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Studies Confirm FLU Vaccines Increase Infections & Have Negative Efficacy. 27% Increase In Contracting Flu Infections. 440% Increase In Contracting Non-Flu Infections Such As COVID & Pneumonia. Multi-Dose Vials Used In Large Corporate Settings Still Contain Thimerosal Mercury. Effectiveness of the Influenza Vaccine During the 2024-2025 Respiratory Viral Season...

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Valerie Anne Smith

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95,893 views • 9 months ago •via X (Twitter)

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FLUZONE Flu Vaccine...Approved For 6 Month Old Infants. Causes Guillain Barre Syndrome Paralysis. Contains Neurotoxin Formaldehyde Which Causes Leukemia. 4 Flu Strains Grown In Fertilized Chicken Egg--Warning For Future Egg Allergy. No Clinical Safety Study Prior To Approval. ---Ingredients--- 4 Strains of influenza Fertilized embryonic chicken egg (causes egg allergy) Formaldehyde (neurotoxin & causes leukemia) Triton X-100 (detergent/hormone disruptor) Hemagglutinin HA Antigen (harmful host cell) Phosphate solution (toxic to bones) ---European Union Bans Triton X-100--- Triton™ X-100, a detergent with a hydrophilic polyethylene oxide chain has found widespread use in the biopharmaceutical industry. Even though it is used heavily throughout the industry, the degradation products from Triton™ X-100 exhibit long-lasting estrogenic properties in fish, birds & mammals, causing chronic harm to their endocrine systems. ---Hemagglutinin HA Antigen--- Influenza virus hemagglutinin facilitates infection by allowing the virus to bind to & enter host cells, making the virus dangerous. ---Warnings & Precautions--- Causal for Guillain Barre Syndrome Paralysis like Polio. Do not administer to anyone with an egg allergy, if egg allergy is known in a 6 month old infant. Emergency procedures must be in place in case of anaphylaxis. ---Clinical Trials--- No clinical trial was done, no safety trial & no placebo. 1,419 children age 6 months thru 35 months were injected & then blood serum tested to check for antibody titers. ---Post Marketing Adverse Events & Injuries--- Guillain-Barré syndrome (GBS) Convulsions Myelitis Encephalomyelitis Transverse myelitis Facial palsy (Bell’s Palsy) Optic neuritis/neuropathy Brachial neuritis (paralysis) Syncope Anaphylaxis Angioedema Thrombocytopenia Lymphadenopathy Vasculitis Stevens Johnson Syndrome High fever Loss of appetite Extreme fatigue Apnea ---Vaxxed Verses Unvaxxed Studies--- 2025 flu vaccine efficacy rate is only 32%. Studies on inactivated influenza vaccines show 4.4 times greater risk of getting the flu after a flu vaccination as compared to those unvaccinated. 👇Fluzone Vaccine Package Insert👇 👇Influenza Vaccine Adverse Events Reports👇 👇Flu Vaccine Increases Risk Of Getting The Flu👇 Speaker: Dr Jeffrey Barke, MD
2:07

FLUZONE Flu Vaccine...Approved For 6 Month Old Infants. Causes Guillain Barre Syndrome Paralysis. Contains Neurotoxin Formaldehyde Which Causes Leukemia. 4 Flu Strains Grown In Fertilized Chicken Egg--Warning For Future Egg Allergy. No Clinical Safety Study Prior To Approval. ---Ingredients--- 4 Strains of influenza Fertilized embryonic chicken egg (causes egg allergy) Formaldehyde (neurotoxin & causes leukemia) Triton X-100 (detergent/hormone disruptor) Hemagglutinin HA Antigen (harmful host cell) Phosphate solution (toxic to bones) ---European Union Bans Triton X-100--- Triton™ X-100, a detergent with a hydrophilic polyethylene oxide chain has found widespread use in the biopharmaceutical industry. Even though it is used heavily throughout the industry, the degradation products from Triton™ X-100 exhibit long-lasting estrogenic properties in fish, birds & mammals, causing chronic harm to their endocrine systems. ---Hemagglutinin HA Antigen--- Influenza virus hemagglutinin facilitates infection by allowing the virus to bind to & enter host cells, making the virus dangerous. ---Warnings & Precautions--- Causal for Guillain Barre Syndrome Paralysis like Polio. Do not administer to anyone with an egg allergy, if egg allergy is known in a 6 month old infant. Emergency procedures must be in place in case of anaphylaxis. ---Clinical Trials--- No clinical trial was done, no safety trial & no placebo. 1,419 children age 6 months thru 35 months were injected & then blood serum tested to check for antibody titers. ---Post Marketing Adverse Events & Injuries--- Guillain-Barré syndrome (GBS) Convulsions Myelitis Encephalomyelitis Transverse myelitis Facial palsy (Bell’s Palsy) Optic neuritis/neuropathy Brachial neuritis (paralysis) Syncope Anaphylaxis Angioedema Thrombocytopenia Lymphadenopathy Vasculitis Stevens Johnson Syndrome High fever Loss of appetite Extreme fatigue Apnea ---Vaxxed Verses Unvaxxed Studies--- 2025 flu vaccine efficacy rate is only 32%. Studies on inactivated influenza vaccines show 4.4 times greater risk of getting the flu after a flu vaccination as compared to those unvaccinated. 👇Fluzone Vaccine Package Insert👇 👇Influenza Vaccine Adverse Events Reports👇 👇Flu Vaccine Increases Risk Of Getting The Flu👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

68,458 views • 11 months ago

"Are the flu shots safe & effective? Absolutely NOT." -Dr Jeff Barke, MD "Stop listening to the media. Stop going to pharmacies. Start taking care of your own body." "We don't have a flu season...we have a drink too much, eat like crap, stay indoors & not enough sleep season." The Peer Reviewed Studies Showing Negative Efficacy... - Cleveland Clinic Study (Shrestha et al., 2024-2025 season): Those Vaccinated had a -26.9% effectiveness against flu. Translation? You are 27% more likely to get the flu. - Cowling study: Flu vaccine recipients faced 4.4X higher rate of non-flu infections...COVID & pneumonia, which is 440%! FLU-ZONE Ingredients... -Thimerosal Mercury in multi-dose vials used in hospital, pharmacy & corporate locations -Formaldehyde -Triton X 100 -Fertilized chicken eggs -Phosphate buffers (bone-toxic) -Lab-grown hemagglutinin antigens from harmful host cells Post-marketing reports adverse events... - Guillain-Barré Syndrome (GBS) - Anaphylaxis & angioedema -Encephalomyelitis -Bell's palsy -Convulsions -Optic neuropathy -Thrombocytopenia -Apnea -Brachial neuritis -Stevens Johnson Syndrome Have you ever gotten a flu shot? Did it harm your health? Share your experience below...
3:42

"Are the flu shots safe & effective? Absolutely NOT." -Dr Jeff Barke, MD "Stop listening to the media. Stop going to pharmacies. Start taking care of your own body." "We don't have a flu season...we have a drink too much, eat like crap, stay indoors & not enough sleep season." The Peer Reviewed Studies Showing Negative Efficacy... - Cleveland Clinic Study (Shrestha et al., 2024-2025 season): Those Vaccinated had a -26.9% effectiveness against flu. Translation? You are 27% more likely to get the flu. - Cowling study: Flu vaccine recipients faced 4.4X higher rate of non-flu infections...COVID & pneumonia, which is 440%! FLU-ZONE Ingredients... -Thimerosal Mercury in multi-dose vials used in hospital, pharmacy & corporate locations -Formaldehyde -Triton X 100 -Fertilized chicken eggs -Phosphate buffers (bone-toxic) -Lab-grown hemagglutinin antigens from harmful host cells Post-marketing reports adverse events... - Guillain-Barré Syndrome (GBS) - Anaphylaxis & angioedema -Encephalomyelitis -Bell's palsy -Convulsions -Optic neuropathy -Thrombocytopenia -Apnea -Brachial neuritis -Stevens Johnson Syndrome Have you ever gotten a flu shot? Did it harm your health? Share your experience below...

