• Vaccines and the Length of Our Lives
    David Bell
    The commercial imperative to extract money from human bodies is playing havoc with medical education, and the body of knowledge through which the medical professions operate. Nowhere is this more apparent than in the field of vaccines, and their place in determining the length of our lives.

    The History of Living Longer

    As a medical student, I was taught that the reason we in wealthy countries now live far longer than our forebears was improvements in living conditions, sanitation, and nutrition. We don’t walk through sewage and horse dung each day, eat fly-blown meat, drink water from below the nearest latrines, or sleep eight to a room on rancid bedding. We get beaten less often and have more leisure time. Antibiotics also helped but came after most of these gains had been achieved.

    Most vaccination came even later, mopping up some residual mortality in ‘vaccine-preventable diseases.’ This was all stated in a lecture hall of 300 medical students, with the relevant data to back it up, and accepted as fact. Because for wealthier countries it was, and is, undeniably true.

    I recently asked a small group of students the major reasons for improved life expectancy, and was told “vaccination.” In a subsequent session, I showed some of the graphs laid out below. The students were shocked and asked where I obtained this information. It was actually fairly difficult to find. I remember searching 20 years ago and readily finding it on the web.

    In 2024, it took a lot of sifting through information explaining how vaccinations have apparently saved humanity, and how those repeating what I was taught as a student were a subversive element undermining the greater good, spreading misinformation or similar daft claims. We have certainly not progressed.

    This does not mean vaccines are not a great idea. Providing some immunity before an infection can mitigate much of its harm by giving the body a head start in fighting back. It just means their usefulness must be understood in context, as must their harms. Somewhat strangely, discussion of vaccines has become increasingly controversial within the medical establishment. It is as if an Inquisition has been imposed over the profession, seeking out anyone still prioritizing calm rational thought over a dogma dictated from above. However, if truth and calm discussion can form an anchor for policy, vaccination will be more effective.

    The charts shown here, from Australia, the United States, and England, reflect those of other wealthy countries. The same findings are reflected in various published papers. Facts are facts, even if they may with time become harder to find, buried under Big Search algorithms to keep us safe. They remain facts even if medical students are taught to believe alternate realities. Such false teaching, coupled with large financial incentives, drive their desire to ensure children be ‘fully vaccinated’ according to their country’s childhood schedule. They increasingly believe a lie, undeniable misinformation, that this is why most children in our countries now grow up without experiencing the death of a friend or sibling.


    Vaccines in Context

    The medical world calls these “vaccine-preventable diseases” because companies sell vaccines that can prevent them. They are vaccine-preventable to a large extent, and vaccines do stop them from killing people. But in wealthy countries, truthfully, the numbers they save are very low.

    Vaccination probably had a major role in the elimination of smallpox. We cannot, of course, be absolutely sure, as there was no control group. Smallpox caused outbreaks that decimated populations isolated for thousands of years from the virus, such as Native Americans, where a vaccine would have made a massive difference.

    However, smallpox also had the hallmarks of a disease that might actually disappear through good public health education and improved living standards; it lacked an animal reservoir, required close contact with body fluids to spread, and was usually easy to recognize. It is probable that the vaccine considerably accelerated its decline, especially in poorer countries.

    Measles is similarly interesting. As the graphic shows, most decline was long before mass vaccination. Like whooping cough, mortality was probably partly reduced through the advent of oxygen therapy, but mainly people just appear to have become less susceptible to its complications.

    It could nonetheless be a devastating disease, which decimated isolated, immunologically-naïve populations in the Pacific Islands and elsewhere that had no history of contact, and still causes avoidable child death in low-income countries today. Measles deaths are often associated with micronutrient malnutrition, such as vitamin A deficiency, and fixing that would also address many other health risks. This used to be emphasized 30 years ago.

    However, the measles vaccine is also very effective at stopping measles deaths in susceptible populations. It has very little impact on mortality in wealthy countries where it mainly stops infection and annoying sickness, as few kids are so micronutrient-deficient to be susceptible to very severe diseases. It is so good at stopping actual infection that mandates for measles vaccines that some countries impose are more about authoritarianism than public health.

    If you don’t want your child to risk measles and decide that vaccination is a lesser risk, you can have your child vaccinated. Your child is now protected from those who are unvaccinated, so there should be no interest in mandating it for them. Rational free people could live with that.


    Hepatitis B and HPV vaccination (for Human Papilloma Virus) are two further curiosities. We schedule Hep B vaccination on the first day of life, even though it is mainly spread in Western countries through sexual contact and intravenous drug use. If the parents are not infected (and all mothers are screened), then there is not really a risk until the late teenage years, when the person can make their own informed choice. For a child born in a country with 30% Hepatitis B positivity rates and poor healthcare, the risk-benefit calculation may produce a different result. Dying of liver failure or liver cancer is not pleasant.

    The HPV vaccine, intended to prevent cervical cancer, has a complicated picture. It will have limited mortality impact in Western countries where cervical cancer mortality has already declined through regular screening. Elsewhere the situation is very different, with over 300,000 women dying annually from this agonizing disease, mostly in regions such as sub-Saharan Africa where only about 12% are screened. This is not through choice but because screening is poorly accessible. As development of cancer can take about 20 years after HPV infection, we must also rely on (reasonable) assumptions about causality when calculating benefits. So, the equation clearly varies between women.

    Calculating risk versus benefit in order to ensure clear informed consent (or even medical ethical competency) would require consideration of age, behavior, access to screening, and adverse event rates. To know adverse event rates, a comparison would logically be necessary between the vaccine and something neutral like saline (rather than other vaccine constituents). Because this is still awaited, women should of course be informed of this data gap. Therefore, a blanket policy on HPV vaccination would be illogical.

    The story of diphtheria suggests that medical management may have had a major role in its decline. The decline coincided with the introduction of antibody therapy (anti-toxin), and later decline with the toxoid vaccine. However, it also coincided with the decline of other respiratory diseases of childhood that did not have such interventions. So, we simply cannot be sure.

    Tetanus toxoid may also have had an impact, especially for people at higher risk, such as plumbers and farmers. However, accountants no longer navigate dung-paved streets on the way to the office and this general cleaning up of the environment will have driven much of the change. For business reasons that are slightly unclear, boosters are available only combined with diphtheria and pertussis vaccines in many Western countries, which adds nothing to an adult’s benefit but adds to their risk. It’s hard to claim safety and benefit are the main drivers in the face of such an anomaly.


    Knowing What We Don’t Know

    All vaccines also have adverse effects. While not discussed here, they are real and I know people whose health was wrecked by vaccination. Assessment of risk is difficult as no childhood vaccines on the US schedule have been through a true placebo-controlled trial – they are usually compared against the rest of the contents of the vial (chemicals such as adjuvants and preservatives but lacking the antigen or inactivated virus – a mixture that may be the cause of most of the side effects) or against another vaccine.

    By doing this, they can be shown to be no worse than the comparator, which would be fine if we actually had decent placebo-controlled trials of the comparators. Most doctors who prescribe vaccines almost certainly don’t know this. (There is a good, evidence-based explanation of this issue which is well worth reading).

    Most doctors probably also pay little attention to the lack of trials determining the effect of giving dozens of doses of immune-stimulating adjuvants and preservatives, including aluminum salts, to growing children across their formative years. It is likely to be relatively harmless to many children, but harmful to some, as biology tends to work that way. However, if the disease that it addresses is hardly ever severe, then that ‘some’ can become very significant. Each ‘some’ is a child whose parents are trying to do the right thing, and trusting the medical establishment that this is indeed being done.


    None of this would be new to a lot of people, as interest in vaccines and their harms and benefits is growing. However, most doctors performing vaccinations are probably unaware of much of the above, especially those graduating in the past couple of decades. If they are aware, they will likely be scared to discuss it as this would risk being labeled a “vaccine denier” or similarly childish term, or seen as promoting “vaccine hesitancy.” Vaccine hesitancy is what we once referred to as informed consent (or thinking before doing). After World War Two, we decided that informed consent was essential for ethical medicine. Now, the World Health Organization considers such independent thought a particularly dangerous threat to their interests and those of their sponsors.

    Many recently trained doctors would consider the lecture I attended 40 years ago a public health risk, and the facts we were shown ‘misinformation.’ They will, at least in the US, also graduate with massive debt and be quite dependent on the subsidies they can receive from medical insurers, which include offering or giving vaccinations. This is why they can be so dismissive of intelligent people who spend time reading up on, and questioning, such things. They are not being aggressive or intentionally batting for Big Pharma; they are just so indoctrinated in the selling of these health commodities, and so financially and professionally dependent on this being the best course, that they are unable to articulate an independent, rational, evidence-based stance.

    Navigating a Rational Path

    To understand the vaccination issue, the public needs to understand that the medical and public health professions have lost their ability to reason. They are experts in repeating what they were taught, but not in deciphering reality. There are also fanatics and dogmatic people on the other side of the vaccine divide that can see the harms, but not the good.

    They downplay a few hundred thousand cervical cancer deaths per year, and have not witnessed the gut-wrenching sight of a baby dying of tetanus in a low-income country with no ability to address her pain. They have not had to send a rabies sufferer home to die because there is simply nothing the local medical system can do for them once they are symptomatic.


    On vaccination policy, the public mostly needs to go it alone. Understand there are real risks and real benefits, like any pharmaceutical. Understand that the main reason why we don’t die from many of the infectious diseases that we used to has little to do with vaccination. Listen to a doctor, then ask them some pointed questions to ascertain whether they are looking at your child in context and weighing both sides or simply reciting a script.

    When the benefits clearly outweigh the risks, vaccines make sense. They are a foolish idea when the opposite applies. It’s difficult to navigate the information out there, but the public must do so until the medical establishment frees itself from the shackles of its sponsors and catches up.

