Supreme Court Will Hear Landmark Pro-Life Challenge

Chief Justice John Roberts

The Supreme Court on Monday agreed to hear Mississippi’s bid to enforce a ban on abortions after 15 weeks, ending almost a full year of suspense and setting the stage for a landmark decision.

Mississippi’s petition is a groundbreaking one, asking the Court to authorize new limits on abortion in the earliest stages of a pregnancy. Abortion advocates warn a victory for Mississippi would rupture 50 years worth of judicial decisions favoring maternal choice before an unborn child is viable.

Monday’s order is a welcome lift for the pro-life movement and a dire signal for abortion advocates. The Mississippi case has lingered on the Court’s docket for months without action. The long delay gave rise to speculation that the newly reinforced conservative majority was wary of abortion disputes, a concern Monday’s news seemed to dispel. And it raised doubts about assumptions that the right-leaning Court would move incrementally to undo pro-abortion precedents.

Jackson Women’s Health Organization, the only abortion clinic in Mississippi, challenged the 15-week ban as soon as it took effect. Judges in the lower courts sparred vigorously over the law.

U.S. District Judge Carlton Reeves pulled no punches in a 2018 decision striking down Mississippi’s law on constitutional grounds. He called the legislature’s justifications for the bill—protecting maternal health and the reputation of the medical profession—"pure gaslighting," and he faulted lawmakers for crafting an attack on abortion while doing nothing "to address the tragedies lurking on the other side of the delivery room."

"Legislation like H.B. 1510 is closer to the old Mississippi—the Mississippi bent on controlling women and minorities," Reeves wrote.

A three-judge panel of the Fifth U.S. Circuit Court of Appeals upheld Reeves’s decision. But Judge James Ho took Reeves to task in a separate opinion, calling his decision "deeply disquieting."

"Instead of respecting all sides, the district court opinion disparages the Mississippi legislation as ‘pure gaslighting,’" Ho wrote. "It equates a belief in the sanctity of life with sexism, disregarding the millions of women who strongly oppose abortion. And, without a hint of irony, it smears Mississippi legislators by linking House Bill 1510 to the state’s tragic history of race relations, while ignoring abortion’s own checkered racial past."

State lawyers highlighted what they called Reeves’s "diatribe" near the top of their petition to the Supreme Court.

There are two legal issues at stake. One is whether state power to regulate abortion should turn on the viability of an unborn child, the framework set out in Roe v. Wade. Mississippi argues the Court should scrap that standard in light of new evidence about fetal development and its capacity to survive outside the womb at earlier stages of a pregnancy.

"Given the many medical advances our scientific community is constantly achieving, it is only a matter of time before development of an artificial womb moves ‘viability’ all the way back to the moment of conception," the state’s petition reads.

Instead, abortion regulations should be tied to the state’s interest in protecting children, maternal health, and the reputation of physicians, the state says.

The other is the test courts ought to use to evaluate restrictions on abortion. Chief Justice John Roberts surprised observers in 2020 when he voted with his four liberal colleagues to strike down a Louisiana regulation that required abortion providers to have admitting privileges at a nearby hospital. That decision, perhaps by the chief justice’s design, seeded division in the lower courts and spawned another major abortion controversy for the Court to resolve.

While Roberts voted with the liberals on the bottom line outcome in the 2020 case, he did not agree with their reasoning. Writing for the four liberal justices, Justice Stephen Breyer said the admitting privileges rule was unconstitutional because the burdens it imposed on abortion access outweighed its benefits for women.

The chief justice pointedly rejected that cost-benefit analysis in a separate, solo opinion. Instead, he voted to strike the law because the Court declared an identical regulation from Texas unconstitutional in a 2016 decision. Roberts wrote he felt compelled to follow precedent and "treat like cases alike." He added, citing an older case, that courts should ask whether an abortion restriction amounts to an "undue burden," a more permissive standard than Breyer’s cost-benefit approach.

