Archive for the ‘Viruses’ Category

Big Tech & Big Pharma Merge: Oracle Takes Over Vaccine Data World

https://childrenshealthdefense.org/defender/big-tech-big-pharma-merge-oracle-takes-over-vaccine-data-world/

01/06/21

Big Tech and Big Pharma Merge: Oracle Takes Over Vaccine Data World

The pandemic handed Oracle CEO Larry Ellison what he’s wanted for decades — the power to curate the vast datasets housing our medical, financial and personal information.

As pandemic countermeasures obliterate the middle class and civil rights, Silicon Valley’s billionaire robber barons are cashing in on the global economic collapse and the rise of the surveillance state.

Now, one of these tech titans — a man with deep ties to the U.S. Central Intelligence Agency (CIA) — has claimed the golden ring: the key contract to manage all the personal, health and financial data that will allow government and industry to keep us in line as they build their New World Order.

Oracle CEO Larry Ellison will curate the vast datasets that house our medical, financial and personal information enabling Big Brother to track and trace our movements, our purchases, our preferences and our vulnerabilities, and use that information to control civil populations, suppress dissent and punish disobedience.

Ellison, whose estimated net worth of $87.7 billion makes him the seventh-richest individual in the world, has just achieved a long-sought milestone. On Dec.15, Oracle, the tech company Ellison founded in 1977 with help from the CIA, issued a press release announcing it “will serve as the CDC’s [U.S. Centers for Disease Control and Prevention] central data repository for all vaccination data in the U.S. This ‘national clearing house’ system will receive data from all U.S. jurisdictions administering vaccinations.”

Almost 20 years since Ellison, in the wake of the 9/11 terrorist attack, offered the government a proposal for a national security database “that collected everything possible to identify someone,” the mogul appears to finally be sitting on cloud nine.

Oracle’s National Electronic Health Records Cloud dates back to the beginnings of the COVID-19 pandemic. In March 2020, a couple of weeks after letting President Trump use his estate near Palm Springs for a $100,000-a-plate golfing fundraiser, Ellison placed a call to the White House. According to a Forbes cover story on Ellison, he “asked Trump if a clearinghouse existed for real-time data about treatment efficacies and outcomes.”

Within a week after the president asked “how much?” and Ellison said, “for free,” the tech titan had brought together a team of Oracle engineers “to build a database and website registering coronavirus cases” and work with the National Institutes of Health (NIH), U.S. Food and Drug Administration (FDA) and other agencies.

The first public acknowledgment of Oracle’s progress came on July 3, 2020, when the NIH’s National Institute for Allergies and Infectious Diseases (NIAID), overseen by Dr. Anthony Fauci, launched the COVID-19 Prevention Trials Network (COVPN), aimed at enrolling thousands of volunteers in large-scale trials for a variety of investigational vaccines and monoclonal antibodies.

Fauci achieved this by merging four existing networks, all researching HIV/AIDS, something they would continue to do. “The network is expected to operate more than 100 clinical trial sites across the United States and internationally,” according to the NIAID press release which also stated “the COVPN website features a customized data collection platform, which Oracle (Redwood Shores, CA) built and donated, to securely identify potential trial participants.”

In August, a paper published by the Johns Hopkins Center for Health Security proposed that the “passive reporting” systems managed by the CDC and FDA ought to be revamped to forge “an active safety surveillance system directed by the CDC that monitors all [COVID-19] vaccine recipients — perhaps by short message service or other electronic mechanisms.”

By September, Operation Warp Speed director Moncef Slaoui was telling the periodical Science: “We’re working super hard on a very active pharmacovigilance system, to make sure that when the vaccines are introduced that we’ll absolutely continue to assess their safety.

In October, Slaoui told the New York Times: “The FDA is proposing that at least 50% of the individuals in the study population have at least two months of follow-up on safety before the vaccines are approved. And secondly, we are working really hard with the FDA and the CDC to make sure we have a very active pharmacovigilance surveillance system to allow us to continue to assess the safety of the vaccines as they are being used in the high risk population.”

And the Wall Street Journal reported in a profile of Slaoui that he’d said “tracking systems will have to be ‘incredibly precise’ to ensure that patients each get two doses of the same vaccine and to monitor them for adverse health effects. Operation Warp Speed has selected the medical-distribution company McKesson and cloud operators Google and Oracle to collect and track vaccine data.”

This marked the first time that Oracle’s role was revealed to have expanded to include Operation Warp Speed.

Oracle Chairman Ellison’s lucrative government arrangements trace back to the data software pioneer’s origins. In 1975, then in his early thirties, Ellison worked on a project for the electronics company Ampex in the Bay area, building a large terabit memory system for the CIA.

Ellison revealed in 2014 that the CIA not only became his firm’s first customer for a “relational database” two years later, but that he adopted the name from a CIA project called Oracle. “The news about our hot little database traveled around the intelligence community pretty quickly,” Ellison was quoted as saying in the 2003 book, “Softwar.” “In a little over six months’ time we had won several deals — the CIA, Navy Intelligence, Air Force Intelligence and the NSA [National Security Agency].”

By the turn of the millennium, Oracle had fought off competition from IBM and Microsoft to reach the financial pinnacle of database management. Two days after 9/11, Ellison met with NSA Director Michael Hayden to talk about his proposed data surveillance system. He then went to see Attorney General John Ashcroft to discuss an idea for a national identification card.

