☆Tadabbur Kalamullah 22 Ramadhan 1445H☆ لَیۡلَةُ ٱلۡقَدۡرِ خَیۡرࣱ مِّنۡ أَلۡفِ شَهۡرࣲ "Malam Lailatul-Qadar lebih baik daripada seribu bulan" [Surah al-Qadr 3] #Menurut Syeikh Ali bin Ubaidillah: "Dinamakan malam al-Qadar kerana diturunkan pada malam tersebut kitab yang mempunyai kemuliaan di samping rahmat dan malaikat juga turun pada malam tersebut". #Kemuliaan apa lagi yang lebih agung dari suatu malam yang menjadi permulaan turunnya cahaya dan petunjuk kepada seluruh manusia setelah berlalunya beberapa abad kaum Quraisy yang berada dalam kesesatan menyembah berhala. #Tidak ada lagi keagungan yang lebih tinggi dari suatu malam yang menjadi saat bersinarnya cahaya pengetahuan Ilahi ke hati Rasulullah saw sebagai bukti rahmat kepada hamba-hambaNya. Berkata Imam Ad-Dahhaq: "Allah tidak takdirkan pada malam tersebut kecuali keselamatan". #Berkata pula Imam Mujahid: "Ia merupakan malam selamat di mana syaitan tidak mampu untuk melakukan sebarang kejahatan pada malam tersebut". #Sebahagian para ulamak telah menyebut dalam kitab masing-masing berkenaan dengan sebahagian tanda dan alamat yang mungkin dapat dilihat oleh sebahagian hamba Allah yang diizinkannya pada setiap tahun daripada bulan Ramadhan, antaranya ialah: 1. Berkata Sayidina Ubadah bin al-Somit r.a: "Sesungguhnya malam tersebut bersih terang, seolah-olah bulan yang menerangi tenang, nyaman tidak terlalu sejuk pada malam tersebut dan tidak terlalu panas dan tiadalah tempat bagi bintang untuk dilihat dengannya hingga ke waktu pagi. Dan daripada tandanya bahawa matahari pada waktu paginya keluar dalam keadaan tidak bercahaya dengan kepanasan seperti bulan penuh purnama dan syaitan tidak ada tempat untuk keluar bersamanya pada hari tersebut. 2. Daripada Sayidina Ubay bin Kaab r.a menyatakan daripada Nabi saw sabdanya: "Sesungguhnya matahari terbit pada hari tersebut tidak mempunyai cahaya dan kepanasan". 3. Riwayat daripada Sayidina Ibn Mas’ud: "Sesungguhnya matahari keluar setiap hari antara dua tanduk syaitan, kecuali pagi malam qadar" (Lihat: Umdah al-Qari) #Antara doa terbaik untuk dibaca pada malam lailatulqadar ialah yang diriwayatkan daripada Sayidatina Aisyah r.ha, bahawa beliau bertanya Nabi saw: “Wahai Nabi Allah, jika aku bertemu dengan malam al-Qadar maka apa yang sepatutnya aku ucapkan. Nabi saw bersabda: اللهُمَّ إِنَّكَ عَفُوٌّ تُحِبُّ الْعَفْوَ، فَاعْفُ عَنِّي "Ya Allah Ya Tuhan Kami, sesungguhnya Kamu Maha Pengampun dan amat suka akan keampunan, maka berikanlah keampunan kepadaku" (HR at-Tirmizi, Ibn Majah dan Ahmad) #Imam an-Nawawi berkata bahawa ashab kami (ulamak Syafieyyah) mengatakan disunatkan memperbanyakkan membaca doa ini pada malam al-Qadar. Begitu juga, disunatkan membaca al-Quran, zikir-zikir dan doa-doa yang disunatkan pada tempat-tempat yang mulia. (Lihat: al-Azkar) ♡Banyakkan beramal di 10 malam terakhir Ramadhan. Moga kita bertemu malam al-Qadar. Aamiiin♡ 🐊Ust naim Klik link ini untuk     http://bit.ly/tadabburkalamullah Facebook:    https://m.facebook.com/tadabburkalamullah

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

Why Does the WHO Make False Claims Regarding Proposals to Seize States’ Sovereignty? By David Bell, Thi Thuy Van Dinh December 11, 2023 Government, Law, Public Health 15 minute read The Director General (DG) of the World Health Organization (WHO) states: No country will cede any sovereignty to WHO, referring to the WHO’s new pandemic agreement and proposed amendments to the International Health Regulations (IHR), currently being negotiated. His statements are clear and unequivocal, and wholly inconsistent with the texts he is referring to. A rational examination of the texts in question shows that: The documents propose a transfer of decision-making power to the WHO regarding basic aspects of societal function, which countries undertake to enact. The WHO DG will have sole authority to decide when and where they are applied. The proposals are intended to be binding under international law. Continued claims that sovereignty is not lost, echoed by politicians and media, therefore raise important questions concerning motivations, competence, and ethics. The intent of the texts is a transfer of decision-making currently vested in Nations and individuals to the WHO, when its DG decides that there is a threat of a significant disease outbreak or other health emergency likely to cross multiple national borders. It is unusual for Nations to undertake to follow external entities regarding the basic rights and healthcare of their citizens, more so when this has major economic and geopolitical implications. The question of whether sovereignty is indeed being transferred, and the legal status of such an agreement, is therefore of vital importance, particularly to the legislators of democratic States. They have an absolute duty to be sure of their ground. We systematically examine that ground here. The Proposed IHR Amendments and Sovereignty in Health Decision-Making Amending the 2005 IHR may be a straightforward way to quickly deploy and enforce “new normal” health control measures. The current text applies to virtually the entire global population, counting 196 States Parties including all 194 WHO Member States. Approval may or may not require a formal vote of the World Health Assembly (WHA), as the recent 2022 amendment was adopted through consensus. If the same approval mechanism is to be used in May 2024, many countries and the public may remain unaware of the broad scope of the new text and its implications to national and individual sovereignty. The IHR are a set of recommendations under a treaty process that has force under international law. They seek to provide the WHO with some moral authority to coordinate and lead responses when an international health emergency, such as pandemic, occurs. Most are non-binding, and these contain very specific examples of measures that the WHO can recommend, including (Article 18): require medical examinations; review proof of vaccination or other prophylaxis; require vaccination or other prophylaxis; place suspect persons under public health observation; implement quarantine or other health measures for suspect persons; implement isolation and treatment where necessary of affected persons; implement tracing of contacts of suspect or affected persons; refuse entry of suspect and affected persons; refuse entry of unaffected persons to affected areas; and implement exit screening and/or restrictions on persons from affected areas. These measures, when implemented together, are generally referred to since early 2020 as ‘lockdowns’ and ‘mandates.’ ‘Lockdown’ was previously a term reserved for people incarcerated as criminals, as it removes basic universally accepted human rights and such measures were considered by the WHO to be detrimental to public health. However, since 2020 it has become the default standard for public health authorities to manage epidemics, despite its contradictions to multiple stipulations of the Universal Declaration of Human Rights (UDHR): Everyone is entitled to all the rights and freedoms set forth in this Declaration, without distinction of any kind including no arbitrary detention (Article 9). No one shall be subjected to arbitrary interference with his privacy, family, home or correspondence (Article 12). Everyone has the right to freedom of movement and residence within the borders of each state, and Everyone has the right to leave any country, including his own, and to return to his country (Article 13). Everyone has the right to freedom of opinion and expression; this right includes freedom to hold opinions without interference and to seek, receive and impart information and ideas through any media and regardless of frontiers (Article 19). Everyone has the right to freedom of peaceful assembly and association (Article 20). The will of the people shall be the basis of the authority of government (Article 21). Everyone has the right to work (Article 23). Everyone has the right to education (Article 26). Everyone is entitled to a social and international order in which the rights and freedoms set forth in this Declaration can be fully realized (Article 28). Nothing in this Declaration may be interpreted as implying for any State, group or person any right to engage in any activity or to perform any act aimed at the destruction of any of the rights and freedoms set forth herein (Article 30). These UDHR stipulations are the basis of the modern concept of individual sovereignty, and the relationship between authorities and their populations. Considered the highest codification of the rights and freedoms of individuals in the 20th century, they may soon be dismantled behind closed doors in a meeting room in Geneva. The proposed amendments will change the “recommendations” of the current document to requirements through three mechanisms on Removing the term ‘non-binding’ (Article 1), Inserting the phrase that Member States will “undertake to follow WHO’s recommendations” and recognize WHO, not as an organization under the control of countries, but as the “coordinating authority” (New Article 13A). States Parties recognize WHO as the guidance and coordinating authority of international public health response during public health Emergency of International Concern and undertake to follow WHO’s recommendations in their international public health response. As Article 18 makes clear above, these include multiple actions directly restricting individual liberty. If transfer of decision-making power (sovereignty) is not intended here, then the current status of the IHR as ‘recommendations’ could remain and countries would not be undertaking to follow the WHO’s requirements. States Parties undertake to enact what previously were merely recommendations, without delay, including requirements of WHO regarding non-State entities under their jurisdiction (Article 42): Health measures taken pursuant to these Regulations, including the recommendations made under Articles 15 and 16, shall be initiated and completed without delay by all State Parties and applied in a transparent, equitable and non-discriminatory manner. State Parties shall also take measures to ensure Non-State Actors operating in their respective territories comply with such measures. Articles 15 and 16 mentioned here allow the WHO to require a State to provide resources “health products, technologies, and know-how,” and to allow the WHO to deploy personnel into the country (i.e., have control over entry across national borders for those they choose). They also repeat the requirement for the country to require the implementation of medical countermeasures (e.g., testing, vaccines, quarantine) on their population where WHO demands it. Of note, the proposed Article 1 amendment (removing ‘non-binding’) is actually redundant if New Article 13A and/or the changes in Article 42 remain. This can (and likely will) be removed from the final text, giving an appearance of compromise without changing the transfer of sovereignty. All of the public health measures in Article 18, and additional ones such as limiting freedom of speech to reduce public exposure to alternative viewpoints (Annex 1, New 5 (e); “…counter misinformation and disinformation”) clash directly with the UDHR. Although freedom of speech is currently the exclusive purview of national authorities and its restriction is generally seen as negative and abusive, United Nations institutions, including the WHO, have been advocating for censoring unofficial views in order to protect what they call “information integrity.” It seems outrageous from a human rights perspective that the amendments will enable the WHO to dictate countries to require individual medical examinations and vaccinations whenever it declares a pandemic. While the Nuremberg Code and Declaration of Helsinki refer specifically to human experimentation (e.g. clinical trials of vaccines) and the Universal Declaration on Bioethics and Human Rights also to the provider-patient relationship, they can reasonably be extended to public health measures that impose restrictions or changes to human behavior, and specifically to any measures requiring injection, medication, or medical examination which involve a direct provider-person interaction. If vaccines or drugs are still under trial or not fully tested, then the issue of being the subject of an experiment is also real. There is a clear intent to employ the CEPI ‘100 day’ vaccine program, which by definition cannot complete meaningful safety or efficacy trials within that time span. Forced examination or medication, outside of a situation where the recipient is clearly not mentally competent to comply or reject when provided with information, is unethical. Requiring compliance in order to access what are considered basic human rights under the UDHR would constitute coercion. If this does not fit the WHO’s definition of infringement on individual sovereignty, and on national sovereignty, then the DG and his supporters need to publicly explain what definition they are using. The Proposed WHO Pandemic Agreement as a Tool to Manage Transfer of Sovereignty The proposed pandemic agreement will set humanity in a new era strangely organized around pandemics: pre-pandemic, pandemic, and inter-pandemic. A new governance structure under WHO auspices will oversee the IHR amendments and related initiatives. It will rely on new funding requirements, including the WHO’s ability to demand additional funding and materials from countries and to run a supply network to support its work in health emergencies (Article 12): In the event of a pandemic, real-time access by WHO to a minimum of 20% (10% as a donation and 10% at affordable prices to WHO) of the production of safe, efficacious and effective pandemic-related products for distribution based on public health risks and needs, with the understanding that each Party that has manufacturing facilities that produce pandemic-related products in its jurisdiction shall take all necessary steps to facilitate the export of such pandemic-related products, in accordance with timetables to be agreed between WHO and manufacturers. And Article 20 (1): …provide support and assistance to other Parties, upon request, to facilitate the containment of spill-over at the source. The entire structure will be financed by a new funding stream separate from current WHO funding – an additional requirement on taxpayers over current national commitments (Article 20 (2)). The funding will also include an endowment of voluntary contributions of “all relevant sectors that benefit from international work to strengthen pandemic preparation, preparedness and response” and donations from philanthropic organizations (Article 20 (2)b). Currently, countries decide on foreign aid on the basis of national priorities, apart from limited funding that they have agreed to allocate to organizations such as WHO under