• PSA: Check Your Ivermectin
    Not all Ivermectin is Created Equal

    Dr. Syed Haider
    Covimectin 12 Ivermectin 12mg Tablets at Rs 250/strip of 10 tablets | Pharmaceutical Capsules in Nagpur | ID: 2852920640491
    Every time I post about ivermectin on Twitter a dozen bots drop into my replies and start directing people to various online direct mail-order pharmacies that don’t require prescriptions.

    These are almost all Indian pharmacies, but could also be located in China or Mexico.

    So it’s important to understand that not all ivermectin is created equal.

    Actually not all ivermectin is even ivermectin at all (same goes for the other meds they sell).

    From a study done by the regulator in Australia:

    "Three products that listed ivermectin on the label were also found to be counterfeit (Iversun-12, Covimectin-12, Ivilife-12)."

    Indians in India don't even trust these pharmacies.

    The only ivermectin that ever gave a patient of mine chest pain came from India.

    She also tried European and American versions and no chest pain.

    Don't trust stuff coming straight from India or China or Mexico.

    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

    Share

    Buy American meds from FDA regulated pharmacies that buy from verified manufacturers.

    It doesn't even matter if the bulk powder the pharmacies are using originates overseas in one of the no-go countries I listed (all of it does), because B2B bulk pharmaceuticals for export to the US are a different ballgame than direct to consumer products.

    The stuff that get’s imported into the country by compounding pharmacies is the real deal from trusted and safe manufacturers - they even exceed our own standards because they are so grateful to be selling into our market they are extra cautious that they don’t harm their reputation by dropping the ball in any way.

    But, what is listed on direct to consumer websites littering social media platforms is going to be diluted because no one’s checking to make sure it’s not and it makes more money if it is.

    It may even have nothing of what’s listed on the label, since they can get away with it. It could have something harmful if taken in prescribed doses, it could have nothing but sand for all we know.

    And there isn’t even any good reason to get meds from those online Indian pharmacies.

    The only possible reason is saving money, but getting ivermectin from a regulated US compounding pharmacy with a prescription is cheaper mg for mg than overseas pharmacies when you use mygotodoc.com (and we beat every one of our competitors with a low price guarantee).

    Last I checked we’re usually even cheaper than buying most US-sourced animal versions of human prescription drugs (eg ivermectin, amoxicillin, ciprofloxacin, etc - these and others are prescribed in our disaster paks, antibiotic medkits and travel paks).

    So when you see people recommending this stuff online, let them know that it’s not safe, it’s probably not real, and it’s not even cheaper.

    Buy American.

    Use mygotodoc: we’re as American as apple pie, and just as sweet.

    140+ Patriotic Apple Pie Stock Photos, Pictures & Royalty ...
    Stock Up On Ivermectin

    Oh and before I forget we also have a huge anniversary sale on our premium vitamins this entire month with 25% off at our sister site mygotostack.com.


    And be sure to check out the bestsellers:

    IMMUNITY [vitamins] the most popular pandemic supplement of the last 3 years, DETOX [spike buster] the most popular spike detox support on the planet and IMMUNITY [herbals] that rounds out what you need for treatment or recovery. The latter two are based on the McCullough and FLCCC protocols for detoxing spike and have to be separated into two products since the spike buster is taken without meals and the herbals are taken with food


    START STACKING VITAMINS

    https://blog.mygotodoc.com/p/psa-check-your-ivermectin
    PSA: Check Your Ivermectin Not all Ivermectin is Created Equal Dr. Syed Haider Covimectin 12 Ivermectin 12mg Tablets at Rs 250/strip of 10 tablets | Pharmaceutical Capsules in Nagpur | ID: 2852920640491 Every time I post about ivermectin on Twitter a dozen bots drop into my replies and start directing people to various online direct mail-order pharmacies that don’t require prescriptions. These are almost all Indian pharmacies, but could also be located in China or Mexico. So it’s important to understand that not all ivermectin is created equal. Actually not all ivermectin is even ivermectin at all (same goes for the other meds they sell). From a study done by the regulator in Australia: "Three products that listed ivermectin on the label were also found to be counterfeit (Iversun-12, Covimectin-12, Ivilife-12)." Indians in India don't even trust these pharmacies. The only ivermectin that ever gave a patient of mine chest pain came from India. She also tried European and American versions and no chest pain. Don't trust stuff coming straight from India or China or Mexico. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share Buy American meds from FDA regulated pharmacies that buy from verified manufacturers. It doesn't even matter if the bulk powder the pharmacies are using originates overseas in one of the no-go countries I listed (all of it does), because B2B bulk pharmaceuticals for export to the US are a different ballgame than direct to consumer products. The stuff that get’s imported into the country by compounding pharmacies is the real deal from trusted and safe manufacturers - they even exceed our own standards because they are so grateful to be selling into our market they are extra cautious that they don’t harm their reputation by dropping the ball in any way. But, what is listed on direct to consumer websites littering social media platforms is going to be diluted because no one’s checking to make sure it’s not and it makes more money if it is. It may even have nothing of what’s listed on the label, since they can get away with it. It could have something harmful if taken in prescribed doses, it could have nothing but sand for all we know. And there isn’t even any good reason to get meds from those online Indian pharmacies. The only possible reason is saving money, but getting ivermectin from a regulated US compounding pharmacy with a prescription is cheaper mg for mg than overseas pharmacies when you use mygotodoc.com (and we beat every one of our competitors with a low price guarantee). Last I checked we’re usually even cheaper than buying most US-sourced animal versions of human prescription drugs (eg ivermectin, amoxicillin, ciprofloxacin, etc - these and others are prescribed in our disaster paks, antibiotic medkits and travel paks). So when you see people recommending this stuff online, let them know that it’s not safe, it’s probably not real, and it’s not even cheaper. Buy American. Use mygotodoc: we’re as American as apple pie, and just as sweet. 140+ Patriotic Apple Pie Stock Photos, Pictures & Royalty ... Stock Up On Ivermectin Oh and before I forget we also have a huge anniversary sale on our premium vitamins this entire month with 25% off at our sister site mygotostack.com. And be sure to check out the bestsellers: IMMUNITY [vitamins] the most popular pandemic supplement of the last 3 years, DETOX [spike buster] the most popular spike detox support on the planet and IMMUNITY [herbals] that rounds out what you need for treatment or recovery. The latter two are based on the McCullough and FLCCC protocols for detoxing spike and have to be separated into two products since the spike buster is taken without meals and the herbals are taken with food START STACKING VITAMINS https://blog.mygotodoc.com/p/psa-check-your-ivermectin
    BLOG.MYGOTODOC.COM
    PSA: Check Your Ivermectin
    Not all Ivermectin is Created Equal
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  • HOW TO GET NINTENDO GIFT CARD CODES
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    Are you a fan of Nintendo games and products? Do you want to get your hands on some free Nintendo gift card codes to use for your favorite games or accessories? Well, you’re in luck because we have some tips on how to easily obtain Nintendo gift card codes without spending a dime!One of the easiest ways to get free Nintendo gift card codes is by participating in online surveys or signing up for rewards programs. Many websites and companies offer rewards for completing surveys or signing up for their services, and these rewards often include gift cards to popular retailers like Nintendo
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  • Dropify AI Review | Activate Your 5-Step Dropshipping System Now

    Welcome To Dropify AI Review. When it comes to e-commerce, success depends on two factors. First, think about the products you are selling. If you sell an unpopular product, you will never convert or sell.

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  • Roblox gift cards are a popular way for players to purchase Robux, the in-game currency used in the online gaming platform. While you can purchase Roblox gift cards at various retailers, there are also ways to get them for free. Here are some methods you can try to get Roblox gift cards without spending any money:
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    Roblox gift cards are a popular way for players to purchase Robux, the in-game currency used in the online gaming platform. While you can purchase Roblox gift cards at various retailers, there are also ways to get them for free. Here are some methods you can try to get Roblox gift cards without spending any money: GET LINK: https://foremostbuy.com/roblox-gift-%f0%9f%8e%81-card-generator/ #RobloxGiftCard #FreeRobloxGiftCard #GetRobloxGiftCard #EarnRobloxGiftCard #RobloxGiftCardForFree
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  • The Silent Shame of Health Institutions
    J.R. Bruning
    For how much longer will health policy ignore multimorbidity, that looming, giant elephant in the room, that propagates and amplifies suffering? For how much longer will the ‘trend’ of increasing diagnoses of multiple health conditions, at younger and younger ages be rendered down by government agencies to better and more efficient services, screening modalities, and drug choices?

    Multimorbidity, the presence of many chronic conditions, is the silent shame of health policy.

    All too often chronic conditions overlap and accumulate. From cancer, to diabetes, to digestive system diseases, to high blood pressure, to skin conditions in cascades of suffering. Heartbreakingly, these conditions commonly overlap with mental illnesses or disorders. It’s increasingly common for people to be diagnosed with multiple mental conditions, such as having anxiety and depression, or anxiety and schizophrenia.

    Calls for equity tend to revolve around medical treatment, even as absurdities and injustices accrue.

    Multimorbidity occurs a decade earlier in socioeconomically deprived communities. Doctors are diagnosing multimorbidity at younger and younger ages.

    Treatment regimens for people with multiple conditions necessarily entail a polypharmacy approach – the prescribing of multiple medications. One condition may require multiple medications. Thus, with multimorbidity comes increased risk of adverse outcomes and polyiatrogenesis – ‘medical harm caused by medical treatments on multiple fronts simultaneously and in conjunction with one another.’

    Side effects, whether short-term or patients’ concerns about long-term harm, are the main reason for non-adherence to prescribed medications.

    So ‘equity’ which only implies drug treatment doesn’t involve equity at all.

    Poor diets may be foundational to the Western world’s health crisis. But are governments considering this?

    The antinomies are piling up.

    We are amid a global epidemic of metabolic syndrome. Insulin resistance, obesity, elevated triglyceride levels and low levels of high-density lipoprotein cholesterol, and elevated blood pressure haunt the people queuing up to see doctors.

    Research, from individual cases to clinical trials, consistently show that diets containing high levels of ultra-processed foods and carbohydrates amplify inflammation, oxidative stress, and insulin resistance. What researchers and scientists are also identifying, at the cellular level, in clinical and medical practice, and at the global level – is that insulin resistance, inflammation, oxidative stress, and nutrient deficiencies from poor diets not only drive metabolic illness, but mental illnesses, compounding suffering.

    There is also ample evidence that the metabolic and mental health epidemic that is driving years lost due to disease, reducing productivity, and creating mayhem in personal lives – may be preventable and reversible.

    Doctors generally recognise that poor diets are a problem. Ultra-processed foods are strongly associated with adult and childhood ill health. Ultra-processed foods are

    ‘formulations of ingredients, mostly of exclusive industrial use, typically created by series of industrial techniques and processes (hence ‘ultra-processed’).’

    In the USA young people under age 19 consume on average 67% of their diet, while adults consume around 60% of their diet in ultra-processed food. Ultra-processed food contributes 60% of UK children’s calories; 42% of Australian children’s calories and over half the dietary calories for children and adolescents in Canada. In New Zealand in 2009-2010, ultra-processed foods contributed to the 45% (12 months), 42% (24 months), and 51% (60 months) of energy intake to the diets of children.

    All too frequently, doctors are diagnosing both metabolic and mental illnesses.

    What may be predictable is that a person is likely to develop insulin resistance, inflammation, oxidative stress, and nutrient deficiencies from chronic exposure to ultra-processed food. How this will manifest in a disease or syndrome condition is reflective of a human equivalent of quantum entanglement.

    Cascades, feedback loops, and other interdependencies often leave doctors and patients bouncing from one condition to another, and managing medicine side effects and drug-drug relationships as they go.

    In New Zealand it is more common to have multiple conditions than a single condition. The costs of having two NCDs simultaneously is typically superadditive and ‘more so for younger adults.’

    This information is outside the ‘work programme’ of the top echelons in the Ministry of Health:

    Official Information Act (OIA) requests confirm that the Ministries’ Directors General who are responsible for setting policy and long-term strategy aren’t considering these issues. The problem of multimorbidity and the overlapping, entangled relationship with ultra-processed food is outside of the scope of the work programme of the top directorates in our health agency.

    New Zealand’s Ministry of Health’s top deputy directors general might be earning a quarter of a million dollars each, but they are ignorant of the relationship of dietary nutrition and mental health. Nor are they seemingly aware of the extent of multimorbidity and the overlap between metabolic and mental illnesses.

    Neither the Public Health Agency Deputy Director-General – Dr Andrew Old, nor the Deputy Director-General Evidence, Research and Innovation, Dean Rutherford, nor the Deputy Director-General of Strategy Policy and Legislation, Maree Roberts, nor the Clinical, Community and Mental Health Deputy Director-General Robyn Shearer have been briefed on these relationships.

    If they’re not being briefed, policy won’t be developed to address dietary nutrition. Diet will be lower-order.

    The OIA request revealed that New Zealand’s Ministry of Health ‘does not widely use the metabolic syndrome classification.’ When I asked ‘How do you classify, or what term do you use to classify the cluster of symptoms characterised by central obesity, dyslipidemia, hypertension, and insulin resistance?’, they responded:

    ‘The conditions referred to are considered either on their own or as part of a broader cardiovascular disease risk calculation.’

    This is interesting. What if governments should be calculating insulin resistance first, in order to then calculate a broader cardiovascular risk? What if insulin resistance, inflammation, and oxidative stress are appearing at younger and younger ages, and ultra-processed food is the major driver?

    Pre-diabetes and Type 2 diabetes are driven by too much blood glucose. Type 1 diabetics can’t make insulin, while Type 2 diabetics can’t make enough to compensate for their dietary intake of carbohydrates. One of insulin’s (many) jobs is to tuck away that blood glucose into cells (as fat) but when there are too many dietary carbohydrates pumping up blood glucose, the body can’t keep up. New Zealand practitioners use the HbA1c blood test, which measures the average blood glucose level over the past 2-3 months. In New Zealand, doctors diagnose pre-diabetes if HbA1c levels are 41-49 nmol/mol, and diabetes at levels of 50 nmol/mol and above.

    Type 2 diabetes management guidelines recommend that sugar intake should be reduced, while people should aim for consistent carbohydrates across the day. The New Zealand government does not recommend paleo or low-carbohydrate diets.

    If you have diabetes you are twice as likely to have heart disease or a stroke, and at a younger age. Prediabetes, which apparently 20% of Kiwis have, is also high-risk due to, as the Ministry of Health states: ‘increased risk of macrovascular complications and early death.’

    The question might become – should we be looking at insulin levels, to more sensitively gauge risk at an early stage?

    Without more sensitive screens at younger ages these opportunities to repivot to avoid chronic disease are likely to be missed. Currently, Ministry of Health policies are unlikely to justify the funding of tests for insulin resistance by using three simple blood tests: fasting insulin, fasting lipids (cholesterol and triglycerides), and fasting glucose – to estimate where children, young people, and adults stand on the insulin resistance spectrum when other diagnoses pop up.

    Yet insulin plays a powerful role in brain health.

    Insulin supports neurotransmitter function and brain energy, directly impacting mood and behaviours. Insulin resistance might arrive before mental illness. Harvard-based psychiatrist Chris Palmer recounts in the book Brain Energy, a large 15,000-participant study of young people from age 0-24:

    ‘Children who had persistently high insulin levels (a sign of insulin resistance) beginning at age nine were five times more likely to be at risk for psychosis, meaning they were showing at least some worrisome signs, and they were three times for likely to already be diagnosed with bipolar disorder or schizophrenia by the time they turned twenty-four. This study clearly demonstrated that insulin resistance comes first, then psychosis.’