Writing an opinion piece for the Wall Street Journal (October 18, 2001), Ellison reminded readers that the government already maintained thousands of databases to keep track of people as well as issuing IDs like Social Security cards and driver’s licenses. Ellison wrote:

“The single thing we could do to make life tougher for terrorists would be to ensure that all the information in myriad government databases was integrated into a single national file. My company … has already offered to provide the necessary software for free … It’s important these donations be made with no strings attached. The database would be maintained and run by the government alone, with no question of corporations benefiting … The good news is that a national database combined with biometrics, thumb prints, hand prints, iris scans or other new technology could detect false identities … We don’t need to trade our liberties for our lives.”

In a follow-up op-ed for the New York Times in January 2002, Ellison thought this could be achieved in a few months because it was “technically simple. All we have to do is copy information from the hundreds of separate law enforcement databases into a single database.”

In April 2002, along with Ashcroft, Ellison was a named recipient of an annual “Big Brother Award” presented by Privacy International to the most notorious individuals who had done the most to threaten such liberties.

By 2003, as the Patriot Act brought an explosion in surveillance and data mining, the federal government accounted for about one-fourth of Oracle’s billions in revenue.

“The information about your banks, your checking balances, your saving balance is stored in an Oracle database,” Ellison was quoted in the 2004 book, “The Naked Crowd.” “Your airline reservation is stored in an Oracle database. What books you bought on Amazon is stored in an Oracle database. Your profile on Yahoo! is stored in an Oracle database …Privacy is already gone.”

That same year, Ashcroft — godfather of the Patriot Act — sued Oracle to prevent its acquisition of a multibillion-dollar intelligence contract. But after Ashcroft resigned from the second Bush administration, he founded a lobbying firm which Oracle then hired in 2005, allowing The Ashcroft Group to hit the ground running. With the group’s help, Oracle went on to acquire the contract.

One program that didn’t last long was called Total Information Awareness (TIA), overseen by the Pentagon’s Defense Advanced Research Projects Agency (DARPA), which would later become a primary funder of COVID-19 vaccine developer Moderna and other of Fauci’s favored companies.

DARPA had conceived of TIA some years earlier. In addition to what Ellison specified needing, TIA wanted to collect Americans’ medical records, drug prescriptions and even DNA, maintaining that the whole population needed surveillance to prevent not only future terrorist attacks, but bioterrorism and even naturally occurring disease outbreaks.

Citizens’ financial, travel and media consumption habits would also be managed in a “public-private partnership” with the NSA, CIA, private sector and academia. In a mirrored scenario to that now surrounding the pandemic, the “invisible enemy” could be conquered.

But the backlash was swift. The ACLU called TIA

“the closest thing to a true ‘Big Brother’ program that has ever been seriously contemplated in the United States. It is based on a vision of pulling together as much information as possible about as many people as possible into an ‘ultra-large-scale’ database.”

A year after its formation by DARPA, Congress defunded TIA in January 2003.

But TIA never really went away. Various of its programs ended up divvied into a web of military and intelligence programs.

In 2013, Ellison told CBS News that the NSA’s domestic spying program was “essential.” A revolving door between Oracle and the CIA, which began with Ellison himself, went on to include Leon Panetta, CIA director and then Defense Secretary under Obama, who joined Oracle’s board in 2015.

Oracle Labs, the research arm, invested in a partnership with DARPA toward “a vision for a ‘macrochip,’ an optically interconnected supercomputer.”

As the FDA revved toward emergency use approval for the Pfizer and Moderna vaccines late in 2020, linkages between the CIA and the Big Tech companies escalated simultaneously. An earlier agency contract had gone to Amazon in 2013, but on Nov. 20, it was reported that the CIA “has awarded its long-awaited Commercial Cloud Enterprise, or C2E, contract to five companies – Amazon Web Services, Microsoft, Google, Oracle and IBM.” These companies “will compete for specific task orders issued by the CIA on behalf of itself and the 16 other agencies that comprise the intelligence community.” At the moment, “Microsoft is the competitor closest to attaining authorization to host top-secret data.”

Procurement documents issued by the CIA in 2019 indicated the expected value of the C2E contract could be worth tens of billions over the next decade-and-a- half.

Then in mid-December, Oracle issued a press release that said:

“By working collaboratively with the CDC and the U.S. Department of Defense during the pandemic, Oracle was able to extend the capabilities of the Public Health Management Applications Suite to help manage nationwide distribution and to collect patient data around COVID-19 vaccines and treatments.”

Moving well beyond its original sketchy mandate with Fauci’s NIAID, not only would Oracle’s National Electronic Health Records Cloud be the CDC’s new central data repository for vaccination data, but the company said it was:

“currently in discussions with dozens of countries around the world to adopt Oracle’s Public Health Management Applications Suite to modernize their national public health infrastructure and thus enable efficient COVID-19 vaccine distribution, therapeutic monitoring and diagnostic testing … This is just the beginning.”

It had been a productive and ultimately very profitable year for Ellison and Oracle. Also in mid-December, Ellison announced that his company was leaving Silicon Valley for a new headquarters in Austin, Texas, while he himself was moving to the Lanai Hawaiian island that he owned. Ellison had stepped down as Oracle CEO in 2014, but stayed on as chief technical officer. At the start of the pandemic, on March 23, his stock in the company (and he owned 35 percent of it) had dropped 11 percent. But shortly before he closed the government deal collecting all the vaccine data, his fortune rose $2.5 billion in a single week, bringing Ellison’s net worth to an estimated $81.5 billion.