existing obligations or treaties. The proposed agreement is remarkable not just in greatly increasing the amount countries must give as treaty requirements, but in setting up a parallel funding structure disconnected from other disease priorities (quite the opposite of previous ideas on integration in health financing). It also gives power to an external group, not directly accountable, to demand or acquire further resources whenever it deems necessary. In a further encroachment into what is normally within the legal jurisdiction of Nation States, the agreement will require countries to establish (Article 15) “…, no-fault vaccine injury compensation mechanism(s),…”, consecrating effective immunity for pharmaceutical companies for harm to citizens resulting from use of products that the WHO recommends under an emergency use authorization, or indeed requires countries to mandate onto their citizens. As is becoming increasingly acceptable for those in power, ratifying countries will agree to limit the right of their public to voice opposition to the WHO’s measures and claims regarding such an emergency (Article 18): …and combat false, misleading, misinformation or disinformation, including through effective international collaboration and cooperation… As we have seen during the Covid-19 response, the definition of misleading information can be dependent on political or commercial expediency, including factual information on vaccine efficacy and safety and orthodox immunology that could impair the sale of health commodities. This is why open democracies put such emphasis on defending free speech, even at the risk of sometimes being misleading. In signing on to this agreement, governments will be agreeing to abrogate that principle regarding their own citizens when instructed by the WHO. The scope of this proposed agreement (and the IHR amendments) is broader than pandemics, greatly expanding the scope under which a transfer of decision-making powers can be demanded. Other environmental threats to health, such as changes in climate, can be declared emergencies at the DG’s discretion, if broad definitions of ‘One Health’ are adopted as recommended. It is difficult to think of another international instrument where such powers over national resources are passed to an unelected external organization, and it is even more challenging to envision how this is seen as anything other than a loss of sovereignty. The only justification for this claim would appear to be if the draft agreement is to be signed on the basis of deceit – that there is no intention to treat it other than as an irrelevant piece of paper or something that should only apply to less powerful States (i.e. a colonialist tool). Will the IHR Amendments and the Proposed Pandemic Agreement be Legally Binding? Both texts are intended to be legally binding. The IHR already has such status, so the impact of the proposed changes on the need for new acceptance by countries are complicated national jurisdictional issues. There is a current mechanism for rejection of new amendments. However, unless a high number of countries will actively voice their oppositions and rejections, the adoption of the current published version dated February 2023 will likely lead to a future shadowed by the permanent risks of the WHO’s lockdown and lockstep dictates. The proposed pandemic agreement is also clearly intended to be legally binding. WHO discusses this issue on the website of the International Negotiating Body (INB) that is working on the text. The same legally binding intent is specifically stated by the G20 Bali Leaders Declaration in 2022: We support the work of the Intergovernmental Negotiating Body (INB) that will draft and negotiate a legally binding instrument that should contain both legally binding and non-legally binding elements to strengthen pandemic PPR…, repeated in the 2023 G20 New Delhi Leaders Declaration: …an ambitious, legally binding WHO convention, agreement or other international instruments on pandemic PPR (WHO CA+) by May 2024, and by the Council of the European Union: A convention, agreement or other international instrument is legally binding under international Law. An agreement on pandemic prevention, preparedness and response adopted under the World Health Organization (WHO) would enable countries around the globe to strengthen national, regional and global capacities and resilience to future pandemics. The IHR already has standing under international law. While seeking such status, WHO officials who previously described the proposed agreement as a ‘treaty” are now insisting neither instrument impacts sovereignty. The implication that it is States’ representatives at the WHA that will agree to the transfer, rather than the WHO, is a nuance irrelevant to its claims regarding their subsequent effect. The WHO’s position raises a real question of whether its leadership is truly ignorant of what is proposed, or is actively seeking to mislead countries and the public in order to increase the probability of acceptance. The latest version dated 30 October 2023 requires 40 ratifications for the future agreement to enter into force, after a two-thirds vote in favor within the WHA. Opposition by a considerable number of countries will therefore be needed to derail this project. As it is backed by powerful governments and institutions, financial mechanisms including IMF and World Bank instruments and bilateral aids are likely to make opposition from lower-income countries difficult to sustain. The Implications of Ignoring the Issue of Sovereignty The relevant question regarding these two WHO instruments should really be not whether sovereignty is threatened, but why any sovereignty would be forfeited by democratic States to an organization that is (i) significantly privately funded and bound to obey the dictates of corporations and self-proclaimed philanthropists and (ii) jointly governed by Member States, half of which don’t even claim to be open representative democracies. If it is indeed true that sovereignty is being knowingly forfeited by governments without the knowledge and consent of their peoples, and based on false claims from governments and the WHO, then the implications are extremely serious. It would imply that leaders were working directly against their peoples’ or national interest, and in support of external interests. Most countries have specific fundamental laws dealing with such practice. So, it is really important for those defending these projects to either explain their definitions of sovereignty and democratic process, or explicitly seek informed public consent. The other question to be asked is why public health authorities and media are repeating the WHO’s assurances of the benign nature of the pandemic instruments. It asserts that claims of reduced sovereignty are ‘misinformation’ or ‘disinformation,’ which they assert elsewhere are major killers of humankind. While such claims are somewhat ludicrous and appear intended to denigrate dissenters, the WHO is clearly guilty of that which it claims is such a crime. If its leadership cannot demonstrate how its claims regarding these pandemic instruments are not deliberately misleading, its leadership would appear ethically compelled to resign. The Need for Clarification The WHO lists three major pandemics in the past century – influenza outbreaks in the late 1950s and 1960s, and the Covid-19 pandemic. The first two killed