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Florida Surgeon General, Dr. Ladipo, has expressed safety concerns regarding the Pfizer and Moderna COVID vaccines. He believes that the discovery of billions of DNA fragments per dose in these vaccines poses a problem that has not been addressed by the FDA or the CDC. Dr. Ladipo has sent letters to the heads of these organizations, questioning the potential risks of DNA integration with the vaccines. He specifically mentions concerns about healthy genes transforming into cancerous cells, chromosomal instability, and the impact on various parts of the body. Local doctor Michael Sparks acknowledges the uncertainty surrounding new medications but emphasizes the importance of discussing the risk-benefit analysis with individual patients. An interview with Dr. Ladipo was requested but not granted.

Health officials are warning of a 5th wave of COVID-19, urging the public to get up-to-date booster vaccinations. The Cleveland Clinic published a paper suggesting that more shots increase the risk of getting COVID. Waning immunity and new hybrid variants are likely contributing to the rise in cases. The virus is expected to mutate and find ways to evade the vaccine. COVID cases have spiked in Auckland, prompting the director of public health to ask for renewed precautions. A new bivalent vaccine offers better protection against Omicron subvariants. Some individuals have experienced adverse reactions after receiving the vaccine, including heart attacks, aneurysms, brain bleeds, and blood clots. Boosters are available for those over 30 and immunocompromised individuals, while under 16s are not eligible unless they have a medical condition. Only half of New Zealanders over 50 have received their second booster.

Twenty percent of Americans did not take the COVID vaccine because it was not safe enough. The mRNA in the Pfizer and Moderna vaccines has been chemically modified to resist breakdown by enzymes. The mRNA and spike protein are found in the heart and brain, and the spike protein circulates in the blood for six to nine months post-vaccination. The speaker claims the lethal part of the virus circulates in the blood of vaccinated individuals, especially after boosters, and that it is a killer protein. The speaker asserts safety trumps efficacy and objects to claims that vaccines, specifically the COVID-19 vaccine, saved millions of lives. They state that consent forms do not guarantee the vaccine will save lives and that there has never been a prospective, randomized, double-blind, placebo-controlled trial showing that COVID-19 vaccines reduce mortality or hospitalization.

Health Canada has authorized the new Moderna Spikevrax COVID-19 vaccine targeting the Omicron XBB1.5 subvariant for individuals aged 6 months and older. This decision follows a thorough independent review confirming the vaccine's safety, efficacy, and quality. The evidence indicates that the benefits of the vaccine outweigh potential risks. For individuals aged 5 and older, one dose is recommended, regardless of their previous COVID-19 vaccination history. Children aged 6 months to 4 years should receive two doses if they have not been previously vaccinated. If they have received one or more doses, they should get a single dose.

The CDC recommends everyone 6 months and older to get the updated COVID-19 vaccine before the fall and winter season. Extensive data and clinical trials support this recommendation. As the head of the CDC and a doctor, I would not recommend anything I wouldn't do for my own family. That's why my husband, parents, and my 9 and 11-year-old daughters will be getting the vaccine. I encourage you to do the same for everyone in your family who is 6 months and older. Don't forget to also get your flu shot. Visit vaccines.gov to find a nearby location and consult your doctor if you have any questions.

There is a new mRNA COVID-19 vaccine, but there is no evidence to support its effectiveness or safety in human trials. Additionally, several studies from different countries suggest that these vaccines may actually increase the risk of contracting COVID-19 over time. This is concerning and not a typical outcome.

The Florida Department of Health released new COVID booster recommendations, citing safety and efficacy concerns regarding mRNA COVID-19 vaccines. According to the recommendations, the mRNA COVID-19 vaccines present a risk of subclinical and clinical myocarditis and other cardiovascular conditions. The vaccines may be associated with an increased risk of postural orthostatic tachycardia syndrome (POTS) and autoimmune diseases including systemic lupus erythematosus (SLE), rheumatoid arthritis, and psoriasis. Studies found the mRNA COVID vaccines are associated with negative effectiveness up to 4 to 6 months, and vaccinated individuals developed an increased risk of infection. Elevated levels of mRNA and spike protein from the mRNA COVID vaccine persist among some individuals for an indefinite period, which may carry health risks. Potential DNA integration from the mRNA COVID-19 vaccines poses a unique and elevated risk to human health and to the integrity of the human genome. There is an unknown risk of potential adverse impacts with each additional dose. The recommendations conclude with self-help measures for optimising health, such as staying physically active, minimising processed foods, prioritising vegetables and healthy fats, and spending time outdoors to support necessary vitamin D levels.

