DJI Mini 3 Pro vs DJI Mini 2 SE Price in India: Which Drone is Better for Indian Consumers? When it comes to choosing a drone, DJI has made its mark with two standout models: the DJI Mini 3 Pro and the DJI Mini 2 SE. Both drones offer exceptional value, but which one is the best choice for Indian consumers? In this article, we'll compare these two popular models based on price, performance, camera quality, and features to help you make an informed decision. 1. Price Breakdown: DJI Mini 3 Pro vs DJI Mini 2 SE in India DJI Mini 3 Pro Price in India The DJI Mini 3 Pro is a premium drone that comes with a higher price tag. As of now, the price for the DJI Mini 3 Pro price in India ranges from ₹91,000 to ₹95,000, depending on the configuration you choose. This price includes advanced features like superior camera quality, obstacle avoidance, and intelligent flight modes, making it a top-tier option for both amateur and professional drone enthusiasts. DJI Mini 2 SE Price in India The DJI Mini 2 SE, on the other hand, is a more affordable alternative. In India, it is priced at around ₹34,999, making it an ideal choice for budget-conscious buyers or beginners who want to experience drone flying without making a large investment. Despite being more affordable, the Mini 2 SE still offers great value with solid performance for its price. 2. Camera Quality: A Key Differentiator DJI Mini 3 Pro Camera The DJI Mini 3 Pro stands out with its impressive 48MP camera and 4K video recording at 60fps, which delivers highly detailed and vibrant footage. Whether you're shooting landscapes, real estate videos, or cinematic content, the Mini 3 Pro offers unparalleled image quality, even in low-light conditions. The three-axis gimbal ensures that your shots remain stable and smooth, even in windy conditions. Camera Resolution: 48MP Video Resolution: 4K at 60fps Gimbal: 3-axis stabilization Low-Light Performance: Excellent DJI Mini 2 SE Camera The DJI Mini 2 SE comes with a 12MP camera, which offers solid quality for casual use and basic content creation. It supports 4K video at 30fps, making it perfect for beginners who want high-definition video without the complexity or price of a professional drone. While the camera resolution isn’t as high as the Mini 3 Pro, it still offers great performance for standard recreational flying and social media content. Camera Resolution: 12MP Video Resolution: 4K at 30fps Gimbal: 2-axis stabilization Low-Light Performance: Good for general use 3. Battery Life: How Long Can You Fly? DJI Mini 3 Pro Battery Life The DJI Mini 3 Pro offers an outstanding flight time of up to 34 minutes with the standard battery and can be extended to 47 minutes with the larger battery option. This extended battery life is ideal for professional use, particularly if you need to capture long aerial shots or need more time to explore larger areas. DJI Mini 2 SE Battery Life The DJI Mini 2 SE provides a slightly shorter flight time, up to 31 minutes per charge. While it’s not as long as the Mini 3 Pro, it still offers a solid duration for casual drone flights, perfect for new pilots or short photography sessions. 4. Flight Features and Performance: What Sets Them Apart? DJI Mini 3 Pro Performance The Mini 3 Pro is packed with advanced features, making it suitable for both hobbyists and more serious drone pilots. It comes with obstacle sensors on the front, back, and bottom, making it safer to fly in tight or cluttered spaces. Obstacle Avoidance: Yes (front, rear, downward) Flight Modes: ActiveTrack, FocusTrack, Mastershots, and more Max Speed: 16 m/s (approximately 57.6 km/h) Advanced Stability: Yes, even in windy conditions DJI Mini 2 SE Performance The Mini 2 SE is designed for beginner and intermediate drone users who want a simple, fun, and safe flying experience. While it lacks advanced obstacle avoidance sensors, it still offers GPS stability and QuickShots, which help capture creative shots with ease. Its maximum speed is slower than the Mini 3 Pro, but still suitable for most recreational flights. Obstacle Avoidance: No Flight Modes: QuickShots (Dronie, Circle, Helix) Max Speed: 8 m/s (approximately 28.8 km/h) Stability: Good for casual flying 5. Which Drone Should You Choose in India? When deciding between the DJI Mini 3 Pro vs DJI Mini 2 SE, it ultimately boils down to your budget and requirements. Choose the DJI Mini 3 Pro if: You need professional-grade camera quality, with 4K video at 60fps and a 48MP camera. You want advanced flight features like obstacle avoidance, ActiveTrack, and FocusTrack. You’re a content creator, real estate agent, or professional photographer looking to elevate your shots. You’re willing to invest in a drone with extended flight time and more powerful performance. You require superior stability and safety features for complex flying environments. Choose the DJI Mini 2 SE if: You are a beginner or hobbyist looking for an affordable and easy-to-use drone. You need a drone with good image quality for casual use, social media content, or fun flights. You’re okay with fewer advanced features, such as the lack of obstacle avoidance and fewer intelligent flight modes. You don’t mind a shorter flight time and a more basic performance compared to the Mini 3 Pro. Conclusion: Which Drone is the Right Choice for You? Both the DJI Mini 3 Pro and DJI Mini 2 SE are excellent drones, but they cater to different types of users. The Mini 3 Pro is the best choice for those seeking a top-tier drone with professional-level performance, while the Mini 2 SE is perfect for beginners or those on a budget who still want a solid drone for recreational flying. If you’re looking for exceptional image quality, advanced flight features, and longer flight time, the DJI Mini 3 Pro in India is the better choice, albeit at a higher price. On the other hand, if you're just starting out or prefer a simpler, more affordable option, the DJI Mini 2 SE offers excellent value at a fraction of the price. Ultimately, both drones provide great performance for their respective price points, making either choice a good investment for Indian consumers looking to explore the world of drone flying. For more information you can visit - https://flyandtech.com/

