Did Trump make a mistake endorsing Luna?!

Today’s blog is not something I saw myself ever writing or posting. During the last election cycle I supported Anna Paulina Luna. Financially and other ways. She was a stated veteran and true conservative I thought. I attended some of her rallies, had her yard signs, spoke with her several times. Promoted her candidacy.

I read the story I am posting here and it seemed like dejavue all over again. Was this yet another swamp creature raising its head? Was it all lies? Did I really misjudge her so badly? Maybe….You judge. You tell me. I mean – look at her campaign photo from a magazine cover!

You read this story and understand that it is because we are too trusting in people’s claims that we do not do due diligence before supporting and voting for candidates whose ethics and story may not be what we understood them to be.

This article is by Roger Stone, a friend and confidante of President Trump for over 40 years. His research seems accurate from what I have looked into. Read this now and understand why we need to do due diligence every time we vote. Our Constitutional Republic depends on it. Become informed voters.

Opinion Roger Stone: Trump Endorsement Of Luna Questionable.

I noticed this morning ( September 15th ) that former President Donald Trump, a friend and client of mine for some 40 years, has endorsed Anna Paulina Luna for Congress for the seat vacated by former Governor Charlie Crist so he can run for Governor.

It’s an odd choice particularly since ‘Luna” as she now calls herself did not run a particularly strong race, losing badly by 30,000 votes, running 5 points behind Trump who only lost the district by 1% while Luna lost by 6%.

As someone who has great loyalty and affection for the President and both knows and understands him and also has a keen understanding of the dynamics surrounding the process in which these endorsement decisions are made,

I can now confidently predict that the President will ultimately withdraw his endorsement long before the Republican Congressional Primary next year. I really doubt that the President has any understanding of Anna Meyerhoffer, the California Democrat who supported Barrack Obama while living in California (where she listed ethnicity on her driver’s license as ‘Caucasian” rather than Hispanic.

There is surely no way President Trump, my friend of 40 years, is aware of her abuse of the Judicial System and her (Luna) habitual filing of restraining orders against her political opponents or anyone who gets in her ambitious way. She filed a restraining order against a member of her own family when he had the audacity to come forward and point out that her entire biography is a fraud.

Luna also filed a restraining order against a woman in Fort Walton Beach which just happens to be in the Matt Gaetz district -when Luna was working at a Gentleman’s club as a dancer. Luna’s denial that she was a dancer and her insistence she was a cocktail waitress is debunked in sworn affidavits from the club owner and two employees. Dancer. Stripper. Read ” Stone’s Rules. No amount of cash to Peter Scorsch Is going to change the facts.

Let me state up front that I have no professional involvement in this congressional race; Matt Tito, a US Marine combat veteran who is going to make a bid for the congressional nomination, is a friend of mine. Unlike Luna who was never deployed outside the country during her time in the Air Force and never saw combat. Matt Tito is a genuine American hero. Matt came to my attention when he made a valiant bid for a Florida State House in an overwhelmingly Democrat district and ran 18% ahead of the President in 2020.

When I was in Tampa, Tito posted a picture of us together on INSTAGRAM. Suddenly my e-mail box blew up with anonymous e-mails attacking Matt Tito, accusing him of a host of unsubstantiated crimes and misdeeds – none of which were accurate or true. Only weeks later an Editor at El American asked me if I would write an OP-ED for July 4th.

When my piece was posted I learned that “Luna”, who has some affiliation with El American, demanded the editors take my piece down because I “tried to poison her.”

I have never met this woman but her nutty claim forced me to dig into who she really is. By the way, I have two sworn affidavits from people working for El American as to this exact course of events because I now know “Luna’s” pattern when confronted with her unhinged unbalanced behavior; she lies and plays the victim.

