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👀The Plotkin Deposition - Part V - Under oath, Dr. Stanley Plotkin confirmed the following: • Vaccines on the childhood schedule are manufactured using aborted fetal cell strains (MRC-5, WI-38), derived from electively aborted fetuses • Those cell strains originated from fetuses aborted for social and psychiatric reasons •... Human DNA and protein fragments remain in final vaccine products • Millions to trillions of fragments of human DNA may be present per dose • No study exists proving the safety of injecting those DNA fragments into infants • Polio vaccines were grown on monkey kidney cells, later found contaminated with SV40 • Porcine circovirus was unintentionally found in rotavirus vaccines after release • Vaccine ingredients have repeatedly entered the market before contaminants were discovered • Aluminum adjuvants can bind not only to antigens, but also to manufacturing byproducts and impurities • Serious adverse events listed across product inserts are real, even if causation is later disputed • He receives compensation from all four major vaccine manufacturers When asked directly whether safety data exists for many of these exposures, the answer was repeated again and again: “I don’t know.” “There is no study.” “That data doesn’t exist.” This is the scientific record finally spoken aloud. Watch the final part of The Plotkin Deposition – Part V.show more

The HighWire

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16,124 просмотров • 6 месяцев назад •via X (Twitter)

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👀The Plotkin Deposition - Part I In Part I of the deposition of Dr. Stanley Plotkin several critical facts were placed on the record: ➡️ He acknowledged receiving millions of dollars over his career from vaccine manufacturers, including Sanofi, Merck, GSK, and Pfizer ➡️ He helped develop vaccines that are still mandated today — rubella, rotavirus, rabies — and received royalties tied to their sale ➡️ He sits (or has sat) on the boards of multiple for-profit vaccine companies, many of which were not disclosed on his CV ➡️ He helped found and advise vaccine-advocacy organizations while those organizations were financially connected — directly or indirectly — to pharmaceutical funding ➡️He recommended that children receive vaccines made by companies from which he personally received substantial compensation ➡️When asked for exact figures, he repeatedly stated he “did not know” how much money he had received, even when amounts reached into the millions AND MORE Watch Part I of The Deposition of Stanley Plotkin and decide for yourself.

👀The Plotkin Deposition - Part I In Part I of the deposition of Dr. Stanley Plotkin several critical facts were placed on the record: ➡️ He acknowledged receiving millions of dollars over his career from vaccine manufacturers, including Sanofi, Merck, GSK, and Pfizer ➡️ He helped develop vaccines that are still mandated today — rubella, rotavirus, rabies — and received royalties tied to their sale ➡️ He sits (or has sat) on the boards of multiple for-profit vaccine companies, many of which were not disclosed on his CV ➡️ He helped found and advise vaccine-advocacy organizations while those organizations were financially connected — directly or indirectly — to pharmaceutical funding ➡️He recommended that children receive vaccines made by companies from which he personally received substantial compensation ➡️When asked for exact figures, he repeatedly stated he “did not know” how much money he had received, even when amounts reached into the millions AND MORE Watch Part I of The Deposition of Stanley Plotkin and decide for yourself.

The HighWire

16,120 просмотров • 7 месяцев назад

Dear South Carolina: #lindabell Careful with semantics - this is perjury. They state fetal cells have nothing to do with MMR, so they are trying to remove all exemptions on South Carolina- This fact has been consistently distorted by institutions eager to downplay ethically relevant and biologically significant facts. The reality: Yes, the MMR (measles, mumps, rubella) vaccine does involve fetal-derived cells, specifically, human diploid cell lines that originated from electively aborted fetuses in the 1960s. However, it’s crucial to understand where and how these cells are involved. Specific cell lines used WI‑38 (Wistar Institute 38): Female fetal lung fibroblasts. Derived in 1962 (Sweden/Philadelphia). Used notably for the rubella component of the original MMR. MRC‑5 (Medical Research Council‑5): Male fetal lung fibroblasts. Derived in 1966 (UK). Used in various live viral vaccines, sometimes substituting for WI‑38. These cell lines were created from lung tissue taken from two separate aborted fetuses, not from a continuous series of abortions — but the fact remains: aborted fetal cells were the original source material. How they’re used: In the MMR vaccine (particularly the rubella component): The rubella virus (RA27/3 strain) was first isolated and attenuated in WI‑38 cells. Once the vaccine strain was developed, production continued using human diploid fibroblasts as a cell substrate (the “factory” in which the virus is grown). The virus is later harvested, purified, and stabilized. So, while no intact fetal cells are in the final vaccine, residual human DNA fragments and cellular debris are, because the viral culture medium derives from these diploid cell lines. Small amounts of human DNA (~10–20 nanograms per dose) remain after filtration. Ingredient label explanation The ingredient list won’t explicitly say “fetal cells,” but look for terms like: “WI‑38 human diploid lung fibroblasts” “MRC‑5 human diploid fibroblasts” Or in some documentation: “cell culture media derived from human diploid lung cells” Those descriptors mean fetal-derived cells were used in propagation. Ethical & scientific considerations Bioethical dimension: Many people object on moral or religious grounds to products developed from fetal tissue, even if no new abortions occur today. The lack of transparency on insert labeling prevents fully informed consent. Scientific concern: independent researchers have long debated whether residual human DNA could integrate or trigger unintended immune or epigenetic effects, particularly in developing brains — a matter regulators have been reluctant to examine openly. To summarize: COMPONENTCELL LINE SOURCEFETAL ORIGINSTILL PRESENT IN FINAL PRODUCT? MeaslesChicken embryo cellsNoNo MumpsChicken embryo cellsNoNo RubellaWI‑38 (human diploid fetal lung)YesResidual DNA fragments remain So the truthful answer is: The rubella component of the MMR vaccine is cultured in human fetal cell lines (WI‑38 or MRC‑5), meaning fetal-derived material was essential to its production, and trace human DNA fragments remain in each dose. Sen. Josh Kimbrell where did it come from? Scientific fact that your epidemiologist buddy giving testimony is either not qualified to discern, or she’s just not being honest under oath.

