Deranged Democrats Outraged as Respected Historian Blisters 1619 Project

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Nothing outrages the Democrats more than truth and accuracy. Hellzapoppin.

Left Upset as Respected Historian Blisters 1619 Project

Daybreak Insider, September 21, 2021:

Princeton historian Sean Wilentz wrote in his lengthy piece regarding the take on the American Revolution

“If it were a high school history paper, that discussion alone would have been grounds for failure. It’s rare, after all, to read a student get every single stated fact perfectly wrong, in support of a proposition for which there is no other evidence cited, on two of the most important topics in all of U.S. history, indeed, all of modern history, the causes of the American Revolution and the origins of antislavery. But this wasn’t a high school paper, it was the New York Times Magazine, and the author was, according to her contributor’s biography, a highly acclaimed journalist. The essay may have been historically fallacious, but it was also inflammatory and attention-getting (Historica).

From Dan McLaughlin:

Wilentz has fired another salvo against the 1619 Project, its editor and lead essayist Nikole Hannah-Jones, Times Magazine editor in chief Jake Silverstein, and more broadly, the intellectual climate of “anti-racist” politics that produce warped history while intimidating serious scholars into silence (National Review).

EDITORS NOTE: This Geller Report column is republished with permission. ©All rights reserved.

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FDA Panel Member on COVID “Vaccines”: “Heart Attacks Happen 71 Times More Often….”

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“I had a heart attack….”

A bit more than a month ago I wrote about “My troubling COVID vaccine story experiences.” Aside from citing a friend who developed heart inflammation after taking a coronavirus genetic-therapy agent (GTA, a.k.a. a “vaccine”; more on this later), I mentioned that I’d had some unusual experiences: I encountered two men within a relatively short period of time, at the same recreational facility, who told me they’d had heart attacks — after taking SARS-CoV-2 GTAs.

One man suspected the GTA induced his coronary; the other fellow was oblivious, though his attack occurred the month after his shot.

At the time, I mentioned that though I’d been reporting on GTA-coincident complications for a while, I aimed to be objective and thus had to consider that my experiences *could* have been mere coincidences. All the men in question are over 60, at ages where heart issues are more common, after all. On the other hand, I pointed out that I wasn’t looking for these stories or asking related questions, and I’m not a social butterfly who regularly interacts with large numbers of people.

But then it happened again. At the same recreational facility approximately two weeks ago, I saw a man I’d met there previously. After extending mutual greetings, one of the first things he said was, “I had a heart attack.”

Sure enough, I learned that he’d taken a GTA.

He didn’t connect the two occurrences; in fact, when I mentioned I’d met other men suffering the same fate, he suggested it was coincidence.

But this thesis appears to have gone out the window.

Consider the testimonial of Steve Kirsch, executive director of the COVID-19 Early Treatment Fund and also identified as a Food and Drug Administration (FDA) panel member. In an eight-hour virtual discussion of the Vaccines and Related Biological Products Advisory Committee released Friday by the FDA, Kirsch said there “are four times as many heart attacks [as is normal] in the treatment group in the Pfizer six-month trial report — that wasn’t bad luck.”

What’s more, “The VAERS [Vaccine Adverse Event Reporting System] shows heart attacks happen 71 times more often following these vaccines compared to any other vaccine,” he continued (video below. It should automatically start at 4:20:17; if it doesn’t, you’ll have to fast-forward to that point).

Among other things, Kirsch presents the following table:

Study source Excess deaths

required to save

COVID life

 Lives saved
Pfizer 6 month* 5 1
VAERS 2 1
Nursing home (booster)* 6 1

*Not statistically significant

Kirsch is, of course, not the only informed person warning about or wary of the GTAs. Though the shot-hesitant are portrayed as knuckle-dragging, medieval scientific obscurantists, a study found that the education-level-defined group least likely to be vaccinated is Ph.D. holders. Even more strikingly, it emerged in May that at least 40 percent (this figure may be different now) of FDA employees and those at Anthony Fauci’s NIAID hadn’t yet been vaccinated. Did they know something Fauci wasn’t telling?

Then there are the nurses choosing to resign in droves rather than take the GTAs. (In fact, a New York hospital was consequently left so short-staffed it had to cease delivering babies.) One such nurse, who faces dismissal for refusing the jab and wishes to remain anonymous, contacted me after reading my first COVID-experiences article. Here’s her explanation for why she won’t take a GTA (edited for punctuation):

I have seen many, many new diagnoses of cancer; many, many new diagnoses of blood clots; many new diagnoses of atrial fibrillation; GI bleeding; and many, many, many new and “unexplained” diagnoses of thrombocytopenia. I have also seen and heard many reports of unexplained neurological events, one of them being my sister who experienced a neurological event out of the blue (she seems ok for now other than she suffered a bad knee injury when she passed out for NO reason!). There are many, many prolonged hospitalizations and readmissions for what I classify as shot-related events. But not one single soul in my circle/…organization is asking questions [or, presumably, recording these as GTA-coincident adverse reactions].

Below are the testimonials of three other people who contacted me and who I’m also keeping anonymous (edited for grammar, style and punctuation).

  • “My 74-year-old wife had a check up in January; found no problem. On March 13 she had her second COVID vaccination; the next day her heart went into afib. She endured three trips to emergency room and one week in the hospital. The ER doctor said she was the second one that day with the same story. Her heart doctor said she is not the only one with her story.”
  • “I am a work-at-home person with limited social contact and also have what I believe is a relatively high number of anecdotal myocarditis and Bell’s Palsy stories of friends and their families, especially after their second prick,” writes a woman. “Most dismiss their conditions as coincidental, so I’m guessing most are not reported, sadly.”

Another woman, in Middle America, mentioned that her family members were rushing to get the GTAs and then wrote, “I have been quietly observing some medical issues that may be related to adverse affects.” She then provided the following list:

Cognitive

  1. My brother’s daughter made a plan to kill herself and had to be hospitalized.
  2. My sister’s husband is having a very sudden noticeable deterioration of cognitive ability.

Immunity

  1. My son is experiencing swelling of the lymph nodes in his neck and arm pits.

Heart related

  1. My very fit athletic 16 year old granddaughter is experiencing swelling of her hands and feet. (This seems related to circulation at least.)

Some of the above is “scientific”; much of it is anecdotal. Yet there’s far, far more evidence of the GTAs’ downsides than I’ve mentioned here (this interview with renowned China virus doctor Peter McCullough is a must-watch). Moreover, dismissing “anecdotes” — even when enough of them, intelligently analyzed, can be tantamount to a scientific sample — is foolishness.

Oh, and here’s why I label the GTAs just that: Traditional vaccines work via introduction of an organism into your system that induces an immune response corresponding to that organism. China virus GTAs work differently: They introduce a genetic code into your bloodstream that programs your body to (supposedly) create an immune response. Yet as Dr. McCullough, one of the most published experts in his field, pointed out, we’ve never asked the human body to do this before.

Making this even more tragic is that becoming a GTA guinea pig is wholly unnecessary. McCullough also informed that COVID has always been treatable, and with early intervention it’s fatal to precious few. In fact, because they’ve demonized efficacious early treatments, Fauci and his feckless medical establishment fellows have blood on their dissembling, unholy hands.

As for Steve Kirsch, he’s firm on where he stands. He said simply and definitively, “The vaccines kill more people than they save.”

Contact Selwyn Duke; follow him on Gab, MeWe, or Parler; or log on to SelwynDuke.com.

©Selwyn Duke. All rights reserved.

Chasing the China Virus Dragon!

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Again I use a guest writer or two for you. The foreword by a very good friend and extremely knowledgeable former Federal Agency official. A true patriot. The second a link to a story from Israel on the ineffectiveness of the China Virus booster vaccinations. It makes interesting reading. Enjoy and share widely please using this blog. As always credits and links at bottom of this article.

1st Writer Pete A. Perhaps, it is because I come from a 15-year world of federal drug enforcement that I fall back on a truism that affects the drug junkie. It is called ‘chasing the dragon.’ Once the victim is ‘hooked’ on heroin, most never escape until they are stone-cold dead. Their addiction is a treadmill they can not get off – a race to attain that ever-greater high until they kill themselves. This is what I see going on, as described in the below article, with the great Covid injection genocide.
Isreal is the forerunner, leading the pack on this treadmill and there will be no getting off until the vaxed have taken their final fix. I have come to believe their bodies are now pumping out spike protein every time their immune system is challenged, which then actually infects them with the spike protein. Most importantly, the public has yet to fully understand that the injections have destroyed the vaxed innate immune systems and the ‘fix’ can do nothing more than forestall the inevitable.
There is hope for those who got the shot. It is now clear that this genocidal experiment was not uniformly administered across all populations. That is, not everyone was injected with the same concoction. The batches were numbered and controlled with different potions being administered across the populace. Therefore, there is a reason for hope, hope that if you received an injection it may have been inert or at least not of the life-threatening kind. What you need to take away as you enter the fall and winter flu season is to at least arm yourself with the commonly recognized therapeutics as if you were unvaccinated or not naturally immune from having had the Covid.

Israeli Researchers Can Confirm Only 12 Days of Protection From COVID-19 Virus with Booster Shot – by Shane Trejo.

Israeli researchers have only been able to demonstrate that the COVID-19 booster shot provides a proven 12 days of protection from the virus after being administered to people aged 60 or above.

However, the vaxx pushers and their captive propagandists in the media are spinning these findings as proof of vaccine efficacy.

The Jerusalem Post is reporting that the third Pfizer vaccine provides a ten-times boost of the immunity within individuals against individuals who have received only two vaccine shots. These findings, of course, presume that there was any real immunity boost given from the vaccines to begin with.

Thus far, nearly three million Israelis have received the third booster shot. Israel has emerged as the world leader in vaccine compliance, and their COVID-19 case totals keep shattering recordsas more Israelis line up to comply.

The authors claim that the study makes it “evident that booster vaccination is very effective at reducing the rate of both confirmed infection and severe illness.” Perhaps they came to these dubious conclusions after making considerations about preserving their budgets and maintaining their prestigious jobs.

Big League Politics has reportedabout how cases are surging in countries that have boasted the most compliance with the vaccine:

“Many countries listed as a high travel risk by the Centers for Disease Control and Prevention (CDC) have enforced vaccine compliance the best according to data from the Johns Hopkins University (JHU) School of Medicine.

The nations of Malta, the United Arab Emirates, Seychelles, Uruguay, Chile, Bahrain, Mongolia, Israel and Ireland are on the CDC’s list of Level 4 countries for COVID-19 risk. This is despite all of these countries vaccinating well over 50 percent of their population, with countries listed reaching as high as 78.8 percent compliance.

The data compiled by JHU omits Gibraltar, which also appears as a Level 4 country by the CDC. Gibraltar has boasted 99 percent rates of vaccine compliance, the highest of any country in the world, which has corresponded with a recent case spike and a renewal of crippling lockdown policies.

The CDC advises Americans to “avoid travel to these destinations,” adding that “if you must travel to these destinations, make sure you are fully vaccinated before travel.” Of course, there is no guarantee that a fully-vaccinated traveler would be protected any more than the individuals in those countries where vaccination levels are high but cases continue to spike.

As the vaccines fail to contain the spread of the virus, pharmaceutical corporations that have already cashed out mightily due to the crisis get ready for their next fear-induced pay day.”

Despite the Big Pharma-owned public health establishment’s spin to the contrary, the vaccine is failing on all the metrics that the public was sold upon. The public must resist because this is only the beginning of a cruel technocracy that will feature unending invasive and nonsensical mandates.

<blockquote class=”wp-embedded-content”><a href=”https://bigleaguepolitics.com/israeli-researchers-can-confirm-only-12-days-of-protection-from-covid-19-virus-with-booster-shot/”>Israeli Researchers Can Confirm Only 12 Days of Protection From COVID-19 Virus with Booster Shot</a></blockquote>

Israeli Researchers Can Confirm Only 12 Days of Protection From COVID-19 Virus with Booster Shot

©Fred Brownbill. All rights reserved.

Biden Bans Selling Covid Anti-body Treatments to Florida, Gov. DeSantis Will Buy Antibodies DIRECT From Manufacturer

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Click here for Information on Monoclonal Antibody Therapy | Florida Department of Health

Biden pulling therapeutics is a death sentence. It’s murder.

SORRY BIDEN! DeSantis To Buy Antibodies DIRECT From Manufacturer After Biden Tried Crippling Florida

In a defiant move against President Joe Biden, Florida Governor Ron DeSantis will be buying antibody treatments against COVID-10 directly from the manufacturer after Biden purposely slowed the supply to Florida, putting many Americans in danger.

By Collin Rugg, TP, September 18, 2021:

“Just last week on September 9th, President Joe Biden said that his administration would be increasing shipments of monoclonal antibodies in September by 50%, and yet on September 13th, HHS announced that it was seizing control of the monoclonal antibody supply and that it would control distribution, and then on September 14th, the announcement was more than 50% of the monoclonal antibodies that had been used in Florida were going to be reduced,” DeSantis said. “So this is a dramatic reduction, and I’d say it’s doubly problematic because what Shane Strum and folks in Tampa General and these other hospital systems that have been doing this, they’re not getting it from the state.”

“What the HHS and the Biden administration is now doing is they’re saying that all of the reduced amount will go to the state, and we’re responsible not only for sourcing our sites, which we’re happy to do, but any infusion center, any provider, any hospital will have to come through the state, and to just spring this on us starting next week, we’re going to have to do that,” DeSantis continued. “There’s going to be a huge disruption and patients are going to suffer as a result of this.”