The statement by the President calling Matt Tito a RINO just adds to the mountain of lies that Luna has told, many of them under oath particularly in the recent contrived publicity stunt in which she accused Matt Tito and her other opponents of plotting together to murder her. In fact, the released Presidential Statement came on the exact day Luna and one of her henchwomen perjured themselves repeatedly as Luna’s ‘Murder Plot PR stunt” began to unravel in a court-ordered deposition.

I can’t imagine who might have urged the President to endorse such a person and wonder if he knows what happens when someone hasn’t told the President the whole truth leading to an action- where he might get embarrassed for not knowing all the facts.

What will the President do when he learns that Anna Paulina Luna is not even her real name and that she has not an iota of Hispanic heritage? What happens when he learns that she used campaign photos of herself in fatigues holding military-grade weapons to imply that she has served her country in combat when she was never deployed; such a claim is stolen valor and illegal in the state of Florida.

What happens when the president learns that Luna, who was a registered Democrat who supported Obama when she lived in California and where she listed her ethnicity as non-Hispanic in her voting records? Or when he learns “Luna” used “LUNA- TRUMP” on her yard signs in the Republican primary but distancing herself from the President switching to ‘LUNA- INDEPENDENT LEADERSHIP yard signs for her dismal general election campaign.

What happens when the President learns that Luna’s campaign operatives illegally recorded telephone conversations with political opponents; a felony for which individuals are regularly prosecuted in Florida and for which Luna’s henchwoman will ultimately be prosecuted herself?

Then there is the police report filed with the Saint Petersburg police in which Luna accused her opponents of “plotting her murder.

By law a police complaint must be cosigned by two witnesses. In this case, Anna  Paulina Luna’s complaint was cosigned by her husband “Brian Luna.” There is no such person. Filing a police complaint under a false name is a felony. Oh, what a tangled web we weave.

I have no doubt that the rigors of a primary campaign will demonstrate that Anna Paulina Luna is mentally unbalanced and a congenital liar whose entire background is essentially falsified. My next move? I am taking out a restraining order to ensure that certified, nut job Diva, Anna Paulina Meyerhoffer, and the camp followers she surrounds herself with stay away from me.

©Fred Brownbill. All rights reserved.

Lyft Puts Anti-Life Ideology on Display with Opposition to Texas’ Heartbeat Law

State legislators have a duty to enact laws supported by their constituents. This foundational principle is core to America’s Constitutional, federalist system. But it’s also somehow controversial to woke social justice warriors, who rail against any state policy that goes against their vision of a progressive cultural utopia.

The latest state to end up in their crosshairs is Texas. Their newly enacted “Heartbeat Law” prohibits abortion after 6 weeks gestation, making it a civil offense to perform or aid in one after the unborn child has a heartbeat.

Never mind that a plurality of Americans support the law. It contradicts the authoritarian woke agenda, so woke corporations have dutifully fallen in line to express their opposition.

One of the most ridiculous responses is from ride-sharing app Lyft (1.00), whose CEO Tweeted that since their drivers could be considered “aiding abortion” by bringing women to their appointments, Lyft would cover legal fees for drivers sued under the law. They also gave a $1 million donation to Planned Parenthood.

For a company that waxes poetic about their employees’ value, Lyft cares little for their freedom of expression. Just weeks ago, they fired a driver for listening to a radio show a passenger deemed “racist.” Ironically, the show featured a Black host accusing Black Lives Matter of ignoring how abortion destroys more Black lives than any other demographic. Clearly, Lyft values their employees only when they dutifully adhere to pro-abortion ideology: acceptance earns applause; dissent gets you fired.

While Lyft put their hypocrisy on display, it isn’t the only company taking a stance against Texas’ new law. Dating app Bumble pledged to help Texas-based employees terminate their pregnancies out of state. GoDaddy Inc. (2.67), a website-hosting service, took down a site used to report violations of the new law.

These companies must get out of the business of policymaking and leave that to lawmakers and the courts. Until they do, take your money elsewhere. Perhaps when we hold Lyft accountable for their support of destroying human life, they’ll get out of politics and back to business.

