Coronavirus

Quote:

---

Originally Posted by Dachsie

Dachsie comment:

They're losing the narrative. Notice how all of them are slyly telling you exactly the opposite of what they were telling you a week ago. That entity named Dr. Leanna Wen is a case in point. What a joke!

There is a big chess game going on and iit's clear and all sides know who the loser is long before the game is actually over. The losing side is just doing everything they can think of to lessen the impact of their fall. It is OK to enjoy watching them fall because they have done such unmitigated evil.

I think there is proof now in documents that have been made available that the Fauci gang followed the DMED data from the beginning and knew the horrible deaths and permanent severe injury being done to our soldiers by the vaccine.

Another big reveal that will start happening very soon is when Pfizer will release the first large tranche of Trial data of the Pfizer BioNTech mRNA vaccine, the entire quantity of which must be released to the public within an eight moth period beginning in March 2022. That information will also damn all the liars in our government and BigPharma companies and should open them up to massive class action law suits. The thing is THEY know this big bad news right now and Pfizer is trying every last ditch effort to not have to release the court-ordered data release.

Like Dr. Stan used to say -- What Did They Know and When Did They Know It ?

What all of this clearly means is that Dr. Fauci and gang knew the lethality of the vaccines all along and yet kept lying and lying to the public and kept pushing the vaccine and boosters anyway. That is nothing other than

CRIMES AGAINST HUMANITY !

_________________________________

https://static-3.bitchute.com/live/c...iF_320x180.jpg
https://www.bitchute.com/profile/mbVsqsUlNPlP/

They Just Admitted ALL OF IT and are Trying to Ba il from a Sinking Ship

15:33 video runtime

First published at 05:13 UTC on February 11th, 2022.


channel image

The Red Elephants - Vincent James

---

"That entity named Dr. Leanna Wen is a case in point. What a joke!"

I grew up in a time when communists, particularly Communist China were recognized as our mortal enemies. Now it is completely opposite with .gov welcoming them with open arms.

https://childrenshealthdefense.org/d...4-4fb3c3f96f32


02/11/22
•

COVID › Views
Breaking: FDA Postpones Meeting on COVID Shots for Kids Under 5 After Pfizer Says Not Enough Data. But Don’t Let Up!

Citing insufficient data, Pfizer today said it will delay applying for Emergency Use Authorization of its COVID vaccine for infants and children 6 months to 4 years old.

Pfizer today said it will delay applying for Emergency Use Authorization (EUA) of its COVID vaccine for infants and children 6 months to 4 years old stating there’s not enough data on the efficiency of a third dose.

The U.S. Food and Drug Administration (FDA) in response postponed a meeting that had been scheduled for Feb. 15 to review Pfizer’s application for the pediatric vaccine.

Two separate clinical trials of Pfizer-BioNTech’s COVID vaccine for the younger age group are in progress: one involving children between the ages of 6 months to 2 years old, the other involving children between ages 2 and 4.

CNBC last month reported two shots did not induce an adequate immune response in children 2 to 4 years old in Pfizer’s clinical trials, leading Dr. Anthony Fauci to predict children in that age group would need a three-dose regimen of the vaccine.

In what the New York Times described as a “highly unusual move,” the FDA urged Pfizer to apply for EUA of the vaccine, even though two doses failed to produce the hoped-for immune response among children 2 to 4 years old and the vaccine maker did not yet have data on the efficacy of a third shot.

Pfizer had planned to submit its application to the FDA next week, then provide additional data in the coming weeks on a third dose, NBC reported.

The FDA did not say when the Feb. 15 meeting would be rescheduled, and Pfizer did not indicate when it would submit the application.

URGENT! TAKE ACTION: Tell the FDA Don't Approve Pfizer’s mRNA Shots for Infants and Children under 5

Keep up the pressure! Tell the FDA ‘Don’t Break Our Hearts’

Despite today’s news that Pfizer is delaying its application, Children’s Health Defense is asking everyone to send a message to the FDA asking the agency to Protect the Kids.

The National Institutes of Health on Feb. 4 urged the public to participate in National Wear Red Day as part of an American Heart Month initiative to spotlight heart disease as the number one killer of Americans.

That same day, the Centers for Disease Control and Prevention’s (CDC) Advisory Committee for Immunization Practices overlooked thousands of reports of myocarditis, heart attacks and other cardiovascular events experienced by people who received COVID vaccines as the panel voted unanimously to recommend Moderna ‘Spikevax’ vaccine for people 18 and older.

