WATCH: NHS Doctor Don't Take Covid Vaccine Because They Will Be PULLED

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A National Health Service doctor in the UK who was speaking with a patient over the phone – and telling her to not take any more doses of the experimental Covid-19 vaccines because the shots are about to be pulled out of circulation, has caused alarm on social media after a video recording of their conversation went viral this week.

In the recording, which was reportedly of a telemedicine appointment out of Chichester UK, a woman is informed by the doctor that because of information that has been hidden from the public that shows the dangerousness of the rushed vaccines, they will likely be halted globally very soon, and therefore she, and everyone else she knows, should not take any more doses – for their own safety.

https://www.thegatewaypundit.com/2022/01/watch-nhs-doctor-tells-patient-not-take-covid-vaccine-will-pulled-soon-warns-vaccine-data-hidden-public/

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Maybe not so tinfoil...........

EEU Regulators, WHO Call for End to COVID Boosters, Citing Evidence Strategy Is Failing

https://www.theepochtimes.com/eeu-regulators-who-call-for-end-to-covid-boosters-citing-evidence-strategy-is-failing_4220673.html

Report
EEU Regulators, WHO Call for End to COVID Boosters, Citing Evidence Strategy Is Failing


EU drug regulators, World Health Organization experts and the former chairman of the UK’s COVID task force all cited mounting evidence mRNA COVID boosters aren’t working and the strategy should be dropped

European Union drug regulators on Tuesday warned frequent COVID boosters could adversely affect the immune system and said there are currently no data to support repeated doses.

This comes a month after EU drug regulators said it made sense to “administer COVID-19 vaccine boosters as early as three months after the initial two-shot regimen,” amid concerns over the Omicron variant.

According to the European Medicines Agency (EMA), continued booster doses every four months could pose a risk of overloading people’s immune systems and lead to fatigue.

Instead, the agency recommended countries space out the intervals between boosters and coordinate their programs with the onset of the cold season in each hemisphere — following blueprints of influenza vaccination strategies.

“While use of additional boosters can be part of contingency plans, repeated vaccinations within short intervals would not represent a sustainable long-term strategy,” the EMA’s head of vaccines strategy, Marco Cavaleri, said Tuesday during a press briefing.

Boosters “can be done once, or maybe twice, but it’s not something that we can think should be repeated constantly,” Cavaleri said. “We need to think about how we can transition from the current pandemic setting to a more endemic setting.”

Cavaleri said more data is needed on the impact of Omicron on vaccines and a better understanding of the evolution of the current wave to decide whether a vaccine specific to the new variant is needed.

“Preliminary results from recently published studies are showing that the vaccine effectiveness against the symptomatic disease is significantly reduced for Omicron and tends to wane over time,” Cavaleri said.

“It is important that there is a good discussion around the choice of the composition of the vaccine to make sure that we have a strategy that is not just reactive … and try to come up with an approach that will be suitable in order to prevent a future variant,” he added.

Just last month, Cavaleri, speaking on behalf of the EMA, said it made sense to administer COVID boosters as early as three months after the initial two-dose regimen due to “extremely worrying” infection numbers.

“While the current recommendation is to administer boosters preferably after six months, the data currently available support safe and effective administration of a booster as early as three months from completion,” Cavaleri said during a press briefing in December.

WHO Warns Repeated Boosters Not Viable Strategy Against New Variants

The World Health Organization’s (WHO) Technical Advisory Group on COVID-19 Vaccine Composition (TAG-CO-VAC) on Jan. 11 warned, “a vaccination strategy based on repeated booster doses of the original vaccine composition is unlikely to be appropriate or sustainable.”

The expert group, created by the WHO to assess the performance of COVID vaccines, said providing fresh doses of already existing vaccines as new strains of the virus emerge is not the best way to fight a pandemic.

TAG-CO-VAC said COVID vaccines that can prevent infection and transmission, in addition to preventing severe disease and death are needed and should be developed.

Until such vaccines are available, and as the SARS-CoV-2 virus evolves, the composition of current COVID vaccines may need to be updated, the group said.

COVID vaccines need to be genetically and antigenically close to the circulating SARS-CoV-2 variants, be more effective in protection against infection, and should elicit an immune response that is broad, strong and long-lasting in order to reduce the need for successive booster doses, TAG-CO-VAC said.

“It’s over, people,”
Alex Berenson, former New York Times reporter and best-selling author, wrote.
“Aside from a few unlucky Israelis, no one is going to receive a fourth dose of the original vaccine.”


