Although there is considerable evidence that a subset of infants has an increased risk of sudden death after receiving vaccines, health authorities eliminated “prophylactic vaccination” as an official cause of death, so medical examiners are compelled to mi-classify and conceal vaccine-related fatalities under alternate cause-of-death classifications.
In this paper, the Vaccine Adverse Event Reporting System (VAERS) database was analyzed to ascertain the onset interval of infant deaths post-vaccination. Of 2605 infant deaths reported to VAERS from 1990 through 2019, 58 % clustered within 3 days post-vaccination and 78.3 % occurred within 7 days post-vaccination, confirming that infant deaths tend to occur in temporal proximity to vaccine administration.
The excess of deaths during these early post-vaccination periods was statistically significant (p < 0.00001). A review of the medical literature substantiates a link between vaccines and sudden unexplained infant deaths. Several theories regarding the pathogenic mechanism behind these fatal events have been proposed, including the role of inflammatory cytokines as neuromodulators in the infant medulla preceding an abnormal response to the accumulation of carbon dioxide; fatal disorganization of respiratory control induced by adjuvants that cross the blood-brain barrier; and biochemical or synergistic toxicity due to multiple vaccines administered concurrently. While the findings in this paper are not proof of an association between infant vaccines and infant deaths, they are highly suggestive of a causal relationship.
by Alexandra Bruce
Ramola D of The Everyday Concerned Citizen is new to me and I love the way she presents information and puts things together.
We’ve previously spoken about the findings of microscopy expert, Dr Robert Young, who published his images of the contents of the four publicly-available jabs using various methods, including Phase Contrast Microscopy, Transmission and Scanning Electron Microscopy and Energy-Dispersive X-Ray Spectroscopy. It was Dr Young who first reported to have found Trypanosoma cruzi in the vaccines.
Ramola reads recent entries in the VAERS system that corroborate Dr Young’s findings. One tells of a woman who is a regular blood donor and that after her second vaccination, her blood donation tested positive for the Trypanosoma cruzi parasite, the same as what Dr Young found in the vaxx.
These parasites are transmissible by blood and organ donation and they cause incurable Chagas disease. Luckily, donor organs and blood are now routinely screened for Chagas antibodies – and that’s how these were discovered.
Myocarditis and fluid accumulation around the heart have been reported in many vaxxed people (often, in the young and athletic). These are known severe symptoms of early-stage Chagas disease.
Ramola finds the three other cases of people reported in VAERS who were screened for this parasite (two teenagers and a 60-year-old) had all presented with heart problems after being vaxxed. She’s then surprised to find it’s now becoming routine to screen all vaxxed patients with heart issues for T. cruzi.
Ramola found an additional three people in the VAERS system, whose symptoms were labeled as “Trypanosoma brucei”. T. brucei is protozoan related to T. cruzi from Africa that causes sleeping sickness in humans.
Patients listed in VAERS as suffering from the symptoms of sleeping sickness are having their symptoms labeled as this exotic parasite species, which does not affect members of the US population. Ramola says this points to an awareness within the medical community that there are parasites in the vaxx.
Interestingly, a primary drug used to treat infection with T. brucei is suramin, which has been touted in the health freedom community for much of 2021 as helpful in mitigating the effects of the vaxx – and of the spike proteins being shed by the vaxxed.
Ramola dives deeper into the transhumanist potentials of Hydra vulgaris and other Cnidaria species and other interesting findings in this most thorough report I’ve yet seen on the topic.
-Forbidden Knowledge TV
by John Kaminski, Florida
We need to rescind all liability shields for all vaccines, bar none, and put the Jewish owners of all these vaccine companies in jail, post haste. Ditto the sorry slugs occupying high political positions who oppress the public with relish while, like our pathetic president, take money under the table from both foreign companies and vaccine makers.
