The WHO Pandemic Agreement: A Guide By David Bell, Thi Thuy Van Dinh March 22, 2024 Government, Society 30 minute read The World Health Organization (WHO) and its 194 Member States have been engaged for over two years in the development of two ‘instruments’ or agreements with the intent of radically changing the way pandemics and other health emergencies are managed. One, consisting of draft amendments to the existing International health Regulations (IHR), seeks to change the current IHR non-binding recommendations into requirements or binding recommendations, by having countries “undertake” to implement those given by the WHO in future declared health emergencies. It covers all ‘public health emergencies of international concern’ (PHEIC), with a single person, the WHO Director-General (DG) determining what a PHEIC is, where it extends, and when it ends. It specifies mandated vaccines, border closures, and other directives understood as lockdowns among the requirements the DG can impose. It is discussed further elsewhere and still under negotiation in Geneva. A second document, previously known as the (draft) Pandemic Treaty, then Pandemic Accord, and more recently the Pandemic Agreement, seeks to specify governance, supply chains, and various other interventions aimed at preventing, preparing for, and responding to, pandemics (pandemic prevention, preparedness and response – PPPR). It is currently being negotiated by the Intergovernmental Negotiating Body (INB). Both texts will be subject to a vote at the May 2024 World Health Assembly (WHA) in Geneva, Switzerland. These votes are intended, by those promoting these projects, to bring governance of future multi-country healthcare emergencies (or threats thereof) under the WHO umbrella. The latest version of the draft Pandemic Agreement (here forth the ‘Agreement’) was released on 7th March 2024. However, it is still being negotiated by various committees comprising representatives of Member States and other interested entities. It has been through multiple iterations over two years, and looks like it. With the teeth of the pandemic response proposals in the IHR, the Agreement looks increasingly irrelevant, or at least unsure of its purpose, picking up bits and pieces in a half-hearted way that the IHR amendments do not, or cannot, include. However, as discussed below, it is far from irrelevant. Historical Perspective These aim to increase the centralization of decision-making within the WHO as the “directing and coordinating authority.” This terminology comes from the WHO’s 1946 Constitution, developed in the aftermath of the Second World War as the world faced the outcomes of European fascism and the similar approaches widely imposed through colonialist regimes. The WHO would support emerging countries, with rapidly expanding and poorly resourced populations struggling under high disease burdens, and coordinate some areas of international support as these sovereign countries requested it. The emphasis of action was on coordinating rather than directing. In the 80 years prior to the WHO’s existence, international public health had grown within a more directive mindset, with a series of meetings by colonial and slave-owning powers from 1851 to manage pandemics, culminating in the inauguration of the Office Internationale d’Hygiene Publique in Paris in 1907, and later the League of Nations Health Office. World powers imposed health dictates on those less powerful, in other parts of the world and increasingly on their own population through the eugenics movement and similar approaches. Public health would direct, for the greater good, as a tool of those who wish to direct the lives of others. The WHO, governed by the WHA, was to be very different. Newly independent States and their former colonial masters were ostensibly on an equal footing within the WHA (one country – one vote), and the WHO’s work overall was to be an example of how human rights could dominate the way society works. The model for international public health, as exemplified in the Declaration of Alma Ata in 1978, was to be horizontal rather than vertical, with communities and countries in the driving seat. With the evolution of the WHO in recent decades from a core funding model (countries give money, the WHO decides under the WHA guidance how to spend it) to a model based on specified funding (funders, both public and increasingly private, instruct the WHO on how to spend it), the WHO has inevitably changed to become a public-private partnership required to serve the interests of funders rather than populations. As most funding comes from a few countries with major Pharma industrial bases, or private investors and corporations in the same industry, the WHO has been required to emphasize the use of pharmaceuticals and downplay evidence and knowledge where these clash (if it wants to keep all its staff funded). It is helpful to view the draft Agreement, and the IHR amendments, in this context. Why May 2024? The WHO, together with the World Bank, G20, and other institutions have been emphasizing the urgency of putting the new pandemic instruments in place earnestly, before the ‘next pandemic.’ This is based on claims that the world was unprepared for Covid-19, and that the economic and health harm would be somehow avoidable if we had these agreements in place. They emphasize, contrary to evidence that Covid-19 virus (SARS-CoV-2) origins involve laboratory manipulation, that the main threats we face are natural, and that these are increasing exponentially and present an “existential” threat to humanity. The data on which the WHO, the World Bank, and G20 base these claims demonstrates the contrary, with reported natural outbreaks having increased as detection technologies have developed, but reducing in mortality rate, and in numbers, over the past 10 to 20 years.. A paper cited by the World Bank to justify urgency and quoted as suggesting a 3x increase in risk in the coming decade actually suggests that a Covid-19-like event would occur roughly every 129 years, and a Spanish-flu repetition every 292 to 877 years. Such predictions are unable to take into account the rapidly changing nature of medicine and improved sanitation and nutrition (most deaths from Spanish flu would not have occurred if modern antibiotics had been available), and so may still overestimate risk. Similarly, the WHO’s own priority disease list for new outbreaks only includes two diseases of proven natural origin that have over 1,000 historical deaths attributed to them. It is well demonstrated that the risk and expected burden of pandemics is misrepresented by major international agencies in current discussions. The urgency for May 2024 is clearly therefore inadequately supported, firstly because neither the WHO nor others have demonstrated how the harms accrued through Covid-19 would be reduced through the measures proposed, and secondly because the burden and risk is misrepresented. In this context, the state of the Agreement is clearly not where it should be as a draft international legally binding agreement intended to impose considerable financial and other obligations on States and populations. This is particularly problematic as the proposed expenditure; the proposed budget is over $31 billion per year, with over $10 billion more on other One Health activities. Much of this will have to be diverted from addressing other diseases burdens that impose far greater burden. This trade-off, essential to understand in public health policy development, has not yet been clearly addressed by the WHO. The WHO DG stated recently that the WHO does not want the power to impose vaccine mandates or lockdowns on anyone, and does not want this. This begs the question of why either of the current WHO pandemic instruments is being proposed, both as legally binding documents. The current IHR (2005) already sets out such approaches as recommendations the DG can make, and there is nothing non-mandatory that countries cannot do now without pushing new treaty-like mechanisms through a vote in Geneva. Based on the DG’s claims, they are essentially redundant, and what new non-mandatory clauses they contain, as set out below, are certainly not urgent. Clauses that are mandatory (Member States “shall”) must be considered within national decision-making contexts and appear against the WHO’s stated intent. Common sense would suggest that the Agreement, and the accompanying IHR amendments, be properly thought through before Member States commit. The WHO has already abandoned the legal requirement for a 4-month review time for the IHR amendments (Article 55.2 IHR), which are also still under negotiation just 2 months before the WHA deadline. The Agreement should also have at least such a period for States to properly consider whether to agree – treaties normally take many years to develop and negotiate and no valid arguments have been put forward as to why these should be different. The Covid-19 response resulted in an unprecedented transfer of wealth from those of lower income to the very wealthy few, completely contrary to the way in which the WHO was intended to affect human society. A considerable portion of these pandemic profits went to current sponsors of the WHO, and these same corporate entities and investors are set to further benefit from the new pandemic agreements. As written, the Pandemic Agreement risks entrenching such centralization and profit-taking, and the accompanying unprecedented restrictions on human rights and freedoms, as a public health norm. To continue with a clearly flawed agreement simply because of a previously set deadline, when no clear population benefit is articulated and no true urgency demonstrated, would therefore be a major step backward in international public health. Basic principles of proportionality, human agency, and community empowerment, essential for health and human rights outcomes, are missing or paid lip-service. The WHO clearly wishes to increase its funding and show it is ‘doing something,’ but must first articulate why the voluntary provisions of the current IHR are insufficient. It is hoped that by systematically reviewing some key clauses of the agreement here, it will become clear why a rethink of the whole approach is necessary. The full text is found below. The commentary below concentrates on selected draft provisions of the latest publicly available version of the draft agreement that seem to be unclear or potentially problematic. Much of the remaining text is essentially pointless as it reiterates vague intentions to be found in other documents or activities which countries normally undertake in the course of running health services, and have no place in a focused legally-binding international agreement. REVISED Draft of the negotiating text of the WHO Pandemic Agreement. 7th March, 2024 Preamble Recognizing that the World Health Organization…is the directing and coordinating authority on international health work. This is inconsistent with a recent statement by the WHO DG that the WHO has no interest or intent to direct country health responses. To reiterate it here suggests that the DG is not representing the true position regarding the Agreement. “Directing authority” is however in line with the proposed IHR Amendments (and the WHO’s Constitution), under which countries will “undertake” ahead of time to follow the DG’s recommendations (which thereby become instructions). As the HR amendments make clear, this is intended to apply even to a perceived threat rather than actual harm. Recalling the constitution of the World Health Organization…highest attainable standard of health is one of the fundamental rights of every human being without distinction of race, religion, political belief, economic or social condition. This statement recalls fundamental understandings of public health, and is of importance here as it raises the question of why the WHO did not strongly condemn prolonged school closures, workplace closures, and other impoverishing policies during the Covid-19 response. In 2019, WHO made clear that these dangers should prevent actions we now call ‘lockdowns’ from being imposed. Deeply concerned by the gross inequities at national and international levels that hindered timely and equitable access to medical and other Covid-19 pandemic-related products, and the serious shortcomings in pandemic preparedness. In terms of health equity (as distinct from commodity of ‘vaccine’ equity), inequity in the Covid-19 response was not in failing to provide a vaccine against former variants to immune, young people in low-income countries who were at far higher risk from endemic diseases, but in the disproportionate harm to them of uniformly-imposed NPIs that reduced current and future income and basic healthcare, as was noted by the WHO in 2019 Pandemic Influenza recommendations. The failure of the text to recognize this suggests that lessons from Covid-19 have not informed this draft Agreement. The WHO has not yet demonstrated how pandemic ‘preparedness,’ in the terms they use below, would have reduced impact, given that there is poor correlation between strictness or speed of response and eventual outcomes. Reiterating the need to work towards…an equitable approach to mitigate the risk that pandemics exacerbate existing inequities in access to health services, As above – in the past century, the issue of inequity has been most pronounced in pandemic response, rather than the impact of the virus itself (excluding the physiological variation in risk). Most recorded deaths from acute pandemics, since the Spanish flu, were during Covid-19, in which the virus hit mainly sick elderly, but response impacted working-age adults and children heavily and will continue to have effect, due to increased poverty and debt; reduced education and child marriage, in future generations. These have disproportionately affected lower-income people, and particularly women. The lack of recognition of this in this document, though they are recognized by the World Bank and UN agencies elsewhere, must raise real questions on whether this Agreement has been thoroughly thought through, and the process of development been sufficiently inclusive and objective. Chapter I. Introduction Article 1. Use of terms (i) “pathogen with pandemic potential” means any pathogen that has been identified to infect a human and that is: novel (not yet characterized) or known (including a variant of a known pathogen), potentially highly transmissible and/or highly virulent with the potential to cause a public health emergency of international concern. This provides a very wide scope to alter provisions. Any pathogen that can infect humans and is potentially highly transmissible or virulent, though yet uncharacterized means virtually any coronavirus, influenza virus, or a plethora of other relatively common pathogen groups. The IHR Amendments intend that the DG alone can make this call, over the advice of others, as occurred with monkeypox in 2022. (j) “persons in vulnerable situations” means individuals, groups or communities with a disproportionate increased risk of infection, severity, disease or mortality. This is a good definition – in Covid-19 context, would mean the sick elderly, and so is relevant to targeting a response. “Universal health coverage” means that all people have access to the full range of quality health services they need, when and where they need them, without financial hardship. While the general UHC concept is good, it is time a sensible (rather than patently silly) definition was adopted. Society cannot afford the full range of possible interventions and remedies for all, and clearly there is a scale of cost vs benefit that prioritizes certain ones over others. Sensible definitions make action more likely, and inaction harder to justify. One could argue that none should have the full range until all have good basic care, but clearly the earth will not support ‘the full range’ for 8 billion people. Article 2. Objective This Agreement is specifically for pandemics (a poorly defined term but essentially a pathogen that spreads rapidly across national borders). In contrast, the IHR amendments accompanying it are broader in scope – for any public health emergencies of international concern. Article 3. Principles 2. the sovereign right of States to adopt, legislate and implement legislation The amendments to the IHR require States to undertake to follow WHO instructions ahead of time, before such instruction and context are known. These two documents must be understood, as noted later in the Agreement draft, as complementary. 3. equity as the goal and outcome of pandemic prevention, preparedness and response, ensuring the absence of unfair, avoidable or remediable differences among groups of people. This definition of equity here needs clarification. In the pandemic context, the WHO emphasized commodity (vaccine) equity during the Covid-19 response. Elimination of differences implied equal access to Covid-19 vaccines in countries with large aging, obese highly vulnerable populations (e.g. the USA or Italy), and those with young populations at minimal risk and with far more pressing health priorities (e.g. Niger or Uganda). Alternatively, but equally damaging, equal access to different age groups within a country when the risk-benefit ratio is clearly greatly different. This promotes worse health outcomes by diverting resources from where they are most useful, as it ignores heterogeneity of risk. Again, an adult approach is required in international agreements, rather than feel-good sentences, if they are going to have a positive impact. 5. …a more equitable and better prepared world to prevent, respond to and recover from pandemics As with ‘3’ above, this raises a fundamental problem: What if health equity demands that some populations divert resources to childhood nutrition and endemic diseases rather than the latest pandemic, as these are likely of far higher burden to many younger but lower-income populations? This would not be equity in the definition implied here, but would clearly lead to better and more equal health outcomes. The WHO must decide whether it is about uniform action, or minimizing poor health, as these are clearly very different. They are the difference between the WHO’s commodity equity, and true health equity. Chapter II. The world together equitably: achieving equity in, for and through pandemic prevention, preparedness and response Equity in health should imply a reasonably equal chance of overcoming or avoiding preventable sickness. The vast majority of sickness and death is due to either non-communicable diseases often related to lifestyle, such as obesity and type 2 diabetes mellitus, undernutrition in childhood, and endemic infectious diseases such as tuberculosis, malaria, and HIV/AIDS. Achieving health equity would primarily mean addressing these. In this chapter of the draft Pandemic Agreement, equity is used to imply equal access to specific health commodities, particularly vaccines, for intermittent health emergencies, although these exert a small fraction of the burden of other diseases. It is, specifically, commodity-equity, and not geared to equalizing overall health burden but to enabling centrally-coordinated homogenous responses to unusual events. Article 4. Pandemic prevention and surveillance 2. The Parties shall undertake to cooperate: (b) in support of…initiatives aimed at preventing pandemics, in particular those that improve surveillance, early warning and risk assessment; .…and identify settings and activities presenting a risk of emergence and re-emergence of pathogens with pandemic potential. (c-h) [Paragraphs on water and sanitation, infection control, strengthening of biosafety, surveillance and prevention of vector-born diseases, and addressing antimicrobial resistance.] The WHO intends the Agreement to have force under international law. Therefore, countries are undertaking to put themselves under force of international law in regards to complying with the agreement’s stipulations. The provisions under this long article mostly cover general health stuff that countries try to do anyway. The difference will be that countries will be assessed on progress. Assessment can be fine if in context, less fine if it consists of entitled ‘experts’ from wealthy countries with little local knowledge or context. Perhaps such compliance is best left to national authorities, who are more in use with local needs and priorities. The justification for the international bureaucracy being built to support this, while fun for those involved, is unclear and will divert resources from actual health work. 6. The Conference of the Parties may adopt, as necessary, guidelines, recommendations and standards, including in relation to pandemic prevention capacities, to support the implementation of this Article. Here and later, the COP is invoked as a vehicle to decide on what will actually be done. The rules are explained later (Articles 21-23). While allowing more time is sensible, it begs the question of why it is not better to wait and discuss what is needed in the current INB process, before committing to a legally-binding agreement. This current article says nothing not already covered by the IHR2005 or other ongoing programs. Article 5. One Health approach to pandemic prevention, preparedness and response Nothing specific or new in this article. It seems redundant (it is advocating a holistic approach mentioned elsewhere) and so presumably is just to get the term ‘One Health’ into the agreement. (One could ask, why bother?) Some mainstream definitions of One Health (e.g. Lancet) consider that it means non-human species are on a par with humans in terms of rights and importance. If this is meant here, clearly most Member States would disagree. So we may assume that it is just words to keep someone happy (a little childish in an international document, but the term ‘One Health’ has been trending, like ‘equity,’ as if the concept of holistic approaches to public health were new). Article 6. Preparedness, health system resilience and recovery 2. Each Party commits…[to] : (a) routine and essential health services during pandemics with a focus on primary health care, routine immunization and mental health care, and with particular attention to persons in vulnerable situations (b) developing, strengthening and maintaining health infrastructure (c) developing post-pandemic health system recovery strategies (d) developing, strengthening and maintaining: health information systems This is good, and (a) seems to require avoidance of lockdowns (which inevitably cause the harms listed). Unfortunately other WHO documents lead one to assume this is not the intent…It does appear therefore that this is simply another list of fairly non-specific feel-good measures that have no useful place in a new legally-binding agreement, and which most countries are already undertaking. (e) promoting the use of social and behavioural sciences, risk communication and community engagement for pandemic prevention, preparedness and response. This requires clarification, as the use of behavioral science during the Covid-19 response involved deliberate inducement of fear to promote behaviors that people would not otherwise follow (e.g. Spi-B). It is essential here that the document clarifies how behavioral science should be used ethically in healthcare. Otherwise, this is also a quite meaningless provision. Article 7. Health and care workforce This long Article discusses health workforce, training, retention, non-discrimination, stigma, bias, adequate remuneration, and other standard provisions for workplaces. It is unclear why it is included in a legally binding pandemic agreement, except for: 4. [The Parties]…shall invest in establishing, sustaining, coordinating and mobilizing a skilled and trained multidisciplinary global public health emergency workforce…Parties having established emergency health teams should inform WHO thereof and make best efforts to respond to requests for deployment… Emergency health teams established (within capacity etc.) – are something countries already do, when they have capacity. There is no reason to have this as a legally-binding instrument, and clearly no urgency to do so. Article 8. Preparedness monitoring and functional reviews 1. The Parties shall, building on existing and relevant tools, develop and implement an inclusive, transparent, effective and efficient pandemic prevention, preparedness and response monitoring and evaluation system. 2. Each Party shall assess, every five years, with technical support from the WHO Secretariat upon request, the functioning and readiness of, and gaps in, its pandemic prevention, preparedness and response capacity, based on the relevant tools and guidelines developed by WHO in partnership with relevant organizations at international, regional and sub-regional levels. Note that this is being required of countries that are already struggling to implement monitoring systems for major endemic diseases, including tuberculosis, malaria, HIV, and nutritional deficiencies. They will be legally bound to divert resources to pandemic prevention. While there is some overlap, it will inevitably divert resources from currently underfunded programs for diseases of far higher local burdens, and so (not theoretically, but inevitably) raise mortality. Poor countries are being required to put resources into problems deemed significant by richer countries. Article 9. Research and development Various general provisions about undertaking background research that countries are generally doing anyway, but with an ’emerging disease’ slant. Again, the INB fails to justify why this diversion of resources from researching greater disease burdens should occur in all countries (why not just those with excess resources?). Article 10. Sustainable and geographically diversified production Mostly non-binding but suggested cooperation on making pandemic-related products available, including support for manufacturing in “inter-pandemic times” (a fascinating rendering of ‘normal’), when they would only be viable through subsidies. Much of this is probably unimplementable, as it would not be practical to maintain facilities in most or all countries on stand-by for rare events, at cost of resources otherwise useful for other priorities. The desire to increase production in ‘developing’ countries will face major barriers and costs in terms of maintaining quality of production, particularly as many products will have limited use outside of rare outbreak situations. Article 11. Transfer of technology and know-how This article, always problematic for large pharmaceutical corporations sponsoring much WHO outbreak activities, is now watered down to weak requirements to ‘consider,’ promote,’ provide, within capabilities’ etc. Article 12. Access and benefit sharing This Article is intended to establish the WHO Pathogen Access and Benefit-Sharing System (PABS System). PABS is intended to “ensure rapid, systematic and timely access to biological materials of pathogens with pandemic potential and the genetic sequence data.” This system is of potential high relevance and needs to be interpreted in the context that SARS-CoV-2, the pathogen causing the recent Covid-19 outbreak, was highly likely to have escaped from a laboratory. PABS is intended to expand the laboratory storage, transport, and handling of such viruses, under the oversight of the WHO, an organization outside of national jurisdiction with no significant direct experience in handling biological materials. 3. When a Party has access to a pathogen [it shall]: (a) share with WHO any pathogen sequence information as soon as it is available to the Party; (b) as soon as biological materials are available to the Party, provide the materials to one or more laboratories and/or biorepositories participating in WHO-coordinated laboratory networks (CLNs), Subsequent clauses state that benefits will be shared, and seek to prevent recipient laboratories from patenting materials received from other countries. This has been a major concern of low-and middle-income countries previously, who perceive that institutions in wealthy countries patent and benefit from materials derived from less-wealthy populations. It remains to be seen whether provisions here will be sufficient to address this. The article then becomes yet more concerning: 6. WHO shall conclude legally binding standard PABS contracts with manufacturers to provide the following, taking into account the size, nature and capacities of the manufacturer: (a) annual monetary contributions to support the PABS System and relevant capacities in countries; the determination of the annual amount, use, and approach for monitoring and accountability, shall be finalized by the Parties; (b) real-time contributions of relevant diagnostics, therapeutics or vaccines produced by the manufacturer, 10% free of charge and 10% at not-for-profit prices during public health emergencies of international concern or pandemics, … It is clearly intended that the WHO becomes directly involved in setting up legally binding manufacturing contracts, despite the WHO being outside of national jurisdictional oversight, within the territories of Member States. The PABS system, and therefore its staff and dependent entities, are also to be supported in part by funds from the manufacturers whom they are supposed to be managing. The income of the organization will be dependent on maintaining positive relationships with these private entities in a similar way in which many national regulatory agencies are dependent upon funds from pharmaceutical companies whom their staff ostensibly regulate. In this case, the regulator will be even further removed from public oversight. The clause on 10% (why 10?) products being free of charge, and similar at cost, while ensuring lower-priced commodities irrespective of actual need (the outbreak may be confined to wealthy countries). The same entity, the WHO, will determine whether the triggering emergency exists, determine the response, and manage the contracts to provide the commodities, without direct jurisdictional oversight regarding the potential for corruption or conflict of interest. It is a remarkable system to suggest, irrespective of political or regulatory environment. 8. The Parties shall cooperate…public financing of research and development, prepurchase agreements, or regulatory procedures, to encourage and facilitate as many manufacturers as possible to enter into standard PABS contracts as early as possible. The article envisions that public funding will be used to build the process, ensuring essentially no-risk private profit. 