Tag Archives: mRNA

COVID – Looking Down the Line

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The Biggest COVID Question: What Will Happen in 10 years?

Analysis by Dr. Joseph MercolaFact Checked

STORY AT-A-GLANCE

  • So far, children have been largely unfazed by COVID-19 because their interferon pathway works really well. Interferon is an immune molecule that protects cells against invading pathogens
  • The COVID jab inhibits the type-1 interferon pathway, so mass injecting young children may actually erase the natural herd immunity against COVID-19 that would develop if all children remained unjabbed
  • Aggressive cancers have exploded among adults who got the shots, even though it’s only been a little over two years since their rollout
  • Analysis of U.S. Morbidity and Mortality Weekly Report (MMWR) data suggests the U.S. Centers for Disease Control and Prevention is redesignating cancer deaths as COVID deaths to eliminate the cancer signal, and has been doing so since April 2021
  • We’ve also seen massive increases in excess mortality from abnormal clotting issues and heart problems since the COVID shots rolled out. If side effects such as cancer, heart disease and stroke are killing working age adults in unprecedented numbers already, what will the excess mortality be, say, 10 years from now if children and teens keep getting mRNA boosters every year?

What will the future hold for people whose exposure to COVID-19 occurs during the first years of life? That question was recently asked by Katherine J. Wu, a staff writer at The Atlantic.1

“To be a newborn in the year 2023 — and, almost certainly, every year that follows — means emerging into a world where the coronavirus is ubiquitous … Beyond a shadow of a doubt, this virus will be one of the very first serious pathogens that today’s infants — and all future infants — meet,” she writes.

“Eventually, the expectation is that the illness will reach a stable nadir, at which point it may truly be ‘another common cold,’ says Rustom Antia, an infectious-disease modeler at Emory.

The full outcome of this living experiment, though, won’t be clear for decades — well after the billions of people who encountered the coronavirus for the first time in adulthood are long gone.

The experiences that today’s youngest children have with the virus are only just beginning to shape what it will mean to have COVID throughout a lifetime, when we all coexist with it from birth to death as a matter of course.”

COVID Jab Prevents Natural Herd Immunity

Wu praises the COVID jab as being part of why we can be hopeful for future generations that have to live with this new virus, but is that really realistic? Right now, everything points to the COVID shot being a disaster, and no one actually knows what the long-term effect will be on children who get it.

Wu highlights the fact that children’s immune systems have the advantage of “marshaling hordes of interferon — an immune molecule that armors cells against viruses.” This is thought to be a primary reason why COVID-19 isn’t nearly as lethal in young children as in older adults.

The problem that Wu completely misses is that the COVID jab inhibits the type-1 interferon pathway,2 so mass injecting young children may actually erase the natural herd immunity against COVID-19 that would develop if all children remained unjabbed. The shots will NOT, as Wu suggests, help us achieve herd immunity at all.

Cancer Rates in Young People Will Likely Rise

Mass injecting children with a drug that impairs their immune system may also (rather predictably) result in exploding cancer rates. Already, aggressive cancers have exploded among adults who got the shots,3 even though it’s only been a little over two years since their rollout.

For example, data from the Defense Medical Epidemiology Database (DMED)4 — historically one of the most well-kept and most heavily relied-upon medical databases in the world — showed that, compared to the previous five-year averages, cancer among Department of Defense (DOD) personnel in 2021 skyrocketed.

Overall, cancers tripled among servicemen and their family members after the rollout of the COVID shots. Breast cancer went up 487%. Exploding cancer rates are also seen elsewhere. Indeed, the explosion of cases is so bad that cancer is now one of the top three leading causes of premature death among young working-age adults — a trend that in turn has driven down U.S. life expectancy by three years.

Cancer Relapses and Metastasis Rates Are Exploding

November 26, 2022, The Daily Sceptic published a letter5,6 to the editor of The BMJ, written by Dr. Angus Dalgleish, professor of oncology at St. George’s University of London, warning that COVID boosters may be causing aggressive metastatic cancers:

“COVID no longer needs a vaccine programme given the average age of death of COVID in the U.K. is 82 and from all other causes is 81 and falling,” Dalgleish wrote. “The link with clots, myocarditis, heart attacks and strokes is now well accepted, as is the link with myelitis and neuropathy …

However, there is now another reason to halt all vaccine programmes. As a practicing oncologist I am seeing people with stable disease rapidly progress after being forced to have a booster, usually so they can travel. Even within my own personal contacts I am seeing B cell-based disease after the boosters.

