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  • 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.

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    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
    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
    BROWNSTONE.ORG
    The WHO Pandemic Agreement: A Guide ⋆ Brownstone Institute
    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.
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  • ALERT: World Health Assembly Meeting on May 27th – Here’s What You Need to Know
    March 22, 2024 • by Meryl Nass, MD


    Introduction

    On May 27th 2024, the 77th World Health Assembly (WHA) of the World Health Organization (WHO) will take place. At this meeting, the WHA may vote, or may approve by consensus or secret ballot, two documents that would transfer health decision-making powers to the WHO, and would give the WHO Director General, Tedros Ghebreyesus, the unilateral ability to declare health emergencies worldwide – with no checks and balances.

    The two documents of concern are amendments to the International Health Regulations (IHR) and the Pandemic Treaty. These two documents give the WHO control over health information, health decision-making, and sharing of pandemic pathogens. They require member states to implement laws enforcing censorship, requiring vaccinations, and controlling movement and quarantine based on WHO directives.

    Call to Action

    We are asking everyone to help get out these messages:

    HR 4665 – Vote on March 22 – defunds the WHO and requires any pandemic treaty to go through Senate ratification process.
    What can you do? Sign the Align Act to contact your congress person

    More info here: https://doortofreedom.org/2024/03/15/federal-watch-hr-4665
    Model legislation: a resolution states can pass reinforcing that the WHO has no jurisdiction. If you have a health-freedom friendly legislator or legislature, please share this model resolution. https://doortofreedom.org/2024/03/15/model-legislation/
    What can Parliamentarians do? This document provides a list that could be used by any concerned member of Parliament or Congress to challenge the WHO.
    https://doortofreedom.org/what-can-parliamentarians-do/
    —————————–

    Email from March 15th, 2024

    Tedros continues to lie about what the WHO is attempting to achieve. His lies get a lot of press. They have been repeated in European Parliaments and by US diplomats in front of the Select Subcommittee on the Coronavirus Pandemic in the House.
    Like the IHR amendments, negotiated in secret for 15 months, or the Pandemic Treaty, which has had 5 different names, there is a concerted, deliberate attempt to confuse and mislead the public about the IHR amendments and pandemic treaty before their anticipated vote in May 2024.

    Here are lies he told at the World Governments Summit last month:
    “The second major barrier [to passage of the documents] is the litany of lies and conspiracy theories about the agreement:

    That it’s a power grab by the World Health Organisation;
    That it will cede sovereignty to WHO;
    That it will give WHO power to impose lockdowns or vaccine mandates on countries;
    That it’s an ‘attack on freedom’;
    That WHO will not allow people to travel;
    And that WHO wants to control people’s lives.
    These are some of the lies that are being spread.

    If they weren’t so dangerous, these lies would be funny. But they put the health of the world’s people at risk. And that is no laughing matter.

    These claims are utterly, completely, categorically false. The pandemic agreement will not give WHO any power over any state or any individual, for that matter.”

    I have shown with the evidence from the documents themselves how this statement is false, here.

    Dr. David Bell and international lawyer Van Dinh (both have PhDs and both have worked for UN agencies) show how these claims are false as well, here:

    https://brownstone.org/articles/why-does-the-who-make-false-claims-regarding-proposals-to-seize-states-sovereignty/

    It is important to point out the lies and obfuscations, for this is likely to lead to people understanding that the WHO cannot be trusted with such agreements, and they may begin to grasp the enormity of what we face.
    I have also compiled a list of 12 ways the WHO can be challenged in national or state parliaments, legislatures and Congress: https://doortofreedom.org/what-can-parliamentarians-do/
    I hope you will spread this information widely.

    Subscribe to DailyClout so you never miss an update!

    https://dailyclout.io/alert-world-health-assembly-meeting-on-may-27th-heres-what-you-need-to-know/
    ALERT: World Health Assembly Meeting on May 27th – Here’s What You Need to Know March 22, 2024 • by Meryl Nass, MD Introduction On May 27th 2024, the 77th World Health Assembly (WHA) of the World Health Organization (WHO) will take place. At this meeting, the WHA may vote, or may approve by consensus or secret ballot, two documents that would transfer health decision-making powers to the WHO, and would give the WHO Director General, Tedros Ghebreyesus, the unilateral ability to declare health emergencies worldwide – with no checks and balances. The two documents of concern are amendments to the International Health Regulations (IHR) and the Pandemic Treaty. These two documents give the WHO control over health information, health decision-making, and sharing of pandemic pathogens. They require member states to implement laws enforcing censorship, requiring vaccinations, and controlling movement and quarantine based on WHO directives. Call to Action We are asking everyone to help get out these messages: HR 4665 – Vote on March 22 – defunds the WHO and requires any pandemic treaty to go through Senate ratification process. What can you do? Sign the Align Act to contact your congress person More info here: https://doortofreedom.org/2024/03/15/federal-watch-hr-4665 Model legislation: a resolution states can pass reinforcing that the WHO has no jurisdiction. If you have a health-freedom friendly legislator or legislature, please share this model resolution. https://doortofreedom.org/2024/03/15/model-legislation/ What can Parliamentarians do? This document provides a list that could be used by any concerned member of Parliament or Congress to challenge the WHO. https://doortofreedom.org/what-can-parliamentarians-do/ —————————– Email from March 15th, 2024 Tedros continues to lie about what the WHO is attempting to achieve. His lies get a lot of press. They have been repeated in European Parliaments and by US diplomats in front of the Select Subcommittee on the Coronavirus Pandemic in the House. Like the IHR amendments, negotiated in secret for 15 months, or the Pandemic Treaty, which has had 5 different names, there is a concerted, deliberate attempt to confuse and mislead the public about the IHR amendments and pandemic treaty before their anticipated vote in May 2024. Here are lies he told at the World Governments Summit last month: “The second major barrier [to passage of the documents] is the litany of lies and conspiracy theories about the agreement: That it’s a power grab by the World Health Organisation; That it will cede sovereignty to WHO; That it will give WHO power to impose lockdowns or vaccine mandates on countries; That it’s an ‘attack on freedom’; That WHO will not allow people to travel; And that WHO wants to control people’s lives. These are some of the lies that are being spread. If they weren’t so dangerous, these lies would be funny. But they put the health of the world’s people at risk. And that is no laughing matter. These claims are utterly, completely, categorically false. The pandemic agreement will not give WHO any power over any state or any individual, for that matter.” I have shown with the evidence from the documents themselves how this statement is false, here. Dr. David Bell and international lawyer Van Dinh (both have PhDs and both have worked for UN agencies) show how these claims are false as well, here: https://brownstone.org/articles/why-does-the-who-make-false-claims-regarding-proposals-to-seize-states-sovereignty/ It is important to point out the lies and obfuscations, for this is likely to lead to people understanding that the WHO cannot be trusted with such agreements, and they may begin to grasp the enormity of what we face. I have also compiled a list of 12 ways the WHO can be challenged in national or state parliaments, legislatures and Congress: https://doortofreedom.org/what-can-parliamentarians-do/ I hope you will spread this information widely. Subscribe to DailyClout so you never miss an update! https://dailyclout.io/alert-world-health-assembly-meeting-on-may-27th-heres-what-you-need-to-know/
    DAILYCLOUT.IO
    ALERT: World Health Assembly Meeting on May 27th - Here's What You Need to Know
    At this meeting, the WHA may vote, or may approve by consensus or secret ballot, two documents that would transfer health
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  • WHO never Discovered SARS-COV-2 Artificial Origin but Promotes VIPs Calling for New Deal on Future Pandemics
    28 Marzo 2024
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    12.285 Views

    by Fabio Giuseppe Carlo Carisio

    VERSIONE IN ITALIANO

    “I love my brother Bobby, but I do not share or endorse his opinions on many issues, including the COVID pandemic, vaccinations, and the role of social media platforms in policing false information,” she said at the time. “It is also important to note that Bobby’s views are not reflected in or influence the mission or work of our organization.”

    These were the sentences about Robert F. Kennedy jr statements released by Kerry Kennedy, former wife of New York Governor Andrea Cuomo and Chair of the Amnesty International USA Leadership Council. Nominated by President Bush and confirmed by the Senate. She serves on the board of directors of the United States Institute of Peace, as well as Human Rights First, and Inter Press Service (Rome, Italy).

    Zuckerberg Confession: “Establishment asked Facebook to ‘censor’ Covid posts”

    Kerry Kennedy, President, Robert F. Kennedy Human Rights, is one of the VIPs who signed the “Call for urgent Agreement on International Deal to Prepare for and prevent future Pandemics” (whole text below) meanwhile World Health Organization is loosing many hopes that WHO Assembly will approve the Pandemic Treaty due to the opposition of Russia an many other nations.

    WHO, EU Launch New Global Vaccine Passport Initiative: “Death Sentence for Millions”

    The appeal was launched by Office of Gordon and Sarah Brown, the website of former UK prime minister., who signed it as Tony Blair, the Former UN General Secretary Ban-ki Moon, New Zealand’s former Prime Minister Helen Cark and Italian former PM Mario Monti, life senator and former manager of New York bank Goldman Sachs in business with Pfizer, nominated as president of Pan-European Commission on Health and Sustainable Development, a body created by the World Health Organization during Covid-19 emergency despite his ties with Wuhan Institute of Virology.

    WUHAN-GATES – 68. THE SMOKING GUN OF MANMADE SARS-COV-2. Fauci, Wuhan & Chinese Military Scientists behind Research on Vaccine for Biodefense

    Indeed Monti was in the European Commission which financed the EPISARS project for the developing of dangerous research on Coronavirus SARS from which, in a huge affair among China and US, emerged the artificial SARS-Cov-2.