NAZI has authorized the use of updated COVID-19 vaccines for age groups, recommending a dose every 6 months after the last dose or infection. Canada has seen the Omicron variant evolve, including subvariants like XBB and BA.2.86. The updated vaccines are expected to provide better protection against circulating strains. If it has been more than 6 months since the last dose or infection, individual protection may have decreased, making it important to get a vaccine dose this fall. This is especially crucial for those at higher risk, such as older adults, individuals with underlying conditions, pregnant people, and those in congregate living settings. Vaccination and personal protective measures are essential in reducing the impact of respiratory illnesses, especially during colder months when indoor activities increase the risk.

The FDA has approved a new mRNA Moderna vaccine, despite known serious adverse events. The speaker expresses disappointment, suggesting the FDA is slow to change course. The approval letter concerns the speaker. The vaccine, MN spike, is an mRNA vaccine that produces spike protein, with lipid nanoparticles that will go everywhere. The manufacturer's data indicates serious adverse events were reported by 2.7% of participants receiving the new vaccine, compared to 2.6% for the older vaccine it replaces. The speaker finds it bemusing that a treatment with a 2.7% risk of serious adverse events would be authorized, unless there was a significant risk-benefit. The new vaccine (mRNA 1283) was compared to the old Moderna vaccine (mRNA 1273), not a placebo.

Florida's surgeon general, Dr. Ladipo, has expressed safety concerns regarding the Pfizer and Moderna COVID vaccines. He has discovered billions of DNA fragments per dose in these vaccines, which have not been addressed by the FDA or CDC. Dr. Ladipo believes that if the risks of DNA integration cannot be resolved, the vaccines should not be used in humans. He has sent letters to the FDA and CDC, questioning the impact on human genes, chromosomal stability, and potential effects on various body parts. Local doctor Michael Sparks acknowledges the conflicting viewpoints between the state surgeon general and the FDA, leaving healthcare providers caught in the middle.

"The FDA recently revoked the emergency youth authorizations for three COVID vaccinations while simultaneously green lighting four new COVID nineteen vaccines with twenty twenty five and twenty twenty six formulas." "The the reason for the revocation of that emergency youth authorization is because obviously the COVID pandemic and the public health emergency is over." "But just to correct the record because there's been a lot of misinformation on this, the FDA's decision does not affect the availability of COVID vaccines for Americans who want them." "We believe in individual choice. That's a promise both the president and the secretary have made, and it's a promise they have now delivered on."

Speaker 0 discusses the FDA approval of a new Moderna COVID vaccine, called MN Spike, for active immunization to prevent coronavirus disease. The speaker notes, “the messenger RNA coronavirus vaccine doesn't prevent infection and doesn't prevent transmission,” and says, “Yet here we are.” In the warnings and precautions section, the speaker states, “This product can cause myocarditis and pericarditis usually within the first week following vaccination.” They remark on ingredients, asserting, “Ingredients include polyethylene glycol, antifreeze,” and add, “Sure. Put that right into your body.” They claim the vaccine “codes for the spike glycoprotein,” and emphasize, “Remember, folks, this is the first time in human history that we have injected a product into the body that have forced our ribosomes, protein manufacturing machinery, to produce a nonhuman protein.” The speaker highlights section 13.1, asserting, “This product has not been evaluated for the potential for it to cause cancer.” They then say, “Well, actually, it has. These products now have been around for several years. Multi boosted people are showing an increased risk of cancer, often termed turbo cancer.” They argue that the warning should be changed to reflect that the product may cause cancer. Regarding studies, they claim, “not a single, not one randomized controlled trial against a placebo,” and ask, “What do they compare it to? The earlier version of their vaccine.” They conclude, “This is perfect. In my opinion, all COVID vaccines should pulled from the market immediately and a thorough investigation be launched.” They add, “Informed consent Friday. I hope this is helpful. Your comments are always appreciated. Take care.”