Dear South Carolina: #lindabell Careful with semantics - this is perjury. They state fetal cells have nothing to do with MMR, so they are trying to remove all exemptions on South Carolina- This fact has been consistently distorted by institutions eager to downplay ethically relevant and biologically significant facts. The reality: Yes, the MMR (measles, mumps, rubella) vaccine does involve fetal-derived cells, specifically, human diploid cell lines that originated from electively aborted fetuses in the 1960s. However, it’s crucial to understand where and how these cells are involved. Specific cell lines used WI‑38 (Wistar Institute 38): Female fetal lung fibroblasts. Derived in 1962 (Sweden/Philadelphia). Used notably for the rubella component of the original MMR. MRC‑5 (Medical Research Council‑5): Male fetal lung fibroblasts. Derived in 1966 (UK). Used in various live viral vaccines, sometimes substituting for WI‑38. These cell lines were created from lung tissue taken from two separate aborted fetuses, not from a continuous series of abortions — but the fact remains: aborted fetal cells were the original source material. How they’re used: In the MMR vaccine (particularly the rubella component): The rubella virus (RA27/3 strain) was first isolated and attenuated in WI‑38 cells. Once the vaccine strain was developed, production continued using human diploid fibroblasts as a cell substrate (the “factory” in which the virus is grown). The virus is later harvested, purified, and stabilized. So, while no intact fetal cells are in the final vaccine, residual human DNA fragments and cellular debris are, because the viral culture medium derives from these diploid cell lines. Small amounts of human DNA (~10–20 nanograms per dose) remain after filtration. Ingredient label explanation The ingredient list won’t explicitly say “fetal cells,” but look for terms like: “WI‑38 human diploid lung fibroblasts” “MRC‑5 human diploid fibroblasts” Or in some documentation: “cell culture media derived from human diploid lung cells” Those descriptors mean fetal-derived cells were used in propagation. Ethical & scientific considerations Bioethical dimension: Many people object on moral or religious grounds to products developed from fetal tissue, even if no new abortions occur today. The lack of transparency on insert labeling prevents fully informed consent. Scientific concern: independent researchers have long debated whether residual human DNA could integrate or trigger unintended immune or epigenetic effects, particularly in developing brains — a matter regulators have been reluctant to examine openly. To summarize: COMPONENTCELL LINE SOURCEFETAL ORIGINSTILL PRESENT IN FINAL PRODUCT? MeaslesChicken embryo cellsNoNo MumpsChicken embryo cellsNoNo RubellaWI‑38 (human diploid fetal lung)YesResidual DNA fragments remain So the truthful answer is: The rubella component of the MMR vaccine is cultured in human fetal cell lines (WI‑38 or MRC‑5), meaning fetal-derived material was essential to its production, and trace human DNA fragments remain in each dose. Sen. Josh Kimbrell where did it come from? Scientific fact that your epidemiologist buddy giving testimony is either not qualified to discern, or she’s just not being honest under oath.

Dr. Lynn Fynn-derella

32,914 просмотров • 4 месяцев назад

👀The Plotkin Deposition - Part IV This is not opinion. This is sworn testimony. In Part IV of the Stanley Plotkin deposition, the record gets uncomfortable. Fast. Under oath, the world’s most celebrated vaccine authority admits: • There has never been a study comparing the total health outcomes of fully vaccinated children vs. completely unvaccinated children • The Institute of Medicine reviewed 158 serious vaccine injury claims, and for 135 of them, concluded the evidence was insufficient to determine causation • He helped review those reports while consulting for multiple vaccine manufacturers, a conflict not disclosed in the reports • Vaccines are recommended even when science cannot determine whether they cause certain injuries • Aluminum adjuvants can persist in the body, be taken up by immune cells, and travel to the brain - something he acknowledged is possible • Studies showing concerning outcomes are dismissed as “predatory,” yet he agrees they warrant larger, better studies • Despite billions in revenue and taxpayer-funded vaccine purchases, no comprehensive safety comparison has ever been done Perhaps most telling: When asked whether doctors should wait for science before declaring vaccines do not cause autism, his answer was clear: “Do I wait? No.” Watch Part IV of The Plotkin Deposition and decide for yourself whether “safe and effective” is science or policy.

👀The Plotkin Deposition - Part IV This is not opinion. This is sworn testimony. In Part IV of the Stanley Plotkin deposition, the record gets uncomfortable. Fast. Under oath, the world’s most celebrated vaccine authority admits: • There has never been a study comparing the total health outcomes of fully vaccinated children vs. completely unvaccinated children • The Institute of Medicine reviewed 158 serious vaccine injury claims, and for 135 of them, concluded the evidence was insufficient to determine causation • He helped review those reports while consulting for multiple vaccine manufacturers, a conflict not disclosed in the reports • Vaccines are recommended even when science cannot determine whether they cause certain injuries • Aluminum adjuvants can persist in the body, be taken up by immune cells, and travel to the brain - something he acknowledged is possible • Studies showing concerning outcomes are dismissed as “predatory,” yet he agrees they warrant larger, better studies • Despite billions in revenue and taxpayer-funded vaccine purchases, no comprehensive safety comparison has ever been done Perhaps most telling: When asked whether doctors should wait for science before declaring vaccines do not cause autism, his answer was clear: “Do I wait? No.” Watch Part IV of The Plotkin Deposition and decide for yourself whether “safe and effective” is science or policy.

The HighWire

23,365 просмотров • 6 месяцев назад

👀The Plotkin Deposition - Part III In Part III, Stanley Plotkin confirms a series of facts that are rarely acknowledged publicly, but matter deeply for informed consent: • Hepatitis B vaccines (Recombivax HB & Engerix-B) were licensed after safety monitoring of 4–5 days, with no placebo control groups • Serious neurological and autoimmune conditions are listed in manufacturer inserts — yet causation was never tested pre-licensure • Once a vaccine is placed on the CDC schedule, Plotkin admits it becomes “ethically difficult” to ever perform a proper placebo-controlled safety study • IPV (polio) safety was monitored for just 48 hours, and it was administered alongside DTP, making attribution of injury impossible • MMR: Plotkin cannot cite a single randomized, placebo-controlled pre-licensure safety trial despite decades of use • Gardasil (HPV) trials combined aluminum-adjuvant controls with saline placebo — masking the fact that the saline-only group showed 0% autoimmune events • Drugs given to sick adults undergo safety follow-up for years, while vaccines given to healthy babies are monitored for days ...AND MORE Watch The Plotkin Deposition – Part III and share your thoughts below.

👀The Plotkin Deposition - Part III In Part III, Stanley Plotkin confirms a series of facts that are rarely acknowledged publicly, but matter deeply for informed consent: • Hepatitis B vaccines (Recombivax HB & Engerix-B) were licensed after safety monitoring of 4–5 days, with no placebo control groups • Serious neurological and autoimmune conditions are listed in manufacturer inserts — yet causation was never tested pre-licensure • Once a vaccine is placed on the CDC schedule, Plotkin admits it becomes “ethically difficult” to ever perform a proper placebo-controlled safety study • IPV (polio) safety was monitored for just 48 hours, and it was administered alongside DTP, making attribution of injury impossible • MMR: Plotkin cannot cite a single randomized, placebo-controlled pre-licensure safety trial despite decades of use • Gardasil (HPV) trials combined aluminum-adjuvant controls with saline placebo — masking the fact that the saline-only group showed 0% autoimmune events • Drugs given to sick adults undergo safety follow-up for years, while vaccines given to healthy babies are monitored for days ...AND MORE Watch The Plotkin Deposition – Part III and share your thoughts below.

The HighWire

15,354 просмотров • 6 месяцев назад

The Plotkin Deposition - Part II: Under oath, Dr. Stanley Plotkin admits what the public is rarely told. He acknowledges that acellular pertussis vaccines lose most of their effectiveness within a few years, leaving many adolescents and adults largely unprotected - even while mandates remain in place He concedes that vaccinated individuals may still carry and transmit pertussis, and that this risk has never been properly studied in humans, relying instead on animal models because human trials were never done He confirms that: • Vaccine makers operate in a liability-free market • Advisory bodies that shape the childhood schedule work through non-public working groups • Billions of taxpayer dollars fund vaccine purchases • Conflicts of interest between regulators, advisors, and manufacturers are real and widespread During the deposition, it was revealed that Paul Offit held a patent on a rotavirus vaccine while sitting as a voting member of ACIP when the first rotavirus vaccine was approved for universal use, a decision that helped open a taxpayer-funded market for future rotavirus vaccines. AND MORE If the system were as settled as we’re told, these answers wouldn’t feel so unsettling. Watch The Deposition of Stanley Plotkin – Part 2 and decide for yourself.