They describe being distinctly unwell a few days to weeks after the booster — one developing leukemia, two work colleagues Non-Hodgkin’s lymphoma, and an old friend who has felt like he has had Long COVID since receiving his booster and who, after getting severe bone pain, has been diagnosed as having multiple metastases from a rare B cell disorder.

I am experienced enough to know that these are not coincidental anecdotes … The reports of innate immune suppression after mRNA for several weeks would fit, as all these patients to date have melanoma or B cell-based cancers, which are very susceptible to immune control — and that is before the reports of suppressor gene suppression by mRNA in laboratory experiments. This must be aired and debated immediately.”

In a December 19, 2022, article7 in Conservative Woman, Dalgleish continued discussing the phenomenon of rapidly spreading cancers in patients who were in stable remission for years before receiving their COVID boosters. He noted that after his letter to The BMJ was published, several oncologists contacted him to say they’re seeing the same thing in their own practices.

“Seeing the recurrence of these cancers after all this time naturally makes me wonder if there is a common cause?” he wrote.8 “I had previously noted that relapse in stable cancer is often associated with severe long-term stress, such as bankruptcy, divorce, etc.

However, I found that none of my patients had any such extra stress during this time, but they had all had booster vaccines and, indeed, a couple of them noted that they had a very bad reaction to the booster which they did not have to the first two injections.

I then noted that some of these patients were not having a normal pattern of relapse but rather an explosive relapse, with metastases occurring at the same time in several sites … Scientifically, I was reading reports that the booster was leading to a big excess of antibodies at the expense of the T-cell response and that this T-cell suppression could last for three weeks, if not more.

To me, this could be causal as the immune system is being asked to make an excessive response through the humoral inflammatory part of the immune response against a virus (the alpha-delta variant) which is no longer in existence in the community.

This exertion leads to immune exhaustion, which is why these patients are reporting up to a 50% greater increase in Omicron, or other variations, than the non-vaccinated.”

Swedish pathologist, researcher and senior physician at Lund’s University, Dr. Ute Krueger, has also observed an explosion in rapidly advancing cancers in the wake of the COVID shots, with the largest increase occurring among 30- to 50-year-olds.9,10 According to Krueger, tumor sizes are also dramatically larger, multiple tumors in multiple organs are becoming more common, and cancer recurrence and metastasis are both increasing.

Cancer Deaths Are Being Intentionally Hidden

Disturbingly, as detailed in “How Cancer Deaths From the COVID Jabs Are Being Hidden,” analysis of U.S. Morbidity and Mortality Weekly Report (MMWR) data suggests the U.S. Centers for Disease Control and Prevention is filtering out and redesignating cancer deaths as COVID deaths to eliminate the cancer signal, and has been doing so since April 2021.

The signal is being hidden by swapping the underlying cause of death with main cause of death. As many as 20% of the weekly so-called COVID deaths are actually cancer deaths.

An Unconscionable Experiment on Humanity

Absolutely no one knows what the long-term ramifications of giving these injections to infants and young children will be. It’s a public health experiment unlike anything we’ve ever seen before. So far, we’ve not seen cancer rates among children skyrocket, but the uptake among young children has also been low.

Since their immune systems are also more robust, children may be protected from cancer for a time even if they do get the jab. The question is how long? The U.S. childhood vaccination schedule now includes the initial series plus an annual COVID booster. How many boosters will it take before a child’s immune system breaks and cancer starts to proliferate?

Excess Mortality Skyrocketing

We’ve also seen massive increases in excess mortality from abnormal clotting issues and heart problems since the COVID shots rolled out. If side effects such as cancer, heart disease and stroke are killing working age adults in unprecedented numbers already, what will the excess mortality be, say, 10 years from now if children and teens keep getting mRNA boosters every year?

I shudder to even think about it. Making matters even worse, drug makers are working overtime to deliver other mRNA-based “vaccines” as well, including one against respiratory syncytial virus (RSV). The U.S. Food and Drug Administration has already fast-tracked it. This, despite the fact that previous attempts to create an RSV vaccine failed because they caused antibody dependent enhancement (ADE).

No Benefit, Massive Cost

Now that we’re more than two years into the COVID injection campaign, the cost-benefit analysis is clearer than ever. The benefit is so small as to be inconsequential, while the costs are enormous. Here’s a quick summary breakdown, based on available evidence:

•Benefit — Short-term (four to six months) protection from severe COVID illness and death.

