Just A little Prick: It’s All Good!

(OK:  WAY TOO LONG FOR A QUICK READ, BUT it is time to acknowledge what we are really dealing with and what you want your future and that of your loved ones to be.)

Propaganda-In-Action: How The Media Minimizes mRNA Vaccine Injuries

“Hurt” by ₡ґǘșϯγ Ɗᶏ Ⱪᶅṏⱳդ is marked with CC0 1.0
Propaganda is the Technocrat way of sowing confusion and doubt about what otherwise is self-evident reality. Some people call this “gaslighting”. Whatever you are seeing with your own eyes is miss-interpreted or miss-represented and therefore you should accept the propaganda as being true. This is blatant fraud, but people fall for it time after time, giving the reason why propaganda continues to be sprayed from a firehose. ⁃ TN Editor

I regard consensus science as an extremely pernicious development that ought to be stopped cold in its tracks. Historically, the claim of consensus has been the first refuge of scoundrels; it is a way to avoid debate by claiming that the matter is already settled. Whenever you hear the consensus of scientists agrees on something or other, reach for your wallet, because you’re being had… Let’s be clear: the work of science has nothing whatever to do with consensus. Consensus is the business of politics. Science, on the contrary, requires only one investigator who happens to be right, which means that he or she has results that are verifiable by reference to the real world. In science consensus is irrelevant. What are relevant are reproducible results. The greatest scientists in history are great precisely because they broke with the consensus. There is no such thing as consensus science. If it’s consensus, it isn’t science. If it’s science, it isn’t consensus. Period.

– MICHAEL CRICHTON, LECTURE AT THE CALIFORNIA INSTITUTE OF TECHNOLOGY, PASADENA, CALIFORNIA, JANUARY 17, 2003. (1)

Within a few months of the SARS-Cov-2 vaccines being injected into millions of people, numerous types of adverse reactions were reported throughout the world. Information about adverse events became an object of intense denial and obfuscation by government agencies and state-funded and corporate-sponsored media, whether the information was in the form of rumors, amateur speculation, or serious scientific inquiry by qualified academics.

However, in 2023, government registries of vaccine injuries now reveal serious deficiencies of the vaccines designed to combat SARS-Cov-2. In a report published in the International Journal of Vaccine Theory, Practice, and Research, the authors analyzed data from regulatory surveillance and self-reporting systems in Germany, Israel, Scotland, the United Kingdom, and the United States “to find long-term adverse events of the COVID products that cannot be captured during the expedited safety analyses.” This extract from the abstract goes on to state:

Our data show, among other trends, increases in adverse event reports if we compare COVID products to influenza and pertussis vaccines and statistically significant higher numbers of hospital encounters in military personnel, as well as increases in incidences of thromboembolic conditions, such as menstrual abnormalities, myocarditis, and cerebrovascular events after the implementation of COVID injection mandates, compared to the preceding five years… Our meta-analysis of both national and international vaccine adverse events emphasizes the importance of re-evaluating public health policies that promote universal mass injection and multiple boosters for all demographic groups. In combination with informal reports from reliable witnesses, limitations of the safety trials, and the decreased lethality of new strains, our research demonstrates that the cost (both monetary and humanitarian) of injecting healthy people, and especially children, outweighs any claimed though unvalidated benefits. (2)

In this late phase of the event that started in 2020, governments and their various propaganda platforms cannot hide these adverse events and are now engaged perhaps in what can be called the “cooling the mark out” phase of the pandemic. An article in The New Yorker in 2015 discussed this sociological phenomenon (3). The term was used in a 1952 study by Erving Goffman to describe an important element of con artistry, but it also describes generally any social mechanism that is needed to help people adjust to material losses and humiliation. When a victim is forced to acknowledge he has been conned or ripped off, the perpetrators have to make some effort to help him adjust. Otherwise, he may do something “irrational” such as pursuing violent revenge, media exposure, criminal charges, or a lawsuit. He needs to be reminded that he still has precious things he could lose, so he has to just accept the loss and humiliation and go back to his wife and children. Governments are doing the same now: “Yes, there have been some rare adverse events. Get in line and fill out this form to apply for your legally entitled compensation. We will be with you shortly.”

Some of the adverse events are mild reactions such as fainting, dizziness, fatigue, and flu-like malaise lasting a few days—just like the viral infection itself, ironically enough. People under age seventy who had a 99.9% chance of recovering quickly from the infection chose instead to suffer this malaise, going along with the social coercion and accepting the unknown risks of vaccination (4). As if it were a scheduled elective surgery, they were simply choosing the timing of when they were going to feel horrible—i.e. “I should get this over with now before my vacation.”

The less mild reactions are myocardial infarction, myocarditis, pericarditis, tachycardia, stroke, blood clots (embolism), aneurysm, tinnitus, Bell’s Palsy, Guillain-Barré Syndrome, transverse myelitis, cancer, heavy bleeding, menstrual irregularities, miscarriage, neurological symptoms, immune system disorders, skin rash, intense pain and numbness, memory loss, “brain fog,” and “inexplicable” sudden death. These conditions can be transitory or, like the last one on the list, permanent.

One can easily find peer-reviewed research papers that confirm the increased rates of these adverse health events after vaccination, yet a curious thing about them is that they often end very tentatively, including a phrase such as the one found in the extract below:

The number of reported cases is relatively very small in relation to the hundreds of millions of vaccinations that have occurred, and the protective benefits offered by COVID-19 vaccination far outweigh the risks. (5)

This tendency was also found in the recent Cochrane review on the efficacy of wearing masks (6). Instead of stating emphatically that in numerous studies there is no evidence to show a benefit in wearing masks, the authors concluded by stating all the ways that the studies they reviewed might contain some undiscovered flaws. It was like they were afraid of having made an important discovery that should change government policy.

Minimization, Exaggeration, Diversion and Distraction in Mass Media and Scientific Journals

Example 1: Putting a Positive Spin on Vaccine-Induced Cancer

Another such example, this one in the popular press, was the story told about the immunologist Dr. Michel Goldman in The Atlantic in September 2022 (7). As an advocate of many vaccines during his career, and in particular as a believer in the salutary effects of the mRNA vaccines, he was confronted with the images on a CT scan that showed lymphatic cancer spreading aggressively in his body soon after his mRNA shots, both after the first two shots and then again after a booster shot a few months later. The cancer connection to the shots was hard to deny because the aggressive growth was extremely rare and also because the first shots were in the left arm and the cancer appeared on the left armpit. The booster was injected in the right arm, then the cancer appeared on the right side.

If the subject matter were not so dark, the article would appear to be a satire of people who can’t think logically or change their views when confronted with new facts. The author, Roxanne Khamsi, goes to extreme lengths to describe the struggle she had to write the story in a way that would not lend support to those who spread “anti-vaccine disinformation.” Dr. Goldman was just as determined, willing to see himself as one of the rare unfortunate ones who must suffer so that so many others may be saved by these supposedly miraculous new drugs.

As Piers Robinson’s lessons on propaganda have taught us, the propagandist doesn’t lie directly. Propaganda operates through exaggeration, omission, incentivization and coercion, and these are in evidence in The Atlantic, in this article, and in all of its coverage of the pandemic (8). Roxanne Khamsi selectively focuses on the most hyperbolic reactions from the “fearmongers [who] have made the problem worse by citing scary-sounding data from the Vaccine Adverse Event Reporting System… with insufficient context.” She also had to mention that a vaccination center was set ablaze in Poland. Nowhere in the long article is there any mention of less radical reactions such as the hundreds of scientific papers describing adverse events—studies written by non-fearmongering sober-minded scientists. Such exaggeration and omission move the reader toward an acceptance of the necessity of mass vaccination.

Another facet of this propaganda is its use of what could be called “The New Yorker” genre of journalism. It is a “long read” piece (4,000 words) of narrative storytelling that uses the methods of fictional literature. It dramatizes the story arc of one individual, going deep into his biographical details, thoughts, and feelings. This is the genre that is natural and expected by the educated professional class of people who wake up on Sunday mornings and look for something serious to read, something that will make them feel smart before going back to the grind the next day. It is also a genre used by documentary filmmakers. They may have an important social problem to expose, but they have to find a person at the center of it and tell a story. Otherwise, the audience will tune out. The TED talks tell us it is hardwired in our brains. Humans are storytellers.

The New Yorker genre makes the educated class feel informed and serious: 4,000 words, a deep read, not the superficial stuff that the deplorables read in the New York Post! The length of the piece makes it likely that readers won’t be using their time to read anything else. Most importantly, the use of this genre diverts attention away from the need for an objective understanding of a phenomenon that involves billions of victims. The writer and the subject, Dr. Goldman, say much about the need to understand the science and not inflame radical reactions from the so-called low-information types, but this genre is itself un-scientific, subjective, sentimental, and narrow in its scope.

The most stunning omission in the article is that neither the author nor Dr. Goldman makes the obvious logical conclusion that, considering both the apparent and the still unknown risks, mandatory or coerced vaccination is unethical, especially for a viral infection that 99.9% of people under age seventy can survive. After learning of what happened to Dr. Goldberg, persons in good health, if not propagandized to think otherwise, would logically decide in favor of taking their chances with an infection that will pass in a few days. This is especially true for people who, unlike Dr. Goldman, don’t have a brother who is head of nuclear medicine at a university hospital and may not have timely access to the high quality of health care that Dr. Goldman had.

The article concludes thus:

And as a longtime immunologist and medical innovator, he’s still considering the question of whether a vaccine that is saving tens of millions of lives each year might have put his own in jeopardy. He remains adamant that COVID-19 vaccines are necessary and useful for the vast majority of people.

Many would disagree and say that the vaccines are, at best, only for the non-vast minority of high-risk individuals who accept them with informed consent. Despite his own experience of suffering vaccine-induced aggressive lymphoma, Dr. Goldman believes that a vast majority of people should subject themselves to the risk of suffering the same fate. In September 2022, the time of publication, it had been officially acknowledged that the mRNA shots had not stopped the spread of the virus, had not induced lasting immunity, and may not have lowered the fatality rate of the illness. Other possible explanations:

(1) The virus harmed most of the vulnerable population before the vaccines arrived.

(2) Doctors learned how to treat the disease without resorting to deadly practices such as delayed treatment, ventilators and Remdesivir.

(3) The virus evolved into less deadly variants.

The purported benefits of the vaccines remain unprovable, and explanations (1)-(3) remain as matters of controversy.

Example 2: The Feint After Post-Vaccination Fainting

Other examples of this genre applied to the Covid-19 event are plentiful and easy to find in the media that have been funded by the Bill and Melinda Gates Foundation or sponsored by Pfizer and other hidden hands. I will describe just one more that shows that it was still being used in April 2023, three years on as the official narrative becomes untenable.

On April 10th, 2023, NBC News published a 3,400-word piece on the “fainting nurse” social media frenzy that occurred in December 2020 when frontline healthcare workers in the US started to receive the mRNA shots (9). The vaccination of nurse Tiffany Dover was recorded by a local television news crew because it was the big day when the savior vaccines had arrived to supposedly end the pandemic. Unfortunately, the cameras recorded her fainting shortly after receiving her injection.

The article describes how “conspiracy theorists” created an episode of “participatory misinformation” as they circulated her story on social media, exaggerated what the fainting meant, spread rumors of her death, and engaged in a campaign of harassment (a.k.a. doxing) (10). Tiffany remained steadfastly supportive of the vaccination program and believed that her fainting was inconsequential, yet she was traumatized by the doxing and chose to remain silent for two full years. Unfortunately, this choice only intensified the rumors of her death or of her enforced silence.

My critique of this article includes no support for the people who engage in doxing and wild speculation. My criticism is that this genre of journalism consistently associates all disagreement with the official narratives as the work of wild-eyed, deplorable bullies. It consistently ignores the hundreds of scientists who are publishing peer-reviewed articles on vaccine injuries and questioning the abandonment of standard public health policy that started in 2020.

Brandy Zadrozny, the author of this article about Tiffany Dover, felt it was necessary to associate Tiffany’s story with other instances of unhinged conspiracy theory such as the 2020 election being stolen from Donald Trump and the denial of the murders at Sandy Hook Elementary School. Thus, the very intentional implication here is that if you are concerned about the accumulation of medical journal articles describing a long list of vaccine-related injuries, think twice. You don’t want to be dismissed as one of those cruel and deranged fools who have lost touch with reality. Your family, friends and colleagues are all being trained to ostracize you for wrongthink, so forget about it. You are the mark that needs to be cooled out.