10. To support operationalization of the PABS System, WHO shall…make such contracts public, while respecting commercial confidentiality. The public may know whom contracts are made with, but not all details of the contracts. There will therefore be no independent oversight of the clauses agreed between the WHO, a body outside of national jurisdiction and dependent of commercial companies for funding some of its work and salaries, and these same companies, on ‘needs’ that the WHO itself will have sole authority, under the proposed amendments to the IHR, to determine. The Article further states that the WHO shall use its own product regulatory system (prequalification) and Emergency Use Listing Procedure to open and stimulate markets for the manufacturers of these products. It is doubtful that any national government could make such an overall agreement, yet in May 2024 they will be voting to provide this to what is essentially a foreign, and partly privately financed, entity. Article 13. Supply chain and logistics The WHO will become convenor of a ‘Global Supply Chain and Logistics Network’ for commercially-produced products, to be supplied under WHO contracts when and where the WHO determines, whilst also having the role of ensuring safety of such products. Having mutual support coordinated between countries is good. Having this run by an organization that is significantly funded directly by those gaining from the sale of these same commodities seems reckless and counterintuitive. Few countries would allow this (or at least plan for it). For this to occur safely, the WHO would logically have to forgo all private investment, and greatly restrict national specified funding contributions. Otherwise, the conflicts of interest involved would destroy confidence in the system. There is no suggestion of such divestment from the WHO, but rather, as in Article 12, private sector dependency, directly tied to contracts, will increase. Article 13bis: National procurement- and distribution-related provisions While suffering the same (perhaps unavoidable) issues regarding commercial confidentiality, this alternate Article 13 seems far more appropriate, keeping commercial issues under national jurisdiction and avoiding the obvious conflict of interests that underpin funding for WHO activities and staffing. Article 14. Regulatory systems strengthening This entire Article reflects initiatives and programs already in place. Nothing here appears likely to add to current effort. Article 15. Liability and compensation management 1. Each Party shall consider developing, as necessary and in accordance with applicable law, national strategies for managing liability in its territory related to pandemic vaccines…no-fault compensation mechanisms… 2. The Parties…shall develop recommendations for the establishment and implementation of national, regional and/or global no-fault compensation mechanisms and strategies for managing liability during pandemic emergencies, including with regard to individuals that are in a humanitarian setting or vulnerable situations. This is quite remarkable, but also reflects some national legislation, in removing any fault or liability specifically from vaccine manufacturers, for harms done in pushing out vaccines to the public. During the Covid-19 response, genetic therapeutics being developed by BioNtech and Moderna were reclassified as vaccines, on the basis that an immune response is stimulated after they have modified intracellular biochemical pathways as a medicine normally does. This enabled specific trials normally required for carcinogenicity and teratogenicity to be bypassed, despite raised fetal abnormality rates in animal trials. It will enable the CEPI 100-day vaccine program, supported with private funding to support private mRNA vaccine manufacturers, to proceed without any risk to the manufacturer should there be subsequent public harm. Together with an earlier provision on public funding of research and manufacturing readiness, and the removal of former wording requiring intellectual property sharing in Article 11, this ensures vaccine manufacturers and their investors make profit in effective absence of risk. These entities are currently heavily invested in support for WHO, and were strongly aligned with the introduction of newly restrictive outbreak responses that emphasized and sometimes mandated their products during the Covid-19 outbreak. Article 16. International collaboration and cooperation A somewhat pointless article. It suggests that countries cooperate with each other and the WHO to implement the other agreements in the Agreement. Article 17. Whole-of-government and whole-of-society approaches A list of essentially motherhood provisions related to planning for a pandemic. However, countries will legally be required to maintain a ‘national coordination multisectoral body’ for PPPR. This will essentially be an added burden on budgets, and inevitably divert further resources from other priorities. Perhaps just strengthening current infectious disease and nutritional programs would be more impactful. (Nowhere in this Agreement is nutrition discussed (essential for resilience to pathogens) and minimal wording is included on sanitation and clean water (other major reasons for reduction in infectious disease mortality over past centuries). However, the ‘community ownership’ wording is interesting (“empower and enable community ownership of, and contribution to, community readiness for and resilience [for PPPR]”), as this directly contradicts much of the rest of the Agreement, including the centralization of control under the Conference of Parties, requirements for countries to allocate resources to pandemic preparedness over other community priorities, and the idea of inspecting and assessing adherence to the centralized requirements of the Agreement. Either much of the rest of the Agreement is redundant, or this wording is purely for appearance and not to be followed (and therefore should be removed). Article 18. Communication and public awareness 1. Each Party shall promote timely access to credible and evidence-based information …with the aim of countering and addressing misinformation or disinformation… 2. The Parties shall, as appropriate, promote and/or conduct research and inform policies on factors that hinder or strengthen adherence to public health and social measures in a pandemic, as well as trust in science and public health institutions and agencies. The key word is as appropriate, given that many agencies, including the WHO, have overseen or aided policies during the Covid-19 response that have greatly increased poverty, child marriage, teenage pregnancy, and education loss. As the WHO has been shown to be significantly misrepresenting pandemic risk in the process of advocating for this Agreement and related instruments, its own communications would also fall outside the provision here related to evidence-based information, and fall within normal understandings of misinformation. It could not therefore be an arbiter of correctness of information here, so the Article is not implementable. Rewritten to recommend accurate evidence-based information being promoted, it would make good sense, but this is not an issue requiring a legally binding international agreement. Article 19. Implementation and support 3. The WHO Secretariat…organize the technical and financial assistance necessary to address such gaps and needs in implementing the commitments agreed upon under the Pandemic Agreement and the International Health Regulations (2005). As the WHO is dependent on donor support, its ability to address gaps in funding within Member States is clearly not something it can guarantee. The purpose of this article is unclear, repeating in paragraphs 1 and 2 the earlier intent for countries to generally support each other. Article 20. Sustainable financing 1. The Parties commit to working together…In this regard, each Party, within the means and resources at its disposal, shall: (a) prioritize and maintain or increase, as necessary, domestic funding for pandemic prevention, preparedness and response, without undermining other domestic public health priorities including for: (i) strengthening and sustaining capacities for the prevention, preparedness and response to health emergencies and pandemics, in particular the core capacities of the International Health Regulations (2005);… This is silly wording, as countries obviously have to prioritize within budgets, so that moving funds to one area means removing from another. The essence of public health policy is weighing and making such decisions; this reality seems to be ignored here through wishful thinking. (a) is clearly redundant, as the IHR (2005) already exists and countries have agreed to support it. 3. A Coordinating Financial Mechanism (the “Mechanism”) is hereby established to support the implementation of both the WHO Pandemic Agreement and the International Health Regulations (2005) This will be in parallel to the Pandemic Fund recently commenced by the World Bank – an issue not lost on INB delegates and so likely to change here in the final version. It will also be additive to the Global Fund to fight AIDS, tuberculosis, and malaria, and other health financing mechanisms, and so require another parallel international bureaucracy, presumably based in Geneva. It is intended to have its own capacity to “conduct relevant analyses on needs and gaps, in addition to tracking cooperation efforts,” so it will not be a small undertaking. Chapter III. Institutional and final provisions Article 21. Conference of the Parties 1. A Conference of the Parties is hereby established. 2. The Conference of the Parties shall keep under regular review, every three years, the implementation of the WHO Pandemic Agreement and take the decisions necessary to promote its effective implementation. This sets up the governing body to oversee this Agreement (another body requiring a secretariat and support). It is intended to meet within a year of the Agreement coming into force, and then set its own rules on meeting thereafter. It is likely that many provisions outlined in this draft of the Agreement will be deferred to the COP for further discussion. Articles 22 – 37 These articles cover the functioning of the Conference of Parties (COP) and various administrative issues. Of note, ‘block votes’ will be allowed from regional bodies (e.g. the EU). The WHO will provide the secretariat. Under Article 24 is noted: 3. Nothing in the WHO Pandemic Agreement shall be interpreted as providing the Secretariat of the World Health Organization, including the WHO Director-General, any authority to direct, order, alter or otherwise prescribe the domestic laws or policies of any Party, or to mandate or otherwise impose any requirements that Parties take specific actions, such as ban or accept travellers, impose vaccination mandates or therapeutic or diagnostic measures, or implement lockdowns. These provisions are explicitly stated in the proposed amendments to the IHR, to be considered alongside this agreement. Article 26 notes that the IHR is to be interpreted as compatible, thereby confirming that the IHR provisions including border closures and limits on freedom of movement, mandated vaccination, and other lockdown measures are not negated by this statement. As Article 26 states: “The Parties recognize that the WHO Pandemic Agreement and the International Health Regulations should be interpreted so as to be compatible.” Some would consider this subterfuge – The Director-General recently labeled as liars those who claimed the Agreement included these powers, whilst failing to acknowledge the accompanying IHR amendments. The WHO could do better in avoiding misleading messaging, especially when this involves denigration of the public. Article 32 (Withdrawal) requires that, once adopted, Parties cannot withdraw for a total of 3 years (giving notice after a minimum of 2 years). Financial obligations undertaken under the agreement continue beyond that time. Finally, the Agreement will come into force, assuming a two-thirds majority in the WHA is achieved (Article 19, WHO Constitution), 30 days after the fortieth country has ratified it. Further reading: WHO Pandemic Agreement Intergovernmental Negotiating Board website: https://inb.who.int/ International Health Regulations Working Group website: https://apps.who.int/gb/wgihr/index.html On background to the WHO texts: Amendments to WHO’s International Health Regulations: An Annotated Guide An Unofficial Q&A on International Health Regulations On urgency and burden of pandemics: https://essl.leeds.ac.uk/downloads/download/228/rational-policy-over-panic Disease X and Davos: This is Not the Way to Evaluate and Formulate Public Health Policy Before Preparing for Pandemics, We Need Better Evidence of Risk Revised Draft of the negotiating text of the WHO Pandemic Agreement: Published under a Creative Commons Attribution 4.0 International License For reprints, please set the canonical link back to the original Brownstone Institute Article and Author. Authors David Bell David Bell, Senior Scholar at Brownstone Institute, is a public health physician and biotech consultant in global health. He is a former medical officer and scientist at the World Health Organization (WHO), Programme Head for malaria and febrile diseases at the Foundation for Innovative New Diagnostics (FIND) in Geneva, Switzerland, and Director of Global Health Technologies at Intellectual Ventures Global Good Fund in Bellevue, WA, USA. View all posts Thi Thuy Van Dinh Dr. Thi Thuy Van Dinh (LLM, PhD) worked on international law in the United Nations Office on Drugs and Crime and the Office of the High Commissioner for Human Rights. Subsequently, she managed multilateral organization partnerships for Intellectual Ventures Global Good Fund and led environmental health technology development efforts for low-resource settings. View all posts Your financial backing of Brownstone Institute goes to support writers, lawyers, scientists, economists, and other people of courage who have been professionally purged and displaced during the upheaval of our times. You can help get the truth out through their ongoing work. https://brownstone.org/articles/the-who-pandemic-agreement-a-guide/ https://www.minds.com/donshafi911/blog/the-who-pandemic-agreement-a-guide-1621719398509187077

SV40, a DNA Altering, Carcinogenic Contaminant, found in Pfizer’s COVID-19 Vaccines The ExposéMarch 17, 2024 It’s not just the spike protein and the mRNA that are a problem. Both Pfizer and Moderna covid injections also have DNA contamination and Pfizer’s covid injection contains SV40 promoters. Microbiologist Kevin McKernan pioneered research on testing some of the covid vaccine vials and discovered unacceptable levels of double-stranded DNA plasmids floating around. This is DNA contamination. He found the contamination in Pfizer and Moderna vials. During an interview with Peter Sweden, Sasha Latypova said that DNA contamination is “a huge problem because this is replication competent plasmid, it can then invade human cells, it can invade the bacterial cells that live in your gut. So, they go into the bacteria they replicate there, they replicate antibiotic-resistant genes…it can cause sepsis, it can cause cancer, all sorts of issues.” The World Council for Health (“WCH”) stated that a red line has been crossed. “DNA contamination of mRNA ‘vaccines’ poses a risk to everyone on the planet,” WCH said. “Replicable DNA, so-called plasmids, in both the monovalent and bivalent vaccines, which should not be there at all … We can only speculate how it will end, but what needs to happen today after the publication of the paper by McKernan et al (2023) is an immediate stop of the ‘covid-19 vaccine’ program.” In Pfizer’s mRNA injection, McKernan also discovered Simian Virus 40 (“SV40”) promoters which are tied to cancer development in humans. He emphasised that the SV40 found is a viral piece, it is not the whole virus. However, it still presents a risk of driving cancer. SV40 or Simian Virus 40 was the 40th virus found in rhesus monkey kidney cells when these cells were used to make the polio vaccine. This virus contaminated both the inactivated polio vaccine (“IPV”) and the oral or “live” polio vaccine (“OPV”) developed by Dr. Albert Sabin. When it was discovered that SV40 was an animal carcinogen that had found its way into the polio vaccines, a federal law was passed in 1961 that required that no vaccines contain this virus. Kanekoa The Great tweeted two audio/video transcripts. One of a recent interview with McKernan explaining his discoveries and another of a Japanese professor expressing his concerns about these discoveries. We have republished these transcripts below. Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… DNA Contamination and SV40 Discovered McKernan joined Conservative Review with Daniel Horowitz on Friday to warn that there is no quality control in the manufacturing process of these vaccines. If his findings turn out to be widespread, it could portend an even greater risk for anaphylaxis, blood clotting, developing resistance to antibiotics, gene integration risk, and long-term production of spike protein within the body. You can listen to an audio of the interview on Apple podcasts HERE. During the interview, McKernan said: “It’s in both Moderna and Pfizer. We looked at the bivalent vaccines for both Moderna and Pfizer and only the monovalent vaccines for Pfizer because we didn’t have access to monovalent vaccines for Moderna. In all three cases, the vaccines contain double-stranded DNA contamination. If you sequence that DNA, you’ll find that it matches what looks to be an expression vector that’s used to make the RNA… “Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there’s any E. coli endotoxin present because that creates anaphylaxis for the injected. And, of course, your viewers and listeners are probably aware there’s a lot of anaphylaxis going on, not only on TV but in the VAERS database. You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA… “At least on the Pfizer side of things, it has what’s known as an SV40 promoter. This is an oncogenic virus piece. It’s not the entire virus. However, the small piece is known to drive very aggressive gene expression. And the concern that people, even at the FDA, have noted in the past whenever injecting double-stranded DNA is that these things can then integrate into the genome. If you’re not careful with how you manufacture these things, and you have excess amounts of this DNA, your concern for genome integration goes up… “If you get an SV40 promoter in front of an oncogene, you will end up with a high expression of a gene that can drive cancer, it will be a very rare event, but you don’t need many of these cells to be hit with something like this for it to take off. SV40 actually plagued, granted it was the full viral genome, not just the promoter, but this has plagued previous vaccine programs. The polio vaccine is one of them that they were concerned that this may have contributed to cancer from that vaccine. So, there’s a history of being concerned over SV40. “Having the promoter inside some of these vectors isn’t necessary. It seems to be superfluous oversight they could have eliminated, yet it’s still there because they ran this out the door so quickly, they didn’t really have time to get rid of superfluous parts of the plasmid. So, that piece of DNA is something we really need to pay attention to. We’ve made quantitative PCR assays to hunt for this. So several researchers around the globe are now running these assays to look for how much of this DNA is floating around after people have been vaccinated.” Further reading: Sequencing the Pfizer monovalent mRNA vaccines also reveals dual copy 72-bp SV40 Promoter, Anandamide (Kevin McKernan), 12 April 2023 dsDNA variance in Pfizer Docs, Anandamide (Kevin McKernan), 20 May 2023 McKernan, K., Helbert, Y., Kane, L. T., & McLaughlin, S. (2023, April 10). Sequencing of bivalent Moderna and Pfizer mRNA vaccines reveals nanogram to microgram quantities of expression vector dsDNA per dose. https://doi.org/10.31219/osf.io/b9t7m Plasmid DNA is a Known Pfizer Ingredient – NOT a Contaminant, Karen Kingston, 14 April 2023 Japanese Professor Expresses Concern Japanese Professor Murakami of Tokyo University expressed his concerns over the alarming discovery of SV40 promoters McKernan had made. He said: “The Pfizer vaccine has a staggering problem. I have made an amazing finding. This figure is an enlarged view of Pfizer’s vaccine sequence. As you can see, the Pfizer vaccine sequence contains part of the SV40 sequence here. This sequence is known as a promoter. Roughly speaking, the promoter causes increased expression of the gene. The problem is that the sequence is present in a well-known carcinogenic virus. “The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine. There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine. This is not the only problem. If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus. “So, it means that the DNA can easily enter the genome. This is such an alarming problem. It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious. This kind of promoter sequence is completely unnecessary for the production of the mRNA vaccine. In fact, SV40 is a promoter of cancer viruses.” https://expose-news.com/2024/03/17/sv40-a-dna-altering-carcinogenic-contaminant-found-in-pfizers-covid-19-vaccines/

Chimaeras and interspecies hybrids; the sinister agenda hiding behind covid Rhoda WilsonMarch 20, 2024 There is something that has quietly slipped through the din of the murderously phoney episode called covid-19, Dr. Mathew Maavak writes. “If the covid-19 vaccines were ‘experimental gene therapies’, what other genetic experimentations continue unhindered out there?” he asks. In May 2020, Dr. Maavak wrote an article about how SARS-CoV-2 was not germinated in a vacuum. The Wuhan Institute of Virology conducted research with alarming global parallels including the pursuit of superintelligence and the development of chimaeras, or interspecies hybrids. What he wrote in May 2020 is still relevant today, he says. So yesterday, Dr. Maavak reposted his now four-year-old article. Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… Coronavirus in a Time of Chimaeras and Beyond By Dr. Mathew Maavak In May 2020, just as the coronavirus made hourly headlines, I had suspected that the virus was part of a much more sinister agenda. What I wrote back then remains just as relevant today. Here it is. Genetically-Enhanced Competitiveness The Sars-Cov-2 virus, which allegedly causes covid-19, was not germinated in a vacuum. The type of research conducted at the Wuhan Institute of Virology had ominous analogues worldwide. These included the quest for super intelligence and the development of interspecies hybrids or chimaeras. What began as a scientific mission to remedy congenital defects has rapidly morphed into a global race to create designer babies, super soldiers and transhumans through the aid of biotechnology, artificial intelligence and/or machine-neuralinking. 21st century eugenics is tacitly justified by the need to boost “national competitiveness.” China leads the way here. In one revealing episode, genome sequencing giant BGI Shenzhen had procured and sequenced the DNA of more than 2,000 people – mostly Americans – with IQ scores of at least 160. According to Stephen Hsu, a theoretical physicist from Michigan State University and scientific adviser to BGI: An exceptional person gets you an order of magnitude more statistical power than if you took random people from the population … BGI Shenzhen intends to become a “bio-Google” that will collate the “world’s biological information and make it universally accessible and useful.” From 2012 onwards, it began collaborating with the Bill & Melinda Gates Foundation (“BMGF”). No surprises there. Scientific endeavours like these are based on the assumption that an assemblage of smart samples can help in the identification and transplantation of optimal bits of genetic material into future generations. Can a virus or vaccine perform this transplantation? Or will such agencies be used to cull the majority of the human population before a “genetic antidote” emerges to reverse their lethal effects? It will be too late for the vast majority of mankind by then. artificial selection, backed by artificial intelligence, may decide who gets this new booster. But is such a hypothetical scenario even realistic? There are too many imponderables here but viruses, nasal swabs and “vaccines” will surely deliver vital data for the “New Human Genome Project.” New Eugenics Zeitgeist The science of eugenics is not dissuaded by the nurture over nature debate, even after exhaustive studies had failed to establish genetic variants associated with intelligence. For example, a 2010 study led by Robert Plomin, a behavioural geneticist at King’s College London, had probed over 350,000 variations in single DNA letters across the genomes of 7,900 children but found no prized variant. Curiously, most of the smart samples procured by BGI Shenzhen were sourced from Plomin’s research activities. Periodic setbacks did not deter the proponents of “procreative beneficence” who argue that it is a human duty to augment the genetic codes of future generations. Failure to do so is couched in terms of “genetic neglect” and even child abuse. If this sounds eerily familiar, look no further than the worldview which once animated the Western world before the Nazis elevated it to a whole new level altogether. The eugenics zeitgeist has gripped China in a big way. Under its Maternal and Infant Health Care Law (1994), foetuses with potential hereditary diseases or deformities are recommended for abortion. At the rate Beijing is building its eugenics utopia, the definition of deformity may ultimately include a genetically pre-diagnosed average IQ. Instead of inciting public outrage, the law precipitated a headlong rush to select “intelligent” babies through methods like preimplantation genetic diagnosis (“PGD”). The idea behind PGD is to screen and identify the most promising embryos for implantation and birth. Combined with CRISPR gene-editing tools, next-generation Chinese citizens are expected to exhibit remarkably higher IQs – at least according to bioethicists who fret over a future marked by the “genetic haves” and “genetic have-nots.” China already has three CRISPR-edited babies whose current fate remains unknown. In the aftermath of the corona psychosis, the availability of “smart samples” would have increased exponentially and may dovetail nicely with the eugenics agenda of the Rockefeller Foundation and BMGF. Incidentally, Bill Gates grew up in a household that was heavily invested in population control and eugenics. Our smart societies may inevitably face the existential question of “live-lets” and “live-nots” down the line. The orchestrated rebellion towards selective extinction, if it occurs, has a tragicomical public face: An autistic Swede who parrots the “listen to the science” and “listen to the experts” mantra. How will future designer babies contribute to society? For one thing, we will be missing individuals like Beethoven (deaf); Albert Einstein (learning disability/late development); John Nash (schizophrenia); Andrea Boccelli (congenital glaucoma) and Vincent van Gogh (chronic depression/anxiety) and a host of others like them. A future Stephen Hawking (motor neurone disease) and Greta Thunberg (Asperger’s Syndrome – allegedly) will be genetically disqualified before birth. It is now inconvenient to consider intelligence as a result of peer interactions, human environment and ingenious reactions to adversity. (I personally define intelligence as an ability to nip the bullsh*t in its foetid bud). Mapping out the complex and sometimes unpredictable interplay between 100 trillion synaptic connections in a human brain may take centuries to accomplish but that does not deter the utopians of today. After all, genetic manipulation is the eugenic wormhole that promises to accelerate the emergence of a super society at warp speed. The late billionaire paedophile, Jeffrey Epstein, was a prominent proponent of this philosophy. Epstein intended to breed a “super race of humans with his DNA by impregnating women at his New Mexico ranch, genetic engineering and artificial intelligence.” Welcome to Lebensborn 2.0! Prominent scientists linked to Epstein’s transhumanist fantasies included “molecular engineer George Church; Murray Gell-Mann, the discoverer of the quark; the evolutionary biologist Stephen Jay Gould; the neurologist and author Oliver Sacks; and the theoretical physicist Frank Wilczek.” The late Stephen Hawking – who will ironically flunk the genetic pre-screenings of tomorrow – was another Epstein associate. Forget about Mars missions; major powers see eugenics as the next great frontier. Its hyper-materialistic focus is encapsulated by the following analogy from Russian scientist Denis Rebrikov: It currently costs about a million roubles (US$15,500 at that time) to genetically change an embryo – more than a lot of cars – but prices will fall with greater use … I can see the billboard now: “You Choose: a Hyundai Solaris or a Super-Child?” You are comparing a child, super or not, with a Hyundai? I mean a Hyundai, really? Sometimes, the road to hell is paved with good intentions but most of the time, it begins with a diabolically silly proposition. But why stop at children? From genetically engineered horses in Argentina that are supposedly faster, stronger and better jumpers to super-dogs in China that are comprehensively superior to the average mutt, the DNA of the entire natural world is being slated for a revolutionary redesign. Crouching Chimaeras, Hideous Hybrids The masters of our universe however cannot create future generations of superhumans without being adept at recombining genetic sequences across species. That is the logic guiding eugenicists. As a result, a slew of chimaeras or interspecies hybrids have been spawned with the aid of CRISPR technology. These include ghastly human-monkey hybrids, monkey-pig hybrids, human-rabbit hybrids and a host of other lab-manufactured monstrosities. Chimaeras are created when human embryonic stem cells are injected into embryos of other species. The goal, for the time being, is to induce growth of targeted human organs. Those facing terminal illnesses will no longer have to worry about long organ waiting lists. Chinese scientists have just transplanted a modified pig liver into a brain-dead human and it seems to have worked. A less controversial approach to human organ replacement is 3D bioprinting or its 4D bioprinting iteration. These techniques involve the “printing” of a replacement organ from the stem cells of a transplant recipient, thereby eliminating the odds of organ rejection. But why stop at replacement organs when we can have “replacement humans” altogether? Future generations must think like Einsteins, be as nimble as leopards and possess owl-like night visions. And, of course, be virus-resistant as well! The manipulation of the human genome is the new “grand response” to the venerable set of “grand challenges” for 2030 and beyond. China is the go-to place for such genetic tinkering as some of these undertakings are technically illegal in the West. And this is where the utility of covid-19 comes into the picture. It provides the perfect pretext to remove such ethical constraints. After all, “Disease X” is just waiting to escape from the belly of some bat or pangolin … Since 2014, the Wuhan Institute of Virology has been the recipient of a two-stage grant worth $7.2 million from the United States government for gain-of-function research into bat coronaviruses. According to a Newsweek report in April 2020: Many scientists have criticised gain of function research, which involves manipulating viruses in the lab to explore their potential for infecting humans because it creates a risk of starting a pandemic from accidental release. Such caution has not deterred a flurry of research into microbial gene manipulation. The Wuhan experiments may have either spawned the Sars-Cov-2 virus or it may have provided a fraudulent context for future tyrannical mandates. But to solely blame China for the coronavirus “pandemic” is a tad unfair. Just as China is the factory of the world for foreign corporations, it is also the genetic incubator for a variety of viruses and chimaeras for foreign governments and foundations. Even so, the human-pig chimaera was the creation of the Salk Institute in California. Research into the world’s first human-mouse hybrid was largely a Japanese affair. The Portuguese in the meantime had created a virus chimaera. The United Kingdom, on their end, had spawned a human-cow hybrid embryo in 2008 – perhaps in keeping with the bovine disposition of those glued to the BBC. It was in Britain where the game-changing Dolly the Sheep was cloned in 1996. The transition from sheep to sheeple may turn out to be a short 21st century Jurassic Park ride. Coincidences and Consequences Before the advent of gene-editing tools and supercomputing, it would have been impossible to create a viable chimaera. The Biotech-Industrial Complex and contact tracing-type panopticons constitute a new growth area for Tech Titans that were once facing bankruptcy. The dangers of genome editing were in fact included in the Worldwide Threat Assessment reports submitted to the United States Congress in 2016 and 2017. These risks were either omitted or glossed over in the 2018 and 2019 reports – just as such risks gravitated to the high impact-high likelihood quadrant. Is it a coincidence that the nations most affected by covid-19 – at least during the first two years of its alleged spread – were the very ones that had either promoted or encouraged a variety of genetic experimentations that are contrary to nature? If – and that is a big “if” – these nations succeed in their quest for “designer babies” and “superhumans,” the rest of mankind will be rendered redundant. Some mass extermination event may transpire under the guise of World War III, food shortages, Disease X or a combination thereof. If everything goes according to plan, however, there will be 500 million potential specimens left for The Great Reset. The Third World, whose leaders are being monetarily incentivised to focus on unattainable Sustainable Development Goals (“SDGs”), will be consigned to the ash heaps of history. It is quite ironic that a new generation of cerebrally deficient “thought leaders” and “experts” are being groomed to promote the demises of their societies and themselves. About the Author Mathew Maavak, with a PhD in Policy Studies, specialises in systems science, global risks, strategic foresight, geopolitics and governance. He is a Malaysian expert on risk foresight and governance. Dr. Maavak has published numerous op-eds on a variety of eclectic subjects for over 20 years – by ‘connecting the dots’ in a disjointed world. He is the author of a Substack page titled ‘The Eye Opener’ which you can subscribe to and follow HERE. https://expose-news.com/2024/03/20/chimaeras-and-interspecies-hybrids/

