The mRNA Vaccine: Clinical Trial on Humans

By  Michelle Edwards, UNCOVERDC

As COVID-19 vaccines—including Moderna and Pfizer-NBioTech’s mRNA “gene-therapy” jabs—continue to be promoted and mandated as the primary “treatment” against SARS-CoV-2, other alternative therapies have been around for just as long as the vaccines but have been heavily censored by government agencies. With substantial funding from the U.S. Defense Department’s Advanced Research Projects Agency (DARPA) since 2011, mRNA vaccine technology took center stage as a treatment for COVID, with both mRNA “vaccines” receiving Emergency Use Authorization (EUA). Still, one element missing from the emerging treatment was clinical proof of its effectiveness. 

Despite Years of Study, mRNA Vaccines Lacked Trial on Large Scale

A 2017 article published in Nature called “The ‘anti-hype’ vaccine” starts by remarking that the idea of “vaccines-on-demand” is an “alluring, yet misleadingly simple, concept,” adding that “such a vaccine would enable rapid-response agents against pandemic threats. Ignored for years, using RNA as a starting point for immunotherapy “ticks many of the boxes for a vaccine-on-demand offering advantages in manufacture, flexibility, scalability, and cost of goods.” Nonethelessclinical validation faced challenging obstacles, “such as antigen discovery, product formulation, and delivery.” 

The first mRNA vaccine to be injected into humans was a prostate cancer product developed by CureVac. Despite $110 million in funding from Bill Gates and German billionaire Dietmar Hopp in 2015, the product failed to improve survival over the standard of care in patients with prostate cancer. With sustained interest across the board—including the commitment from DARPA, specifically its Biological Technology Office (BTO) in D.C.— the failure of Curevac’s mRNA prostate vaccine didn’t stop funding, and research continued. At the time, Matt Hepburn, program manager at DARPA’s BTO, whose primary focus is having “platforms in place that can respond quickly in the case of a pandemic,” commented:

“We like to think of ourselves as [funders of] early-breakthrough, high-risk, things that would not normally be funded. If you were going to do a safe biomedical research program with incremental approaches to solving a problem, that would not be us. Our mindset, day, night, 24/7, is what do we need to do to be ready for the next pandemic.” 

2013 mRNA Pre-Clinical Trial on Rats

mRNA vaccines had their first opportunity to halt a pandemic in 2013 during an outbreak of H7N9, a deadly strain of Asian lineage Avian Influenza A in China. With funding from DARPA and Biomedical Advanced Research and Development Authority (aka BARDA, which supports the application and delivery side as opposed to the development side), scientists at Novartis took a gene sequence deposited in GenBank by the Chinese Center for Disease Control and Prevention and endeavored to make a vaccine “based on the electronic sequence.” Andrew Geall, who was managing Novartis’s mRNA vaccine program at the time, said:

“We were lucky enough to be collaborating with Craig Venter’s teams, so we made a vaccine in 8 days, put it in mice in 13 days, and showed that, indeed, it works.” 

Interestingly, Venter’s companies, Synthetic Genomics (whose research also focuses on synthetic biofuels and animal products, along with Bill Gates) and Synthetic Genomics Vaccines, began working on “next-generation synthetic RNA replicon platforms” to develop vaccines for livestock in 2017. The same year, Synthetic Genomics partnered with Duke Human Vaccine Institute on DARPA’s recently funded Pandemic Prevention Platform (P3), which “aimed at establishing a system capable of halting viral pandemics within 60 days.” An October 26, 2017 press release announced:

The Duke Human Vaccine Institute has received a $12.8 million, 30-month grant from the U.S. Department of Defense, Defense Advanced Research Projects Agency (DARPA) to develop a system capable of halting viral pandemics within 60 days.

The program, called DARPA Pandemic Prevention Platform (P3), seeks to combine expertise in virology, immunology and clinical manufacturing to rapidly identify and respond to disease outbreaks such as SARS, pandemic influenza and Zika before they spread widely.

As noted by Geall, the Novartis mRNA vaccine “worked” in that it raised neutralizing antibodies after “one injection of 1 mg and all protect mice had HI titers considered protective after two doses.” The study results were thrilling to DARPA, who had just handed its recently funded Moderna Zika program to BARDA. Hepburn stated:

“What you are seeing in the field now is that using a nucleic acid to get the body to do what you want it to do, whether it’s a vaccine or other responses, is really exploding. We find that profoundly exciting.”

Human mRNA Clinical Trial Continues

Fast forward three years to 2020 and the introduction of the COVID-19 pandemic, and, even with all of DARPA’s research and funding, a system was not in place capable of halting a viral pandemic in three months. As we close in on year two of the pandemic, the safety and efficacy of the two mRNA vaccines against COVID-19 continue to wane, and uncertainty about the vaccines persists. Meanwhile, as promising alternative treatments options remain censored by government agencies, funding for mRNA vaccines and mRNA therapeutics continues to take center stage.