less than die each year today from tuberculosis, whilst the reported deaths from Covid-19 never reached the level of cancer or cardiovascular disease and remained almost irrelevant in low-income countries compared to endemic infectious diseases including tuberculosis, malaria, and HIV/AIDs. No other non-influenza outbreak recorded by the WHO that fits the definition of a pandemic (e.g., rapid spread across international borders for a limited time of a pathogen not normally causing significant harm) has caused greater mortality in total than a few days of tuberculosis (about 4,000/day) or more life-years lost than a few days of malaria (about 1,500 children under 5 years old every day). So, if it is indeed the case that our authorities and their supporters within the public health community consider that powers currently vested within national jurisdictions should be given over to external bodies on the basis of this level of recorded harm, it would be best to have a public conversation as to whether this is sufficient basis for abandoning democratic ideals in favor of a more fascist or otherwise authoritarian approach. We are, after all, talking about restricting basic human rights essential for a democracy to function. 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/why-does-the-who-make-false-claims-regarding-proposals-to-seize-states-sovereignty/

☆Tadabbur Kalamullah 21 Ramadhan 1445H☆ لَیۡلَةُ ٱلۡقَدۡرِ خَیۡرࣱ مِّنۡ أَلۡفِ شَهۡرࣲ "Malam Lailatul-Qadar lebih baik daripada seribu bulan" [Surah al-Qadr 3] #Imam Ibn Qudamah rahimahullah berpendapat malam al-Qadar ialah malam yang mulia, diberkati, diagungkan dan mempunyai banyak kelebihan. (Lihat: al-Mughni) #Menurut Imam Abu Bakar al-Warraq, dinamakan al-Qadar kerana siapa yang tidak mempunyai kemuliaan akan mendapat kemuliaan dengan melakukan ibadat pada malam tersebut. #Berkata as-Syahid Sayid Qutub rahimahullah: "Terdapat ayat-ayat al-Quran yang menyebut peristiwa malam ini berkilauan memancarkan cahaya, ia melimpahkan cahaya yang tenang, indah dan mesra iaitu cahaya Allah yang gemilang di dalam al-QuranNya" #Imam Ibn Kathir berkata: "Zahir ayat menunjukkan bahawa malam Qadar lebih afdal daripada malam Jumaat. Walaupun begitu, ada juga pendapat yang mengatakan malam Jumaat lebih afdal". #Imam al-Qurtubi rahimahullah berkata: "Malam Qadar mempunyai kelebihan kerana banyaknya keistimewaan dan malam tersebut dibahagikan kebaikan yang banyak yang tidak terdapat seumpamanya pada seribu bulan. Ramai ulama dan ahli tafsir berpendapat amalan dilakukan pada malam Qadar lebih baik daripada seribu bulan yang tiada padanya malam Qadar". #Malam al-Qadar itu merupakan perayaan bagi umat Islam di mana telah turunnya al-Quran dan merupakan malam kesyukuran, kebajikan dan kenikmatan. Malaikat menyertai manusia pada malam itu dan mereka mengetahui kelebihan malam tersebut dan betapa besarnya kelebihan manusia atas diri mereka. Seterusnya, Allah swt menjadikan manusia sebagai khalifah di atas muka bumi. تَنَزّلُ الْمَلاَئِكَةُ وَالرُّوحُ فِيْهَا بِإِذْنِ رَبِّهِمْ مِنْ كُلِّ أَمْـرٍ﴿٤﴾ سَلاَمٌ هِيَ حَتَّى مَطْلَعِ الْفَجْرِ "Pada malam itu turun malaikat-malaikat dan malaikat Jibril dengan izin  TuhanNya untuk mengatur segala urusan. Malam itu (penuh) kesejahteraan sehingga terbit fajar" [Surah al-Qadr 4-5] #Menurut Imam al-Qurtubi rahimahullah: "Mereka (malaikat) turun daripada setiap langit dan juga Sidratul Muntaha ke langit dunia untuk mengaminkan doa orang yang memohon pada malam tersebut hingga waktu fajar". ♡Sepatutnya umat Islam menjadikan malam kemuliaan ini sebagai malam perayaan! Malam inilah permulaan turunnya perundangan samawi (langit), yang membimbing umat Islam ke arah yang baik. Jom hidupkan malam dengan ibadah!!♡ 🐊Ust naim Klik link ini untuk     http://bit.ly/tadabburkalamullah Facebook:    https://m.facebook.com/tadabburkalamullah

Israeli occupation forces are committing the actual rapes of Palestinians in Gaza Lawyer behind 'Hamas rape' claims exposed as fraud Employees of Israeli ministries claim that Cochav Elkayam-Levy has spread fake news and sought to make millions off her false claims about Hamas carrying out mass rapes on 7 October Israeli officials have "dissociated themselves" from a lawyer who has played a vital role in promoting false claims that Hamas carried out systematic rape and sexual abuse on 7 October, Yedioth Ahronoth reported on 24 March. The Israeli newspaper reported claims by Israeli ministry officials that lawyer Cochav Elkayam-Levy had produced inaccurate research, spread false stories about Hamas atrocities, and sought to collect millions of dollars in donations for a so-called ‘civic commission’ of which she is the only member. Elkayam-Levy, who is the head of the Deborah Institute and a lecturer in the Department of International Relations at the Hebrew University, was among the first to spread false claims that Hamas had carried out systematic rape during Operation Al-Aqsa Flood. As The Grayzone detailed, Elkayam-Levy presented images of female Kurdish fighters killed in Syria while claiming they were Jewish Israeli women who had been killed and raped by Hamas fighters at the Nova Music Festival on 7 October. The Grayzone further noted that Elkayam-Levy gained significant public attention in December after being interviewed by CNN's Jake Tapper and meeting with members of the White House National Security Council and Assistant to the President and Director of the Gender Policy Council Jennifer Klein in Washington. "People disassociated themselves from her because her research is inaccurate," explained an official in one of the government offices speaking with Yedioth Ahronoth. "After all, the whole story is that they [Palestinians] want to accuse us of spreading fake news, and her methodology was neither good nor accurate." Elkayam-Levy spread the story in the international press "about the pregnant woman who had her stomach cut open – a story that was proven to be untrue," one official complained. "It's no joke. Little by little, professionals began to distance themselves from her because she is unreliable." She also created a ‘civilian commission’ to investigate alleged Hamas atrocities. While the commission's name suggests it was a government-established body, it consisted only of Elkayam-Levy herself. She then solicited millions of dollars in donations for the fake commission, claiming a budget of $8 million, including $1.5 million for administrative fees, was needed. "Rahm Emanuel, the US ambassador to Japan, donated money to her. She took donations from many people and started asking for money for lectures," said the same official in the government office. The critical report from Yeditoh Ahronoth comes just days after Elkayam-Levy was given the Israel Prize for her efforts to ‘raise awareness’ about alleged Hamas atrocities on 7 October. The Israeli government has sought to use seemingly neutral third parties, including the volunteer rescue services, ZAKA and United Hatzalah, to spread propaganda regarding the events of 7 October. These groups have fabricated wild tales of Hamas crimes in an effort to justify Israel's ongoing Genocide in Gaza. https://thecradle.co/articles-id/24093

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

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 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/