Valerie Anne Smith

16,571 views • 6 months ago

The Truth Is Out... The Flu Vaccine Not Only DOESN'T Prevent Influenza & DOESN'T Lessen It's Symptoms... If You Get The Flu Vaccine You Are 27% MORE Likely To Get Influenza. A Recent Cleveland Clinic Study Reveals The Influenza Vaccine Carries A Negative Efficacy Of 26.9%! From The Study..."53,402 Cleveland Clinic employees were followed & studied for 25 weeks during the 2024-2025 flu season. Over the course of the study the cumulative incidence of influenza increased more rapidly among the vaccinated than the unvaccinated. Yielding a calculated vaccine effectiveness of −26.9%." The flu shot not only primes you for flu, it primes you for Coronavirus at 36% increased rate. Nordic Cochrane Group & British Medical Journal both have found, people are 4.4 times more likely to get a non flu infection. Many people get the flu shot & then get sick. They are getting an indistinguishable illness from the flu. The flu shot gives you pathogenic priming. It injures your immune system so that you're more likely to get a non flu viral upper respiratory infection. In fact, the PENTAGON published a study, in which they said the flu shot not only primes you for flu, it primes you for coronavirus. To determine military readiness, they had a placebo group & a vaccine group, to determine if the flu shot was protective against Coronavirus. The results showed those who received the flu shot were 36% more likely to get Coronavirus. That is not a lone study, there are at least 6 other major studies showing the same thing, if you get the flu shot, you're more likely to get Coronavirus. Flu Shot Ingredients: If you wouldn't eat or drink it, you wouldn't want to inject it either. MDCK: Canine Cocker Spaniel Kidney DNA M59 Adjuvant Squalene Oil: GMO Microbial caused 95% Gulf War Syndrome to Soldiers. MSG: Neurotoxin, Reproductive & Developmental Harm. Formaldehyde: Carcinogen & Poisonous to Internal Organs. Thimerosal Mercury: One of The Most Poisonous Substances Known. Even Minute Amounts Cause Damage. Aluminum: Cause of brain damage, dementia, seizures, coma & autism. Baculovirus Cell DNA: Virus insect pathogens. Neomycin Sulfate: Antibiotic that blocks B6 absorption causing uptake error epilepsy & antibiotic resistance. Polysorbate 80: Carcinogen that crosses the blood brain barrier. Phosphates: Toxic to bones & organs 👇Flu Vaccine 2024-2025 Negative Efficacy👇 👇Dept Of Defense Flu Vaccine Study👇 👇Flu Vaccine Causes 4.4 Times More Illness👇 Speakers: The Jimmy Dore Show & Dr John Campbell
1:23

The Truth Is Out... The Flu Vaccine Not Only DOESN'T Prevent Influenza & DOESN'T Lessen It's Symptoms... If You Get The Flu Vaccine You Are 27% MORE Likely To Get Influenza. A Recent Cleveland Clinic Study Reveals The Influenza Vaccine Carries A Negative Efficacy Of 26.9%! From The Study..."53,402 Cleveland Clinic employees were followed & studied for 25 weeks during the 2024-2025 flu season. Over the course of the study the cumulative incidence of influenza increased more rapidly among the vaccinated than the unvaccinated. Yielding a calculated vaccine effectiveness of −26.9%." The flu shot not only primes you for flu, it primes you for Coronavirus at 36% increased rate. Nordic Cochrane Group & British Medical Journal both have found, people are 4.4 times more likely to get a non flu infection. Many people get the flu shot & then get sick. They are getting an indistinguishable illness from the flu. The flu shot gives you pathogenic priming. It injures your immune system so that you're more likely to get a non flu viral upper respiratory infection. In fact, the PENTAGON published a study, in which they said the flu shot not only primes you for flu, it primes you for coronavirus. To determine military readiness, they had a placebo group & a vaccine group, to determine if the flu shot was protective against Coronavirus. The results showed those who received the flu shot were 36% more likely to get Coronavirus. That is not a lone study, there are at least 6 other major studies showing the same thing, if you get the flu shot, you're more likely to get Coronavirus. Flu Shot Ingredients: If you wouldn't eat or drink it, you wouldn't want to inject it either. MDCK: Canine Cocker Spaniel Kidney DNA M59 Adjuvant Squalene Oil: GMO Microbial caused 95% Gulf War Syndrome to Soldiers. MSG: Neurotoxin, Reproductive & Developmental Harm. Formaldehyde: Carcinogen & Poisonous to Internal Organs. Thimerosal Mercury: One of The Most Poisonous Substances Known. Even Minute Amounts Cause Damage. Aluminum: Cause of brain damage, dementia, seizures, coma & autism. Baculovirus Cell DNA: Virus insect pathogens. Neomycin Sulfate: Antibiotic that blocks B6 absorption causing uptake error epilepsy & antibiotic resistance. Polysorbate 80: Carcinogen that crosses the blood brain barrier. Phosphates: Toxic to bones & organs 👇Flu Vaccine 2024-2025 Negative Efficacy👇 👇Dept Of Defense Flu Vaccine Study👇 👇Flu Vaccine Causes 4.4 Times More Illness👇 Speakers: The Jimmy Dore Show & Dr John Campbell

Valerie Anne Smith

38,938 views • 1 year ago

The American Academy of Pediatrics Wants To Ban All Religious & Philosophical Vaccine Exemptions. Mandating The 72 Doses On The Childhood Vaccine Schedule Assures Pediatricians Of Their Continued 50% Revenue Stream. Making Vaxelis 6-in-1 Vaccine Mandatory Is Criminal & Unjust. If Parents Read The Package Insert, No One In Their Right Mind Would Ever Inject Their Child Again. Not A Single Safety Study Against A Placebo & 6 Infants Died During The Trial. Anaphylaxis & Allergy Warning: Epinephrine & other appropriate agents & equipment must be available for immediate use in case an anaphylactic or acute hypersensitivity reaction occurs. 'Institute Of Medicine' Review: Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Ingredients: Each dose, in a 3 injection series Diphtheria Vaccine Tetanus Toxoid Vaccine Pertussis Vaccine Polio Vaccine HIB & Hep-B Vaccines Polysorbate 80 Formaldehyde Aluminum Phosphate Amorphous Aluminium Hydroxyphosphate Sulfate Recombinant DNA Yeast Vero African Green Monkey Kidney cell line, Ammonium Thiocyanate Glutaraldehyde Neomycin Streptomycin Polymyxin B Bovine serum albumin Clinical Safety Trial Studies: 6 clinical trials were all run without an inert placebo. One group received the Vaxelis 6 in 1 experimental vaccine. The other group received the 5 in 1 Penta vaccine with added Hep-B. Both groups received the same 6 vaccines. There was no placebo group to compare vaccine injuries. Clinical Safety Trial Deaths: In one of the 6 safety studies, 68 infants suffered a serious adverse event. Of these adverse event injuries, 6 infants died. The reported 'causes of death' were: Sepsis, SIDS & Hydrocephalus. Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Bell's palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder 👇AAP Calls To Ban Vaccine Exemptions👇 👇Hexavalent Vaccines & Sudden Death👇 👇National Vaccine Information Center👇 👇Vaxelis Vaccine Package Insert For Physicians👇 Speaker: Dr Jeffrey Barke, MD
2:33

