Sue got back to me and said this:
“DALE CAME THROUGH SURGERY FINE. THEY DID FIND A SMALL BALLOON IN THE SMALL INTESTINES AND THEY REMOVED IT. THE COLON WAS FINE. WHEN I CALLED THE VA, DALE WAS STILL IN ICU. THEY WERE PLANNING TO MOVE HIM TODAY TO THE SURGERY FLOOR.”
KEEP PRAYING BRETHREN!
I don’t think I need to interpret the abstract below for this audience, as most of you are very educated on the subject of the toxicities associated with these jabs – just read the bolded text in the concluding paragraphs.
Biomedicines 2023 Vol. 11 Issue 8
Abstract
The COVID-19 pandemic caused much illness, many deaths, and profound disruption to society. The production of ‘safe and effective’ vaccines was a key public health target. Sadly, unprecedented high rates of adverse events have overshadowed the benefits. This two-part narrative review presents evidence for the widespread harms of novel product COVID-19 mRNA and adenovectorDNA vaccines and is novel in attempting to provide a thorough overview of harms arising from the new technology in vaccines that relied on human cells producing a foreign antigen that has evidence of pathogenicity.
This first paper explores peer-reviewed data counter to the ‘safe and effective’ narrative attached to these new technologies. Spike protein pathogenicity, termed ‘spikeopathy’, whether from the SARS-CoV-2 virus or produced by vaccine gene codes, akin to a ‘synthetic virus’, is increasingly understood in terms of molecular biology and pathophysiology. Pharmacokinetic transfection through body tissues distant from the injection site by lipid-nanoparticles or viral-vector carriers means that ‘spikeopathy’ can affect many organs.
The inflammatory properties of the nanoparticles used to ferry mRNA; N1-methylpseudouridine employed to prolong synthetic mRNA function; the widespread biodistribution of the mRNA and DNA codes and translated spike proteins, and autoimmunity via human production of foreign proteins, contribute to harmful effects.
This paper reviews autoimmune, cardiovascular, neurological, potential oncological effects, and autopsy evidence for spikeopathy. With many gene-based therapeutic technologies planned, a re-evaluation is necessary and timely.
Immun Inflamm Dis 2023 Vol. 11 Issue 3 Pages e807
BACKGROUND AND OBJECTIVES: Since publishing successful clinical trial results of mRNA coronavirus disease 2019 (COVID-19) vaccines in December 2020, multiple reports have arisen about cardiovascular complications following the mRNA vaccination.
This study provides an in-depth account of various cardiovascular adverse events reported after the mRNA vaccines’ first or second dose including pericarditis/myopericarditis, myocarditis, hypotension, hypertension, arrhythmia, cardiogenic shock, stroke, myocardial infarction/STEMI, intracranial hemorrhage, thrombosis (deep vein thrombosis, cerebral venous thrombosis, arterial or venous thrombotic events, portal vein thrombosis, coronary thrombosis, microvascular small bowel thrombosis), and pulmonary embolism.
METHODS: A systematic review of original studies reporting confirmed cardiovascular manifestations post-mRNA COVID-19 vaccination was performed. Following the PRISMA guidelines, electronic databases (PubMed, PMC NCBI, and Cochrane Library) were searched until January 2022. Baseline characteristics of patients and disease outcomes were extracted from relevant studies.
RESULTS: A total of 81 articles analyzed confirmed cardiovascular complications post-COVID-19 mRNA vaccines in 17,636 individuals and reported 284 deaths with any mRNA vaccine. Of 17,636 cardiovascular events with any mRNA vaccine, 17,192 were observed with the BNT162b2 (Pfizer-BioNTech) vaccine, 444 events with mRNA-1273 (Moderna).
Thrombosis was frequently reported with any mRNA vaccine (n = 13,936), followed by stroke (n = 758), myocarditis (n = 511), myocardial infarction (n = 377), pulmonary embolism (n = 301), and arrhythmia (n = 254). Stratifying the results by vaccine type showed that thrombosis (80.8%) was common in the BNT162b2 cohort, while stroke (39.9%) was common with mRNA-1273 for any dose.
The time between the vaccination dosage and the first symptom onset averaged 5.6 and 4.8 days with the mRNA-1273 vaccine and BNT162b2, respectively. The mRNA-1273 cohort reported 56 deaths compared to the 228 with BNT162b2, while the rest were discharged or transferred to the ICU.