These experimental COVID vaccines may pose more risk than benefit to the nearly 20 million American infants and preschool-aged children who will be eligible.

The shots don’t work

Pfizer’s clinical trial data showed that two doses failed to produce a “non-inferiority” immune response in 2- to 4 year-olds. According to partner BioNtech’s press release:

“Compared to the 16- to 25-year-old population in which high efficacy was demonstrated, non-inferiority was met for the 6- to 24-month-old population but not for the 2- to under 5-year-old population in this analysis …The decision to evaluate a third dose of 3 µg for children 6 months to under 5 years of age reflects the companies’ commitment to carefully select the right dose to maximize the risk-benefit profile. If the three-dose study is successful, Pfizer and BioNTech expect to submit data to regulators to support an Emergency Use Authorization (EUA) for children 6 months to under 5 years of age in the first half of 2022.”

In other words, Pfizer and BioNTech are evaluating a third dose because they have not yet found the right dose to maximize the risk-benefit profile for our youngest vaccine recipients.

And they won’t know if three doses will work until after the first two doses are approved. This is concerning. These are our babies.

Pfizer’s December 2021 press release noted the updates to its clinical trial were “informed by the effectiveness data for three doses of the vaccine for people 16 years and older, and the early laboratory data observed with Delta and other variants of concern, including Omicron, which suggest that people vaccinated with three doses of a COVID- 19 vaccine may have a higher degree of protection.”

However, breakthrough infections and hospitalizations have become commonplace among the vaccinated since that time. And we don’t know whether a third dose of this vaccine will increase the likelihood of adverse events.

What we do know is that there is no public health emergency for this age group. Children are at extremely low risk of serious outcomes from COVID.

Multiple studies attribute this to a stronger innate immune response in the upper respiratory tract that prevents viral replication early on. This may explain why children are also far less likely to contribute to disease transmission.

CDC data indicate deaths among children make up a fraction of a percentage of those who have died from COVID.

A study by Johns Hopkins showed a mortality rate of zero among 48,000 children without preexisting conditions and a large COVID study conducted in Germany found the case fatality rate among children is three out of a million, and zero deaths occurred in children under five.

But data about adverse events following Pfizer’s COVID vaccines continues to accumulate.

A Hong Kong study showed 1 out of 2,700 boys got myocarditis after receiving the Comirnaty vaccine. Among male adolescents, the incidence of myocarditis after the second dose was 37.32% per 100,000 people vaccinated.

A study from Kaiser found the same rate of myocarditis in 12- to 17-year-old American boys, 1 out of 2,700. This is alarming.

The Vaccine Adverse Event Reporting System (VAERS) has recorded more than 1,000,000 adverse events following COVID vaccinations: 31,545 of those were in children 17 and under.

Of the more than 23,000 reported deaths, including U.S. and foreign reports, 62 were children under age 17. VAERS also lists 829 cases of myocarditis and pericarditis in children following COVID shots.

With long-term health impacts still unknown and growing evidence of risks of myocarditis, neurological events, thrombosis and other serious side effects, the potential risks to our children likely outweigh any potential benefits.

We must act now!

Pfizer’s pediatric vaccine, if the FDA authorizes it for emergency use, will be available to more than 19 million children under the age of 5, many of whom already have robust natural immunity.

It also will be an important milestone in the pharmaceutical industry’s ultimate goal of getting COVID shots added to the CDC’s recommended childhood vaccine schedule, which means vaccine makers will have permanent immunity from liability for injuries and deaths caused by the vaccines.

If you’re seeing red, you’re not alone.

If the color red and the month of February are about love and heart health, then it’s time we reclaim those values to protect the hearts and health of those we love the most: our children.

What can you do?

Reach out to the regulatory authorities, local health departments, legislative offices and public officials and demand they join the “Don’t Break Our Heart. Protect our Health” campaign to stop the EUA of these experimental pediatric shots.

URGENT! TAKE ACTION: Tell the FDA Don't Approve Pfizer’s mRNA Shots for Infants and Children under 5

Here are five ways to remind regulators that red also means STOP:

1. Send a letter of opposition, mailed in red envelopes to the public health officials and VRBPAC members involved in this decision-making process. Cover their desks in a sea of red envelopes! Use this letter CHD sent to the members of the VRBPAC committee from our advocacy portal or write your own.

