Covid-19 News

  • Prof Francois Balloux: ‘The pandemic has created a market for gloom and doom’


    Prof Francois Balloux: ‘The pandemic has created a market for gloom and doom’ | Coronavirus | The Guardian


    Prof Francois Balloux is director of the University College London Genetics Institute. His work focuses on the reconstruction of disease outbreaks and epidemics. With his colleague Dr Lucy van Dorp, he led the first large-scale sequencing project of the Sars-CoV2 genome. During the pandemic, he has become a prominent scientist on Twitter, where he describes himself as a “militant corona centrist”.


    Would you say a new variant of concern is still the major threat to our way out of this pandemic?

    We haven’t had one in a while. The four variants of concern all emerged in the second half of 2020, and it’s important to keep in mind that viruses evolve all the time at a fairly regular pace.

    However, with Alpha, something unexpected happened: there was a sudden accumulation of mutations. One reasonable hypothesis is that Alpha emerged from an infection of an immunocompromised person or someone who was infected for a very long period. The other three variants of concern (Beta, Gamma, Delta) emerged through gradual accumulation of mutations.


    So it’s not always predictable?

    It’s extraordinarily difficult to predict a shock like the Alpha variant. What is easy to predict is that mutations will continue to appear and the virus will progressively drift, with the vaccines becoming less effective over time.

    There was a suggestion in a Sage paper that a very lethal variant could emerge, while other scientists suggest that the virus has reached its “maximum fit”, that if it evolves further it will lose the ability to coexist with its human hosts.

    It’s important to balance the scariness of predictions with their likelihood. The likelihood of a lineage emerging that is 50 times more lethal is extraordinarily implausible. I say that because we have 200 respiratory viruses in circulation and most of us get infected on a regular basis. We’ve never seen that kind of sudden change in mortality. I’m not saying it’s impossible, but you may have a better chance of winning the lottery jackpot many times over.


    Where does the emergence of the alpha and delta variants sit on your jackpot-winning measure?

    That’s such a difficult question. It is somewhat comparable to asking what the chances of someone winning the jackpot are, without having any idea about how many numbers there are on the lottery ticket.


    The Alpha and Delta variants emerged, and they obviously were winning combinations of mutations for the virus – though we also know that no other comparably transmissible viral lineage has emerged so far, despite millions of infections and a constant influx of mutations.



    Another concern is a mutation that enables the virus to “escape” the vaccines…

    Over two million viral samples have been sequenced, and we’ve probably already seen all the mutations that are technically possible. From our observations, we know that vaccine escape will not appear after one or two mutations – it will require an accumulation giving rise to the right combination. We will not go from one day everyone being protected to everyone being vulnerable the next. We will have time to update the vaccines.


    Also, while a vaccine-escape variant would indeed be able to infect vaccinated people far more easily, it would not nullify the protection against severe disease and death provided by the vaccine and prior infection.


    Where do you stand on vaccinating teenagers?

    This is the mother of all questions. There are people who are very passionate on both sides. Given the data available – and not many teenagers have been immunised – I think the JCVI has probably been right to err on the side of caution by first recommending the vaccine for healthy over-18s, and as more data has become available, to healthy over-16s. There is an issue with heart inflammation in younger males administered mRNA vaccines. One possible solution could be to give teenagers only one dose – most of the side-effects have been registered after the second dose. However, a single-dose regime hasn’t been trialled or approved yet.


    You have stated that a “non-trivial” number of long-Covid cases are psychosomatic.

    We know that infections such as Covid lead to post-viral syndromes. At the risk of being insensitive, I would be surprised if there wasn’t a link between disease severity and the severity of follow-up symptoms. Like tuberculosis or influenza, people who have a severe case should expect to take a long time to recover fully. And sometimes recovery is never complete.


    I would like to stress: if you have a serious infection, do not necessarily expect to be back to full fitness in three months

    The situation is more complicated with a mild infection. Post-viral symptoms can happen but it seems relatively implausible to me that this would happen very frequently. In all likelihood, some cases are psychosomatic – though this doesn’t make the suffering less real for those affected or reduce the cost to society. All disease is real, irrespective of its root cause.



    There is a mental component to health and disease. Just the fear of something bad happening to us can make us feel unwell. A remarkable example of this process can be seen in the way over 30% of the people who were enrolled in the control arm of the Pfizer vaccine trial reported headaches and fatigue, despite not being injected with a vaccine.


    You had a bad bout of Covid – does this inform your view?

    I try to discount my own experience when I think about public health issues. That said, I would probably be included as having long Covid because six months later I haven’t fully recovered my sense of smell or taste. I think we need a meaningful definition that captures whether you have regained full fitness. I would like to stress: if you have a serious infection, do not necessarily expect to be back to full fitness in three months.



    Your Twitter bio states you are a “militant corona centrist”. What do you mean by that?

    From the start, the pandemic has been polarising. Some people thought we should “let it rip” or “take it on the chin” and others thought we should fight to eliminate it everywhere. These camps have fought for 16 months and it’s pretty toxic. Both are pretty extreme and unrealistic. I always thought very careful mitigation could keep the pandemic under control until vaccines arrived. A few countries have come close, such as Singapore, Norway and Denmark.


    The scientist is supposed to revise their conclusions as the evidence evolves. Do you feel that scientists on both sides of the debate have been holding on to their views in spite of the evidence?

    It’s self-serving to say “they don’t change their mind, I do” – despite the fact that I didn’t. Our brains work in a Bayesian way – we have priors that influence how we regard new information. As a scientist, it is very important not to have overwhelmingly strong priors – you need to be open to surprise and to let your priors be updated by new data. It’s important to engage with new evidence. Being dogmatic is problematic.


    This issue is amplified when, as now, scientists are talking directly to the public…

    Before the pandemic, scientists were rarely asked anything, or we were listened to in a polite, slightly bored way. But now people are clinging to the words of scientists, which can make it more difficult for them to change their mind. Few scientists have changed their views on Covid but when they do it’s often not well received – there’s an element of groupthink and for more media-savvy scientists, an expectation from their adoring crowd that they’re not meant to do that

    Neil Ferguson has been criticised for his predictions of 100,000 cases a day after the easing of restrictions on 19 July.

    I know Neil, he was my boss for five years. His predictions were quite pessimistic but he tends to be pessimistic – which isn’t a criticism. If you are in a position of authority giving advice to the government you really want to err on the side of caution.



    Can you explain what you mean by “scientific populism”?

    As the pandemic has advanced the mood of the public has become darker and more fearful and this has created a market for gloom and doom. It’s as bad as the effects of the super-optimism at the beginning – stay at home for two weeks, it’s a mild disease or wear a mask and it will be gone. So I kind of captured the market for corona centrism – not to be systematically optimistic or pessimistic and to make it clear there are major uncertainties. And this is empowering, because understanding things is.


    You’ve often stated that the pandemic will be over by mid to late 2021. Do you stand by this?

    Depends on how you quantify it. I would say the pandemic is over when Covid-19 doesn’t cause significantly more mortality than other respiratory viruses in circulation. This will happen first in places such as the UK that have been privileged to get vaccine coverage – I expect at the latest early next year.

  • COVID face masks (blue surgical masks and white cloth masks/man made masks) are largely ineffective and potentially harmful: be careful what we do to our children


    COVID face masks (blue surgical masks and white cloth masks/man made masks) are largely ineffective and potentially harmful: be careful what we do to our children
    Note that views expressed in this opinion article are the writer’s personal views and not necessarily those of TrialSite. Paul Elias Alexander, PhD,
    trialsitenews.com



    Note that views expressed in this opinion article are the writer’s personal views and not necessarily those of TrialSite.


    Paul Elias Alexander, PhD, Howard Tenenbaum, PhD, DDS, Parvez Dara, MD, MBA


    Where do we begin? We begin by stating that masking our children is tragic, unscientific, and very damaging. Our careful prior review suggested that masks do not work! We will revisit this again now with updated evidence below. We are underpinned by the evidence that children do not readily acquire SARS-CoV-2 (very low risk) including the Delta variant, do not readily spread it to other children or teachers, or endanger parents or others at home. This is the settled science globally and for over one year now. There is no reason to believe it will be otherwise for the Delta variant and we have looked and have found no evidence to suggest otherwise. In the rare cases where a child contracts Covid virus it is very unusual for the child to get severely ill or die. Masking can do positive harm to children – as it can to some adults. But the cost benefit analysis is entirely different for adults and children – particularly younger children. Whatever arguments there may be for consenting adults – children should not be required to wear masks to prevent the spread of Covid-19. Of course, zero risk is not attainable – with or without masks, vaccines, therapeutics, distancing or anything else medicine may develop or government agencies may impose.


    The mask has become so very politicized that it prevents rational consideration of the evidence (even across political lines) and drives levels of acrimony, invidious actions, disdain, and villainy among wearers to each other who feel threatened by the individual who will not or cannot wear a mask.


    Look at the insanity in August 2021 where the US government is again discussing COVID-19 lockdowns and imposing face mask mandates, especially on our children. This illogical, irrational, and unscientific, and an absurd nonsensical renewed push to mask our children when the World Health Organization is on record stating that masks in children under 5 years old is not warranted, “Children aged 5 years and under should not be required to wear masks. This is based on the safety and overall interest of the child…”. “The WHO admitted to the BBC that its June 2020 mask policy update was due not to new evidence but “political lobbying”: “We had been told by various sources WHO committee reviewing the evidence had not backed masks but they recommended them due to political lobbying. This point was put to WHO who did not deny.” (D. Cohen, BBC Medical Correspondent)”.