•Cost — Negative effectiveness after a few months (meaning the risk of infection, hospitalization and death from COVID is higher than before the injection). It also doesn’t prevent infection or spread of the virus, so vaccine-induced herd immunity can never be achieved.

The shots destroy immune function, making people more prone to all types of infections and chronic diseases, which in turn puts pressure on the health care system, raises disability rates and excess mortality, and lowers life expectancy. On top of all that, there’s evidence suggesting the shots have adverse effects on fertility, which could potentially result in a population collapse.

Evidence mRNA Jabs Cause Fertility Problems

By December 2021, at which time the COVID jabs had only been out for one year, reports of surges in menstrual changes and stillbirths were already proliferating. And, while health officials were, and still are, adamant that the COVID shot is safe for pregnant women, the data tell a very different story.

The study11 most widely used to support the U.S. recommendation for pregnant women to get injected was sponsored by the Centers for Disease Control and Prevention and published in The New England Journal of Medicine (NEJM) in April 2021. According to this study, the miscarriage rate among COVID jab recipients was 13.9%.

However, there was a MAJOR mistake made in this study, which was highlighted in a rapid communication12 from the Institute for Pure and Applied Knowledge (IPAK). The authors are Aleisha Brock, Ph.D. of New Zealand, and Simon Thornley, Ph.D., a senior lecturer in the section of epidemiology and biostatistics at the University of Auckland.

They explained that the NEJM study “presents falsely reassuring statistics related to the risk of spontaneous abortion in early pregnancy, since the majority of women in the calculation were exposed to the mRNA product after the outcome period was defined (20 weeks’ gestation).”13

When the risk of spontaneous abortion (miscarriage) was recalculated based on the cohort that was injected prior to 20 weeks’ gestation, the incidence of miscarriage was seven to eight times higher than the original study indicated, with a cumulative incidence of miscarriage ranging from 81.9% to 91.2%!

What’s more, 12.6% women who received the jab in the third trimester reported Grade 3 adverse events, which are severe or medically significant but not immediately life-threatening.

Another 8% also reported a fever of 38 degrees C (100.4 degrees F), which can lead to miscarriage or premature labor.14 Another problem with the NEJM study is that follow-up only continued for 28 days after birth, meaning the long-term effects of prenatal exposure to babies is still unknown.

A Pfizer-BioNTech rat study also showed the injection more than doubled the incidence of preimplantation loss. Birth defects, specifically mouth/jaw malformations, gastroschisis (a birth defect of the abdominal wall) and abnormalities in the right-sided aortic arch and cervical vertebrae, were also observed.15

Transhumanist Cabal Intend to Change Humanity

It’s become quite clear that the technocratic, transhumanist cabal that it trying to seize worldwide control is aggressively trying to genetically alter humanity. But to what end? Considering all the negative effects we’re seeing in adults, just two years in, what will happen to the infants and children who have been jabbed over the next decade or two? Especially if they start getting mRNA boosters every year?

Transhumanism is “sold” as the way of the future — a future in which everyone is in perfect health and can live as long as they want. We already see how the COVID shots are advertised as a simple “software update” for your immune system. The idea is that, eventually, any health issue will be solved this way.

The problem with this utopia is manifold, however. First of all, considering how disastrous this first mRNA injection is, it seems clear the reengineering of an already perfect biological system isn’t as easy as they make it out to be, and I for one doubt they’ll ever perfect it.

Secondly, while they say this transhumanist utopia is for everyone, it’s absolutely not. Do you really believe they want 8 billion people to be in perfect health and live for hundreds of years?

Perfect health means perfect reproductive capacity, so the number of offspring would be staggering. Clearly, they don’t want this, seeing how these same individuals are already complaining that the world is overpopulated. So, perfect health for everyone is a pipedream.

Extreme life extension for the masses also isn’t in the cards. Already, they want people to die as close to retirement age as possible, to minimize payouts. Do you really think they’d be willing to pay billions of people to spend 100 years in retirement?

Even if the retirement age was pushed way back to, say, 150, and the average life span is 175, who’s going to employ all these people? Remember, robots and artificial intelligence are already slated to take over most jobs, making most humans obsolete. There’s simply no incentive to extend the health span and life span of billions of people.