To encourage people to join in, post a picture of your red envelope to social media before you mail them with #DontBreakOurHearts and #SeeingRed and let’s get these hashtags trending! Red envelopes are available at many retailers including Staples, Office Depot, Walmart and Amazon.

Phone calls and emails also are important.

2. Email all the decision-makers directly from our Advocacy Portal. Fill out this form to email all the members of the VRBPAC committee and the other public officials listed on this page. Make sure to follow up with phone calls to each person asking if they’ve received your email. Phone numbers can be found at the bottom of this page.

3. Get Ready, Get Set … TWEET! Take part in our Twitter storm. Follow the CHD Twitter account and re-tweet our tweets targeting the FDA, public health officials and VRBPAC members to convince them to vote no at the likely upcoming meeting. Be sure to use the hashtags #DontBreakOurHearts and #SeeingRed.

4. Organize a Convoy for Kids. Keep on Truckin’ in your own neighborhood by organizing your own convoy. Decorate your cars with red signs and messages, including the hashtags #DontBreakOurHearts #SeeingRed. Drive to the FDA, Pfizer Headquarters, Washington, DC, your state capital, legislative offices or your Board of Health meetings. Wear red and wave red signs. Deliver handmade “Don’t Break Our Hearts, Protect Our Health” Valentine messages and hand out CHD’s Second Opinion Fact Sheets.

5. Get Social and Share, Share, Share! Over the next few days, you’ll see a series of social media graphics as well as our video from Mary Holland, CHD president and general counsel. Share any content we put out there to combat censorship and help educate others. Be our army of truth and help get this crucial information to the world.

Let’s make Valentine’s Day a “Red Letter Day” for children’s health! You can find a sample letter in CHD’s Protect the Kids Campaign page.


By
The Defender Staff


https://childrenshealthdefense.org/w...re-800x417.jpg

https://catholicvote.org/dhs-to-inve...al-terrorists/

https://catholicvote.org/wp-content/...ce-800x467.jpg
https://catholicvote.org/dhs-to-inve...al-terrorists/

DHS To Investigate Vaccine Dissenters As Potential Terrorists

CV NEWS FEED // The Department of Homeland Security (DHS) issued a new national terrorism advisory statement Monday that suggests federal law enforcement will investigate and monitor citizens who share so-called “misinformation” about COVID-19.

“The United States remains in a heightened threat environment fueled by several factors, including an online environment filled with false or misleading narratives and conspiracy theories, and other forms of mis- dis- and mal-information (MDM) introduced and/or amplified by foreign and domestic threat actors,” the advisory states:

These threat actors seek to exacerbate societal friction to sow discord and undermine public trust in government institutions to encourage unrest, which could potentially inspire acts of violence.

The advisory goes on to state that factors such as “the proliferation of false or misleading narratives,” calls for “violence directed at” both government institutions and “the media,” and “calls by foreign terrorist organizations for attacks on the United States based on recent events” have “increased the volatility, unpredictability, and complexity of the threat environment.”

“The convergence of violent extremist ideologies, false or misleading narratives, and conspiracy theories have and will continue to contribute to a heightened threat of violence in the United States,” the advisory states. “For example, there is widespread online proliferation of false or misleading narratives regarding unsubstantiated widespread election fraud and COVID-19.”

The document also notes that “COVID-19 mitigation measures—particularly COVID-19 vaccine and mask mandates—have been used by domestic violent extremists to justify violence since 2020 and could continue to inspire these extremists to target government, healthcare, and academic institutions that they associate with those measures.”

In addition:

Some domestic violent extremists have continued to advocate for violence in response to false or misleading narratives about unsubstantiated election fraud. The months preceding the upcoming 2022 midterm elections could provide additional opportunities for these extremists and other individuals to call for violence directed at democratic institutions, political candidates, party offices, election events, and election workers.

The DHS document has riled many commentators, who point out that the agency seems to be threatening to take action against people who merely share information and opinions on social media or between friends.

Throughout the DHS statement, there are many indications that the federal government intends to monitor or investigate citizens who have not committed crimes, framing them as “potential” terrorist threats because of their public speech on controversial topics such as election integrity and COVID-19 mandates.