The Plotkin Deposition - Part II: Under oath, Dr. Stanley Plotkin admits what the public is rarely told. He acknowledges that acellular pertussis vaccines lose most of their effectiveness within a few years, leaving many adolescents and adults largely unprotected - even while mandates remain in place He concedes that vaccinated individuals may still carry and transmit pertussis, and that this risk has never been properly studied in humans, relying instead on animal models because human trials were never done He confirms that: • Vaccine makers operate in a liability-free market • Advisory bodies that shape the childhood schedule work through non-public working groups • Billions of taxpayer dollars fund vaccine purchases • Conflicts of interest between regulators, advisors, and manufacturers are real and widespread During the deposition, it was revealed that Paul Offit held a patent on a rotavirus vaccine while sitting as a voting member of ACIP when the first rotavirus vaccine was approved for universal use, a decision that helped open a taxpayer-funded market for future rotavirus vaccines. AND MORE If the system were as settled as we’re told, these answers wouldn’t feel so unsettling. Watch The Deposition of Stanley Plotkin – Part 2 and decide for yourself.

The HighWire

11,256 просмотров • 6 месяцев назад

In 1986, There Were Only 3 Vaccines. They Were So Harmful That The Manufacturers Faced Bankruptcy Because of Vaccine Injury Lawsuits. The U.S. Congress...Instead Of Forcing Vaccine Makers To Make A Safe Product, They Chose To Give Full Immunity For Those 3 & All Future Vaccines. There Are Now 72 Doses Of Vaccines On The Childhood Vaccination Schedule & 13 Vaccines On The Adult Vaccination Schedule Totaling 24 Doses. With No Liability & Full Legal Immunity, Vaccine Manufacturers Have The Right To Make & Inject You With 100s Of Unsafe & Toxic Ingredients Such As These: Polysorbate 80 Thimerosal Mercury Aluminum Formaldehyde M59 Squalene Acetone Sodium Borate (Borax) 2-Phenoxyethanol SV40 Triton X-100 Bovine Calf Serum Porcine Gelatin Poultry Serum Poultry Byproducts Yeast Latex mRNA DNA Fragments Animal Organ DNA In Vaccines: MDCK: Madin Darby Canine Kidney, female Cocker Spaniel VERO: African Green Monkey Kidney FRHL: Fetal Rhesus Monkey Lung CHO: Chinese Hamster Ovary PK-15: Pork Kidney RK-13: Rabbit Kidney SIRC: Rabbit Cornea The vaccine industry is built on the use of aborted babies organs to produce the vaccines we use today…and they have to replace these lines with current aborted organs. The most recent harvested human organ for vaccine research is WALVAX-2 which is a harvested lung from a 3 month old unborn baby taken in 2015. This was one baby of 10 in total, in which organs were harvested for research & vaccine development. ⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in: HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A & Shingles RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid IMR-90: Lung from a 16 week old fetus; to replace the WI-38 line WALVAX-2: Lung from a 3 month old fetus; to replace the WI-38 and MRC-5 line 👇2015 Organs Harvested For WALVAX-2👇 👇Human Fetal Tissue & Organ Trafficking👇 👇Vaccine Excipient Summary List👇 Speaker: Aaron Siri Podcast: Russell Brand

Valerie Anne Smith

115,279 просмотров • 1 год назад

Aaron Siri Exposes Shocking Truth About Fetal Cell Lines in MMR Vaccines In a recent conversation, attorney Aaron Siri broke down why many parents are deeply disturbed by how vaccines like the MMR are produced. He pointed to official CDC ingredient lists showing that cultured cell lines such as MRC-5 and WI-38—originally derived from aborted fetal tissue—are used in the growth process of certain viral vaccines. Siri explained that viruses cannot replicate on their own; they must be grown in living cells. According to him, the rubella virus used in MMR was cultured using human fetal lung fibroblasts. This claim traces back to historical studies where researchers examined tissue samples from dozens of aborted fetuses to determine which body parts could best sustain viral growth. Siri referenced his deposition of Dr. Stanley Plotkin—often called the “godfather of vaccines”—and described it as one of the most disturbing records available for public review. The deposition, according to him, detailed studies involving normal, healthy fetuses used for experimental virus culture research. Many listeners reacted with disbelief and moral outrage, calling the practice a “sacrificial” aspect of modern vaccine production—something they say crosses ethical and religious boundaries. Siri emphasized that his goal is transparency and informed consent, urging Americans to see the original court deposition for themselves before forming conclusions.

Aaron Siri Exposes Shocking Truth About Fetal Cell Lines in MMR Vaccines In a recent conversation, attorney Aaron Siri broke down why many parents are deeply disturbed by how vaccines like the MMR are produced. He pointed to official CDC ingredient lists showing that cultured cell lines such as MRC-5 and WI-38—originally derived from aborted fetal tissue—are used in the growth process of certain viral vaccines. Siri explained that viruses cannot replicate on their own; they must be grown in living cells. According to him, the rubella virus used in MMR was cultured using human fetal lung fibroblasts. This claim traces back to historical studies where researchers examined tissue samples from dozens of aborted fetuses to determine which body parts could best sustain viral growth. Siri referenced his deposition of Dr. Stanley Plotkin—often called the “godfather of vaccines”—and described it as one of the most disturbing records available for public review. The deposition, according to him, detailed studies involving normal, healthy fetuses used for experimental virus culture research. Many listeners reacted with disbelief and moral outrage, calling the practice a “sacrificial” aspect of modern vaccine production—something they say crosses ethical and religious boundaries. Siri emphasized that his goal is transparency and informed consent, urging Americans to see the original court deposition for themselves before forming conclusions.

Camus

45,102 просмотров • 8 месяцев назад

American nurse says “I don’t care anymore.” She’s learned the truth about our vaccines system and she’s speaking out “I feel like I've just unlocked a new level of awakening, and normally I would be so scared to talk about vaccines because someone's gonna label me anti-vax, but I literally don't care anymore because the truth is out there and it's right in front of our faces” “You can look on the inserts and it's literally aborted fetuses in the vaccine ingredient list and all these other animal cells — I looked everything up myself and it's all true — long story short, Roe v. Wade was not meant for women's rights — The propaganda is real. It all makes sense, and it's so disgusting that they're using aborted fetuses to make our vaccines” “Anyone who thinks otherwise, like, I don't care anymore. Yes, I'm anti-vaccine.” She’s telling the truth, aborted fetus are used for our vaccines. Using human cell lines originally derived from elective abortions in the 1960s. Now today these are immortalized cell lines maintained in labs The viruses are grown in these cells, then purified. Trace DNA may remain in minute amounts This is why there is legitimate cause for religious exemption These cell lines were chosen in the 1960s because they grow viruses well in a sterile environment Major religious bodies including the Vatican have addressed moral concerns I included examples of current vaccines still using this method

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American nurse says “I don’t care anymore.” She’s learned the truth about our vaccines system and she’s speaking out “I feel like I've just unlocked a new level of awakening, and normally I would be so scared to talk about vaccines because someone's gonna label me anti-vax, but I literally don't care anymore because the truth is out there and it's right in front of our faces” “You can look on the inserts and it's literally aborted fetuses in the vaccine ingredient list and all these other animal cells — I looked everything up myself and it's all true — long story short, Roe v. Wade was not meant for women's rights — The propaganda is real. It all makes sense, and it's so disgusting that they're using aborted fetuses to make our vaccines” “Anyone who thinks otherwise, like, I don't care anymore. Yes, I'm anti-vaccine.” She’s telling the truth, aborted fetus are used for our vaccines. Using human cell lines originally derived from elective abortions in the 1960s. Now today these are immortalized cell lines maintained in labs The viruses are grown in these cells, then purified. Trace DNA may remain in minute amounts This is why there is legitimate cause for religious exemption These cell lines were chosen in the 1960s because they grow viruses well in a sterile environment Major religious bodies including the Vatican have addressed moral concerns I included examples of current vaccines still using this method