    How did we arrive at the confusion and misinformation surrounding mask use which is our focus, yet by extension, the crushing societal lockdowns and harmful school closures? There are serious harms and downsides due to these crushing restrictive policies and we understand that one would think reflexively if there is a pathogen, we should just lock and shut everything down and away. We understand this initial instinct. But the evidence quickly accumulated in spring and summer 2020 that showed that the polices were all flawed and failed. That they were killing people and not helping. That they shifted the morbidity and mortality burden on the poorer in society, to persons least able to afford them. That they benefitted the ‘laptop café latte’ class.


    There are benefits and risks to any action and the harms of these lockdowns and school closures (and masking) far outweighed the benefits based on what has transpired. We even knew this soon after implementing lockdowns yet we continued catastrophic policies and are still continuing (and planning to re-engage). How did we get here societally? How have our government bureaucratic leaders failed so disastrously? We lay heavy blame on our government leaders but argue that the so-called ‘medical experts’ who are part of Covid Task Forces and guidance panels have been largely unscientific, illogical, and irrational in their guidance and statements.


    Untethered from the reality of things. In many instances these Task Forces and medical experts have been just flat out misleading and wrong! The incessant campaign by the media (especially on this infectious but non-lethal Delta variant) that has worked to drive fear, panic, and hysteria in the public is also partly to blame. There appears to be an unholy alliance between the government bureaucrats, the aforementioned ‘medical experts,’ and a willing print and digital media. A vast lot of what these experts say on Covid makes no sense anymore, at times unhinged and lacking of any credibility. In such incredibly important Covid-related input and guidance, these television medical experts and many government leaders have failed in profound and often unimaginable ways and we are left asking how they got things so very wrong. Is it that these medical experts do not read the science or data? Or maybe cannot understand the data or science? Which? Are they blinded to it by politics? By their own biases? They, these specious medical experts on television and in our governments, talk about following the science but seem blinded to it. They clearly don’t follow the science else we would not be here. They seem to not understand the evidence and the devastation that they have visited upon the lives of so many (and are preparing to revisit again).


    We continue to confront highly irrational, punitive, capricious, and groundless societal restrictions for a virus with an infection fatality rate (IFR), based on Stanford University John Ioannidis’s calculations, of 0.05% in persons under 70 years old (across different global nations). Ioannidis’s research was followed up recently by a reported non-institutionalized IFR in the state of Indiana (persons aged > 12 years) of 0.12% (95% CI 0.09 to 0.19) when age 40-59/60 years (reported in the Annals of Internal Medicine), and an IFR when < 40 years old of 0.01% (95% CI 0.01 to 0.02). Persons 60 or older had an IFR of 1.71% (overall IFR was 0.26%). So why would we and did we continue this way with these unsound and very punitive restrictive policies and for so long once the factual characteristics of this virus became evident and as alluded to above, we finally realized that its infection fatality rate (IFR) which is a more accurate and realistic reflection of mortality than CFR, was really no worse than annual influenza? Why this now insane unsound push to lockdown and re-mask?


    Where is the evidence by these scientific experts that masks work? We say they have none and this Delta variant (and others) are and will be used to continue the baseless fear mongering within the society, and mainly now to drive persons to vaccinate (especially our children) with an untested vaccine that remains investigational and experimental. Where the safety testing was not done, and we are being asked to submit our children to this risk, where there is no opportunity for benefit but only opportunity for harms for our children. No one, not one prior Trump administration official nor current Biden administration official can point to any evidence that warrants children being subjected to these vaccines. None. And this is frightening given children may be set up for a life-time of possible disability and ill effect given we do not know the long-term effects of the vaccines because the vaccine developers did not study this. This last sentence is an incredible one if you ponder it carefully! That we would put out a vaccine that was not safety tested!


    We argue that the messaging by the media and medical experts initially suggested that all persons are of equal risk of severe illness from Covid infection. This is where it all went wrong and where societies were greatly deceived by those who should not have done that. We were never ‘all’ at equal risk. This was deeply flawed and has crippled the US and global nations since day one of this pandemic. This messaging continues today with the push to scare the population into vaccinating. This was and remains a flat-out falsehood (untrue) and it has driven irrational fear by the public. This clearly erroneous intimation has stuck in the minds of the public and severely impacted the public’s perception of their risk and how they would move forward. This falsehood along with the falsehood on the prominence of asymptomatic spread as a driver of the infection and re-current infection being extensive. These are very rare occurrences if any, yet if you listened to the television medical experts, you would take your teddy bear and go hide under your mother’s bed for the next 25 years. They have subverted science by their unscientific messages. This caused irrational fear and hysteria and it has held on. This type of deception and the resulting unfounded fear has been driven by the media despite “a thousandfold difference in risk between old and young.”


    The use of face masks is our focus in this op-ed. What is the current best evidence (comparative effectiveness research and any type of higher-quality reporting) and what does it tell us about face masks and especially for our children in terms of harms? There are potentially catastrophic harms due to mask use (references 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33). A recent study report published in JAMA indicated that wearing a mask can expose children to very dangerous levels of carbon dioxide in 3 minutes. We are seeking clarification for this study may have been retracted due to the current political and biased research publication era we are operating in. We will update as needed. The sum total of the evidence, even if we torture it and say it is ‘neutral’, states conclusively that masks do not work in this COVID emergency and will not work for the Delta variant etc. At least how they have been used and the type of masks that have been used. Certainly, this does not apply to a properly fitted seal tested N95 mask in the proper environment and with other protective equipment. Masks based on the evidence, are ineffective and a waste of time in stopping transmission or curbing deaths. We thus provide the ineffectiveness of masks based on references 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42. We also know of the failure of mask mandates (references 1, 2, 3, 4, 5, 6, 7, 8). While the recent report by Blazemedia shreds the Delta variant narrative of it being a lethal variant etc., it actually showcases that masks do not work given India has among the highest mask use globally yet is/was ineffective against the Delta variant. These masks do not work and something other than science is at play in terms of the prior catastrophically failed lockdowns, school closures, and masking!


    As an example, a particularly important seminal research study by the CDC published in Emerging Infectious Diseases (EID) in May 2020 and looking at nonpharmaceutical measures for pandemic influenza in nonhealthcare settings (personal protective and environmental measures using 10 RCTs), found that use of masks did not reduce the rate of laboratory-proven infections with the respiratory influenza virus. “In pooled analysis, we found no significant reduction in influenza transmission with the use of face masks”.


    Similarly, a strong argument against the use of masks in the current Covid-19 pandemic gained traction when a recent CDC case-control study reported that well over 80% of cases always or often wore masks. This CDC study further called into question the utility of masks in the Covid-19 emergency. This CDC study showed that the majority of persons infected wore face masks, and still got infected.


    Again, even if we tried to tease out ‘minimal help’ and say that ‘they may help a little,’ these COVID-19 masks are largely ineffective. As an example, a very recent publication stated that face masks become nonconsequential and do not function after 20 minutes due to saturation. “Those masks are only effective so long as they are dry,” said Professor Yvonne Cossart of the Department of Infectious Diseases at the University of Sydney.” As soon as they become saturated with the moisture in your breath, they stop doing their job and pass on the droplets.” In a similar light, there are indications that wearing a mask that has already been used, which is very common as we tend to reuse our masks, is riskier than if one wore no mask at all.


    What can we say about the harms? We are limited by space but we wish to raise some key issues. We have also published on harms elsewhere. During April to October 2020 in the US, emergency room visits linked to mental health problems (e.g. anxiety) for children aged 5-11 increased by nearly 25% and increased by 31% for those aged 12-17 years old as compared to the same period in 2019. During the month of June 2020, 25% of persons aged 18 to 24 in the US reported suicidal ideation. While some of this may be related to the pandemic, we suspect that it is largely a function of our response to the pandemic. Child suicides have escalated in the US due to the lockdowns and school closures.


    One of the most starkly revealing and troubling observations come from Dr. Margarite Griesz-Brisson MD, PhD, who is one of Europe’s leading neurologists and neurophysiologists focused on neurotoxicology, environmental medicine, neuro-regeneration and neuroplasticity. She has gone on record stating: “The rebreathing of our exhaled air will without a doubt create oxygen deficiency and a flooding of carbon dioxide. We know that the human brain is very sensitive to oxygen deprivation.” There are neurons, for example in the hippocampus that cannot survive more than 3 minutes without an adequate supply of oxygen. Given that such cells are so sensitive to oxygen deprivation, their functionality must be affected by low oxygen levels.


    Oxygen deprivation can cause metabolic changes and the metabolic changes that happen in neuronal cells are vitally important for cognitive functioning and brain plasticity and it is known that when drastic metabolic shifts occur in the brain, there are consequent changes of oxidative stress (cellular oxidative state) and these have a significant role in managing neuron functioning (we do not claim that masking would produce complete absence of oxygen of course).


    The acute warning symptoms are headaches, drowsiness, dizziness, reduced ability to concentrate and reductions in cognitive function. Given that the development of neurodegenerative diseases can take years to develop, then what are the potentially deleterious effects of the use of masks, especially in children, when masks are used over the majority of their day? We and particularly parents, must consider this and weigh the benefits versus the harms. Are there benefits enough to warrant use relative to the potential harms? If the harms outweigh the benefits, then we cannot in good conscience advocate for mask use. Moreover, the continual and stressful impacts of masking (and school closures) will also have a known and deleterious impact on the immune systems in children (and adults).


    Other medical harms relate to the notion that children and adolescents have an extremely active and adaptive immune system, a robust developing immune system that must be challenged in order to retain functionality. Yet by severely restricting children’s activities because of lockdowns and masking (physical activity/fitness exercises are almost impossible whilst wearing a mask), we are probably hobbling their immune systems. We may be setting our children up for future ‘excess’ morbidity due to these societal restrictions by weakening their immune systems. Evidence indicates that regular physical activity and frequent exercise enhance immune competency and regulation.