    Psychiatrist Georgia Ede suggests that high blood glucose and high insulin levels act like a ‘deadly one-two punch’ for the brain, triggering waves of inflammation and oxidative stress. The blood-brain barrier becomes increasingly resistant to chronic high insulin levels. Even though the body might have higher blood insulin, the same may not be true for the brain. As Ede maintains, ‘cells deprived of adequate insulin ‘sputter and struggle to maintain normal operations.’

    Looking at the relationship between brain health and high blood glucose and high insulin simply might not be on the programme for strategists looking at long-term planning.

    Nor are Directors General in a position to assess the role of food addiction. Ultra-processed food has addictive qualities designed into the product formulations. Food addiction is increasingly recognised as pervasive and difficult to manage as any substance addiction.

    But how many children and young people have insulin resistance and are showing markers for inflammation and oxidative stress – in the body and in the brain? To what extent do young people have both insulin resistance and depression resistance or ADHD or bipolar disorder?

    This kind of thinking is completely outside the work programme. But insulin levels, inflammation, and oxidative stress may not only be driving chronic illness – but driving the global mental health tsunami.

    Metabolic disorders are involved in complex pathways and feedback loops across body systems, and doctors learn this at medical school. Patterns and relationships between hormones, the brain, the gastrointestinal system, kidneys, and liver; as well as problems with joints and bone health, autoimmunity, nerves, and sensory conditions evolve from and revolve around metabolic health.

    Nutrition and diet are downplayed in medical school. What doctors don’t learn so much – the cognitive dissonance that they must accept throughout their training – is that metabolic health is commonly (except for some instances) shaped by the quality of dietary nutrition. The aetiology of a given condition can be very different, while the evidence that common chronic and mental illnesses are accompanied by oxidative stress, inflammation, and insulin resistance are primarily driven by diet – is growing stronger and stronger.

    But without recognising the overlapping relationships, policy to support healthy diets will remain limp.

    What we witness are notions of equity that support pharmaceutical delivery – not health delivery.

    What also inevitably happens is that ‘equity’ focuses on medical treatment. When the Ministry of Health prefers to atomise the different conditions or associate them with heart disease – they become single conditions to treat with single drugs. They’re lots of small problems, not one big problem, and insulin resistance is downplayed.

    But just as insulin resistance, inflammation, and oxidative stress send cascading impacts across body systems, systemic ignorance sends cascading effects across government departments tasked with ‘improving, promoting, and protecting health.’

    It’s an injustice. The literature solidly points to lower socio-economic status driving much poorer diets and increased exposures to ultra-processed food, but the treatments exclusively involve drugs and therapy.

    Briefings to Incoming Ministers with the election of new Governments show how ignorance cascades across responsible authorities.

    Health New Zealand, Te Whatu Ora’s November 2023 Briefing to the new government outlined the agency’s obligations. However, the ‘health’ targets are medical, and the agency’s focus is on infrastructure, staff, and servicing. The promotion of health, and health equity, which can only be addressed by addressing the determinants of health, is not addressed.

    The Māori Health Authority and Health New Zealand Joint Briefing to the Incoming Minister for Mental Health does not address the role of diet and nutrition as a driver of mental illness and disorder in New Zealand. The issue of multimorbidity, the related problem of commensurate metabolic illness, and diet as a driver is outside scope. When the Briefing states that it is important to address the ‘social, cultural, environmental and economic determinants of mental health,’ without any sound policy footing, real movement to address diet will not happen, or will only happen ad hoc.

    The Mental Health and Wellbeing Commission, Te Hiringa Mahara’s November 2023 Briefing to Incoming Ministers that went to the Ministers for Health and Mental Health might use the term ‘well-being’ over 120 times – but was silent on the related and overlapping drivers of mental illness which include metabolic or multimorbidity, nutrition, or diet.

    Five years earlier, He Ara Ora, New Zealand’s 2018 Mental Health and Addiction enquiry had recognised that tāngata whaiora, people seeking wellness, or service users, also tend to have multiple health conditions. The enquiry recommended that a whole of government approach to well-being, prevention, and social determinants was required. Vague nods were made to diet and nutrition, but this was not sufficiently emphasised as to be a priority.

    He Ara Ora was followed by 2020 Long-term pathway to mental well-being viewed nutrition as being one of a range of factors. No policy framework strategically prioritised diet, nutrition, and healthy food. No governmental obligation or commitment was built into policy to improve access to healthy food or nutrition education.

    Understanding the science, the relationships, and the drivers of the global epidemic, is ‘outside the work programmes’ of New Zealand’s Ministry of Health and outside the scope of all the related authorities. There is an extraordinary amount of data in the scientific literature, so many case studies, cohort studies, and clinical trials. Popular books are being written, however government agencies remain ignorant.

    In the meantime, doctors must deal with the suffering in front of them without an adequate toolkit.

    Doctors and pharmacists are faced with a Hobson’s choice of managing multiple chronic conditions and complex drug cocktails, in patients at younger and younger ages. Ultimately, they are treating a patient whom they recognise will only become sicker, cost the health system more, and suffer more.

    Currently there is little support for New Zealand medical doctors (known as general practitioners, or GPs) in changing practices and recommendations to support non-pharmaceutical drug treatment approaches. Their medical education does not equip them to recognise the extent to which multiple co-existing conditions may be alleviated or reversed. Doctors are paid to prescribe, to inject, and to screen, not to ameliorate or reverse disease and lessen prescribing. The prescribing of nutrients is discouraged and as doctors do not have nutritional training, they hesitate to prescribe nutrients.

    Many do not want to risk going outside treatment guidelines. Recent surges in protocols and guidelines for medical doctors reduce flexibility and narrow treatment choices for doctors. If they were to be reported to the Medical Council of New Zealand, they would risk losing their medical license. They would then be unable to practice.

    Inevitably, without Ministry of Health leadership, medical doctors in New Zealand are unlikely to voluntarily prescribe non-drug modalities such as nutritional options to any meaningful extent, for fear of being reported.

    Yet some doctors are proactive, such as Dr Glen Davies in Taupo, New Zealand. Some doctors are in a better ‘place’ to work to alleviate and reverse long-term conditions. They may be later in their career, with 10-20 years of research into metabolism, dietary nutrition, and patient care, and motivated to guide a patient through a personal care regime which might alleviate or reverse a patient’s suffering.

    Barriers include resourcing. Doctors aren’t paid for reversing disease and taking patients off medications.

    Doctors witness daily the hopelessness felt by their patients in dealing with chronic conditions in their short 15-minute consultations, and the vigilance required for dealing with adverse drug effects. Drug non-compliance is associated with adverse effects suffered by patients. Yet without wrap-around support changing treatments, even if it has potential to alleviate multiple conditions, to reduce symptoms, lower prescribing and therefore lessen side effects, is just too uncertain.

    They saw what happened to disobedient doctors during Covid-19.

    Given such context, what are we to do?

    Have open public discussions about doctor-patient relationships and trust. Inform and overlay such conversations by drawing attention to the foundational Hippocratic Oath made by doctors, to first do no harm.

    Questions can be asked. If patients were to understand that diet may be an underlying driver of multiple conditions, and a change in diet and improvement in micronutrient status might alleviate suffering – would patients be more likely to change?

    Economically, if wrap-around services were provided in clinics to support dietary change, would less harm occur to patients from worsening conditions that accompany many diseases (such as Type 2 diabetes) and the ever-present problem of drug side-effects? Would education and wrap-around services in early childhood and youth delay or prevent the onset of multimorbid diagnoses?

    Is it more ethical to give young people a choice of treatment? Could doctors prescribe dietary changes and multinutrients and support change with wrap-around support when children and young people are first diagnosed with a mental health condition – from the clinic, to school, to after school? If that doesn’t work, then prescribe pharmaceutical drugs.

    Should children and young people be educated to appreciate the extent to which their consumption of ultra-processed food likely drives their metabolic and mental health conditions? Not just in a blithe ‘eat healthy’ fashion that patently avoids discussing addiction. Through deeper policy mechanisms, including cooking classes and nutritional biology by the implementation of nourishing, low-carbohydrate cooked school lunches.

    With officials uninformed, it’s easy to see why funding for Green Prescriptions that would support dietary changes have sputtered out. It’s easy to understand why neither the Ministry of Health nor Pharmac have proactively sourced multi-nutrient treatments that improve resilience to stress and trauma for low-income young people. Why there’s no discussion on a lower side-effect risk for multinutrient treatments. Why are there no policies in the education curriculum diving into the relationship between ultra-processed food and mental and physical health? It’s not in the work programme.

    There’s another surfacing dilemma.

    Currently, if doctors tell their patients that there is very good evidence that their disease or syndrome could be reversed, and this information is not held as factual information by New Zealand’s Ministry of Health – do doctors risk being accused of spreading misinformation?

    Government agencies have pivoted in the past 5 years to focus intensively on the problem of dis- and misinformation. New Zealand’s disinformation project states that

    Disinformation is false or modified information knowingly and deliberately shared to cause harm or achieve a broader aim.
    Misinformation is information that is false or misleading, though not created or shared with the direct intention of causing harm.
    Unfortunately, as we see, there is no division inside the Ministry of Health that reviews the latest evidence in the scientific literature, to ensure that policy decisions correctly reflect the latest evidence.

    There is no scientific agency outside the Ministry of Health that has flexibility and the capacity to undertake autonomous, long-term monitoring and research in nutrition, diet, and health. There is no independent, autonomous, public health research facility with sufficient long-term funding to translate dietary and nutritional evidence into policy, particularly if it contradicted current policy positions.

    Despite excellent research being undertaken, it is highly controlled, ad hoc, and frequently short-term. Problematically, there is no resourcing for those scientists to meaningfully feedback that information to either the Ministry of Health or to Members of Parliament and government Ministers.

    Dietary guidelines can become locked in, and contradictions can fail to be chewed over. Without the capacity to address errors, information can become outdated and misleading. Government agencies and elected members – from local councils all the way up to government Ministers, are dependent on being informed by the Ministry of Health, when it comes to government policy.

    When it comes to complex health conditions, and alleviating and reversing metabolic or mental illness, based on different patient capacity – from socio-economic, to cultural, to social, and taking into account capacity for change, what is sound, evidence-based information and what is misinformation?

    In the impasse, who can we trust?

    Published under a Creative Commons Attribution 4.0 International License
    For reprints, please set the canonical link back to the original Brownstone Institute Article and Author.

    Author

    J.R. Bruning is a consultant sociologist (B.Bus.Agribusiness; MA Sociology) based in New Zealand. Her work explores governance cultures, policy and the production of scientific and technical knowledge. Her Master’s thesis explored the ways science policy creates barriers to funding, stymying scientists’ efforts to explore upstream drivers of harm. Bruning is a trustee of Physicians & Scientists for Global Responsibility (PSGR.org.nz). Papers and writing can be found at TalkingRisk.NZ and at JRBruning.Substack.com and at Talking Risk on Rumble.