Bisikan Ruh Ramadhan 2 Ramadhan adalah bulan diturunkan Al Quran. Al Quran telah mensifatkan dirinya dengan berbagai nama dan sifat yang mulia agar manusia mudah mengenalinya. Sayugianya Al Quran lebih dikenali, didekati dan diingati. 1. Al-Quran adalah As-Shirath Al-Mustaqim ( jalan lurus ) وَأَنَّ هَٰذَا صِرَاطِي مُسْتَقِيمًا فَاتَّبِعُوهُ. ﴿ الأنعام : ١٥٣﴾ “Dan sungguh, inilah jalan–Ku yang lurus, maka ikutilah!.” (Al-An’am: 153) 2. Al-Quran adalah Al–Hablu al-Matin ( Tali agama yang kukuh ) وَاعْتَصِمُوا بِحَبْلِ اللهِ جَمِيعًا ﴿أل عمران : ١٠٣ ﴾ “Maka berpegang teguhlah kamu semuanya pada tali (agama) Allah.” (Ali ‘Imran: 103) 3. Al-Quran adalah Al-Mizan ( Neraca nilaian ) فَإِن تَنَازَعْتُمْ فِي شَيْءٍ فَرُدُّوهُ إِلَى اللهِ وَالرَّسُولِ ﴿ النساء : ٥٩ ﴾ “Kemudian jika kamu berbeda pendapat tentang sesuatu, maka kembalikanlah kepada Allah dan Rasul.” (An Nisa’: 59) “Kembali kepada Allah” maknanya adalah kembali kepada Al-Qur’an, sedangkan “kembali kepada Rasulullah sallallahu ‘alaihi wa sallam” adalah kembali kepada As-Sunnah. 4. Al-Quran adalah Al–‘Urwatul Wutsqa ( Pegangan yang kukuh ) لَا إِكْرَاهَ فِي الدِّينِ قَد تَّبَيَّنَ الرُّشْدُ مِنَ الْغَيِّ فَمَن يَكْفُرْ بِالطَّاغُوتِ وَيُؤْمِن بِاللهِ فَقَدِ اسْتَمْسَكَ بِالْعُرْوَةِ الْوُثْقَىٰ لَا انفِصَامَ لَهَا وَاللهُ سَمِيعٌ عَلِيمٌ ﴿ البقرة : ٢٥٦ ﴾ “Tidak ada paksaan dalam (menganut) agama (Islam), sesungguhnya telah jelas (perbedaan) antara jalan yang benar dengan jalan yang sesat. Barangsiapa yang ingkar kepada thaghut dan beriman kepada Allah, maka sungguh dia telah berpegang (teguh) pada tali yang sangat kuat, yang tidak akan putus. Allah Maha Mendengar, Maha Mengetahui.” (Al-Baqarah: 256) 5. Al-Quran adalah al- Burhan ( bukti kebenaran ) dan An-Nur al-Mubin ( Cahaya yang terang ) يَا أَيُّهَا النَّاسُ قَدْ جَاءَكُم بُرْهَانٌ مِّن رَّبِّكُمْ وَأَنزَلْنَا إِلَيْكُمْ نُورًا مُّبِينً ﴿ النساء : ١٧٤ ﴾ “Wahai manusia! Sesungguhnya telah sampai kepadamu bukti kebenaran dari Tuhanmu (Muhammad dengan mukjizatnya), dan telah Kami turunkan kepadamu cahaya yang terang benderang.” (An-Nisa’: 174) وَكَذَٰلِكَ أَوْحَيْنَا إِلَيْكَ رُوحًا مِّنْ أَمْرِنَا مَا كُنتَ تَدْرِي مَا الْكِتَابُ وَلَا الْإِيمَانُ وَلَٰكِن جَعَلْنَاهُ نُورًا نَّهْدِي بِهِ مَن نَّشَاءُ مِنْ عِبَادِنَا وَإِنَّكَ لَتَهْدِي إِلَىٰ صِرَاطٍ مُّسْتَقِيمٍ ﴿ الشورى : ٥٢ ﴾ “Dan demikianlah Kami wahyukan kepadamu (Muhammad) ruh (Al–Qur’an) dengan perintah Kami. Sebelumnya engkau tidak mengetahui apakah kitab (Al-Qur’an) dan apakah iman itu, tetapi Kami jadikan Al-Qur’an itu cahaya, dengan itu Kami memberi petunjuk siapa yang Kami kehendaki diantara hamba-hamba Kami. Dan sungguh, engkau benar-benar membimbing (manusia) kepada jalan yang lurus.” (Asy-Syura: 52) 6. Al-Quran adalah Al–Huda ( Petunjuk ) إِنَّ هَٰذَا الْقُرْآنَ يَهْدِي لِلَّتِي هِيَ أَقْوَمُ وَيُبَشِّرُ الْمُؤْمِنِينَ الَّذِينَ يَعْمَلُونَ الصَّالِحَاتِ أَنَّ لَهُمْ أَجْرًا كَبِيرًا ﴿ الإسراء : ٩ ﴾ “Sungguh, Al–Qur’an ini memberi petunjuk ke (jalan) yang paling lurus dan memberi kabar gembira kepada orang mukmin yang mengerjakan kebajikan, bahwa mereka akan mendapat pahala yang besar." (Al-Isra’: 9) وَنَزَّلْنَا عَلَيْكَ الْكِتَابَ تِبْيَانًا لِّكُلِّ شَيْءٍ وَهُدًى وَرَحْمَةً وَبُشْرَىٰ لِلْمُسْلِمِينَ ﴿ النحل : ٨٩ ﴾ “Dan Kami turunkan Al–Kitab (Al–Qur’an) kepadamu untuk menjelaskan segala sesuatu, sebagai petunjuk serta rahmat dan kabar gembira bagi orang yang berserah diri (muslim).” (An-Nahl: 89) 7. Al-Quran adalah Asy–Syifa’ ( Penawar dan penyembuhan) يَا أَيُّهَا النَّاسُ قَدْ جَاءَتْكُم مَّوْعِظَةٌ مِّن رَّبِّكُمْ وَشِفَاءٌ لِّمَا فِي الصُّدُورِ وَهُدًى وَرَحْمَةٌ لِّلْمُؤْمِنِينَ. ﴿ يونس : ٥٧ ﴾ “Wahai manusia! Sungguh telah dating kepadamu pelajaran (Al–Qur’an) dari Tuhanmu, penyembuh bagi penyakit yang ada dalam dada, dan petunjuk serta rahmat bagi orang yang beriman.” (Yunus: 57) وَلَوْ جَعَلْنَاهُ قُرْآنًا أَعْجَمِيًّا لَّقَالُوا لَوْلَا فُصِّلَتْ آيَاتُهُ أَأَعْجَمِيٌّ وَعَرَبِيٌّ قُلْ هُوَ لِلَّذِينَ آمَنُوا هُدًى وَشِفَاءٌ ﴿ فصلت : ٤٤ ﴾

Bisikan Ruh Ramadhan 1 Ramadhan adalah bulan teristimewa yang berbeza dari bulan-bulan yang lain. Ianya adalah : 1. Bulan diturunkan Al Quran dan kitab-kitab samawiyyah. Allah ta’ala berfirman, شَهْرُ رَمَضَانَ الَّذِي أُنْزِلَ فِيهِ الْقُرْآَنُ هُدًى لِلنَّاسِ وَبَيِّنَاتٍ مِنَ الْهُدَى وَالْفُرْقَانِ فَمَنْ شَهِدَ مِنْكُمُ الشَّهْرَ فَلْيَصُمْهُ{البقرة: ١٨٥} “(Beberapa hari yang ditentukan itu ialah) bulan Ramadhan, bulan yang di dalamnya diturunkan (permulaan) Al Quran sebagai petunjuk bagi manusia dan penjelasan-penjelasan mengenai petunjuk itu dan pembeza (antara yang hak dan yang bathil). Kerana itu, barangsiapa di antara kamu hadir (di negeri tempat tinggalnya) di bulan itu, maka hendaklah ia berpuasa pada bulan itu.” (Al Baqarah: 185)   إِنَّا أَنْزَلْنَاهُ فِي لَيْلَةِ الْقَدْرِ (1) وَمَا أَدْرَاكَ مَا لَيْلَةُ الْقَدْرِ (2) لَيْلَةُ الْقَدْرِ خَيْرٌ مِنْ أَلْفِ شَهْرٍ(3){القدر: ١-٣} ”Sesungguhnya Kami telah menurunkannya (Al Quran) pada lailatul qadar (malam kemuliaan). Dan tahukah kamu apakah malam kemuliaan itu? Malam kemuliaan itu lebih baik dari seribu bulan.” (Al Qadr: 1-3).   Allah ta’ala juga berfirman, إِنَّا أَنْزَلْنَاهُ فِي لَيْلَةٍ مُبَارَكَةٍ إِنَّا كُنَّا مُنْذِرِينَ {الدخان: ٣} ”Sesungguhnya Kami menurunkannya pada suatu malam yang diberkati dan sesungguhnya Kami-lah yang memberi peringatan.” ( Ad-Dukhan: 3)   2. Bulan untuk qiyamullail dengan solat tarawih dan tahajjud. Nabi ﷺ bersabda, من قام رمضان إيمانا واحتسابا غفر له ما تقدم من ذنبه (رواه البخاري ومسلم).  ”Barangsiapa yang berdiri (menunaikan salat) di bulan Ramadan dengan iman dan mengharap (pahala), maka dosa-dosanya yang telah lalu akan diampuni”. 3. Bulan pengampunan dan penghapus dosa. Nabi ﷺ bersabda, من صام رمضان إيمانا واحتسابا غفر له ما تقدم من ذنبه (رواه البخاري ومسلم) Barangsiapa yang berpuasa di bulan Ramadhan dengan penuh keimanan dan pengharapan, maka akan diampunkan dosanya yang telah lalu.” (HR al-Bukhari dan Muslim) 4. Bulan pembebasan dari api neraka. Nabi ﷺ bersabda, (ولله عتقاء من النار وذلك في كل ليلة) رواه الترمذي وابن ماجه. Dan bagi Allah membebaskan sejumlah orang dari neraka. Hal itu terjadi pada setiap malam.” (HR. Tirmizi dan Ibn Majah) 5. Bulan ihsan kasihan belas dan pemurah. Nabi ﷺ bersabda, عن ابن عباس رضي الله عنهما قال: كان النبي صلى الله عليه وسلم أجود الناس وكان أجود ما يكون في رمضان حين يلقاه جبريل فيدارسه القرآن. (رواه البخاري ومسلم) Nabi ‎ﷺ adalah orang yang paling dermawan. Dan Baginda lebih dermawan lagi di bulan Ramadhan saat Baginda bertemu Jibril. Jibril menemuinya setiap malam untuk mengajarkan Al Qur’an. (HR. Bukhari,Muslim) 6. Bulan dibuka pintu-pintu syurga, ditutup pintu-pintu neraka dan dibelenggu para syaitan. Nabi ﷺ bersabda, إذا جاء رمضان فتحت أبواب الجنة، وغلقت أبواب النار، وصفدت الشياطين (رواه البخاري ومسلم) Bila datang Ramadhan, dibuka pintu-pintu syurga, ditutup pintu-pintu neraka, dibelenggu para syaitan. ( HR Bukhari, Muslim) 7. Bulan doa-doa dimakbulkan oleh Allah ta’ala. Dalam surah Al Baqarah selepa ayat kewajipan berpuasa, Allah ta’ala menyatakan tentang diriNya sebagai Pemakbul Doa dari para hambaNya. وَإِذَا سَأَلَكَ عِبَادِي عَنِّي فَإِنِّي قَرِيبٌ أُجِيبُ دَعْوَةَ الدَّاعِ إِذَا دَعَانِ فَلْيَسْتَجِيبُوا لِي وَلْيُؤْمِنُوا بِي لَعَلَّهُمْ يَرْشُدُونَ ‎ ﴿البقرة: ١٨٦﴾‏ Dan apabila hamba-hambaKu bertanya kepadamu mengenai Aku maka (beritahu kepada mereka): sesungguhnya Aku (Allah) sentiasa hampir (kepada mereka); Aku perkenankan permohonan orang yang berdoa apabila ia berdoa kepadaKu. Maka hendaklah mereka menyahut seruanku (dengan mematuhi perintahKu), dan hendaklah mereka beriman kepadaKu supaya mereka menjadi baik serta betul. (186) (Al Baqarah: 186) Nabi ﷺ bersabda, ثَلاَثَةٌ لاَ تُرَدُّ دَعْوَتُهُمُ الصَّائِمُ حَتَّى يُفْطِرَ وَالإِمَامُ الْعَادِلُ وَدَعْوَةُ الْمَظْلُومِ “Tiga orang yang do’anya tidak tertolak: orang yang berpuasa sampai ia berbuka, pemimpin yang adil, dan do’a orang yang dizalimi”. (HR Tirmizi) 8. Bulan yang digandakan pahala amal ibadah dan kebaikan. Nabi ﷺ bersabda, فَإِذَا جَاءَ رَمَضَانُ فَاعْتَمِرِي ، فَإِنَّ عُمْرَةً فِيهِ تَعْدِلُ حَجَّةً Sekiranya telah tiba bulan Ramadhan, maka hendaklah kamu mengerjakan umrah. Ini kerana umrah pada bulan tersebut menyamai pahalanya seperti mengerjakan haji. (HR al-Bukhari) 9. Bulan berlakunya lailatul qadar iaitu malam yang paling mulia. Allah ta’ala berfirman, إِنَّا أَنْزَلْنَاهُ فِي لَيْلَةِ الْقَدْرِ (1) وَمَا أَدْرَاكَ مَا لَيْلَةُ الْقَدْرِ (2) لَيْلَةُ الْقَدْرِ خَيْرٌ مِنْ أَلْفِ شَهْرٍ(3) ”Sesungguhnya Kami telah menurunkannya (Al Quran) pada lailatul qadar (malam kemuliaan). Dan tahukah kamu apakah malam kemuliaan itu? Malam kemuliaan itu lebih baik dari seribu bulan.” (Al Qadr: 1-3).   