CMNnews -- Your Credible Medical News Network -- Update 27th February 2024 From Global sources -- Updated Twice Weekly -- CMNNEWS -- We roam the planet for the best Medical News Stories CMNnews THE DOCTORS MONKEY NOT SEE — MONKEY NOT HEAR — MONKEY NOT SPEAK HISTORIC AUSTRALIAN SUPREME COURT DECISION STATE GOVERNMENT FOUND “ACTED UNLAWFULLY” IN REGARD TO VACCINE MANDATES ON POLICE AND AMBULANCE WORKERS Supreme Court bombshell: Queensland’s mandatory Covid vaccine orders ‘unlawful’ Excerpts: Dozens of police and health workers have won a mammoth legal battle over mandatory Covid vaccination orders. Vanda Carson court reporter Courier Mail Newspaper Queensland, Australia 2 min read In a 115-page decision handed down by Justice Glenn Martin on Tuesday he declared police commissioner Katarina Carroll’s direction for mandatory Covid-19 vaccination issued in December 2021 was unlawful under the Human Rights Act and banned her from taking any steps to enforce the direction. He also ruled that a similar order by John Wakefield, the director general of Queensland Health’s equivalent vaccination policy “is of no effect” and Mr Wakefield be blocked from forcing paramedics to have the injection. The workers did not have to be vaccinated while their legal fight was underway. Ms Carroll and Mr Wakefield are also banned from disciplining any of the paramedics and police officers. “I am not satisfied that the (police) Commissioner has demonstrated that she gave proper consideration to the human rights that might have been affected by her decisions,” Justice Martin said in relation to the police staff. “I do not accept that the Commissioner had … considered whether the decision would be compatible with human rights,” he noted in his 115-page decision. “By failing to give proper consideration, the making of each of those decisions was unlawful. “Despite the revocation of the QPS Directions, a finding of unlawfulness is still available.” Link: https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb Share CMNNews -- The Credible Medical News Network Update Article: Supreme Court bombshell: Qld’s mandatory Covid vaccine orders ‘unlawful’ Excerpts: Dozens of police and health workers including paramedics have won a mammoth legal battle over mandatory ­vaccination orders after the Supreme Court declared they were unlawful. A spokeswoman for the Nurses’ Professional Association of Queensland (NPAQ) said the Supreme Court ruling “ highlighted how Queensland Health has violated thousands of healthcare workers’ rights”. The association highlighted that during a workforce crisis there were members who were stood due to the vaccine mandate who are dying to return to work. “We have nurses and midwives sitting at home during a workforce crisis and the healthcare system’s unlawful decisions are directly to blame,” the spokeswoman said. “NPAQ is currently liaising with our legal team to explore legal avenues for our members in light of today’s Supreme Court outcome.” https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb COVID-19 vaccine mandates 'unlawful' for emergency services, court finds The court on Tuesday delivered its judgments in three lawsuits brought by 86 parties against Queensland Police Service and Queensland Ambulance Service for their directions to workers issued in 2021 and 2022. The court found Police Commissioner Katarina Carroll failed to give proper consideration to human rights relevant to the decision to issue the vaccine mandate. “The court also found the directions limited the human rights of workers because they were required to undergo a medical procedure without full consent ….” Australian Senate finally acknowledge excess deaths are concerning : Letter from Australian Senator Ralph Babet SENATOR RALPH BABET — IS THIS THE GREATEST SENATE DECISION IN HISTORY? TWO MINUTE VIDEO JIM FERGUSON – “THIS IS GENOCIDE – MURDER OF MILLIONS AND POSSIBLY BILLIONS OF PEOPLE” – “THE PRIME MINISTER COULD BE INVOLVED” -- “THESE ARE CRIMES AGAINST HUMANITY” “Explosive allegations against top Government officials in the UK Government update. As Member of Parliament Andrew Bridgen prepares to present evidence of potential criminal conduct involving Prime Minister Rishi Sunak and his cabinet to London's Metropolitan Police Commissioner Mark Rowley, we explore the mindset of others who might be implicated in alleged widespread wrongdoing, including potential mass genocide and profiteering. Will they now do the right thing and blow the lid on whats really been going on! If the gatekeepers in our Security Services and Police are compromised or complicit in what is arguably the greatest potential crime against humanity of all time then all bets are off as to what happens next.” https://twitter.com/i/status/1761505188056072263 DR DAVID MARTIN EXPLAINS WHO THEY ARE AND HOW THEY ARE DOING THIS TO US “THEY WERE CONVICTED OF ANTI-TRUST CRIMES” “THIS IS A CRIMINAL CONSPIRACY” “WHO IS MOVING THE STICK – WELLCOME, GATES AND ROCKEFELLER” “THIS IS A VIOLATION OF SWISS LAW” Dr. David Martin Reveals Who Is Pulling the Strings Behind the World Health Organization Who are “THEY”? “We have to name the names” in the worst miscarriage of medical science in history. Is it the World Health Organization? Dr. David Martin says Tedros is just a puppet with a “giant stick up his ass, which is what’s making his mouth move… 18 days ago · 446 likes · 136 comments · The Vigilant Fox BILL GATES DONATION TO WORLD HEALTH ORGANIZATION JIM FERGUSON INTERVIEWS ANDREW BRIDGEN -- “Exclusive Breaking News: Evidence to be presented that criminal activity has been committed by the very top of Government in the UK. Rishi Sunak British Prime Minister may face a criminal investigation and face potential criminal charges of the most egregious kind. British MP Andrew Bridgen has written to Mark Rowley Commissioner of the Metropolitan Police and the most senior of Police officers to have a three hour meeting where experts and whistle blowers will lay out the evidence where potential criminal activity has been conducted by the very top of Government and the civil service in the UK Parliament has been deliberately misled over the vaccine contracts. This matter may be taken to Parliamentary standards in addition to the presentation of evidence to the Police and the Security services. "heads of governments around the world and others below them have engaged in what is tantamount to treason against the public" Office of National Statistics (ONS) figures on Excess Deaths are being covered up. "there is a huge coverup going on" In August 2019 a member of the security services stated that there was a pandemic coming and not to take any of the vaccines. Bill gates and Rishi Sunak invested heavily into the Pharma companies like Pfizer and Moderna prior to the pandemic. Did they have insider knowledge about what was being planned in a coming pandemic! 75% of congressmen and woman in the United States have investments in Big Pharma. A Pfizer executive stated that a senator could be bought for $10,000. The journalists are complicit in the cover up. Main Stream Media are bought and paid for. A court case has been launched against the former health secretary Matt Hancock for defamation against Andrew Bridgen and this will take place in the Royal Court of Justice.” https://twitter.com/i/status/1761393940874293335 THESE EVIL PEOPLE ARE COMING AFTER OUR PETS – YOUR DOGS AND CATS – A SECURITY CHIEF WARNED “DO NOT TAKE THE VACCINE” – “THE PRIME MINISTER OF THE UK, RISHI SUNAK, INVESTED HALF A BILLION DOLLARS INTO MODERNA TWO TO THREE YEARS BEFORE COVID OCCURRED” – “HE MUST HAVE HAD PRIOR KNOWLEDGE” https://rumble.com/v4ew676-these-evil-monsters-are-coming-after-our-pets.html JIM FERGUSON ON TWITTER @JimFergusonUK “British PM and #WEF2030Agenda devotee #Sunak invested $500 million of his private funds into Moderna through a company called Thelema Partners in a notorious tax haven in the Caymen Islands. Afterwards he stated in parliament that the vaccine was "safe and effective" while then going on to roll out further permissions for Moderna to set up further vaccine producing interests within the UK. Did he use his position as Prime Minister to make massive personal profits while knowingly or even unknowingly causing harm to the British people and has he broken the National Security Act which states "if you're working in secret for a foreign power to use or abuse your knowledge in a way that causes harm to our citizens you will be a criminal." Former Head of MI6 Sir Alex Younger.” 2024 Is the Last Year of Free Speech and Democracy in the Western World https://www.paulcraigroberts.org/2024/02/19/2024-is-the-last-year-of-free-speech-and-democracy-in-the-western-world/ To Understand The Globalists We Must Understand Their Psychopathic Religion https://alt-market.us/to-understand-the-globalists-we-must-understand-their-psychopathic-religion/ TWO BRAVE AND COURAGEOUS DOCTORS #141 - Dr Charles Hoffe, A Persecuted Ethical Doctor Or Dangerous Misinformation Spreader? FREEDOM - LIBERTY - HAPPINESS SUPPORT DOC MALIK About this conversation - Dr Charles Hoffe is a family doctor who lives and works in British Columbia, Canada. He has worked in general practice and emer… 14 days ago · 34 likes · 5 comments · Doc Malik New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023) VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023) VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023… 14 days ago · 122 likes · 57 comments · Dr. William Makis MD LIST OF LAWYERS NOW AVAILABLE FOR LAWSUITS ON COVID VACCINE INJURY https://deeprootsathome.com/list-of-attorneys-worldwide-now-available-for-lawsuits/ Kaboom! — Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3 "We've just seen this in the last 2 years... but we didn’t see this before the vaccines. The doctor noticed this between two years to one year ago, in about 50% of the patients," Kaboom! Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3 It’s taking a long time folks, but the worms are crawling out of the cans, and corrupt institutions and politicians are scrambling to seal them back in! Perhaps due to a significant decrease in mRNA vaccine sales influencing pharmaceutical companies… 18 days ago · 103 likes · 30 comments · Aussie17 mRNA VACCINE SHEDDING OF SPIKE PROTEIN As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s 2015 document on Gene Product Shedding Studies and all other gene therapy products on the market list shedding as a risk in their [package] insert (Luxterna, Roctavian, Zolgensma) and shed from 7 days to 6 months.” phillip.altman’s Substack mRNA VACCINE SHEDDING OF SPIKE PROTEIN There has been considerable concern about the potential for the vaccinated to shed Spike Protein to the unvaccinated. See Dr. Piere Kory’s Substack of 20 Feb. CLICK HERE to view. As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s… Read more 18 days ago · 64 likes · 9 comments · phillip.altman WORLDWIDE CENSORSHIP IS UNDER WAY – “Google Isn’t Just Trying to Rewrite History. It’s at the Centre of a Worldwide Web of Censorship” https://dailysceptic.org/2024/02/25/google-isnt-just-trying-to-rewrite-history-its-at-the-centre-of-a-worldwide-web-of-censorship/ TUCKER CARLSON INTERVIEW – JUST 6 MINUTES Steve Kirsch Tags the COVID Jab as the ‘Most Dangerous Vaccine of All Time’ The VAERS system has identified 770 safety signals related to the COVID-19 vaccine. “That is mind-blowing. That is not a three-alarm fire. That is a 770-alarm fire.” So, what did the CDC do? “They said nothing.” https://twitter.com/VigilantFox/status/1761369027685793810 FOREIGN DNA SHOULD NOT BE IN THE VACCINES – IT CAN ENTER THE DNA IN THE NUCLEUS OF EACH CELL Kevin McKernan testifies about how the FDA and Regulators, funded by those who profit from the deception in a great conflict of interest, put the human genome at risk by downplaying the risk of DNA integration. Crimes Against Humanity Case Phase 1 Starts At The Same Time We Learn That Covid "Vaccine" DNA Integration Into Ovaries Chromosomes 19 & 12 Is Now Confirmed! Lying Health Ministers, CDC, W.H.O. OH MY! This video needs to go viral! SHARE! IoJ is filing an injunction to stop the shots pronto based on the evidence in this Substack article. Our Donation Drive is now open!!! We can win this! Everyone’s going down dammit. This is just unacceptable. The human genome, heritage of humanity is at risk from the WHO and regulators cow towing to Big Pharma’s covi… Read more 13 days ago · 84 likes · 34 comments · Interest of Justice MICROPLASTICS – WHAT ARE THEY? Humanity United Now - Ana Maria Mihalcea, MD, PhD Microplastics - aka Nanotechnological Self Assembly Polymers - Are Everywhere - Poisoning Our Biosphere, Food Supply And Humans The use of the word microplastics is once again to normalize the self assembly polymers that have been sprayed via illegal Geoengineering and bioengineering operations to transform our biosphere according to the transhumanist agenda. This is literally killing our planet, killing all life and humanity. This microplastics cover story is to explain why the… Read more 5 months ago · 141 likes · 53 comments · Ana Maria Mihalcea, MD, PhD TRICKS AND TREATS FOR A COVID JAB IN NEW ZEALAND VIDEO - New Zealand Vax Propaganda & subsequent Sudden Deaths "Get the jab, get the treats" (Oct.16, 2021 Super Saturday Vaxathon) VIDEO - New Zealand Vax Propaganda & Sudden Deaths "Get the jab, get the treats" (Source: Coronavirus Plushie) Get the jab, get the treats . . . Incentivizing Kiwis to get jabbed by offering them cash prizes, food, free tickets for the rugby, and other kinds of 'treats', was a big part of the 16 Oct, 2021 'Super Saturday Vaxathon… 19 days ago · 101 likes · 65 comments · Dr. William Makis MD 99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree. A multinational Global Vaccine Data Network (GVDN) cohort study of 99 million vaccinated individuals concludes that the benefits of COVID outweigh the risks. My colleagues and I disagree. 99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree. Executive summary A new study of over 99 million vaccinated people has been highly promoted in the press with headlines like “Covid Vaccines Linked To Small Increase In Heart And Brain Disorders, Study Finds—But Risk From Infection Is Far Higher.” I’m going to convince you that this is bullshit… Read more 18 days ago · 525 likes · 334 comments · Steve Kirsch “All of the harms from the COVID-19 injectable products were predictable, and preventable” There are no 'desired proteins' with regard to the modified spike mRNA “All of the harms from the COVID-19 injectable products were predictable, and preventable.” Jessica Rose, PhD A Nature publication by Mulroney et al. entitled N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting was published on December 6, 2023. The authors showed that N1-methylpseudouridine affects the fidelity of mRNA translation via ri… Read more 3 months ago · 272 likes · 67 comments · Jessica Rose Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians COVID Chronicles Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians The Epoch Times, a media outlet that is not state-funded, released an article yesterday that was updated today. Everyone around the world should read it. You can find it here. The journalist, Noé Chartier, did an excellent job writing a well-balanced, objective, and factual account. I do not have much to add… Read more 15 days ago · 370 likes · 104 comments · Dr. Byram W. Bridle Subscribe to CMNNews - The Credible Medical News Network News From Around the Globe -- Updated Twice Weekly Disclaimer: All content is presented for educational and/or entertainment purposes only. Under no circumstances should it be mistaken for professional advice, nor is it at all intended to be taken as such. The contents simply reflect current newsworthy items that are freely available. It is subject to error and change without notice.The presence of a link to a website does not indicate approval or endorsement of that web site or any services, products, or opinions that may be offered by them. Neither CMNnews nor any of its principals or contributors are under any obligation to update or keep current the information contained herein. Although the information contained is derived from sources which are believed to be reliable, they cannot be guaranteed. Disclosure: We accept no advertising or compensation, and have no material connection to any products, brands, topics or companies mentioned anywhere on the site. Fair Use Notice: This site contains copyrighted material the use of which has not always been specifically authorized by the copyright owner. We are making such material available in our efforts to advance understanding of issues of social significance. We believe this constitutes a ‘fair use’ of any such copyrighted material as provided for in section 107 of the US Copyright Law. In accordance with Title 17 U.S.C. Section 107, the material on this site is distributed without profit. If you wish to use copyrighted material from this site for purposes of your own that go beyond ‘fair use’, you must obtain permission from the copyright owner. Share CMNNews -- The Credible Medical News Network Thank you for reading CMNNews -- The Credible Medical News Network. This post is public so feel free to share it. Share https://open.substack.com/pub/cmnnews/p/cmnnews-your-credible-medical-news-a60?r=29hg4d&utm_medium=ios https://telegra.ph/CMNnews----Your-Credible-Medical-News-Network----Update-27th-February-2024-03-11

Will Disease X be Leaked in 2025? All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name (only available in desktop version). To receive Global Research’s Daily Newsletter (selected articles), click here. Click the share button above to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. New Year Donation Drive: Global Research Is Committed to the “Unspoken Truth” *** The WHO’s pandemic treaty is the gateway to a global, top-down totalitarian regime, a one world government. The reason we can be sure there will be additional pandemics, whether manufactured using either fear and hype alone or an actual bioweapon created for this very purpose, is because the takeover plan, aka The Great Reset, is based on the premise that we need global biosecurity surveillance and centralized response A new contagion will likely be born in 2025, and media are already preparing us for it January 15-19, 2024, global leaders met at the World Economic Forum’s (WEF) Davos summit where the key topic of discussion was “Preparing for Disease X,” a hypothetical new pandemic predicted to kill 20 times more people than COVID-19 In August 2023, a new vaccine research facility was set up in Wiltshire, England, to begin work on a vaccine against the unknown “Disease X” The U.S. Congress introduced the “Disease X Act of 2023” (H.R.3832) in June 2023. The bill calls for the establishment of a BARDA program to develop “medical countermeasures for viral threats with pandemic potential.” The bill was referred to the Subcommittee on Health in early June 2023 but has not yet been passed * The COVID-19 pandemic allowed for an unprecedented shift in power and wealth distribution across the world and, as predicted, it was not to be a one-off event. A new contagion will likely be born in 2025, and media are already preparing us for it. January 15-19, 2024, global leaders met at the World Economic Forum’s (WEF) Davos summit where the key topic of discussion was “Preparing for Disease X,”1 a hypothetical new pandemic predicted to emerge in 2025 and kill 20 times more people than COVID-19.2 As reported by the Mirror:3 “The World Health Organization (WHO) has warned of a potential Disease X since 2017, a term indicating an unknown pathogen that could cause a serious international epidemic … Public speakers at the ‘Preparing for Disease X’ event next Wednesday [January 17, 2024] include Tedros Adhanom Ghebreyesus, director-general of the WHO, Brazilian minister of health Nisia Trindade Lima, and Michel Demaré, chair of the board at AstraZeneca. In their first post-pandemic meeting held in November 2022, the WHO brought over 300 scientists to consider which of over 25 virus families and bacteria could potentially create another pandemic. The list the team came up with included: the Ebola virus, the Marburg virus disease, Covid-19, SARS, and the Middle East respiratory syndrome coronavirus (MERS-CoV). Others included lassa fever, nipah and henipaviral diseases, zift Valley fever, and zika — as well as the unknown pathogen that would cause ‘Disease X.’” I’ve interviewed Meryl Nass about how the WHO is trying to take over aspects of everyone’s lives. She just published an important piece over the weekend, Why Is Davos So Interested in Disease? about how the WEF and the WHO have become partners to terrify the world. Alexis Baden-Mayer, Esq., political director for the Organic Consumers Association, did some digging into the participants of this WEF event, and the two things they all have in common are 1) dumping the AstraZeneca COVID shot on the developing world (primarily India and Brazil) after rich countries rejected it due to its admitted blood clotting risk, and 2) pushing for the implementation of medical AI systems that will eliminate doctors along with patient choice and privacy. Practice Runs or Responsible Planning? In a January 11, 2024, tweet, Fox News analyst and former assistant secretary for public affairs for the U.S. Treasury Department, Monica Crowley, wrote:4 “From the same people who brought you COVID-19 now comes Disease X: Next week in Davos, the unelected globalists at the World Economic Forum will hold a panel on a future pandemic 20x deadlier than COVID … Just in time for the election, a new contagion to allow them to implement a new WHO treaty, lock down again, restrict free speech and destroy more freedoms. Sound far-fetched? So did what happened in 2020. When your enemies tell you what they’re planning and what they’re planning FOR, believe them. And get ready.” Dr. Stuart Ray, vice chair of medicine for data integrity and analytics at Johns Hopkins’ Department of Medicine, dismissed such warnings, telling Fortune magazine5 that “Coordination of public health response is not conspiracy, it’s simply responsible planning.” I’d be willing to believe him if it wasn’t for a now-obvious trend: Whatever the globalists claim will happen actually does happen at a remarkable frequency, and their prognostic capabilities become easier to explain when you consider that most lethal pandemics have been caused by manmade viruses, the products of gain-of-function research. It’s pretty easy to predict a new viral outbreak if you have said virus waiting in the wings. With that in mind, recent research from China certainly raises concern, to say the least. According to a January 3, 2024, preprint,6 a SARS-CoV-2-related pangolin coronavirus — described as a “cell culture-adapted mutant” called GX_P2V that was first cultured in 2017 — was found to kill 100% of the humanized mice (ACE2-transgenic mice) infected with it.7 The primary cause of death was brain inflammation. According to the authors, “this is the first report showing that a SARS-CoV-2-related pangolin coronavirus can cause 100% mortality in hACE2 mice, suggesting a risk for GX_P2V to spill over into humans.” However, if this virus mutated as a result of passaging through cell cultures, then it’s not likely to emerge in the wild. It’s another unnatural lab creation, so rather than saying it may spill over from pangolins to humans, it would be more accurate to admit that it may pose a (rather serious) risk to humans were a lab escape to occur. COVID Dress Rehearsals In 2017, Johns Hopkins Center of Health Security held a coronavirus pandemic simulation called the SPARS Pandemic 2025-2028 scenario.8 Importantly, the exercise stressed “communication dilemmas concerning medical countermeasures that could plausibly emerge” in a pandemic scenario. Then, in October 2019, less than three months before the COVID-19 outbreak, the Bill & Melinda Gates Foundation in collaboration with Johns Hopkins and the World Economic Forum hosted Event 201. The name itself suggests it may have been a continuation of the SPARS Pandemic exercise. College courses are numbered based on their prerequisites. A 101 course does not require any prior knowledge whereas 201 courses require prior familiarity with the topic at hand. As in the SPARS Pandemic scenario, Event 201 involved an outbreak of a highly infectious coronavirus, and the primary (if not sole) focus of the exercise was, again, how to control information and keep “misinformation” in check, not how to effectively discover and share remedies. Social media censorship played a prominent role in the Event 201 plan, and in the real-world events of 2020 through the present, accurate information about vaccine development, production and injury has indeed been effectively suppressed around the world, thanks to social media companies and Google’s censoring of opposing viewpoints. In March 2021, an outbreak of “an unusual strain of monkeypox virus” was simulated.9 In late July the following year, the WHO director-general declared that a multi-country outbreak of monkeypox constituted a public health emergency of international concern,10 against his own advisory group. ‘Catastrophic Contagion’ Exercise Considering both of these simulations, SPARS (“Event 101”?) and Event 201, foreshadowed what eventually occurred in real life during COVID, when Gates hosts yet another pandemic exercise, it’s worth paying attention to the details. October 23, 2022, Gates, Johns Hopkins and the WHO cohosted “a global challenge exercise” dubbed “Catastrophic Contagion,”11,12 involving a fictional pathogen called “severe epidemic enterovirus respiratory syndrome 2025” (SEERS-25). Enterovirus D6813 is typically associated with cold and flu-like illness in infants, children and teens. In rare cases, it’s also been known to cause viral meningitis and acute flaccid myelitis, a neurological condition resulting in muscle weakness and loss of reflexes in one or more extremities. Enteroviruses A71 and A6 are known to cause hand, foot and mouth disease,14 while poliovirus, the prototypical enterovirus, causes polio (poliomyelitis), a potentially life-threatening type of paralysis that primarily affects children under age 5. So, the virus they modeled in this simulation appears to be something similar to enterovirus D68, but worse. Vaccine Drug Trials Begin for Deadly Nipah Virus One known virus that bears some resemblance to the fictional SEERS-25 is the Nipah virus. This virus has a kill rate of about 75%,15 and survivors oftentimes face long-term neurological issues stemming from the infection. Nipah is also said to affect children to a greater degree than adults.16 Incidentally, human trials for a vaccine against the deadly Nipah virus were recently launched.17Volunteers received their first shots in early January 2024. The experimental injection uses the same viral vector technology used to produce AstraZeneca’s COVID shot. The trial is reportedly being carried out by the University of Oxford in an undisclosed area where Nipah is actively infecting victims. (India seems to be indicated, as an outbreak in Kerala killed two people and hospitalized three in September 2023.18) The disease is thought to spread via interaction with infected animals such as goats, pigs, cats and horses. It may also spread via tainted blood products and food. Symptoms can emerge anywhere from a few days after exposure to as long as 45 days. Initial symptoms include fever, headache and respiratory illness, which can rapidly progress to encephalitis (brain swelling), seizures and coma within just a couple of days. According to the WHO, pigs are known to be “highly contagious” during the incubation period, and it’s possible that humans may be as well, although that has yet to be confirmed. Training African Leaders to Go Along with the Narrative Tellingly, the Catastrophic Contagion exercise focused on getting leadership in African countries involved and trained in following the script. African nations went “off script” more often than others during the COVID pandemic, and didn’t follow in the footsteps of developed nations when it came to pushing the jabs. As a result, vaccine makers now face the problem of having a huge control group, as the COVID jab uptake on the African continent was only 6%,19 yet it fared far better than developed nations in terms of COVID-19 infections and related deaths.20 The Catastrophic Contagion exercise predicts SEERS-25 will kill 20 million people worldwide, including 15 million children, and many who survive the infection will be left with paralysis and/or brain damage. In other words, the “cue” given is that the next pandemic may target children rather than the elderly, as was the case with COVID-19. Vaccine Against Unknown ‘X’ Pathogen Is Already in the Works In August 2023, a new vaccine research facility was set up in Wiltshire, England, fully staffed with more 200 scientists, to begin work on a vaccine against the unknown “Disease X.” As reported by Metro:21 “It took 362 days to develop the Covid-19 vaccine. But the Vaccine Development and Evaluation Centre team wants to reduce that time to 100 days. Scientists at the facility will develop a range of prototype vaccines and tests. The new lab is a part of a global effort to respond to global health threats. The UK and other G7 countries signed up to the ‘100 Days Mission’ in 2021. The government has invested £65 million into the lab. Professor Dame Jenny Harries, the head of the UK Health Security Agency, said the new facility would ‘ensure that we prepare so that if we have a new Disease X, a new pathogen, we have as much of that work in advance as possible.’” In the U.S., Congress also introduced the “Disease X Act of 2023” (H.R.383222) back in June 2023. The bill calls for the establishment of a BARDA program to develop “medical countermeasures for viral threats with pandemic potential.” The bill was referred to the Subcommittee on Health in early June 2023 but has not yet been passed. The Disease X Act amends a section of the Public Health Service Act with two new clauses that call for “the identification and development of platform manufacturing technologies needed for advanced development and manufacturing of medical countermeasures for viral families which have significant potential to cause a pandemic,” and “advanced research and development of flexible medical countermeasures against priority respiratory virus families and other respiratory viral pathogens with a significant potential to cause a pandemic, with both pathogen-specific and pathogen-agnostic approaches …” Needless to say, since it’s impossible to customize vaccines using the conventional method of growing viruses in eggs or some other cell media in 100 days, it seems inevitable that all these efforts are about the expansion of gene-based technologies. This, despite the fact that the mRNA technology used for the COVID jabs has proven to be disastrous from a safety standpoint, and ineffective to boot. Why Manufactured Pandemics Will Continue At this point, it’s quite clear that “biosecurity” is the chosen means by which the globalist cabal intends to seize power over the world. The WHO is working on securing sole power over pandemic response globally through its international pandemic treaty which, if implemented, will eradicate the sovereignty of all member nations. The WHO’s pandemic treaty is the gateway to a global, top-down totalitarian regime, a one world government. Ultimately, the WHO intends to dictate all health care. But to secure that power, they will need more pandemics. COVID-19 alone was not enough to get everyone onboard with a centralized pandemic response unit, and they probably knew that from the start. So, the reason we can be sure there will be additional pandemics, whether manufactured using either fear and hype alone or an actual bioweapon created for this very purpose, is because the takeover plan, aka The Great Reset, is based on the premise that we need global biosecurity surveillance and centralized response. Biosecurity, in turn, is the justification for an international vaccine passport, which the G20 has signed on to, and that passport will also be your digital identification. That digital ID, then, will be tied to your social credit score, personal carbon footprint tracker, medical records, educational records, work records, social media presence, purchase records, your bank accounts and a programmable central bank digital currency (CBDC). Once all these pieces are fully connected, you’ll be in a digital prison, and the ruling cabal — whether officially a one world government by then or not — will have total control over your life from cradle to grave. We’re Already Suffering Under a Pseudo-One World Government We actually already have a pseudo-one world government, in the form of Bill Gates’ nongovernmental organizations (NGOs). They are making health care decisions that should be left to individual nations and/or states, and they’re making decisions that will line their own pockets, regardless of what happens to the public health-wise. They coordinate and synchronize pandemic communication during simulated practice runs, and then, when the real-world situation emerges that fits the bill, the preplanned script is played out more or less verbatim. Between the G20 declaration to implement an international vaccine passport under the auspice of the WHO, and the WHO’s pandemic treaty, everything is lined up to take control of the next pandemic, and in so doing, further securing the foundation for a one world government. As discussed in my 2021 article, “COVID-19 Dress Rehearsals and Proof of the Plan,” the pandemic measures rolled out for COVID-19 were the culmination of decades of careful planning to radically and permanently alter the governance and social structures of the world. The medical system has been used in the past to drive forward a New World Order agenda — now rebranded as “The Great Reset” — and it’s now being used to implement the final stages of that longstanding plan. COVID-19 was a real-world practice run, and showed just how effectively a pandemic can be used to shift the balance of power, and strip the global population of its wealth and individual freedoms. So, there’s no doubt in my mind that additional pandemics will be declared, because they’re the means to the globalists’ ends. To prevent this global coup, we need everyone to speak and share the truth to the point that you’re able. Only then will our voices outnumber the voices of the propaganda machine. Door To Freedom (doortofreedom.org), an organization founded by Dr. Meryl Nass, has a poster that explains how the pandemic treaty and International Health Regulations (IHR) amendments will change life as we know it and strip us of every vestige of freedom. Please download this poster and share it with everyone you know. Also put it up on public billboards and places where communities share information. * Note to readers: Please click the share button above. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. Notes 1, 21 Metro January 15, 2024 2, 3 Mirror January 13, 2024 4 Twitter/X Monica Crowley January 11, 2024 5 Fortune January 12, 2024 6 ResearchGate January 2024 DOI: 10.1101/2024.01.03.574008 7 MSN January 15, 2024 8 SPARS Pandemic Scenario 9 NTI Paper November 2021 10 UN News July 23, 2022 11 Catastrophic Contagion 12 Catastrophic Contagion Videos 13 CDC Enterovirus D68 14 CDC Enteroviruses 15 Forbes September 15, 2023 16 Intractable & Rare Diseases Research February 2019; 8(1): 1-8 17 Forbes January 11, 2024 18 BBC September 14, 2023 19 First Post November 19, 2021 20 Yahoo News November 19, 2021 22 HR 3832 The Disease X Act of 2023 Featured image source https://www.globalresearch.ca/will-disease-x-leaked-2025/5847210 https://donshafi911.blogspot.com/2024/01/will-disease-x-be-leaked-in-2025-all.html

Elon Musk says Neuralink implanted wireless brain chip 10 hours ago CEO of Tesla, Chief Engineer of SpaceX and CTO of X Elon Musk speaks during the New York Times annual DealBook summit on 29 November 2023 in New York City, USGetty Images By Patrick Jackson & Tom Gerken BBC News Tech billionaire Elon Musk has claimed his Neuralink company has successfully implanted one of its wireless brain chips in a human. In a post on X, formerly Twitter, he said "promising" brain activity had been detected after the procedure and the patient was "recovering well". The company's goal is to connect human brains to computers to help tackle complex neurological conditions. A number of rival firms have already implanted similar devices. "For any company producing medical devices, the first test in humans is a significant milestone," said Professor Anne Vanhoestenberghe of King's College London. "For the brain computer interface community, we must place this news in the context that whilst there are many companies working on exciting products, there are only a few other companies who have implanted their devices in humans, so Neuralink has joined a rather small group." However, she also suggested there needed to be a note of caution as "true success" could only be evaluated in the long-term. "We know Elon Musk is very adept at generating publicity for his company," she added. Among the other companies to make similar advances in the field is the École Polytechnique Fédérale in Lausanne (EPFL), in Switzerland, which has successfully enabled a paralysed man to walk just by thinking. That was achieved by putting electronic implants on his brain and spine which wirelessly communicate thoughts to his legs and feet. Details of the breakthrough were published in the peer-reviewed journal Nature in May 2023. There has been no independent verification of Mr Musk's claims, nor has Neuralink provided any information about the procedure he says has taken place. BBC News has approached both Neuralink and the US's medical regulator, the Food and Drug Administration (FDA), for comment. Neuralink testing Neuralink has been criticised in the past, with Reuters reporting in December 2022 that the company engaged in testing which resulted in the deaths of approximately 1,500 animals, including sheep, monkeys and pigs. In July 2023, the head of the US Department of Agriculture - which investigates animal welfare concerns - said it had not found any violations of animal research rules at the firm. However, a separate investigation by the agency is ongoing. Mr Musk's company was given permission to test the chip on humans by the FDA in May 2023. That gave the green light for the start of the six-year study during which a robot is being used to surgically place 64 flexible threads, thinner than a human hair, on to a part of the brain that controls "movement intention", according to Neuralink. The company says that these threads allow its experimental implant - powered by a battery that can be charged wirelessly - to record and transmit brain signals wirelessly to an app that decodes how the person intends to move. "[It] has great potential to help people with neurological disorders in future and is an excellent example of how fundamental neuroscience research is being harnessed for medical advances," said Professor Tara Spires-Jones, president of the British Neuroscience Association. "However, most of these interfaces require invasive neurosurgery and are still in experimental stages thus it will likely be many years before they are commonly available." Telepathy In another post on X, Mr Musk said Neuralink's first product would be called Telepathy. Telepathy, he said, would enable "control of your phone or computer, and through them almost any device, just by thinking". "Initial users will be those who have lost the use of their limbs," he continued. Referring to the late British scientist who had motor neurone disease, he added: "Imagine if Stephen Hawking could communicate faster than a speed typist or auctioneer. That is the goal." While Mr Musk's involvement raises the profile of Neuralink, some of his rivals have a track record dating back two decades. Utah-based Blackrock Neurotech implanted its first of many brain-computer interfaces in 2004. Precision Neuroscience, formed by a Neuralink co-founder, also aims to help people with paralysis. And its implant resembles a very thin piece of tape that sits on the surface of the brain and can be implanted via a "cranial micro-slit", which it says is a much simpler procedure. Existing devices have also generated results. In two separate recent US scientific studies, implants were used to monitor brain activity when a person tried to speak, which could then be decoded to help them communicate. Related Topics Elon Musk Health United States https://www.bbc.com/news/technology-68137046 https://donshafi911.blogspot.com/2024/01/elon-musk-says-neuralink-implanted.html