The American Academy of Pediatrics Wants To Ban All Religious & Philosophical Vaccine Exemptions. Mandating The 72 Doses On The Childhood Vaccine Schedule Assures Pediatricians Of Their Continued 50% Revenue Stream. Making Vaxelis 6-in-1 Vaccine Mandatory Is Criminal & Unjust. If Parents Read The Package Insert, No One In Their Right Mind Would Ever Inject Their Child Again. Not A Single Safety Study Against A Placebo & 6 Infants Died During The Trial. Anaphylaxis & Allergy Warning: Epinephrine & other appropriate agents & equipment must be available for immediate use in case an anaphylactic or acute hypersensitivity reaction occurs. 'Institute Of Medicine' Review: Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Ingredients: Each dose, in a 3 injection series Diphtheria Vaccine Tetanus Toxoid Vaccine Pertussis Vaccine Polio Vaccine HIB & Hep-B Vaccines Polysorbate 80 Formaldehyde Aluminum Phosphate Amorphous Aluminium Hydroxyphosphate Sulfate Recombinant DNA Yeast Vero African Green Monkey Kidney cell line, Ammonium Thiocyanate Glutaraldehyde Neomycin Streptomycin Polymyxin B Bovine serum albumin Clinical Safety Trial Studies: 6 clinical trials were all run without an inert placebo. One group received the Vaxelis 6 in 1 experimental vaccine. The other group received the 5 in 1 Penta vaccine with added Hep-B. Both groups received the same 6 vaccines. There was no placebo group to compare vaccine injuries. Clinical Safety Trial Deaths: In one of the 6 safety studies, 68 infants suffered a serious adverse event. Of these adverse event injuries, 6 infants died. The reported 'causes of death' were: Sepsis, SIDS & Hydrocephalus. Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Bell's palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder 👇AAP Calls To Ban Vaccine Exemptions👇 👇Hexavalent Vaccines & Sudden Death👇 👇National Vaccine Information Center👇 👇Vaxelis Vaccine Package Insert For Physicians👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

317,432 views • 11 months ago

2.23 Million-Person Study Finds Pneumococcal Vaccines Increase Risk Of Pneumonia & Death. Rather Than Prevention, Risk Of Pneumonia Increased +83% & Risk Of Death Increased +91%. There Have Been 5 Pneumonia Vaccines, All Were 'Safety Tested' Using Another Vaccine As 'Placebo.' The pneumococcal vaccines that are given to nearly every US child & senior adult are linked to higher pneumonia & death rates in one of the largest real-world studies ever conducted. Health authorities have promoted getting a Pneumonia Vaccine as a 'crucial' tool to prevent serious bacterial pneumonia. Tens of millions of doses are given every year. Infants receive a 4 dose series & adults over 50 are urged to get vaccinated. Now, a landmark population-based study published in BMC Infectious Diseases has completely dismantled the rationale for current pneumococcal conjugate vaccine (PCV) recommendations. The study authors found that recipients were significantly more likely to be hospitalized for pneumonia & more likely to die from pneumonia-related causes compared to their unvaccinated counterparts. Risk of pneumonia increased +83% & risk of death increased +91%. All 5 Pneumococcal Vaccines are built on the same biological platform. Each newer version contains all of the same serotypes included in PCV13, plus additional ones, using the same diphtheria-derived carrier protein (CRM197) & aluminum adjuvant system. Safety Study Placebos Used For Each Vaccine... Pneumovax 23 used the HEP-A & HEP-B vaccines as placebo. Prevnar 20 used the Prevnar 13 vaccine as placebo. Prevnar 13 used the Prevnar 9 vaccine as placebo. Prevnar 9 used the Prevnar 7 vaccine as placebo. Prevnar 7 used the DTP-HIB vaccine as placebo. Harmful Ingredients In Each Of The Pneumonia Vaccines... 1⃣ Pneumonia Strains conjugated to diphtheria toxoid CRM197 protein, which carries the risk of Bovine Spongiform Encephalopathy also known as Mad Cow Disease, because of how the diphtheria toxoid is 'grown.' 2⃣ Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant, is a known neurotoxin. The amount in the vaccine, 125 mcg, is 8X the limit of aluminum safe for a 7lb infant for direct injection, per FDA own standards of 5 mcg/per kg of weight as max aluminum limit. 3⃣ Polysorbate 80 weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions & adverse Cardiac Events. Post Marketing Injuries... 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. In the infant, the death will be classified as SIDS. In the adult, the death will be classified as SUDS or SADS, Sudden Unexpected Death Syndrome & Sudden Adult Death Syndrome. Serious Adverse Events... Guillain Barre Syndrome(full body paralysis) Cyanosis(cardiac distress) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant & Adult Sudden Apnea Heart Palpitations Acute Disseminated Encephalomyelitis (ADEM) Convulsions Seizure Transverse myelitis Systemic Inflammatory Response System (SIRS) 👇Vaccines Increase Risk Of Pneumonia & Death👇 👇Prevnar 20 Package Insert👇 👇Pneumonia Vaccine/Guillain Barre Syndrome👇 Speaker: Dr Jeffrey Barke, MD
0:58

2.23 Million-Person Study Finds Pneumococcal Vaccines Increase Risk Of Pneumonia & Death. Rather Than Prevention, Risk Of Pneumonia Increased +83% & Risk Of Death Increased +91%. There Have Been 5 Pneumonia Vaccines, All Were 'Safety Tested' Using Another Vaccine As 'Placebo.' The pneumococcal vaccines that are given to nearly every US child & senior adult are linked to higher pneumonia & death rates in one of the largest real-world studies ever conducted. Health authorities have promoted getting a Pneumonia Vaccine as a 'crucial' tool to prevent serious bacterial pneumonia. Tens of millions of doses are given every year. Infants receive a 4 dose series & adults over 50 are urged to get vaccinated. Now, a landmark population-based study published in BMC Infectious Diseases has completely dismantled the rationale for current pneumococcal conjugate vaccine (PCV) recommendations. The study authors found that recipients were significantly more likely to be hospitalized for pneumonia & more likely to die from pneumonia-related causes compared to their unvaccinated counterparts. Risk of pneumonia increased +83% & risk of death increased +91%. All 5 Pneumococcal Vaccines are built on the same biological platform. Each newer version contains all of the same serotypes included in PCV13, plus additional ones, using the same diphtheria-derived carrier protein (CRM197) & aluminum adjuvant system. Safety Study Placebos Used For Each Vaccine... Pneumovax 23 used the HEP-A & HEP-B vaccines as placebo. Prevnar 20 used the Prevnar 13 vaccine as placebo. Prevnar 13 used the Prevnar 9 vaccine as placebo. Prevnar 9 used the Prevnar 7 vaccine as placebo. Prevnar 7 used the DTP-HIB vaccine as placebo. Harmful Ingredients In Each Of The Pneumonia Vaccines... 1⃣ Pneumonia Strains conjugated to diphtheria toxoid CRM197 protein, which carries the risk of Bovine Spongiform Encephalopathy also known as Mad Cow Disease, because of how the diphtheria toxoid is 'grown.' 2⃣ Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant, is a known neurotoxin. The amount in the vaccine, 125 mcg, is 8X the limit of aluminum safe for a 7lb infant for direct injection, per FDA own standards of 5 mcg/per kg of weight as max aluminum limit. 3⃣ Polysorbate 80 weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions & adverse Cardiac Events. Post Marketing Injuries... 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. In the infant, the death will be classified as SIDS. In the adult, the death will be classified as SUDS or SADS, Sudden Unexpected Death Syndrome & Sudden Adult Death Syndrome. Serious Adverse Events... Guillain Barre Syndrome(full body paralysis) Cyanosis(cardiac distress) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant & Adult Sudden Apnea Heart Palpitations Acute Disseminated Encephalomyelitis (ADEM) Convulsions Seizure Transverse myelitis Systemic Inflammatory Response System (SIRS) 👇Vaccines Increase Risk Of Pneumonia & Death👇 👇Prevnar 20 Package Insert👇 👇Pneumonia Vaccine/Guillain Barre Syndrome👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