    A child unexposed to nature has little defense against a minor illness, which can become overwhelming due to the lack of a primed ‘tuned-up’ and ‘taxed’ immune system. A robust immune system shortens an illness as a consequence of the presence of preprogrammed anamnestic immunity. Preventing children from such interactions with nature and germs can and does lead to overwhelming infections and serious consequences to the health and life of a child. We might be setting up our children for future disaster when they emerge from societal restrictions fully and with no masks, to then be at the mercy of normally benign opportunistic infections with a now weakened immune system. This cannot be disregarded as we consider the consequences of our actions today in this pandemic and the questionable lockdowns, school closures, and mask policies.


    A German-wide registry (not the optimal highest-quality study) used by 20,353 parents who reported on data from almost 26,000 children, found that the “average wearing time of the mask was 270 minutes per day. Impairments caused by wearing the mask were reported by 68% of the parents. These included irritability (60%), headache (53%), difficulty concentrating (50%), less happiness (49%), reluctance to go to school/kindergarten (44%), malaise (42%) impaired learning (38%) and drowsiness or fatigue (37%).”


    Concerns are being raised regarding psychological damage and why a mask is not ‘just a mask.’ There is tremendous psychological damage to infants and children, with potential catastrophic impacts on the cognitive development of children. This is even more critical in relation to children with special needs or those within the autism spectrum who need to be able to recognize facial expressions as part of their ongoing development. The accumulating evidence also suggests that prolonged mask use in children or adults can cause harms, so much so that Dr. Blaylock states “the bottom line is that [if] you are not sick, you should not wear a mask.” Furthermore, Dr. Blaylock writes, “By wearing a mask, the exhaled viruses will not be able to escape and will concentrate in the nasal passages, enter the olfactory nerves and travel into the brain.”


    In sum, as mentioned, the optimal comparative research on harms has not sufficiently accumulated but what has been reported is sufficient to inform and guide us in our debate on the potential harms of mask use (surgical and cloth), especially in children. But we do have real-world evidence. While additional evidence will help clarify the extent of risk, the existing details are sobering enough and of tremendous utility as we consider the benefits versus the harms of mask use. Even the potential of minimal harm is enough to prevent justification of such use.


    The public remains confused by the all of the mask messaging from senior medical experts across the US, and up to today, August 7th 2021, with the renewed push to mask in light of the non-lethal Delta variant. This can be exemplified by comments made by Dr. Anthony Fauci very early on in the pandemic (March 2020) as part of his Covid-19 Task Force role when he stated categorically that (para), “wearing a mask might make people feel a little bit better” but “it’s not providing the perfect protection that people think it is.” Then and now, he actually echoed the current scientific consensus and this was in line with the World Health Organization’s guidance.


    The guidance coming from experts was confusing at best and downright unscientific and flawed at worst. Interestingly, this type of advice (also given by others including Canada’s Chief Medical Officer, Dr. Theresa Tam), was changed (initially dismissive of mask use) under the notion that in fact the experts were intentionally saying these things so as to prevent runs on surgical masks that were in short supply at the time and needed by healthcare workers. We put forward the notion that this is not the case and that in fact at that time, the experts actually were relying on available data as alluded to above. All this is to say that such changes in advice provided by top medical experts only served to confuse a public desperately in need of honesty and optimal guidance.


    In relation to the above we point out that the World Health Organization (WHO) stated that “the widespread use of masks by healthy people in the community setting is not yet supported by high quality or direct scientific evidence and there are potential benefits and harms to consider.”


    We argue strongly against the masking of our children especially as they prepare to re-enter school, as it is ineffective and can be potentially very harmful. I/we challenge any prior Task Force member or medical expert (Trump administration) or current Task Force member (Biden administration), to provide for us, the evidence that masks and mandates work and are effective in curbing transmission or deaths, and that they are not harmful. We have searched long and hard and cannot find any such evidence.


    Orofecal transmission?

    Understanding the transmission of this respiratory SARS-CoV-2 pathogen is also evolving given evidence of orofecal spread as having a potentially larger contributor role in non-respiratory transmission of Covid. As an example, a recent open-evidence review brief by Oxford researchers (Jefferson, Brassey, Heneghan) and its publication in CEBM, reveals the growing recognition that SARS-CoV-2 can infect and be shed from the gastrointestinal (GI) tract of humans. Orofecal spread demands urgent study and if orofecal spread is shown to be definitive and more consequential in Covid transmission, then this could (could have) impacted mitigation strategies beyond those for respiratory transmission. Is there a stronger role for orofecal spread? We remain at a loss as to why this orofecal route of transmission was not focused on initially or at the least, conjointly.


    Let us close with some key points we wish to raise that could guide your thinking and decision-making, even in light of the Delta variant:


    i) No governments must ever be allowed ‘emergency powers’ alike how they were for this pandemic; this was not an emergency as it was made to be


    ii) Initial false narrative painted by governments, their COVID Task Force advisors, and television medical experts that all of population was at equal risk of severe outcomes and/or death if infected; forced to stick to the narrative but this remains the rate limiting step that has damaged responding and keeps populations scared and panicked


    iii) COVID-19 did not kill all age-groups equally and remains focused on elderly persons with medical conditions; younger persons with medical conditions, and obese persons, as well as diabetics


    iv) Life expectancy is about 79-80 years and average age of death from COVID is 82 years so it kills persons beyond their life expectancy


    v) In December 2020, 35% of Americans believed that half of the people with COVID-19 required hospitalization. The correct figure was 1%-5%.


    vi) As a result of mistaken prognostications like this, the media compared COVID-19 to the 1918 influenza pandemic, for which the average age of death was 28. For COVID-19 the average age of death is 73, and about half of all deaths are in people 80 or older.


    vii) While the CDC projected a one-year decrease in life expectancy for the U.S. population, the overall decrease in life expectancy was only five days, and the U.S.’s excess mortality in 2017 was greater than its excess mortality in 2020.


    viii) We knew very early on that COVID-19 was very amenable to risk-stratification, age being the strongest determinant of mortality


    ix) Your outcome depends on your baseline risk; baseline risks were strong determinants for mortality, even more than age


    x) Obesity emerged as a major risk ‘super-loaded’ factor for mortality with age; we knew quickly those <50, no risks, would be very fine; public service message should have been the daily norm


    xi) We argue that it is best to ignore the CDC, as of this writing June 2021, more than one-half Americans (more than 150 million) already immune naturally (from natural exposure)


    xii) We knew early on that those persons under the age of 50, 55 or so, with no underlying illness, would do very well if infected


    xiii) Initially, 60-80% and greater of persons had T-cells (immunity) reactive to SARS-CoV-2 virus; large parts of populations were immune to COVID virus from day one


    xiv) We have strong evidence that survivors of the 1918 flu pandemic retained immunity; near 100 years, a lifetime


    xv) Health services/hospitals did not collapse and this falsehood is being used again to scare you to vaccinate


    xvi) We argue that we may have been able to handle this pandemic without these vaccines, via the use of early drug treatment (multi-drug sequenced combination protocols with ivermectin, hydroxychloroquine and other anti-virals along with zinc and immune-modulatory anti-inflammatory corticosteroids to tame the hyper dysregulated ARDS florid pneumonia phase, and anti-platelet anti-thrombotic drugs to handle micro thrombi in this vascular COVID illness etc.), natural immunity (COVID recovered and prior cross-reactive cross-protection), public service messaging on Vitamin D and C, and strong protections of the elderly high-risk persons that were always neglected. Along with this, we should have allowed the low-risk, healthy, well in society to face the pathogen and develop immunity naturally and harmlessly. Vaccines were not needed for this pathogen and disease if management of the response was not a political one and stayed within the confines of a public health one.

  • CDC’s Walensky on Record that Vaccines Don’t Stop SARS-CoV-2 Transmission While Other Societies Show An Alternative Pathway


    CDC's Walensky on Record that Vaccines Don’t Stop SARS-CoV-2 Transmission While Other Societies Show An Alternative Pathway
    Although the inhibition of transmission in pursuit of herd immunity was a fundamental premise underlying the COVID-19 vaccine program, the reality,
    trialsitenews.com


    Although the inhibition of transmission in pursuit of herd immunity was a fundamental premise underlying the COVID-19 vaccine program, the reality, according to CDC Director Rochelle Walensky, is very different from that. That’s right; the vaccine doesn’t stop the vaccinated from becoming vectors or transmitters themselves. A core foundational question emerges: are the vaccines instrumental as a matter of public health or more of a personal preference? This discussion unfolded on Friday as CNN’s Wolf Blitzer interviewed the CDC director Walensky who declared that although, of course, the vaccines were protecting people from more severe illness “…But what they can’t do anymore is prevent transmission.” This was very different from Walensky’s position back in March, when she made the claim that vaccinated people would nearly never get infected, of course now an obviously false statement. How could she make such claims back then? There was no actual scientific proof for such a declaration. Back then Walensky declared, “Our data from the CDC suggest that vaccinated people do not carry the virus.” Of course, this was completely wrong.


    Health Passport Advocate

    By late July, the CDC director emphasized the importance of vaccine passports as a means to transition out of the pandemic crisis. Looking to Europe and their “health passes,” Walensky coveted the European models as a path forward.


    But what is the CDC not telling us? Take India, where low-cost generic drugs such as ivermectin were used in states like Uttar Pradesh to turn around the Delta-driven pandemic completely. India’s low vaccination rate (about 8% of the population is fully vaccinated) and low fatality rate plummeted without any COVID-19 vaccines. Instead, ivermectin and other treatments were used yet completely suppressed by global health agencies, such as the World Health Organization (WHO) and the mainstream media.