August 31, 2021 | 28 Comments »

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  1. I am wondering whether all these “vaccinated people catching COVID” are, in fact, suffering from their vaccine spike protein surge and not from COVID.

    That COVID keeps getting misdiagnosed and other diseases keep getting labeled as COVID at a drop of a hat (or at a setting of the PCR test) is a given.

    BTW, those serological tests they are starting to use in Israel, wouldn’t they also show false results for the immune people because the antibody level is supposed to drop even in those who have acquired natural immunity because then the T-cells take over?

  2. @Michael

    Fully Vaccinated People are dropping dead during Delta surge:

    The vax is failing. One of the problems, one of the worse problems, of CDC claiming the vax is 95% effective when they knew since April that this was declining, is that it gave the vaccinated people the false sense of being protected. Don’t misunderstand me, masks don’t work, so they would not have been protected using them. I am referring to maintaining a high level of hygiene, washing your hands often(VERY VERY HELPFUL TO PREVENT EXPOSURE) for instance. But more so than even this, since they were protected by the shot, when they first felt the crashing headache(hallmark early sign of Delta), they would assume it was anything but Covid,and by the time they were showing symptoms they were likely spreading the disease to everyone they contacted for days.

    Now, finally, 4 months later we all know that the vax is failing, because the CDC could not smother the truth any longer, and vaccinated people are more readily getting tested, and so we have increased number of people getting the disease and dying from it. What will be concerning, and by that I mean we just jumped off a cliff concerning, is if the vaccinated ever are found to be dying in numbers exceeding their representation in the general public – for example if 75% of deaths are in vaccinated patients in a state where the vaccinated are only 50%, that would be really really bad. Otherwise, all this hysteria that “an increase of 25% of death in vaccinated people” is just further revaluations to the fact that the vax is failing.

    It would be good if the governor would allow his people to be treated with effective drugs and save both the vaccinated and the unvaccinated alike, as this disease has killed millions, and will kill millions more if we treat it as a mild headache instead of a killer virus needing immediate medical care. The false concerns and misplaced attentions will never replace the lack of medical treatment.

  3. @peloni

    This is scary.

    Can you imagine the coming crisis in organ transplantation and blood transfusions?!

    People dying by tens of thousands who could have been saved just a year ago?

    We are ruled by the criminally insane – this is the only conclusion that makes sense to me.

    Unless I give them too much credit for brains.

  4. @Reader

    “Anyone who has received their Vaccine cannot donate convalescent plasma to other Covid patients.”

    This is an important point. The last thing you would want to happen is to have an unwanted immune reaction to occur when you are administering a plasma/whole blood transfusion. One thing that I would advise people to consider is to have your own blood pulled and kept aside so you will have it if you need it. No complications with matching blood types or spike antibody types. This spike thing is really complicating matters. They are not accepting organ donations from vaccinated patients either, or they weren’t as of about 2 months ago. Everything changes by the hour, so it is hard to keep up with all the changes that CDC and her sister autocrat agencies have mandated.

  5. Thanks, Peloni.

    Here is more stuff about what the mRNA vaccinated cannot do (it’s in the comments under the article):

    https://www.jpost.com/health-and-wellness/coronavirus/covid-jabbed-abroad-need-shot-in-israel-to-be-exempt-from-quarantine-678323

    16 hours ago
    Red Cross: Anyone who has received their Vaccine cannot donate convalescent plasma to other Covid patients.

    The Vaccine wipes out natural Covid antibodies making the convalescent plasma ineffective for treatment.

    Once people are vaccinated, they cannot donate plasma. The vaccine causes spike antibodies, and for convalescent plasma, they need nucleocapsid antibodies.

    Only the plasma from the UNVACCINATED meets their requirements:

    Red Cross website:

    “One of the Red Cross requirements for plasma from routine blood and platelet donations that test positive for high-levels of antibodies to be used as convalescent plasma is that it must be from a donor that has not received a COVID-19 vaccine. This is to ensure that antibodies collected from donors have sufficient antibodies directly related to their immune response to a COVID-19 infection and not just the vaccine, as antibodies from an infection and antibodies from a vaccine are not the same.”

  6. @Reader

    Seems a bit heavy handed, doesn’t it?

    When you become accustomed to solving problems using a hammer, every problem will come to appear more and more like a nail. That is until you try hammering a square glass into a round hole.