41,343 views • 8 months ago

PENTACEL 5-in-1 Vaccine...approved for 6 week old infants. 4 dose series includes aluminum, polysorbate 80 & formaldehyde. No safety study against a placebo & 5 infants died during clinical trials. 'Institute of Medicine' cautions it causes guillain barre syndrome paralysis. ---Ingredients--- Diphtheria Tetanus Toxoid Pertussis Polio HIB Polysorbate 80 Streptomycin Glutaraldehyde Formaldehyde Aluminum Vero African Green Monkey Kidney cell line Neomycin Polymyxin B Bovine Calf Serum MRC-5 Human Lung ---Institute Of Medicine Review--- Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. ---Risk Of Apnea--- SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. ---Clinical Safety Trial Studies--- Clinical trials were all run without an inert placebo. One group received the Pentacel 5-in-1 vaccine. The other group received the 4-in-1 Quadrivalent vaccine with added HIB. Both groups received the same 5 vaccines. There was no placebo group to compare vaccine injuries. ---Safety Trial Deaths & Adverse Events--- Across all safety studies, 3.9% of infants suffered an SAE serious adverse event, such as pneumonia, asthma, bronchiolitis & gastroenteritis. Of these adverse event injuries, 5 infants died. The reported 'causes of death' was SIDS & Neuroblastoma. 8 infants suffered seizures. 2 cases of encephalopathy were documented. ---Post Marketing Adverse Events--- Cyanosis, Apnea, Anaphylaxis, Meningitis, Screaming, Inconsolable Crying, Depressed Nervous System. 👇Penta 5-in-1 Vaccines Death Study👇 👇Pentacel Vaccine Package Insert👇 👇Vaccine Excipient Summary List👇 Speaker: Dr Jeffrey Barke, MD
2:37

PENTACEL 5-in-1 Vaccine...approved for 6 week old infants. 4 dose series includes aluminum, polysorbate 80 & formaldehyde. No safety study against a placebo & 5 infants died during clinical trials. 'Institute of Medicine' cautions it causes guillain barre syndrome paralysis. ---Ingredients--- Diphtheria Tetanus Toxoid Pertussis Polio HIB Polysorbate 80 Streptomycin Glutaraldehyde Formaldehyde Aluminum Vero African Green Monkey Kidney cell line Neomycin Polymyxin B Bovine Calf Serum MRC-5 Human Lung ---Institute Of Medicine Review--- Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. ---Risk Of Apnea--- SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. ---Clinical Safety Trial Studies--- Clinical trials were all run without an inert placebo. One group received the Pentacel 5-in-1 vaccine. The other group received the 4-in-1 Quadrivalent vaccine with added HIB. Both groups received the same 5 vaccines. There was no placebo group to compare vaccine injuries. ---Safety Trial Deaths & Adverse Events--- Across all safety studies, 3.9% of infants suffered an SAE serious adverse event, such as pneumonia, asthma, bronchiolitis & gastroenteritis. Of these adverse event injuries, 5 infants died. The reported 'causes of death' was SIDS & Neuroblastoma. 8 infants suffered seizures. 2 cases of encephalopathy were documented. ---Post Marketing Adverse Events--- Cyanosis, Apnea, Anaphylaxis, Meningitis, Screaming, Inconsolable Crying, Depressed Nervous System. 👇Penta 5-in-1 Vaccines Death Study👇 👇Pentacel Vaccine Package Insert👇 👇Vaccine Excipient Summary List👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

209,935 views • 11 months ago

Shingles SHINGRIX Vaccine...grown in Chinese Hamster Ovary cells with an SV40 promoter. FDA Warning: Causes Guillain Barre Syndrome 'polio like' paralysis. 2025 Study: Shingrix causes 11X increase in vaccine induced Shingles. SV40 In The Production of Glaxosmithkline SHINGRIX...'Scientific Reports Journal (2016) Article 26446, Impact Of Promoters CHO & SV40' "The Shingrix vaccine is produced using immortalized Chinese hamster ovary (CHO) cells that contain a plasmid with an SV40 promoter to express the viral antigen." Description & ingredients...The mRNA gE antigen is obtained by culturing GMO genetically engineered Chinese Hamster Ovary cells. Shingrix contains AS01B, Phosphates, DOPC, MPL from the cell wall of Salmonella, QS21, Polysorbate 80 & Host Cell Protein & DNA. Post marketing serious adverse events... Guillain Barre Syndrome Lupus Gout Shingles Arthritis Myalgia Optic Ischemic Neuropathy Autoimmune Disease Death GI distress Arthralgia Neuropathy Pneumonia Influenza Neuralgia 2025 research study results...The primary care SCCS analysis found an 11X increase in shingles presentations within 21 days post vaccination. Precautions & warnings...Guillain Barré syndrome was observed during the 42 days following vaccination with SHINGRIX & Black Box Warning added in 2021. Anaphylaxis & Syncope is linked to SHINGRIX. Documented Lupus cases induced by the Shingrix vaccine.
2:47

Shingles SHINGRIX Vaccine...grown in Chinese Hamster Ovary cells with an SV40 promoter. FDA Warning: Causes Guillain Barre Syndrome 'polio like' paralysis. 2025 Study: Shingrix causes 11X increase in vaccine induced Shingles. SV40 In The Production of Glaxosmithkline SHINGRIX...'Scientific Reports Journal (2016) Article 26446, Impact Of Promoters CHO & SV40' "The Shingrix vaccine is produced using immortalized Chinese hamster ovary (CHO) cells that contain a plasmid with an SV40 promoter to express the viral antigen." Description & ingredients...The mRNA gE antigen is obtained by culturing GMO genetically engineered Chinese Hamster Ovary cells. Shingrix contains AS01B, Phosphates, DOPC, MPL from the cell wall of Salmonella, QS21, Polysorbate 80 & Host Cell Protein & DNA. Post marketing serious adverse events... Guillain Barre Syndrome Lupus Gout Shingles Arthritis Myalgia Optic Ischemic Neuropathy Autoimmune Disease Death GI distress Arthralgia Neuropathy Pneumonia Influenza Neuralgia 2025 research study results...The primary care SCCS analysis found an 11X increase in shingles presentations within 21 days post vaccination. Precautions & warnings...Guillain Barré syndrome was observed during the 42 days following vaccination with SHINGRIX & Black Box Warning added in 2021. Anaphylaxis & Syncope is linked to SHINGRIX. Documented Lupus cases induced by the Shingrix vaccine.