Please reach out to LyftBumble, and GoDaddy to share your collective thoughts on the pro-life issue and let your voice be heard!

EDITORS NOTE: This 2nd Vote column is republished with permission. ©All rights reserved.

Summary: Covid-19 Vaccine Concerns

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

Exclusive Summary: Covid-19 Vaccine Concerns

  • 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.”

ItalyRestricted 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:
https://www.cdc.gov/coronavirus/2019-ncov/cases-updates/burden.html 

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 

Krammer F, Srivastava K, Simon V, the PARIS team. Robust spike antibody responses and increased reactogenicity in seropositive individuals after a single dose of SARS-CoV-2 mRNA vaccine [Internet]. bioRxiv. medRxiv; 2021. Available from: http://medrxiv.org/lookup/doi/10.1101/2021.01.29.21250653 

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 

European Medicines Agency. Assessment Report. COVID-19 Vaccine Moderna (COVID-19 mRNA Vaccine (nucleoside-modified)), EMA/15689/2021 Corr.1 [Internet]. 2021 Mar [cited 2021 Apr 13]. Available from: https://www.ema.europa.eu/en/documents/assessment-report/covid-19-vaccine- moderna-epar-public-assessment-report_en.pdf#page=47

European Medicines Agency. Assessment Report. COVID-19 Vaccine Janssen, EMA/158424/2021 [Internet]. 2021 Mar [cited 2021 Apr 13]. Available from: https://www.ema.europa.eu/en/documents/assessment-report/covid-19-vaccine-janssen-epar- public-assessment-report_en.pdf#page=50

Pfizer. SARS-CoV- 2 mRNA Vaccine (BNT162, PF-07302048) 2.6.4 Yakubutsu dōtai shiken no gaiyō bun [summary of pharmacokinetic studies] [Internet]. 2021 [cited 2021 May 28]. Available from: https://www.pmda.go.jp/drugs/2021/P20210212001/672212000_30300AMX00231_I100_1.pdf#pa ge=16

CDC. Selected adverse events reported after COVID-19 vaccination [Internet]. 2021 [cited 2021 May 28]. Available from: https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/adverse- events.html 

Doshi P. FDA response to BMJ on reports of death after covid-19 vaccination [Internet]. 2021 [cited 2021 May 28]. Available from: https://www.bmj.com/content/372/bmj.n149/rr-25

Wyller TB, Kittang BR, Ranhoff AH, Harg P, Myrstad M. Nursing home deaths after COVID-19 vaccination. Tidsskr Nor Laegeforen [Internet]. 2021 May 20;141. Available from: http://dx.doi.org/10.4045/tidsskr.21.0383

Torjesen I. Covid-19: Pfizer-BioNTech vaccine is “likely” responsible for deaths of some elderly patients, Norwegian review finds. BMJ [Internet]. 2021 May 27 [cited 2021 May 28];373. Available from: https://www.bmj.com/content/373/bmj.n1372 

Food and Drug Administration. Coronavirus (COVID-19) update: FDA Issues Policies to guide medical product developers addressing virus variants [Internet]. 2021 [cited 2021 May 28]. Available from: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19- update-fda-issues-policies-guide-medical-product-developers-addressing-virus

Owens C. Vaccine boosters could be necessary as soon as September [Internet]. Axios. 2021 [cited 2021 May 28]. Available from: https://www.axios.com/coronavirus-vaccines-boosters-pfizer- moderna-e8d6bed6-8238-4e52-9959-ca4c6a6e0d5a.html

Polack FP, Thomas SJ, Kitchin N, Absalon J, Gurtman A, Lockhart S, et al. Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine. N Engl J Med [Internet]. 2020 Dec 31;383(27):2603–15. Available from: http://dx.doi.org/10.1056/NEJMoa2034577