  7. @Reader
    No, it was a DNA retrovirus vaccine which is rendered less lethal than the actual normal virus – ie it was more in line with the usual vaccines types. The Israeli vaccine was a genetically modified retro-Vesicular Stomatitis Virus which has a substituted Spike protein, of course, on the virus. The virus was attenuated, which is a more normal type vaccine. It is just a virus which has the toxic spike on it that will act as any virus and generate an immune response for a few days and then it would be gone. This retro-Vesicular Stomatitis Virus was used to create a vaccine to Ebola and I think they are working with it on HIV. The Vesicular Stomatitis Virus causes a disease that affects large animals such as horses, cows, goats, pigs, etc. It can infect humans where it causes limited flu like symptoms. This vax would fail to create any protection to anyone who had been previously exposed to this Vesicular Stomatitis Virus, but few humans are infected by this virus, usually just veterinarians and farm workers would have any possible exposure.

    The researchers did work on hampsters and their prototype appeared to be successful in protecting the animal trials – wow, they actually did animal trials, how normal – no wonder they didn’t make the cut.

    A major advantage with the Israeli vax, if it had worked in human trials, is that the virus has no lipid-nanoparticles, which has very serious consequences beyond the spike. And then the other, more important issue is the enduring presence of the vaccine in the body creating an unknown perpetual immune stimulation. Vaccines all have a given dosage. That amount of vaccine will have the potential to generate a certain known amount of protein, usually a very small amount. Even in a virus vaccine as this one is, you could calculate how much protein could be created over the 4-8 days the virus would be present in the body. But with the mRNA vaccines, you are taking over the cells and generating untold numbers of proteins and this process could be ongoing for weeks or months. They just found a case where the spike was found in a blood sample 9months post-vax(needs to be verified still). Previous reports have the spike still present 5months-post vax in some patients. That is a rediculously long time to clear a vaccine. And nobody knows how much protein is being generated in that time – but it is a LOT. Also, the mRNA in the vaccines doesn’t break down, like human mRNA does, after it makes a copy – it just keeps making more and more copies, and it can wind up in the blood system where it can create a prion disease in the brain. So not sure of the downsides of the Israeli vax but it could not have been as concerning as the mRNA vax. But it also might not have been protective at all.

    The mRNA vax were very good at making a very strong immune response, ie it generated very strong antibody levels, because it flooded the body with excessive amounts of spike protein as described above. I heard recently that the researchers had info 10yrs back that the spike was dangerous, but I haven’t seen that report, just heard it mentioned recently from McCullough or Malone.

  8. @peloni

    Was Israel’s vaccine also mRNA?

    Head of Israel’s Biological Institute: Our COVID vaccine was sabotaged
    Professor Shmuel Shapira says his institute was half way to developing an Israeli made vaccine when the government opted to turn country into Pfizer’s experimental laboratory; ‘We may not be chosen by the pharma industry next time and must rely on ourselves,’ he says
    Sarit Rosenblum |
    Updated: 08.31.21, 19:13

    Still, the man who headed one of the country’s most secretive and important institutions for the better part of a decade will never forget the phone call he received on February 1, 2020.

    On the other side of the line was the office of then-Prime Minister Benjamin Netanyahu, who summoned Shapira to an urgent meeting on the development of an Israeli made COVID vaccine.

    A year and a half after that call, over 5 million Israelis had already received the Pfizer vaccine – which many around the country regard as nothing less than an economy-saving lifeline.

    Shapira, though, still believes in his institution’s own vaccine, the development of which, he claims, was suspended for reasons unknown.

    https://www.ynetnews.com/magazine/article/byemibz11k?utm_source=Taboola_internal&utm_medium=organic

  9. @Adam
    The C.1.2 isn’t taking off because it has no evolutionary benefit that would allow it to displace Delta. Delta was around since Feb-Mar 2020 and for nearly a full year, Delta was only able to maintain a very low presence in cases. It was only due to the vaccines that Delta gained an evolutionary advatage by Alfa/Beta/Gamma all being very sensitive to the vaccines while Delta was not. This is how Delta came to become the dominant variant. Now, Delta is not being killed effectively by the vax, so C.1.2 will have to wait til something gives it an advatage over Delta before it can dominate. Perhaps the booster vax will be effective, to some significant level, but only if it is effective against Delta and not C.1.2. Only then will C.1.2 become dominant strain. .

    The waiting period for people, who have had Covid-19, is 30 days before they can be vaccinated.

    It is very concerning that they are vaccinating Covid recovered people. They are very susceptible to serious adverse reactions to the vax and a plurality of the serioius adverse reactions are experienced by Covid recovered patients. Furthermore, the Covid recovered people were not included in the EUA studies. In addition to this, the Covid recovered people are immune to every part of the virus and their immunity is maintained while the vax are failing, hence there is no benefit to them taking the risk of the vax adverse reactions.