    Everyone should be hesitant to have stuff injected into them for commercial profit. We should hesitate more when the person injecting it is also rewarded for their compliance. Doctors should be hesitant about injecting chemicals and metal salts into anyone unless they have strong expectations of net benefit. With vaccines, as with antibiotics and almost any other pharmaceutical, sometimes they will have and sometimes they won’t.

    Obviously, governments should not be mandating the injection of commercial chemicals as a requirement to participate in society – that would be ridiculous. A State can never make such individual cost-benefit assessments, and in a democracy, we certainly don’t pay the government to own and direct our bodies.

    This is all so obvious, and inline with conventional evidence-based practice, that you really wonder what all the fuss is about.

    Author

    David Bell, Senior Scholar at Brownstone Institute, is a public health physician and biotech consultant in global health. David is a former medical officer and scientist at the World Health Organization (WHO), Programme Head for malaria and febrile diseases at the Foundation for Innovative New Diagnostics (FIND) in Geneva, Switzerland, and Director of Global Health Technologies at Intellectual Ventures Global Good Fund in Bellevue, WA, USA.

    View all posts

    https://brownstone.org/articles/vaccines-and-the-length-of-our-lives/

    https://donshafi911sars-cov-2.blogspot.com/2024/10/vaccines-and-length-of-our-lives-david.html
    Vaccines and the Length of Our Lives David Bell The commercial imperative to extract money from human bodies is playing havoc with medical education, and the body of knowledge through which the medical professions operate. Nowhere is this more apparent than in the field of vaccines, and their place in determining the length of our lives. The History of Living Longer As a medical student, I was taught that the reason we in wealthy countries now live far longer than our forebears was improvements in living conditions, sanitation, and nutrition. We don’t walk through sewage and horse dung each day, eat fly-blown meat, drink water from below the nearest latrines, or sleep eight to a room on rancid bedding. We get beaten less often and have more leisure time. Antibiotics also helped but came after most of these gains had been achieved. Most vaccination came even later, mopping up some residual mortality in ‘vaccine-preventable diseases.’ This was all stated in a lecture hall of 300 medical students, with the relevant data to back it up, and accepted as fact. Because for wealthier countries it was, and is, undeniably true. I recently asked a small group of students the major reasons for improved life expectancy, and was told “vaccination.” In a subsequent session, I showed some of the graphs laid out below. The students were shocked and asked where I obtained this information. It was actually fairly difficult to find. I remember searching 20 years ago and readily finding it on the web. In 2024, it took a lot of sifting through information explaining how vaccinations have apparently saved humanity, and how those repeating what I was taught as a student were a subversive element undermining the greater good, spreading misinformation or similar daft claims. We have certainly not progressed. This does not mean vaccines are not a great idea. Providing some immunity before an infection can mitigate much of its harm by giving the body a head start in fighting back. It just means their usefulness must be understood in context, as must their harms. Somewhat strangely, discussion of vaccines has become increasingly controversial within the medical establishment. It is as if an Inquisition has been imposed over the profession, seeking out anyone still prioritizing calm rational thought over a dogma dictated from above. However, if truth and calm discussion can form an anchor for policy, vaccination will be more effective. The charts shown here, from Australia, the United States, and England, reflect those of other wealthy countries. The same findings are reflected in various published papers. Facts are facts, even if they may with time become harder to find, buried under Big Search algorithms to keep us safe. They remain facts even if medical students are taught to believe alternate realities. Such false teaching, coupled with large financial incentives, drive their desire to ensure children be ‘fully vaccinated’ according to their country’s childhood schedule. They increasingly believe a lie, undeniable misinformation, that this is why most children in our countries now grow up without experiencing the death of a friend or sibling. Vaccines in Context The medical world calls these “vaccine-preventable diseases” because companies sell vaccines that can prevent them. They are vaccine-preventable to a large extent, and vaccines do stop them from killing people. But in wealthy countries, truthfully, the numbers they save are very low. Vaccination probably had a major role in the elimination of smallpox. We cannot, of course, be absolutely sure, as there was no control group. Smallpox caused outbreaks that decimated populations isolated for thousands of years from the virus, such as Native Americans, where a vaccine would have made a massive difference. However, smallpox also had the hallmarks of a disease that might actually disappear through good public health education and improved living standards; it lacked an animal reservoir, required close contact with body fluids to spread, and was usually easy to recognize. It is probable that the vaccine considerably accelerated its decline, especially in poorer countries. Measles is similarly interesting. As the graphic shows, most decline was long before mass vaccination. Like whooping cough, mortality was probably partly reduced through the advent of oxygen therapy, but mainly people just appear to have become less susceptible to its complications. It could nonetheless be a devastating disease, which decimated isolated, immunologically-naïve populations in the Pacific Islands and elsewhere that had no history of contact, and still causes avoidable child death in low-income countries today. Measles deaths are often associated with micronutrient malnutrition, such as vitamin A deficiency, and fixing that would also address many other health risks. This used to be emphasized 30 years ago. However, the measles vaccine is also very effective at stopping measles deaths in susceptible populations. It has very little impact on mortality in wealthy countries where it mainly stops infection and annoying sickness, as few kids are so micronutrient-deficient to be susceptible to very severe diseases. It is so good at stopping actual infection that mandates for measles vaccines that some countries impose are more about authoritarianism than public health. If you don’t want your child to risk measles and decide that vaccination is a lesser risk, you can have your child vaccinated. Your child is now protected from those who are unvaccinated, so there should be no interest in mandating it for them. Rational free people could live with that. Hepatitis B and HPV vaccination (for Human Papilloma Virus) are two further curiosities. We schedule Hep B vaccination on the first day of life, even though it is mainly spread in Western countries through sexual contact and intravenous drug use. If the parents are not infected (and all mothers are screened), then there is not really a risk until the late teenage years, when the person can make their own informed choice. For a child born in a country with 30% Hepatitis B positivity rates and poor healthcare, the risk-benefit calculation may produce a different result. Dying of liver failure or liver cancer is not pleasant. The HPV vaccine, intended to prevent cervical cancer, has a complicated picture. It will have limited mortality impact in Western countries where cervical cancer mortality has already declined through regular screening. Elsewhere the situation is very different, with over 300,000 women dying annually from this agonizing disease, mostly in regions such as sub-Saharan Africa where only about 12% are screened. This is not through choice but because screening is poorly accessible. As development of cancer can take about 20 years after HPV infection, we must also rely on (reasonable) assumptions about causality when calculating benefits. So, the equation clearly varies between women. Calculating risk versus benefit in order to ensure clear informed consent (or even medical ethical competency) would require consideration of age, behavior, access to screening, and adverse event rates. To know adverse event rates, a comparison would logically be necessary between the vaccine and something neutral like saline (rather than other vaccine constituents). Because this is still awaited, women should of course be informed of this data gap. Therefore, a blanket policy on HPV vaccination would be illogical. The story of diphtheria suggests that medical management may have had a major role in its decline. The decline coincided with the introduction of antibody therapy (anti-toxin), and later decline with the toxoid vaccine. However, it also coincided with the decline of other respiratory diseases of childhood that did not have such interventions. So, we simply cannot be sure. Tetanus toxoid may also have had an impact, especially for people at higher risk, such as plumbers and farmers. However, accountants no longer navigate dung-paved streets on the way to the office and this general cleaning up of the environment will have driven much of the change. For business reasons that are slightly unclear, boosters are available only combined with diphtheria and pertussis vaccines in many Western countries, which adds nothing to an adult’s benefit but adds to their risk. It’s hard to claim safety and benefit are the main drivers in the face of such an anomaly. Knowing What We Don’t Know All vaccines also have adverse effects. While not discussed here, they are real and I know people whose health was wrecked by vaccination. Assessment of risk is difficult as no childhood vaccines on the US schedule have been through a true placebo-controlled trial – they are usually compared against the rest of the contents of the vial (chemicals such as adjuvants and preservatives but lacking the antigen or inactivated virus – a mixture that may be the cause of most of the side effects) or against another vaccine. By doing this, they can be shown to be no worse than the comparator, which would be fine if we actually had decent placebo-controlled trials of the comparators. Most doctors who prescribe vaccines almost certainly don’t know this. (There is a good, evidence-based explanation of this issue which is well worth reading). Most doctors probably also pay little attention to the lack of trials determining the effect of giving dozens of doses of immune-stimulating adjuvants and preservatives, including aluminum salts, to growing children across their formative years. It is likely to be relatively harmless to many children, but harmful to some, as biology tends to work that way. However, if the disease that it addresses is hardly ever severe, then that ‘some’ can become very significant. Each ‘some’ is a child whose parents are trying to do the right thing, and trusting the medical establishment that this is indeed being done. None of this would be new to a lot of people, as interest in vaccines and their harms and benefits is growing. However, most doctors performing vaccinations are probably unaware of much of the above, especially those graduating in the past couple of decades. If they are aware, they will likely be scared to discuss it as this would risk being labeled a “vaccine denier” or similarly childish term, or seen as promoting “vaccine hesitancy.” Vaccine hesitancy is what we once referred to as informed consent (or thinking before doing). After World War Two, we decided that informed consent was essential for ethical medicine. Now, the World Health Organization considers such independent thought a particularly dangerous threat to their interests and those of their sponsors. Many recently trained doctors would consider the lecture I attended 40 years ago a public health risk, and the facts we were shown ‘misinformation.’ They will, at least in the US, also graduate with massive debt and be quite dependent on the subsidies they can receive from medical insurers, which include offering or giving vaccinations. This is why they can be so dismissive of intelligent people who spend time reading up on, and questioning, such things. They are not being aggressive or intentionally batting for Big Pharma; they are just so indoctrinated in the selling of these health commodities, and so financially and professionally dependent on this being the best course, that they are unable to articulate an independent, rational, evidence-based stance. Navigating a Rational Path To understand the vaccination issue, the public needs to understand that the medical and public health professions have lost their ability to reason. They are experts in repeating what they were taught, but not in deciphering reality. There are also fanatics and dogmatic people on the other side of the vaccine divide that can see the harms, but not the good. They downplay a few hundred thousand cervical cancer deaths per year, and have not witnessed the gut-wrenching sight of a baby dying of tetanus in a low-income country with no ability to address her pain. They have not had to send a rabies sufferer home to die because there is simply nothing the local medical system can do for them once they are symptomatic. On vaccination policy, the public mostly needs to go it alone. Understand there are real risks and real benefits, like any pharmaceutical. Understand that the main reason why we don’t die from many of the infectious diseases that we used to has little to do with vaccination. Listen to a doctor, then ask them some pointed questions to ascertain whether they are looking at your child in context and weighing both sides or simply reciting a script. When the benefits clearly outweigh the risks, vaccines make sense. They are a foolish idea when the opposite applies. It’s difficult to navigate the information out there, but the public must do so until the medical establishment frees itself from the shackles of its sponsors and catches up. Everyone should be hesitant to have stuff injected into them for commercial profit. We should hesitate more when the person injecting it is also rewarded for their compliance. Doctors should be hesitant about injecting chemicals and metal salts into anyone unless they have strong expectations of net benefit. With vaccines, as with antibiotics and almost any other pharmaceutical, sometimes they will have and sometimes they won’t. Obviously, governments should not be mandating the injection of commercial chemicals as a requirement to participate in society – that would be ridiculous. A State can never make such individual cost-benefit assessments, and in a democracy, we certainly don’t pay the government to own and direct our bodies. This is all so obvious, and inline with conventional evidence-based practice, that you really wonder what all the fuss is about. Author David Bell, Senior Scholar at Brownstone Institute, is a public health physician and biotech consultant in global health. David is a former medical officer and scientist at the World Health Organization (WHO), Programme Head for malaria and febrile diseases at the Foundation for Innovative New Diagnostics (FIND) in Geneva, Switzerland, and Director of Global Health Technologies at Intellectual Ventures Global Good Fund in Bellevue, WA, USA. View all posts https://brownstone.org/articles/vaccines-and-the-length-of-our-lives/ https://donshafi911sars-cov-2.blogspot.com/2024/10/vaccines-and-length-of-our-lives-david.html
    BROWNSTONE.ORG
    Vaccines and the Length of Our Lives ⋆ Brownstone Institute
    Imperative to extract money is playing havoc. Nowhere is this more apparent than vaccines and their place in determining length of our lives.
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  • Cured Meat: Curse or Cure?
    Nitrites and Nitrates have been vilified, but they've been used for 1000s of years.