In the ensuing months, lower courts have disagreed with one another about which opinion they’re bound to follow. Some have cited Breyer’s opinion as precedential, while others have used the chief’s more lenient test. Mississippi said that was a reason to hear their case in legal papers filed last September.

"Absent this Court’s immediate intervention, there will be many dozens of cases splitting along the same lines," the brief reads. "Only half of them will be correct. This Court should not let the issue percolate even another day."

The case, which will be heard near the end of this year, is No. 19-1392 Dobbs v. Jackson Women’s Health Organization.

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BOOM! CDC Director Finally Admits that COVID Cases are Hugely Over-Counted — Just as Gateway Pundit and Donald Trump Reported in August

In August 2020 The Gateway Pundit’s Joe Hoft posted an article about COVID-19 that sent shockwaves throughout the internet — The CDC website admitted that only around 6% of COVID recorded deaths were due entirely to the Coronavirus-

SHOCK REPORT: This Week CDC Quietly Updated COVID-19 Numbers – Only 9,210 Americans Died From COVID-19 Alone – Rest Had Different Other Serious Illnesses

The gist of the reporte was that COVID-19 is not nearly as deadly as first projected by the WHO and then by Dr. Tony Fauci and Dr. Debra Birx.  Based on CDC numbers in Ausust  only 6% of all deaths attributed to COVID-19 were instances where the only factor in the individual’s death was due to COVI9-19.

From the CDC website.

For all the other deaths reported by the CDC linked to COVID-19, the individuals who passed away had 2-3 other serious illnesses or co-morbidities.

This came from actual data from the CDC and was tweeted by Mel Q on Twitter.

Twitter user Mel Q shared a calculation which showed that 6% of all COVID-19 deaths as reported by the CDC turned out to be 9,201 deaths at the time. 

Only 9,201 people died in the US according to August numbers where COVID-19 was the only cause of death.

We used Mel Q’s tweet in our report and the President of the United States retweeted Mel Q’s tweet as well.

But  Twitter took down the tweet claiming fake news.  They notified Mel Q that the tweet that used actual CDC data “violated their policy on misleading information about COVID-19.”  Her account was suspended from posting for 12 hours.

Then the far left hacks at CNN wrote an article about this calculation, the President’s retweet and our article entitled – Twitter removes QAnon supporter’s false claim about coronavirus death statistics that Trump had retweeted. They refused to look at the science.

On Sunday CDC Director Rochelle Walensky finally admitted that “many, many hospitals” were counting COVID deaths to include cases that were not COVID deaths.

The Gateway Pundit was right.
Trump was right.
The tech giants and CNN were wrong again pushing fake news.

But we were the ones who were punished.
We see this a lot.

The Epoch Times reported:

Of the people who died after being fully vaccinated, 42 were asymptomatic or not related to COVID-19, according to the CDC. Additionally, 342 of the hospitalizations were asymptomatic or not related to COVID-19.

“Many, many hospitals are screening people for COVID when they come in, so not all of those 223 cases who had COVID actually died of COVID. They may have had mild disease, but died, for example, of a heart attack,” CDC Director Rochelle Walensky said on CNN’s “State of the Union” on Sunday.

Under the usual counting program, people who have not been vaccinated but who die of heart attacks or other causes are typically listed as a COVID-19 death.

Here is the video of CDC Director Walensky on CNN.

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Ted Cruz Knocks Biden’s Comments On Chauvin Trial

President Joe Biden’s comments on the Chauvin trial, in which he suggested he was “praying” for a guilty verdict, prompted a sharp rebuke from Sen. Ted Cruz (R-TX), who argued that such comments could lead to a mistrial.

“I’m praying the verdict is the right verdict,” Biden said on Tuesday. “Which is — I think it is overwhelming in my view. I wouldn’t say that unless the jury is sequestered.”

Ted Cruz denounced Joe Biden’s rhetoric as being equally as irresponsible as Rep. Maxine Waters (D-CA).

“Joe Biden decides that Maxine Waters shouldn’t be the only politician foolishly providing grounds for a mistrial or a possible basis on appeal to challenge any guilty conviction,” Cruz tweeted.