Berenson wrote:

“Everyone with eyes can see it doesn’t work against Omicron — and if you haven’t gotten a third dose, at this point, why would you? You are getting at most weeks of marginally improved protection for potentially severe side effects.

“Instead the WHO is now promising/demanding vaccines based on whatever the dominant Sars-Cov-2 strain is at the moment. That promise is as empty as all the others the health bureaucrats and vaccine companies have made.”


Berenson noted there have been at least five major “variants of concern” in the last year alone, two of which became globally dominant.

“Even the mRNA vaccines cannot be cooked up and delivered fast enough to match whatever strain of virus becomes dominant,” Berenson said. “COVID is faster than the scientists.”

UK Expert Calls for COVID to Be Treated as an Endemic Virus Similar to Flu

COVID should be treated as an endemic virus similar to the flu and mass vaccination should end after the booster campaign, said Dr. Clive Dix, former chairman of the UK’s vaccine task force.

According to the Centers for Disease Control and Prevention, an endemic refers to “the constant presence and/or usual prevalence of a disease or infectious agent in a population within a geographic area,” whereas a pandemic is an “out of control” epidemic that has spread over several countries or continents, usually affecting a large number of people.

“We need to analyze whether we use the current booster campaign to ensure the vulnerable are protected if this is seen to be necessary,” he said. “Mass population-based vaccination in the UK should now end.”

Calling for a “major rethink” of the UK’s COVID strategy, Dix encouraged the ministers to “urgently back research into COVID immunity beyond antibodies” to include B-cells and white blood cells, called T-cells.

Dix said there should be a shift to disease management from viral spreading, and “stopping progression to severe disease in vulnerable groups” should be the future objective.

Written by Megan Redshaw childrenshealthdefense.org This article was originally published on GreenMedInfo.com

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Researcher Calls Out Censorship After Journal Pulls COVID-19 Vaccine Adverse Events Analysis

https://www.theepochtimes.com/researcher-calls-out-censorship-after-journal-pulls-covid-19-vaccine-adverse-events-analysis_4221081.html



Jessica Rose didn’t ask for any of this. She started to analyze data on adverse reactions after COVID-19 vaccines simply as an exercise to master a new piece of software. But she couldn’t ignore what she saw and decided to publish the results of her analysis. The next thing she knew, she was in a “bizzarro world,” she told The Epoch Times.

A paper she co-authored based on her analysis was withdrawn by the academic journal Elsevier under circumstances that raised eyebrows among her colleagues. The journal declined to comment on the matter.

Rose received her PhD in computational biology from the Bar-Ilan University in Israel. After finishing her post-doctoral studies on molecular dynamics of certain proteins, she was looking for a new challenge. Switching to a new statistical computing software, she was looking for an interesting data set to sharpen her skills on. She picked the Vaccine Adverse Event Reporting System (VAERS), a database of reports of health problems that have occurred after a vaccination and may or may not have been caused by it.

She said she wasn’t looking for anything in particular in the data.

“I don’t go in with questions,” she said.

What she found, however, was disturbing to her.

VAERS has been in place since 1990 to provide an early warning signal that there might be a problem with a vaccine. Anybody can submit the reports, which are then checked for duplicates. They are largely filed by health care personnel, based on previous research. Usually, there would be around 40,000 reports a year, including several hundred deaths.

But with the introduction of the COVID-19 vaccines, VAERS reports went through the roof. By Jan. 7, there were over a million reports, including more than 21,000 deaths. Other notable issues include over 11,000 heart attacks, nearly 13,000 cases of Bell’s palsy, and over 25,000 cases of myocarditis or pericarditis.

Rose found the data alarming, only to realize authorities and even some experts were generally dismissing it.

“Clearly, there’s no concern [among these authorities and experts] for people who are suffering adverse events,”
she said.

The usual arguments against the VAERS data have been that it’s unverified and unreliable.

Rose, however, sees such arguments as irrelevant—VAERS was never meant to provide definitive answers, it’s meant to give early warning and, as she sees it, it’s doing just that.

“It’s emitting so many safety signals and they’re being ignored,” she said.

She teamed up with Peter McCullough, an internist, cardiologist, and epidemiologist, to write a paper on VAERS reports of myocarditis in youth—an issue already acknowledged as a side effect of the vaccination, though usually described as rare.

As of July 9, they found 559 VAERS reports of myocarditis, 97 among children ages 12–15. Some of them may have been related to COVID itself, which can also cause heart problems, but there were too many cases to dismiss the likelihood the vaccines were involved, according to the authors.

