TruthArchive.ai - Related Video Feed

They didn't see safety signals because they didn't want to see them and wouldn't report them. They lied about the vaccine staying in the arm, when they knew it wouldn't. They said the mRNA would dissolve in hours or days, but they knew it was modified RNA that stayed in the body with the spike protein. They continue to push this, despite evidence to the contrary. The science has been corrupted and the agencies have been corrupted, so they have no credibility.

The speaker outlines a series of alarming claims regarding mRNA vaccination and female fertility. They state that in a study involving rats, mRNA-vaccinated subjects exhibited a 60% reduction in primordial (premortial) follicles. The speaker emphasizes that primordial follicles represent a finite resource with no regenerative capacity, noting that women are born with a limited number of these follicles. The implication drawn is that the mRNA shots can reach the ovaries and instruct the ovarian tissue to produce toxic spike protein. According to the speaker, the body's response to this production is to attack the spike protein, leading to tissue damage and destruction of eggs. The destruction of eggs is presented as irreversible, given that primordial follicles do not regenerate, which the speaker asserts has direct consequences for fertility. Further, the speaker cites human data indicating a 33% lower birth rate among vaccinated women, linking this observation to the ovarian damage described in the animal model. They combine these points to argue that a pattern of reduced reproductive capacity is occurring and that this pattern is supported by both the animal study and the human data referenced. The speaker portrays these findings as extraordinarily worrisome and asserts that regulators have failed to address the issue. They argue that regulatory inaction is contributing to what they describe as an ongoing decline in humanity’s fertility. The overarching message is a call for regulatory attention and intervention in response to what they characterize as significant risks to fertility associated with mRNA vaccination. In summary, the speaker claims: - Rats given mRNA vaccines showed a 60% reduction in primordial follicles. - Women are born with a finite, non-regenerating pool of these follicles. - mRNA vaccines purportedly reach the ovaries and cause production of toxic spike protein, provoking an immune attack that damages ovarian tissue and eggs. - This damage allegedly leads to a 33% lower birth rate in vaccinated women, as suggested by cited human data. - The combination of these factors is described as highly concerning and in need of regulatory action, warned against as contributing to a potential future decline in human fertility.

Fertility clinics report unusual issues with sperm and eggs of vaccinated individuals. A study shows an 80% miscarriage rate in women who received the Pfizer vaccine during pregnancy. Reports of menstrual cycle abnormalities, clotting, and even deaths in young girls are emerging. Concerns about potential long-term fertility effects are raised.

Before the emergency use authorization of the vaccines, significant concerns were already known. The Pfizer technical document revealed that these vaccines caused widespread distribution of the encoded protein in major tissues and were associated with inflammatory reactions due to lipid nanoparticles. It was understood that these nanoparticles could deliver RNA and DNA into cells, and the use of pseudo uridine was intended to enhance the immune response and prolong the product's effectiveness. However, critical investigations regarding potential shedding, reproductive toxicity, and the presence of contaminants were not conducted. These omissions are concerning, especially considering previous FDA regulations that recognized the risks of genotoxicity related to manufacturing processes.

Many labs, including Medicinal Genomics, found DNA contamination in Pfizer and Moderna mRNA vaccines. Regulators like the FDA and EMA admitted to this, but downplayed its significance. The SP 40 sequences omitted by Pfizer are crucial. DNA contamination can cause insertional mutagenesis, as stated in Moderna's patents. Regulatory agencies were deceived and failed to properly address the issue. This poses a serious risk that cannot be ignored.