Baden LR, El Sahly HM, Essink B, Kotloff K, Frey S, Novak R, et al. Efficacy and Safety of the mRNA- 1273 SARS-CoV-2 Vaccine. N Engl J Med [Internet]. 2021 Feb 4;384(5):403–16. Available from: http://dx.doi.org/10.1056/NEJMoa2035389

Thacker PD. Covid-19: How independent were the US and British vaccine advisory committees? BMJ [Internet]. 2021 May 26;373:n1283. Available from: http://dx.doi.org/10.1136/bmj.n1283

Moderna. SARS-CoV- 2 mRNA Vaccine (Moderna) 2.6.4 Yakubutsu dōtai shiken no gaiyō bun [summary of pharmacokinetic studies] [Internet]. 2021 [cited 2021 May 29]. Available from: https://www.pmda.go.jp/drugs/2021/P20210519003/400256000_30300AMX00266_I100_1.pdf#pa ge=7

RELATED VIDEO: Turning their own data back on the traitors.

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.

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

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]

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

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

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.

Gen. Milley: BLM Riots Causing $1 Billion in Damage Were Trivial

Traitorous Gen. Mark Milley reportedly suggested the 2020 Black Lives Matter (BLM) riots, which caused an estimated one billion dollars in damage, were trivial, according to authors Bob Woodward and Robert Costa in the book Peril.

“Mr. President, they are not burning it down,” Milley told former President Trump about the riots sparked by George Floyd’s death. “We’re a country of 330 million people. You’ve got these penny packet protests,” Milley reportedly said, using a phrase for something trivial. “They used spray paint, Mr. President, that’s not an insurrection.”

One billion dollars of damage, not to mention the dozens of lives lost, including law enforcement officers, is not a “penny packet protest.” It is revolution.

According to the New York Post, Milley reportedly told Trump the U.S. military should not be involved in the 2020 riots because the “protests were understandable given systemic racism,” which he claimed was “pent up in communities that have been experiencing what they perceive to be police brutality.”

Milley, you may recall, is the same general who told the House Armed Services Committee, “I want to understand White rage. And I’m White. I’ve read Mao Zedong. I’ve read Karl Marx. I’ve read Lenin. That doesn’t make me a communist. So what is wrong with understanding… the country which we are here to defend?”

Milley is not here to defend this country. He is here to subvert it.


Black Lives Matter (BLM)

130 Known Connections

Founder of BLM Utah Chapter Says American Flag Is “Symbol of Hatred”

In a July 4, 2021 Facebook post, Lex Scott, the founder of Utah’s Black Lives Matter chapter, wrote:

“When we Black Americans see this flag we know the person flying it is not safe to be around. When we see this flag we know the person flying it is a racist. When we see this flag we know that the person flying it lives in a different America than we do. When we see this flag, we question your intelligence. We know to avoid you. It is a symbol of hatred.”

Ms. Scott subsequently told Fox News:

“Ever since we put up the post, our page has been flooded with hatred from people who fly the flag. And we want to thank those people for proving our point.” When asked how she would respond to people who say the American flag represents all Americans, Scott replied: “I would ask those people if they ever showed outrage when the Ku Klux Klan marched down the street holding that flag, if they ever showed outrage last week when Patriot Front, a White supremacist group, was marching through Philadelphia holding that flag, if they feel outraged that the Three Percenters have co-opted their flag, that the Proud Boys have co-opted their flag. If they have never shown outrage when hate groups use their symbol for hatred, then they need to not come to us – they need to go directly to those groups. When you allow a hate group to fly that flag in the name of hatred, and you say nothing, and you do nothing, you send a message to us that you agree with their messaging. You agree with that hate, and you condone it.”

To learn more about Black Lives Matter, click here.

EDITORS NOTE: This Discover the Networks column is republished with permission. ©All rights reserved.

India Announces State Is COVID-19 Free Proving the Effectiveness of IVERMECTIN

The “Horse” Drug Democrats Mocked And LIED About.