DeSantis made it perfectly clear that he is going to “work like hell to make sure” that Florida “can overcome the obstacles that HHS and the Biden administration” are imposing against his state, adding that the treatment has saved lives.

“To just kind of pull the rug out from anyone a week after the president himself said they were going to be increasing the distributions by 50%, it’s very, very problematic,” DeSantis said. “What I am doing though, is we’re going to try to cover the bases.”

DeSantis noted that he had a call with GlaxoSmithKline executives and believes Florida will be able to purchase the antibody directly from them.

Donald Trump Jr. reacted to the news of how Biden was limiting treatment options for COVID-19, accusing him of putting Americans in danger.

“Americans will die because of Biden’s despicable decision to punish his political enemies in red states by restricting their ability to secure life-saving monoclonal antibody treatments for all that need them,” Trump tweeted. “Their blood is directly on Joe’s hands.”

“Antibody treatments aren’t a substitute for vaccines But they have prevented thousands of hospitalizations including in breakthrough cases,” Sen. Marco Rubio (R-FL) also noted. “Now in a move that reeks of partisan payback against states like Florida, the Biden administration is rationing these treatments.”

RELATED ARTICLE: Effectiveness Gap Between Moderna’s, Pfizer’s COVID-19 Vaccines Widens Over Time: Study

EDITORS NOTE: This Geller Report column is republished with permission. ©All rights reserved.

Quick note: Tech giants are shutting us down. You know this. Twitter, LinkedIn, Google Adsense, Pinterest permanently banned us. Facebook, Google search et al have shadow-banned, suspended and deleted us from your news feeds. They are disappearing us. But we are here. We will not waver. We will not tire. We will not falter, and we will not fail. Freedom will prevail.

Subscribe to Geller Report newsletter here — it’s free and it’s critical NOW when informed decision making and opinion is essential to America’s survival. Share our posts on your social channels and with your email contacts. Fight the great fight.

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COVID Vaccines: The Dog Is Chasing Its Tail.

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Today’s blog comes from a friend Chris Wright and I found it interesting, as well as relevant and I wanted to share it with you – my readers! It is well written and you may see more of his writing as the time goes on. There are many links that are worth your time hitting as you read. As always please share from here and share far and wide!! In liberty. Fred B!

The Story of Ivermectin:

Hi all,

I have questioned the integrity of public health officials concerning their pronouncements on COVID many times in previous commentaries.  I have asserted the whole subject has become completely politicized and we’re not getting the straight story.  I’ve given you story after story about how the number of COVID cases is being overstated.  I’ve questioned why authorities continue to push masks when masks have not been shown to be of much use.  I’ve talked about the now over 14,000 deaths in the U.S. from adverse reactions to COVID vaccines.  With respect to the latter, I’ve been accused of misusing the data and spreading misinformation, but I wrote a rebuttal to my accusers [Daily Skirmish – 9/1/21] and nobody on a health policy listserv or my other accusers answered.  As of this moment, my rebuttal stands unrebutted.

And so it is I have concluded we’re not getting the straight story about the vaccines, either.  In the first place, there are recent reports immunity from vaccines can wear off after six months.  When they said ‘get vaccinated and you can go back to a normal life’, they didn’t say, ‘and, oh by the way, it’s just for six months,’ did they?  Secondly, a published medical doctor is sounding the alarm about “vaccine chasing”, the idea that mass vaccination causes new variants to emerge, just like the overuse of antibiotics causes antibiotic-resistant strains to emerge.

Dr. Richard Fleming writes there is “no statistically significant difference in the number of people who died who were un-vaccinated compared with those who received the vaccines.”  Then, in discussing breakthrough cases after vaccination, “there was no statistical difference in the number of people who were diagnosed with COVID independent of whether they were vaccinated or not.”  This is true for Pfizer and Moderna.  Johnson & Johnson did a little better, but the comparatively good results shown at 14 days disappeared by 28 days after vaccination.

For all that trouble, in 33 countries – notably Israel and the U.K. – Delta and other new variants emerged after mass vaccination.  As a result, the overall number of cases did not decrease in any of those countries despite mass vaccination  So, mass vaccination is basically a failure.  Not only that, Fleming writes, there are concerns the vaccines are causing vascular disease and neurological symptoms.  Then comes the kicker:   “There is of course also the mounting number of deaths associated with the use of these Drug Vaccine Biologics,” Fleming writes, referring to the same government data for which my detractors came after me.

Fleming sums it up this way:  “As we continue the Mass Vaccination program of using these Drug Vaccine Biologics, that according to the EUA data itself fail to show a statistical reduction in COVID-19 cases or death, with an increasing number of adverse events including death; we are simultaneously producing a Pressure Selection of Variants that will produce what appears to be a never ending cycle of Pressure Selection-Vaccination.”

A never-ending cycle, like a dog chasing its tail.  The more we vaccinate, the more variants we get.  The more variants we get, the more vaccines we need.  Meanwhile, the people pushing the party line on vaccines are getting rich, careers are being made, and public health authorities get to feel oh, so important.

And now you want to tie me down, stick a needle in my arm, and tell me I can’t work or travel out of state if I don’t comply?  Stop this train, I want to get off.

Dr. Fleming discussed his work further on Secure Freedom Radio on 9/16/21.

Visit The Daily Skirmish

Best wishes,
-Chris

©Fred Brownbill. All rights reserved.

Tipping Point – Daniel Horowitz on Vaccine Mandates [Video]

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Rumble — Daniel Horowitz on Vaccine Mandates.

©OANN – Tipping Point. All rights reserved.

RELATED VIDEO: RNC ad shows Fauci flip-flopping on vaccine mandates.

VIDEO: Fraudulent Biden Told OSHA to Hide Info on Vaccine Side Effects

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Strong-arming and lying — it’s what the Democrats do.

Lara Logan Video: Biden Told OSHA to Hide Info on Vaccine Side Effects

Strong-arming and lying — it’s the Democrat way.

By: Front Page Magazine, September 17, 2021

In the short video below, Fox News’ Lara Logan explores President Biden’s manipulation of the Occupational Safety and Health Administration (OSHA) to promote the COVID vaccine: “Joe Biden didn’t even bother to ask Congress. He said the new mandate is justified because COVID is an ‘emergency.’ Then he walked away without taking questions, once again.”

Check out the video:

And more here:

“As a result, OSHA will not enforce 29 CFR part 1904’s recording requirements to require any employers to record worker side effects from COVID-19 vaccination at least through May 2022. OSHA will reevaluate the agency’s position at that time to determine the best course of action moving forward. Individuals may choose to submit adverse reactions to the federal Vaccine Adverse Event Reporting System.”

See edit here: https://www.osha.gov/coronavirus/safework

See OSHA page in Way back machine internet archive at beginning of the year before edit: https://web.archive.org/web/20210201160820/https://www.osha.gov/coronavirus/safework

It is the latest event showing an organized conspiracy racket between the big pharmaceutical and state governments to promote sales and use of vaccination across the world.

In the conspiracy, any alternative treatment including government approved medications like monoclonal antibodies, have been suppressed with the vaccine pathway being the only one advertised and now mandated with increasing distribution even to kids with a reported risky health benefit-risk ratio.

The World Health Organisation, WHO has also in the past been accused of conspiring with and on big pharma’s payroll to inflate the H1N1 epidemic.

This happened back in 2010.

RELATED VIDEO: Rand Paul weighs in on COVID-19 antibody treatments

RELATED ARTICLES:

FDA PANEL DISCUSSION: “COVID Vaccines Are Killing More People Than They’re Saving”

FDA Panel Overwhelmingly REJECTS BIDEN’S BOOSTER SHOT Plan For All Americans

EDITORS NOTE: This Geller Report column is republished with permission. ©All rights reserved.

Quick note: Tech giants are shutting us down. You know this. Twitter, LinkedIn, Google Adsense, Pinterest permanently banned us. Facebook, Google search et al have shadow-banned, suspended and deleted us from your news feeds. They are disappearing us. But we are here. We will not waver. We will not tire. We will not falter, and we will not fail. Freedom will prevail.

Subscribe to Geller Report newsletter here — it’s free and it’s critical NOW when informed decision making and opinion is essential to America’s survival. Share our posts on your social channels and with your email contacts. Fight the great fight.

Follow me on Gettr. I am there, click here. It’s open and free.

Remember, YOU make the work possible. If you can, please contribute to Geller Report.

Summary: Covid-19 Vaccine Concerns

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Huge props to Sharyl Attkisson for researching the critical data assembled in this comprehensive report.

Exclusive Summary: Covid-19 Vaccine Concerns

 by Sharyl Attkisson

  • Updated Sept. 12, 2021 with study finding teenage boys face much higher heart risk from vaccine than Covid
  • Updated Sept.10,2021 with Israel study on majority of hospitalized being vaccinated
  • Updated Sept. 9, 2021 with CDC study about increased myocarditis/heart inflammation risk, lymphadenopathy, appendicitis, and herpes zoster infection
  • Updated Sept. 4, 2021 with acute CNS demyelination after Pfizer and Moderna vaccines
  • Updated Aug. 30, 2021 with Functional Neurological Disorder
  • Updated Aug. 24, 2021 with waning immunity
  • Updated Aug. 17, 2021 with Bell’s Palsy analysis, Hong Kong
  • Updated Aug. 16, 2021 with Antibody Dependent Enhancement (ADE) study
  • Updated Aug. 5, 2021 with heart disorders more common than CDC reported from database
  • Updated July 22, 2021 with EU warning about Guillain-Barre autoimmune paralysis after Johnson and Johnson vaccination.
  • Updated July 12, 2021 with new FDA warning of Guillain-Barre autoimmune paralysis cases after vaccination.
  • Updated July 12, 2021 with reports of Graves disease autoimmune disorder after vaccination.
  • Updated July 1, 2021 with reports of Guillain-Barre paralysis cases after vaccination.
  • Updated June 30, 2021 with news of first case of blood clot disorder in double-dose RNA vaccine.

If you find yourself confused about the mixed guidance when it comes to Covid-19 vaccines and safety concerns, you’re not alone.

While the Centers for Disease Control (CDC) is marketing widespread use of the emergency-use vaccines in the U.S. for both old and young alike, many other countries are limiting Covid-19 vaccine use. Health officials around the world are giving varying advice on safety issues as Covid-19 vaccines are given to more people, and more information can be collected.

Read CDC’s information here.

Below are summaries of some of the concerns that have emerged or been raised by medical officials.

Click here to jump to: Summary by safety concern

Click here to jump to: Summary by vaccine

Click here to jump to: Summary by country

Click here to jump to: Additional reading and studies

Summary by safety concern

General

In the UK, some scientists analyzed adverse event reports and called upon the Medicines and Healthcare Products Regulatory Agency to stop the Covid-19 vaccines as “not safe for human use” due to reports of issues with bleeding/clotting, pain, immune system, neurological, loss of sight/hearing/smell/speech, and questions about impact in pregnant women.

A petition of scientists led by Linda Wastila, Professor, Pharmaceutical Health Services Research University of Maryland School of Pharmacy is calling for Covid-19 vaccines to be disapproved.

Fifty-seven authors from 17 countries have signed an endorsement urging that Covid-19 vaccinations be stopped unless new safety mechanisms are immediately implemented.

The authors include Dr. Peter McCullough, cardiologist and former Vice Chief of Medicine at Baylor University Medical Center in Dallas, Texas, who has called for a halt to vaccinating 30-year olds due to “no clinical benefit” and safety concerns. [McCullough is currently Senior Professor of Internal Medicine at the Texas A&M University Health Sciences Center.]

Lymphadenopathy

Updated Sept. 9, 2021: The Pfizer COVID-19 mRNA vaccine was found to be associated with an increased risk of lymphadenopathy, swelling or inflammation of lymph nodes according to a real-world case-control study from Israel.

Appendicitis

Updated Sept. 9, 2021: The Pfizer COVID-19 mRNA vaccine was found to be associated with increased risk of appendicitis, according to a real-world case-control study from Israel.

Herpes Zoster Infection

Updated Sept. 9, 2021: The Pfizer COVID-19 mRNA vaccine was found to be associated with an increased risk of herpes zoster infection, according to a real-world case-control study from Israel.

Acute CNS Demyelination and Multiple Sclerosis

A new study in Journal of Neurology examines possible links between Pfizer and Moderna vaccines, and acute Central Nervous System (CNS) demyelination, including Multiple Sclerosis (MS).

Demyelinating diseases damage the protective covering surrounding nerve fibers in the brain, optic nerves and spinal cord, causing neurological problems. In the study, four patients had the Pfizer vaccine and three had the Moderna vaccine. Within 21 days of the first or second dose, the patients developed active CNS demyelination of the optic nerve, brain, and/or spinal cord leading to “visual loss, dysmetria, gait instability, paresthesias, sphincter disturbance, and limb weakness.”

Age ranged from 24 to 64 years old. Four patients were ultimately diagnoses with exacerbation of their stable MS.

Two were diagnosed with new cases of MS.

One was diagnosed with neuromyelitis optica.

Functional Neurological Disorder (FND)

Researchers in the United Kingdom are studying two additional cases of Functional Neurological Disorder (FND) in women in their 30s after receiving Covid-19 vaccines.

FND is a neurological disorder involving malfunctioning of the nervous system and how the brain and body transmit signals. Symptoms can include limb weakness, paralysis, tremor, spasms, problems walking, speech problems, tingling, vision loss, seizures, fatigue, anxiety, chronic pain, memory symptoms, and blackouts.

An analysis of Covid-19 vaccine adverse events showed hundreds of thousands of reports of such symptoms.