No, the transhumanist utopia is intended to be reserved for a select few, and this is something to keep in mind as they continue these genetic experiments on humanity. They’re not for our benefit.

What Are They Turning Us Into?

In closing, here’s a snippet from a November 22, 2022, Truth Talk article, in which blogger Katrina Wicks ponders the reasons behind the transhumanist push:16

“They make no secret of it, it’s not some wild conspiracy theory and is in fact being implemented in front of us and around us. Changing humans from what we are, into something else. Augmented humans seem to be on the horizon, as well as disrupted, corrupted and spliced humans too …

‘The Island of Dr. Moreau’ … by H.G. Wells … highlights an obsession with making animals more human through ‘medical intervention’ … I wonder if they are trying to do the opposite … to make humans more animal like? …

A certain international organization seems to have a nominated mascot who is the mouthpiece of how they want us to be bio-mechanical beings essentially, being constantly monitored, tested, observed and upgraded. Weird huh? Yet they gleefully put these plans forward and explain how and when. Just not really covering the why, or at least the real reasons for it.

But you can make up your own mind on what their purpose really is … what is out there for everyone to see is that they do want control.

Of your daily activities, thoughts, fears, aspirations … and generally of your future. So that is where you do get to take an active role, unless you already consider your life forfeit and have already accepted their new regime and landscape. But if you do not … and you have chosen to live, then now is the time.”

from:    https://articles.mercola.com/sites/articles/archive/2023/03/20/covid-question-what-will-happen-in-10-years.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1HL&cid=20230320&cid=DM1366943&bid=1750595981

What’s In Your Salad?

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RIVERSIDE, Calif. — Vaccinations can be a controversial subject for many people, especially when it comes to injections. So what if you could replace your next shot with a salad instead? Researchers at the University of California-Riverside are working on a way to grow edible plants that carry the same medication as an mRNA vaccine.

The COVID-19 vaccine is one of the many inoculations which use messenger RNA (mRNA) technology to defeat viruses. They work by teaching cells from the immune system to recognize and attack a certain infectious disease. Unfortunately, mRNA vaccines have to stay in cold storage until use or they lose stability. The UC-Riverside team says if they’re successful, the public could eat plant-based mRNA vaccines — which could also survive at room temperature.

Thanks to a $500,000 grant from the National Science Foundation, researchers are now looking accomplish three goals. First, the team will try to successfully deliver DNA containing mRNA vaccines into plant cells, where they can replicate. Next, the study authors want to show that plants can actually produce enough mRNA to replace a traditional injection. Finally, the team will need to determine the right dosage people will need to eat to properly replace vaccinations.

“Ideally, a single plant would produce enough mRNA to vaccinate a single person,” says Juan Pablo Giraldo, an associate professor in UCR’s Department of Botany and Plant Sciences, in a university release.

“We are testing this approach with spinach and lettuce and have long-term goals of people growing it in their own gardens,” Giraldo adds. “Farmers could also eventually grow entire fields of it.”

Plants are capable of growing more vaccines

Giraldo and a team of scientists from UC-San Diego and Carnegie Mellon University say the key to making edible vaccines are chloroplasts. These are small organs inside plant cells which help convert sunlight into energy.

“They’re tiny, solar-powered factories that produce sugar and other molecules which allow the plant to grow,” Giraldo explains. “They’re also an untapped source for making desirable molecules.”

Previous studies have shown that it’s possible for chloroplasts to express genes which are not a natural part of that plant. Giraldo’s team accomplished this by sending genetic material inside of a protective casing into plant cells.

In the new study, Giraldo teamed with UC-San Diego’s Professor Nicole Steinmetz to use nanotechnology to deliver more genetic material into chloroplasts.

“Our idea is to repurpose naturally occurring nanoparticles, namely plant viruses, for gene delivery to plants,” Steinmetz says. “Some engineering goes into this to make the nanoparticles go to the chloroplasts and also to render them non-infectious toward the plants.”

“One of the reasons I started working in nanotechnology was so I could apply it to plants and create new technology solutions. Not just for food, but for high-value products as well, like pharmaceuticals,” Giraldo adds.

from:   https://www.studyfinds.org/vaccines-salad-growing-plants/

THey Will Pay You to Vaccinate Your Child

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FDA Lets Pfizer Test Experimental COVID-19 Vaccine on U.S. Children

Pfizer becomes first company in U.S. to include children in Phase 3 COVID vaccine trials.

