Courtesy of Matt at The DC Patriot
The following is a statement from the 45th President of the United States, Donald J. Trump. In the following statement the 45th President addresses …
Statement by Donald J. Trump, 45th President of the United States of America on Arizona Attorney General and Review of Audits
A document prepared for the FDA Advisory Committee meeting, in which members voted seventeen to zero in favour of giving emergency use authorisation for the administration of the Pfizer Covid-19 injection to children aged 5 to 11, confirms that Pfizer have modified the formulation of their injection for children to include an ingredient that reduces the acidity of blood and is used to stabilise people who have suffered a heart attack.
By Patricia Harrity
The FDA Briefing Document titled ‘EUA amendment request for Pfizer-BioNTech COVID-19 Vaccine for use in children 5 though 11 years of age‘ states the following on page 14 –
“Authorization is being requested for a modified formulation of the Pfizer‑BioNTech COVID-19 Vaccine. Each dose of this formulation contains 10 μg of a nucleoside-modified messenger RNA (mRNA) encoding the viral spike (S) glycoprotein of SARS-CoV-2 that is formulated in lipid particles and supplied as a frozen suspension in multiple dose vials.”
“To provide a vaccine with an improved stability profile, the Pfizer-BioNTech COVID-19 Vaccine for use in children 5-11 years of age uses tromethamine (Tris) buffer instead of the phosphatebuffered saline (PBS) as used in the previous formulation and excludes sodium chloride and potassium chloride”.
The Food and Drug Administration (FDA) granted emergency use authorization (EUA) to Pfizer’s COVID-19 vaccine for children aged between 5 to 11 years old on October 29th 2021. The authorisation was based on what the FDA believes was their “thorough and transparent evaluation of the data” which included input from independent advisory committee experts, and the vote was overwhelmingly in favour of making the vaccine available to all children in this age group.
However, with overwhelming evidence against the safety of the vaccine and now a change in the formula used in clinical trials EUA should never have been granted.
The Pfizer risk and benefit analysispresented to the FDA for EUA approval, states that resulting from their clinical trials they have found the COVID-19 vaccine to be 90.7% effective at preventing symptomatic disease in children ages five to 11. The UKs Joint Committee on Vaccination and Immunisation (JCVI) have said that the evidence strongly indicates that almost all children and young people are at very low risk from COVID-19.
Where symptoms are seen in children and young people, they are “typically mild, and little different from other mild respiratory viral infections which circulate each year”. Children also recover from these infections quickly and according to many studies develop a robust broad spectrum immunity.
The rates in 5 to 11 are so low that there were no “cases” of severe COVID-19 or death from either the treatment (n= 1,518) or control group(n= 750), this renders the “90% effective” claim, meaningless. This should have stopped an EUA application in its tracks, as clearly there is no emergency for this age group in particular and therefore no benefit either.
Additionally, Pfizer admit that the number of participants in the current clinical development program is too small to detect any potential risks of myocarditis associated with vaccination or long-term safety of COVID-19 vaccine in participants 5 to 11 years old.
The FDA had addressed this earlier in the year and asked Pfizer to expand the clinical trials, nevertheless, this had not happened., Pfizer just ignored them and instead “fudged it by importing data from a different study” according to experienced risk and benefit analyser Toby Rogers PHD.
In his article, “Ten red flags in the FDA risk benefit” Toby Rogers simplified, “if the rate of particular adverse outcome in kids as a result of the vaccine is 1 in 5,000 and the trial only enrols 1,518 in the treatment group then it is unlikely to spot this particular harm in the clinical trial”.
The study that was added “polluted data rather than clarified outcomes” as participants from cohort 1, which was 95.1% of the trial had safety follow-ups up to 2 months after Dose 2 and cohort 2 were only monitored for adverse events for a mere 17 days at the time of the September 6, 2021 data cut-off.”
According to Dr Robert Malone, inventor of mRNA technology, the harms of myocarditis from these vaccines will likely unfold over the course of years the risks of “adverse events such as cardiomyopathy will be cumulative.” They will likely have to be repeated twice for each school year, at approx. six-month intervals.
For minimal if any direct clinical benefit to the child and will not prevent infection”. Therefore, the trials did not allow nearly adequate time to analyse the long-term effects, but also the other 4.9% who did not have a safety follow up after dose 2 with no indication of whether they were in the control group or the treatment group, potentially skews the results.
Pfizer-BioNTech do admit however, that Myocarditis and Pericarditis have occurred in some people who have received the vaccine. A first dose of Pfizer’s vaccine comes with a risk of 3 to 17 cases of vaccine-induced Myocarditis and a second dose risks an additional 12 to 34 cases of myocarditis.
How can this be deemed safe? Yet through the recording of adverse events following vaccination, we have been made aware of the many other risks there have been 837,593 reports to date to the US VAERS site alone. There is a remote chance that the vaccine could cause a severe allergic reaction according to Pfizer-BioNTech . A severe allergic reaction would usually occur within a few minutes to one hour after getting a dose of the vaccine.
Signs of a severe allergic reaction can include:
• Difficulty breathing • Swelling of the face and throat • A fast heartbeat • A bad rash all over the body • Dizziness and weakness
— Read on
Brevard County Florida school employees used nylon rope to tie a mask onto a female nonverbal down syndrome student every day for 6 weeks.
One day they forgot to remove it and sent her home, which is how her dad found out.
THIS IS ANOTHER REASON WHY MASKS MANDATES ARE NOT ONLY UNNECESSARY BUT DANGEROUS!
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A new report is revealing that the Amish community has made it through the coronavirus pandemic without experiencing a catastrophic loss of life despite their refusal to adopt many of the safety precautions as necessary to prevent widespread loss of life.