This was despite a delay in his pending buy-in to the global social media platform TikTok, “an app for teens, filled with goofy dancing and lip-synching videos” as the Wall Street Journal described it — but a highly lucrative, and controversial, one.

Last spring, around the time he started calling COVID-19 the “China virus,” President Trump had ordered TikTok’s Chinese parent company Bytedance to either sell its American operation or be banned on U.S. shores, because the data it gathered somehow threatened national security. Suddenly Microsoft, Twitter and Oracle were reportedly negotiating bids to China’s billionaire entrepreneur Zhang Yming.

One aspect of TikTok that would doubtless have interested Ellison is the app’s use of artificial intelligence to shoot people news based upon their reading habits. “Powered by algorithms that can make its video feed addictive,” TikTok had turned into a global sensation, downloaded more than 2 billion times worldwide and with a $100 billion valuation. For more than a year, according to a Wall Street Journal analysis, “the app tracked users using a tactic banned by Google, which enabled it to collect unique identifiers from millions of mobile devices without letting users opt out.” While TikTok said it had stopped the practice and “promised to create a firewall between China and overseas users,” that’s apparently why Trump got so worried about possible Chinese government access to TikTok’s American user data.

In September 2020, Oracle announced it had reached agreement with TikTok for a 12.5 percent stake in the U.S. operation while also providing cloud services and security for the app. Walmart bought an additional 7.5 percent, and Trump declared victory for the new TikTok Global, which will likely go public once the dust settles and the sales are approved by the U.S. and China.

Oracle hopes to use the TikTok deal as another model to provide security and cloud services to other companies down the road,” CNBC reported in September. Or, as happened less than two months later, to the federal government.

Could there have been an ulterior motive behind Oracle’s plunge into kiddie social media? At the end of August, the Journal of Adolescent Health published an article headlined “Tik Tok and Its Role in Covid-19 Information Propagation.” The NIH website would reprint it in November. Noting that the pandemic had generated the near-complete sudden closure of U.S. educational institutions in the spring,

“noneducational screen time among young people has greatly escalated” and “social media have played a large role in youth resocialization in a pandemic society … Given social media’s ability to propagate factually inaccurate medical information at an alarming rate,” and given TikTok’s more than 45.6 million active users in the U.S., the paper’s authors decided to analyze the 100 most popular videos earmarked with hashtags for COVID-19 and coronavirus.

These had reached as many as 93.1 billion views, “demonstrating the platform’s immense ability to encourage sharing.” Only a handful seemed to have provided misleading information, while “videos by healthcare professionals were few in number … [but] often among the most widely ‘liked’ and shared across the board. The distribution suggests that demand on TikTok for more healthcare-related voices currently outpaces supply. TikTok has shown itself to be a viable means for practitioners to educate and dispel myths about COVID-19 to a broad and diverse adolescent demographic,” according to the article.

Some in the public health community took notice.

“A growing number of scientists and doctors are making viral videos on TikTok to provide information on COVID-19 vaccines,” Scripps reported on Jan. 1. The group called itself Team Halo, with a goal “to try and reduce hesitancy.”

One of the “dozens of health experts from all over the world,” director of the Harvard Immunology Graduate Program, Dr. Shiv Pillai, went into a great deal about the messenger mRNA used to develop the Pfizer and Moderna vaccines, explaining “why it’s safe and effective, as well as the side effects that would be simple to pinpoint.” Pillaj used poetry to get his message across: “The vaccine it will change our lives. To get a shot is to be smart. To make this virus bite the dust, let us all just do our part.”

According to Scripps, in other videos, Pillai talks about a child he treated as an intern. The boy died in his hands from tetanus because he wasn’t vaccinated.

The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children’s Health Defense.

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**Comment**

This explains a lot.

Moderna Admits: COVID Vaccines Inject an Operating System into Your Body

https://healthimpactnews.com/2021/the-new-mrna-covid-vaccines-inject-an-operating-system-into-your-body-not-a-conspiracy-theory-moderna-admits-it/

The New mRNA COVID Vaccines Inject an Operating System into Your Body – Not a Conspiracy Theory, Moderna Admits It

Comments by Brian Shilhavy
Editor, Health Impact News

Excerpts of article below:

mRNA Platform: Enabling Drug Discovery & Development

modernatx.com

Enabling Drug Discovery & Development

We built Moderna on the guiding premise that if using mRNA as a medicine works for one disease, it should work for many diseases. And, if this is possible – given the right approach and infrastructure – it could meaningfully improve how medicines are discovered, developed and manufactured.

Our Operating System

Recognizing the broad potential of mRNA science, we set out to create an mRNA technology platform that functions very much like an operating system on a computer. It is designed so that it can plug and play interchangeably with different programs. In our case, the “program” or “app” is our mRNA drug – the unique mRNA sequence that codes for a protein.

We have a dedicated team of several hundred scientists and engineers solely focused on advancing Moderna’s platform technology. They are organized around key disciplines and work in an integrated fashion to advance knowledge surrounding mRNA science and solve for challenges that are unique to mRNA drug development. Some of these disciplines include mRNA biology, chemistry, formulation & delivery, bioinformatics and protein engineering.