Speaker claims COVID is a respiratory infection, but Pfizer documents show 'a three sixty degree obsessive focus on ruining human reproduction.' They say researchers studied 'ruining fallopian tubes, ruining ova, ruining placentas, ruining fetuses in utero, ruining the birth process, ruining lactation' and ask, 'Why is that?' They assert lipid nanoparticles 'traverse the placenta' and cause placental calcifications 'which prevent the baby from getting nutrients and oxygen.' They report babies born early because placentas cannot grow normally, and that 'placentas are flat.' They say lipid nanoparticles would go into the baby, 'degrading the Leydig cells and Sertoli cells of baby boys of vaccinated moms,' noting 'Sertoli cells and Leydig cells are the factories of masculinity.' An andrology report allegedly 'confirmed that the injection killed the ants and motility of sperm in men.' Pfizer allegedly warns not to have intercourse with unvaccinated women of childbearing age, 'two reliable forms of contraception.' They state 'two seventy women got pregnant in the study of vaccinated women' and 'two thirty four of them, the records of what happened to that pregnancy were lost,' and 'of the thirty six women who gave birth, over eighty percent of them lost their babies.'

We found that the FDA lied about a maternal rat study that was testing the safety of mandating a vaccine to pregnant women. In every litter, individual pups had horrible bone deformities. This signal was extremely prominent. Moderna submitted the rat study, as they were required to do. The FDA then lied about the study results by claiming there were no problems. It was a huge enterprise in lying.

Doctors administered untested gene therapy to infants, toddlers, and pregnant women, claiming it was safe. However, the mRNA jab was deemed the most dangerous medical product for pregnant individuals. Traditional medical principles were disregarded, including giving experimental drugs to pregnant patients and assuming any death or injury post-intervention was related. Regulatory authorities worldwide dismissed adverse events as unrelated until proven otherwise, leading to disastrous consequences.

Pfizer’s definition of “exposure to the vaccine” is described as including skin contact, breath, and body fluids such as semen. The transcript states that “shedding is supposed to be a conspiracy theory,” and it contrasts that with the claim that, “to this day,” the specific meaning of what Pfizer says is not known. The transcript then asserts that there are reports—described as anecdotal—that women are experiencing “horrible cramps” and “real problems” when they have intercourse with vaccinated husbands. It says that the audience does not know why Pfizer said “don’t do that,” referring to advice given in relation to sexual contact. A “hypothetical” is then introduced as further context. According to the transcript, in the study, Pfizer told women not to get pregnant. Despite that instruction, 270 vaccinated women got pregnant in the study. The transcript then claims that 234 of those cases had their records of what happened to the pregnancy “lost,” describing this as illegal, and says Pfizer was supposed to follow these pregnancies through to their outcomes. It further states that, among the remaining women who gave birth, there were 36 women who delivered. The transcript reports that over 80% of those pregnancies resulted in loss of the babies, and it emphasizes “Over 80%.” It concludes this section by stating, “Pfizer knew that.” Overall, the transcript links three main points: Pfizer’s stated inclusion of exposure mechanisms (skin contact, breath, semen/body fluids), reported sexual-contact-related symptoms attributed to vaccinated partners and the lack of an explanation for Pfizer’s advice not to engage in that behavior, and alleged study outcome handling—specifically, pregnancies occurring despite instructions not to become pregnant, a large portion of pregnancy outcome records being “lost,” and a reported rate of baby loss among those who gave birth, followed by the claim that Pfizer knew of these outcomes.

A recent study suggests that Pfizer may have excluded known deaths in the vaccine arm of its clinical trial from its data filing with the FDA in 2020. The study also found that trial subjects vaccinated with Pfizer's COVID-19 vaccine experienced a significant increase in cardiovascular deaths compared to placebo controls. This information was not disclosed by Pfizer when the FDA was evaluating the vaccine for emergency use. Additionally, researchers identified instances where Pfizer attributed potential vaccine-associated deaths to other causes, undermining vaccine safety data. The data presented to the FDA prior to the authorization of Pfizer's vaccine did not include all the deaths that occurred during the trial. The speaker raises concerns about the prioritization of profit over lives and warns against trusting Big Pharma.

Pfizer marketed its vaccine as safe for pregnant women, but reports showed adverse events and miscarriages. They denied a link between their vaccine and heart conditions, despite evidence. Pfizer claimed effectiveness against variants, but data showed otherwise. They also misled about transmission and censored criticism on social media. Pfizer avoided government oversight in vaccine development. Despite these issues, Pfizer successfully marketed their vaccine in Kansas. Multiple states are filing suits against Pfizer.

mRNA vaccinated rats experienced a 60% reduction in primordial follicles, which are essential for life and do not regenerate. mRNA shots are allegedly getting into the ovaries, instructing them to produce toxic spike protein. The body attacks this protein, resulting in tissue damage and egg destruction. This follicle damage allegedly leads to 33% lower birth rates in vaccinated women, as seen in human data. This combination of factors is considered worrisome and demands attention from regulators. It is claimed that humanity's fertility is being run off a cliff.

