WELCOME TO THE NWO GULAG — James Perloff

SGT Report – Feb 2nd, 2023


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James Perloff returns to SGT Report to expose the United Nations Agenda 2030 New World Order World Economic Forum plan for 15-minute gulags where human freedom will go to die.
https://jamesperloff.net/


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Meanwhile in Australia they’re pushing the 5th dose

Free Your Mind – January 30th, 2023



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WE THOUGHT THE ANTI-VAXXERS WERE SILLY THEN MY DAUGHTER DROPS DEAD

OH MY GOD – January 30th, 2023


IT IS OUR CIVIL AND MORAL DUTY TO DO OUR BEST TO BREAK THE WALL OF CENSORSHIP AND TELL THE TRUTH TO THOSE WHO HAVE NOT SEEN IT YET.


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THE PATH TO VICTORY OVER EVIL — Dr. Mark Sherwood

SGT Report – Jan 28th, 2023


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Dr. Mark Sherwood joins me to discuss the bioweapon, the cognitive dissonance of the sheeple and our path to victory over the profound evil of the rulers of the darkness of this world.

Mark’s website:
Sherwood.tv


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Brought To You By Pfizer!

BANNED.VIDEO – January 24th, 2023


Brought To You By Pfizer!


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Elon Musk Shares Personal Experience with Serious JAB Side Effects



Elon Musk Shares Personal Experience with Serious Vaccine Side Effects

‘Hopefully, No Permanent Damage’

BECKER NEWS

Count billionaire tech entrepreneur Elon Musk among those Americans who are concerned about serious Covid mRNA vaccine side effects.

Musk on Friday revealed that he had taken a second booster shot and immediately experienced “major” side effects.

“I had major side effects from my second booster shot,” Musk wrote on Twitter. “Felt like I was dying for several days. Hopefully, no permanent damage, but I dunno.”

The Twitter chief also related a story about his cousin who went to the hospital with a serious case of myocarditis.

“And my cousin, who is young & in peak health, had a serious case of myocarditis,” Musk added. “Had to go to the hospital.”

Elon Musk’s remarks provoked a strong response from people who have had similar experiences, as well as those whom Big Tech silenced when discussing such matters.

“That’s actually crazy,” ALX commented. “What’s sad is that you’d be deplatformed or Fact Checked on Facebook, Instagram, or YouTube for sharing that because it’s not in line with the WHO or ‘independent fact checkers’.”

But Scott Adams, whose post triggered the thread, was skeptical about the claim

“No one gets deplatformed for saying something happened to their cousin,” Adams argued.

“Replies to this say otherwise,” ALX responded. “People often get banned from platforms for *no* reason and their policies have changed so much over time on the subject of vaccines. Just because they’re smaller accounts. Doesn’t mean it isn’t happening.”

Interestingly, Adams’ post had gotten the conversation going by showing the polling disparity between Americans who claim vaccine side effects and the “official” narrative that such adverse events are “rare.”

“How do we interpret this?” he asked.

The post showed a Rasmussen poll where about 7% of the respondents claimed “serious” side effects from the Covid mRNA shots, which considerably exceeds the typical medical threshold for “rare.”

“Question: 68% of 260M Adults (177M) indicate they received the COVID-19 VAX and 7% of those reported major side effects. That translates (177 x .07) into approx 12M people. The CDC says major side effects are ‘rare.’ How many people does CDC estimate had major side effects?” Rasmussen asked while citing a 2009 definition from the European Medicines Agency.

The Vaccine Adverse Event Reporting System (VAERS) is a “passive” system used by the CDC that allows medical providers and the public to report adverse events. There have been over 670,000 adverse events reported after taking the Covid-19 vaccine, according to the VAERS website.

Richard Baris in November polled the self-reporting of “serious adverse effects” from the Covid vaccines – described as events so serious they “prevent daily activity.” This was reported to be 5.2% among all groups: Democrat, Republican, and Independent voters. Independent voters had the highest reported serious adverse effect rate at 6.5%.

There is also medical evidence that the mRNA shots are linked to adverse events.