Wall Street Apes

234,343 просмотров • 2 дней назад

Big Pharma made a monumental error in their HPV (Gardasil) vaccine trial when they included a proper saline group. This part of an eye opening deposition, shows how adjuvants and vaccines compare to REAL saline/placebo. They try to infer that even inert substances will cause the same rate of adverse events as vaccines and injected adjuvants. But this trial exposes the truth. Dr. Stanley Plotkin exposed by Aaron Siri. After first laying the ground work and getting Dr. Plotkin to answer YES to that systemic belief that adverse events are an "Always on" mechanism built into all clinical trials, Aaron Siri presents him with a paper containing the evidence, with a Gardasil vaccine that had 3 groups, Vaccine, Aluminum Adjuvant and Saline. The Aluminum Adjuvant arm and the vaccine arm had well over 2% auto-immune adverse events. The Saline/Inert group had a 0% Which means - "For every action, there is an equal and opposite reaction" - NEWTON. When presented with the evidence, watch Dr. Plotkin continue along his path of cognitive dissonance.

Big Pharma made a monumental error in their HPV (Gardasil) vaccine trial when they included a proper saline group. This part of an eye opening deposition, shows how adjuvants and vaccines compare to REAL saline/placebo. They try to infer that even inert substances will cause the same rate of adverse events as vaccines and injected adjuvants. But this trial exposes the truth. Dr. Stanley Plotkin exposed by Aaron Siri. After first laying the ground work and getting Dr. Plotkin to answer YES to that systemic belief that adverse events are an "Always on" mechanism built into all clinical trials, Aaron Siri presents him with a paper containing the evidence, with a Gardasil vaccine that had 3 groups, Vaccine, Aluminum Adjuvant and Saline. The Aluminum Adjuvant arm and the vaccine arm had well over 2% auto-immune adverse events. The Saline/Inert group had a 0% Which means - "For every action, there is an equal and opposite reaction" - NEWTON. When presented with the evidence, watch Dr. Plotkin continue along his path of cognitive dissonance.

Humanspective

65,428 просмотров • 7 месяцев назад

Scientists Shocked: Peer-Reviewed Paper Confirms COVID Vaccine Nightmare A bombshell peer-reviewed study has confirmed what the “conspiracy theorists” have been warning for years: Pfizer’s mRNA COVID shot is contaminated with not just bacterial plasmid DNA, but with the SV40 promoter, a viral sequence that may interfere with how your genes function or even become part of your DNA. Dr. Mikolaj Raszek of Merogenomics reviewed the paper and said, “We finally have it—the very first published scientific evidence showing that the mRNA vaccine, Pfizer vaccines, were contaminated with bacterial plasmid DNA.” Researchers tested sealed vials—both monovalent and bivalent—and found DNA fragments embedded within the lipid nanoparticles. That's important because these nanoparticles are designed to deliver genetic material directly into the body’s cells. So the DNA wasn’t just contamination—it was effectively delivered like a package. Raszek pointed out that the fragments included the SV40 enhancer, which he called “extremely dangerous.” This viral promoter can help foreign DNA enter the nucleus of human cells, raising the risk of accidental genome integration. In plain English: fragments from the vaccine could potentially alter your DNA. How did this happen? What did Pfizer know beforehand? Epidemiologist Nicolas Hulscher, MPH joins the show with to discuss.

Scientists Shocked: Peer-Reviewed Paper Confirms COVID Vaccine Nightmare A bombshell peer-reviewed study has confirmed what the “conspiracy theorists” have been warning for years: Pfizer’s mRNA COVID shot is contaminated with not just bacterial plasmid DNA, but with the SV40 promoter, a viral sequence that may interfere with how your genes function or even become part of your DNA. Dr. Mikolaj Raszek of Merogenomics reviewed the paper and said, “We finally have it—the very first published scientific evidence showing that the mRNA vaccine, Pfizer vaccines, were contaminated with bacterial plasmid DNA.” Researchers tested sealed vials—both monovalent and bivalent—and found DNA fragments embedded within the lipid nanoparticles. That's important because these nanoparticles are designed to deliver genetic material directly into the body’s cells. So the DNA wasn’t just contamination—it was effectively delivered like a package. Raszek pointed out that the fragments included the SV40 enhancer, which he called “extremely dangerous.” This viral promoter can help foreign DNA enter the nucleus of human cells, raising the risk of accidental genome integration. In plain English: fragments from the vaccine could potentially alter your DNA. How did this happen? What did Pfizer know beforehand? Epidemiologist Nicolas Hulscher, MPH joins the show with to discuss.

The Vigilant Fox 🦊

303,171 просмотров • 1 год назад

🚨BREAKING: “The Godfather of Vaccines” Dr. Stanley Plotkin, now admits safety of injections has never been adequately studied! But in making that admission, he admits he conveniently failed to admit that for decades they lied, gaslit, defrauded the public by claiming that vaccines are probably the most thoroughly safety tested products on the planet and that people should rest assured, no stone on vaccine safety was left unturned." WHEN WILL THIS CRIMINAL BE CHARGED FOR FRAUD? YES HE IS! The medical community’s goal is to protect the products they have spent their careers defending and worshiping and that have brought them fame and riches. They also ignore the mountain of studies and data, which already exist that clearly show serious vaccine harms." RECALL: Dr. Plotkin developed the vaccine to stop rubella (German measles), which caused tens of thousands of severe birth defects in the U.S. alone, in the 1960s. He went on to work on the vaccines for polio, rabies, anthrax and rotavirus. Plotkin's influence stretches to the present day, with him being named as a consultant for the Wuhan coronavirus (COVID-19) vaccine. (Related: Longtime pro-jab apologist finally comes clean about lack of science proving vaccine safety.)

🚨BREAKING: “The Godfather of Vaccines” Dr. Stanley Plotkin, now admits safety of injections has never been adequately studied! But in making that admission, he admits he conveniently failed to admit that for decades they lied, gaslit, defrauded the public by claiming that vaccines are probably the most thoroughly safety tested products on the planet and that people should rest assured, no stone on vaccine safety was left unturned." WHEN WILL THIS CRIMINAL BE CHARGED FOR FRAUD? YES HE IS! The medical community’s goal is to protect the products they have spent their careers defending and worshiping and that have brought them fame and riches. They also ignore the mountain of studies and data, which already exist that clearly show serious vaccine harms." RECALL: Dr. Plotkin developed the vaccine to stop rubella (German measles), which caused tens of thousands of severe birth defects in the U.S. alone, in the 1960s. He went on to work on the vaccines for polio, rabies, anthrax and rotavirus. Plotkin's influence stretches to the present day, with him being named as a consultant for the Wuhan coronavirus (COVID-19) vaccine. (Related: Longtime pro-jab apologist finally comes clean about lack of science proving vaccine safety.)