Cruz was referring to the incendiary comments made by Congresswoman Maxine Waters over the weekend, before the jury was sequestered, when she said people should “get more confrontational” if a guilty verdict is not delivered in the Chauvin trial.

“We’re looking for a guilty verdict. We’re looking for a guilty verdict. And we’re looking to see if all of this [inaudible] that took place and has been taking place after they saw what happened to George Floyd,” Waters said. “If nothing does not happen, then we know, that we’ve got to not only stay in the street, but we’ve got to fight for justice, but I am very hopefully and I hope that we’re going to get a verdict that will say guilty, guilty, guilty. And if we don’t, we cannot go away.”

“We’ve got to get more active. [We’ve] got to get more confrontational,” she added. “[We’ve] got to make sure that they know we mean business.”

Chauvin’s defense attorney later requested a mistrial due to Waters’ comments. Though Hennepin County District Judge Peter Cahill denied the motion for a mistrial, he did reluctantly admit that the congresswoman’s comments may create an avenue for defense to appeal a guilty verdict.

“And it is so pervasive that it is I just don’t know how this jury it can really be said to be that they are free from the taint of this,” the lawyer representing Derek Chauvin said. “And now that we have U.S. representatives, threatening acts of violence in relation to the specific case, it’s mind-boggling to me, judge.”

“Well, I’ll give you that Congresswoman Waters may have given you something on appeal that may result in this whole trail being overturned,” Cahill responded.

Cahill, however, did not believe that the congresswoman’s comments ultimately mattered.

“I think if they want to give their opinions, they should do so in a respectful and in a manner that is consistent with their oath to the Constitution, to respect a co-equal branch of government,” he said. “Their failure to do so I think is abhorrent, but I don’t think it has prejudices with additional material that would prejudice history, they have been told not to watch the news. I trust they are following those instructions, and that there is not in any way a prejudice to the defendant beyond the articles that we’re talking specifically about the facts of this case. A Congress woman’s opinion really doesn’t matter a whole lot. Anyway, so motion for mistrial is denied.”

RELATED: Joe Biden On Chauvin Trial: ‘I’m Praying For The Right Verdict,’ Evidence Is ‘Overwhelming’

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House Democrats Unanimously Support Waters’ Calls For “More Confrontation”, Block GOP Censure Vote

House Democrats Unanimously Support Waters’ Calls For "More Confrontation", Block GOP Censure Vote

In what is perhaps not a shocking vote at all in this insanely partisan world in which we live, The House has just rejected a Republican resolution to censure Rep. Maxine Waters for saying that “we’ve got to get more confrontational” about police brutality against African Americans.

Republicans argued that Waters incited violence with her remarks at a protest over the weekend in Minneapolis.

House Minority Whip Steve Scalise (R-La.) commented ahead of the vote that:

“Right now I haven’t heard any Democrats speaking out against what Maxine has said. And it’s time for Democrats to speak out when they see it on both sides. They only want to speak out on one side of the aisle, not on both. And that hypocrisy, I think, is starting to shine through.”

As The Hill reports, lawmakers voted along party lines 216-210, with no defections on either side, to table the resolution from Minority Leader Kevin McCarthy (R-Calif.) that would have issued the chamber’s harshest disapproval short of expulsion.

…impeachment for thee, but not for me.

Tyler Durden
Tue, 04/20/2021 – 16:46

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Watch: FL Sheriff Uses 2 Photos to Show Difference Between a Peaceful Protest and a Riot

Riots and peaceful protests — there’s a clear difference between the two, right? The question is simple enough, but some on the left still can’t seem to make the distinction. (Consider the establishment media’s riot coverage, for instance.) Polk County, Florida, Sheriff Grady Judd employed two photographs to help illustrate the difference at a Monday…

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AOC reintroduces the Green New Deal to fundamentally transform the US economy

Congressional Democrats, led by Rep. Alexandria Ocasio-Cortez (D-N.Y.) and Sen. Ed Markey (D-Mass.), reintroduced the Green New Deal on Tuesday, a sweeping progressive legislative agenda designed to fundamentally transform the U.S. economy to end capitalism while promoting so-called racial, economic, and climate "justice."