In January, videos showing vaccine patients suffering such symptoms were treated by media outlets such as Wired as if they were fake news and “dangerous” misinformation.

In fact, the videos garnered the attention of scientists who investigated and concluded they were early warnings of what happens to some who get Covid-19 vaccines.

The newest cases are outlined in the journal NeuroPsychiatry and include:

  • A 38-year old woman who got her first dose of Pfizer’s vaccine and quickly developed weakness around her ear, mouth, left arm and leg. She went to the ER the next day and was diagnosed with Bell’s palsy or a transient ischemic attack. Problems continued months later, including memory issues, and she was diagnosed with FND.
  • A 36-year-old woman who got her second dose of Moderna and quickly noticed weakness in right hand and right leg limping. A day later she reported severe leg heaviness, fatigue, movement difficulties. After physical therapy her right-side weakness improved but she awoke weeks later with left-side weakness, tightness and heaviness in neck, difficulties with daily living, rapid muscle fatigue, dragging right foot, and tremor. She was diagnosed with FND.

Antibody Dependent Enhancement (ADE)

Updated (read more here). According to studies:

  • Antibody Dependent Enhancement (ADE) can make vaccinated people more susceptible to serious infection from the virus
  • “ADE may be a concern” for those who have been vaccinated for Covid-19
  • With ADE, after people get vaccinated for an initial virus, infection by a subsequent variant or strain of the virus can result in “increased viral replication and more severe disease, leading to major safety risks”
  • ADE can also “occur when neutralizing antibodies (which bind the virus and stop it from causing infection) are present at low enough levels that they don’t protect against infection. Instead, they can form immune complexes with viral particles, which in turn leads to worse illness”
  • This concern was initially described by some scientists who were subsequently banned from media platforms that incorrectly claimed the scientists were disseminating disinformation

Guillain-Barre syndrome autoimmune paralysis

Update July 22, 2021: The European Union added Guillain-Barré syndrome, an autoimmune paralysis disorder, as a possible side effect from Johnson and Johnson’s Covid-19 vaccine.

Update July 12, 2021: The FDA added warnings about Guillain-Barre autoimmune paralysis, in which the immune system attacks the body’s nerves, after Johnson and Johnson vaccine. According to reports, the cases have primarily been reported about two weeks after vaccination, mostly in men, and “any aged 50 and older.”

Numerous case reports of Guillain-Barre syndrome paralysis after Covid-19 vaccine have prompted scientists to warn that “all physicians” should be “vigilant in recognizing Guillain-Barré syndrome in patients who have received the AstraZeneca vaccine… our observations suggest that this clinically distinct [Guillain-Barré syndrome] variant is more severe than usual and may require mechanical ventilation.” In the U.K., scientists flagged “bifacial weakness and normal facial sensation in four men between 11 and 22 days after their first doses of the Astra-Zeneca vaccine.” A case has also been reported in a patient who got the Pfizer vaccine. In India, there are reports of seven severe cases of Guillain-Barré syndrome 10 to 14 days after the first dose of AstraZeneca’s vaccine. Six were women, all had facial paralysis, “all progressed to quadriplegia, and six required respiratory support. Patients’ ages ranged from 43 to 70. Four developed other cranial neuropathies, including abducens palsy and trigeminal sensory nerve involvement.”

Guillain-Barre syndrome has been reported after other vaccinations. The cause is believed to be damage to the immune system. The disorder can be extremely serious and can lead to total paralysis with dependence on artificial respiration. Even those who recover may have serious muscle wasting and may have to slowly teach the body to relearn most every normal task, such as walking. One in 20 cases is fatal.

Bell’s Palsy

Updated Aug. 17: An analysis in Hong Kong shows risk of Bell’s palsy is higher with CoronaVac (Sinovac Biotech) shot, a vaccine formulation not currently used in U.S. Bell’s palsy is facial paralysis, muscle twitching, or weakness. It may include change in taste, and pain around the ear, increased sensitivity to sound known as hyperacusis. An adverse event analysis of U.S. reports shows 4,154 Bell’s Palsy after Covid-19 vaccination.

Heart Issues

Updated Sept. 9, 2021: The Pfizer COVID-19 mRNA vaccine was found to be associated with a threefold increased risk of myocarditis, according to a real-world case-control study from Israel. “Vaccination had a strong association with an increased risk of myocarditis as well as increased risks of lymphadenopathy [swelling or inflammation of lymph nodes], appendicitis, and herpes zoster infection.”

The Food and Drug Administration has added a new warning to Pfizer and Moderna Covid-19 vaccines about risk of heart inflammation.

As of June of 2021, CDC said that more than 1,200 cases of heart inflammation (myocarditis or pericarditis) in young people had been reported after Pfizer and Moderna Covid-19 vaccination.

  • More than half were after the second dose.
  • Most of the injuries are in males under age 30.

Updated Aug. 4: A new, independent study of medical records found the incidences of myocarditis and pericarditis are more than five times more common than CDC reported.

The Israeli Ministry of Health announced it’s monitoring for heart inflammation after Pfizer’s vaccine due to reports of problems.

Myocarditis and Other Cardiovascular Complications of the mRNA-Based COVID-19 Vaccines [Pfizer-BioNTech, Moderna] in a number of patients are described in a scientific article:

  • Two patients with clinically suspected myocarditis
  • One patient with stress cardiomyopathy
  • Two patients with pericarditis

According to the research:

  • The two patients with clinically suspected myocarditis were otherwise healthy young men who presented with acute substernal chest pressure and/or dyspnea after receiving the second dose of the vaccine and were found to have diffuse ST elevations on electrocardiogram (ECG), elevated cardiac biomarkers and inflammatory markers, and mildly reduced left ventricular (LV) function on echocardiography. Both patients met the modified Lake Louise Criteria for acute myocarditis by cardiac magnetic resonance imaging.
  • A case of stress cardiomyopathy occurred in a 60-year-old woman with known coronary artery disease (CAD) and previously normal LV function, who presented with new exertional symptoms, ECG changes, and apical akinesis following the second dose of the vaccine.
  • The two patients with pericarditis who presented with chest pain, elevated inflammatory markers, and pericardial effusions after receiving the vaccine.

Updated Sept.9, 2021: An August 10 study in JAMA Cardiology confirms the previously identified Pfizer vaccine’s myocarditis (heart inflammation) risk in young boys.

Read the study here.

Updated Sept. 12, 2021: A study of Pfizer and Moderna vaccines finds teenage boys are six times more likely to suffer heart issues from Covid-19 vaccination than from Covid. (However, in both instances, the risk is considered slight.)

Blood Clots and Blood Disorders

In late June, the first case of a blood clot disorder called “thrombosis with thrombocytopenia” after an RNA double-dose vaccine was been reported in the Annals of Internal Medicine. The case was that of a 65-year-old man who developed symptoms ten days after his second dose of the Moderna vaccine. Because the blood clot disorder was not previously warned about in the Moderna and Pfizer vaccines, doctors treated the patient with heparin, the very drug that’s not supposed to be used in post-vaccine patients suffering from the disorder because it could actually worsen the condition.

The Johnson and Johnson Covid-19 vaccine was temporarily removed from the market in the U.S. on April 16, 2021 while health officials studied reports of blood clot injuries. Among them was an 18-year old teen named Emma Burkey, who got sick about a week after the Johnson and Johnson Covid-19 vaccine and ended up having three brain surgeries related to blood clots and seizures.

Read: BBC radio news anchor dies of blood clots after Covid vaccine

The Johnson and Johnson vaccine was allowed back on the market April 27, 2021 with new warnings about the disorder.

Swedish health officials determined that people under age 65 should not get the Johnson and Johnson vaccine due to reports of blood clots.

An editorial published in the Journal of the American Medical Association recommended women under age 50 avoid the Johnson and Johnson Covid-19 vaccine due to concerns about blood clots. The recommendation discussed 12 case reports of a blood disorder known as cerebral venous sinus thrombosis (CVST) with thrombocytopenia following the Johnson and Johnson vaccine.

The AstraZeneca Covid-19 vaccine (not currently approved in the U.S.) has been linked to a dangerous disorder involving blood clots with low blood platelets. On April 7, 2021, the European Medicines Agency says it made the association after it analyzed 62 cases of cerebral venous sinus thrombosis and 24 cases of splanchnic vein thrombosis reported in the EU drug safety database (EudraVigilance) as of March 22, 2021; 18 of which were fatal.

An otherwise healthy South Florida doctor, Gregory Michael, died of a brain hemorrhage 16 days after he got Pfizer’s Covid-19 vaccine. Authorities concluded he died of a blood disorder called “immune thrombocytopenia” (ITP) that can prevent blood from clotting and cause internal bleeding. His wife said a blood test showed the level of his platelets to be at “zero.” She said before the shot, Dr. Michael had “absolutely no medical issues” and no underlying conditions. However, authorities later categorized his death as “natural.”

In Spain, the AstraZeneca shot has been restricted in people under age 60 due to reports of blood clots in younger people.

Bulgaria, Iceland and Norway have halted AstraZeneca shots.

Austria, Italy and Romania banned certain “lots” or batches of the AstraZeneca shots.

Denmark stopped using the AstraZeneca Covid-19 vaccine altogether as well as the Johnson and Johnson vaccine after investigations into blood clots, saying “the benefits of using the COVID-19 vaccine from Johnson & Johnson do not outweigh the risk of causing the possible adverse effect in those who receive the vaccine.”

The Italian government recently restricted AstraZeneca Covid-19 vaccine to adults over age 60 after a teenager who got the shot died from a rare form of blood clotting. Eighteen-year-old Camilla Canepa died after getting vaccinated May 25, 2021.

Several other European countries have also stopped giving the AstraZeneca Covid-19 vaccine to people below a certain age, usually ranging from 50 to 65.

Updated Sept. 9, 2021: An August 10 study in JAMA Cardiology urged caution in giving Covid-19 vaccine to certain high risk patients due to the vaccine link to a serious blood disorder: thrombocytopenia with thrombosis. “One of the devastating manifestations of this syndrome, termed vaccine-induced immune thrombotic thrombocytopenia (VITT), is cerebral venous sinus thrombosis (CVST),” say the study authors. The link involves the AstraZeneca/Oxford and Johnson & Johnson vaccines, according to the study. The AstraZeneca vaccine is not administered in the U.S. currently.

Read the study here.

Graves disease autoimmune disorder

Studies in Mexico and Turkey link the autoimmune thyroid disorder Graves disease to Covid-19 vaccination in numerous female health care workers, including two who were breastfeeding. Pfizer-BioNTech was the vaccine given in Mexico. A Chinese vaccine was given in Turkey. Read more at the link below.

https://sharylattkisson.com/2021/07/two-studies-covid-19-vaccines-trigger-graves-disease-in-some-female-health-care-workers/

Frail, elderly

Health officials in Norway sounded the alarm after 23 patients died shortly after getting the Pfizer Covid-19 vaccine. They advise doctors to use caution in administering the shot to “very frail elderly patients.”

After investigating 13 of the deaths, the Norwegian authorities concluded that common side effects from so-called “RNA” vaccines may be too much for a frail elderly person to handle, and may contribute to their death.

“There is a possibility that these common adverse reactions, that are not dangerous in fitter, younger patients and are not unusual with vaccines, may aggravate underlying disease in the elderly,” said Steinar Madsen, medical director of the Norwegian Medicines Agency.

CDC said it is monitoring the impact of the vaccines on already-frail patients such as the chronically ill in nursing homes.

Several clusters of elderly patients in U.S. nursing homes died after Pfizer or Moderna Covid-19 vaccine. In one group, a number of the patients who died tested positive for Covid-19 after vaccination.

Pregnant women

Several Brazilian states suspended use of AstraZeneca’s Covid-19 vaccine for pregnant women in May 2021 after a pregnant woman died after getting vaccinated. The decisions follow the recommendation of the country’s National Health Surveillance Agency, which recommended “immediate suspension” of the AstraZeneca Covid-19 vaccine for pregnant women after results of vaccine adverse events monitoring in the country.

CDC says that with limited data on impact of Covid-19 vaccine in pregnant women and on their unborn children, the decision on whether to vaccinate while pregnant is an individual decision to be made between a woman and her physician.

Previously-infected

CDC falsely claimed that studies showed Covid-19 vaccines are effective for those who already had Covid-19. In fact, studies showed the opposite.

Manufacturing problems

On June 11, the European Union’s drug regulator announced it will not use batches of the Johnson & Johnson COVID-19 vaccine that were made at a Baltimore, Maryland-based plant around the time that cross-contamination manufacturing problems were reported at the facility.

Anonymous sources claimed that up to 60 million doses of the Johnson and Johnson vaccine had to be thrown out. But the FDA issued a news release saying that two batches from the Baltimore plant were safe to use. The FDA said “several other batches are not suitable for use, but additional batches are still under review.”

Waning immunity, Breakthrough Infections

Israel announced that about half of the adults infected with Covid-19 during its outbreak in the June 2021 time period were fully vaccinated. The fully-vaccinated individuals had gotten Pfizer’s shots.

According to Epoch Times, in June 2021 nearly 4,000 fully vaccinated people in Massachusetts tested positive for Covid-19. On April 30, “the CDC reported that some 10,626 breakthrough cases were reported in 46 states and territories.” Breakthrough cases are where fully vaccinated people still end up infected with Covid-19.

Scientists hoped that Covid-19 vaccines would be effective in variants of Covid-19, which are mutations that occur naturally with viruses and were always expected with Covid-19. However, the vaccine effectiveness against variants may be limited. CDC and vaccine makers are studying the medical landscape to find out more.

