Lawyer breaks media silence on Ottawa Detective’s probe into sudden infant death increase

An Ottawa police detective is facing trial for allegations of misconduct after investigating a series of unusual sudden infant deaths in the region, in 2021 and 2022.

Detective Helen Grus, who was working at the time for the sexual assault and child abuse unit (SACA) for the Ottawa Police Service (OPS), is accused of unauthorized access of an internal database while researching a potential link between the novel COVID-19 mRNA vaccines and an uptick in sudden infant deaths after their roll out.

During her tribunal defence hearing in May of this year, Grus presented evidence of a roughly 97% fatality rate among unborn babies in Pfizer’s clinical trial data. This full disclosure could not be heard because Grus was interrupted and silenced by the hearing officer, retired superintendent Chris Renwick, who has no legal training.

The defence suspects that the police and the hearing officer are politically motivated to silence and prosecute Grus, disregarding potential criminality around this alarming trend affecting the most vulnerable population.

Grus’ lawyer, Bath-Sheba van den Berg, describes the unsettling incident as unlike anything she has witnessed in proceedings before.

“She’s sitting there in front of me, facing me,” details van den Berg, “and she’s stating simply that, 31 out of 32 [babies died]. And as she was stating that, the hearing officer lurched forward and said ‘stop.’”

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1/200 chance of death in context of new bird flu injection – 5 times higher than placebo according to clinical trial

On June 26, 2024, Reuters wrote a piece announcing the looming threat of plans to offer preemptive bird flu injection to the people of Finland who work with animals.

It’s important that the people of the world understand something about the so-called AUDENZ™ (Influenza A (H5N1) Monovalent Vaccine, Adjuvanted), another product in clinical trials that will soon be offered to the public to fight ‘bird flu’.

Some details: It’s a 2-doser – 21 days apart. Anaphylaxis is counter-indicated and a precautionary warning pertaining to Guillain-Barré syndrome is listed in the prescribing information sheet.

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Stroke Risk: COVID Shots 200 Times More Likely to Cause Blood Clots in Brain

The COVID-19 vaccines carry a much higher risk of blood clots in the brain compared with other vaccines, according to a new study by Dr. Peter McCullough and colleagues.

The researchers looked at reports in the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) from January 1990 through December 2023.

They counted the number of cerebral thromboembolism events — as in, blood clots of the brain’s veins or arteries — reported in people who received a COVID-19 shot compared with those who received a flu shot or other vaccines.

Blood clots that block blood flow to the brain account for roughly 87% of all strokes, according to the American Stroke Association, a division of the American Heart Association.

McCullough — a cardiologist with over 1,000 publications and over 685 citations in the National Library of Medicine — told The Defender the study showed “an unacceptable risk of catastrophic thrombotic injuries to the brain” in individuals who took one or more COVID-19 shots.

McCullough summarized the study’s results on Substack:

“Compared to influenza vaccines given over 34 years, COVID-19 vaccines in 36 months of use had over 1000-fold increased risk of most blood clot events, and compared to all vaccines combined administered over 34 years, this risk remained at over 200-times greater with COVID-19 vaccination.”

Prior research has suggested that the spike protein in both the SARS-CoV-2 virus and the COVID-19 vaccine can cause serious blood clotting, McCullough and his co-authors noted in their report.

Blood clots in the brain are difficult to treat, McCullough told The Defender, and “oftentimes leave patients with devastating disabilities.”

“This and other sources of data,” he added, “support calls to remove all COVID-19 vaccines from public use.”

The study — co-authored with Claire Rogers, Dr. James Thorp and Kirstin Cosgrove — is under peer review and available online as a preprint.

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Guillain-Barré Syndrome ‘More Common Than Expected’ in Early RSV Vaccine Trial

Reports of the nervous system disorder Guillain-Barré syndrome (GBS) were “more common than expected” in the older adult population who received the new vaccine for respiratory syncytial virus (RSV). The data, reported by the U.S. Centers for Disease Control and Prevention (CDC), matched trial data reported earlier this year.1

GBS is a “polio-like” inflammatory autoimmune disorder in which a person’s immune system damages nerve cells, which can result in muscle weakness and paralysis of the face, respiratory system and limbs, including full body paralysis and can lead to death. GBS usually develops after an infection and symptoms include numbness and tingling, throbbing pain, heart rhythm problems, high blood pressure, slurred speech, difficulty swallowing and shortness of breath. Most people recover but, in some cases, the nerve damage is permanent.2

Current recommendations state that patients over the age of 60 should talk to their doctor to decide whether they should get the new RSV vaccine. Government officials still say that the benefits of the vaccine outweigh the risks and that they do not plan to change their recommendations.1

The most recent CDC report highlighted 28 cases of RSV vaccine-related GBS and all but one developed symptoms of GBS within 21 days after being vaccinated. Data from the Vaccine Adverse Event Reporting System (VAERS) revealed that there were 1.5 cases per one million in people who received GlaxoSmithKline’s (GSK) Arexvy RSV vaccine, and five cases per one million in people who received Pfizer’s Abrysvo RSV vaccine.