Valerie Anne Smith

147,839 views • 4 months ago

MenQuadfi Meningitis Vaccine...Newly Approved For 6 Week Old Infants. If People Read The Package Insert, No One Would Consent To This Injection. Another Vaccine That's Causative For Guillain Barre Syndrome & Bell's Palsy. Another Vaccine NOT Safety Tested Against A Placebo. --Ingredients-- 40 mcg (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate --Tetanus Toxoid Protein Carrier-- Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-has never been safety tested nor studied in a vaccine trial. --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of MenQuadfi was the Meningitis Vaccine Menveo. The safety trial 'placebo' used to prove the safety of Menveo was the Meningitis Vaccine Menactra The safety trial 'placebo' used to prove the safety of Menactra was the Meningitis Vaccine Menomune. Menomune never underwent a placebo controlled trial either. Menomune used Menactra as it's safety trial 'placebo.' --Adverse Reactions & Post Marketing Injuries-- Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis --30% Of Meningitis Cases Not Covered By This Vaccine-- This vaccine covers 4 of the 5 strains of Meningitis, types A, C, W & Y. 30% of meningitis cases are caused by strain B, which this vaccine does not contain. --Carcinogenic Cancer Risk-- MenQuadfi has not been evaluated or safety tested for cancer or if it interferes with reproductive health. --Long Term Efficacy-- Quadrivalent (4 strain) Meningitis Vaccines lose effectiveness within 5yrs. The CDC recommends MenQuadfi & all Quadrivalent Meningitis Vaccines be readministered every 5yrs for life. 👇MenQuadfi Package Insert👇 👇SIRVA Shoulder Injury From Meningitis Vaccine👇 👇Quad Meningitis Vaccine Adverse Events👇 Speaker: Dr Jeffrey Barke, MD
2:30

MenQuadfi Meningitis Vaccine...Newly Approved For 6 Week Old Infants. If People Read The Package Insert, No One Would Consent To This Injection. Another Vaccine That's Causative For Guillain Barre Syndrome & Bell's Palsy. Another Vaccine NOT Safety Tested Against A Placebo. --Ingredients-- 40 mcg (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate --Tetanus Toxoid Protein Carrier-- Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-has never been safety tested nor studied in a vaccine trial. --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of MenQuadfi was the Meningitis Vaccine Menveo. The safety trial 'placebo' used to prove the safety of Menveo was the Meningitis Vaccine Menactra The safety trial 'placebo' used to prove the safety of Menactra was the Meningitis Vaccine Menomune. Menomune never underwent a placebo controlled trial either. Menomune used Menactra as it's safety trial 'placebo.' --Adverse Reactions & Post Marketing Injuries-- Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis --30% Of Meningitis Cases Not Covered By This Vaccine-- This vaccine covers 4 of the 5 strains of Meningitis, types A, C, W & Y. 30% of meningitis cases are caused by strain B, which this vaccine does not contain. --Carcinogenic Cancer Risk-- MenQuadfi has not been evaluated or safety tested for cancer or if it interferes with reproductive health. --Long Term Efficacy-- Quadrivalent (4 strain) Meningitis Vaccines lose effectiveness within 5yrs. The CDC recommends MenQuadfi & all Quadrivalent Meningitis Vaccines be readministered every 5yrs for life. 👇MenQuadfi Package Insert👇 👇SIRVA Shoulder Injury From Meningitis Vaccine👇 👇Quad Meningitis Vaccine Adverse Events👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

22,944 views • 1 year ago

"Not A SINGLE Childhood Vaccine Has Gone Through A Placebo Controlled Clinical Trial Before Being Injected Into Millions Of Children In America." Aaron Siri "It's Time For The Gov't To Be Honest...The 1st Hep-B Vaccine Was Only Tested For 5 Days On 147 Children With No Placebo!" 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. List Of 'Placebos' Used In Vaccine Clinical Trials: Hepatitis B Clinical Trial...Placebo Was Aluminum Adjuvant & Only Tested For 5 Days. Vaxelis 6 in 1 Vaccine Trial...Placebo Was DTaP, Polio, HIB & Hep-B Vaccines. HPV Gardasil Clinical Trial...Placebo Was Aluminum Adjuvant & Hep-A Vaccine. Hepatitis A Clinical Trial...Placebo Was Hep-B Vaccine. Influenza A Clinical Trial...Placebo Was Influenza B Vaccine. Meningitis Vaccine Clinical Trial...Placebo Was DTaP Vaccine. Pertussis Vaccine Clinical Trial...Placebo Was Diphtheria & Tetanus Vaccine. Prevnar-13 Pneumonia Clinical Trial...Placebo Was Prevnar-7 Vaccine. Prevnar-9 Pneumonia Clinical Trial...Placebo Was DTP-Hib Vaccine. Prevnar-23 Pneumonia Vaccine...Placebo Was Hep A & Hep-B Vaccine. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine. Chicken Pox Vaccine Clinical Trial...Placebo Was Diluted Chicken Pox Vaccine. Shingles Vaccine Clinical Trial...Placebo Was Diluted Shingles Vaccine. COVID-19 Vaccine Clinical Trial...Placebo Was Meningitis Vaccine. No true placebo in a vaccine clinical trial skews all results & makes all vaccines appear "safe & effective" because the adverse events, side effects & Injuries in both groups are the same. The absolute risk of suffering a serious adverse event from any vaccine is 1 in 20. We now know, because of vaccinated vs unvaccinated studies, unvaccinated children are always healthier & experience little to no chronic conditions compared to those who are vaccinated. Health Condition-- Vaccinated / Unvaccinated: • All Chronic Conditions -- 60% / 5.71% • Arthritis -- 16.67% / 0% • Heart Disease -- 48% / 0% • Diabetes -- 10% / 0% • Asthma -- 7.7% / 0% • Autism -- 3.2% / 0% • ADHD -- 9.4% / 0.47% • Cancer -- 6.0% / 0% Vaccinated children have: *⃣ 14X the rate of gastrointestinal disorders. *⃣ 21X the rate of ADD/ADHD. *⃣ 28X the rate of ear infections. 👇Pediatric Vaccine Clinical Trial Placebos👇 👇Vaccine Trial Placebo Development👇 👇Vaccinated Versus Unvaccinated Study👇 Speakers: Del Bigtree & Aaron Siri Podcast: The HighWire
1:57