    Dr. Syed Haider

    I was never convinced meat was inherently unhealthy, but anti-meat propaganda did get me to avoid cured meat for years, then one day I realized that people have been curing meat for centuries, basically using the same method we use today - i.e. adding nitrogen in the form of nitrate to meat, which is converted by bacteria within the meat into nitrite. The nitrite acts as an antioxidant, dries out the meat and inhibits the growth of bacteria.

    The Phoenicians, Romans and Ancient Greeks used various naturally occurring nitrate salts to cure their meat going back 1000s of years.

    However, like so many other things that people have done for millennia, curing meat was singled out as harmful in the last century when Big Business and Big Government started to meddle with what people since time immemorial knew to be true about nutrition and health. Studies seemed to show a correlation between meat consumption, especially processed meats, and various chronic diseases. It was postulated that the harm came from nitrosamines that were formed by the combination of nitrites/nitrates with amino acids when the cured meat was cooked.

    However there are some inconvenient holes in this theory.

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

    Share

    First nitrites & nitrates are much more common in plants than in meat. And many plants also contain amino acids, the building blocks of proteins, so cooking them should also form the supposedly harmful nitrosamines. Yet plants aren’t demonized like meat is.

    We also need nitrites/nitrates to form nitric oxide, which is an essential signaling molecule and very important for vascular health. In fact nitrates are the name of an entire class of medications with nitrate in them, that are used for heart disease to increase the bodies nitric oxide levels.

    People think hot dogs are unhealthy, but they still can't resist them
    But perhaps the biggest reason this theory of nitrites/nitrates in meat being harmful holds no water is that our own bodies make far more of the supposedly harmful nitrosamines than we can ever possibly eat.

    So basically it was a bad psyop all along that collapses under the most cursory examination (and yet there are so many of these types of dysinformation psyops out there no one has time to examine them all and they mostly go unnoticed).

    If there is no coherent theoretical mechanism for harm and many different people have done it forever it’s likely that any signal you find in a study is from systemic bias (Ioannidis, 2005).

    "Why Most Published Research Findings are False" Part III
    There is clear anti-meat bias in the scientific establishment because the government funds most science and the government needs science that helps it to cover up and minimize the inflation it causes by printing too many dollars.

    As inflation causes the prices of healthy food to climb and normal people can no longer afford it, the government is incentivized to convince everyone that it’s not actually good for you anyway, which is why in 1966 then US president Lyndon Johnson called the Surgeon General and said he needed some “science” showing that eggs were bad for you.

    Shortly thereafter the media spread the myth that cholesterol and therefore eggs high in it, were bad. Many generations of Americans were thoroughly convinced that not only were cholesterol and saturated animal fats bad, but that cheap grains, seed oils and sugar were good.

    So now I have a useful rule of thumb: if government funded science (most science nowadays) says anything it’s almost always, if not always, agenda driven, statistically manipulated garbage that is very likely to be in gross error.

    A few minutes on the search engine of your choice is usually long enough to discover the truth, unless its a topic that really scares the establishment like an unusually effective therapy that threatens Big Pharma profits (I’ll be writing about one of those for heart disease soon so stay tuned and subscribe if you haven’t don’t do so already).

    While nitrites and nitrates appear to be benign (and perhaps even health promoting via nitric oxide), it’s important to acknowledge that not all processed and preserved meats are created equal.

    Many processed meats are of low quality, and contain various chemicals, unnatural preservatives, colorings and flavorings that should be avoided. Some can hardly be recognized as meat during their excessive processing (highly processed foods are generally acknowledged by everyone to be less healthy than minimally, traditionally processed ones). For example there is a famous video of pink sludge making it’s way through a large factory before it ends up as sliced deli meat. I for one don’t think my final meat product should begin it’s life as a liquid pink sludge.

    Ham production screenshots from TikTok
    So curing is fine, but what about the meat itself?

    That was the broader psyop, of which the nitrite/nitrate controversy was but a side note.

    The primary focus was on the saturated fat in meat and animal products like milk and butter.

    But we now know for a fact that all the research was severely tainted. Early research by Alan Keys was clearly cherry picked to create a false narrative.

    It’s since been pretty conclusively shown that saturated fat is healthy, dietary cholesterol does not usually influence blood cholesterol levels, and moreover blood cholesterol is not the cause of coronary artery disease. It’s actually the only solution some peoples bodies can find for their badly inflamed and damaged arteries, given the bad hand they’ve dealt themselves.

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

    Share

    People in “blue zones” who are purported to live longer than anyone else and were supposed to eat little meat, actually eat more meat than researchers let on. For example Okinawans eat more meat than their closest co-ethnic neighbors who live shorter lives. There’s evidence that groups like the 7th Day Adventists who say they don’t eat meat for religious reasons actually do. On Sardinia they don’t eat what the media portrays as a “Mediterranean Diet” - generally high in carbs and low in saturated fats. They actually eat more fish, meat, and full fat dairy products, while consuming relatively less grains than we’ve been led to believe.

    But just because cured meat and meat in general isn’t inherently bad, doesn’t mean it’s necessarily good for a particular person either.

    For example it may be better for many of the chronically ill to prioritize fatty fish over meat for their DHA content and other important nutrients. For someone who has overeaten Omega 6 rich seed oils for years they may not benefit from focusing on chicken or grain fed beef that is also rich in Omega 6 fats. For someone seriously depressed it’s usually best to avoid the meat of stressed out and depressed animals, because their psychological state also imbues their meat (stress hormones and water memory). For someone with cancer, its usually best to avoid anabolic foods like meat all together.

    But in general, fresh or cured meat is an important part of a healthy, balanced diet and theres nothing wrong with enjoying it.