  10. The C.1.2 Covid-19 variant hasn’t taken off like the Delta variant, according to Sahpra board chairperson Helen Rees.
    Vaccines are monitored for its effectiveness against new variants.
    The waiting period for people, who have had Covid-19, is 30 days before they can be vaccinated.
    The new C.1.2 Covid-19 variant has fortunately not “taken off” like the Delta variant, the board chairperson of the South African Health Products Regulatory Authority (Sahpra), Helen Rees, told Parliament’s Portfolio Committee on Health on Wednesday morning.

    She says South Africa is very fortunate to have a highly active group of academics, who are picking up new variants of the virus.

    The new C.1.2 variant was detected in May.

    “It only represents about 2% of the current testing that is going on, but it’s been detected in eight of our nine provinces. It has also been detected in eight countries around the world, from Europe, Asia, other countries in the African region and the Western Pacific region. So, it’s widely detected… it is not doing, at the moment, what we were seeing the Delta variant do, which has really taken off, which we are all familiar with now,” she said.

    READ | SA’s potential Covid-19 variant of interest ‘a signal that the pandemic is not over’ – expert

    “But the changes in this particular variant we’ve seen in earlier variants. And the concern is that some of the changes, the mutations that we see, suggests that this might be a variant that could be more transmissible, or could be better at evading our immune system, at resisting our immune response.”

    She says that is why they are watching it very closely.

    But at the moment, we have not seen that it has been taking off.

    This Dr. Rees is very much an “establishment” doctor and a strong advocate of the Covid vaccines. She downplays the importance of the new South African variant. However, she does provide some interesting and concerning information about it.

  11. @Adam
    I agree with everything you have stated here, but the statistics for Alfa are recorded at 2%. I will add two points to your observation that also act as additional confounding issues. The PCR testing and the lack of any useful treatment.

    PCR Testing
    The PCR testing which would diagnose the Rock of Gibraltar with Covid using the rediculously false positive testing regimine, which caused two separate tragedies:
    1. We will never know what number of people ever actually had Covid, not by any margin or grade.
    2. Every poor soul who had cancer, or heart disease, or the flu or a stomach virus or any treatable condition was denied any treatment once they were diagnosed with Covid. They were denied any out-patient care and then when they were hospitalized, they were then placed in the Covid wards, where they could actually contract the disease. They recieved no treatment until they couldn’t breath due to the resulting pneumonia. At that point they were placed on oxygen and they recieved Remdisivir as their only treatment. I have read that some hospitals administered morphine to help with the pain, but morphine suppresses respiration(very bad thing to do for pneumonia cases), so I hope that report was false. In any event, that was all the treatment they recieved due to the CDC guidance. This means not only the people accurately diagnosed of Covid died a needless death, but anyone who was misdiagnosed with Covid due to that useless test that is still being used to sentence people to this same fate.

    Lack of any useful treatment
    The lack of any useful treatment resulted in the overwhelming deaths everywhere. As you say, a pittance of the lives lost were beyond saving. Likely everyone who could receive prophylaxis would have been spared disease or at least reduce the severity of disease such that they would likely recover. This tragic deception has already acted to murder millions of people and we are far from a rational treatment plan that will prevent this continuing towards a much worse outcome.

  12. New COVID variant detected in South Africa, most mutated variant so far
    The C.1.2 variant first detected in South Africa is more mutated compared to the original virus than any other known variant.
    By TZVI JOFFRE SEPTEMBER 1, 2021 21:20

    This article in the Jerusalem Post some of what Dr. (Ph.D.) Penny Moore reported to a recent seminar on Covid variants, but leaves out a lot of what Dr. Moore reported. She reports several, not just one, variants of the Covid virus that have “escaped” from the mRNA vaccines, and to a lesser extent, from the more “traditional covid vaccines, such as Johnson @ Johnsons and Astrazenica, as well. She did find that the “conventional” vaccines that employ traditional vaccine technology did reduce the number of cases that became serious or lethal, at least to some extent. However, the mRNA vaccines were not effective at all against these new “African” variants

  13. Peloni, I have my doubts as to whether the “Alpha” variation killed as many people as the CDC-John Hopkins statistics claim. After all, hospitals were paid extra if they reported a death as Covid. Because hospitals have been claiming for years that they are short of money, it seems to me inevitable that they reported a huge number of false Covid deaths–mainly people who died of pneumonia that was not caused by Covid. Doctors were instructed to report a death as caused by Covid if the person tested positive for Covid within a certain period of time (30 days, I think) whatever other illnesses they may have had, and even if they were hospitalized for accidents or gunshot wounds. Doctors were “coached” to report people who died of unknown causes and were never tested for Covid as Covid deaths, if a relative or friend of the deceased told them that the deceased had been “in contact” with someone who had Covid.
    Then there was the “mysterious” disappearance of flu deaths as soon as the supposed “pandemic” began. It is highly likely that many, perhaps most, of the supposed Covid victims died of influenza and its “complications,” mainly pneumonia. Influenza and pseumonia always take a heavy toll in the late winter and early spring, which is when the supposed “pandemic” began.

