stop playing politics and theater,” and “start governing” instead “to better support his military and local governments.” The third point, related to establishing an oversight mechanism, has apparently irked Kiev the most.
“Congress has to establish proper oversight of critical infrastructure and delivery of weapons and aid,” Spartz stated.
Establishing an oversight mechanism into how money destined to help would be actually spent had been demanded by US politicians before. Back in May, for instance, Kentucky Sen. Rand Paul delayed the passage of the behemoth $40 billion Ukraine bill, urging the creation of the oversight mechanism.
Uruguay Halts COVID-19 Vaccine for Kids Under 13, Judge Demands Officials Turn Over Pfizer Contracts
By Megan Redshaw | The Defender | July 8, 2022
Uruguay suspended COVID-19 vaccines for children under 13 after a judge on Thursday issued an injunction halting vaccinations in that age group until government officials turn over its contracts with Pfizer.
Uruguayan government officials and Pfizer were ordered on Wednesday to appear in court after judge Alejandro Recarey gave them 48 hours to present detailed information on Pfizer’s COVID-19 vaccine while the court considered an injunction request to halt COVID-19 vaccinations for children 5 and older.
The government said a confidentiality clause in the contract prevents it from producing the documents, The Washington Post reported.
According to ABC News, the judge received answers to 18 questions about the safety and chemical composition of COVID-19 vaccines, signed by Health Minister Daniel Salinas, but did not turn over the contracts.
It is unknown whether the answers provided by government officials adequately addressed the questions posed by the judge, who ultimately ordered an injunction based on what was provided.
Salinas, after the court’s ruling, strongly defended the government’s vaccination plan and criticized the judge for questioning the safety of vaccines.
Alvaro Delgado, the secretary of the presidency, said the halt is a threat to public health.
“We’re convinced that it’s crazy to suspend voluntary vaccination because it has a strong scientific backing,” Delgado said at a news conference.
Vaccinations for those older than 13 will continue, the Health Ministry said in a statement.
The government plans to appeal the decision, according to ABC News.
As The Defender reported Wednesday, judge Recarey of the Administrative Litigation Tribunal used his inquisitorial powers to demand the Uruguayan Ministry of Public Health, State Health Services Administration and the President’s Office submit all information regarding the contracts for the purchase of COVID-19 vaccines, including contractual information related to any clauses of civil indemnity or criminal impunity of the suppliers in the event of adverse effects.
The judge is seeking, among other things, to know whether there are clauses in the contracts that promised pharmaceutical companies like Pfizer civil and criminal immunity for adverse effects caused by their vaccines.
Judge Recarey posed a series of questions to government officials and Pfizer regarding the chemical composition, efficacy and safety of COVID-19 vaccines, and required Pfizer to state whether it has “admitted, in any area, internal or external to it and its partners, the verification of adverse effects” of its COVID-19 vaccines in children.
© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
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.
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
Warning: many people will die because of these COVID injections, many healthy children WILL die due to these shots…
“FDA, CDC, NIH, Moderna, & Pfizer secretly told me this”
By Dr. Paul Alexander | June 30, 2022
They said, follow the $CIENCE. Fauci said he is the $CIENCE.
I have been trying to warn. I have written on this here in stack. I try again.
Everything you have been told by government, by CDC, by NIH, by Fauci, by Birx, by Bourla, by Pfizer, by all your government officials, were lies, distortions, exaggerations, meant to mislead you. All pure lies on everything about lockdowns and these failed COVID gene injections. All, every single part was a lie. A deception. This entire COVID pandemic, was a lie! Yes, we had an emergency, but everything done to us the last over 2 years was a fraud hoax, a lie. Every single COVID policy failed. Canada, US, UK, everywhere.
The entire lockdown lunacy failed! All school closures failed, just killed children. Everything was a lie! They knew it would never work but knew one thing, that you as people, as the population, crazily thought, that they as health officials and medical doctors, wanted to do good by them and they could ‘trust’ you. You would do them no harm.
Little did they know. Little did we know the corruptible malfeasants we were dealing with. I include many medical doctors in this.
Trump was right when he early on said it was hoax. He did not mean the virus was a fraud or hoax. He meant the repose. The response was, and he saw what the deepstate and media, and CDC and NIH and Fauci and Birx were doing to him. But he could not stop them. He could, he could have, but he was weak. He then did the unthinkable. He allowed Fauci and Birx to lead a crazy lockdown lunatic policy that harmed and killed thousands of Americans. None of it worked! Not one!
You will come to learn, that 2.5 years of your life was taken away, for a lie! A greed, power drunk lie! By sick malfeasant people. Their motives. That must all be investigated and if it is shown they did this deliberately and caused deaths, we jail them all! Yes, 2.5 years lost to these malfeasants. The COVID injection is a failed ineffective dangerous injection.