Instead of treating the “participatory misinformation” campaign as a problem of the deplorables that the righteous must struggle to solve, the writers of such articles could start to wonder if there is some legitimate anger driving such regrettable phenomena. There were very sound reasons to worry about a pharmaceutical product being rushed to market in less than a year, especially one that was based on a novel biotechnology. Additionally, fainting, after all, is not always a minor incident, and it is rational to be concerned about it happening so soon after a medical treatment. Furthermore, it would not be unreasonable for a healthy person to decide he would rather risk infection with the virus than suffer side-effects from an unproven vaccine. Not everyone has the good fortune to faint “into the arms of two nearby doctors” (as the fainting was described in the article). Some people break bones and sustain skull fractures. Some people have their adverse reaction after they leave the clinic and are driving home. Some have it months later.

After more than two years since vaccinations began, it should have been clear that, because the mRNA treatments were not as safe and effective as promised, no one should have ever been coerced into taking them. Their heavy promotion, backed by well-funded propaganda campaigns of half-truths and bold lies, was unethical, as was the gaslighting, shaming and shunning of the people who demanded bodily autonomy.

However, at this late date, after so much has been officially admitted about the adverse effects, including death, the author claimed that Tiffany’s story became a rallying point for those “who falsely believe that vaccines are killing and injuring people in droves.” (italics added) Those last two words were probably chosen carefully because without them one could not say they “falsely believe.” It is a fact that they are killing and injuring people, but “in droves” may be ambiguous enough to make the statement passable for a quibbling fact checker. The sentence is now “partially true” if one wants to see it that way.

One can denounce the campaign of coercion and still let Tiffany have her proclaimed “belief” in the vaccines. The issue that should be discussed is the failure of medical ethics in public policy that led to the vilification of people who had a different belief. They did not want to submit themselves to a medical therapy that had been rushed to market with no long-term safety data to support its use. Despite the facts, this issue remains utterly invisible to the writers who specialize in this genre.

The final thing to mention about this article is that, like the article in The Atlantic, it uses the devices of fiction. It focuses on the emotional and physical condition of the subject and thus leads the reader to an engagement with her story. Her eyes are “wide and bright and terribly blue.” They are described again at the end of the article as “electric blue.” The writer emphasizes this because a post-vaccination photo of her was not lit well and her eye color was not visible, and this is what set off rumors that it was not really her in the photo. Nonetheless, the descriptions are unnecessary embellishments. Readers don’t need to know her hair dye choices, either, but these too were described. This news article about a controversial pharmaceutical product could also be reported without the accompanying glamor photos of the very photogenic victim. There are, after all, less glamorous and less fortunate victims of vaccination who suffered fates worse than fainting (11). Tiffany is alive and healthy, and she did not refuse to be filmed on the day of her vaccination. This isn’t really about a story about her fainting and its aftermath, however. The purpose of this genre is the feint—the fake out and distraction from what the public should really be paying attention to.

Example 3: Minimization in Scientific Journal Articles

Let’s return to the scientific journal articles. Concluding statements in scientific papers are not always about objective findings. They are interpretations and opinions by the authors, and they often seem to go in the direction of minimizing the problems revealed by the study. It has always been standard practice for researchers to be humble about the impact of their work, for their conclusions may be disproven by subsequent research. Nonetheless, when it comes to any research related to Covid-19, excessive hesitancy and even fear are evident.

For some reason, the medical specialists authoring these papers never express alarm or suggest a halt to vaccination of individuals who are at low risk of suffering serious harm from the viral infection. Recall that the infectious mortality rate was found to be about 0.1%, more or less, depending on one’s age. It is this low for healthy individuals and higher for the elderly and the unhealthy. As mentioned above, the rate became lower as doctors learned how to treat the infection and abandoned dangerous interventions. Another factor was the virus itself becoming less deadly.

Readers might respond that I am ignoring the millions of cases of “long covid,” but my response is that there is no clinical definition for it, and it may be no different than the post-viral syndrome associated with influenza—a phenomenon which never aroused alarm in society before 2020. The alleged symptoms of long covid also overlap with adverse reactions to the vaccine, so if we must be concerned about long covid, we also have to object to the continued use of therapies that use the spike protein to induce immunity. Doctors are developing treatments for reactions to the spike protein, whether they came from the virus or the mRNA jabs. It is also likely that “long covid” is a side effect of “long type 2 diabetes” and various other chronic (i.e. long duration) illnesses that are the root causes of death by SARS-Cov-2.

The ritualistic minimization of vaccine injuries in the scientific reports is obviously an essential bow of fealty to the scientific priesthood. It is the modern equivalent of Galileo in the 17th century affirming the existence and greatness of God in order to, hopefully, have heliocentrism taken seriously. These researchers may feel privately that the matter is urgent, but they know that in order to shine any light on the issue in a respected medical journal, they will have to bow down to the official doctrine. They justify it as the only way to shine some light on the problem and change the system from within. If they really thought the matter was so trivial, they wouldn’t study it. Medical personnel could just treat their patients without worrying about the speculative role vaccines might have played in their illnesses. A doctor treating a cancer rarely worries about whether it was caused by fallout from nuclear weapons testing because identifying this cause would make no difference in the treatment. Her job is to treat the patient. However, in the late 1950s, some doctors saw a reason to speak out and create the political pressure that halted nuclear tests in the atmosphere in 1963.

The paper cited in the appendix below, to conclude this long essay, was chosen as an example of this minimization. It is concerned with liver diseases following vaccination. I found this one because recently I took note of the 15th mRNA-jabbed person in my social circles to suffer a severe health crisis since January 2021. In the two years before then, I knew of only one medical emergency among friends, family, and colleagues. In the 15th person’s case, it was a pyogenic liver abscess that put him in the ICU and almost killed him.

In studies like this that conclude by minimizing the problem, there is an obvious problem in saying the number of cases is “very small in relation to the hundreds of millions of vaccinations.” When one considers all of the research on adverse events in all other organ systems, one starts to think, as Yogi Berra said, “Little things are big.” Yogi Bear was smarter than the average bear, and Yogi Berra, the “dumb” sage of baseball legend, was, it seems, far smarter than the average immunologist. Little things do start to add up. One case of lymphoma, or fainting, or liver disease may seem insignificant when seen is isolation, but when all the adverse events are seen together from a distance, along with a sharp rise in all-cause mortality, we can start to ask the right questions (12). They are similar to the questions we should ask about the compounding effects of numerous environmental toxicants and pollutants humans are exposed to. One chemical might be declared safe at a certain exposure, but what is the combined effect of hundreds of such chemicals? It looks like the harms are extremely rare only when cases and types of injuries are studied in isolation and the victims are also kept isolated.

We could also add Yogi Berra’s other gems of wisdom that apply to the entire Covid phenomenon. When we find that not much has changed since Galileo’s time, recall that Yogi Berra said, “it’s like déjà vu all over again,” and when you think about all that has happened since March 2020, remember he said, “the future ain’t what it used to be.”

References


  1. J.R. Barrio, “Consensus science and the peer review.” Molecular Imaging and Biology. April 2009, 11(5): 293. doi: 10.1007/s11307-009-0233-0. PMID: 19399558; PMCID: PMC2719747.
  2. E. Romero, S. Fry, S., and B. Hooker, “Safety of mRNA Vaccines Administered During the First Twenty-Four Months of the International COVID-19 Vaccination Program,” International Journal of Vaccine Theory, Practice, and Research, 2023, 3(1), 891–910. https://doi.org/10.56098/ijvtpr.v3i1.7
  3. Louis Menand, “Crooked Psychics and Cooling the Mark Out,” The New Yorker, June 18, 2015. “The classic exposition of the practice of helping victims of a con adapt to their loss is the sociologist Erving Goffman’s 1952 article ‘On Cooling the Mark Out.’ … ‘After the blowoff has occurred,’ Goffman explained, about the operation of a con, ‘one of the operators stays with the mark and makes an effort to keep the anger of the mark within manageable and sensible proportions. The operator stays behind his team-mates in the capacity of what might be called a cooler and exercises upon the mark the art of consolation. An attempt is made to define the situation for the mark in a way that makes it easy for him to accept the inevitable and quietly go home. The mark is given instruction in the philosophy of taking a loss.’ What happened stays out of the paper.”
  4. Angelo Maria Pezzullo, Cathrine Axfors, Despina G. Contopoulos-Ioannidis, Alexandre Apostolatos, John P.A. Ioannidis, “Age-stratified infection fatality rate of COVID-19 in the non-elderly informed from pre-vaccination national seroprevalence studies,” Environmental Research, January 2023. This study found that Covid-19’s infection fatality rate (IFR) by age was under 0.1% for those under 70. The breakdown by age was 0.0003% at 0-19 years, 0.003% at 20-29 years, 0.011% at 30-39 years, 0.035% at 40-49 years, 0.129% at 50-59 years, and 0.501% at 60-69 years.
  5. S. Alhumaid et al., “New-onset and relapsed liver diseases following COVID-19 vaccination: a systematic review.” BMC Gastroenterology, October 2022; 22(1):433. doi: 10.1186/s12876-022-02507-3. PMID: 36229799; PMCID: PMC9559550. The abstract states, “Mortality was reported in any of the included cases.” Was the erroneous use of any in this sentence a typographical error or a deliberate ambiguity put into the abstract? There are three options for a correct interpretation: 1. Mortality was not reported in any of the included cases… 2. Mortality was reported in many of the included cases… 3. Mortality was reported in all of the included cases. It is difficult to know the authors’ intended meaning regarding this significant finding from their research. The sample sizes (six figures indicated as sample sizes, n=x) total 41 cases out of the 275 cases studied. This is a fatality rate of 15%, but it is difficult to know what the intended meaning of the 32 authors is, due to the ambiguity described above. One can conclude that any ofmany ofall of, or not any of the authors read the abstract carefully before it went to press. In any case, even if there were no deaths, one could take issue with the statement that “patients were easily treated without any serious complications, recovered and did not require long-term hepatic therapy.” Many patients would not feel so optimistic about having had such damage inflicted on a vital organ which is, considering the contemporary food supply and environment, already exposed to enough harm.
  6. Tom Jefferson et al., “Physical Interventions to Interrupt or Reduce the Spread of Respiratory Viruses,” Cochrane, January 30, 2023.
  7. Roxanne Khamsi, “Did a Famous Doctor’s COVID Shot Make His Cancer Worse? A Lifelong Promoter of Vaccines Suspects He Might Be the Rare, Unfortunate Exception.” The Atlantic, September 24, 2022.
  8. “David Miller and Piers Robinson, Propaganda—An introduction by David Miller and Piers Robinson.” YouTube Channel. (3:25~), accessed April 15, 2023.
  9. Brandy Zadrozny, “Conspiracy theorists made Tiffany Dover into an anti-vaccine icon. She’s finally ready to talk about it,” NBC News, April 10, 2023.
  10. It is important to note that this phenomenon has many precedents that occurred long before social media existed. The Dreyfus Affair (1890s) and the death of Azaria Chamberlain in Australia (1980) are just two examples one could refer to. The latter one was the butt of several jokes in poor taste broadcast on mainstream media outlets (referencing the apocryphal phrase “A dingo ate my baby!”) Back then, the incident was referred to benignly by the mass media as a regrettable “media circus.” The panic in the mainstream media about the new panics is interesting in the way it views professional journalism as beyond reproach and “participatory misinformation” as an urgent new threat posed by irresponsible, out-of-control social media platforms and a monstrous new type of people that apparently did not exist in the past.
  11. Megan Redshaw, “Vaccine-Injured Speak Out, Feel Abandoned by Government Who Told Them COVID Shot Was Safe,” Childrens Health Defense Fund, November 3, 2021.
  12. Ed Dowd, “Cause Unknown”: The Epidemic of Sudden Deaths in 2021 & 2022 (Skyhorse, 2022). Website: https://www.theyliedpeopledied.com/: “Between March of 2021 and February of 2022, 61,000 millennials died excessively above the prior 5-year base trend line… The relative timespan and rate of change into the fall of 2021 is a signal that a harmful event occurred to this 25-44 age group. This means that millennials started dying in large numbers at the same times when vaccines and boosters were rolled out. The vaccine clearly had a role, as many previously hesitant folks were forced into compliance.” Or see Aubrey Marcus, “Why Are Healthy People Dying Suddenly Since 2021? w/ Ed Dowd,” January 5, 2023. (31:40~).

Read full story here…

July 3, 2023. READING

There is going to be a big push towards ….  Controlling all of humanity in many inhumane ways, but the tide has turned, and those who are forcing the control are not seeing that.  They live within an environment of their own making, and they bolster one another up with the lie that all is well, but that is not true.

There is also coming on some very intense environmental aspects which will be in the form of weather and earthquakes as well as things coming from the sun.  There will be “accidents’ that will be occurring because the machines that are being used to manipulate weather are based on ancient and outdated models so that when they are turned on, they will not react in the way that they thought.  You see, they have modified things on the Earth in such a way that they no longer work according to the old paradigms.  There will be problems which ultimately refer back to the perpetrators, and you can expect to see a shake up within their ranks, perhaps even some passing on.