    Even so, the official statistics. if one reads them carefully, attributes most of the supposed Covid deaths to “complications” of Covid, not to Covid directly. And as I have already said, the “complications” of Covid can just as likely be complications of other illnesses, such as pneumonia and the “common cold.” This ‘common cold,” it should be pointed out, is a serious and life-threatening illness for those who already are suffering from a serious illness (such as a heart condition or cancer) and for the very elderly.

    To the extent that there were some people who have died of Covid or complications arising from it, intentional decisions of politicians, most notably Andrew Cuomo, caused them to beome infected with the illness, and/or to receive minimally adequate care for it. Cuomo’s decision to send people with active Covid cases to nursing homes, where they quickly infected numerous other patients as well as some staff, resulting in thousands of unnecessary deaths. And while Cuomo’s behavior was eventually exposed, it is possible that other politicians took similar disasterous actions in the early stages of the supposed pandemic.

    In a little-noticed action, Congress passed a law giving nearly all doctors and nurses the same income that they reported on their tax returns in 2019 above and beyond whatever they actually earned from their medical practices in 2020. Naturally, many of the doctors and nurses decided to take theyear off. Numerous medical offices either closed down or were drastically understaffed. Hospitals, too, suffered from severe staff shortages. Since people who were sick, whether with Covid or other illnesses, had no place to go but the emergency room of the nearest hospital, they are likely to have contracted either Covid or some other infectious disease that always thrive and are easily transmitted in hospital environments. Hospitals insisted on admitting anyone who had or seemed to have Covid, which is the reverse of their “normal” practice of sending people home from emergency rooms, and also sending them home from the regular hospital wards at the earliest possible moment. That also must have resulted in a huge increase of people who developed infectious diseases while in the hospital and died of them. Of course, hospitals received extra payments from the government depending on how many hospital beds they filled, and if they claimed they were overwhelmed with patients.

    To summarize, I think that “Alpha” was not an especially serious illness, and that the high death rate reported from it was partly the result of false reporting, and partly the result of irrational responses and panic by governments and the medical community. Had governments not pressured or bribed doctors and hospitals into making false reports, and had the medical community and hospitals responded to the new infectious disease the same way they had always responded to seasonally epidemics, the death toll would have been very small–a few thousand deaths at most. Well under 1 per cent of those infected would have died. And even with all of the government-encouraged medical malpractice, the actual death toll was still probably less than half of what the government’s and WHO’s statistics reported, or under 1 per cent.

  14. @Adam

    Alabama, Georgia, Florida, and Texas …ICU beds are filled at 90% capacity or more.

    The US manages healthcare ICU beds on a very marginal basis. This means anytime there is an epidemic the ICU beds will quickly fill. This is the worry, it was always the worry, with Delta. Delta is not Alfa. Alfa made few(relatively) sick and killed many of them – 2% of cases as opposed to 0.2% of cases with Delta. It is terrible to state such things out loud, but the deaths made the hospital management easier, as it freed up beds. But Delta doesn’t kill people, remember Delta has a very high infectivitiy rate. Hence, it makes them sick, it makes lots and lots of them sick – all at the same time, and the sick linger in the hospital beds for weeks. So this is what happened in India in May. The only reason India turned into the snowball in July, ie the story went away, was because of widely dispersed Medical Prophylaxis and Early Treatment, so everything was better by June, in India at least.

    For the US, the money in the bank which turned out to be counterfeit chump change was the vax. Everyone assumed, upto a month ago, the vaccinated public would not become sick, so the only ones that would become ill and need beds were the unvaccinated. Only the assumption that the vax would have at least 50% effecicy or last at least a year were both false – nevermind that by law they have to meet both these standards in order to be labled as a vaccine. Hence, the US is now looking at having to provide beds for extended stays for a large part of the public….and they just don’t have the beds. This will fill the hospitals and these reports will terrify the public to get the new untested vax booster – just released and never tested – and when/if people become sick from the booster vax, where the heck are they going to put them?

    The vax failures has the potential to create a great deal of social unrest due to the incompetency of the medical establishment to treat a disease that is fully treatable. And the overfilling of hospitals is a fatal event, all by itself, ie people will die simply due to the overwhelmed medical community/hospitals. Good news is that for Covid they won’t need a lot of drugs in the hospitals because the only thing they can treat the patients with are Remdisivir, which has been shown to not help but only prolong the hosptital stay(!!!) and monoclonal antibodies which has been demonstrated to generate variants in live time as the antibodies are administered(!!!)…. Welcome to the worse case scenario. Let’s hope this report is Fake News as it was almost every-time it was reported last year in each of those same states. They do of course have the opportunity to, as last year, create field hospitals, if the states call for it, which I suspect would be the case if this report was real, but it probably isn’t.