"Not A SINGLE Childhood Vaccine Has Gone Through A Placebo Controlled Clinical Trial Before Being Injected Into Millions Of Children In America." Aaron Siri "It's Time For The Gov't To Be Honest...The 1st Hep-B Vaccine Was Only Tested For 5 Days On 147 Children With No Placebo!" 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. List Of 'Placebos' Used In Vaccine Clinical Trials: Hepatitis B Clinical Trial...Placebo Was Aluminum Adjuvant & Only Tested For 5 Days. Vaxelis 6 in 1 Vaccine Trial...Placebo Was DTaP, Polio, HIB & Hep-B Vaccines. HPV Gardasil Clinical Trial...Placebo Was Aluminum Adjuvant & Hep-A Vaccine. Hepatitis A Clinical Trial...Placebo Was Hep-B Vaccine. Influenza A Clinical Trial...Placebo Was Influenza B Vaccine. Meningitis Vaccine Clinical Trial...Placebo Was DTaP Vaccine. Pertussis Vaccine Clinical Trial...Placebo Was Diphtheria & Tetanus Vaccine. Prevnar-13 Pneumonia Clinical Trial...Placebo Was Prevnar-7 Vaccine. Prevnar-9 Pneumonia Clinical Trial...Placebo Was DTP-Hib Vaccine. Prevnar-23 Pneumonia Vaccine...Placebo Was Hep A & Hep-B Vaccine. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine. Chicken Pox Vaccine Clinical Trial...Placebo Was Diluted Chicken Pox Vaccine. Shingles Vaccine Clinical Trial...Placebo Was Diluted Shingles Vaccine. COVID-19 Vaccine Clinical Trial...Placebo Was Meningitis Vaccine. No true placebo in a vaccine clinical trial skews all results & makes all vaccines appear "safe & effective" because the adverse events, side effects & Injuries in both groups are the same. The absolute risk of suffering a serious adverse event from any vaccine is 1 in 20. We now know, because of vaccinated vs unvaccinated studies, unvaccinated children are always healthier & experience little to no chronic conditions compared to those who are vaccinated. Health Condition-- Vaccinated / Unvaccinated: • All Chronic Conditions -- 60% / 5.71% • Arthritis -- 16.67% / 0% • Heart Disease -- 48% / 0% • Diabetes -- 10% / 0% • Asthma -- 7.7% / 0% • Autism -- 3.2% / 0% • ADHD -- 9.4% / 0.47% • Cancer -- 6.0% / 0% Vaccinated children have: *⃣ 14X the rate of gastrointestinal disorders. *⃣ 21X the rate of ADD/ADHD. *⃣ 28X the rate of ear infections. 👇Pediatric Vaccine Clinical Trial Placebos👇 👇Vaccine Trial Placebo Development👇 👇Vaccinated Versus Unvaccinated Study👇 Speakers: Del Bigtree & Aaron Siri Podcast: The HighWire

Valerie Anne Smith

40,853 views • 1 year ago

Meningitis Vaccine...Newly Approved For 6 Week Old Infants. The 'Safety Trials' Caused 1 Child Out Of Every 20 To Suffer A Serious Vaccine Injury. The Injection Was Never Tested Against A Placebo & It Causes Anaphylaxis, Infant Death & Guillain Barre 'Polio Like Paralysis.' --MenQuadfi Meningitis Vaccine--Ingredients-- 40 mcg (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate --Tetanus Toxoid Protein Carrier-- Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow, causing a risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-has never been safety tested nor studied in a vaccine trial. --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of MenQuadfi was the Meningitis Vaccine Menveo. --Adverse Reactions & Post Marketing Injuries-- Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea (Sudden Infant Death) Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis --Recommended Frequency Of Injection-- The CDC recommends MenQuadfi & all Quadrivalent Meningitis Vaccines be readministered every 5yrs for life. 👇MenQuadfi Package Insert👇 👇Quad Meningitis Vaccine Adverse Events👇 👇SIRVA Shoulder Injury From Meningitis Vaccine👇 Speakers: Del Bigtree & Jefferey Jaxen Podcast: The HighWire
1:20

Meningitis Vaccine...Newly Approved For 6 Week Old Infants. The 'Safety Trials' Caused 1 Child Out Of Every 20 To Suffer A Serious Vaccine Injury. The Injection Was Never Tested Against A Placebo & It Causes Anaphylaxis, Infant Death & Guillain Barre 'Polio Like Paralysis.' --MenQuadfi Meningitis Vaccine--Ingredients-- 40 mcg (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate --Tetanus Toxoid Protein Carrier-- Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow, causing a risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-has never been safety tested nor studied in a vaccine trial. --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of MenQuadfi was the Meningitis Vaccine Menveo. --Adverse Reactions & Post Marketing Injuries-- Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea (Sudden Infant Death) Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis --Recommended Frequency Of Injection-- The CDC recommends MenQuadfi & all Quadrivalent Meningitis Vaccines be readministered every 5yrs for life. 👇MenQuadfi Package Insert👇 👇Quad Meningitis Vaccine Adverse Events👇 👇SIRVA Shoulder Injury From Meningitis Vaccine👇 Speakers: Del Bigtree & Jefferey Jaxen Podcast: The HighWire

Valerie Anne Smith

46,316 views • 1 year ago

Dr. Robert W Malone, MD explains to me why he voted to recommend the removal of thimerosal, a mercury-based preservative, from influenza vaccines during the recent CDC advisory panel meeting: "97% of all influenza vaccines currently administered in the United States are administered using single dose vials. That means that it comes in a little vial and it's got the rubber nib at the top, and the physician puts the syringe and the needle into that, draws out that one dose, hopefully changes the needle otherwise the needle's a little dull and it hurts more, and then administers it to the child or the adult. What that does is it minimizes the chance of introducing contamination by going through that rubber stopper - that nib, again and again and again, which is what you do with a multi-dose vial. So multi-dose vials are a little bit cheaper, but they are considerably more risky in terms of introducing contaminants into the jar that then get drawn out and injected into another patient. That could be a virus like Hepatitis B, it could be a bacterial contamination, it could be a fungal contamination, etc, etc. So, that's why in a multi-dose vial you have to put in some sort of preservative—and there are other approved preservatives other than thimerosal. So, in the interest of doing our best at this stage to take another move forward in eliminating the added dose of mercury to patients that receive an influenza vaccine - remember that they're going to get a vaccine every year, and the people that get it from a multi-dose vial today are likely to be the same ones that get from a multi-dose vial next year. So, the mercury doesn't get excreted very well. There is a cumulative effect. And so, the [ACIP] committee, I think wisely, voted to just say no to thimerosal containing multi-dose vials. Now, for some reason, the pharmaceutical industry and corporate media see this as some sort of existential threat - that eliminating 3% of the influenza doses that contain thimerosal is a crisis for the entire vaccine industry and their academic and media supporters. I don't get it, but that seems to be the meme, and the strange thing is that it has left media and pharma arguing in favor of injecting mercury into Americans. It just is horrible optics, it's not the right decision, and I think I applaud the committee for having the temerity to just say no."
3:46

Dr. Robert W Malone, MD explains to me why he voted to recommend the removal of thimerosal, a mercury-based preservative, from influenza vaccines during the recent CDC advisory panel meeting: "97% of all influenza vaccines currently administered in the United States are administered using single dose vials. That means that it comes in a little vial and it's got the rubber nib at the top, and the physician puts the syringe and the needle into that, draws out that one dose, hopefully changes the needle otherwise the needle's a little dull and it hurts more, and then administers it to the child or the adult. What that does is it minimizes the chance of introducing contamination by going through that rubber stopper - that nib, again and again and again, which is what you do with a multi-dose vial. So multi-dose vials are a little bit cheaper, but they are considerably more risky in terms of introducing contaminants into the jar that then get drawn out and injected into another patient. That could be a virus like Hepatitis B, it could be a bacterial contamination, it could be a fungal contamination, etc, etc. So, that's why in a multi-dose vial you have to put in some sort of preservative—and there are other approved preservatives other than thimerosal. So, in the interest of doing our best at this stage to take another move forward in eliminating the added dose of mercury to patients that receive an influenza vaccine - remember that they're going to get a vaccine every year, and the people that get it from a multi-dose vial today are likely to be the same ones that get from a multi-dose vial next year. So, the mercury doesn't get excreted very well. There is a cumulative effect. And so, the [ACIP] committee, I think wisely, voted to just say no to thimerosal containing multi-dose vials. Now, for some reason, the pharmaceutical industry and corporate media see this as some sort of existential threat - that eliminating 3% of the influenza doses that contain thimerosal is a crisis for the entire vaccine industry and their academic and media supporters. I don't get it, but that seems to be the meme, and the strange thing is that it has left media and pharma arguing in favor of injecting mercury into Americans. It just is horrible optics, it's not the right decision, and I think I applaud the committee for having the temerity to just say no."