The Amish community in Lancaster, Pennsylvania, has made it through the coronavirus pandemic without experiencing a catastrophic loss of life despite their refusal to adopt many of the safety precautions portrayed as necessary to prevent widespread loss of life, according to a new report.
While officials in most U.S. cities ordered businesses and churches to close for several months in an attempt to slow the spread of COVID-19, the Amish continued working and never stopped worshiping together at church.
She described the Amish as a “Christian group that emphasizes the virtuous over the superficial.” In an effort to live a “virtuous” life, many in the group refrain from driving and using electricity.
Attkisson traveled to Lancaster County, well-known for its large Amish population, to talk to locals about how they handled the pandemic. One person she spoke to, an Amish Mennonite named Calvin Lapp, explained: “There are three things the Amish don’t like: And that’s government; they won’t get involved in government. They don’t like the public education system; they won’t send their children to education. And … they also don’t like the health system.”
“Those three things are all part of what COVID is,” he said. Attkisson noted that “after a short shutdown last year, the Amish chose a unique path that led to COVID-19 tearing through at warp speed.” The community gathered for a religious celebration in May 2020, where they all took communion.
Lapp then described how the Amish take communion: “They dunk their wine into a cup, and they take turns to drink out of the cup. So you go the whole way down the line and everybody drinks out of that cup, so if one person has coronavirus, the rest of the church is going to get coronavirus.”
While he acknowledged that “everybody got coronavirus,” Lapp defended the community’s approach: “It’s a worse thing to quit working than dying. But to shut down and say that we can’t go to church, we can’t get together with family, we can’t see our old people in the hospital, we got to quit working … it’s going completely against everything that we believe.”
About a year after the coronavirus pandemic first broke out in the U.S., national news outlets and The Associated Press wire service reported that the Lancaster County Amish community had reached herd immunity, meaning that “a large part of the population had been infected with COVID-19 and became immune.” However, precise data is difficult to come across because the Amish were hesitant to publicize coronavirus cases in their community.
Steve Nolt, a scholar on Amish and Mennonite culture, told Attkisson that in some cases, “Amish people … refused to go to the hospital, even when they were very sick because if they went there, they wouldn’t be able to have visitors, and it was more important to be sick, even very sick, at home and have the ability to have some people around you than to go to the hospital and be isolated.”
Nolt added that “even those who … believed that they had COVID tended not to get tested. Their approach tended to be ‘I’m sick, I know I’m sick, I don’t have to have someone else tell me I’m sick,’ or a concern that if they … got a positive test, they would then be asked to really dramatically limit what they were doing in a way that … might be uncomfortable for them.”
“There’s no evidence of any more deaths among the Amish than in places that shut down tight. Some claim there were fewer here,” Attkisson maintained. “That’s without masking, staying at home” or taking the coronavirus vaccine.
Lapp highlighted that the absence of a prolonged shutdown meant that the Amish “made more money in the last year than we ever did” as the rest of the country experienced economic hardships because of lockdowns. He described 2020 as “our best year ever.”
Ryan Foley is a reporter for The Christian Post. He can be reached at: ryan.foley@christianpost.com
— Read on www.christianpost.com/news/amish-survived-covid-19-better-than-most-by-not-locking-down.html
Copied this from a post Simon….x Mike Yeadon, ex-Pfizer scientist sent this out Thursday.
We are approaching Stage 5 – Phase 5: Establish chaos and Martial law. (November 2021-March 2022)
and most people still think we are going back to normal!?
Phase 1: Simulate a threat and create fear. (December 2019-March 2020)
Phase 2: Sow the tares and division. (March 2020-December 2020)
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Phase 3: Bring a treacherous and deadly solution. (December 2020-June 2021)
Phase 4: Install Apartheid and the QR code. (June 2021-October 2021)
Phase 5: Establish chaos and Martial law. (November 2021-March 2022)
Phase 6: Cancel the debts and dematerialize the money. (March 2022-September 2022)
Here are the bioweapon details of the stealthy Covid plot to poison and mass murder most of humanity! (EVERYONE Must View This Video | SOTN: Alternative News, Analysis & Commentary
This New World Order globalist scheme has many facets to it, but there are two primary components that work closely in tandem with each other.
First, there was the launch of the different generations of the COVID-19 bioweapon as well as its variants targeting certain nations across the planet. In other word, Wuhan, Milan, Tehran, New York City, Moscow and Guayaquil, Ecuador all experienced different variations of the COVID-19 bioweapon whose main pathogenic micro-organism was a parasite.
Secondly, there was the roll-out of the various weaponized Covid vaccine programs around the globe each of which was designed to provide more vectors of dissemination of the extremely deadly and damaging spike proteins. The bioweapon spike proteins bioengineered in the COVID-19 bioweapon were then super-charged by the spike weapons put into the Covid injections.
Both of these depopulation and debilitation phases of the Covid Plandemic were designed to produce a slow-motion mass murder of the targeted populations as well as a gradual sickening of a large swath of humanity.
What follows is an excellent description of this one-two knockout punch thrown at the entire human race. This detailed explanation is rendered by a very smart Indian physician who appears to have read SOTN for many months since this Alt Media platform has posted many of the same pieces of the Covid crime puzzle.
In fact, this Covid one-two punch was presented by SOTN as a very similar dissection of the COVID-19 crime scene during the first few months of the Plandemic several months, before the vaccines were even approved on an emergency basis by the FDA. The first big clue came when the research team from India published their scientific paper (early in 2020) that identified the dangerous spike proteins found in COVID-19.
Now here is the highly informative video which should be posted and sent out everywhere post-haste, especially to all healthcare professionals—Thank you!
State of the Nation
November 10, 2021
— Read on stateofthenation.co/
The Trailblazing Patriot 