As for the outsiders, the ET,s as you call them, they have been waiting and watching, and while the government is attempting to control the whole project of disclosure, they are not in charge of the Outsiders’ actions. There will be a large kerfuffle this month in which some things will be coming forth from unknown sources which can lead to a lot of head scratching as well as head rolling, but those who sought to control disclosure will find out that they re not in charge, and that their powers are limited and being more limited. 

Things are not going to work the way they used, and this is in all areas, the grid, travel, weather, even your CERN is going to find itself somewhat out of control of those scientists who are supposed to be controlling it.  They will not, however be revealing this to the public other than as a leak, and as a result, there will be a shift in the leadership of CERN and some unfortunate “accidents’.

“Who’s Yo’ Daddy?”

Synthetic human embryos created in groundbreaking advance

Exclusive: Breakthrough could aid research into genetic disorders but raises serious ethical and legal issues

Scientists have created synthetic human embryos using stem cells, in a groundbreaking advance that sidesteps the need for eggs or sperm.

Scientists say these model embryos, which resemble those in the earliest stages of human development, could provide a crucial window on the impact of genetic disorders and the biological causes of recurrent miscarriage.

However, the work also raises serious ethical and legal issues as the lab-grown entities fall outside current legislation in the UK and most other countries.

The structures do not have a beating heart or the beginnings of a brain, but include cells that would typically go on to form the placenta, yolk sac and the embryo itself.

Prof Magdalena Żernicka-Goetz, of the University of Cambridge and the California Institute of Technology, described the work in a plenary address on Wednesday at the International Society for Stem Cell Research’s annual meeting in Boston.

“We can create human embryo-like models by the reprogramming of [embryonic stem] cells,” she told the meeting.

There is no near-term prospect of the synthetic embryos being used clinically. It would be illegal to implant them into a patient’s womb, and it is not yet clear whether these structures have the potential to continue maturing beyond the earliest stages of development.

The motivation for the work is for scientists to understand the “black box” period of development that is so called because scientists are only allowed to cultivate embryos in the lab up to a legal limit of 14 days. They then pick up the course of development much further along by looking at pregnancy scans and embryos donated for research.

Robin Lovell-Badge, the head of stem cell biology and developmental genetics at the Francis Crick Institute in London, said: “The idea is that if you really model normal human embryonic development using stem cells, you can gain an awful lot of information about how we begin development, what can go wrong, without having to use early embryos for research.”

Previously, Żernicka-Goetz’s team and a rival group at the Weizmann Institute in Israel showed that stem cells from mice could be encouraged to self-assemble into early embryo-like structures with an intestinal tract, the beginnings of a brain and a beating heart. Since then, a race has been under way to translate this work into human models, and several teams have been able to replicate the very earliest stages of development.

The full details of the latest work, from the Cambridge-Caltech lab, are yet to be published in a journal paper. But, speaking at the conference, Żernicka-Goetz described cultivating the embryos to a stage just beyond the equivalent of 14 days of development for a natural embryo.

The model structures, each grown from a single embryonic stem cell, reached the beginning of a developmental milestone known as gastrulation, when the embryo transforms from being a continuous sheet of cells to forming distinct cell lines and setting up the basic axes of the body. At this stage, the embryo does not yet have a beating heart, gut or beginnings of a brain, but the model showed the presence of primordial cells that are the precursor cells of egg and sperm.

“Our human model is the first three-lineage human embryo model that specifies amnion and germ cells, precursor cells of egg and sperm,” Żernicka-Goetz told the Guardian before the talk. “It’s beautiful and created entirely from embryonic stem cells.”

The development highlights how rapidly the science in this field has outpaced the law, and scientists in the UK and elsewhere are already moving to draw up voluntary guidelines to govern work on synthetic embryos. “If the whole intention is that these models are very much like normal embryos, then in a way they should be treated the same,” Lovell-Badge said. “Currently in legislation they’re not. People are worried about this.”

There is also a significant unanswered question on whether these structures, in theory, have the potential to grow into a living creature. The synthetic embryos grown from mouse cells were reported to appear almost identical to natural embryos. But when they were implanted into the wombs of female mice, they did not develop into live animals. In April, researchers in China created synthetic embryos from monkey cells and implanted them into the wombs of adult monkeys, a few of which showed the initial signs of pregnancy but none of which continued to develop beyond a few days. Scientists say it is not clear whether the barrier to more advanced development is merely technical or has a more fundamental biological cause.

“That’s very difficult to answer. It’s going to be hard to tell whether there’s an intrinsic problem with them or whether it’s just technical,” Lovell-Badge said. This unknown potential made the need for stronger legislation pressing, he said.

from:    https://www.theguardian.com/science/2023/jun/14/synthetic-human-embryos-created-in-groundbreaking-advance

New Info on Just What is in those Jabs

Green Monkey DNA Found in COVID-19 Shots

Analysis by Dr. Joseph MercolaFact Checked
May 31, 2023
Link for Video of Sucharit Bhakdti dscussing this issue:   https://rumble.com/v2owij0-why-the-covid-mrna-vaccines-are-actually-dna-gene-therapies-that-must-be-re.html

STORY AT-A-GLANCE

  • Microbiologist Kevin McKernan — a former researcher and team leader for the MIT Human Genome project — has discovered massive DNA contamination in the mRNA COVID shots, including simian virus 40 (SV40) promoters
  • SV40 has been linked to cancer in humans, including mesotheliomas, lymphomas and cancers of the brain and bone. In 2002, the Lancet published evidence linking polio vaccines contaminated with SV40 to Non-Hodgkin’s lymphoma. According to the authors, the vaccine may be responsible for up to 50% of the 55,000 Non-Hodgkin’s lymphoma cases diagnosed each year
  • The level of contamination varies depending on the platform used to measure it, but no matter which method is used, the level of DNA contamination is significantly higher than the regulatory limits in both Europe and the U.S. The highest level of DNA contamination found was 30%
  • The finding of DNA means the mRNA COVID shots may have the ability to alter the human genome
  • Even if genetic modification does not occur, the fact that you’re getting foreign DNA into your cells poses a risk in and of itself. Partial expression could occur, or it might interfere with other transcription translations that are already in the cell. Cytoplasmic transfection can also allow for genetic manipulation, as the nucleus disassembles and exchanges cellular components with the cytosol during cell division

In the video1 above, Dr. Steven E. Greer interviews microbiologist Kevin McKernan — a former researcher and team leader for the MIT Human Genome project2 — and Dr. Sucharit Bhakdi about the DNA contamination McKernan’s team has found in the Pfizer and Moderna mRNA shots.

As it turns out, spike protein and the mRNA are not the only hazards of these injections. McKernan’s team have also discovered simian virus 40 (SV40) promoters that, for decades, have been suspected of causing cancer in humans, including mesotheliomas, lymphomas and cancers of the brain and bone.3 The findings4,5,6,7 were posted on OSF Preprints in early April 2023. As explained in the abstract:8

“Several methods were deployed to assess the nucleic acid composition of four expired vials of the Moderna and Pfizer bivalent mRNA vaccines. Two vials from each vendor were evaluated … Multiple assays support DNA contamination that exceeds the European Medicines Agency (EMA) 330ng/mg requirement and the FDAs 10ng/dose requirements …”

As noted by Greer,9 this means that governments and drug companies “have misled the world to a far greater extent than previously known.” If these findings are correct, it would also mean that “the so-called ‘vaccines’ are actually altering the human genome and causing permanent production of the deadly spike protein,” and this internal production of spike protein would, in turn, “trigger the immune system to attack its own cells,” Greer says.

In the interview, McKernan explains how the DNA contaminants found in the COVID jabs can result in the genetic modification of the human genome, and Bhakdi reviews how and why the shots can trigger autoimmune diseases.

Background: What Is SV40?

In 2002, the Lancet published10 evidence linking polio vaccines contaminated with SV40 to Non-Hodgkin’s lymphoma. According to the authors, the vaccine may be responsible for up to half the 55,000 Non-Hodgkin’s lymphoma cases diagnosed each year.

How did this simian (monkey) virus get into the human population? According to the late Dr. Maurice Hilleman, a leading vaccine developer, Merck inadvertently unleashed the virus via their polio vaccine.11 It’s unclear exactly when SV40 was eliminated from the polio vaccine. The timing also varies from country to country. For example, SV40-contaminated polio vaccines were administered in Italy as recently as 1999.12

As reported in a Lancet book review of “The Virus and the Vaccine: The True Story of a Cancer-Causing Money Virus, Contaminated Polio Vaccine and the Millions of Americans Exposed”:13

“By 1960, scientists and vaccine manufacturers knew that monkey kidneys were sewers of simian viruses. Such contamination often spoiled cultures, including those of an NIH researcher named Bernice Eddy, who worked on vaccine safety … Her discovery … threatened one of the USA’s most important public-health programs …

Eddy tried to get word out to colleagues but was muzzled and stripped of her vaccine regulatory duties and her laboratory … [Two] Merck researchers, Ben Sweet and Maurice Hilleman, soon identified the rhesus virus later named SV40 — the carcinogenic agent that had eluded Eddy.

In 1963, U.S. authorities decided to switch to African green monkeys, which are not natural hosts of SV40, to produce polio vaccine. In the mid-1970s, after limited epidemiological studies, authorities concluded that although SV40 caused cancer in hamsters, it didn’t seem to do so in people.

Fast forward to the 1990s: Michele Carbone, then at NIH, was working on how SV40 induces cancers in animals. One of these was mesothelioma, a rare cancer of the pleura thought in people to be caused mainly by asbestos. The orthodoxy held that SV40 didn’t cause human cancers.

Emboldened by a 1992 NEJM paper that found DNA ‘footprints’ of SV40 in childhood brain tumors, Carbone tested human mesothelioma tumor biopsies at the National Cancer Institute: 60% contained SV40 DNA. In most, the monkey virus was active and producing proteins.

He published his results in Oncogene in May, 1994, but the NIH declined to publicize them … Carbone … moved to Loyola University. There he discovered how SV40 disables tumor suppressor genes in human mesothelioma, and published his results in Nature Medicine in July, 1997. Studies in Italy, Germany, and the USA also showed associations between SV40 and human cancers.”

mRNA COVID Jabs Contaminated With Double-Stranded DNA

With that background, let’s get back to McKernan’s findings, which in addition to the featured video are also discussed in Daniel Horowitz’s podcast above. In short, his team discovered elevated levels of double-stranded DNA plasmids, including SV40 promoters (DNA sequence that is essential for gene expression) that are known to trigger cancer development when encountering an oncogene (a gene that has the potential to cause cancer).

The level of contamination varies depending on the platform used to measure it, but no matter which method is used, the level of DNA contamination is significantly higher than the regulatory limits in both Europe and the U.S., McKernan says. The highest level of DNA contamination found was 30%, which is rather astounding.

As explained by McKernan, when using a typical PCR test, you’ll be considered positive if the test detects the SARS-CoV-2 virus using a cycle threshold (CT) of about 40. In comparison, the DNA contamination is detected at CTs below 20.

That means the contamination is a million-fold greater than the amount of virus you’d need to have in order to test positive for COVID. “So, there’s an enormous difference here with regards to the amount of material that’s in there,” McKernan says.

In his Substack article,14 he also points out that people who argue that double-stranded DNA and viral RNA is a false equivalency because viral RNA is replication competent, are wrong.

“The majority of the sgRNA you are detecting in a nasal swab in your nose is NOT REPLICATION COMPETENT as shown in Jaafar et al.15 It is just an RNA fragment that should have lower longevity in your cells than dsDNA contaminating fragments,” he writes.

In that Substack article, McKernan has also copied a 2009 study discussing how DNA in vaccines can cause cancer and highlighted the most relevant parts. It’s a helpful resource if you want to learn more.

Quality Control Is Sorely Lacking

As for how SV40 promoters ended up in the mRNA shots, it appears to be related to poor quality control during the manufacturing process, although it’s unclear where in the development SV40 might have sneaked in. Quality control deficiencies may also be responsible for the high rate of anaphylactic reactions we’ve been seeing. McKernan tells Greer:

“It’s in both Moderna and Pfizer. We looked at the bivalent vaccines for both Moderna and Pfizer and only the monovalent vaccines for Pfizer because we didn’t have access to monovalent vaccines for Moderna. In all three cases, the vaccines contain double-stranded DNA contamination.

If you sequence that DNA, you’ll find that it matches what looks to be an expression vector that’s used to make the RNA … Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there’s any E. coli endotoxin present because that creates anaphylaxis for the injected.

