Children’s Health Defense Supports the Motion Against U.S. Department of Health and Human Services Alleging Fraud in Omnibus Autism Proceeding

Children’s Health Defense (CHD) Senior Staff Attorney Rolf Hazlehurst filed a motion in the U.S. Court of Federal Claims alleging that the U.S. Department of Justice (DOJ), representing the U.S. Department of Health and Human Services (HHS), committed fraud in its representation of HHS in the Omnibus Autism Proceeding (OAP) in the National Vaccine Injury Compensation Program (NVICP).

The OAP was established to consolidate and adjudicate the approximately 5,400 claims filed on behalf of children who regressed into autism following vaccination.

In 2003, Hazlehurst filed a claim in the program on behalf of his son Yates, diagnosed with autism after suffering adverse reactions following routine childhood vaccines. Hazlehurst’s claim was one of six original “test cases” in 2007 that would decide the fate of all the other claims in the OAP.

According to the newly filed motion, the DOJ attorneys engaged in a series of acts of fraud upon the courts, beginning in the NVICP and ultimately impacting the Supreme Court of the United States.

In the NVICP, DOJ attorneys concealed from the special masters and petitioners that the government’s top expert witness, a world-renowned pediatric neurologist, revised his opinion on whether vaccines can cause autism.

The expert explained to the DOJ attorneys that vaccines can cause autism in a subset of children. The witness had been scheduled to testify in the first test case in the OAP.

However, the DOJ abruptly dismissed him as a witness once they learned of his clarification. Without the witness’s knowledge, DOJ attorneys repeatedly misrepresented his prior case-specific written opinion in the OAP to argue there is no scientific basis that vaccines cause autism.

Ultimately, all of the 5,400 OAP claims were dismissed, leaving vaccine-injured children and their families with no recourse.

“The DOJ’s first act of fraud upon the court snowballed into a massive scheme of deception with far-reaching implications. Their fraudulent scheme denied justice to Yates and the thousands of other children in the OAP,” said Hazlehurst.

“By hiding that their own expert’s opinion had changed to favor Yates and other children in the OAP, the DOJ effectively closed the NVICP’s doors to the injured children with similar claims who have followed.”

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SHOCKING: USA has recorded over 1 Million Excess Deaths among the over 65’s since the FDA “approved” the COVID-19 Vaccine

The FDA granted Emergency Use Authorization (EUA) for the Pfizer-BioNTech COVID-19 vaccine on December 11, 2020, making it the first COVID-19 vaccine to receive such authorization in the United States.

Following that, the Moderna COVID-19 vaccine received EUA on December 18, 2020, and the Janssen (Johnson & Johnson) COVID-19 vaccine received EUA on February 27, 2021.

The elderly were offered the COVID-19 vaccine first and the number of excess deaths recorded was astounding. During the first 20 weeks of 2021 150,085 excess deaths were recorded among people aged over 65’s compared to the 2015 to 2019 five-year average.

Then from week 21 to week 40 of 2021, an astounding 165,387 excess deaths were recorded among people aged 65 and over. This brought the total excess deaths from week 1 to week 40 of 2021 to 315,472 among those most likely to get the COVID-19 vaccine.

The remainder of 2021 saw 133,268 excess deaths recorded. Bringing the total excess deaths for the year among the over 65’s to 448,740.

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Vaccinated People Show Long COVID-Like Symptoms With Detectable Spike Proteins: Preprint Study

Spike protein could remain in immune cells for more than 245 days following vaccination, according to a recent preprint. The study evaluated 50 patients who developed long COVID-like symptoms after the COVID-19 vaccine; none had been infected with the virus.

The authors extracted immune cells from 14 post-vaccine patients and found that 13 had spike protein in their immune cells. Asymptomatic vaccinated people had no spike present.

Researchers from InCellDx, a research company that produces panels and protocols that test for and treat long COVID and post-vaccine syndrome, authored the paper.

Their previous study published in 2022 showed that unvaccinated long-COVID patients could have spike protein persist in their immune cells for 15 months.

In both papers, the spike proteins were detected in monocytes, immune cells that circulate the body.

These findings indicate that the persistence of these spike proteins was likely the driver for the symptoms of long COVID and post-vaccine syndrome, InCellDx founder and lead study author Dr. Bruce Patterson told The Epoch Times.

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Whoops! FOIA response from Santa Clara County reveals that the COVID shots INCREASED your risk of getting COVID!

Based on new data I just got from a FOIA request, it appears that the public health epidemiologists in Santa Clara County knew in January 2022 that the vaccines made people more likely to get COVID, but they remained silent.

I predict that there will be further silence on this matter: no accountability and no opportunity for public challenges. They will continue to push the shots as if nothing had happened and the mainstream media will ignore this important data.

Here is the data for you to download yourself

Download it here. When you click the link, it will silently download the Excel file to your Downloads folder.

Summary of the data

The data in the spreadsheet is from January 2022 and contains a line for each person who was diagnosed with COVID in that month.

N means unvaccinated. Y means vaccinated. U means unknown. Blank means unknown.