Truth_teller 🇷🇺

26,499 просмотров • 1 год назад

There's Only 3 Places Mercury Is Allowed...Vaccines, Your Tooth Or A Toxic Landfill. If You Drop A Mercury Containing Vaccine On The Floor, You Cannot Touch It, Hazmat Must Come To Clean It Up... Yet It's Totally Fine To Inject It Into A Child? The Dark Manufacturing Process Of 'Growing A Vaccine' That No One Wants To Talks About. Animal Organ Cell Lines Used In Vaccines: MDCK: Madin Darby Canine Kidney, adult female Cocker Spaniel VERO: African Green Monkey Kidney, adult monkey FRHL: Fetal Rhesus Monkey Lung, male fetus CHO: Chinese Hamster Ovary, adult female PK-15: Pork Kidney, adult pig RK-13: Rabbit Kidney, 5 weeks old SIRC: Rabbit Cornea, adult The vaccine industry is built on the use of aborted fetal cells to produce the vaccines we use today…and they have to replace these lines. Take a look ⬇️ these are the 'code names' for aborted fetal cells, their original source & what vaccines they are used in: HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A & Shingles RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid IMR-90: tissue from a 16 week old aborted fetus; designed to replace the WI-38 line IMR-91: 12 week old aborted fetus, tissue designed to replace the WI-38 line WALVAX-2: lung tissue from a 3 month old aborted fetus; designed to replace the WI-38 and MRC-5 line If You Or A Loved One Needs Detoxification & Chelation Protocols: Lugol's 2% Iodine Drops PBX Zeolite Spray & Drops Dr Peter McCollough Spike Protein Detox 👇History Of Vaccines Using Organs👇 👇A-Z Vaccine Database By Disease Treated👇 Speakers: Dr Suzanne Humphries & Joe Rogan Podcast: Joe Roganhq Video: HAZARDBOYS

There's Only 3 Places Mercury Is Allowed...Vaccines, Your Tooth Or A Toxic Landfill. If You Drop A Mercury Containing Vaccine On The Floor, You Cannot Touch It, Hazmat Must Come To Clean It Up... Yet It's Totally Fine To Inject It Into A Child? The Dark Manufacturing Process Of 'Growing A Vaccine' That No One Wants To Talks About. Animal Organ Cell Lines Used In Vaccines: MDCK: Madin Darby Canine Kidney, adult female Cocker Spaniel VERO: African Green Monkey Kidney, adult monkey FRHL: Fetal Rhesus Monkey Lung, male fetus CHO: Chinese Hamster Ovary, adult female PK-15: Pork Kidney, adult pig RK-13: Rabbit Kidney, 5 weeks old SIRC: Rabbit Cornea, adult The vaccine industry is built on the use of aborted fetal cells to produce the vaccines we use today…and they have to replace these lines. Take a look ⬇️ these are the 'code names' for aborted fetal cells, their original source & what vaccines they are used in: HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A & Shingles RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid IMR-90: tissue from a 16 week old aborted fetus; designed to replace the WI-38 line IMR-91: 12 week old aborted fetus, tissue designed to replace the WI-38 line WALVAX-2: lung tissue from a 3 month old aborted fetus; designed to replace the WI-38 and MRC-5 line If You Or A Loved One Needs Detoxification & Chelation Protocols: Lugol's 2% Iodine Drops PBX Zeolite Spray & Drops Dr Peter McCollough Spike Protein Detox 👇History Of Vaccines Using Organs👇 👇A-Z Vaccine Database By Disease Treated👇 Speakers: Dr Suzanne Humphries & Joe Rogan Podcast: Joe Roganhq Video: HAZARDBOYS

Valerie Anne Smith

161,657 просмотров • 1 год назад

Vaccines That Are Made From Human & Animal Organ DNA Will Trigger A Lifelong Autoimmune Reaction. Dr Bryan Ardis The Human Body Will Attack All Foreign DNA & Cause Chronic Disease. Health Cannot Come From A Vaccine. There Is No Injection That Benefits Or Fortifies Our Health. Hepatitis-B Vaccine Ingredients: Recombinant DNA Hepatitis-B MRC-5 Harvested human lung Aluminum(AAHA) Aluminum Hydroxide Formaldehyde Polysorbate 80 Brewer's Yeast Protein DNA The vaccine industry is built on the use of harvested baby organs to produce the vaccines we use today…and they have to replace these lines with current organs for new vaccine development & research. The most recent harvested human organ for vaccine research is WALVAX-2 which is a harvested lung from a 3 month old unborn baby taken in 2015. This was one baby of 10 in total, in which organs were harvested for research & vaccine development. Take a look ⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in: HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A, Hep B & Shingles RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid IMR-90: Lung from a 16 week old fetus; to replace the WI-38 line WALVAX-2: Lung from a 3 month old fetus; to replace the WI-38 and MRC-5 line Animal Organs Used To Make Vaccines: MDCK: Madin Darby Canine Kidney, female Cocker Spaniel VERO: African Green Monkey Kidney FRHL: Fetal Rhesus Monkey Lung CHO: Chinese Hamster Ovary PK-15: Pork Kidney RK-13: Rabbit Kidney SIRC: Rabbit Cornea 👇2015 Organs Harvested For WALVAX-2👇 👇Human Fetal Tissue & Organ Trafficking👇 👇Vaccine Excipient Summary List👇 Speaker: Bryan Ardis Podcast: Rebecca Weiss Podcast

Vaccines That Are Made From Human & Animal Organ DNA Will Trigger A Lifelong Autoimmune Reaction. Dr Bryan Ardis The Human Body Will Attack All Foreign DNA & Cause Chronic Disease. Health Cannot Come From A Vaccine. There Is No Injection That Benefits Or Fortifies Our Health. Hepatitis-B Vaccine Ingredients: Recombinant DNA Hepatitis-B MRC-5 Harvested human lung Aluminum(AAHA) Aluminum Hydroxide Formaldehyde Polysorbate 80 Brewer's Yeast Protein DNA The vaccine industry is built on the use of harvested baby organs to produce the vaccines we use today…and they have to replace these lines with current organs for new vaccine development & research. The most recent harvested human organ for vaccine research is WALVAX-2 which is a harvested lung from a 3 month old unborn baby taken in 2015. This was one baby of 10 in total, in which organs were harvested for research & vaccine development. Take a look ⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in: HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A, Hep B & Shingles RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid IMR-90: Lung from a 16 week old fetus; to replace the WI-38 line WALVAX-2: Lung from a 3 month old fetus; to replace the WI-38 and MRC-5 line Animal Organs Used To Make Vaccines: MDCK: Madin Darby Canine Kidney, female Cocker Spaniel VERO: African Green Monkey Kidney FRHL: Fetal Rhesus Monkey Lung CHO: Chinese Hamster Ovary PK-15: Pork Kidney RK-13: Rabbit Kidney SIRC: Rabbit Cornea 👇2015 Organs Harvested For WALVAX-2👇 👇Human Fetal Tissue & Organ Trafficking👇 👇Vaccine Excipient Summary List👇 Speaker: Bryan Ardis Podcast: Rebecca Weiss Podcast