    https://blog.mygotodoc.com/p/cured-meat-curse-or-cure

    https://donshafi911sars-cov-2.blogspot.com/2024/07/cured-meat-curse-or-cure-nitrites-and.html
    Cured Meat: Curse or Cure? Nitrites and Nitrates have been vilified, but they've been used for 1000s of years. Dr. Syed Haider I was never convinced meat was inherently unhealthy, but anti-meat propaganda did get me to avoid cured meat for years, then one day I realized that people have been curing meat for centuries, basically using the same method we use today - i.e. adding nitrogen in the form of nitrate to meat, which is converted by bacteria within the meat into nitrite. The nitrite acts as an antioxidant, dries out the meat and inhibits the growth of bacteria. The Phoenicians, Romans and Ancient Greeks used various naturally occurring nitrate salts to cure their meat going back 1000s of years. However, like so many other things that people have done for millennia, curing meat was singled out as harmful in the last century when Big Business and Big Government started to meddle with what people since time immemorial knew to be true about nutrition and health. Studies seemed to show a correlation between meat consumption, especially processed meats, and various chronic diseases. It was postulated that the harm came from nitrosamines that were formed by the combination of nitrites/nitrates with amino acids when the cured meat was cooked. However there are some inconvenient holes in this theory. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share First nitrites & nitrates are much more common in plants than in meat. And many plants also contain amino acids, the building blocks of proteins, so cooking them should also form the supposedly harmful nitrosamines. Yet plants aren’t demonized like meat is. We also need nitrites/nitrates to form nitric oxide, which is an essential signaling molecule and very important for vascular health. In fact nitrates are the name of an entire class of medications with nitrate in them, that are used for heart disease to increase the bodies nitric oxide levels. People think hot dogs are unhealthy, but they still can't resist them But perhaps the biggest reason this theory of nitrites/nitrates in meat being harmful holds no water is that our own bodies make far more of the supposedly harmful nitrosamines than we can ever possibly eat. So basically it was a bad psyop all along that collapses under the most cursory examination (and yet there are so many of these types of dysinformation psyops out there no one has time to examine them all and they mostly go unnoticed). If there is no coherent theoretical mechanism for harm and many different people have done it forever it’s likely that any signal you find in a study is from systemic bias (Ioannidis, 2005). "Why Most Published Research Findings are False" Part III There is clear anti-meat bias in the scientific establishment because the government funds most science and the government needs science that helps it to cover up and minimize the inflation it causes by printing too many dollars. As inflation causes the prices of healthy food to climb and normal people can no longer afford it, the government is incentivized to convince everyone that it’s not actually good for you anyway, which is why in 1966 then US president Lyndon Johnson called the Surgeon General and said he needed some “science” showing that eggs were bad for you. Shortly thereafter the media spread the myth that cholesterol and therefore eggs high in it, were bad. Many generations of Americans were thoroughly convinced that not only were cholesterol and saturated animal fats bad, but that cheap grains, seed oils and sugar were good. So now I have a useful rule of thumb: if government funded science (most science nowadays) says anything it’s almost always, if not always, agenda driven, statistically manipulated garbage that is very likely to be in gross error. A few minutes on the search engine of your choice is usually long enough to discover the truth, unless its a topic that really scares the establishment like an unusually effective therapy that threatens Big Pharma profits (I’ll be writing about one of those for heart disease soon so stay tuned and subscribe if you haven’t don’t do so already). While nitrites and nitrates appear to be benign (and perhaps even health promoting via nitric oxide), it’s important to acknowledge that not all processed and preserved meats are created equal. Many processed meats are of low quality, and contain various chemicals, unnatural preservatives, colorings and flavorings that should be avoided. Some can hardly be recognized as meat during their excessive processing (highly processed foods are generally acknowledged by everyone to be less healthy than minimally, traditionally processed ones). For example there is a famous video of pink sludge making it’s way through a large factory before it ends up as sliced deli meat. I for one don’t think my final meat product should begin it’s life as a liquid pink sludge. Ham production screenshots from TikTok So curing is fine, but what about the meat itself? That was the broader psyop, of which the nitrite/nitrate controversy was but a side note. The primary focus was on the saturated fat in meat and animal products like milk and butter. But we now know for a fact that all the research was severely tainted. Early research by Alan Keys was clearly cherry picked to create a false narrative. It’s since been pretty conclusively shown that saturated fat is healthy, dietary cholesterol does not usually influence blood cholesterol levels, and moreover blood cholesterol is not the cause of coronary artery disease. It’s actually the only solution some peoples bodies can find for their badly inflamed and damaged arteries, given the bad hand they’ve dealt themselves. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share People in “blue zones” who are purported to live longer than anyone else and were supposed to eat little meat, actually eat more meat than researchers let on. For example Okinawans eat more meat than their closest co-ethnic neighbors who live shorter lives. There’s evidence that groups like the 7th Day Adventists who say they don’t eat meat for religious reasons actually do. On Sardinia they don’t eat what the media portrays as a “Mediterranean Diet” - generally high in carbs and low in saturated fats. They actually eat more fish, meat, and full fat dairy products, while consuming relatively less grains than we’ve been led to believe. But just because cured meat and meat in general isn’t inherently bad, doesn’t mean it’s necessarily good for a particular person either. For example it may be better for many of the chronically ill to prioritize fatty fish over meat for their DHA content and other important nutrients. For someone who has overeaten Omega 6 rich seed oils for years they may not benefit from focusing on chicken or grain fed beef that is also rich in Omega 6 fats. For someone seriously depressed it’s usually best to avoid the meat of stressed out and depressed animals, because their psychological state also imbues their meat (stress hormones and water memory). For someone with cancer, its usually best to avoid anabolic foods like meat all together. But in general, fresh or cured meat is an important part of a healthy, balanced diet and theres nothing wrong with enjoying it. https://blog.mygotodoc.com/p/cured-meat-curse-or-cure https://donshafi911sars-cov-2.blogspot.com/2024/07/cured-meat-curse-or-cure-nitrites-and.html
    BLOG.MYGOTODOC.COM
    Cured Meat: Curse or Cure?
    Nitrites and Nitrates have been vilified, but they've been used for 1000s of years.
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  • Lithium Orotate Dietary Supplement Is Pharmaceutical Snakeoil
    Dr. Ariyana Love (ND)
    I was asked by a client to investigate lithium orotate, lithium chloride and sodium citrate as health supplementation, and determine if these substances are safe for human consumption and if they have any medicinal benefits.

    These substances are being promoted by medical doctors, Naturopathic doctors and other health care practitioners as health miracles, but are they?

    Michael Nehls, MD, PHD writes:

    “The key element against brain fog, long-COVID/post-vac syndrome, chronic fatigue syndrome, depression, Alzheimer's – and even indoctrination?”


    Is Dr. Nehls talking about the organic and naturally occurring trace mineral lithium or is he promoting the synthetic pharmaceutical perversion? It’s difficult to say because he doesn’t actually specify the difference in his Substack article.

    Lithium in its pure form exists as a trace mineral found in nature. Lithium (Li), discovered in 1817, is a naturally occurring metal in the earth’s crust (0.0017%). Naturally occurring lithium in drinking water is beneficial in appropriate quantities and may have the potential to reduce the risk of suicide and may possibly even stabilize your mood.

    Leave it to nature to provide natural remedies to every ailment, but leave it to pharmaceutical companies to pervert nature’s purity, which leads to untold self-harm.

    Pharma would have you believe that moderate amounts of their synthetic lithium poison is therapeutic but “chronic toxicity occurs when you slowly take a little too much of a lithium prescription every day for a while”. Lithium is cumulative poison, meaning the longer you use it, the more damage it causes to your body system.

    The most common pharmaceutical lithium drug is lithium carbonate, which is synthesized by reacting lithium salts with soda or potash, followed by purification of the synthetic salt. It’s used to treat manic and bipolar disorders and has many toxic side effects.

    Lithium toxicity is in fact a life-threatening condition that causes intestinal and neurological symptoms. It can also lead to kidney damage. 75 to 90 percent of patients treated with lithium have signs or symptoms of toxicity at some point during their treatment, according to studies. This is because synthetic lithium is a neurotoxin, which means essentially that no amount is safe.

    Studies like this one make Lithium sound so absolutely amazing and full of wondrous potential, but you can be sure they tested a synthetic “lithium serum”.

    According to the NIH, lithium toxicity leads to a range of gastrointestinal and neurologic signs and symptoms and can ultimately be fatal.

    “…lithium toxicity can lead to coma, brain damage, or even death.”

    Lithium orotate

    Lithium Orotate is available as a synthetic salt of synthetic lithium and synthetic orotic acid, as a monohydrate, LiC5H3N2O4·H2O (Lithium chloride monohydrate). The only source of Lithium Orotate (C5H3LiN2O4) is a synthetic salt of orotic acid and lithium.

    Fischer Science Safety Data Sheet reveals that the target organs of Lithium Orotate are the central nervous system and the cardiovascular system.

    “May be harmful if swallowed. May cause central nervous system effects. May cause respiratory and digestive tract irritation. Contact with skin causes irritation and possible burns, especially if the skin is wet or moist.”

    Orotic acid in its natural form, is known as vitamin B-13. Orotic acid is found naturally in high quantities in beets. By using organic beet powder supplementation, you can obtain the B-13 that your body needs.

    Naturally occuring orotic acid acts as a transporter that carries magnesium into cells and may reduce the severity of chronic myocardial dysfunction and structural damage in cardiomyopathy. It also helps resolve gut microbiome issues. This will be true in its natural form.

    First patented in the 1990s, synthetic Lithium Orotate has been patented and mainstreamed by pharmaceutical companies as a treatment for mental health conditions. It’s mutagenic in somatic cells, which means it alters the human genome. Lithium Orotate is also mutagenic for bacteria and yeast, which means that it increases the replication of bad bacteria, ultimately disrupting your healthy microbiome balance. This explains the GI issues associated with taking this drug.

    In 1976, Lonza, LTD patented a synthetic version of Orotic Acid made from trichloroacetyl chloride and ketene. Trichloroacetyl chloride is a colorless volatile liquid with a strong odor that’s denser than water. Contact severely irritates skin, eyes and mucous membranes and “may be very toxic by ingestion and inhalation”. Ketene will cause “severe damage to the lungs at the alveolar level and may manifest as long as 24 hours post exposure”.

    High levels of Orotic Acid can be dangerous and, as a synthetic pharmaceutical drug, it can be deadly or induce Orotic Aciduria, which is an autosomal recessive disorder characterized by megaloblastic anemia and orotic acid crystalluria that is frequently associated with some degree of physical and mental retardation. Other side effects are heart abnormalities, seizures, coma, and possibly even death.

    A Chinese patent from the Shenghai Institute of Organic Chemistry of CAS to synthesize Orotic Acid uses sodium bromide, chlorine and maleylurea; then, the 5-bromine-2, 6-dioxo-hexahydropyrimidime-4-carboxylic acid and sodium hydroxide. Sodium bromide is a pesticide with reproductive toxicity as demonstrated in rat studies.

    Chlorine is, of course, an extremely dangerous industrial poison. Maleylurea is another toxic substance. 5-bromine-2 induces methemoglobinemia and delayed encephalopathy. 6-dioxo-hexahydropyrimidime-4-carboxylic acid is toxic while sodium hydroxide is corrosive to all body tissues.