Americans have been following COVID-19 vaccine trial developments for weeks, watching companies jockey for frontrunner status like contestants in a reality TV show. And though participants in some of the studies (by Moderna, Oxford, Johnson & Johnson and Pfizer) have surfaced with reactions serious enough to pause several of the trials, market analysts remain “bullish” about the near-term prospects for approval of these liability-free products by the U.S. Food and Drug Administration (FDA).

On Oct. 16, Pfizer’s CEO indicated the company would likely file for FDA Emergency Use Authorization for its experimental BNT162b2 vaccine in late November. That statement came three days after Pfizer announced that it had received FDA permission to administer the unproven vaccine to children as young as 12, becoming the first company in the U.S. to include young participants in Phase 3 trials. In the UK, Oxford and AstraZeneca gained approval to test their vaccine in children aged 5-12 back in May, a couple of months before two of their adult clinical trial participants developed transverse myelitis.

To date, Pfizer has administered two doses of vaccine to almost 35,000 adult participants in five countries. Unworried by the dramatic side effects reported by some of these adults — including high fever, pounding headaches, body aches, exhaustion and shivering intense enough to crack teeth — more than 90 parents have already expressed interest in volunteering their teenagers.

Are these parents (perhaps left unemployed by coronavirus restrictions) tempted by the financial incentives offered to clinical trial participants, reportedly anywhere from $1200 to $2000? Otherwise, their motivation for wanting to throw their children into the experimental fray is unclear; as the director of the Cincinnati Children’s Hospital stated, “most of the time, what a coronavirus causes is a cold” that does not even make children “sick enough to where a parent says they need to go to a doctor.”

The Cincinnati physician has, nonetheless, just started giving Pfizer’s shot to 16- and 17-year-olds (and soon to 12-15-year-olds). To entice additional young participants, he tells parents that the COVID-19 death rate in children is “not zero” — but declines to spell out that, according to the Centers for Disease Control and Prevention, the survival rate in those age 19 and under is 99.997%. Using similarly vague language, a Memorial Sloan-Kettering health policy expert said that a COVID-19 vaccine’s benefits for the young would likely be “secondary’ in nature” but characterized the gesture as “an act of service to help protect others.”

However, reports in Pediatrics and other journals assert that children are not a source of infection and are far more likely to acquire COVID-19 from adults “rather than transmitting it to them.” In other words, policymakers expect children to accept a risk-benefit equation heavily tilted toward risk.

Corporate bad guy

Pharmaceutical giant Pfizer — the second-largest drug and biotech company in the world and the fourth-highest earner of vaccine revenues — has seen a 7% increase in its share value this year. However, though Pfizer claims to be a standard-bearer for “quality, safety and value,” it has a corporate rap sheet a mile long. Pfizer is routinely mired in controversies involving alleged price-fixing, bribery, kickbacks, tax avoidance, regulatory misdirection and other unsavory practices and has also repeatedly paid fines for environmental violations at its research and manufacturing plants.

Critics point to decades of aggressive and questionable marketing. In 2009, this behavior earned Pfizer the dubious distinction of paying the largest-ever criminal fine at the time — $2.3 billion — for fraudulent and illegal promotion of four drugs, including a painkiller marketed at “dangerously high” doses. In 2016, a British regulator levied a $106 million fine against Pfizer for a 2600% increase in the price of a widely prescribed anti-epilepsy drug that increased the National Health Services’ expenditures from one year to the next — for a single drug—from $2.5 million to $63 million.

Perhaps to compensate for its unpleasant track record, Pfizer is the top drug company spender in state elections, even outspending the industry’s own lobbying group, Pharmaceutical Research and Manufacturers of America (PhRM). As a just-published analysis of drug company political spending by STAT and the National Institute on Money and Politics shows, Pfizer’s “prolific” state-level spending ($778,000 since January 2019) “mirrors its behavior at the federal level, where its [political action committee] was also the top political spender among drug companies” — roughly $1 million over the same time period. The report pointedly notes that while the amounts paid out to legislators represent a “pittance” for a company earning tens of billions a year, “those small chunks of corporate change can have a significant impact.”

Pfizer’s vaccines

Pfizer is responsible for two vaccines on the U.S. childhood and adolescent vaccine schedule: the pneumococcal vaccine Prevnar-13 (given to children under 5 and also to older adults) and the meningococcal vaccine Trumenba (approved for 10 – 25-year-olds). Package inserts link the two vaccines to a large number of serious adverse events, including anaphylaxis and other allergic reactions, severe headaches and chronic muscle and joint pain. Among the roughly 40 harms listed in the Prevnar-13 insert are sudden infant death syndrome (SIDS) and half a dozen other fatal outcomes.