“Domestic threat actors who seek to exacerbate societal friction to sow discord and undermine public trust in government institutions to encourage unrest, which could potentially inspire acts of violence,” wrote CatholicVote President Brian Burch, citing the DHS statement. “In other words, if you criticize the government, as determined by the government, you are a terrorist. Basically the exact opposite of everything America was founded on.”

Feb. 11 Friday 7:00 pm 186,271

Feb. 12 Saturday 5:15 am 186,267 ? ? ? total down 4 points (second time this happened recently)
__________________________________________________ __

Coronavirus
Started by Dachsie, 23rd January 2020 08:25 PM

1 2 3 ... 271

18 Deleted Post(s) You are subscribed to this thread

Replies: 2,702
Views: 186,267

Dachsie
Today, 05:04 AM Go to last post

THIS IS EXTREMELY IMPORTANT VIDEO.

https://static-3.bitchute.com/live/c...ql_320x180.jpg

https://x22report.com/aiovg_videos/t...g-pharma-fauci

36:54 VIDEO RUNTIME

VIDEO IS AL SO ON RUMBLE

https://rumble.com/vurelj-thomas-ren...wn-big-ph.html

X22 Report Published February 12, 2022

also viewable on x22report Bitchute channel

https://www.bitchute.com/video/6EkGUlABGgql/





Thomas Renz – The Coverup Phase Has Begun, The Evidence Will Bring Down Big Pharma & Fauci




Today’s Guest: Thomas Renz
Website: Renz Law
https://renz-law.com

Attorney Thomas Renz is the lead Attorney in several major cases brought in Ohio, New Mexico, Maine, and Nationally against the CDC and DHHS regarding the COVID-19 lockdowns, mask mandates, business closures, false PCR data, fraudulent death numbers and more. Thomas begins the conversation discussing DOD database and how they are tracking the effects of the vaccine. Big Pharma has been forced to produce the documentation in 6-8 months. Big Pharma, the [DS] are now trying to cover it all up, the coverup always gets you in the end.
SPREAD THE WORD

Prepare Today
$50 OFF 4-WEEK KIT
My Patriot Supply
http://preparewithx22.com

Today’s Guest: Thomas Renz
Website: Renz Law
https://renz-law.com

Regarding posting # 2705


Partial transcript:
Video
https://x22report.com/aiovg_videos/t...g-pharma-fauci

Thomas Renz – The Coverup Phase Has Begun, The Evidence Will Bring Down Big Pharma & Fauci

Video posted on February 12, 2022

Begin transcript at 27:12 of the video track
____________
Tom Renz: Because remember, the PCR test, most of them, are in “Class 1 Recall” * because the PCR was testing for the presence of the spike protein. Well, if your body is producing it, of course you’re going to test positive. Right?

And even though they changed it –one of the things really interesting-- …

So with Fauci, being the crook that he is, he’s running those PCR tests for unvaccinated people at around 45 cycles. Each cycle is an amplification, so every time you run a cycle, it’s like blowing up the number of these particles, you know, bigger. Right?

For vaccinated people, he only running it at 28 cycles, yet they’re still having all these vaccinated people show up COVID-positive. Ask the NFL.

Dave of X22 Report: I can see why he’s doing it, because he wants to show the unvaccinated –‘You have COVID’ – and he was trying to minimize the people that got the vaccine – ‘Oh no, they don’t have it.’ But it seems like it backfired on him.
End of transcript at 28:19

__________________________________

*


https://www.newswars.com/fda-announces-that-cdcs-pcr-test-failed-review-will-have-emergency-use-authorization-revoked/

By Jamie White | INFOWARS.COM Sunday, July 25, 2021

https://www.newswars.com/wp-content/...cr-test325.jpg

The Centers for Disease Control and Prevention (CDC) announced this week that its PCR test has failed its full review and will have its Emergency Use Authorization revoked.

The Innova SARS-CoV-2 Antigen Rapid Qualitative Test, the CDC’s benchmark COVID diagnostic testing system, will be withdrawn for Emergency Use by the end of 2021 due to an inordinate frequency of false positive and negative results.

“The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death,” the FDA stated on its website.