Jan Jekielek

69,666 views • 1 year ago

🚨PENTACEL 5-in-1 Vaccine...approved for 6 week old infants. 4 dose series includes aluminum, polysorbate 80 & formaldehyde. No safety study against a placebo & 5 infants died during clinical trials. 'Institute of Medicine' cautions it causes guillain barre syndrome paralysis. ---Ingredients--- Diphtheria Tetanus Toxoid Pertussis Polio HIB Polysorbate 80 Streptomycin Glutaraldehyde Formaldehyde Aluminum Vero African Green Monkey Kidney cell line Neomycin Polymyxin B Bovine Calf Serum MRC-5 Human Lung ---Institute Of Medicine Review--- Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. ---Risk Of Apnea--- SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. ---Clinical Safety Trial Studies--- Clinical trials were all run without an inert placebo. One group received the Pentacel 5-in-1 vaccine. The other group received the 4-in-1 Quadrivalent vaccine with added HIB. Both groups received the same 5 vaccines. There was no placebo group to compare vaccine injuries. ---Safety Trial Deaths & Adverse Events--- Across all safety studies, 3.9% of infants suffered an SAE serious adverse event, such as pneumonia, asthma, bronchiolitis & gastroenteritis. Of these adverse event injuries, 5 infants died. The reported 'causes of death' was SIDS & Neuroblastoma. 8 infants suffered seizures. 2 cases of encephalopathy were documented. ---Post Marketing Adverse Events--- Cyanosis, Apnea, Anaphylaxis, Meningitis, Screaming, Inconsolable Crying, Depressed Nervous System.
2:31

🚨PENTACEL 5-in-1 Vaccine...approved for 6 week old infants. 4 dose series includes aluminum, polysorbate 80 & formaldehyde. No safety study against a placebo & 5 infants died during clinical trials. 'Institute of Medicine' cautions it causes guillain barre syndrome paralysis. ---Ingredients--- Diphtheria Tetanus Toxoid Pertussis Polio HIB Polysorbate 80 Streptomycin Glutaraldehyde Formaldehyde Aluminum Vero African Green Monkey Kidney cell line Neomycin Polymyxin B Bovine Calf Serum MRC-5 Human Lung ---Institute Of Medicine Review--- Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. ---Risk Of Apnea--- SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. ---Clinical Safety Trial Studies--- Clinical trials were all run without an inert placebo. One group received the Pentacel 5-in-1 vaccine. The other group received the 4-in-1 Quadrivalent vaccine with added HIB. Both groups received the same 5 vaccines. There was no placebo group to compare vaccine injuries. ---Safety Trial Deaths & Adverse Events--- Across all safety studies, 3.9% of infants suffered an SAE serious adverse event, such as pneumonia, asthma, bronchiolitis & gastroenteritis. Of these adverse event injuries, 5 infants died. The reported 'causes of death' was SIDS & Neuroblastoma. 8 infants suffered seizures. 2 cases of encephalopathy were documented. ---Post Marketing Adverse Events--- Cyanosis, Apnea, Anaphylaxis, Meningitis, Screaming, Inconsolable Crying, Depressed Nervous System.

Valerie Anne Smith

21,459 views • 22 days ago

Pertussis (Whooping Cough) Vaccine...Shocking Facts Everyone Should Know. The Vaccine Does Not Stop Infection Or Transmission. It Has Never Been Safety Tested With A Placebo & The Risk Of Serious Adverse Injury Is 1 in 25. Whooping Cough Outbreaks Occur Within The Vaccinated. Pertussis (Whooping Cough) Vaccine is part of the multi vaccination of TDaP &/or DTaP. Pertussis Vaccine is only available combined with Tetanus Toxoid & Diphtheria. Anaphylaxis & Allergy Warning: Epinephrine & other appropriate agents & equipment must be available for immediate use in case an anaphylactic or acute hypersensitivity reaction occurs. Institute Of Medicine Review: Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. Tetanus Toxoid Vaccine Manufacture: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. Minced beef heart is heated to boiling & the putrid environment allows the tetanus toxin to grow. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Diphtheria Toxin Vaccine Manufacture: C. Diphtheriae grown on fetal bovine serum then treated with Formaldehyde. Pertussis Antigen Vaccine Manufacture: B. Pertussis bacteria grown on dairy casein fermentation broth then treated with glutaraldehyde & formaldehyde. Warning To Those With Dairy & Latex Allergies: Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP & DTaP Vaccines. Many cases of fatal anaphylaxis are caused by this. Ingredients Of DTaP & TDaP Vaccines: Tetanus Toxoid Diphtheria Toxin Pertussis Antigen Polysorbate 80 Formaldehyde Glutaraldehyde Aluminum Adjuvant Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Facial palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder Placebo Safety Testing In Clinical Trials: Neither DTaP nor TDap were clinical safety tested against a true saline placebo. Each individual component was safety tested against the other 2 used as placebo. Pertussis safety trials used Diphtheria Toxoid & Tetanus Toxoid as placebos, thus skewing results with vaccine injuries in both groups making the pertussis vaccine appear safe. NNV Number Needed To Vaccinate For Efficacy: (The number of people needed to receive vaccination in order to prevent death or hospitalization.) 1,000,000 million people need to be vaccinated to prevent 1 death from pertussis. 100,000 people need to be vaccinated to prevent 1 ICU hospital admission. 10,000 people need to be vaccinated to prevent 1 hospital admission. 👇Pertussis Outbreaks Occur In The Vaccinated👇 👇Pertussis Vaccine Does Not Prevent Spread👇 👇Pertussis Vaccine Not Effective Against Infection👇 Speaker: Ted Kuntz & Nico Laganiere Video: Vaccine Choice Canada
0:54

