La fertilité des femmes :une cible du vaccin Arn m touchant même les femmes non vaccinées ?
Lien vers la vidéo d’origine :
Cette vidéo est le premier extrait doublée de cet échange entre 5 médecins le 22 avril 2021 autour des conséquences de la vaccination ARNm sur les personnes non vaccinées. En effet, Depuis que des rapports ont fait surface ces derniers jours selon lesquels des personnes qui ont choisi de NE PAS recevoir les injections expérimentales de COVID-19 mais ont été exposées à ceux qui les ont reçues et ont souffert de ce qui semble être des infections provenant de ces personnes entièrement «vaccinées», affectant principalement les femmes qui ont signalé des problèmes de menstruation, des saignements abondants, des fausses couches et une réduction du lait maternel…
Le reste des interventions notamment de Carrie Madej et Lee Merrit sur ces questions feront l’objet d’une diffusion très prochaine.
Vous pouvez me soutenir financièrement dans ce travail de réinformation et de doublage de vidéo :
IDENTIFYING POST-VACCINATION COMPLICATIONS & THEIR CAUSES: AN ANALYSIS OF COVID-19 PATIENT DATA
April 26, 2021Dain Pascocello
An AFLDS Issue Brief for Citizens, Policymakers and Physicians
STATEMENT OF POSITION
After several months dealing with capacity-related issues in COVID-19 vaccine administration, US states are set to find themselves with a supply of Pfizer, Moderna, and Johnson & Johnson immunizations outstripping demand for the experimental shots. According to a recent report by the Kaiser Family Foundation, by about mid-May states will reach a “tipping point where demand for rather than supply of vaccines is our primary challenge.” One official with the American Public Health Association put it this way: “Anybody who’s ever done a public health program knows that the last 20-30% of your target is the hardest.” Perhaps anticipating the challenge, the Biden administration dedicated $48 billion in its stimulus legislation to “implement a national, evidence-based strategy for testing, contact tracing, surveillance, and mitigation with respect to SARS-CoV-2 and COVID-19.” By means of comparison, the National Intelligence Program budget, which includes the CIA and parts of the FBI, will spend about $62 billion in the current year – just 29% more than a single COVID-related line item in the president’s “American Rescue Plan.”
On April 24, state health authorities in Indiana, New York, Virginia, Missouri, and Michigan resumed administering Johnson & Johnson’s COVID vaccine following an 11-day federal “pause” on the single-shot inoculation. According to published reports, a review by the Centers for Disease Control and Prevention’s (CDC) advisory committee, known as ACIP, uncovered 15 cases of vaccine side effects involving potentially fatal blood clots. All were women, most under 50 years old. Three died and seven remain hospitalized. ACIP ultimately decided to lift the pause and recommended attaching a warning label to the experimental injection, to which J&J’s chief medical officer agreed to add at a later date.
The CDC’s early warning system for vaccine side effects, its 30-year-old Vaccine Adverse Event Reporting System, or VAERS, has captured thousands of other “adverse events” since the COVID-19 vaccination effort began in late 2020. Yet these complications have received a fraction of the attention paid to J&J’s blood-clotting controversy. Why? America’s Frontline Doctors (AFLDS) opposes attempts by state and federal jurisdictions to mandate vaccination for COVID-19 and supports further study by independent health officials before the Food and Drug Administration (FDA) replaces its conditional “emergency use authorization” (EUA) for the immunizations with full approval, known as a biologics license, a decision which could come as early as April or May 2021. This AFLDS Issue Brief is intended to provide additional information for concerned citizens, health experts, and policymakers about adverse events and other post-vaccination issues resulting from the three experimental COVID-19 vaccines currently administered under EUA. As always, potential vaccine recipients should weigh the available evidence on medical side effects against their particular needs free of third-party coercion, intimidation, and threats.
TAKING PATIENT EXPERIENCES SERIOUSLY
Drugmaker Pfizer expects to collect $15 billion in 2021 from sales of its mRNA experimental COVID vaccine. There is an irrepressible economic incentive among pharmaceutical companies for childhood COVID vaccines, boosters, and the like. Public health experts should stop and assess data on possible vaccine side effects and related post-vaccination questions before it is too late. Here are some major categories of concern as-yet publicly unaddressed by either the FDA or CDC. AFLDS believes these patient concerns ought to be taken more seriously by health regulators in the United States and abroad. Failing to consider these and other “known unknowns” is a dereliction of basic medical research.
