Biden and these nefarious companies Pfizer, Moderna & Johnson & Johnson are not exempt from being sued by millions of families of those who died from these shots/jabs or were left severely disabled by these experimental shots and most importantly did not have Emergency Use Authorization because people gave consent to UNKNOWN dangerous adverse events including a high probability of death as indicated in a screenshot from Pfizer’s adverse event report from its clinical trials, where we can see how many types of autoimmune diseases may be caused by a Pfizer, Moderna and J&J jabs.

Pfizer, Moderna and J&J including Biden and his administration, Dr Anthony Fauci, Bill Gates and George Soros should be held accountable for the millions of lives that were taken or left permanently debilitated due to these dangerously experimental shots.

A vaccine takes at minimum 10 years to half a century to make an effective vaccine with gold standard trials during a long process.

Every cell contains a nucleus in the nucleus are our chromosomes which are made up of our DNA 🧬. What these pharmaceutical companies did was nefarious, where DNA is made from RNA. This is not normal. The normal transcription process involves a portion of the DNA serving as a template to make an mRNA molecule inside the nucleus.

In the abnormal reverse transcription the mRNA leaves the nucleus and enters the cell’s cytoplasm, where it translates into LINE-1 protein. A segment of the protein called the open reading frame-1, (ORF-1), then goes back into the nucleus, where it attaches to the vaccine’s mRNA and then the Spike protein DNA travels to every part of the body to major organs. Even through the blood stream.

Teenagers who are athletes in school are being diagnosed with Myocarditis an inflammation of the heart. This is an example of the Spike protein damaging the heart.

These shots/jabs are NOT “vaccines” and were never meant to prevent people from getting COVID-19. In fact most people after the jab are contagious and spreads the COVID-19. They were meant to create the extremely harmful SPIKE protein that lowers the immune system by up to 75% then the spike protein travels to every major organ and tissue damaging organs and tissues forming behemoth blood clots. The boosters contain all kinds of illnesses. Under a microscope, scientists were in shock at the different live viruses detected.

Below a screenshot from Pfizer’s adverse event report from its clinical trials, where we can see how many types of autoimmune diseases may be caused by a Pfizer jab. Pfizer was not transparent and hid these serious autoimmune diseases from the public to trick them into thinking these experimental jabs were safe. This was a criminally insane and a crime against humanity. 

It’s critically important to read the following link to the most  important article defining all the countless adverse events and deaths. ~ Natalie

🚨🚨🚨🚨 What COVID Jabs Are Doing to the Immune System

The CEO of pharmaceutical and biotechnology company Moderna, Stéphane Bancel, said the company is having to “throw away” millions of doses of COVID-19 vaccines because “nobody wants them.”

Bancel made the comments during an appearance at the World Economic Forum on Monday, while noting his concerns over the lack of people getting vaccinated and waning immunity among those who have had the shots but declined to get boosters.

“It’s sad to say, I’m in the process of throwing 30 million doses in the garbage because nobody wants them. We have a big demand problem,” Bancel said.

The Moderna chief explained that his company has contacted a number of governments across the globe to see if anyone wants to take the vaccines but it has proven unsuccessful.

“We right now have governments—we tried to contact … through the embassies in Washington. Every country and nobody wants to take them,” he said. “And so the challenge we have right now is very different to the one we had two years ago.”

“The issue in many countries is that people don’t want vaccines,” Bancel added, while referencing populations in countries like China and the United States.

Bancel’s comments come as Moderna is set to release its “superior” Omicron- and subvariant-specific COVID-19 vaccine booster by the fall.

Moderna Chief Medical Officer Paul Burton told CBS earlier this month, “We are confident that by the fall of this year, we should have large amounts of that new booster vaccine that will protect against Omicron and other variants, and really protect Americans and people around the world as we go into the fall of 2022.”

However, deaths from COVID-19 have declined in recent months while hospitalizations remain relatively low. Meanwhile, COVID-19 vaccines have remained a polarizing topic amid reports of adverse effects.

In recent months, a string of European countries have found themselves stuck with vaccines that they simply cannot use because of a lack of demand, while tighter finances in the aftermath of the war in Ukraine mean some nations simply cannot afford to purchase more. Those nations are now looking to amend their contracts with producers including Pfizer, Bloomberg reported.