    I should note that the potential for such a disaster actually occuring with Delta is real due to its high infectivity rate, but again with Delta the disease is not very lethal and most of the cases are much more mild than the Alpha cases.

  15. From the New York haredi newspaper Hamodia:

    As Covid Fills Hospitals, Other Patients Care at Risk

    By Sara MarcusWednesday, September 1, 2021 at 11:27 am | ?”? ???? ???”?Updated Wednesday, September 1, 2021 at 1:01 pm

    A man arrives at Starr County Memorial Hospital, in Rio Grande City, Texas. (AP Photo/Eric Gay)
    NEW YORK –
    As overwhelmed hospitals in the South rapidly run out beds due to an influx of coronavirus patients, the care of others is suffering.

    Alabama, Georgia, Florida, and Texas ICUs are running out of hospital beds, Insider reported. Each state’s ICU beds are filled at 90% capacity or more. In Alabama, the ICUs are over 100% full; there were 1,621 patients in need of beds, but only 1,537 available.

  16. From today’s Jerusalem Post:

    BREAKING NEWS
    Japan finds stainless steel in suspended Moderna doses
    By REUTERS SEPTEMBER 1, 2021 16:51

  17. We conclude that SARS-CoV-2 spike glycoprotein…can exploit the [Cardiac Muscle] to drive heart damage directly, …from lymphocytic myocarditis, often suspected but rarely confirmed in COVID-19.

    So Spike protein can cause myocarditis. Given the Spike protein in the vax are identical to the Spike protein of the original(more lethal) viruses, it should be concluded that the vax are also saddled with the same cardiac dilemna, possibly more so due to dosing. The recent study that showed the 324% increase in myocarditis associated with the vax would support this conclusion. Hence, this should be accepted as a further reason to pursue the use of Medical Prophylaxis, ie, to prevent any heart injury by preventing any infection or exposure to the toxic Spike.

    SARS-CoV-2 direct cardiac damage through spike-mediated cardiomyocyte fusion

  18. When Obamacare became law it had many consequences. A very large consequence was the inability of small local physician practices to compete. Consequently, they were largely acquired by larger hospital systems which became ever larger as a consequence. There was a small number(relatively) of small local practices that remained in private hands outside the control of these large hospital systems . This PREP Act waver waives any liability for lawsuits for these small local physicians practices, but only so long as the only treatments employed at these clinics are the “Covered Countermeasure”, ie FDA authorized medications. For Covid this includes the use of monoclonal antibodies and Remdisivir and that is all. They are absolutely commited to letting these people wither with pneumonia til they either self-heal or die. The waiver will not apply for these small practices if Early-Treatment or neutriceticals are prescribed for Covid – recall that since April most of the neutriceuticals that would be beneficial to support Covid patients are available by prescription only.

    Dr. Ardis claims he has evidence that Remdisivir is actually toxic to patients. I have not seen anything to support that claim conclusively, but there has been recent evidence shown from clinical studie that Remdisivir does not reduce Covid deaths but does increase hospital stays – this alone indicates its use should be discontinued.

    The monoclonal antibodies were designed against the early SARS-Cov2 virus, just as the vax was, and I have not seen a study recently to assess its use on the current variants. There was some work done in South Africa in June where it was shown, in an immune suppressed patient, that these antibodies stimulated the generation of multiple variants in the same patient over a 4month period til the patient died. That patient, of course, recieved only the full FDA protocol of treatment of Remdisivir and monoclonal antibodies during that time.

    HHS Amends PREP Act Liability Waiver To Cover Only NIH Approved Treatments for COVID-19
    August 31, 2021 | Sundance | 246 Comments

    There have been some recent reports about hospitals, doctors and health officials now refusing to treat U.S. patients with vitamin D, ivermectin, hydroxychloroquine and another effective therapeutics. A recent notation about HHS changing liability waivers under the PREP Act, might provide some insight.

    “Enacted in December 2005, the PREP Act authorizes the Secretary of HHS (Secretary) to issue a declaration (called a PREP Act declaration) that provides immunity from tort liability (except for willful misconduct) for claims of loss caused, arising out of, relating to, or resulting from administration or use of countermeasures to diseases, threats and conditions determined by the Secretary to constitute a present, or credible risk of a future public health emergency to entities and individuals involved in the development, manufacture, testing, distribution, administration, and use of such countermeasures.” (link)

    A PREP Act declaration is specifically for the purpose of providing immunity from tort liability, and is different from, and not dependent on, other emergency declarations.