    Now, in India, according to recent Reuters reports, nearly 70% of the population of India produce SARS-CoV-2 antibodies, again contributing to lower fatality rates and transmission. While the COVID-19 vaccines were touted as the key to transcending the pandemic, they will more than likely become nothing more than equivalent to annual flu shots.


    (this article was updated to correct inaccuracies identified in the comments)

  • We argue that the messaging by the media and medical experts initially suggested that all persons are of equal risk of severe illness from Covid infection. This is where it all went wrong and where societies were greatly deceived by those who should not have done that. We were never ‘all’ at equal risk. This was deeply flawed and has crippled the US and global nations since day one of this pandemic. This messaging continues today with the push to scare the population into vaccinating.

    Debunked vaccine terrorist claims:


    If you vaccinate then:


    - You protect others. Complete rubbish you may be become the ideal super spreader. Best fully vaccinated spreader so far known caused 70 infections. Delta infects vaccinated and unvaccinated (CDC,Israel) with same magnitude.

    - You help society. NO, best case you help yourself, worst case you damage yourself and thus the society.

    - All need the vaccine. Wrong up to 80% of the population have T-cell protection from classic corona. Mortality, damage risk among healthy and younger is larger from the vaccine than from COV-19...

    - Vaccines are safe! tells this the > 100'000 vaccine deaths and even a larger number of permanently crippled.

    - Vaccines are tested. No this never happened in a proper way. Only very few tests have been done.

    - Vaccines are the only way to immunity: NO - see Uttar Pradesh. Natural infection protects at least 7x better than a vaccine and is far longer lasting.

    - Phase III study did show high protection. Wrong. E.g. the Pfizer data was highly fudged (>200 early infections kicked out) and even 95% ( 3 months) would mean 80% over one year what is the best case we know from today's data.

    - Wearing masks: Makes no sense. Is good for worrying people and setting up a panic mind. All masks up to FP2 offer only marginal (5..20%) protection. You must start with a FP95 (FP3) at least.

    - We have no drugs to fight CoV-19: Lie! True: Big pharma has no expensive drugs that work. But Ivermectin 1'000'000'000 Indian folks did take it, Budenoside (Austria 5000+), HCQ + combo all did work very well with far less damage than vaccines.


    Vaccines can be a solution for people with many comorbidity. For people that without will show a fast increase in severe symptoms. People that have no access to working anti viral drugs. People that live alone or want/must live a risky way.


    But no vaccine protects you from an infection.

  • But no vaccine protects you from an infection.

    Last night running/walking our dog along the shores of Lake Ontario, I came across someone in the near dark who was also walking his dog. As we approached I recognized him, and he cautioned that I should not get too close, as he suspected he had Covid. (His symptoms apparently checked all the right boxes.) He wasn't wearing a mask, but then he wasn't expecting to be bumping into an acquaintance like me in the middle of nowhere at night. He said that although he was double vaxxed he was really feeling the effects of covid. We got to talking and he shared that he was an academic, a professor at a university outside of Toronto. He was discouraged about the attitudes of many of his fellow academics, the elitism, the 'rules are made for the masses, not for us' type of attitude. Very humble and down to earth fellow, who is being crushed by a combination of elitism and wokeness at the university. Although we had briefly chatted before, this was all new to me, and I felt for the guy. Anyway, we walked about twenty minutes back to our homes together chatting, as he lives about two blocks away from me. I made sure I was a little ahead of him as we walked together, to lessen any virus dosage I might receive. So I probably got a little booster shot last night.

    Just a little something to brighten Jed and THH's day.

  • Has Delta mutated to become more deadly to overweight, diabetic children in the US? Something seems to be happening here, that is not happening in the UK:


    Why so many children in America are in hospital with Covid
    Children's hospitals in Alabama, Arkansas, Louisiana and Florida have all reported more under-18s with Covid-related conditions in their care than at any other…
    www.dailymail.co.uk


    -Children's hospitals in Alabama, Arkansas, Louisiana and Florida have all reported more under-18s with Covid-related conditions in their care than at any other point in the pandemic.


    -Most were said to be suffering from pneumonia or paediatric inflammatory multisystem syndrome, or PIMS, a rare complication of Covid that affects only children


    -In Arkansas, just 38 per cent of the population is fully vaccinated. In Louisiana it is 37 per cent, and levels are similarly low in many areas of Florida – and these are areas where kids are worst hit.


    -Dr Rochelle Walensky, director of the Centers for Disease Control, dubbed the outbreaks a 'pandemic of the unvaccinated'. She said: 'We are seeing outbreaks of cases in parts of the country that have low vaccination coverage because unvaccinated people are at risk.'


    -As children with PIMS in the UK are promptly treated, our death rate is roughly 0.2 per cent. In America, between two and three per cent of youngsters with it die.

  • Most were said to be suffering from pneumonia or paediatric inflammatory multisystem syndrome, or PIMS

    How many vaccines did these kid already get before >20 >30? May be antibody enhancement factors play a role. Next problem. Where do the children live? Playing outdoors, in own room or together with a super spreader in the same room.

    Overweight from high carb diet leads to insulin resistance and then diabetes liver problems. Going fat from burgers (meat, vegi) is not the big problem.


    Ivermectin works very well for kids, but you cannot expect that the over all world ranked 34? US health care system can afford such expensive drugs....

  • Last night running/walking our dog along the shores of Lake Ontario, I came across someone in the near dark who was also walking his dog. As we approached I recognized him, and he cautioned that I should not get too close, as he suspected he had Covid. (His symptoms apparently checked all the right boxes.) He wasn't wearing a mask, but then he wasn't expecting to be bumping into an acquaintance like me in the middle of nowhere at night. He said that although he was double vaxxed he was really feeling the effects of covid. We got to talking and he shared that he was an academic, a professor at a university outside of Toronto. He was discouraged about the attitudes of many of his fellow academics, the elitism, the 'rules are made for the masses, not for us' type of attitude. Very humble and down to earth fellow, who is being crushed by a combination of elitism and wokeness at the university. Although we had briefly chatted before, this was all new to me, and I felt for the guy. Anyway, we walked about twenty minutes back to our homes together chatting, as he lives about two blocks away from me. I made sure I was a little ahead of him as we walked together, to lessen any virus dosage I might receive. So I probably got a little booster shot last night.

    Just a little something to brighten Jed and THH's day.

    Maybe you can expand on if he was in the sciences, and what he meant by "rules are for the masses"? Did he mean they didnt want to play ball with the One Gov dictates from WHO?

  • How many vaccines did these kid already get before >20 >30? May be antibody enhancement factors play a role. Next problem. Where do the children live? Playing outdoors, in own room or together with a super spreader in the same room.

    Overweight from high carb diet leads to insulin resistance and then diabetes liver problems. Going fat from burgers (meat, vegi) is not the big problem.


    Ivermectin works very well for kids, but you cannot expect that the over all world ranked 34? US health care system can afford such expensive drugs....

    Whatever the reason these kids are suddenly vulnerable, IMO these new developments are changing the benefit/risk analyses to favor vaccinating the younger people who are obese, or have some of the other underlying health issues.


    This virus has shown incredible adaptation and looks to be with us for a long time to come, so perhaps it is time to be realistic and accept vaccines as part of the arsenal to combat it?


    I believe, as do you, that had Iver+ been included in the US Standard of Care, it would have helped these kids avoid hospitalization, but after being so thoroughly stigmatized, it's being accepted here in the US is not going to happen anytime soon. Maybe in time, after the countries which embraced it, or one of the THH approved RCT's, show beyond doubt it's efficacy, it will be adopted here. Until then, the only option is the vaccine.

  • Do as we say, not as we do. Masks for thee, but not for me. This is just one of many examples:


    https://www.dailymail.co.uk/ne…irthday-brunch-Oprah.html

    Shane, you are old enough now to understand how the world works. Obama and the political middle men are are right behind the police and military (strong man) - they know that the true elite (guy with the dark suit) - will let them get away with hypocracy and establish confusion so that the middle class cheers for them or gets angry at them in a constant psychodrama to take away your energy. You and me are the guys with the loaf of bread - we get by.


    The people on this board promoting vaccines? They are in minor cults created by the dark suited guy. They don't know they are in a cult, that's how programmed they can be.


    I didn't draw this, the dark suited guys drew this.


    I leave it to you to figure out who announces with revelry the coming of the dark suited guy (his plans for you are what is announced - "His arrival" not his presence at your dinner table haha -- like The Great Reset or Build Back Better


  • Maybe you can expand on if he was in the sciences, and what he meant by "rules are for the masses"? Did he mean they didnt want to play ball with the One Gov dictates from WHO?

    He didn't say outright, and I didn't ask. I gathered however it was related to the social sciences, probably political science, cultural studies and history. The guy I would say was approaching 50.

    He spoke of his academic peers generally as elitist and arrogant, that they saw themselves as qualified to craft the rules which everyone else should follow for their own good because they didn't know any better. He said outright that universities like his were the epicentres of wokeness (such as identity politics and cancel culture), and that it was like a cult. Discussion or even clarification of certain issues was forbidden, off limits, and those who suggested having a conversation - say, about race issues - was suspected of being racist and then cancelled in one way or another. The pressure to fall in line is enormous. Nuance is lost to a type of dogmatism. It's a new kind of fundamentalism.


    I asked if he was familiar with Brett Weinstein and Jordan Peterson, other academics who have faced such things. He certainly was, and was pleased that I knew about them.


    So it wasn't about the WHO dictates, it was about what is coming out of our universities, a far greater threat than a virus.