The Surgeon General of Florida, Dr. Joseph Laudipo, has called for a halt to the use of mRNA COVID-19 vaccines due to concerns about DNA integration with the human genome. He argues that the vaccines contain DNA that hangs on with the mRNA and enters cells, which is a problem because each dose likely contains billions of DNA fragments. The FDA's own guidelines state that testing should be done to ensure foreign DNA does not integrate into the human genome, but the FDA has not provided a clear answer on whether they have conducted such tests. Dr. Laudipo finds it concerning that something as precious as human DNA is not being treated with more care.

FDA, I don't know why, just approved a new Moderna COVID vaccine. Here is the package insert. It's called MN Spike. It's a vaccine indicated for active immunization to prevent coronavirus disease. This product can cause myocarditis and pericarditis, usually within the first week following vaccination. Ingredients include polyethylene glycol, antifreeze. And it codes for the spike glycoprotein. This is the first time in human history that we have injected a product into the body that have forced our ribosomes, protein manufacturing machinery, to produce a nonhuman protein. This product has not been evaluated for the potential for it to cause cancer. not a single, not one randomized controlled trial against a placebo. What do they compare it to? The earlier version of their vaccine. In my opinion, all COVID vaccines should be pulled from the market immediately and a thorough investigation be launched.

During the pandemic, researchers found that all-cause mortality increased in countries after COVID-19 vaccine rollouts. A study showed 17 million deaths worldwide were linked to vaccines, with a higher fatality rate among the elderly. No evidence of vaccine benefits was found in the data. Booster rollouts coincided with peaks in deaths across multiple countries, including the US. The report suggests sharing this information with those considering the vaccine to help them make an informed decision.

The TGA approved the Moderna COVID pediatric vaccine for high-risk children based on the results of the KidCOVE clinical trial. The trial evaluated the vaccine's effectiveness in healthy children aged 6 months to 12 years. The TGA relied on clinical data provided by the vaccine sponsor and did not require patient-level data. The TGA's approval was based on interim clinical data, as part of the provisional pathway. The TGA does not have exact numbers on the reports of deaths or adverse events waiting to be checked. There is no evidence of a vaccine-associated increase in cancer risk. The TGA does not support vaccine mandates, but some agencies and states have implemented them. The TGA rejects any suggestion of misfeasance and has not taken a position on vaccine mandates.

Florida Surgeon General, Dr. Ladipo, has expressed safety concerns about the Pfizer and Moderna COVID vaccines due to the discovery of DNA fragments in each dose. He believes these concerns have not been addressed by the FDA or CDC. Dr. Ladipo questions the potential risks of DNA in the vaccines, including the transformation of healthy genes into cancerous cells, chromosomal instability, and the impact on various parts of the body. He has sent letters to the FDA and CDC seeking clarification. Local doctor Michael Sparks acknowledges the conflicting messages between the state surgeon general and the FDA, leaving healthcare providers in a difficult position.

Florida Surgeon General Dr. Ladipo is recommending that people stop getting the COVID vaccine due to safety concerns. He states that billions of DNA fragments were discovered per dose in the Pfizer and Moderna COVID vaccines. He claims that these concerns have not been addressed by the FDA or CDC. Dr. Ladipo says that if the risks of DNA integration with COVID vaccines cannot be addressed, then the vaccines aren't appropriate for use in humans. He sent letters to the heads of the FDA and the CDC questioning how this would impact humans in three areas: healthy human genes being transformed into cancerous cells, chromosomal instability, and how the integration could affect unintended parts of the body such as the heart, brain, lungs, and the injection site. A local doctor, Michael Sparks, says health providers are stuck in the middle with the state surgeon general saying one thing and the FDA saying another.

The Surgeon General of Florida, Dr. Joseph Laudipo, has called for a halt to the use of mRNA COVID-19 vaccines due to concerns about DNA integration with the human genome. He explains that these vaccines contain DNA, which is not necessarily a problem on its own, but becomes an issue because the DNA hangs on with the mRNA and enters people's cells. This is different from other products that have DNA. The FDA's failure to test for DNA integration, despite their own guidelines, is deemed intolerable. Dr. Laudipo emphasizes the need for specific tests to confirm that foreign DNA is not integrating into the human genome.