Expert Sewer Main Repair and Installation: Everything You Need to Know for a Smooth Flow The sewer main is one of the most critical components of any plumbing system, ensuring the smooth flow of wastewater away from your home or business. When this essential system is damaged or improperly installed, it can lead to costly repairs and significant disruptions. Whether you’re considering sewer main installation or require repair services, understanding the process is key to making informed decisions. Here’s your ultimate guide to sewer main repair and installation, with key points to ensure a smooth experience. Key Points to Remember Signs of Sewer Main Problems: Gurgling sounds, slow drainage, or foul odors can indicate issues in your sewer main. Professional Installation is Non-Negotiable: Proper installation ensures long-term reliability. Advanced Repair Techniques: Modern methods like trenchless repair minimize disruption. Regular Maintenance Saves Money: Periodic inspections can catch problems early. When Do You Need Sewer Main Repair? Identifying sewer main issues early can save you time, money, and stress. Common signs include: Slow Drains: If multiple drains in your home are slow, it’s likely a sewer main issue. Backups: Frequent backups in toilets or sinks often point to blockages or damage in the sewer line. Lush Spots in Your Yard: Patches of overly green grass may indicate a leak in the sewer line beneath. Foul Smells: Persistent odors in or around your property could mean wastewater isn’t flowing properly. Ignoring these signs can lead to more extensive damage, so it’s crucial to address them promptly. The Importance of Proper Sewer Main Installation Whether you’re building a new property or replacing an old sewer line, the installation process is crucial to its performance. Professional installation ensures: Accurate Placement: Correct alignment and slope are essential for optimal wastewater flow. Durability: High-quality materials and techniques prevent frequent repairs. Compliance with Local Codes: Professional plumbers understand local regulations, ensuring your system is up to code. Investing in expert installation upfront can save you from costly repairs down the line. Modern Sewer Repair Methods Gone are the days of digging up entire yards to repair a sewer main. Advanced techniques now offer efficient and less invasive solutions, including: Trenchless Pipe Repair: This method uses minimal excavation, preserving your landscape while fixing the problem. Pipe Bursting: A new pipe is pulled through the old one, replacing it without major disruption. Cured-In-Place Pipe (CIPP): A resin-coated liner is inserted into the damaged pipe, creating a new pipe within the old one. These techniques save time and reduce the mess typically associated with sewer repairs. Why Hire Professionals for Sewer Main Services? Sewer main repair and installation require specialized expertise and tools. Here’s why professional services are a must: Accurate Diagnosis: Professionals use advanced equipment like cameras to pinpoint problems. Quality Workmanship: Certified plumbers ensure repairs and installations meet high standards. Safety: Handling sewer lines involves health risks and potential damage to other utilities. Cost Efficiency: Professionals complete the job right the first time, avoiding repeat issues. Maintaining Your Sewer Main Regular maintenance can extend the life of your sewer main and prevent unexpected repairs. Consider scheduling periodic inspections and cleaning to remove debris, tree roots, and other potential blockages. Conclusion Sewer main repair and installation don’t have to be overwhelming. By staying informed about the signs of damage, choosing professional services, and opting for modern techniques, you can ensure your sewer system operates efficiently for years to come. When you need expert sewer main services, don’t compromise—choose a trusted professional to get the job done right. Ensure your home or business enjoys the smooth flow it deserves! For More Information Visit Us Email: [email protected] Contact : (785) 917–1616 Location: Lawrence, Kansas Website: www.risingsonplumbing.com

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Dr. Pierre Kory about Covid-19 vaccine during pregnancy: "It's the most dangerous medical product in history for anyone in and around pregnancy. They broke the golden rule....the golden rule of pregnancy: you never give an experimental drug to a pregnant patient and we suddenly now recommended almost no data, our public health agents who recommended for the entire population of pregnant women in this country. And then the thing that they threw out which is the regulatory standard for 20 years is that anytime a death or an injury is reported associated with a novel, a just released medical intervention, you assume that it's caused by that intervention until proven otherwise. what did regulatory authorities do around the world? They simply dismissed everything as unrelated until you could prove it was related, which is a complete flip of our regulatory safety approaches to medical interventions..." Join ➣ 👉@COVID19VACCINEVICTIMSANDFAMILIES

🧪 Federal Judge Upholds Florida Ban on Lab-Grown Meat, as Other States Propose Similar Bans “The dangers of cultivated meat far outweigh any misleading environmental claims. Floridians will not be lectured by billionaires like Bill Gates on how to feed their families.” @JayCollinsFL Lab-grown or cultivated meat is produced from cultured stem cells taken from live animals or an animal cell bank and then reproduced in bioreactors using techniques borrowed from Big Pharma. Don't let Big Pharma control your food. https://childrenshealthdefense.org/defender/federal-judge-upholds-florida-ban-lab-grown-meat-cultivated-chicken/ Federal Judge Upholds Florida Ban on Lab-Grown Meat, as Other States Propose Similar Bans The ban will remain in place while the lawsuit challenging its legality moves through the courts. Upside Foods, which makes a cultivated chicken product, sued to overturn the ban, which was signed into law on May 1. florida flag, lab grown chicken and gavel Toxic Exposures by Brenda Baletti, Ph.D. October 23, 2024 florida flag, lab grown chicken and gavel 5411 Pageviews Listen to this article A federal judge earlier this month rejected a request by California-based Upside Foods for a preliminary injunction against Florida’s new law banning the manufacture, distribution and sale of “cultivated,” or lab-grown meat. Florida Gov. Ron DeSantis signed the ban into law on May 1, making it a second-degree misdemeanor to produce or sell lab-grown meat in the state. The law took