CONCLUSION: Available literature includes more studies with the BNT162b2 vaccine than mRNA-1273. Future studies must report mortality and adverse cardiovascular events by vaccine types.
(Caveat: In the USA, the inoculations were unequally distributed and the formulations of the initial shot and the booster were not the same. So, it is difficult to compare adverse event frequencies and even the adverse events).
The article above documents cardiovascular complications post-COVID-19 mRNA vaccines in 17,636 individuals and reported 284 deaths with any mRNA vaccine. This is just those cases found in the literature.
In a recent Epoch Times Article, Senator Ron Johnson – one of the few people in government actually tracking the VAERS system reports:
Mr. Johnson “Sadly, we passed two milestones on VAERS. Over 1 million advisers events and over 21,000 deaths, 30 percent of those deaths occurred on day 0, 1, or 2 following vaccination.
“When will federal agencies start being transparent with Americans? Why do they continue to ignore early treatment?” he concluded.
The US Government Health Resources and Services Administration Data as of August 1, 2023 is below.
This table displays the alleged countermeasure, alleged injury, and amount of compensation paid for each compensated CICP claim filed between Fiscal Years 2010 through 2023. Data is current through August 1, 2023.
The chart has been clipped to show COVID-19 vaccine compensation paid by the US Government (the full chart can be viewed at this link):
That is it folks. A grand total of four people have been compensated. The government has paid out a total of $8,592.55 for the entire injury compensation program. Which is an average of $2,148. per person.
This is sickening.
Beyond sickening. This is infuriating.
In the documented peer reviewed literature (above), there are 17,636 individuals with cardiovascular adverse events (and an unknown number of other adverse events) and 284 deaths.
The VAERS reports shows over 1 million adverse events and over 21,000 deaths. Which evidently only four of those adverse events been investigated by the US government and paid out on. The other 999,996 adverse events have not been assessed yet…
These are real people, who are unable to work. Who have suffered terrible injuries. Young adults who have damaged hearts. Other people who have lost family members and our government is making a mockery of their ruined lives. They are mocking the families of people who have died from these inoculations.
There are no words to express how disgusting this is. Where is Congress? Why is there no investigation into this scandal?
Why is there no public outcry?
What do we have to do to wake people up?
MARANATHA!
Couldn’t happen to a nicer state!
The state of Massachusetts seems to be in a state of panic. Many are wondering what will happen next.
And the Massachusetts Governor has made a decision that left many Democrats shocked.
Massachusetts has been having a hard time dealing with Joe Biden’s border crisis.
They have requested federal aid as their state has become flooded with illegal immigrants from the southern border.
Now, the Massachusetts Governor, Maura Healey, has activated the National Guard in order to get the crisis under control.
The state continues to be flooded with thousands of illegal aliens every day and the state is starting to get desperate.
Fellow Democrats have begged Joe Biden to provide aid and help with the crisis in any way he can.
However, in true form, Joe Biden continues to send billions in aid to foreign countries but refuses to do anything to aid his own allies.
Governor Healey has finally had enough though and has now activated the National Guard.
More than 200 national guardsmen have been activated to help at hotels and shelters providing the “basic needs” for immigrants.
Massachusetts has declared a state of emergency and Governor Healey said that “we need all hands on deck to meet this moment and ensure families have access to safe shelter and basic services.”
There are currently more than 20,000 people living in the emergency shelters in Massachusetts and the majority of these individuals are illegal aliens.
The solution to this ongoing crisis seems to be obvious: shut down the border.
Instead, Joe Biden and even the complaining Democrat leaders of overwhelmed states continue to destroy their own citizens’ lives for the benefit of foreigners entering and living in the US illegally.
The left’s “open border policy” is doing nothing but making things worse for everyone.
Democrats are asking for even more taxpayer money to pay for illegal immigrants’ cost of living.
This model is destroying our country and everything it stands for.
Illegal immigrants should not be allowed in the country in the first place even!
This situation could have easily been avoided if there was a competent President in the White House.
Instead, we have a brain-dead bumbling buffoon who hates America.
Stay tuned to the Federalist Wire as we bring more updates on this story and more. source
I was laughing as I posted this piece. <my bad>
COME LORD JESUS!!