I am no anti-vaxxer, but I am against these injections.
I was told by these officials (FDA, CDC, NIH, Moderna, & Pfizer), in confidential secret discussions, that in about 6 to 6.5 years from roll-out, in those who take the injections, they feared mass auto-immune disease and deaths, they feared viral immune escape and very problematic variants, and they anticipated constant deaths from the injections but a major number of deaths to emerge. I could not even understand exactly what they did for it was so haphazard, but these were officials. And they wanted to talk to me. To tell me ‘their truths’.
They said based on all they knew, that the COVID injections could never work, especially the mRNA platform. It never worked in the animal model and was pathological. They told me that in about 6 to 6.5 years, there will be a surge in deaths in persons who take the injections (then about 1 year ago). This was their projection. They advised me they nor their families will never (especially their children) take any of the COVID injections.
The key is the injection works for some people and I argue we do not know how long and what the effects are and this is what I was told. But you understand that too. You cannot take a 15 year process and boil it down to a few months and declare it is safe. They were never safety tested to exclude harms and deaths longer term. We do not know exactly what is coming. But it certainly does not work for a whole bunch of people. Look around, you know people who have been harmed by these injections and died. Do you not? Something is very wrong with these injections. Very wrong and they just will not stop.
I am being open with you to inform you. I am sick and tired, years now, of the lies and fraud and disaster put out by the media, the alphabet health agencies etc. You trusted your public health officials, you think ‘they care about you’, well, they never cared about you, your family, or the truth. It is to them about the $CIENCE.
I think I shared prior that my office was on the 6th floor of the HHS building in DC, Operation warp speed and Moderna were stationed on the 7th floor. FDA, CDC etc. have sub-satellite offices at HHS. At least when I was there and Hahn, Redfield etc. came there daily after congress or White House to see their staff, various persons, persons in various offices.
These people I talked with, came to me out of anger and fear too, they knew who I was and wanted to tell me their stories and how worried they were for the population, and fearful for their lives and own careers as to the COVID injections (and other issues). If they spoke out openly so had to talk secretly.
They were very very dismayed and angered and worried as to why the agencies they worked for e.g. FDA and NIH and CDC etc. and the pharmaceuticals were not properly regulating and conducting the proper safety studies, proper durations of follow-up. They felt the COVID injection program was a pure disaster and should be stopped back then. This is 6 months or so before roll-out. They felt no healthy children should ever be given the very injections they were working on. They were that concerned.
I want to be clear again, based on all I know today, based on what I was told, many many children will die due to these injections. Healthy children will die, not ‘if’, but ‘will die. Healthy children, healthy people, normal people never needed and do not need these injections. I have told you before that (strong research and scholarship by Geert) we will be in a pandemic for 100 years if we continue these injections. It is the COVID injection itself that is driving the variants and these CDC, NIH, Moderna, and Pfizer officials are malfeasants IMO who are continuing this. There is no sound justification. These malfeasants know that they are vaccinating with the Wuhan strain (legacy strain) that has been gone many months now and omicron dominates. The vaccinal antibodies are to the original Wuhan strain and will not hit the omicron spike antigen (original antigenic sin (OAS)).
It is the COVID injection (and consequent non-neutralizing antibodies pressuring the spike antigen) that is causing the vaccinated to become infected, hospitalized, and die. The data is clear. Massive antibody-dependent enhancement, some refer to this as antibody mediated viral enhancement. Some pathogenic priming. All IMO the very same. The recall antibodies are to something that does not exist today. The key is to reduce viral pressure, infectious pressure on the population, so that the sub-optimal injections have less virus to put under pressure. We have effective chemoprophylaxis, we can do this. We have early treatment. This can worked effectively and this can thus help reduce viral transmission. At the same time, the best step is to stop these filed injections.
I want all of these people investigated in proper public and legal inquiries, and if it is shown they did wrong, in proper inquiries, I want them arrested. I want all who made policy decisions that costed lives, to be jailed! All their monies taken!
Dr. Rogers looked at the FDA June 28th meeting and his takeaway is bang on and what we have been saying here for near a year now here:
‘‘Yesterday, the FDA’s Vaccines and Related Biological Products Advisory Committee approved a bivalent Covid-19 shot with the Wuhan strain and the Omicron variant.
The vote was:
19 yes.
2 no.
A few thoughts:
The Wuhan strain is no longer in circulation. So they are vaccinating against a strain that no longer exists.
The Omicron variant that they are going to put into this shot is Omicron BA.4/BA.5:
1. By the time it gets to market in the fall, Omicron BA.4/BA.5 will likely no longer be in circulation.
2. There is no efficacy data whatsoever on vaccines against Omicron BA.4/5.
3. There is no safety data whatsoever on vaccines against Omicron BA.4/5.
4. They do not intend to gather any efficacy or safety data between now and when these shots will be released in the fall:
At the meeting, the manufacturers (Moderna, Pfizer, and Novavax) were asked what their production timelines are… and they said out loud, “So long as we don’t have to provide any clinical data, we’ll have them ready by fall.”