Pfizer developed its COVID-19 vaccine — which uses experimental messenger RNA (mRNA) technology — in partnership with the German biopharma company BioNTech. Although mRNA vaccines must be stored in special ultra-low-temperature freezers that pose certain logistic obstacles, Pfizer is gung-ho on the never-before-approved approach because it bypasses the more costly and difficult methods used in traditional vaccine production. It does this by essentially turning recipients into “vaccine factories” — with long-term risks that are unknown.

Pfizer and BioNTech brought their COVID-19 vaccine candidates “from concept into clinical development” in under three months, perhaps helped along by the current Pfizer CEO’s efforts to restructure Pfizer into a more “nimble” company. At the same time, observers who now place Pfizer at the head of the pack for COVID-19 vaccines credit the company’s “well-oiled system,” remarking that “Pfizer’s incredibly organized and is always … a couple steps ahead, planning where they want to go.”

Conflicts of interest and revolving doors

In the summer of 2019, after having served as the Trump administration’s FDA commissioner for two years, Scott Gottlieb passed through the revolving door to join Pfizer’s board of directors as well as becoming a regular contributor on CNBC. For the past four decades, stepping onto pharmaceutical boards has been par for the course for departing FDA commissioners, though Gottlieb may have upped the ante by also joining the boards of the AI- and big-data-reliant genetic testing start-up, Tempus, and the biotech company Illumina.

While at the FDA, Gottlieb presided over a record number of drug approvals. According to one commentator, this “trail-blazing” FDA stint and Gottlieb’s focus on “hustling up the [drug approval] process … helped endear him to the industry, making him one of the most popular commissioners in FDA history.” As the director of a consumer watchdog group put it, “He’s basically been a shill for pharmaceutical corporations for much of his career.” Two months before stepping down from the agency, Gottlieb attracted notice when he strongly denied any link between vaccines and autism while publicly threatening that the federal government might be “forced” to intervene in states with vaccine exemptions to make vaccines mandatory across the board.

Gottlieb’s affiliation with CNBC may explain why he has been a frequent public face during the coronavirus pandemic, promoting the U.S. as a world leader in the vaccine race but also vocally endorsing measures like universal masking, universal testing and restaurant and school shutdowns. On October 19, Gottlieb dourly told Americans that the U.S. is “entering a pretty difficult period” and that “the hardest part is probably [still] ahead.” Ironically, around the same time that Gottlieb was using positive test results to hype ongoing restrictive measures, a former Pfizer vice-president and chief science officer in the UK characterized mass testing as “inappropriate,” asserting that “it is impossible for the positives to be much other than false.” Discussing the harsh policies that have been particularly disastrous for children, the former Pfizer executive agreed that they have essentially been based on “completely fake data.”

Kids at risk

Reporter Whitney Webb recently outlined how Operation Warp Speed is awarding contracts to vaccine companies through a nongovernmental defense contractor intermediary, a tactic that shields the contracts from oversight and federal regulation. Meanwhile, Moncef Slaoui — who heads up the Operation Warp Speed initiative — stated that after a round of testing in adolescents, he expects the leading coronavirus vaccines to also be tested in toddlers and babies. Parents would do well to keep their children on the sidelines of these experiments. If vaccine clinical trials, including Pfizer’s, are already generating concerning results in adults capable of describing their symptoms, what will happen when preverbal babies experience similar adverse outcomes?

from:    https://childrenshealthdefense.org/defender/fda-pfizer-experimental-covid-vaccine-children/?utm_source=salsa&eType=EmailBlastContent&eId=b18c0c6e-fe4c-4d23-b98f-d41da6147716

Rewriting Your RNA

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A DARPA-Funded Implantable Biochip To Detect COVID-19 Could Hit Markets By 2021    September 21, 2020

Raul Diego, Mint Press News
Waking Times

The most significant scientific discovery since gravity has been hiding in plain sight for nearly a decade and its destructive potential to humanity is so enormous that the biggest war machine on the planet immediately deployed its vast resources to possess and control it, financing its research and development through agencies like the National Institutes of Health (NIH), the Defense Advanced Research Projects Agency (DARPA) and HHS’ BARDA.