Allah ta’ala juga berfirman, إِنَّا أَنْزَلْنَاهُ فِي لَيْلَةٍ مُبَارَكَةٍ إِنَّا كُنَّا مُنْذِرِينَ   ”Sesungguhnya Kami menurunkannya pada suatu malam yang diberkati dan sesungguhnya Kami-lah yang memberi peringatan.” ( Ad-Dukhan: 3) Justeru, ambillah dan rebutlah ruang dan peluang yang Allah ta’ala telah berikan padamu dengan hadirnya Ramadhan tahun ini. Kerana engkau tidak pasti lagi dapat menemuinya pada tahun hadapan. ABi

Australia challenged on ‘moral failure’ of weapons trade with Israel Regular protests have been taking place outside Australian firms making crucial components for the F-35 fighter jet. Ali MC Protesters sitting outside the HTA factory in the Melbourne suburbs,. There is a large placard reading 'Stop arming Israel" Weekly protests have been taking place for months [Ali MC/Al Jazeera] Melbourne, Australia – Israel’s continued assault on Gaza has highlighted a hidden yet crucial component of the world’s weapons manufacturing industry – suburban Australia. Tucked away in Melbourne’s industrial north, Heat Treatment Australia (HTA) is an Australian company that plays a vital role in the production of F-35 Joint Strike Fighters; the same model that Israel is using to bomb Gaza. Weekly protests of about 200 people have been taking place for months outside the nondescript factory, where heat treatment is applied to strengthen components for the fighter jet a product of US military giant Lockheed Martin. While protesters have sometimes brought production to a halt with their pickets, they remain concerned about what’s going on inside factories like HTA. “We decided to hold the community picket to disrupt workers, and we were successful in stopping work for the day,” Nathalie Farah, protest organiser with local group Hume for Palestine, told Al Jazeera. “We consider this to be a win.” “Australia is absolutely complicit in the genocide that is happening,” said 26-year-old Farah, who is of Syrian and Palestinian origin. “Which is contrary to what the government might have us believe.” More than 32,000 Palestinians have been killed since Israel launched its war in Gaza six months ago after Hamas killed more than 1,000 people in a surprise attack on Israel. The war, being investigated as a genocide by the International Court of Justice (ICJ), has left hundreds of thousands on the brink of starvation, according to the United Nations. HTA – which did not respond to Al Jazeera for comment – is just one of an increasing number of companies in Australia engaged in the weapons manufacturing industry. Community organiser Nathalie Farah. She's wearing a Palestinian scarf and a black T-shirt saying Australia. Nathalie Farah has been organising regular protests outside HTA’s factory [Ali MC/Al Jazeera] According to Lockheed Martin, “Every F-35 built contains some Australian parts and components,” with more than 70 Australian companies having export contracts valued at a total 4.13 billion Australian dollars ($2.69bn). Protesters have also picketed Rosebank Engineering, in Melbourne’s southeast, the world’s only producer of the F-35’s “uplock actuator system”, a crucial component of the aircraft’s bomb bay doors. Sign up for Al Jazeera Weekly Newsletter protected by reCAPTCHA Defence industry push In recent years, the Australian government has sought to increase defence exports to boost the country’s flagging manufacturing industry. In 2018, former Prime Minister Malcolm Turnbull announced Australia aimed to become one of the world’s top 10 defence exporters within a decade. It is currently 30th in global arms production, according to the Stockholm International Peace Institute. It is an aspiration that appears set to continue under the government of Anthony Albanese after it concluded a more than one-billion-Australian-dollar deal with Germany to supply more than 100 Boxer Heavy Weapon Carrier vehicles in 2023 – Australia’s single biggest defence industry deal. Since the Gaza war began, the industry and its business relationship with Israel have come increasingly under the spotlight. Last month, Deputy Prime Minister Richard Marles insisted that there were “no exports of weapons from Australia to Israel and there haven’t been for many, many years”. However, between 2016 and 2023 the Australian government approved some 322 export permits for military and dual-use equipment to Israel. The Department of Foreign Affairs and Trade’s own data – available to the public online – shows that Australian exports of “arms and ammunition” to Israel totalled $15.5 million Australian dollars ($10.1m) over the same period of time. Officials now appear to be slowing the export of military equipment to Israel. In a recent interview with Australia’s national broadcaster ABC, the Minister for International Development and the Pacific Pat Conroy insisted the country was “not exporting military equipment to Israel” and clarified this meant “military weapons, things like bombs”. However, defence exports from Australia fall into two categories, items specifically for military use – such as Boxer Heavy Weapons vehicles for Germany – and so-called ‘dual use’ products, such as radar or communications systems, that can have both civilian and military uses. Australia’s Department of Defence did not respond to Al Jazeera’s requests about whether the halt to defence exports to Israel also included dual-use items. What is certain is that companies such as HTA and Rosebank Engineering are continuing to manufacture components for the F-35, despite the risk of deployment in what South Africa told the International Court of Justice in December amounted to “genocidal acts“. In the Netherlands – where parts for the jet are also manufactured – an appeal court last month ordered the Dutch government to block such exports to Israel citing the risk of breaching international law. The Australian government has also come under scrutiny for its lax “end-use controls” on the weapons and components it exports. As such, while the F-35 components are exported to US parent company Lockheed Martin, their ultimate use is largely outside Australia’s legal purview. Lauren Sanders, senior research fellow on law and the future of war at the University of Queensland, told Al Jazeera that the “on-selling of components and military equipment through third party states is a challenge to global export controls. “Once