    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-silent-shame-of-health-institutions/
    The Silent Shame of Health Institutions J.R. Bruning For how much longer will health policy ignore multimorbidity, that looming, giant elephant in the room, that propagates and amplifies suffering? For how much longer will the ‘trend’ of increasing diagnoses of multiple health conditions, at younger and younger ages be rendered down by government agencies to better and more efficient services, screening modalities, and drug choices? Multimorbidity, the presence of many chronic conditions, is the silent shame of health policy. All too often chronic conditions overlap and accumulate. From cancer, to diabetes, to digestive system diseases, to high blood pressure, to skin conditions in cascades of suffering. Heartbreakingly, these conditions commonly overlap with mental illnesses or disorders. It’s increasingly common for people to be diagnosed with multiple mental conditions, such as having anxiety and depression, or anxiety and schizophrenia. Calls for equity tend to revolve around medical treatment, even as absurdities and injustices accrue. Multimorbidity occurs a decade earlier in socioeconomically deprived communities. Doctors are diagnosing multimorbidity at younger and younger ages. Treatment regimens for people with multiple conditions necessarily entail a polypharmacy approach – the prescribing of multiple medications. One condition may require multiple medications. Thus, with multimorbidity comes increased risk of adverse outcomes and polyiatrogenesis – ‘medical harm caused by medical treatments on multiple fronts simultaneously and in conjunction with one another.’ Side effects, whether short-term or patients’ concerns about long-term harm, are the main reason for non-adherence to prescribed medications. So ‘equity’ which only implies drug treatment doesn’t involve equity at all. Poor diets may be foundational to the Western world’s health crisis. But are governments considering this? The antinomies are piling up. We are amid a global epidemic of metabolic syndrome. Insulin resistance, obesity, elevated triglyceride levels and low levels of high-density lipoprotein cholesterol, and elevated blood pressure haunt the people queuing up to see doctors. Research, from individual cases to clinical trials, consistently show that diets containing high levels of ultra-processed foods and carbohydrates amplify inflammation, oxidative stress, and insulin resistance. What researchers and scientists are also identifying, at the cellular level, in clinical and medical practice, and at the global level – is that insulin resistance, inflammation, oxidative stress, and nutrient deficiencies from poor diets not only drive metabolic illness, but mental illnesses, compounding suffering. There is also ample evidence that the metabolic and mental health epidemic that is driving years lost due to disease, reducing productivity, and creating mayhem in personal lives – may be preventable and reversible. Doctors generally recognise that poor diets are a problem. Ultra-processed foods are strongly associated with adult and childhood ill health. Ultra-processed foods are ‘formulations of ingredients, mostly of exclusive industrial use, typically created by series of industrial techniques and processes (hence ‘ultra-processed’).’ In the USA young people under age 19 consume on average 67% of their diet, while adults consume around 60% of their diet in ultra-processed food. Ultra-processed food contributes 60% of UK children’s calories; 42% of Australian children’s calories and over half the dietary calories for children and adolescents in Canada. In New Zealand in 2009-2010, ultra-processed foods contributed to the 45% (12 months), 42% (24 months), and 51% (60 months) of energy intake to the diets of children. All too frequently, doctors are diagnosing both metabolic and mental illnesses. What may be predictable is that a person is likely to develop insulin resistance, inflammation, oxidative stress, and nutrient deficiencies from chronic exposure to ultra-processed food. How this will manifest in a disease or syndrome condition is reflective of a human equivalent of quantum entanglement. Cascades, feedback loops, and other interdependencies often leave doctors and patients bouncing from one condition to another, and managing medicine side effects and drug-drug relationships as they go. In New Zealand it is more common to have multiple conditions than a single condition. The costs of having two NCDs simultaneously is typically superadditive and ‘more so for younger adults.’ This information is outside the ‘work programme’ of the top echelons in the Ministry of Health: Official Information Act (OIA) requests confirm that the Ministries’ Directors General who are responsible for setting policy and long-term strategy aren’t considering these issues. The problem of multimorbidity and the overlapping, entangled relationship with ultra-processed food is outside of the scope of the work programme of the top directorates in our health agency. New Zealand’s Ministry of Health’s top deputy directors general might be earning a quarter of a million dollars each, but they are ignorant of the relationship of dietary nutrition and mental health. Nor are they seemingly aware of the extent of multimorbidity and the overlap between metabolic and mental illnesses. Neither the Public Health Agency Deputy Director-General – Dr Andrew Old, nor the Deputy Director-General Evidence, Research and Innovation, Dean Rutherford, nor the Deputy Director-General of Strategy Policy and Legislation, Maree Roberts, nor the Clinical, Community and Mental Health Deputy Director-General Robyn Shearer have been briefed on these relationships. If they’re not being briefed, policy won’t be developed to address dietary nutrition. Diet will be lower-order. The OIA request revealed that New Zealand’s Ministry of Health ‘does not widely use the metabolic syndrome classification.’ When I asked ‘How do you classify, or what term do you use to classify the cluster of symptoms characterised by central obesity, dyslipidemia, hypertension, and insulin resistance?’, they responded: ‘The conditions referred to are considered either on their own or as part of a broader cardiovascular disease risk calculation.’ This is interesting. What if governments should be calculating insulin resistance first, in order to then calculate a broader cardiovascular risk? What if insulin resistance, inflammation, and oxidative stress are appearing at younger and younger ages, and ultra-processed food is the major driver? Pre-diabetes and Type 2 diabetes are driven by too much blood glucose. Type 1 diabetics can’t make insulin, while Type 2 diabetics can’t make enough to compensate for their dietary intake of carbohydrates. One of insulin’s (many) jobs is to tuck away that blood glucose into cells (as fat) but when there are too many dietary carbohydrates pumping up blood glucose, the body can’t keep up. New Zealand practitioners use the HbA1c blood test, which measures the average blood glucose level over the past 2-3 months. In New Zealand, doctors diagnose pre-diabetes if HbA1c levels are 41-49 nmol/mol, and diabetes at levels of 50 nmol/mol and above. Type 2 diabetes management guidelines recommend that sugar intake should be reduced, while people should aim for consistent carbohydrates across the day. The New Zealand government does not recommend paleo or low-carbohydrate diets. If you have diabetes you are twice as likely to have heart disease or a stroke, and at a younger age. Prediabetes, which apparently 20% of Kiwis have, is also high-risk due to, as the Ministry of Health states: ‘increased risk of macrovascular complications and early death.’ The question might become – should we be looking at insulin levels, to more sensitively gauge risk at an early stage? Without more sensitive screens at younger ages these opportunities to repivot to avoid chronic disease are likely to be missed. Currently, Ministry of Health policies are unlikely to justify the funding of tests for insulin resistance by using three simple blood tests: fasting insulin, fasting lipids (cholesterol and triglycerides), and fasting glucose – to estimate where children, young people, and adults stand on the insulin resistance spectrum when other diagnoses pop up. Yet insulin plays a powerful role in brain health. Insulin supports neurotransmitter function and brain energy, directly impacting mood and behaviours. Insulin resistance might arrive before mental illness. Harvard-based psychiatrist Chris Palmer recounts in the book Brain Energy, a large 15,000-participant study of young people from age 0-24: ‘Children who had persistently high insulin levels (a sign of insulin resistance) beginning at age nine were five times more likely to be at risk for psychosis, meaning they were showing at least some worrisome signs, and they were three times for likely to already be diagnosed with bipolar disorder or schizophrenia by the time they turned twenty-four. This study clearly demonstrated that insulin resistance comes first, then psychosis.’ Psychiatrist Georgia Ede suggests that high blood glucose and high insulin levels act like a ‘deadly one-two punch’ for the brain, triggering waves of inflammation and oxidative stress. The blood-brain barrier becomes increasingly resistant to chronic high insulin levels. Even though the body might have higher blood insulin, the same may not be true for the brain. As Ede maintains, ‘cells deprived of adequate insulin ‘sputter and struggle to maintain normal operations.’ Looking at the relationship between brain health and high blood glucose and high insulin simply might not be on the programme for strategists looking at long-term planning. Nor are Directors General in a position to assess the role of food addiction. Ultra-processed food has addictive qualities designed into the product formulations. Food addiction is increasingly recognised as pervasive and difficult to manage as any substance addiction. But how many children and young people have insulin resistance and are showing markers for inflammation and oxidative stress – in the body and in the brain? To what extent do young people have both insulin resistance and depression resistance or ADHD or bipolar disorder? This kind of thinking is completely outside the work programme. But insulin levels, inflammation, and oxidative stress may not only be driving chronic illness – but driving the global mental health tsunami. Metabolic disorders are involved in complex pathways and feedback loops across body systems, and doctors learn this at medical school. Patterns and relationships between hormones, the brain, the gastrointestinal system, kidneys, and liver; as well as problems with joints and bone health, autoimmunity, nerves, and sensory conditions evolve from and revolve around metabolic health. Nutrition and diet are downplayed in medical school. What doctors don’t learn so much – the cognitive dissonance that they must accept throughout their training – is that metabolic health is commonly (except for some instances) shaped by the quality of dietary nutrition. The aetiology of a given condition can be very different, while the evidence that common chronic and mental illnesses are accompanied by oxidative stress, inflammation, and insulin resistance are primarily driven by diet – is growing stronger and stronger. But without recognising the overlapping relationships, policy to support healthy diets will remain limp. What we witness are notions of equity that support pharmaceutical delivery – not health delivery. What also inevitably happens is that ‘equity’ focuses on medical treatment. When the Ministry of Health prefers to atomise the different conditions or associate them with heart disease – they become single conditions to treat with single drugs. They’re lots of small problems, not one big problem, and insulin resistance is downplayed. But just as insulin resistance, inflammation, and oxidative stress send cascading impacts across body systems, systemic ignorance sends cascading effects across government departments tasked with ‘improving, promoting, and protecting health.’ It’s an injustice. The literature solidly points to lower socio-economic status driving much poorer diets and increased exposures to ultra-processed food, but the treatments exclusively involve drugs and therapy. Briefings to Incoming Ministers with the election of new Governments show how ignorance cascades across responsible authorities. Health New Zealand, Te Whatu Ora’s November 2023 Briefing to the new government outlined the agency’s obligations. However, the ‘health’ targets are medical, and the agency’s focus is on infrastructure, staff, and servicing. The promotion of health, and health equity, which can only be addressed by addressing the determinants of health, is not addressed. The Māori Health Authority and Health New Zealand Joint Briefing to the Incoming Minister for Mental Health does not address the role of diet and nutrition as a driver of mental illness and disorder in New Zealand. The issue of multimorbidity, the related problem of commensurate metabolic illness, and diet as a driver is outside scope. When the Briefing states that it is important to address the ‘social, cultural, environmental and economic determinants of mental health,’ without any sound policy footing, real movement to address diet will not happen, or will only happen ad hoc. The Mental Health and Wellbeing Commission, Te Hiringa Mahara’s November 2023 Briefing to Incoming Ministers that went to the Ministers for Health and Mental Health might use the term ‘well-being’ over 120 times – but was silent on the related and overlapping drivers of mental illness which include metabolic or multimorbidity, nutrition, or diet. Five years earlier, He Ara Ora, New Zealand’s 2018 Mental Health and Addiction enquiry had recognised that tāngata whaiora, people seeking wellness, or service users, also tend to have multiple health conditions. The enquiry recommended that a whole of government approach to well-being, prevention, and social determinants was required. Vague nods were made to diet and nutrition, but this was not sufficiently emphasised as to be a priority. He Ara Ora was followed by 2020 Long-term pathway to mental well-being viewed nutrition as being one of a range of factors. No policy framework strategically prioritised diet, nutrition, and healthy food. No governmental obligation or commitment was built into policy to improve access to healthy food or nutrition education. Understanding the science, the relationships, and the drivers of the global epidemic, is ‘outside the work programmes’ of New Zealand’s Ministry of Health and outside the scope of all the related authorities. There is an extraordinary amount of data in the scientific literature, so many case studies, cohort studies, and clinical trials. Popular books are being written, however government agencies remain ignorant. In the meantime, doctors must deal with the suffering in front of them without an adequate toolkit. Doctors and pharmacists are faced with a Hobson’s choice of managing multiple chronic conditions and complex drug cocktails, in patients at younger and younger ages. Ultimately, they are treating a patient whom they recognise will only become sicker, cost the health system more, and suffer more. Currently there is little support for New Zealand medical doctors (known as general practitioners, or GPs) in changing practices and recommendations to support non-pharmaceutical drug treatment approaches. Their medical education does not equip them to recognise the extent to which multiple co-existing conditions may be alleviated or reversed. Doctors are paid to prescribe, to inject, and to screen, not to ameliorate or reverse disease and lessen prescribing. The prescribing of nutrients is discouraged and as doctors do not have nutritional training, they hesitate to prescribe nutrients. Many do not want to risk going outside treatment guidelines. Recent surges in protocols and guidelines for medical doctors reduce flexibility and narrow treatment choices for doctors. If they were to be reported to the Medical Council of New Zealand, they would risk losing their medical license. They would then be unable to practice. Inevitably, without Ministry of Health leadership, medical doctors in New Zealand are unlikely to voluntarily prescribe non-drug modalities such as nutritional options to any meaningful extent, for fear of being reported. Yet some doctors are proactive, such as Dr Glen Davies in Taupo, New Zealand. Some doctors are in a better ‘place’ to work to alleviate and reverse long-term conditions. They may be later in their career, with 10-20 years of research into metabolism, dietary nutrition, and patient care, and motivated to guide a patient through a personal care regime which might alleviate or reverse a patient’s suffering. Barriers include resourcing. Doctors aren’t paid for reversing disease and taking patients off medications. Doctors witness daily the hopelessness felt by their patients in dealing with chronic conditions in their short 15-minute consultations, and the vigilance required for dealing with adverse drug effects. Drug non-compliance is associated with adverse effects suffered by patients. Yet without wrap-around support changing treatments, even if it has potential to alleviate multiple conditions, to reduce symptoms, lower prescribing and therefore lessen side effects, is just too uncertain. They saw what happened to disobedient doctors during Covid-19. Given such context, what are we to do? Have open public discussions about doctor-patient relationships and trust. Inform and overlay such conversations by drawing attention to the foundational Hippocratic Oath made by doctors, to first do no harm. Questions can be asked. If patients were to understand that diet may be an underlying driver of multiple conditions, and a change in diet and improvement in micronutrient status might alleviate suffering – would patients be more likely to change? Economically, if wrap-around services were provided in clinics to support dietary change, would less harm occur to patients from worsening conditions that accompany many diseases (such as Type 2 diabetes) and the ever-present problem of drug side-effects? Would education and wrap-around services in early childhood and youth delay or prevent the onset of multimorbid diagnoses? Is it more ethical to give young people a choice of treatment? Could doctors prescribe dietary changes and multinutrients and support change with wrap-around support when children and young people are first diagnosed with a mental health condition – from the clinic, to school, to after school? If that doesn’t work, then prescribe pharmaceutical drugs. Should children and young people be educated to appreciate the extent to which their consumption of ultra-processed food likely drives their metabolic and mental health conditions? Not just in a blithe ‘eat healthy’ fashion that patently avoids discussing addiction. Through deeper policy mechanisms, including cooking classes and nutritional biology by the implementation of nourishing, low-carbohydrate cooked school lunches. With officials uninformed, it’s easy to see why funding for Green Prescriptions that would support dietary changes have sputtered out. It’s easy to understand why neither the Ministry of Health nor Pharmac have proactively sourced multi-nutrient treatments that improve resilience to stress and trauma for low-income young people. Why there’s no discussion on a lower side-effect risk for multinutrient treatments. Why are there no policies in the education curriculum diving into the relationship between ultra-processed food and mental and physical health? It’s not in the work programme. There’s another surfacing dilemma. Currently, if doctors tell their patients that there is very good evidence that their disease or syndrome could be reversed, and this information is not held as factual information by New Zealand’s Ministry of Health – do doctors risk being accused of spreading misinformation? Government agencies have pivoted in the past 5 years to focus intensively on the problem of dis- and misinformation. New Zealand’s disinformation project states that Disinformation is false or modified information knowingly and deliberately shared to cause harm or achieve a broader aim. Misinformation is information that is false or misleading, though not created or shared with the direct intention of causing harm. Unfortunately, as we see, there is no division inside the Ministry of Health that reviews the latest evidence in the scientific literature, to ensure that policy decisions correctly reflect the latest evidence. There is no scientific agency outside the Ministry of Health that has flexibility and the capacity to undertake autonomous, long-term monitoring and research in nutrition, diet, and health. There is no independent, autonomous, public health research facility with sufficient long-term funding to translate dietary and nutritional evidence into policy, particularly if it contradicted current policy positions. Despite excellent research being undertaken, it is highly controlled, ad hoc, and frequently short-term. Problematically, there is no resourcing for those scientists to meaningfully feedback that information to either the Ministry of Health or to Members of Parliament and government Ministers. Dietary guidelines can become locked in, and contradictions can fail to be chewed over. Without the capacity to address errors, information can become outdated and misleading. Government agencies and elected members – from local councils all the way up to government Ministers, are dependent on being informed by the Ministry of Health, when it comes to government policy. When it comes to complex health conditions, and alleviating and reversing metabolic or mental illness, based on different patient capacity – from socio-economic, to cultural, to social, and taking into account capacity for change, what is sound, evidence-based information and what is misinformation? In the impasse, who can we trust? Published under a Creative Commons Attribution 4.0 International License For reprints, please set the canonical link back to the original Brownstone Institute Article and Author. Author J.R. Bruning is a consultant sociologist (B.Bus.Agribusiness; MA Sociology) based in New Zealand. Her work explores governance cultures, policy and the production of scientific and technical knowledge. Her Master’s thesis explored the ways science policy creates barriers to funding, stymying scientists’ efforts to explore upstream drivers of harm. Bruning is a trustee of Physicians & Scientists for Global Responsibility (PSGR.org.nz). Papers and writing can be found at TalkingRisk.NZ and at JRBruning.Substack.com and at Talking Risk on Rumble. 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-silent-shame-of-health-institutions/
    BROWNSTONE.ORG
    The Silent Shame of Health Institutions ⋆ Brownstone Institute
    There is no scientific agency outside the Ministry of Health that has flexibility and the capacity to undertake autonomous, long-term monitoring and research in nutrition, diet and health.
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  • Firm helping Israel spy on Gaza includes genocide advocate
    Michael F. Brown Rights and Accountability 28 March 2024

    Palestinian children and adults try to secure food
    Giora Eiland, a retired Israeli major general, has pushed for a humanitarian crisis in Gaza, a position which has contributed to desperate scenes of Palestinians trying to secure food.
    Mahmoud Issa DPA
    The Israeli military is using Corsight facial recognition technology to collect information about Palestinians in Gaza according to The New York Times.

    “The facial recognition program, which is run by Israel’s military intelligence unit, including the cyber-intelligence division Unit 8200, relies on technology from Corsight, a private Israeli company, four intelligence officers said.”


    The Israeli military also employs Google Photos.

    Israel’s apartheid army detained, interrogated and beat Palestinian poet Mosab Abu Toha, a graduate of Syracuse University, with the assistance of Corsight’s facial recognition technology. Other Palestinians have been similarly detained via Corsight technology.
    Abu Toha notes Palestinians have died in Israeli custody.

    There is little complaint from western politicians. Corsight’s complicity isn’t seen as an urgent matter.

    Nor, for that matter, do most of these politicians give sufficient attention to Israel’s genocidal policies in Gaza.

    Board of directors

    Unmentioned by the Times is that Giora Eiland, a retired Israeli major general, serves on the board of directors of Corsight.

    When Eiland joined the board in January 2021, Igal Raichelgauz, chairman and founder of the Cortica Group, stated, “We are excited to add Giora to the company board, we believe that due to his extensive experience in the national security field, Corsight will continue growing into new markets and territories and lead the face recognition market in Israel and in the world.” Corsight is a subsidiary of Cortica, a firm focused on artificial intelligence.

    Eiland is a proponent of the ethnic cleansing of the occupied territory of Gaza.

    He wrote for the Israeli publication Ynet on 12 October that “One option is a massive and complex ground operation, with no regard to duration and cost, while the second option is to create conditions where life in Gaza becomes unsustainable.”