There were 18 reported deaths after RSV vaccinations that were attributed to “a variety of reasons,” two of which were associated with GBS. Other reported causes of death included severe respiratory illness and failure, cardiovascular events, hepatic encephalopathy, RSV infection, and sepsis, among others.3

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Lawsuit On Behalf Of Vaccine-injured Seeks To Strike Down ‘Unconstitutional’ PREP Act

lawsuit filed Tuesday seeks to strike down the PREP Act — the federal law that granted legal immunity to companies such as Pfizer and Moderna for injuries caused by their COVID-19 vaccines and other COVID-19 countermeasures.

The lawsuit, filed in the U.S. District Court for the Middle District of Florida, Tampa Division, alleges the Public Readiness and Emergency Preparedness (PREP) Act violates the U.S. Constitution and the Administrative Procedure Act, which governs how federal agencies develop and issue regulations.

Plaintiffs in the suit include the nonprofit Moms for America and individual plaintiffs who were injured by a COVID-19 vaccine, or whose loved one suffered injury or death from a COVID-19 vaccine.

According to the complaint, “This case is about the government’s failure to resolve conflicts involving Americans killed or grievously harmed while receiving healthcare during the COVID-19 pandemic.”

Defendants are the U.S. Department of Health and Human Services (HHS), the U.S. Health Resources and Services Administration, HHS Secretary Xavier Becerra and President Joe Biden.

“As even The New York Times has recently acknowledged,” Jeff Childers, attorney for the plaintiffs, told The Defender, “too many Americans have been injured by the COVID vaccines and other rushed treatments, and now have no recourse, no help and no support. They can’t sue anybody, thanks to PREP.”

“PREP was poorly conceived, badly executed, and gave far too much power to unelected bureaucrats and executive agencies,” he added.

Childers wrote on Substack today that the PREP Act should “be crushed and burned to a cinder in the incinerator of history’s worst ideas.”

The lawsuit asks the court to declare the PREP Act unconstitutional and to declare that the HHS secretary’s actions in implementing the act violate the Administrative Procedure Act.

The suit also asks the court to declare that the plaintiffs can sue companies like Pfizer and Moderna in federal and state courts. It also seeks compensation for attorney fees.

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Study Finds Alarming Surge In Deaths From Neurological Disease Among Young Adults

A recent preprint study which relies on extensive data from the Centers for Disease Control and Prevention (CDC) paints a concerning picture of the neurological health landscape in the United States. The study, which focuses on those aged 15-44, reveals a disturbing increase in deaths from neurological diseases both as the primary cause and among multiple contributing factors.

This uptick in mortality rates, which is particularly significant among younger adults, could have profound implications for the nation’s public health policies, especially in the wake of the COVID-19 pandemic.

Perhaps most concerning, the study found an increase in neurological complications following COVID-19 vaccinations, including conditions such as Guillain-Barré syndrome and acute disseminated encephalomyelitis.

According to Phinance principal Ed Dowd, “The results show a clear break from the prior historical trend in death rates from neurological diseases.”

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Peer Reviewed Study: Infants Who Receive Multiple Vaccines At Greater Risk Of Injury

The more vaccines an infant receives at once, the greater the chance the infant will develop an infection, a respiratory illness or developmental delays following their shots, according to a peer-reviewed study published Wednesday in the International Journal of Vaccine Theory, Practice, and Research.

“If safety signals sounded alarms, the results would be deafening,” lead author Karl Jablonowski, Ph.D., senior research scientist at Children’s Health Defense (CHD), told The Defender. “The sheer number of diseases increases exponentially with every added vaccine.”

Jablonowski and CHD’s Chief Scientific Officer Brian Hooker, Ph.D., analyzed 20 years’ worth of data from 1,542,076 vaccine combinations administered to infants under age 1.

The data, collected from July 1, 1991, to May 31, 2011, came from the publicly available Florida Medicaid Database, which contains more than 460 million billing claims from over 10 million people.