“Within 8 weeks of the public offering of COVID-19 products to the 12–15-year-old age group, we found 19 times the expected number of myocarditis cases in the vaccination volunteers over background myocarditis rates for this age group,” the paper said.

After two weeks, on Oct. 15, the paper disappeared from the Elsevier website, replaced by a notice of “Temporary Removal.” Not only weren’t the authors told why, they weren’t informed at all, according to Rose.

“It’s unprecedented in the eyes of all of my colleagues,” she said.

When they brought up the issue with the journal, they were first told the paper was pulled because it wasn’t “invited,” Rose said. That was shot down as irrelevant by McCullough, who threatened to sue for breach of contract. The journal then turned to its terms of use, saying it has the right to refuse any paper for any reason.

It’s still not clear why the paper was pulled.

“I do apologise, but Elsevier cannot comment on this enquiry,” said Jonathan Davis, the journal’s communications officer, in an email to The Epoch Times.

In late November, the paper was replaced by a notice that the “article has been withdrawn at the request of the author(s) and/or editor.”

“It just feels like weird censorship that isn’t really justified,” Rose said.

The paper’s conclusions are not necessarily controversial. A recent Danish study concluded, for example, an elevated risk of myocarditis for young people following the Moderna COVID vaccine.

It’s common, however, even for papers that examine potential issues with the vaccines to frame their results in a way that still endorses vaccination.

“That’s what you have to say to get your work published these days,” Rose said.

Her paper did no such thing.

“As part of any risk/benefit analysis which must be completed in the context of experimental products, the points herein must be considered before a decision can be made pertaining to agreeing to 2-dose injections of these experimental COVID-19 products, especially into children and by no means, should parental consent be waived under any circumstances to avoid children volunteering for injections with products that do not have proven safety or efficacy,” the paper said.

The paper also called the vaccines “injectable biological products”—a reference to the fact that they are distinct from all other traditional vaccines.

A traditional vaccine uses “whole live or attenuated pathogens” while the COVID vaccines use “mRNA in lipid nanoparticles,” Rose explained via email. She said the lipid nanoparticles include “cationic lipids which are highly toxic.” Pfizer, the manufacturer of the most popular COVID-19 vaccine in many countries, addressed the issue by saying the dose is sufficiently low to ensure “an acceptable safety margin,” according to the European drug authority, the Committee for Medicinal Products for Human Use (pdf).

Rose also noted that the COVID-19 vaccines haven’t gone “through the 10-15 years of safety testing that vaccines have always had to go through … for obvious reasons.”

By this point, Rose is no longer a dispassionate observer. Reading through countless VAERS reports gave her a window into the hardships of those who believe they’ve been harmed by the vaccines.

“I speak for all of those people,” she said.

In the past, 50 reports of deaths in VAERS would prompt authorities to hit the breaks and investigate, Rose said. In her view, that should have happened with the COVID-19 vaccines a year ago.

Not only has that not happened, but it isn’t even clear what would be enough to convince the authorities to do so.

“What’s the cut-off number for the number of deaths?”
Rose asked.

The counterargument is that the vaccines save more lives than they cost. But in Rose’s view, this logic is flawed since the vaccines haven’t been around long enough and studied thoroughly enough to tell how many lives they may cost.

It is known, however, that VAERS understates adverse events following vaccination—by a factor of anywhere between 5 and as much as 100, based on some estimates.

Submitting a VAERS report takes about 30 minutes and many medical practitioners simply don’t have the time, Rose said. Some may feel that filing the report may get them labeled as “anti-vaxxers.” Some may simply not associate whatever health issue they’re facing with the vaccination. Some may not even be aware VAERS exists.

It’s unlikely that any significant number of the reports would be fraudulent, she suggested, noting it’s a federal offense to submit a false report.

Rose has now joined the ranks of dissident doctors and researchers skeptical of the official line on the vaccines and the pandemic in general. She described it as something she’s compelled to do despite the disincentives involved.

“We don’t want to be doing this. But it is our duty. Doctors swore an oath to do no harm. And researchers with integrity cannot look away from this,”
she said via email.

[Piratesailor]

But it’s amazing how many supposedly smart individuals, and conservatives, will continue to get the vax and the booster.

I gave all this information to a friend and he still went and got a booster.

[red442joe]

My two best friends got the jab. One is the most intelligent person I've ever known. (Dont tell him)
It is interesting, when I told them "every one I talked to that got the jab has been arrogant af", neither commented on my assertions.
They both got my meaning but doubled-down on their insistence everyone should get it.
"Who the **** you trying to convince?"

Joe