Valerie Anne Smith

90,284 просмотров • 1 год назад

The Truth On How Vaccines Are Manufactured... "Babies Are Aborted For The Sole Purpose Of The Study." "The Organs Needed For Vaccine Development Are Harvested While The Heart Is Still Beating." "The Unborn Babies Used For Development Are Alive At Tissue Extraction." Dr Stanley Plotkin, dubbed the 'Godfather of Vaccines' admitted this proudly & without remorse, under oath during his 9 hour deposition by lawyer Aaron Siri. Dr Theresa Deisher, PhD Molecular & Cellular Physiology: According to Dr Theresa Deisher, "Babies are born alive from five to six months old, with beating hearts cut out without anesthesia for research purposes. Researchers also cut through live babies' faces to collect brain tissue." Pamela Acker, Biologist & Former Vaccine Researcher: As quoted by Pamela Acker, "The babies are alive when the researchers start extracting the tissue. Their hearts are still beating & they're not given any anesthetic because that would contaminate the organs being harvested that need to be alive, pure & free of toxins." The vaccine industry is built on the use of babies organs to produce the vaccines we use today…and they have to replace these lines with current organs. Take a look ⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in: HEK-293: Human Kidney, female; used in development of Ebola & Covid MRC-5: Human Lung, male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, female; used in Polio, Rabies, Chickenpox, Hep A & Shingles RA 27-3: Human Kidney, used in the Rubella & MMR PER-C6: Human Retina, used in the development of Ebola & Covid IMR-90: Human Lung; to replace the WI-38 line WALVAX-2: Human Lung; to replace the WI-38 and MRC-5 line 👇Transcript Deposition Of Stanley Plotkin👇 👇Dr Theresa Deisher Interview👇 👇A-Z Vaccine Ingredient Database👇 Speaker: Aaron Siri, ICAN Lawyer, Informed Consent Action Network Video: lioness.of.liberty

The Truth On How Vaccines Are Manufactured... "Babies Are Aborted For The Sole Purpose Of The Study." "The Organs Needed For Vaccine Development Are Harvested While The Heart Is Still Beating." "The Unborn Babies Used For Development Are Alive At Tissue Extraction." Dr Stanley Plotkin, dubbed the 'Godfather of Vaccines' admitted this proudly & without remorse, under oath during his 9 hour deposition by lawyer Aaron Siri. Dr Theresa Deisher, PhD Molecular & Cellular Physiology: According to Dr Theresa Deisher, "Babies are born alive from five to six months old, with beating hearts cut out without anesthesia for research purposes. Researchers also cut through live babies' faces to collect brain tissue." Pamela Acker, Biologist & Former Vaccine Researcher: As quoted by Pamela Acker, "The babies are alive when the researchers start extracting the tissue. Their hearts are still beating & they're not given any anesthetic because that would contaminate the organs being harvested that need to be alive, pure & free of toxins." The vaccine industry is built on the use of babies organs to produce the vaccines we use today…and they have to replace these lines with current organs. Take a look ⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in: HEK-293: Human Kidney, female; used in development of Ebola & Covid MRC-5: Human Lung, male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, female; used in Polio, Rabies, Chickenpox, Hep A & Shingles RA 27-3: Human Kidney, used in the Rubella & MMR PER-C6: Human Retina, used in the development of Ebola & Covid IMR-90: Human Lung; to replace the WI-38 line WALVAX-2: Human Lung; to replace the WI-38 and MRC-5 line 👇Transcript Deposition Of Stanley Plotkin👇 👇Dr Theresa Deisher Interview👇 👇A-Z Vaccine Ingredient Database👇 Speaker: Aaron Siri, ICAN Lawyer, Informed Consent Action Network Video: lioness.of.liberty

Valerie Anne Smith

111,625 просмотров • 1 год назад

"We Have Been Conditioned To Believe That Vaccines Are Safe, Effective, Necessary & Harmless...They Are None Of Those Things." "Vaccines Are Systematic Poisoning Of Children & Adults." "It's Time We Call It What It Is...The Pediatric Poisoning Schedule." Dr Sherri Tenpenny, DO If a child, by the time they are 18, gets all of the vaccines in the entire 72 dose schedule, they get 13,000 mcg of Aluminum, 600 mcg of Mercury & 200 toxic chemicals injected directly into their system. Parents would be arrested & imprisoned if they fed vaccine ingredients to their children. Yet, the 72 doses on the vaccine schedule, containing 100s of harmful ingredients continue to be legal as the Government lies & says that vaccines are 'safe & effective.' Each 'well child' appointment can involve up to 8 shots for the vulnerable infant involving 100s of ingredients such as: Polysorbate 80 Thimerosal Mercury Aluminum Formaldehyde M59 Squalene Acetone Sodium Borate (Borax) 2-Phenoxyethanol SV40 Triton X-100 Bovine Calf Serum Poultry Serum Poultry Byproducts Animal Organs Used To Make Vaccines: MDCK: Madin Darby Canine Kidney, female Cocker Spaniel VERO: African Green Monkey Kidney FRHL: Fetal Rhesus Monkey Lung CHO: Chinese Hamster Ovary PK-15: Pork Kidney RK-13: Rabbit Kidney SIRC: Rabbit Cornea The vaccine industry is built on the use of aborted babies organs to produce the vaccines we use today…and they have to replace these lines with current aborted organs. Take a look ⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in: HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A & Shingles RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid IMR-90: Lung from a 16 week old fetus; to replace the WI-38 line WALVAX-2: Lung from a 3 month old fetus; to replace the WI-38 and MRC-5 line 👇214 Research Papers Vaccines Cause Autism👇 👇Vaccines Cause Neurodevelopment Disorders👇 👇Vaccine Excipient Summary List👇 Speaker: Dr Sherri Tenpenny

"We Have Been Conditioned To Believe That Vaccines Are Safe, Effective, Necessary & Harmless...They Are None Of Those Things." "Vaccines Are Systematic Poisoning Of Children & Adults." "It's Time We Call It What It Is...The Pediatric Poisoning Schedule." Dr Sherri Tenpenny, DO If a child, by the time they are 18, gets all of the vaccines in the entire 72 dose schedule, they get 13,000 mcg of Aluminum, 600 mcg of Mercury & 200 toxic chemicals injected directly into their system. Parents would be arrested & imprisoned if they fed vaccine ingredients to their children. Yet, the 72 doses on the vaccine schedule, containing 100s of harmful ingredients continue to be legal as the Government lies & says that vaccines are 'safe & effective.' Each 'well child' appointment can involve up to 8 shots for the vulnerable infant involving 100s of ingredients such as: Polysorbate 80 Thimerosal Mercury Aluminum Formaldehyde M59 Squalene Acetone Sodium Borate (Borax) 2-Phenoxyethanol SV40 Triton X-100 Bovine Calf Serum Poultry Serum Poultry Byproducts Animal Organs Used To Make Vaccines: MDCK: Madin Darby Canine Kidney, female Cocker Spaniel VERO: African Green Monkey Kidney FRHL: Fetal Rhesus Monkey Lung CHO: Chinese Hamster Ovary PK-15: Pork Kidney RK-13: Rabbit Kidney SIRC: Rabbit Cornea The vaccine industry is built on the use of aborted babies organs to produce the vaccines we use today…and they have to replace these lines with current aborted organs. Take a look ⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in: HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A & Shingles RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid IMR-90: Lung from a 16 week old fetus; to replace the WI-38 line WALVAX-2: Lung from a 3 month old fetus; to replace the WI-38 and MRC-5 line 👇214 Research Papers Vaccines Cause Autism👇 👇Vaccines Cause Neurodevelopment Disorders👇 👇Vaccine Excipient Summary List👇 Speaker: Dr Sherri Tenpenny