And notice how no one mentions Sweden any more, the one country that did not lock down, did not force masks on schools etc. They are doing swimmingly, in fact. The Democrats will throw you and you mom in front of a bus to keep control using the COVID hoax. They have all but declared war on COVID cures and therapeutics.

India Announces State Is COVID-19 Free Proving the Effectiveness of “Deworming Drug” IVERMECTIN

By Jim Hoft, Gateway Pundit, September 15, 2021:

The Gateway Pundit previously reported that COVID cases are plummeting in India thanks to new rules that promote Ivermectin and hydroxychloroquine to its massive population. The 33 districts in Uttar Pradesh, India have now become free from COVID-19 government informed on Friday. The recovery rate has increased up to 98.7% proving the effectiveness of IVERMECTIN as part of the “Uttar Pradesh Covid Control Model.” Of course, the media won’t mention that Ivermectin is being used for the treatment of COVID-19.

This state has an estimated population of 241 million people in 2021 and has the highest population in India.  This is almost two-thirds of the United States population in 2021 and yet it is now a COVID-19 free nation.

So what could the United States be doing wrong? Let’s ask Dr. Fauci.

Hindustan Times reported on this big development:

Overall, the state has a total of 199 active cases, while the positivity rate came down to less than 0.01 per cent. The recovery rate, meanwhile, has improved to 98.7 per cent. As per the state’s health bulletin, Uttar Pradesh reported only 11 new Covid-19 cases and zero deaths in the last 24 hours.

India Today also reported on this last August 31:

The active caseload in Uttar Pradesh is down to 269, while the percentage of active cases against the total confirmed cases is 0 per cent.

The active caseload, which was at a high of 3,10,783 in April, has reduced by over 99 per cent.

Fresh Covid-19 cases in the state have remained below 100 for 50 consecutive days.
Of the 1,87,638 samples tested in the last 24 hours, 21 tested positive. In the same period, another 17 patients recovered from the infection, adding to the recovery of over 16,86,182 people so far. (These numbers are in lakh so the comma placement is different in the US. 1,87,638 lakh is 187,638)

Uttar Pradesh is the leading state in India to use Ivermectin as early and preventatively in all family contacts. And this state is one of the five lowest COVID cases of all states in India despite having only a low vaccination rate of 5.8% fully vaccinated compared to the USA that has 54% fully vaccinated.

The USA has 179,289,983 fully vaccinated as of September 14 while Uttar Pradesh has 15,236,150 who got their second dose. 

Here’s a little background on the use of Ivermectin in UP, The Indian Express reported:

Uttar Pradesh was the first state in the country to introduce large-scale prophylactic and therapeutic use of Ivermectin. In May-June 2020, a team at Agra, led by Dr. Anshul Pareek, administered Ivermectin to all RRT team members in the district on an experimental basis. It was observed that none of them developed Covid-19 despite being in daily contact with patients who had tested positive for the virus,” Uttar Pradesh State Surveillance Officer Vikssendu Agrawal said.

He added that based on the findings from Agra, the state government sanctioned the use of Ivermectin as a prophylactic for all the contacts of Covid patients and later cleared the administration of therapeutic doses for the treatment of such patients.

Claiming that timely introduction of Ivermectin since the first wave has helped the state maintain a relatively low positivity rate despite its high population density, he said, “Despite being the state with the largest population base and a high population density, we have maintained a relatively low positivity rate and cases per million of population”.

He said that apart from aggressive contact tracing and surveillance, the lower positivity and fatality rates may be attributed to the large-scale use of Ivermectin use in the state, adding that the drug has recently been introduced in the National Protocol for Covid treatment and management. “Once the second wave subsides, we would conduct our own study as there has been an emerging body of evidence to substantiate our timely use of Ivermectin from the first wave itself,” Vikasendu told The Indian Express.”

