Tag: vaccine injury

Doctors Confirm Vaccine Connection after Young Ontario Woman Paralyzed after Moderna Shot – Then Offer Her Euthanasia as Remedy

A young mother’s life has been turned upside down in the wake of receiving her Moderna COVID-19 booster shot, which has left her paralyzed from the neck down, The Canadian Independent reported.

Kayla Pollock, a 37-year-old from Mount Albert, Ontario, has had her vibrant life of motherhood and community involvement brought to a sudden halt due to what doctors have diagnosed as a severe vaccine-related reaction.

Kayla, who suffered an abusive childhood, had overcome her past to find joy in her work as a behavioral trainer for exotic animals and later as an educational assistant. The single mother, known for her active lifestyle, was compelled to get vaccinated to ensure she could continue visiting her father in his long-term care facility.

However, after receiving her booster shot on January 11, 2022, Kayla began experiencing alarming symptoms, culminating in her complete paralysis less than two weeks later. Despite initial skepticism from emergency department staff, an MRI revealed a significant lesion on her spinal cord.

A neurologist, documented on an audio recording, expressed his belief that the vaccine was the likely cause of Kayla’s condition, a view later confirmed with a diagnosis of transverse myelitis – a rare inflammatory disorder caused by damage to the spinal cord.

The once active mother has since spent several months in hospital and rehabilitation centers, even being offered MAID – Medical Assistance in Dying – which she refused.

Medical Assistance in Dying (MAID) in Canada is a legal and voluntary form of euthanasia, allowing eligible adults to request assistance from a medical practitioner to end their lives.

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Vaccinated are susceptible to viral infections and “covid vaccine heart syndrome”

A recent paper examined the mechanisms that cause “covid vaccine heart syndrome.”

It raised the possibility of many mechanisms explaining the broad array of cardiac complications and the varying times from injection to presentation.  While they consider several causative factors, the researchers also speculate the known cardiotoxicity of adjuvants is involved.

Dr. Kevin Stillwagon points out what the researchers failed to mention; adjuvants focus white blood cells, known as T-cells, on what was injected and miss other things which allow them to get through the epithelial barrier.

Epithelial barriers – such as such as the skin, the gastrointestinal mucosal membrane and tissue lining the respiratory tract – are an important line of our bodies’ defence preventing the invasion of microorganisms and their products. Epithelial barriers are essential in protecting the body from the environment, covering internal cells, secretion and excretion, absorption and filtration.

Focusing T-cells to detect constituents of injections while ignoring everything else, means that infections will continue to occur as SARS-CoV-2 naturally mutates and viruses associated with other communicable diseases will get through our bodies’ natural barriers as well.

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Biden Admin. pressured Amazon to censor books about vaccine safety risks during Covid

White House officials pressured Amazon in 2021 to censor and minimize access to books on its online site that questioned the safety or efficacy of vaccines, according to e-mails released earlier this month by House Judiciary Committee Chairman, U.S. Representative Jim Jordan of Ohio.

The campaign to curtail any vaccine-related book sales during the height of the pandemic was led by President Biden’s Senior Advisor for Covid-19 Response, Andrew Slavitt, and sought to avoid the spread of “propaganda and misinformation.”

“Who can we talk to about the high levels of propaganda and misinformation and disinformation of [sic] Amazon?” Slavitt wrote to Amazon in a Mar. 2, 2021, e-mail.

In initial discussions, Amazon officials discouraged “a manual intervention” to censor or remove certain book titles from populating in search results, concerned that it would be too obvious and lead to further criticism. “We will not be doing a manual intervention today,” one e-mail between Amazon executives read. “The team/PR feels very strongly that it is too visible, and will further compound the Harry/Sally narrative (which is getting the Fox News treatment today apparently), and won’t fix the problem long-term … because of customer behavior associates.”

The Amazon officials, whose names were redacted from the e-mails, reveal that another individual at the company “gave very direct guidance to the teams to be boring and not do anything that is visible and will draw more attention.”

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Study of Nearly 100 Million COVID-19 Vaccine Recipients Reveals a Host of Adverse Events

A multinational study of over 99 million vaccinated people has identified higher incidences of neurological, cardiovascular, and blood disorder complications than what the researchers expected.

