The U.S. Department of Health and Human Services (HHS) has announced that the agency is amending an emergency declaration under the Public Readiness and Emergency Preparedness Act (PREP Act) to authorize additional medical professionals to administer experimental COVID-19 vaccines being distributed under an Emergency Use Authorization (EUA). This announcement was made after President Biden stated that he intends to provide directives to all the states and territories to make all adults over the age of 18 eligible for the experimental COVID-19 vaccines by May 1, 2021. Acting HHS Secretary Norris Cochran said: "As President Biden said last night, the key to getting us back to our lives is increasing vaccinations, and in order to do that, we need more vaccinators. … As vaccine supply ramps up, we want to be sure communities have the help they need to get shots into arms for anyone in the U.S. who wants to be vaccinated against COVID-19." The expanded COVID-19 vaccine administration workforce includes the following health professionals, who are currently or previously active within the last five years (retired or non-practicing health providers): dentists, emergency medical technicians (EMT), midwives, nurses, optometrists, paramedics, pharmacists, pharmacy interns, pharmacy technicians, physicians, physician assistant, podiatrist, respiratory therapists and veterinarians.
Fully Vaccinated People Testing Positive for COVID – So How Does the “Benefit” of Experimental Vaccines “Outweigh the Risk”?
What are being called "breakthrough" cases of COVID-19 are popping up across the U.S. They're people who test positive 14 days or more after receiving their last dose of the vaccine. “It still is shocking that I’m positive. I have no symptoms," home health worker Hanna Rewerts said. The 27-year-old's vaccination card shows she received her second dose of the Pfizer vaccine on January 12. She said she found out she was positive on March 18 from one of the routine tests she takes weekly for work. Believing it might be a false positive, Rewerts said she took a rapid test, which also came back positive. She said her mother and two other family members – all fully vaccinated – also tested positive this week. They are experiencing symptoms. “My biggest question right now is – is it still effective in my system?" Rewerts asked of the vaccine. Rewerts is currently isolating. She said she was told by the health department that she can resume normal activities on March 25, as long as she's not experiencing symptoms. “I think I’d just want people to continue to educate themselves about the vaccine and what’s best for them and their family. I still am happy that I got it, but I really would like there to be more research on the effectiveness," she said. In addition to media reports of breakthrough cases in Florida outside Tampa Bay, the Minnesota Health Department released an advisory earlier this month saying it was investigating instances in that state. It's asking health care providers to report breakthrough cases so that it can look into them further, along with the Centers for Disease Control and Prevention. What exactly are the "benefits" that "outweigh the risk" of being permanently disabled or killed by one of these shots then?
UK Government Changes Recommendations on Pregnant Women Getting Experimental COVID Injections Causing at Least 20 Miscarriages So Far
It saddens us to have to report that as a result of receiving a dose of either the Pfizer / BioNTech MRNA vaccine or the Oxford / Astrazeneca Viral Vector (still MRNA technology), a total of twenty women have now had to suffer the grief of having a miscarriage and losing their unborn child. Adverse reactions to both jabs reported to the MHRA Yellow Card scheme up to the 21st February shows that the number has almost doubled in just seven days when compared with the previous weeks data, which included adverse reactions to both jabs. When the Pfizer jab was first approved for emergency use only in the United Kingdom, meaning the manufacturer is not liable for any harm or injury caused by their product, the Government’s advice was: "There are no or limited amount of data from the use of COVID-19 mRNA Vaccine BNT162b2. Animal reproductive toxicity studies have not been completed. COVID-19 mRNA Vaccine BNT162b2 is not recommended during pregnancy. For women of childbearing age, pregnancy should be excluded before vaccination. In addition, women of childbearing age should be advised to avoid pregnancy for at least 2 months after their second dose." However the Government has since updated it’s advice within the document, for reasons unknown to the following: "There is limited experience with use of the COVID-19 mRNA Vaccine BNT162b2 in pregnant women. Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryo/foetal development, parturition or post-natal development. Administration of the COVID-19 mRNA Vaccine BNT162b2 in pregnancy should only be considered when the potential benefits outweigh any potential risks for the mother and foetus." So now we know why pregnant women have started to be inoculated with the experimental jabs, because the Government quietly changed its own advice based on zero evidence to support it. Even going as far as to remove the recommendation that women of child bearing age being told to avoid pregnancy for at least two months after their second dose. Statistically these women stood no chance of suffering from serious illness due to the alleged SARS-CoV-2 virus and the alleged resulting disease Covid-19, now sadly they have to suffer the misery of losing their unborn children. How many more women need to suffer a miscarriage to stop this madness?