New research in pre-print publication at the American Heart Association’s journal Circulation shows a link between free spike antigens produced by the mRNA Covid shots and a form of heart inflammation known as myocarditis. In December, the Food and Drug Administration uncovered a risk of blood clotting and pulmonary embolism. The CDC recently announced an “investigation” into an elevated risk of strokes, but quickly shut it down by claiming there was no risk.

The scientific evidence and accumulating personal testimonies are causing a major rift between the American public’s experience of vaccine side effects and the U.S. government’s official narrative that it is all our imagination.

Now that at least one major social media platform is open to citizens sharing their personal experiences, there is reason to believe that the dam is about to break.

*********

(TLB) published this article from Becker News as compiled and written by Kyle Becker

Header featured image (edited) credit: Elon Musk/orginal BN article

Emphasis added by (TLB) editors

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Big Pharma C-19 JAB under FDA harsh glare on Serious Side Effects

Big Pharma C-19 JAB under FDA harsh glare on Serious Side Effects


Lawyer in FOIA suit suggests CDC steered early vaccine recipients to surveys where it could control reported side effects better.

By Greg Piper

Research by the FDA and Taiwanese medical institutions is casting a pall over Pfizer’s mRNA COVID-19 vaccine for both elderly and young populations, raising fresh questions about the CDC’s omission of known severe “adverse events of special interest” (AESIs) from post-vaccination surveys.

Big Pharma has kept political scrutiny at bay by doling out campaign checks. A STAT analysis in 2021 showed two-thirds of federal lawmakers received payouts in 2020, with Pfizer alone funding 228 members.

Last month, Pfizer gave the Kentucky GOP $1 million for its building fund, an indirect boon to Senate Republican Leader Mitch McConnell, the namesake of the state party’s headquarters. The Kentucky Lantern said it may be the biggest party donation in Kentucky history, more than three times larger than the next biggest donor last month.

The FDA research published in the Elsevier journal Vaccine, which was first submitted in May, is notable for focusing on the oldest Americans rather than young people, now widely understood to have greater post-vaccination risk for heart inflammation.

Researchers reviewed Centers for Medicare & Medicaid Services data covering more than 30 million elderly people, looking for 14 “outcomes of interest” following COVID vaccination.

Initial evaluation found Pfizer’s vaccine alone “met the threshold for a statistical signal” on increased risk for pulmonary embolism (54%), acute myocardial infarction (42%), “disseminated intravascular coagulation,” or full-body blood clots, (91%) and “immune thrombocytopenia,” or plunging platelet levels, (44%), they wrote.

When the researchers used “background rates from the flu-vaccinated population as the historical comparator,” AMI and PE still met the signal threshold (41% and 48%).

“After further evaluation, only the RR [relative risk] for PE still met the statistical threshold for a signal,” they said. The RR for pulmonary embolism was more than twice as likely in the “inpatient setting.”

The FDA researchers emphasized that “more robust epidemiologic studies with adjustment for confounding, including age and nursing home residency, are underway to further evaluate these signals.” The agency “strongly believes the potential benefits” of vaccination outweigh the risks of infection.

“If FDA reported any other drug increased lung blood clots 50% can you imagine our media staying silent?” tweeted emergency room doctor Joseph Fraiman, who coauthored an earlier study in Vaccine on severe AESIs in the mRNA vaccine trials and sits on Florida’s new Public Health Integrity Committee.

In a November listserv message, Fraiman explained that the FDA’s October study of insurance databases did not corroborate his Vaccine study because the former ensured “no false positives occur at the expense of false negatives … the opposite of how a surveillance analysis should be conducted.”

The Vaccine study’s corresponding author, University of Maryland pharmaceutical research professor Peter Doshi, has also spoken about it. He’s also a senior editor at the British Medical Journal, which has questioned data integrity in Pfizer’s vaccine trial.

A new study of nearly 5,000 predominantly male Taiwanese teenagers in Springer’s European Journal of Pediatrics adds to the global evidence base that young men have an elevated risk of post-vaccination heart irregularities. The only dispute is what counts as “rare” and “mild.”

The Taiwanese medical researchers found that after the second Pfizer dose in the primary series 17% “had at least one cardiac symptom,” 1% had “abnormal” electrocardiograms, and 0.1% “significant arrhythmias and myocarditis.” None needed hospitalization, “and all of these symptoms improved spontaneously.”