EXCLUSIVEInside NIH virus lab in Montana - that has eerie ties to Wuhan - where US scientists inject pigs and monkeys with EBOLA and other dangerous bio-agents By Alexa Lardieri U.S. Deputy Health Editor Dailymail.Com 14:57 GMT 27 Jan 2024 , updated 14:57 GMT 27 Jan 2024 Photos obtained by a watchdog group show experiments performed on animals NIH lab in Montana was previously found to have been experimenting with SARS REVEALED: NIH lab experimented with coronaviruses from Wuhan in 2018 Photos and videos obtained exclusively by DailyMail.com show US government-funded researchers experimenting on animals at a controversial lab in Montana where risky virus research is carried out. Advertisement Advertisement Images and video footage obtained through a Freedom of Information Act request and shared exclusively with this website show researchers sedating monkeys and pigs and giving them injections, as well as piglets housed in small and unsanitary cages. Top Stories by Daily Mail 01:00 Admiral Rob Bauer: 'The next 20 years will not be hunky dory' MailOnline explains the top myths and facts surrounding Diabetes Prince William visits Kate as she spends her third day in hospital Crack appears in block of flats where 88 homes are being bulldozed Kate in hospital after undergoing abdominal surgery PETER HITCHENS: We don't wantdeath or blackouts, end the march to war While there is no suggestion any of the footage shows illegal activity, it gives an eerie glimpse into what goes on at the National Institutes of Health's Rocky Mountain Lab (RML), which has come under scrutiny in recent months. Last year, this website revealed that RML in Montana had been experimenting with SARS-like viruses a year before the Covid pandemic, and while that research has stopped, current projects involving other deadly pathogens with the potential to spark a new pandemic are still being carried out at the lab. These include injecting pigs with Ebola and infecting monkeys with Covid-19 and studying how they react to Hemorrhagic Fever, which involves vomiting blood, internal bleeding, bleeding in the brain and from the eyes, nose and mouth. The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, for a project to take place between 2017 and 2020 The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, for a project to take place between 2017 and 2020 The White Coat Waste project obtained photos of animal experiments on monkeys and pigs at the National Institutes of Health's Rocky Mountain Lab in Montana The White Coat Waste project obtained photos of animal experiments on monkeys and pigs at the National Institutes of Health's Rocky Mountain Lab in Montana The National Institutes of Health's Rocky Mountain Lab in Montana was previously found to have been experimenting with SARS-like viruses in 2018 The National Institutes of Health's Rocky Mountain Lab in Montana was previously found to have been experimenting with SARS-like viruses in 2018 Piglet experiments were to be carried in two parts, first infecting the pigs with REBOV via their noses - as seen in the photos above Piglet experiments were to be carried in two parts, first infecting the pigs with REBOV via their noses - as seen in the photos above The footage was obtained through a FOIA request by the White Coat Waste Project (WCW), which has campaigned against risky virus research and cruel animal experiments. The RML was first revealed to be experimenting with deadly pathogens in WCW's first batch of documents provided to this website last year. Previous documents from WCW revealed that in 2018, NIH researchers infected bats at the Rocky Mountain Lab with a 'SARS-like' virus as part of a collaboration with the Wuhan Institute of Virology, which is at the center of the Covid cover-up scandal. They showed US taxpayer money was used to experiment with coronaviruses from the Chinese lab thought to be the source of the Covid pandemic more than a year before the global outbreak. The NIH, under Dr Anthony Fauci's leadership, infected 12 Egyptian fruit bats with a 'SARS-like' virus called WIV1 at RML. The WIV1-coronavirus was shipped from the Wuhan lab the FBI believes caused the Covid pandemic and was tested on bats acquired from a 'roadside' Maryland zoo. Senators probe Fauci-run virus lab in Montana where US scientists were infecting bats with Covid-like viruses shipped in from WUHAN in 2018 - years before the pandemic Senators are demanding answers about a laboratory in Montana where US taxpayer money was used to manipulate coronaviruses before the pandemic. The research determined the novel virus could not cause a 'robust infection,' but is more evidence of ties between the US government and the Wuhan lab, as well as the funding of dangerous virus research across the globe. Advertisement Advertisement Following the WCW's investigation and DailyMail.com's reporting, Republican Senators Joni Ernst, from Iowa, and Eric Schmitt, from Missouri, sent a letter to the NIH demanding 'to learn more about potentially risky research' carried out by scientists at RML. Most recently, Sen Ernst wrote another letter, along with Rep Mike Gallagher, to the Pentagon demanding a review of the $50million in grants the US is sending to Chinese pandemic research institutions, including those based in Wuhan. The senator said in a statement: 'Taxpayers deserve to know how much of their money is being shipped to China and why Washington continues collecting and creating deadly super viruses — both of which could pose threats to our national security.' While the 'SARS-like' virus research has stopped, current projects involving other deadly pathogens with the potential to spark a new pandemic are still being carried out at the lab. As part of WCW's current lawsuit, the NIH was compelled to send the group records of its experiments taking place at RML. The documents reveal NIH scientists proposed infecting two- to three-week old piglets with reston virus (REBOV), a family of pathogens that could cause Ebola, a virus with a death rate of up to 90 percent, for a project to take place between 2017 and 2020. The project, 'The role of Arterivirus co-infection in the pathogenesis of Reston Ebola Virus in swine', was to test how the co-infection of Porcine Reproductive and Respiratory Syndrome (PRRS) and REBOV increased the virus' transmissibility and severity. The experiment was to be carried out in two parts, first infecting the pigs with REBOV via their noses - as seen in photos. On day three and between days five and 10 after inoculation, four animals were to be euthanized so necropsies could be performed. The remaining animals were to be euthanized on day 28. Then, researchers proposed inoculating pigs with PRRSV and REBOV several days later to observe their behavior and take vitals then euthanize them on day 28. One study was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth One study was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19 In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19 In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19 In documents obtained by WCW, scientists proposed experimenting on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever and Covid-19 Advertisement Advertisement While experimental 'manipulations' were to take place while the pigs were under anesthesia, the researchers said, 'Since we are evaluating these animals as potential models of disease progression, we are unable to alleviate the signs of disease.' Symptoms of these diseases include fever, breathing problems, weight loss, diarrhea, excessive or internal bleeding, coughing up or vomiting blood and neurological disorders that could be fatal. Researchers said: 'The illness experienced by animals exposed to these viruses must not be treated with analgesics because treatment will interfere with studying the disease manifestation and ultimate outcomes of infection.' In additional documents obtained by WCW, scientists proposed experiments between 2019 and 2022 on non-human primate that included infecting monkeys with Crimean-Congo hemorrhagic fever, a tick-borne virus that causes a life-threatening fever, muscle and joint pain, liver and kidney failure or pulmonary failure. The proposal said: 'In previous studies animals were scored for... reduced movement in cage and edema that on rare instances was of severity sufficient to impair function of internal organs such as the lungs and intestines. 'Since the objective of this study is to evaluate the efficacy of DNA vaccine candidates against CCHFV and contains necessary irrelevant DNA control group it is expected that some or animals will develop clinical signs and may suffer pain and distress. 'The illness experienced by the animals exposed to CCHFV must not be treated with analgesics because treatment could interfere with the disease manifestation and the outcome of vaccination.' Photos show piglets housed in small and unsanitary cages Photos show piglets housed in small and unsanitary cages Photos show piglets housed in small and unsanitary cages Photos show piglets housed in small and unsanitary cages A third proposal for experiments between 2020 and 2023 was titled 'Nonhuman primate model development for the novel coronavirus emerging in Wuhan, China.' The aim was to evaluate up to three species of nonhuman primates as potential animal models for Covid-19. For each species, one group of eight animals would be inoculated with a high dose of the virus via the eyes, nose or mouth - as seen in photos. The primates were to be evaluated and have their vitals taken and on day three, four would be euthanized. The remaining were to be monitored for disease progression. Advertisement Advertisement The proposal read: 'Infection with 2019-nCoV may cause mild to severe disease in nonhuman primates. Signs of illness may include fever, malaise, fatigue cough and heavy breathing potentially resulting in acute respiratory distress; the infection may be fatal. 'However, in this study we are unable to alleviate the disease manifestations potentially associated with 2019-nCoV infection as treatment would interfere with the outcome of the study.' Justin Goodman, the senior vice president of the White Coat Waste Project told DailyMail.com: 'Our successful lawsuit has pierced the veil of secrecy around the NIH’s dangerous, wasteful, and cruel maximum pain animal experiments with deadly bioagents that have up to 100 percent kill rates in humans. 'We’ve uncovered how NIH gain-of-function researchers linked to EcoHealth and the Wuhan lab import primates to the Rocky Mountain Lab from Fauci’s Monkey Island in South Carolina, infect them with viruses including Ebola and COVID, and then completely withhold pain relief while the animals suffer excruciating deaths. 'Taxpayers have a right to know how their money is being spent in barbaric NIH animal labs that can cause a devastating lab leak and pandemic right here in the US.' https://www.dailymail.co.uk/health/article-13008119/montana-lab-scientists-experimenting-dangerous-pathogens.html

WEF Admits Disease X Will Be Leaked in 2025 Sean Adl-Tabatabai Fact checked January 23, 2024 30 Comments WEF admits Disease X will be unleashed in 2025. The World Economic Forum (WEF) has declared that ‘Disease X’ will be unleashed onto the public by the year 2025 – and the consequences will be devastating for humanity. Last week, global elites met at the WEF Davos summit where the key topic of discussion was “Preparing for Disease X,”1 a hypothetical new deadly pandemic predicted to emerge in 2025 and kill 20 times more people than COVID-19.2 As reported by the Mirror:3 BYPASS THE CENSORS Sign up to get unfiltered news delivered straight to your inbox. You can unsubscribe any time. By subscribing you agree to our Terms of Use “The World Health Organization (WHO) has warned of a potential Disease X since 2017, a term indicating an unknown pathogen that could cause a serious international epidemic … Public speakers at the ‘Preparing for Disease X’ event next Wednesday [January 17, 2024] include Tedros Adhanom Ghebreyesus, director-general of the WHO, Brazilian minister of health Nisia Trindade Lima, and Michel Demaré, chair of the board at AstraZeneca. In their first post-pandemic meeting held in November 2022, the WHO brought over 300 scientists to consider which of over 25 virus families and bacteria could potentially create another pandemic. The list the team came up with included: the Ebola virus, the Marburg virus disease, Covid-19, SARS, and the Middle East respiratory syndrome coronavirus (MERS-CoV). Others included lassa fever, nipah and henipaviral diseases, zift Valley fever, and zika — as well as the unknown pathogen that would cause ‘Disease X.’” Mercola.com reports: I’ve interviewed Meryl Nass about how the WHO is trying to take over aspects of everyone’s lives. She just published an important piece over the weekend, Why Is Davos So Interested in Disease? about how the WEF and the WHO have become partners to terrify the world. Alexis Baden-Mayer, Esq., political director for the Organic Consumers Association, did some digging into the participants of this WEF event, and the two things they all have in common are 1) dumping the AstraZeneca COVID shot on the developing world (primarily India and Brazil) after rich countries rejected it due to its admitted blood clotting risk, and 2) pushing for the implementation of medical AI systems that will eliminate doctors along with patient choice and privacy. Practice Runs or Responsible Planning? In a January 11, 2024, tweet, Fox News analyst and former assistant secretary for public affairs for the U.S. Treasury Department, Monica Crowley, wrote:4 “From the same people who brought you COVID-19 now comes Disease X: Next week in Davos, the unelected globalists at the World Economic Forum will hold a panel on a future pandemic 20x deadlier than COVID … Just in time for the election, a new contagion to allow them to implement a new WHO treaty, lock down again, restrict free speech and destroy more freedoms. Sound far-fetched? So did what happened in 2020. When your enemies tell you what they’re planning and what they’re planning FOR, believe them. And get ready.” Dr. Stuart Ray, vice chair of medicine for data integrity and analytics at Johns Hopkins’ Department of Medicine, dismissed such warnings, telling Fortune magazine5 that “Coordination of public health response is not conspiracy, it’s simply responsible planning.” I’d be willing to believe him if it wasn’t for a now-obvious trend: Whatever the globalists claim will happen actually does happen at a remarkable frequency, and their prognostic capabilities become easier to explain when you consider that most lethal pandemics have been caused by manmade viruses, the products of gain-of-function research. It’s pretty easy to predict a new viral outbreak if you have said virus waiting in the wings. With that in mind, recent research from China certainly raises concern, to say the least. According to a January 3, 2024, preprint,6 a SARS-CoV-2-related pangolin coronavirus — described as a “cell culture-adapted mutant” called GX_P2V that was first cultured in 2017 — was found to kill 100% of the humanized mice (ACE2-transgenic mice) infected with it.7 JOIN THE FIGHT: BECOME A CITIZEN JOURNALIST TODAY! The primary cause of death was brain inflammation. According to the authors, “this is the first report showing that a SARS-CoV-2-related pangolin coronavirus can cause 100% mortality in hACE2 mice, suggesting a risk for GX_P2V to spill over into humans.” However, if this virus mutated as a result of passaging through cell cultures, then it’s not likely to emerge in the wild. It’s another unnatural lab creation, so rather than saying it may spill over from pangolins to humans, it would be more accurate to admit that it may pose a (rather serious) risk to humans were a lab escape to occur. COVID Dress Rehearsals In 2017, Johns Hopkins Center of Health Security held a coronavirus pandemic simulation called the SPARS Pandemic 2025-2028 scenario.8 Importantly, the exercise stressed “communication dilemmas concerning medical countermeasures that could plausibly emerge” in a pandemic scenario. Then, in October 2019, less than three months before the COVID-19 outbreak, the Bill & Melinda Gates Foundation in collaboration with Johns Hopkins and the World Economic Forum hosted Event 201. The name itself suggests it may have been a continuation of the SPARS Pandemic exercise. College courses are numbered based on their prerequisites. A 101 course does not require any prior knowledge whereas 201 courses require prior familiarity with the topic at hand. As in the SPARS Pandemic scenario, Event 201 involved an outbreak of a highly infectious coronavirus, and the primary (if not sole) focus of the exercise was, again, how to control information and keep “misinformation” in check, not how to effectively discover and share remedies. Social media censorship played a prominent role in the Event 201 plan, and in the real-world events of 2020 through the present, accurate information about vaccine development, production and injury has indeed been effectively suppressed around the world, thanks to social media companies and Google’s censoring of opposing viewpoints. In March 2021, an outbreak of “an unusual strain of monkeypox virus” was simulated.9 In late July the following year, the WHO director-general declared that a multi-country outbreak of monkeypox constituted a public health emergency of international concern,10 against his own advisory group. ‘Catastrophic Contagion’ Exercise Considering both of these simulations, SPARS (“Event 101”?) and Event 201, foreshadowed what eventually occurred in real life during COVID, when Gates hosts yet another pandemic exercise, it’s worth paying attention to the details. October 23, 2022, Gates, Johns Hopkins and the WHO cohosted “a global challenge exercise” dubbed “Catastrophic Contagion,”11,12 involving a fictional pathogen called “severe epidemic enterovirus respiratory syndrome 2025” (SEERS-25). Enterovirus D6813 is typically associated with cold and flu-like illness in infants, children and teens. In rare cases, it’s also been known to cause viral meningitis and acute flaccid myelitis, a neurological condition resulting in muscle weakness and loss of reflexes in one or more extremities. Enteroviruses A71 and A6 are known to cause hand, foot and mouth disease,14 while poliovirus, the prototypical enterovirus, causes polio (poliomyelitis), a potentially life-threatening type of paralysis that primarily affects children under age 5. So, the virus they modeled in this simulation appears to be something similar to enterovirus D68, but worse. Vaccine Drug Trials Begin for Deadly Nipah Virus One known virus that bears some resemblance to the fictional SEERS-25 is the Nipah virus. This virus has a kill rate of about 75%,15 and survivors oftentimes face long-term neurological issues stemming from the infection. Nipah is also said to affect children to a greater degree than adults.16 Incidentally, human trials for a vaccine against the deadly Nipah virus were recently launched.17 Volunteers received their first shots in early January 2024. The experimental injection uses the same viral vector technology used to produce AstraZeneca’s COVID shot. The trial is reportedly being carried out by the University of Oxford in an undisclosed area where Nipah is actively infecting victims. (India seems to be indicated, as an outbreak in Kerala killed two people and hospitalized three in September 2023.18) The disease is thought to spread via interaction with infected animals such as goats, pigs, cats and horses. It may also spread via tainted blood products and food. Symptoms can emerge anywhere from a few days after exposure to as long as 45 days. Initial symptoms include fever, headache and respiratory illness, which can rapidly progress to encephalitis (brain swelling), seizures and coma within just a couple of days. According to the WHO, pigs are known to be “highly contagious” during the incubation period, and it’s possible that humans may be as well, although that has yet to be confirmed. Training African Leaders to Go Along With the Narrative Tellingly, the Catastrophic Contagion exercise focused on getting leadership in African countries involved and trained in following the script. African nations went “off script” more often than others during the COVID pandemic, and didn’t follow in the footsteps of developed nations when it came to pushing the jabs. As a result, vaccine makers now face the problem of having a huge control group, as the COVID jab uptake on the African continent was only 6%,19 yet it fared far better than developed nations in terms of COVID-19 infections and related deaths.20 The Catastrophic Contagion exercise predicts SEERS-25 will kill 20 million people worldwide, including 15 million children, and many who survive the infection will be left with paralysis and/or brain damage. In other words, the “cue” given is that the next pandemic may target children rather than the elderly, as was the case with COVID-19. Vaccine Against Unknown ‘X’ Pathogen Is Already in the Works In August 2023, a new vaccine research facility was set up in Wiltshire, England, fully staffed with more 200 scientists, to begin work on a vaccine against the unknown “Disease X.” As reported by Metro:21 “It took 362 days to develop the Covid-19 vaccine. But the Vaccine Development and Evaluation Centre team wants to reduce that time to 100 days. Scientists at the facility will develop a range of prototype vaccines and tests. The new lab is a part of a global effort to respond to global health threats. The UK and other G7 countries signed up to the ‘100 Days Mission’ in 2021. The government has invested £65 million into the lab. Professor Dame Jenny Harries, the head of the UK Health Security Agency, said the new facility would ‘ensure that we prepare so that if we have a new Disease X, a new pathogen, we have as much of that work in advance as possible.’” In the U.S., Congress also introduced the “Disease X Act of 2023” (H.R.383222) back in June 2023. The bill calls for the establishment of a BARDA program to develop “medical countermeasures for viral threats with pandemic potential.” The bill was referred to the Subcommittee on Health in early June 2023 but has not yet been passed. The Disease X Act amends a section of the Public Health Service Act with two new clauses that call for “the identification and development of platform manufacturing technologies needed for advanced development and manufacturing of medical countermeasures for viral families which have significant potential to cause a pandemic,” and “advanced research and development of flexible medical countermeasures against priority respiratory virus families and other respiratory viral pathogens with a significant potential to cause a pandemic, with both pathogen-specific and pathogen-agnostic approaches …” Needless to say, since it’s impossible to customize vaccines using the conventional method of growing viruses in eggs or some other cell media in 100 days, it seems inevitable that all these efforts are about the expansion of gene-based technologies. This, despite the fact that the mRNA technology used for the COVID jabs has proven to be disastrous from a safety standpoint, and ineffective to boot. Why Manufactured Pandemics Will Continue At this point, it’s quite clear that “biosecurity” is the chosen means by which the globalist cabal intends to seize power over the world. The WHO is working on securing sole power over pandemic response globally through its international pandemic treaty which, if implemented, will eradicate the sovereignty of all member nations. The WHO’s pandemic treaty is the gateway to a global, top-down totalitarian regime, a one world government. Ultimately, the WHO intends to dictate all health care. But to secure that power, they will need more pandemics. COVID-19 alone was not enough to get everyone onboard with a centralized pandemic response unit, and they probably knew that from the start. So, the reason we can be sure there will be additional pandemics, whether manufactured using either fear and hype alone or an actual bioweapon created for this very purpose, is because the takeover plan, aka The Great Reset, is based on the premise that we need global biosecurity surveillance and centralized response. Biosecurity, in turn, is the justification for an international vaccine passport, which the G20 has signed on to, and that passport will also be your digital identification. That digital ID, then, will be tied to your social credit score, personal carbon footprint tracker, medical records, educational records, work records, social media presence, purchase records, your bank accounts and a programmable central bank digital currency (CBDC). Once all these pieces are fully connected, you’ll be in a digital prison, and the ruling cabal — whether officially a one world government by then or not — will have total control over your life from cradle to grave. We’re Already Suffering Under a Pseudo-One World Government We actually already have a pseudo-one world government, in the form of Bill Gates’ nongovernmental organizations (NGOs). They are making health care decisions that should be left to individual nations and/or states, and they’re making decisions that will line their own pockets, regardless of what happens to the public health-wise. They coordinate and synchronize pandemic communication during simulated practice runs, and then, when the real-world situation emerges that fits the bill, the preplanned script is played out more or less verbatim. Between the G20 declaration to implement an international vaccine passport under the auspice of the WHO, and the WHO’s pandemic treaty, everything is lined up to take control of the next pandemic, and in so doing, further securing the foundation for a one world government. As discussed in my 2021 article, “COVID-19 Dress Rehearsals and Proof of the Plan,” the pandemic measures rolled out for COVID-19 were the culmination of decades of careful planning to radically and permanently alter the governance and social structures of the world. The medical system has been used in the past to drive forward a New World Order agenda — now rebranded as “The Great Reset” — and it’s now being used to implement the final stages of that longstanding plan. COVID-19 was a real-world practice run, and showed just how effectively a pandemic can be used to shift the balance of power, and strip the global population of its wealth and individual freedoms. So, there’s no doubt in my mind that additional pandemics will be declared, because they’re the means to the globalists’ ends. To prevent this global coup, we need everyone to speak and share the truth to the point that you’re able. Only then will our voices outnumber the voices of the propaganda machine. Door To Freedom (doortofreedom.org), an organization founded by Dr. Meryl Nass, has a poster that explains how the pandemic treaty and International Health Regulations (IHR) amendments will change life as we know it and strip us of every vestige of freedom. Please download this poster and share it with everyone you know. Also put it up on public billboards and places where communities share information. Not only a healthy way to eat but also the most sustainable, eating nose to tail provides you with some of the most nutritionally dense sources of valuable minerals and fat-soluble vitamins from organ meats. Help balance the nutritional shortcomings of muscle meats with Grass Fed Beef Organ Complex, offering five of the most valuable organs — liver, heart, kidney, pancreas and spleen — from roaming, healthy New Zealand cows with year-round access to grasslands. 1, 21 Metro January 15, 2024 2, 3 Mirror January 13, 2024 4 Twitter/X Monica Crowley January 11, 2024 5 Fortune January 12, 2024 6 ResearchGate January 2024 DOI: 10.1101/2024.01.03.574008 7 MSN January 15, 2024 8 SPARS Pandemic Scenario 9 NTI Paper November 2021 10 UN News July 23, 2022 11 Catastrophic Contagion 12 Catastrophic Contagion Videos 13 CDC Enterovirus D68 14 CDC Enteroviruses 15 Forbes September 15, 2023 16 Intractable & Rare Diseases Research February 2019; 8(1): 1-8 17 Forbes January 11, 2024 18 BBC September 14, 2023 19 First Post November 19, 2021 20 Yahoo News November 19, 2021 22 HR 3832 The Disease X Act of 2023 https://thepeoplesvoice.tv/wef-admits-disease-x-will-be-leaked-in-2025/

Who Wants The Next Pandemic And Why? Who Wants The Next Pandemic And Why? #COVID-19#RUSSIA 16.01.2024 - 1789 views 8 1 0 Share1 12 Support SouthFrontPDF Download Who Wants The Next Pandemic And Why? Click to see the full-size image Written by Drago Bosnic, independent geopolitical and military analyst It’s been nearly two years since Russia uncovered the extremely disturbing truth about American involvement in bioweapons testing in Ukraine. However, the institutions of the so-called “rules-based world order” (posing as the “international community”) have completely ignored these findings, while the mainstream propaganda machine has done everything in its power to present them as supposed “conspiracy theories”. Still, the world has been demanding answers from the US-led political West. This includes non-aligned countries, often dubbed the “fence sitters” by the United States, although there have been far worse descriptions used by the European Union. American diplomacy (if one could even call it that way) is too busy meddling in the internal affairs of other countries, so it usually refuses to comment on allegations regarding the Pentagon-run “biological research facilities” in Ukraine. Luckily for the world, the Russian military never stopped investigating this issue, despite constant attempts to prevent, sabotage and/or discredit these efforts. On January 15, TASS reported that the Russian Ministry of Defense (MoD) identified over 50 participants in America’s bioweapons program in Ukraine last year alone. During a briefing held on the same day, Lieutenant General Igor Kirillov, Head of the Russian Armed Forces’ Nuclear, Biological and Chemical (NBC) Protection Troops, warned about the dangers of these US-sponsored illicit activities. Kirillov revealed that an event that can only be described as a false flag training exercise was held in Lvov back in August 2023. The goal was to accuse Russia of supposed bioweapons usage in Ukraine, likely as a way for the US/NATO to both incriminate Moscow and divert attention away from itself and its illegal biological warfare activities in the war-torn country. “I would like to note the work carried out in 2023 to identify the organizers and participants of military-biological activities on the territory of Ukraine. As a result of the analysis of the documentation obtained, more than 50 people were identified, including officials of US and Ukrainian government agencies, and employees of intermediary organizations and private companies,” Kirillov said at the briefing. Among others, he named Kenneth Myers, Robert Pope and Joanna Wintrol, employees of the US DoD’s Cooperative Threat Reduction Program, as well as representatives of the companies Battelle and EcoHealth Alliance, Kevin Olival, Karen Saylors and Lewis von Thaer. “The [false flag] event [in Lvov] was attended by Filippa Lentzos; Gemma Bowsher; and Irina Demchyshyna, Head of the Reference Laboratories of the Public Health Center of the Ukrainian Health Ministry; as well as Darya Ponomarenko, Head of the Department of Biological Safety and Biological Protection of the Public Health Center of the Ukrainian Health Ministry,” Kirillov said. He added that R&D on pathogens that could cause massive economic damage was extensively conducted in these biolabs, including research on mechanisms for their more efficient distribution and spreading. The program was conducted under the leadership of Denis Muziyka. In addition, Viktor Gavrilenko and Alexander Mezinov were involved in the collection and shipment of materials. It can be argued the report essentially shows that the endgame was to cause long-term damage to the Russian economy (particularly its massive agricultural potential). In turn, this was supposed to cause instability in the country, possibly even a famine that could destabilize the Russian government. Needless to say, such activities are tantamount to a declaration of war. And yet, those conducting them are completely unmoved by the possibility of a direct confrontation between nuclear-armed superpowers. In further reports published later that day, TASS revealed additional goals of these US-run biolabs. General Kirillov touched upon the US strategy of (ab)using its publicly stated goals of supposedly “monitoring infectious diseases and providing assistance to developing countries” to further expand its biological warfare capabilities. “Over the past year, the Pentagon has developed and adopted a number of conceptual documents that involve expanding the foreign network of US-controlled biological laboratories and continuing military biological research beyond national jurisdiction. <…> While the stated goals are monitoring infectious diseases and providing assistance to developing countries, using the example of Ukraine, it became clear how the military-biological potential of the United States is being built up,” he stated. Kirillov also recalled that Washington DC created new administrative and technical agencies last year – the Office of Pandemic Preparedness and Response Policy, and the Bureau of Global Health Security and Diplomacy. These two agencies are supposed to serve as fronts for further bioweapons programs, not only in Ukraine, but around the world. Kirillov also reiterated previous findings uncovered after the start of the special military operation (SMO). He specifically mentioned the Pentagon’s two major projects in Ukraine, aimed at studying the causative agents of particularly dangerous pathogens and diseases such as tularemia, anthrax and hantavirus infections. “The research was carried out in three main areas. These are monitoring the biological situation, collecting endemic strains, and studying the susceptibility of the local population,” Kirillov said. In an additional report by the South Front, the Russian military revealed that the US Department of Defense conducted a series of experiments with smallpox viruses, which is prohibited by the World Health Assembly. This also includes research on the use of the monkeypox virus as a bioweapon, as well as R&D on the usage of agent-based simulators of smallpox viruses. Two strains of this pathogen are used in the course of aerobic studies. The World Health Assembly allows only two organizations to conduct such research – the Vector State Scientific Center in Russia and the Center for Disease Control in the US. However, these experiments were conducted by the employees of the Institute of Infectious Diseases, which is subordinate to the Pentagon. The US DoD was also engaged in studying other orthopoxviruses that are deadly and pose great danger to human life and health. Interestingly (or perhaps “terrifyingly” would be a much more fitting term), concurrently with the Russian military’s briefings, the infamous World Economic Forum announced it would discuss the new unspecified deadly pathogen that causes what they call the “Disease X”, which the WEF claims is “10 times deadlier than the COVID-19”. Considering the fact that the WEF is deeply intertwined with the political West and its vaunted “rules-based world order”, the timing is rather peculiar. Why are the WEF and the so-called “international community” so “worried” about an unknown disease, but they keep ignoring clear-cut evidence of America’s massive (and rapidly expanding) bioweapons program? Why is the US military conducting this sort of research (on a global scale, at that), although any official civilian public health institution could easily do so on its own and without such deadly biohazard risks? MORE ON THE TOPIC: US Military Conducts Dangerous Experiments With Prohibited Viruses Kiev Sold Ukrainian Land For Disposal Of Hazardous Chemical Waste Of US Companies – Report Moscow Accuses Washington Of Preparing For New Pandemic 8 1 0 Share1 12 Support SouthFrontPDF Download https://southfront.press/who-wants-the-next-pandemic-and-why/