    In fact, Israel has done both.

    Eiland noted, without voicing dissent, that “Israel has already begun suspending the supply of diesel, fuel, electricity and water, as well as closing the border crossings. Yet, it remains uncertain whether these measures are enough.”

    He then moved to ethnic cleansing.

    “Israel issued a stern warning to Egypt and made it clear that it would not permit humanitarian aid from Egypt to enter Gaza. Israel needs to create a humanitarian crisis in Gaza, compelling tens of thousands or even hundreds of thousands to seek refuge in Egypt or the Gulf.”

    He said nothing of wanting such an arrangement to be temporary.

    Eiland then jumped beyond an ethnic cleansing of “tens of thousands or even hundreds of thousands.” He wrote: “The entire population of Gaza will either move to Egypt or move to the Gulf.”

    The retired general also recommended targeting civilian vehicles in Gaza.

    “Every vehicle in Gaza is considered a military vehicle transporting combatants. Therefore, there is no vehicular traffic, and it does not matter whether it is transporting water or other critical supplies.”

    Such rhetoric amounts to abetting war crimes and has had real consequences for Palestinian children such as 6-year-old Hind Rajab who, according to the Palestine Red Crescent, the Israeli military killed earlier this year in a car along with other family members.

    Eiland pushed collective punishment of Palestinians in Gaza as well.

    “The UN secretary-general has initiated humanitarian aid to Gaza. The Israeli condition for any aid should be a visit by the Red Cross to Israeli hostages and especially the civilians among them. Until this happens, no aid of any kind will be permitted to enter into Gaza.”

    Hinting at the overwhelming violence to come against Palestinian civilians, Eiland wrote of the developing Israeli attack: “It is comparable to the Japanese attack on Pearl Harbor, which led to the launch of an atomic bomb in Japan.”

    The Israeli military has killed over 32,000 Palestinians in Gaza since 7 October, including more than 13,000 children. The International Court of Justice deems it plausible that Israel is engaged in genocidal actions in the small coastal territory.

    Eiland wrapped up his opinion piece by declaring, “As a result, Gaza will become a place where no human being can exist, and I say this as a means rather than an end. I say this because there is no other option for ensuring the security of the state of Israel. We are fighting an existential war.”

    This goes beyond ethnic cleansing to genocide talk when speaking of “a place where no human being can exist.”


    Omer Bartov, a professor of Holocaust and genocide studies at Brown University, documented this and more from Eiland in a November opinion piece in The New York Times.
    He cited a column Eiland wrote in the Israeli newspaper Yedioth Ahronoth. The Brown University professor quoted Eiland as writing, “The state of Israel has no choice but to turn Gaza into a place that is temporarily or permanently impossible to live in.”

    Bartov also quoted Eiland for maintaining, “Creating a severe humanitarian crisis in Gaza is a necessary means to achieving the goal.”

    Then he cited the same Ynet quote noted above that “Gaza will become a place where no human being can exist.”

    Bartov commented, “Apparently, no army representative or politician denounced this statement.”

    Eiland continued with the genocidal talk in November when he wrote, “The international community warns of a humanitarian catastrophe in Gaza and of severe epidemics. We must not shy away from it, as hard as it is. After all, severe epidemics in the south of the Strip will hasten victory.”


    Corsight, with its invasive technology against a largely refugee population dispossessed in 1948, should expect heavy criticism with a board member calling for the ethnic cleansing of Gaza and to make the place uninhabitable.
    Of course, Democratic Majority for Israel received scant attention when it came to light that its board member Archie Gottesman once issued her own genocidal call against Palestinians in Gaza when she tweeted: “Gaza is full of monsters. Time to burn the whole place.”

    Ethnic cleansing and genocide against Palestinians don’t properly register with most western politicians who, of course, are providing weapons to Israel to carry out the devastation in Gaza.

    That Corsight carries out “global operations and support in the US, UK, Singapore, Australia, and R&D in Israel” with the backing of a board member proponent of ethnic cleansing and genocide will not be a significant concern in Washington.

    Popular concern, however, may prove to be a different matter.


    Corsight
    The New York Times
    Google Photos
    Mosab Abu Toha
    Syracuse University
    Igal Raichelgauz
    Cortica Group
    Giora Eiland
    Ynet
    ethnic cleansing
    Hind Rajab
    Palestine Red Crescent Society
    collective punishment
    International Court of Justice
    Gaza genocide
    Omer Bartov
    Brown University
    Democratic Majority for Israel
    Archie Gottesman
    Yediot Ahronot

    https://electronicintifada.net/blogs/michael-f-brown/firm-helping-israel-spy-gaza-includes-genocide-advocate
    Firm helping Israel spy on Gaza includes genocide advocate Michael F. Brown Rights and Accountability 28 March 2024 Palestinian children and adults try to secure food Giora Eiland, a retired Israeli major general, has pushed for a humanitarian crisis in Gaza, a position which has contributed to desperate scenes of Palestinians trying to secure food. Mahmoud Issa DPA The Israeli military is using Corsight facial recognition technology to collect information about Palestinians in Gaza according to The New York Times. “The facial recognition program, which is run by Israel’s military intelligence unit, including the cyber-intelligence division Unit 8200, relies on technology from Corsight, a private Israeli company, four intelligence officers said.” The Israeli military also employs Google Photos. Israel’s apartheid army detained, interrogated and beat Palestinian poet Mosab Abu Toha, a graduate of Syracuse University, with the assistance of Corsight’s facial recognition technology. Other Palestinians have been similarly detained via Corsight technology. Abu Toha notes Palestinians have died in Israeli custody. There is little complaint from western politicians. Corsight’s complicity isn’t seen as an urgent matter. Nor, for that matter, do most of these politicians give sufficient attention to Israel’s genocidal policies in Gaza. Board of directors Unmentioned by the Times is that Giora Eiland, a retired Israeli major general, serves on the board of directors of Corsight. When Eiland joined the board in January 2021, Igal Raichelgauz, chairman and founder of the Cortica Group, stated, “We are excited to add Giora to the company board, we believe that due to his extensive experience in the national security field, Corsight will continue growing into new markets and territories and lead the face recognition market in Israel and in the world.” Corsight is a subsidiary of Cortica, a firm focused on artificial intelligence. Eiland is a proponent of the ethnic cleansing of the occupied territory of Gaza. He wrote for the Israeli publication Ynet on 12 October that “One option is a massive and complex ground operation, with no regard to duration and cost, while the second option is to create conditions where life in Gaza becomes unsustainable.” In fact, Israel has done both. Eiland noted, without voicing dissent, that “Israel has already begun suspending the supply of diesel, fuel, electricity and water, as well as closing the border crossings. Yet, it remains uncertain whether these measures are enough.” He then moved to ethnic cleansing. “Israel issued a stern warning to Egypt and made it clear that it would not permit humanitarian aid from Egypt to enter Gaza. Israel needs to create a humanitarian crisis in Gaza, compelling tens of thousands or even hundreds of thousands to seek refuge in Egypt or the Gulf.” He said nothing of wanting such an arrangement to be temporary. Eiland then jumped beyond an ethnic cleansing of “tens of thousands or even hundreds of thousands.” He wrote: “The entire population of Gaza will either move to Egypt or move to the Gulf.” The retired general also recommended targeting civilian vehicles in Gaza. “Every vehicle in Gaza is considered a military vehicle transporting combatants. Therefore, there is no vehicular traffic, and it does not matter whether it is transporting water or other critical supplies.” Such rhetoric amounts to abetting war crimes and has had real consequences for Palestinian children such as 6-year-old Hind Rajab who, according to the Palestine Red Crescent, the Israeli military killed earlier this year in a car along with other family members. Eiland pushed collective punishment of Palestinians in Gaza as well. “The UN secretary-general has initiated humanitarian aid to Gaza. The Israeli condition for any aid should be a visit by the Red Cross to Israeli hostages and especially the civilians among them. Until this happens, no aid of any kind will be permitted to enter into Gaza.” Hinting at the overwhelming violence to come against Palestinian civilians, Eiland wrote of the developing Israeli attack: “It is comparable to the Japanese attack on Pearl Harbor, which led to the launch of an atomic bomb in Japan.” The Israeli military has killed over 32,000 Palestinians in Gaza since 7 October, including more than 13,000 children. The International Court of Justice deems it plausible that Israel is engaged in genocidal actions in the small coastal territory. Eiland wrapped up his opinion piece by declaring, “As a result, Gaza will become a place where no human being can exist, and I say this as a means rather than an end. I say this because there is no other option for ensuring the security of the state of Israel. We are fighting an existential war.” This goes beyond ethnic cleansing to genocide talk when speaking of “a place where no human being can exist.” Omer Bartov, a professor of Holocaust and genocide studies at Brown University, documented this and more from Eiland in a November opinion piece in The New York Times. He cited a column Eiland wrote in the Israeli newspaper Yedioth Ahronoth. The Brown University professor quoted Eiland as writing, “The state of Israel has no choice but to turn Gaza into a place that is temporarily or permanently impossible to live in.” Bartov also quoted Eiland for maintaining, “Creating a severe humanitarian crisis in Gaza is a necessary means to achieving the goal.” Then he cited the same Ynet quote noted above that “Gaza will become a place where no human being can exist.” Bartov commented, “Apparently, no army representative or politician denounced this statement.” Eiland continued with the genocidal talk in November when he wrote, “The international community warns of a humanitarian catastrophe in Gaza and of severe epidemics. We must not shy away from it, as hard as it is. After all, severe epidemics in the south of the Strip will hasten victory.” Corsight, with its invasive technology against a largely refugee population dispossessed in 1948, should expect heavy criticism with a board member calling for the ethnic cleansing of Gaza and to make the place uninhabitable. Of course, Democratic Majority for Israel received scant attention when it came to light that its board member Archie Gottesman once issued her own genocidal call against Palestinians in Gaza when she tweeted: “Gaza is full of monsters. Time to burn the whole place.” Ethnic cleansing and genocide against Palestinians don’t properly register with most western politicians who, of course, are providing weapons to Israel to carry out the devastation in Gaza. That Corsight carries out “global operations and support in the US, UK, Singapore, Australia, and R&D in Israel” with the backing of a board member proponent of ethnic cleansing and genocide will not be a significant concern in Washington. Popular concern, however, may prove to be a different matter. Corsight The New York Times Google Photos Mosab Abu Toha Syracuse University Igal Raichelgauz Cortica Group Giora Eiland Ynet ethnic cleansing Hind Rajab Palestine Red Crescent Society collective punishment International Court of Justice Gaza genocide Omer Bartov Brown University Democratic Majority for Israel Archie Gottesman Yediot Ahronot https://electronicintifada.net/blogs/michael-f-brown/firm-helping-israel-spy-gaza-includes-genocide-advocate
    ELECTRONICINTIFADA.NET
    Firm helping Israel spy on Gaza includes genocide advocate
    Retired general Giora Eiland has promoted making Gaza “a place where no human being can exist.”
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  • Ukrainian ‘Caliphate’: What the West prefers not to notice when blaming ISIS for the terrorist attack in Moscow
    Kiev’s connections with terrorist groups and Islamists are recognized even in the West. Could Ukrainians be behind the massacre in Crocus City Hall?

    Jonas E. Alexis, Senior EditorMarch 27, 2024

    VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel

    $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts
    Source: Embassy of Israel, Washington, D.C. and US Department of State.

    On March 22, Russia suffered one of the worst terrorist attacks in recent history, in the course of which 137 people were killed and 182 others were injured. The four terrorists who carried out the attack chose one of the largest exhibition and concert venues in the country, Crocus City Hall, in the city of Krasnogorsk on the outskirts of Moscow, which hosts large events every day.

    Even though the investigation is still ongoing, the West has already claimed that the Islamic State (IS) is responsible for the tragedy. This was first reported by some media outlets, including Reuters and CNN, and was later picked up by Western officials. For example, on Monday, this was stated by White House Press Secretary Karine Jean-Pierre.

    However, when we compare this terrorist attack with other IS attacks, we notice more differences than similarities.

    How IS kills

    On that fateful Friday night, a concert by Picnic, a St. Petersburg rock band, was supposed to take place in Crocus City Hall. This fact gave rise to comparisons with the horrible terrorist attack in France in November 2015. Back then, terrorists broke into the Bataclan Theater in Paris, where a concert of the US band Eagles of Death Metal was taking place. IS claimed responsibility for the crime, which left 89 people dead.

    Weapon of mass distraction: Is the West scapegoating Islamic State over Moscow attack?

    Read more

    Weapon of mass distraction: Is the West scapegoating Islamic State over Moscow attack?

    In those years, IS became increasingly active throughout the world – but this was actually a sign of its decline. In its heyday, IS didn’t urge its supporters to carry out terrorist attacks, but instead called on them to “fulfill the hijrah” – i.e., move to the territories controlled by the organization. Over ten years ago, this was quite easy to do, since part of the Syrian border with Turkey was controlled by the jihadists, which allowed people to freely cross it and join their ranks.

    However, as the terrorists lost many of their territories, their rhetoric changed. Through its information resources, IS urged its followers to commit terrorist acts in places where they lived. This caused an upsurge in violence in Europe: a wave of terror swept through France, Belgium, Germany, the UK, and other countries. In Russia, the North Caucasus became a point of tension.

    The strategy was simple – anyone who supported the jihadists, wherever they lived, could record a video with an oath of allegiance to the “caliph,” send it via an automated feedback bot, and then commit a terrorist act. Often it was only the perpetrator who died, but for IS, this didn’t matter – it only cared about being mentioned in connection with the terrorist activity, which is why the organization occasionally took responsibility for crimes that it had nothing to do with.

    The terrorist attack in Krasnogorsk, however, doesn’t match this straightforward strategy usually adopted by IS. In fact, the choice of a rock concert as the site of the terrorist attack is almost the only common feature between this attack and other acts of terror it has committed.

    What preceded the events at Crocus City Hall

    Four people who had not previously known each other were recruited to carry out the terrorist attack. One of them, Shamsidin Fariduni, was in Türkiye in February, and from there he flew to Russia on March 4. He spent at least ten days in Türkiye and investigators are currently determining who he communicated with while there.

    According to unofficial information, he met with a certain “Islamic preacher” in Istanbul. However, it is also known that the terrorists corresponded with the “preacher’s assistant.” According to Fariduni, this anonymous person sponsored and organized the terrorist attack.

    RT

    After arriving in Russia, Fariduni visited Crocus City Hall on March 7 in order to see the site where the crime was to be committed. From this, we may conclude that the attack was to take place soon after his arrival from Türkiye. On the same day, the US embassy in Russia warned its citizens to avoid large gatherings “over the next 48 hours” due to possible attacks by extremists.

    The next concert at Crocus City Hall was given by the singer Shaman, who is known for his patriotism. However, his concert on Saturday, March 9 passed without incident. In the following days, there were other performances at the venue, but apparently the terrorists were forced to adjust their plans.

    As a result, they chose the concert by the band Picnic, scheduled for March 22. Although this band is not as popular as Shaman, it is also known for its patriotic stance and for donating funds for the needs of the Russian Armed Forces in Ukraine.

    ‘The Moscow terror attack was an inside job!’ The strange and twisted world of the West’s political and media Russia haters

    Read more

    ‘The Moscow terror attack was an inside job!’ The strange and twisted world of the West’s political and media Russia haters

    What happened afterwards

    None of the terrorists planned to “join the Houris in paradise,” as is usual for IS followers. After shooting people in Crocus City Hall and setting the building on fire, they did not attack the special forces which arrived at the scene and instead got in a car and fled from Moscow. Neither did they wear “suicide belts” – a characteristic detail of IS followers who are ready to die after committing their crime.