    WUHAN-GATES – 65. L’ANELLO MANCANTE DEL DIABOLICO COMPLOTTO NWO-UE: Dal SARS da Laboratorio di Monti al Vaccino COVID col Grafene di Capua

    Although WHO has not yet been able to prove the laboratory origin of the Covid-19 virus, also because it has entrusted the investigations to doctors with enormous conflicts of interest for having worked in the Wuhan Institute of Virology, today it continues to insist on launch the global agreement on pandemics thanks to those same people who supported Bill Gates’ global immunization plan and the “Covid-19 pandemic planned for decades” as declared by the lawyer Robert F. Kennedy jr and as demonstrated by the patents expert David Martin on the role of Anthony Fauci, and detailed by the Gospa News investigations of the “Wuhan-Gates” cycle.

    WHO claims to develop more and major researches on viruses when it is now well established that the Covid-19 pandemic was caused by man precisely because of research on biological weapons.

    Fabio Giuseppe Carlo Carisio
    © COPYRIGHT GOSPA NEWS
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    GOSPA NEWS – WUHAN-GATES INVESTIGATIONS

    GOSPA NEWS – COVID, BIG PHARMA, VACCINES

    WHO: “Call for urgent Agreement on International Deal to Prepare for and prevent future Pandemics”

    Article originally published on World Health Organization

    All links to Gospa News articles have been added aftermath, in relation to the topics highlighted

    Subscribe to the Gospa News Newsletter to read the news as soon as it is published

    A high-powered intervention by 23 former national Presidents, 22 former Prime Ministers, a former UN General Secretary and 3 Nobel Laureates is being made today to press for an urgent agreement from international negotiators on a Pandemic Accord, under the Constitution of the World Health Organizaion, to bolster the world’s collective preparedness and response to future pandemics.

    WUHAN-GATES – 69. How and Why the Spy of Biden & Gates Hid ManMade SARS-Cov-2 in US Intelligence Dossier

    Former UN General Secretary Ban-ki Moon, New Zealand’s former Prime Minister Helen Cark, former UK Prime Ministers Gordon Brown and Tony Blair, former Malawi President Joyce Banda, former Peru President Franciso Sagasti, and 3 former Presidents of the UN General Assembly are amongst 100+ global leaders, from all continents and fields of politics, economics and health management who today issued a joint open letterurging accelerated progress in current negotiations to reach the world’s first ever multi-lateral agreement on pandemic preparedness and prevention.

    “A pandemic accord is critical to safeguard our collective future. Only a strong global pact on pandemics can protect future generations from a repeat of the COVID-19 crisis, which led to millions of deaths and caused widespread social and economic devastation, owing not least to insufficient international collaboration,” the leaders write in their joint letter.

    WUHAN-GATES – 60. NEW SCANDAL INTO WHO. French Co-Chair of Investigative Group on SARS-2 Worked in the China Bio-lab which Enhanced Coronavirus

    In the throes of the COVID-19 disaster which, officially, claimed 7 million lives and wiped $2 trillion from the world economy, inter-governmental negotiations to reach international agreement on future pandemic non-proliferation were begun in December 2021 between 194 of the world’s 196 nations. Nations set themselves the deadline of May 2024 by which they should reach agreement on what would be the world’s first ever Pandemic Accord.

    The Ninth round of Pandemic Accord negotiations are underway this week and next. Signatories of today’s open letter hope their combined influence willencourage all 194 nations to maintain the courage of their Covid-years conviction and make their own collective ambition of an international pandemic protocol a reality by the intended May deadline to enable ratification by the World Health Assembly at its May 2024 Annual General Assembly.

    And they urge negotiators “to redouble their efforts” to meet the imminent deadline and not let their efforts be blown off course by malicious misinformation campaigning against the WHO, the international organisation which would be tasked with implementing the new health accord.

    Taking a swipe at those who wrongly believe national sovereignty may be undermined by this major international step forward for public health the signatories say “there is no time to waste” and they call on the leaders of the 194 nations taking part in the current negotiations to “redouble their efforts to complete the accord by the May deadline.”

    WUHAN-GATES – 72. THE SUMMARY: WHO Intrigues on the SARS-Cov-2 Bioweapon & Vaccine Plots – McCullough reveals

    The letter, hosted on the website of The Office of Gordon and Sarah Brown states, “Countries are doing this not because of some dictum from the WHO – like the negotiations, participation in any instrument would be entirely voluntary – but because they need what the accord can and must offer. In fact, a pandemic accord would deliver vast and universally shared benefits, including greater capacity to detect new and dangerous pathogens, access to information about pathogens detected elsewhere in the world, and timely and equitable delivery of tests, treatments, vaccines, and other lifesaving tools.

    “As countries enter what should be the final stages of the negotiations, governments must work to refute and debunk false claims about the accord. At the same time, negotiators must ensure that the agreement lives up to its promise to prevent and mitigate pandemic-related risks. This requires, for example, provisions aimed at ensuring that when another pandemic threat does arise, all relevant responses – from reporting the identification of risky pathogens to delivering tools like tests and vaccines on an equitable basis – are implemented quickly and effectively. As the COVID-19 pandemic showed, collaboration between the public and private sectors focused on advancing the public good is also essential.”

    WUHAN-GATES – 24. WHO & Pandemic in Gates-China’s Puppet Hands: Dr. Tedros Leader of TPLF, Islamic-Communist Rebels blamed of Last Massacre in Ethiopia by Amnesty

    “A new pandemic threat will emerge; there is no excuse not to be ready for it. It is thus imperative to build an effective, multisectoral, and multilateral approach to pandemic prevention, preparedness, and response. Given the unpredictable nature of public-health risks, a global strategy must embody a spirit of openness and inclusiveness. There is no time to waste, which is why we are calling on all national leaders to redouble their efforts to complete the accord by the May deadline.”

    “Beyond protecting countless lives and livelihoods, the timely delivery of a global pandemic accord would send a powerful message: even in our fractured and fragmented world, international cooperation can still deliver global solutions to global problems.”

    Article originally published on World Health Organization

    Joint letter to leaders of WHO member states calling for an urgent agreement on a pandemic accord

    Originally published on the Office of Gordon and Sarah Brown website on March, 20, 2024

    The overwhelming lesson we learned from COVID-19 is that no one is safe anywhere until everyone is safe everywhere – and that can only happen through collaboration. In response, the 194 countries which are members of the World Health Organization decided in December 2021 to launch negotiations for a new international instrument on pandemic prevention, preparedness and response, a Pandemic Accord, as a “global framework” to work together to prepare for and stem any new pandemic threat, including by achieving equitable access to vaccines, therapeutics and diagnostics.

    WUHAN-GATES – 62. MANMADE SARS-Cov-2 FOR GOLDEN VACCINES: Metabiota, CIA, Biden, Gates, Rockefeller intrigued in Ukraine, China and Italy

    Negotiation of an effective pandemic accord is a much needed opportunity to safeguard the world we live in. Countries themselves have proposed this instrument, individual countries are negotiating it, and only countries will ultimately be responsible for its requirements and its success or failure.

    Establishing a strong global pact on pandemics will protect future generations from a repeat of the millions of deaths and the social and economic devastation which resulted from a lack of collaboration during theCOVID-19 pandemic. All countries need what the accord can offer: the capacity to detect and share pathogens presenting a risk, and timely access to tests, treatments and vaccines.

    An agreement is meant to be reached just two and a half months from now – countries imposed a deadline of May 2024, in time for the 77th World Health Assembly.

    WUHAN-GATES – 73. Half of Century of Covert Bioweapon Development Leading to Fauci’s SARS-Cov-2 and to mRNA Lethal Vaccines

    As countries now enter what should be the final stages of the negotiations, they must ensure that they are agreeing on actions which will do the job required: to prevent and mitigate pandemic threats. We urge solutions which ensure both speed in reporting and sharing pathogens, and in access – in every country – to sufficient tools like tests and vaccines to protect lives and minimise harm. The public and private sectors must work together towards the public good. This global effort is being threatened by misinformation and disinformation. Among the falsehoods circulating are allegations that the WHO intends to monitor people’s movements through digital passports; that it will take away the national sovereignty of countries; and that it will have the ability to deploy armed troops to enforce mandatory vaccinations and lockdowns. All of these claims are wholly false and governments must work to disavow them with clear facts.

    WUHAN-GATES – 47. SARS-2 BIOWEAPON. Pentagon’s DARPA Stopped a Risky Test in US but Funded a Secret one in UK with Gates

    It is imperative now to build an effective, multisectoral and multilateral approach to pandemic prevention,preparedness, and response marked by a spirit of openness and inclusiveness. In doing so we can send a message that even in this fractured and fragmented world, cross-border co-operation can deliver global solutions to global problems.

    We call on leaders of all countries to step up their efforts and secure an effective pandemic accord by May. A new pandemic threat will emerge – and there is no excuse not to be ready for it.