effect in July. Upside Foods, which makes cultivated chicken, sued Florida in August, alleging the ban is unconstitutional and violates two federal laws that preempt Florida from imposing the ban. A preliminary injunction is typically issued in a lawsuit if the court finds the plaintiff has a good chance of winning its case — a “substantial likelihood of success on the merits,” However, Chief U.S. District Judge Mark Walker said Upside’s argument, which boiled down to “if it’s a poultry product, states can’t ban it,” was insufficient. Just because a product falls within the scope of the federal Poultry Products Inspection Act and is under the U.S. Department of Agriculture’s (USDA) regulatory authority does not mean a state is “expressly preempted from banning the sale of that particular kind of poultry product,” Walker wrote. Upside argued that the ban imposed ingredient and manufacturing requirements that clashed with provisions of the Poultry Products Inspection Act. However, Walker said Upside was unable to identify any federal law or regulation that created an “ingredient requirement” for cultivated meat. He also said that because the company didn’t produce its lab-grown meat in Florida, the manufacturing ban didn’t affect its premises, operations or facilities. scales of justice Your support helps fund this work, and CHD’s related advocacy, education and scientific research. Donate Now The ruling means the ban will remain in place while the lawsuit challenging its legality moves through the courts. “We are not surprised by the judge’s rejection of Upside’s preliminary injunction,” Florida Sen. Jay Collins, who co-sponsored the original bill, told The Defender. “The dangers of cultivated meat far outweigh any misleading environmental claims. Floridians will not be lectured by billionaires like Bill Gates on how to feed their families.” Upside’s attorney, Suranjen Sen from the Institute for Justice, said in a press release that the company plans to appeal the decision and is “confident that the courts will ultimately recognize that Florida cannot ban products simply to protect local industries from honest competition.” A bench trial is set for Monday, Aug. 18, 2025. Upside struggled to become profitable Lab-grown or cultivated meat is produced from cultured stem cells taken from live animals or an animal cell bank and then reproduced in bioreactors using techniques borrowed from Big Pharma. The cells are “fed” a mixture of sugars, amino and fatty acids, salts and vitamins to make them proliferate quickly. Once they’ve grown into a mass or a sheet — depending on the manufacturer — they are formed into meat-looking shapes like cutlets or nuggets. Although the companies promote lab-grown meat in part by claiming it has environmental benefits, the process is energy-intensive. Research from the University of California, Davis, found that cultured meat’s environmental impact is likely “orders of magnitude” higher than real meat, based on current production methods. Attorney Ray Flores, who worked in the natural health industry for 35 years, told The Defender that even if it provides environmental benefits, “Any environmental benefit is greatly outweighed by the possible dangers that these cutting-edge products may pose to one’s health.” An investigation by The New York Times revealed several incidents during the development of some of Upside’s products that raised safety concerns. The company in 2018 found its chicken cell line contaminated with mouse cells. And in 2019, the cell line was found to be contaminated with rat cells. Yet, the U.S. Food and Drug Administration (FDA) said Upside’s meat was safe for human consumption in 2022, and the USDA approved the sale of products by Upside Foods and Good Meat — the first two companies to go through the regulatory approval process — in June 2023. That approval made the U.S. the second country in the world, behind Singapore, to allow sales of lab-grown meat. In January, Israel green-lighted the sale of steaks made from cultivated beef cells, The Associated Press reported. Since the USDA approval, however, Upside has struggled to become profitable. Upside doesn’t have products available in stores. Partnerships with restaurants are primarily how the company gets its products to consumers. It had sold its lab-grown chicken to one restaurant in Miami and was planning to showcase it at Miami’s Art Basel event before the ban took effect, according to the judgment. However, Crunchbase reported that the company halted its plans to develop a major facility in Glenview, Illinois, and restaurants that had tried it out have since pulled it from their menus. San Francisco Michelin-star restaurant Bar Crenn, its final sale venue, confirmed it was pulling the lab-grown meat from the menu in February. In the original complaint, Upside and the Institute for Justice claim that the “growing patchwork of conflicting state laws governing cultivated meat” makes it more difficult for Upside to partner with national meat distributors “who generally will not carry products they cannot lawfully sell in every state.” It also makes it more difficult for them to partner with restaurants. If not for the ban, they said, they would be reaching out to several restaurants to create partnerships. Following the Florida ban, Upside laid off 26 workers. TVs stacked on each other 10 a.m. ET 
Monday, Dec. 2 to noon ET
Wednesday, Dec. 4 Donate Now More states move to ban lab-grown meat, federal regulators eye labeling requirements A few weeks after Florida passed its bill, Alabama passed a similar law making the manufacture, sale or distribution of food products made from cultured animal cells a Class C misdemeanor, with fines ranging from $100 to $10,000. Iowa’s governor in May signed a bill prohibiting schools from buying lab-grown meat products and requiring clear labeling for lab-grown meats sold in other venues. Five other states have proposed similar laws. And in August, Nebraska Gov. Jim Pillen signed an executive order banning the state government from purchasing it. The USDA and the FDA share regulatory responsibility for cultivated meat products. Under the Biden administration’s 2022 plan to advance biotechnology and biomanufacturing innovation, the USDA also announced plans to issue draft guidance on the pre-approval consultation process and the agencies plan to propose rules for labeling cell-cultured meat and poultry sometime in 2024.