    Another detail which is uncharacteristic for IS is the monetary reward promised to the terrorists. The payment was supposed to be made in two installments – before and after the attack. The terrorists had already received the first payment, amounting to 250,000 rubles ($2,700).

    The most important detail is the location where the terrorists were detained. Traffic cameras allowed intelligence services to monitor where they were headed. They were eventually detained on the federal highway M-3 Ukraine – a route which used to connect Russia and Ukraine but lost much of its international importance after the deterioration of relations between the two countries in 2014, and particularly after the start of Russia’s military operation in 2022.

    The terrorists were detained after passing the turn to route A240, which leads to Belarus. At that moment, it became obvious that there was only one place where they could be headed: Ukraine.

    Despite the fact that the terrorists were armed, only one of them, Mukhammadsobir Fayzov, put up resistance. All of the terrorists were detained alive, which was most likely an order given to the security forces involved in the operation. However, as we mentioned above, the terrorists themselves did not want to die.

    RT

    Moreover, they knew where to go to save their lives: to the Ukrainian border. Later, in his address to the nation, Russian President Vladimir Putin said that a “window” for passage had been opened for them on the Ukrainian side.

    This, too, is uncharacteristic for IS, since someone who carries out a terrorist act, especially an outsider, is always considered “disposable.” Even if he makes it out alive, no one will help him. Moreover, in earlier years, IS usually didn’t take responsibility for an attack if the perpetrator remained alive, as this could harm him during the investigation. However, later the organization no longer cared about this due to the deplorable state in which it found itself.

    All this comes down to the fact that compared to other attacks carried out by IS in the past few years, this one is strikingly different when it comes to the level of preparation, detailed planning, and financial compensation.

    Dmitry Trenin: The American explanation for the Moscow terror attack doesn’t add up

    Read more

    Dmitry Trenin: The American explanation for the Moscow terror attack doesn’t add up

    What does Ukraine have to do with it?

    Having already mentioned Ukraine several times, we must note its links with terrorists. Since 2015, it has been known that the Security Service of Ukraine tried to recruit radical Islamists with the goal of carrying out sabotage and terrorist attacks, etc. on Russian territory. Ukraine’s intelligence services were also active among the terrorists in Syria. This cooperation was marked in particular by the arrival in Ukraine of Chechen terrorist Rustam Azhiev, who served in the International Legion controlled by the Main Directorate of Intelligence of Ukraine’s Defense Ministry.

    Azhiev participated in the second Chechen campaign against the Russian Armed Forces and eventually fled to Türkiye. In 2011, he moved to Syria, where he headed the terrorist group Ajnad Al-Kavkaz. Under his command, the militants participated in hostilities against the Syrian Armed Forces and were noted for terrorist attacks directed against civilians. Azhiev operated side-by-side with groups that are recognized as terrorist organizations not only in the United States, but throughout the world. The main ally of Ajnad Al-Kavkaz was Jabhat Al-Nusra in Syria.

    Over time, the Russian Armed Forces and Syrian Armed Forces liberated territories from terrorists and significantly reduced their supply base. As a result, Azhiev and his associates became involved in contract killings, extortion, torture, and racketeering. In 2019, Azhiev even had to publicly apologize for the actions of his associates, who kidnapped the wrong person.

    The terrorists had been “unemployed” for several years when in 2022, Azhiev and his associates were approached by Ukrainian intelligence services through an intermediary – field commander Akhmed Zakayev. Azhiev and his associates took part in combat operations against the Russian Armed Forces and as a reward, Azhiev was given a Ukrainian passport.

    RT

    In 2024, led by Azhiev, the terrorists participated in an attack on border settlements in Belgorod Region. In a video, Azhiev publicly admitted that the purpose of the operation was to destabilize the situation in Russia before and during the presidential elections. This was confirmed by the fact that the attacks stopped right after the elections.

    After the terrorist attack in Crocus City Hall, the Austrian newspaper Heute discovered another link between Ukraine and radical Islamists. According to the publication, which cites information from intelligence services, many suspected terrorists had entered the EU from Ukraine. For example, in December 2023, a Tajik citizen and his wife, along with an accomplice, were detained in Vienna. They were preparing an attack on St. Stephen’s Cathedral. The couple had come to the EU from Ukraine in February 2022.

    ***

    Ukraine is the place of residence not only for many terrorists, but also IS administrators and those who sympathize with the terrorists. Some of these people are actively involved in raising funds for imprisoned IS fighters in Syria and Iraq. Some of this money goes to purchasing food and medicines. But quite often, it is spent on buying weapons to carry out attacks inside prisons, and for bribing guards. Since some of the terrorists are officially “employed” in Ukraine’s Defense Ministry and others work for the Security Service of Ukraine, they can both push their employers to organize a terrorist attack or do so on their own, without formally consulting the authorities. Currently, one of the versions is that an employee of the Ukrainian intelligence services could’ve been hiding under the guise of the “preacher’s assistant.”



    Moreover, Kiev has prior experience in carrying out terrorist acts on Russian territory – both directly, as in the case of Daria Dugina, and through intermediaries, as in the case of Vladlen Tatarsky. Therefore, using radical Islamists, such as IS followers, to carry out terrorist attacks fully corresponds to Ukraine’s strategy, which comes down to inflicting maximum damage on Russia and its residents.


    ATTENTION READERS

    We See The World From All Sides and Want YOU To Be Fully Informed
    In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion.

    About VT - Policies & Disclosures - Comment Policy
    Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT.

    https://www.vtforeignpolicy.com/2024/03/krainian-caliphate-what-the-west-prefers-not-to-notice-when-blaming-isis-for-the-terrorist-attack-in-moscow/
    Ukrainian ‘Caliphate’: What the West prefers not to notice when blaming ISIS for the terrorist attack in Moscow Kiev’s connections with terrorist groups and Islamists are recognized even in the West. Could Ukrainians be behind the massacre in Crocus City Hall? Jonas E. Alexis, Senior EditorMarch 27, 2024 VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $ 280 BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation; $ 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. On March 22, Russia suffered one of the worst terrorist attacks in recent history, in the course of which 137 people were killed and 182 others were injured. The four terrorists who carried out the attack chose one of the largest exhibition and concert venues in the country, Crocus City Hall, in the city of Krasnogorsk on the outskirts of Moscow, which hosts large events every day. Even though the investigation is still ongoing, the West has already claimed that the Islamic State (IS) is responsible for the tragedy. This was first reported by some media outlets, including Reuters and CNN, and was later picked up by Western officials. For example, on Monday, this was stated by White House Press Secretary Karine Jean-Pierre. However, when we compare this terrorist attack with other IS attacks, we notice more differences than similarities. How IS kills On that fateful Friday night, a concert by Picnic, a St. Petersburg rock band, was supposed to take place in Crocus City Hall. This fact gave rise to comparisons with the horrible terrorist attack in France in November 2015. Back then, terrorists broke into the Bataclan Theater in Paris, where a concert of the US band Eagles of Death Metal was taking place. IS claimed responsibility for the crime, which left 89 people dead. Weapon of mass distraction: Is the West scapegoating Islamic State over Moscow attack? Read more Weapon of mass distraction: Is the West scapegoating Islamic State over Moscow attack? In those years, IS became increasingly active throughout the world – but this was actually a sign of its decline. In its heyday, IS didn’t urge its supporters to carry out terrorist attacks, but instead called on them to “fulfill the hijrah” – i.e., move to the territories controlled by the organization. Over ten years ago, this was quite easy to do, since part of the Syrian border with Turkey was controlled by the jihadists, which allowed people to freely cross it and join their ranks. However, as the terrorists lost many of their territories, their rhetoric changed. Through its information resources, IS urged its followers to commit terrorist acts in places where they lived. This caused an upsurge in violence in Europe: a wave of terror swept through France, Belgium, Germany, the UK, and other countries. In Russia, the North Caucasus became a point of tension. The strategy was simple – anyone who supported the jihadists, wherever they lived, could record a video with an oath of allegiance to the “caliph,” send it via an automated feedback bot, and then commit a terrorist act. Often it was only the perpetrator who died, but for IS, this didn’t matter – it only cared about being mentioned in connection with the terrorist activity, which is why the organization occasionally took responsibility for crimes that it had nothing to do with. The terrorist attack in Krasnogorsk, however, doesn’t match this straightforward strategy usually adopted by IS. In fact, the choice of a rock concert as the site of the terrorist attack is almost the only common feature between this attack and other acts of terror it has committed. What preceded the events at Crocus City Hall Four people who had not previously known each other were recruited to carry out the terrorist attack. One of them, Shamsidin Fariduni, was in Türkiye in February, and from there he flew to Russia on March 4. He spent at least ten days in Türkiye and investigators are currently determining who he communicated with while there. According to unofficial information, he met with a certain “Islamic preacher” in Istanbul. However, it is also known that the terrorists corresponded with the “preacher’s assistant.” According to Fariduni, this anonymous person sponsored and organized the terrorist attack. RT After arriving in Russia, Fariduni visited Crocus City Hall on March 7 in order to see the site where the crime was to be committed. From this, we may conclude that the attack was to take place soon after his arrival from Türkiye. On the same day, the US embassy in Russia warned its citizens to avoid large gatherings “over the next 48 hours” due to possible attacks by extremists. The next concert at Crocus City Hall was given by the singer Shaman, who is known for his patriotism. However, his concert on Saturday, March 9 passed without incident. In the following days, there were other performances at the venue, but apparently the terrorists were forced to adjust their plans. As a result, they chose the concert by the band Picnic, scheduled for March 22. Although this band is not as popular as Shaman, it is also known for its patriotic stance and for donating funds for the needs of the Russian Armed Forces in Ukraine. ‘The Moscow terror attack was an inside job!’ The strange and twisted world of the West’s political and media Russia haters Read more ‘The Moscow terror attack was an inside job!’ The strange and twisted world of the West’s political and media Russia haters What happened afterwards None of the terrorists planned to “join the Houris in paradise,” as is usual for IS followers. After shooting people in Crocus City Hall and setting the building on fire, they did not attack the special forces which arrived at the scene and instead got in a car and fled from Moscow. Neither did they wear “suicide belts” – a characteristic detail of IS followers who are ready to die after committing their crime. Another detail which is uncharacteristic for IS is the monetary reward promised to the terrorists. The payment was supposed to be made in two installments – before and after the attack. The terrorists had already received the first payment, amounting to 250,000 rubles ($2,700). The most important detail is the location where the terrorists were detained. Traffic cameras allowed intelligence services to monitor where they were headed. They were eventually detained on the federal highway M-3 Ukraine – a route which used to connect Russia and Ukraine but lost much of its international importance after the deterioration of relations between the two countries in 2014, and particularly after the start of Russia’s military operation in 2022. The terrorists were detained after passing the turn to route A240, which leads to Belarus. At that moment, it became obvious that there was only one place where they could be headed: Ukraine. Despite the fact that the terrorists were armed, only one of them, Mukhammadsobir Fayzov, put up resistance. All of the terrorists were detained alive, which was most likely an order given to the security forces involved in the operation. However, as we mentioned above, the terrorists themselves did not want to die. RT Moreover, they knew where to go to save their lives: to the Ukrainian border. Later, in his address to the nation, Russian President Vladimir Putin said that a “window” for passage had been opened for them on the Ukrainian side. This, too, is uncharacteristic for IS, since someone who carries out a terrorist act, especially an outsider, is always considered “disposable.” Even if he makes it out alive, no one will help him. Moreover, in earlier years, IS usually didn’t take responsibility for an attack if the perpetrator remained alive, as this could harm him during the investigation. However, later the organization no longer cared about this due to the deplorable state in which it found itself. All this comes down to the fact that compared to other attacks carried out by IS in the past few years, this one is strikingly different when it comes to the level of preparation, detailed planning, and financial compensation. Dmitry Trenin: The American explanation for the Moscow terror attack doesn’t add up Read more Dmitry Trenin: The American explanation for the Moscow terror attack doesn’t add up What does Ukraine have to do with it? Having already mentioned Ukraine several times, we must note its links with terrorists. Since 2015, it has been known that the Security Service of Ukraine tried to recruit radical Islamists with the goal of carrying out sabotage and terrorist attacks, etc. on Russian territory. Ukraine’s intelligence services were also active among the terrorists in Syria. This cooperation was marked in particular by the arrival in Ukraine of Chechen terrorist Rustam Azhiev, who served in the International Legion controlled by the Main Directorate of Intelligence of Ukraine’s Defense Ministry. Azhiev participated in the second Chechen campaign against the Russian Armed Forces and eventually fled to Türkiye. In 2011, he moved to Syria, where he headed the terrorist group Ajnad Al-Kavkaz. Under his command, the militants participated in hostilities against the Syrian Armed Forces and were noted for terrorist attacks directed against civilians. Azhiev operated side-by-side with groups that are recognized as terrorist organizations not only in the United States, but throughout the world. The main ally of Ajnad Al-Kavkaz was Jabhat Al-Nusra in Syria. Over time, the Russian Armed Forces and Syrian Armed Forces liberated territories from terrorists and significantly reduced their supply base. As a result, Azhiev and his associates became involved in contract killings, extortion, torture, and racketeering. In 2019, Azhiev even had to publicly apologize for the actions of his associates, who kidnapped the wrong person. The terrorists had been “unemployed” for several years when in 2022, Azhiev and his associates were approached by Ukrainian intelligence services through an intermediary – field commander Akhmed Zakayev. Azhiev and his associates took part in combat operations against the Russian Armed Forces and as a reward, Azhiev was given a Ukrainian passport. RT In 2024, led by Azhiev, the terrorists participated in an attack on border settlements in Belgorod Region. In a video, Azhiev publicly admitted that the purpose of the operation was to destabilize the situation in Russia before and during the presidential elections. This was confirmed by the fact that the attacks stopped right after the elections. After the terrorist attack in Crocus City Hall, the Austrian newspaper Heute discovered another link between Ukraine and radical Islamists. According to the publication, which cites information from intelligence services, many suspected terrorists had entered the EU from Ukraine. For example, in December 2023, a Tajik citizen and his wife, along with an accomplice, were detained in Vienna. They were preparing an attack on St. Stephen’s Cathedral. The couple had come to the EU from Ukraine in February 2022. *** Ukraine is the place of residence not only for many terrorists, but also IS administrators and those who sympathize with the terrorists. Some of these people are actively involved in raising funds for imprisoned IS fighters in Syria and Iraq. Some of this money goes to purchasing food and medicines. But quite often, it is spent on buying weapons to carry out attacks inside prisons, and for bribing guards. Since some of the terrorists are officially “employed” in Ukraine’s Defense Ministry and others work for the Security Service of Ukraine, they can both push their employers to organize a terrorist attack or do so on their own, without formally consulting the authorities. Currently, one of the versions is that an employee of the Ukrainian intelligence services could’ve been hiding under the guise of the “preacher’s assistant.” Moreover, Kiev has prior experience in carrying out terrorist acts on Russian territory – both directly, as in the case of Daria Dugina, and through intermediaries, as in the case of Vladlen Tatarsky. Therefore, using radical Islamists, such as IS followers, to carry out terrorist attacks fully corresponds to Ukraine’s strategy, which comes down to inflicting maximum damage on Russia and its residents. ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/03/krainian-caliphate-what-the-west-prefers-not-to-notice-when-blaming-isis-for-the-terrorist-attack-in-moscow/
    WWW.VTFOREIGNPOLICY.COM
    Ukrainian ‘Caliphate’: What the West prefers not to notice when blaming ISIS for the terrorist attack in Moscow
    Kiev’s connections with terrorist groups and Islamists are recognized even in the West. Could Ukrainians be behind the massacre in Crocus City Hall?
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  • DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA

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

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

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

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

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

    TLDR

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

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

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

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

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

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

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

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

    Now, the first results are in.