1. Why is there concern surrounding this particular vaccine?
The COVID-19 vaccines are still experimental. They are currently being used on an “emergency” basis and are not FDA approved. It takes years to be sure something new is safe. The vaccines are new as is the technology they employ. This new biotechnology introduces something called a “spike protein” instead of the traditional attenuated antigen response in a conventional vaccine. No one knows definitively the long-term health implications for the body and brain, especially among the young, related to this spike protein. In addition, if documented problems with the protein do arise, there will never be any way to reverse the adverse effects in those already vaccinated.
2. What about the reported neurological issues?
There are two major neurological concerns related to the COVID vaccines. These are the spike proteins and the lipid nanoparticles which carry the mRNA into the cell. They are both capable of passing through the “blood-brain barrier” which typically keeps the brain and spinal cord completely insulated from entrants into the body. There simply has not been enough time to know what brain problems and how often a brain problem will develop from that. There is concern amongst many scientists for prion disease (neurodegenerative brain disease).
Traditional vaccines do not pass through the blood-brain barrier. Crossing the blood-brain barrier places patients at risk of chronic inflammation and thrombosis (clotting) in the neurological system, contributing to tremors, chronic lethargy, stroke, Bell’s Palsy and ALS-type symptoms. The lipid nanoparticles can potentially fuse with brain cells, resulting in delayed neuro-degenerative disease. And the mRNA-induced spike protein can bind to brain tissue 10 to 20 times stronger than the spike proteins that are (naturally) part of the original virus.
3. Can the unvaccinated get sick from contact with the vaccinated?
The vaccine produces many trillions of particles of spike proteins in the recipient. Patients who are vaccinated can shed some of these (spike protein) particles to close contacts. The particles have the ability to create inflammation and disease in these contacts. In other words, the spike proteins are pathogenic (“disease causing”) just like the full virus. What is most worrisome is that a person’s body is being suddenly flooded with 13 trillion of these particles and the spike proteins bind more tightly than the fully intact virus. Because of the biomimicry (similarity) on the spike, shedding appears to be causing wide variety of autoimmune disease (where the body attacks its own tissue) in some persons. Worldwide cases of pericarditis, shingles, pneumonia, blood clots in the extremities and brain, Bell’s Palsy, vaginal bleeding and miscarriages have been reported in persons who are near persons who have been vaccinated. In addition, we know the spike proteins can cross the blood brain barrier, unlike traditional vaccines.
4. What about interaction between unvaccinated children and vaccinated adults?
AFLDS is concerned that some children will become COVID symptomatic after their parents and teachers get vaccinated. This concern does not relate to risk from infection. Indeed, according to the American Academy of Pediatrics and the Children’s Hospital Association, approximately “1.6% of children with a known case of COVID-19 have been hospitalized and 0.01% have died.” Rather, public health bureaucrats might use these cases of breakthrough transmission or symptoms to speculate that a child’s illness is related to a SARS-CoV-2 “variant,” when in reality it is a reaction to the vaccine. Our other concern is that children could develop long-term chronic autoimmune disease including neurological problems due to the fact that children have decades ahead of them and trillions of the spike proteins mentioned above.
5. Is there a post-vaccination menstrual bleeding risk?
AFLDS is aware of thousands of reports involving vaginal bleeding, post-menopausal vaginal bleeding, and miscarriages following COVID-19 vaccination as well as anecdotal reports of similar adverse events among those in close contact with the vaccinated. We cannot comment definitively on the close contacts yet, other than to say we have heard reports of this worldwide. But there is so much reporting of vaginal bleeding post-vaccination that it is clear a connection between the vaccine and irregular bleeding exists. Despite this clear-cut evidence, menstrual-cycle changes were not listed among the FDA’s common side effects in its phase-three clinical participants. Women’s reproductive health needs to be taken seriously rather than waved away by agenda-driven public health officials.
CONCLUSION
The continued rollout of COVID-19 vaccines moves along without due consideration of patient side effects and post-inoculation complications. AFLDS calls on state and federal health regulators to release more adverse-event-related data and conduct additional follow-up studies before the FDA fully licenses any of the vaccines currently administered under emergency use authorization. The growing body of evidence is too compelling to ignore.
Source : americasfrontlinedoctors.org
3 Reasons Miami School Might Be Right About Asking Teachers Not to Get COVID Vaccine
Centner Academy, a private school in Miami, faced a global media assault after asking staff not to get vaccinated, but these three facts about the vaccines lend support to the school’s decision.