Other states, such as Maine, are noting Covid-19 deaths occurring in fully vaccinated people.

Update Aug. 24, 2021: With evidence of seriously-waning immunity at the five- to six-month mark, CDC is now recommending a third “booster” shot. In highly-vaccinated Israel, recognition that vaccination likely does not confer protection beyond a few months, the country has reimagined its vaccine passports. They will only apply to people who have had three shots, and only be good for a six month period of time.

Update Sept. 10, 2021: An analysis of data in Israel, which has one of the world’s highest Covid-19 vaccination levels, showed almost 60% of those hospitalized for Covid were fully vaccinated. “This is a very clear warning sign for the rest of the world,” said Ran Balicer, CIO at Clalit Health Services, Israel’s largest health maintenance organization. “If it can happen here, it can probably happen anywhere.” The Pfizer vaccine is given in Israel.

Summary by vaccine

Pfizer and Moderna

Acute CNS Demyelination and Multiple Sclerosis

A new study in Journal of Neurology examines possible links between Pfizer and Moderna vaccines, and acute Central Nervous System (CNS) demyelination, including Multiple Sclerosis (MS).

Demyelinating diseases damage the protective covering surrounding nerve fibers in the brain, optic nerves and spinal cord, causing neurological problems. In the study, four patients had the Pfizer vaccine and three had the Moderna vaccine. Within 21 days of the first or second dose, the patients developed active CNS demyelination of the optic nerve, brain, and/or spinal cord leading to “visual loss, dysmetria, gait instability, paresthesias, sphincter disturbance, and limb weakness.”

Age ranged from 24 to 64 years old. Four patients were ultimately diagnoses with exacerbation of their stable MS.

Two were diagnosed with new cases of MS.

One was diagnosed with neuromyelitis optica.

Waning Immunity, Breakthrough Infections

Update Aug. 24, 2021: With evidence of seriously-waning immunity at the five- to six-month mark, CDC is now recommending a third “booster” shot. In highly-vaccinated Israel, recognition that vaccination likely does not confer protection beyond a few months, the country has reimagined its vaccine passports. They will only apply to people who have had three shots, and only be good for a six month period of time.

Update Sept. 10, 2021: An analysis of data in Israel, which has one of the world’s highest Covid-19 vaccination levels, showed almost 60% of those hospitalized for Covid were fully vaccinated. “This is a very clear warning sign for the rest of the world,” said Ran Balicer, CIO at Clalit Health Services, Israel’s largest health maintenance organization. “If it can happen here, it can probably happen anywhere.” The Pfizer vaccine is given in Israel.

Functional Neurological Disorder (FND)

Updated Aug. 30, 2021: Researchers in the United Kingdom are studying two additional cases of Functional Neurological Disorder (FND) in women in their 30s after receiving Covid-19 vaccines.

FND is a neurological disorder involving malfunctioning of the nervous system and how the brain and body transmit signals. Symptoms can include limb weakness, paralysis, tremor, spasms, problems walking, speech problems, tingling, vision loss, seizures, fatigue, anxiety, chronic pain, memory symptoms, and blackouts.

An analysis of Covid-19 vaccine adverse events showed hundreds of thousands of reports of such symptoms.

In January, videos showing vaccine patients suffering such symptoms were treated by media outlets such as Wired as if they were fake news and “dangerous” misinformation.

In fact, the videos garnered the attention of scientists who investigated and concluded they were early warnings of what happens to some who get Covid-19 vaccines.

The newest cases are outlined in the journal Neurology and include:

  • A 38-year old woman who got her first dose of Pfizer’s vaccine and quickly developed weakness around her ear, mouth, left arm and leg. She went to the ER the next day and was diagnosed with Bell’s palsy or a transient ischemic attack. Problems continued months later, including memory issues, and she was diagnosed with FND.
  • A 36-year-old woman who got her second dose of Moderna and quickly noticed weakness in right hand and right leg limping. A day later she reported severe leg heaviness, fatigue, movement difficulties. After physical therapy her right-side weakness improved but she awoke weeks later with left-side weakness, tightness and heaviness in neck, difficulties with daily living, rapid muscle fatigue, dragging right foot, and tremor. She was diagnosed with FND.

Antibody Dependent Enhancement (ADE)

Updated (read more here). According to studies:

  • Antibody Dependent Enhancement (ADE) can make vaccinated people more susceptible to serious infection from the virus
  • “ADE may be a concern” for those who have been vaccinated for Covid-19
  • With ADE, after people get vaccinated for an initial virus, infection by a subsequent variant or strain of the virus can result in “increased viral replication and more severe disease, leading to major safety risks”
  • ADE can also “occur when neutralizing antibodies (which bind the virus and stop it from causing infection) are present at low enough levels that they don’t protect against infection. Instead, they can form immune complexes with viral particles, which in turn leads to worse illness”
  • This concern was initially described by some scientists who were subsequently banned from media platforms that incorrectly claimed the scientists were disseminating disinformation

Guillain-Barre autoimmune paralysis

Numerous case reports of Guillain-Barre syndrome paralysis after Covid-19 vaccine have prompted scientists to warn that “all physicians” should be “vigilant in recognizing Guillain-Barré syndrome in patients who have received the AstraZeneca vaccine… our observations suggest that this clinically distinct [Guillain-Barré syndrome] variant is more severe than usual and may require mechanical ventilation.” In the U.K., scientists flagged “bifacial weakness and normal facial sensation in four men between 11 and 22 days after their first doses of the Astra-Zeneca vaccine.” A case has also been reported in a patient who got the Pfizer vaccine. In India, there are reports of seven severe cases of Guillain-Barré syndrome 10 to 14 days after the first dose of AstraZeneca’s vaccine. Six were women, all had facial paralysis, “all progressed to quadriplegia, and six required respiratory support. Patients’ ages ranged from 43 to 70. Four developed other cranial neuropathies, including abducens palsy and trigeminal sensory nerve involvement.”

Guillain-Barre syndrome has been reported after other vaccinations. The cause is believed to be damage to the immune system. The disorder can be extremely serious and can lead to total paralysis with dependence on artificial respiration. Even those who recover may have serious muscle wasting and may have to slowly teach the body to relearn most every normal task, such as walking. One in 20 cases is fatal.

Blood Clots

In late June, the first case of a blood clot disorder called “thrombosis with thrombocytopenia” after an RNA double-dose vaccine was been reported in the Annals of Internal Medicine. The case was that of a 65-year-old man who developed symptoms ten days after his second dose of the Moderna vaccine. Because the blood clot disorder was not previously warned about in the Moderna and Pfizer vaccines, doctors treated the patient with heparin, the very drug that’s not supposed to be used in post-vaccine patients suffering from the disorder because it could actually worsen the condition.

Heart inflammation

Updated Sept. 9, 2021: The Pfizer COVID-19 mRNA vaccine was found to be associated with a threefold increased risk of myocarditis, according to a real-world case-control study from Israel. “Vaccination had a strong association with an increased risk of myocarditis as well as increased risks of lymphadenopathy [swelling or inflammation of lymph nodes], appendicitis, and herpes zoster infection.”

The Food and Drug Administration has added a new warning to Pfizer and Moderna Covid-19 vaccines about risk of heart inflammation.

As of June of 2021, CDC said that more than 1,200 cases of heart inflammation (myocarditis of pericarditis) in young people had been reported after Pfizer and Moderna Covid-19 vaccination.

  • More than half were after the second dose.
  • Most of the injuries are in males under age 30.

Updated Aug. 4: A new, independent study of medical records found the incidences of myocarditis and pericarditis are more than five times more common than CDC reported.

The Israeli Ministry of Health announced it’s monitoring for heart inflammation after Pfizer’s vaccine due to reports of problems.

Myocarditis and Other Cardiovascular Complications of the mRNA-Based COVID-19 Vaccines [Pfizer-BioNTech, Moderna] in a number of patients are described in a scientific article:

  • Two patients with clinically suspected myocarditis
  • One patient with stress cardiomyopathy
  • Two patients with pericarditis

According to the research:

  • The two patients with clinically suspected myocarditis were otherwise healthy young men who presented with acute substernal chest pressure and/or dyspnea after receiving the second dose of the vaccine and were found to have diffuse ST elevations on electrocardiogram (ECG), elevated cardiac biomarkers and inflammatory markers, and mildly reduced left ventricular (LV) function on echocardiography. Both patients met the modified Lake Louise Criteria for acute myocarditis by cardiac magnetic resonance imaging.
  • A case of stress cardiomyopathy occurred in a 60-year-old woman with known coronary artery disease (CAD) and previously normal LV function, who presented with new exertional symptoms, ECG changes, and apical akinesis following the second dose of the vaccine.
  • The two patients with pericarditis who presented with chest pain, elevated inflammatory markers, and pericardial effusions after receiving the vaccine.

An otherwise healthy South Florida doctor, Gregory Michael, died of a brain hemorrhage 16 days after he got Pfizer’s Covid-19 vaccine. Authorities concluded he died of a blood disorder called “immune thrombocytopenia” (ITP) that can prevent blood from clotting and cause internal bleeding. His wife said a blood test showed the level of his platelets to be at “zero.” She said before the shot, Dr. Michael had “absolutely no medical issues” and no underlying conditions. However, authorities later categorized his death as “natural.”

Updated Sept. 12, 2021: A study of Pfizer and Moderna vaccines finds teenage boys are six times more likely to suffer heart issues from Covid-19 vaccination than from Covid. (However, in both instances, the risk is considered slight.)

Frail, elderly

Health officials in Norway sounded the alarm after 23 patients died shortly after receiving the Pfizer Covid-19 vaccine. They advise doctors to use caution in administering the shot to “very frail elderly patients.”

After investigating 13 of the deaths, the Norwegian authorities concluded that common side effects from so-called “RNA” vaccines may be too much for a frail elderly person to handle, and may contribute to their death.

“There is a possibility that these common adverse reactions, that are not dangerous in fitter, younger patients and are not unusual with vaccines, may aggravate underlying disease in the elderly,” said Steinar Madsen, medical director of the Norwegian Medicines Agency.

CDC said it is monitoring the impact of the vaccines on already-frail patients such as the chronically ill in nursing homes.

Several clusters of elderly patients in U.S. nursing homes died after Pfizer or Moderna Covid-19 vaccine. In one group, a number of the patients who died tested positive for Covid-19 after vaccination.

Israel announced that about half of the adults infected with Covid-19 during its outbreak in the June 2021 time period were fully vaccinated. The fully-vaccinated individuals had gotten Pfizer’s shots.

Graves Disease

Studies in Mexico and Turkey link the autoimmune thyroid disorder Graves disease to Covid-19 vaccination in numerous female health care workers, including two who were breastfeeding. Pfizer-BioNTech was the vaccine given in Mexico. A Chinese vaccine was given in Turkey. Read more at the link here.

Johnson and Johnson

Update Sept. 9, 2021: An August 10 study in JAMA Cardiology urged caution in giving Johnson and Johnson Covid-19 vaccine to certain high risk patients due to the vaccine link to a serious blood disorder: thrombocytopenia with thrombosis. “One of the devastating manifestations of this syndrome, termed vaccine-induced immune thrombotic thrombocytopenia (VITT), is cerebral venous sinus thrombosis (CVST),” say the study authors.

Read the study here.

Update July 22, 2021: The European Union added Guillain-Barré syndrome, an autoimmune paralysis disorder, as a possible side effect from Johnson and Johnson’s Covid-19 vaccine.

Update July 12, 2021: The FDA added warnings about Guillain-Barre autoimmune paralysis, in which the immune system attacks the body’s nerves, after Johnson and Johnson vaccine. According to reports, the cases have primarily been reported about two weeks after vaccination, mostly in men, and “any aged 50 and older.”

The Johnson and Johnson Covid-19 vaccine was temporarily removed from the market in the U.S. on April 16, 2021 while health officials studied reports of blood clot injuries.

Updated Aug. 4: A new, independent study of medical records found the incidences of myocarditis and pericarditis are more than five times more common than CDC reported.

The Johnson and Johnson vaccine was allowed back on the market April 27, 2021 with new warnings about the disorder.

Swedish health officials determined that people under age 65 should not get the Johnson and Johnson vaccine due to reports of blood clots.

An editorial in the Journal of the American Medical Association recommended women under age 50 avoid the Johnson and Johnson Covid-19 vaccine due to concerns about blood clots: a blood disorder known as cerebral venous sinus thrombosis (CVST) with thrombocytopenia following the Johnson and Johnson vaccine.

On June 11, the European Union’s drug regulator announced it will not use batches of the Johnson & Johnson COVID-19 vaccine that were made at a Baltimore, Maryland-based plant around the time that cross-contamination manufacturing problems were reported at the facility.

Anonymous sources claimed that up to 60 million doses of the Johnson and Johnson vaccine had to be thrown out. But the FDA issued a news release saying that two batches from the Baltimore plant were safe to use. The FDA said “several other batches are not suitable for use, but additional batches are still under review.”

Denmark  banned the Johnson and Johnson vaccine altogether saying “the benefits of using the COVID-19 vaccine from Johnson & Johnson do not outweigh the risk of causing the possible adverse effect in those who receive the vaccine”.

AstraZeneca (not given in the U.S.)

Update: Sept. 9, 2021: An August 10 study in JAMA Cardiology urged caution in giving AstraZeneca Covid-19 vaccine to certain high risk patients due to the vaccine link to a serious blood disorder: thrombocytopenia with thrombosis. “One of the devastating manifestations of this syndrome, termed vaccine-induced immune thrombotic thrombocytopenia (VITT), is cerebral venous sinus thrombosis (CVST),” say the study authors.