    Originally published on the Office of Gordon and Sarah Brown website on March, 20, 2024

    Name Title
    Carlos Alvarado* President of Costa Rica (2018-2022)
    Michelle Bachelet* President of Chile (2006-2010)
    Jan Peter Balkenende* Prime Minister of The Netherlands (2002-2010)
    Ban Ki-moon* Eighth Secretary General of the United Nations
    Joyce Banda* President of Malawi (2012-2014)
    Kjell Magne Bondevik* Prime Minister of Norway (1997-2000; 2001-2005)
    Kim Campbell* Prime Minister of Canada (1993)
    Alfred Gusenbauer* Chancellor of Austria (2007-2008)
    Seung-Soo Han* Prime Minister of the Rep. of Korea (2008-2009)
    Mehdi Jomaa* Prime Minister of Tunisia (2014-2015)
    Horst Köhler* President of Germany (2004-2010)
    Rexhep Meidani* President of Albania (1997-2002)
    Mario Monti* Prime Minister of Italy (2011-2013)
    Francisco Sagasti* President of Peru (2020-2021)
    Jenny Shipley* Prime Minister of New Zealand (1997-1999)
    Juan Somavía* Ninth Director of the International Labour Organization
    Helen Clark** Former Prime Minister of New Zealand
    Micheline Calmy-Rey** Former President of the Swiss Confederation
    Baroness Lynda Chalker** Former Minister of Overseas Development of the UK
    Chester A. Crocker** Former Assistant Secretary for African Affairs, USA
    Marzuki Darusman** Former Attorney General of Indonesia
    Mohamed ElBaradei** Former Vice President of Egypt
    Gareth Evans** Former Foreign Minister of Australia
    Lawrence Gonzi** Former Prime Minister of Malta
    Lord George Robertson** Former Secretary General of NATO
    Gordon Brown Former Prime Minister of the UK 2007-2010
    Vaira Vike-Freiberga*** Co-Chair, NGIC; President of Latvia 1999-2007
    Ismail Serageldin*** Co-Chair, NGIC; Vice President of the World Bank 1992-2000
    Kerry Kennedy*** President, Robert F. Kennedy Human Rights
    Rosen Plevneliev*** President of Bulgaria 2012-2017
    Petar Stoyanov*** President of Bulgaria 1997-2002
    Chiril Gaburici*** Prime Minister of Moldova 2015
    Mladen Ivanic*** Member of the Presidency of Bosnia and Herzegovina 2014-2018
    Zlatko Lagumdzija*** Permanent Representative of Bosnia and Herzegovina to the UN; Prime Minister 2001-2002; Deputy Prime Minister 1993-1996, 2012-2015
    Rashid Alimov*** Secretary-General Shanghai Cooperation Organization 2016-2018
    Jan Fisher*** Prime Minister of the Czech Republic 2009-2010
    Sir Tony Blair Prime Minister of the UK 1997-2007
    Csaba Korossi*** 77th President of the UN General Assembly
    Maria Fernanda Espinosa*** 73rd President of the UN General Assembly
    Volkan Bozkir*** 75th President of the UN General Assembly
    Ameenah Gurib Fakim*** President of Mauritius 2015-2018
    Filip Vujanovic*** President of Montenegro 2003-2018
    Borut Pahor*** President of Slovenia 2012-2022; Prime Minister 2008-2012
    Ivo Josipovic*** President of Croatia 2010-2015
    Petru Lucinschi*** President of Moldova 1997-2001
    Boris Tadic*** President of Serbia 2004-2012
    Mirko Cvetkovic*** Prime Minister of Serbia 2008-2012
    Dumitru Bragish*** Prime Minister of Moldova 1999-2001
    Emil Constantinescu*** President of Romania 1996-2000
    Nambaryn Enkhbayar*** President of Mongolia 2005-2009
    Kolinda Grabar-Kitarovic*** President of Croatia 2015-2020
    Gjorge Ivanov*** President of North Macedonia 2009-2019
    Valdis Zatlers*** President of Latvia 2007-2011
    Ana Birchall*** Deputy Prime Minister of Romania 2018-2019
    Hikmet Cetin*** Minister of Foreign Affairs of Turkey 1991-1994
    Jewel Howard Taylor*** Vice President of Liberia 2018-2024
    Djoomart Otorbayev*** Prime Minister of Kyrgyzstan 2014-2015
    Julio Cobos*** Vice President of Argentina 2007-2011
    Ouided Bouchmani*** Nobel Peace Prize Laureate 2015
    Abdul Rauf AlRawabdeh*** Prime Minister of Jordan 1999-2000
    Jadranka Kosor*** Prime Minister of Montenegro 2009-2011
    Milica Pejanovic*** Minister of Defense of Montenegro 2012-2016
    Mats Karlsson*** Former Vice-President of the World Bank
    Laimdota Straujuma*** Prime Minister of Latvia 2014-2016
    Eka Tkeshelashvili*** Deputy Prime Minister of Georgia 2010-2012, Minister of Foreign Affairs 2010
    Moushira Khattab*** Former Minister of State for Family and Population of Egypt
    Raimonds Vejonis*** President of Latvia 2015-2019
    Ilir Meta*** President of Albania 2017-2022
    Edmond Panariti*** Former Minister of Foreign affairs, Minister of Agriculture and Rural Development of Albania
    Andris Piebalgs*** European Commissioner for Development 2010-2014, European Commissioner for Energy 2004-2010
    Manuel Pulgar Vidal*** Climate and Energy Global Leader at the World Wide Fund for Nature, Minister of Environment of Peru 2011-2016, President of COP20
    Yves Leterme*** Yves Leterme, Prime Minister of Belgium 2008, 2009-201
    Rovshan Muradov*** Secretary-General of the Nizami Ganjavi International Center
    Professor Erik Berglof London School of Economics and Political Science
    Professor Justin Lin Beijing University
    Professor Bai Chong-En Tsinghua School of Economics and Management Studies
    Professor Robin Burgess London School of Economics and Political Science
    Professor Shang-jin Wei Columbia University
    Professor Harold James Princeton University
    Ahmed Galal Former Minister of Finance, Egypt
    Professor Jong-Wha Lee Korea University
    Professor Leonhard Wantchekon African School of Economics, Benin
    Professor Ernst-Ludwig von Thadden Mannheim University
    Professor Kaushik Basu Cornell University
    Professor Bengt Holmstrom Massachusetts Institute of Technology
    Professor Mathias Dewatripont Université Libre de Bruxelles
    Professor Dalia Marin University of Munich
    Professor Richard Portes London Business School
    Professor Chris Pissarides London School of Economics and Political Science
    Professor Diane Coyle University of Cambridge
    Mustapha Nabli Former Governor, Central Bank of Tunisia
    Professor Wendy Carlin University College London
    Professor Gerard Roland University of California, Berkeley
    Professor Nora Lustig Tulane University
    Piroska Nagy-Mohacsi London School of Economics and Political Science
    Professor Philippe Aghion College de France
    Professor Devi Sridhar University of Edinburgh
    Yu Yongding Former President of China Society in the World Economy
    Muhammad Yunus, Nobel Peace Prize Laureate 2006
    Kailash Satyarthe, Nobel Peace Prize Laureate 2014
    Sir Ivor Roberts Former UK Ambassador
    Sir Suma Chakrabarti Former EBRD President
    Sir Tim Hitchens Former UK Ambassador
    Alistair Burt Former Minister for Health/International Development
    Tom Fletcher Former UK Ambassador
    Julian Braithwaite Former UK Perm Rep to WHO
    John Casson Former UK Ambassador
    *indicates membership of Club de Madrid