    Speaking of the WHO, as beholden to special interests as they may be, the WHO actually had and has a more conservative approach in its pandemic recommendations, akin to Sweden. But a global network of 'health' administrators have decided to go far beyond what the WHO would recommend, inspired by China. I'm talking about things like lockdowns and isolation of the healthy. For your viewing (dis)pleasure


    Sydney, Australia: Police Helicopter Reminds Citizens to Only Exercise with 2 People
    Sydney, Australia: Police Helicopter Reminds Citizens to Only Exercise with 2 People. Strict lockdowns have occured in Australia despite 0 covid deaths in 7…
    rumble.com

  • Norway System of Patient Injury Compensation Authorizes First COVID-19 Vaccine Damages Claims


    Norway System of Patient Injury Compensation Authorizes First COVID-19 Vaccine Damages Claims
    The Scandinavian nation of Norway has a special compensation program associated with the nationwide COVID-19 mass vaccination program.  Known as the
    trialsitenews.com


    The Scandinavian nation of Norway has a special compensation program associated with the nationwide COVID-19 mass vaccination program. Known as the Norwegian System of Patient Injury Compensation (NPE) this organization has identified three cases approved for compensation due to serious adverse events or death. Involving two female health care workers and a male—all in their 30s—two of the individuals have long lasting adverse events while one of the women died. A total of 77 people in Norway have made claims that are now under consideration by the NPE for compensation. A majority of the incidents are associated with the AstraZeneca vaccine, originally developed at University of Oxford and known as ChAdOx1 nCoV-19. Much hope was associated with this vaccine as it’s properties and price point has made it easier to distribute around the world, especially to low-and-middle-income countries (LMICs). The investigational vaccine candidate ran into delays during clinical trials due to adverse events and in fact the studies in the United States never led to emergency use authorization (EUA). The use of this vaccine in several Northern European countries, including those in Scandinavia were put on hold due to some reported safety incidents. Other incidents here involved the mRNA-based vaccines from Pfizer-BioNTech (BNT162b2) and Moderna (mRNA-1273).


    TrialSite provides a brief breakdown of this situation for the global community. The NPE reminded the reader that that nation had halted the national vaccination program’s use of the AstraZeneca vaccine due to a number of serious adverse events.


    The Most Common COVID-19 Vaccine Side Effects

    The NPE reports that the most common side effects associated with the COVID-19 vaccines include dizziness, fatigue, headache, and pain. But others reported bleeding stomach ulcers, cramps, rashes, spasms, paralysis, anaphylactic reaction, blood clots and decreased platelet count.


    NPE reminds us that all vaccines carry some risk, some more than others. In the overwhelming number of cases most side effects associated with COVID-19 vaccines are mild and dissipate shortly. These majority cases are precluded from the NPE compensation program.


    Norwegian Assessment

    Importantly assessments of COVID-19 vaccine safety such as this effort out of Norway isn’t covered by mainstream press, considered an off subject matter as it’s perceived any negative news can impact vaccination programs. The COVID-19 vaccines are still experimental as they are making their way through the regulatory approval process in various countries. They are for the most part safe and effective but there have been incidents given the total volumes associated with mass vaccination.


    Transparency and full disclosure are vital for not only adhering to ethics and legal principles, but also as a matter of empowerment for healthcare consumers to fully understand the risks and benefits associated with specific COVID-19-related products.


    Norway’s NPE went on the record on Friday August 6 that the AstraZeneca vaccine triggered a series of “Serious side effects” at least in some recipients. An advanced economy with sophisticated health system, Norway investigated the matters thoroughly, involving one of the nation’s top academic medical centers called Oslo University Hospital Rikshospitalet (Rikshospitalet). Specifically Rikshospitalet conducted sophisticated analyses into the special immune reactions observed in association with the AstraZeneca vaccinations. Due to these findings NPE’s director Rolf Gunnar Jørstad, went on the record that the organization would “uphold the applicants” moving on now to calculating the damages for compensation. That is the reimbursement for the financial loss and damage associated with the events. For deaths the NPE compensates as well for funerals and loss of income.


    The First Claimants’ Experience

    A couple of female health workers were hospitalized back in March immediately after vaccination with severe blood clots and reduced platelet counts. One of these women died a few weeks after the incident while a man still battles with major side effects associated with the vaccine. The male declared “I was admitted with great pains. It was frightening to follow the news about others who had just died from the same vaccine I had received.”


    The surviving women declared “I had a severe cerebral hemorrhage and a blood clot. At the hospital, I received many calls from friends and family wondering if I was still alive.”


    All three of the claimants were in their 30s. The two surviving claimants still cannot work. Thus the first three claimants, two survivors and the relatives of the deceased woman will receive compensation for vaccine injuries.


    77 Claimants

    The NPE reported that the government organization has received 77 applications for compensation for COVID-19 vaccine-related adverse effects. 53 of the 77 received the AstraZeneca vaccine, eleven received the Pfizer-BioNTech vaccine known as BNT162b2 and six received Moderna’s mRNA-1273. NPE declares there are still seven cases where it’s unclear which vaccine was used.


    Eight of these Norwegian individuals died from the jabs. The deaths can be broken down to four deceased from the AstraZeneca vaccine, one from mRNA-1273 and two from BNT162b2 with two unresolved deaths—that is, it’s not known for certain which vaccine is associated with the event.


    According to NPE’s director Jørstad the organization has confirmed absolute causality with one of the eight deaths and now are probing for causation with the other seven deaths.


    Norway COVID-19 & Vaccination Updates

    Norway experienced a few waves during the COVID-19 pandemic, now entering what is its fourth wave. The Nordic nation of about 5.5 million inhabitants has recorded approximately 140,466 total SARS-CoV-2 cases with 804 deaths. Most recently the Delta variant triggered this present wave, starting in late July and into August the average number of daily cases, based on the seven-day mean, has gone up to 406 new cases per day. Few deaths have occurred since the spring but they do occur from time to time.


    About 35.5% of Norway’s population is fully vaccinated while nearly 70% of the population has received at least one jab.


    Since earlier this summer breakthrough cases, that is fully vaccinated people getting infected with SARS-CoV-2 has become more common. One prominent early breakthrough cluster of cases was reported on in early July when 450 fully vaccinated people were infected with the coronavirus. According to local public health research here, such as Norwegian Institute of Public Health chief physician Sara Viksmoen Watle, such incidents still represent low probability events. While others there emphasize that at least one in ten of the vaccinated will fall to infection. The good news: few infections progress to serious levels. But disease progression does happen in the vaccinated. Out of the 450 breakthrough cases reported, 21 of the infected were hospitalized. In those cases it most often involves the elderly, that is those over 75.

  • Whatever the reason these kids are suddenly vulnerable, IMO these new developments are changing the benefit/risk analyses to favor vaccinating the younger people who are obese, or have some of the other underlying health issues.

    I agree that for the US situation (obese kids short from diabetes II) a vacciantion is a good option albeit it will kill/disable 100x more kids than PIMS if the RNA gen therapy is used. Best would be to take take a vector vaccine = Sinovac. But as said the ranked 34 health system with a clear agenda to kill patients for money...

  • I agree that for the US situation (obese kids short from diabetes II) a vacciantion is a good option albeit it will kill/disable 100x more kids than PIMS if the RNA gen therapy is used. Best would be to take take a vector vaccine = Sinovac. But as said the ranked 34 health system with a clear agenda to kill patients for money...

    Why is it so hard to give a Kid ivermectin. Or monoclonal antibodies. I think you guys forget, the danger is not the corona it is the spike in the corona. You can read 10,20,30,40 pages of refutation by the Towne Criers but it won't change the simple fact. The toxin is the spike protein.

  • He spoke of his academic peers generally as elitist and arrogant, that they saw themselves as qualified to craft the rules which everyone else should follow for their own good because they didn't know any better. He said outright that universities like his were the epicentres of wokeness (such as identity politics and cancel culture), and that it was like a cult. Discussion or even clarification of certain issues was forbidden, off limits, and those who suggested having a conversation - say, about race issues - was suspected of being racist and then cancelled in one way or another. The pressure to fall in line is enormous. Nuance is lost to a type of dogmatism. It's a new kind of fundamentalism.


    I asked if he was familiar with Brett Weinstein and Jordan Peterson, other academics who have faced such things. He certainly was, and was pleased that I knew about them.

    Universities, like other places, have many different people, some good, some bad. Wokeness is an idea at the epicentre of political culture wars - I can see you are an activist here on the anti-wokeness side. The university departments I know (admittedly STEM) are no more woke than any other place. University students everywhere do seem to have some weird ideas (including wokeness) as well as good noble ideas. When has it been other?


    I've never really understood what wokeness is. I try to make sense of it and:


    (1) When somone with known very extreme views on an issue wants to come to a Uni to promote them - what do you do? Personally, I'd want that person to come if they want, but in circumstances where they got very strong refutation. It is not easy to mange that - such people are often good demagogues and countering a rabble-rousing and poisonous speech with voices of reason can be difficult. Leaving such uncountered seems wrong. So this is "maybe don't invite neo-Nazis or Stalinists just because you want to seem on the side of free-speech ideology". Unfortunately students are idiots and sometimes invite such people not realising the full horror. Would I want to de-platform in that case? probably not - it would send the wrong message. But it would be a real headache and I'd rather such people were not invited unless I had really good speakers willing and ready to take them on.


    (2) Safe spaces. I've never empathised with this, or understood it. I can see having a loathsome creep speaking in a Uni cafeteria while everyone else has to be there would be very wrong. I can't see a well-advertised meeting for a speaker putting points of view that are non-violent in a closed hall is a problem.


    (3) But personally, when somone here says things that are dangerous and false, like the anti-vax stuff, I just feel I should correct the most obvious falsities and correct the record. It does not damage me emotionally. Whereas i know there are many people in the world not like me where false words can hurt them. What compassion do we have for such people, and how much should it affect what we say, or invite others to say? I am on the fence here, partly because I feel I'm not really qualified to see both sides of the issue. My instincts are - let people say what they want - if they say hurtful things point out how problematic that is for some people.