Our mRNA Medicines – The ‘Software of Life’

When we have a concept for a new mRNA medicine and begin research, fundamental components are already in place.

Generally, the only thing that changes from one potential mRNA medicine to another is the coding region – the actual genetic code that instructs ribosomes to make protein. Utilizing these instruction sets gives our investigational mRNA medicines a software-like quality. We also have the ability to combine different mRNA sequences encoding for different proteins in a single mRNA investigational medicine.

We are leveraging the flexibility afforded by our platform and the fundamental role mRNA plays in protein synthesis to pursue mRNA medicines for a broad spectrum of diseases.

Overcoming Key Challenges

Using mRNA to create medicines is a complex undertaking and requires overcoming novel scientific and technical challenges. We need to get the mRNA into the targeted tissue and cells while evading the immune system.

If the immune system is triggered, the resultant response may limit protein production and, thus, limit the therapeutic benefit of mRNA medicines.

We also need ribosomes to think the mRNA was produced naturally, so they can accurately read the instructions to produce the right protein. And we need to ensure the cells express enough of the protein to have the desired therapeutic effect.

Our multidisciplinary platform teams work together closely to address these scientific and technical challenges.

This intensive cross-functional collaboration has enabled us to advance key aspects of our platform and make significant strides to deliver mRNA medicines for patients.

Sourcemodernatx.com

Why Bill Gates Switched From Microsoft to Vaccines – Extracted from the full film Plandemic, by Mikki Willis.

https://www.bitchute.com/embed/ZUZ1zkxC4GP1/ (Video here) Vaccine information first, then at about 13:00, the video goes into:

  • Gates’ efforts to block out the sun in which calcium carbonate and other materials are released into the atmosphere in an effort to control ‘global warming’. It’s been called a “global genocide experiment” by environmental scientists.
  • He’s also invested over 1 billion dollars in “Earth Now” global surveillance project putting hundreds of satellites into space for the for the 24/7 monitoring of people everywhere.
  • In partnership with MIT, Gates has developed new technology (quantum dot tattoo) allowing vaccines to be injected under your skin along with your medical records. Authorities can access this with an app on a phone.
  • The Gates Foundation has funded Oxitec, the company releasing GMO mosquitoes allowing people to become vaccinated through mosquitoes.  Science Magazine called them “Flying Syringes.”
  • And then there’s the connection with Jeffry Epstein…..
  • Since the COVID-19 is under the PREP Act, if you are injured, “you are on your own.”

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For more:

Clinical Considerations for COVID-19 Vaccines & WHO, Fauci Warn Vaccine May Not Prevent Infection and Transmission

https://www.cdc.gov/vaccines/covid-19/info-by-product/clinical-considerations.html

Clinical Considerations for Use of mRNA COVID-19 Injections 

(See link for entire article)

An important consideration for Lyme/MSIDS patients is the fact doctors have seen a reactivation of symptoms after vaccination:  https://madisonarealymesupportgroup.com/2017/12/02/scottish-doctor-gives-insight-on-lyme-msids/

 And to balance out the CDC’s continued denial of vaccine harm:  https://www.greenmedinfo.com/blog/attacking-ourselves-top-doctors-reveal-vaccines-turn-our-immune-system-against-us

Excerpts for Lyme/MSIDS patients from CDC website:

Immunocompromised persons

Persons with HIV infection or other immunocompromising conditions, or who take immunosuppressive medications or therapies might be at increased risk for severe COVID-19. Data are not currently available to establish vaccine safety and efficacy in these groups.

Persons with autoimmune conditions

No data are currently available on the safety and efficacy of mRNA COVID-19 vaccines in persons with autoimmune conditions.

Persons with a history of Bell’s palsy (a symptom of Lyme disease)

Cases of Bell’s palsy were reported following vaccination in participants in both the Pfizer-BioNTech and Moderna COVID-19 vaccines clinical trials.

Pregnant people

Pregnant people with COVID-19 have an increased risk of severe illness, including illness resulting in intensive care admission, mechanical ventilation, or death. Additionally, they might be at an increased risk of adverse pregnancy outcomes, such as preterm birth.  There are currently few data on the safety of COVID-19 vaccines, including mRNA vaccines, in pregnant people.

Lactating people

There are no data on the safety of COVID-19 vaccines in lactating people or the effects of mRNA COVID-19 vaccines on the breastfed infant or milk production/excretion.

Children and Adolescents

Vaccine safety and efficacy data in this age group are limited. Children and adolescents younger than 16 years of age are not authorized to receive the Pfizer-BioNTech COVID-19 vaccine at this time.

Contraindications & Precautions

Anaphylactic reactions have been reported following vaccination with mRNA COVID-19 vaccines. Persons with a history of an immediate allergic reaction (of any severity) to an mRNA COVID-19 vaccine or any of its components might be at greater risk for anaphylaxis upon re-exposure to either of the currently authorized mRNA COVID-19 vaccines. An immediate allergic reaction to a vaccine or medication is defined as any hypersensitivity-related signs or symptoms such as urticaria, angioedema, respiratory distress (e.g., wheezing, stridor), or anaphylaxis that occur within four hours following administration.