Virology - The Damning Evidence The Stake In The Heart For This Pseudoscientific Profession dpl Introduction One never realize how big the task of writing on a subject is until you start. One thing you can be assured of is how much you learn by writing about your findings or thoughts. My stance on virology has been clarified in two previous posts as follows: The Gatekeepers Club. Virus Lie - The Result of 4 Years of Study. Another thing you quickly realize on this journey is how easy it is to censor someone, especially if you start hitting a nerve. I have documented some of it underneath the conclusion of the The Gatekeepers Club article. It is very important to make copies of your work, as shadow banning is one thing, but if these platforms decide to terminate your channel and all the work you have done is on it, you will obviously lose it all. We were in that same position about a year ago when Discord decided to terminate our channel. Twenty of the smartest people you would ever know had been working on it for close to two years, and it was gone overnight. Therefore, this post will serve as safekeeping for some of the best information that I have come across in the last few weeks proving that virology is pseudoscience. Update - 18 September 2023 The order of the sections of this article has been rearranged to introduce the most important information first. As mentioned in my most recent article titled: Hacking at the Root of the Virus Issue it was explained that for the longest time I thought that failure to “isolate” viruses was the most important evidence to focus on. This is however not the case as explained in detail in the “Hacking at the Root of the Virus Issue” article. Transmission is the fundamental assumption on which virology rest. Without proof of transmission, nothing downstream matters. Even though understanding these downstream concepts will never be a waste of time one must consider that the normal man on the street will not be interested in complicated terminology and processes. It is of crucial importance for the no virus community to find easier ways to explain the fallacy that is virology. Seeing as no one need a laboratory to assess whether transmission is possible and because we can observe this phenomena ourselves (Inductive reasoning) this is the linchpin for virology. A twitter space where we discussed this can be viewed here (*Note: Jamie was cut off during his talk and his section was not included). As discussed during the twitter space, we have reviewed the available transmission studies and a summary of these studies can be seen below. Transmission / Infection One of the funniest things you will see while debating the trolls on Twitter is that they will provide studies conducted to prove the efficacy of vaccines. The people that undertake these studies assume that transmission or infection has already been proven, but nothing could be further from the truth. That is why it is important for us to list the peer-reviewed studies that disprove transmission or infection to further demonstrate that virology is a pseudoscience. The list of studies was compiled with the help of Jamie, georgie&donny, and Aldhissla (also see Aldhissla’s list on polio here). (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment). The Journal of Infectious Diseases, Vol. 2, No. 2 (Mar. 1, 1905): - Chapman, 1801: Tried to transmit measles using the blood, tears, the mucus of the nostrils and bronchia, and the eruptive matter in the cuticle without any success. - Willan, 1809: Inoculated three children with vesicle fluids of measles but without success. - Albers, 1834: Attempted to infect four children with measles without success. He quoted Alexander Monro, Bourgois, and Spray as also having made unsuccessful inoculations with saliva, tears, and cutaneous scales. - Themmen, 1817: Tried to infect 5 children with measles. 0/5 children became sick. Charles Creighton, 1837 (A history of epidemics in Britain). "No proof of the existence of any contagious principles by which it was propagated from one individual to another." EH Ackernecht, writing about Anticontagionism between 1821 and 1867 - “That the anticontagionists were usually honest men and in deadly earnest is shown, among other things, by the numerous self-experiments to which they submitted themselves to prove their contentions.” also see “Famous are the plague self-experiments of Clot-Bey, the offers for plague self-experiment by Chervin, Lassis, Costa, Lapis, and Lasserre, and the cholera self-experiments of Fay, Scipio Pinel, Wayrot, and J.L. Guyon. The amazing thing is that almost all of these experiments failed to produce the disease.” Note on Hospitals by Florence Nightingale, 1858 - "Suffice it to say, that in the ordinary sense of the word, there is no proof, such as would be admitted in any scientific inquiry, that there is any such thing as 'contagion." also see "Just as there is no such thing as 'contagion,' there is no such thing as inevitable 'infection." Andreas Christian Bull, 1868 - “It does not seem apparent in this small [polio] epidemic that contagion played any role, because the disease occurred here and there in the different places of the district without the possibility of establishing any relation between the various cases or the families of the same.” Karl-Oskar Medin, 1887 - A Swedish pediatrician who was the first to examine a polio outbreak, concluded that it was an infectious, but not contagious, disease. Charles Caverly, 1894 - Investigated the first US polio epidemic: ”it is very certain that it was non-contagious.” Journal of American Medical Association, Volume 72, Number 3, 1919 (or additional link here): - Warschawsky, 1895 - Injected small pigs and rabbits with blood taken in the eruptive stage. All results were negative. - Belila, 1896 - Placed warm nasal mucus and saliva from measles patients on the nasal and oral mucous membrane of rabbits, guinea-pigs, cats, mice, dogs and lambs, but without any positive results. - Josias, 1898 - Rubbed measles secretions over the throat, nose and eyes of several young pigs, but without any effects. - Geissler, 1903 - Inoculated sheep, swine, goats, dogs and cats in various ways with the bodily fluids from patients with measles; including smearing, spraying, rubbing. All results were negative. - Pomjalowsky, 1914 - Injected measles blood into guineapigs, rabbits and small pigs. All results were negative. - Jurgelunas, 1914 - Inoculated blood from patients with measles into suckling pigs and rabbits, but without effect. Leegaard, 1899 - Was not able to prove a single case of patient-to-patient contagion in a polio outbreak in Norway. "Infantile paralysis is of an infectious, but not of a contagious nature. As a matter of fact no indisputable instance of contagion could be proved." Dr. Rodermund, 1901 - From his diary of SmallPox experiments. For 15 years he smeared the pus of smallpox patients on his face and used to go home with his family, play cards at the gentleman’s club and treat other patients and never got sick or saw a single other person get sick. Walter Reed, 1902 - “Without entering into details, I may say that, in the first place, the Commission saw, with some surprise, what had so often been noted in the literature, that patients in all stages of yellow fever could be cared for by non-immune nurses without danger of contracting the disease. The non-contagious character of yellow fever was, therefore, hardly to be questioned.” Landsteiner & Popper, 1909 - "Attempts to transmit the disease [polio] to the usual laboratory animals, such as rabbits, guinea pigs, or mice, failed." F.E. Batten, (1909) - “Against the infectivity of the disease may be urged, first, the absence of spread of infection in hospital. The cases of poliomyelitis admitted to hospital freely mixed with other cases in the ward without any isolation or disinfection, some 70 children came in contact, but no infection took place. (p. 208, last paragraph)” The Boston medical and surgical journal, 1909 - An inquiry a 1908 polio outbreak found the following: “A large number of children were in intimate contact with those that were sick, and of these children an insignificant minority developed the disease.” 244 children were in intimate contact with those who were afflicted with polio. Of those 244 children, an "insignificant minority" developed the disease. Massachusetts State board of health, 1909 - "Poliomyelitis prevailed in epidemic form in Kansas during the summer of 1909 … No method of contagion could be found, and the author does not consider the disease contagious." Flexner & Lewis, 1910 - Multiple unsuccessful polio transmission attempts. "Many guinea-pigs and rabbits, one horse, two calves, three goats, three pigs, three sheep, six rats, six mice, six dogs, and four cats have had active virus introduced in the brain but without causing any appreciable effect whatever. These animals have been under observation for many weeks." A Washinton, 1911 - “I have not seen any cases of Polio contagion. We put the patients on one side and typhoid cases on the other, and no nurse or mother was infected. If the disease was so contagious, I don't see why the nurses and mothers would not have been infected.” J.J. Moren, 1912 - "Monkeys suffering from polio in the same cage with healthy monkeys, do not infect others." P. H. Römer, 1913 - "No proofs of the contagiousness of the disease [polio] could be obtained in the great epidemic in New York in 1907, nor in the epidemic in the Steiermark (Furntratt, Potpeschnigg) nor in Pomerania (Peiper). H. W. Frauenthal, 1914 - "Advocates of the contagion theory were at a loss to account for the fact that spontaneous [polio] transmission among laboratory monkeys was never known to occur ... There is no proof that spontaneous transmission of acute poliomyelitis, without an inoculation wound, can take place. There is no proof that contact contagion takes place. Spontaneous development of the disease among laboratory animals is unknown." W.H. Frost, 1916 - "The disease [polio] develops in a such a small proportion of people known to have been intimately associated with acute cases of polio." ... "The majority of cases of poliomyelitis can not be traced to known contact, either direct or indirect, with any previous case." W. L. Holt, 1916 - Investigated an epidemic of polio and found that he was "surprised that I could trace hardly any cases to personal contact with others, there rarely being successive cases." Dr. I. D. Rawlings, 1916 - "Any one who has had much experience with poliomyelitis is struck by the infrequency, relatively, of the secondary cases among direct contacts ... there were approximately 1,500 direct contacts, and yet but one possible case occurred among them. Also among the large number of people that came from New York and other infected areas not a single case occurred.” H. L. Abramson, 1917 - Attempts to induce polio in a monkey by injecting the spinal fluid of 40 polio patients (rather than the ground cord) into the brain failed. Dold et al. 1917 (Original paper in German from Muenchener Medizinische Wochenschrift 64 ( 1917), bottom of p 143) - Injected healthy people with the nasal secretions taken from one ill person, 1/40 healthy people became ill. A review of the investigations concerning the etiology of measels, A. W. Sellards harvard Medical School. Boston, Massachusetts as seen below: - Jurgelunas, 1914: Tried to produce measles in monkeys using inoculations of the blood and mucus secretions from measles patients as well as by exposing the animals to patients in measles wards. All results were negative. - Sellards, 1918: Tried to transmit measles to 8 healthy volunteers without a prior history of measles exposure. 0/8 men became sick after multiple failed attempts. - Sellards and Wenworth, 1918: Inoculated 3 monkeys in various ways, including intensive injections of blood from measles patients. The animals remained well. - Sellards and Wenworth, 1918: Blood from measles patients was injected simultaneously into 2 men and 2 monkeys. Both men remained symptom-free. One of the two monkeys developed symptoms that were not suggestive of measles. Milton Rosenau, 1918 - Professor of preventive medicine and hygiene at Harvard, notes that "monkeys have so far never been known to contract the disease [polio] spontaneously, even though they are kept in intimate association with infected monkeys." Page 341. Hess & Unger, 1918 - "In three instances the nasal secretion of varicella patients was applied to the nostrils; in three others the tonsillar secretion to the tonsils, and in six, the tonsillar and pharyngeal secretions were transferred to the nose, the pharynx, and the tonsils. In none of these twelve cases was there any reaction whatsoever, either local or systemic." Hess & Unger, 1918 - The vesicle fluids from people with chickenpox was injected intravenously into 38 children. 0/38 became sick. Published in the Journal - American Medical Association, 1919 - Need Of Further Research On The Transmissibility Of Measles And Varicella. “Evidently in our experiments we do not, as we believe, pursue nature's mode of transmission; either we fail to carry over the virus, or the path of infection is quite different from what it is commonly thought to be.” Milton J. Rosenau, March 1919 - Conducted 9 separate experiments in a group of 49 healthy men, to prove contagion. In all 9 experiments, 0/49 men became sick after being exposed to sick people or the bodily fluids of sick people. More information on the Rosenau studies here. Wahl et al, 1919 - Conducted 3 separate trials on six men attempting to infect them with different strains of Influenza. Not a single person got sick. Schmidt et al, 1920 (Original paper in German here) - Conducted two controlled experiments, exposing healthy people to the bodily fluids of sick people. Of 196 people exposed to the mucous secretions of sick people, 21 (10.7%) developed colds and three developed grippe (1.5%). In the second group, of the 84 healthy people exposed to mucous secretions of sick people, five developed grippe (5.9%) and four colds (4.7%). Of forty-three controls who had been inoculated with sterile physiological salt solutions eight (18.6%) developed colds. A higher percentage of people got sick after being exposed to saline compared to those being exposed to the “virus”. Williams et al, 1921 - Tried to experimentally infect 45 healthy men with the common cold and influenza, by exposing them to mucous secretions from sick people. 0/45 became ill. Mahatma Gandhi, 1921 - "and the poison that accumulates in the system is expelled in the form of small-pox. If this view is correct, then there is absolutely no need to be afraid of small-pox" also see "This has given rise to the superstition that it is a contagious disease, and hence to the attempt to mislead the people into the belief that vaccination is an effective means of preventing it." Blanc and Caminopetros, 1922 (original paper in French here) - Material from nine cases of shingles was inoculated into the eyes, cornea, conjunctiva, skin, brain, and spinal cord of a series of animals, including rabbits, mice, sheep, pigeons, monkeys, and a dog. All results were negative. Robertson & Groves, 1924 - Exposed 100 healthy individuals to the bodily secretions from 16 different people suffering from influenza. 0 people of 100 whom they deliberately tried to infect with Influenza got sick That is because Viruses don't cause disease. Bauguess, 1924 - "A careful search of the literature does not reveal a case in which the blood from a patient having measles was injected into the blood stream of another person and produced measles." The problem of the etiology of herpes zoster, 1925 - "Many other authors report entirely negative results following the inoculation of herpes zoster material into the sacrified corneas of rabbits: Kraupa (18); Baum (19); LSwenstein (8), Teissier, Gastinel, and Reilly (20) ; Kooy (21) ; Netter and Urbain (22); Bloch and Terris (23); Simon and Scott (24); and Doerr (25). It is evident, therefore, that the results of attempts to inoculate animals with material from cases of herpes zoster must be considered at present to be inconclusive." Volney S and Chney M.D., 1928 - A study where it is clearly stated that cold is not infectious. Dochez et al, 1930 - Attempted to infect 11 men with intranasal influenza. Not a single person got sick. Most strikingly one person got very sick when he accidently found out that is what they were trying to do. His symptoms disappeared when they told him he was misinformed. L. L. Lumsden, 1935 - “Painstaking efforts were made throughout the studies to obtain all traces of transmission of the disease through personal contact, but it appears that in this outbreak in Louisville evidence of personal association between the cases of poliomyelitis, suggestive of cause and effect, was no more common than that which might have been found if histories had been taken of personal association between cases of broken bones occurring in the city in the same period.” Thomas Francis Jr et al, 1936 - Gave 23 people influenza via 3 different methods. 0 people got sick.. They gave 2 people already "suffering from colds" the influenza who also did not get sick Burnet and Lush, 1937 - 200 people given "Melbourne type" Influenza . 0 people showed any symptoms of disease. 200/0. Lumsden, 1938 - "It is quite usual in small [polio] outbreaks in rural counties for individual cases to develop in separate homes three or for miles apart without there being any evidence of direct or indirect personal contact having operated between persons afflicted." L. L Lumsden, 1938 - ”The general and usual epidemiological features of the disease [polio] all appear opposed to the hypothesis that poliomyelitis is a contagious disease spread among human beings by nose-to-nose or any other direct personal contact.” Burnet and Foley, 1940 - Attempted to experimentally infect 15 university students with influenza. The authors concluded their experiment was a failure. Thomas Francis Jr, 1940 - Gave 11 people "Epidemic Influenza" 0 people got sick. That is because viruses don't cause disease. John Toomey, 1941 - A veteran polio researcher: "no animal gets the disease from another, no matter how intimately exposed." A. R. Kendall, 1945 - “The epidemiological facts of poliomyelitis are these: … (2) A majority of cases of clinically diagnosable poliomyelitis (polioparalysis) occur sporadically, with no history of contact with previous cases. (3) Two cases of polioparalysis in one family are unusual, even though no precautions are taken to prevent cross infection. (4) Clinically diagnosable cases of poliomyelitis (polioparalysis) show little tendency to spread, even in schools or other places of public gathering. (5) Incidence of polioparalysis is no greater among doctors and nurses, in intimate contact with acute cases than it is among the civil population, even though the former are exposed freely to infection.” […] “Polioparalysis is not contagious.” E. B. Shaw & H. E. Thelander, 1949 - “The epidemiology of the disease [polio] remains obscure. There has been a tendency to depart from an early theory that the disease spreads by means of direct contact.” Albert Sabin, 1951 (inventor of the polio vaccine). "There is no evidence for the transmission of poliomyelitis by droplet nuclei." Archibald L. Hoyne, 1951 (alternative link here) - “However, in the Cook County Contagious Disease Hospital where the latter procedure has not been used there has never been a doctor, intern, nurse or any other member of the personnel who contracted poliomyelitis within a period of at least thirty-five years, nor has any patient ever developed poliomyelitis after admission to the hospital.” Ralph R. Scobey, 1951 - ”Although poliomyelitis is legally a contagious disease, which implies that it is caused by a germ or virus, every attempt has failed conclusively to prove this mandatory requirement of the public health law.” Professor of clinical pediatrics and president of the Poliomyelitis Research Institute, Syracuse, N.Y. Ralph R. Scobey, 1952 - "In addition to the failure to prove contagiousness of human poliomyelitis, it has likewise been impossible to prove contagiousness of poliomyelitis in experimental animals." Douglas Gordon et al, 1975 - This study gave 10 people English type Influenza and 10 people a placebo. The study was negative. Most telling is they admit that mild symptoms were seen in the placebo group, proving that the inoculation methods cause them. Beare et al 1980 (refer to reference 6 in the linked paper). Quote from John J Cannell, 2008 as follows - “An eighth conundrum – one not addressed by Hope-Simpson – is the surprising percentage of seronegative volunteers who either escape infection or develop only minor illness after being experimentally inoculated with a novel influenza virus.” Nancy Padian, 1996 - A study which followed 176 discordant couples (1 HIV positive and the other negative) for 10 years. These couples regularly slept together and had unprotected sex. There were no HIV transmissions from the positive partner to the negative partner during the entirety of the study. John Treanor et al, 1999 - Gave 108 people Influenza A. Only 35% recorded mild symptoms such as stuffy nose. Unfortunately 35% of the placebo control group also developed mild symptoms proving the methods of inoculation are causing them. Bridges et al, 2003 - "Our review found no human experimental studies published in the English-language literature delineating person-to-person transmission of influenza... Thus, most information on human-to-human transmission of influenza comes from studies of human inoculation with influenza virus and observational studies." The Virology Journal, 2008 - ”There were five attempts to demonstrate sick-to-well influenza transmission in the desperate days following the pandemic [1918 flu] and all were ’singularly fruitless’ … all five studies failed to support sick-to-well transmission, in spite of having numerous acutely ill influenza patients, in various stages of their illness, carefully cough, spit, and breathe on a combined total of >150 well patients.” Public Health Reports, 2010 - ”It seemed that what was acknowledged to be one of the most contagious of communicable diseases [1918 flu] could not be transferred under experimental conditions.” Jasmin S Kutter, 2018, - Our observations underscore the urgent need for new knowledge on respiratory virus transmission routes and the implementation of this knowledge in infection control guidelines to advance intervention strategies for currently circulating and newly emerging viruses and to improve public health. - There is a substantial lack of (experimental) evidence on the transmission routes of PIV (types 1–4) and HMPV. - Extensive human rhinovirus transmission experiments have not led to a widely accepted view on the transmission route [35, 36, 37, 38, 39, 40]. - However, until today, results on the relative importance of droplet and aerosol transmission of influenza viruses stay inconclusive and hence, there are many reviews intensively discussing this issue [10, 45, 46, 47, 48, 49, 50]. - Despite this, the relative importance of transmission routes of respiratory viruses is still unclear, depending on the heterogeneity of many factors like the environment (e.g. temperature and humidity), pathogen and host [5, 19]. Jonathan Van Tam, 2020 - Conducted these human trials of Flu A in 2013. 52 people were intentionally given "Flu A" and made to live in controlled conditions with 75 people. 0 people sick. 0 PCR positive. J.S. Kutter, 2021 - “Besides nasal discharge, no other signs of illness were observed in the A/H1N1 virus-positive donor and indirect recipient animals.” The animals were subsequently euthanized after the animals experienced what the scientist describe as having breathing difficulties (no further details were given to describe their condition). *Refer to Note 1. Ben Killingley, 2022 - Gave 36 people what he considered to be purified Covid Virus Intranasally. The Results: Nobody got sick. *Refer to Note 2. Notes *Note 1 - Jasmin Kutter, 2021: From the Results section: “Throat and nasal swabs were collected from the donor and indirect recipient animals on alternating days.” This on its own can lead to nasal discharge which is the only “sign of illness” that was noted in this study. *Note 2 - Ben Killingley, 2022: See the video explanation by Jamie here. Ben Killingley also conducted a study in the early 2010's in which he had inoculated people in a room with 75 others some wearing masks others as a control. Not a single person even tested PCR positive. Some links to his previous studies include a 2011, 2019 and a 2020 study. It is assumed that his latest, 2022 study, is a follow up to cover the findings of his previous findings. Some additional notes on the study referenced include: - They gave 10 people the potent nephrotoxin Remdisivir. - They measure sickness by means of a PCR test which isn't indicative of disease because it can tests positive with “asymptomatic” cases as well. - Even if you say that a runny nose after swabbing is Covid. A 50% outcome to a direct challenge of something is a negative result. It doesn't suggest causation which would need to be at least 90%. - The very methods of inoculation used during the study could cause the nasal congestion/discharge (which is their measure of whether someone is sick or not). This has been shown in previous studies. - Lastly nobody was given "regeneron" because nobody got "sick". *Note 3 - Dr Robert Willner, 1994: December 7th 1994 Hollywood Roosevelt Hotel, Greensboro, N.C., Dr Willner (a medical doctor of 40 years experience) an outspoken whistleblower of the AIDS hoax. In front of a gathering of about 30 alternative-medicine practitioners and several journalists, Willner stuck a needle in the finger of Andres, 27, a Fort Lauderdale student who says he has tested positive for HIV. Then, wincing, the 65-year-old doctor stuck himself. In 1993, Dr. Willner stunned Spain by inoculating himself with the blood of Pedro Tocino, an HIV positive hemophiliac. This demonstration of devotion to the truth and the Hippocratic Oath he took, nearly 40 years before, was reported on the front page of every major newspaper in Spain. His appearance on Spain’s most popular television show envoked a 4 to 1 response by the viewing audience in favor of his position against the “AIDS hypothesis.” When asked why he would put his life on the line to make a point, Dr. Willner replied: “I do this to put a stop to the greatest murderous fraud in medical history. By injecting myself with HIV positive blood, I am proving the point as Dr. Walter Reed did to prove the truth about yellow fever. In this way it is my hope to expose the truth about HIV in the interest of all mankind.” He tested negative multiple times. He died of a Heart attack 4 months later 15th April 1995 (yeh right, funny how these naysayers all die suddenly. Link to the presentation here. Ludicrous “Transmission” Studies The picture of virology’s ludicrousy won’t be complete without a list of studies showing the insanity of what virologists claim to be transmission of disease. This include the injection of fluids into the brains and lungs of animals and we may just include some epidemiological studies to show how these are also not proof of anything. Joe Hendry mostly put it together and the papers we have are as follows (*Please note that this section is open to comments at the moment and anyone that want to add notes or studies are free to leave a comment): Louis Pasteur, 1881 - For rabies, tried to demonstrate transmission by injecting diseased brain tissue "directly onto the surface of the brain of a healthy dog through a hole drilled into its skull." Simon Flexner and Paul A. Lewis, 1910 - Spinal cords from deceased children were ground up and emulsified to be injected into the brains of monkeys. Study explained in detail here. John F. Anderson and Joseph Goldberger, 1911 - Injected blood from a measles patient directly into the heart and brains of monkeys. Carl Tenbroeck, 1918 - A mixture of ground up rat's livers, spleens, kidneys, testicles, lungs, hearts, and brains was injected into the brains of other rats. Claus W. Jungeblut, 1931 - Ground up monkey spinal cord was injected into the brains of other monkeys. Wilson Smith, 1933 - “The infected animal is killed when showing symptoms, often at the beginning of the second temperature rise. The turbinates are scraped out, ground up with sand, and emulsified in about 20 c.cm. of equal parts of broth and saline. The emulsion is lightly centrifuged, and about 1 c.cm. of the supernatant fluid is dropped into the nostrils of another ferret.” Thomas Francis and Jr, T. P. Magill, 1935 - Ground up ferret lung tissue was injected into the brains of rabbits. Ann G. Kuttner and T'sun T'ung, 1935 - Ground up kidney and brain of a guinea pig was injected into the brain of another guinea pig. Erich Traub. April 01 1936 - Ground up mouse brain was injected into the brains of guinea pigs. Albert B. Sabin and Peter K. Olitsky, 1937 - Ground up mouse brain was injected into the brains of other mice. G. John Buddingh, 1938 - Ground up chick embryo was injected into the brains 2 or 3 day old chicks. Gilbert Dalldorf, 1939 - Ground up ferret spleens was injected into the brains of mice. Claus W. Jungeblut et al, 1942 - Ground up brain or spinal cord of paralyzed mice was injected into the brains of 13 monkeys. Henry Pinkerton and Vicente Moragues, 1942 - Ground up brain tissue from dying mice was injected into the brains of pigeons. C. Kling et al, 1942 - Injected sewage sludge into the brains and abdomen of monkeys. This convinced him that he had isolated a virus and proven that the sewer is a vehicle for polio transmission. D.M. Horstmann, 1944 - Allegedly "proved" that the feces of polio patients contained "poliovirus" by injecting fecal samples into monkeys' brains and spines. Joseph E. Smadel et al, 1945 - Ground up pigeon spleen was injected into the brains of mice. F. Sargent Cheever et al, 1949 - Ground up mouse brain was injected into the brains of rats and hamsters. Isolation Isolation has been well defined in Virus Lie - The Result of 4 Years of Study and to this day there has not been a single paper presented that could show the isolation of a virus without first contaminating the sample. This is shown in detail in the virus lie article and will not be repeated here again. One interesting point that can be captured here is all the studies showing a control test proving that the isolation method used for viruses is flawed. They can be listed as follows: John F Enders, 1954 - Under other agents isolated during the study. "A second agent was obtained from an uninoculated culture of monkey kidney cells. The cytopathic changes it induced in the unstained preparations could not be distinguished with confidence from the viruses isolated from measles." It is highlighted here. Refer to the video explanation here. Image It is further discussed in the paper that "While there is no ground for concluding that the factors in vivo (in the body) are the same as those which underlie the formation of giant cells and the nuclear disturbances in vitro (outside a living organism), the appearance of these phenomena in cultured cells is consistent with the properties that a priori might be associated with the virus of measles.” Image Rustigian et al, 1955 - This paper is described in an article by Viroliegy here (look under Rustigain in the article). Cohen et al, 1955 - This paper is also described in the same article by Viroliegy here (look under Cohen in the article). Bech and von Magnus, 1959 - This paper is also described in the same article by Viroliegy here (look under Von Magnus in the article). F Rapp et al, 1959 - This paper is described in a video by Spacebusters here. Most noteworthy is “Monkey kidney cells, however, are unsuitable for the investigations of the type reported here; Peebles et al. and Ruckle showed that monkeys, and cell cultures derived from them, are often infected with an agent serologically indistinguishable from human measles virus, which causes cytopathic changes in monkey kidney cell cultures almost identical with those caused by human measles virus.” Image Carl J. O’Hara et al, 1988 - The study demonstrated "HIV" particles in 18 out of 20 (90% of) AIDS-related lymph node enlargements but also in 13 out of 15 (88% of) non-AIDS-related enlargements. Which means that particles claimed to be HIV virions are non-specific since identical particles can be found in the majority of patients with enlarged lymph nodes not attributed to AIDS, and at no risk for developing AIDS. Refer to @Aldhissla45’s tweet here. P Gluschankof et al, 1997 - This paper described in a video here with additional notes by Jamie here. Julian W. Bess Jr., 1997 - This paper described in a video here with additional notes by Jamie here. C.A. Cassol, 2020 - This paper is described by Andrew Kaufman here as well as by Thomas Cowan here. “Unofficially” we can also add the Lanka 3 phase control experiment that can be seen here or searched for it here. A further indication of the isolation procedure fallacy is shown in a study during which the CPE becomes more well defined with the addition of specific substances. The study is as follows: Leon Caly et al, 2020 - “Following several failures to recover virions with the characteristic fringes of surface spike proteins, it was found that adding trypsin to the cell culture medium immediately improved virion morphology.” See a video explanation here. Recent Requests and Statements Further and more recent requests and statements that were sent to me by my good friend Courtenay are as follows: May 5, 2022: U.S. CDC and Agency for Toxic Substances and Disease Registry confirmed that a search of their records failed to find any that describe anyone on Earth finding an alleged “avian influenza virus” in the bodily fluids of any diseased diseased host (animal or human) and purifying “it”… which is necessary so that “it” could be sequenced, characterized and studied with controlled experiments. This can be viewed here. May 20, 2022: Public Health Agency of Canada confirmed that they have no record of any alleged “avian influenza virus” having been found and purified from the bodily fluid/tissue/excrement of any diseased “host” on the planet (in order for “it” to be sequenced, characterized and studied with controlled experiments) by anyone, anywhere, ever. Insanely, they insist that: “Viruses” are in hosts despite their utter inability to find them there,. It’s necessary to “grow them” in non-host cells (as if “they” would grow better there than they allegedly grew in the diseased host lol). They pretend that mixing complex substances together results in purification. This can be viewed here. December 20, 2021: Public Health Agency of Canada confirmed that they have no record of any alleged “virus” having been purified from a sample taken from any diseased human on Earth, by anyone, ever, period. To be viewed here. March 11, 2022: U.S. Centers for Disease Control and Prevention and Agency for Toxic Substances and Disease Registry respond to a FOIA request for all studies / reports in their possession, custody or control describing the purification of any “virus” addressed by any “vaccine” on either their childhood or adult U.S. “immunization” schedule, directly from a sample taken from any diseased "host" on Earth where the sample was not first combined with any other source of genetic material. CDC/ATSDR provided 5 studies on “rotavirus” (thereby admitting they have no records for any other alleged viruses). None of these 5 studies actually describe isolation/purification of a “rotavirus” from a human. Request, response, studies to be viewed here. March 8, 2023: Italy 2020: Inside Covid’s “Ground zero” in Europe - Three years ago the Western World came to a standstill. The official Covid-19 narrative depicted a strange suddenly-super-spreading, deadlier-than-flu virus hailing from China that landed in Northern Italy. On February 20, 2020 the first alleged case of Covid-19 was discovered in the West in the Lombardy town of Codogno, Italy. Later that day the Italian government reported their first “Covid-19 death.” Dramatic media reports emerging from Northern Italy were hammered into and onto the Western psyche giving the impression there was a mysterious “super spreading” and “super lethal” novel virus galloping across the region infecting and killing scores of people. Read the rest of the report here. Conclusion The above list will be worked on over the coming years. If you think that any corrections need to be made or if you want to add additional studies, please leave a comment. Share Leave a comment https://open.substack.com/pub/dpl003/p/virology-the-damning-evidence?r=29hg4d&utm_medium=ios&utm_campaign=post

BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy donshafi911 BOMBSHELL! Inside mRNA Vaccines a Human Molecule Diabolically Altered | VT Foreign Policy January 6, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. In the cover image, the Canadian researcher Jessica Rose, author of an excellent biochemical analysis of an article from the University of Cambridge commenting a study by some of its researchers on the toxicity of manipulated human nucleoside in mRNA genetic sera by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell». With this phrase to be engraved in the history of the massive Covid vaccination campaign, the esteemed Canadian researcher, biochemist, immunologist and molecular biologist Jessica Rose (Source 1), author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridge in relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule” because it is a biological human component modified twice in the laboratory. (Source 1). UPDATE! Florida State Surgeon General Calls for Halt of mRNA Vaccines due to Dangerous, Oncogenes DNA Fragments Author of multiple fundamental discoveries on the contamination of mRNA genetic sera, best describes the disturbing importance of an article published by University of Cambridgein relation to an enlightening scientific research which confirmed to the global scientific community the dangerous experimental use in the Pfizer-Biontech and Moderna mRNA vaccines of what we do not hesitate to define as the “Diabolical Molecule”because it is a biological human component modified twice in the laboratory. Billions of Dangerous Spike DNA’s Molecules inside Covid mRNA Vaccines. They can Reproduce the Toxic Protein in Human Cells for a Long Time This is the double alteration of Uridinetransformed into Pseudourine with the first synthetic biochemical alteration and then into N1-methylpseudouridine initialed “m1Ψ” as an acronym for N1-methyl-Ψ in which the Greek letter “Psi” was used to name Psueudoridine . Uridine is an organic compound, nucleoside,made up of the coupling of a molecule of ribose and one of uracil. Uracil is one of the two pyrimidine nitrogenous bases that form the nucleotides of RNA nucleic acid. This manipulation was designed by the Hungarian biochemist Katalin Karikó,awarded the 2023 Nobel Prize for Medicine precisely for having laid the foundations of mRNA vaccines, in order to “deceive” human cells into recognizing the synthetic mRNA as harmless human RNA … I apologize to the biochemistry experts for any transcription mistakes I may make trying to translate from a difficult chemical language the portentous scientific essence of the abundant technical quotations in the article published by Rose on her Substack, from which we will only extrapolate its introduction. Bombshell from US! FDA “Hides” Toxicity on DNA Fragments inside mRNA Vaccines despite Danger of Cancer Highlighted in its Guidance too Martin: “Pseudouridine Killer in the Vaccines for Depopulation” This analysis comes surprisingly providential as on Gospa News International we have just reported the summary of a conference by the famous patent expert David E. Martin in which he narrated in recent weeks the story of SARS-Cov-2 as a bacteriological weapon built in 58 years of military research on coronaviruses and that of mRNA vaccines, in his opinion, knowingly spread in a mass experiment for the search for vaccines against HIV-AIDS and cancer but also aimed at global depopulation. WUHAN-GATES – 73. Half of Century of Covert Bioweapon Development Leading to Fauci’s SARS-Cov-2 and to mRNA Lethal Vaccines In a very detailed article the American osteopath doctor Joseph Mercola wrote that «Martin points out that even if they don’t unleash any other bioweapons, the desired death toll may still be achieved, because they used pseudouridine in the mRNA shots, which is causing “turbo cancers”». Because: «Pseudouridine suppresses cancer-controlling agents and promotes oncogenic activity in the body, and this has been known since 2018, so its inclusion was hardly an accident. It’s a conspiracy, alright. But not a conspiracy theory in the dismissive sense. It’s a global conspiracy by identifiable agents who have, for nearly 60 years, plotted to commit, and profit from, the greatest genocide the world has ever seen, while hiding behind the false veneer of “public health.”». Well today, both the University of Cambridge and other authoritative scientists from around the world implicitly confirm that all those vaccinated with Covid mRNA with Moderna’s Spikevax and Pfizer-Biontech’s Comirnaty have been and continue to be unpaid and, above all, unaware human guinea pigs. Precisely because of this altered nucleoside… The Disturbing Article from Cambridge University The comment by the researcher Rose that we reported in the incipit of the article referred to the text of the University of Cambridge(Source 2) in relation to the study “N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting” by Mulroney et al.published on December 6, 2023 by Nature after more than a month of review. «Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses» is the eloquent title of the scientific text published by the British university. «The latest developments, led by biochemist Professor Anne Willis and immunologist Dr James Thaventhiran from the MRC Toxicology Unit at the University of Cambridge, build upon previous advances to ensure the prevention of any safety issues linked with future mRNA-based therapeutics. Their report is published today in the journal Nature» we read in the unsigned article. «The researchers identified that bases with a chemical modification called N1-methylpseudouridine – which are currently contained in mRNA therapies – are responsible for the ‘slips’ along the mRNA sequence» adds the university website. In collaboration with researchers at the Universities of Kent, Oxford and Liverpool, the MRC Toxicology Unit team«tested for evidence of the production of ‘off-target’ proteins in people who received the mRNA Pfizer vaccine against COVID-19. They found an unintended immune response occurred in one third of the 21 patients in the study who were vaccinated – but with no ill-effects, in keeping with the extensive safety data available on these COVID-19 vaccines». SCIENCE Magazine Finally Admitted the mRNA Vaccines Dangerous Side Effects! Shots linked to Long Covid, Neurologic Damages and POTS Despite disturbing the article already appears biased as it is aimed at “minimizing” the adverse reactions, even lethal one, that are accumulating in pharmacovigilance systems around the world, which have been confirmed by an alarming article in the journal Science, by the regulatory bodies from all over the world (EMA, FDA, etc.) and which led Moderna and Pfizer-Biontech to include the risk of lethal myocarditis in the information leaflets of their genetic drugs… 7 EURODEPUTATI CHIEDONO IL RITIRO DEI VACCINI COVID. Per Miocarditi Letali, Malori Improvvisi e Sicurezza Incerta nei Fragili British Study: “Incorrect mRNA Translation may Increase Toxicity” But it is the same authors of the study whose first signatory is Thomas E. Mulroney (Source 3), associate researcher of the Toxicology Unit of the MRC in Cambridge, who wrote the shocking considerations from a biochemical point of view in the conclusions. «We show that 1-methylΨ is a modified ribonucleotide that significantly increases +1 ribosomal frameshifting during mRNA translation and that cellular immunity to +1 frameshifted products can occur following vaccination with mRNA containing 1-methylΨ. To our knowledge, this is the first report that mRNA modification affects ribosomal frameshifting. Alongside this impact on host T cell immunity, the off-target effects of ribosomal frameshifting could include increased production of new B cell antigens». And they further add: «These findings are of particular importance to our fundamental understanding of how ribonucleotide modification affects mRNA translation, and for designing and optimizing future mRNA-based therapeutics to avoid mistranslation events that may decrease efficacy or increase toxicity». We will not delve further into the technical references but return to the analysis published by Jessica Rose in her Substack, making an extreme summary of it and advising professionals to read the text full of important images. Billions of DNA Fragments of Toxic Spike Protein and SV40 gene in the mRNA Vaccines. New Study: “They may Cause Turbo-Cancer” Let’s start with the comment added under the research published by Nature by her together with David Wiseman, L. Maria Gutschi, David J. Speicher, Kevin McKernan. Alongside the Canadian biologist they were already co-authors of the study “DNA fragments detected in the monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: exploratory dose-response relationship with serious adverse events” which induced the EMA to confess that Pfizer hid the use of the very dangerous SV40 gene in its vaccine, which can cause tumors. The same research encouraged the bioimmunologist Robert Malone to denounce the presence of the antibiotic resistance gene in the Moderna one, pointing out also that the pharmaceutical company was aware of the tumor risks of mRNA biotechnology as reported in its own patent. Bomba Mondiale! “NEI VACCINI COVID GENE DI RESISTENZA AGLI ANTIBIOTICI”. Studio Spagnolo lo Conferma. Ministro Schillaci lo CELA nell’Allarme Morti AMR We have written extensively about these topics in three investigations, one of which – on antibiotic resistance gene – is a world exclusive. Alarm of American Scientists for the New Research Let us therefore see the content of the comment by Rose and colleagues (Source 1)on Cambridge’s research: The paper provides evidence for the formation “off-target” or unintended proteins following vaccination with BNT162b2 due to frameshifting. Given the proposed mechanism, a similar problem is likely to exist for the Moderna product. While the authors have not isolated samples of these proteins from vaccinated patients or animals, their existence is evidenced by the specific cellular immune responses elicited to frameshifted proteins the authors synthesized. It is not clear why B cell – antibody responses were not studied. The authors state that “Although there is no evidence that frameshifted products in humans generated from BNT162b2 vaccination are associated with adverse outcomes.” BOMBSHELL: mRNA COVID jabs can Damage Children’s Immune Response to OTHER Viruses as well, Study finds It is unclear how it is possible to make this statement, given: • The small number of vaccinated subjects (n=21) providing samples. • This was not a controlled trial. • None of these subjects had reported undue effects of vaccination. Accordingly, the sample is subject to selection bias. • The toxicology of these unintended proteins must be studied. • The authors acknowledge the misdirected immunity “has huge potential to be harmful.” Translated into simpler words, no one has verified the selection methods of the samples which may have been chosen precisely because they did not have serious adverse reactions. SPIKE-DEMIC among Vaccinated: 83 % hit by PCVS Syndrome. Indian Study confirmed Gates, Big Pharma’s Health Disaster Furthermore, in the interests of expertise we read that the two Cambridge scientists Thomas E. Mulroney and Anne E. Willis «are inventors of a pending patent application (2305297.0) relating to mRNA technology» while in the information on the authors it is discovered that Alexander J Mentzer works at the Wellcome Center for Human Genetics, University of Oxford. Wellcome, with the Bill & Melinda Gates Foundation and the World Economic Forum, is among the founders of the Ngo CEPI(Coalition for Epidemic Preparedness Innovations) which has already launched the SKYCovion vaccine together with the London-based GSK, managed by CEO Emma Walmsley who is also director of Microsoft, and SK Bioscience. WUHAN-GATES – 73. BILL III A CACCIA DI CAVIE UMANE PER VACCINO COVID COREANO. “Genotossicità non Studiata” ma OMS & UK danno OK a SkyCovione con Spike Tossica e Adiuvante GSK da Pericoloso Squalene But let’s go back to the analysis made by Jessica Rose on the Cambridge researchers’ study: «The authors write that N1-methylpseudouridine affects the fidelity of mRNA translation via ribosome stalling that induces frameshifting. Frameshifting results in the production multiple, unique and potentially aberrant proteins». «The modified mRNAs for use in the COVID-19 products were codon-optimized for maximal protein expression in humans. Codon optimization, or synonymous codon replacement, rests on the idea that one can induce mutations throughout a gene of interest (like spike) based on an organism’s (like humans) codon usage bias, to increase translational efficiency and protein expression without altering the sequence of the protein. But, it is well-known that codon-optimization can lead to protein conformation, folding and stability problems». COVID: SCOPERTA LA PROTEINA CHE RIVELA I LETALI COAGULI DI SANGUE. Ma Nessuno Indaga sulla Correlazione coi Vaccini The Canadian immunologist further notes: «Codon optimization could affect protein conformation, folding and stability, change post-translational modification sites and even affect protein function.Different rates of translation by different tRNAs, including those that exhibit wobble base-pairing (a tRNA that can recognize multiple synonymous codons) may actually be critical for determining the rate of translation. The ribosome may slow and pause during elongation which may actually be necessary for proper protein folding. Therefore, codon optimization may disrupt the fine-tuned timing of translation and ultimately protein function». The Prophetic Seneff Study on Autoimmune and Neurocerebral Damage He then refers to other studies that had reported the dangers of this biochemical manipulation (Source 1): «Codon optimization can also lead to misfolding of mRNAs due to increased Guanine/Cytosine (GC content). Please read McKernan et al.’s preprint, Xia et al.’s paper and Seneff et al.’s paper to learn more about potential problems relating to codon optimization and GC content changes. The latter group write: Synonymous codon replacement also results in a change in the multifunctional regulatory and structural roles of resulting proteins». ONE in THREE Covid Vaccinated with Neurological Complications. Alarming Study from Italian National Research Council The risks to the human organism are clearly highlighted: «There is, in fact, a significant enrichment of GC content (17% and 25% enrichments as per Pfizer and Moderna, respectively, as compared to SARS-CoV-2) as a result of the codon optimization that was done, and this can lead to “dysregulation of the G4-RNA-protein binding system and a wide range of potential disease-associated cellular pathologies including suppression of innate immunity, neurodegeneration, and malignant transformation”. Increased GC content significantly alters mRNA secondary structure as well, and this can also lead to ribosomal pausing or stalling». These considerations were expressed in a study published by illustrious scientists such as Stephanie Seneff, Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA, USA, Greg Nigh, Immersion Health, Portland, OR, USA, Anthony M. Kyriakopoulos, Nasco AD Biotechnology Laboratory, Department of Research and Development, Piraeus, Greece and Peter A. McCullough, for Health Foundation, Tucson, AZ, USA, which was the subject of enormous censorship by specialized medical journals but we published in Gospa News thanks to an excellent summary by Dr. Mercola. Dangerous RNA Manipulation with N1-methyl-Ψ Below are the quotes from Seneff et al.(Source 4) useful for understanding the connection with uridine modified in N1-methyl-Ψ: «The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein». «However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance». The COVID Jabs’ Mechanisms of Injury: Sudden Death, Blood Cloths, Human Mad Cow and Autoimmune Diseases In the study entitled “Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs” the scientists added: «These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines questions them as positive contributors to public health». The late biologist Luc Montagnier, in a study published posthumously by his research friends Jean-Claude Perez and Claire Moret-Chalmin with a review contribution from Seneff biophysics, proved without a shadow of a doubt the correlation between killer prions caused by vaccines and rapid deaths for neurocerebral Creutzfeldt-Jacob disease, human mad cow disease. PRIONS as KILLERS: 25 Deaths due to a New Mad-Cow from Covid Vaccines. Shocking Research by Montagnier (RIP), Perez & Moret-Chalmin on CJD Brain Damages In detail Seneff and the other scientists also refer to specific alterations: «Impaired type I IFN signaling is linked to many disease risks, most notably cancer, as type I IFN signaling suppresses proliferation of both viruses and cancer cells by arresting the cell cycle, in part through upregulation of p53, a tumor suppressor gene, and various cyclin- dependent kinase inhibitors (Musella et al., 2017; Matsuoka et al., 1998). IFNα also induces major histocompatibility (MHC) class 1 antigen presentation by tumor cells, causing them to be more readily recognized by the cancer surveillance system (Heise et al., 2016)». They then delve into the problem of the uridine molecule. To understand its importance we report a note from Rose: «Pseudouridines (Ψs) are a normal and essential part of our biology. They have been called the 5th nucleotide, in fact, and “are a ubiquitous constituent of structural RNA (transfer, ribosomal, small nuclear (snRNA) and small nucleolar), and present in coding RNA, across the three phylogenetic domains of life”and “accounts for about 1.4% of all bases in human rRNAs”». “mRNA COVID-19 Vaccines are Like Gene Therapy Products” French Study highlighted Omitted Controls on Genotoxicity Here’s what Seneff and his colleagues wrote about vaccines: «A breakthrough came when it was discovered experimentally that the mRNA coding for the spike protein could be modified in specific ways that would essentially fool the human cells into recognizing it as harmless human RNA. A seminal paper by Karikó et al. (2005) demonstrated through a series of in vitro experiments that a simple modification to the mRNA such that all uridines were replaced with pseudouridine could dramatically reduce innate immune activation against exogenous mRNA». Cancer Risk pointed out by the Nobel Inventor of mRNA Vaccines Precisely for this discovery, Hungarian researcher Katalin Karikó, long-time at Biontech, recently received the Nobel Prize for Medicine together with her American colleague Drew Weissman, although both warned of the dangers of the new mRNA biotechnology. Medicine Nobel to mRNA Covid Vaccines’ Scientists, both Sponsored by Gates, Fauci and Zuckerberg In particular, on January 6, Karikó declared to the German newspaper Welt (Source 5): «Every day I receive many emails from people who write to me about their experiences. One woman wrote to me that two days after the vaccination she developed a large lump in her breast. Vaccination caused cancer, it was her conclusion. But the cancer was already there, only vaccination gave an extra boost to the immune system, so that the immune defense cells rushed in large numbers towards the enemy». The Gospa News investigations on Turbo-Cancer based now on seven published scientific studies have highlighted a very strong correlation between mRNA gene sera and the appearance or reactivation of tumor phenomena with abnormal degeneration resulting in lethal outcomes. TURBO-CANCER – 2. Many Lethal/Serious Cases and New Researches on Covid mRNA Vaccines Risks. Melatonin Hope… Karikó herself adds: «Vaccination provides a strong boost to the immune system. It can happen that a dormant infection breaks out in people with an already weakened immune system. The extent to which this is the case for shingles will need to be examined more closely». Gospa News did so by discovering 27 thousand cases of Herpes Zoster, in the European Union only, as adverse reactions to vaccines reported by EMA pharmacovigilance database even in children, who are more exposed to damage to the natural immune system as confirmed by recent research. Esclusivo! EPIDEMIA DI HERPES DOPO I VACCINI COVID. 27mila Casi nell’UE: 31 Morti da Zoster. Lo Studio: “Per danni al Sistema Immunitario” Let’s go back to Seneff’s conclusions: «Andries et al. (2015) later discovered that 1-methylpseudouridine as a replacement for uridine was even more effective than pseudouridine and could essentially abolish the TLR response to the mRNA, preventing the activation of blood-derived dendritic cells. This modification is applied in both the mRNA vaccines on the market (Park et al., 2021)». To put it simply, the dendritic cell plays the role of sentinel and if it senses the presence of a pathogen in the body, it stimulates the immune response of B and T lymphocytes, specific against that antigen. If its action is limited or suppressed, it may become incapable of dealing with viral or bacterial enemies but also tumor dangers. Critical Role of Pseudouridine in mRNA Vaccines A study published by Pedro Morais, Director (Pseudouridylation Technology) ProQR Therapeutics, Leiden, Netherlands, and by Department of Biochemistry and Biophysics, Center for RNA Biology, University of Rochester Medical Center, Rochester, NY, US, entitled “The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines” highlighted the fundamental role of the laboratory alteration of this protein in the Comirnaty and Spikevax genetic sera (source 6). «Both consisted of N1-methyl-pseudouridine-modified mRNA encoding the SARS-COVID-19 Spike protein and were delivered with a lipid nanoparticle (LNP) formulation. Because the delivery problem of ribonucleic acids had been known for decades, the success of LNPs was quickly hailed by many as the unsung hero of COVID-19 mRNA vaccines». “European Medicines Agency Knew Toxicity of Pfizer Covid Vaccine”. Bombshell Study Published in US by an Italian BioChemist on Dangers mRNA-LNPs But the scholars, one of whom has a clear conflict of interest because he is director of the Pseudouridylation Technology project, have highlighted another very interesting fact: «However, the clinical trial efficacy results of the Curevac mRNA vaccine (CVnCoV) suggested that the delivery system was not the only key to the success. CVnCoV consisted of an unmodified mRNA (encoding the same spike protein as Moderna and Pfizer-BioNTech’s mRNA vaccines) and was formulated with the same LNP as Pfizer-BioNTech’s vaccine (Acuitas ALC-0315).However, its efficacy was only 48%. This striking difference in efficacy could be attributed to the presence of a critical RNA modification (N1-methyl-pseudouridine) in the Pfizer-BioNTech and Moderna’s mRNA vaccines (but not in CVnCoV)». “Toxic Nanoforms inside Pfizer-Biontech Covid Vaccine”. Vital Study by Italian Biochemist on US Journal of Virology highlights an Alleged Crime However, the same researchers highlight a significant note: «The intrinsic immunogenicity of non-modified mRNA was once considered a potential advantage for its use in vaccines(Ishii and Akira, 2005) as it would encode the antigen and concomitantly serve as an adjuvant while permitting a low dose. In fact, the unmodified COVID-19 mRNA vaccine candidate in late-stage clinical trials (CVnCoV, developed by Curevac) had a maximum dose of 12 µg». Curevac was developed by Curevac NV of Tubingen, together with the Ngo CEPI founded by Bill Gates with Wellcome and WEF, which initiated an authorization process before the CHMP committee of the European Medicines Agency (EMA) but withdrew it due to its low efficacy on October 12, 2021 (source 7) in view of the arrival of a new pharmacological product developed with GSK financed by Gates himself. MINISTRO SCHILLACI SPECULA SU BIG PHARMA FINANZIATA DA GATES. €700mila Investiti in Biomediche USA che Testano anche Vaccini DNA Covid Here is another cryptic phrase in which we talk about the “safety” of vaccines, implicitly implying that it is not clear in the current vaccines which therefore make all those who take them into “human guinea pigs”from the laboratory as the immunologist Rose clearly highlights in her final bioethical considerations. Rose: “Unpredictable Health Effects of Manipulated Codons” «Ehden Biber also wrote a great article about the pitfalls of codon optimization that you can read here. In a Nature article published in 2011 entitled: “Breaking the silence”, the author writes on the potential danger of fiddling with codons in therapeutic proteins whereby it “could have unpredictable effects on people’s health”» Rose wrote in her comment on the Cambridge research quoting many sentences by scientific journalist Alla Katsnelson which we report below. Bombshell! Texas Attorney General sues Pfizer on Covid Vaccine Efficacy and Conspiring In detail, the Canadian researcher adds: «She points to a study where the authors show that a synonymous codon change found in the most common form of cystic fibrosis results in mRNA misfolding. (Keep this in mind.) She also points out that in the context of the multi-drug resistance 1 gene (MDR1) (the gene that encodes P-glycoprotein), that a codon change may interfere with the pauses that characterize RNA passing through the ribosome, thereby changing how the growing amino acid chain folds». «But perhaps the most timely and spine-tingly relevant statement in this article is found at the end, and I quote: “At the moment, companies developing recombinant therapies must verify that the DNA sequence designed by their scientists is the one that’s producing their proteins, but they aren’t required to note how different that is from the native genetic code”». European Regulator: Pfizer Hid Dangerous Cancer Gene! It Kept Secret the SV40 DNA Sequence In COVID-19 Vaccine We do not have any guidance with regard to the [DNA] sequence,” Kimchi-Sarfaty notes. While it was the Italian bioimmunologist Mauro Mantovani who demonstrated how the “double Proline” inserted in mRNA vaccines makes the toxic Spike protein dangerously persistent in the human body. «That’s one piece of data that could be tracked by the system she is proposing. Such knowledge, in turn, could ultimately help define better strategies for optimization and possibly even make biologic drugs safer for people» adds Alla Katsnelson while the immunologist asks herself a question: «I wonder if the FDA ever took her advice to track the differences in codons and the resulting potential adverse effects?» Covid Vaccines Killer Pathologies in a Name Only: Spikeopathy! Huge, Chilling Study on mRNA Genic Serums’ Serious Adverse Reactions Therefore Rose quoted the article which we analyzed before: «In addition to our comment on the Nature paper, a University of Cambridge write-up entitled: Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses was penned. They make it clear that the most relevant conclusion from the Nature paper is that we can make more products similarly insanely dangerous as the ones pumped into billions of bodies because we can simply ‘reduce the production of frameshifted products’ by ‘synonymous targeting of slippery sequences’». So she wrote her milestone sentence: «Well of course! Now that we know that billions of people’s cells might be making aberrant proteins, for unknown periods of time, we can simply sweep these people under the rug, ‘fix’ the product, and keep on makin’ money. Let’s go slidin’ down the slippery sequence slope of gene therapy straight to the Gates of hell». Moderna AWARE that mRNA Jabs cause CANCER due to DNA Fragments. Malone Unveils Patent The Canadian molecular biologist concludes before going into detail about a biochemical analysis that is too technical for non-experts: «The manufacturers might have thought to explore options to prevent potentially harmful responses from their products prior to injecting billions of people with them. It is criminal that these products continue to be forced onto newborns and infants by mandate, to this day». And then she report an emblematic quote about the risks of “Fooling with Mother Nature” by an evolutionary cell biologist at the University of Chicago: “Please do not monkey with these sites; they are optimized for some reason”, in reference to codon bias in mammals. Fabio Giuseppe Carlo Carisio © COPYRIGHT GOSPA NEWS prohibition of reproduction without authorization follow Fabio Carisio Gospa News director on Twitter follow Gospa News on Telegram MAIN SOURCES SOURCE 1 – JESSICA ROSE – That Substack about N1-methylpseudouridines and frameshifting SOURCE 2 – UNIVERSITY OF CAMBRIDGE – Researchers redesign future mRNA therapeutics to prevent potentially harmful immune responses SOURCE 3 – NATURE – N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting SOURCE 4– PUBMED – Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs SOURCE 5 – WELT – “Das ist der wirkliche Grund, warum man unter neuen Varianten nicht mehr so krank wird“ SOURCE 6 – FRONTIERS IN – The Critical Contribution of Pseudouridine to mRNA COVID-19 Vaccines SOURCE 7 – EMA ends rolling review of CVnCoV COVID-19 vaccine following withdrawal by CureVac AG Fabio G. C. Carisio Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal. His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more… Most popolar investigation on VT is: Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting. For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime. With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians. In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence. In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates His investigations was quoted also by The Gateway Pundit, Tasnim and others He worked for many years for the magazine Art & Wine as an art critic and curator. VETERANS TODAY OLD POSTS www.gospanews.net/ ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/01/bombshell-inside-mrna-vaccines-a-human-molecule-diabolically-altered/