Last August, the government of UP issued a notification to have Ivermectin (12 mg) tablets. The Dialogue reported:

“The government notification reads, “Doctors are advising to take ivermectin 12 mg to contain the impact of pandemic. This medicine is quite effective in protecting from covid-19. Therefore, we appeal each and every citizen to have this tablet.”

The notification then goes on to explain the dosage: For positive patients isolated at home (one tablet per day for three days and for primary and secondary contacts (one tablet each on the first and 7th day).”

Even Australian MP Craig Kelly praises UP’s Chief Minister for introducing Ivermectin as a preventive measure in a tweet last July.

Both Uttar Pradesh and Delhi have seen an incredible drop in COVID-19 cases because they use Ivermectin early and preventatively. Whereas Kerala, a tiny state located in southern India that is over-dependent on vaccines and less dependent on Ivermectin, has been reporting a significant increase in COVID-19 cases. Keep in mind that Uttar Pradesh has eight times larger population than Kerala.

More information on Kerala’s COVID- 19 cases on The Desert Review:

“While Kerala included Ivermectin in their state’s guideline in April, they restricted it’s use to only in Class B – severe cases or those with associated disease, making its use much less than if mild cases were allowed. This meant it was reserved as a late treatment if used at all.

Finally, Kerala abandoned Ivermectin use altogether on August 5, 2021.

Juan Chamie, the Cambridge-based data analyst who has provided graphical insight and published on COVID, provided his answer to why Kerala’s COVID cases have spun out of control.

“My main current explanation is the lack of early treatment. Kerala’s COVID protocol from April 2021 included Ivermectin, but not as an early treatment. As a result, only a small group qualified, those in Category B patients having high-risk factors. The new protocol from August 5 is even worse. They removed Ivermectin (completely).”

Despite a widespread attempt by the media and WHO to convince the world that India has dropped Ivermectin by citing the DGHS, the ICMR and AIIMS have not changed their position, and Ivermectin remains in the India National Protocol.”

Of course, the WHO, pharmaceutical companies, fake news media, and Fauci are not happy with this big development. New York Times will have a meltdown with this news.

RELATED ARTICLES:

Heavily vaccinated state accounts for 65% of India’s COVID cases after rejecting ivermectin

LARGEST REAL WORLD ANALYSIS STUDY: Natural Immunity Best Defense Against COVID, Vaxxed

People At “Greater Risk of Hospitalization”More on Ivermectin

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.

Texas Hospital Faces Closure Over COVID-19 Vaccine Mandate

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.

TRAITOR: Pelosi IN UK Launches Disgusting Attack Overseas, Trashes Millions Of Americans, Compares Capitol Protest To Civil War

As if America’s reputation hadn’t been dragged enough by Democrats these past months. Ironically, it may take a civil war to remove this illegitimate regime.

Pelosi in the U.K. compares Capitol riot to the Civil War

Mrs. Pelosi then launched into a Civil War analogy.

By: Washington Times, September 17, 2021

House Speaker Nancy Pelosi on Friday told a British audience that the political environment in the U.S. that led to the Jan. 6 riot was similar to the Civil War era.

Mrs. Pelosi, California Democrat, made the remarks in a livestreamed forum in London with Robin Niblett, Director of the British think tank Chatham House.

The host noted that the most recent presidential transition in the U.S. was “rough and tumble.”

“There’ve been in the past the rough and tumble of politics, but nothing like what we are suffering now. I mean, of course, there was a Civil War,” she said. “But in terms of politics, at the time of the civil war, President Lincoln was building the dome of the Capitol — this symbol of democracy for the world, a beacon of hope to the world.”

She continued, “The fact that that dome with all of its symbolism and all that went into constructing it at a time of disunity in our country would be assaulted the way it was, was not just an assault on a physical structure. It was on an institution.”

The speaker also told Dr. Nibblet that she believes the events that happened that day were rooted in “white supremacy, antisemitism, and Islamophobia.”