"Not only do we refuse to leave any community behind but those who have been left behind come first," Ocasio-Cortez said at a news conference announcing the reintroduction of the Green New Deal. "We’re going to transition to a 100% carbon-free economy that is more unionized, more just, more dignified and that guarantees more health care and housing than we’ve ever had before. That’s our goal."

More than 100 Democrats are co-sponsoring the reintroduction of the Green New Deal resolution in the House, which comes ahead of a virtual international summit hosted by President Joe Biden to discuss climate change on Earth Day, this Friday.

While President Biden’s administration has not officially endorsed the Green New Deal, the president has signed several executive actions to curb U.S. oil and gas production and increase renewable energy production.

Sen. Markey urged Biden to be willing to go further to address climate change.

"We are going to be calling for the highest aspirations that our country can reach," he said Tuesday. "We want to go big. Even bigger."

Rep. @AOC reintroduces the Green New Deal: ’The climate crisis is a crisis born of injustice and it is a crisis bor… https://t.co/239OuAhpVf

— NowThis (@NowThis)1618932272.0

Ocasio-Cortez first introduced the Green New Deal in 2019 as a nonbinding resolution in the House that broadly outlined a Democratic legislative agenda to remake the economy. The plan sets a goal of "net-zero greenhouse gas emissions" which will be met after a "10-year national mobilization" that would restructure government social programs, vastly expand government power to centrally plan the economy, and dramatically increase federal taxes and spending to fund it all.

The Green New Deal calls for "100 percent of the power demand in the United States" to be met through "clean, renewable, and zero-emission energy sources." Infrastructure and public transportation would be overhauled to the point where "air travel stops becoming necessary," relying on boondoggles like "high speed rail" and mandates requiring the public to use electric cars to meet the government’s standards. The resolution calls for "all existing buildings" in the United States to be upgraded for maximum energy efficiency.

But the "all hands on deck approach" of the Green New Deal goes well beyond climate policy. Ocasio-Cortez said the Democratic initiative must "rectify the injustices of the past" by providing free higher education for all Americans, "affordable, safe, and adequate" housing, free health care, and millions of "union jobs."

She further added that Green New Deal legislation must address the "systemic cause of climate change."

"While climate change is a planetary crisis, it does not have a random or environmental genesis," she asserted. "It’s not just human-caused, it’s societally-caused. The climate crisis is a crisis born of injustice. And it is a crisis born of the pursuit of profit at any and all human and ecological cost.

"We must recognize in legislation that the trampling of indigenous rights is a cause of climate change. That the trampling of racial justice is a cause of climate change," she continued. "We are allowing folks to deny ourselves human rights and deny people the right to health care, the right to housing and education."

Green New Deal legislation is likely to remain aspirational for Democrats as Republicans are adamantly opposed to these policies, arguing they would make Americans poorer. Sen. John Barasso (R-Wyo.) called it the "Green New Disaster" in a statement responding to Markey and Ocasio-Cortez’s news conference.

The Green New Disaster is back.And if you’re somebody who pays taxes, heats your home, or drives a car…you’re g… https://t.co/DQtnDwQsa0

— Senate Republicans (@Senate Republicans)1618943219.0

"It’s about massively increasing the size of government and dictating how Americans live their lives," Barasso said. "The last thing we need now is to double down on the punishing policies we have already seen from the Biden administration."

Various bills related to Green New Deal policies that have already passed the Democratic-controlled House and have gone nowhere in the U.S. Senate. The Democrats’ narrowest possible 50-50 majority cannot overcome a filibuster threat from Republicans, leaving the viability of a plan to fundamentally restructure the U.S. economy very much in doubt.

For now, the Green New Deal serves as a messaging tool for Democrats to rally their progressive base and Republicans to attack ahead of the 2022 midterm elections.

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COVID-19 And Vaccines: What Do We Really Know?