    Other processes for producing Orotic Acid use Corynebacterium. This is a lethal exotoxin that induces diphtheria.

    Orotic Acid, a promoter of liver carcinogenesis, induces DNA damage in rat livers. It also induces hypertension associated with impaired endothelial Nitric Oxide synthesis, ultimately disrupting your redox balance.

    There was toxic and vascular nephropathy associated with Orotic Acid administration in laboratory cats. It destroys the liver of rats. In other studies, it induced fatty liver, causing weight gain.

    Please see the toxicity data sheet for Orotic Acid. It’s suggested to “avoid using Lithium Orotate until more is known”.

    Lithium Orotate supplements

    Some synthetic Lithium Orotate supplements boast of being organic or natural. I’ve noticed that Medical Doctors’ definition of organic or natural may vary greatly from the facts.

    Dr. Edward Group, D.C. from Global Healing, advertises a Lithium Orotate supplement as “natural trace minerals” for mood stabilization.


    Dr. Ed was interviewed by Mike Adams of Natural news, where he convincingly boasted about their “all natural” products and heavy metal detox protocols. The company went so far as to register their Lithium Orotate product on Amazon as “organic” and then later removed their false advertising and fake medical claim.

    However, things remain forever on the Internet. Oops!


    I reached out to Global Healing to give them a chance and asked directly if Global Healing is using “all natural” lithium and “all natural” orotic acid in their Lithium Orotate supplement. They responded by telling me that they derive their Lithium Orotate ingredients from all natural sources. When I pressed them for more information, asking what their sources are, they vaguely answered me with “it varies”. Oops, again!

    On their Lithium Orotate label, Global Healing only states that their lithium source comes “from lithium orotate”. Lithium does not naturally contain orotic acid, so this doesn’t make sense if it were “natural”. If it were natural, they would have two sources not one, because lithium and orotic acid are not naturally found together.


    If Global healing’s lithium source is from “lithium orotate”, then this is the patented pharmaceutical Lithium Orotate synthetic salt and this is false advertising.

    Dr. Edward’s Group is also selling and promoting EDTA and C-60 as health supplements. They claim that Calcium Disodium EDTA promotes “cardiovascular and immune health” but there’s no scientific evidence to support this claim.



    Please read: Is C60 And EDTA Safe? Clinical Review


    Lithium chloride

    Lithium chloride metal chloride salt is a toxic, inorganic synthetic compound. Please see the safety data sheet.

    Lithium chloride is produced by treatment of lithium carbonate with hydrochloric acid. A single exposure to hydrochloric acid causes organ toxicity and there are cases of lithium toxicity from Internet dietary supplements. Please avoid this at all costs.

    Sodium Citrate

    Sodium citrate (citric acid) is another toxic preservative. It’s a synthetic chemical that induces symptoms such as paresthesia, hypotension and possible cardiac arrhythmia. It’s being touted as an “anti-coagulant” and prooted on Karl.C’s Substack. But honestly, the blood results are not good.

    Sodium citrate contains propylene glycol which is neurotoxic. Read more here.

    Superior, natural anti-coagulants can be found in my premium detox and repair protocol.


    Please see: Dr. Ariyana Love's Anti-Aging Premium Detox Protocol


    Lithium and Graphene weapon systems

    On a side note, during my research I came across some pertinent information.

    Synthetic graphite is used for lithium-ion batteries. Pharmaceutical lithium is being used with reduced graphene oxide-based electrodes to produce a higher capacity of electrical conductivity. Nanocomposites based on hydroxyapatite/lithium oxide and graphene oxide nanosheets are indeed being used for medical applications. Lithium batteries have served as the predominant power source for implantable medical devices such as nanowires, which are used in tissue scaffolding technology.

    Scientists are using scaffolds made from conductive silicon nanowires to reconstruct artificial heart tissue. Nanowired organoids are used to accelerate the development of stem cells into healthy, well-functioning heart tissue. They create an organoid from a mixture of stem-cell-derived heart cells, stromal connective tissue cells, and endothelial cells – which line the walls of blood vessels.

    Incidentally, Methylene Blue is used to kick-start the growth of the stem cells used in tissue scaffolding.


    Please see: Methylene Blue Is Pharmaceutical Poison


    Polymers-ceramic nonwoven compositions supercapacitors with electrical storage capacity are self-organized and have tinsel strength. They’re not implanted into the body per se, they are grown inside the body using graphene oxide and lithium-fueled nanowires. Highly porous membranes with self-organized Nanopores are used for rapid sequencing of genes.

    The long, white “fibrous clots” that embalmers are finding in the veins of dead vaccinated individuals, is part of this transhumanist agenda to turn people into a new species of super-conducting robots.

    Karen Kingston recently exposed that Moderna is using Graphene Oxide Nanoparticles in DARPA’s hydrogel lipid-payloads.


    Please read: The Covid-19 Vaccine “Antigen” is Anthrax


    Graphene oxide–silver Nanowire nanocomposites are being used for enhanced sensing of Hg2+ (mercuric cations). These are energy harvesting devices and hybrid materials using carbon nanotubes (graphene oxide hydrogels) and polyethylene glycol nanocomposites. They’re highly toxic, as a 2019 study demonstrates, but they’re being used none-the-less for internal biosensor and bioimaging. The patent holders can essentially read the internal biometric data of “vaccinated” individuals without their Informed Consent.


    Please read: EDTA Snakeoil! Ana Maria Mihalcea's Medical Malfeasance Exposed


    Conclusion

    There’s no reason under the sun to use any experimental pharmaceutical drugs. 100 years ago humanity got along just fine with natural cures. None of the pharmaceuticals mentioned in this article are effective at heavy metal chelation. I have many clients who were very sick after using EDTA especially, along with other experimental drugs that will not achieve detox. It’s simply not logical to treat poisoning with more poison! To achieve an affectiv detox, you must eliminate toxins.

    Superior heavy metal chelators exist, and I help people to learn how to use them. You can schedule a consultation with me here for truly all natural health protocols that contain the greatest breakthroughs in medical science and heavy metal chelation.

    Let’s be Pharma free.