It’s truly shocking to see how unethical some doctors have become. From pushing Covid shots with no long safety data, to pushing medical mutilation “sex-change” surgeries—many physicians don’t offer informed consent or discuss the serious risks involved. This has to stop. Subscribe and share ➡️➡️ @DrSimoneGoldLA

EU Ministers reject Israeli Arms BAN despite Gaza War Crimes and Genocide Evidence Fabio G. C. CarisioDecember 30, 2024 Become a VT Supporting Member Today Please keep VT Radio and VT Foreign Policy alive! Donate today to make sure VT stays on the internet free and clear of Big Tech control! Donate today: Please Donate - Click Here The Intercept on Tuesday revealed that European Union foreign ministers rejected a proposal to halt arms exports to “Israel” last month, despite being presented with evidence of war crimes and genocide in an internal EU assessment. The 35-page report, authored by Olof Skoog, the EU’s special representative for human rights, was sent to ministers ahead of a council meeting on November 18. The document, which had not been disclosed before, presented findings from United Nations sources on violations of international humanitarian law committed by “Israel” and Hamas since the start of the war in October 2023. The report emphasized the disproportionate toll on civilians in Gaza, with an estimated 45,000 deaths, more than half of whom were women and children. BLOODY CHRISTMAS. Gaza Worse than Auschwitz because of NATO Demons Supporting Netanyahu’s Zionist Genocide. UN: “14,500 Children Exterminated” “War has rules,” the assessment stated. “Given the high level of civilian casualties and human suffering, allegations focus mainly on how duty bearers, including the Israeli [Occupation] Forces (IOF), have seemingly failed to distinguish between civilians and combatants and to take all feasible precautions to protect civilians and civilian objects against the effects of the attacks, in violation of the fundamental principles of IHL.” The report also cited “dehumanizing language” used by Israeli officials, warning that it might “contribute to evidence of intent” to commit genocide. “Incitement to discrimination, hostility or violence — such as that made in statements by Israeli officials — constitutes a serious violation of international human rights law and may amount to the international crime of incitement to genocide,” it added. EU complicity Despite Skoog’s call for EU countries to deny arms export licenses where there was a clear risk of misuse in war crimes, the proposal to suspend political dialogue with “Israel” and ban arms sales was ultimately rejected by EU ministers. POPE: “GENOCIDE IN GAZA”. International Court issues NETANYAHU ARREST WARRANT! Here IMAGES of Chilling Crimes and ICC Paper Former Greek finance minister Yanis Varoufakis underscored the legal implications of the report for EU officials. “They cannot plausibly deny that they were privy to the facts given the contents of the EU’s special representative’s report that they had a duty to take under consideration,” he told The Intercept. “The world now knows that they knew they were in breach of international law because they were explicitly told so by the EU’s own special representative on human rights. History will judge them harshly. And perhaps so will the ICC.” European Commission president accused of Complicity in Israel’s War Crimes at ICC The EU report also drew attention to economic interests tied to the EU-“Israel” Association Agreement, which facilitated €46.8 billion in trade in 2022. Although Spain and Ireland requested a review of whether “Israel’s” actions breached human rights clauses in the agreement, European Commission President Ursula von der Leyen declined to act. Read more – ICC warrants expose ‘Israel’ and US defenders: WashPo Legal experts and humanitarian groups have criticized EU member states for their continued arms sales to “Israel” despite the report’s findings. Agnès Bertrand-Sanz, a humanitarian expert with Oxfam, called it “a blatant case of criminal collusion.” She added, “Even when their own services presented them with the facts, they refused to act.” The report’s conclusions also warned that indiscriminate attacks on Gaza, including targeting hospitals, could amount to crimes against humanity. It called on “Israel” to adhere to its responsibilities as an occupying power to ensure the safety and health of civilians under its control. However, as Diana Buttu, a former Palestinian negotiator, noted, “It was a question of whether the politics would match with the law, and unfortunately, they did not.” Originally published by Al Mayadeen English RELATED TOPICS FREEMASONRY & ZIONISM – 3. Devilish Roots of HOLOCAUST IN HOLY LAND. 70 % of Exterminated are Children, Women by Netanyahu thanks Western NeoNazis “CHRIST still under RUBBLE”: Palestinian Pastor referred on Christians in Gaza mark another Christmas amid genocide The Grim NATO’S JIHADs. How Atlantic Intelligence “14 Eyes” uses ISLAMIC TERRORISTS: from Italy to Libya, Ukraine and Syria Fabio G. C. Carisio Fabio is investigative journalist since 1991. Now geopolitics, intelligence, military, SARS-Cov-2 manmade, NWO expert and Director-founder of Gospa News: a Christian Information Journal. His articles were published on many international media and website as SouthFront, Reseau International, Sputnik Italia, United Nation Association Westminster, Global Research, Kolozeg and more… Most popolar investigation on VT is: Rumsfeld Shady Heritage in Pandemic: GILEAD’s Intrigues with WHO & Wuhan Lab. Bio-Weapons’ Tests with CIA & Pentagon Fabio Giuseppe Carlo Carisio, born on 24/2/1967 in Borgosesia, started working as a reporter when he was only 19 years old in the alpine area of Valsesia, Piedmont, his birth region in Italy. After studying literature and history at the Catholic University