The Pfizer COVID vaccine was not tested for its ability to stop the transmission of the virus before it entered the market. The speaker acknowledges that they had to work quickly to understand the situation and move at the speed of science.

Four studies are cited as showing significant lot variability in the vaccine batches. The speaker notes that the variability is substantial across lots, with some batches from the early 2021 period appearing to be the most dangerous. They state that some lots are linked to large numbers of adverse events, while other lots are linked to no adverse events at all, describing these as “duds.” According to the speaker, these problematic batches may result from several issues: the mRNA being degraded, or the cold-chain failure such as being left out of the refrigerator for too long, or problems in the manufacturing process that rendered the batch ineffective. The implication is that these dud batches were not manufactured properly. The speaker emphasizes that some of these batches had devastating effects on individuals. They further claim that these batches were probably contaminated with high levels of DNA plasmids from the manufacturing process, extremely high levels of mRNA, and even heavy metal contamination. The range of issues is described as broad, indicating multiple types of contamination or quality problems in different batches. The overall assertion is that not a single batch appears to be the same as another; there is clear heterogeneity across batches, with some batches causing major adverse events and others causing none.

Pfizer documents show an 80% miscarriage rate in pregnant women. 236 out of 270 records were lost. Babies in utero were exposed to the vaccine, leading to deaths. Breast milk was poisoned by vaccine components, causing convulsions and deaths. Newborns may have air sacs between lungs and chest walls, leading to respiratory distress. Pfizer knew about this issue 2 years prior.

Moderna has a patent on the use of RNA for vaccines (patent number 2019-024-0317-A1). In that patent, Moderna explicitly acknowledges that RNA is superior to DNA for vaccine purposes because of “problems” including the possibility of insertional immunogenesis, which could lead to the activation of oncogenes or the integration of tumor suppressor genes. The transcript says that while the FDA says it is not aware of any concerns, Moderna’s own patent lays out the same concerns about DNA and insertional immunogenesis and genotoxicity, and that Moderna “knows it.” The discussion then turns to DNA as a contaminant. The transcript says DNA is left in because, in “process two,” circular DNA is purified from bacteria to make RNA; RNA makes protein; then the DNA is degraded and must be purified away from the RNA. It says the process is apparently not very good, and that DNA fragments were detected after some scientists in the U.S. and Canada obtained unopened vials with clear chain of custody, sampled them, and performed deep sequencing to reconstruct what circular plasmid DNA looked like in the RNA preparation. The transcript claims that these DNA fragments were not disclosed to the public. It adds that the reconstructed sequences include sequences “normally not allowed” in anything going into humans, including an antibiotic resistance gene for kanamycin or neomycin. It also says sequences from simian virus 40 (SV40) are present, specifically highly active promoter sequences. The transcript states that FDA older regulations said these must be avoided because they confer additional risk for insertional mutagenesis. The transcript further claims that when Pfizer provided documents to the FDA, EMA, and Health Canada, Pfizer took standard plasmid maps generated by publicly accessible programs and deleted the notation indicating SV40 sequences. It then says that the FDA did not reconstruct raw DNA sequences to check these maps and instead relied on Pfizer’s submissions. The transcript attributes the emergence of these findings to researchers performing work “akin to the lot release testing that is not happening.” When asked about downstream bad outcomes, the transcript says the outcomes associated with DNA damage include birth defects and cancer.