Last week, UncoverDC reported on the FDA and CDC’s pause of Johnson & Johnson’s (J&J) COVID-19 vaccine due to complications from a severe but rare clotting condition known as cerebral venous sinus thrombosis (CVST), which appeared in combination with a condition called thrombocytopenia (often referred to as immune thrombocytopenic purpura, or ITP).
Essentially, ITP causes the immune system to malfunction and produces antibodies that attack the body’s platelets. The most dangerous complication of ITP is bleeding in the brain, causing a cerebral hemorrhage and catastrophic brain damage or death.

In explaining the pause, the CDC reported seven women suffered thrombotic complications following the J&J vaccine. Although evidence establishes a relationship between COVID-19, thrombolysis and clotting, which is one of the main reasons for sudden decline and death with the virus, the connection between clotting and the three available COVID-19 vaccines in the United States—Pfizer-BioNTech, Moderna, and Johnson & Johnson—is less explicit.

As pandemic research continues, scientists concede that vaccine development against SARS-CoV-2 within a timeframe as tight as the ongoing COVID-19 vaccine campaign makes it difficult to thoroughly understand the long-term effectiveness and potential side effects of the current vaccines. Therefore, it is not unexpected to see complications, including death. The United States, in just four months, has administered approximately 212 million COVID-19 vaccines, with 85.3 million people now fully vaccinated, or 25.7% of the population. According to CDC data, around 85% of those receiving the Moderna COVID-19 vaccine experienced some type of reaction.

Armed with the knowledge, or lack thereof, we have thus far; most scientists would agree that when navigating through catastrophic, life-altering events that transpire quickly, it is important to pause, reflect upon, and study “how did we get here” and “what would we do differently?”

The Vaccine Road That Led Us To Where We Are Now

In Jan. 2020, immediately after China released the genetic sequence of SARS-CoV-2, the race to produce a vaccine got underway. There are close to a dozen COVID-19 vaccines currently approved for use around the world. While there are many different kinds and types of vaccines, they all have the same objective—tricking a healthy body into thinking it is under assault by a particular disease so the immune system will learn to create the cells and proteins needed to immediately fight off the disease if it becomes a threat. Simply put, vaccines are designed to create antibodies that allow the body to protect itself from future infections without actually getting sick.

The current COVID-19 vaccines approved for emergency use in the United States (and therefore do not need FDA approval) are manufactured by J&J, Pfizer, and Moderna. They each work by fooling cells into making spike proteins—the sharp bumps that protrude from the surface of the outer envelope of the coronavirus. These proteins are the pathogens needed to cause the immune system to develop resistance to the virus. For this to happen, DNA or RNA must be injected and delivered to the inside of the cells.

Johnson & Johnson and AstraZeneca’s vaccines use genetically engineered viruses called adenovirus vectors to serve as a Trojan horse and carry the genetic material to the cells to create spike proteins. The J&J vaccine uses a form of human adenovirus called Ad26, and the AstraZeneca vaccine uses a genetically engineered version of a chimpanzee adenovirus. However, despite being over thirty years in the making, other than for military personnel, no approved adenovirus vaccine is available to the general public, with the technology existing commercially only in a rabies vaccine.

And while not “vaccines” in the traditional sense, using nascent technology, the Pfizer and Moderna shots are gene-modifying agents that insert synthetic, chemically protected mRNA into cells (using a chemical called polyethylene glycol, or PEG). Never before used in an approved vaccine, PEG may be the culprit behind severe allergic reactions in mRNA COVID-19 vaccines. Once in the cell, the synthetic mRNA instructs it to produce a protein matching the spike protein found on the outer surface of a SARS-CoV-2 virus molecule. The cells then eject this protein out, which triggers the creation of COVID-19 antibodies.

Hoping to achieve the same goal, both Pfizer and Moderna, who are fierce competitors, are making every effort to be the first company to bring this synthetic mRNA technology to life in a vaccine against COVID-19.