From leohohmann.com
Pharmaceutical giant Pfizer tested its Covid “boosters” on fewer than two dozen people before Joe Biden’s Food and Drug Administration approved the mRNA shots for full public use, explosive new documents reveal.
The watchdog group Judicial Watch obtained documents through a Freedom of Information Act lawsuit which forced the government to turn over the information.
The organization has published the first batch of those documents and they expose Pfizer’s lax testing practices.
According to the documents, Pfizer only tested the safety and efficacy of its Covid vaccine booster on 23 people in 2021 before putting in a request with the FDA to approve the shots for nationwide public use.
Biden’s FDA immediately approved the Covid booster shot and pushed it out to the public at the end of September 2021.
The participants included 11 people aged 18 to 55 and 12 people aged 65 to 85, Judicial Watch reported. Of the younger group, there were nine females and two males; eight of whom were white, one was black and two were Asian. Of the older group, six were female, six were males, and all were white.
The FDA said it based its decision to approve the shots on the documents presented by Pfizer, as well as input from the CDC, the Israeli Ministry of Health and the University of Bristol in the UK.
Based on those paltry numbers of just 23 human guinea pigs and then checking in with the Israelis and a single British university, the FDA gave its rubber stamp and a total of 8.9 million people across America were injected with Covid boosters within three weeks.
Judicial Watch released 58 pages of records from the FDA showing that a Pfizer “study” administered the shots to just 23 people in 2021 to gauge reactions to its “booster.” The FDA indicated that this production of records “represents our complete response to your request; no additional productions are anticipated.”
The records were obtained in response to a March 2022 lawsuit filed after the Department of Health and Human Services refused to respond to an August 2021 Freedom of Information Act (FOIA) request. (Judicial Watch Inc. v. U.S. Department of Health and Human Services (No. 1:22-cv-00730).
The request was for records “submitted by Pfizer and BioNTech to the FDA, including BARDA, relating to ‘booster’ vaccinations for the SARS-CoV-2 virus.”
Biomedical Advanced Research and Development Authority, BARDA, has been heavily involved with the development of the COVID-19 vaccine. According to its website:
The Biomedical Advanced Research and Development Authority (BARDA) provides an integrated, systematic approach to the development of the necessary vaccines, drugs, therapies, and diagnostic tools for public health medical emergencies such as chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks; pandemic influenza (PI), and emerging infectious diseases (EID).
These documents are just the latest confirmation of Robert F. Kennedy Jr.’s statement about the safety of “vaccines.” None of them are put through the sort of rigorous, double-blind placebo-controlled testing protocols that other medicines are required to go through. And we know that, even with these rigorous testing protocols, there are many examples of medicines that slip through and end up injuring and killing people, forcing companies to pull them from the market.
But with vaccines, none of these rigorous and lengthy testing protocols are followed.
RFK Jr. explains why in the 2-minute video below.
Kennedy explains that vaccines are not considered “medicines” but rather “biologics” which are developed under quasi-military conditions as part of a national defense program against potential biological warfare.
Once Congress created this loophole, corporate pharma companies rushed in to take advantage of a system that allows them to bring vaccines to market very quickly without rigorous pre-licensing safety tests. That’s one reason why there are so many vaccines, 72 of them now “recommended” by the CDC as part of the childhood vaccine schedule between birth and age 16. They are extremely profitable and the manufacturers are not accountable for the safety of their products. It’s virtually impossible to sue them for wrongful death or serious injury.
“There’s not a single vaccine that’s ever been tested in a pre-licensing safety study that’s part of that 72,” said Kennedy.
What kind of nation throws its children to a profit-driven pharmaceutical industry without any safeguards? This is criminal.
But when it comes to the “boosters,” this affects not only children but Americans of every age.
A new Covid booster will be released later this month, just in time for a new round of Covid hysteria being cranked up in the mainstream corporate media, which is largely funded by corporate pharmaceutical makers. You just can’t make this stuff up, folks.
Judicial Watch President Tom Fitton issued a statement warning the American people to carefully examine the documents his organization has made available before being pressured by the Biden administration to take another booster.
“With the planned push for new boosters by the Biden administration, the public would do well to examine these troubling documents about the shotgun approval of prior COVID boosters,” said Fitton.
These documents prove that everything you’ve heard about “safe and effective” is a smokescreen designed to deceive. All of this talk in the corporate media about “the Covid vaccines are the most rigorously tested vaccines in history,” is nothing but lies.
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