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

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

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

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

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

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

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

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


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

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

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


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

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

    ‘Major advance,’ but clinical implications are limited

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

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

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

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

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

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

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

    LNPs deliver contaminant DNA straight to the cells

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

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

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


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

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

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

    Regulators unconcerned

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

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

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

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

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

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

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

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

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

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

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

    ‘No excuse’ for ignoring ‘screaming hot signal’

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

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

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

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

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


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

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

    Scientists pick up regulators’ slack

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

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

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

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

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

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

    Decentralisation the future of science?

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

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

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

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


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

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

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

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


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

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

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

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

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

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

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


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    Follow me on X

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

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

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

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

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

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

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

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


    https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows It also appears that the contamination enters the cell nucleus and integrates with human DNA Rebekah Barnett Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can. The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells. Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say. And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say. However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA. TLDR 1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable) 2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient) 3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination 4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA. Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process. McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.” Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients. But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan. While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration. Now, the first results are in. In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine. The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites. “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says. “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.” To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls. The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan. Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA. This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with. Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA. “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.” Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan. Source: Kevin McKernan’s Substack Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line. You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’ ‘Major advance,’ but clinical implications are limited McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.” “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries. The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells. McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately. At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan. The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety. Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English). LNPs deliver contaminant DNA straight to the cells A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur. This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes. This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems. Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021 From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.” It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis. Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines. Regulators unconcerned I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment. The TGA did not address the new findings, but a spokesperson from the TGA responded, “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.” However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims. Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised. Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted. In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year. Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories. Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning. Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further. The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk. ‘No excuse’ for ignoring ‘screaming hot signal’ Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan. Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.” “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?” There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years. “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.” Source: National Human Genome Research Institute DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination. “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.” Scientists pick up regulators’ slack In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton. “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.” Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites. In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in. “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said. McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present. Decentralisation the future of science? McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust. “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan. “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“ In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world. Source: X For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation. “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan. Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet. Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct. Source: X In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.” But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa. Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not. The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received. View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files. Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina. Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account. To support my work, make a one-off contribution to DDU via my Kofi account and/or subscribe. Thanks! Follow me on X Follow me on Instagram 1 From an article I wrote for Umbrella News on this topic last year: The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News, “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.” “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.” With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected). As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims. The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken. Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed. https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    NEWS.REBEKAHBARNETT.COM.AU
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA
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  • FDA Loses its War on Ivermectin: Agrees to Remove All Related Social Media Content and Consumer Advisories on Ivermectin Usage for COVID-19
    by Jim Hᴏft Mar. 22, 2024 8:30 am
    In December 2021, the FDA warned Americans not to use Ivermectin, which “is intended for animals” to treat or prevent COVID-19.

    “Never use medications intended for animals on yourself or other people. Animal ivermectin products are very different from those approved for humans. Use of animal ivermectin for the prevention or treatment of COVID-19 in humans is dangerous,” FDA said at the time.

    This was a very controversial statement at the time since the FDA pushed the drug on African migrants back in 2015, and the drug was praised in several scientific journals.

    There have now been 101 Ivermectin COVID-19 controlled studies that show a 62% lower risk in early treatment in COVID-19 patients.

    New Deals At The Gateway Pundit Discounts Page At MyPillow – Up to 71% Off With Promo Code TGP

    A group of brave doctors had filed a federal lawsuit against the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) over the agencies’ unlawful attempts to block the use of ivermectin in treating COVID-19.

    The lawsuit, filed in the U.S. Southern District of Texas in Galveston, argues that the FDA has overstepped its authority and unjustifiably interfered with their medical practice.

    The plaintiffs, Drs. Mary Talley Bowden, Paul E. Marik, and Robert L. Apter, are contesting the FDA’s portrayal of ivermectin as dangerous for human consumption. They note that the FDA has approved ivermectin for human use since 1996 for a variety of diseases. However, they allege that with the advent of the COVID-19 pandemic, the FDA began releasing documents and social media posts discouraging the use of the anti-viral drug for COVID-19 treatment.

    “We’re suing the FDA for lying to the public about ivermectin,” said Dr. Bowden.

    Claims were made that the initial article misrepresented the law by stating the FDA’s official stance against Ivermectin use without mentioning that doctors were allowed to administer the medicine.

    U.S. law is cited in the complaint, including the provision that the FDA “may not interfere with the authority of a health care provider to prescribe or administer any legally marked device to a patient for any condition or disease within a legitimate health care practitioner-patient relationship.”

    On Thursday, the U.S. Food and Drug Administration (FDA) reportedly agreed to remove all its previous social media posts and consumer advisories that specifically addressed the use of ivermectin for the treatment or prevention of COVID-19.

    “FDA loses its war on ivermectin and agrees to remove all social media posts and consumer directives regarding ivermectin and COVID, including its most popular tweet in FDA history. This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship,” Dr. Bowden wrote on her social media.

    Emily Post News reported:

    The FDA agreed to delete the Twitter, LinkedIn, and Facebook posts from August 21, 2021 that read, “You are not a horse. You are not a cow. Seriously, y’all. Stop it.” (A screencap of the X/twitter one is above and still online here.)

    It will also remove the Twitter post (below) from April 26, 2022 that reads, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.

    Further, the FDA will delete all other social media posts on FDA accounts that link to its website (below) called “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19.”

    It will “retire” this website (called a consumer update) originally posted on March 5, 2021 and revised on September 7, 2021. The FDA retains the right to post a revised update.

    Bowden said she and her co-plaintiffs Dr. Paul E. Marik and Dr. Robert L. Apter decided to drop the lawsuit they got what they wanted.

    “After nearly two years and a resounding rebuke by the Fifth Circuit Court of Appeals, the FDA has agreed to remove its misleading social media posts and consumer directives regarding ivermectin and Covid-19,” said Bowden.

    Trending: MAGA Beauty Isabella DeLuca’s Arrest Is Proof Positive That Biden’s Weaponized Justice System Has Become Outright Despotic Against Political Dissidents


    The Gateway Pundit previously reported that during a hearing, the agency’s lawyers argued that the FDA was only giving advice and it was not mandatory when it told people to “stop” taking Ivermectin for COVID-19.

    “The cited statements were not directives,” said Isaac Belfer, one of the lawyers. “They were not mandatory. They were recommendations. They said what parties should do. They said, for example, why you should not take ivermectin to treat COVID-19. They did not say you may not do it, you must not do it. They did not say it’s prohibited or it’s unlawful. They also did not say that doctors may not prescribe ivermectin.”

    “They use informal language, that is true… It’s conversational but not mandatory,” he continued.

    However, the statement from the lawyer contradicted the FDA’s social media post, stating, “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” and another tweet says, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.”

    Both tweets displayed the title of “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19” and included a link to that publication.

    Last year, Doctors Mary Talley Bowden, Paul Marik, & Robert Apter appeared in the Fifth Circuit Court of Appeals as part of their lawsuit.

    “The FDA is not your doctor. Yesterday we took them to court to remind them of that,” Dr. Bowden wrote.

    “A pharmacist cites CDC and US FDA as why she will continue to deny filling prescriptions for ivermectin. On Tuesday, the FDA’s attorney declared the FDA has no problem with doctors prescribing ivermectin off-label. It’s time for them to make a formal announcement and set the record straight,” Bowden wrote on Thursday.

    During the oral argument, Ashley Cheung Honold, a Department of Justice lawyer representing the FDA stated that the agency “explicitly recognizes” that doctors do have the authority to administer ivermectin to treat COVID.

    “”FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” said Honold.

    “FDA made these statements in response to multiple reports of consumers being hospitalized, after self-medicating with ivermectin intended for horses, which is available for purchase over the counter without the need for prescription,” Honold said.

    “In some contexts, those words could be construed as a command,” Ms. Honold said. “But in this context, where FDA was simply using these words in the context of a quippy tweet meant to share its informational article, those statements do not rise to the level of a command.”

    “FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” she said.

    It can be recalled that Houston Methodist launched an investigation into Bowden and suspended her for defying health authorities and exercising free speech.

    The hospital excoriated Bowden for “using her social media accounts to express her personal opinions about the COVID-19 vaccine and treatments,” NBC News reports. The suspension barred the physician from admitting or treating patients at the hospital.

    Bowden repeatedly warned that it is “wrong” to mandate the experimental mRNA vaccines and continuously touted Ivermectin as a safe and effective treatment amid threats from public health officials against prescribing the drug.

    Bowden was forced to resign. In her resignation letter, Bowden doubled down on the efficacy of Ivermectin.

    “I have worked hard to provide early treatment for victims of COVID-19. My efforts have been successful. I have treated more than 200 COVID-19 patients, including many with co-morbidities, and none of these patients have required hospitalization. This is a testament to the success of my treatment methods,” she wrote. “Throughout this pandemic, there has been no FDA-approved treatment for COVID. Therefore I have done my best to care for patients and save lives in the absence of a clear scientific consensus.”

    “Early treatment must still be part of any strategy for patient care. That is why physicians and hospitals should pay more attention to medications such as Ivermectin, which significant research and my clinical experience indicate is effective,” she continued. “I have decided to part ways with Houston Methodist because of the accusation that I have been spreading “dangerous information.” This is false and defamatory. I do not spread misinformation, and my opinions are supported by science. There is substantial evidence for the efficacy of Ivermectin in treating COVID-19, and no evidence for serious or fatal side effects associated with the doses used to treat COVID-19.”


    The U.S. FDA was sued over its false statements about ivermectin and now has to remove those false statements from their social media posts https://www.thegatewaypundit.com/2024/03/fda-loses-its-war-ivermectin-agrees-remove-all/. I wonder if the Singapore MOH is following this development.


    FDA Loses its War on Ivermectin: Agrees to Remove All Related Social Media Content and Consumer Advisories on Ivermectin Usage for COVID-19 by Jim Hᴏft Mar. 22, 2024 8:30 am In December 2021, the FDA warned Americans not to use Ivermectin, which “is intended for animals” to treat or prevent COVID-19. “Never use medications intended for animals on yourself or other people. Animal ivermectin products are very different from those approved for humans. Use of animal ivermectin for the prevention or treatment of COVID-19 in humans is dangerous,” FDA said at the time. This was a very controversial statement at the time since the FDA pushed the drug on African migrants back in 2015, and the drug was praised in several scientific journals. There have now been 101 Ivermectin COVID-19 controlled studies that show a 62% lower risk in early treatment in COVID-19 patients. New Deals At The Gateway Pundit Discounts Page At MyPillow – Up to 71% Off With Promo Code TGP A group of brave doctors had filed a federal lawsuit against the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) over the agencies’ unlawful attempts to block the use of ivermectin in treating COVID-19. The lawsuit, filed in the U.S. Southern District of Texas in Galveston, argues that the FDA has overstepped its authority and unjustifiably interfered with their medical practice. The plaintiffs, Drs. Mary Talley Bowden, Paul E. Marik, and Robert L. Apter, are contesting the FDA’s portrayal of ivermectin as dangerous for human consumption. They note that the FDA has approved ivermectin for human use since 1996 for a variety of diseases. However, they allege that with the advent of the COVID-19 pandemic, the FDA began releasing documents and social media posts discouraging the use of the anti-viral drug for COVID-19 treatment. “We’re suing the FDA for lying to the public about ivermectin,” said Dr. Bowden. Claims were made that the initial article misrepresented the law by stating the FDA’s official stance against Ivermectin use without mentioning that doctors were allowed to administer the medicine. U.S. law is cited in the complaint, including the provision that the FDA “may not interfere with the authority of a health care provider to prescribe or administer any legally marked device to a patient for any condition or disease within a legitimate health care practitioner-patient relationship.” On Thursday, the U.S. Food and Drug Administration (FDA) reportedly agreed to remove all its previous social media posts and consumer advisories that specifically addressed the use of ivermectin for the treatment or prevention of COVID-19. “FDA loses its war on ivermectin and agrees to remove all social media posts and consumer directives regarding ivermectin and COVID, including its most popular tweet in FDA history. This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship,” Dr. Bowden wrote on her social media. Emily Post News reported: The FDA agreed to delete the Twitter, LinkedIn, and Facebook posts from August 21, 2021 that read, “You are not a horse. You are not a cow. Seriously, y’all. Stop it.” (A screencap of the X/twitter one is above and still online here.) It will also remove the Twitter post (below) from April 26, 2022 that reads, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19. Further, the FDA will delete all other social media posts on FDA accounts that link to its website (below) called “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19.” It will “retire” this website (called a consumer update) originally posted on March 5, 2021 and revised on September 7, 2021. The FDA retains the right to post a revised update. Bowden said she and her co-plaintiffs Dr. Paul E. Marik and Dr. Robert L. Apter decided to drop the lawsuit they got what they wanted. “After nearly two years and a resounding rebuke by the Fifth Circuit Court of Appeals, the FDA has agreed to remove its misleading social media posts and consumer directives regarding ivermectin and Covid-19,” said Bowden. Trending: MAGA Beauty Isabella DeLuca’s Arrest Is Proof Positive That Biden’s Weaponized Justice System Has Become Outright Despotic Against Political Dissidents The Gateway Pundit previously reported that during a hearing, the agency’s lawyers argued that the FDA was only giving advice and it was not mandatory when it told people to “stop” taking Ivermectin for COVID-19. “The cited statements were not directives,” said Isaac Belfer, one of the lawyers. “They were not mandatory. They were recommendations. They said what parties should do. They said, for example, why you should not take ivermectin to treat COVID-19. They did not say you may not do it, you must not do it. They did not say it’s prohibited or it’s unlawful. They also did not say that doctors may not prescribe ivermectin.” “They use informal language, that is true… It’s conversational but not mandatory,” he continued. However, the statement from the lawyer contradicted the FDA’s social media post, stating, “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” and another tweet says, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.” Both tweets displayed the title of “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19” and included a link to that publication. Last year, Doctors Mary Talley Bowden, Paul Marik, & Robert Apter appeared in the Fifth Circuit Court of Appeals as part of their lawsuit. “The FDA is not your doctor. Yesterday we took them to court to remind them of that,” Dr. Bowden wrote. “A pharmacist cites CDC and US FDA as why she will continue to deny filling prescriptions for ivermectin. On Tuesday, the FDA’s attorney declared the FDA has no problem with doctors prescribing ivermectin off-label. It’s time for them to make a formal announcement and set the record straight,” Bowden wrote on Thursday. During the oral argument, Ashley Cheung Honold, a Department of Justice lawyer representing the FDA stated that the agency “explicitly recognizes” that doctors do have the authority to administer ivermectin to treat COVID. “”FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” said Honold. “FDA made these statements in response to multiple reports of consumers being hospitalized, after self-medicating with ivermectin intended for horses, which is available for purchase over the counter without the need for prescription,” Honold said. “In some contexts, those words could be construed as a command,” Ms. Honold said. “But in this context, where FDA was simply using these words in the context of a quippy tweet meant to share its informational article, those statements do not rise to the level of a command.” “FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” she said. It can be recalled that Houston Methodist launched an investigation into Bowden and suspended her for defying health authorities and exercising free speech. The hospital excoriated Bowden for “using her social media accounts to express her personal opinions about the COVID-19 vaccine and treatments,” NBC News reports. The suspension barred the physician from admitting or treating patients at the hospital. Bowden repeatedly warned that it is “wrong” to mandate the experimental mRNA vaccines and continuously touted Ivermectin as a safe and effective treatment amid threats from public health officials against prescribing the drug. Bowden was forced to resign. In her resignation letter, Bowden doubled down on the efficacy of Ivermectin. “I have worked hard to provide early treatment for victims of COVID-19. My efforts have been successful. I have treated more than 200 COVID-19 patients, including many with co-morbidities, and none of these patients have required hospitalization. This is a testament to the success of my treatment methods,” she wrote. “Throughout this pandemic, there has been no FDA-approved treatment for COVID. Therefore I have done my best to care for patients and save lives in the absence of a clear scientific consensus.” “Early treatment must still be part of any strategy for patient care. That is why physicians and hospitals should pay more attention to medications such as Ivermectin, which significant research and my clinical experience indicate is effective,” she continued. “I have decided to part ways with Houston Methodist because of the accusation that I have been spreading “dangerous information.” This is false and defamatory. I do not spread misinformation, and my opinions are supported by science. There is substantial evidence for the efficacy of Ivermectin in treating COVID-19, and no evidence for serious or fatal side effects associated with the doses used to treat COVID-19.” The U.S. FDA was sued over its false statements about ivermectin and now has to remove those false statements from their social media posts https://www.thegatewaypundit.com/2024/03/fda-loses-its-war-ivermectin-agrees-remove-all/. I wonder if the Singapore MOH is following this development.
    0 Comments 0 Shares 16392 Views
  • Lawsuit Drops Bombshell on FDA’s Orwellian Lie About Ivermectin
    The FDA has lost its war on ivermectin and agreed to remove all related social media content and consumer advisories on ivermectin usage for COVID-19.

    vnninfluencersMarch 22, 2024
    This article originally appeared on The Gateway Pundit and was republished with permission.