In this new era of massive profits totally in the billions, Big Pharma needs to pay the hospital bills and/or funeral expenses for all the innocent victims it has injured or killed. In addition, those legislators who voted to establish liability shields for pharmaceutical companies needed to be indicted, tried, convicted and jailed (or executed) for conspiracy to commit mass murder of unsuspecting victims of these irresponsible medical trials, as well as to assume appropriate financial responsibility for their knowingly irresponsible actions.
The great COVID scamdemic is like the red scare of the 1950s, when schoolchildren were ordered to hide under their desks during civil defense scares, a maneuver that was supposed to protect them if the Soviets dropped an atomic bomb on them at that moment. It was all a fearful fiction put into their minds by mass media hypnosis, much as the masks and lockdowns are used today to keep people terrified and thus compliant. Those bombs never fell. And this disease does not exist.
But the poisoned injections, now responsible for endless chapters of so-called variant plagues, certainly do.
How many deaths will it take?
The same people who counted the votes recently seem to be ones counting the deaths from these diabolical inoculations. The accuracy at both is total fiction, the first illegally overcounted, the second maliciously undercounted.
So what the Heck is the Harvard Pilgrim Study and what did it really say that about the underreporting of vaccine adverse events?
A 2011 report by Harvard Pilgrim Health Care, Inc. for the U.S. Department of Health and Human Services (HHS) stated that fewer than 1 percent of all vaccine adverse events are reported to the government.
Translation? The 12,000 or so vaccine-related deaths reported to VAERS likely represents only 1 percent of the total number of deaths that have actually occurred. That makes the real number of people who have been murdered by the poison vaccines
This is a number that absolutely dwarfs the total of people who supposedly have died of the fictitious COVID plague, whatever that fabricated figure happens to be these days.
So the cure being worse than the disease is a fantastic understatement.
Similarly, if 100,000 reports of permanent disabilities have been reported to VAERS, that number likely is closer to 10 million. https://thevaccinereaction.org/2020/01/only-one-percent-of-vaccine-reactions-reported-to-vaers/
Although the 1986 Act legally requires doctors and other medical workers who administer vaccines in the U.S. to report vaccine reactions, Congress did not include legal penalties in the law for those who refuse to comply with the reporting requirement.
Therefore, VAERS is really a “passive” reporting system because there is no mechanism to compel compliance and hold vaccine administrators accountable for failing to report serious health problems, hospitalizations, injuries and deaths that occur after vaccination to the government.
You would hope that if a new vaccine wound up getting more death reports in five months than all the others combined over the entire previous 28 years, that might warrant some attention.
The bottom line
Dr. Sean Brooks has a message for you
This coordinated campaign of falsehoods emanating from all mainstream media should really be legally actionable considering all the needless deaths it has caused by its promotion of provably false information. So it’s not just Gates and Fauci and all the other felonious dissemblers with fancy titles who should be prejudicially punished for their premeditated lies, but these harsh penalties should also be extended to every journalist in the world who has repeated these injurious misstatements as well as every doctor who has forsaken his Hippocratic oath in order to keep his job.
We’re talking not only about their complicity in betraying the very people they have sworn to serve, but in being accessories to an unprecedented mass murder of innocents by participating in a lie they pretended — and still do to this very moment — was the truth, which is why sleepwalking people keep dying and the curdled masterminds of our decaying society keep smiling.
John Kaminski is a writer who lives on the Gulf Coast of Florida, constantly trying to figure out why we are destroying ourselves, and pinpointing a corrupt belief system as the engine of our demise. Solely dependent on contributions from readers, please support his work by mail: 6871 Willow Creek Circle #103, North Port FL 34287 USA.
Letter to the Editor
Moderna mRNA gene therapy has just been rubber stamped for use in Australia, is still an Experimental Test Vaccine in America under Emergency Protocol.:
Covid vaccine maker Moderna received 300,000 reports of side effects after vaccinations over a three-month period following the launch of its shot, according to an internal report from a company that helps Moderna manage the reports.