And, of course … there’s a lot of anaphylaxis going on, not only on TV but in the VAERS database. You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA …”

Regulatory Agencies Knew There Was a Contamination Problem

In a May 20, 2023, Substack article,16 McKernan points out that Pfizer itself submitted evidence to the European Medicines Agency (EMA) showing sampled lots contained vast differences in the levels of double-stranded DNA contamination.

The arbitrary limit for dsDNA that the EMA came up with was 330 nanograms per milligram (ng/mg). Data submitted to the EMA by Pfizer shows sampled lots had anywhere from 1 ng/mg to 815 ng/mg of DNA. McKernan adds:17

“This limit likely did not consider the potency of this dsDNA contamination if it was packaged in an LNP [lipid nanoparticle]. Packaged dsDNA is more potent as a gene therapy. We now know this DNA is packaged and transfection ready.18 Even lower limits should be applied if the DNA is packaged in transfection ready LNPs …

Even with Pfizer being able to cherry pick the data they provided to the EMA for 10 lots, they see a 1 to 815ng/mg variance. If you were to expand this study to 100 or 1000 lots, you’d likely see another order or two of magnitude variance.”

Double-Stranded DNA May Integrate Into Your Genome

The presence of double-stranded DNA also brings up another major concern, and that is the possibility of genomic integration.

“At least on the Pfizer side of things, it has what’s known as an SV40 promoter. This is an oncogenic virus piece. It’s not the entire virus. However, the small piece is known to drive very aggressive gene expression.

And the concern that people, even at the FDA, have noted in the past whenever injecting double-stranded DNA, is that these things can integrate into the genome,” McKernan says.

While McKernan’s paper does not present evidence of genome integration, it does point out that it’s possible, especially in the presence of SV40 promoters:19

“There has been a healthy debate about the capacity for SARs-CoV-2 to integrate into the human genome … This work has inspired questions regarding the capacity for the mRNA vaccines to also genome integrate. Such an event would require LINE-1 driven reverse transcription of the mRNA into DNA as described by Alden et al.

dsDNA [double-stranded DNA] contamination of sequence encoding the spike protein wouldn’t require LINE-1 for Reverse Transcription and the presence of an SV40 nuclear localization signal in Pfizer’s vaccine vector would further increase the odds of integration.”

Manifold Risks

That said, even if genetic modification does not occur, the fact that you’re getting foreign DNA into your cells poses a risk in and of itself, McKernan says. For example, partial expression could occur, or it might interfere with other transcription translations that are already in the cell.

Bhakdi also points out that the SV40 promoters do not need to be present in the nucleus of the cell for problems to occur. Cytoplasmic transfection can, in and of itself, allow for genetic manipulation, because the nucleus disassembles and exchanges cellular components with the cytosol during cell division.

In addition to having DNA floating around and causing potential problems, the RNA in the COVID jab is also modified to resist breakdown. “So, we have TWO versions of the spike protein floating around that can persist longer than anticipated,” McKernan says, and the spike protein, of course, is the most toxic part of the virus that can cause your body to attack itself.

Both McKernan and Bhakdi are adamant that ALL mRNA “vaccines” must be immediately stopped, whether for human or animal use, due to the magnitude of the risks involved.

‘Alarming Problems’

In the video above,20 Yusuke Murakami, a professor at Tokyo University, expresses alarm over the finding of SV40 promoters in the COVID jabs. The interview is in Japanese but has English subtitles. I’ve included it because I think he does a good job of putting the problem into layman’s terms:

“The Pfizer vaccine has a staggering problem,” Murakami says. “This figure is an enlarged view of Pfizer’s vaccine sequence. As you can see, the Pfizer vaccine sequence contains part of the SV40 sequence here. This sequence is known as a promoter.

Roughly speaking, the promoter causes increased expression of the gene. The problem is that the sequence is present in a well-known carcinogenic virus. The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine.

There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine.

This is not the only problem. If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus. So it means that the DNA can easily enter the genome. This is such an alarming problem.

It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious. This kind of promoter sequence is completely unnecessary for the production of the mRNA vaccine. In fact, SV40 is a promoter of cancer viruses.”

Resources for Those Injured by the COVID Jab

The more we learn about the COVID jabs, the worse they appear. While they suck as vaccines, they’re truly masterful bioweapons, as they’re capable of destroying health in any number of ways, through myriad mechanisms.

If you got one or more jabs and are now reconsidering, first and foremost, never ever take another COVID booster, another mRNA gene therapy shot or regular vaccine. You need to end the assault on your body. Even if you haven’t experienced any obvious side effects, your health may still be impacted long-term, so don’t take any more shots.

If you’re suffering from side effects, your first order of business is to eliminate the spike protein that your body is producing. Two remedies that can do this are hydroxychloroquine and ivermectin. Both of these drugs bind and facilitate the removal of spike protein.

The Front Line COVID-19 Critical Care Alliance (FLCCC) has developed a post-vaccine treatment protocol called I-RECOVER. Since the protocol is continuously updated as more data become available, your best bet is to download the latest version straight from the FLCCC website at covid19criticalcare.com21 (hyperlink to the correct page provided above).

For additional suggestions, check out the World Health Council’s spike protein detox guide,22 which focuses on natural substances like herbs, supplements and teas. To combat neurotoxic effects of spike protein, a March 2022 review paper23 suggests using luteolin and quercetin. Time-restricted eating (TRE) and/or sauna therapy can also help eliminate toxic proteins by stimulating autophagy.

from:    https://articles.mercola.com/sites/articles/archive/2023/05/31/dna-contamination-mrna-covid-shots.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1ReadMore&cid=20230531&cid=DM1408714&bid=1815660384

“Doctor”(?) Chelsea Clinton Wants Your Kids

‘The Big Catch-Up’: Chelsea Clinton Pushes ‘Largest Childhood Immunization Effort Ever’

Chelsea Clinton aims to provide childhood immunizations to as many children as possible with a new initiative called “The Big Catch-Up” that she touted as “the largest childhood immunization effort ever.” The WHO, UNICEF, GAVI, the Vaccine Alliance and the Bill & Melinda Gates Foundation, along with Immunization Agenda 2030, announced “The Big Catch-Up” last month, which WHO characterized as a “targeted global effort to boost vaccination among children following declines driven by the COVID-19 pandemic.” Clinton complained about the lack of trust in science and public health officials and said that she thinks we need the public sector to stop stripping away  public health emergency powers from state public health agencies.

Chelsea Clinton aims to provide childhood immunizations to as many children as possible with a new initiative called “The Big Catch-Up.”

Speaking at the Brainstorm Health conference hosted by Fortune Magazine last month in Marina del Rey, Calif., the daughter of Bill and Hillary Clinton called the initiative “the largest childhood immunization effort ever.”

“A new effort that we’re a part of is the new initiative launched by the WHO last week to try to catch kids up on their routine immunizations. In 2021 alone more than 25 million kids under the age of 1 missed at least 1 routine immunization and so we’re working with WHO and the Gates Foundation and others to kind of hopefully have the largest childhood immunization effort ever over the next 18 months to catch as many kids up as possible, because no one should die of polio, measles, or pneumonia—including in this country, where we also need people to vaccinate their kids,” she said.

The WHO, UNICEF, GAVI, the Vaccine Alliance and the Bill & Melinda Gates Foundation, along with Immunization Agenda 2030 announced “The Big Catch-Up” last month, which WHO characterized as a “targeted global effort to boost vaccination among children following declines driven by the COVID-19 pandemic.”

“This effort aims to reverse the declines in childhood vaccination recorded in over 100 countries since the pandemic, due to overburdened health services, closed clinics, and disrupted imports and exports of vials, syringes and other medical supplies,” WHO described in a press release.

Read full article here…

from:    https://needtoknow.news/2023/05/the-big-catch-up-chelsea-clinton-pushes-largest-childhood-immunization-effort-ever/

I thought you Wanted Long telomeres….

The Telomere Scam

Analysis by Dr. Joseph MercolaFact Checked
May 22, 2023
the telomere scam

STORY AT-A-GLANCE

  • Shorter telomeres are said to indicate increased risk of premature death; longer telomere length has therefore been assumed to represent health and longevity
  • Research published in The New England Journal of Medicine (NEJM) revealed long telomeres are linked to cancer and clonal hematopoiesis of indeterminate potential (CHIP), a blood disorder
  • Shorter telomere length is linked to degenerative diseases such as Alzheimer’s disease and heart disease, while longer telomere length is associated with increased cancer risks
  • Cells with long telomeres accumulate mutations, promoting tumors that might otherwise be prevented via normal telomere shortening processes
  • Rather than relying on telomere length as a measure of longevity or disease, harness the power of lifestyle strategies to slow the aging process and improve your health span

Telomeres are repetitive nucleotide sequences at the end of each chromosome. Sometimes compared to the plastic tip on a shoelace, telomeres help protect DNA, preserving chromosome stability and preventing “molecular contact with neighboring chromosomes.”1

Evidence suggests telomere length may predict morbidity and mortality, with shorter telomeres linked to an increased risk of premature death.2 Longer telomere length has therefore been assumed to represent health and longevity, but the link is controversial. New research suggests, in fact, that telomeres’ link to aging may have been wrong all along.3

Is Telomere Attrition a Hallmark of Aging?

The idea that telomere length serves as a marker of aging has become scientific dogma. Writing in the journal Cell, researchers described telomere attrition as one of the hallmarks of aging that lead to most age-related disorders.4 Telomeres, they noted, are especially vulnerable to age-related deterioration, and telomere shortening occurs during the normal aging process in humans and animals, such as mice.

When DNA damage occurs at telomeres, it leads to persistent harm and “deleterious cellular effects including senescence and/or apoptosis.”5

Further, the team explained, when telomerase, a key maintenance mechanism of telomere length, is deficient in humans, it’s associated with premature disease development, including those involving loss of regenerative capacity in tissues, such as pulmonary fibrosis, dyskeratosis congenita and aplastic anemia.6 According to the Cell study:

“Genetically-modified animal models have established causal links between telomere loss, cellular senescence and organismal aging. Thus, mice with shortened or lengthened telomeres exhibit decreased or increased lifespan, respectively. Recent evidence also indicates that aging can be reverted by telomerase activation.

In particular, the premature aging of telomerase-deficient mice can be reverted when telomerase is genetically reactivated in these aged mice.

Moreover, normal physiological aging can be delayed without increasing the incidence of cancer in adult wild-type mice by pharmacological activation or systemic viral transduction of telomerase. In humans, recent meta-analyses have indicated a strong relation between short telomeres and mortality risk, particularly at younger ages.”

Risks Revealed for Short or Long Telomeres

Just because short telomeres have been linked to aging and disease, it doesn’t mean long telomeres have the opposite effect. In fact, research published in The New England Journal of Medicine (NEJM) revealed long telomeres are linked to cancer and clonal hematopoiesis of indeterminate potential (CHIP) — a blood disorder.7

“Short telomeres were thought to be bad — people with premature aging syndromes had short telomeres — so, by analogy, long telomeres were thought to be good,” study author Dr. Mary Armanios, professor of oncology at Johns Hopkins University School of Medicine, told The New York Times. “And the longer the better.”8

Previous research by Armanios, who also directs the telomere center at Johns Hopkins University School of Medicine, and colleagues revealed, however, that the reality is much more complicated. While short telomere length (TL) was linked to disease, longer telomere length increased the risk of cancers, including lung, melanoma and glioma.9

“The upper threshold that increases the risk of these cancers is not known, but these recent findings add significant warning to the oversimplified interpretation of short TL being linked to aging and long telomeres to youth,” they concluded in 2018. It seemed that having either very short or very long telomeres may be a risk factor for disease.

Researchers with UCSF School of Medicine and Stanford echoed this sentiment in 2020, revealing that shorter telomere length is linked to degenerative diseases such as Alzheimer’s disease and heart disease, while longer telomere length is associated with increased cancer risks.10

“Genetically determined long and short telomere length are associated with disease risk and burden of approximately equal magnitude,” they concluded.

Long Telomeres Linked to Cancer, Disease

The NEJM study involved 17 people with a POT1 genetic mutation, known to not only lengthen telomeres but also increase cancer risk. The study participants ranged in age from 7 to 83 and had a variety of tumors, ranging from benign uterine fibroids to melanoma. They also had significantly longer telomeres than the average population — 90% longer in 13 participants and 99% longer in nine.11

While six of the participants had some signs of youth, including no gray hair even in their 70s, many had high rates of clonal hematopoiesis-related mutations. The mutations are linked to the development of blood and other cancers, and existed at much higher rates than expected in the general population.

One participant had cells with 1,000 mutations per clone, which the researchers believe began when the person was just 4 years old. “The long telomere length allowed the blood cell propagation since then,” Armanios said.