    Guest post by Jim Hᴏft

    In December 2021, the FDA warned Americans not to use Ivermectin, which “is intended for animals” to treat or prevent COVID-19.

    “Never use medications intended for animals on yourself or other people. Animal ivermectin products are very different from those approved for humans. Use of animal ivermectin for the prevention or treatment of COVID-19 in humans is dangerous,” FDA said at the time.

    This was a very controversial statement at the time since the FDA pushed the drug on African migrants back in 2015, and the drug was praised in several scientific journals.

    There have now been 101 Ivermectin COVID-19 controlled studies that show a 62% lower risk in early treatment in COVID-19 patients.



    A group of brave doctors had filed a federal lawsuit against the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) over the agencies’ unlawful attempts to block the use of ivermectin in treating COVID-19.

    The lawsuit, filed in the U.S. Southern District of Texas in Galveston, argues that the FDA has overstepped its authority and unjustifiably interfered with their medical practice.

    The plaintiffs, Drs. Mary Talley Bowden, Paul E. Marik, and Robert L. Apter, are contesting the FDA’s portrayal of ivermectin as dangerous for human consumption. They note that the FDA has approved ivermectin for human use since 1996 for a variety of diseases. However, they allege that with the advent of the COVID-19 pandemic, the FDA began releasing documents and social media posts discouraging the use of the anti-viral drug for COVID-19 treatment.

    “We’re suing the FDA for lying to the public about ivermectin,” said Dr. Bowden.

    Claims were made that the initial article misrepresented the law by stating the FDA’s official stance against Ivermectin use without mentioning that doctors were allowed to administer the medicine.

    U.S. law is cited in the complaint, including the provision that the FDA “may not interfere with the authority of a health care provider to prescribe or administer any legally marked device to a patient for any condition or disease within a legitimate health care practitioner-patient relationship.”

    On Thursday, the U.S. Food and Drug Administration (FDA) reportedly agreed to remove all its previous social media posts and consumer advisories that specifically addressed the use of ivermectin for the treatment or prevention of COVID-19.

    “FDA loses its war on ivermectin and agrees to remove all social media posts and consumer directives regarding ivermectin and COVID, including its most popular tweet in FDA history. This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship,” Dr. Bowden wrote on her social media.

    The plaintiffs have recently received the signed court order and are preparing to issue a press release about it later today.


    The Gateway Pundit previously reported that during a hearing, the agency’s lawyers argued that the FDA was only giving advice and it was not mandatory when it told people to “stop” taking Ivermectin for COVID-19.

    “The cited statements were not directives,” said Isaac Belfer, one of the lawyers. “They were not mandatory. They were recommendations. They said what parties should do. They said, for example, why you should not take ivermectin to treat COVID-19. They did not say you may not do it, you must not do it. They did not say it’s prohibited or it’s unlawful. They also did not say that doctors may not prescribe ivermectin.”

    “They use informal language, that is true… It’s conversational but not mandatory,” he continued.

    However, the statement from the lawyer contradicted the FDA’s social media post, stating, “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” and another tweet says, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.”

    Both tweets displayed the title of “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19” and included a link to that publication.




    Last year, Doctors Mary Talley Bowden, Paul Marik, & Robert Apter appeared in the Fifth Circuit Court of Appeals as part of their lawsuit.

    “The FDA is not your doctor. Yesterday we took them to court to remind them of that,” Dr. Bowden wrote.

    “A pharmacist cites CDC and US FDA as why she will continue to deny filling prescriptions for ivermectin. On Tuesday, the FDA’s attorney declared the FDA has no problem with doctors prescribing ivermectin off-label. It’s time for them to make a formal announcement and set the record straight,” Bowden wrote on Thursday.

    During the oral argument, Ashley Cheung Honold, a Department of Justice lawyer representing the FDA stated that the agency “explicitly recognizes” that doctors do have the authority to administer ivermectin to treat COVID.

    “”FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” said Honold.

    “FDA made these statements in response to multiple reports of consumers being hospitalized, after self-medicating with ivermectin intended for horses, which is available for purchase over the counter without the need for prescription,” Honold said.

    “In some contexts, those words could be construed as a command,” Ms. Honold said. “But in this context, where FDA was simply using these words in the context of a quippy tweet meant to share its informational article, those statements do not rise to the level of a command.”

    “FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” she said.

    It can be recalled that Houston Methodist launched an investigation into Bowden and suspended her for defying health authorities and exercising free speech.

    The hospital excoriated Bowden for “using her social media accounts to express her personal opinions about the COVID-19 vaccine and treatments,” NBC News reports. The suspension barred the physician from admitting or treating patients at the hospital.

    Bowden repeatedly warned that it is “wrong” to mandate the experimental mRNA vaccines and continuously touted Ivermectin as a safe and effective treatment amid threats from public health officials against prescribing the drug.

    Bowden was forced to resign. In her resignation letter, Bowden doubled down on the efficacy of Ivermectin.

    “I have worked hard to provide early treatment for victims of COVID-19. My efforts have been successful. I have treated more than 200 COVID-19 patients, including many with co-morbidities, and none of these patients have required hospitalization. This is a testament to the success of my treatment methods,” she wrote. “Throughout this pandemic, there has been no FDA-approved treatment for COVID. Therefore I have done my best to care for patients and save lives in the absence of a clear scientific consensus.”

    “Early treatment must still be part of any strategy for patient care. That is why physicians and hospitals should pay more attention to medications such as Ivermectin, which significant research and my clinical experience indicate is effective,” she continued. “I have decided to part ways with Houston Methodist because of the accusation that I have been spreading “dangerous information.” This is false and defamatory. I do not spread misinformation, and my opinions are supported by science. There is substantial evidence for the efficacy of Ivermectin in treating COVID-19, and no evidence for serious or fatal side effects associated with the doses used to treat COVID-19.”

    Copyright 2024 The Gateway Pundit


    https://vigilantnews.com/post/lawsuit-drops-bombshell-on-fdas-orwellian-lie-about-ivermectin/
    Lawsuit Drops Bombshell on FDA’s Orwellian Lie About Ivermectin The FDA has lost its war on ivermectin and agreed to remove all related social media content and consumer advisories on ivermectin usage for COVID-19. vnninfluencersMarch 22, 2024 This article originally appeared on The Gateway Pundit and was republished with permission. Guest post by Jim Hᴏft In December 2021, the FDA warned Americans not to use Ivermectin, which “is intended for animals” to treat or prevent COVID-19. “Never use medications intended for animals on yourself or other people. Animal ivermectin products are very different from those approved for humans. Use of animal ivermectin for the prevention or treatment of COVID-19 in humans is dangerous,” FDA said at the time. This was a very controversial statement at the time since the FDA pushed the drug on African migrants back in 2015, and the drug was praised in several scientific journals. There have now been 101 Ivermectin COVID-19 controlled studies that show a 62% lower risk in early treatment in COVID-19 patients. A group of brave doctors had filed a federal lawsuit against the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) over the agencies’ unlawful attempts to block the use of ivermectin in treating COVID-19. The lawsuit, filed in the U.S. Southern District of Texas in Galveston, argues that the FDA has overstepped its authority and unjustifiably interfered with their medical practice. The plaintiffs, Drs. Mary Talley Bowden, Paul E. Marik, and Robert L. Apter, are contesting the FDA’s portrayal of ivermectin as dangerous for human consumption. They note that the FDA has approved ivermectin for human use since 1996 for a variety of diseases. However, they allege that with the advent of the COVID-19 pandemic, the FDA began releasing documents and social media posts discouraging the use of the anti-viral drug for COVID-19 treatment. “We’re suing the FDA for lying to the public about ivermectin,” said Dr. Bowden. Claims were made that the initial article misrepresented the law by stating the FDA’s official stance against Ivermectin use without mentioning that doctors were allowed to administer the medicine. U.S. law is cited in the complaint, including the provision that the FDA “may not interfere with the authority of a health care provider to prescribe or administer any legally marked device to a patient for any condition or disease within a legitimate health care practitioner-patient relationship.” On Thursday, the U.S. Food and Drug Administration (FDA) reportedly agreed to remove all its previous social media posts and consumer advisories that specifically addressed the use of ivermectin for the treatment or prevention of COVID-19. “FDA loses its war on ivermectin and agrees to remove all social media posts and consumer directives regarding ivermectin and COVID, including its most popular tweet in FDA history. This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship,” Dr. Bowden wrote on her social media. The plaintiffs have recently received the signed court order and are preparing to issue a press release about it later today. The Gateway Pundit previously reported that during a hearing, the agency’s lawyers argued that the FDA was only giving advice and it was not mandatory when it told people to “stop” taking Ivermectin for COVID-19. “The cited statements were not directives,” said Isaac Belfer, one of the lawyers. “They were not mandatory. They were recommendations. They said what parties should do. They said, for example, why you should not take ivermectin to treat COVID-19. They did not say you may not do it, you must not do it. They did not say it’s prohibited or it’s unlawful. They also did not say that doctors may not prescribe ivermectin.” “They use informal language, that is true… It’s conversational but not mandatory,” he continued. However, the statement from the lawyer contradicted the FDA’s social media post, stating, “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” and another tweet says, “Hold your horses, y’all. Ivermectin may be trending, but it still isn’t authorized or approved to treat COVID-19.” Both tweets displayed the title of “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19” and included a link to that publication. Last year, Doctors Mary Talley Bowden, Paul Marik, & Robert Apter appeared in the Fifth Circuit Court of Appeals as part of their lawsuit. “The FDA is not your doctor. Yesterday we took them to court to remind them of that,” Dr. Bowden wrote. “A pharmacist cites CDC and US FDA as why she will continue to deny filling prescriptions for ivermectin. On Tuesday, the FDA’s attorney declared the FDA has no problem with doctors prescribing ivermectin off-label. It’s time for them to make a formal announcement and set the record straight,” Bowden wrote on Thursday. During the oral argument, Ashley Cheung Honold, a Department of Justice lawyer representing the FDA stated that the agency “explicitly recognizes” that doctors do have the authority to administer ivermectin to treat COVID. “”FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID,” said Honold. “FDA made these statements in response to multiple reports of consumers being hospitalized, after self-medicating with ivermectin intended for horses, which is available for purchase over the counter without the need for prescription,” Honold said. “In some contexts, those words could be construed as a command,” Ms. Honold said. “But in this context, where FDA was simply using these words in the context of a quippy tweet meant to share its informational article, those statements do not rise to the level of a command.” “FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” she said. It can be recalled that Houston Methodist launched an investigation into Bowden and suspended her for defying health authorities and exercising free speech. The hospital excoriated Bowden for “using her social media accounts to express her personal opinions about the COVID-19 vaccine and treatments,” NBC News reports. The suspension barred the physician from admitting or treating patients at the hospital. Bowden repeatedly warned that it is “wrong” to mandate the experimental mRNA vaccines and continuously touted Ivermectin as a safe and effective treatment amid threats from public health officials against prescribing the drug. Bowden was forced to resign. In her resignation letter, Bowden doubled down on the efficacy of Ivermectin. “I have worked hard to provide early treatment for victims of COVID-19. My efforts have been successful. I have treated more than 200 COVID-19 patients, including many with co-morbidities, and none of these patients have required hospitalization. This is a testament to the success of my treatment methods,” she wrote. “Throughout this pandemic, there has been no FDA-approved treatment for COVID. Therefore I have done my best to care for patients and save lives in the absence of a clear scientific consensus.” “Early treatment must still be part of any strategy for patient care. That is why physicians and hospitals should pay more attention to medications such as Ivermectin, which significant research and my clinical experience indicate is effective,” she continued. “I have decided to part ways with Houston Methodist because of the accusation that I have been spreading “dangerous information.” This is false and defamatory. I do not spread misinformation, and my opinions are supported by science. There is substantial evidence for the efficacy of Ivermectin in treating COVID-19, and no evidence for serious or fatal side effects associated with the doses used to treat COVID-19.” Copyright 2024 The Gateway Pundit https://vigilantnews.com/post/lawsuit-drops-bombshell-on-fdas-orwellian-lie-about-ivermectin/
    VIGILANTNEWS.COM
    Lawsuit Drops Bombshell on FDA’s Orwellian Lie About Ivermectin
    The FDA has lost its war on ivermectin and agreed to remove all related social media content and consumer advisories on ivermectin usage for COVID-19.
    1 Comments 0 Shares 12363 Views
  • ISIS claims responsibility for attack at Moscow-area concert venue that left at least 60 dead
    CNN — normal
    ISIS has claimed responsibility for an attack at a popular concert hall complex near Moscow Friday after assailants stormed the venue with guns and incendiary devices, killing at least 60 people and injuring 145.

    The terror group took responsibility for the attack in a short statement published by ISIS-affiliated news agency Amaq on Telegram on Friday. It did not provide evidence to support the claim.

    Video footage from the Crocus City Hall shows the vast complex, which is home to both the music hall and a shopping center, on fire with smoke billowing into the air. State-run RIA Novosti reported the armed individuals “opened fire with automatic weapons” and “threw a grenade or an incendiary bomb, which started a fire.” They then “allegedly fled in a white Renault car,” the news agency said.

    State media Russia 24 reported the roof of the venue has partially collapsed.

    The fire had been brought largely under control more than six hours later. “There are still some pockets of fire, but the fire has been mostly eliminated,” Moscow governor Andrey Vorobyov said on Telegram.

    The deadliest terror attack on Moscow in decades, Friday’s assault came less than a week after President Vladimir Putin won a stage-managed election by an overwhelming majority to secure another term in office, tightening his grip on the country he has ruled since the turn of the century.

    With attention focused on the country’s war with neighboring Ukraine, Putin had trumpeted a message of national security before Russians went to the polls.

    The carnage broke out before a concert by the band Picnic, according to Russia 24.