During a virtual meeting with health officials from EU members nations including Poland, Slovakia, Romania, Bulgaria, Luxembourg, Finland, and others, organized by Polish Health Minister Adam Niedzielski on May 18, officials agreed to write a joint letter to the European Commission regarding the need to renegotiate the vaccine contracts.

“We hope that the discussion with the commission and among member states will allow flexibility in the vaccine agreements,” the joint letter states, adding, “We are also counting on vaccine producers to show understanding to the exceptional challenges that Poland is facing supporting Ukraine and giving shelter to millions of Ukrainian citizens fleeing the war.”

In a separate letter to commission President Ursula von der Leyen in April, the prime ministers of Estonia, Latvia, and Lithuania noted that vaccines are still being delivered to the Baltic states and other member states despite dwindling administration.

“This puts pressure not only on logistics networks and storage but also has budgetary implications,” the presidents wrote.

Negotiating with the vaccine manufacturers in an effort to amend deals with suppliers could grant member states the right to “re-phase, suspend, or cancel altogether vaccine deliveries with short shelf life,” they noted.

Meanwhile, in another letter, the health ministry of Bulgaria called for an “open dialog” with the commission and pharmaceutical companies, pointing to the fact that the current arrangement leaves member states forced to “purchase quantities of vaccines they don’t need.”

From The New York Post By Callie Patteson June 2, 2022

Kids under 5 could get COVID vaccine in June, Dr. Ashish Jha says

Children under 5 years old could receive their first COVID-19 shot before the end of this month, White House pandemic response coordinator Dr. Ashish Jha said Thursday.

“We expect that vaccinations will begin in earnest as early as Tuesday, June 21,” Jha told reporters during a White House press briefing.

Jha, who joined the Biden administration in April, warned that it could take some time for doses to reach vaccination sites across the country, but added that he expected that “within weeks, every parent that wants their child to get vaccinated will be able to get an appointment.”

The announcement came one day after Pfizer revealed it had filed its emergency use application with the Food and Drug Administration to administer their COVID-19 vaccine for children as young as 6 months old.

“We recognize parents are anxious to have their young children vaccinated against COVID-19 and while the FDA cannot predict how long its evaluation of the data and information will take, we will review any EUA request we receive as quickly as possible using a science-based approach,” the agency said.

“We recognize parents are anxious to have their young children vaccinated against COVID-19 and while the FDA cannot predict how long its evaluation of the data and information will take, we will review any EUA request we receive as quickly as possible using a science-based approach,” the agency said.

Pfizer’s shot for young children would provide just one-tenth of the vaccine dose given to adults.

The FDA’s Vaccine and Related Biological Products Advisory Committee (VRBAC) meet to discuss the emergency use authorization on June 14 and 15th, Jha said Thursday, indicating that the FDA will make their decision “soon thereafter.”

However, states can begin to order initial vaccine doses starting Friday. To jump start the program, the administration will me 10 million doses available to pharmacies, community health centers and federal entities.

“We expect some of the shipments to start arriving to — in their destinations over that long weekend,” Jha said, noting that most doctor’s offices will be closed for the Juneteenth holiday. “We can’t ship vaccines until the FDA has authorized these vaccines.“

In April, Moderna revealed it would also ask the FDA to approve its coronavirus vaccine for children under 6 years old. It is seeking to greenlight two small-dose shots. In a clinical trial, the company found that quarter-dosed-sized vaccinations were just as effective for children under 6 as regular-sized shots were for adults.

Its potential use for young children will also be discussed in the VRBAC meetings later this month.

So far, the FDA has only authorized the Pfizer vaccine to be administered to children between the ages of 5 and 11. As of May 25, 10 million children within that age range had received at least one dose of the vaccine — approximately 35% of all kids aged 5 to 11.

Children currently represent approximately 18.9% of all COVID-19 cases reported in the US — more than 13.3 million infections, the American Academy of Pediatrics reported late last month. Cases among children dramatically spiked during the Omicron winter surge earlier this year and while they have decreased significantly since, AAP found that cases among children have increased for the past seven weeks.

Generally, coronavirus symptoms in young children are milder than adult cases and hospitalization rates remain extremely low. AAP has reported that among states reporting, children only made up between 1.3% and 4.6% of their total hospitalizations while the children hospitalized only made up between 0.1% and 1.5% of all COVID-19 cases reported.

05.27.2022.13