Read the study here.

The AstraZeneca Covid-19 vaccine has been linked to a dangerous disorder involving blood clots with low blood platelets.

On April 7, 2021: The European Medicines Agency says it made the association after it analyzed 62 cases of cerebral venous sinus thrombosis and 24 cases of splanchnic vein thrombosis reported in the EU drug safety database (EudraVigilance) as of March 22, 2021, 18 of which were fatal.

In Spain, the AstraZeneca shot has been restricted in people under age 60 due to reports of blood clots in younger people.

Bulgaria, Iceland and Norway have halted AstraZeneca shots.

Austria, Italy and Romania banned certain “lots” or batches of the AstraZeneca shots.

Denmark stopped using the AstraZeneca Covid-19 vaccine altogether after investigations into blood clots.

The Italian government recently restricted AstraZeneca Covid-19 vaccine to adults over age 60 after a teenager who got the shot died from a rare form of blood clotting. Eighteen-year-old Camilla Canepa died after getting vaccinated May 25, 2021.

Several other European countries have also stopped giving the AstraZeneca COVID-19 vaccine to people below a certain age, usually ranging from 50 to 65.

Several Brazilian states suspended use of AstraZeneca’s Covid-19 vaccine for pregnant women in May 2021 after a pregnant woman died after getting vaccinated. The decisions follow the recommendation of the country’s National Health Surveillance Agency, which recommended “immediate suspension” of the AstraZeneca Covid-19 vaccine for pregnant women after results of vaccine adverse events monitoring in the country.

Numerous case reports of Guillain-Barre syndrome paralysis after Covid-19 vaccine have prompted scientists to warn that “all physicians” should be “vigilant in recognizing Guillain-Barré syndrome in patients who have received the AstraZeneca vaccine… our observations suggest that this clinically distinct [Guillain-Barré syndrome] variant is more severe than usual and may require mechanical ventilation.” In the U.K., scientists flagged “bifacial weakness and normal facial sensation in four men between 11 and 22 days after their first doses of the Astra-Zeneca vaccine.” A case has also been reported in a patient who got the Pfizer vaccine. In India, there are reports of seven severe cases of Guillain-Barré syndrome 10 to 14 days after the first dose of AstraZeneca’s vaccine. Six were women, all had facial paralysis, “all progressed to quadriplegia, and six required respiratory support. Patients’ ages ranged from 43 to 70. Four developed other cranial neuropathies, including abducens palsy and trigeminal sensory nerve involvement.”

Guillain-Barre syndrome has been reported after other vaccinations. The cause is believed to be damage to the immune system. The disorder can be extremely serious and can lead to total paralysis with dependence on artificial respiration. Even those who recover may have serious muscle wasting and may have to slowly teach the body to relearn most every normal task, such as walking. One in 20 cases is fatal.

Summary by country

Austria: Banned certain “lots” or batches of AstraZeneca shots.

Brazil: Several Brazilian states suspended use of AstraZeneca’s Covid-19 vaccine for pregnant women in May 2021 after a pregnant woman died after getting vaccinated. The decisions follow the recommendation of the country’s National Health Surveillance Agency, which recommended “immediate suspension” of the AstraZeneca Covid-19 vaccine for pregnant women after results of vaccine adverse events monitoring in the country.

Bulgaria: Halted AstraZeneca shots.

Denmark: stopped using the AstraZeneca Covid-19 vaccine and the Johnson and Johnson vaccine altogether after investigations into blood clots.

European Union: July 22, 2021: The European Union added Guillain-Barré syndrome, an autoimmune paralysis disorder, as a possible side effect from Johnson and Johnson’s Covid-19 vaccine.

The AstraZeneca Covid-19 vaccine (not currently approved in the U.S.) has been linked to a dangerous disorder involving blood clots with low blood platelets. On April 7, 2021, the European Medicines Agency says it made the association after it analyzed 62 cases of cerebral venous sinus thrombosis and 24 cases of splanchnic vein thrombosis reported in the EU drug safety database (EudraVigilance) as of March 22, 2021, 18 of which were fatal.

On June 11, the European Union’s drug regulator announced it will not use batches of the Johnson & Johnson COVID-19 vaccine that were made at a Baltimore, Maryland-based plant around the time that cross-contamination manufacturing problems were reported at the facility.

Several European countries have stopped giving the AstraZeneca COVID-19 vaccine to people below a certain age, usually ranging from 50 to 65.

Numerous case reports of Guillain-Barre syndrome paralysis after Covid-19 vaccine have prompted scientists to warn that “all physicians” should be “vigilant in recognizing Guillain-Barré syndrome in patients who have received the AstraZeneca vaccine… our observations suggest that this clinically distinct [Guillain-Barré syndrome] variant is more severe than usual and may require mechanical ventilation.” In the U.K., scientists flagged “bifacial weakness and normal facial sensation in four men between 11 and 22 days after their first doses of the Astra-Zeneca vaccine.” A case has also been reported in a patient who got the Pfizer vaccine. In India, there are reports of seven severe cases of Guillain-Barré syndrome 10 to 14 days after the first dose of AstraZeneca’s vaccine. Six were women, all had facial paralysis, “all progressed to quadriplegia, and six required respiratory support. Patients’ ages ranged from 43 to 70. Four developed other cranial neuropathies, including abducens palsy and trigeminal sensory nerve involvement.”

Guillain-Barre syndrome has been reported after other vaccinations. The cause is believed to be damage to the immune system. The disorder can be extremely serious and can lead to total paralysis with dependence on artificial respiration. Even those who recover may have serious muscle wasting and may have to slowly teach the body to relearn most every normal task, such as walking. One in 20 cases is fatal.

Hong-Kong: Updated Aug. 17: An analysis in Hong Kong shows risk of Bell’s palsy is higher with CoronaVac (Sinovac Biotech) shot, a vaccine formulation not currently used in U.S. Bell’s palsy is facial paralysis, muscle twitching, or weakness. It may include change in taste, and pain around the ear, increased sensitivity to sound known as hyperacusis. An adverse event analysis of U.S. reports shows 4,154 Bell’s Palsy after Covid-19 vaccination.

Iceland: Has halted AstraZeneca shots.

India: Numerous case reports of Guillain-Barre syndrome paralysis after Covid-19 vaccine have prompted scientists to warn that “all physicians” should be “vigilant in recognizing Guillain-Barré syndrome in patients who have received the AstraZeneca vaccine… our observations suggest that this clinically distinct [Guillain-Barré syndrome] variant is more severe than usual and may require mechanical ventilation.” In the U.K., scientists flagged “bifacial weakness and normal facial sensation in four men between 11 and 22 days after their first doses of the Astra-Zeneca vaccine.” A case has also been reported in a patient who got the Pfizer vaccine. In India, there are reports of seven severe cases of Guillain-Barré syndrome 10 to 14 days after the first dose of AstraZeneca’s vaccine. Six were women, all had facial paralysis, “all progressed to quadriplegia, and six required respiratory support. Patients’ ages ranged from 43 to 70. Four developed other cranial neuropathies, including abducens palsy and trigeminal sensory nerve involvement.”

Guillain-Barre syndrome has been reported after other vaccinations. The cause is believed to be damage to the immune system. The disorder can be extremely serious and can lead to total paralysis with dependence on artificial respiration. Even those who recover may have serious muscle wasting and may have to slowly teach the body to relearn most every normal task, such as walking. One in 20 cases is fatal.

Israel: The Israeli Ministry of Health announced it’s monitoring for heart inflammation after Pfizer’s vaccine due to reports of problems.

Announced that about half of the adults infected with Covid-19 during its outbreak in the June 2021 time period were fully vaccinated. The fully-vaccinated individuals had gotten Pfizer’s shots.

Update Aug. 24, 2021: In highly-vaccinated Israel, recognition that vaccination likely does not confer protection beyond a few months, the country has reimagined its vaccine passports. They will only apply to people who have had three shots, and only be good for a six month period of time.

Updated Sept. 9 2021: The Pfizer COVID-19 mRNA vaccine was found to be associated with a threefold increased risk of myocarditis, according to a real-world case-control study from Israel. “Vaccination had a strong association with an increased risk of myocarditis as well as increased risks of lymphadenopathy [swelling or inflammation of lymph nodes], appendicitis, and herpes zoster infection.”

Italy: Restricted AstraZeneca Covid-19 vaccine to adults over age 60 after a teenager who got the shot died from a rare form of blood clotting. Eighteen-year-old Camilla Canepa died after getting vaccinated May 25, 2021.

Banned certain “lots” or batches of the AstraZeneca shots.

Mexico: Studies in Mexico and Turkey link the autoimmune thyroid disorder Graves disease to Covid-19 vaccination in numerous female health care workers, including two who were breastfeeding. Pfizer-BioNTech was the vaccine given in Mexico. A Chinese vaccine was given in Turkey. Read more at the link here.

Norway: Halted AstraZeneca shots. Cautioned use of the vaccine in “very frail elderly patients” after nearly two dozen deaths.

“There is a possibility that these common adverse reactions, that are not dangerous in fitter, younger patients and are not unusual with vaccines, may aggravate underlying disease in the elderly,” said Steinar Madsen, medical director of the Norwegian Medicines Agency.

Romania: Banned certain “lots” or batches of the AstraZeneca shots.

Spain: The AstraZeneca shot has been restricted in people under age 60 due to reports of blood clots in younger people.

Sweden: Health officials determined that people under age 65 should not get the Johnson and Johnson vaccine due to reports of blood clots.

Turkey: Studies in Mexico and Turkey link the autoimmune thyroid disorder Graves disease to Covid-19 vaccination in numerous female health care workers, including two who were breastfeeding. Pfizer-BioNTech was the vaccine given in Mexico. A Chinese vaccine was given in Turkey. Read more at the link here.

UK: Some scientists analyzed adverse event reports and called upon the Medicines and Healthcare products Regulatory Agency to stop the Covid-19 vaccines as “not safe for human use” due to reports of issues with bleeding/clotting, pain, immune system, neurological, loss of sight/hearing/smell speech, and questions about impact in pregnant women.

Updated: Researchers in the United Kingdom are studying two additional cases of Functional Neurological Disorder (FND) in women in their 30s after receiving Covid-19 vaccines.

FND is a neurological disorder involving malfunctioning of the nervous system and how the brain and body transmit signals. Symptoms can include limb weakness, paralysis, tremor, spasms, problems walking, speech problems, tingling, vision loss, seizures, fatigue, anxiety, chronic pain, memory symptoms, and blackouts.

An analysis of Covid-19 vaccine adverse events showed hundreds of thousands of reports of such symptoms.

In January, videos showing vaccine patients suffering such symptoms were treated by media outlets such as Wired as if they were fake news and “dangerous” misinformation.

In fact, the videos garnered the attention of scientists who investigated and concluded they were early warnings of what happens to some who get Covid-19 vaccines.

The newest cases are outlined in the journal Neurology and include:

  • A 38-year old woman who got her first dose of Pfizer’s vaccine and quickly developed weakness around her ear, mouth, left arm and leg. She went to the ER the next day and was diagnosed with Bell’s palsy or a transient ischemic attack. Problems continued months later, including memory issues, and she was diagnosed with FND.
  • A 36-year-old woman who got her second dose of Moderna and quickly noticed weakness in right hand and right leg limping. A day later she reported severe leg heaviness, fatigue, movement difficulties. After physical therapy her right-side weakness improved but she awoke weeks later with left-side weakness, tightness and heaviness in neck, difficulties with daily living, rapid muscle fatigue, dragging right foot, and tremor. She was diagnosed with FND.

issues from Covid-19 vaccination than from Covid. (However, in both instances, the risk is considered slight.)

Update Sept. 9, 2021: An August 10 study in JAMA Cardiology confirms the previously identified Pfizer vaccine’s myocarditis (heart inflammation) risk in young boys.

Read the study here.

Update Sept. 4, 2021: Acute CNS Demyelination and Multiple Sclerosis: A new study in Journal of Neurology examines possible links between Pfizer and Moderna vaccines, and acute Central Nervous System (CNS) demyelination, including Multiple Sclerosis (MS).

Demyelinating diseases damage the protective covering surrounding nerve fibers in the brain, optic nerves and spinal cord, causing neurological problems. In the study, four patients had the Pfizer vaccine and three had the Moderna vaccine. Within 21 days of the first or second dose, the patients developed active CNS demyelination of the optic nerve, brain, and/or spinal cord leading to “visual loss, dysmetria, gait instability, paresthesias, sphincter disturbance, and limb weakness.”

Age ranged from 24 to 64 years old. Four patients were ultimately diagnoses with exacerbation of their stable MS.

Two were diagnosed with new cases of MS.

One was diagnosed with neuromyelitis optica.

Update Aug. 24, 2021: With evidence of seriously-waning immunity at the five- to six-month mark, CDC is now recommending a third “booster” shot. In highly-vaccinated Israel, recognition that vaccination likely does not confer protection beyond a few months, the country has reimagined its vaccine passports. They will only apply to people who have had three shots, and only be good for a six month period of time.