    (4) identity wars. I try not to engage in these though I'm aware many young people think differently. That would include in the type of activism which is "my identity requires me to buy and carry large anti-personnel weapons, because this is my inalienable right".


    Getting back on topic. When somone argues strongly that other people should do something that will possibly damage them, saying that this is harmless, and appearing to be an expert - or quoting experts, and appearing convincing, what do you do?

  • Heavily Vaccinated & Masked Hawaii’s Pandemic the Worse Ever as Conventional Wisdom Out the Window


    Heavily Vaccinated & Masked Hawaii’s Pandemic the Worse Ever as Conventional Wisdom Out the Window
    Hawaii shouldn't be here given conventional wisdom promulgated from the U.S. Centers for Disease Control and Prevention (CDC), the National Institutes of
    trialsitenews.com


    Hawaii shouldn’t be here given conventional wisdom promulgated from the U.S. Centers for Disease Control and Prevention (CDC), the National Institutes of Health (NIH) and other federal health-related agencies. Why? Hawaii follows strict masking mandates and is heavily vaccinated with at least 54% of the state’s population fully vaccinated and approximately 70% of the state’s 1.4 million receiving at least one dose of either Pfizer-BioNTech, Moderna or the Johnson and Johnson COVID-19 vaccine. Yet the State is now experiencing the worst stage of the COVID-19 pandemic since the onset of the entire crisis over a year-and-a-half ago. New cases by Thursday August 5 the state experienced an all time record of 655 new cases and by August 7th another 600 were recorded. The good news is deaths are incredibly low confirming that the Delta’s variant’s transmissibility is muted by its far lower mortality rate. But the premise that heavily vaccinated societies are the key to non-disease transmission have been shattered by the Delta variant and waning vaccine strength, perhaps or other data not discovered as of yet. Is the COVID-19 pandemic merely “a pandemic of the unvaccinated” heard endlessly on liberal to centrist media platforms and POTUS administrators?


    More than likely not as the situation in Hawaii evidence not only the Delta variant’s strength and ability to trigger breakthrough infections, that is the infection of vaccinated persons, but also penetrate the fortress defense of mask mandates, social distancing, and other measures. TrialSite confirms that those who are vaccinated are less likely to experience a severe illness but again the fundamental premise of mass vaccination programs was to eradicate the pathogen, via first and foremost stopping transmission.


    That paradigm of course has shifted and the NIH, CDC and others aren’t looking that deeply into the mirror to acknowledge that much of their assumptions were off. Rather they double down on whatever the most pressing and relevant contextual messaging of the day is, e.g. you will not get as sick.


    Hawaii, a beautiful paradise in many ways with sound pandemic policies, is having a very tough time with a growth in infections per capita that beats nearly every other state. The state’s test-positive rate grew to its highest at 6.9% according to the health department as reported recently by MSN.


    Yes, the mainstream media will continue to pound on the fact that the unvaccinated will get hospitalized more than those vaccinated (and they are correct) yet will they question the fundamental underlying premise of the global push for SARS-CoV-2 eradication?


    That mass vaccination is the only answer? Could that be the case in the short run? Probably not given a number of assumptions that would all have to come together worldwide for that to become true.


    That’s because unless the entire world can A) access safe and effective vaccines in a timely manner (a faulty assumption given the nature and structure of world markets, health inequity, corruption, etc.); B) that people unilaterally are forced to receive the vaccines; C) that the vaccines don’t in fact contribute to variant evolution as some studies may suggest; and D) that continuous morphing won’t make vaccines less effective—as can be seen with the Delta variant.


    Breakthrough infections show that vaccinated individuals can transmit the pathogen with ease challenging the conventional wisdom basis for argument as is obvious in Hawaii.


    Based on this point of view the argument that everyone around the world simply needs to get vaccinated is in reality a far over-simplified, theoretical exercise rather than a pragmatic global public health policy. Hence global and national health authorities must be more creative, offering not only safe and effective vaccines but also early onset treatment, options for people to isolate and not lose out economically and take other sound measures to avoid ongoing global pandemic contagion, while better ensuring growing numbers of economically challenged people don’t sink further. That latter situation will lead to even more polarized and extreme politics.

  • Long-term perturbation of the peripheral immune system months after SARS-CoV-2 infection


    Long-term perturbation of the peripheral immune system months after SARS-CoV-2 infection
    Increasing evidence suggests immune dysregulation in individuals recovering from SARS- CoV-2 infection. We have undertaken an integrated analysis of immune…
    www.medrxiv.org


    Abstract

    Increasing evidence suggests immune dysregulation in individuals recovering from SARS- CoV-2 infection. We have undertaken an integrated analysis of immune responses at a transcriptional, cellular, and serological level at 12, 16, and 24 weeks post-infection (wpi) in 69 individuals recovering from mild, moderate, severe, or critical COVID-19. Anti-Spike and anti-RBD IgG responses were largely stable up to 24wpi and correlated with disease severity. Deep immunophenotyping revealed significant differences in multiple innate (NK cells, LD neutrophils, CXCR3+ monocytes) and adaptive immune populations (T helper, T follicular helper and regulatory T cells) in COVID-19 convalescents compared to healthy controls, which were most strongly evident at 12 and 16wpi. RNA sequencing suggested ongoing immune and metabolic dysregulation in convalescents months after infection. Variation in the rate of recovery from infection at a cellular and transcriptional level may explain the persistence of symptoms associated with long COVID in some individuals.


    Discussion

    Recovery from SARS-CoV-2 infection is frequently associated with persistent symptoms months after infection including fatigue, muscle weakness, sleep impairment and anxiety or depression (4, 5, 45). These data suggest ongoing immune dysregulation in COVID-19 convalescents which has been supported by several recent studies profiling the immune system in individuals recovering from COVID-19 using multi-parameter flow cytometry, bulk and single-cell transcriptomics, and other approaches (15, 16, 46–49). Our study extends on these recently published studies, which have mostly assessed immune responses at 2-12 weeks post-infection. Here, we report an integrated analysis of immune responses at a transcriptional, cellular and serological level, in individuals recovering from mild/moderate or severe/critical COVID-19 at 12, 16, and 24 weeks post-infection, in comparison to age- matched HCs.


    Anti-Spike and anti-RBD serology data demonstrated heterogeneity of antibody responses to SARS-CoV-2 consistent with previously published reports showing long-lasting IgG and IgG1 antibody responses to at least 6 months post-infection which were correlated with disease severity (23, 50, 51). Our cohort is particularly well-suited to the assessment of the durability of antibody responses due to the negligible risks of re-infection in South Australia where, due to strict border restrictions and public health measures, community transmission was eliminated during the sample collection period. Despite the anticipated decay in IgA and IgM (52–54) a large percentage of convalescents remained seropositive for both RBD- and Spike-specific Ig (all isotypes) for the duration of the study. This decay was less pronounced at 24 wpi in the severe COVID-19 convalescents compared to the mild cohort, with significant differences in RBD-specific IgM and IgG3 isotypes between the two groups. Recently, declining levels of SARS-CoV-2 Spike-specific IgM in mild COVID-19 convalescents were found to strongly correlate with serum virus neutralisation activity (55), findings that were further confirmed in experiments with purified IgM fractions and IgM- depleted sera from similar patients (27, 56). In COVID-19 convalescents, IgM, similarly to IgG1, preferentially targets the S1 domain of the Spike protein (57), the region that contains the RBD and N-terminus domains and the target of most neutralising antibodies and regions of high interest for developing passive immunotherapies to deal with new SARS-CoV-2 variants of concern (58). Conversely, less abundant SARS-CoV-2-specific IgG3, targets the S2 domain more efficiently (57), which suggests that its ability to neutralise the virus is, by comparison, reduced. Yet, S2 contains the sequences that allow SARS-CoV-2 membrane fusion with the cell host membrane, a key step in virus entry (2). In fact, the ability of antibodies targeting S2 regions involved in membrane fusion to block Spike protein-mediated cell-cell fusion has been confirmed experimentally (59). In the future it will be necessary to elucidate the particular roles of IgM and IgG3 in neutralising SARS-CoV-2 but, perhaps too, blocking virus infection by other mechanisms such as blockade of membrane fusogenic regions of the Spike protein. This will provide further insights into the overall importance of specific Ig isotypes in determining disease severity and outcomes.


    In addition to our serological analysis of COVID-19 convalescents, we extensively and longitudinally profiled immune cell populations in the same individuals using a multi-panel approach that enabled the identification and enumeration of ∼130 different sub-populations including deep phenotyping of the CD4 and CD8 compartments. Differences in immune cell populations compared with HCs were most strongly evident at 12 wpi, but some populations were still significantly different at 24 wpi. CD56++ NK cells, granulocytes, LD neutrophils and tissue-homing CXCR3+ monocytes were significantly increased in convalescents at 12 wpi. Many of these changes persisted until at least 16 or 24 weeks. Consistent with our data, increased NK cells (46) and granulocytes (49) have been reported in other cohorts of convalescents and scRNAseq has revealed that increased non-classical monocytes are associated with more severe disease during active infection (60). In contrast to our study, a study of 109 Austrian convalescents at 10 weeks post-infection, did not find neutrophils, monocytes, CD3+ T cells, CD56+ NK cells or CD19+ B cells to be significantly different in convalescents (49). Other studies have also reported significant decreases in the frequencies of invariant NKT and NKT-like cells (47), which we and others (20) did not observe.