    ** Indicates membership of Global Leadership Forum

    *** Indicates membership of NGIC

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    https://www.gospanews.net/en/2024/03/28/who-never-discovered-sars-cov-2-artificial-origin-but-promotes-vips-calling-for-new-deal-on-future-pandemics/
    WHO never Discovered SARS-COV-2 Artificial Origin but Promotes VIPs Calling for New Deal on Future Pandemics 28 Marzo 2024 FacebookTwitterWhatsAppEmailLinkedInTelegramCondividi 12.285 Views by Fabio Giuseppe Carlo Carisio VERSIONE IN ITALIANO “I love my brother Bobby, but I do not share or endorse his opinions on many issues, including the COVID pandemic, vaccinations, and the role of social media platforms in policing false information,” she said at the time. “It is also important to note that Bobby’s views are not reflected in or influence the mission or work of our organization.” These were the sentences about Robert F. Kennedy jr statements released by Kerry Kennedy, former wife of New York Governor Andrea Cuomo and Chair of the Amnesty International USA Leadership Council. Nominated by President Bush and confirmed by the Senate. She serves on the board of directors of the United States Institute of Peace, as well as Human Rights First, and Inter Press Service (Rome, Italy). Zuckerberg Confession: “Establishment asked Facebook to ‘censor’ Covid posts” Kerry Kennedy, President, Robert F. Kennedy Human Rights, is one of the VIPs who signed the “Call for urgent Agreement on International Deal to Prepare for and prevent future Pandemics” (whole text below) meanwhile World Health Organization is loosing many hopes that WHO Assembly will approve the Pandemic Treaty due to the opposition of Russia an many other nations. WHO, EU Launch New Global Vaccine Passport Initiative: “Death Sentence for Millions” The appeal was launched by Office of Gordon and Sarah Brown, the website of former UK prime minister., who signed it as Tony Blair, the Former UN General Secretary Ban-ki Moon, New Zealand’s former Prime Minister Helen Cark and Italian former PM Mario Monti, life senator and former manager of New York bank Goldman Sachs in business with Pfizer, nominated as president of Pan-European Commission on Health and Sustainable Development, a body created by the World Health Organization during Covid-19 emergency despite his ties with Wuhan Institute of Virology. WUHAN-GATES – 68. THE SMOKING GUN OF MANMADE SARS-COV-2. Fauci, Wuhan & Chinese Military Scientists behind Research on Vaccine for Biodefense Indeed Monti was in the European Commission which financed the EPISARS project for the developing of dangerous research on Coronavirus SARS from which, in a huge affair among China and US, emerged the artificial SARS-Cov-2. WUHAN-GATES – 65. L’ANELLO MANCANTE DEL DIABOLICO COMPLOTTO NWO-UE: Dal SARS da Laboratorio di Monti al Vaccino COVID col Grafene di Capua Although WHO has not yet been able to prove the laboratory origin of the Covid-19 virus, also because it has entrusted the investigations to doctors with enormous conflicts of interest for having worked in the Wuhan Institute of Virology, today it continues to insist on launch the global agreement on pandemics thanks to those same people who supported Bill Gates’ global immunization plan and the “Covid-19 pandemic planned for decades” as declared by the lawyer Robert F. Kennedy jr and as demonstrated by the patents expert David Martin on the role of Anthony Fauci, and detailed by the Gospa News investigations of the “Wuhan-Gates” cycle. WHO claims to develop more and major researches on viruses when it is now well established that the Covid-19 pandemic was caused by man precisely because of research on biological weapons. 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 Subscribe to the Gospa News Newsletter to read the news as soon as it is published MAIN SOURCES GOSPA NEWS – WUHAN-GATES INVESTIGATIONS GOSPA NEWS – COVID, BIG PHARMA, VACCINES WHO: “Call for urgent Agreement on International Deal to Prepare for and prevent future Pandemics” Article originally published on World Health Organization All links to Gospa News articles have been added aftermath, in relation to the topics highlighted Subscribe to the Gospa News Newsletter to read the news as soon as it is published A high-powered intervention by 23 former national Presidents, 22 former Prime Ministers, a former UN General Secretary and 3 Nobel Laureates is being made today to press for an urgent agreement from international negotiators on a Pandemic Accord, under the Constitution of the World Health Organizaion, to bolster the world’s collective preparedness and response to future pandemics. WUHAN-GATES – 69. How and Why the Spy of Biden & Gates Hid ManMade SARS-Cov-2 in US Intelligence Dossier Former UN General Secretary Ban-ki Moon, New Zealand’s former Prime Minister Helen Cark, former UK Prime Ministers Gordon Brown and Tony Blair, former Malawi President Joyce Banda, former Peru President Franciso Sagasti, and 3 former Presidents of the UN General Assembly are amongst 100+ global leaders, from all continents and fields of politics, economics and health management who today issued a joint open letterurging accelerated progress in current negotiations to reach the world’s first ever multi-lateral agreement on pandemic preparedness and prevention. “A pandemic accord is critical to safeguard our collective future. Only a strong global pact on pandemics can protect future generations from a repeat of the COVID-19 crisis, which led to millions of deaths and caused widespread social and economic devastation, owing not least to insufficient international collaboration,” the leaders write in their joint letter. WUHAN-GATES – 60. NEW SCANDAL INTO WHO. French Co-Chair of Investigative Group on SARS-2 Worked in the China Bio-lab which Enhanced Coronavirus In the throes of the COVID-19 disaster which, officially, claimed 7 million lives and wiped $2 trillion from the world economy, inter-governmental negotiations to reach international agreement on future pandemic non-proliferation were begun in December 2021 between 194 of the world’s 196 nations. Nations set themselves the deadline of May 2024 by which they should reach agreement on what would be the world’s first ever Pandemic Accord. The Ninth round of Pandemic Accord negotiations are underway this week and next. Signatories of today’s open letter hope their combined influence willencourage all 194 nations to maintain the courage of their Covid-years conviction and make their own collective ambition of an international pandemic protocol a reality by the intended May deadline to enable ratification by the World Health Assembly at its May 2024 Annual General Assembly. And they urge negotiators “to redouble their efforts” to meet the imminent deadline and not let their efforts be blown off course by malicious misinformation campaigning against the WHO, the international organisation which would be tasked with implementing the new health accord. Taking a swipe at those who wrongly believe national sovereignty may be undermined by this major international step forward for public health the signatories say “there is no time to waste” and they call on the leaders of the 194 nations taking part in the current negotiations to “redouble their efforts to complete the accord by the May deadline.” WUHAN-GATES – 72. THE SUMMARY: WHO Intrigues on the SARS-Cov-2 Bioweapon & Vaccine Plots – McCullough reveals The letter, hosted on the website of The Office of Gordon and Sarah Brown states, “Countries are doing this not because of some dictum from the WHO – like the negotiations, participation in any instrument would be entirely voluntary – but because they need what the accord can and must offer. In fact, a pandemic accord would deliver vast and universally shared benefits, including greater capacity to detect new and dangerous pathogens, access to information about pathogens detected elsewhere in the world, and timely and equitable delivery of tests, treatments, vaccines, and other lifesaving tools. “As countries enter what should be the final stages of the negotiations, governments must work to refute and debunk false claims about the accord. At the same time, negotiators must ensure that the agreement lives up to its promise to prevent and mitigate pandemic-related risks. This requires, for example, provisions aimed at ensuring that when another pandemic threat does arise, all relevant responses – from reporting the identification of risky pathogens to delivering tools like tests and vaccines on an equitable basis – are implemented quickly and effectively. As the COVID-19 pandemic showed, collaboration between the public and private sectors focused on advancing the public good is also essential.” WUHAN-GATES – 24. WHO & Pandemic in Gates-China’s Puppet Hands: Dr. Tedros Leader of TPLF, Islamic-Communist Rebels blamed of Last Massacre in Ethiopia by Amnesty “A new pandemic threat will emerge; there is no excuse not to be ready for it. It is thus imperative to build an effective, multisectoral, and multilateral approach to pandemic prevention, preparedness, and response. Given the unpredictable nature of public-health risks, a global strategy must embody a spirit of openness and inclusiveness. There is no time to waste, which is why we are calling on all national leaders to redouble their efforts to complete the accord by the May deadline.” “Beyond protecting countless lives and livelihoods, the timely delivery of a global pandemic accord would send a powerful message: even in our fractured and fragmented world, international cooperation can still deliver global solutions to global problems.” Article originally published on World Health Organization Joint letter to leaders of WHO member states calling for an urgent agreement on a pandemic accord Originally published on the Office of Gordon and Sarah Brown website on March, 20, 2024 The overwhelming lesson we learned from COVID-19 is that no one is safe anywhere until everyone is safe everywhere – and that can only happen through collaboration. In response, the 194 countries which are members of the World Health Organization decided in December 2021 to launch negotiations for a new international instrument on pandemic prevention, preparedness and response, a Pandemic Accord, as a “global framework” to work together to prepare for and stem any new pandemic threat, including by achieving equitable access to vaccines, therapeutics and diagnostics. WUHAN-GATES – 62. MANMADE SARS-Cov-2 FOR GOLDEN VACCINES: Metabiota, CIA, Biden, Gates, Rockefeller intrigued in Ukraine, China and Italy Negotiation of an effective pandemic accord is a much needed opportunity to safeguard the world we live in. Countries themselves have proposed this instrument, individual countries are negotiating it, and only countries will ultimately be responsible for its requirements and its success or failure. Establishing a strong global pact on pandemics will protect future generations from a repeat of the millions of deaths and the social and economic devastation which resulted from a lack of collaboration during theCOVID-19 pandemic. All countries need what the accord can offer: the capacity to detect and share pathogens presenting a risk, and timely access to tests, treatments and vaccines. An agreement is meant to be reached just two and a half months from now – countries imposed a deadline of May 2024, in time for the 77th World Health Assembly. WUHAN-GATES – 73. Half of Century of Covert Bioweapon Development Leading to Fauci’s SARS-Cov-2 and to mRNA Lethal Vaccines As countries now enter what should be the final stages of the negotiations, they must ensure that they are agreeing on actions which will do the job required: to prevent and mitigate pandemic threats. We urge solutions which ensure both speed in reporting and sharing pathogens, and in access – in every country – to sufficient tools like tests and vaccines to protect lives and minimise harm. The public and private sectors must work together towards the public good. This global effort is being threatened by misinformation and disinformation. Among the falsehoods circulating are allegations that the WHO intends to monitor people’s movements through digital passports; that it will take away the national sovereignty of countries; and that it will have the ability to deploy armed troops to enforce mandatory vaccinations and lockdowns. All of these claims are wholly false and governments must work to disavow them with clear facts. WUHAN-GATES – 47. SARS-2 BIOWEAPON. Pentagon’s DARPA Stopped a Risky Test in US but Funded a Secret one in UK with Gates It is imperative now to build an effective, multisectoral and multilateral approach to pandemic prevention,preparedness, and response marked by a spirit of openness and inclusiveness. In doing so we can send a message that even in this fractured and fragmented world, cross-border co-operation can deliver global solutions to global problems. We call on leaders of all countries to step up their efforts and secure an effective pandemic accord by May. A new pandemic threat will emerge – and there is no excuse not to be ready for it. Originally published on the Office of Gordon and Sarah Brown website on March, 20, 2024 Name Title Carlos Alvarado* President of Costa Rica (2018-2022) Michelle Bachelet* President of Chile (2006-2010) Jan Peter Balkenende* Prime Minister of The Netherlands (2002-2010) Ban Ki-moon* Eighth Secretary General of the United Nations Joyce Banda* President of Malawi (2012-2014) Kjell Magne Bondevik* Prime Minister of Norway (1997-2000; 2001-2005) Kim Campbell* Prime Minister of Canada (1993) Alfred Gusenbauer* Chancellor of Austria (2007-2008) Seung-Soo Han* Prime Minister of the Rep. of Korea (2008-2009) Mehdi Jomaa* Prime Minister of Tunisia (2014-2015) Horst Köhler* President of Germany (2004-2010) Rexhep Meidani* President of Albania (1997-2002) Mario Monti* Prime Minister of Italy (2011-2013) Francisco Sagasti* President of Peru (2020-2021) Jenny Shipley* Prime Minister of New Zealand (1997-1999) Juan Somavía* Ninth Director of the International Labour Organization Helen Clark** Former Prime Minister of New Zealand Micheline Calmy-Rey** Former President of the Swiss Confederation Baroness Lynda Chalker** Former Minister of Overseas Development of the UK Chester A. Crocker** Former Assistant Secretary for African Affairs, USA Marzuki Darusman** Former Attorney General of Indonesia Mohamed ElBaradei** Former Vice President of Egypt Gareth Evans** Former Foreign Minister of Australia Lawrence Gonzi** Former Prime Minister of Malta Lord George Robertson** Former Secretary General of NATO Gordon Brown Former Prime Minister of the UK 2007-2010 Vaira Vike-Freiberga*** Co-Chair, NGIC; President of Latvia 1999-2007 Ismail Serageldin*** Co-Chair, NGIC; Vice President of the World Bank 1992-2000 Kerry Kennedy*** President, Robert F. Kennedy Human Rights Rosen Plevneliev*** President of Bulgaria 2012-2017 Petar Stoyanov*** President of Bulgaria 1997-2002 Chiril Gaburici*** Prime Minister of Moldova 2015 Mladen Ivanic*** Member of the Presidency of Bosnia and Herzegovina 2014-2018 Zlatko Lagumdzija*** Permanent Representative of Bosnia and Herzegovina to the UN; Prime Minister 2001-2002; Deputy Prime Minister 1993-1996, 2012-2015 Rashid Alimov*** Secretary-General Shanghai Cooperation Organization 2016-2018 Jan Fisher*** Prime Minister of the Czech Republic 2009-2010 Sir Tony Blair Prime Minister of the UK 1997-2007 Csaba Korossi*** 77th President of the UN General Assembly Maria Fernanda Espinosa*** 73rd President of the UN General Assembly Volkan Bozkir*** 75th President of the UN General Assembly Ameenah Gurib Fakim*** President of Mauritius 2015-2018 Filip Vujanovic*** President of Montenegro 2003-2018 Borut Pahor*** President of Slovenia 2012-2022; Prime Minister 2008-2012 Ivo Josipovic*** President of Croatia 2010-2015 Petru Lucinschi*** President of Moldova 1997-2001 Boris Tadic*** President of Serbia 2004-2012 Mirko Cvetkovic*** Prime Minister of Serbia 2008-2012 Dumitru Bragish*** Prime Minister of Moldova 1999-2001 Emil Constantinescu*** President of Romania 1996-2000 Nambaryn Enkhbayar*** President of Mongolia 2005-2009 Kolinda Grabar-Kitarovic*** President of Croatia 2015-2020 Gjorge Ivanov*** President of North Macedonia 2009-2019 Valdis Zatlers*** President of Latvia 2007-2011 Ana Birchall*** Deputy Prime Minister of Romania 2018-2019 Hikmet Cetin*** Minister of Foreign Affairs of Turkey 1991-1994 Jewel Howard Taylor*** Vice President of Liberia 2018-2024 Djoomart Otorbayev*** Prime Minister of Kyrgyzstan 2014-2015 Julio Cobos*** Vice President of Argentina 2007-2011 Ouided Bouchmani*** Nobel Peace Prize Laureate 2015 Abdul Rauf AlRawabdeh*** Prime Minister of Jordan 1999-2000 Jadranka Kosor*** Prime Minister of Montenegro 2009-2011 Milica Pejanovic*** Minister of Defense of Montenegro 2012-2016 Mats Karlsson*** Former Vice-President of the World Bank Laimdota Straujuma*** Prime Minister of Latvia 2014-2016 Eka Tkeshelashvili*** Deputy Prime Minister of Georgia 2010-2012, Minister of Foreign Affairs 2010 Moushira Khattab*** Former Minister of State for Family and Population of Egypt Raimonds Vejonis*** President of Latvia 2015-2019 Ilir Meta*** President of Albania 2017-2022 Edmond Panariti*** Former Minister of Foreign affairs, Minister of Agriculture and Rural Development of Albania Andris Piebalgs*** European Commissioner for Development 2010-2014, European Commissioner for Energy 2004-2010 Manuel Pulgar Vidal*** Climate and Energy Global Leader at the World Wide Fund for Nature, Minister of Environment of Peru 2011-2016, President of COP20 Yves Leterme*** Yves Leterme, Prime Minister of Belgium 2008, 2009-201 Rovshan Muradov*** Secretary-General of the Nizami Ganjavi International Center Professor Erik Berglof London School of Economics and Political Science Professor Justin Lin Beijing University Professor Bai Chong-En Tsinghua School of Economics and Management Studies Professor Robin Burgess London School of Economics and Political Science Professor Shang-jin Wei Columbia University Professor Harold James Princeton University Ahmed Galal Former Minister of Finance, Egypt Professor Jong-Wha Lee Korea University Professor Leonhard Wantchekon African School of Economics, Benin Professor Ernst-Ludwig von Thadden Mannheim University Professor Kaushik Basu Cornell University Professor Bengt Holmstrom Massachusetts Institute of Technology Professor Mathias Dewatripont Université Libre de Bruxelles Professor Dalia Marin University of Munich Professor Richard Portes London Business School Professor Chris Pissarides London School of Economics and Political Science Professor Diane Coyle University of Cambridge Mustapha Nabli Former Governor, Central Bank of Tunisia Professor Wendy Carlin University College London Professor Gerard Roland University of California, Berkeley Professor Nora Lustig Tulane University Piroska Nagy-Mohacsi London School of Economics and Political Science Professor Philippe Aghion College de France Professor Devi Sridhar University of Edinburgh Yu Yongding Former President of China Society in the World Economy Muhammad Yunus, Nobel Peace Prize Laureate 2006 Kailash Satyarthe, Nobel Peace Prize Laureate 2014 Sir Ivor Roberts Former UK Ambassador Sir Suma Chakrabarti Former EBRD President Sir Tim Hitchens Former UK Ambassador Alistair Burt Former Minister for Health/International Development Tom Fletcher Former UK Ambassador Julian Braithwaite Former UK Perm Rep to WHO John Casson Former UK Ambassador *indicates membership of Club de Madrid ** Indicates membership of Global Leadership Forum *** Indicates membership of NGIC (Visited 37 times, 3 visits today) FacebookTwitterWhatsAppEmailLinkedInTelegramCondividi 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    WHO never Discovered SARS-COV-2 Artificial Origin but Promotes VIPs Calling for New Deal on Future Pandemics
    by Fabio Giuseppe Carlo CarisioVERSIONE IN ITALIANO"I love my brother Bobby, but I do not share or endorse his opinions on many issues, including the COVID pandemic, vaccinations, and the role of social media platforms in policing false information," she said at the time. "It is also importa
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  • DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA

    Rebekah Barnett
    Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can.

    The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells.

    Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say.

    And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say.

    However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA.

    TLDR

    1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable)

    2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient)

    3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination

    4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA.
    Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process.

    McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.”

    Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients.

    But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan.

    While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration.

    Now, the first results are in.

    In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine.

    The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites.

    “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says.

    “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.”

    To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls.

    The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan.

    Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA.

    This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with.


    Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack
    Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA.

    “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.”

    Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan.


    Source: Kevin McKernan’s Substack
    Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line.

    You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’

    ‘Major advance,’ but clinical implications are limited

    McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.”

    “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries.

    The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells.

    McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately.

    At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan.

    The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety.

    Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English).

    LNPs deliver contaminant DNA straight to the cells

    A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur.

    This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes.

    This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems.


    Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021
    From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.”

    It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis.

    Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines.

    Regulators unconcerned

    I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment.

    The TGA did not address the new findings, but a spokesperson from the TGA responded,

    “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.”

    However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims.

    Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised.

    Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted.

    In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year.

    Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories.

    Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning.

    Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further.

    The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk.

    ‘No excuse’ for ignoring ‘screaming hot signal’

    Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan.

    Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.”

    “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?”

    There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years.

    “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.”


    Source: National Human Genome Research Institute
    DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination.

    “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.”

    Scientists pick up regulators’ slack

    In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton.

    “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.”

    Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites.

    In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in.

    “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said.

    McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present.

    Decentralisation the future of science?

    McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust.

    “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan.

    “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“

    In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world.


    Source: X
    For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation.

    “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan.

    Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet.

    Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct.


    Source: X
    In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.”

    But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa.

    Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not.

    The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received.

    View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files.

    Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina.

    Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account.


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    1
    From an article I wrote for Umbrella News on this topic last year:

    The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News,

    “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.”

    “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.”

    With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected).

    As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims.

    The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken.

    Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed.


    https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows It also appears that the contamination enters the cell nucleus and integrates with human DNA Rebekah Barnett Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can. The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells. Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say. And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say. However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA. TLDR 1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable) 2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient) 3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination 4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA. Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process. McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.” Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients. But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan. While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration. Now, the first results are in. In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine. The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites. “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says. “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.” To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls. The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan. Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA. This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with. Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA. “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.” Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan. Source: Kevin McKernan’s Substack Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line. You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’ ‘Major advance,’ but clinical implications are limited McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.” “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries. The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells. McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately. At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan. The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety. Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English). LNPs deliver contaminant DNA straight to the cells A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur. This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes. This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems. Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021 From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.” It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis. Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines. Regulators unconcerned I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment. The TGA did not address the new findings, but a spokesperson from the TGA responded, “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.” However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims. Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised. Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted. In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year. Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories. Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning. Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further. The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk. ‘No excuse’ for ignoring ‘screaming hot signal’ Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan. Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.” “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?” There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years. “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.” Source: National Human Genome Research Institute DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination. “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.” Scientists pick up regulators’ slack In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton. “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.” Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites. In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in. “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said. McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present. Decentralisation the future of science? McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust. “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan. “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“ In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world. Source: X For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation. “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan. Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet. Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct. Source: X In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.” But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa. Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not. The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received. View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files. Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina. Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account. To support my work, make a one-off contribution to DDU via my Kofi account and/or subscribe. Thanks! Follow me on X Follow me on Instagram 1 From an article I wrote for Umbrella News on this topic last year: The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News, “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.” “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.” With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected). As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims. The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken. Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed. https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    NEWS.REBEKAHBARNETT.COM.AU
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA
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  • Medical Researchers Call for Urgent Actions to Deal with Mass Contamination of Blood Supply
    "Japanese researchers have published disturbing evidence that blood transfusions from individuals who received COVID-19 shots are tainted with a myriad of dangers." - Jeff Dornik

    Karen Kingston
    March 22, 2024: Japanese researchers published a meta-analysis on the dangers of using blood donated from people who were injected with the COVID-19 ‘vaccines,’ increasing the risks for acute health conditions and severe diseases in recipients of blood donations. The researchers provide testing and screening recommendations, and proposed regulations to reduce these risks.


    Share

    Jeff Dornik published an excellent article summarizing the scientific meta-analysis, declaring;

    “The blood supply, once deemed a lifeline, has now become a conduit for harm.” - Jeff Dornik


    In his article entitled, Japanese Researchers Sound Alarm on Deadly Risks of Vaccinated Blood Transfusions, Jeff writes, “In a shocking revelation, Japanese researchers have unearthed disturbing evidence that could change the way we view COVID-19 Injections forever. According to their findings, blood transfusions from individuals who have received COVID-19 shots are tainted with a myriad of dangers, potentially wreaking havoc on both vaxxed and unvaxxed recipients. This discovery has sparked urgent calls for action from the global medical community, as the ramifications of this contamination could be catastrophic.”

    I recommend reading and sharing Jeff’s breaking news article.

    You Can Make an Impact

    The COVID-19 injections have not only contaminated the blood of those who are injected, but due to shedding and blood donations, all individuals are at risk of being inoculated with gene-editing nanoparticle technologies and toxic biosynthetic spike proteins. These toxic biosynthetic nanoparticles are proven to increase the risk for cardiovascular, neurological, auto-immune, and pulmonary diseases, and can induce permanent changes to the human genome.


    For the safety of the public, the use of mRNA nanoparticle injections must be banned from every county and state in America.

    Every American has standing in their state to demand that the COVID-19 mRNA nanoparticle ‘vaccines’ be banned from their state. You can send a demand letter to your governor, attorney general, and even local sheriff. If they fail to take action, you can petition your state’s Supreme Court to order the governor and attorney general to seize the injections and ban the use of mRNA nanoparticle injections.

    Hebrews 10:35-36

    So do not throw away your confidence; it will be richly rewarded. You need to persevere so that when you have done the will of God, you will receive what he has promised.

    Pending Florida Supreme Court Case: Will DeSantis & AG Moody Be Court-Ordered to Remove ALL mRNA Injections from Florida?

    Pending Florida Supreme Court Case: Will DeSantis & AG Moody Be Court-Ordered to Remove ALL mRNA Injections from Florida?
    March 5, 2024: When I first began this endeavor, God put on my heart to have the mRNA shots removed from every community across the United States and around the world. I’m honored that I was integral in sending Dr. Joseph Sansone the document that I updated from the

    Read full story

    The Kingston Report. TRUTH WINS.

    Ways to Support My Work

    Mail: Karen Kingston/miFight Inc., 960 Postal Way #307, Vista, CA 92085

    Buy me a coffee (Ko-fi)

    Consider becoming a free or paid subscriber.

    email: [email protected]

    Get a FREE $99 Wellness Company Membership

    You can keep a full armamentarium of prescriptions on-hand for bacterial, viral, or parasite infections through The Wellness Company. Use the code FREEMEMBER at checkout and SAVE $45.


    Here is the direct link to Emergency Prescription Kit, which contains prescriptions for the above listed acute (not chronic) conditions and infections. Use the code FREEMEMBER at checkout and SAVE $45 PLUS Receive a FREE TWC Membership ($99 Value)


    https://karenkingston.substack.com/p/medical-researchers-call-for-urgent
    Medical Researchers Call for Urgent Actions to Deal with Mass Contamination of Blood Supply "Japanese researchers have published disturbing evidence that blood transfusions from individuals who received COVID-19 shots are tainted with a myriad of dangers." - Jeff Dornik Karen Kingston March 22, 2024: Japanese researchers published a meta-analysis on the dangers of using blood donated from people who were injected with the COVID-19 ‘vaccines,’ increasing the risks for acute health conditions and severe diseases in recipients of blood donations. The researchers provide testing and screening recommendations, and proposed regulations to reduce these risks. Share Jeff Dornik published an excellent article summarizing the scientific meta-analysis, declaring; “The blood supply, once deemed a lifeline, has now become a conduit for harm.” - Jeff Dornik In his article entitled, Japanese Researchers Sound Alarm on Deadly Risks of Vaccinated Blood Transfusions, Jeff writes, “In a shocking revelation, Japanese researchers have unearthed disturbing evidence that could change the way we view COVID-19 Injections forever. According to their findings, blood transfusions from individuals who have received COVID-19 shots are tainted with a myriad of dangers, potentially wreaking havoc on both vaxxed and unvaxxed recipients. This discovery has sparked urgent calls for action from the global medical community, as the ramifications of this contamination could be catastrophic.” I recommend reading and sharing Jeff’s breaking news article. You Can Make an Impact The COVID-19 injections have not only contaminated the blood of those who are injected, but due to shedding and blood donations, all individuals are at risk of being inoculated with gene-editing nanoparticle technologies and toxic biosynthetic spike proteins. These toxic biosynthetic nanoparticles are proven to increase the risk for cardiovascular, neurological, auto-immune, and pulmonary diseases, and can induce permanent changes to the human genome. For the safety of the public, the use of mRNA nanoparticle injections must be banned from every county and state in America. Every American has standing in their state to demand that the COVID-19 mRNA nanoparticle ‘vaccines’ be banned from their state. You can send a demand letter to your governor, attorney general, and even local sheriff. If they fail to take action, you can petition your state’s Supreme Court to order the governor and attorney general to seize the injections and ban the use of mRNA nanoparticle injections. Hebrews 10:35-36 So do not throw away your confidence; it will be richly rewarded. You need to persevere so that when you have done the will of God, you will receive what he has promised. Pending Florida Supreme Court Case: Will DeSantis & AG Moody Be Court-Ordered to Remove ALL mRNA Injections from Florida? Pending Florida Supreme Court Case: Will DeSantis & AG Moody Be Court-Ordered to Remove ALL mRNA Injections from Florida? March 5, 2024: When I first began this endeavor, God put on my heart to have the mRNA shots removed from every community across the United States and around the world. I’m honored that I was integral in sending Dr. Joseph Sansone the document that I updated from the Read full story The Kingston Report. TRUTH WINS. Ways to Support My Work Mail: Karen Kingston/miFight Inc., 960 Postal Way #307, Vista, CA 92085 Buy me a coffee (Ko-fi) Consider becoming a free or paid subscriber. email: [email protected] Get a FREE $99 Wellness Company Membership You can keep a full armamentarium of prescriptions on-hand for bacterial, viral, or parasite infections through The Wellness Company. Use the code FREEMEMBER at checkout and SAVE $45. Here is the direct link to Emergency Prescription Kit, which contains prescriptions for the above listed acute (not chronic) conditions and infections. Use the code FREEMEMBER at checkout and SAVE $45 PLUS Receive a FREE TWC Membership ($99 Value) https://karenkingston.substack.com/p/medical-researchers-call-for-urgent
    KARENKINGSTON.SUBSTACK.COM
    Medical Researchers Call for Urgent Actions to Deal with Mass Contamination of Blood Supply
    "Japanese researchers have published disturbing evidence that blood transfusions from individuals who received COVID-19 shots are tainted with a myriad of dangers." - Jeff Dornik
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  • "Unwrap Joy: Gift Card and Cash App Giveaway Blessing!

    Unlock the magic of giving and receiving with our exclusive Gift Card and Cash App Giveaway! It's time to spread joy and cheer with a chance to win exciting prizes that will brighten your day and elevate your spirits.