RELATED ARTICLES:

Biden Vomits Marxist Talking Points In Defending Obscene Tax Hikes

Pelosi Launches Disgusting Attack Overseas Against Trump Supporters, Refers to Them as a “Cult”

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.

TEXAS: Iranian National Heading to Prison for Illegally Exporting Military Equipment to Iran

He should have been patient. Old Joe Biden’s handlers will give the mullahs everything they want soon enough.

Iranian National In Texas Heading To Prison For Illegally Exporting Military Equipment

CBSDFW, September 15, 2021:

SAN ANTONIO (CBSDFW.COM) — A court in the Western District of Texas has sentenced a man pf [sic] Iranian descent to more than five years in prison for violating the International Emergency Economic Powers Act.

Mehrdad Ansari, a resident of the United Arab Emirates and Germany, was sentenced to 63 months in prison, followed by three years of supervised release for his role in a scheme to obtain military-sensitive parts for Iran.

“This case reaffirms HSI’s resolve and commitment in securing the homeland by targeting foreign actors attempting to procure sensitive technology by exploiting the U.S. export laws,” said HSI San Antonio acting Special Agent in Charge Craig Larrabee.

In coordination with his co-conspirators, Ansari obtained and attempted to obtain parts that had dual military and civilian capability and could be used in such systems as nuclear weapons, missile guidance and development, secure tactical radio communications, offensive electronic warfare, military electronic countermeasures (radio jamming), and radar warning and surveillance systems.

On May 7, a San Antonio federal jury convicted Ansari on one count of conspiracy to violate the Iranian Transaction Regulations, one count of conspiracy to commit wire fraud, one count of conspiracy to defraud the U.S. Department of the Treasury, and two counts of aiding and abetting the making of false statements.

Evidence presented during trial revealed that the 40-year-old attempted to transship testing equipment obtained from the U.S. by co-defendants, Taiwanese citizen Susan Yip, and Iranian citizen Mehrdad Foomanie, using Ansari’s companies, Gulf Gate Sea Cargo L.L.C., and Global Merchant L.L.C., based in Dubai.

From Oct. 9, 2007, to June 15, 2011, Yip and Foomanie obtained or attempted to obtain from companies worldwide more than 105,000 parts valued at approximately $2,630,800, involving more than 1,250 transactions. The defendant’s main role was to get a particular set of parts from a Central Texas company that was key for the Iranian government’s testing of all other parts…..

RELATED ARTICLES:

Iran: Security guards sexually assaulted female International Atomic Energy Agency inspectors

Biden’s handlers admit their drone strike in Afghanistan killed 10 civilians, including 7 children, and no jihadis

Reza Aslan: ‘America desperately needs to see Afghans as people with hopes and dreams and triumphs and tragedies’

India: Married Muslim man lures two Hindu women into relationship, kills both

UK: Councillor warns that some Afghan evacuees will soon be ‘blowing us up,’ then retracts and apologizes

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

Indian Bar Association Sues WHO Scientist Over Ivermectin!

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.

Schooling Mark Milley: A General Idea of Critical Race Theory for the Chair of the Joint Chiefs

Bill Whittle takes on schooling Gen. Mark Milley, the Chair of the Joint Chiefs of Staff, on the general idea of critical race theory, and other critical subjects.

Moving Back to America is a production of the Members at https://BillWhittle.com.

©Bill Whittle. All rights reserved.

New Plan Would Push Top Tax Rate to Almost 60 Percent In These 4 States

If Congress’s new tax hikes come through, successful residents in high-tax states will be placed in a terrible position.


Successful residents of high-tax states are in for an ugly surprise if new tax legislation passes in Congress. Democratic legislators are currently proposing a multi-trillion-dollar tax hike to raise revenue for a massive welfare and climate change spending plan. Proposed tax hikes include raising the corporate tax rate, higher taxes on cigarettes and vaping products, raising the capital gains tax rate, and higher individual income tax rates.