Moderna’s Top Scientist on mRNA Technology in COVID Shots: “We are Actually Hacking the Software of Life”
Veteran investigative reporter Leo Hohmann has discovered a 2017 Ted Talk presentation by Dr. Tal Zaks, the chief medical officer at Moderna Inc., where he clearly explains in layperson's language just what the mRNA technology does in vaccines. (Thanks to Patrick Wood of Technocracy News for publishing this.) As Dr. Zaks clearly states, they are "hacking the software of life," by injecting their own genetic code into humans. What we are witnessing in this new class of "vaccines" is clearly the wedding together of digital technology born out of the computer age, with Darwinian biology and medicine. In short, the new technocrats of medicine actually believe they can improve the design plan of human beings, replacing God. This is not a conspiracy theory, as they are very arrogant and very open about just what they dream about achieving. This is first and foremost a belief system, with very little to no science involved to back up their claims. We are quickly moving from the realm of science fiction and entertainment, as we see in Hollywood presentations such as Star Trek, where humans can be disassembled and transported (beamed) through space and miraculously put back together instantly, or food can be "replicated" at the push of a button, to real life experiments based on these beliefs by Billionaire psychopaths who have nothing better to do with their wealth other than try to improve upon the human race. Welcome to the brave new world of post-COVID, and the transhumanist agenda. The software engineers of yesterday, who cannot even create a virus-free computer operating system, are now in charge of the "software of life" and working together with the Big Pharma criminal cartel. They also fund and control what is broadcast in the corporate media. What could possibly go wrong?
Johnson and Johnson Has Paid $BILLIONS in Criminal Settlements and Never Produced a Vaccine Before – Why Would We Trust Them for a New Experimental COVID Vaccine?
From its humble beginnings in the 1880s, making cotton gauze dressings and eventually band aids, baby powder and shampoo, J&J has expanded into one of the most powerful multinational pharmaceutical and medical device companies in the world. But how is it that a drug and household health product company, with no prior history in vaccine development, can develop and rush to market its first vaccine against a viral strain that was only identified 14 months ago? Developing a vaccine requires many years and necessitates the establishment of an R&D infrastructure vastly different than conventional drug development. The other major companies developing Covid-19 vaccines have been in the business for decades. But not J&J. There is something more to this story that demands investigation. And if the company’s long rap sheet offers any warning, it is that we must be wary of any claims J&J publicly states about the efficacy and safety of its products. Especially when the pandemic promises to increase the profits of numerous shareholders.
Whistleblower Reveals Many Pregnancy Complications following Experimental COVID Injections – “Vaccine Leaving a Trail of Devastated Mothers”
When the Pfizer experimental COVID "vaccines" were given emergency use authorization (EUA) in the U.S. in December, 2020, Health Impact News reported that while the U.K.'s EUA for the Pfizer shot had warnings for pregnant women, nursing women, and women planning on becoming pregnant, to NOT get the shot, the U.S. FDA's guidelines for the same Pfizer shot failed to include any such warnings. We also reported previously of at least one case where a pregnant doctor received the experimental COVID shots, and then reported that she had a miscarriage three days later. According to a pro-life group out of New Mexico, a whistleblower who sits on a COVID-19 task force is claiming that many pregnancy complications, including preterm birth, miscarriage, and spontaneous abortions following COVID vaccines are being concealed from the public.
Experimental COVID Vaccine Trials Expanded: Children as Young as 6 to be Injected in Trials in Israel
The University of Oxford plans to test its AstraZeneca-produced COVID-19 vaccine on children for the first time, it was announced on Saturday. The trial seeks to recruit 300 volunteers between the ages of 6 and 17, with up to 240 receiving the COVID-19 vaccine and the remainder a control meningitis vaccine. The trial will begin this month at the university and additional sites in London, Southampton and Bristol, Sky News reported. Andrew Pollard, chief researcher on the Oxford vaccine trial, says that while most children don’t get severely ill from COVID-19, “it is important to establish the safety and immune response to the vaccine in children and young people as some children may benefit from vaccination.’’ Other drug companies are also testing the COVID-19 vaccines in children. Pfizer, whose vaccine has already been authorized for use in people 16 and older, began testing its shot in children as young as 12 in October. Moderna in December began testing its vaccine on children as young as 12. Pollard said the Oxford trial should help policymakers decide whether at some point in the future they want to extend mass vaccination programs to children as they seek to ensure schools are safe and combat the spread of the virus in the wider population. “For most children, for themselves, COVID is really not a big problem…,’’ Pollard told The Associated Press. “However, it is certainly possible that wider use to try and curb the progress of the pandemic might be considered in the future, so here we’re just trying to establish the data that would support that if indeed policymakers wanted to go in that direction.”
Pfizer and Moderna COVID Vaccine Results NOT based on Peer-Reviewed Science – ZERO Liability to Companies if Vaccine Kills or Injures due to FDA Fast-track Approval
VAXXED film producer Polly Tomney and attorney Mary Holland of Children's Health Defense discuss the two most recent COVID vaccine press releases from Pfizer and Moderna which both claimed over "90% effective" and just what this means. Because these vaccines are expected to apply for FDA fast-track approval due to the COVID "emergency," they do not go through the same peer-reviewed process, and if the vaccines end up injuring or killing anyone, they are immune from any legal liability.