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Centner Academy, a private school in Miami, has made international headlines for directing its employees who have not yet received the experimental COVID-19 vaccine, to wait until the end of the school year, as a precautionary step to protect the health of their school community, given both concerning new anecdotal reports that the vaccinated can adversely affect the health of the un-vaccinated, and that clinical safety and efficacy data for the mRNA vaccines will not be completed until sometime in 2023.
Thus far, mainstream media reporting has focused and railed against the following statement made by Leila Centner, co-founder and CEO of Centner Academy, to her employees (in an internal email later leaked to the press) as being the most controversial and contestable:
“Tens of thousands of women all over the world have recently been reporting adverse reproductive issues simply from being in close proximity with those who have received any one of the COVID-19 injections, e.g., irregular menses, bleeding, miscarriages, post-menopausal hemorrhaging and amenorrhea (complete loss of menstruation).
“No one knows exactly what may be causing these irregularities, but it appears that those who have received the injections may be transmitting something from their bodies to those with whom they come in contact. Until more is known, we must err on the side of caution when it comes to the welfare of our students and the school team.”
You can read Leila’s entire letter and comment which she posted to Instagram here.
Leila Centner’s private communication, now a matter of global public scrutiny, even reaching the White House press secretary for comment on April 27, came under fire by a number of conventional allopathic physicians, including Dr. Aileen Marty, a physician and infectious disease specialist with Florida International University’s Wertheim College of Medicine, who commented as follows:
“But there’s not one citation, there’s not one physician or scientist whose name is spelled out in there. There’s no references. There’s nothing. There is no scientific evidence provided. Rumor is the only thing that’s there, and if you look at the reality, there’s zero, zero science behind those allegations.
“If they believe it, and they then share this big lie, it has a horrific impact on our entire community.”
While these comments by Dr. Marty, and now hundreds of other mainstream media reports have attempted to dismiss Leila Centner’s statements as a “source of misinformation, without basis in science,” we believe they have significant merit, and are at the least worth exploring further.Ask Congress to Investigate COVID Origins – Take Action
Fact #1: Vaccines make some sick. Sick people are more likely to compromise the health of others
Whereas the mainstream media and government health authorities have been dogmatically pushing the unequivocal narrative that the COVID-19 (and all) vaccines are “safe and effective” a priori, it is undeniable that the COVID-19 vaccines are presently only approved for distribution to the public under an Emergency Use Authorization, in lieu of proper clinical safety and efficacy trial data being available, and which are not estimated to be completed until April 2023 for the Pfizer vaccine.
This makes COVID-19 vaccines, by definition, experimental, as Leila Centner has repeatedly offered as an explanation for her precautionary stance as to their unintended, adverse effects they may have to the health and well-being of her school staff, faculty, children and larger community.
Human medical experimentation, as defined by the Nuremberg code of medical ethics (1947), must not only be voluntary, but the participant needs to be fully informed of both the risks and benefits, in order to be able to give their full legal consent. Also, if the medical experimenter has reason to believe an intervention may cause harm, disability or death he or she must suspend the experiment immediately.
In the case of the experimental mRNA COVID-19 vaccine rollouts, government data reveals the COVID-19 vaccines are having profound, adverse health effects on a subpopulation of recipients, as documented in the Vaccine Adverse Events Reporting System (VAERS), which as of April 28, lists a total of 85,926 reports of the vaccinated experiencing adverse effects, ranging from death to hundreds of other symptoms and life-threatening conditions.
Moreover, VAERS is known to be highly ineffective in capturing the true extent of the actual number of vaccine adverse events, due to its highly passive, post-marketing surveillance methodology. Peer-reviewed research indicates that the rate of report capture is as low as 1% for thrombocytopenic purpura (low blood platelet related bleeding disorder) following the MMR vaccine and hypotonic hyporesponsive (bluish skin; reduced consciousness) episodes following the DTP vaccine.
The implication is that the actual scale of adverse effects within the vaccinated, which include immune dysregulation and suppression, may be several orders of magnitude higher than the already alarming scale of events reported through the conservative numbers offered by VAERS — which are almost universally ignored by the very same media attempting to discredit, defame and make an example out of the Centner Academy.
Given that those who are experiencing immune dysfunction as a result of being vaccinated are more likely to express virus reactivation, such as a cluster of cases recently reported for vaccine-induced Herpes Zoster, or may also experience a disrupted microbiome leading the the overgrowth of opportunistic bacteria, fungi, virusess, i.e., so-called “pathogens,” the health risks to those around them may also increase significantly. It should be noted that this phenomenon of vaccine-induced adverse health effects is not solely associated with the COVID-19 or mRNA vaccines.