Dr. Rogers is a smart guy.
His work:
Snake Oil: the most vaxxed country in Europe now has its worst COVID outcomes
Are those two things related?
By Jordan Schachtel | The Dossier | June 29, 2022
Virtually every single adult in Portugal has taken at least two doses of “miracle cure” COVID vaccine, with the vast majority “boosted” as well. Yet this month, the most vaxxed country in Europe has consistently reported its worst outcomes.
Once thought to be the best positioned nation in Europe to deal with future bouts with the coronavirus, a nuclear bomb of reality has hit Lisbon.
Out of all the countries in Europe, “Portugal has experienced the most dramatic wave,” the Guardian reports. “With infections per million remaining at a seven-day average of 2,043 on Monday – the second highest new case rate in the world.”
It appears the “miracle cure” vaccines have not only not failed to curb the COVID issue, but has potentially made it worse.
US should pull out of NATO: Rep. Marjorie Taylor Greene
Samizdat | July 1, 2022
Washington should pull out of NATO instead of sending billions of taxpayer dollars to Ukraine and risking a nuclear war, according to a Republican congresswoman who has been highly critical of Washington’s response to the Ukraine crisis.
Georgia Representative Marjorie Taylor Greene, a strong supporter of former President Donald Trump, made the case in a series of tweets on Thursday.
Ukraine is the “new Iraq wrapped up with a pretty little NATO bow, with a nuclear present inside,” she wrote.
“The American people do not want war with Russia, but NATO & our own foolish leaders are dragging us into one. We should pull out of NATO.”
She described the provision of military aid to Ukraine, which she voted against in Congress, as a “proxy war” against Russia that Americans have no appetite for.
“Grinding up Ukraine to fight with Russia is disgusting, they could have been an ally,” she tweeted.
Marjorie Taylor Greene also listed a host of problems that she sees as more pressing for the American people, from soaring inflation to fentanyl overdoses and rampant crime. The only people vying for a conflict with Russia are “those who make money off of it,” she claimed.
“NGOs, defense contracts of all kinds, grants, business deals, even humanitarian aid, political consultants, & more,” she wrote. “War is an industry. A deadly profitable industry.”
Warmongers in Washington seeking war with Russia “should suit up and go fight it” themselves, she suggested. “Send your kids and leave ours alone. Pay for it yourself.”
EU chief can’t find texts with Pfizer CEO
Samizdat | June 30, 2022
The European Commission said it is unable to locate text messages sent between its president, Ursula von der Leyen, and Pfizer CEO Albert Bourla during talks for a massive vaccine deal last year, but denied prior charges of “maladministration” from an EU watchdog.
The commission issued a letter on Wednesday stating that an expanded search for the missing messages had “not yielded any results,” following months of dispute between the EU’s executive body and oversight officials. It argued that due to the “short-lived and ephemeral nature” of texts, they typically “do not contain important information” and are therefore rarely stored.
While von der Leyen revealed in an April 2021 interview that she and Bourla privately communicated for several weeks while negotiating a contract for nearly 2 billion vaccine doses, a journalist’s public information request for the texts was later shot down, with the commission claiming it could not find the messages in question.
The denial triggered a rebuke from the European ombudsman, Emily O’Reilly, who followed up with an investigation last year and blasted EU officials over poor administration and a lack of transparency, saying that “no attempt was made to identify if any text messages existed.” The ombudsman then urged the commission to “search again,” asking it to broaden its criteria in a way that might actually locate the records.
The commission doubled down in its latest response to O’Reilly, however, insisting it had handled the matter properly and made every effort to find the texts. It reiterated that it does not register material that contains no “important information,” and that such documents “are not kept, and, as a consequence, are not in the possession of the institution.”
“The European Commission is of the opinion that it has not treated this request in a ‘narrow way’ and that the search and handling of documents for the purpose of public requests for access to documents … is justified and follows the established practice,” it continued.
The body added that it intends to “issue further guidance on modern communication tools” in hopes of avoiding similar mix-ups in the future, but nonetheless held that its actions were “in line with the applicable legislation and the relevant case law on access to documents.”
The office of the ombudsman, which published the commission’s letter on Wednesday, declared that the response was “problematic on several points,” and noted that a “full analysis” of the case would follow in the coming weeks.
The controversy over the missing texts is not the first dispute regarding a lack of transparency in the EU’s vaccine dealings, as the commission was sued in April by several MEPs, who claimed the negotiations were overly secretive. Though contracts were eventually published, they were heavily redacted in a way that “made it impossible to understand the content of the agreements,” the lawmakers alleged, insisting secrecy “has no place in public agreements with pharmaceutical companies.”