Ten New Year’s Resolutions to Restore Medical Freedom Clayton J. Baker, MD As 2023 staggers to its conclusion, leaving behind a world of brutal wars, tenuous economies, corrupt governments, and tyrannical elites, perhaps the most unsettling aspect of the year’s end is a strange silence. Some things always generate plenty of noise. The 2024 US Presidential election promises to be even more hysterical than the last two. It will probably be a rematch, pitting a widely hated octogenarian incumbent President with obvious, rapidly progressing dementia against a widely hated late-septuagenarian former President facing dozens of felony indictments. Still almost a year away, the commotion surrounding this impending showdown of the senescent is already continuous, cacophonous, and confounding. However, regarding the most important historical event since World War II, there is almost total silence. The Covid-19 debacle is the defining event of the 21st century. It is at once the worst act of biological warfare in human history and the greatest mass violation of civil liberties since the Iron Curtain. Even more importantly, it is the self-evident template for the establishment of the technocratic soft-core totalitarianism advocated by globalist entities such as the World Health Organization and the World Economic Forum. And yet virtually no one in the mainstream will discuss it. The legacy media shows near zero curiosity regarding Covid’s origins, the disastrous response, or the toxic vaccines. Both the Biden and Trump camps pretend it never happened. Out of the 4 Republican debates held to date, only one question has been asked about Covid vaccines. And that single exchange, between journalist Megyn Kelly and candidate Vivek Ramaswamy, was mysteriously blacked out, even from supposedly “free speech” platform Rumble’s livestream of the event, with Rumble’s CEO later blaming the blackout on “the source feed from a 3rd party” which he did not name. Nothing to see here. Among the other presidential candidates, former Democrat Robert F. Kennedy, Jr. and Republican Ron DeSantis have spoken up repeatedly and honestly about Covid. As a result, they have both been aggressively reviled and ostracized by both the mainstream media and the establishments of both political parties. Advocates for civil rights in general, and for medical freedom in particular, should be deeply disturbed by this attempt to cast the whole Covid-19 catastrophe down the memory hole. Medical freedom is rapidly developing as a philosophical, intellectual, and ethical concept. However, theoretical efforts to promote medical freedom – and by extension, to re-enforce all fundamental civil liberties – will come to naught if the greatest assault on freedom in modern history is allowed to be forgotten, and the perpetrators are allowed to continue as if nothing happened. As a prominent man once asked: “What is to be done?” In my attempt to answer that question, here are 10 New Year’s Resolutions for Medical Freedom advocates. 1. Speak the Truth About Covid at Every Opportunity. Honest and informed citizens, politicians, and public figures must plainly tell truthful narratives about Covid every chance they get. A brief, factual account might sound something like this: a. SARS CoV-2 is a man-made bioweapon developed through US Government funding, which got out of the lab and into the human population. b. The mRNA Covid vaccines are essentially pre-planned antidotes to that bioweapon, which were hastily produced and aggressively pushed on the population for profit, with an appalling and criminal disregard for safety. c. The lockdowns, masking, school closures, mandates, censorship, scapegoating, etc., were deliberate and illegal assaults on citizens’ civil rights – blatant power grabs that governments made under the pretense of a declared emergency. Medical freedom advocates must explain to people that they have been repeatedly lied to for the past 4 years, by virtually every authority. Then, tell them the truth – coolly, rationally, and politely. If they don’t want to hear it, tell them anyway. For decades, every citizen in modern Western society has been browbeaten with leftist and globalist propaganda, ranging from countless Global Warming false prophecies, to risible DEI nonsense, to Baskin-Robbinsesque gender insanity, to fascistic vaccine absolutism. Then came Covid. At this late date, it is reasonable and salutary to present one’s neighbor with a brief smattering of truth. 2. Encourage and Petition Politicians to Commit to Medical Freedom Policies. The Pharma industry spent a reported $379 million on political lobbying in 2022 alone. It’s going to take a lot of grassroots work with politicians to combat the pernicious influence of that much purchased influence. There is evidence that this can be done. People such as Dr. Mary Talley Bowden in Texas are leading the way in this regard. As of December 23, 2023, Bowden and colleagues have convinced 40 candidates and 25 elected officials from 17 states to publicly state that “the Covid shots must be pulled off the market.” Per Dr. Bowden, “many of these are also pledging not to take donations from Big Pharma.” Those committed to medical freedom should set all their elected officials and relevant appointed government bureaucrats on speed dial. These individuals in positions of power – at all levels, local to national – must hear regularly from their constituents. Constituents must tell these people exactly what they know, as well as what they want. It is now up to constituents to teach their officials the facts about the world. As Andrew Lowenthal has demonstrated in detail, the Censorship Industrial Complex is real, and because of it, many elected officials and bureaucrats suffer from the same lack of accurate information on policy matters as the majority of their constituents. 3. Work to Outlaw all Gain-of-Function Research. All research regarding the genetic manipulation of viruses needs to end. Robert F. Kennedy, Jr. and others have pointed out that such research is really bioweapons research, in which our tax dollars are misused to fund the development of a bioweapon and its antidote vaccine in concert. In Florida, Governor Ron DeSantis and the state legislature have passed laws banning gain-of-function research in that state. The Covid era displayed in high relief the disastrous wages of such “research.” It needs to be completely outlawed everywhere, and all labs involved in such work, from the Wuhan Institute of Virology, to the Ralph Baric lab at the University of North Carolina, to illegal labs in the rural USA or allegedly in places like the Ukraine, need to be permanently shut down. Key to achieving this is not falling prey to the intentionally confusing semantic arguments about what technically constitutes “Gain-of-function” and what doesn’t. The word games Anthony Fauci played with Congress need to be called out as the dishonest prevarications they are, and rejected as a defense for those involved in such wicked “research.” (Of note, the Florida laws included language to prevent this deception, outlawing all “enhanced potential pandemic pathogen research.”) 4. Work to Get the USA out of the World Health Organization. The WHO’s newly proposed pandemic agreement and amendments to the existing International Health Regulations (IHR) unfortunately are bald-faced, bad-faith attempts to usurp power from sovereign nations by an unelected globalist elite, all in the nebulous name of “global health.” As David Bell and Thi Thuy Van Dinh have written, despite claims by WHO Director General Tedros Ghebreyesus that “no country will cede any sovereignty to [the] WHO,” in fact The documents propose a transfer of decision-making power to the WHO regarding basic aspects of societal function, which countries undertake to enact. The WHO Director-General will have sole authority to decide when and where they are applied. The proposals are intended to be binding under international law. Furthermore, the proposed amendments to the IHR will change WHO directives during declared health emergencies from non-binding recommendations to dictates with the force of international law. As Bell and Dinh state, “It seems outrageous from a human rights perspective that the amendments will enable the WHO to dictate countries to require individual medical examinations and vaccinations whenever it declares a pandemic.” And the potential incursions to medical freedom hardly end there, potentially including all the items in Article 18 of the existing IHR, which already directly contradict the UN’s own Universal Declaration of Human Rights in multiple places. Most current debate on the matter surrounds the question of whether individual countries should accept or reject these proposals. However, in the wake of the Covid disaster, the WHO’s current proposals reveal that its intention is not to step back, learn from the catastrophe, and account for the mistakes it and other authorities made. Rather, it seeks to consolidate its own power by permanently encoding the top-down, public-health-by-totalitarian-diktat approach that caused so much destruction. Not only these policies, but the organization proposing them should be categorically rejected. The WHO is a classic wolf in sheep’s clothing. It is an unelected globalist cabal of profiteering elites, heavily funded by Bill Gates and closely associated with the World Economic Forum. It is engaged in blatant political power-grabbing while masquerading as a benevolent public health institution. It is insufficient for nations to merely reject the WHO’s proposed pandemic agreement and amendments to its IHR. The USA and every sovereign nation should leave the WHO entirely, and medical freedom advocates should lead the way in the struggle to make this happen. 5. Join the Fight to Remove the Covid mRNA Vaccines From the Market. The Covid-19 mRNA vaccines have demonstrated toxicities far more common, more varied, and more severe than numerous conventional medicines that have been appropriately pulled from the market in the past. Dr. Peter McCollough and numerous other leaders in the fight for medical freedom have rightly called for the Covid mRNA vaccines to be removed from the market. Despite the intense efforts of Big Pharma, the growing Censorship Industrial Complex, and captured government agencies, public awareness of the numerous and often deadly toxicities of the Covid mRNA injections is growing. This is reflected in both reduced public “uptake” for recurrent “boosters” per CDC data and the falling stock price of Pfizer, Inc. A small but growing number of politicians, as described above, are committing to the fight to remove the vaccines from the market, demonstrating that this is becoming a tenable and perhaps winning political position to hold. Encouraging as these trends may be, they are insufficient on their own. Medical freedom advocates should speak out supporting the removal of the Covid mRNA vaccines from the market. They should recruit, support, and vote for elected officials and candidates taking this position, and support legal actions toward this goal. 6. Push for a Moratorium on the mRNA-Based Pharmaceutical Platform as a Whole. Even if the Covid mRNA vaccines are removed from the market, a widely overlooked corollary question remains: how much of the toxicity from these products is Covid-specific, i.e. due to the spike protein, and how much is due to the deeply problematic and incompletely understood mRNA platform itself? There is certainly plenty of toxicity to go around, as numerous mechanisms of injury have been identified from these injections. These include toxicities to the heart, immune system, skin, reproductive organs, blood clotting cascade, and cancer promotion, among others. It is willful denial at best and criminal negligence at worst to assume that the mRNA platform does not contribute to these problems. mRNA vaccines are currently in use in food animals, notably swine. Furthermore on its own website, Moderna describes a pipeline of mRNA vaccines currently in development for Influenza, Respiratory Syncytial Virus (RSV), Cytomegalovirus (CMV), Epstein-Barr Virus (EBV), Human Immunodeficiency Virus (HIV), Norovirus, Lyme disease, Zika virus, Nipah virus, Monkeypox, and others. Meanwhile, the trial for its EBV vaccine has reportedly been halted in adolescents due to a case of – you guessed it – myocarditis. The human population will soon be inundated with mRNA-based drugs on a scale and with an imposed intensity that will make the Covid era seem positively quaint. The safety record for the sole mRNA product currently in human use – the Covid vaccines – is abysmal. A moratorium of at least several years, combined with an open, thorough, and publicly debated inquiry into the likely and possible toxicities inherent to the mRNA platform is essential to human safety, and if done, will save countless lives in coming years. 7. Work to Have the 1986 Vaccine Act Repealed. The toxicity of vaccines was so well-established even decades ago, that a Federal law – the National Childhood Vaccine Injury Act (NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) was passed to specifically exempt vaccine manufacturers from product liability, based on the legal principle that vaccines are “unavoidably unsafe” products. Since the 1986 NCVIA act protecting vaccine manufacturers from liability, there has been a dramatic increase in the number of vaccines on the market, as well as the number of vaccines added to the CDC vaccine schedules, with the number of vaccines on the CDC Child and Adolescent schedule rising from 7 in 1986 to 21 in 2023. The National Childhood Vaccine Injury Act (NCVIA) of 1986 should be repealed, returning vaccines to the same liability status as other drugs. 8. Work to End Vaccine Mandates at Every Level of Society. According to the National Center for Education Statistics, in the 2019-20 academic year there were 3,982 degree-granting colleges and universities in the United States. In the fall of 2021, all but approximately 600 of these institutions mandated Covid-19 vaccination for their students. Since then, nearly all such institutions have dropped their student Covid vaccine mandates. However, at this writing, 71 colleges and universities, or approximately 1.7%, continue to mandate the Covid vaccines for students to attend. The number of mandating schools reduced gradually, largely through the intense, extremely labor intensive work of a very few small, newly-formed, grassroots organizations like No College Mandates. While the effectiveness of such efforts is undeniable, the 71 holdouts (which include “elite” institutions such as Harvard and Johns Hopkins) demonstrate just how deeply entrenched the mandating of vaccines remains in certain segments of society. As a result of the hubris and abuse it displayed during Covid, the entire vaccine mega-industry has suffered tremendous (and richly deserved) damage to its formerly unquestioned, “safe and effective” image. However, from education to healthcare to the military, gains made against vaccine mandates have been partial and temporary at most. A concerted effort to further educate the public about the immense problems with vaccines and to restore individual choice must be joined by a great many more people if this fundamental imposition on basic bodily autonomy is to be overcome. 9. Work to End Direct-to-Consumer Advertising of Pharmaceuticals. The United States is one of only 2 countries in the world that allows direct-to-consumer advertising of pharmaceuticals. The dangers of this utterly ill-advised policy are multiple. First, as we all can see by simply turning on the television, Big Pharma abuses this privilege to aggressively yet seductively hawk every product it feels it can make a buck off of. The “pill for every ill” mindset shifts into hyperdrive, with an expensive, proprietary, pharmacological cure for everything from your morbid obesity to your “bent carrot.” The situation on social media is, if anything, even worse. It is no coincidence that black markets for overhyped, purported wonder drugs such as semaglutide develop, nor that dangerous misuse, such as thousands of reported overdoses have been reported. Perhaps more importantly, direct-to-consumer advertising provides Big Pharma with a convenient and legal way to capture media. Big Pharma was the second-largest television advertising industry in 2021, spending $5.6 billion. No legacy media outlet dares to go against the wishes of those providing that level of funding. This effectively muzzles any and all dissenting voices from appearing on those platforms. A free society requires freedom of the press and media. The Covid era has demonstrated that direct-to-consumer pharmaceutical advertising stifles freedom of the press and media to a dangerous and unacceptable degree. 10. Play Offense. If all you do is play defense, the best result you can hope for is a draw. During the lockdowns, with courts closed, businesses shuttered, and citizens isolated from one another, it was extremely difficult to mount even a solid defense against the gross incursions on our civil rights. A few courageous individuals, often acting alone and at tremendous personal cost, managed to counterpunch effectively. Their contributions to saving our “free” societies (if indeed they are eventually saved) will perhaps never be adequately recognized. Today, despite the mainstream silence, the tide is turning in favor of medical freedom and civil liberties in multiple areas. It is time for the masses to join in and help those who managed to make these early advances, and who continue to fight on behalf of all citizens. For example, New York attorney Bobbie Anne Cox continues her David v. Goliath legal struggle to defeat Governor Kathy Hochul’s extralegal and grossly unconstitutional quarantine camp order. This case may eventually reach the Supreme Court. I don’t want to declare that Ms. Cox can’t do it alone, because that’s pretty much what she has done so far, and having followed that case, I wouldn’t bet against her. But hell, even Hercules had a sidekick. Medical freedom advocates would do well by actively and generously supporting her. After surviving his own trial by fire, Texas Attorney General Ken Paxton has announced a lawsuit against Pfizer for “unlawfully misrepresenting the Covid-19 vaccine’s effectiveness, and attempting to censor public discussion of the product.” Citizens of other states would do well to aggressively petition their attorneys general to take similar action, including removing the mRNA vaccines from the market in their states on the grounds of their demonstrated adulteration with potentially harmful DNA. If medical freedom advocates want the concept to prevail, they must go on offense. Get involved. There is no need to reinvent the wheel at this point. Adopt one or more of the organizations or causes above as your personal project, join, and contribute. Add your light to the sum of light, and the darkness will not overcome it. In summary, those of us seeking to secure and ensure medical freedom for ourselves and future generations must become vocal, persistent advocates, as well as courageous people of action. Furthermore, we must not allow the abuses and evils of the Covid era to vanish down the memory hole, which of course is exactly what every politician, bureaucrat, Deep State apparatchik, and globalist elite who perpetrated those deeds wants to happen. Some cliches are true, and this is one of them: if we allow ourselves to forget history, we will be doomed to repeat it. Covid-19 was the defining event of the century. It was a destructive, deadly catastrophe, but it does have one remarkable silver lining. It peeled the veneer off our governments, institutions, corporations, and society as a whole. It revealed how the powerful plan to strip us of our freedoms – medical and otherwise. We now know what we face. May we, the ordinary citizens, have the courage and intelligence to act effectively to regain and retain our freedoms, dignity, and fundamental human rights. Published under a Creative Commons Attribution 4.0 International License For reprints, please set the canonical link back to the original Brownstone Institute Article and Author. Author C.J. Baker, M.D. is an internal medicine physician with a quarter century in clinical practice. He has held numerous academic medical appointments, and his work has appeared in many journals, including the Journal of the American Medical Association and the New England Journal of Medicine. From 2012 to 2018 he was Clinical Associate Professor of Medical Humanities and Bioethics at the University of Rochester. View all posts Your financial backing of Brownstone Institute goes to support writers, lawyers, scientists, economists, and other people of courage who have been professionally purged and displaced during the upheaval of our times. You can help get the truth out through their ongoing work. https://brownstone.org/articles/ten-new-years-resolutions-to-restore-medical-freedom/

Ten New Year’s Resolutions to Restore Medical Freedom Clayton J. Baker, MD As 2023 staggers to its conclusion, leaving behind a world of brutal wars, tenuous economies, corrupt governments, and tyrannical elites, perhaps the most unsettling aspect of the year’s end is a strange silence. Some things always generate plenty of noise. The 2024 US Presidential election promises to be even more hysterical than the last two. It will probably be a rematch, pitting a widely hated octogenarian incumbent President with obvious, rapidly progressing dementia against a widely hated late-septuagenarian former President facing dozens of felony indictments. Still almost a year away, the commotion surrounding this impending showdown of the senescent is already continuous, cacophonous, and confounding. However, regarding the most important historical event since World War II, there is almost total silence. The Covid-19 debacle is the defining event of the 21st century. It is at once the worst act of biological warfare in human history and the greatest mass violation of civil liberties since the Iron Curtain. Even more importantly, it is the self-evident template for the establishment of the technocratic soft-core totalitarianism advocated by globalist entities such as the World Health Organization and the World Economic Forum. And yet virtually no one in the mainstream will discuss it. The legacy media shows near zero curiosity regarding Covid’s origins, the disastrous response, or the toxic vaccines. Both the Biden and Trump camps pretend it never happened. Out of the 4 Republican debates held to date, only one question has been asked about Covid vaccines. And that single exchange, between journalist Megyn Kelly and candidate Vivek Ramaswamy, was mysteriously blacked out, even from supposedly “free speech” platform Rumble’s livestream of the event, with Rumble’s CEO later blaming the blackout on “the source feed from a 3rd party” which he did not name. Nothing to see here. Among the other presidential candidates, former Democrat Robert F. Kennedy, Jr. and Republican Ron DeSantis have spoken up repeatedly and honestly about Covid. As a result, they have both been aggressively reviled and ostracized by both the mainstream media and the establishments of both political parties. Advocates for civil rights in general, and for medical freedom in particular, should be deeply disturbed by this attempt to cast the whole Covid-19 catastrophe down the memory hole. Medical freedom is rapidly developing as a philosophical, intellectual, and ethical concept. However, theoretical efforts to promote medical freedom – and by extension, to re-enforce all fundamental civil liberties – will come to naught if the greatest assault on freedom in modern history is allowed to be forgotten, and the perpetrators are allowed to continue as if nothing happened. As a prominent man once asked: “What is to be done?” In my attempt to answer that question, here are 10 New Year’s Resolutions for Medical Freedom advocates. 1. Speak the Truth About Covid at Every Opportunity. Honest and informed citizens, politicians, and public figures must plainly tell truthful narratives about Covid every chance they get. A brief, factual account might sound something like this: a. SARS CoV-2 is a man-made bioweapon developed through US Government funding, which got out of the lab and into the human population. b. The mRNA Covid vaccines are essentially pre-planned antidotes to that bioweapon, which were hastily produced and aggressively pushed on the population for profit, with an appalling and criminal disregard for safety. c. The lockdowns, masking, school closures, mandates, censorship, scapegoating, etc., were deliberate and illegal assaults on citizens’ civil rights – blatant power grabs that governments made under the pretense of a declared emergency. Medical freedom advocates must explain to people that they have been repeatedly lied to for the past 4 years, by virtually every authority. Then, tell them the truth – coolly, rationally, and politely. If they don’t want to hear it, tell them anyway. For decades, every citizen in modern Western society has been browbeaten with leftist and globalist propaganda, ranging from countless Global Warming false prophecies, to risible DEI nonsense, to Baskin-Robbinsesque gender insanity, to fascistic vaccine absolutism. Then came Covid. At this late date, it is reasonable and salutary to present one’s neighbor with a brief smattering of truth. 2. Encourage and Petition Politicians to Commit to Medical Freedom Policies. The Pharma industry spent a reported $379 million on political lobbying in 2022 alone. It’s going to take a lot of grassroots work with politicians to combat the pernicious influence of that much purchased influence. There is evidence that this can be done. People such as Dr. Mary Talley Bowden in Texas are leading the way in this regard. As of December 23, 2023, Bowden and colleagues have convinced 40 candidates and 25 elected officials from 17 states to publicly state that “the Covid shots must be pulled off the market.” Per Dr. Bowden, “many of these are also pledging not to take donations from Big Pharma.” Those committed to medical freedom should set all their elected officials and relevant appointed government bureaucrats on speed dial. These individuals in positions of power – at all levels, local to national – must hear regularly from their constituents. Constituents must tell these people exactly what they know, as well as what they want. It is now up to constituents to teach their officials the facts about the world. As Andrew Lowenthal has demonstrated in detail, the Censorship Industrial Complex is real, and because of it, many elected officials and bureaucrats suffer from the same lack of accurate information on policy matters as the majority of their constituents. 3. Work to Outlaw all Gain-of-Function Research. All research regarding the genetic manipulation of viruses needs to end. Robert F. Kennedy, Jr. and others have pointed out that such research is really bioweapons research, in which our tax dollars are misused to fund the development of a bioweapon and its antidote vaccine in concert. In Florida, Governor Ron DeSantis and the state legislature have passed laws banning gain-of-function research in that state. The Covid era displayed in high relief the disastrous wages of such “research.” It needs to be completely outlawed everywhere, and all labs involved in such work, from the Wuhan Institute of Virology, to the Ralph Baric lab at the University of North Carolina, to illegal labs in the rural USA or allegedly in places like the Ukraine, need to be permanently shut down. Key to achieving this is not falling prey to the intentionally confusing semantic arguments about what technically constitutes “Gain-of-function” and what doesn’t. The word games Anthony Fauci played with Congress need to be called out as the dishonest prevarications they are, and rejected as a defense for those involved in such wicked “research.” (Of note, the Florida laws included language to prevent this deception, outlawing all “enhanced potential pandemic pathogen research.”) 4. Work to Get the USA out of the World Health Organization. The WHO’s newly proposed pandemic agreement and amendments to the existing International Health Regulations (IHR) unfortunately are bald-faced, bad-faith attempts to usurp power from sovereign nations by an unelected globalist elite, all in the nebulous name of “global health.” As David Bell and Thi Thuy Van Dinh have written, despite claims by WHO Director General Tedros Ghebreyesus that “no country will cede any sovereignty to [the] WHO,” in fact The documents propose a transfer of decision-making power to the WHO regarding basic aspects of societal function, which countries undertake to enact. The WHO Director-General will have sole authority to decide when and where they are applied. The proposals are intended to be binding under international law. Furthermore, the proposed amendments to the IHR will change WHO directives during declared health emergencies from non-binding recommendations to dictates with the force of international law. As Bell and Dinh state, “It seems outrageous from a human rights perspective that the amendments will enable the WHO to dictate countries to require individual medical examinations and vaccinations whenever it declares a pandemic.” And the potential incursions to medical freedom hardly end there, potentially including all the items in Article 18 of the existing IHR, which already directly contradict the UN’s own Universal Declaration of Human Rights in multiple places. Most current debate on the matter surrounds the question of whether individual countries should accept or reject these proposals. However, in the wake of the Covid disaster, the WHO’s current proposals reveal that its intention is not to step back, learn from the catastrophe, and account for the mistakes it and other authorities made. Rather, it seeks to consolidate its own power by permanently encoding the top-down, public-health-by-totalitarian-diktat approach that caused so much destruction. Not only these policies, but the organization proposing them should be categorically rejected. The WHO is a classic wolf in sheep’s clothing. It is an unelected globalist cabal of profiteering elites, heavily funded by Bill Gates and closely associated with the World Economic Forum. It is engaged in blatant political power-grabbing while masquerading as a benevolent public health institution. It is insufficient for nations to merely reject the WHO’s proposed pandemic agreement and amendments to its IHR. The USA and every sovereign nation should leave the WHO entirely, and medical freedom advocates should lead the way in the struggle to make this happen. 5. Join the Fight to Remove the Covid mRNA Vaccines From the Market. The Covid-19 mRNA vaccines have demonstrated toxicities far more common, more varied, and more severe than numerous conventional medicines that have been appropriately pulled from the market in the past. Dr. Peter McCollough and numerous other leaders in the fight for medical freedom have rightly called for the Covid mRNA vaccines to be removed from the market. Despite the intense efforts of Big Pharma, the growing Censorship Industrial Complex, and captured government agencies, public awareness of the numerous and often deadly toxicities of the Covid mRNA injections is growing. This is reflected in both reduced public “uptake” for recurrent “boosters” per CDC data and the falling stock price of Pfizer, Inc. A small but growing number of politicians, as described above, are committing to the fight to remove the vaccines from the market, demonstrating that this is becoming a tenable and perhaps winning political position to hold. Encouraging as these trends may be, they are insufficient on their own. Medical freedom advocates should speak out supporting the removal of the Covid mRNA vaccines from the market. They should recruit, support, and vote for elected officials and candidates taking this position, and support legal actions toward this goal. 6. Push for a Moratorium on the mRNA-Based Pharmaceutical Platform as a Whole. Even if the Covid mRNA vaccines are removed from the market, a widely overlooked corollary question remains: how much of the toxicity from these products is Covid-specific, i.e. due to the spike protein, and how much is due to the deeply problematic and incompletely understood mRNA platform itself? There is certainly plenty of toxicity to go around, as numerous mechanisms of injury have been identified from these injections. These include toxicities to the heart, immune system, skin, reproductive organs, blood clotting cascade, and cancer promotion, among others. It is willful denial at best and criminal negligence at worst to assume that the mRNA platform does not contribute to these problems. mRNA vaccines are currently in use in food animals, notably swine. Furthermore on its own website, Moderna describes a pipeline of mRNA vaccines currently in development for Influenza, Respiratory Syncytial Virus (RSV), Cytomegalovirus (CMV), Epstein-Barr Virus (EBV), Human Immunodeficiency Virus (HIV), Norovirus, Lyme disease, Zika virus, Nipah virus, Monkeypox, and others. Meanwhile, the trial for its EBV vaccine has reportedly been halted in adolescents due to a case of – you guessed it – myocarditis. The human population will soon be inundated with mRNA-based drugs on a scale and with an imposed intensity that will make the Covid era seem positively quaint. The safety record for the sole mRNA product currently in human use – the Covid vaccines – is abysmal. A moratorium of at least several years, combined with an open, thorough, and publicly debated inquiry into the likely and possible toxicities inherent to the mRNA platform is essential to human safety, and if done, will save countless lives in coming years. 7. Work to Have the 1986 Vaccine Act Repealed. The toxicity of vaccines was so well-established even decades ago, that a Federal law – the National Childhood Vaccine Injury Act (NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) was passed to specifically exempt vaccine manufacturers from product liability, based on the legal principle that vaccines are “unavoidably unsafe” products. Since the 1986 NCVIA act protecting vaccine manufacturers from liability, there has been a dramatic increase in the number of vaccines on the market, as well as the number of vaccines added to the CDC vaccine schedules, with the number of vaccines on the CDC Child and Adolescent schedule rising from 7 in 1986 to 21 in 2023. The National Childhood Vaccine Injury Act (NCVIA) of 1986 should be repealed, returning vaccines to the same liability status as other drugs. 8. Work to End Vaccine Mandates at Every Level of Society. According to the National Center for Education Statistics, in the 2019-20 academic year there were 3,982 degree-granting colleges and universities in the United States. In the fall of 2021, all but approximately 600 of these institutions mandated Covid-19 vaccination for their students. Since then, nearly all such institutions have dropped their student Covid vaccine mandates. However, at this writing, 71 colleges and universities, or approximately 1.7%, continue to mandate the Covid vaccines for students to attend. The number of mandating schools reduced gradually, largely through the intense, extremely labor intensive work of a very few small, newly-formed, grassroots organizations like No College Mandates. While the effectiveness of such efforts is undeniable, the 71 holdouts (which include “elite” institutions such as Harvard and Johns Hopkins) demonstrate just how deeply entrenched the mandating of vaccines remains in certain segments of society. As a result of the hubris and abuse it displayed during Covid, the entire vaccine mega-industry has suffered tremendous (and richly deserved) damage to its formerly unquestioned, “safe and effective” image. However, from education to healthcare to the military, gains made against vaccine mandates have been partial and temporary at most. A concerted effort to further educate the public about the immense problems with vaccines and to restore individual choice must be joined by a great many more people if this fundamental imposition on basic bodily autonomy is to be overcome. 9. Work to End Direct-to-Consumer Advertising of Pharmaceuticals. The United States is one of only 2 countries in the world that allows direct-to-consumer advertising of pharmaceuticals. The dangers of this utterly ill-advised policy are multiple. First, as we all can see by simply turning on the television, Big Pharma abuses this privilege to aggressively yet seductively hawk every product it feels it can make a buck off of. The “pill for every ill” mindset shifts into hyperdrive, with an expensive, proprietary, pharmacological cure for everything from your morbid obesity to your “bent carrot.” The situation on social media is, if anything, even worse. It is no coincidence that black markets for overhyped, purported wonder drugs such as semaglutide develop, nor that dangerous misuse, such as thousands of reported overdoses have been reported. Perhaps more importantly, direct-to-consumer advertising provides Big Pharma with a convenient and legal way to capture media. Big Pharma was the second-largest television advertising industry in 2021, spending $5.6 billion. No legacy media outlet dares to go against the wishes of those providing that level of funding. This effectively muzzles any and all dissenting voices from appearing on those platforms. A free society requires freedom of the press and media. The Covid era has demonstrated that direct-to-consumer pharmaceutical advertising stifles freedom of the press and media to a dangerous and unacceptable degree. 10. Play Offense. If all you do is play defense, the best result you can hope for is a draw. During the lockdowns, with courts closed, businesses shuttered, and citizens isolated from one another, it was extremely difficult to mount even a solid defense against the gross incursions on our civil rights. A few courageous individuals, often acting alone and at tremendous personal cost, managed to counterpunch effectively. Their contributions to saving our “free” societies (if indeed they are eventually saved) will perhaps never be adequately recognized. Today, despite the mainstream silence, the tide is turning in favor of medical freedom and civil liberties in multiple areas. It is time for the masses to join in and help those who managed to make these early advances, and who continue to fight on behalf of all citizens. For example, New York attorney Bobbie Anne Cox continues her David v. Goliath legal struggle to defeat Governor Kathy Hochul’s extralegal and grossly unconstitutional quarantine camp order. This case may eventually reach the Supreme Court. I don’t want to declare that Ms. Cox can’t do it alone, because that’s pretty much what she has done so far, and having followed that case, I wouldn’t bet against her. But hell, even Hercules had a sidekick. Medical freedom advocates would do well by actively and generously supporting her. After surviving his own trial by fire, Texas Attorney General Ken Paxton has announced a lawsuit against Pfizer for “unlawfully misrepresenting the Covid-19 vaccine’s effectiveness, and attempting to censor public discussion of the product.” Citizens of other states would do well to aggressively petition their attorneys general to take similar action, including removing the mRNA vaccines from the market in their states on the grounds of their demonstrated adulteration with potentially harmful DNA. If medical freedom advocates want the concept to prevail, they must go on offense. Get involved. There is no need to reinvent the wheel at this point. Adopt one or more of the organizations or causes above as your personal project, join, and contribute. Add your light to the sum of light, and the darkness will not overcome it. In summary, those of us seeking to secure and ensure medical freedom for ourselves and future generations must become vocal, persistent advocates, as well as courageous people of action. Furthermore, we must not allow the abuses and evils of the Covid era to vanish down the memory hole, which of course is exactly what every politician, bureaucrat, Deep State apparatchik, and globalist elite who perpetrated those deeds wants to happen. Some cliches are true, and this is one of them: if we allow ourselves to forget history, we will be doomed to repeat it. Covid-19 was the defining event of the century. It was a destructive, deadly catastrophe, but it does have one remarkable silver lining. It peeled the veneer off our governments, institutions, corporations, and society as a whole. It revealed how the powerful plan to strip us of our freedoms – medical and otherwise. We now know what we face. May we, the ordinary citizens, have the courage and intelligence to act effectively to regain and retain our freedoms, dignity, and fundamental human rights. Published under a Creative Commons Attribution 4.0 International License For reprints, please set the canonical link back to the original Brownstone Institute Article and Author. Author C.J. Baker, M.D. is an internal medicine physician with a quarter century in clinical practice. He has held numerous academic medical appointments, and his work has appeared in many journals, including the Journal of the American Medical Association and the New England Journal of Medicine. From 2012 to 2018 he was Clinical Associate Professor of Medical Humanities and Bioethics at the University of Rochester. View all posts Your financial backing of Brownstone Institute goes to support writers, lawyers, scientists, economists, and other people of courage who have been professionally purged and displaced during the upheaval of our times. You can help get the truth out through their ongoing work. https://brownstone.org/articles/ten-new-years-resolutions-to-restore-medical-freedom/