Health Canada has authorized the new Moderna Spike Brax COVID-19 vaccine for individuals aged 6 months and older. The vaccine underwent a thorough scientific review for safety, efficacy, and quality. The data showed strong evidence that the benefits of the vaccine outweigh the potential risks. People aged 5 and above should receive one dose, regardless of their COVID-19 vaccination history. Children aged 6 months to 4 years should receive two doses if they haven't been previously vaccinated, and if they have, they should receive a single dose.

Initially, all vaccines released under emergency use authorization by the FDA were considered outstanding. The J&J vaccine carries a risk of life-threatening blood clots. Despite claims that COVID poses zero threat to healthy children, vaccination for children was urged. Two mRNA vaccines were considered a three-dose vaccine. Two doses were found to be insufficient for emergency room visits and hospitalizations, necessitating a third immunization. A fourth immunization was suggested as a potential innovative solution. The numbers are trending up again, so a new bivalent booster is recommended for everyone ages 12 and older. Those over 50 who have had two boosters more than 2-4 months prior may need a third booster, a fifth immunization. Boosters may not be holding up as well as desired, potentially requiring boosters every few months. Disinformation campaigns have promoted fake concepts of herd immunity and discredited masks. Vaccinating is considered our last hope. The single most impactful thing is to be fully boosted, preferably twice boosted. Monkeypox is accelerating among men who have sex with men, though sources disagree on whether it is sexually transmitted.

The Florida Surgeon General expressed concerns about the safety of Pfizer and Moderna COVID vaccines due to DNA fragments found in each dose. He believes the risks of DNA integration could lead to cancerous cells, chromosomal instability, and other health issues. The FDA and CDC have not addressed these concerns. With conflicting information from health officials, providers are unsure about vaccine safety. The Surgeon General warns against assuming new medications are safe, citing past instances of harmful effects.

The CDC recommends everyone 6 months and older to get the updated COVID-19 vaccine before the fall and winter season. Extensive data and clinical trials support this recommendation. As the head of the CDC and a doctor, I would not recommend anything I wouldn't recommend for my own family. That's why my husband, parents, and my 9 and 11-year-old daughters will all be getting the vaccine. I encourage you to do the same for yourself and your family members. Don't forget to also get your flu shot if you haven't already. Visit vaccines.gov to find a nearby location and consult your doctor if you have any questions.

The first speaker argues that messenger RNA vaccines were unprecedented compared to anything previously developed. They state there was never any justification given for not using a traditional vaccine, and there was never any evidence that the messenger RNA vaccine was as good as a ground-up virus—the old-fashioned type of vaccine—whose safety, efficiency, and cost are well known. They emphasize the importance of that point and note that a recent Korean study in young boys compared a booster using an antigen vaccine with a messenger RNA vaccine, and found the antigen vaccine to be more protective than the messenger RNA vaccine. From this, they conclude that there are currently data indicating there are no ongoing advantages to using these genetic vaccines. The second speaker adds that this situation is a huge mystery, questioning why the genetic RNA route was chosen in the first place. They suggest that someone made a lot of money, acknowledging that money is a factor, but saying they have never heard a scientific explanation for the decision-making process, describing it as a complete black box. They further point out that there are ongoing efforts by many people to transform vaccines beyond traditional forms to include self-replicating RNA, and that this discussion continues. They argue that the red flags from the first round have not been sorted out, and that there is no evidence these approaches are better; in fact, they imply they are clearly not better.

Florida is sending a letter to nurses and doctors regarding informed consent for COVID-19 mRNA vaccines. The letter informs patients that the vaccines are for the wrong variant and are dangerous, citing prolonged spike protein circulation, respiratory infection risk, and autoimmune disease risk. The Florida Surgeon General recommends against mRNA vaccine use and advises nurses and doctors to recommend against the vaccine. The speaker expresses happiness about this and anticipates other states will follow suit, except for "blue" states.