I am one of the scientists involved in a study on the safety and dependency of vaccine batches. We found three types of side effects: mild, severe, and even death. These adverse effects were present in the initial batches, which were later changed, possibly due to Pfizer altering the product or during transportation. Patients were not informed of the risks and some received poor-quality batches. The study also reveals a safety issue that both Pfizer and regulatory institutions should have addressed. Pfizer had already informed the European Medicines Agency (EMA) about the safety problem in August 2021. Our data from Sweden indicates that this is a European issue, not just a Danish one. We are concerned about long-term side effects and their potential links to cancer and increased mortality rates. The EMA should have taken action based on the data and informed the public. The vice-president of Pfizer's statement about building the plane while flying is apt, as we have shown that one wing has fallen off.

Pfizer's claim of 96% efficacy for their vaccine was questioned. The study and data were not independently verified, and Pfizer wanted to keep the data hidden for 75 years. The true effectiveness of the vaccine, based on absolute risk reduction, is less than 1%. More people died and were harmed in their trials compared to the placebo group. The vaccine's safety was questionable from the start, and it is not effective. Additionally, appropriate studies were not conducted for new variants.

Pfizer documents reveal an 80% miscarriage rate among pregnant women who received the vaccine. However, 236 out of 270 records of pregnant women were lost. The documents also show that Pfizer knew the vaccine was being transmitted to babies in utero, leading to their deaths. The vaccine was found to contaminate breast milk, causing convulsions and deaths. Additionally, the documents from two years prior indicated that newborns could experience respiratory distress due to air sacks between their lungs and chest walls. Despite this knowledge, babies were still being sent home and later returning with the same issue.

The evidence shows that out of 344 babies in a Pfizer trial, only 3 completed it, with reasons like hospitalization and death leading to discontinuation. Less than 1% of babies finished the trial, yet it's claimed to be safe. The speaker questions the safety of these injections, citing reports of babies experiencing symptoms similar to sudden infant death syndrome.

Pregnant women who received COVID-19 shots experienced concerning effects, according to maternal fetal medicine expert Dr. Against Thorpe. The shots quickly spread throughout the body, crossing barriers like the placenta and blood-brain barriers in both the mother and fetus. Compared to the flu vaccine, COVID-19 shots led to more adverse events in women of reproductive age. Data showed a 27-fold higher risk of miscarriage and over twice the risk of negative fetal outcomes across six categories. Additionally, birth rates in several European countries dropped significantly after widespread COVID-19 vaccination. As a result, researchers are urging the immediate suspension of COVID-19 vaccination for individuals of childbearing and reproductive age.

We observed potential safety issues with coronavirus vaccines similar to past respiratory virus vaccines. In the 1960s, some children had adverse reactions, even deaths, due to immune enhancement when exposed to the virus after vaccination. This led to the abandonment of the RSV vaccine program for decades. The same immune pathology was seen in laboratory animals during coronavirus vaccine development, raising concerns about safety.

Pfizer documents show an 80% miscarriage rate among pregnant women, with 236 out of 270 records lost. Babies exposed to the vaccine in utero experienced transplacental exposure. The vaccine was found in breast milk, causing convulsions and deaths. Newborns were known to have air sacs between lungs and chest walls, leading to respiratory distress. Despite this, babies appeared fine initially but later returned due to air pocket issues.

Pfizer has been forced to release previously secret documents, including FDA approval packages, due to court orders and successful FOIA requests. These documents reveal that Pfizer tested different versions of their vaccine during preclinical and clinical trials, which goes against FDA guidance. The different versions included modified RNA, unmodified RNA, self-amplifying RNA, and Spike protein alone. Surprisingly, all these versions were tested under the same investigational new drug number, despite FDA guidance stating that multiple versions should have their own individual numbers. Additionally, the toxicity of the mRNA active ingredient in the COVID-19 vaccines was never studied. This raises concerns about the regulatory process and the lack of safety testing.

On COVID, there's a perception that credit isn't given where it's due. While the vaccines were developed quickly, they don't prevent infection or transmission and may have serious side effects. In hindsight, would anything be done differently? Studies on the vaccines are ongoing, and results will emerge over time. It's important to note that Pfizer marketed its vaccine as safe for pregnant women, but reports indicated that over half of the 458 pregnant women who received the vaccine experienced adverse events. The ongoing studies will help clarify these concerns.