CDC considers a history of the following to be a contraindication to vaccination:

  • Severe allergic reaction (e.g., anaphylaxis) after a previous dose of an mRNA COVID-19 vaccine or any of its components
  • Immediate allergic reaction of any severity to a previous dose of an mRNA COVID-19 vaccine or any of its components (including polyethylene glycol [PEG])*  They should not receive additional doses.
  • Immediate allergic reaction of any severity to polysorbate (due to potential cross-reactive hypersensitivity with the vaccine ingredient PEG)*
Precautions

CDC considers a history of any immediate allergic reaction to any other vaccine or injectable therapy (i.e., intramuscular, intravenous, or subcutaneous vaccines or therapies not related to a component of mRNA COVID-19 vaccines or polysorbate) as a precaution but not a contraindication to vaccination for both the Pfizer-BioNTech and Moderna COVID-19 vaccines. These persons should be counseled about the unknown risks of developing a severe allergic reaction and balance these risks against the benefits of vaccination. 

Observation periods following vaccination (for persons without contraindications to mRNA COVID-19 vaccines)

CDC recommends an observation period following vaccination with mRNA COVID-19 vaccines. Persons with a history of an immediate allergic reaction of any severity to a vaccine or injectable therapy and persons with a history of anaphylaxis due to any cause should be observed for 30 minutes. All other persons should be observed for 15 minutes.

Reporting of vaccine adverse events

Adverse events that occur in a recipient following mRNA COVID-19 vaccination should be reported to VAERS. Vaccination providers are required by the Food and Drug Administration to report the following that occur after mRNA COVID-19 vaccination under Emergency Use Authorization:

  • Vaccine administration errors
  • Serious adverse events
  • Cases of Multisystem Inflammatory Syndrome
  • Cases of COVID-19 that result in hospitalization or death

Reporting is encouraged for any other clinically significant adverse event even if it is uncertain whether the vaccine caused the event. Information on how to submit a report to VAERS is available at https://vaers.hhs.govexternal icon or by calling 1-800-822-7967.

In addition, CDC has developed a new, voluntary smartphone-based tool, v-safe. This tool uses text messaging and web surveys to provide near real-time health check-ins after patients receive COVID-19 vaccination. Reports to v-safe indicating a medically significant health impact, including pregnancy, are followed up by the CDC/v-safe call center to collect additional information to complete a VAERS report, if appropriate. 

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https://thevaccinereaction.org/2021/01/who-fauci-warn-covid-19-vaccines-may-not-prevent-infection-and-disease-transmission/

WHO, Fauci Warn COVID-19 Injections May Not Prevent Infection and Disease Transmission

 
 
 
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**Comment**
 
If you mistakenly believe getting this touted injection will solve all your problems and allow you to once again live freely, think again.  It was never about returning to normal.  
 
BTW: HHS is launching a $250M Propaganda campaign with massive ad blitz slated for January:  https://www.fiercepharma.com/marketing/hhs-readies-vaccine-confidence-campaign-massive-ad-blitz-rollout-january  Excerpt:
 
The Ad Council video leads with Anthony Fauci, M.D., director of the National Institute of Allergy and Infectious Diseases, who says: “My primary message to healthcare professionals is please get vaccinated. It’s important to protect yourselves, to protect your family, but as important symbolically as healthcare providers to show confidence in the vaccine so that other people in this country follow suit and get vaccinated.”
 
Please remember, this isn’t a “vaccine.”
 
Here is a list of the lies that are being told to the American people through this video (Source):
 
  • LIE #1: “It’s important to note that none of these vaccines can give you COVID19 since they only express a protein from the virus that allows your body’s immune system to generate antibodies.”  FALSE. The fact is, the COVID19 SARS virus has never been fully identified, and the PCR test to test for COVID19 is inaccurate. Even if what they say is true about there not being a COVID19 virus in the vaccine, since they can only at this point identify fragments from the faulty PCR test, who is to say that a “protein” from the virus that affects the body’s immune system would not produce symptoms of COVID19 and test positive?Also, in Israel, which at the time of publication of this article has had the largest amount of people vaccinated with the experimental COVID vaccines, has reported that 240 people have come down with COVID right after being vaccinated. See: 4 People Died and 240 Got COVID19 in Israel After Being Injected with Pfizer Experimental mRNA Vaccine
  • LIE #2: “Because vaccines are given to millions of healthy people to prevent serious diseases, they’re held to very high safety standards. Both the FDA and the CDC have to ensure the safety and efficacy of the vaccines before they are recommended for use in the United States. The COVID19 vaccine, just like all others, are undergoing a rigorous process...”FALSE. The COVID19 vaccines are NOT approved by the FDA like every other vaccine currently in the market, and the typical time it takes to bring a vaccine to market is 5-7 years. (Source.)  The experimental COVID vaccines should NOT be compared to vaccines that have full FDA approval, but to other times a vaccine was rushed to market under emergency use authorization, and the last time that happened was in 1976 with the Swine Flu “epidemic.”  But the “epidemic” never panned out. Only one death and 13 cases were attributed to the Swine Flu, while 25 people died from the vaccine and another 500 or so developed Guillain-Barre syndrome. The vaccine was withdrawn from the market after 10 weeks.  https://healthimpactnews.com/2020/healthcare-workers-in-the-u-s-suffer-serious-reactions-from-illegal-pfizer-experimental-vaccine-others-fake-vaccination-on-tv/
  • LIE #3: “So far, we haven’t seen any trends of serious side effects.”  FALSE. They are trying to be clever by using the word “trends” so that specific cases of serious side effects, including DEATH, can be excused as “abnormal” or not a result of the vaccine.  But they got caught in their own lie here, as even the FDA has stated that they are investigating why so many people are experiencing anaphylactic shock after receiving the vaccine, focusing on the polyethylene glycol component of the vaccine. (Source.)  Not to mention that several people have now died after receiving the experimental vaccines, including one healthcare worker in Portugal, and apparently Nurse Tiffany Dover from Tennessee as well.  There were deaths in the vaccine trials as well, before the FDA EUA was issued. (Source.)