    A COVID watchdog group recently noted: “It appears that the Prep Act had been amended such that private hospitals and entities were covered in their actions taken with Covid-19 patients and relieved of all liability as long as they were prescribing ‘Covered Countermeasures’. ie. NIH approved medications. This may be why hospitals are refusing to use effective COVID treatments like vitamin D, ivermectin, hydroxychloroquine, etc” (link)

    Under the HHS Notification, the PREP Act has been modified: “The amended Section VII adds that PREP Act liability protections also extend to Covered Persons for Recommended Activities that are related to any Covered Countermeasure that is:

    licensed, approved, cleared, or authorized by the Food and Drug Administration (FDA) (or that is permitted to be used under an Investigational New Drug Application or an Investigational Device Exemption) under the Federal Food, Drug, and Cosmetic (FD&C) Act or Public Health Service (PHS) Act to treat, diagnose, cure, prevent, mitigate or limit the harm from COVID–19, or the transmission of SARS–CoV–2 or a virus mutating therefrom; (link)

    The attachment of a liability or tort waiver to only cover FDA approved therapeutics likely explains a shift amid the medical community to stop patients treatment due to coverage restrictions on their malpractice insurance. Additionally, Big Pharma -the group who controls NIH- wouldn’t make as much money if their mandatory vaccines had a less costly alternative. So there’s that.

  19. @Adam
    Thanks for sharing that video. I am not sure if you noticed but that was from a Feb. lecture. Info is still relavent of course. They have known about the variants since the vaccine rollout began. This is why Dr. Vander Bosshe was able to make his predictions about the ultimate eventuality of vaccine escape which we are seeing today, as well the immune-cell hijacking, on which we all hope he is not proven correct. Interesting that they found this new variant which is related to a variant not seen since Jan.

    There is another lecture in June which is about 15min. which and the speaker is pretty easily understood. He talks about the vax and the variants. He discribes one patient who was immuno-suppressed and died after 4months of treatments with only Remdesivir and the immunoclonal antibodies. They tracked the progression in this one patient of a series of mutations that took place after each course of the monoclonal antibodies. These antibodies act just as a patient’s own antibodies. The result of these administered antibodies was seen to drive the mutations each time they were administered and they were seen to give rise to a series of evolving variants. This parallels exactly what we spoke of yesterday, as these administered antibodies act exactly as the body’s own immune system’s antibodies.

    Here is his lecture:
    https://academicmedicaleducation.com/meeting/covid-19-vaccine-development-implementation-workshop-2021-june-edition/video/sars-cov-2-0

    One point on these lectures, if you are having trouble understanding them, not a unique issue, turn on the close caption on the control bar at the bottom of the video box. The CC is not always accurate, but it has been for these two speakers, with an occasional screw-up such as ‘titus’ being written instead of ‘titer’ which was spoken. Just FYI.

  20. https://www.youtube.com/watch?v=5Od2bmr-grw&t=133s. This is an important video that I ask everyone to check out. A Ph.D. medical researcher with considerable experience testing vaccines, named Penny Moore, descibes several new variants of of the cv19 virus that have developed in different areas of Africa over the past year that are resistant to the mRNA vaccines. They are also highly contagious, and one, active in South Africa, has a high death rate associeted with it.

    Today’s Jerusalem Post has a story today that reports some of what Dr. Moore says.

    Listening to Dr. Moore is a frustrating experience, because she speaks in a very low voice, fast and in a monotone. Very often I could understand what she was saying as a result. But I unserstood enough to get the main points of her talk.

    Yet another example of the poor communications skills of expert scientists when they attempt to speak to the general public–something they are not used to doing.

  21. Big:

    BREAKING: In a major blow to vaccine efforts, senior FDA leaders stepping down
    Zachary Brennan
    Senior Editor
    Marion Gruber

    Two of the FDA’s most senior vaccine leaders are exiting from their positions, raising fresh questions about the Biden administration and the way that it’s sidelined the FDA.

    Marion Gruber, director of the FDA’s Office of Vaccines Research & Review and 32-year veteran of the agency, will leave at the end of October, and OVRR deputy director Phil Krause, who’s been at FDA for more than a decade, will leave in November. The news, first reported by BioCentury, is a massive blow to confidence in the agency’s ability to regulate vaccines.

    The bombshell announcement comes at a particularly crucial moment, as boosters and children’s shots are being weighed by the regulator. The departures also come as the administration has recently jumped ahead of the FDA’s reviews of booster shots, announcing that they might be available by the week of Sept. 20.

    A former senior FDA leader told Endpoints that they’re departing because they’re frustrated that CDC and their ACIP committee are involved in decisions that they think should be up to the FDA. The former FDAer also said he’s heard they’re upset with CBER director Peter Marks for not insisting that those decisions should be kept inside FDA. What finally did it for them was the White House getting ahead of FDA on booster shots.