Update Aug. 16, 2021: Antibody Dependent Enhancement (ADE) (read more here). According to studies:

  • Antibody Dependent Enhancement (ADE) can make vaccinated people more susceptible to serious infection from the virus
  • “ADE may be a concern” for those who have been vaccinated for Covid-19
  • With ADE, after people get vaccinated for an initial virus, infection by a subsequent variant or strain of the virus can result in “increased viral replication and more severe disease, leading to major safety risks”
  • ADE can also “occur when neutralizing antibodies (which bind the virus and stop it from causing infection) are present at low enough levels that they don’t protect against infection. Instead, they can form immune complexes with viral particles, which in turn leads to worse illness”
  • This concern was initially described by some scientists who were subsequently banned from media platforms that incorrectly claimed the scientists were disseminating disinformation

Update Aug. 4, 2021: A new, independent study of medical records found the incidences of myocarditis and pericarditis are more than five times more common than CDC reported.

Update July 12, 2021: The FDA added warnings about Guillain-Barre autoimmune paralysis, in which the immune system attacks the body’s nerves, after Johnson and Johnson vaccine. According to reports, the cases have primarily been reported about two weeks after vaccination, mostly in men, and “any aged 50 and older.”

In late June, the first case of a blood clot disorder called “thrombosis with thrombocytopenia” after an RNA double-dose vaccine was been reported in the Annals of Internal Medicine. The case was that of a 65-year-old man who developed symptoms ten days after his second dose of the Moderna vaccine. Because the blood clot disorder was not previously warned about in the Moderna and Pfizer vaccines, doctors treated the patient with heparin, the very drug that’s not supposed to be used in post-vaccine patients suffering from the disorder because it could actually worsen the condition.

Dr. Peter McCullough, cardiologist and Vice Chief of Medicine at Baylor University Medical Center in Dallas, Texas, has called for a halt to vaccinating 30-year olds due to “no clinical benefit” and safety concerns.

A petition of scientists led by Linda Wastila, Professor, Pharmaceutical Health Services Research University of Maryland School of Pharmacy is calling for Covid-19 vaccines to be disapproved.

The Food and Drug Administration has added a new warning to Pfizer and Moderna Covid-19 vaccines about risk of heart inflammation.

As of June of 2021, CDC said that more than 1,200 cases of heart inflammation (myocarditis of pericarditis) in young people had been reported after Pfizer and Moderna Covid-19 vaccination.

  • More than half were after the second dose.
  • Most of the injuries are in males under age 30.

Myocarditis and Other Cardiovascular Complications of the mRNA-Based COVID-19 Vaccines [Pfizer-BioNTech, Moderna] in a number of patients are described in a scientific article:

  • Two patients with clinically suspected myocarditis
  • One patient with stress cardiomyopathy
  • Two patients with pericarditis

According to the research:

  • The two patients with clinically suspected myocarditis were otherwise healthy young men who presented with acute substernal chest pressure and/or dyspnea after receiving the second dose of the vaccine and were found to have diffuse ST elevations on electrocardiogram (ECG), elevated cardiac biomarkers and inflammatory markers, and mildly reduced left ventricular (LV) function on echocardiography. Both patients met the modified Lake Louise Criteria for acute myocarditis by cardiac magnetic resonance imaging.
  • A case of stress cardiomyopathy occurred in a 60-year-old woman with known coronary artery disease (CAD) and previously normal LV function, who presented with new exertional symptoms, ECG changes, and apical akinesis following the second dose of the vaccine.
  • The two patients with pericarditis who presented with chest pain, elevated inflammatory markers, and pericardial effusions after receiving the vaccine.

The Johnson and Johnson Covid-19 vaccine was temporarily removed from the market in the U.S. on April 16, 2021 while health officials studied reports of blood clot injuries. Among them was an 18-year old teen named Emma Burkey, who got sick about a week after the Johnson and Johnson Covid-19 vaccine and ended up having three brain surgeries related to blood clots and seizures.

The Johnson and Johnson vaccine was allowed back on the market April 27, 2021 with new warnings about the disorder.

An editorial published in the Journal of the American Medical Association recommended women under age 50 avoid the Johnson and Johnson Covid-19 vaccine due to concerns about blood clots. The recommendation discussed 12 case reports of a blood disorder known as cerebral venous sinus thrombosis (CVST) with thrombocytopenia following the Johnson and Johnson vaccine.

An otherwise healthy South Florida doctor, Gregory Michael, died of a brain hemorrhage 16 days after he got Pfizer’s Covid-19 vaccine. Authorities concluded he died of a blood disorder called “immune thrombocytopenia” (ITP) that can prevent blood from clotting and cause internal bleeding. His wife said a blood test showed the level of his platelets to be at “zero.” She said before the shot, Dr. Michael had “absolutely no medical issues” and no underlying conditions. However, authorities later categorized his death as “natural.”

Several clusters of elderly patients in U.S. nursing homes died after Pfizer or Moderna Covid-19 vaccine. In one group, a number of the patients who died tested positive for Covid-19 after vaccination.

CDC falsely claimed that studies showed Covid-19 vaccines are effective for those who already had Covid-19. In fact, studies showed the opposite.

Anonymous sources claimed that up to 60 million doses of the Johnson and Johnson vaccine had to be thrown out. But the FDA issued a news release saying that two batches from the Baltimore plant were safe to use. The FDA said “several other batches are not suitable for use, but additional batches are still under review.”

According to Epoch Times, in June 2021 nearly 4,000 fully vaccinated people in Massachusetts tested positive for Covid-19. On April 30, “the CDC reported that some 10,626 breakthrough cases were reported in 46 states and territories.” Breakthrough cases are where fully vaccinated people still end up infected with Covid-19.

Scientists hoped that Covid-19 vaccines would be effective in variants of Covid-19, which are mutations that occur naturally with viruses and were always expected with Covid-19. However, the vaccine effectiveness against variants may be limited. CDC and vaccine makers are studying the medical landscape to find out more.

Other states, such as Maine, are noting Covid-19 deaths occurring in fully vaccinated people.

Additional reading and studies

Additional case studies of myocarditis in people after Pfizer and Moderna Covid-19 vaccines, Aug. 18, 2021: https://www.nejm.org/doi/full/10.1056/NEJMc2109975

Zuckerman DM. Emergency Use Authorizations (EUAs) Versus FDA Approval: Implications for COVID-19 and Public Health. Am J Public Health [Internet]. 2021 Jun;111(6):1065–9. Available from: http://dx.doi.org/10.2105/AJPH.2021.306273 

Food and Drug Administration. Development and Licensure of Vaccines to Prevent COVID-19: Guidance for Industry [Internet]. 2020 [cited 2020 Oct 6]. Available from: https://www.fda.gov/media/139638/download

Food and Drug Administration. FDA Briefing Document. Janssen Ad26.COV2.S Vaccine for the Prevention of COVID-19 [Internet]. 2021 [cited 2021 May 28]. Available from: https://www.fda.gov/media/146217/download

CDC. Risk for COVID-19 infection, hospitalization, and death by age group [Internet]. 2021 [cited 2021 May 28]. Available from: https://www.cdc.gov/coronavirus/2019-ncov/covid- data/investigations-discovery/hospitalization-death-by-age.html

CDC. COVID-19 Pandemic Planning Scenarios [Internet]. 2021 [cited 2021 May 28]. Available from:
https://www.cdc.gov/coronavirus/2019-ncov/hcp/planning-scenarios.html 

CDC. Estimated disease burden of COVID-19 [Internet]. 2021 [cited 2021 May 28]. Available from:
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Dan JM, Mateus J, Kato Y, Hastie KM, Yu ED, Faliti CE, et al. Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection. Science [Internet]. 2021 Feb 5;371(6529). Available from: http://dx.doi.org/10.1126/science.abf4063

Turner JS, Kim W, Kalaidina E, Goss CW, Rauseo AM, Schmitz AJ, et al. SARS-CoV-2 infection induces long-lived bone marrow plasma cells in humans. Nature [Internet]. 2021 May 24; Available from: http://dx.doi.org/10.1038/s41586-021-03647-4 

Breton G, Mendoza P, Hagglof T, Oliveira TY, Schaefer-Babajew D, Gaebler C, et al. Persistent Cellular Immunity to SARS-CoV-2 Infection. bioRxiv [Internet]. 2020 Dec 9; Available from: http://dx.doi.org/10.1101/2020.12.08.416636

Hall VJ, Foulkes S, Charlett A, Atti A, Monk EJM, Simmons R, et al. SARS-CoV-2 infection rates of antibody-positive compared with antibody-negative health-care workers in England: a large, multicentre, prospective cohort study (SIREN). Lancet [Internet]. 2021 Apr 17;397(10283):1459–69. Available from: http://dx.doi.org/10.1016/S0140-6736(21)00675-9 

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Samanovic MI, Cornelius AR, Wilson JP, Karmacharya T, Gray-Gaillard SL, Allen JR, et al. Poor antigen-specific responses to the second BNT162b2 mRNA vaccine dose in SARS-CoV-2-experienced individuals. medRxiv [Internet]. 2021 Feb 9; Available from: http://dx.doi.org/10.1101/2021.02.07.21251311 

Camara C, Lozano-Ojalvo D, Lopez-Granados E, Paz-Artal E, Pion M, Correa-Rocha R, et al. Differential effects of the second SARS-CoV-2 mRNA vaccine dose on T cell immunity in naïve and COVID-19 recovered individuals [Internet]. bioRxiv. 2021 [cited 2021 May 28]. p. 2021.03.22.436441. Available from: https://www.biorxiv.org/content/10.1101/2021.03.22.436441v1

Levi R, Azzolini E, Pozzi C, Ubaldi L, Lagioia M, Mantovani A, et al. A cautionary note on recall vaccination in ex-COVID-19 subjects [Internet]. bioRxiv. medRxiv; 2021. Available from: http://medrxiv.org/lookup/doi/10.1101/2021.02.01.21250923

Ogata AF, Cheng C-A, Desjardins M, Senussi Y, Sherman AC, Powell M, et al. Circulating SARS-CoV-2 Vaccine Antigen Detected in the Plasma of mRNA-1273 Vaccine Recipients. Clin Infect Dis [Internet]. 2021 May 20; Available from: http://dx.doi.org/10.1093/cid/ciab465

Kuba K, Imai Y, Rao S, Gao H, Guo F, Guan B, et al. A crucial role of angiotensin converting enzyme 2 (ACE2) in SARS coronavirus-induced lung injury. Nat Med [Internet]. 2005 Aug;11(8):875–9. Available from: http://dx.doi.org/10.1038/nm1267

Chen I-Y, Chang SC, Wu H-Y, Yu T-C, Wei W-C, Lin S, et al. Upregulation of the chemokine (C-C motif) ligand 2 via a severe acute respiratory syndrome coronavirus spike-ACE2 signaling pathway. J Virol [Internet]. 2010 Aug;84(15):7703–12. Available from: http://dx.doi.org/10.1128/JVI.02560-09

Patra T, Meyer K, Geerling L, Isbell TS, Hoft DF, Brien J, et al. SARS-CoV-2 spike protein promotes IL- 6 trans-signaling by activation of angiotensin II receptor signaling in epithelial cells. PLoS Pathog [Internet]. 2020 Dec;16(12):e1009128. Available from: http://dx.doi.org/10.1371/journal.ppat.1009128

Zhang S, Liu Y, Wang X, Yang L, Li H, Wang Y, et al. SARS-CoV-2 binds platelet ACE2 to enhance thrombosis in COVID-19. J Hematol Oncol [Internet]. 2020 Sep 4;13(1):120. Available from: http://dx.doi.org/10.1186/s13045-020-00954-7

Suresh SJ, Suzuki YJ. SARS-CoV-2 Spike Protein and Lung Vascular Cells. Journal of Respiration [Internet]. 2020 Dec 31 [cited 2021 May 25];1(1):40–8. Available from: https://www.mdpi.com/2673-527X/1/1/4

Angeli F, Spanevello A, Reboldi G, Visca D, Verdecchia P. SARS-CoV-2 vaccines: Lights and shadows. Eur J Intern Med [Internet]. 2021 Apr 30; Available from: http://dx.doi.org/10.1016/j.ejim.2021.04.019

Han M, Pandey D. ZMPSTE24 Regulates SARS-CoV-2 Spike Protein-enhanced Expression of Endothelial Plasminogen Activator Inhibitor-1. Am J Respir Cell Mol Biol [Internet]. 2021 May 18; Available from: http://dx.doi.org/10.1165/rcmb.2020-0544OC

Rhea EM, Logsdon AF, Hansen KM, Williams LM, Reed MJ, Baumann KK, et al. The S1 protein of SARS-CoV-2 crosses the blood-brain barrier in mice. Nat Neurosci [Internet]. 2021 Mar;24(3):368– 78. Available from: http://dx.doi.org/10.1038/s41593-020-00771-8

Idrees D, Kumar V. SARS-CoV-2 spike protein interactions with amyloidogenic proteins: Potential clues to neurodegeneration. Biochem Biophys Res Commun [Internet]. 2021 May 21;554:94–8. Available from: http://dx.doi.org/10.1016/j.bbrc.2021.03.100 

Lei Y, Zhang J, Schiavon CR, He M, Chen L, Shen H, et al. SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE 2. Circ Res [Internet]. 2021 Apr 30;128(9):1323–6. Available from: http://dx.doi.org/10.1161/CIRCRESAHA.121.318902 

Zhang L, Richards A, Barrasa MI, Hughes SH, Young RA, Jaenisch R. Reverse-transcribed SARS-CoV-2 RNA can integrate into the genome of cultured human cells and can be expressed in patient- derived tissues. Proc Natl Acad Sci U S A [Internet]. 2021 May 25;118(21). Available from: http://dx.doi.org/10.1073/pnas.2105968118