The research suggests long telomeres are leading to CHIP and giving more time for cancer-causing mutations to develop. According to Armanios:12

“Our findings challenge the idea that long telomeres protect against aging. Rather than long telomeres protecting against aging, long telomeres allowed cells with mutations that arise with aging to be more durable … Cells with very long telomeres accumulate mutations and appear to promote tumors and other types of growths that would otherwise be put in check by normal telomere shortening processes.”

Telomere shortening, for instance, is said to represent a “major measurable molecular characteristic of aging of cells in vitro and in vivo,” which may have developed as a mechanism to protect against tumors in long-lived species.13

Is DNA Methylation a Better Measure of Your Biological Age?

It’s possible to determine your biological age, as opposed to your chronological age, by measuring your DNA methylation, and in head-to-head comparisons, DNA methylation is significantly more correlated to the aging process than telomeres.

DNA methylation is the silencing of gene transcription. Your genes have promoter sites at the beginning of the DNA strand, and methylation is measured at those sites. The level of methylation at the promoter site correlates to the degree of expression of that particular gene.

Ryan Smith is the founder of TruDiagnostic, a commercial testing system that measures DNA methylation. What’s being measured is not your ability to methylate or not methylate. Rather, it measures the actual expression of your DNA. And, contrary to conventional genetic testing like 23andMe, which is done once, DNA methylation can be measured multiple times as the actual expression of your DNA is alterable and changes over time.

DNA methylation is a better marker of disease risk and health span than telomere length, Smith said during our 2022 interview.

“If you were to make sure that the telomere length never decreased in a cell, you’d still see methylation-related biological aging. If you made sure that the methylation age was reset, you would still see telomere length aging. So, there’s two separate processes.

In a recent review, they actually looked at twins and tried to ascribe how much of the difference in their aging process was affected by these different markers. They said right around 2% of the variance in phenotypic aging was due to telomere length, whereas right around 35% of that was based on these epigenetic methylation clocks.

So, while they both might be important, we definitely would think that the DNA methylation clocks are significantly better.”

Antiaging Strategies That Work

While measuring your rate of aging, or biological age, is intriguing, harnessing the power of lifestyle strategies to slow the aging process and ward off disease can improve your health span and quality of life. Simple antiaging strategies you can implement today include:

Vitamin D optimization — Ideally, you want to maintain a blood level of 60 ng/mL to 80 ng/mL. Smith cited an interventional trial in which overweight participants reduced their biological age by 1.8 years on average, taking just 4,000 IUs of oral vitamin D a day for 16 weeks.

Optimize your metabolic flexibility — Core strategies include time-restricted eating or intermittent fasting, and eating a diet high in healthy fats and low in refined carbs to optimize your insulin sensitivity. Also, eat your last meal each day at least three hours before bed.

Get regular exercise and daily movement — In one study, among 1,481 older women included in the study, those who sat the longest were, on average, eight years older, biologically speaking, than women who moved around more often.14

Another study touted exercise as a “possible cure” for the declines in mitochondrial biogenesis and mitochondrial protein quality commonly seen with aging. Not only did exercise training reverse or lessen age-associated declines in mitochondrial mass, but it also “decreased the gap between young and old animals in other measured parameters.”15

Stress management — According to Smith, people who meditate or engage in other stress-reduction strategies on a regular basis tend to age at a slower rate than those who don’t.

Limit consumption of unsaturated fats — Omega-6 linoleic acid (LA) is particularly harmful. It’s highly susceptible to oxidation, causing oxidative stress, and can remain in your cells for up to a decade. So, you want to eliminate vegetable/seed oils, which are high in LA.

In terms of supplement options, glycine is a powerful longevity enhancer that’s inexpensive and has a pleasant, slightly sweet taste. Research shows glycine extends lifespan in worms, mice and rats while improving health in models of age-related disease.16

If there were any doubt about its importance, consider that collagen — the most abundant protein in your body17 — is made mostly of glycine. It’s also a precursor to glutathione, a powerful antioxidant that declines with age. To gain all of glycine’s healing potential, doses of 10, 15, or 20 grams a day may be necessary. I personally take three teaspoons of it a day.

Collagen is also an outstanding source of glycine. You can boost your collagen intake by making homemade bone broth using bones and connective tissue from grass fed, organically raised animals. But remember, there’s no magic potion to stop the aging process.

Methods that claim to stop aging by lengthening your telomeres appear to be misguided. And if your telomeres are too long — or too short — it could be indicative of disease. The fact remains that the best longevity benefits come from leading a comprehensively healthy lifestyke.

from:    https://articles.mercola.com/sites/articles/archive/2023/05/22/the-telomere-scam.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art2ReadMore&cid=20230522_HL2&cid=DM1403765&bid=1807324684

Resources for Real Vaccine Information

Think Globally, Act Locally

National vaccine policy recommendations in the U.S. are made at the federal level but vaccine laws are made at the state level. It is at the state level where your action to protect your vaccine choice rights can have the greatest impact.

It is critical for EVERYONE to get involved now in standing up for the legal right to make voluntary vaccine choices in America because those choices are being seriously threatened.

Not only are lobbyists representing drug companies, medical trade associations and public health officials trying to persuade legislators to strip all vaccine exemptions from public health laws, but global political operatives lobbying the United Nations and World Health Organization are determined to take away the human right to autonomy and protection of bodily integrity.

We must take action to defend our constitutional republic and civil liberties, including the right to autonomy, in America. That includes reforming oppressive mandatory vaccination laws and stopping the digital health ID that will make vaccine passports a reality for us, our children and grandchildren if we don’t take action today.

Signing up to use the free online Advocacy Portal sponsored by the National Vaccine Information Center (NVIC) at www.NVICAdvocacy.org gives you immediate, easy access to your own state and federal legislators on your smartphone or computer so you can make your voice heard.

NVIC will keep you up to date on the latest bills threatening to eliminate — or expand — your legal right to make vaccine choices and give you guidance about what you can do to support or oppose those bills. So, please, as your first step, sign up for the NVIC Advocacy Portal.

CLICK HERE TO JOIN!

Internet Resources Where You Can Learn More

I encourage you to visit the four websites of the National Vaccine Information Center, at www.NVIC.org, a nonprofit charity that has been educating the public about the need to prevent vaccine injuries and deaths since 1982. The information you get on their websites is fully referenced and will help you become an effective vaccine choice advocate in your community:

  • NVIC.org — This website was established in 1995 and is the oldest and largest consumer operated website publishing information on diseases and vaccines on the internet. Learn about vaccine reactions, injuries and deaths and the history and current status of vaccine science, policy, law and ethics in the U.S. on more than 2,000 web pages.
  • NVICAdvocacy.org — This communications and advocacy network, established in 2010, is your gateway to taking action to protect your right to make vaccine choices where you live.
  • TheVaccineReaction.org — This weekly journal newspaper published by NVIC since 2015 is dedicated to encouraging an “enlightened conversation about vaccination, health and autonomy.”
  • MedAlerts.org — This is a user-friendly search engine for the federal Vaccine Adverse Event Reporting System (VAERS) established under the 1986 National Childhood Vaccine Injury Act and sponsored by NVIC since 2006. Search for descriptions of vaccine injuries and deaths reported to VAERS on this popular website.

Find a Doctor Who Will Listen and Care

If your doctor or pediatrician refuses to provide medical care to you or your child unless you agree to get vaccines you don’t want, I strongly encourage you to have the courage to find another doctor. Harassment, coercion and refusal to provide medical care to someone declining one or more doses of government recommended vaccines is a violation of the informed consent ethic.

Unfortunately, it is becoming routine among members of the medical establishment to be reluctant to share vaccine decision-making power with patients and parents of minor children, especially during the aggressive push for all Americans to get COVID shots.

There are doctors out there who respect the precautionary and informed consent principles, so take the time to locate a doctor who treats you with compassion and is willing to listen and respect the health care choices you make for yourself or your child.

 

from:    https://articles.mercola.com/sites/articles/archive/2023/05/23/why-pediatricians-push-vaccines.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1HL&cid=20230523&cid=DM1404352&bid=1808248248

How Much Money Is In Your Kid’s Vaccine?

Is This Why Pediatricians Push Vaccines?

Analysis by Dr. Joseph MercolaFact Checked
why pediatricians push vaccines

STORY AT-A-GLANCE

  • Primary care providers across the U.S. were bribed with incentive programs to coerce patients into getting the toxic COVID shot. Anthem Blue Cross and Blue Shield paid doctors $50 for each Medicaid patient aged 6 months and older, who got the experimental jab
  • Doctors have been financially incentivized to vaccinate children for a long time. In 2016, Blue Cross Blue Shield paid pediatricians a $400 bonus for each patient that completed 10 vaccinations before their second birthday, provided 63% of their patients were fully vaccinated
  • “Client and family incentives” also exist. In 2015, the Community Preventive Services Task Force recommended boosting vaccination rates by giving small, inexpensive incentive rewards to patients
  • Bribery is also par for the course when it comes to vaccine mandates. Pfizer paid undisclosed sums to front groups that advocated for COVID jab mandates, thereby hiding their conflict of interest
  • While the COVID-19 pandemic furthered many globalist goals, it inadvertently tanked childhood vaccination rates. To get childhood vaccination rates back on track, a global alliance has launched “The Big Catch-Up” initiative. It’s touted as the largest childhood immunization effort ever

In April 2023, I reported how primary care providers across the U.S. were bribed with incentive programs to coerce patients into getting the toxic COVID shot. Since there was no medical malpractice liability, doctors profited while patients risked their lives as participants in an unprecedented medical experiment, all while being lied to about the safety and effectiveness of these injections.

Even more egregiously, once the U.S. Food and Drug Administration authorized the COVID shot for children, similar vaccination incentives were extended to pediatricians as well. As detailed in an Anthem Blue Cross and Blue Shield Medicaid provider bulletin1 dated July 2022, doctors received $50 for each Medicaid patient aged 6 months and older, who got the experimental jab.

Pediatricians Are Financially Incentivized to Vaccinate

As it turns out, doctors have been financially incentivized to vaccinate children for a long time. According to a 1999 JAMA Pediatrics article,2 the average patient load of American pediatricians is 1,546, although the number of patients was “significantly higher in less populated areas and solo practices.”

Of these, 8.3% were younger than 1 year, 9.5% were 1 year old and 8.6% were 2 years old.3 That means approximately 26.4% of the average pediatrician’s patients were 2 years old and younger. More recent data,4 published in 2021, show 75% of pediatricians have between 1,000 and 1,800 patients and 21% have around 1,200 patients; most practices, 65%, are in the 1,000 to 1,500 range.

As shown in the 2016 provider incentive program document from Blue Cross Blue Shield below,5,6 pediatricians were getting $400 for each pediatric patient that completed all the 10 vaccinations listed — 25 doses in all7 — before their second birthday. (Keep in mind that incentives can vary by state. The example provided is part of Michigan’s Blue Cross Blue Shield Performance Recognition Program.)8

How Much Money Is at Stake?

The math from there is pretty straight-forward (although keep in mind that we’re dealing with presumed averages and aged statistics here). Just multiply the number of patients under age 2 times $400. Using the average statistics from 1999, if a pediatrician has 1,000 patients, 264 can be expected to be 2 years old or younger. If all are fully vaccinated, the pediatrician would be eligible for a $105,600 year-end bonus.

childhood immunization - combo 10

While $400 per fully vaccinated child might seem incentivizing enough, there’s an added pressure here, because Blue Cross Blue Shield also has (or at least had, in 2016) a “target” level of 63%.

This means that if the pediatrician fails to vaccinate 63% of his eligible patients, he or she gets nothing. So, the pediatrician has a VERY high incentive to get as many toddlers fully vaccinated as possible, so as not to miss that target. It’s not just $400 that is at stake when parents decline one or more shots. Tens of thousands of dollars could be on the line. As noted by Dr. Bob Sears:9

“Such incentives … end up forcing a doctor to consider the financial implications of accepting patients who even just want to opt out of one vaccine … Maybe a few such families wouldn’t make them fail the chart reviews, but if they have too many, there goes their year-end bonus.”

Why Pediatricians Become Adversaries

Anytime financial incentives are part of the equation, one can reasonably assume that the lure of self-enrichment will win. With tens of thousands of dollars at stake, pediatricians can easily be lulled into complacency when it comes to digging deeper into the science.

After all, who wants to see evidence that what they’re doing is causing more harm than good? These kinds of incentives also encourage pediatricians to simply toss questioning parents out of their practice, to make room for more compliant patients that don’t put their income at risk. As reported by Children’s Health Defense back in 2018:10

“… the 11 well-child visits recommended by the AAP over a child’s first 30 months (with annual visits thereafter through age 21) ensure a steady stream of repeat customers and revenue for pediatricians.