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Why was mRNA the Government Vaccine of Choice for COVID-19?

John Solomon on Real America’s Voice Just the News asked me why was mRNA chosen over traditional vaccines for the COVID-19 pandemic? My answer goes back many years to the US Department of Defense Biomedical Advanced Research and Development Authority (DARPA) ADEPT PROTECT P3 program which stated in 2012 the US will use mRNA vaccines to end pandemics in 60 days.

Former president Trump and the White House Task Force should have done their homework with a phone calls to DARPA and a few clicks on the internet and told America that mRNA was the plan for many years. It was not developed during the few months of Operation Warp Speed.

mRNA has a scientific “seduction” that lathers up molecular biologists unlike any other product I have ever witnessed with 9,613 patents licensed to giants in biotech and the US government. The National Institutes of Health Biomedical Advanced Research and Development Authority (BARDA) and DARPA have had a torrid love affair with mRNA for decades. Note how both agencies end with the designation “Authority.” The speed from sequencing a novel virus to production of a mRNA vaccine is breathtaking. However, seduction leads to blunder and that is exactly what happened with the Pfizer/BioNTech and Moderna mRNA vaccine programs.

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Heart Scarring Detected Over 1 Year After COVID-19 Vaccination: Studies

Heart scarring was detected more than one year after COVID-19 vaccination in some people who suffered myocarditis following receipt of a shot, researchers reported in new studies.

A third of 60 patients with follow-up cardiac imaging done more than 12 months after their myocarditis diagnosis had persistent late gadolinium enhancement (LGE), which is, in the majority of cases, reflective of heart scarring, Australian researchers reported in a preprint of a new study, published on March 22.

Myocarditis is a form of heart inflammation.

The median time from receipt of a vaccine to follow-up imaging was 548 days, with the longest interval being 603 days.

“We found that the incidence of persistent myocardial fibrosis is high, seen in almost a third of patients at >12 months post diagnosis, which could have implications for the management and prognosis of this predominantly young cohort,” the researchers wrote.

“The long-term clinical implications of LGE in this condition are as yet unknown, but LGE has been demonstrated to confer worse prognosis in non-COVID-19 vaccine-associated myocarditis, especially if it persists beyond six months,” they added later, pointing to severalpreviouspapers.

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A WORLD FIRST ! AUSTRALIAN SENATE TO INVESTIGATE EXCESS DEATHS !

You would think that any Federal Government would jump at the chance to launch an inquiry to investigate why there are so many unexplained non-COVID Excess Deaths in Australia and around the world following the release of the COVID-19 “vaccines”.

But no, the Labor Party voted against Senator Ralph Babet’s motion to investigate Excess Deaths. The Albanese Labor Government obviously does not care if you live or die but, fortunately, they were defeated!

Congratulations Senator Babet!

CLICK HERE to watch a 2 minute video of the vote and announcement. It was a narrow victory – 31 to 30.

Below are the details from Senator Babet.

Finally!! Excess deaths to be investigated by the Senate

I’ve been trying repeatedly for two years and yesterday the Senate finally voted in favour of investigating excess deaths. 

For the past few years Australians have been dying in excess numbers without adequate explanation. 

Excess mortality is not just a transitory phenomenon. In 2022 we experienced our highest excess death rate since World War Two. The Therapeutic Goods Administration (TGA) provisional mortality statistics released last month confirm that to November 2023 there were 15,114 or 10% more deaths than the baseline average. 

My successful motion means that the Community Affairs References Committee will be tasked with the job of investigating the factors contributing to excess mortality. 

Submissions will be requested from the general public with public hearings expected to follow. The committee will prepare a report by 31st August 2024. 

Fifth time’s the charm! This is the fifth time I have moved a motion on excess deaths. Finally, the Senate has agreed an investigation is warranted. 

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Moderna Vaccine Recipients Have Greater Risk Of Developing Chronic Condition: Study

People who receive Moderna’s COVID-19 vaccine have a greater risk of developing chronic hives, according to researchers in Denmark.

The Danish Medicines Agency review of data from Denmark and the European Union validated a safety signal that arose for chronic hives, or chronic urticaria, and Moderna’s shot, the agency said on March 20.

Of 360 cases reported in Europe following the Moderna or Pfizer-BioNTech vaccine, 58 were deemed probably caused by vaccination and 228 were determined to be possibly caused by the vaccination, Martin Zahle Larsen from the Danish Medicines Agency said in a statement.

Most of the cases were reported by patients, doctors, or pharmaceutical companies.

The study found that in Denmark, it was expected based on background rates of chronic hives that 175 people who received Pfizer’s shot would experience chronic hives following vaccination and that 18 people who received Moderna’s shot would experience the issue.

While the 105 reported cases after Pfizer vaccination came in under the expected number, the 55 reported cases following Moderna vaccination came in well above the expected number.

The risk of developing chronic hives was calculated to be three times higher for Moderna recipients, compared to the general population. Researchers also stratified the risk by gender and age and found the risk was the highest—5.2 times higher than the background rate—among young men.