Facts About the Experimental COVID Vaccines they Do NOT Tell You

In addition to their lies, the people in this video are failing to give full disclosure about all the facts regarding these experimental COVD vaccines.

  1. These vaccines are NOT approved by the FDA.  This is stated multiple times in the vaccine guidelines that are supposed to be given to everyone. Therefore, it is illegal to require anyone to take them. They are 100% voluntary, because you are basically participating in the last part of their vaccine trials in order to get FDA approval.
  2. Emergency Use Authorization was issued by the FDA illegally, because other therapeutics to treat COVID19 are available.  Hydroxychloroquine and Ivermectin are two older drugs already approved by the FDA that tens of thousands of doctors have used successfully to treat and cure COVID19.  In addition, the experimental COVID19 vaccines used the faulty PCR test in their trials, and therefore should never have been approved until accurate testing was used. An Administrative Stay of Action was filed against the FDA, but they simply ignored it. See:  https://healthimpactnews.com/2020/stay-of-action-filed-against-fda-to-stop-approval-of-covid-vaccine-for-using-faulty-pcr-tests-in-trials/
  3. Warnings of Potential Infertility due to These Experimental Vaccines are NOT Being Issued by the FDA.  The UK guidelines for the Pfizer vaccine warn of potential infertility of women and also do NOT recommend pregnant women receive the vaccine, while neither warnings are issued for the same vaccine for Americans. See:  https://healthimpactnews.com/2020/unlike-uk-u-s-fda-allows-pregnant-and-lactating-women-to-receive-experimental-pfizer-covid-vaccine/  Also, the University of Miami is investigating the effects of the COVID-19 vaccines on male fertility. See:  https://www.local10.com/news/local/2020/12/20/study-investigates-effects-of-covid-19-vaccine-on-male-fertility/
  4. The other thing that the U.S. Government and Big Pharma never disclose, is the revolving door between both. Former FDA Chief Scott Gottlieb, for example, now sits on the Board of Directors for Pfizer. See:  https://healthimpactnews.com/2020/former-fda-director-gottlieb-now-pfizer-board-member-secures-1-95billion-for-covid-vaccine/  The CDC, FDA, and HHS have become primarily marketing branches of Big Pharma. And now, the U.S. Government is going to give the corporate media and Big Tech a quarter of a million dollars to try and brainwash you into getting the unapproved experimental COVID vaccine, which is a mere drop in the bucket of the $TRILLIONS of American wealth that has been transferred to Big Pharma in 2020 all in the name of the “pandemic.” Don’t be fooled by their lies! Turn off your TVs and stop watching these Hollywood-style actors and actresses posing as journalists spew forth this dangerous propaganda.
  5. Corporate Media is owned by Big Pharma.  While in years past the primary advertisers funding the corporate media were Wall Street conglomerates heavily invested in tobacco and the oil industry, today it is Big Pharma.  See: https://healthimpactnews.com/2020/brainwashing-the-masses-6-companies-own-almost-all-of-the-media-in-the-u-s-using-medical-doctors-to-sell-their-message/  Protecting their financial interest in the pharmaceutical trade is Big Tech, as now even Google is a pharmaceutical company, and they filter their search results to censor anything that challenges pharmaceutical products like vaccines. See:  https://healthimpactnews.com/2019/vaccine-scientific-denialism-the-vaccine-deep-states-control-over-public-policy-by-ignoring-real-science/

For more on the COVID-19 vaccine:

 

Fareed/Tyson COVID-19 Treatment Protocol

https://www.thedesertreview.com/news/dr-george-fareed-and-dr-brian-tyson-share-early-treatment-protocol/article

Dr. George Fareed and Dr. Brian Tyson share early treatment protocol

Updated

Dr. George Fareed, Imperial Valley frontline doctor fighting against the COVID-19 pandemic locally, has been fielding phone calls from across the nation helping those afflicted but unable to get early treatment from their medical establishments.

“I’m really busy, but I’m willing to help anyone,” Fareed said.