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    "Unwrap Joy: Gift Card and Cash App Giveaway Blessing! Unlock the magic of giving and receiving with our exclusive Gift Card and Cash App Giveaway! It's time to spread joy and cheer with a chance to win exciting prizes that will brighten your day and elevate your spirits. Gift Card and Cash App Giveaway Blessing! Join Here 👇👇 https://cutt.ly/4w2uRsHF In a world where generosity knows no bounds, we believe in celebrating the spirit of giving. That's why we're thrilled to announce our special giveaway, where lucky winners will be treated to an array of gift cards and cash prizes through the convenience of Cash App. Imagine the possibilities as you unwrap the gift of choice with a variety of gift cards from leading retailers, covering everything from fashion and electronics to dining and entertainment. Whether you're treating yourself to a shopping spree or surprising a loved one with a thoughtful gesture, these gift cards are your ticket to endless smiles and memorable moments. But that's not all – we're taking it up a notch by including Cash App prizes in the mix! With Cash App, you have the power to send, spend, and save money effortlessly. And now, you could be one of the lucky winners to receive cash prizes directly into your Cash App account, giving you the freedom to use it however you please. Entering our giveaway is as simple as can be. Just follow a few easy steps, and you could be on your way to winning big: 1.Visit our official giveaway page and follow the instructions to enter👇👇 https://cutt.ly/4w2uRsHF 2.Spread the word by sharing our giveaway with your friends and family. 3.Keep an eye on your inbox – winners will be notified via email and announced on our social media channels. Whether you're dreaming of a shopping spree, craving a delicious meal, or simply looking to brighten someone's day, our Gift Card and Cash App Giveaway is your chance to make it happen. Don't miss out on this incredible opportunity to unwrap joy and spread kindness in the most delightful way possible. Join us in celebrating the magic of giving and receiving – enter our giveaway today and let the blessings flow! #Cashapp #Cashappblessing #Cashmoney #Cashappgiveaway #Giftcard #Giftcardgiveaway #freegiftcard #makemoney #Makemoneyonline #onlinemoney #digitalmoney #Makemoneyathome
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  • WE all know that mainstream media has been CONTROLLED by the deep state for decades..it's how the levels of LIES and DECEPTION were accepted by so many.....I do still pay attention to mainstream because I choose to know what the "masses" are being fed...I believe we have been watching a lot of "REVERSE Operation Mockingbird" over the last few years...slowly leaking TRUTH for folks to digest...just my opinion That said, last night IMHO was a HUGE WIN for We the People! Regardless if you LIke FOX - Dislike FOX - Like Jesse- Dislike Jesse- the fact remains that last night March 19, 2024 at 8pm the TRUTH about Operation Mockingbird and the "Deep State" was being put out on Jesse Watters Primetime...including video clips we have been sharing for years on Telegram and other social media platforms....For me, it's more validation that the Storm IS upon us.... https://www.foxnews.com/video/6349280028112
    💥💥💥WE all know that mainstream media has been CONTROLLED by the deep state for decades..it's how the levels of LIES and DECEPTION were accepted by so many.....I do still pay attention to mainstream because I choose to know what the "masses" are being fed...I believe we have been watching a lot of "REVERSE Operation Mockingbird" over the last few years...slowly leaking TRUTH for folks to digest...just my opinion 🤷‍♀️ That said, last night IMHO was a HUGE WIN for We the People! 😊 Regardless if you LIke FOX - Dislike FOX - Like Jesse- Dislike Jesse- the fact remains that last night March 19, 2024 at 8pm the TRUTH about Operation Mockingbird and the "Deep State" was being put out on Jesse Watters Primetime...including video clips we have been sharing for years on Telegram and other social media platforms....For me, it's more validation that the Storm IS upon us.... https://www.foxnews.com/video/6349280028112
    WWW.FOXNEWS.COM
    Jesse Watters: The 'deep state' is preparing for war | Fox News Video
    Fox News host Jesse Watters gives his take on how the term ‘deep state’ has changed throughout the years on ‘Jesse Watters Primetime.’
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  • Fasting On The White Days
    Definition, benefits and steps on observing the fasting of White days

    Definition, benefits and steps on observing the fasting of White days
    Have you tried voluntary fasting on Monday or Thursday? Do you know that you can also fast on the White days? Do you know which days are White days? Today, the practice of fasting on the White days is often forgotten by many. This article intends to reintroduce this beautiful prophetic practice in hopes that it will not be considered a forgotten Sunnah.

    Fasting of White days during Full moon

    What are the White days?

    The White days, or known as 'Al-Ayyam al-Bid' in Arabic, are the three consecutive days that fall on every 13th, 14th and 15th day of the Islamic month. It is called white days because the full moon shines brightly throughout the 3 mentioned days. Hence, the radiant full moon at night symbolises the White days.

    Scientifically, the Islamic month begins with a new moon, and then it gradually expands from a crescent moon for 12 nights until it becomes a full moon which is when it radiates the brightest out of any other night, for three consecutive days. Afterwards, the moon will slowly fade away until it turns into a crescent once again and the cycle continues. One of the reasons why the Messenger of Allah s.a.w. and his companions r.a. fasted on the White days was to show gratitude towards Allah s.w.t.

    Muslims are encouraged to fast during these three days on every Islamic month except for the 13th Zulhijjah as Muslims are prohibited to fast on the days of Tashriq. Prophet Muhammad s.a.w. has observed the fasting of White days and has encouraged his companions r.a. to fast along as reported by Abu Hurairah r.a. that the Prophet Muhammad s.a.w. has advised him to do three things, which are;

    صِيَامِ ثَلاَثَةِ أَيَّامٍ مِنْ كُلِّ شَهْرٍ، وَرَكْعَتَي الضُّحَى، وَأَنْ أُوتِرَ قَبْلَ أَنْ أَنَامَ

    “Fasting for three days every month, performing two rakaats of Dhuha prayers and praying witr before sleep.”

    (Sahih Al-Bukhari)

    What are the merits of fasting on the White days?

    The rewards gained from fasting during the full moon are equivalent to that of fasting the whole month as reported by Abdullah Bin Amr Bin Al-As r.a. that the Messenger of Allah s.a.w. said:

    صَوْمُ ثَلاَثَةِ أَيَّامٍ صَوْمُ الدَّهْرِ كُلِّهِ

    “Observing fasting on three days of every month is equivalent to fasting the whole year”

    (Sahih Al-Bukhari)

    The Prophet Muhammad s.a.w. himself has never failed to observe white days fasting as reported by Mu’adhah Al-‘Adawiyah r.a, that she asked the Prophet’s wife, Aisyah r.a

    أَكَانَ رسولُ اللَّهِ صلَّى اللَّهُ عليهِ وسلَّمَ يصومُ ثلاثةَ أيَّامٍ مِن كلِّ شهرٍ قالت نعَم

    “Did the Messenger of Allah s.a.w. observed three days of fasting for every month?”, She replied: “Yes”

    (Sunan At-Tirmizi)

    Fasting of White days, glass of water and dates

    Thus, following in the steps of Prophet Muhammad s.a.w. fasting on White days will help us gain immense rewards. Furthermore, the greatness of the rewards of fasting is made only known to Allah s.w.t. as mentioned in a Hadith Qudsi:

    كُلُّ عَمَلِ ابْنِ آدَمَ له، إلَّا الصِّيَامَ؛ فإنَّه لي، وأَنَا أجْزِي به

    “Every good deed of Adam’s son is for him except fasting; it is for Me and I shall reward (the person fasting) for it”

    (Sahih Al-Bukhari)

    How do we observe the fasting of White Days?

    To begin fasting on white days, one must make the niyyah (intention) as follows and then observe fasting as usual, from sunrise to sunset:

    نَوَيتُ صَومَ أَيَّامِ البِيض سُنَّةً لله تَعَالَى

    Nawaytu Sauma Ayyamil Bidh Sunnatan Lillahi Taa’la

    I intend to observe the Sunnah fast of the White days for Allah the Most High

    You may also establish your intention in your heart through the language that you understand. Once you have tried fasting on White days, try to continue to fast on the following month too and eventually, InsyaAllah, it will turn into a habit, just like how the Messenger of Allah s.a.w. has the habit of observing voluntary fasting.

    Fasting of white days with full moon

    Let us revive and practice this forgotten Sunnah together, following the Prophet Muhammad s.a.w. in pursuit of Allah s.w.t’s love and blessings as well as collecting rewards along the way.

    To be honest, I myself am trying to observe fasting on white days, though some months I did not manage to do so, nevertheless, it feels great to practice the Sunnah and I enjoyed sharing about it with the people around me. I highly encourage my fellow readers to try it out. So, come join me, let’s challenge ourselves to observe these 3 days of fasting and May Allah s.w.t. grant us the strength to ace this challenge. Amin.

    And Allah knows best.