Greenmedinfo.com has a database of over 1300 studies indicating over 150 potential adverse health effects from vaccines presently in the CDC vaccine schedule. Therefore any vaccine could, in theory, weaken or disrupt the immune system of a vaccine recipient, increasing the likelihood that they may transmit infection or disease-provoking aspects of either their microbiome or cell contents (mediated via extracellular vesicles) to those around them, which will be explained in greater detail in section #3.
Fact #2: The Pfizer mRNA vaccine clinical trial study design warns against proximity (shared air inhalation or skin contact) between vaccine participants and the unvaccinated as a possible vectors of harm
Titled, “A Phase 1/2/3 Study to Evaluate the Safety, Tolerability, Immunogenicity, and Efficacy of RNA Vaccine Candidates Against COVID-19 in Healthy Individuals,” the Pfizer COVID-19 mRNA vaccine study protocol document explicitly identifies in section 8.3.5. the need for monitoring what it calls “Exposure During Pregnancy or Breastfeeding, and Occupational Exposure.” A concern they take seriously enough that they require any incident to be reported within 24 hours to the Pfizer Safety system.
According to the document an EDP [environmental exposure during pregnancy] occurs if, for example: “a male vaccine recipient exposes a female partner prior to or around the time of conception.”
Exposure to the study intervention is defined as “inhalation or skin contact,” indicating that physical proximity between the vaccinated and unvaccinated is recognized by the Pfizer study protocol to be a cause for concern for transmission of potential side effects of the vaccine.
The document also gives the following example of an EDP scenario: “A male family member or healthcare provider who has been exposed to the study intervention by inhalation or skin contact then exposes his female partner prior to or around the time of conception.” Clearly, in this case Pfizer is acknowledging that something as simple as a healthcare provider or family member who has been exposed to an mRNA vaccine recipient through “inhalation or skin contact” (i.e., physical proximity) could generate an adverse event and/or affect the study outcomes.
Another example provided in section 8.3.5.2 titled, “Exposure During Breastfeeding,” gives the following example of what constitutes such an exposure:
“An example of environmental exposure during breastfeeding is a female family member or healthcare provider who reports that she is breastfeeding after having been exposed to the study intervention by inhalation or skin contact.”
Finally, in section 8.3.5.3., an “Occupational Exposure” occurs,
“when a person receives unplanned direct contact with the study intervention, which may or may not lead to the occurrence of an AE. Such persons may include healthcare providers, family members and other roles that are involved in the trial participant’s care.”
Clearly, the Pfizer mRNA vaccine protocol design reveals that concerns for how the vaccinated may adversely affect the health, and even reproductive outcomes, of the unvaccinated simply by being within physical proximity, are being taken extremely seriously by the manufacturer of the vaccine itself. In light of this, Leila Centner’s expressed concerns quoted at the beginning of this article are, in fact, backed by the most authoritative document we have on the experimental vaccine, and the nature of the human experiments being conducted on their behalf.
So far, there has been no acknowledgment or reporting on this fact by the global mainstream media, the vaccine manufacturers nor government health authorities. It will be up to the reader to share this article, and get the word out.
Fact #3: There is a plausible epigenetic molecular mechanism in biology whereby the vaccinated may affect the health status of the unvaccinated
The third major substantiating factor behind identifying the potential harm the vaccinated may have on the unvaccinated concerns the discovery of so-called horizontal information transfer within biological systems mediated by extracellular vesicles, which include a virus-like phenomenon known as microvesicle shedding and/or exosome-mediated transfer of nucleic acids. This falls within the category of epigenetics, which the apologists and shills for the mRNA vaccines’ purported safety and efficacy conveniently ignore in order to make their claim that was debunked in 1970 with the discovery of the enzyme reverse transcriptase.
Reverse transcriptase is able to transcribe RNA to DNA, essentially destroying the fundamental dogma of molecular biology, namely, the undirectional flow of information from the cell nucleus to mRNA to protein can not be reversed. This dogma is still being used half-a-century later to make the false claim that the only health risk a genetically modified vaccine has worth discussing is the possibility that it may affect the structure or function of nuclear, protein-coding genes.
We’ve even seen, through the discovery of exosomes, that the Weismann barrier has been penetrated, and somatic cells can communicate heritable information to the germline cells in what amounts to real-time, essentially devalidating the risk models presently used by vaccine manufacturers and regulators which do not account for the power epigenetic processes have to amplify the unintended adverse effects of genetically modified technologies and interventions.