(See link for article)

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Excerpt:

Fareed/Tyson COVID-19 Treatment Protocol
  • HCQ 200 mg tabs #16 (HCQ = hydroxychloroquine)
  • Zinc sulfate 22O mg (or elemental Zinc 50 mg) # 15
  • Azithromycin 500 mg # 5 (or Z pack) or
  • Doxycycline 100 mg # 10)
  • Ivermectin 3 mg tabs #8
  • Aspirin 325 mg tabs #30 
Day 1
  • HCQ 2 tabs twice a day
  • Zinc sulfate tab twice a day
  • (Azithromycin tab one per day or doxycycline cap twice a day)
  • Ivermectin 12 mg on day 1 only
  • Aspirin 325 mg 
Days 2-5 
  • HCQ tab 3 times a day
  • Zinc sulfate 3 times a day
  • (Azithromycin tab daily or doxycycline cap twice a day)
  • Aspirin 325 mg daily
  • Ivermectin 12 mg on day 3 if symptoms warrant 
  • Prednisone 60 mg daily x 5-7 days or
  • Dexamethasone 4 mg bid if wheezing /SOB
  • Budesonide 0.5-1mg/2ml vía nebulizer bid 
  • Vitamin D3 5000 iu daily
  • Pepcid 20 mg daily
  • Continue daily Aspirin 325 mg
Over the counter prevention:
  • Elemental Zinc 25 mg once a day
  • Vitamin D 4000 iu once a day
  • Vitamin C 1000 mg once a day 
  • Quercetin 500 mg once a day. If Quercetin is unavailable, then use Epigallocatechin-gallate (EGCG) 400mg once a day

Protocols for low, medium, and high risk patients are also included.

For more on COVID treatments:  

 

Artemisinin from Sweet Wormwood Inhibits SARS-CoV-2

https://articles.mercola.com/sites/articles/archive/2021/01/04/artemisinin-from-sweet-wormwood-inhibits-sars-cov-2.aspx

Artemisinin From Sweet Wormwood Inhibits SARS-CoV-2

Analysis by Dr. Joseph MercolaFact Checked

STORY AT-A-GLANCE

  • An antimalarial treatment made from the plant Artemisia annua (Sweet Wormwood) shows promise as a COVID-19 treatment
  • The drug artesunate — which contains two compounds found in Artemisia annua: artemisinin and dihydroartemisinin — is a first-line treatment for malaria
  • In a recent in vitro study, both pretreatment and treatment with artemisinin extracts, synthetic artemisinin and the drug artesunate were able to inhibit SARS-CoV-2 infection. However, artesunate was the most potent in terms of treatment, and from a clinical perspective may be the only one worth pursuing
  • Artesunate’s mechanism of action against SARS-CoV-2 is as yet unknown, but artemisinin does have confirmed antiviral activity
  • The World Health Organization has come out in opposition to artemisinin-based products, warning their use can bolster drug-resistant strains of malaria parasites. For this reason, people living in malaria-prone areas should be cautious about using this plant remedy

A second antimalarial treatment is now being seriously considered and evaluated for its efficacy against COVID-19. The treatment is made from the plant Artemisia annua, which most people know as Sweet Wormwood. Other names for this plant include Annual Sagewort and Sweet Annie.

Research over the past few decades has revealed multiple health benefits from this medicinal herb, which has a centuries-long history of use in folk medicine. In 2015, Chinese scientist Tu Youyou received a partial Nobel Prize in Physiology or Medicine for his discovery of artemisinin and dihydroartemisinin,1 both of which have potent malaria-fighting properties.

As reported by the University of Kentucky,2 “The popular malaria drug artesunate was developed from those compounds and is still used as a first-line treatment for the disease today.”

Artemisinin — A Viable COVID-19 Remedy?

Interestingly, in addition to having a long-standing history of being used as a highly effective antiparasitic, it also has anticancer properties. Additionally, artemisia annua has antiviral activity that might be helpful against SARS-CoV-2.

In an April 8, 2020, press release Mateon Therapeutics reported3 that “Artemisinin is highly potent at inhibiting the ability of the COVID-19 causing virus (SARS-CoV-2) to multiply while also having an excellent safety index.”

After testing the plant’s antiviral effects in a laboratory setting for a couple of years, University of Kentucky researchers are also exploring its use for the treatment of COVID-19,4 as are researchers in Denmark and Germany.5 According to the University of Kentucky:6

“Surprisingly, results showed that the plant’s leaves, when extracted with absolute ethanol or distilled water, provided more antiviral activity than the actual drug itself — meaning that an Artemisia annua-blended coffee or tea could possibly be more effective than taking the drug.”

Based on these findings, researchers have decided to test artemisinin in patients diagnosed with COVID-19. Some of the first human studies, set to investigate both the extract blended into coffee and tea, as well as the drug artesunate, were implemented by UK HealthCare.

University of Kentucky researchers have founded a company called ArtemiFlow to develop and manufacture the drug, in collaboration with the Kentucky Tobacco Research & Development Center.7 A sister company, ArtemiLife, is marketing Artemisia tea and coffee to raise research funds.

Mechanism of Action Remains Unknown

As for its mechanism of action, such details still remain to be discovered. C&EN explains:8

When countering malaria, artemisinin exploits the parasite’s taste for hemoglobin in its host’s blood. As the parasite digests hemoglobin, it frees the iron-porphyrin heme complex from the protein.

Because this heme is toxic to the parasite, the organism normally converts the complex to a more benign crystalline form. ‘But artemisinin corrupts this heme-detoxification pathway,’ says Paul O’Neill, a medicinal chemist at the University of Liverpool.

If artemisinin does have any effect against SARS-CoV-2, though, it likely relies on a completely different mechanism than the one it uses against the malaria parasite, Harvard’s [malaria researcher Dyann F.] Wirth says.”

In Vitro Study Reports Positive Results

An in vitro study9,10 looking at the efficacy of artemisinin-based treatments against SARS-CoV-2, posted on the prepublication server bioRxiv, October 5, 2020, report promising results.