The peer-reviewed observational cohort study, published in the Vaccine journal on Feb. 12, aimed to evaluate the risk of 13 adverse events of special interest (AESI) following COVID-19 vaccination. The AESIs spanned three categories—neurological, hematologic (blood), and cardiovascular.

It reviewed data collected from more than 99 million vaccinated people from eight nations—Argentina, Australia, Canada, Denmark, Finland, France, New Zealand, and Scotland—looking at risks up to 42 days after getting the shots.

The study looked at three vaccines—Pfizer and Moderna’s mRNA vaccines as well as AstraZeneca’s viral vector jab.

Researchers found higher than expected cases that they deemed met the threshold to be potential safety signals for multiple AESIs, including for Guillain-Barre syndrome (GBS), cerebral venous sinus thrombosis (CVST), myocarditis, and pericarditis. A safety signal refers to information that could suggest a potential risk or harm that may be associated with a medical product.

  • GBS is a disorder in which a body’s immune system attacks the nerves, and can eventually paralyze the whole body. Most people with the condition require hospitalization. A “statistically significant increase” in GBS cases was observed after the first AstraZeneca shot. The researchers had expected 76 GBS events in the observational cohort study but ended up identifying 190.
  • Acute disseminated encephalomyelitis (ADEM) is a condition that typically occurs after a bacterial or viral infection. It causes inflammation of the central nervous system. Two cases were expected. However, the study identified seven events after the first Moderna jab.
  • Bell’s palsy is a weakness or paralysis of facial muscles. Higher than expected Bell’s palsy cases were identified after the first dose of the Pfizer and Moderna vaccines.
  • CVST is a condition in which blood clots form in the brain, blocking the blood from draining out. This can end up causing a hemorrhage. While 21 events were expected, researchers identified over three times the number of cases at 69 following the first dose of AstraZeneca vaccine. CVST cases were also higher than expected after the first and second Pfizer shots.
  • Myocarditis is inflammation of the heart muscle. Higher than expected cases of myocarditis that met the threshold for “prioritized safety signals” for the condition were “consistently identified following a first, second, and third dose of mRNA vaccines,” both Pfizer and Moderna, according to the study.
  • Pericarditis is an inflammation of the outer lining of the heart. The number of pericarditis cases exceeded expectations following “all doses of all the three vaccines,” researchers wrote.

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US Officials Concede No Active Surveillance On Long-Term Effects Of COVID-19 Vaccines

In a Feb. 15 hearing by the Select Subcommittee on the Coronavirus Pandemic, U.S. health officials side-stepped a question when asked whether the U.S. Food and Drug Administration (FDA) is actively conducting extended safety surveillance on those who received early COVID-19 vaccines.

Rep. Nicole Malliotakis (R-N.Y.) asked Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, whether the FDA is conducting active surveillance and if there are any specific health markers they’re studying that may signal trends requiring further inquiry.

“Every time we go through and do the safety surveillance, we start back, and it goes back to 2020. In some cases where we’re looking for certain things, we might use a different window, but indeed, we have to look from the beginning of the period of surveillance. I can turn it over to Dr. Jernigan because he can speak for CDC [Centers for Disease Control and Prevention] in that regard,” Dr. Marks said.

“So with regard to myocarditis, we certainly have been monitoring the issue with various different data systems. I think the most recent data really demonstrates that you’re about eight times less likely to get myocarditis if you’re vaccinated compared to those that are unvaccinated,” Dr. Daniel Jernigan, director of the National Center for Emerging and Zoonotic Infectious Diseases at the CDC responded.

Rep. Malliotakis told Jernigan she wanted to know about “everything,” not just myocarditis.

Dr. Jerrigan asked her to repeat the question, and she asked again whether the FDA was conducting extended safety surveillance on early recipients of COVID-19 vaccines.

“Most of the reports that we get of adverse events are in the few weeks following the vaccination,” Jernigan said. In terms of monitoring these over time, Jernigan said the agency has “vaccine effectiveness” systems in place at the CDC.