__________________


https://www.fda.gov/medical-devices/medical-device-recalls/innova-medical-group-recalls-unauthorized-sars-cov-2-antigen-rapid-qualitative-test-risk-false-test

Innova Medical Group Recalls Unauthorized SARS-CoV-2 Antigen Rapid Qualitative Test with Risk of False Test Results


The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Recalled Product

Innova SARS-CoV-2 Antigen Rapid Qualitative Test (also distributed under the names Innova COVID-19 Self-Test Kit (3T Configuration), Innova SARS-CoV-2-Antigen Rapid Qualitative Test (7T Configuration), and Innova SARS-CoV-2-Antigen Rapid Qualitative Test (25T Configuration))
Lot codes:
25T (25 tests per box) - U2101750, U2101751, X2006004, X2008001, X2008010, X2009002, X2009004, X2009013, X2009016, X2010004, X2010010, X2011005, X2011006, X2011007, X2011008, X2011009, X2011012, X2011013, X2011015, X2011016, X2011017, X2011025, X2011051, X2011052, X2012001, X2012002, X2012004, X2012005, X2012008, X2101002, X2101004, X2101014, X2101031, X2101038
3T (3 tests per box) - U2102003, X2012310
7T (7 tests per box) - U2101748, U2102001, U2102002, X2012711, X2103792
Manufacturing Dates: September 1, 2020 to March 3, 2021
Distribution Dates: November 2, 2020 to March 22, 2021
Devices Recalled in the U.S.: At least 77,339
Date Initiated by Firm: March 24, 2021

Device Description

The Innova SARS-CoV-2 Antigen Rapid Qualitative Test claimed to determine if a person has an active COVID-19 infection. The test used a nasal swab sample and test strip to detect specific proteins, called antigens, from the SARS-CoV-2 virus. If the nasal sample had SARS-CoV-2 antigens, a colored test line should have appeared on the test strip, indicating that the person may have COVID-19. If the nasal sample did not have SARS-CoV-2 antigens, a colored line should not have appeared on the test strip. The test has not been authorized, cleared, or approved by FDA for commercial distribution in the United States.
Reason for Recall

Innova Medical Group is recalling its SARS-CoV-2 Antigen Rapid Qualitative Test. Labeling distributed with certain configurations of the test includes performance claims that did not accurately reflect the performance estimates observed during the clinical studies of the tests. The performance characteristics of the test have not been adequately established, presenting a risk of false results.

False-negative results may lead to delayed diagnosis or inappropriate treatment of SARS-CoV-2, which may cause patient harm including serious illness and death. False-negative results can also lead to further spread of the SARS-CoV-2 virus, including when presumed negative patients are grouped into cohorts in health care, long-term care, and other facilities based on false test results.
False-positive results could lead to a delay in the correct diagnosis and the initiation of an appropriate treatment for the actual cause of patient illness, which could be another life-threatening disease that is not SARS-CoV-2. False-positive results could also lead to further spread of the SARS-CoV-2 virus when presumed positive patients are grouped into cohorts based on false test results.

Who May Be Affected

People who were tested using these devices
Health care providers who may have access to and use these tests or whose patients have used these tests
Organizers of large testing programs, such as on college campuses, who may be using and distributing these tests for diagnostic use

What to Do

On April 23, 2021, Innova Medical Group sent all affected device users an Urgent Medical Device Recall letter. The letter provided the following information:

Do not use these tests to screen for or diagnose COVID-19.
Identify and remove all affected tests from inventory.
Either destroy the tests by placing them in the trash or return the tests using the FedEx return label that was included with the letter Innova sent to its customers.
Complete and return the form Innova sent to its customers, indicating the number of destroyed or returned tests.

The FDA also recommends:

Test users and caregivers: Talk to your health care provider if you think you were tested with the Innova SARS-CoV-2 Antigen Rapid Qualitative Test and you have concerns about your test results.
Health care providers: If the test was given less than two weeks ago, consider retesting your patients using a different SARS-CoV-2 diagnostic test if you suspect an inaccurate result. If testing was performed more than two weeks ago and there is no reason to suspect current SARS-CoV-2 infection, it is not necessary to retest.
Testing program organizers: Notify participants in your testing program to discontinue diagnostic use of these tests and to use an FDA-authorized test to continue testing. For listings of FDA-authorized tests, see:
FDA-Authorized Molecular Diagnostic Tests for SARS-CoV-2
FDA-Authorized Antigen Diagnostic Tests for SARS-CoV-2
Report any problems you experience with the Innova SARS-CoV-2 Antigen Rapid Test to the FDA, including suspected false results.