That figure is far higher than the number of side effect reports about Moderna’s vaccine publicly available in the federal system that tracks such adverse events.
Washington: In a first, a new study has pointed out that those taking the Moderna vaccine have reported more side effects than people who get the Pfizer/BioNTech jabs….
Vaccine manufacturers like Moderna are legally required to forward all side effect reports they receive to the Vaccine Adverse Events Reporting System, where they are made public each week.
Run by the Centers for Disease Control and Food & Drug Administration, the VAERS system is crucial to tracking potential problems with vaccines. It helped scientists determine the Covid vaccines may cause heart problems in young adults.
The reason for the gap is not clear. Moderna may simply still be processing the reports, though the number of reports about Moderna’s vaccine in VAERS from the first half of 2021 remained almost flat this week.
Moderna and IQVIA, the company that works with Moderna to handle the reports, did not return emails for comment.
The 300,000 figure comes from an internal update provided to employees by IQVIA, a little-known but enormous company that helps drugmakers manage clinical trials. Headquartered in North Carolina, IQVIA has 74,000 employees worldwide and had $11 billion in sales last year.
Earlier this week, Richard Staub, the president of IQVIA’s Research & Development Solutions division, sent a “Q2 2021 update” which was labeled “Confidential – For internal distribution only.”
A person with access to the presentation provided screenshots of the relevant slide, which clearly explains the 300,000 side effect reports were received over “a three-month span” – not since the introduction of the vaccine in December – and differentiates between them and “medical information queries.”
The slide does not make clear what three months are covered but refers to the “global launch” of the vaccine, which essentially took place in the first quarter of 2021. Whether the slide is referring to January through March or April through June, the 300,000 figure dwarfs the number of reports in VAERS for the Moderna vaccine for either period.
A query of VAERS this morning reveals roughly 110,500 adverse events reports worldwide for Spikevax completed from January through March. All but 650 were in the United States. VAERS also includes 78,000 reports completed from April through June, including 71,400 in the United States.
Those figures overstate the number of reports Moderna has provided, because they include many reports from patients, physicians, and other health-care providers, as well as those from Moderna.
VAERS was established in 1990 and is jointly managed by the CDC and FDA, which contract with General Dynamics to administer it. It has struggled to keep up with the hundreds of thousands of reports it has received about the Covid vaccines since their rollout began in December. For much of the spring, it lagged months behind in making reports public.
VAERS is usually characterized as a voluntary system. But physicians and healthcare providers are required to report certain serious post-vaccine side effects, including deaths. However, the CDC and FDA have no real way to check if they are doing so.
Healthcare providers do have discretion over whether they report less serious side effects. Many have decided not to do so for the Covid vaccines, because the volume of reports is already so high.
However, vaccine manufacturers must forward ALL reports they receive, as the VAERS Website makes clear. It distinguishes between healthcare providers, who are “strongly encouraged” to report various events, and manufacturers like Moderna, who “are required [emphasis added] to report to VAERS all adverse events that come to their attention.”
Moderna’s stock has nearly quadrupled this year as sales of the Covid vaccine have soared. On Thursday, the company reported $4.4 billion in sales and $2.8 billion in profits for the second quarter.
As of today’s update, VAERS contains more than “3,000 reports of deaths” following Moderna vaccinations.
from Alex Berenson, NSW
The active substance in each dose is 0.10 mg mRNA encoding the pre-fusion stabilized Spike glycoprotein of SARS-CoV-2 embedded in lipid nanoparticles. It also contains polyethylene glycol/macrogol (PEG) as part of PEG2000-DMG and is a multidose vial which contains 10 doses of 0.5 mL.