In accordance with the Centers for Disease Control and Prevention’s vaccine schedule, pediatric practices are expected to administer vaccines (often as many as six at a time) at about half of well-child visits through the adolescent years, making vaccination a foundational bread-and-butter component of pediatricians’ job description …

It is quite common for pediatricians (and family doctors) to encounter parents who refuse one or more infant vaccines, most often due to safety concerns. These concerns also mean that pediatricians frequently get requests to modify or delay the vaccine schedule — nearly three-fifths (58%) of pediatricians reported such requests in a 2014 AAP survey …

Rather than recognize the validity of parents’ safety concerns or admit to their own ambivalence about some of the newer vaccines, many pediatricians — nearly two in five according to some estimates — choose to boot uncooperative families out of their practice …

Ultimately … subtle and not-so-subtle financial incentives and social pressures are likely to maintain widespread adherence by pediatricians to the vaccine schedule — even in instances where contraindications are present.

Although pediatricians have a legal duty to fully inform patients about vaccine risks and side effects, the lure of monetary perks and the desire to fit in may lessen their motivation to do so.”

Patients Are Bribed Too

In addition to the financial incentives given to physicians, “client and family incentives” also exist. A nongovernmental panel of public health and prevention experts called the “Community Preventive Services Task Force”11 in 2015 published a guide12 on how to boost vaccination rates using incentive rewards for patients.

The task force was established by the U.S. Department of Health and Human Services in 1996 “to develop guidance on which community-based health promotion and disease prevention intervention approaches work and which do not work, based on available scientific evidence.”13 As explained by this task force:14

“The Community Preventive Services Task Force recommends client or family incentive rewards, used alone or in combination with additional interventions, to increase vaccination rates in children and adults.

Client or family incentive rewards are used to motivate people to obtain recommended vaccinations. Rewards may be monetary or non-monetary, and they may be given to clients or families in exchange for keeping an appointment, receiving a vaccination, returning for a vaccination series, or producing documentation of vaccination status. Rewards are typically small (e.g., food vouchers, gift cards, lottery prizes, baby products).”

The scientific evidence supporting bribery of patients with food vouchers, gift cards and other products of limited value was said to be 4 out of 4, meaning very strong. In other words, incentives, even near-worthless ones, work.

Indeed, we saw this during COVID-19 as well. People were lining up for experimental COVID shots in return for a doughnut, hamburger and fries or even a free lap dance at the local strip club. The pattern is the same. Throw the patient a bone and they’ll agree to things that bring others big profits.

As patients, we need to get savvier about these kinds of tricks and interpret them for what they are. These kinds of “gifts” are not given out of kindness or concern for your well-being. It’s a compliance bribe, and your compliance is making someone rich. Meanwhile, any risks involved are on you.

Bribery and Vaccine Mandates

Bribery is also par for the course when it comes to vaccine mandates. As detailed in a previous article, Pfizer paid undisclosed sums to front groups that advocated for COVID jab mandates, thereby hiding their conflict of interest. In part due to the fake “grassroots” work of these groups, Pfizer was able to rake in a record-breaking $100 billion in sales in 2022.15

Of course, the U.S. government also paid news media a staggering $1 billion to promote and build public confidence in the jab, and Pfizer itself spent $2.8 billion on ads in 2022 alone.

But the pressure from consumer groups, civil rights groups, patient groups and doctors’ groups — all of which had been paid off — was probably why COVID jab mandates could even be officially considered by the government. They created a false consensus that people desperately wanted vaccine mandates to keep everyone “safe.”

Special interest groups paid by Pfizer16 to push for COVID jab mandates and coercive vaccine policies included the Chicago Urban league (which argued that the jab mandate would benefit the Black community), the National Consumers League, the Immunization Partnership, the Advertising Council and a long list of universities and cancer, liver diseases, cardiology, rheumatology and medical science organizations.

Each of these organizations received anywhere from several thousand to hundreds of thousands of dollars from Pfizer in 2021 alone. Is it any wonder, then, that more than 50 major health care organizations called for vaccine mandates that year, including for their own workers?17

Childhood Vaccination Rates Tanked During COVID

While the COVID-19 pandemic furthered many globalist goals, it inadvertently tanked childhood vaccination rates, as many parents ended up missing routine well-child visits due to clinic closures, lockdowns and fear of taking their children outside. As reported by the American Medical Association (AMA) in November 2021:18

“… recently published research sheds new light on how the COVID-19 pandemic has disrupted some of those routine vaccinations, as parents and their children didn’t just stay home — they stayed away from the doctor.

The JAMA Pediatrics study19 … found that vaccine-administration rates were significantly lower across all pediatric age groups as the pandemic first surged in the U.S. … For example, only 74% of infants turning 7 months old in September 2020 were up to date on their vaccinations, a drop from 81% in September 2019.

And just 57% of infants who hit the 18-month mark in September 2020 were up to date, down from 61% the year before. The proportion of children up to date for routine vaccinations was lowest among Black children, with inequities more pronounced in the 18-month-old group.”

The Big Catch-Up Initiative

To get childhood vaccination rates back on track, Chelsea Clinton is now making the rounds promoting a new vaccine initiative called “The Big Catch-Up.” In a recent interview with Fortune Magazine,20 Clinton promised it would be “the largest childhood immunization effort ever.” Over the next 18 months, this initiative will attempt to “catch as many kids up as possible,” she said.

Partners in this effort include the World Health Organization, UNICEF, Gavi, the Vaccine Alliance, the Bill & Melinda Gates Foundation, Immunization Agenda 2030, and several other “global and national health partners.” As reported by the WHO, April 24, 2023:21

“The pandemic saw essential immunization levels decrease in over 100 countries, leading to rising outbreaks of measles, diphtheria, polio and yellow fever. ‘The Big Catch-up’ is an extended effort to lift vaccination levels among children to at least pre-pandemic levels and endeavors to exceed those …

While calling on people and governments in every country to play their part in helping to catch up by reaching the children who missed out, The Big Catch-up will have a particular focus on the 20 countries where three quarters of the children who missed vaccinations in 2021 live …

The 20 countries where three quarters of the children who missed vaccinations in 2021 live are: Afghanistan, Angola, Brazil, Cameroon, Chad, DPRK [Democratic People’s Republic of Korea], DRC [Democratic Republic of the Congo], Ethiopia, India, Indonesia, Nigeria, Pakistan, Philippines, Somalia, Madagascar, Mexico, Mozambique, Myanmar, Tanzania, Viet Nam.”

Vaccine Program Is Run ‘Soft Mafia’ Style

When you look at all these areas of bribery and financial incentives, doesn’t it seem as though the entire vaccine program runs on financial coercion? A sort of “soft mafia” kind of operation, where the threats and promises all revolve around money and public/professional shaming versus accolades.

What would happen if all financial incentives were removed? All the performance bonuses paid to doctors, the freebies given to patients, the “charitable donations” to industry-friendly organizations and payments to front groups?

What would happen if parents were simply given unbiased evidence and no one was financially driven to pressure them either way? I don’t have the answer. It’s a thought experiment. But I suspect that vaccination rates would drop dramatically.

from:  https://articles.mercola.com/sites/articles/archive/2023/05/23/why-pediatricians-push-vaccines.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1HL&cid=20230523&cid=DM1404352&bid=1808248248JAMA

Pediac

What’s In Your Beauty Product?

The 10 Most Hazardous Cosmetic Products

Analysis by Dr. Joseph MercolaFact Checked
  • An analysis of personal care and cleaning products found the top 10 most hazardous products include a children’s shampoo, JLo Glow perfume, Kaboom with OxiClean, Axe body spray and Organix Shampoo
  • Over-the-counter products are not inherently safe as there are nearly 13,000 chemicals used in cosmetics and only 10% have been tested for safety. This loophole was created by the Fair Packaging and Labeling Act, which does not force companies to disclose trade secrets
  • The Environmental Working Group found perfumes typically contain a dozen or more potentially hazardous chemicals, some of which are derived from petroleum. This chemical cocktail may be responsible for the rising number of adverse events reported after exposure to personal care products
  • Look for products without dangerous chemicals, including parabens, “fragrance,” triclosan and toluene, or consider making your own products at home from safe and natural ingredients

Editor’s Note: This article is a reprint. It was originally published October 24, 2018.

Unfortunately, just because it’s sold over-the-counter does not mean a product is safe for you. In fact, of the nearly 13,000 chemicals used in cosmetics, only 10% have been tested for safety. While the U.S. Food and Drug Administration (FDA) has the authority to regulate ingredients in cosmetics and personal care products, they often do not exercise it.1

Adding insult to injury, the FDA tasks companies manufacturing and marketing cosmetics with ensuring their safety. Not only is this an obvious conflict of interest, but “neither the law nor FDA regulations require specific test to demonstrate the safety of individual products or ingredients.”2

So, while cosmetic companies are responsible for substantiating safety, there are no required tests and the companies do not have to share safety data. In fact, the FDA isn’t even authorized to order recalls of hazardous chemicals from the market.

Cosmetic3 companies may also fall back on a loophole in the Fair Packaging and Labeling Act,4 which allows companies to withhold information relating to “trade secrets,” under which fragrances and flavor ingredients fall.5

Participating with Environmental Defense and other U.S. groups, the Breast Cancer Prevention Partners (BCPP) tested personal care products and cleaning products sold at major Canadian retailers in order to identify undisclosed fragrance ingredients.6 A lack of federal regulation in Canada and the U.S. results in an increased risk of exposure to consumers.

Your Right to Know

The Campaign for Safe Cosmetics, a project of the BCPP, is a broad-based national coalition of nonprofit organizations whose mission it is to protect the health of consumers by securing reforms necessary to eliminate dangerous chemicals linked to adverse health effects.7

The research project was triggered by scientific literature and prior product testing indicating chemicals linked to cancer, birth defects, endocrine disruption and other adverse effects were used heavily in beauty, personal care and cleaning products.

However, despite research evidence, there continues to be a lack of legislatively mandated labeling requirements, leaving consumers uninformed of the dangers in products they bring into their homes every day. For this test, BCPP and their partners purchased 140 different beauty, personal care and cleaning products for testing.

Of particular concern were products marketed to children, women of color and products marketed by celebrities as “good for the environment” or “green.” One of the more concerning results was that many of the personal care products tested contained more hazardous chemicals than the cleaning products.8

Millions of dollars and countless hours of lobbying have been poured into the industry’s fight against legislatively mandated ingredient disclosure. Fragrance is a big business as they are used in personal care products and cleaning products.

The value of the North American flavor and fragrance market is nearly $6 billion and forecast to reach $7.42 billion by 2020.9

Top 10 Most Hazardous Products Tested

The fragrance industry has nearly 4,000 fragrance chemicals at its disposal, which companies are not mandated to disclose. BCPP hired two independent third-party testing laboratories. The first assessed volatile organic compounds and the other performed two-dimensional gas chromatography on a subset of 32 products, including shampoo, deodorant, multipurpose cleaners and lotions.

There was an average of 136 chemicals in the cleaning products and an average of 146 in personal care products. The team then compared the product name against the type of chemicals triggering hormone disruption, asthma, developmental toxins and cancer.

From this data they ranked the top 10 products with the most hazardous chemicals in terms of the highest number linked to these health effects.10 The products making the top 10 dangerous products directly from the BCPP report were:11

Just for Me Shampoo — A children’s shampoo, from a hair-relaxing kit marketed to kids of color by Strength of Nature.
JLo Glow Perfume — A fine fragrance made by Coty and endorsed by music, television and film icon Jennifer Lopez.
Kaboom with OxiClean Shower Tub & Tile Cleaner — Marketed as a “great cleaner that is safe and friendly to use,” made by Church & Dwight Co.
Olay Luminous Tone Body Lotion — Made by Procter & Gamble and marketed for its antiaging qualities.
Axe Phoenix Body Spray — A body spray made by Unilever and marketed to young men using an overtly sexual ad campaign.
Marc Jacobs Daisy Perfume — Another Coty fragrance carrying the famous designer’s name and using beatific, radiant young girls in its marketing campaigns.
Taylor Swift Wonderstruck Perfume — A Revlon fine fragrance endorsed by the beloved pop country singer Taylor Swift.
Organix (OGX) Shampoo — A Johnson & Johnson product marketed as part of a “green/sustainable” line of products to young women.
Formulation 64-RP — An industrial cleaner and disinfectant used by custodians firefighters and others.
White Linen Perfume — Created by Estée Lauder in 1978, marketed as “a beautiful perfume” for women young and old.

While these were the top 10 products, it is important to remember the team conducted tests on 140 personal care and cleaning products, the lowest of which, yellow soap, had 46 chemicals. Other cleaning products such as Kaboom with OxiClean Shower, Tub and Tile Cleaner had 229. Of the 25 personal care products tested, only three had less than 100 and none had less than 75.