Zelensky demands $5 billion “every month” from NATO, cites security in Europe
Samizdat | June 29, 2022
Ukrainian President Volodymyr Zelensky has urged the US-led NATO bloc to ramp up support of his country amid the ongoing conflict with Russia, claiming that Kiev’s defeat would result in a “delayed” war between Moscow and the whole West. Zelensky made the remarks as he addressed the NATO summit in Madrid via a video link on Wednesday.
“It’s either urgent aid to Ukraine sufficient for victory, or a delayed war between Russia and you,” Zelensky told NATO leaders.
The country needs both direct military and financial aid, Zelensky stated, adding that some $5 billion a month was needed to cover its budget deficit. Top Ukrainian officials have repeatedly called upon the West to provide financial support.
“Financial aid for Ukraine has no less significance than arms deliveries,” Zelensky said. “We need some $5 billon every month, you know that. And this is a fundamental thing, needed for defense and protection.”
To help Ukraine now end this war with a victory on the battlefield, that is, to give a really strong response to Russia’s actions – this is what we, and the entire alliance, the whole Euro-Atlantic community need.
Once the conflict is over, Ukraine must be provided with a decent place in the Western security architecture, Zelensky insisted, rejecting the prospect of Ukraine remaining in a “gray zone” between Russia and the NATO bloc. “We need security guarantees, and you must find a place for Ukraine in the common security space,” he stressed.
Russia sent troops into Ukraine on February 24, citing Kiev’s failure to implement the Minsk agreements, designed to give the regions of Donetsk and Lugansk special status within the Ukrainian state. The protocols, brokered by Germany and France, were first signed in 2014. Former Ukrainian President Petro Poroshenko has since admitted that Kiev’s main goal was to use the ceasefire to buy time and “create powerful armed forces.”
In February 2022, the Kremlin recognized the Donbass republics as independent states and demanded that Ukraine officially declare itself a neutral country that will never join any Western military bloc. Kiev insists the Russian offensive was completely unprovoked.
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As Hillary Clinton kisses up to Henry Kissinger, RT looks at 4 of his most heinous acts
RT | September 3, 2016
… While Clinton retains the ultimate warmongering seal, RT examines some of Kissinger’s most memorable acts… Read full article
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Aletho News- IRAN WALKS OUT ON PEACE DEAL DUE TO TRUMP’S THREATS – w/ Prof. Seyed Mohammad Marandi
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- UK Speech Regulator’s Telegram Questions Point Toward Private Chats
- Cuban FM blasts Rubio for ‘chronically lying’ about US fuel blockade
- Al-Jazeera demands punishment for Israeli officials following latest assassination of cameraman
- Iran opens hundreds of legal cases over US, Israeli aggression: Prosecutor general
- Iran delegation protests Trump’s threat at Switzerland talks, weighs ‘proper’ response: Source
- Terms of US capitulation to Iran presage new era for the region
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- The Story the Media — and the Government — Don’t Want You to Hear
- If Americans Knew
- JNS Policy Summit to kick off in Israel
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- ‘Reproductive genocide’ in Gaza; death toll in Lebanon tops 4,000 (during a ceasefire) – Daily Update
- Israelis Invaded Lebanon And Then Cried Victim When Their Soldiers Got Killed
- FARA Docs: Israel is Spying On Millions Of Christian Americans In Their Churches
- Why US presidents from both parties end up cursing Benjamin Netanyahu
- Israel Asked Facebook to Censor Iran War Content, Internal Documents Show
- Deaths in Gaza undercounted, possibly by 100s of thousands; “Psychopath” Ben-Gvir talks trash – Daily Update
- UNICEF: “Trauma is woven into the very fabric of childhood in Gaza”
- 15 articles a day: The extent of the Israeli army’s media interference
- No Tricks Zone
- THE TRANSCEIVER PARADOX: Why Organoid Intelligence (OI) Could Become Our Ultimate Alien Predator
- German Wind Turbines Face Regulatory Shutdown Due To Excessive Noise
- New Study: Chile’s Relative Sea Level Was 3.2 Meters Higher Than Today During The Mid-Holocene
- Beyond The Pitch: Why FIFA’s World Cup Is One Of Humanity’s Best Investments
- Climate Alarmists Now Using Natural Phenomena To Support Their Claims
- New Study: Significant CO2 Fluxes From Non-Volcanic Sources Are Largely Neglected In Carbon Budgets
- Women Climate Scientists Being Harassed, Insulted By Skeptics, Claims Berkeley Earth Researcher
- Germany’s Longterm Spring Climate Data Show “No Climate Trend”
- New Study: Solar Photovoltaic, Wind Power Fail To Meet Annual Energy Demands 62% Of The Time
- Germany’s Die Welt: “Too Much Is Too Much” … Green Energies Are Cannabalizing Each Other!
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