of the Sacred Heart in Milan, he became director of the local newspaper Notizia Oggi Vercelli and specialized in judicial reporting. For about 15 years he is a correspondent from Northern Italy for the Italian newspapers Libero and Il Giornale, also writing important revelations on the Ustica massacre, a report on Freemasonry and organized crime. With independent investigations, he collaborates with Carabinieri and Guardia di Finanza in important investigations that conclude with the arrest of Camorra entrepreneurs or corrupt politicians. In July 2018 he found the counter-information web media Gospa News focused on geopolitics, terrorism, Middle East, and military intelligence. In 2020 published the book, in Italian only, WUHAN-GATES – The New World Order Plot on SARS-Cov-2 manmade focused on the cycle of investigations Wuhan-Gates His investigations was quoted also by The Gateway Pundit, Tasnim and others He worked for many years for the magazine Art & Wine as an art critic and curator. VETERANS TODAY OLD POSTS www.gospanews.net/ VT Condemns the ETHNIC CLEANSING OF PALESTINIANS by USA/Israel $280+ BILLION US TAXPAYER DOLLARS INVESTED since 1948 in US/Israeli Ethnic Cleansing and Occupation Operation 150B direct "aid" and $ 130B in "Offense" contracts Source: Embassy of Israel, Washington, D.C. and US Department of State. ATTENTION READERS We See The World From All Sides and Want YOU To Be Fully Informed In fact, intentional disinformation is a disgraceful scourge in media today. So to assuage any possible errant incorrect information posted herein, we strongly encourage you to seek corroboration from other non-VT sources before forming an educated opinion. About VT - Policies & Disclosures - Comment Policy Due to the nature of uncensored content posted by VT's fully independent international writers, VT cannot guarantee absolute validity. All content is owned by the author exclusively. Expressed opinions are NOT necessarily the views of VT, other authors, affiliates, advertisers, sponsors, partners, or technicians. Some content may be satirical in nature. All images are the full responsibility of the article author and NOT VT. https://www.vtforeignpolicy.com/2024/12/eu-ministers-reject-israeli-arms-ban-despite-gaza-war-crimes-and-genocide-evidence/

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CDC Scientist: We Tried To ‘Destroy Vaccine-Autism Study Documents’ Sharryl AtkissonJune 25, 2020 Written by on . Posted in Current News A Centers for Disease Control (CDC) senior scientist has made an unprecedented admission: he and his colleagues–he says– committed scientific misconduct to cover up a meaningful link between vaccines and autism in black boys. [PSI editor note: this article was first published in June 2016] Just as startling, the CDC scientist, Dr. William Thompson, says the study co-authors “scheduled a meeting to destroy documents related to the study. The remaining four co-authors all met and brought a big garbage can into the meeting room, and reviewed and went through all the hardcopy documents that we had thought we should discard, and put them into a huge garbage can.” “The…co-authors…brought a big garbage can into the meeting room… [and put the documents]…into a huge garbage can.” –CDC Senior Scientist Dr. William Thompson Despite this whistleblower testimony, which Dr. Thompson provided to Rep. Bill Posey, R-Florida, there is little chance of a meaningful hearing or investigation. In an untainted news environment, the allegations would make headlines in most legitimate publications and would trigger federal inquiries. However, the interests of the powerful pharmaceutical industry reach deeply into Congress and the news media through lobbyists, propaganda and advertising dollars. “The omitted data suggested that African American males who received the MMR vaccine before age 36 months were at increased risk for autism.” –CDC Senior Scientist Dr. William Thompson That’s why Congressman Posey resorted to simply reading some of Dr. Thompson’s statement today on the House floor…including the part in which Dr. Thompson says he retained the evidence that had been thrown in the garbage can, in the unlikely event that a neutral investigative or scientific body would like to see it today. “[B]ecause I assumed it was illegal and would violate both FOIA [Freedom of Information Act] and DOJ [Department of Justice] requests, I kept hardcopies of all documents in my office, and I retain all associated computer files,” Posey quotes Dr. Thompson as reporting. The CDC and Thompson’s co-author Dr. Frank DeStefano, CDC Director of Immunization Safety, have defended the controversial study as originally published. Dr. DeStefano explains why here in detail. One final note: Rep. Posey unequivocally states that he is pro-vaccine. However, the propaganda campaign typically falsely portrays anyone who addresses vaccine safety issues as “anti-vaccine.” Listen to Rep. Posey’s statement by pasting the link below into your browser and going to 1:02:24 http://www.c-span.org/video/?327309-1/us-house-morning-hour&live CDC responds to allegations it omitted vaccine-autism study link AUDIO CDC: Possibility that vaccines rarely trigger autism Rep. Posey’s entire statement about Dr. Thompson: “I rise today on matters of scientific integrity and research. To begin with, I am absolutely, resolutely, pro-vaccine. Advancements in medical immunization have saved countless and greatly benefitted public health. That being said, it’s troubling to me that in a recent Senate hearing on childhood vaccinations, it was never mentioned that our government has paid out over $3 billion through a vaccine injury compensation program for children who have been injured by vaccinations. “Regardless of the subject matter, parents making decisions about their children’s health deserve to have the best information available to them. They should be able to count on federal agencies to tell them the truth. For these reasons, I bring the following matter to the House floor. “In August 2014, Dr. William Thompson, a senior scientist at the Centers for Disease Control and Prevention, worked with a whistleblower attorney to provide my office with documents related to a 2004 CDC study that examined the possibility of a relationship between [the] mumps, measles, rubella vaccine and autism. In a statement released in August, 2014, Dr. Thompson stated, ‘I regret that my co-authors and I omitted statistically significant information in our 2004 article published in the journal Pediatrics.’ “Mr. Speaker, I respectfully request the following excepts from the statement written by Dr. Thompson be entered into the record. “Now quoting Dr. Thompson. “‘My primary job duties while working in the immunization safety branch from 2000 to 2006, were to later co-lead three major vaccine safety studies. The MADDSP, MMR autism cases control study was being carried out in response to the Wakefield-Lancet study that suggested an association between the MMR vaccine and an autism-like health outcome. There were several major concerns among scientists and consumer advocates outside the CDC in the fall of 2000, regarding the execution of the Verstraeten Study. One of the important goals that was determined up front, in the spring of 2001, before any of these studies started, was to have all three protocols vetted outside the CDC prior to the start of the analyses so consumer advocates could not claim that we were presenting analyses that suited our own goals and biases. We hypothesized that if we found statistically significant effects at either 18 or 36 month thresholds, we would conclude that vaccinating children early with MMR vaccine could lead to autism-like characteristics or features. We all met and finalized the study protocol and analysis plan. The goal was to not deviate from the analysis plan to avoid the debacle that occurred with the Verstraeten thimerosal study published in Pediatrics in 2003. ‘At the Sept 5th meeting we discussed in detail how to code race for both the sample and the birth certificate sample. At the bottom of table 7, it also shows that for the non-birth certificate sample, the adjusted race effect statistical significance was huge. ‘All the authors and I met and decided sometime between August and September 2002, not to report any race effects from the paper. Sometime soon after the meeting, we decided to exclude reporting any race effects. The co-authors scheduled a meeting to destroy documents related to the study. The remaining four co-authors all met and brought a big garbage can into the meeting room, and reviewed and went through all the hardcopy documents that we had thought we should discard, and put them into a huge garbage can. However, because I assumed it was illegal and would violate both FOIA and DOJ requests, I kept hardcopies of all documents in my office, and I retain all associated computer files. I believe we intentionally withheld controversial findings from the final draft of the Pediatrics paper.’ “Mr. Speaker, I believe it is our duty to insure that the documents that Dr. Thompson are not ignored. Therefore I will provide them to members of Congress and the House Committees upon request. Considering the nature of the whistleblower’s documents as well as the involvement of the CDC, a hearing and a thorough investigation is warranted. “So I ask, Mr. Speaker, I beg, I implore my colleagues on the appropriations committees to please, please take such action.” Read CDC Vaccine Safety Info here Read other vaccine news reports here About the author: Sharyl Atkisson is an American writer and host of the TV show Full Measure with Sharyl Attkisson. She is a five-time Emmy Award winner, and an Radio Television Digital News Association Edward R. Murrow Award recipient. Read more at sharylattkisson.com PRINCIPIA SCIENTIFIC INTERNATIONAL, legally registered in the UK as a company incorporated for charitable purposes. Head Office: 27 Old Gloucester Street, London WC1N 3AX. Please DONATE TODAY To Help Our Non-Profit Mission To Defend The Scientific Method. Trackback from your site. https://principia-scientific.com/cdc-scientist-we-tried-to-destroy-vaccine-autism-study-documents/

Dr. Sherri Tenpenny Reveals in 1 Minute How Much Aluminum, Mercury, and Chemicals Children Ingest Through Vaccines One-time or recurring donations can be made through Ko-Fi: By RAIR Foundation December 21, 2024 When Dr. Sherri Tenpenny worked in the emergency room, she believed vaccines contained only weakened viruses and saline. That assumption shattered in September 2000 when she read the package insert of a vaccine for the first time. What she discovered set her on a path to uncover the shocking truth behind vaccine ingredients—information hidden in plain sight but ignored by most. A Shocking Discovery Dr. Tenpenny was horrified by what she found. “If a child receives every vaccine on the current U.S. vaccine schedule, they are injected with almost 13,000 micrograms of aluminum, nearly 600 micrograms of mercury, and over 200 other chemicals,” she explained in a recent interview with Jonathan Patrick Sears at the premiere of The Great Awakening. “I didn’t know that.” This level of chemical exposure raises profound questions about safety—questions that, according to Tenpenny, remain unanswered because vaccines have never been proven safe. “That’s why,” she said, “they’ve never been proven to be safe. Giving your child a vaccination is like injecting foreign matter into a little baby—the most precious little thing in your life.” What’s Missing from Vaccine Labels? Nicole Shanahan, former running mate of Robert F. Kennedy Jr., echoes these concerns, highlighting that even the