Some offspring of Moderna mRNA vaccine test rats born with skeletal deformities

Pharmaceutical company Moderna informed the Food and Drug Administration that a “statistically significant” number of rats whose mothers received the company’s mRNA COVID-19 vaccine were born with skeletal deformities, according to data from the Department of Health and Human Services that a watchdog group obtained.

Judicial Watch announced on Tuesday that HHS had handed over 699 pages of records pertaining to data Moderna sent the FDA. Said handover followed a Freedom of Information Act lawsuit the group filed to obtain the records after the relevant agencies failed to respond to the initial FOIA request.

A “nonclinical overview” included in the records the group obtained noted that “mRNA-1273 [Moderna vaccine]-related variations in skeletal examination included statistically significant increases in the number of F1 rats with 1 or more wavy ribs and 1 or more rib nodules. Wavy ribs appeared in 6 fetuses and 4 litters with a fetal prevalence of 4.03% and a litter prevalence of 18.2%. Rib nodules appeared in 5 of those 6 fetuses.”

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The CIA Code Word for Bioweapon is ‘Vaccine’

Andrew Huff, former VP of EcoHealth Alliance, a CIA operated organization per Huff’s own testimony, is making the media rounds promoting both his new book and the CIA propaganda that SARS-CoV-2 is a chimeric gain-of-function virus that accidentally leaked from the Wuhan lab.

Huff appeared on Stew Peters on Friday, December 9, 2022, and when asked if a chimeric gain-of-function virus could event infect humans or be of pandemic potential without being delivered in some kind of nanoparticle technology, Huff dodged the question. He responded by saying that the nanoparticles are in the vaccine and EcoHealth and Wuhan would have to develop the antidote or cure while they were developing the bioweapon.

Huff blatantly lied when he said the pandemic was cause by the SARS-CoV-2 virus. The pandemic was caused by the nanoparticle bioweapon technology, not a virus.

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UK government asked Twitter and Facebook to “tweak” algorithms during Covid

Former United Kingdom Health Secretary Matt Hancock, self-styled as an official who was at the forefront of Britain’s battle against Covid, didn’t seem to feel like he had done enough in 2020 and 2021, so he felt compelled to milk the pandemic cow by writing a book about that “battle.”

But he wasn’t laboring alone, since he had a co-author, Isabel Oakeshott, who reports say is actually opposed to Hancock’s policies and is a lockdown skeptic.

And now, Oakeshott, who had access to official records and Hancock’s notes exchanged with “all the key players in Britain’s Covid-19 story” – as the book’s blurb states – has penned her own “story,” an article based on the collaboration published by the Spectator, whose content draws from the material used for the book.

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FDA Says Ivermectin Doesn’t Work Against COVID-19 But Points To Studies That Show It Does

The U.S. Food and Drug Administration (FDA) says a drug called ivermectin does not work against COVID-19 but links to studies that show it does, an Epoch Times review has found.

The FDA’s website states, “Currently available data do not show ivermectin is effective against COVID-19.”

But half of the studies to which the FDA points support using ivermectin against COVID-19, according to the review.

The papers cut against the drug agency’s repeated exhortations for people not to take ivermectin for COVID-19. In Twitter posts, public statements, and emails, FDA officials have repeatedly warned against ivermectin. Some of those statements triggered a lawsuit from doctors who say the agency’s role is to approve drugs, not to issue recommendations. The suit was dismissed this week.

Dr. Pierre Kory, who frequently prescribes ivermectin for COVID-19 and co-authored a meta-analysis that concluded the drug is effective against the illness, told The Epoch Times that the government’s position on ivermectin “is one of the most glaring examples of the corruption of modern evidence based medicine.”

There’s one message they want everyone to understand. And that message is that ivermectin doesn’t work,” Kory said. “That’s not a scientific conclusion, that’s theirs. That’s their perverted and distorted interpretation of the data.”

The FDA’s media office did not respond to a request for comment.

Dr. Janet Woodcock, a top official at the agency who was its commissioner from January 2021 to February 2022, told The Epoch Times via email that “ivermectin has been shown to be ineffective against COVID in large randomized trials.”