Most cases of chronic hives occurred from 7 to 13 days following vaccination.

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Kids Ages 2-5 Had Higher Rate of Convulsions After mRNA COVID Shots

Children ages 2-5 who received the COVID-19 mRNA vaccine faced an increased risk of febrile seizures immediately following vaccination, according to a new study led by researchers at the U.S. Food and Drug Administration (FDA).

The preprint study found children who received the Moderna shot were 2.5 times more likely to have a febrile seizure within a day of being vaccinated than they were to have one between eight and 63 days following vaccination.

The incidence rate ratio was “significantly elevated,” the researchers wrote, but the “absolute risk” — the risk of having a seizure following vaccination, was low within the first day following vaccination.

FDA researchers also found a higher risk of febrile seizures among children ages 2-4 on the first day following the Pfizer vaccine than in the 8-63 days following vaccination. However, that increased risk was not statistically significant, the researchers reported.

“Based on the current body of scientific evidence, the safety profile of the monovalent mRNA vaccines remains favorable for use in young children,” the researchers concluded.

Dr. Michelle Perro, a pediatrician and co-author of “What’s Making our Children Sick?” told The Defender that the way the authors mixed different measures of risk in their reporting obfuscated the findings.

“This paper buried itself in statistical gymnastics and made it difficult to assess their true findings,” despite their claim that the safety profile remains favorable, Perro said.

“Based on their own data, I would advise that this vaccination is risky due to the probability of the occurrence of non-febrile seizures in a small population of vaccinated children, along with the fact that we don’t know what other future effects might be,” Perro said.

The FDA’s Richard A. Forshee, Ph.D., led the team of researchers who came largely from commercial health claim database companies — Carelon Research, CVS Health and Optum — that contributed data to the analysis.

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Experts Discover Over 200Billion DNA Fragments in a Single Dose of Pfizer’s COVID-19 mRNA Vaccine

Dr. Phillip Buckhaults is a Professor at the University of South Carolina.  He has a PhD in biochemistry and molecular biology and conducts cancer genomics research.  What that effectively means is he and his team are specialists at detecting foreign pieces of DNA in places where they are not supposed to be.

On 12 September, he testified before the South Carolina Senate Medical Affairs Ad-Hoc Committee on the Department of Health and Environmental Control (“DHEC”).

“The Pfizer vaccine is contaminated with plasmid DNA. It’s not just mRNA, it’s got bits of DNA in it.” Prof. Buckhaults said.

A colleague who was in charge of the vaccination programme in Columbia, South Carolina,  kept all the Pfizer vials, containing remnants of the contents, from the two batches that were used.  From the remnants, Prof. Buckhaults sequenced all the DNA that was in these vials. “I can see what’s in [the vaccines] and it’s surprising that there’s any DNA in there. And you can kind of work out what it is and how it got there and I’m kind of alarmed about the possible consequences of this both in terms of human health and biology,” he said.

“This DNA, in my view, it could be causing some of the rare, but serious, side effects like death from cardiac arrest.

“This DNA can and likely will integrate into the genomic DNA of cells that got transfected with the vaccine mix … we do this in the lab all the time; we take pieces of DNA, we mix them up with a lipid complex, like the Pfizer vaccine is in, we pour it onto cells and a lot of it gets into the cells.  And a lot of it gets into the DNA of those cells and it becomes a permanent fixture of the cell.  It’s not just a temporary thing.  It is in that cell from now on and all of its progeny from now on and forever more …  So, that’s why I’m kind of alarmed about this DNA being in the vaccine. It’s different from RNA because it can be permanent.”

Based on solid molecular biology, it is a theoretical but reasonable concern that this DNA could cause a sustained autoimmune attack towards that tissue, he said.

“It’s also a very real theoretical risk of future cancer in some people. Depending on where in the genome this foreign piece of DNA lands it can interrupt a tumour suppressor or activate an oncogene,” he added. “I think it’ll be rare but I think the risk is not zero.”

“DNA is a long-lived,” Prof. Buckhaults explained.  “What you were born with you’re going to die with and pass on to your kids. DNA lasts for hundreds of thousands of years … So, alterations to the DNA – they stick around.”

Prof. Buckhaults explained that there are a LOT of pieces of DNA in Pfizer’s vaccines.  Although some are 5,000 and 500 base pairs long, most of the pieces are around 100 base pairs. But this is irrelevant because the probability of a piece of DNA integrating into the human genome is unrelated to its size.  “Your genome risk is just a function of how many particles there are,” he said. “All these little pieces of DNA that are in the vaccine [give] many many thousands of opportunities to modify a cell of a vaccinated person.”

“The pieces are very small because during the process they chopped them up to try to make them go away – but they actually increased the hazard of genome modification in the process.”

Prof. Buckhaults’ team took all these little pieces of DNA and “glued them together” to try to establish its source.  After putting together 100,000 pieces of DNA they were able to establish it came from a plasmid that can be purchased online from Agilent, a Californian life sciences company which was established in 1999 as a spin-off from Hewlett Packard.

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