something is out of a state’s control, it becomes more difficult to trace, and to prevent it being passed on to another country,” she said. Sanders said Australia’s “end use controls” were deficient in comparison with other exporters such as the United States. “The US has hundreds of dedicated staff – with appropriate legal authority to investigate – to chase down potential end-use breaches,” she said. “Australia does not have the same kind of end-use controls in place in its legislation, nor does it have the same enforcement resources that the US does.” A protester carrying a Palestinian flag at a picket outside an Australian arms company. They have wrapped a Palesinian scarf around their face so only their eyes are visible, Other protesters are behind them. They have placards. Some are sitting on the ground. The protesters say they will continue their action until manufacturing of F-35 components is stopped [Ali MC/Al Jazeera] In fact, under legislation passed in November 2023, permits for defence goods are no longer required for exports to the United Kingdom and the US under the AUKUS security agreement. In a statement, the government argued the exemption would “deliver 614 million [Australian dollars; $401m] in value to the Australian economy over 10 years, by reducing costs to local businesses and unlocking investment opportunities with our AUKUS partners”. International law This new legislation may provide more opportunities for Australian weapons manufacturers, such as NIOA, a privately owned munitions company that makes bullets at a factory in Benalla, a small rural town in Australia’s southeast. The largest supplier of munitions to the Australian Defence Force, NIOA – which did not respond to Al Jazeera for comment – also has aspirations to break into the US weapons market. At a recent business conference, CEO Robert Nioa said that “the goal is to establish greater production capabilities in both countries so that Australia can be an alternative source of supply of weapons in times of conflict for the Australian and US militaries”. Greens Senator David Shoebridge told Al Jazeera that the government needed to “publicly and immediately refute the plan to become a top 10 global arms dealer and then to provide full transparency on all Australian arms exports including end users. “While governments in the Netherlands and the UK are facing legal challenges because of their role in the global supply chain, the Australian Labor government just keeps handing over weapons parts as though no genocide was happening,” he said. “It’s an appalling moral failure, and it is almost certainly a gross breach of international law.” The Australian government also recently announced a 917 million Australian dollar ($598m) deal with controversial Israeli company Elbit Systems. A court in the Netherlands hearing a case brought in relation to military exports. The room is wood panelled and there is a portrait on the wall. The Dutch government has faced legal action over the export of F-35 fighter jet parts to Israel [File: Piroschka van de Wouw/Reuters] Elbit has come under fire for its sale of defence equipment to the Myanmar military regime, continuing sales even after the military, which seized power in a 2021 coup, was accused of gross human rights violations – including attacks on civilians – by the United Nations and others. Despite a recent joint announcement between the Australian and UK governments for an “immediate cessation of fighting” in Gaza, some say Australia needs to go further and cut defence ties with Israel altogether. “The Australian government must listen to the growing public calls for peace and end Australia’s two-way arms trade with Israel,” Shoebridge said. “The Albanese government is rewarding and financing the Israeli arms industry just at the moment they are arming a genocide.” Protests have continued both at the HTA factory in Melbourne and their premises in Brisbane, with organisers pledging to continue until the company stops manufacturing components for the F-35. https://www.aljazeera.com/news/2024/3/28/australia-challenged-on-moral-failure-of-weapons-trade-with-israel

COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers. COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher (CROCOTHERY/Shutterstock) Following his discovery of DNA contamination in COVID-19 mRNA vaccines, genomic researcher Kevin McKernan has recently found that the DNA in these vaccines can potentially integrate into human DNA. The COVID-19 vaccine spike sequence was detected in two types of chromosomes in cancer cell lines following exposure to the COVID-19 mRNA vaccine. Mr. McKernan’s findings, which he presents on his Substack blog, haven’t been peer-reviewed. These are expected to be “rare events,” but they can happen, Mr. McKernan told The Epoch Times. DNA Integration Since the introduction of the COVID-19 mRNA vaccines, some members of the public have been concerned that the vaccines may modify human DNA by combining their sequences with the human genome. Story continues below advertisement “Fact-checkers” refuted this, saying mRNA cannot be changed into DNA. Yet Mr. McKernan’s earlier work shows that DNA in the vaccine vials may be capable of changing human DNA. Ulrike Kämmerer, a professor of human biology at the University Hospital of Würzburg in Germany, conducted earlier stages of this research. Exposing breast and ovarian human cancer cells to Pfizer and Moderna mRNA vaccines, Ms. Kämmerer found that about half of the cells expressed the COVID-19 spike protein on their cellular surface, indicating that they had absorbed the vaccines. Mr. McKernan then performed gene sequencing and found that these cells and their descendant cells contained vaccine DNA. Story continues below advertisement After this, he tested to see whether any vaccine DNA combined with the cancer cell DNA, a process known as DNA integration. Integration is more of a concern in healthy cells than cancer cells because it disrupts cells’ genetic stability and integrity, increasing cancer risk. However, because cancer cells already have unstable DNA, the effects of DNA integration are less clear. Currently, in biomedical research, most experiments are carried out in cancer cell lines, as they are easier to obtain, experiment on, and maintain in the laboratory. Mr. McKernan detected vaccine DNA sequences on two chromosomes in the cancer cell lines: chromosome 9 and chromosome 12. The sequencing machine detected both instances of integration twice. It is important to get two readings of the DNA integration to ensure that the integration is not a result of misreading or random error, he said. Story continues below advertisement “The integration of ‘vaccine’ genetic information into the genome of cells was not such a surprise for me—more the confirmation of what we had to expect, unfortunately,” he told The Epoch Times. Mr. McKernan said it is unsurprising that integration was detected on only two chromosomes with two readings of each integration. This is because integration is rare, and the genes must be sequenced many times to get more sensitive results. The current findings are still preliminary, he said. More tests are also needed to determine whether DNA integration could be passed on to descendant cancer cells and whether this may affect cancer patients. Also, since the test was conducted in cancer cells and not in healthy human cells, it does not suggest the same integration