Neither Jernigan nor Marks referenced any active surveillance initiatives being undertaken by their agencies to monitor people who received the original COVID-19 vaccines for long-term health effects.

“There is no system in place for long-term vaccine safety surveillance in this country,” Ms. Liz Willner, founder of OpenVAERS, told The Epoch Times.

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BREAKING: FIRST LOOK AT THE “FREE-TEXT” COVID VACCINE SAFETY DATA THE CDC WANTED TO HIDE

When the CDC created V-Safe as a way to track individuals who received the experimental COVID-19 “vaccines,” the agency vowed to be completely transparent. Remember—despite forcing millions of frightened human beings to take the jab—there were subpar clinical trials. One recipient shared, “The only reason I took this b******* vaccination is because my job gave me two choices. Sign a waiver or get the shot. I [got] the shot in fear of losing any benefits.” So it makes sense, and seems mandatory, that the CDC create a system for individuals to share how they feel after receiving the experimental, mRNA-driven “vaccines.” To build trust in that system, the CDC touted V-Safe as “the most intensive safety monitoring effort in U.S. history.” Yet, as severe adverse events, including death, rapidly ascended following the EUA-pushed jabs, the CDC failed to be transparent with the data, releasing, when ordered by the Court in 2022, only superficial details. But persistence paid off. Last month, a federal judge ordered the CDC to release all 7.8 million detailed “free-text” data entries over the next 12 months. The “free-text” section is the only place in V-Safe for participants to potentially report serious adverse events. Yesterday, the CDC released the initial batch of data containing symptoms reported after being injected. The eye-opening entries are telling.

The free-text entries are critical because, shockingly, despite having an index of “adverse events of special interest” listed in its protocol, V-Safe entirely omitted those same adverse events from being tracked. As explained by ICAN, instead of asking V-safe participants about whether, for example, they experienced things such as anaphylaxis, myocarditis, or coagulopathy after taking an entirely experimental “vaccine” based on technology never before used, the CDC carelessly only asked about minor and generalized reactions, such as “chills,” “headache,” “fatigue or tiredness,” and “vomiting.” Thus, for users who may have wanted to report more serious adverse events, they must use the “free-text” field, which allows up to 250 characters. This data is crucial to understanding the safety profile of the COVID-19 “vaccines.” The fact the CDC had not thus far voluntarily released this critical data is indicative of the overall failure of the federal government’s responsibility to protect the health of Americans.

ICAN’s initial win in two previous lawsuits opened the door to obtaining V-Safe data. However, the taxpayer-funded CDC argued that producing the “free-text” entries was too burdensome an endeavor for them to be responsible for. Nevertheless, the Court strongly disagreed, noting that the “Production of the free-text data will permit independent researchers to put the government agencies to their proof by considering all of the available data.” Reporting on this outstanding victory  brought by the lawyers that regularly represent ICAN on behalf of the Freedom Coalition of Doctors for Choice, ICAN explained the Court recognized that:

“The development and distribution of the COVID-19 vaccine was one of the greatest endeavors in recent history. Predictably, the American public now seeks access to COVID-related papers to ensure that relevant government policies were — and still are — supported and justified by the available data. That is precisely what FOIA contemplates and facilitates.”

Indeed, District Court Judge Matthew Kacsmaryk’s ruling is a huge win for transparency, and yesterday’s first production of at 390,000 entries outlining what users experienced in the first two days of receiving the “vaccine” is telling. And unfortunately, it’s indicative of what’s to follow. Indeed, the “free-text” data, which is available here, has an overall theme of uneasiness. Users reported “anaphylaxis”—a severe, potentially life-threatening allergic reaction—numerous times, detailing experiences such as, “Emergency room visit for anaphylaxis … went to the ER … I had repeat facial swelling.” One user wrote, “Anaphylaxis within 10 min. of being vaccinated. Throat swollen almost shut.” Another user wrote:

“After receiving the shot (within 15 mins) I had an allergic reaction (tightening of the throat, dizziness, confusion, elevated heart rate) and was taken to the ER. Received steroid shot, Benadryl shot, and ephephrine shot. Was released to go home.” The user later wrote, “Feeling of mild allergic reaction in the throat. Elevated heart rate.”