The researchers examined the medical diagnoses given to vaccinated infants within 30 days after vaccination. They excluded diagnoses made on the day the babies received the shots, to eliminate any possible preexisting conditions.

The study compared babies who received three “base vaccines” to babies who received those same vaccines plus others in a single pediatrician visit.

The control group consisted of 227,231 cases of infants who in one visit only received the DTP, Haemophilus influenzae type b (Hib) and the inactivated poliovirus vaccine (IPV).

They compared medical outcomes among that group to outcomes for cohorts of infants who also received either the hepatitis B (HepB) vaccine, the pneumococcal vaccine (PCV), or the rotavirus vaccine, or different combinations of two or three of those vaccines administered together.

The researchers found seven cohorts of infants in the database who received different vaccine combinations — ranging, for example, from base vaccines plus HepB to base vaccines plus HepB, PCV and rotavirus — and compared those to the control group.

They used the Fisher’s Exact Test statistical model to compare the frequency of a particular disease following the shots in one cohort with the frequency of the same disease in another cohort.

They also used Bonferroni correction, a powerful statistical tool, to eliminate any random results and implemented a high bar for identifying statistical significance.

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Explosive Study Once Removed by Lancet within 24 Hours, Now Peer-Reviewed and Public: Reveals 74% of Deaths Directly Linked to COVID-19 Shot

A previously censored paper from The Lancet has now undergone peer review and is available online.

The study, titled “A Systematic Review of Autopsy Findings in Deaths After COVID-19 Vaccination,” analyzed 325 autopsy cases and found that a staggering 73.9% of deaths were either directly due to or significantly contributed to by the COVID-19 vaccination.

The paper’s lead author, Dr. Nicolas Hulscher, faced significant opposition in bringing these findings to light. After initially being downloaded over 100,000 times, The Lancet removed the paper within 24 hours, according to Dr. William Makis. 

According to The Daily Sceptic, the reason given at the time was, “This preprint has been removed by Preprints with the Lancet because the study’s conclusions are not supported by the study methodology.”

The news outlet added:

“Without further detail from the Preprints with the Lancet staff who removed the paper it is hard to know what substance the claim that the conclusions are not supported by the methodology really has. A number of the authors of the paper are at the top of their fields so it is hard to imagine that the methodology of their review was really so poor that it warranted removal at initial screening rather than being subject to full critical appraisal. It smacks instead of raw censorship of a paper that failed to toe the official line. Keep in mind that the CDC has not yet acknowledged a single death being caused by the Covid mRNA vaccines. Autopsy evidence demonstrating otherwise is clearly not what the U.S. public health establishment wants to hear.”

In a post on X Friday, Dr. William Makis shared the exciting news.

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Biden Seeks to Delay COVID Vaccine Safety Data Release Until 2026.

The Biden government is seeking an 18-month delay in releasing COVID-19 vaccine safety data, pushing potential disclosure until at least 2026. This regime claims an influx of pandemic-related information requests is overwhelming the Food and Drug Administration (FDA) and that releasing vaccine records requires extensive staff training and onboarding, which could take up to two years.

“This is a typical government excuse which is,’ Oh, we’re so busy, we don’t have the resources to help provide you, the American people with the information that you need,’” says America First Legal lawyer, Gene Hamilton, representing Just the News, which is requesting vaccine safety records under freedom of information laws.

Hamilton characterizes the regime’s position on the vaccination records as, “you just need to wait until 18 months from now. And maybe you’ll get to see it, maybe you won’t. And what they’re hoping to do is stretch this out to the point where everybody forgets about it.”

America First Legal and Just the News are suing the FDA and the Centers for Disease Control and Prevention (CDC) for data on Covid vaccine reactions “kept in a back-end, nonpublic system.” This is separate from the public Vaccine Adverse Event Reporting System (VAERS).

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We Now Have Proof The COVID Vaccines Damage Cognition

When the COVID-19 vaccines were brought to market, due to their design I expected them to have safety issues, and I expected over the long term, a variety of chronic issues would be linked to them. This was because there were a variety of reasons to suspect they would cause autoimmune disorders, fertility issues and cancers—but for some reason (as shown by the Pfizer EMA leaks), the vaccines had been exempted from being appropriately tested for any of these issues prior to being given to humans.

Since all new drugs are required to receive that testing, I interpreted it to be a tacit admission it was known major issues would emerge in these areas, and that a decision was made that it was better to just not officially test any of them so there would be no data to show Pfizer “knew” the problems would develop and hence could claim plausible deniability. Sadly, since the time the vaccines entered the market, those three issues (especially autoimmunity) have become some of the most common severe events associated with the vaccines.

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