    Several previous studies have reported that T and B cell activation/exhaustion markers remain elevated following SARS-CoV-2 infection (15). Furthermore, CD4+ and CD8+ EM T cells have been reported to be significantly higher in convalescents at 10 wpi (49). Consistent with reports in active infection and convalescence (15), convalescent individuals in our study had lymphopenia until at least 16 wpi, however, CD3+ T cells were significantly increased at 12 wpi. We also observed significantly increased CD19+ B cells at 12 and 16 wpi and CD38+CD27+ memory B cells at 16 wpi in convalescents. Recent studies have shown that increased activation and exhaustion of memory B cells observed during COVID-19 correlates with CD4+ T cell functions (61), and consistent with this we observed reduced CD4+ EM cell proportions in COVID-19 convalescents at 12 wpi. We were particularly interested in the role of regulatory T cells (Tregs) in COVID-19, as there have been conflicting reports of Tregs being either increased or decreased in convalescents. Significantly increased Foxp3+ Tregs were observed in 49 convalescents from Wuhan at ∼112 days post-recovery (47), however, another study observed that CD25+Foxp3+ Tregs were significantly reduced 10 weeks after COVID-19 (49). We observed no significant difference in the total (CD4+CD25+CD127low) Treg pool at any timepoint, but when we interrogated Tregs for their memory/maturation status, we observed that the naïve and TEMRA Treg compartment was significantly expanded at 12 and 16 wpi, while EM and CM Tregs were significantly reduced, mirroring a similar reduction in the proportion of CD4+ EM and CM pools at 12 and 16 wpi.


    Interestingly, a number of the Th lineage subsets including Th2, Th22, Th2/22, and Th17 had an increased proportions of CM vs EM, revealing subtle skewing of the Th memory formation. The expansion of naïve Tregs could be an attempt to restore the balance in the Treg pool in the face of both inflammation and tissue damage, which is supported by emerging evidence of a dual role for Tregs in supressing immune responses and promoting tissue repair (62). Increased TEMRA Tregs, which are often associated with exhaustion, but are in fact a poly-functional effector Treg population with characteristics of cytotoxic cells, migratory T cells and tissue repair cells (63, 64), further suggest a competition between classical immune suppression and tissue repair by these cells in response to tissue damage in COVID-19 convalescents.


    Each Th subset has a paired regulatory subset (28), and this includes Tfh subsets, as B cell help in germinal centres also requires regulation in the steady state (65). In a stereotypical antiviral immune response, Th1 cells migrate to sites of viral infection to establish an adaptive response, and regulatory cells co-migrate to limit chronic inflammation once the pathogen levels decline, however, there is an emerging function of tissue resident Treg cells in tissue repair (62, 66). We did not observe increased Th1 cells, but we did observe a reduction of Th9 cells, which are believed to home to the gut mucosa (67), potentially suggesting a diversion of Th cells to other sites. We also observed that the maturation of Th pools was enhanced in both Th17 and Th22 subsets, where CM marker proportions were increased at all timepoints post-infection. This may suggest that epithelial homing and tissue damage trigger activation and form part of the COVID-19 T cell recall response. It is intriguing that the Treg partners of these lineages, including ThR2, ThR22 and ThR2/22 were all significantly reduced over the same time course post-infection, suggesting that the signal recruiting Th cells to tissue locations are persistent long after COVID infection. A similar imbalance in follicular help vs follicular regulation was also observed, whereby Tfh1 and Tfh2/22 cells were significantly elevated post COVID-19, but total TfhR, TfhR2, TfhR22 and TfhR2/22 cells were reduced. Other studies have demonstrated that CXCR5+ Tfh populations are significantly elevated in individuals recovering from COVID-19 and correlate with robust humoral immunity (68), however this previous study did not analyse the regulatory arm in this compartment. Another previous study has reported a decline in Tfh cells at 4 months post-infection (53).


    In addition to immunophenotyping by flow cytometry, we performed RNA sequencing of total RNA from 138 blood samples collected from convalescent individuals at 12, 16 and 24 wpi, as well as HCs. To our knowledge, no other study has profiled transcriptome-wide changes in COVID-19 convalescents for such a long period post-infection. We found that the blood transcriptome of convalescents was significantly perturbed compared to HCs, with the largest numbers of DEGs being identified at 12 wpi. Transcriptional dysregulation persisted until at least 24 weeks. There was a very strong enrichment for pathways and BTMs related to transcription, translation, and ribosome biosynthesis among genes up-regulated in recovering individuals, at all 3 timepoints. Many viruses upregulate rRNA synthesis during infection [42, 43], but why rRNA gene expression remains up-regulated months after infection is currently unknown. Other statistically enriched pathways among up-regulated genes included neutrophil degranulation, antimicrobial peptides, immune system and pathways related to other viral infections. These data suggest ongoing inflammatory responses and immune dysregulation in COVID-19 convalescents weeks-to-months after infection. Consistent with these data, neutrophil degranulation has reported to be significantly up-regulated in active infection (69, 70), suggesting that certain signatures of active infection persist well into convalescence.


    We also found evidence for dysregulated expression of genes involved in oxidative phosphorylation, a signature which has also been identified in one other recent study of convalescents to occur irrespective of whether elevated inflammatory markers persist or not (20), but whose functional significance is currently unknown. While some changes in gene expression were associated with variation in specific immune cell populations between individuals, differences in gene expression were not solely explained by changes in the frequency of any single immune cell population. A patient-specific analysis of the gene expression activity of pre-annotated BTMs enabled a more thorough assessment of the variation in gene expression responses. There was a broad spectrum in the recovery of gene expression responses in both mild/moderate and severe/critical convalescents. Variation in the rate of recovery from infection at a cellular and transcriptional level may explain the persistence of symptoms, such as fatigue, associated with long COVID in some convalescent individuals, although data related to ongoing symptoms was unfortunately not collected for this cohort. Interestingly, a link between gene expression in peripheral blood and fatigue following infectious mononucleosis has been previously reported (71), with at least some of the same genes differentially expressed in COVID-19 convalescents. These data may point towards common mechanisms regulating ‘long COVID’ and post-viral infection fatigue more generally. Finally, we also uncovered significant inverse correlations between dysregulated BTMs and anti-Spike and anti-RBD antibody responses suggesting that prolonged transcriptional dysregulation may be associated with reduced antibody responses with potential consequences for the durability of protective immunity. Further work is now needed to assess whether dysregulated immunity following COVID-19 has implications for responses to other infections, vaccination or in the management of chronic diseases.

  • Worse than the disease? Reviewing some possible unintended consequences of mRNA vaccines against Covid-19

    There has been considerable chatter on the Internet about the possibility of vaccinated people causing disease in unvaccinated people nearby. While this may seem hard to believe, there is a plausible process by which it could occur


    Worse than the disease? Reviewing some possible unintended consequences of mRNA vaccines against Covid-19 | The Rio Times
    While the promises of mRNA technology have been widely heralded, the objectively assessed risks and safety concerns have received far less detailed attention.
    riotimesonline.com


    RIO DE JANEIRO, BRAZIL – No, this article will not be an easy read for you. We apologize. Reviewing a scientific study is always a challenge. However, if you are interested and concerned about Covid-19 vaccination, we recommend that you try to read it anyway. It might be worth the effort.


    While the promises of mRNA technology have been widely heralded, the objectively assessed risks and safety concerns have received far less detailed attention.


    Stephanie Seneff and Greg Nigh from the Computer Science and Artificial Intelligence Laboratoryof MIT intended to review several highly concerning aspects of infectious disease-related mRNA technology and correlate these with both documented and potential pathological effects.

    The development of mRNA vaccines against infectious diseases is unprecedented in many ways.


    In a 2018 publication sponsored by the Bill and Melinda Gates Foundation, vaccines were divided into three categories: Simple, Complex, and Unprecedented. Simple and Complex vaccines represented standard and modified applications of existing vaccine technologies.


    Unprecedented represents a category of a vaccine against a disease for which there has never before been a suitable vaccine.


    Read also: Deaths occurring after Covid-19 vaccinations have become hot topic in the U.S.


    In sum, an unprecedented vaccine was predicted to have a 2% probability of success at the stage of Phase III clinical trial. As the authors bluntly put it, there is a “low probability of success, especially for unprecedented vaccines.”


    With that in mind, two years later, we have an unprecedented vaccine with reports of 90-95% efficacy. In fact, these reports of efficacy are the primary motivation behind public support of vaccination adoption (U.S. Department of Health and Human Services, 2020).


    This defies not only predictions but also expectations. There are indeed reasons to believe that estimations of efficacy need re-evaluation.


    Others have brought up important additional questions regarding Covid-19 vaccine development, questions with direct relevance to the mRNA vaccines reviewed here. For example, Haidere, et al. (2021) identify four “critical questions” related to the development of these vaccines, questions that are germane to both their safety and their efficacy:


    • Will Vaccines Stimulate the Immune Response?

    • Will Vaccines Provide Sustainable Immune Endurance?

    • How Will SARS-CoV-2 Mutate?

    • Are We Prepared for Vaccine Backfires?


    The media has generated a great deal of excitement about this revolutionary technology. However, there are also concerns that we may not realize the complexity of the body’s potential for reactions to foreign mRNA and other ingredients in these vaccines that go far beyond the simple goal of tricking the body into producing antibodies to the spike protein.

    The Pfizer/BioNTech and Moderna mRNA vaccines are based on similar technologies encoding the spike protein. This process has now been commoditized, so it’s relatively straightforward to obtain a DNA molecule from a specification of the sequence of nucleotides.


    Moderna executives have a grand vision of extending the technology for many applications where the body can be directed to produce therapeutic proteins not just for antibody production but also to treat genetic diseases and cancer, among others.


    They are developing a generic platform where DNA is the storage element, messenger RNA is the “software,” and the RNA’s proteins represent diverse application domains.