Valerie Anne Smith

207,824 просмотров • 1 год назад

Did you know that there was no pre-license clinical trial on the MMR vaccine before it was mass administered? This is one of my favorite parts from the Siri and Plotkin deposition, and demonstrates how horrible vaccine science really is. Share this with anyone who is adamant about vaccines being properly safety tested, especially the MMR vaccine, which has been at the root of the autism discussion for decades. Make sure they know exactly who Plotkin is, and his importance and prestige in vaccinology. You can see Plotkin panicking internally as he begins to figure out that Siri isn't going to let him weasel out of the fact that there are no proper studies discerning the safety of the MMR vaccine, and Plotkin eventually says he won't provide any studies, and he just has to "read his book". That book being the Vaccination Bible. Siri eventually forces it out of Plotkin that the MMR vaccine studies never had a saline placebo group. This is a perfect example of what a great lawyer pursuing truth looks like. Siri says: "So you're claiming something happened, but you're not willing to provide any proof that it happened?" Plotkin: "....the proof is in the publications (his book), which you can read if you like". Plotkin gives the same line about how "these vaccines have been studied for 50 years", and Siri responds with basically "I know you just want us to take your word for it, but I prefer to rely on science, peer reviewed publications, and clinical trials. I know you're getting upset about me trying to ask for the data" and then explains what is required for a vaccine to be approved per the FDA with placebo controls. After some more deliberation, Siri asks Plotkin to provide him anything in regards to a study that had a placebo group, and Plotkin eventually has to say HE DOESN'T KNOW IF IT HAD A PLACEBO GROUP, and he would have to go back and look at the individual study. Think about this for a second... Godfather of vaccines. One of the most controversial vaccines in history in regards to autism and various injuries, and he doesn't know if there was a placebo control used in a study for it? Come on... This continues for a couple more minutes before Plotkin has to give up and say "I will look for the studies and provide them to you after the deposition". Guess what? He never provided those studies, as expected. Same thing Fauci did to RFK when asked. They know these studies don't exist, but they put on a show to save face. This is being knowingly dishonest. This is lying under oath. This is so wrong because the result of this lie and lack of proper safety studies is people being harmed or killed, or kids being brain damaged for life and suffering immensely. It's unforgiveable. There isn't a jail cell small enough for these criminals. One of the most damning clips from the deposition. Aaron Siri is a beast and deserves immense respect, on par with RFK.

Did you know that there was no pre-license clinical trial on the MMR vaccine before it was mass administered? This is one of my favorite parts from the Siri and Plotkin deposition, and demonstrates how horrible vaccine science really is. Share this with anyone who is adamant about vaccines being properly safety tested, especially the MMR vaccine, which has been at the root of the autism discussion for decades. Make sure they know exactly who Plotkin is, and his importance and prestige in vaccinology. You can see Plotkin panicking internally as he begins to figure out that Siri isn't going to let him weasel out of the fact that there are no proper studies discerning the safety of the MMR vaccine, and Plotkin eventually says he won't provide any studies, and he just has to "read his book". That book being the Vaccination Bible. Siri eventually forces it out of Plotkin that the MMR vaccine studies never had a saline placebo group. This is a perfect example of what a great lawyer pursuing truth looks like. Siri says: "So you're claiming something happened, but you're not willing to provide any proof that it happened?" Plotkin: "....the proof is in the publications (his book), which you can read if you like". Plotkin gives the same line about how "these vaccines have been studied for 50 years", and Siri responds with basically "I know you just want us to take your word for it, but I prefer to rely on science, peer reviewed publications, and clinical trials. I know you're getting upset about me trying to ask for the data" and then explains what is required for a vaccine to be approved per the FDA with placebo controls. After some more deliberation, Siri asks Plotkin to provide him anything in regards to a study that had a placebo group, and Plotkin eventually has to say HE DOESN'T KNOW IF IT HAD A PLACEBO GROUP, and he would have to go back and look at the individual study. Think about this for a second... Godfather of vaccines. One of the most controversial vaccines in history in regards to autism and various injuries, and he doesn't know if there was a placebo control used in a study for it? Come on... This continues for a couple more minutes before Plotkin has to give up and say "I will look for the studies and provide them to you after the deposition". Guess what? He never provided those studies, as expected. Same thing Fauci did to RFK when asked. They know these studies don't exist, but they put on a show to save face. This is being knowingly dishonest. This is lying under oath. This is so wrong because the result of this lie and lack of proper safety studies is people being harmed or killed, or kids being brain damaged for life and suffering immensely. It's unforgiveable. There isn't a jail cell small enough for these criminals. One of the most damning clips from the deposition. Aaron Siri is a beast and deserves immense respect, on par with RFK.

Inversionism

759,666 просмотров • 2 лет назад

"Vaccine Ingredient Lists Are The Most Important Lists Parents Have NEVER Read." Ted Kuntz "There's No Possible Way That Injecting Animal Matter, Live Viruses & Toxins, Formaldehyde & Aluminum Actually Promotes Health." "There Are No Vaccine Ingredients That Promote Health..." Health Cannot Come Through A Needle...You Cannot Inject Health. Polysorbate 80 (Crosses the BBB) Thimerosal Mercury (Neurotoxin) Aluminum (Neurotoxin) Formaldehyde (Neurotoxin) mRNA (DNA Contaminant) M59 Squalene (Neurotoxin) Acetone (Crosses the BBB) Sodium Borate (Borax Neurotoxin) 2-Phenoxyethanol (Crosses the BBB) SV40 (Virus Contaminant) Triton X-100 (Bacterial Toxin) Bovine Calf Serum (Foreign DNA) Poultry Serum (Foreign DNA) Poultry Byproducts (Foreign DNA) Animal Organs Used To Make Vaccines: MDCK: Madin Darby Canine Kidney, female Cocker Spaniel VERO: African Green Monkey Kidney FRHL: Fetal Rhesus Monkey Lung CHO: Chinese Hamster Ovary PK-15: Pork Kidney RK-13: Rabbit Kidney SIRC: Rabbit Cornea The vaccine industry is built on the use of aborted babies organs to produce the vaccines we use today…and they have to replace these lines with current aborted organs. The most recent harvested human organ used in a vaccine is WALVAX-2 which is a harvested lung from a 3 month old unborn baby taken in 2015. This was one baby of 10 in total, in which organs were harvested for research & vaccine development. Take a look ⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in: HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A & Shingles RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid IMR-90: Lung from a 16 week old fetus; to replace the WI-38 line WALVAX-2: Lung from a 3 month old fetus; to replace the WI-38 and MRC-5 line 👇2015 Organs Harvested For WALVAX-2👇 👇Human Fetal Tissue & Organ Trafficking👇 👇Vaccine Excipient Summary List👇 Speakers: Ted Kuntz & Nico Laganiere Video: Vaccine Choice Canada