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FDA approves unpopular bivalent Covid shot for BABIES and ‘encourages parents to get their child vaccinated before the holidays’

US health officials today approved Pfizer and Moderna‘s bivalent Covid vaccines for babies, in a move bound to draw criticism.

The Food and Drug Administration (FDA) has green-lit plans for the updated shots to be given as part of a three-dose course for children aged six months to four years.

Agency officials said they ‘encourage parents and caregivers’ to get their child vaccinated ‘especially as we head into the holidays and winter months’.

It comes after a study found the bivalent vaccines are significantly weaker against a rising Covid variant expected to become dominant in the US in months.

Pre-school-aged children were already allowed to receive three extra-small doses of Pfizer’s original Covid vaccine, instead of the standard two-dose regimen for adults.

The move will see them given the Omicron-specific booster – made by either Pfizer of Moderna – as their third and final shot.

Officials recommend the children to receive the bivalent shot from the same brand they received their first two vaccine shots from.

So a child who receive the Pfizer vaccine for their first two doses should get the Pfizer bivalent shot as well. 

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Fauci deposition: Fauci says no one from his office pushed for social media censorship. Documents show they did.

Dr. Anthony Fauci’s deposition, taken as part of the lawsuit filed by Missouri and Louisiana’s Attorneys General alleging collusion between government and online platforms to censor certain viewpoints, has details about Dr. Fauci’s attitude towards Covid topics that were censored on social media platforms.

Read the full deposition transcript here.

Fauci, the retiring director of the National Institute of Allergy and Infectious Diseases, was deposed under oath on November 23.
During the deposition, Fauci said that he did not have the expertise to say whether or not COVID-19 originated from a laboratory or nature. However, he repeatedly dismissed the lab-leak theory.

Social media companies also censored content and accounts suggesting the virus originated from a lab.

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World Health Organization meets to discuss granting of increased surveillance powers under pandemic treaty

The unelected global health agency the World Health Organization (WHO) is currently meeting to consider a draft version of a controversial international pandemic treaty that will give the WHO increased surveillance powers.

The new surveillance powers are detailed in Article 10 (“Strengthening and sustaining capacities for pandemic prevention, preparedness, response and recovery of health systems”) and Article 17 (“One Health”) of the draft treaty. They include requirements for the WHO’s member states to “build and reinforce surveillance systems” across both the public and private sector and to strengthen the WHO’s “One Health surveillance systems.”

In its fact sheet on One Health, the WHO cites Covid-19 as one of the main drivers for expanding its One Health approach and notes that the COVID-19 pandemic “put a spotlight on the need for a global framework for improved surveillance and a more holistic, integrated system.”

While the draft treaty doesn’t mention contact tracing and testing, these were two of the main surveillance tools that were used to track the spread of Covid-19 during the pandemic and create a mass surveillance dragnet. Not only did this result in many citizens being forced to use surveillance apps and devices but the data was often abused by governments and third parties.

Not only does this treaty grant the WHO new surveillance powers but it also recognizes “the central role of WHO” and deems it to be “the directing and coordinating authority on international health work.”

We obtained a copy of the draft international pandemic treaty for you here.

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Duke University Refuses Kidney Transplant To Dying Girl For Refusing COVID Vaccine

Two Christian parents, Chrissy and Lee Hicks, both North Carolina Army veterans, have 11 children, including a 14-year-old girl, Yulia, who is a rescued orphan from Ukraine.  Yulia has been shuffled around the US and transferred between caretakers several times and has been finally adopted by the Hicks, who feel a strong determination and sense of duty to give their daughter some stability and justice in life. Despite coming this far, Yulia is now being denied a critical organ transplant due to her vaccination status.

Tragically, Yulia’s health has been slipping due to a genetic kidney disorder.  The Hicks family has sought help and had been embraced and encouraged by Durham Duke medical staff for being a serious-minded family that cared well for Yulia and who followed all medical procedures and guidelines given to them, getting Yulia closer to the transplant process.

But on November 29, something went wrong for the family.