    The vision is grandiose, and the theoretical potential applications are vast (Moderna, 2020). The technology is impressive, but manipulation of the code of life could lead to completely unanticipated negative effects, potentially long-term or even permanent.

    ACTIVATION OF LATENT HERPES ZOSTER


    An observational study conducted at Tel Aviv Medical Center and the Carmel Medical Center in Haifa, Israel, found a significantly increased herpes zoster incidence following the Pfizer vaccination.


    This observational study monitored patients with pre-existing autoimmune inflammatory rheumatic diseases (AIIRD). Among the 491 patients with AIIRD over the study period, 6 (1.2%) were diagnosed with herpes zoster as a first-ever diagnosis between 2 days and 2 weeks after the first or second vaccination. In the control group of 99 patients, there were no herpes zoster cases identified.


    The CDC’s VAERS database, queried on April 19, 2021, contains 278 reports of herpes zoster following either the Moderna or Pfizer vaccinations. Given the documented under-reporting to VAERS and the associational nature of VAERS reports, it is impossible to prove any causal link between the vaccinations and the zoster reports. However, the authors of the study believe the occurrence of zoster is another important ‘signal’ in VAERS.


    Multiple studies have shown that patients with primary or acquired immune deficiency are more susceptible to severe herpes zoster infection. This suggests that the mRNA vaccines may be suppressing the innate immune response.


    SPIKE PROTEIN TOXICITY


    The picture is now emerging that SARS-CoV-2 has serious effects on the vasculature (arrangement and distribution of blood vessels) in multiple organs, including the brain.


    In a series of papers, Yuichiro Suzuki, in collaboration with other authors, presented a strong argument that the spike protein by itself can cause a signaling response in the vasculature with potentially widespread consequences. These authors observed that, in severe cases of Covid-19, SARS-CoV-2 causes significant morphological changes to the pulmonary vasculature.


    STROKE


    They speculated that these effects would not be restricted to the lung vasculature. The signaling cascade triggered in the heart vasculature would cause coronary artery disease, and activation in the brain could lead to stroke.


    Systemic hypertension would also be predicted. They hypothesized that this ability of the spike protein to promote pulmonary arterial hypertension could predispose patients who recover from SARS-CoV-2 to develop right ventricular heart failure later.


    Furthermore, they suggested that a similar effect could happen in response to the mRNA vaccines, and they warned of potential long-term consequences to both children and adults who received Covid-19 vaccines based on the spike protein.


    In an in vitro study of the blood-brain barrier, the S1 component of the spike protein promoted loss of barrier integrity, suggesting that the spike protein acting alone triggers a pro-inflammatory response in brain endothelial cells, which could explain the neurological consequences of the disease.


    The implications of this observation are disturbing because the mRNA vaccines induce a synthesis of the spike protein, which could theoretically act in a similar way to harm the brain.

    A POSSIBLE LINK TO PRION DISEASES AND NEURODEGENERATION


    Prion diseases are a collection of neurodegenerative diseases induced by the misfolding of important bodily proteins, which form toxic oligomers that eventually precipitate out as fibrils causing widespread damage to neurons.


    The best-known prion disease is MADCOW disease, which became an epidemic in European cattle beginning in the 1980s. The CDC website on prion diseases states that “prion diseases are usually rapidly progressive and always fatal.” (Centers for Disease Control and Prevention, 2018).


    A paper published by J. Bart Classen (2021) proposed that the spike protein in the mRNA vaccines could cause prion-like diseases through its ability to bind to many known proteins and induce their misfolding into potential prions. Idrees and Kumar (2021) have proposed that the spike protein’s S1 component is prone to act as functional amyloid and form toxic aggregates.


    1. LESSONS FROM PARKINSON’S DISEASE


    There are many parallels between α-synuclein and the spike protein, suggesting prion-like disease following vaccination. The authors have already shown that the mRNA in the vaccine ends up in high concentrations in the liver and spleen, two organs that are well connected to the vagus nerve.


    The cationic lipids in the vaccine create an acidic pH conducive to misfolding, and they also induce a strong inflammatory response, another predisposing condition.


    However, this also means that mRNA vaccines induce an ideal situation for prion formation from the spike protein and its transport via exosomes along the vagus nerve to the brain.

    Studies have shown that prion spread from one animal to another first appears in the lymphoid tissues, particularly the spleen. Differentiated follicular dendritic cells are central to the process as they accumulate misfolded prion proteins (Al-Dybiat et al., 2019).


    An inflammatory response upregulates the synthesis of α-synuclein in these dendritic cells, increasing the risk of prion formation.


    2. VACCINE SHEDDING


    There has been considerable chatter on the Internet about the possibility of vaccinated people causing disease in unvaccinated people nearby.


    Contrary to what is stated on many so-called knowledge databases on the internet, study authors Stephanie Seneff and Greg Nigh of MIT’s Computer Science and Artificial Intelligence Laboratory, say that ‘vaccine shedding’ is not mere misinformation from so-called anti-vaccine activists, but a real possibility that should not be disregarded.


    While this may seem hard to believe, there is a plausible process by which it could occur by releasing exosomes from dendritic cells in the spleen containing misfolded spike proteins, in complex with other prion reconfirmed proteins.


    A Phase 1/2/3 study undertaken by BioNTech on the Pfizer mRNA vaccine implied in their study protocol that they anticipated the possibility of secondary exposure to the vaccine (BioNTech, 2020).


    They even suggested two levels of indirect exposure: “A male family member or healthcare provider who has been exposed to the study intervention by inhalation or skin contact then exposes his female partner before or around the time of conception.”


    3. EMERGENCE OF NOVEL VARIANTS


    An interesting hypothesis has been proposed in a paper published in Nature, which described a case of serious Covid-19 disease in a cancer patient who was taking immune-suppressing cancer chemotherapy drugs.


    The patient survived for 101 days after admission to the hospital, finally succumbing in the battle against the virus. The patient constantly shed viruses over the entire 101 days, and therefore he was moved to a negative-pressure high air-change infectious disease isolation room to prevent contagious spread.


    During the course of the hospital stay, the patient was treated with Remdesivir and subsequently with two rounds of antibody-containing plasma taken from individuals who had recovered from Covid-19 (convalescent plasma).


    It was only after the plasma treatments that the virus began to mutate rapidly, and a dominant new strain eventually emerged, verified from samples taken from the nose and throat of the patient.


    An in-vitro experiment demonstrated that this mutant strain had reduced sensitivity to multiple units of convalescent plasma taken from several recovered patients. The authors proposed that the administered antibodies had actually accelerated the mutation rate in the virus because the patient was unable to clear the virus due to their weak immune response fully.


    There are at least two concerns that the authors have regarding this experiment in relation to the mRNA vaccines. The first is that, via continued infection of immune-compromised patients, one can expect continued emergence of more novel strains that are resistant to the antibodies induced by the vaccine, such that the vaccine may quickly become obsolete.

    The vaccine was only 2/3 more effective against the South African strain than against the original strain (Liu et al., 2021).


    The second more ominous consideration is to ponder what will happen with an immune-compromised patient following vaccination. It is conceivable that they will respond to the vaccine by producing antibodies, but those antibodies will be unable to contain the disease following exposure to Covid-19.


    CONCLUSION


    Experimental mRNA vaccines have been heralded as having the potential for great benefits, but they also harbor the possibility of potentially tragic and even catastrophic unforeseen consequences. The mRNA vaccines against SARS-CoV-2 have been implemented with great fanfare, but many aspects of their widespread utilization merit concern.


    The authors of the study have reviewed some, but not all, of those concerns here, and they want to emphasize that these concerns are potentially serious and might not be evident for years or even transgenerationally.


    To rule out the adverse potentialities described in this paper, they recommend, at a minimum, that the following research and surveillance practices be adopted:


    A national effort to collect detailed data on adverse events associated with the mRNA vaccines with abundant funding allocation tracked well beyond the first couple of weeks

    after vaccination.

    Repeated autoantibody testing of the vaccine-recipient population. The autoantibodies tested could be standardized and based upon previously documented antibodies and

    autoantibodies potentially elicited by the spike protein.

    Immunological profiling related to cytokine balance and related biological effects. Tests

    should include, at a minimum, IL-6, INF-α, D-dimer, fibrinogen, and C-reactive protein.

    Studies comparing populations who were vaccinated with the mRNA vaccines and those

    who did not confirm the expected decreased infection rate and milder symptoms of the vaccinated group, while at the same time comparing the rates of various autoimmune diseases and prion diseases in the same two populations.

    Studies to assess whether an unvaccinated person can acquire vaccine-specific

    forms of the spike proteins from a vaccinated person nearby.

    In vitro studies to assess whether the mRNA nanoparticles can be taken up by sperm and converted into cDNA plasmids.

    Animal studies to determine whether vaccination shortly before conception can result in

    offspring carrying spike-protein-encoding plasmids in their tissues, possibly integrated into their genome.

    In vitro studies aimed to better understand the toxicity of the spike protein to the brain,

    heart, testes, etc.

    The authors conclude that public policy around mass vaccination has generally proceeded on the assumption that the risk/benefit ratio for the novel mRNA vaccines is a “slam dunk.” With the massive vaccination campaign well underway in response to the declared international emergency of Covid-19, we have rushed into vaccine experiments on a worldwide scale.


    At the very least, societies, countries, and rulers should take advantage of the data that are available from these experiments to learn more about this new and previously untested technology. And, in the future, they so urge governments to proceed with more caution in the face of new biotechnologies.


    Source: International Journal of vaccine theory practice and research, May 2021


    Stephanie Seneff and Greg Nigh – Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge MA, 02139, USA, E-mail: [email protected]

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