Suzuki YJ, Nikolaienko SI, Dibrova VA, Dibrova YV, Vasylyk VM, Novikov MY, et al. SARS-CoV-2 spike protein-mediated cell signaling in lung vascular cells. Vascul Pharmacol [Internet]. 2021 Apr;137:106823. Available from: http://dx.doi.org/10.1016/j.vph.2020.106823

Suzuki YJ, Gychka SG. SARS-CoV-2 Spike Protein Elicits Cell Signaling in Human Host Cells: Implications for Possible Consequences of COVID-19 Vaccines. Vaccines (Basel) [Internet]. 2021 Jan 11;9(1). Available from: http://dx.doi.org/10.3390/vaccines9010036

Ogata AF, Maley AM, Wu C, Gilboa T, Norman M, Lazarovits R, et al. Ultra-sensitive Serial Profiling of SARS-CoV-2 Antigens and Antibodies in Plasma to Understand Disease Progression in COVID-19 Patients with Severe Disease. Clin Chem [Internet]. 2020 Sep 8; Available from: http://dx.doi.org/10.1093/clinchem/hvaa213

Kloc M, Uosef A, Kubiak JZ, Ghobrial RM. Exaptation of Retroviral Syncytin for Development of Syncytialized Placenta, Its Limited Homology to the SARS-CoV-2 Spike Protein and Arguments against Disturbing Narrative in the Context of COVID-19 Vaccination. Biology [Internet]. 2021 Mar 19;10(3). Available from: http://dx.doi.org/10.3390/biology10030238 

Khan I, Hatiboglu MA. Can COVID-19 induce glioma tumorogenesis through binding cell receptors? Med Hypotheses [Internet]. 2020 Nov;144:110009. Available from: http://dx.doi.org/10.1016/j.mehy.2020.110009

Singh N, Bharara Singh A. S2 subunit of SARS-nCoV-2 interacts with tumor suppressor protein p53 and BRCA: an in silico study. Transl Oncol [Internet]. 2020 Oct;13(10):100814. Available from: http://dx.doi.org/10.1016/j.tranon.2020.100814

Madla CM, Gavins FKH, Merchant H, Orlu M, Murdan S, Basit AW. Let’s Talk About Sex: Differences in Drug Therapy in Males and Females. Adv Drug Deliv Rev [Internet]. 2021 May 17; Available from: http://dx.doi.org/10.1016/j.addr.2021.05.014 

European Medicines Agency. Assessment Report. Comirnaty (COVID-19 mRNA vaccine (nucleoside- modified)), EMA/707383/2020 Corr.1 [Internet]. 2021 Feb [cited 2021 Apr 13]. Available from: https://www.ema.europa.eu/en/documents/assessment-report/comirnaty-epar-public- assessment-report_en.pdf#page=45 

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Local Detroit TV Asks For Stories of Unvaxxed Dying from COVID – Gets over 182K Responses of Vaccine Injured and Dead Instead

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More life and death news the Democrat-media-entertainment-academia-complex militantly forbids from the public.

Local Detroit TV Asks for Stories of Unvaxxed Dying from COVID – Gets over 180K Responses of Vaccine Injured and Dead Instead

By Brian Shilhavy, Editor, Health Impact News September 14, 2021:

The corporate media narrative that unvaccinated people are filling up the hospitals and dying from COVID is quickly falling apart, perhaps faster than they even expected.

WXYZ TV Channel 7 in Detroit asked their viewers on their Facebook Page last Friday to direct message them if they lost a loved one due to COVID-19 if they refused to get one of the COVID-19 vaccines.

This is a clear indication that they are getting desperate to find these stories, and are having a difficult time finding them.

I don’t know if they got any such stories through direct messaging, but the post on their Facebook Page, as of the time of publication today, had received over 182,000 comments, and they seem to be all comments of those who have lost loved ones after receiving a COVID shot, and comments asking them why they are not covering that story.

I paged through many dozens of the comments and did not see a single one stating that they lost someone to COVID after refusing a COVID-19 shot.

People who have been silenced and censored on Facebook and other Big Tech platforms took advantage of the opportunity to share their stories instead. It is amazing that Facebook left these up, but after so many had commented, it would probably have been an even bigger story if they had taken down the post and comments.

I wonder what WXYZ will do now? Will they do what most corporate media companies do, fueled by almost unlimited resources from their billionaire Wall Street owners who are almost all connected to the pharmaceutical industry, and just go out and hire actors instead to do the story and make them up?

Here are a few screen shots of the comments that are representative of what people are posting, in case they do take this down.

CLICK HERE TO VIEW SCREEN SHOTS

RELATED ARTICLE: Summary: Covid-19 Vaccine Concerns

EDITORS NOTE: This Geller Report column is republished with permission. ©All rights reserved.

Quick note: Tech giants are shutting us down. You know this. Twitter, LinkedIn, Google Adsense, Pinterest permanently banned us. Facebook, Google search et al have shadow-banned, suspended and deleted us from your news feeds. They are disappearing us. But we are here. We will not waver. We will not tire. We will not falter, and we will not fail. Freedom will prevail.

Subscribe to Geller Report newsletter here — it’s free and it’s critical NOW when informed decision making and opinion is essential to America’s survival. Share our posts on your social channels and with your email contacts. Fight the great fight.

Follow me on Gettr. I am there. It’s open and free.

Remember, YOU make the work possible. If you can, please contribute to Geller Report.

Biden Restricts Life-Saving Coronavirus Meds In Feud With GOP Governors [+Video]

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Take action. Please go online to their websites and send an email to Senator Rubio, Senator Scott, Rep. Franklin, and Rep Soto that asks the following question.

Could you please explain to me what you are doing about Biden’s federal Department of Health restricting doses of life saving monoclonal antibody treatments to FL which also prevent hospitalizations ?

Outrage Builds as Biden Denies Life-Saving Coronavirus Meds in Feud with GOP Governors

By CHARLIE SPIERING

President Joe Biden continues facing criticism for restricting shipments of monoclonal antibody treatments for the coronavirus to Southern states.

The treatment for the Chinese coronavirus is in high demand in Southern states where some residents are still not vaccinated, as well as for those who are vaccinated but still contracted the virus.

But the Department of Health and Human services has restricted shipments of the treatment to Florida and other southern states.

In Florida, HHS provided less than 31,000 doses this week — half of the 70,000 doses requested by the state.

That prompted Florida Gov. Ron DeSantis to publicly condemn the Biden administration.

Read more.

©All rights reserved.

RELATED ARTICLE: CDC Panel: Heart Attacks Happen 71 Times More Often After mRNA Vaxx

VIDEO: Biden Isn’t Joe-King with Mandate

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Attorneys general in 24 states sent a letter to President Biden yesterday, threatening legal action if he follows through on his threat to mandate private companies with more than 100 employees to require their employees either take the coronavirus vaccine, submit to weekly testing, or be fired. One of those attorneys general, Dave Yost of Ohio, explained further on “Washington Watch.”

“What the president said he wanted to do,” said Yost, “seems clearly beyond his authority.” President Biden plans to define coronavirus as an occupational safety hazard to be enforced by the Department of Labor, a step clearly outside the intended purpose of the law, the letter argued.

“Congress writes the laws, not the president. He doesn’t get to govern by dictate,” said Yost. “The difference between a democracy and a monarchy or a dictatorship is that in a democracy laws have to be written by a representative body, a congress or a parliament. In a monarchy or a dictatorship, one executive decides what the rules are and they enforce them. That is just fundamentally opposite our constitutional order.”

Not only is President Biden circumventing Congress’ authority to write laws, said Yost, but he is interfering with health issues which are properly considered “part of the police power that belongs to the states.” (Thus, to date, the CDC has issued only recommended guidelines, which state health departments have adopted, modified, or rejected. Mask mandates and lockdowns were widely issued by state governors, but the federal government only issued a mask mandate covering areas of federal jurisdiction, like federal property and air travel.)

Everyone, even the Biden administration, understands the president lacks the authority for such a mandate. “They know they don’t have the legal authority,” Yost explained, “but they do it knowing it’ll be in the courts forever.” President Biden’s strategy seems strikingly similar to one he employed only weeks ago, when he unilaterally extended an illegal moratorium on evictions, in direct violation of a Supreme Court ruling. Then, Biden admitted his action was illegal, but he was simply buying time for his policies. He said he sought the “ability to, if we have to appeal, to keep this going for a month at least. I hope longer.”

In striking down Biden’s eviction moratorium, the Supreme Court stated clearly that the Constitution “does not permit agencies to act unlawfully even in pursuit of desirable ends.” They added, “we expect Congress to speak clearly when authorizing an agency to exercise powers of ‘vast economic and political significance.'” It seems President Biden is simply calculating he can force many businesses to comply with his diktat before the Supreme Court obliterates it.

Yost said the attorneys general would likely ask for a temporary restraining order — when the administration actually produces a regulation. “Right now, it’s not in effect.” (Some private companies have begun requiring vaccination as a condition of employment, but that is their own decision.)

The silver lining of President Biden’s brazen lawlessness is that it serves to highlight the checks and balances of America’s federal system. When you don’t live in a monarchy ruled by King Joseph the First. When 1600 Pennsylvania Avenue overreaches, it triggers a reaction across town at the Supreme Court. But it also triggers a larger wave of resistance from those governments outside the Washington beltway that actually listen to the American people.

COLUMN BY

Joshua Arnold

Media Coordinator. As media coordinator, Joshua serves under the Vice President of Communications in a number of ways, including coordinating interview requests, editing op-eds and press releases, and assisting in various capacities with the Washington Watch radio show.

Joshua hails from Clemson, South Carolina, where he was homeschooled with his five siblings. He graduated from Patrick Henry College with a B.A. in Government and a special emphasis in American Politics and Policy. He later attended the Pepperdine University School of Public Policy and graduated as valedictorian with a Master’s in Public Policy, emphasizing Economics and American Policy. Before joining Family Research Council, Joshua also worked for the National Pro-Life Alliance and parentalrights.org, as well as interning in the White House Office of Speechwriting.

Joshua is passionate about policy research and analysis, specifically about developing innovative solutions to the day’s greatest policy challenges from a biblical perspective. He enjoys participating in the life of his local church and exploring a variety of nerdy hobbies ranging from strategy board games to sci-fi television and book series.

EDITORS NOTE: This FRC-Action video and column are republished with permission. ©All rights reserved.

VIDEO: FDA Bought Fetal Organs, Heads and Tissue for ‘Humanized Mice’ Project

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Judicial Watch has uncovered more documents detailing the evil activities of your federal government – the trafficking of the remains of unborn human beings killed by abortion.

We received another 198 pages of records and communications from the U.S. Food and Drug Administration (FDA) involving “humanized mice” research with human fetal heads, organs and tissue, including communications and contracts with human fetal tissue provider Advanced Bioscience Resources (ABR).

Most of the records are communications and related attachments between Perrin Larton, a procurement manager for ABR, and research veterinary medical officer Dr. Kristina Howard of the FDA.

We received the records through a March 2019 FOIA lawsuit against the U.S. Department of Health and Human Services, of which the FDA is a part (Judicial Watch v. U.S. Department Health and Human Services (No. 1:19-cv-00876)).

Our lawsuit asks for all contracts and related documentation on disbursement of funds, procedural documents and communications between FDA and ABR for the provision of human fetal tissue to be used in humanized mice research. After we successfully opposed the FDA’s redaction of certain information from its records, a federal court ordered HHS to release additional information about its purchases of organs harvested from aborted human fetuses – including “line item prices,” or the price per organ the government paid to ABR. The court also found “there is reason to question” whether the transactions violate federal law barring the sale of fetal organs. Documents previously uncovered in this lawsuit show that the federal government demanded the purchased fetal organs be “fresh and never frozen.”)

The records include an FDA generated contract with ABR, based on a “requisition” it issued on July 27, 2012, for $12,000 worth of “tissue procurement for humanized mice,” which indicates the requisition was for a “non-competitive award.” Although the initial award was for $12,000, the total estimated amount of funds allocated for the requisition was $60,000. Under “Justification for Other than Full and Open Competition,” the FDA writes:

Scientists within the FDA and in the larger field of humanized mouse research have searched extensively over the past several years, and ABR is the only company in the U.S. capable of supplying tissues suitable for HM research. No other company or organization is capable of fulfilling the need.

Costs are estimated [for the fetal parts] at $230 per tissue x two tissues per shipment = $460 plus $95 shipping = $555 per shipment. A total of 21 shipments = $11,655.00.

An April 1, 2013, “Amendment of Solicitation/Modification of Contract” form that shows the FDA purchased fetal livers and thymuses from ABR going back to at least October 2012, billing $580 per liver/thymus set, but later paying a unit price of $685.

A January 1, 2013, “Fees for Services Schedule” provided by ABR to the FDA includes:

FETAL CADAVEROUS PROCUREMENT                           SERVICE FEE
2nd trimester D&E
[Dilation and Evacuation abortion]
(13-24 weeks)                                                                      per specimen     $275
1st trimester aspiration [abortion] (8-12 weeks)          per specimen     $515
Intact Calvarium [baby’s skull] (8-24 weeks)”                per specimen     $515

The fees for services schedule also includes “Special Processing/Preservation” of the fetal parts, such as “Tissue ‘Cleaning,’” “Snap freezing,” and “Passive freezing (Dry ice).”

In a September 9, 2014, “Order for Supplies or Services,” the FDA writes regarding a $9,900 order:

The Contractors shall ship 2nd Trimester thymus $325, 2nd Trimester liver $325. Overnight deliver $150 and EFT wire transfer fee $25, for a total per delivery of $825. Total of this contract not to exceed $9,900.00.