The U.S. government is poised to withdraw longstanding warnings about cholesterol Peter Whoriskey Time to put eggs back on the menu? (Deb Lindsey for The Washington Post) The nation’s top nutrition advisory panel has decided to drop its caution about eating cholesterol-laden food, a move that could undo almost 40 years of government warnings about its consumption. The group’s finding that cholesterol in the diet need no longer be considered a “nutrient of concern” stands in contrast to the committee’s findings five years ago, the last time it convened. During those proceedings, as in previous years, the panel deemed the issue of excess cholesterol in the American diet a public health concern. The finding follows an evolution of thinking among many nutritionists who now believe that, for healthy adults, eating foods high in cholesterol may not significantly affect the level of cholesterol in the blood or increase the risk of heart disease. Story continues below advertisement The greater danger in this regard, these experts believe, lies not in products such as eggs, shrimp or lobster, which are high in cholesterol, but in too many servings of foods heavy with saturated fats, such as fatty meats, whole milk, and butter. [Scientists have figured out what makes Indian food so delicious] The new view on cholesterol in food does not reverse warnings about high levels of “bad” cholesterol in the blood, which have been linked to heart disease. Moreover, some experts warned that people with particular health problems, such as diabetes, should continue to avoid cholesterol-rich diets. While Americans may be accustomed to conflicting dietary advice, the change on cholesterol comes from the influential Dietary Guidelines Advisory Committee, the group that provides the scientific basis for the “Dietary Guidelines.” That federal publication has broad effects on the American diet, helping to determine the content of school lunches, affecting how food manufacturers advertise their wares, and serving as the foundation for reams of diet advice. Story continues below advertisement The panel laid out the cholesterol decision in December, at its last meeting before it writes a report that will serve as the basis for the next version of the guidelines. A video of the meeting was later posted online and a person with direct knowledge of the proceedings said the cholesterol finding would make it to the group’s final report, which is due within weeks. After Marian Neuhouser, chair of the relevant subcommittee, announced the decision to the panel at the December meeting, one panelist appeared to bridle. “So we’re not making a [cholesterol] recommendation?” panel member Miriam Nelson, a Tufts University professor, said at the meeting as if trying to absorb the thought. “Okay ... Bummer.” Story continues below advertisement Members of the panel, called the Dietary Guidelines Advisory Committee, said they would not comment until the publication of their report, which will be filed with the Department of Health and Human Services and the Department of Agriculture. [Here’s what the government’s dietary guidelines should really say] While those agencies could ignore the committee’s recommendations, major deviations are not common, experts said. Five years ago, “I don’t think the Dietary Guidelines diverged from the committee’s report,” said Naomi K. Fukagawa, a University of Vermont professor who served as the committee’s vice chair in 2010. Fukagawa said she supports the change on cholesterol. Story continues below advertisement Walter Willett, chair of the nutrition department at the Harvard School of Public Health, also called the turnaround on cholesterol a “reasonable move.” “There’s been a shift of thinking,” he said. But the change on dietary cholesterol also shows how the complexity of nutrition science and the lack of definitive research can contribute to confusion for Americans who, while seeking guidance on what to eat, often find themselves afloat in conflicting advice. Cholesterol has been a fixture in dietary warnings in the United States at least since 1961, when it appeared in guidelines developed by the American Heart Association. Later adopted by the federal government, such warnings helped shift eating habits -- per capita egg consumption dropped about 30 percent -- and harmed egg farmers. Story continues below advertisement Yet even today, after more than a century of scientific inquiry, scientists are divided. Some nutritionists said lifting the cholesterol warning is long overdue, noting that the United States is out-of-step with other countries, where diet guidelines do not single out cholesterol. Others support maintaining a warning. The forthcoming version of the Dietary Guidelines -- the document is revised every five years -- is expected to navigate myriad similar controversies. Among them: salt, red meat, sugar, saturated fats and the latest darling of food-makers, Omega-3s. As with cholesterol, the dietary panel’s advice on these issues will be used by the federal bureaucrats to draft the new guidelines, which offer Americans clear instructions -- and sometimes very specific, down-to-the-milligram prescriptions. But such precision can mask sometimes tumultuous debates about nutrition. Story continues below advertisement “Almost every single nutrient imaginable has peer reviewed publications associating it with almost any outcome,” John P.A. Ioannidis, a professor of medicine and statistics at Stanford and one of the harshest critics of nutritional science, has written. “In this literature of epidemic proportions, how many results are correct?” Now comes the shift on cholesterol. Even as contrary evidence has emerged over the years, the campaign against dietary cholesterol has continued. In 1994, food-makers were required to report cholesterol values on the nutrition label. In 2010, with the publication of the most recent “Dietary Guidelines,” the experts again focused on the problem of "excess dietary cholesterol." Story continues below advertisement Yet many have viewed the evidence against cholesterol as weak, at best. As late as 2013, a task force arranged by the American College of Cardiology and the American Heart Association looked at the dietary cholesterol studies. The group found that there was “insufficient evidence” to make a recommendation. Many of the studies that had been done, the task force said, were too broad to single out cholesterol. “Looking back at the literature, we just couldn’t see the kind of science that would support dietary restrictions,” said Robert Eckel, the co-chair of the task force and a medical professor at the University of Colorado. The current U.S. guidelines call for restricting cholesterol intake to 300 milligrams daily. American adult men on average ingest about 340 milligrams of cholesterol a day, according to federal figures. That recommended figure of 300 milligrams, Eckel said, is " just one of those things that gets carried forward and carried forward even though the evidence is minimal.” Story continues below advertisement "We just don't know," he said. Other major studies have indicated that eating an egg a day does not raise a healthy person’s risk of heart disease, though diabetic patients may be at more risk. “The U.S. is the last country in the world to set a specific limit on dietary cholesterol,” said David Klurfeld, a nutrition scientist at the U.S. Department of Agriculture. “Some of it is scientific inertia.” The persistence of the cholesterol fear may arise, in part, from the plausibility of its danger. As far back as the 19th century, scientists recognized that the plaque that clogged arteries consisted, in part, of cholesterol, according to historians. It would have seemed logical, then, that a diet that is high in cholesterol would wind up clogging arteries. In 1913, Niokolai Anitschkov and his colleagues at the Czar’s Military Medicine Institute in St. Petersburg, decided to try it out in rabbits. The group fed cholesterol to rabbits for about four to eight weeks and saw that the cholesterol diet harmed them. They figured they were on to something big. “It often happens in the history of science that researchers ... obtain results which require us to view scientific questions in a new light,” he and a colleague wrote in their 1913 paper. But it wasn’t until the 1940s, when heart disease was rising in the United States, that the dangers of a cholesterol diet for humans would come more sharply into focus. Experiments in biology, as well as other studies that followed the diets of large populations, seemed to link high cholesterol diets to heart disease. Public warnings soon followed. In 1961, the American Heart Association recommended that people reduce cholesterol consumption and eventually set a limit of 300 milligrams a day. (For comparison, the yolk of a single egg has about 200 milligrams.) Eventually, the idea that cholesterol is harmful so permeated the country's consciousness that marketers advertised their foods on the basis of "no cholesterol." What Anitschkov and the other early scientists may not have foreseen is how complicated the science of cholesterol and heart disease could turn out: that the body creates cholesterol in amounts much larger than their diet provides, that the body regulates how much is in the blood and that there is both “good” and “bad” cholesterol. Adding to the complexity, the way people process cholesterol differs. Scientists say some people -- about 25 percent -- appear to be more vulnerable to cholesterol-rich diets. “It’s turned out to be more complicated than anyone could have known,” said Lawrence Rudel, a professor at the Wake Forest University School of Medicine. As a graduate student at the University of Arkansas in the late 1960s, Rudel came across Anitschkov’s paper and decided to focus on understanding one of its curiosities. In passing, the paper noted that while the cholesterol diet harmed rabbits, it had no effect on white rats. In fact, if Anitschkov had focused on any other animal besides the rabbit, the effects wouldn't have been so clear -- rabbits are unusually vulnerable to the high-cholesterol diet. “The reason for the difference -- why does one animal fall apart on the cholesterol diet -- seemed like something that could be figured out,” Rudel said. “That was 40 or so years ago. We still don’t know what explains the difference.” In truth, scientists have made some progress. Rudel and his colleagues have been able to breed squirrel monkeys that are more vulnerable to the cholesterol diet. That and other evidence leads to their belief that for some people -- as for the squirrel monkeys -- genetics are to blame. Rudel said that Americans should still be warned about cholesterol. “Eggs are a nearly perfect food, but cholesterol is a potential bad guy,” he said. “Eating too much a day won’t harm everyone, but it will harm some people.” Scientists have estimated that, even without counting the toll from obesity, disease related to poor eating habits kills more than half a million people every year. That toll is often used as an argument for more research in nutrition. Currently, the National Institutes of Health spends about $1.5 billion annually on nutrition research, an amount that represents about 5 percent of its total budget. The turnaround on cholesterol, some critics say, is just more evidence that nutrition science needs more investment. Others, however, say the reversal might be seen as a sign of progress. “These reversals in the field do make us wonder and scratch our heads,” said David Allison, a public health professor at the University of Alabama at Birmingham. “But in science, change is normal and expected.” When our view of the cosmos shifted from Ptolemy to Copernicus to Newton and Einstein, Allison said, “the reaction was not to say, ‘Oh my gosh, something is wrong with physics!’ We say, ‘Oh my gosh, isn’t this cool?’ ” Allison said the problem in nutrition stems from the arrogance that sometimes accompanies dietary advice. A little humility could go a long way. “Where nutrition has some trouble,” he said, “is all the confidence and vitriol and moralism that goes along with our recommendations.” Did the government’s dietary guidelines help make us fat? A local's guide to Mumbai, India 5 simple Indian recipes to make at home Scientists have figured out what makes Indian food so delicious Ghee has been an Indian staple for millennia. Now the rest of the world is catching on. https://www.washingtonpost.com/news/wonk/wp/2015/02/10/feds-poised-to-withdraw-longstanding-warnings-about-dietary-cholesterol/?utm_term=.1982832f86fa

Do You Know What’s in a Vaccine? Chemical Ingredients Addendum to the Childhood Vaccination Series All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name. To receive Global Research’s Daily Newsletter (selected articles), click here. Click the share button above to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. *** Over the last few decades, the number of chemicals added to foods and other products has skyrocketed. Chemicals are added to “enhance flavor”, make fruits and vegetables look fresh, extend the shelf life of packaged foods and for other invented reasons. A cornucopia of chemicals are also found in lotions and beauty products with the ostensible reason that these chemicals make beauty products feel, look, and smell nice. Along with this increase in heavily processed foods has come increased skepticism about the necessity of inserting chemical additives into everything we touch and taste. A significant and growing segment of the US population are beginning to examine the health consequences of ingesting and absorbing these chemical-laden products. This growing awareness about the adverse effects of ingesting and absorbing synthetic ingredients and the public’s understanding of the attendant health benefits of consuming products free from synthetic chemicals has prompted consumers to seek out organic ingredient-based items in their foods and skin lotions. More people are showing interest in knowing about the ingredients in their food and striving to ‘eat clean.’ This increased awareness is evidenced in the steady growth of the organic food industry and trends in the natural and organic cosmetic industry where demand is higher than ever. This same level of concern has begun to seep into the public conscience regarding a certain medical product that has mostly avoided scrutiny – the vaccine. Having been trained to accept that this product is a customary aspect of everyday life, most people haven’t given much thought to what’s inside the vaccine vials. Rarely will the vaccine ritual in the doctor’s office include a discussion about the ingredients which are about to be injected into the patient’s body. It’s highly likely the physicians and nurses themselves don’t know the ingredients of each vaccine. So what’s in that vial? What’s coming through that needle? A Partial List of Ingredients Aluminum: Aluminum salts are used in some vaccine formulations as an adjuvant. An adjuvant is a substance added to vaccines to ostensibly enhance the immune response. Examples of aluminum salts in some vaccines are aluminum hydroxide, aluminum phosphate, alum (potassium aluminum sulfate) or mixed aluminum salts. In a 2011 study Canadian scientists Professor Christopher Shaw and Dr. Lucija Tomljenovic stated the following: “Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences.” Multiple studies have shown that the intramuscularly injected aluminum vaccine adjuvant is absorbed into the systemic circulation and travels to different sites in the body, such as the brain, joints, and the spleen, where it accumulates and is retained for years post-vaccination. Mercury (thimerosal): Thimerosal is an ethyl mercury-based preservative used in vials that contain more than one dose of a vaccine (multi-dose vials) to prevent germs, bacteria and/or fungi from contaminating the vaccine. While in decline some flu vaccines and childhood vaccines in multi-dose vials still utilize thimerosal. Mercury is known to be a genotoxic agent, even in minute concentrations, which can damage the genetic information within a cell causing mutations, which may lead to cancer. A meta-analysis epidemiological study suggested thimerosal containing vaccines significantly increased the risk of neurodevelopmental disorders. A 2011 study suggested there may be higher rates of blood and brain mercury levels in monkeys exposed to vaccines containing thimerosal. The American Academy of Pediatrics and the U.S. Public Health Service (1999) published a joint statement that urged “all government agencies to work rapidly toward reducing children’s exposure to mercury from all sources.” Gelatin: Gelatin is used as a stabilizer in some vaccines licensed in the U.S. Stabilizers are added to vaccines to protect the active ingredients from degrading during manufacture, transport and storage. Gelatin is a protein obtained from cows or pigs and produced by the partial hydrolysis of collagen extracted by boiling animal parts such as cartilage, tendons, skin, bones and ligaments in water. Some people might have a severe allergic reaction to it. Certain vaccine viruses are grown on gelatin derived from the ligaments of pigs fed heavy doses of glyphosate in their feed. Gelatin comes from collagen which has lots of glycine. Gelatin is one of the most commonly identified causes of allergic reactions to vaccines. A 1999 Japanese study showed most anaphylactic reactions and some urticarial reactions to gelatin-containing measles, mumps, and rubella monovalent vaccines were associated with gelatin allergy. Based on these findings Japan removed gelatin from vaccines in 2000. Formaldehyde: Formaldehyde is used during the manufacture of some vaccines to inactivate viruses (like polio and hepatitis A viruses) or bacterial toxins (like diphtheria and tetanus toxins). Formaldehyde is a human carcinogen based on evidence from cancer studies in humans and is listed as aknown to be human carcinogen in the National Toxicology Program’s (NTP) Twelfth Report on Carcinogens(2011). Phenol/Phenoxyethanol: Phenoxyethanol is used in vaccines and biologics as a preservative to prevent microbial growth. A 2010 study, The relative toxicity of compounds used as preservatives in vaccines and biologics, assessed the relative cytotoxicity of the levels of the compounds commonly used as preservative in US licensed vaccines and found that for phenoxyethanol it was 4.6-fold, for phenol 12.2-fold and for Thimerosal >330-fold. They concluded, “None of the compounds commonly used as preservatives in US licensed vaccine/biological preparations can be considered an ideal preservative, and their ability to fully comply with the requirements of the US Code of Federal Regulations (CFR) for preservatives is in doubt.” Case reports (here, here and here) have suggested a link between phenoxyethanol and urticaria (hives), eczema and anaphylaxis. Triton X-100: Triton X –100 or octylphenol ethoxylate (OPE) is a surfactant (reducing the surface tension of liquids) and stabilizer present in some influenza vaccines. OPEs are endocrine disruptors and break down relatively easily into Octylphenols (OPs), which are more harmful. Endocrine disruptors can alter reproductive function, increase incidences of breast cancer, affect growth patterns and neurodevelopment in children and change immune function. Squalene: Squalene is a naturally-occurring substance derived primarily from shark liver oil. When combined with other ingredients it becomes an adjuvant, which, like aluminum, is added to vaccines to elicit a stronger immune response from the body. A 2000 study demonstrated that one intradermal injection of squalene adjuvant produced arthritis in rats. Some believe that Gulf War Syndrome was linked to the presence of squalene in certain lots of the anthrax vaccine. Beta-propiolactone: Beta-propiolactone (BPL) is a commonly used reagent for the inactivation of viruses for use in vaccine preparations. It has recently been used in the development of an inactivated SARS-CoV-2 vaccine preparation. Beta-propiolactone is a known carcinogen. Local sarcomas have been produced by subcutaneous injection of beta-propiolactone in rats. In the laboratory sarcomas and squamous papillomas in mice were produced by a single subcutaneous injection of a minute amount of beta-propiolactone. Polysorbate 80: Polysorbate 80 is present in some vaccines to stop the vaccine from separating into its component parts. In a PubMed study Polysorbate 80 was described as, “a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.” In a pharmacological study on mice and rats Polysorbate 80 produced, “mild to moderate depression of the central nervous system with a marked reduction in locomotor activity and rectal temperature, exhibited ataxia and paralytic activity and potentiated the pentobarbital sleeping time.” The results of that study concluded, “The results of the present study indicate that polysorbate 80 can neither be used as a solvent for isolated tissue experiments nor when considered for intravenous administration.” Another study from the American Association for Cancer Research (AACR) suggested the dietary emulsifier polysorbate 80 may induce low-grade inflammation which may contribute to metabolic diseases and increase the potential for development in colon cancer. Genetically modified yeast: S. cerevisiae, a species of yeast, is used in vaccines in a variety of ways. It is used as an adjuvant and now through genetic manipulation it is being used to create artificial antibodies Studies have suggested that genetically engineered yeast used in vaccines may be a contributing factor to autoimmune disorders. Monosodium Glutamate (MSG): Monosodium Glutamate is used in small amounts in some vaccines to keep them stable and protect them from losing potency even when exposed to heat and light. In a study that looked at rat fertility and MSG consumption the authors found there was a negative impact on the rats’ fertility. In another study it was noted that chronic MSG intake caused kidney dysfunction and renal oxidative stress in the animal model. Cells From Aborted Fetus: Fetal cell lines are used to grow viruses which are then collected from the cell cultures and processed further to produce the vaccine itself. The cell lines are propagated from lung tissue of mature aborted and used in the current manufacture of a number of routine vaccines, including measles, mumps and rubella (MMRV), diphtheria, tetanus, pertussis and polio, (DTaP-IPV), Hepatitis A and chickenpox. Aborted fetal cells are listed on vaccine package inserts as “Human Fetal Diploid Cells.” Two aborted fetal cell lines, WI-38 and MRC-5, have been grown under laboratory conditions since the 1960s. Diploid cells (WI-38, MRC-5) vaccines have their origin in induced abortions. The use of such cell lines can be profoundly objectionable to segments of the population who hold certain religious and/or philosophical beliefs. The Italian vaccine research and advocacy organization Corvelva released a study in 2019 regarding the use of aborted fetal cell lines in vaccines. In their summary they highlighted the following: The human genomic DNA contained in this vaccine is clearly, undoubtedly abnormal, presenting important inconsistencies with a typical human genome, that is, with that of a healthy individual. 560 genes known to be associated with forms of cancer were tested and all underwent major modifications. There are variations whose consequences are not even known, not yet appearing in the literature, but which still affect genes involved in the induction of human cancer. What is also clearly abnormal is the genome excess showing changes in the number of copies and structural variants. Serum From Aborted Calf Fetus Blood: The purpose for the fetal bovine serum is to provide a nutrient broth for viruses to grow in cells. Humane Research Australia describes the process of how the blood is collected, “The blood is collected after the slaughter of a mature female cow, the mother’s uterus containing the calf fetus is removed during the evisceration process and transferred to the blood collection room. A needle is then inserted between the fetus’s ribs directly into its heart and the blood is vacuumed into a sterile collection bag. Only fetuses over the age of three months are used otherwise the heart is considered too small to puncture. Once collected, the blood is allowed to clot at room temperature and the serum separated through a process known as refrigerated centrifugation.” Beyond certain ethical considerations scientists have found that different bovine tissues contain different amounts of the BSE agent. Antibiotics: Antibiotics are used during the manufacturing process of some vaccines to stop bacteria growing and contaminating the vaccine. Antibiotics found in some vaccines include neomycin, streptomycin, polymyxin b, gentamicin and kanamycin. Polymyxin B comes with a warning that, “This medicine has not been fully studied in pregnant women. This medicine may cause kidney problems. This medicine may cause nerve problems”, as well as a laundry list of side effects. Similar warnings are found with streptomycin, neomycin, gentamicin, and kanamycin. A study out of Finland raised concerns about excessive antibiotic use in early childhood which may lead to weight gain and altered gut bacteria. What Else Could be in That Needle? The list above is not a complete account of all the ingredients found in various vaccine cocktails. A comprehensive manufacturers’ catalog of ingredients can be found here, here and here. The reality is that even a complete list issued by the producer doesn’t tell the entire story of what is found in vaccines. Using an Environmental Scanning Electron Microscope equipped with an X-ray microprobe a group of Italian scientists examined 44 samples of 30 different vaccines and found dangerous contaminants, including metal toxicants in 43 of the 44 samples tested. In the study, published in the International Journal of Vaccines and Vaccination, the researchers detected lead, chromium, nickel and other metals in every adjuvant sample tested. Additional metal contaminants identified in 25 of the human vaccines included platinum, silver, bismuth, iron, and chromium. Foreign impurities such as zirconium, hafnium, strontium, tungsten, antimony, bismuth, cerium and were also detected in many of the vaccines tested. The researchers commenting on their unexpected findings reported: The quantity of foreign bodies detected and, in some cases, their unusual chemical compositions baffled us. In most circumstances, the combinations detected are very odd as they have no technical use, cannot be found in any material handbook and look like the result of the random formation occurring….In any case, whatever their origin, they should not be present in any injectable medicament, let alone in vaccines, more in particular those meant for infants. [Emphasis added] When interviewed lead scientist Dr. Antonietta Gatti, of the National Council of Research of Italy and Scientific Director of Nanodiagnostics, explained that the discovery of vaccine impurities shocked the researchers: Those particles should not have been there. We had never questioned the purity of vaccines before. In fact, for us the problem did not even exist. All injectable solutions had to be perfectly pure and that was an act of faith on which it seemed impossible to have doubts. For that reason, we repeated our analyses several times to be certain. In the end, we accepted the evidence. Speculating on the potential consequences of these foreign impurities Dr. Gatti stated: The particles, be they isolated, aggregated or clustered, are not supposed to be there… Our tissues perceive these foreign bodies as potential enemies…Unfortunately, though, the particles we found in vaccines, are not biodegradable. So, all the macrophages’ efforts will be useless, and depending on the exact chemicals involved, the particles may be especially toxic. Cytokines and pro-inflammatory substances in general are released and granulated tissue forms, enveloping the particles. This provokes inflammation which, in the long run, if locally persistent, is known to be a precursor to cancer. Along with unlisted metal contaminants another unlisted contaminant was noted in some vaccines when a preliminary screening result from Microbe Inotech Laboratories Inc. detected glyphosate in the childhood vaccines they tested. Merck’s MMR II vaccine had 2.671 parts per billion (ppb) of glyphosate, Sanofi Pasteur’s DTap Adacel vaccine had 0.123 ppb, Novartis’ Influenza Fluvirin had 0.331 ppb, Glaxo Smith Kline’s HepB Energix-B vaccine had 0.325 ppb, Merck’s Pneumococcal Vax Polyvalent Pneumovax 23 had 0.107 ppb of glyphosate. These findings prompted Moms Across America to send a letter to the FDA, CDC, EPA,NIH and California Department of Health requesting that they test vaccines for glyphosate and recall contaminated vaccines. MIT scientist Dr. Stephanie Seneff remarked on the route by which glyphosate could get into vaccines: Collagen is a protein found in large amounts in the ligaments of cows, and these ligaments are often used in the production of gelatin. The MMR vaccine and flu vaccine viruses are grown as live cultures on gelatin sourced from cows fed high concentrations of glyphosate in their GMO Roundup­Ready feed. What to Do? Given the complex nature of the composition of vaccines and the paucity of information volunteered to the public on the manufacturing processes and ingredients that go into these products, how does one go about navigating this subject? Conventional wisdom might suggest, “Ask your doctor.” But how independent are these doctors? Where do you turn when you discover physicians and pediatricians, who have a legal duty to fully inform patients about vaccine risks and side effects, have ideological and material incentives to avoid presenting specific information that might cause a parent to question a vaccine? What about educational materials and advice from the agencies tasked with protecting public health? Can we trust the FDA and the CDC to provide detailed and unbiased information when it is known that they get substantial amounts of money from vaccine manufacturers? Informed consent is a principle in medical ethics and medical law that a patient must have sufficient information and understanding before making decisions about their medical care.This includes being given a thorough account of the risks and benefits of treatments, alternative treatments, the patient’s role in treatment, and their right to refuse treatment. Informed and individualized health care decisions about any product one puts into their or their children’s body starts with being fully informed with what is in that product. * Note to readers: Please click the share button above. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles. This article was originally published on Health Freedom Defense Fund. Featured image is from HFDF https://www.globalresearch.ca/do-you-know-what-vaccine/5839377