For more information, please see the FDA's June 2021 safety communication, Stop Using Innova SARS-CoV-2 Antigen Rapid Qualitative Test.
Contact Information

Customers with questions about this recall should contact Linda Weinreb at Linda.Weinreb@innovamedgroup.com or call 747-494-0852.
How do I report a problem?

Health care professionals and consumers may report adverse reactions or quality problems they experienced using these devices to MedWatch: The FDA Safety Information and Adverse Event Reporting Program using an online form, regular mail, or FAX.

Quote:

---

Originally Posted by Dachsie

https://catholicvote.org/dhs-to-inve...al-terrorists/

https://catholicvote.org/wp-content/...ce-800x467.jpg
https://catholicvote.org/dhs-to-inve...al-terrorists/

DHS To Investigate Vaccine Dissenters As Potential Terrorists

CV NEWS FEED // The Department of Homeland Security (DHS) issued a new national terrorism advisory statement Monday that suggests federal law enforcement will investigate and monitor citizens who share so-called “misinformation” about COVID-19.

“The United States remains in a heightened threat environment fueled by several factors, including an online environment filled with false or misleading narratives and conspiracy theories, and other forms of mis- dis- and mal-information (MDM) introduced and/or amplified by foreign and domestic threat actors,” the advisory states:

These threat actors seek to exacerbate societal friction to sow discord and undermine public trust in government institutions to encourage unrest, which could potentially inspire acts of violence.

The advisory goes on to state that factors such as “the proliferation of false or misleading narratives,” calls for “violence directed at” both government institutions and “the media,” and “calls by foreign terrorist organizations for attacks on the United States based on recent events” have “increased the volatility, unpredictability, and complexity of the threat environment.”

“The convergence of violent extremist ideologies, false or misleading narratives, and conspiracy theories have and will continue to contribute to a heightened threat of violence in the United States,” the advisory states. “For example, there is widespread online proliferation of false or misleading narratives regarding unsubstantiated widespread election fraud and COVID-19.”

The document also notes that “COVID-19 mitigation measures—particularly COVID-19 vaccine and mask mandates—have been used by domestic violent extremists to justify violence since 2020 and could continue to inspire these extremists to target government, healthcare, and academic institutions that they associate with those measures.”

In addition:

Some domestic violent extremists have continued to advocate for violence in response to false or misleading narratives about unsubstantiated election fraud. The months preceding the upcoming 2022 midterm elections could provide additional opportunities for these extremists and other individuals to call for violence directed at democratic institutions, political candidates, party offices, election events, and election workers.

The DHS document has riled many commentators, who point out that the agency seems to be threatening to take action against people who merely share information and opinions on social media or between friends.

Throughout the DHS statement, there are many indications that the federal government intends to monitor or investigate citizens who have not committed crimes, framing them as “potential” terrorist threats because of their public speech on controversial topics such as election integrity and COVID-19 mandates.

“Domestic threat actors who seek to exacerbate societal friction to sow discord and undermine public trust in government institutions to encourage unrest, which could potentially inspire acts of violence,” wrote CatholicVote President Brian Burch, citing the DHS statement. “In other words, if you criticize the government, as determined by the government, you are a terrorist. Basically the exact opposite of everything America was founded on.”

---

This should drive home the reason the Founders declared the #2A Militia of the several States are NECESSARY TO THE SECURITY OF A FREE STATE, and as Art. II §2 Clause 1,Art. I §8 Clauses 15, 16 indicate the Milita are supposed to be permanent institutions of the federal system, as permanent as Congress but were unconstitutionally disestablished and replaced by the National Guard, an adjunct of the military, Troops and Ships of War.

Any State can revitalize her #2A Constitutional Militia without the consent of Congress.

The #2A Militia composed of a great body of the people possess police powers, and have the power to arrest and remove from office tyrants who violate the Constitution. With what we have been put through the last 2 years it should be a wake up call

Mis dos centavos.

Edit: As the Freedom Convoys are proving it is obvious what may be accomplished by the People uniting.

Dachsie comment:

It's too late for these serial killers.

These people will be held to account.

This is a war against humanity.

We need Nuremberg 2 trials.


__________________________________________________ ____________________

https://www.newswars.com/not-normal-...e-on-same-day/

There are three embedded videos in this article.