As the result of an August 21, 2015, “Amendment of Solicitation/Modification of Contract,” ABR bumped up the price of baby livers and thymuses from $325 each to $340 each.

A “Tissue Acquisition Quote” sent by ABR to Howard on July 5, 2017, provided a quote of $5,440 each to provide 16 sets of second trimester (16-24 weeks) livers and 16 sets of second trimester (16-24 weeks) thymuses at $340 per “sample.” The request for the quote notes that “tissue known to be positive for HIV, HepA, HepB, HepC or chromosomal abnormalities are not acceptable.”

On June 28, 2017, a redacted FDA contract specialist sends Larton at ABR a request for a quote (RFQ) of pricing for human fetal tissue, aged “16-24 weeks,” including a “Statement of Needs”:

The HM [humanized mice] are created by surgical implantations of human tissue into mice that have multiple genetic mutations that block the development of the mouse immune system at a very early stage. The absence of the mouse immune system allows the human tissues to grow and develop into functional human tissues…. In order for the humanization to proceed correctly we need to obtain fetal tissue with a specific set of specialized characteristics.

A May 2018, report from a company named “LABS,” which was employed by ABR to test fetal parts and their mothers for hepatitis and HIV, notes in its “methodology description” that they are approved by the FDA “for living and cadaveric donor screening.”

The records include a recitation of requirements by the FDA for “Payment by Electronic Funds Transfer,” in which ABR must adhere to regulations relating to “Convict Labor” and “Child Labor-Cooperation with Authorities and Remedies.”

On September 24, 2018, the Trump FDA terminated its contract with ABR for human tissue purchases and began an audit of its acquisitions of baby body parts. The records include the FDA’s letter terminating the contract:

Based on the terms and conditions of the Purchase Order as awarded to Advanced Bioscience Resources, Inc. (“ABR”) on July 27, 2018, the Government is not sufficiently assured that the human tissue provided to the Government to humanize the immune systems of mice will comply with the prohibitions set forth under 42 U.S.C. § 289g- 2. Furthermore, the Government has concerns with the sufficiency of the sole-source justification. Therefore, pursuant to FAR [Federal Acquisition Regulation] clause 52.213-4(f), the Purchase Order is being terminated effective September 24, 2018.

Here’s some background.

In February 2020, we first uncovered through this lawsuit hundreds of pages of records from the National Institutes of Health (NIH) showing that the agency paid thousands of dollars to a California-based firm to purchase organs from aborted human fetuses to create “humanized mice” for HIV research.

In May 2021, this lawsuit uncovered FDA records showing the agency spent tens of thousands of taxpayer dollars to buy human fetal tissue from ABR. The tissue was used in creating “humanized mice” to test “biologic drug products.” The records indicated the FDA wanted tissue purchases “Fresh; shipped on wet ice.”

On August 3, 2021, we announced that The Center for Medical Progress (CMP) and Judicial Watch, through a separate lawsuit, received 252 pages of new documents from the U.S. Department of Health and Human Services that reveal nearly $3 million in federal funds were spent on the University of Pittsburgh’s quest to become a “Tissue Hub” for human fetal tissue ranging from 6 to 42 weeks’ gestation. The Pitt scientists note that, “All fetal tissue is collected through a collaborative process including Family Planning, Obstetrics and Pathology.” Pitt anticipated “being able to harvest and distribute quality tissue and cells … [and] do not anticipate any major problems related to the acquisition and distribution of the tissues.” Pitt’s target goal “is to have available a minimum of 5 cases (tissues and if possible other biologicals) per week of gestational age for ages 6-42 weeks.”

Chopping up aborted human beings for their organs and tissue is a moral and legal outrage. This issue should be front and center in any debate about America’s barbaric abortion industry.

EDITORS NOTE: This Judicial Watch column is republished with permission. ©All rights reserved.

CDC Panel: Heart Attacks Happen 71 Times More Often After mRNA Vaxx

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The FDA’s official YouTube channel posted a livestream hours ago where a panel member admits COVID vaccines are killing more people than they’re saving, effectively declaring them ineffective and highly dangerous.

Watch:

©All rights reserved.

RELATED ARTICLES:

Summary: Covid-19 Vaccine Concerns

Local Detroit TV Asks For Stories of Unvaxxed Dying from COVID – Gets over 182K Responses of Vaccine Injured and Dead Instead

Texas Hospital Faces Closure Over COVID-19 Vaccine Mandate

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The Democrats are taking a wrecking ball to …….. everything. Their hatred for this country is heinous and evil.

Texas Hospital Faces Closure Over COVID-19 Vaccine Mandate: CEO

By Jack Phillips, September 15, 2021

The chief executive of a hospital in Texas warned that his facility faces closure after President Joe Biden’s announcement last week that most healthcare workers get the COVID-19 vaccine.

If the mandate goes through, Brownfield Regional Medical Center CEO Jerry Jasper said that “20 percent of my, probably 20 to 25 percent of my staff will have to go away if that’s the case,” reported KCBD. Losing those workers, he said, would likely cause his hospital to shut down, and losing Medicare and Medicaid money isn’t an option either.

A White House stipulates that healthcare workers who work at hospitals and facilities that receive either Medicaid or Medicare funds will have to get the COVID-19 vaccine.

“It’s huge in our rural community as all the other rural communities. We all have high poverty levels and stuff like that, so a lot of Medicaid usage in our communities and stuff like that,” Jasper remarked to the station.

Another local hospital executive said that the mandate echoed Jasper’s sentiments.

“Well, it would be devastating for the community, frankly. We have a large percentage of our revenue that comes from Medicare, Medicaid, and those kinds of products,” Larry Gray, the CEO of the Seminole Hospital District, told the station.

While Gray said he encourages vaccines, mandates don’t work.

“I think the mandate is just a terrible message because if the vaccinations are working, why do you have to mandate people to get the vaccines?” Gray asked. “What happens to individual choice and medical decisions between the patient and their doctor, which is all of the things that we’re trying to support.”

Other than mandates for healthcare workers, Biden also announced he would direct the federal Occupational Safety and Health Administration to enforce a rule against companies with 100 or more workers that employees either get the vaccine or submit to weekly COVID-19 testing. Federal workers and contractors will also have to get the vaccine, he said.

In Upstate New York, a regional hospital’s executive said that the facility will have to at least temporarily close down its maternity unit and will not be able to deliver babies due to a mandate that was handed down by former Gov. Andrew Cuomo. Lewis County Health System Chief Executive Officer Gerald Cayer said that six employees who were employed in the unit resigned, according to local media reports.

“If we can pause the service and now focus on recruiting nurses who are vaccinated, we will be able to reengage in delivering babies here in Lewis County,” Cayer said at a news conference on Sept. 10.

EDITORS NOTE: This Geller Report column is republished with permission. ©All rights reserved.

Quick note: Tech giants are shutting us down. You know this. Twitter, LinkedIn, Google Adsense, Pinterest permanently banned us. Facebook, Google search et al have shadow-banned, suspended and deleted us from your news feeds. They are disappearing us. But we are here. We will not waver. We will not tire. We will not falter, and we will not fail. Freedom will prevail.

Subscribe to Geller Report newsletter here — it’s free and it’s critical NOW when informed decision making and opinion is essential to America’s survival. Share our posts on your social channels and with your email contacts. Fight the great fight.

Follow me on Gettr. I am there. It’s open and free.

Remember, YOU make the work possible. If you can, please contribute to Geller Report.

Indian Bar Association Sues WHO Scientist Over Ivermectin!

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Today’s blog comes from an article from India. It is about the Indian Bar Association suing the WHO ( World Health Organization ) for lying about the ineffectiveness of Ivermectin.

It is an interesting take and a strong step other states, countries and governments need to be taking. As I keep mentioning this whole china virus thing is about money, power, enslaving and more money and power. Making citizens around the world dependent on the government and to destroy all vestiges of liberty and freedom including freedom of choice. You will belong to the government from cradle to grave.

They will decide your job, religion, healthcare and every other aspect including what media you listen to and your freedom to choose for your kids will be removed. Read this story posted below and feel free to share this blog far and wide.

Indian Bar Association sues WHO scientist over Ivermectin – by Justus R. Hope, MD. (Updated September 08.)

The Indian Bar Association (IBA) sued WHO Chief Scientist Dr. Soumya Swaminathan on May 25, accusing her in a 71-point brief of causing the deaths of Indian citizens by misleading them about Ivermectin.

Point 56 states, “That your misleading tweet on May 10, 2021, against the use of Ivermectin had the effect of the State of Tamil Nadu withdrawing Ivermectin from the protocol on May 11, 2021, just a day after the Tamil Nadu government had indicated the same for the treatment of COVID-19 patients.”

Advocate Dipali Ojha, lead attorney for the Indian Bar Association, threatened criminal prosecution against Dr.  Swaminathan “for each death” caused by her acts of commission and omission. The brief accused Swaminathan of misconduct by using her position as a health authority to further the agenda of special interests to maintain an EUA for the lucrative vaccine industry.

Specific charges included the running of a disinformation campaign against Ivermectin and issuing statements in social and mainstream media to wrongfully influence the public against the use of Ivermectin despite the existence of large amounts of clinical data showing its profound effectiveness in both prevention and treatment of COVID-19.

In particular, the Indian Bar brief referenced the peer-reviewed publications and evidence compiled by the ten-member Front Line COVID-19 Critical Care Alliance (FLCCC) group and the 65-member British Ivermectin Recommendation Development (BIRD) panel headed by WHO consultant and meta-analysis expert Dr. Tess Lawrie.

The brief cited US Attorney Ralph C. Lorigo’s hospital cases in New York where court orders were required for dying COVID patients to receive the Ivermectin. In multiple instances of such comatose patients, following the court-ordered Ivermectin, the patients recovered. In addition, the Indian Bar Association cited previous articles published in this forum, The Desert Review.

Advocate Ojha accused the WHO and Dr. Swaminathan in Points 60 and 61 as having misled and misguided the Indian people throughout the pandemic from mask wear to exonerating China as to the virus’s origins.

“The world is gradually waking up to your absurd, arbitrary and fallacious approach in presenting concocted facts as ‘scientific approach.’ While the WHO flaunts itself like a ‘know it all,’ it is akin to the vain Emperor in new clothes while the entire world has realized by now, the Emperor has no clothes at all.”

The brief accused the WHO of being complicit in a vast disinformation campaign. Point 61 states, “The FLCCC and the BIRD have shown exemplary courage in building a formidable force to tackle the challenge of disinformation, resistance, and rebuke from pharma lobbies and powerful health interests like WHO, NIH, CDC, and regulators like the US FDA.”

Dr. Swaminathan was called out for her malfeasance in discrediting Ivermectin to preserve the EUA for the vaccine and pharmaceutical industry. Point 52 reads,  “It seems you have deliberately opted for deaths of people to achieve your ulterior goals, and this is sufficient grounds for criminal prosecution against you.”

The Indian Bar Association posted an update on their website June 5, 2021, noting that Dr. Swaminathan had deleted her now-infamous tweet. They wrote, “However, deleting the tweet will not save Dr. Soumya Swaminathan and her associates from the criminal prosecution which is to be launched by the citizens with active support from the Indian Bar Association.”

https://indianbarassociation.in/blogs-iba/

In this update, Advocate Dipali Ojha clarified the nature of the planned action,

“The Indian Bar Association has warned action under section 302 etc. of the Indian Penal Code against Dr. Soumya Swaminathan and others, for murder of each person dying due to obstruction in treatment of COVID-19 patient effectively by Ivermectin. Punishment under section 302 of the Indian Penal Code is death penalty or life imprisonment.”

He further wrote, “After receiving the said notice, Dr. Soumya Swaminathan went on the back foot and deleted her tweet. This has proved the hollowness of the WHO’s recommendation against Ivermectin for COVID-19. The dishonesty of  WHO and the act of Dr. Soumya Swaminathan in deleting her contentious tweet was witnessed by citizens across the world, as the news got a wide coverage on social media. By deleting the tweet, Dr. Soumya Swaminathan has proved her mala fide intentions.”

The entire world witnessed the effectiveness of Ivermectin against India’s deadly second surge as the locations that adopted it saw their outbreaks quickly extinguished in stark contrast to those states that did not.

Among the most prominent examples include the Ivermectin areas of Delhi, Uttar Pradesh, Uttarakhand, and Goa where cases dropped 98%, 97%, 94%, and 86%, respectively. By contrast, Tamil Nadu opted out of Ivermectin. As a result, their cases skyrocketed and rose to the highest in India. Tamil Nadu deaths increased ten-fold.

https://www.thedesertreview.com/news/national/ivermectin-obliterates-97-percent-of-delhi-cases/article_6a3be6b2-c31f-11eb-836d-2722d2325a08.html

Tamil Nadu publicly relied upon Dr. Swaminathan’s advice in revoking their initial choice of Ivermectin the day after she recommended against it in her May 10 tweet on social media. As a direct result, Tamil Nadu experienced a surge in COVID death and sickness that continues to this day.

The Indian Bar Association dared to initiate a landmark court case against a Public Health Authority (PHA) to call out corruption and to save lives. As the courts in the United States proved to be the life-saving force to ensure a patient’s right to receive Ivermectin, a court in India is now doing the same.

Criminal prosecution of public health officials will send a powerful signal that disinformation campaigns resulting in death carry consequences. Perhaps this pathway will ultimately break the disinformation and censorship stranglehold around repurposed drug use to save lives. Maybe we will witness other countries following India’s example, both in medicine and in law.

Signed, Justus R. Hope, MD

©Fred Brownbill. All rights reserved.