A Closer Look At Moderna, Bill Gates, and Dr. Anthony Fauci

For years, Moderna, under the leadership of Stéphane Bancel (who, along with Pfizer CEO Albert Bourla, just announced that a booster shot will probably be necessary for the company’s mRNA vaccines), has been quietly working on advanced protein therapies—a multi-billion dollar industry responsible for drugs like Humara. Confident its technology would level the playing field by creating therapeutic proteins inside the body instead of in a lab and manufacturing facility, Moderna’s mission has hinged on one feat that no biotech facility has successfully accomplished—harnessing mRNA

National Institutes of Health Director Dr. Francis Collins and National Institute of Allergy and Infectious Diseases Director Dr. Anthony Fauci meet with Bill Gates of the Bill and Melinda Gates Foundation to discuss research opportunities in global health in June 2017 at NIH. Credit: National Institutes of Health | FlickrCC

Long before the pandemic, Moderna (who shares ownership of its vaccine with Dr. Fauci’s National Institute of Allergy and Infectious Disease, or NIAID) received awards from the federal government, including DARPA, to conduct research on mRNA. In 2016, the notoriously secretive Moderna—a Flagship Pioneering company since 2010, with twenty-one mRNA programs in its pipeline—announced a partnership with the Bill and Melinda Gates Foundation.

According to Moderna, the purpose of its collaboration with the Gates Foundation (who also funds the pandemic policy-dictating entity the Institute for Health Metrics and Evaluation, tied to Dr. Anthony Fauci) is “to advance the development of a novel, affordable combination of mRNA-based antibody therapeutics to help prevent HIV infection,” with the potential for future follow-on projects of up to $100 million to “support the development of additional mRNA based projects for various infectious diseases.” At the time of the partnership, Moderna was valued at close to $5 billion, making it worth more than any other private biotech lab in the country.

The Bill and Melinda Gates Foundation, along with the Johns Hopkins Center for Health Security and the World Economic Forum, sponsored the ‘Global Pandemic Exercise’ Event 201 on Oct. 18, 2019. The pandemic tabletop exercise “simulated a series of dramatic, scenario-based facilitated discussions, confronting difficult, true-to-life dilemmas associated with response to a hypothetical, but scientifically plausible, pandemic.” Three days prior, on Oct. 15, 2019, the Coalition for Epidemic Preparedness Innovations (CEPI) launched a call for proposals to attract funding applications for ground-breaking platform technologies in order to:

“develop vaccines and other immunoprophylactics to rapidly respond to future outbreaks of emerging infectious diseases and unknown pathogens, known as ‘Disease X’.” 

Interestingly, CEPI—which supported the production of Moderna’s vaccine candidate for the Phase 1 clinical trial and is supported by the Biden administration’s National Strategy—was co-founded in 2017 by the governments of Norway and India, the Bill & Melinda Gates Foundation, Wellcome, (funded in part by Gates, Wellcome has a £29.1 billion investment portfolio, and is a partner with the ChanZuckerberg Initiative) and the World Economic Forum. Dr. Richard Hatchett, CEO of CEPI, had this to say of the initiative:

“We can be sure that another epidemic is on the horizon. It is not a case of if, but when. We need to be prepared. We need to invest in platform technologies that can be used to quickly respond to the emergence of a pathogen with epidemic potential.”

For decades, Dr. Anthony Fauci, Director of the NIAID, has been conducting research on the coronavirus, which was first characterized in the 1960s. Throughout the current pandemic, there have been critical observations surrounding a controversial type of research banned in the U.S. by the Obama administration in 2014, called gain-of-function. The risky research requires taking wild viruses and passing them through live animals until they mutate into a form that could pose a pandemic threat. According to Dr. Peter Navarro, this research genetically engineers a virus to make it more deadly and dangerous—“to weaponize it.”

Effectively side-stepping Obama’s ban on gain-of-function research, Dr. Anthony Fauci and Dr. Francis Collins, at the expense of the U.S. taxpayer, intentionally moved the experiment to China. In fact, an expanding body of evidence suggests that Dr. Fauci funded scientists at the Chinese Communist Party’s Wuhan Institute of Virology and other institutions to work on gain-of-function research on bat coronaviruses.