[SIZE=4]https://www.newswars.com/wp-content/...-alto-chic.jpg

By Kelen McBreen | INFOWARS.COM Thursday, February 10, 2022

A pair of teenagers from different states both collapsed and died during their high school basketball games on Tuesday.

embedded video

By Kelen McBreen | INFOWARS.COM Thursday, February 10, 2022

A pair of teenagers from different states both collapsed and died during their high school basketball games on Tuesday.

Texas sophomore Devonte Mumphrey and Illinois Senior Cameran Wheatley tragically passed away while doing what they loved.

Mumphrey, who attended Alto High School, was named All-District 22-2A Newcomer of the Year in 2021.

“You couldn’t have met a better kid,” Mumphrey’s cousin Jessica told the Tyler Morning Telegraph. “He had respect. I never saw him with an attitude.”

“He was the kind of kid that touched everybody. Family and friends were most important to Vonte,” she added. “He was a good kid. This all feels like a dream; it doesn’t feel real.”

The same night Mumphrey collapsed, nearly one thousand miles away, Bremen High School’s Cameran Wheatley also fell onto the court and was later pronounced dead.

“That’s tragic as I don’t know what,” a parent with children attending the school said. “I wouldn’t think anything like that would happen at a high school to anyone that young.”
Release the warrior in you by capitalizing on hot deals you won't find anywhere else!

ABC 7 reported that Wheatley’s father confirmed his son had a clean bill of health and had played several sports for almost 10 years.

Cameran’s friend Hugo Silva remembered his pal, saying, “You could always go up to him, say hi to him, ask him how he was, how are you feeling. He was always there for you if you needed him as well, and I will miss him.”

The teens’ vaccination statuses are unknown, and autopsy reports have yet to be released.

However, healthy athletes don’t often collapse and die, and cases of this happening have been increasing since the experimental vaccine rollout began.

Earlier this week, Infowars covered a County Coroner’s autopsy report claiming 24-year-old New York college student George Watts Jr. died in direct relation to the Pfizer Covid shot.

Last month, Infowars reported on a 26-year-old man named Joseph Keating who died from myocarditis after a Pfizer Covid-19 vaccine booster jab.

According to the certificate of death, Keating died from “multifocal myocarditis involving the left ventricle and septum,” with the second cause of death listed as “Recent Pfizer Covid-19 booster vaccine.”

In October of 2021, Police in Sonoma County, California blamed Pfizer’s experimental mRNA jab for causing the sudden death of a local teen.

The teenager’s death report states that after a postmortem examination was conducted by a forensic pathologist, “the cause of death was determined to be: ‘STRESS CARDIOMYOPATHY WITH PERIVASCULAR CORONARY ARTERY INFLAMMATION (hours to days), due to, UNKOWN ETIOLOGY IN SETTING OF RECENT PFIZER-BIONTECH COVID-19 VACCINATION (days).’” [emphasis theirs]

http://By Kelen McBreen | INFOWARS.C...phasis theirs]

Texas sophomore Devonte Mumphrey and Illinois Senior Cameran Wheatley tragically passed away while doing what they loved.

Pasting the article 3 times seems excessive. Sort of like repeating gossip.

Look at these filthy lying murdering bottom dwelling slugs !

The Surgeon General is going to murder his 5-year old too.

_________________________________

https://www.youtube.com/watch?v=owy8uHfFo4s&list=PLbpi6ZahtOH71a6AQn1p3XGQ 2CQSlfPIU

https://www.youtube.com/watch?v=owy8...p3XGQ2CQSlfPIU

The Truth About COVID Vaccines For Kids ft. Surgeon General

Doctor Mike

8.89M subscribers

Dr. Vivek Murthy is the Surgeon General of the United States and a leading expert on COVID-19. I sat down with him to discuss his recently released A Community Toolkit for Addressing Health Misinformation which provides resources and education to battle medical misinformation, such as how to spot bad actors and even talk to loved ones when we believe they’re being mislead. We also dove deep into the recently approved COVID-19 vaccine from Pfizer that has been approved for children ages 5-11. We talked about side effects, myocarditis, the quality of the research, and so much more. We’re simply here to provide you with as many facts as possible so you can make the best decision for you and your family.

A Community Toolkit for Addressing Health Misinformation: https://www.hhs.gov/sites/default/fil...

More information on COVID-19 vaccination for children: https://www.cdc.gov/coronavirus/2019-...