Interestingly, thousands of users reported an odd “metallic taste” in their mouth, often accompanied by a tingling feeling in their tongue, lasting anywhere from a few minutes to hours or longer. Equally as many people—in the thousands—experienced rapid and concerning heart rates. Likewise, in addition to ongoing feelings of intense anxiety, numbness, dizziness, stiffness, fatigue, and diarrhea, thousands went to the emergency room within 24 to 48 hours of receiving the “vaccine.” One user described their experience at the ER, stating, “3 to 5 days after my shot, I experienced a rash around my eye that was painful and burning. I reported to the emergency room on Thursday, 12/24, diagnosed with shingles/herpes zoster, which I’ve never had before, so I’m just suspicious if that could have been a result of my first dose of the COVID vaccine.” Sadly, over 600 users specifically noted they were pregnant when they received the shot. Did the CDC monitor them more closely? They should have. Twenty-two users reported having a miscarriage that coincided with receiving the “vaccine.” One such user wrote:

“I had a miscarriage. I should’ve been 8 weeks pregnant but the baby stopped  growing at 6 weeks which would’ve been very close to when I received my vaccine.”

It will take weeks to sift through the disturbing “free-text” entries detailing the myriad of troubling symptoms users experienced within the first couple of days after getting the “vaccine.” The 390,000 initial entries emphasize the potential for more serious adverse event symptoms like myocarditis that may be revealed as more “free-text” data files are released. Despite the unsettling entries, given the disaster that has been the COVID-19 “vaccine” campaign, reviewing the data is a massive step in the right direction. ICAN remarked, “This ruling sends a clear message to our federal agencies: we are not moving on and forgetting about the pandemic or the actions they took. ICAN will not stop until ALL the data is released to the public and there is true transparency and accountability around COVID-19.”

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Conspiracy Theory Debunker Finds Real Conspiracies

The 2023 book Misbelief by Dan Ariely belongs to a genre I would label “debunking Covid conspiracy theories.” The book is meant to explore the thought process of people who subscribe to conspiracy theories, especially about Covid and the Covid vaccines. 

Thus I was surprised to encounter in the book two stories in which the author uncovered real conspiracies to hide information about Covid from the public. 

Ariely, a professor of psychology at Duke University, played a bit part in promoting Covid lockdowns around the world. By his own description, he worked 

…on projects related to Covid-19 with the Israeli government and a bit with the British, Dutch, and Brazilian governments as well…I was mostly working to try to get the police to use rewards to incentivize good mask-wearing behavior and observance of social distancing instead of using fines… (p. 4) 

The first genuine conspiracy he describes involved the US Food and Drug Administration (FDA) manipulating data in the Vaccine Adverse Events Reporting System (VAERS).

The second involved a newspaper editor-in-chief refusing to report about vaccine side effects observed by a hospital. The author reports these situations matter-of-factly, and even gives the conspirators the benefit of the doubt, saying maybe they did the right thing! 

Let’s look at the VAERS conspiracy (recounted on pp. 274-276). Ariely says he got this information directly from a person who works “in the information technology department of the FDA.” The agency, according to the story, determined that: 

…foreign powers, mostly Russian and Iranian, had found a way to spread disinformation using VAERS. So when the FDA identified cases that had clearly come from such sources, it removed them from the system…

Not only did it delete this data, but it did so silently. Ariely only found out by accident: Parents of vaccine-injured children maintained their own copy of the VAERS data, downloaded from the FDA site. They noticed that cases appearing in their downloaded data later disappeared from the government copy of the database, and they told Ariely about this. 

Supposedly the FDA tried to keep these actions secret because it “did not want to announce to the foreign powers that it was onto them,” the FDA employee told him. But to anyone reasonably well-versed in information technology, keeping such acts secret is an obvious mistake. The bad guys will figure out what is going on; the folks we are trying to protect are left in the dark about possible mischief affecting data they rely on. And that’s the most charitable assessment of their actions. It could be worse: the FDA might have removed valid information inadvertently (putting aside possible nefarious intentions at this point). How might that come about? 