There are also well-documented concerns, examined by Dr. David E. Martin, surrounding COVID-19 and pre-pandemic research, patents, and associations between the NIAID, the University of Chapel Hill (UNC), Harvard University, Emory University, Vanderbilt University, University of Pennsylvania, and Tsinghua University. Martin’s investigation also points to many other research institutions and their commercial affiliations, including that of Peter Daszak, a self-proclaimed “virus hunter” and long-time president of EcoHealth Alliance, a New York-based non-profit whose claimed focus is the business of pandemic prevention.

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FDA Aware of Concerns over Clotting after mRNA Vaccines

A Dec. 17, 2020 FDA Briefing Document from Moderna stated numerous times that there were “no known neurologic, neuro-inflammatory, and thrombotic events, that would suggest a causal relationship to the Moderna COVID-19 vaccine.”

Prior to that, on Dec. 8, 2020, in response to an FDA request for comments regarding Pfizer-BioNTech’s COVID-19 vaccine, Patrick Whelan, M.D., Ph.D., submitted a report intended to alert the agency to the possibility that, instead of creating immunity, COVID-19 mRNA vaccines have the potential to cause injury when instructing the body to make spike proteins. In his letter to the FDA, Whelan, who urged particular caution in the mass vaccination of children before actual safety data is available, stated:

“I am concerned about the possibility that the new vaccines aimed at creating immunity against the SARS-CoV-2 spike protein (including the mRNA vaccines of Moderna and Pfizer) have the potential to cause microvascular injury (inflammation and small blood clots called microthrombi) to the brain, heart, liver, and kidneys in a way that is not currently being assessed in safety trials of these potential drugs.”

The CDC and the FDA have not issued another statement following their announcement pausing the Johnson & Johnson vaccine.

Researchers Indicate Possible Connection Between Vaccines & Clots

Scientists have offered no conclusive answer to the exact cause of COVID-19 or the reason why a handful of thrombotic events following the receipt of COVID-19 vaccines completely shut down two vaccine trials. Immediately following the pause of its vaccine, J&J released a statement that was met with criticism, declaring:

“We are aware that thromboembolic events including those with thrombocytopenia have been reported with all COVID-19 vaccines.”

Well‐documented cases of ITP have been reported following other drugs and vaccinations, including MMR. However, research suggests that in the absence of testing pre‐vaccination platelet counts prior to COVID-19 vaccination, combined with the time it takes to discover thrombocytopenia, it is difficult to accurately estimate the percentage of secondary ITP incidences following vaccination.

Most recently, on April 16, the New England Journal of Medicine issued an article indicating the cause of blood clots that may be linked with certain coronavirus vaccines, adding that their findings have important implications for treating the condition, regardless of whether vaccines cause it. Even though the link is not yet firm, they’re calling the condition vaccine-induced immune thrombotic thrombocytopenia or VITT. It’s characterized by unusual blood clotting combined with a low number of platelets. Patients suffer from dangerous clots and, sometimes, hemorrhaging at the same time.

Where Does All of This Leave Us Right Now?

On average, it takes between ten and twelve years to develop a safe and effective vaccine. In fact, researchers have been searching for a vaccine against HIV—a project supported by the Bill and Melinda Gates Foundation, CEPI, BARDA, and Dr. Anthony Fauci—since the early 1980s. Unfortunately, so far, they have not been successful. Citing the pandemic, scientists have raced to shorten the time to find a COVID-19 vaccine and suggest accelerating or limiting the typical time it takes to get vaccines approved. Once COVID-19 vaccines are FDA approved and produced, researchers will begin observing the progress of the vaccinated patients, which is Phase IV of vaccine development.

As the current clinical trials on current COVID-19 vaccines continue and new emerging variants spark talks of new vaccines, the bigger question remains—what other circumstances and side effects, besides blood clots, are we overlooking or not yet fully aware of?

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