    “Unidentified people in camouflage broke into Crocus City Hall and started shooting before the start of the concert,” the Prosecutor General’s Office said, cited by TASS.

    This screen grab from video shows armed men inside the Crocus City Hall concert venue in Moscow region, Russia. CNN can not verify whether these are the armed attackers or Russian authorities moving in.
    Video footage showed panic as the attack unfolded, with crowds of people huddling together, screaming and ducking behind cushioned seats as gunshots started echoing in the vast hall. One group sheltering next to a large wall of windows outside the concert venue were forced to break them to escape the gunfire, video obtained by CNN shows.

    Footage geolocated by CNN shows an armed individual starting at least one fire inside the venue. The individual is seen carrying something in their hand and, as they walk off-screen, a bright flash of light from a large flame is seen in the video.

    A SWAT team was called to the area and more than 70 ambulance teams and doctors assisted victims.

    One hundred and forty-five people have been hospitalized, TASS reported. Sixty people are in a “serious condition.”

    According to the Kremlin, Putin was informed about the attack and is being kept updated on measures on the ground.

    The president on Saturday wished those injured in the attack a speedy recovery, the state-run RIA-Novosti news agency said. He also “conveyed his gratitude to the doctors,” RIA added.

    Around 100 people were evacuated from the building by firefighters, TASS reported.

    Moscow Mayor Sergei Sobyanin called the attack a “terrible tragedy.”

    “My condolences to the loved ones of the victims. I gave orders to provide all necessary assistance to everyone who suffered during the incident,” Sobyanin said in a statement.

    Sobyanin said on Telegram that he was canceling all sports, cultural and other public events in Moscow this weekend.

    Picnic’s manager told state media that the performers were unharmed.

    Shaman, the band’s singer, said he would pay for the funerals of the victims and treatment for those injured.

    “We are all one big family. And in a family there is no such thing as somebody else’s grief,” the singer, known for his nationalistic views, said in a video posted on the Russian social media network Vkontakte to his more than 600,000 followers.

    “My people, any troubles and misfortunes have always united our country. They have made Russia tougher and stronger. It will not be possible to frighten and break us this time either.”

    ISIS claims responsibility for Moscow attack that killed 40

    02:51 - Source: CNN
    US had warned of potential attack

    Earlier this month, the US embassy in Russia said it was “monitoring reports that extremists have imminent plans to target large gatherings in Moscow,” including concerts. The embassy warned US citizens to avoid large gatherings. On Friday, following reports of the Crocus City Hall attack, it advised US citizens not to travel to Russia.

    Starting in November, there has been a steady stream of intelligence that ISIS-K was determined to attack in Russia, according to two sources familiar with the information.

    ISIS-K stands for ISIS-Khorasan, the terror organization’s affiliate that is active in Afghanistan and the surrounding region.

    US National Security Council spokesperson Adrienne Watson said the US government had had information about a planned terrorist attack in Moscow – potentially targeting large gatherings, to include concerts – and that this is what prompted the State Department to issue the public advisory.

    “The US government also shared this information with Russian authorities in accordance with its longstanding ‘duty to warn’ policy,” Watson said.

    In a speech Tuesday, Putin had blasted the American warnings as “provocative,” saying “these actions resemble outright blackmail and the intention to intimidate and destabilize our society.”

    In March alone, Russian authorities had thwarted several ISIS-related incidents, according to RIA. On March 3, RIA reported that six ISIS members were killed in a counter-terrorist operation in the Ingush Karabulak; on March 7, it said security services had uncovered and “neutralized” a cell of the banned organization Vilayat Khorasan in the Kaluga region, whose members were planning an attack on a synagogue in Moscow; and on March 20, it said the commander of an ISIS combat group had been detained.

    A US official said Friday that Washington had no reason to doubt ISIS’ claim that it was responsible for the latest attack.

    International response

    Ukraine, which has been embroiled in a war with Russia for more than two years, denied any involvement in the attack.

    “Ukraine has never resorted to the use of terrorist methods,” Ukrainian presidential adviser Mykhailo Podolyak wrote, in part, in a post on X. He said he believed Russia would use the attack to justify the ongoing conflict and scale up operations as part of “military propaganda” in Ukraine.

    United Nations Secretary-General Antonio Guterres late Friday condemned “in the strongest possible terms today’s terrorist attack” according to a statement released by his deputy spokesperson, Farhan Haq.

    “The secretary-general conveys his deep condolences to the bereaved families and the people and the government of the Russian Federation. He wishes those injured a speedy recovery,” the statement said.

    In a separate statement, the UN Security Council called the attack “heinous and cowardly.”

    Chinese leader Xi Jinping offered his condolences to Putin on Saturday “over the serious terrorist attack that caused heavy casualties,” according to a report from Chinese state media.

    French President Emmanuel Macron also condemned the attack. “France expresses its solidarity with the victims, their loved ones and all the Russian people,” the Elysee Palace said, AFP and Reuters reported.

    India’s Prime Minister Narendra Modi and Saudi Arabia’s Crown Prince Mohammed bin Salman both also denounced the attack.

    CNN’s Eva Rothenberg, Paul Murphy and Hannah Strange contributed to this reporting.

    https://www.cnn.com/2024/03/22/europe/crocus-moscow-shooting/index.html
    ISIS claims responsibility for attack at Moscow-area concert venue that left at least 60 dead CNN — normal ISIS has claimed responsibility for an attack at a popular concert hall complex near Moscow Friday after assailants stormed the venue with guns and incendiary devices, killing at least 60 people and injuring 145. The terror group took responsibility for the attack in a short statement published by ISIS-affiliated news agency Amaq on Telegram on Friday. It did not provide evidence to support the claim. Video footage from the Crocus City Hall shows the vast complex, which is home to both the music hall and a shopping center, on fire with smoke billowing into the air. State-run RIA Novosti reported the armed individuals “opened fire with automatic weapons” and “threw a grenade or an incendiary bomb, which started a fire.” They then “allegedly fled in a white Renault car,” the news agency said. State media Russia 24 reported the roof of the venue has partially collapsed. The fire had been brought largely under control more than six hours later. “There are still some pockets of fire, but the fire has been mostly eliminated,” Moscow governor Andrey Vorobyov said on Telegram. The deadliest terror attack on Moscow in decades, Friday’s assault came less than a week after President Vladimir Putin won a stage-managed election by an overwhelming majority to secure another term in office, tightening his grip on the country he has ruled since the turn of the century. With attention focused on the country’s war with neighboring Ukraine, Putin had trumpeted a message of national security before Russians went to the polls. The carnage broke out before a concert by the band Picnic, according to Russia 24. “Unidentified people in camouflage broke into Crocus City Hall and started shooting before the start of the concert,” the Prosecutor General’s Office said, cited by TASS. This screen grab from video shows armed men inside the Crocus City Hall concert venue in Moscow region, Russia. CNN can not verify whether these are the armed attackers or Russian authorities moving in. Video footage showed panic as the attack unfolded, with crowds of people huddling together, screaming and ducking behind cushioned seats as gunshots started echoing in the vast hall. One group sheltering next to a large wall of windows outside the concert venue were forced to break them to escape the gunfire, video obtained by CNN shows. Footage geolocated by CNN shows an armed individual starting at least one fire inside the venue. The individual is seen carrying something in their hand and, as they walk off-screen, a bright flash of light from a large flame is seen in the video. A SWAT team was called to the area and more than 70 ambulance teams and doctors assisted victims. One hundred and forty-five people have been hospitalized, TASS reported. Sixty people are in a “serious condition.” According to the Kremlin, Putin was informed about the attack and is being kept updated on measures on the ground. The president on Saturday wished those injured in the attack a speedy recovery, the state-run RIA-Novosti news agency said. He also “conveyed his gratitude to the doctors,” RIA added. Around 100 people were evacuated from the building by firefighters, TASS reported. Moscow Mayor Sergei Sobyanin called the attack a “terrible tragedy.” “My condolences to the loved ones of the victims. I gave orders to provide all necessary assistance to everyone who suffered during the incident,” Sobyanin said in a statement. Sobyanin said on Telegram that he was canceling all sports, cultural and other public events in Moscow this weekend. Picnic’s manager told state media that the performers were unharmed. Shaman, the band’s singer, said he would pay for the funerals of the victims and treatment for those injured. “We are all one big family. And in a family there is no such thing as somebody else’s grief,” the singer, known for his nationalistic views, said in a video posted on the Russian social media network Vkontakte to his more than 600,000 followers. “My people, any troubles and misfortunes have always united our country. They have made Russia tougher and stronger. It will not be possible to frighten and break us this time either.” ISIS claims responsibility for Moscow attack that killed 40 02:51 - Source: CNN US had warned of potential attack Earlier this month, the US embassy in Russia said it was “monitoring reports that extremists have imminent plans to target large gatherings in Moscow,” including concerts. The embassy warned US citizens to avoid large gatherings. On Friday, following reports of the Crocus City Hall attack, it advised US citizens not to travel to Russia. Starting in November, there has been a steady stream of intelligence that ISIS-K was determined to attack in Russia, according to two sources familiar with the information. ISIS-K stands for ISIS-Khorasan, the terror organization’s affiliate that is active in Afghanistan and the surrounding region. US National Security Council spokesperson Adrienne Watson said the US government had had information about a planned terrorist attack in Moscow – potentially targeting large gatherings, to include concerts – and that this is what prompted the State Department to issue the public advisory. “The US government also shared this information with Russian authorities in accordance with its longstanding ‘duty to warn’ policy,” Watson said. In a speech Tuesday, Putin had blasted the American warnings as “provocative,” saying “these actions resemble outright blackmail and the intention to intimidate and destabilize our society.” In March alone, Russian authorities had thwarted several ISIS-related incidents, according to RIA. On March 3, RIA reported that six ISIS members were killed in a counter-terrorist operation in the Ingush Karabulak; on March 7, it said security services had uncovered and “neutralized” a cell of the banned organization Vilayat Khorasan in the Kaluga region, whose members were planning an attack on a synagogue in Moscow; and on March 20, it said the commander of an ISIS combat group had been detained. A US official said Friday that Washington had no reason to doubt ISIS’ claim that it was responsible for the latest attack. International response Ukraine, which has been embroiled in a war with Russia for more than two years, denied any involvement in the attack. “Ukraine has never resorted to the use of terrorist methods,” Ukrainian presidential adviser Mykhailo Podolyak wrote, in part, in a post on X. He said he believed Russia would use the attack to justify the ongoing conflict and scale up operations as part of “military propaganda” in Ukraine. United Nations Secretary-General Antonio Guterres late Friday condemned “in the strongest possible terms today’s terrorist attack” according to a statement released by his deputy spokesperson, Farhan Haq. “The secretary-general conveys his deep condolences to the bereaved families and the people and the government of the Russian Federation. He wishes those injured a speedy recovery,” the statement said. In a separate statement, the UN Security Council called the attack “heinous and cowardly.” Chinese leader Xi Jinping offered his condolences to Putin on Saturday “over the serious terrorist attack that caused heavy casualties,” according to a report from Chinese state media. French President Emmanuel Macron also condemned the attack. “France expresses its solidarity with the victims, their loved ones and all the Russian people,” the Elysee Palace said, AFP and Reuters reported. India’s Prime Minister Narendra Modi and Saudi Arabia’s Crown Prince Mohammed bin Salman both also denounced the attack. CNN’s Eva Rothenberg, Paul Murphy and Hannah Strange contributed to this reporting. https://www.cnn.com/2024/03/22/europe/crocus-moscow-shooting/index.html
    WWW.CNN.COM
    ISIS claims responsibility for attack in busy Moscow-area concert venue that left at least 40 dead | CNN
    At least 40 people were killed and more than 100 were injured after armed attackers stormed a popular concert venue complex near Moscow and opened fire, according to preliminary information from the Federal Security Service in Russia, state media TASS reported.
    2 Comments 0 Shares 14997 Views
  • A dark circles eliminator product can be particularly beneficial for 40-year-old women in the USA for several reasons:

    Age-related Concerns: As individuals age, the skin tends to lose elasticity and collagen, which can exacerbate the appearance of dark circles under the eyes. A targeted dark circles eliminator can help address these concerns specific to aging skin.

    Busy Lifestyle: Many women in their 40s lead busy lives, juggling work, family, and personal commitments. This can lead to stress, lack of sleep, and fatigue, all of which contribute to the formation of dark circles. A product that effectively reduces dark circles can help them maintain a refreshed and youthful appearance despite their hectic schedules.

    Skin Sensitivity: With age, the skin becomes more sensitive and prone to irritation. A dark circles eliminator designed for mature skin will likely contain gentle yet effective ingredients suitable for women in their 40s, helping to minimize the risk of adverse reactions.

    Targeted Formulation: Products formulated specifically for mature skin often contain ingredients that address multiple concerns simultaneously. In addition to reducing dark circles, they may also target fine lines, wrinkles, and puffiness, providing comprehensive skincare benefits tailored to the needs of women in their 40s.

    Visible Results: Women in their 40s are often looking for skincare products that deliver visible results. A dark circles eliminator that effectively reduces the appearance of dark circles can boost confidence and enhance the overall appearance, making it a popular choice among this demographic.

    Professional and Social Engagements: As women progress in their careers and social lives, maintaining a youthful and vibrant appearance becomes increasingly important. A dark circles eliminator can help them look well-rested and rejuvenated, whether they're attending important meetings, social events, or simply enjoying time with family and friends.

    Overall, a dark circles eliminator tailored to the specific needs of 40-year-old women in the USA can offer a combination of age-defying benefits, convenience, and visible results, making it an ideal choice for this demographic.

    https://www.digistore24.com/redir/474960/sarafraz/




    A dark circles eliminator product can be particularly beneficial for 40-year-old women in the USA for several reasons: Age-related Concerns: As individuals age, the skin tends to lose elasticity and collagen, which can exacerbate the appearance of dark circles under the eyes. A targeted dark circles eliminator can help address these concerns specific to aging skin. Busy Lifestyle: Many women in their 40s lead busy lives, juggling work, family, and personal commitments. This can lead to stress, lack of sleep, and fatigue, all of which contribute to the formation of dark circles. A product that effectively reduces dark circles can help them maintain a refreshed and youthful appearance despite their hectic schedules. Skin Sensitivity: With age, the skin becomes more sensitive and prone to irritation. A dark circles eliminator designed for mature skin will likely contain gentle yet effective ingredients suitable for women in their 40s, helping to minimize the risk of adverse reactions. Targeted Formulation: Products formulated specifically for mature skin often contain ingredients that address multiple concerns simultaneously. In addition to reducing dark circles, they may also target fine lines, wrinkles, and puffiness, providing comprehensive skincare benefits tailored to the needs of women in their 40s. Visible Results: Women in their 40s are often looking for skincare products that deliver visible results. A dark circles eliminator that effectively reduces the appearance of dark circles can boost confidence and enhance the overall appearance, making it a popular choice among this demographic. Professional and Social Engagements: As women progress in their careers and social lives, maintaining a youthful and vibrant appearance becomes increasingly important. A dark circles eliminator can help them look well-rested and rejuvenated, whether they're attending important meetings, social events, or simply enjoying time with family and friends. Overall, a dark circles eliminator tailored to the specific needs of 40-year-old women in the USA can offer a combination of age-defying benefits, convenience, and visible results, making it an ideal choice for this demographic. https://www.digistore24.com/redir/474960/sarafraz/
    WWW.DIGISTORE24.COM
    Dark Spots Eliminator
    Eliminates the Look of Dark Circles - Restores nourishment in form of hydration to the under-eye area removing puffiness.
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