    https://substack.com/home/post/p-145685685
    Lithium Orotate Dietary Supplement Is Pharmaceutical Snakeoil Dr. Ariyana Love (ND) I was asked by a client to investigate lithium orotate, lithium chloride and sodium citrate as health supplementation, and determine if these substances are safe for human consumption and if they have any medicinal benefits. These substances are being promoted by medical doctors, Naturopathic doctors and other health care practitioners as health miracles, but are they? Michael Nehls, MD, PHD writes: “The key element against brain fog, long-COVID/post-vac syndrome, chronic fatigue syndrome, depression, Alzheimer's – and even indoctrination?” Is Dr. Nehls talking about the organic and naturally occurring trace mineral lithium or is he promoting the synthetic pharmaceutical perversion? It’s difficult to say because he doesn’t actually specify the difference in his Substack article. Lithium in its pure form exists as a trace mineral found in nature. Lithium (Li), discovered in 1817, is a naturally occurring metal in the earth’s crust (0.0017%). Naturally occurring lithium in drinking water is beneficial in appropriate quantities and may have the potential to reduce the risk of suicide and may possibly even stabilize your mood. Leave it to nature to provide natural remedies to every ailment, but leave it to pharmaceutical companies to pervert nature’s purity, which leads to untold self-harm. Pharma would have you believe that moderate amounts of their synthetic lithium poison is therapeutic but “chronic toxicity occurs when you slowly take a little too much of a lithium prescription every day for a while”. Lithium is cumulative poison, meaning the longer you use it, the more damage it causes to your body system. The most common pharmaceutical lithium drug is lithium carbonate, which is synthesized by reacting lithium salts with soda or potash, followed by purification of the synthetic salt. It’s used to treat manic and bipolar disorders and has many toxic side effects. Lithium toxicity is in fact a life-threatening condition that causes intestinal and neurological symptoms. It can also lead to kidney damage. 75 to 90 percent of patients treated with lithium have signs or symptoms of toxicity at some point during their treatment, according to studies. This is because synthetic lithium is a neurotoxin, which means essentially that no amount is safe. Studies like this one make Lithium sound so absolutely amazing and full of wondrous potential, but you can be sure they tested a synthetic “lithium serum”. According to the NIH, lithium toxicity leads to a range of gastrointestinal and neurologic signs and symptoms and can ultimately be fatal. “…lithium toxicity can lead to coma, brain damage, or even death.” Lithium orotate Lithium Orotate is available as a synthetic salt of synthetic lithium and synthetic orotic acid, as a monohydrate, LiC5H3N2O4·H2O (Lithium chloride monohydrate). The only source of Lithium Orotate (C5H3LiN2O4) is a synthetic salt of orotic acid and lithium. Fischer Science Safety Data Sheet reveals that the target organs of Lithium Orotate are the central nervous system and the cardiovascular system. “May be harmful if swallowed. May cause central nervous system effects. May cause respiratory and digestive tract irritation. Contact with skin causes irritation and possible burns, especially if the skin is wet or moist.” Orotic acid in its natural form, is known as vitamin B-13. Orotic acid is found naturally in high quantities in beets. By using organic beet powder supplementation, you can obtain the B-13 that your body needs. Naturally occuring orotic acid acts as a transporter that carries magnesium into cells and may reduce the severity of chronic myocardial dysfunction and structural damage in cardiomyopathy. It also helps resolve gut microbiome issues. This will be true in its natural form. First patented in the 1990s, synthetic Lithium Orotate has been patented and mainstreamed by pharmaceutical companies as a treatment for mental health conditions. It’s mutagenic in somatic cells, which means it alters the human genome. Lithium Orotate is also mutagenic for bacteria and yeast, which means that it increases the replication of bad bacteria, ultimately disrupting your healthy microbiome balance. This explains the GI issues associated with taking this drug. In 1976, Lonza, LTD patented a synthetic version of Orotic Acid made from trichloroacetyl chloride and ketene. Trichloroacetyl chloride is a colorless volatile liquid with a strong odor that’s denser than water. Contact severely irritates skin, eyes and mucous membranes and “may be very toxic by ingestion and inhalation”. Ketene will cause “severe damage to the lungs at the alveolar level and may manifest as long as 24 hours post exposure”. High levels of Orotic Acid can be dangerous and, as a synthetic pharmaceutical drug, it can be deadly or induce Orotic Aciduria, which is an autosomal recessive disorder characterized by megaloblastic anemia and orotic acid crystalluria that is frequently associated with some degree of physical and mental retardation. Other side effects are heart abnormalities, seizures, coma, and possibly even death. A Chinese patent from the Shenghai Institute of Organic Chemistry of CAS to synthesize Orotic Acid uses sodium bromide, chlorine and maleylurea; then, the 5-bromine-2, 6-dioxo-hexahydropyrimidime-4-carboxylic acid and sodium hydroxide. Sodium bromide is a pesticide with reproductive toxicity as demonstrated in rat studies. Chlorine is, of course, an extremely dangerous industrial poison. Maleylurea is another toxic substance. 5-bromine-2 induces methemoglobinemia and delayed encephalopathy. 6-dioxo-hexahydropyrimidime-4-carboxylic acid is toxic while sodium hydroxide is corrosive to all body tissues. Other processes for producing Orotic Acid use Corynebacterium. This is a lethal exotoxin that induces diphtheria. Orotic Acid, a promoter of liver carcinogenesis, induces DNA damage in rat livers. It also induces hypertension associated with impaired endothelial Nitric Oxide synthesis, ultimately disrupting your redox balance. There was toxic and vascular nephropathy associated with Orotic Acid administration in laboratory cats. It destroys the liver of rats. In other studies, it induced fatty liver, causing weight gain. Please see the toxicity data sheet for Orotic Acid. It’s suggested to “avoid using Lithium Orotate until more is known”. Lithium Orotate supplements Some synthetic Lithium Orotate supplements boast of being organic or natural. I’ve noticed that Medical Doctors’ definition of organic or natural may vary greatly from the facts. Dr. Edward Group, D.C. from Global Healing, advertises a Lithium Orotate supplement as “natural trace minerals” for mood stabilization. Dr. Ed was interviewed by Mike Adams of Natural news, where he convincingly boasted about their “all natural” products and heavy metal detox protocols. The company went so far as to register their Lithium Orotate product on Amazon as “organic” and then later removed their false advertising and fake medical claim. However, things remain forever on the Internet. Oops! I reached out to Global Healing to give them a chance and asked directly if Global Healing is using “all natural” lithium and “all natural” orotic acid in their Lithium Orotate supplement. They responded by telling me that they derive their Lithium Orotate ingredients from all natural sources. When I pressed them for more information, asking what their sources are, they vaguely answered me with “it varies”. Oops, again! On their Lithium Orotate label, Global Healing only states that their lithium source comes “from lithium orotate”. Lithium does not naturally contain orotic acid, so this doesn’t make sense if it were “natural”. If it were natural, they would have two sources not one, because lithium and orotic acid are not naturally found together. If Global healing’s lithium source is from “lithium orotate”, then this is the patented pharmaceutical Lithium Orotate synthetic salt and this is false advertising. Dr. Edward’s Group is also selling and promoting EDTA and C-60 as health supplements. They claim that Calcium Disodium EDTA promotes “cardiovascular and immune health” but there’s no scientific evidence to support this claim. Please read: Is C60 And EDTA Safe? Clinical Review Lithium chloride Lithium chloride metal chloride salt is a toxic, inorganic synthetic compound. Please see the safety data sheet. Lithium chloride is produced by treatment of lithium carbonate with hydrochloric acid. A single exposure to hydrochloric acid causes organ toxicity and there are cases of lithium toxicity from Internet dietary supplements. Please avoid this at all costs. Sodium Citrate Sodium citrate (citric acid) is another toxic preservative. It’s a synthetic chemical that induces symptoms such as paresthesia, hypotension and possible cardiac arrhythmia. It’s being touted as an “anti-coagulant” and prooted on Karl.C’s Substack. But honestly, the blood results are not good. Sodium citrate contains propylene glycol which is neurotoxic. Read more here. Superior, natural anti-coagulants can be found in my premium detox and repair protocol. Please see: Dr. Ariyana Love's Anti-Aging Premium Detox Protocol Lithium and Graphene weapon systems On a side note, during my research I came across some pertinent information. Synthetic graphite is used for lithium-ion batteries. Pharmaceutical lithium is being used with reduced graphene oxide-based electrodes to produce a higher capacity of electrical conductivity. Nanocomposites based on hydroxyapatite/lithium oxide and graphene oxide nanosheets are indeed being used for medical applications. Lithium batteries have served as the predominant power source for implantable medical devices such as nanowires, which are used in tissue scaffolding technology. Scientists are using scaffolds made from conductive silicon nanowires to reconstruct artificial heart tissue. Nanowired organoids are used to accelerate the development of stem cells into healthy, well-functioning heart tissue. They create an organoid from a mixture of stem-cell-derived heart cells, stromal connective tissue cells, and endothelial cells – which line the walls of blood vessels. Incidentally, Methylene Blue is used to kick-start the growth of the stem cells used in tissue scaffolding. Please see: Methylene Blue Is Pharmaceutical Poison Polymers-ceramic nonwoven compositions supercapacitors with electrical storage capacity are self-organized and have tinsel strength. They’re not implanted into the body per se, they are grown inside the body using graphene oxide and lithium-fueled nanowires. Highly porous membranes with self-organized Nanopores are used for rapid sequencing of genes. The long, white “fibrous clots” that embalmers are finding in the veins of dead vaccinated individuals, is part of this transhumanist agenda to turn people into a new species of super-conducting robots. Karen Kingston recently exposed that Moderna is using Graphene Oxide Nanoparticles in DARPA’s hydrogel lipid-payloads. Please read: The Covid-19 Vaccine “Antigen” is Anthrax Graphene oxide–silver Nanowire nanocomposites are being used for enhanced sensing of Hg2+ (mercuric cations). These are energy harvesting devices and hybrid materials using carbon nanotubes (graphene oxide hydrogels) and polyethylene glycol nanocomposites. They’re highly toxic, as a 2019 study demonstrates, but they’re being used none-the-less for internal biosensor and bioimaging. The patent holders can essentially read the internal biometric data of “vaccinated” individuals without their Informed Consent. Please read: EDTA Snakeoil! Ana Maria Mihalcea's Medical Malfeasance Exposed Conclusion There’s no reason under the sun to use any experimental pharmaceutical drugs. 100 years ago humanity got along just fine with natural cures. None of the pharmaceuticals mentioned in this article are effective at heavy metal chelation. I have many clients who were very sick after using EDTA especially, along with other experimental drugs that will not achieve detox. It’s simply not logical to treat poisoning with more poison! To achieve an affectiv detox, you must eliminate toxins. Superior heavy metal chelators exist, and I help people to learn how to use them. You can schedule a consultation with me here for truly all natural health protocols that contain the greatest breakthroughs in medical science and heavy metal chelation. Let’s be Pharma free. https://substack.com/home/post/p-145685685
    SUBSTACK.COM
    Lithium Orotate Dietary Supplements Are Pharmaceutical Snakeoil
    I was asked by a client to investigate lithium orotate, lithium chloride and sodium citrate as health supplementation, and determine if these substances are safe for human consumption and if they have any medicinal benefits. These substances are being promoted by medical doctors, Naturopathic doctors and other health care practitioners as health miracles, but are they?
    Like
    1
    0 Comments 0 Shares 13914 Views
  • The COVID-19 Vaccine Antigen Is ANTHRAX
    Dr. Ariyana Love
    By Dr. Ariyana Love

    Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein.

    We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX?

    “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.”

    Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention.

    A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more.

    According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast).

    Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.”

    The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out.


    Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides


    In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”.

    Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible.

    Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects.


    PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses


    The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare.

    In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg.

    Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs.

    Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant.

    The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels.

    Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax.

    Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

    SPIKE PROTEIN IS AEROSOLIZED ANTHRAX

    There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.”

    The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”.

    “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.”

    The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions.

    The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells.

    The following quote about the Anthrax “protective antigen” is particularly revealing:

    “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).”

    Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”.

    Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized.

    This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic.

    This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality.

    ALHYDROGEL

    According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel.

    Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health.

    In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

    In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death.

    Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network.

    Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system.

    This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from?

    This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

    “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA.

    Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public.

    Alhydrogel was improved and transformed into the Nanoalum adjuvant.

    Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor.

    Alhydrogel is also carried in the lipid coating of nanoparticles.

    The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites.


    Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector!


    ANTHRAX SYMPTOMS AND TREATMENT

    Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs.

    Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance).

    Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time.


    Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review


    Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers.

    The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis?

    Anthrax also coagulates the blood.

    “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.”

    Read more here and here.

    Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax.

    It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation.


    This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia.

    All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal.

    Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen.

    Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI.

    Heroine users in Europe have been tested with Injection Anthrax.

    Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind:

    “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.”

    TREATMENT

    If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax.

    Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning.

    Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol.

    I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system.

    Please follow me on Telegram @drloveariyana and X @drloveariyana.

    If you would like to donate to my research, please do so here.


    UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE.