They cited previous studies that found second-dose Pfizer myocarditis rates up to 1.51 per 10,000 in 16-19 year-old males in Israel and increased cardiac arrhythmia in ages 16 and up in the U.K. after second-dose Moderna, whose “safety profile” they called worse than Pfizer’s.

The scope of post-vaccination heart problems might have surfaced earlier, had the CDC included its list of severe AESIs in check boxes for mobile app v-safe, which surveys users after vaccination. It drew 8.5 million participants between its start in December 2020 and April 2021, after which new enrollment slid.

Newly obtained documents in Freedom of Information Act litigation by the Informed Consent Action Network show that the CDC’s “prespecified medical conditions” chart — including heart attacks, myocarditis, stroke and spinal-cord inflammation — appeared in the first version of the v-safe protocol Nov. 19, 2021, predating the launch, ICAN’s lawyer Aaron Siri wrote.

The second version, dated January 28, 2021 but released first in legal discovery, has the same chart. “Despite the foregoing, v-safe was launched without, and was never updated, to include any check-the-box fields for these conditions,” Siri wrote.

That meant v-safe users had to manually write unlisted adverse events in free-text fields, preventing the agency from “clearly calculat[ing] a rate for each harm,” he said. ICAN is still litigating to obtain free-text field entries.

The CDC’s actions raise the possibility it guided the earliest vaccine recipients to v-safe, where it could highlight preferred side effects, so as to keep them from reporting serious AESIs in the publicly searchable Vaccine Adverse Events Reporting System, Siri said.

He noted the CDC told v-safe users to consider VAERS as a backup and also changed its v-safe protocol between January and May 2021 to only call back users who reported a “significant, medically attended health impact,” at which point the agency would decide whether to make a VAERS report. Siri deemed this a “shell game.”

Even when it followed up with v-safe users, the agency could take months to respond, he wrote. One participant filed months of worsening reports, including brain swelling, abnormal heart rhythm, chest pain and nausea, only getting a CDC response more than 200 days later.

“It was clear the CDC representative had not even read her v-safe reports” because the staffer asked when she had recovered, despite her reports indicating she was still on disability, Siri said.

The CDC told Just the News it couldn’t respond to Siri’s characterization of the v-safe decisions “due to ongoing litigation involving this individual and related to this subject matter.”

Pfizer and McConnell’s office did not respond to queries.

__________

RELATED

CDC identifies potential side effects in Pfizer COVID-19 vaccine Does not recommend any changes to its vaccine practices at this time.

*********

(TLB) published  this article  with permission of John Solomon at Just the News.  Click Here to read about the staff at Just the News

Header featured image (edited) credit:  Pfizer CEO/Getty Images

Emphasis and pictorial content added by (TLB) editors

••••

••••

Stay tuned to …

••••

The Liberty Beacon Project is now expanding at a near exponential rate, and for this we are grateful and excited! But we must also be practical. For 7 years we have not asked for any donations, and have built this project with our own funds as we grew. We are now experiencing ever increasing growing pains due to the large number of websites and projects we represent. So we have just installed donation buttons on our websites and ask that you consider this when you visit them. Nothing is too small. We thank you for all your support and your considerations … (TLB)

••••

Comment Policy: As a privately owned web site, we reserve the right to remove comments that contain spam, advertising, vulgarity, threats of violence, racism, or personal/abusive attacks on other users. This also applies to trolling, the use of more than one alias, or just intentional mischief. Enforcement of this policy is at the discretion of this websites administrators. Repeat offenders may be blocked or permanently banned without prior warning.

••••

Disclaimer: TLB websites contain copyrighted material the use of which has not always been specifically authorized by the copyright owner. We are making such material available to our readers under the provisions of “fair use” in an effort to advance a better understanding of political, health, economic and social issues. The material on this site is distributed without profit to those who have expressed a prior interest in receiving it for research and educational purposes. If you wish to use copyrighted material for purposes other than “fair use” you must request permission from the copyright owner.

••••

Disclaimer: The information and opinions shared are for informational purposes only including, but not limited to, text, graphics, images and other material are not intended as medical advice or instruction. Nothing mentioned is intended to be a substitute for professional medical advice, diagnosis or treatment.

Source

Zero Trust Access

thecrowhouse – January 13th, 2023


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