On the last front, the proposed income tax increase would apply to income over $400,000 for an individual and raise the rate from its current 37 percent to 39.6 percent. The proposal also includes a 3 percent surcharge on all income above $5 million. The tax hikes could push Americans in states like New York, California, New Jersey, and Hawaii up to nearly 60 percent top income tax rates.

“For New Yorkers earning more than $5 million, the combined city, state and federal tax rate would skyrocket to 61.2% under the House plan,” Fox Business reports. “The combined rate in California, meanwhile, would spike to 59.7%, while the wealthiest individuals living in New Jersey could pay a rate as high as 57.2%. In Hawaii, the combined marginal rate would be an estimated 57.4%.”

That’s right: High-earning residents of these states could end up paying nearly 60 percent tax rates on their income earned above a certain level. That’s an obscene and fundamentally unfair level of taxation. But such punitive levels of taxation are also highly impractical and certain to have adverse economic consequences.

For one thing, successful residents can simply move to another state. It is only the combination of high federal income taxes and high state-level income taxes that leads to these combined rates of nearly 60 percent. Yet some states, such as New Hampshire and Florida, have no income tax at all.

We’ve already seen an exodus of wealth, people, and major businesses from states like California, and that trend will only accelerate if taxes are sent even higher by this new plan. It’s only logical: states that heavily tax something are discouraging it, while states that don’t tax it at all are welcoming it. Why would anyone want to discourage income-earning?

Punitive taxation has ramifications for more than just the high-earning individuals and families directly impacted by higher tax rates. If they leave the state, they take with them jobs, investment funds, and spending that would otherwise go back into their communities.

It’s true that not all high-earners will flee states with these punitively high taxes. Some, for a variety of reasons, will stay. But even for these individuals, the high tax rates will backfire, because they’ll create perverse incentives and discourage economic activity above a certain level.

Why?

Well, people make economic decisions “on the margin.” What this means is that they evaluate each additional hour worked on the basis of whether the potential benefits exceed the costs. Then, they work up until the point where the costs begin to exceed the benefits.

When the government applies 60 percent tax rates to income above a certain point, it drastically reduces the benefits of additional labor subject to that tax. Yet the costs of working remain the same. As a result, far less economic activity will happen beyond that threshold.

Think about it like this. A successful entrepreneur founded a restaurant and when it did well, opened up two other locations. Does he add a fourth or rest on his laurels?

Well, if he will only get to keep 40 percent of the income he earns from new locations, because he’s now already making $400,000, he probably won’t bother to expand. Who would want to work more and hustle harder only to hand over 60 cents of every dollar to the government? This economic disincentive hurts more than one entrepreneur—it means jobs never created, customers never satisfied, income never earned, and a community never enriched.

Another problem with highly progressive tax rates is that they discourage economic investment. The same “rich” citizens who would face these 60 percent tax rates are those who would otherwise save and invest that money into the economy. (Rather than simply spend it as low-earners tend to do). As the economist Ludwig von Mises put it, “Progressive taxation of income and profits means that precisely those parts of the income which people would have saved and invested are taxed away.”

Ultimately, 60 percent tax rates are confiscatory, unfair, and economically indefensible. If Congress’s new tax hikes come through, successful residents in high-tax states will be placed in a terrible position. Luckily, they have the option to move to less hostile states. Don’t be surprised when many take it.

WATCH: New Biden Vax Mandate Doesn’t Make ANY Sense (Here’s Why)

COLUMN BY

Brad Polumbo

Brad Polumbo (@Brad_Polumbo) is a libertarian-conservative journalist and Policy Correspondent at the Foundation for Economic Education.

Like this story? Click here to sign up for the FEE Daily and get free-market news and analysis like this from Policy Correspondent Brad Polumbo in your inbox every weekday.

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