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ASIAN MEDICAL EXPERTS CALL FOR IMMEDIATE HALT TO COVID JABS

A panel of experts in Japan called the ‘Vaccine Issues Study Group’ is calling for an immediate halt to the use of COVID mRNA gene therapy, marketed to the public as ‘vaccines.’

The group includes eminent medical and science academics, such as Masanori Fukushima (Professor Emeritus, Kyoto University), Yasufumi Murakami (Professor of Science at Tokyo University) and Masayasu Inoue (Professor Emeritus, School of Medicine at Osaka City University).

The group said they had identified 201 diseases which are caused by the mRNA gene therapy, in addition to 3,071 side effect papers. The documented side effects and diseases were from ‘all fields of medicine’, and affected ‘all organs without exception.’

As a cancer specialist Fukushima said he was well aware of the side effects from chemotherapy, but the pattern of those were ‘pre-determined and well-known.’

The side effects from COVID ‘vaccination’ however were not ‘pre-determined’ with multiple side effects and diseases occuring ‘simultaneously throughout the entire body.’

Murakami noted the tendency for mulitple COVID jab side effects to present simultaneously and affect ‘whole families.’

According to the panel, the cause of the side effects and disease was well-known – the spike protein found in the ‘vaccines’ was toxic. The Lipid Nanoparticles (LNP) used to deliver it were also highly dangerous to human health.

‘The major problem is we are injecting two toxic substances into people, one of which makes human cells produce the spike proteins. Since the immune system will attack this, this causes very violent reactions.’

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CDC’s 2024 Child Vax Schedule: All Risks, No Liability

Childhood vaccines stand as a unique consumer product, enjoying unparalleled liability protection from the government. Given the corruption of the healthcare apparatus, it is no wonder that the U.S. Centers for Disease Control and Prevention (CDC) keeps expanding the list of recommended childhood vaccines, as happened in early 2024, says attorney Aaron Siri.

In his interview with The New American, Siri explains how the number of vaccine doses recommended for children under one year, including in-utero, surged from three to ninety over thirty-seven years, now including three doses of Covid-19 genetic therapy. This increase stems directly from the National Childhood Vaccine Injury Act of 1986, which granted legal immunity to vaccine manufacturers for injuries and deaths caused by CDC-recommended childhood vaccines.

Despite the CDC’s claims of rigorous safety trials, the truth is starkly different, according to the openly available information provided by the vaccine makers to the U.S. Food and Drug Administration (FDA). Shockingly, most safety trials last for only several days, in contrast to the several years spent on drugs that are liable to lawsuits. Furthermore, trials for childhood vaccines are conducted against other vaccines, not placebos, raising questions about the reliability of the results. Thus, a complete safety profile for these products is unknown, as highlighted by the attorney.

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COVID Vaccine Injuries Deserve a Day in Court

Some 270 million Americans received at least one COVID-19 vaccine dose. Tens of thousands have since claimed they suffered a COVID vaccine injury, ranging from minor side effects to severe adverse reactions. Around 9,000 of those people have requested compensation through the only legal avenue available to them—the federal government’s Countermeasures Injury Compensation Program (CICP).

To date, the CICP has paid only $30,855 to just eight claimants. Another 1,588 people have had their claims turned down—making for a 98 percent rejection rate. Thousands more have been left waiting with no response. If their claims are also rejected by the program, they have no other means of ever getting compensation.

Typically, someone who’s been injured by a product, medical or otherwise, would be within his rights to sue the manufacturer in a state court. Since the 1980s, federal liability protections prevent people from suing vaccine makers.

But under the decades-old National Vaccine Injury Compensation Program (VICP), people claiming an injury from a non-COVID vaccine are given an alternative to standard civil litigation. Injured patients instead sue the federal government in special vaccine courts, where both sides have lawyers, a special master (judge) decides claims, and people can appeal rejected compensation requests to higher courts. VICP petitioners need only show a preponderance of the evidence that they were injured by a vaccine—a relatively low burden of proof. The VICP approves about half of all claims and pays out $200 million a year (all funded by an excise tax levied on vaccine doses).

The CICP is nothing like this. The program has its origins in a piece of war on terror legislation intended to create liability protections for makers of novel, emergency countermeasures to bioweapon attacks and the like.

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