    FDA’s former acting chief scientist Luciana Borio added on Twitter, “FDA is losing two giants who helped bring us many safe and effective vaccines over decades of public service.”[FINALLY]

    These two are the leaders for Biologic (vaccine) review in the US. They have a great team, but these two are the true leaders of CBER. A huge global loss if they both leave,” Former BARDA director Rick Bright wrote, weighing in on the news. “Dr. Gruber is much more than the Director. She is a global leader. Visionary mastermind behind global clinical regulatory science for flu, Ebola, Mers, Zika, Sars-cov-2, many others.
    Phil Krause

    Janet Woodcock[FDA Commisioner] told Endpoints that she wishes Gruber and Krause well and thanks them for their significant service.

    You may be unfamiliar with a revolt within the FDA that took place some 20yrs ago, but it was over a drug that was clearly harmful and was not being removed from the market, but rather its use was being expanded. The revolt within the FDA completely upended FDA policy on that drug. This was a critical shift against the current policy with the vax. I really never thought to see this happen.

  22. Molly McCann returns from her sojourn as a law clerk whith a pivotal piece on the Covid “crisis”. I have missed her commentary over the past several months but her ability to capture the essence of a subject has not been dulled by her successful clerkship, it seems.

    Pretending COVID Is An Emergency Is Killing America
    There is no justification for the continued suspension of the American form of self-government that secures all our individual rights and liberties.
    Molly McCann
    By Molly McCann
    August 30, 2021

    The Western world is living a massive COVID lie. That lie is strangling the life out of liberty, and it will destroy our constitutional order if we do not end this horrifying charade.

    A recent article in The Guardian discussing France’s vaccine passport unconsciously provides the perfect example. It describes the Great Plague that struck Marseille in 1720 (the final contortion of the Black Death), noting that it “kill[ed] more than half of the city’s population.”

    “[S]truggl[ing] to find a delicate balance between halting the spread of the disease and damaging vital commerce,” the city authorities, The Guardian tells us, ordered travelers “to carry a ‘bill of health’ and ships arriving at the Mediterranean port underwent a 40-day cordon sanitaire or quarantine.”

    “Three hundred years on,” The Guardian seriously intones, “President Emmanuel Macron is walking an equally tricky tightrope . . .” Hopefully, you spotted the glaring problem with this comparison. In 1720, the Great Plague in Marseille killed more than half the city’s population.

    We have gotten to the point in this “pandemic” where government leaders and a worryingly high percentage of the American people are acting like COVID is a crisis on par with Marseille’s Great Plague. We have been buried in facts, figures, mountains of data, constantly shifting information, misinformation, and more. We are relentlessly briefed by the media about rising infection rates or the current capacity of local ICUs.

    But cut through it all and ask — how many Americans are dying? According to Johns Hopkins, the fatality rate of COVID in the United States is 1.7 percent, which means that 98.3 percent survive. That takes into account all deaths, including people who had underlying conditions and the elderly. Excluding those who are obviously high-risk, the survival rate is close to 100 percent.

    If COVID ever were an emergency, it is no longer one now, and it has not been for a long time. It is a nasty disease, to be sure, but it is one that we are going to have to live with and learn to treat.

    Instead, we have all assumed roles in a live rendition of Hans Christian Andersen’s folktale “The Emperor’s New Clothes.” The government plays the lying emperor, whose hubris resulted in him parading naked in public while declaring he wore clothes. The American people play the silly subjects who disregarded reality to humor the monarch’s farce.[READ THAT AGAIN]

    If we do not say the truth and end this false emergency, we will lose our liberty forever. In March 2020, we foolishly locked down and ceded our constitutional system of government (three independent branches with checks and balances) to rule by the executive. The executives and attendant bureaucrats assumed the powers of the legislature, issuing lockdown orders, mask mandates, and now vaccine passports.

    The end of the article can be read here:
    https://thefederalist.com/2021/08/30/pretending-covid-is-an-emergency-is-killing-america/?fbclid=IwAR0rNYBLuBxvJY3bOxuTxhsNAkmTeDpT5lJs1cajgqxxgKHl0IgpVELK_7k

  23. @Raphael
    It is believed that SARS-Cov2 was actually formulated towards a more lethal outcome to the Asian population given their genetic disposition. The irony is quite unavoidable when we consider that this very treatable plague, that is believed quite plague-like to the Asian populations, has been transformed into a managed plague upon the non-Asian populations, by simply convincing the Westerners in their managed hysteria to forego treatment, and, hence, while create the self-fulfilling prophecy that this plague is really a lethal death-storm. The CCP are not to be trifled with, as they are in a managed position where they are trapped by circumstances of their own making, but quite desperate to change the board upon which they currently stand to lose everything should their public become discounted with their overlords.

  24. Having read this morning that China is working on developing pathogens that specifically target foreigners, while ignoring Chinese, (yes, it’s theoretically possible), one can see why, perhaps, the government is going to such great lengths to validate mRNA vaccines, as a method of rapidly responding to such a bio attack. The possible moves in this chess game are becoming more than can be anticipated by even the best tactician.