The revolutionary breakthrough came to a Canadian scientist named Derek Rossi in 2010 purely by accident. The now-retired Harvard professor claimed in an interview with the National Post that he found a way to “reprogram” the molecules that carry the genetic instructions for cell development in the human body, not to mention all biological lifeforms.

These molecules are called ‘messenger ribonucleic acid’ or mRNA and the newfound ability to rewrite those instructions to produce any kind of cell within a biological organism has radically changed the course of Western medicine and science, even if no one has really noticed yet. As Rossi, himself, puts it: “The real important discovery here was you could now use mRNA, and if you got it into the cells, then you could get the mRNA to express any protein in the cells, and this was the big thing.”

It was so big that by 2014, Rossi was able to retire after the company he co-founded with Flagship Pioneering private equity firm to exploit his innovation, – Moderna Inc., attracted almost a half billion dollars in federal award monies to begin developing vaccines using the technology. No longer affiliated with Moderna beyond his stock holdings, Rossi is just “watching for what happens next” and if he’s anything like the doting “hockey dad” he is portrayed to be, he must be horrified.

Remote Control biology

As early as 2006, DARPA was already researching how to identify viral, upper respiratory pathogens through its Predicting Health and Disease (PHD) program, which led to the creation of the agency’s Biological Technologies Office (BTO), as reported by Whitney Webb in a May article for The Last American Vagabond. In 2014, DARPA’s BTO launched its “In Vivo Nanoplatforms” (IVN) program, which researches implantable nanotechnologies, leading to the development of ‘hydrogel’.

Hydrogel is a nanotechnology whose inventor early on boasted that “If [it] pans out, with approval from FDA, then consumers could get the sensors implanted in their core to measure their levels of glucose, oxygen, and lactate.” This contact lens-like material requires a special injector to be introduced under the skin where it can transmit light-based digital signals through a wireless network like 5G.

Once firmly implanted inside the body, human cells are at the mercy of any mRNA program delivered via this substrate, unleashing a nightmare of possibilities. It is, perhaps, the first true step towards full-on transhumanism; a “philosophy” that is in vogue with many powerful and influential people, such as Google’s Ray Kurzweil and Eric Schmidt and whose proponents see the fusion of technology and biology as an inevitable consequence of human progress.

The private company created to market this technology, that allows for biological processes to be controlled remotely and opens the door to the potential manipulation of our biological responses and, ultimately, our entire existence, is called Profusa Inc and its operations are funded with millions from NIH and DARPA. In March, the company was quietly inserted into the crowded COVID-19 bazaar in March 2020, when it announced an injectable biochip for the detection of viral respiratory diseases, including COVID-19.

A wholly-owned subsidiary

In July, a preliminary report funded by Fauci’s NIAID and the NIH on an mRNA Vaccine against SARS-CoV-2 was published in The New England Journal of Medicine, concluding that mRNA-1273 vaccine. provided by Moderna for the study, “induced anti–SARS-CoV-2 immune responses in all participants, and no trial-limiting safety concerns were identified,” and supported “further development of this vaccine.”

A month earlier, the NIH had claimed a joint stake in Moderna’s mRNA COVID-19 vaccine, citing a contract signed in December, 2019, stipulating that the “mRNA coronavirus vaccine candidates [are] developed and jointly owned” by both parties. Moderna disputes the federal government’s position, stating that the company “has a broad owned and licensed IP estate” and is “not aware of any IP that would prevent us from commercializing our product candidates, including mRNA-1273.”

The only obstacle is a delivery system, which though Moderna claims to be developing separately, is unlikely to get FDA approval before the federal government’s own DARPA-developed hydrogel technology, in tandem with Profusa’s DARPA-funded light sensor technology, which is expected to receive fast track authorization from the Food and Drug Administration by early 2021 and, more than likely, used to deploy a coronavirus vaccine with the capacity to literally change our DNA.

In addition, the Department of Health and Human Services (HHS), is currently investigating Moderna’s patent filings, claiming it failed to disclose “federal government support” in its COVID vaccine candidate patent applications, as required by law. The technicality could result in the federal government owning a 100 percent stake in mRNA-1273.

 

 

About the Author

Raul Diego is a MintPress News Staff Writer, independent photojournalist, researcher, writer and documentary filmmaker.

from:    https://www.wakingtimes.com/2020/09/21/a-darpa-funded-implantable-biochip-to-detect-covid-19-could-hit-markets-by-2021/