While mRNA vaccines are designed using genetically modified processes not dependent on live cell substrates, thereby precluding conventional problems with shedding associated with first generation vaccines like the MMR, it is possible that they do, in fact, contribute to microvesicle shedding, which represents an even greater, more persistent threat than live-cell vaccine shedding when it comes to the persistent biological impact the vaccinated can have on the un-vaccinated.
Microvesicle, which range in size between 0.1–1.0 μm are a type of extracellular vesicle, that are secreted by many different cell types within the body, both in times of health and disease, and are known to reflect the antigenic content of the cell of origin. They have stunningly similar characteristics to viruses. For instance, like SARS-COV-2, microvesicles have a lipid bilayer formed from the budding off from host cell membranes, and they can incorporate and reproduce aspects of a vaccinated or infected cells’ immunogenicity, such as including functional mRNA, viral proteins and other nucleic acids capable of profoundly altering the structure and function of the cells to which they are transmitted.
For instance, it is theoretically feasible that a vaccine recipient’s cells expressing COVID-19 spike protein as a result of transfection with mRNA from a COVID-19 vaccine may secrete microvesicles containing components “originally alien to the cell, such as proteins and nucleic acids that are transiently or constitutively expressed via plasmid or viral vector.” These microvesicles, like viruses, and other extracellular vesicles known as exosomes, can be transmitted to other individuals (inter-individual transmission) through both normal or diseased physiological processes.
Extracellular exosomes have even been found to transfer nucleic acids cross kingdoms (plant > animal, fungal > bacterial), affecting the phenotypic expression of the target species. Therefore, it is plausible that microvesicles can transmit mRNA from a recently vaccinated individual to those within close proximity, and therefore could, in fact, “shed” mRNA and related biomolecules induced from the mRNA vaccination process to non-vaccinated individuals, inducing symptoms similar to those experienced by the vaccinated.
Indeed, microvesicles may have a profound affect on the immune status of those who both produce them, and are exposed to them. A recent study concluded that research “strongly suggests that MVs may function as strong regulators of both innate and adaptive immune systems.” Microvesicles and exosomes have also been researched and developed as vaccine candidates, further indicating that they are already being looked at by the scientific community as potential vectors of immunogenicity and carriers of viral-like and disease-modulating if not also disease-promoting bio-information.
Given the plausible mechanism through which a COVID-19 vaccine recipient’s body produces vaccine antigen (e.g., spike protein), and can package and transmit these antigens through viral-like microvesicles (and perhaps also exosomes) to others, Leila Centner’s statement “it appears that those who have received the injections may be transmitting something from their bodies to those with whom they come in contact,” has a plausible mechanism of action. Especially considering the aforementioned fact that Pfizer’s study protocol itself acknowledges that an unknown factor or mechanism may cause the unvaccinated to be adversely affected by the vaccinated.
Either way, Leila Centner’s decision was made in the spirit of the precautionary principle, and her call for further investigation and information on the vaccines before proceeding with what amounts to a reckless human medical experimentation should not be identified as “fringe,” “irrational” nor “crazy.” To the contrary, the medical establishment and would-be government regulators should themselves be raising the red flag over the tens of thousands of adverse effects that have already been reported to the government VAERS database.
We live in a time and age where protecting our children from coerced and increasingly mandatory medical interventions that carry the risk of death and disability, is perhaps the most important advocacy of our lives. It takes great courage, conviction and love to stand up and make a decision that is in the best interest of your community, and not your bottom line or public relations image. The Centner Academy’s prioritization of the precautionary principle, and Leila Center’s call for more research into the exploding number of adverse events that the mainstream media either ignores or actively covers up, is extremely honorable and worth everyone who follows our work and advocacy getting behind in support.
Please support the Centner Academy through the following actions:
- Share this article with friends and family, in order to support our health freedom advocate, Leila Center, who is undergoing unprecedented media attack.
- Support Instagram Leila Centner (send her some love). Comment here at Leila’s instagram account.
- Learn more about the incredibly positive philosophy of the Centner Academy, focusing on happiness as the centerpiece of a child’s success and cultivating leaders with HEART.
Also, please join us at www.StandforHealthFreedom.com, as we build a grassroots army of millions who believe in informed consent, parental rights, human and medical rights for everyone.
This work is reproduced and distributed with the permission of GreenMedInfo LLC.
The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children’s Health Defense.
Source : CHD