    The Covid-19 Vaccine Antigen Is ANTHRAX

    Read more:
    https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true


    https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    The COVID-19 Vaccine Antigen Is ANTHRAX Dr. Ariyana Love By Dr. Ariyana Love Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX? “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.” Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention. A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more. According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast). Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.” The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out. Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects. PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare. In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg. Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant. The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels. Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax. Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero SPIKE PROTEIN IS AEROSOLIZED ANTHRAX There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.” The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”. “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.” The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions. The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells. The following quote about the Anthrax “protective antigen” is particularly revealing: “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).” Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized. This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic. This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality. ALHYDROGEL According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel. Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health. In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”. In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death. Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network. Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system. This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from? This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel. “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA. Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public. Alhydrogel was improved and transformed into the Nanoalum adjuvant. Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor. Alhydrogel is also carried in the lipid coating of nanoparticles. The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites. Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector! ANTHRAX SYMPTOMS AND TREATMENT Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs. Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance). Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time. Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers. The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis? Anthrax also coagulates the blood. “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.” Read more here and here. Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax. It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation. This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia. All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal. Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen. Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI. Heroine users in Europe have been tested with Injection Anthrax. Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind: “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.” TREATMENT If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax. Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning. Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol. I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system. Please follow me on Telegram @drloveariyana and X @drloveariyana. If you would like to donate to my research, please do so here. UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE. The Covid-19 Vaccine Antigen Is ANTHRAX Read more: https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
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  • Doctors don't know the functionality of the immune system.
    Our immune function is perfect. Our bodies are created by intelligent design. Our body is programmed to solve every embalance, naturally.
    In a state of poisoning, also accute poisoning, you must treat the body gently but firm. Only when a person achieves detox by boosting alkalinity can homeostasis return.
    Pharmaceuticals destroy vital functions of our immune system, often permanently. Genetic modifications are occurring and this phenomenon is aerosolized, we know from early studies on CONVID-DEMOCIDE101.
    Unless MD's realize we can work together and accomplish our goals faster (saving humanity one life at a time) then things can begin to change in the world of medicine.
    A patient or client must remain in detox daily to push to self-replication of the nanoparticles back, until the immune system is fully rescued and cancelation is achieved. Then chelation continues for several months with a good protocol, also tackling parasites and bacterium while turbo charging the immune system with superior medicines; essential oils, salts, super antioxidants. The right combo of things is critical.

    https://t.me/drloveariyana/1613
    Doctors don't know the functionality of the immune system. Our immune function is perfect. Our bodies are created by intelligent design. Our body is programmed to solve every embalance, naturally. In a state of poisoning, also accute poisoning, you must treat the body gently but firm. Only when a person achieves detox by boosting alkalinity can homeostasis return. Pharmaceuticals destroy vital functions of our immune system, often permanently. Genetic modifications are occurring and this phenomenon is aerosolized, we know from early studies on CONVID-DEMOCIDE101. Unless MD's realize we can work together and accomplish our goals faster (saving humanity one life at a time) then things can begin to change in the world of medicine. A patient or client must remain in detox daily to push to self-replication of the nanoparticles back, until the immune system is fully rescued and cancelation is achieved. Then chelation continues for several months with a good protocol, also tackling parasites and bacterium while turbo charging the immune system with superior medicines; essential oils, salts, super antioxidants. The right combo of things is critical. https://t.me/drloveariyana/1613
    T.ME
    Dr. Ariyana Love (new channel)
    Doctors don't know the functionality of the immune system. Our immune function is perfect. Our bodies are created by intelligent design. Our body is programmed to solve every embalance, naturally. In a state of poisoning, also accute poisoning, you must treat the body gently but firm. Only when a person achieves detox by boosting alkalinity can homeostasis return. Pharmaceuticals destroy vital functions of our immune system, often permanently. Genetic modifications are occurring and this phenomenon is aerosolized, we know from early studies on CONVID-DEMOCIDE101. Unless MD's realize we can work together and accomplish our goals faster (saving humanity one life at a time) then things can begin to change in the world of medicine. A patient or client must remain in detox daily to push to self-replication of the nanoparticles back, until the immune system is fully rescued and cancelation is achieved. Then chelation continues for several months with a good protocol, also tackling parasites and bacterium while turbo…
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  • Do You Know What’s in a Vaccine? Chemical Ingredients
    Addendum to the Childhood Vaccination Series


    All Global Research articles can be read in 51 languages by activating the Translate Website button below the author’s name.

    To receive Global Research’s Daily Newsletter (selected articles), click here.

    Click the share button above to email/forward this article to your friends and colleagues. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles.

    ***

    Over the last few decades, the number of chemicals added to foods and other products has skyrocketed. Chemicals are added to “enhance flavor”, make fruits and vegetables look fresh, extend the shelf life of packaged foods and for other invented reasons. A cornucopia of chemicals are also found in lotions and beauty products with the ostensible reason that these chemicals make beauty products feel, look, and smell nice.

    Along with this increase in heavily processed foods has come increased skepticism about the necessity of inserting chemical additives into everything we touch and taste. A significant and growing segment of the US population are beginning to examine the health consequences of ingesting and absorbing these chemical-laden products.

    This growing awareness about the adverse effects of ingesting and absorbing synthetic ingredients and the public’s understanding of the attendant health benefits of consuming products free from synthetic chemicals has prompted consumers to seek out organic ingredient-based items in their foods and skin lotions.

    More people are showing interest in knowing about the ingredients in their food and striving to ‘eat clean.’ This increased awareness is evidenced in the steady growth of the organic food industry and trends in the natural and organic cosmetic industry where demand is higher than ever.

    This same level of concern has begun to seep into the public conscience regarding a certain medical product that has mostly avoided scrutiny – the vaccine.

    Having been trained to accept that this product is a customary aspect of everyday life, most people haven’t given much thought to what’s inside the vaccine vials. Rarely will the vaccine ritual in the doctor’s office include a discussion about the ingredients which are about to be injected into the patient’s body. It’s highly likely the physicians and nurses themselves don’t know the ingredients of each vaccine.

    So what’s in that vial? What’s coming through that needle?

    A Partial List of Ingredients

    Aluminum: Aluminum salts are used in some vaccine formulations as an adjuvant. An adjuvant is a substance added to vaccines to ostensibly enhance the immune response. Examples of aluminum salts in some vaccines are aluminum hydroxide, aluminum phosphate, alum (potassium aluminum sulfate) or mixed aluminum salts.

    In a 2011 study Canadian scientists Professor Christopher Shaw and Dr. Lucija Tomljenovic stated the following:

    “Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences.”

    Multiple studies have shown that the intramuscularly injected aluminum vaccine adjuvant is absorbed into the systemic circulation and travels to different sites in the body, such as the brain, joints, and the spleen, where it accumulates and is retained for years post-vaccination.

    Mercury (thimerosal): Thimerosal is an ethyl mercury-based preservative used in vials that contain more than one dose of a vaccine (multi-dose vials) to prevent germs, bacteria and/or fungi from contaminating the vaccine. While in decline some flu vaccines and childhood vaccines in multi-dose vials still utilize thimerosal.

    Mercury is known to be a genotoxic agent, even in minute concentrations, which can damage the genetic information within a cell causing mutations, which may lead to cancer.

    A meta-analysis epidemiological study suggested thimerosal containing vaccines significantly increased the risk of neurodevelopmental disorders.

    A 2011 study suggested there may be higher rates of blood and brain mercury levels in monkeys exposed to vaccines containing thimerosal.

    The American Academy of Pediatrics and the U.S. Public Health Service (1999) published a joint statement that urged “all government agencies to work rapidly toward reducing children’s exposure to mercury from all sources.”

    Gelatin: Gelatin is used as a stabilizer in some vaccines licensed in the U.S. Stabilizers are added to vaccines to protect the active ingredients from degrading during manufacture, transport and storage.

    Gelatin is a protein obtained from cows or pigs and produced by the partial hydrolysis of collagen extracted by boiling animal parts such as cartilage, tendons, skin, bones and ligaments in water. Some people might have a severe allergic reaction to it.

    Certain vaccine viruses are grown on gelatin derived from the ligaments of pigs fed heavy doses of glyphosate in their feed. Gelatin comes from collagen which has lots of glycine.

    Gelatin is one of the most commonly identified causes of allergic reactions to vaccines.

    A 1999 Japanese study showed most anaphylactic reactions and some urticarial reactions to gelatin-containing measles, mumps, and rubella monovalent vaccines were associated with gelatin allergy. Based on these findings Japan removed gelatin from vaccines in 2000.

    Formaldehyde: Formaldehyde is used during the manufacture of some vaccines to inactivate viruses (like polio and hepatitis A viruses) or bacterial toxins (like diphtheria and tetanus toxins).

    Formaldehyde is a human carcinogen based on evidence from cancer studies in humans and is listed as aknown to be human carcinogen in the National Toxicology Program’s (NTP) Twelfth Report on Carcinogens(2011).

    Phenol/Phenoxyethanol: Phenoxyethanol is used in vaccines and biologics as a preservative to prevent microbial growth.

    A 2010 study, The relative toxicity of compounds used as preservatives in vaccines and biologics, assessed the relative cytotoxicity of the levels of the compounds commonly used as preservative in US licensed vaccines and found that for phenoxyethanol it was 4.6-fold, for phenol 12.2-fold and for Thimerosal >330-fold.

    They concluded, “None of the compounds commonly used as preservatives in US licensed vaccine/biological preparations can be considered an ideal preservative, and their ability to fully comply with the requirements of the US Code of Federal Regulations (CFR) for preservatives is in doubt.”

    Case reports (here, here and here) have suggested a link between phenoxyethanol and urticaria (hives), eczema and anaphylaxis.

    Triton X-100: Triton X –100 or octylphenol ethoxylate (OPE) is a surfactant (reducing the surface tension of liquids) and stabilizer present in some influenza vaccines.

    OPEs are endocrine disruptors and break down relatively easily into Octylphenols (OPs), which are more harmful. Endocrine disruptors can alter reproductive function, increase incidences of breast cancer, affect growth patterns and neurodevelopment in children and change immune function.