    https://www.muslim.sg/articles/fasting-on-the-white-days
    Fasting On The White Days Definition, benefits and steps on observing the fasting of White days Definition, benefits and steps on observing the fasting of White days Have you tried voluntary fasting on Monday or Thursday? Do you know that you can also fast on the White days? Do you know which days are White days? Today, the practice of fasting on the White days is often forgotten by many. This article intends to reintroduce this beautiful prophetic practice in hopes that it will not be considered a forgotten Sunnah. Fasting of White days during Full moon What are the White days? The White days, or known as 'Al-Ayyam al-Bid' in Arabic, are the three consecutive days that fall on every 13th, 14th and 15th day of the Islamic month. It is called white days because the full moon shines brightly throughout the 3 mentioned days. Hence, the radiant full moon at night symbolises the White days. Scientifically, the Islamic month begins with a new moon, and then it gradually expands from a crescent moon for 12 nights until it becomes a full moon which is when it radiates the brightest out of any other night, for three consecutive days. Afterwards, the moon will slowly fade away until it turns into a crescent once again and the cycle continues. One of the reasons why the Messenger of Allah s.a.w. and his companions r.a. fasted on the White days was to show gratitude towards Allah s.w.t. Muslims are encouraged to fast during these three days on every Islamic month except for the 13th Zulhijjah as Muslims are prohibited to fast on the days of Tashriq. Prophet Muhammad s.a.w. has observed the fasting of White days and has encouraged his companions r.a. to fast along as reported by Abu Hurairah r.a. that the Prophet Muhammad s.a.w. has advised him to do three things, which are; صِيَامِ ثَلاَثَةِ أَيَّامٍ مِنْ كُلِّ شَهْرٍ، وَرَكْعَتَي الضُّحَى، وَأَنْ أُوتِرَ قَبْلَ أَنْ أَنَامَ “Fasting for three days every month, performing two rakaats of Dhuha prayers and praying witr before sleep.” (Sahih Al-Bukhari) What are the merits of fasting on the White days? The rewards gained from fasting during the full moon are equivalent to that of fasting the whole month as reported by Abdullah Bin Amr Bin Al-As r.a. that the Messenger of Allah s.a.w. said: صَوْمُ ثَلاَثَةِ أَيَّامٍ صَوْمُ الدَّهْرِ كُلِّهِ “Observing fasting on three days of every month is equivalent to fasting the whole year” (Sahih Al-Bukhari) The Prophet Muhammad s.a.w. himself has never failed to observe white days fasting as reported by Mu’adhah Al-‘Adawiyah r.a, that she asked the Prophet’s wife, Aisyah r.a أَكَانَ رسولُ اللَّهِ صلَّى اللَّهُ عليهِ وسلَّمَ يصومُ ثلاثةَ أيَّامٍ مِن كلِّ شهرٍ قالت نعَم “Did the Messenger of Allah s.a.w. observed three days of fasting for every month?”, She replied: “Yes” (Sunan At-Tirmizi) Fasting of White days, glass of water and dates Thus, following in the steps of Prophet Muhammad s.a.w. fasting on White days will help us gain immense rewards. Furthermore, the greatness of the rewards of fasting is made only known to Allah s.w.t. as mentioned in a Hadith Qudsi: كُلُّ عَمَلِ ابْنِ آدَمَ له، إلَّا الصِّيَامَ؛ فإنَّه لي، وأَنَا أجْزِي به “Every good deed of Adam’s son is for him except fasting; it is for Me and I shall reward (the person fasting) for it” (Sahih Al-Bukhari) How do we observe the fasting of White Days? To begin fasting on white days, one must make the niyyah (intention) as follows and then observe fasting as usual, from sunrise to sunset: نَوَيتُ صَومَ أَيَّامِ البِيض سُنَّةً لله تَعَالَى Nawaytu Sauma Ayyamil Bidh Sunnatan Lillahi Taa’la I intend to observe the Sunnah fast of the White days for Allah the Most High You may also establish your intention in your heart through the language that you understand. Once you have tried fasting on White days, try to continue to fast on the following month too and eventually, InsyaAllah, it will turn into a habit, just like how the Messenger of Allah s.a.w. has the habit of observing voluntary fasting. Fasting of white days with full moon Let us revive and practice this forgotten Sunnah together, following the Prophet Muhammad s.a.w. in pursuit of Allah s.w.t’s love and blessings as well as collecting rewards along the way. To be honest, I myself am trying to observe fasting on white days, though some months I did not manage to do so, nevertheless, it feels great to practice the Sunnah and I enjoyed sharing about it with the people around me. I highly encourage my fellow readers to try it out. So, come join me, let’s challenge ourselves to observe these 3 days of fasting and May Allah s.w.t. grant us the strength to ace this challenge. Amin. And Allah knows best. https://www.muslim.sg/articles/fasting-on-the-white-days
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  • Here’s some interesting insight about the Israeli occupation of Palestine that’s worth sharing.

    I will add that Moses came to Minister to the Jews and lead them away from blood sacrifice, back into worship of the truth living God. This inspired the Torah which authentic Jews follow today.

    Islam is the finalisation of God’s living message for humanity.

    https://www.tiktok.com/@gnostic_alchemy/video/7345923446641020180?_r=1&_t=8kmGRU2Kmqm
    Here’s some interesting insight about the Israeli occupation of Palestine that’s worth sharing. I will add that Moses came to Minister to the Jews and lead them away from blood sacrifice, back into worship of the truth living God. This inspired the Torah which authentic Jews follow today. Islam is the finalisation of God’s living message for humanity. https://www.tiktok.com/@gnostic_alchemy/video/7345923446641020180?_r=1&_t=8kmGRU2Kmqm
    Like
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  • Sending This Notice of Liability To Your Doctors May Wake Them Up And Stop Them Causing More Harm
    Feel free to adapt this letter template as you see fit

    Dr Tess Lawrie, MBBCh, PhD​
    This is just a quick post to share a letter that we have drafted with the help of a valued solicitor as a first notice of liability to your doctor or vaccinating health practitioner.


    We felt it was best to keep to a page so that it will be read!

    This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below

    Feel free to copy, paste and adapt as you see fit. If you want to add links, for example to the DNA contamination independent expert hearing, please share suggestions to others in the comments below. Let us know what your doctor’s response too!

    Sharing with paid subscribers today and all for free tomorrow! Thank you so much for supporting our work. We could not do it without you.

    I hope this template inspires you to get active! We are not helpless. There are many things one can do. Your actions today will help others.


    Share

    [Enter Address]

    [Enter Date]

    Dear Sir/Madam/Doctor

    Re: Administration of SARS CoV2 vaccines:

    I write to put you on notice that your practice/NHS Trust/clinic may be liable for gross negligence in administering the SARS CoV2 vaccine.

    A clinician has to obtain free and informed consent before carrying out any medical procedure. A failure to obtain free and informed consent can be both a breach of the duty of care as well as a battery. To obtain a patient’s consent a clinician has to advise the patient of the material risks of the procedure. Material risks will vary from person to person. A doctor is under a legal obligation to inform patients of material risks so that patients can then decide autonomously whether they wish to run those material risks.

    The reason why the practice is at risk is that in relation to the mRNA vaccines, patients have not been advised of the following:

    The long term material risks of SARS CoV2 vaccines are unknown. The mRNA platform is a gene therapy where material risks are identified over a period up to 15 years. Patients have not been advised that the vaccine is a gene therapy.

    Follow up studies are awaited on medium term material risks.

    The Pfizer vaccine that is being rolled out uses a different manufacturing process, process two, to the vaccine that was authorised which was developed via process one. There has been no large RCT of process two vaccines and material risks are only being identified during the roll out.

    SV40 plasmids have been found in Pfizer SARS CoV2 vaccines. At least two regulators have now acknowledged the presence of SV40. SV40 inhibits cancer suppressing cells and promotes cancer forming cells.

    In the circumstances I would be grateful if you would confirm in writing that patients are being advised by your clinicians about the known material risks, including plasmid contamination, and the fact that there are unknown material risks relating to gene therapies and that such material risks are identified over time.

    Yours sincerely

    [insert name]

    Thanks for your collaboration to make a better world!

    Value Exchange

    If you find value in these Substack articles and videos, please recommend it to others. All proceeds from paid subscriptions go to the work of the World Council for Health. You can also make a one-off donation or become a regular monthly donor in 2024 to support our expanding WCH team and humanitarian work.

    Share A Better Way with Dr Tess Lawrie




    WCH Notice of Liability to Covid Vaccinators

    The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs.

    "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links"

    https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
    Sending This Notice of Liability To Your Doctors May Wake Them Up And Stop Them Causing More Harm Feel free to adapt this letter template as you see fit Dr Tess Lawrie, MBBCh, PhD​ This is just a quick post to share a letter that we have drafted with the help of a valued solicitor as a first notice of liability to your doctor or vaccinating health practitioner. We felt it was best to keep to a page so that it will be read! This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below Feel free to copy, paste and adapt as you see fit. If you want to add links, for example to the DNA contamination independent expert hearing, please share suggestions to others in the comments below. Let us know what your doctor’s response too! Sharing with paid subscribers today and all for free tomorrow! Thank you so much for supporting our work. We could not do it without you. I hope this template inspires you to get active! We are not helpless. There are many things one can do. Your actions today will help others. Share [Enter Address] [Enter Date] Dear Sir/Madam/Doctor Re: Administration of SARS CoV2 vaccines: I write to put you on notice that your practice/NHS Trust/clinic may be liable for gross negligence in administering the SARS CoV2 vaccine. A clinician has to obtain free and informed consent before carrying out any medical procedure. A failure to obtain free and informed consent can be both a breach of the duty of care as well as a battery. To obtain a patient’s consent a clinician has to advise the patient of the material risks of the procedure. Material risks will vary from person to person. A doctor is under a legal obligation to inform patients of material risks so that patients can then decide autonomously whether they wish to run those material risks. The reason why the practice is at risk is that in relation to the mRNA vaccines, patients have not been advised of the following: The long term material risks of SARS CoV2 vaccines are unknown. The mRNA platform is a gene therapy where material risks are identified over a period up to 15 years. Patients have not been advised that the vaccine is a gene therapy. Follow up studies are awaited on medium term material risks. The Pfizer vaccine that is being rolled out uses a different manufacturing process, process two, to the vaccine that was authorised which was developed via process one. There has been no large RCT of process two vaccines and material risks are only being identified during the roll out. SV40 plasmids have been found in Pfizer SARS CoV2 vaccines. At least two regulators have now acknowledged the presence of SV40. SV40 inhibits cancer suppressing cells and promotes cancer forming cells. In the circumstances I would be grateful if you would confirm in writing that patients are being advised by your clinicians about the known material risks, including plasmid contamination, and the fact that there are unknown material risks relating to gene therapies and that such material risks are identified over time. Yours sincerely [insert name] Thanks for your collaboration to make a better world! Value Exchange If you find value in these Substack articles and videos, please recommend it to others. All proceeds from paid subscriptions go to the work of the World Council for Health. You can also make a one-off donation or become a regular monthly donor in 2024 to support our expanding WCH team and humanitarian work. Share A Better Way with Dr Tess Lawrie WCH Notice of Liability to Covid Vaccinators The World Council for Health have put together a useful template Notice of Liability for the public to use to educate and serve on those healthcare professionals who are still vaccinating people with the Covid-19 jabs. "This text for this full Letter Template to Doctors and Health Practitioners administering, promoting or facilitating Covid-19 injections can be found and copied below. Feel free to copy, paste and adapt as you see fit. If you want to add links" https://drtesslawrie.substack.com/p/this-notice-of-liability-to-your
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