Perfumes Tied to Chronic Disease

Are perfumes really the scent of danger? The Environmental Working Group (EWG) found the most popular perfumes, colognes and body sprays may contain trace amounts of natural essence, but they typically contain dozen or more potentially hazardous chemicals. Some of the synthetic chemicals are derived from petroleum.

In an independent laboratory test, the Campaign for Safe Cosmetics12 found 38 secret chemicals in 17 leading fragrances including top offenders from American Eagle, Coco Chanel, Britney Spears and Giorgio Armani. Following an analysis of the data, EWG commented:13

“The average fragrance product tested contained 14 secret chemicals not listed on the label. Among them are chemicals associated with hormone disruption and allergic reactions, and many substances that have not been assessed for safety in personal care products.”

Makers of these popular perfumes often use marketing terms such as “floral,” “exotic” or “musky” without disclosing the complex cocktail of synthetic chemicals used to create the scent.

The average fragrance product tested by the Campaign for Safe Cosmetics contains 14 chemicals not listed on the label, among those associated with hormone disruption, allergic reactions and substances without safety testing.

Undisclosed ingredients also include chemicals that accumulate in the human tissue, such as diethyl phthalates, found in nearly 97% of Americans and linked to sperm damage.

Their report14 also found the FDA was similarly uninformed, as a review of government records revealed a vast majority of the chemicals used in fragrances were not assessed for safety when used in spray-on personal care products.

Phthalates Continue To Be Used in Personal Care Products

However, it isn’t only the undisclosed chemicals under the generic label “fragrance” that are cause for concern. Some chemicals listed included ultraviolet protector chemicals associated with hormone disruption and nearly 24 chemical sensitizers responsible for triggering allergic reactions.

Some manufacturing companies are moving toward restricting or eliminating certain chemicals from fragrances, such as phthalates.15 Although phthalates are only one chemical of concern in fragrances, this is a step in the right direction.

Findings from a multicenter study made a strong correlation between a mother’s exposure to phthalates during pregnancy and changes to the development in a baby boy’s genitals.

Another study at an infertility clinic demonstrated exposure was correlated to DNA damage in sperm and a third study in children aged 4 to 9 linked behavioral problems to higher maternal exposure to low molecular-weight phthalates.16

Adverse Event Reports on the Rise

While FDA regulation is weak at best, it is completely ineffective when adverse effects are not reported. The FDA has an adverse event reporting system containing information on product complaints submitted to the FDA. The database is designed to support safety surveillance programs and includes symptoms, product information and patient outcome.17

The FDA Center for Food Safety and Applied Nutrition (CFSAN) adverse event reporting system was made publicly available in 2016.18 An analysis of events dated between 2004 and 2016, including voluntary submissions by consumers and health care professionals, showed over 5,000 events reported, at an average of 396 events per year.

However, the average number hides a growing trend. For instance, in 2015 there were 706 events reported and in 2016 there were over 1,500. The three most commonly reported products were hair care, skin care and tattoos. The authors of the report suggest more surveillance is needed, saying:19

“Unlike devices, pharmaceuticals and dietary supplements, cosmetic manufacturers have no legal obligation to forward adverse events to the FDA; CFSAN reflects only a small portion of all events. The data suggests that consumers attribute a significant portion of serious health outcomes to cosmetics.”

The spike in adverse effects reported to the FDA in 2016 occurred only after the agency appealed to consumers and physicians to report events related to products manufactured by Chaz Dean Cleansing Conditioners under the brand name Wen.20

When adverse event complaints are made to a manufacturer they are not legally obligated to pass the reports to the FDA. Following an investigation, the FDA uncovered another 21,000 complaints made to Chaz Dean.21 It is highly likely adverse effects are commonly reported to the manufacturer and not to the FDA, indicating the total numbers in the CFSAN system are underreported.

Avoid These Toxic Chemicals in Your Personal Care Products

Despite over 21,000 consumer complaints to the contrary, Guthy-Renker, WEN’s marketing company, told NPR:22

“We welcome legislative and regulatory efforts to further enhance consumer safety across the cosmetic products industry. However, there is no credible evidence to support the false and misleading claim that WEN products cause hair loss.”

Until control improves over chemicals used in personal care products, safety testing and regulation protecting the consumer, it’s important you read the label on every personal care and cosmetic product you purchase. Here’s a list of some of the more hazardous chemicals found in many personal care products:23,24

Parabens — This chemical, found in deodorants, lotion, hair products and cosmetics, is a hormone disruptor mimicking the action of the female hormone estrogen, which can drive the growth of human breast tumors. A study published in 2012 found parabens from antiperspirants and other cosmetics appear to increase your risk of breast cancer.25
BHA and BHT — These chemicals are used as preservatives in makeup and moisturizers and are suspected endocrine disruptors.26
Synthetic colors — FD&C or D&C are the labels used to represent artificial colors. The letters are preceded by a color and number, such as D&C Red 27. The colors are derived from coal tar or petroleum sources and are suspected carcinogens. They are also linked to ADHD in children.
Fragrance — This is a large category of chemicals protected as proprietary information, and manufacturers do not have to release the chemical cocktails used to produce the scents in fabric sheets, perfumes, shampoos, body washes — anything having an ingredient called “fragrance.”
Formaldehyde-releasing preservatives — While adding formaldehyde is banned as it is a known carcinogen, manufacturers have found other chemicals act as preservatives and release formaldehyde. Chemicals such as quaternium-15, diazolidinyl urea, methenamine and hydantoin are used in a variety of cosmetics and slowly release formaldehyde as they age.
Sodium lauryl sulfate and sodium laureth sulfate — These are surfactants found in more than 90% of cleaning products and personal care products to make the product foam. They are known to irritate your eyes, skin and lungs and may interact with other chemicals to form nitrosamines, a known carcinogen.
Toluene — Toluene is made from petroleum or coal tar, and found in most synthetic fragrances and nail polish. Chronic exposure is linked to anemia, lowered blood cell count, liver or kidney damage, and may affect a developing fetus.
Triclosan — This antibacterial ingredient found in soaps and other products has been linked to allergies, endocrine disruption, weight gain and inflammatory responses, and may aggravate the growth of liver and kidney tumors.
Propylene glycol — This small organic alcohol is used as a skin conditioning agent and found in moisturizers, sunscreen, conditioners, shampoo and hairspray. It has also been added to medications to help your body absorb the chemicals more quickly and to electronic cigarettes. It is a skin irritant, is toxic to your liver and kidneys, and may produce neurological symptoms.27,28,29

Prevent Exposure by Making Your Own

Your skin is an excellent drug delivery system, so what goes on your body is as important as what goes in your mouth. Chemicals you ingest may be filtered through a health gut microbiome, a protection you don’t get when they are absorbed through your skin.

Consider preventing exposure by making many of your own personal care products at home and consulting the EWG Skin Deep searchable database30 to help you find personal care products free of potentially dangerous chemicals. Products bearing the “USDA 100% Organic” seal are among your safest bets if you want to avoid potentially toxic ingredients.

Seek out recipes to make your own homemade bath and handwashing products that don’t contain additional by-products and preservatives. For instance, coconut oil is a healthy skin moisturizer with natural antibacterial properties. Coconut oil may also be used as a leave in conditioner on your hair — be sure to start with very little.

Consider a 25% dilution of apple cider vinegar and water to wash your hair. Spritz your hair with the solution and leave it in for five minutes before thoroughly rinsing. You may have to tweak the dilution for your hair type as apple cider vinegar is a conditioning agent.

from:    https://articles.mercola.com/sites/articles/archive/2023/05/23/top-10-most-hazardous-products.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art3ReadMore&cid=20230523&cid=DM1404352&bid=1808248248

What to Know About Protecting Your Choice in the Hospital

How to Save Your Life and Those You Love When Hospitalized

Analysis by Dr. Joseph MercolaFact Checked

STORy AT-A-GLANCE

  • Laura Bartlett and Greta Crawford have founded an organization to address the forced treatments patients receive when they’re hospitalized for COVID-19, but the same strategy can be used to protect yourself against other medical hazards as well
  • The Caregivers and Consent document they created is an “advance decision” document. So, the moment you enter the hospital, the hospital staff know what they can and cannot do to you; they are legally required to respect your current care decisions. And unlike an Advance Directive (which only kicks in when you are incapacitated) the Caregivers and Consent document goes into effect immediately
  • It’s important to complete and notarize your Caregivers and Consent document BEFORE you ever need to go to the hospital
  • Make sure you send the completed, signed and notarized document to the CEO of the hospital in two ways: (1) via a professional courier (one that specializes in delivering legal documents); and (2) via the Postal system with certified mail, return receipt requested. The CEO is responsible for all legal business relating to the hospital, including the medical records, so the CEO, not your attending physician, is the one whose responsibility it is to get your consent document entered into your electronic medical record
  • Make at least 10 copies of the signed, notarized document and keep one copy on your person, in case you ever have an accident or acute illness requiring hospitalization. Also provide copies to the attending physician and nurse once hospitalized
  • Also, should you become hospitalized (and therefore unable to personally send the document to the CEO), designate a family member or friend to send your Caregivers and Consent document on your behalf. Additional recommendations to ensure your safety are included

In this interview, Laura Bartlett and Greta Crawford detail how you can protect yourself from one of the top contributors to premature death, namely conventional hospital care. The key here is to understand what the dangers are and take proactive measures to guard yourself and your family from them.

Nearly 10 years ago, I interviewed Dr. Andrew Saul, author of “Hospitals and Health: Your Orthomolecular Guide to a Shorter, Safer Hospital Stay,” in which he details how to minimize your risk of being a victim of a medical error.

First and foremost, Saul recommended making sure you have a patient advocate, someone who can speak on your behalf if you’re incapacitated and make sure you’re receiving the correct medication and treatment. During COVID, however, family or friends were not allowed into the hospital, and patients were routinely bullied into treatments they did not want or consent to.

The good news is, Bartlett and Crawford have developed a legal document that, when served to the hospital in the proper way, can ensure that your medical wishes are honored. By eliminating any confusion about your consent (or denial of consent), this document can literally save your life.

Why ProtocolKills.com Was Created

Bartlett and Crawford have founded an organization to address the lethal and, in many cases, forced treatments patients receive when they’re hospitalized for COVID-19, but the same strategy can be used to protect yourself against other medical hazards as well. Crawford explains:

“I created a website called ProtocolKills.com. This came after I was in the hospital with COVID. In the process of going to the hospital, I was denied informed consent and was completely unaware of some of the things they were doing to me. I was given five rounds of remdesivir, which nearly took my life, and I did not even know that I was being poisoned at the time …

During that time in the hospital, I went from thinking I was going to go home after I got oxygen to actually feeling like that I was going to die. I was almost certain I was going to die after being given just the first dose of remdesivir …

[And then there was] the constant push for the vaccine in the hospital, the harassment for not getting vaxxed, and the fact that I was given medication without my knowledge at all, which led me to start the website to not only inform people about what was going on, but [as] a platform to allow other victims who were not as fortunate as me.

Many of them, the majority of them, did not make it out alive. So, it’s a platform for them to share their story. We have over 250 stories on there about what they faced in the hospital. We really wanted to get this information out there to the public, but we also wanted to give a solution, not just to scare people. And that’s where I ended up meeting Laura.”

National Hospital Hostage Hotline to the Rescue

Bartlett continues:

“Before I met Greta at the beginning of COVID, in early 2020, I started helping my brother, Dr. Richard Bartlett, who had a protocol utilizing inhaled budesonide steroid as part of his protocol to treat COVID early. We also found it very effective once people were in the hospital to help reverse [the infectious process] and also the scarring and the inflammation of the lungs.

There are instances where it even helped people who were on ventilators as long as 30 days come off the ventilator and go home. So, I was helping him get that message out in early 2020. I’m not a doctor. I’m not a nurse. I’m just somebody who could help get that known around the world. My background is in media PR …

In the process, people who knew my brother, knew me, started reaching out to both of us with stories that they were in the hospital and they were having a hard time getting the doctor to respect their right to informed consent. It was an overwhelming number of instances where people just felt like they were being bullied or coerced, that their right to try budesonide, for instance, was just dismissed.

And it was almost as if informed consent didn’t exist. But in fact, it never went away. Even during the COVID shielding for hospitals, informed consent between the doctor and the patient never went away. You always had the right to informed consent.

So that’s where my work started. In the process, since there were so many people reaching out for help, I thought, ‘Well, why doesn’t somebody come up with a way for people to quickly access some information of what their rights are and their patient rights?’