    Squalene: Squalene is a naturally-occurring substance derived primarily from shark liver oil. When combined with other ingredients it becomes an adjuvant, which, like aluminum, is added to vaccines to elicit a stronger immune response from the body.

    A 2000 study demonstrated that one intradermal injection of squalene adjuvant produced arthritis in rats.

    Some believe that Gulf War Syndrome was linked to the presence of squalene in certain lots of the anthrax vaccine.

    Beta-propiolactone: Beta-propiolactone (BPL) is a commonly used reagent for the inactivation of viruses for use in vaccine preparations. It has recently been used in the development of an inactivated SARS-CoV-2 vaccine preparation.

    Beta-propiolactone is a known carcinogen. Local sarcomas have been produced by subcutaneous injection of beta-propiolactone in rats. In the laboratory sarcomas and squamous papillomas in mice were produced by a single subcutaneous injection of a minute amount of beta-propiolactone.

    Polysorbate 80: Polysorbate 80 is present in some vaccines to stop the vaccine from separating into its component parts. In a PubMed study Polysorbate 80 was described as, “a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.”

    In a pharmacological study on mice and rats Polysorbate 80 produced, “mild to moderate depression of the central nervous system with a marked reduction in locomotor activity and rectal temperature, exhibited ataxia and paralytic activity and potentiated the pentobarbital sleeping time.”

    The results of that study concluded, “The results of the present study indicate that polysorbate 80 can neither be used as a solvent for isolated tissue experiments nor when considered for intravenous administration.”

    Another study from the American Association for Cancer Research (AACR) suggested the dietary emulsifier polysorbate 80 may induce low-grade inflammation which may contribute to metabolic diseases and increase the potential for development in colon cancer.

    Genetically modified yeast: S. cerevisiae, a species of yeast, is used in vaccines in a variety of ways. It is used as an adjuvant and now through genetic manipulation it is being used to create artificial antibodies

    Studies have suggested that genetically engineered yeast used in vaccines may be a contributing factor to autoimmune disorders.

    Monosodium Glutamate (MSG): Monosodium Glutamate is used in small amounts in some vaccines to keep them stable and protect them from losing potency even when exposed to heat and light.

    In a study that looked at rat fertility and MSG consumption the authors found there was a negative impact on the rats’ fertility.

    In another study it was noted that chronic MSG intake caused kidney dysfunction and renal oxidative stress in the animal model.

    Cells From Aborted Fetus: Fetal cell lines are used to grow viruses which are then collected from the cell cultures and processed further to produce the vaccine itself.

    The cell lines are propagated from lung tissue of mature aborted and used in the current manufacture of a number of routine vaccines, including measles, mumps and rubella (MMRV), diphtheria, tetanus, pertussis and polio, (DTaP-IPV), Hepatitis A and chickenpox.

    Aborted fetal cells are listed on vaccine package inserts as “Human Fetal Diploid Cells.” Two aborted fetal cell lines, WI-38 and MRC-5, have been grown under laboratory conditions since the 1960s. Diploid cells (WI-38, MRC-5) vaccines have their origin in induced abortions.

    The use of such cell lines can be profoundly objectionable to segments of the population who hold certain religious and/or philosophical beliefs.

    The Italian vaccine research and advocacy organization Corvelva released a study in 2019 regarding the use of aborted fetal cell lines in vaccines.

    In their summary they highlighted the following:

    The human genomic DNA contained in this vaccine is clearly, undoubtedly abnormal, presenting important inconsistencies with a typical human genome, that is, with that of a healthy individual.
    560 genes known to be associated with forms of cancer were tested and all underwent major modifications.
    There are variations whose consequences are not even known, not yet appearing in the literature, but which still affect genes involved in the induction of human cancer.
    What is also clearly abnormal is the genome excess showing changes in the number of copies and structural variants.
    Serum From Aborted Calf Fetus Blood: The purpose for the fetal bovine serum is to provide a nutrient broth for viruses to grow in cells.

    Humane Research Australia describes the process of how the blood is collected, “The blood is collected after the slaughter of a mature female cow, the mother’s uterus containing the calf fetus is removed during the evisceration process and transferred to the blood collection room. A needle is then inserted between the fetus’s ribs directly into its heart and the blood is vacuumed into a sterile collection bag.

    Only fetuses over the age of three months are used otherwise the heart is considered too small to puncture. Once collected, the blood is allowed to clot at room temperature and the serum separated through a process known as refrigerated centrifugation.”

    Beyond certain ethical considerations scientists have found that different bovine tissues contain different amounts of the BSE agent.

    Antibiotics: Antibiotics are used during the manufacturing process of some vaccines to stop bacteria growing and contaminating the vaccine.

    Antibiotics found in some vaccines include neomycin, streptomycin, polymyxin b, gentamicin and kanamycin.

    Polymyxin B comes with a warning that, “This medicine has not been fully studied in pregnant women. This medicine may cause kidney problems. This medicine may cause nerve problems”, as well as a laundry list of side effects.

    Similar warnings are found with streptomycin, neomycin, gentamicin, and kanamycin.

    A study out of Finland raised concerns about excessive antibiotic use in early childhood which may lead to weight gain and altered gut bacteria.

    What Else Could be in That Needle?

    The list above is not a complete account of all the ingredients found in various vaccine cocktails. A comprehensive manufacturers’ catalog of ingredients can be found here, here and here.

    The reality is that even a complete list issued by the producer doesn’t tell the entire story of what is found in vaccines.

    Using an Environmental Scanning Electron Microscope equipped with an X-ray microprobe a group of Italian scientists examined 44 samples of 30 different vaccines and found dangerous contaminants, including metal toxicants in 43 of the 44 samples tested.

    In the study, published in the International Journal of Vaccines and Vaccination, the researchers detected lead, chromium, nickel and other metals in every adjuvant sample tested.

    Additional metal contaminants identified in 25 of the human vaccines included platinum, silver, bismuth, iron, and chromium. Foreign impurities such as zirconium, hafnium, strontium, tungsten, antimony, bismuth, cerium and were also detected in many of the vaccines tested.

    The researchers commenting on their unexpected findings reported:

    The quantity of foreign bodies detected and, in some cases, their unusual chemical compositions baffled us. In most circumstances, the combinations detected are very odd as they have no technical use, cannot be found in any material handbook and look like the result of the random formation occurring….In any case, whatever their origin, they should not be present in any injectable medicament, let alone in vaccines, more in particular those meant for infants. [Emphasis added]

    When interviewed lead scientist Dr. Antonietta Gatti, of the National Council of Research of Italy and Scientific Director of Nanodiagnostics, explained that the discovery of vaccine impurities shocked the researchers:

    Those particles should not have been there. We had never questioned the purity of vaccines before. In fact, for us the problem did not even exist. All injectable solutions had to be perfectly pure and that was an act of faith on which it seemed impossible to have doubts. For that reason, we repeated our analyses several times to be certain. In the end, we accepted the evidence.

    Speculating on the potential consequences of these foreign impurities Dr. Gatti stated:

    The particles, be they isolated, aggregated or clustered, are not supposed to be there… Our tissues perceive these foreign bodies as potential enemies…Unfortunately, though, the particles we found in vaccines, are not biodegradable. So, all the macrophages’ efforts will be useless, and depending on the exact chemicals involved, the particles may be especially toxic. Cytokines and pro-inflammatory substances in general are released and granulated tissue forms, enveloping the particles. This provokes inflammation which, in the long run, if locally persistent, is known to be a precursor to cancer.

    Along with unlisted metal contaminants another unlisted contaminant was noted in some vaccines when a preliminary screening result from Microbe Inotech Laboratories Inc. detected glyphosate in the childhood vaccines they tested.

    Merck’s MMR II vaccine had 2.671 parts per billion (ppb) of glyphosate, Sanofi Pasteur’s DTap Adacel vaccine had 0.123 ppb, Novartis’ Influenza Fluvirin had 0.331 ppb, Glaxo Smith Kline’s HepB Energix-B vaccine had 0.325 ppb, Merck’s Pneumococcal Vax Polyvalent Pneumovax 23 had 0.107 ppb of glyphosate.

    These findings prompted Moms Across America to send a letter to the FDA, CDC, EPA,NIH and California Department of Health requesting that they test vaccines for glyphosate and recall contaminated vaccines.

    MIT scientist Dr. Stephanie Seneff remarked on the route by which glyphosate could get into vaccines:

    Collagen is a protein found in large amounts in the ligaments of cows, and these ligaments are often used in the production of gelatin. The MMR vaccine and flu vaccine viruses are grown as live cultures on gelatin sourced from cows fed high concentrations of glyphosate in their GMO Roundup­Ready feed.

    What to Do?

    Given the complex nature of the composition of vaccines and the paucity of information volunteered to the public on the manufacturing processes and ingredients that go into these products, how does one go about navigating this subject?

    Conventional wisdom might suggest, “Ask your doctor.” But how independent are these doctors?

    Where do you turn when you discover physicians and pediatricians, who have a legal duty to fully inform patients about vaccine risks and side effects, have ideological and material incentives to avoid presenting specific information that might cause a parent to question a vaccine?

    What about educational materials and advice from the agencies tasked with protecting public health? Can we trust the FDA and the CDC to provide detailed and unbiased information when it is known that they get substantial amounts of money from vaccine manufacturers?

    Informed consent is a principle in medical ethics and medical law that a patient must have sufficient information and understanding before making decisions about their medical care.This includes being given a thorough account of the risks and benefits of treatments, alternative treatments, the patient’s role in treatment, and their right to refuse treatment.

    Informed and individualized health care decisions about any product one puts into their or their children’s body starts with being fully informed with what is in that product.

    *

    Note to readers: Please click the share button above. Follow us on Instagram and Twitter and subscribe to our Telegram Channel. Feel free to repost and share widely Global Research articles.

    This article was originally published on Health Freedom Defense Fund.

    Featured image is from HFDF



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