“To think that a committee can determine someone’s life is terrifying. This is, without a doubt, medical tyranny. What has become of the medical community? How does the refusal of a shot that is known to cause many health issues AND does NOT stop the spread of a disease deny a 14-year lifesaving therapy? How does that happen in America? Today we are sad. Tomorrow is a new day, and God is there with an answer for us,” Chrissy Hicks posted on Yulia’s website.  

The question on their minds is, what if they get the lifesaving surgery for Yulia, and she has complications from the vaccine? Chrissy Hicks shared her concerns with National File.

Up to the late November phone call between the Hicks and the Duke medical staff, the Hicks family believed the vaccination for Yulia was an option and that they could opt out and still get the surgery.

Lee Hicks wrote about the timeline of events that got them to the phone call.

” Oct 7, we had an 8-hour appt at Duke to talk to many doctors. Dr. Chambers was the biggest one pushing the vaccine. Dr. Chang said he highly recommended it, but it was not mandatory and that families had gotten transplants without it. 

Then we got an email from Catherine Thomas, a wellness coordinator, on Nov 9, stating what vaccines Yulia needed.

The First email was what they recommended. Then in a second email, the verbiage changed to what she must have or what was required. Yulia was presented to the committee on 10 Nov and denied because of a lack of the vaccine.

During the uncomfortable conference call, the staff made it clear that without the vaccination, Yulia would not be considered for surgery. After skirting the issue, one medical staff answered decidedly when asked if the shot was a requirement, saying ‘yes’.

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Chinese Cybercriminal Hacker Group Stole $20 Million In COVID Relief Funds, Secret Service Says

U.S. Secret Service officials confirmed an exclusive report Monday alleging prolific cybercriminal hackers tied to the Chinese Communist Party have stolen nearly $20 million worth of COVID pandemic relief benefits.

Secret Service officials did not comment further upon corroborating the NBC News report. However, U.S. law enforcement officials and cybersecurity experts, who spoke on the condition of anonymity, said the pandemic fraud instance is the first publicly acknowledged example of theft linked to foreign and state-sponsored cybercriminals.

Officials said the hacker group in question is APT41, which they described as a “Chinese state-sponsored, cyber threat group that is highly adept at conducting espionage missions and financial crimes for personal gain” that operates out of the southwestern Chinese city of Chengdu.

APT41 — also known as Winnti, Barium, and Wicked Panda — allegedly began stealing COVID relief money in mid-2020 from approximately 2,000 accounts associated with more than 40,000 financial transactions, including Small Business Administration loans and unemployment insurance funds in more than at least a dozen states.

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Pfizer and BioNTech Submit Application to U.S. FDA for Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine in Children Under 5 Years

Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced that the companies have submitted an application to the U.S. Food and Drug Administration (FDA) for emergency use authorization (EUA) of their Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine as the third 3-µg dose in the three-dose primary series for children 6 months through 4 years of age. With the high level of respiratory illnesses currently circulating among children under 5 years of age, updated COVID-19 vaccines may help prevent severe illness and hospitalization.

If authorized, children in this age group would receive a primary series consisting of two 3-µg doses of the original Pfizer-BioNTech COVID-19 Vaccine followed by a third 3-µg dose of the Omicron BA.4/BA.5-adapted bivalent vaccine. An application to extend Pfizer and BioNTech’s Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine marketing authorization in the EU to include children ages 6 months through 4 years is under discussion with the European Medicines Agency (EMA).

The Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine is currently authorized as a booster dose for ages 5 years and older in the U.S. and European Union (EU).

The Pfizer-BioNTech COVID-19 Vaccines (COMIRNATY®) are based on BioNTech’s proprietary mRNA technology and were developed by both BioNTech and Pfizer. BioNTech is the Marketing Authorization Holder for BNT162b2 (Original) and BNT162b2 Bivalent (Original/Omicron BA.4/BA.5) in the United States, the European Union, the United Kingdom, Canada and other countries, and the holder of emergency use authorizations or equivalents in the United States (jointly with Pfizer) and other countries.

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