disclosed ingredients on package inserts tell only part of the story. The production process itself introduces additional contaminants—and vaccine manufacturers aren’t required to report them. “The vaccine insert covers the disclosed, known ingredients,” Shanahan explained. “It doesn’t mention the host of possible contaminants. For example, manufacturers can use cyanylating agents during processing—substances known to cause motor impairment, as seen in diseases like Konzo—and they aren’t required to report residual cyanide contamination.” Shanahan called for greater transparency and accountability. “This is something the next administration can change. As many of us have said, including Donald Trump, it isn’t about taking away vaccines—we just want them to be safe. We want full disclosure of each shot’s risk profile so American citizens can make informed decisions. These are standards of care that are well-established in science and medicine.” The Broader Context Dr. Tenpenny’s revelations align with Robert F. Kennedy Jr.’s stance that vaccines are not inherently the issue—unsafe vaccines are. “I’ve heard Robert F. Kennedy Jr. say he’s not necessarily against vaccines. He’s just against unsafe vaccines,” Dr. Tenpenny said. “He’s just never found a safe one. I think that’s a pretty good way of putting it.” Tenpenny’s journey from ER physician to vaccine researcher has exposed a reality parents deserve to know. Vaccines are far more than a little virus and saline. They contain heavy metals, toxic chemicals, and hidden contaminants—none of which belong in a child’s body. A Call for Accountability This is not about rejecting science. It’s about demanding better science. Transparency. Accountability. Safety. Parents deserve the truth, not half-truths shrouded in medical jargon and marketing campaigns. They deserve the full picture of what’s being injected into their children—so they can make decisions with their eyes wide open. The next administration must act to bring this truth to light and hold vaccine manufacturers accountable. Anything less is a betrayal of the most vulnerable among us: our children. Share Related articles: Doctors Reveal What They’ve Learned During Their Medical Training About ‘Vaccines’ Read full story The Depopulation Industrial Complex: FDA Licensed Vaccines Are Not Evaluated for Carcinogenesis, Mutagenesis, Impairment of Fertility Read full story FDA: “Vaccines Do NOT Require Demonstration of the Prevention of Infection or Transmission” Read full story ZERO Evidence of Transmission of Respiratory “Viruses” - ScienceDirect Read full story MIND-BLOWING REVELATION: Why It's IMPOSSIBLE to "Vaccinate" Against Anything and Why "Vaccines" Are the PERFECT POISONS Read full story You Are Not Sick. You Are Being POISONED: 3D Graphene Oxide Nanoparticles for Cloud Seeding Patent US 2022/0002159 A1 Read full story Satanic Frankensteins: Pfizer and Moderna CEOs Reveal Cabal’s True Intention – Destruction of God’s Creation Read full story https://substack.com/home/post/p-153508323

Press Release: Pfizer Papers - Covid-19 vaccine must be immediately withdrawn Ahmad Jufliz bin Dato' Faiza Murray Hunter Press Release.24.12.2024 1.PRM calls for the immediate formation of a Special People's Task Force consisting of 20 medical experts selected from the Ministry of Health Malaysia and another 20 independent international medical experts to investigate the book "Pfizer Papers: Pfizer's Crimes Against Humanity" edited by Naomi Wolf & Amy Kelly in 2024. Based on primary source Pfizer clinical trial documents that have been revealed through court order, the Pfizer Papers have revealed that the Pfizer Covid-19 mRNA clinical trial was DEEPLY FLAWED; that Pfizer knew from November 2020 that the Covid-19 mRNA "vaccine" was not safe or effective; knew from February 2021, that Covid-19 mRNA injections can cause various serious side effects including death; knew from April 2021 that Covid-19 mRNA injections can cause damage to the hearts of young people; 3. The order of US District Judge in the Northern District of Texas Mart T Pittman in disclosing Pfizer's clinical trial documents including Pfizer's post-marketing documents shows the people that the public disclosure of Pfizer documents is very important; "A popular Government, without popular information, or the means of acquiring it, is but a Prologue to a Farce or a Tragedy"; "A nation that is afraid to let its people judge the truth and falsehood in an open market is a nation that is afraid of its people". 4. PRM urges that all forms of mRNA "vaccines" or any "vaccines" for the use of Malaysians must be discontinued pending the investigation and decision of the People's Special Task Force later. 5. This People's Special Power Position is important to restore the People's Trust Deficit towards Public Health Policy which has been seen to have committed negligence, fraud and medical malpractice on a large scale since the Covid-19 Pandemic and the country needs the scientific community from within and outside the Government to respond to the serious current issue regarding the use of mRNA "vaccines" especially since the Covid-19 Pandemic and also any future national vaccine immunization program. 6. PRM is aware that there are more than 450,000 pages related to the detailed clinical trials that Pfizer conducted regarding the Covid 19 mRNA injection and also including post-marketing documents made for 3 months from 1.12.2020 to 28.2.2021 and the Pfizer Papers have at least succeeded in exposing the flaws in Pfizer's clinical trials. 