Other ingredients listed include:
- Lipid SM-102, cholesterol
- 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC)
- 1,2-Dimyristoyl-rac-glycero-3-methoxypolyethylene glycol-2000 (PEG2000-DMG)
- Trometamol (tris)
- Trometamol hydrochloride (tris HCl)
- Acetic acid
- Sodium acetate trihydrate
- Water for injection
Uncommon side effects
Some of the more uncommon/rare or unknown side effects that may still occur include:
- Temporary one-sided facial drooping (Bell’s palsy)
- Swelling of the face (It should be noted that swelling of the face can occur in patients who have had facial cosmetic injections.)
- Severe allergic reactions (anaphylaxis)
from Open Access Government https://www.openaccessgovernment.org/what-are-the-side-effects-of-the-moderna-vaccine/106767/
The LNP/ALP/Deep State triumvirate is having trouble getting anyone to take an experimental mRNA shot. It is falling into a heap in Australia
New VAERS Data Include 584 More Reports of Deaths After COVID Vaccines. VAERS data released today (04/23/21) showed 86,080 reports of adverse events following COVID vaccines, including 3,186 deaths and 10,152 serious injuries between Dec. 14, 2020 and April 16, 2021.
Letter to the Editor
CDC Reports 1,637 Deaths Following COVID-19 Vaccinations by Celia Farber, March 13, 2021
Vaccination, Risk & Failure Reports CDC Reports 1,637 Deaths Following COVID-19 Vaccinations The Centers for Disease Control and Prevention (CDC) told The Epoch Times in an e-mail that as of Mar. 8, 2021 over 92 million doses of mRNA vaccines for COVID-19 have been injected, with 1,637 deaths occurring following the injections. The CDC claims the vaccines are safe, but a comparison between the rates of deaths following the vaccines for COVID and those for influenza raises questions.
The Epoch Times hasn’t been able independently to confirm the CDC’s numbers. The publicly available Vaccine Adverse Events Reporting System (VAERS) website shows 1,136 deaths through Feb. 26. Details of these deaths are in a spreadsheet linked at the bottom of this article: symptoms before death, age, gender, time between injection and death, and so forth. (In America) Between Dec. 14 and Feb. 26, 25,072 reports were made to the VAERS system of immunizations with either the Moderna or Pfizer/BioNTech mRNA vaccines (the only two vaccines given during the time period assessed).
The 1,136 deaths represent 4.5 percent of the total number of adverse events reports. Of those who died, 94, or 8.3 percent, died on the same day they got the shot. An additional 150 (13.2 percent) died the day after. Another 105 died two days after, and 68 died three days after. A total of 587 (51.7 percent) died within a week, 215 died within 7 to 13 days, and 124 within 14 to 20 days. 85.8 percent of deaths occurred in people over 60. There were five deaths among those aged 20–29; 10 in those aged 30–39; 23 in those aged 40–49; and 69 aged 50–59.
If you download the numbers and add them to the English yellow card system, it will give a rough idea of how many deaths have occurred so far (that we know about) and a reflection of how bad these test vaccines are – insurance companies voiding 841,000 Australian insurance policies, so far, was a doosie and that was only for life policies, so why would they insure all of the other polices a holder might have too, for example:
Driving a car and have an unexpected reaction from the test virus, or drop dead, causing a multi car pileup, or a fire caused by someone who had the test vaccine that caused a fire, that took out that multi story building in England a last year (something to do with the cladding) or a guy smoking downstairs, who went to sleep and the resulting fire took out 31 apartments, in a block, near where I was living, but if “he was a test vaccine person, what then and I called the fire brigade when the person beneath me went out and left his tea cooking on the gas stove – it was all ready to explode into a fireball, by the time the fire brigade arrived and put it out, but, for the sake of argument, if he was a person who has had a test vaccine…. and so the list of insurances goes on – overseas injury, insurance defaulted because of a test vaccine which might have been the cause of the injury and so on.
Seems to me, not being able to get any insurance, because of a test experimental vaccine, does seem a bit risky these days and would an insurer insure a home you had a mortgage on, or even bought outright for cash, after you have had a test, experimental vaccine – I doubt it – after all, your earning capability might not last the length of the policy and what then?