So, I started a nationwide hotline, called the Hospital Hostage Hotline [call or text 888-c19-emergency, or 888-219-3637]. It’s still in effect. I still get calls from all over the country. And I’ve been able to help people who went in even for non-COVID reasons like a urinary tract infection that was [also] diagnosed as COVID, and they were being pushed towards a protocol and told they couldn’t leave the hospital.

They needed to know they could, that they always had the right to leave AMA — Against Medical Advice — if that’s what they chose. They also have the right to either consent or not consent to things and it should be respected. I realized that one of the biggest tools for getting that informed consent notice to the doctor was not to just verbally say it, but to have it in writing. These aren’t my original ideas.

I actually had a hospital insider reach out … somebody who had been in the system and knew how to navigate the system at a high level in administration, give me some tips and tools on how to navigate the hospital system to make sure that informed consent was not only documented and delivered effectively to get into the electronic medical record, but also, what their basic patient rights were and how to advocate for them.”

You Have the Right to Leave

One drawback of signing an AMA is that insurance won’t pay for your treatment. That threat will often keep patients in the hospital because they’ll have to pay out of pocket. So, it can be used against you.

“Profit has been a big factor in a lot of suffering,” Bartlett says. “Patients were afraid to leave because they were told, like in the instance of a gentleman that I was helping in New Jersey who went in for a urinary tract infection.

He was an elderly man. This was early 2020. They quickly tested him for COVID and started him on that road towards a ventilator. And they told him flat out, ‘If you leave, none of this will be covered by insurance.’ So that was a big factor.”

Hospitals may also misinform you about your AMA rights, as we’ve seen repeatedly during COVID. More often than not, the hospital’s reluctance to release a patient has to do with protecting its revenues. Bartlett offers the following story to illustrate:

“Somebody that I was helping advocate for said the doctor actually said to them, ‘You cannot leave.’ This person was 15 or 16 days into their COVID diagnosis and they were feeling better. They were likely not COVID positive …

That’s where the name of the hotline came from. They actually felt like hostages. That’s what they were reporting to me. ‘I feel like I’m held prisoner.’ But in fact, they always had the right to leave a hospital whenever they chose to. It’s not up to the doctor when they can leave. They have to make that medical choice for themselves, whether or not they feel like they can leave.”

A Novel Consent Document That Can Save Your Life

Patients clearly need a way to put themselves back in the driver’s seat, and the novel medical consent document Bartlett and Crawford created, available on OurPatientRights.com, is the most powerful way I’ve seen so far to do that. As explained by Bartlett:

“What we learned from this whole ordeal over the last couple of years is that there was a need for a novel document that did not exist, to our knowledge, that covers your written consent. A document that documents your current consent, not an advance directive that kicks in after you’re incapacitated.

Before you go into the hospital, write down your consent wishes so that everybody involved in your care within the hospital will have eyes on it because it’s put into your electronic medical record. It’s notarized. It’s signed before you go in. That’s the key. So do it while you have full capacity.

It’s a novel strategy. I’m so grateful to the hospital insider who saw the problem and helped us navigate the system, so that we have an insider’s perspective on how to do this to keep people safe.”

As noted by Crawford, while COVID-19 may seem like a distant memory, people are still being hospitalized and diagnosed with COVID, and are being held hostage by a hostile medical system seemingly intent on milking them for all their worth, until death, if need be.

This is where filing a written medical consent form can help save your life. No doctor can override your written decision (consent) declining certain medications or treatments. Verbal communication is not enough. It must be in writing, notarized and delivered in a manner that formally serves the hospital and puts their physicians on notice.

General Consent Vs. Specific Consent

As explained by Bartlett, when you enter a hospital, you must sign a general consent authorization form. This is basically a contract between you and the hospital. Since you have bodily autonomy, they need your consent before they can do anything to you.

Typically, the general consent form authorizes hospital staff to test, treat and care for you in whatever way they see fit — and when a patient signs the general consent authorization, physicians feel justified that they can implement a hospital protocol without further explaining the risks, benefits or alternatives of that protocol to the patient.

Now, if you’re well enough to read the entire document, and see something in there that you don’t agree with, you can strike the sentence or paragraph and initial it, to indicate that you do not consent to that specific detail. However, that still doesn’t offer you much protection.

What you need is a much more specific document where you detail the types of treatments you consent to and the ones you don’t. You need to carve out a niche from the general consent form that specifies exactly what you do (and do not) consent to. And you need to be clear. Fortunately, the Caregivers and Consent document carves out that niche to communicate clearly to all physicians your exact consent wishes.

“You need a written consent document that, in addition to just the general consent, is a contract between you and the doctor, so he knows, he’s put on notice, what it is that you absolutely do not consent to. For instance, a COVID injection, if that’s your wishes,” Bartlett explains.

“They have a code of ethics, the American Medical Association guidance to physicians, per the ethics opinion 2.1.1, that when the patient surrogate has provided specific written consent, the consent form should be included in the record. This is key. Write it down. You don’t need an attorney. You don’t need any fancy training. You don’t need to be a doctor, don’t need to be a nurse.

You can write it down, and then, when you deliver it in our specific way — and it’s very important how you deliver it — it gets put into the electronic medical record for everybody to see. Now you’ve got receipts, that if you do something against consent, it’s intentional. OK?

So, here’s the website you can find a template for that. It’s called OurPatientRights.com. What you’ll see there are two PDF documents. [On one of the PDFs there are two pages.] One is the actual template, the other one is instructions on how to deliver it. And you can edit the document by the way. You can write your own. It’s just a template. But there’s also very specific instructions on how you are going to deliver this so it’s not disregarded.

Here’s what you’re going to see in the document. ‘I [your name] advise all physicians, nurses, and other caregivers that this Caregivers and Consent document reflects my current wishes for my care and are carefully planned and intentional wishes.’ That’s very important because it’s current. It’s not going to kick in when I’m incapacitated.”

Your Written Consent Must Be Respected

Advance medical directives don’t kick in until or unless you’re incapacitated, so that’s another completely different kind of document reflecting current consent wishes. What Bartlett and Crawford have created is an “advance decision” document. So, the moment you enter the hospital, they know what they can and cannot do to you. And, they are legally required to respect your written directives. The following section of the document reads:

“Receipt of this Caregivers and Consent document by the hospital serves as notice that I will report to the Medical Board any physician who violates my carefully planned and intentional wishes that are based upon my deeply held religious and spiritual beliefs and are delineated within this Caregivers and Consent document.”

This puts the doctor on notice. This isn’t a threat. It’s merely a factual statement that if anyone goes against your wishes, they’re intentionally disregarding your consent. Once it’s in your electronic medical record, they can’t say they didn’t know that you did not consent to a specific test, drug, vaccine or procedure. So, ignoring your written consent is then actually a criminal offense akin to assault and battery. It’s also medical malpractice.

“Let me tell you, there are good physicians and they are clamoring for something like this,” Bartlett says. “They are thankful there is something they can use to push back against administration and say, ‘I’m not going to violate this person’s written consent. I’m not going to do this to this person …’

With these documents, if you are blatantly refusing to honor a patient’s wishes and religious beliefs, and you’re doing it against these documented legal forms, then you risk losing your license altogether as a physician and never working in medicine again …

But you need it in writing … and it needs to be served in a very specific way. You need to do this before you ever go to the hospital. Have it handy in case you get yourself into a predicament, like a multi-car pileup on the highway and an ambulance transports you to the hospital. The time to have this done is before there’s a problem.”

The document also specifies that “All items in this Caregivers and Consent document shall remain in effect unless I choose to revoke in writing; no one else may alter or amend this Caregivers and Consent document.” So there can be no misunderstanding. Your doctor or nurse cannot claim you gave implied consent because you mumbled something incoherent in your sleep. In other words, if you didn’t change your consent wishes in writing, you didn’t change your consent wishes. Period.

What’s in the Caregivers and Consent Document Template

As mentioned, you can customize your Caregivers and Consent document any way you like. But to give people a starting point, the template, available on OurPatientRights.com, includes things like:

  • “I do not consent to the use of medications without my being informed of each medication’s risks, benefits and alternatives before they are ordered. Only after that information is communicated shall I choose to either grant consent or to not grant consent for each and every medication that is ordered.”
  • “I do not consent to receiving any vaccine or booster for COVID-19 or COVID-19 variant.”
  • “I do not consent to receiving the seasonal flu vaccine.”
  • “I request and consent to the use of 1 mg of budesonide via nebulizer every 4 to 6 hours for COVID-19 or COVID-19 variant diagnosis with respiratory issues.”

If you want to, you could change the verbiage to state that you do not consent to ANY vaccine. If you have allergies, add that to the list. Personally, I would recommend adding the following dietary notice:

  • “I do not consent to receiving ANY processed food, such as high-fructose corn syrup or seed oils. The only acceptable oil for me is butter, ghee, beef tallow or coconut oil. Acceptable forms of protein would be eggs, lamb, bison, beef or non-farmed seafood; but they must not be prepared with seed oils. If the hospital is unable to provide this food for me, my family or friends will bring it for me.
  • Additionally, I do not consent to not being able to take my normal supplements while in the hospital.”

I would strongly recommend that you integrate this additional clause because it’s a stealth form of abuse. These kinds of foods can only impair your effort to get well, no matter what your problem is. You may also want to add a notice saying you do not consent to receive blood donations from COVID-19 vaccinated donors, and that all blood donations must be from donors confirmed to have not received any COVID-19 vaccines.

Important: Follow Proper Procedure!

As mentioned multiple times in this interview, it’s crucial to follow the proper procedure. Here’s a summary of the necessary steps:

1.Complete your customized and personalized Caregivers and Consent form BEFORE you ever need to go to the hospital.

2.Get the form notarized. Make sure you sign the form in front of the notary.

3.Send the completed, signed, notarized form to the CEO of the hospital in two ways: (1) via a professional courier (one that specializes in delivering legal documents); and (2) via the Postal system with certified mail, return receipt requested.

The CEO is responsible for all legal business relating to the hospital, including the medical records, so the CEO, not your attending physician, is the one whose responsibility it is to get your consent forms entered into your electronic medical record.

4.Make at least 10 copies of the signed, notarized form and keep one copy on your person or in your wallet or purse, and another in the glove compartment of your car, in case you ever have an accident. Also provide copies to family or friends. If you happen to be hospitalized before you’ve had the chance to send the documents, have one of them follow the delivery procedure outlined on the General Instructions form.

5.Once you’re hospitalized, you or one of your contacts will give one copy to your attending physician and another to your nurse, and inform them that this document is already in your electronic medical record, or that the hospital will be served the documents shortly. Distribute additional copies to other care providers as needed.

6.Also, upon hospitalization, request to see your electronic medical record to make sure your Caregivers and Consent form has been entered. It is your right to see your electronic medical record, and it’s available through an online portal, so don’t let anyone tell you otherwise.

Also routinely check your medical record (or have your patient advocate do it for you) to make sure your wishes are being followed and that you’re not being given something you’ve denied consent for.

Crawford notes:

“What we’ve experienced using these documents is a complete change in the attending physician, from being aggressive and maybe trying to push you, to being very helpful and efficient. Once they receive these documents, they just do a 180. As a matter of fact, one patient’s brother told me he’s getting treated better than he’s ever been treated at a hospital before.”

Again, having this document in your medical record virtually guarantees that they cannot harm you by doing something you don’t agree with. Of course, some psychopath might ignore your directives, but they’ll have to pay a hefty price, as they’re guaranteed to lose a malpractice suit and be stripped of their medical license. The legal consequences are so severe that the person doing it would have to be beyond irrational.

Keep in mind that while you can request and consent to certain treatments, such as ivermectin, for example, this document CANNOT force your doctor or hospital to use that treatment. They can still refuse to administer something you’ve consented to.

They cannot, however, administer something that you’ve declined consent for. The ace up your sleeve at that point is that you can still sign out AMA (against medical advice), get out alive, and seek desired treatment elsewhere. Getting out alive is the key goal.

More Information

Again, here are the three resources created by Bartlett and Crawford:

  • ProtocolKills.com — Here you can find a hospital protocol for COVID, information about remdesivir, patient rights information, alternative health care options and patient testimonies
  • OurPatientRights.com — Here you can download the template for the Caregivers and Consent document and general instructions
  • Hospital Hostage Hotline — Call or text 888-c19-emergency, or 888-219-3637

In closing, please share this information with everyone you know. Bring it to your church, synagogue and local community groups. Everyone needs to know they can secure their patient right to informed consent and how to do it so that their wishes cannot be ignored. This is the most effective way to empower yourself when it comes to your medical care. So please, help spread the word.

from:  https://articles.mercola.com/sites/articles/archive/2023/05/21/bartlett-and-crawford-consent-form.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art2ReadMore&cid=20230521_HL2&cid=DM1403018&bid=1806109132