"Vaccine Ingredient Lists Are The Most Important Lists Parents Have NEVER Read." Ted Kuntz "There's No Possible Way That Injecting Animal Matter, Live Viruses & Toxins, Formaldehyde & Aluminum Actually Promotes Health." "There Are No Vaccine Ingredients That Promote Health..." Health Cannot Come Through A Needle...You Cannot Inject Health. Polysorbate 80 (Crosses the BBB) Thimerosal Mercury (Neurotoxin) Aluminum (Neurotoxin) Formaldehyde (Neurotoxin) mRNA (DNA Contaminant) M59 Squalene (Neurotoxin) Acetone (Crosses the BBB) Sodium Borate (Borax Neurotoxin) 2-Phenoxyethanol (Crosses the BBB) SV40 (Virus Contaminant) Triton X-100 (Bacterial Toxin) Bovine Calf Serum (Foreign DNA) Poultry Serum (Foreign DNA) Poultry Byproducts (Foreign DNA) Animal Organs Used To Make Vaccines: MDCK: Madin Darby Canine Kidney, female Cocker Spaniel VERO: African Green Monkey Kidney FRHL: Fetal Rhesus Monkey Lung CHO: Chinese Hamster Ovary PK-15: Pork Kidney RK-13: Rabbit Kidney SIRC: Rabbit Cornea The vaccine industry is built on the use of aborted babies organs to produce the vaccines we use today…and they have to replace these lines with current aborted organs. The most recent harvested human organ used in a vaccine is WALVAX-2 which is a harvested lung from a 3 month old unborn baby taken in 2015. This was one baby of 10 in total, in which organs were harvested for research & vaccine development. Take a look ⬇️ these are the 'code names' for harvested organs used to make vaccines, their original source & what vaccines they are used in: HEK-293: Human Embryo Kidney, aborted female; used in development of Ebola & Covid MRC-5: Human Lung, 14 week old aborted male; used in Polio, Rabies, Chickenpox, Hep A & Shingles WI-38: Human Lung, 12 week old aborted female; used in Polio, Rabies, Chickenpox, Hep A & Shingles RA 27-3: Human Kidney, 6 weeks old, used in the Rubella & MMR PER-C6: Human Retina, 18 weeks old, used in the development of Ebola & Covid IMR-90: Lung from a 16 week old fetus; to replace the WI-38 line WALVAX-2: Lung from a 3 month old fetus; to replace the WI-38 and MRC-5 line 👇2015 Organs Harvested For WALVAX-2👇 👇Human Fetal Tissue & Organ Trafficking👇 👇Vaccine Excipient Summary List👇 Speakers: Ted Kuntz & Nico Laganiere Video: Vaccine Choice Canada

Valerie Anne Smith

44,276 просмотров • 1 год назад

Listen to this horrifying discussion between RFK and Dr. Theresa Deisher about the use of aborted fetuses in vaccine research. Did you know that the fetal cells used to study vaccines and "grow viruses" are harvested from the hearts of fetuses that are still alive? They literally crank open their chest, harvest cells from the heart while it's still beating, and do all this WITHOUT any anesthesia. It has it be from an alive beating heart. You can see how dumbfounded and disgusted RFK is when learning the full scope of this. Every part of the aborted fetus is sold once it's euthanized as well. The heart, thymus, kidney, etc, are sold for various types of scientific research, much of it for vaccines and drug research, but some of it is sold for beauty products, food flavoring research, and numerous other industries. We have an entire economy built around the use of dead fetuses. It's treated like a commodity, and the organizations performing these abortions are making immense amounts of money from it, while also lobbying for "women's right to choose". What if the abortion issue has nothing to do with women's rights, but is instead driven by just profit motive and this barbaric and evil vaccine industry? How can anyone consider this acceptable? How cold and soulless do you have to be to think this is okay?

Listen to this horrifying discussion between RFK and Dr. Theresa Deisher about the use of aborted fetuses in vaccine research. Did you know that the fetal cells used to study vaccines and "grow viruses" are harvested from the hearts of fetuses that are still alive? They literally crank open their chest, harvest cells from the heart while it's still beating, and do all this WITHOUT any anesthesia. It has it be from an alive beating heart. You can see how dumbfounded and disgusted RFK is when learning the full scope of this. Every part of the aborted fetus is sold once it's euthanized as well. The heart, thymus, kidney, etc, are sold for various types of scientific research, much of it for vaccines and drug research, but some of it is sold for beauty products, food flavoring research, and numerous other industries. We have an entire economy built around the use of dead fetuses. It's treated like a commodity, and the organizations performing these abortions are making immense amounts of money from it, while also lobbying for "women's right to choose". What if the abortion issue has nothing to do with women's rights, but is instead driven by just profit motive and this barbaric and evil vaccine industry? How can anyone consider this acceptable? How cold and soulless do you have to be to think this is okay?

Inversionism

455,978 просмотров • 2 лет назад

Dr. Suzanne Humphries: What if the very method of vaccine creation was its greatest flaw? We're told vaccines are a miracle of modern science. But how are they actually made? It starts by extracting a virus from a sick human or animal. This live, virulent virus then must be "attenuated" – weakened. How? By serial passage. They incubate it through a series of foreign cell lines to force it to mutate. Think: human amniotic cells, chicken embryo cells, and most notoriously... monkey kidney cells. But then, they need to mass-produce it. This is where it gets even more concerning. To multiply the virus for millions of doses, they grow it on rapidly dividing cell cultures. Some of these are: ➡️ Madin-Darby Canine Kidney (MDCK) cells (from a cocker spaniel, made tumorigenic so they multiply forever). ➡️ WI-38 & MRC-5 cells (fibroblasts from human fetal lung tissue, originating from elective abortions in the 1960s). These aren't conspiracy theories. They are listed right on the package inserts. You are not just being injected with a "weakened virus." You are being injected with a biological soup of foreign animal DNA, cell debris, and growth medium residuals. The obvious question: What unknown pathogens hitch a ride? History gives us the answer. For 30 years, a cancer-causing monkey virus—SV40—was injected into millions via the polio vaccine before it was "discovered" and acknowledged. It is now heavily associated with human tumors. And SV40 is not alone. Third-party researchers have repeatedly found stray viruses, retroviruses, and other contaminants that were not tested for. Why? Because you can't test for something you don't know exists. The entire process is built on a foundation of biological cross-contamination. We are playing a complex game of genetic roulette, trusting that no new unknown virus is silently passed along. This isn't anti-science. This is PRO-transparency and real safety. It's time to ask the hard questions they don't want to answer. What are we really injecting? What long-term effects are we ignoring?

Dr. Suzanne Humphries: What if the very method of vaccine creation was its greatest flaw? We're told vaccines are a miracle of modern science. But how are they actually made? It starts by extracting a virus from a sick human or animal. This live, virulent virus then must be "attenuated" – weakened. How? By serial passage. They incubate it through a series of foreign cell lines to force it to mutate. Think: human amniotic cells, chicken embryo cells, and most notoriously... monkey kidney cells. But then, they need to mass-produce it. This is where it gets even more concerning. To multiply the virus for millions of doses, they grow it on rapidly dividing cell cultures. Some of these are: ➡️ Madin-Darby Canine Kidney (MDCK) cells (from a cocker spaniel, made tumorigenic so they multiply forever). ➡️ WI-38 & MRC-5 cells (fibroblasts from human fetal lung tissue, originating from elective abortions in the 1960s). These aren't conspiracy theories. They are listed right on the package inserts. You are not just being injected with a "weakened virus." You are being injected with a biological soup of foreign animal DNA, cell debris, and growth medium residuals. The obvious question: What unknown pathogens hitch a ride? History gives us the answer. For 30 years, a cancer-causing monkey virus—SV40—was injected into millions via the polio vaccine before it was "discovered" and acknowledged. It is now heavily associated with human tumors. And SV40 is not alone. Third-party researchers have repeatedly found stray viruses, retroviruses, and other contaminants that were not tested for. Why? Because you can't test for something you don't know exists. The entire process is built on a foundation of biological cross-contamination. We are playing a complex game of genetic roulette, trusting that no new unknown virus is silently passed along. This isn't anti-science. This is PRO-transparency and real safety. It's time to ask the hard questions they don't want to answer. What are we really injecting? What long-term effects are we ignoring?

Camus

60,406 просмотров • 11 месяцев назад