would occur in healthy human cells. Story continues below advertisement However, Hiroshi Arakawa, a researcher at the Institute of Molecular Oncology who has a doctorate in molecular biology and immunology, wrote in his blog that “what happens in cultured cells can also occur in normal cells” after examining Mr. McKernan’s data. His review of Mr. McKernan’s data also found signs of DNA integration at chromosomes 9 and 12. “A wide variety of abnormalities can occur [in normal cells] depending on the site of genome integration,” Mr. Arakawa said. Not Random Events The two integration events into chromosome 9 occurred at the same place, as did the integration events into chromosome 12. Mr. McKernan said the odds of this occurring are one in 3 billion, highlighting that where the DNA integrates may not be random. Story continues below advertisement “There’s likely hotspots for this,” he told The Epoch Times, highlighting that in the human genome, jumping genes—short segments of DNA sequences—tend to “jump” into highly activated areas of DNA. Highly activated DNA tends to play important roles in the human body. The DNA integration into chromosome 12 occurred within the FAIM2 gene. Once activated, this gene creates a protein involved in programmed cell death. Since cancer cells evade cell death, the integration at chromosome 12 may be a survival-driven change. Vaccine DNA Is Active in the Cells Mr. McKernan said he believes that vaccine DNA is highly active in cancer cells. His sequencing machine detected the DNA of cancer cells 30 times but detected spike DNA 3,000 times. Not only did he detect much higher levels of vaccine DNA, but he also detected new variants in certain segments of the vaccine DNA. Story continues below advertisement These new DNA variations were not observed in unvaccinated cancer cells nor in the vaccine not exposed to the cancer cells. Mr. McKernan said he believes that these new gene variants likely occurred because the cancer cell made copies of the vaccine DNA and created small errors. What he and his team have found contradicts the latest arguments from fact-checkers claiming that the DNA from the mRNA vaccines cannot get into the cell, nor can it be active, he said. DNA Contamination From mRNA Vaccine Manufacturing DNA is present in the COVID-19 mRNA vaccines because of the manufacturing process. This has been verified by the U.S. Food and Drug Administration (FDA), Health Canada, and the European Medicines Agency. The mRNA vaccines are made from DNA; some of this DNA persists in the final product because of insufficient clearance. Initially, Pfizer reported that it would use a PCR machine to produce the DNA for its mRNA vaccine. The PCR machine first makes many copies of DNA, which is then sequenced into RNA. However, because this process wouldn’t be fast enough to meet demands, the vaccine manufacturers switched to using bacteria to mass-produce DNA as the template for the mRNA vaccine. In this process, vaccine manufacturers introduce bacterial DNA containing the vaccine spike sequences. The bacteria make many copies of this spike DNA as they divide. This spike DNA is then harvested and transcribed into mRNA in a machine. The mRNA is then packaged into lipid nanoparticles for use in vaccination. However, some bacterial DNA containing spike protein and other sequences could be packaged into lipid nanoparticles during the process, which would then be transported into cells during vaccination. Mr. McKernan’s earlier works have demonstrated this. Works by molecular virologist David Speicher have shown that the amount of DNA in the mRNA vaccine vials is higher than the FDA’s allowable threshold of 10 nanograms per vaccine dose. Mr. McKernan highlighted that compared with previous vaccines, mainly composed of naked DNA that had difficulty entering the cells, the DNA carried in the mRNA vaccines presents greater health risks, as it is packed into lipid nanoparticles and delivered straight into the cells. https://www.theepochtimes.com/health/covid-vaccine-gene-could-integrate-into-human-cancer-cells-researcher-5604184

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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. 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

PERKONGSIAN 1 HARI 1 HADIS Paling Baik, Berani dan Dermawan عَنْ أَنَسٍ رَضِيَ اللَّهُ عَنْهُ قَالَ كَانَ النَّبِيُّ صَلَّى اللَّهُ عَلَيْهِ وَسَلَّمَ أَحْسَنَ النَّاسِ وَأَشْجَعَ النَّاسِ وَأَجْوَدَ النَّاسِ Daripada Anas RA berkata; Nabi SAW adalah orang yang paling baik, paling berani dan paling dermawan. (HR Bukhari No: 2813) Status: Hadis Sahih Pengajaran: 1.  Rasulullah SAW adalah manusia yang paling baik, paling berani dan paling dermawan. 2.  Mencontohi sifat Rasulullah SAW sebagai orang yang paling dermawan khususnya di bulan Ramadan. عَنْ أَنَسٍ قَالَ سُئِلَ النَّبِيُّ صَلَّى اللَّهُ عَلَيْهِ وَسَلَّمَ أَيُّ الصَّوْمِ أَفْضَلُ بَعْدَ رَمَضَانَ فَقَالَ شَعْبَانُ لِتَعْظِيمِ رَمَضَانَ قِيلَ فَأَيُّ الصَّدَقَةِ أَفْضَلُ قَالَ صَدَقَةٌ فِي رَمَضَانَ Daripada Anas RA, Nabi SAW ditanya tentang puasa yang paling utama setelah puasa Ramadan. Baginda menjawab: "puasa di bulan Syaban untuk memuliakan Ramadan, " Baginda ditanya lagi, lalu sedekah apakah yang paling utama? Baginda menjawab: "Sedekah di bulan Ramadan." Sunan Tirmizi No 663 Dar Kutub Ilmiyyah. Status Hadis: Daif 3.  Amalan bersedekah sebagai satu daripada cara untuk menjauhkan daripada api neraka. Rasulullah SAW bersabda عَنْ عَدِيِّ بْنِ حَاتِمٍ قَالَ ذَكَرَ النَّبِيُّ صَلَّى اللَّهُ عَلَيْهِ وَسَلَّمَ النَّارَ فَتَعَوَّذَ مِنْهَا وَأَشَاحَ بِوَجْهِهِ … قَالَ اتَّقُوا النَّارَ وَلَوْ بِشِقِّ تَمْرَةٍ فَإِنْ لَمْ تَجِدْ فَبِكَلِمَةٍ طَيِّبَ Daripada Adi bin Hatim dia berkata; "Nabi SAW menyebutkan tentang neraka, lalu baginda meminta berlindungan darinya sambil mengusap wajahnya, baginda bersabda …. "Takutlah kalian kepada neraka walau dengan setengah biji kurma, jika tiada, hendaknya dengan perkataan yang baik." (HR Bukhari No: 5677) Status: Hadis Sahih 4.  Sifat suka bersedekah adalah pengikat dan penghubung kasih sayang kita dengan orang lain 5.  Allah akan menggantikan apa yang disedekahkan dengan keberkahan harta di dunia dan pahala yang besar di akhirat. Firman Allah: وَمَا أَنْفَقْتُمْ مِنْ شَيْءٍ فَهُوَ يُخْلِفُهُ وَهُوَ خَيْرُ الرَّازِقِينَ “Dan apa saja yang kamu sedekahkan, maka Allah akan menggantinya, dan Dia-lah Pemberi rezeki yang sebaik-baiknya” (Sabaa’:39). 6.  Sedekah akan menjadi penghindar daripada api neraka walaupun sebiji buah kurma. Renunglah kisah ini: Daripada Aisyah RA  bahawa keluarga Rasulullah SAW  pernah menyembelih seekor kambing, kemudian disedekahkan kepada orang-orang miskin, lalu Rasulullah  bertanya: “Apa yang tertinggal daripada (daging) kambing tersebut?”. ‘Aisyah  menjawab: “Tidak ada yang tertinggal darinya kecuali (bahagian) bahu (dari) kambing tersebut”. Maka Rasulullah SAW bersabda: “Itu bererti semua daging kambing tersebut tertinggal tetap dan kekal pahalanya kecuali bahagian bahunya” Tingkatkan sedekah, derma, wakaf kerana itulah yang kekal dan menetap pahala kebaikannya untuk kita, meskipun secara mata kasarnya harta tersebut berkurang. Negara Rahmah Ummah Sejahtera #BangunkanJiwaTaqwa #TeguhkanUkhuwahSebarkanRahmah #BinaNegaraRahmah #PertubuhanIKRAMMalaysiaNegeriJohor #PalestinMerdeka 24hb Mac 2024 13hb Ramadan 1445H Utk dapatkan 1 Hari 1 Hadis Pertubuhan Ikram Malaysia Negeri Johor, sila klik link di bawah : telegram.me/hadisharian_ikram