The study was a collaboration between researchers from Germany, Denmark and Hong Kong, led by Kerry Gilmore, Ph.D., from the Max Planck Institute for Colloids and Interfaces in Potsdam, Germany.

Three artemisinin extracts, as well as pure, synthetic artemisinin, artesunate and artemether were evaluated. During the initial screening for antiviral activity, a German SARS-CoV-2 strain obtained from Munich was used.

Later on, during the concentration-response phase of the trial, they used a Danish SARS-CoV-2 strain from Copenhagen. These two strains are said to be “more closely related to the majority of SARS-CoV-2 strains circulating worldwide than the Wuhan strain.”11,12

In summary, they found that both pretreatment and treatment with artemisinin extracts, synthetic artemisinin and the drug artesunate were able to inhibit SARS-CoV-2 infection of Vero E6 cells and human hepatoma Huh7.5 cells. That said, artesunate was the most potent in terms of treatment, and from a clinical perspective may be the only one worth pursuing.13,14

World Health Organization Warns Against Its Use

While the world is eager to add another remedy to its COVID-19 treatment list, the World Health Organization has come out in opposition to artemisinin-based products. In a May 27, 2020, article, C&EN reported:15

“One of the most high-profile advocates for using the herbal remedy against the novel coronavirus is Madagascar president Andry Rajoelina, who has been touting Covid-Organics, a tonic containing A. annua that the Malagasy Institute of Applied Research developed …

But health officials are deeply concerned about the promotion and use of these herbal remedies for three principal reasons. First, no evidence exists that A. annua extracts can prevent or cure COVID-19 …

Second, A. annua preparations such as teas, tonics, or herbal capsules also contain a cocktail of bioactive compounds in addition to artemisinin that can have side effects such as dizziness, hearing problems, and vomiting.

Third, and perhaps most worrying of all, widespread use of A. annua herbal extracts could bolster drug-resistant strains of malaria parasites such as Plasmodium falciparum.16

For people living in regions where malaria is endemic, exposure to subtherapeutic doses of artemisinin in A. annua may be enough to kill off some of the parasites in their bodies, but not all of them. Clearing out weakling parasites leaves more room for drug-resistant siblings to proliferate, rendering vital ACTs [artemisinin-based combination therapies] ineffective.”

According to Pascal Ringwald, who heads up the drug resistance and response unit of the WHO Global Malaria Program, artemisinin resistance is a significant problem in Southeast Asia, where Artemisia readily grows and is commonly used.17

That said, this risk is bound to be slight for Americans and people in many other Western countries where malaria is exceedingly rare. According to C&EN,18:

“Scientists interviewed by C&EN agree that although this use is against WHO recommendations, it does not risk accelerating resistance because there are so few cases of malaria in the U.S.”

+ Sources and References
 
 
The antiviral activity of artemisinin, which is normally thought of as an anti-parasitic, is as amazing as the antiviral activity of ivermectin, which is normally thought of as a dewormer.  The very interesting aspect of artemisinin; however, is it’s ability to:
 
‘corrupt the heme-detoxification pathway.’  
 
The reason that this is interesting, is that within this video, Dr. Northrup describes how radiation from 5G (60gh) can adversely affect hemoglobin making it difficult to be oxygenated, and that this actually happened in both NY and China. The first case of COVID-19 occurred 1 month after the 5G rollout in Wuhan, China – people were actually blue from lack of oxygen.
 
Also, if you remember the post from April, a NY doctor describes how ventilators were harming COVID patients who were described as suffering severe hypoxemia and that the usual treatments were failing because they:
 
result in severe hemodynamic impairment and fluid retention.” 
 
These details seem to continue to implicate 5G in this saga:  https://madisonarealymesupportgroup.com/2020/04/25/coronavirus-science-policy-politics-5g/
Excerpt:

RF radiation and COVID-19 cause similar disease. In my last newsletter (“Is the Sky Really Falling?”), I noted some effects of COVID-19 that are similar to effects of radio waves. The list of effects in common has grown, and includes:

  • headaches
  • dizziness
  • nausea
  • digestive problems
  • muscle pain
  • tachycardia
  • hypotension
  • cardiac arrhythmias
  • strokes
  • seizures

As many as two-thirds of people who test positive for COVID-19 have lost their sense of smell, often without any other symptoms. Patients are presenting with mental confusion, without any respiratory symptoms at all. Patients are presenting with diarrhea, vomiting, and abdominal pain. When patients with any of these symptoms test positive for the coronavirus, their illnesses are being attributed to that virus. But these are all classic symptoms of radio wave sickness.

WHEN BOTH THE VIRUS AND RF RADIATION ARE PRESENT, THE DISEASE SHOULD BE ATTRIBUTED TO BOTH.

And RF radiation and COVID-19 both cause hypoxia. COVID-19 impairs oxygen absorption by the blood, and RF radiation impairs oxygen use by the cells. COVID-19 would not be so severe were it not for the radiation.

Recently, there is a new symptom that is being attributed to the virus that is exactly what one would expect to see from millimeter waves: a “fizzing” sensation throughout the body. It is being described as a “buzzing sensation,” “a burning feeling,” and “an electric sensation in the skin.” It is probably wrongly being attributed to the virus, and is due instead to 5G.