7. With this disclosure, PRM urges the Ministry of Health Malaysia to no longer repeat the mistakes made by the US FDA. Many who have taken the injection until now, are unaware that the normal safety tests for any new vaccine; the test took 10 -12 years - but in the case of the Covid 19 Pandemic, it was only through a mechanism called EUA/Emergency Use Authorization/Authorized for Emergency Reasons by the FDA; Malaysia at that time just followed the American FDA, with conditional approval. What the People did not know was that the test was actually done on all of us, the People of the World, as if the People were being tested like Lab Rats; And without informed consent; And Pfizer and the FDA knew before the "roll out" and after the "roll out" that the effects of taking this injection were dangerous and could cause death; It was even more surprising when we learned that the FDA initially applied to the court not to disclose Pfizer's data for 75 years. Why does this government agency want to cover up important documents until the current generation, who are affected by what is in this document, die and will not be around anymore? It is also very strange when the FDA approved Pfizer's application within 108 days on 23.8.2021 when Pfizer provided all these clinical trial reports but to disclose to the public, they applied to disclose the reports within 75 years? 8. PRM is very concerned that even though the FDA tried to hold back the disclosure of Pfizer documents, when this disclosure was allowed by the court, the FDA still tried to hide this data from the public and let many Americans and us in Malaysia be injected with the Pfizer mRNA Covid-19 "vaccine" which is dangerous and can cause death without informed consent. Although there were situations where the vaccine was mandatory at that time but in the case of Malaysia even though it was voluntary -- the excessive promotion of the Malaysian Ministry of Health at that time caused many people to take the Covid 19 vaccine injection in the PICK program without informed consent and those who did not have a passport vaccine were discriminated against so that they could not work, were fired, could not cross the border, enter supermarkets or worship at mosques etc. 9. Regarding PFIZER's post-marketing report, it has recorded serious side effects and deaths due to the experimental use of mRNA gene therapy for Covid-19. There are 1291 side effects in appendix 1 of the report.9. The report also states that: I. Within 90 days of the test being conducted on 1.12.2020, there were 1,223 deaths but Pfizer still concluded in the report that there were no new safety issues; II. Out of 42,086 cases, side effects in women [29,914/71%] were 3 times more common than in men [9,182/21.8%]; III. There were 175 cases for those under the age of 17 where it is not known how many doses were given to children under 12 years old without informed consent during that time; Side effects found in children include Bell's palsy in a 1-year-old child, stroke in a 7-year-old child and renal failure in a baby less than 23 months old; IV. For the category of pregnant mothers, 56 fetuses and babies died; 54 cases of pregnancy, the baby was no longer alive at birth; BNT162b2 has never been approved for use during pregnancy or lactation during the collection of data for post-marketing; V. No informed consent was made by the FDA during the ‘roll out’ to the public despite knowing beforehand that there were serious side effects regarding the Covid19 mRNA ‘vaccine’, and in fact did not provide this information to the public; VI. The clinical trial results are divided into 4 parts, namely "Unknown" there are 9,400/22%, "Recovered/Recovering" cases there are 19,582/47% cases, "Not recovered at time of report" there are 11,361 cases & "Recovered with sequele" there are 520 cases in total 27% cases and Fatal 1,223/2.9 cases; If we add all this up, almost 97% of cases, the effects are unknown but 2.9% of cases we know the effects are death; In short, why is "recovered/recovering" combined? It seems that Pfizer is trying to show that the category that has been "recovered" looks good; And how do we distinguish between "Recovering" and "Not recovered at time of report"? 10. Finally, PRM would like to emphasize that as an Executive government administration that upholds the principles of Integrity, Accountability and Good Governance, it is obligatory for the Madani government and the Ministry of Public Health not to hide under the Official Secrets Act in this issue, in fact the People are worried because the Covid-19 mRNA "vaccine" product is protected by the government; Why is the liability product by the manufacturer and the "middleman" who gives the Covid-19 mRNA "vaccine" to the People as consumers protected by the government? "This is unprecedented" Many People are discriminated against to the point of being fired and cannot worship in the Mosque etc. just because there is no passport vaccine; In fact, this violates the fundamental rights guaranteed by Article 5 of the Federal Constitution where no People can be deprived of their life and personal freedom. This right has no constitutional limits whether from the perspective of security, public order, morality or on the basis of public health. In fact, the rights of the People from the perspective of religion or belief must always be respected; What is even worse is that because the government protects the manufacturer Pfizer and the "middlemen" [who have made huge profits in the sale of this "vaccine"] how can the People as consumers obtain compensation for injuries and deaths caused by taking the Covid-19 mRNA "vaccine"?; With the interests of the manufacturers to make huge profits but the safety of their products is protected by the government, this "creates a moral hazard and departs from the product liability doctrine"; This is also a violation under the Consumer Protection Act. Ahmad Jufliz bin Dato' Faiza President of the Malaysian People's Party 24.12.2024. Subscribe Below: https://murrayhunter.substack.com/p/press-release-pfizer-papers-covid

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