Pertussis (Whooping Cough) Vaccine...Shocking Facts Everyone Should Know. The Vaccine Does Not Stop Infection Or Transmission. It Has Never Been Safety Tested With A Placebo & The Risk Of Serious Adverse Injury Is 1 in 25. Whooping Cough Outbreaks Occur Within The Vaccinated. Pertussis (Whooping Cough) Vaccine is part of the multi vaccination of TDaP &/or DTaP. Pertussis Vaccine is only available combined with Tetanus Toxoid & Diphtheria. Anaphylaxis & Allergy Warning: Epinephrine & other appropriate agents & equipment must be available for immediate use in case an anaphylactic or acute hypersensitivity reaction occurs. Institute Of Medicine Review: Tetanus Toxoid Vaccine causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. Tetanus Toxoid Vaccine Manufacture: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. Minced beef heart is heated to boiling & the putrid environment allows the tetanus toxin to grow. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Diphtheria Toxin Vaccine Manufacture: C. Diphtheriae grown on fetal bovine serum then treated with Formaldehyde. Pertussis Antigen Vaccine Manufacture: B. Pertussis bacteria grown on dairy casein fermentation broth then treated with glutaraldehyde & formaldehyde. Warning To Those With Dairy & Latex Allergies: Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP & DTaP Vaccines. Many cases of fatal anaphylaxis are caused by this. Ingredients Of DTaP & TDaP Vaccines: Tetanus Toxoid Diphtheria Toxin Pertussis Antigen Polysorbate 80 Formaldehyde Glutaraldehyde Aluminum Adjuvant Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Facial palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder Placebo Safety Testing In Clinical Trials: Neither DTaP nor TDap were clinical safety tested against a true saline placebo. Each individual component was safety tested against the other 2 used as placebo. Pertussis safety trials used Diphtheria Toxoid & Tetanus Toxoid as placebos, thus skewing results with vaccine injuries in both groups making the pertussis vaccine appear safe. NNV Number Needed To Vaccinate For Efficacy: (The number of people needed to receive vaccination in order to prevent death or hospitalization.) 1,000,000 million people need to be vaccinated to prevent 1 death from pertussis. 100,000 people need to be vaccinated to prevent 1 ICU hospital admission. 10,000 people need to be vaccinated to prevent 1 hospital admission. 👇Pertussis Outbreaks Occur In The Vaccinated👇 👇Pertussis Vaccine Does Not Prevent Spread👇 👇Pertussis Vaccine Not Effective Against Infection👇 Speaker: Ted Kuntz & Nico Laganiere Video: Vaccine Choice Canada

Valerie Anne Smith

34,879 views • 1 year ago

MEASLES MMR VACCINE...Informed Consent Straight From The Package Insert. The 2nd Listed Side Effect Is Vaccine Induced MEASLES. 'Safety Tested' For Only 42 Days Prior To US FDA Approval. This Live Virus Vaccine 'Sheds' For 30 Days, Causing Measles To Transmit To Other People. Banned In Japan For Causing Meningitis & Death. --Ingredients & Allergy Warnings-- Chicken Embryo cell culture (live fertilised chicken) Hydrolyzed Pig Gelatin (porcine origin) Human WI-38 Lung (3 month old Female) Wistar RA 27/3 (27th human fetus, 3rd harvested kidney) Recombinant GMO Human Albumin (Yeast origin) Fetal Bovine Serum (blood collected pregnant cow fetus) Neomycin (FDA banned in 2019 as unsafe) *⃣ The use of Fetal Bovine Serum carries contamination risk of endotoxins, mycoplasma virus & prion disease. --CONTRAINDICATIONS-- Anaphylaxis Reactions to those with allergies to the following ingredients: Egg, Chicken, Pork, Neomycin & Yeast. Those with low immunity can experience vaccine induced measles, mumps & rubella, febrile seizures, encephalitis, pneumonia & death. Do not administer MMR live vaccine to individuals who are pregnant or plan to become pregnant. Do not administer MMR live vaccine to individuals with temperatures above 101 degrees or to anyone with TB Tuberculosis. --ADVERSE REACTIONS-- Panniculitis (painful inflammatory bumps in skin) Measles (live vaccine induced) Vasculitis (autoimmune disease) Pancreatitis (acute pancreas damage) Thrombocytopenia (dangerous low platelet count) Anaphylaxis (fatal reactions) Chronic Bronchial Spasm (asthma) Arthritis (autoimmune disease) Encephalitis (fatal brain inflammation) GBS Guillain Barre Syndrome (autoimmune paralysis) Transverse Myelitis (spinal cord inflammation) Pneumonia & Stevens Johnson Syndrome Infant Hemorrhagic Edema (brain bleed stroke) Ear Nerve Deafness & Optic Eye Disease Severe Neurological Deformities --PREGNANCY RISKS-- MMR live vaccine is contraindicated for pregnancy as the live viruses transmit to the fetus resulting in adverse outcomes such as spontaneous abortion, stillbirth, premature delivery, congenital deformities & maternal harm. In 1993, Japan banned the MMR live vaccine after many injuries occurred in their child population. Serious injuries of Meningitis & sudden deaths prompted the Japanese health authorities to quickly pull the MMR vaccine from their childhood vaccination schedule. 👇MMR Live Vaccine Package Insert👇 👇MMR Live Vaccine Sheds For 30 Days👇 👇MMR Live Vaccine Causes Epilepsy & Autism👇 Speaker: Dr Jeffrey Barke, MD
3:36

MEASLES MMR VACCINE...Informed Consent Straight From The Package Insert. The 2nd Listed Side Effect Is Vaccine Induced MEASLES. 'Safety Tested' For Only 42 Days Prior To US FDA Approval. This Live Virus Vaccine 'Sheds' For 30 Days, Causing Measles To Transmit To Other People. Banned In Japan For Causing Meningitis & Death. --Ingredients & Allergy Warnings-- Chicken Embryo cell culture (live fertilised chicken) Hydrolyzed Pig Gelatin (porcine origin) Human WI-38 Lung (3 month old Female) Wistar RA 27/3 (27th human fetus, 3rd harvested kidney) Recombinant GMO Human Albumin (Yeast origin) Fetal Bovine Serum (blood collected pregnant cow fetus) Neomycin (FDA banned in 2019 as unsafe) *⃣ The use of Fetal Bovine Serum carries contamination risk of endotoxins, mycoplasma virus & prion disease. --CONTRAINDICATIONS-- Anaphylaxis Reactions to those with allergies to the following ingredients: Egg, Chicken, Pork, Neomycin & Yeast. Those with low immunity can experience vaccine induced measles, mumps & rubella, febrile seizures, encephalitis, pneumonia & death. Do not administer MMR live vaccine to individuals who are pregnant or plan to become pregnant. Do not administer MMR live vaccine to individuals with temperatures above 101 degrees or to anyone with TB Tuberculosis. --ADVERSE REACTIONS-- Panniculitis (painful inflammatory bumps in skin) Measles (live vaccine induced) Vasculitis (autoimmune disease) Pancreatitis (acute pancreas damage) Thrombocytopenia (dangerous low platelet count) Anaphylaxis (fatal reactions) Chronic Bronchial Spasm (asthma) Arthritis (autoimmune disease) Encephalitis (fatal brain inflammation) GBS Guillain Barre Syndrome (autoimmune paralysis) Transverse Myelitis (spinal cord inflammation) Pneumonia & Stevens Johnson Syndrome Infant Hemorrhagic Edema (brain bleed stroke) Ear Nerve Deafness & Optic Eye Disease Severe Neurological Deformities --PREGNANCY RISKS-- MMR live vaccine is contraindicated for pregnancy as the live viruses transmit to the fetus resulting in adverse outcomes such as spontaneous abortion, stillbirth, premature delivery, congenital deformities & maternal harm. In 1993, Japan banned the MMR live vaccine after many injuries occurred in their child population. Serious injuries of Meningitis & sudden deaths prompted the Japanese health authorities to quickly pull the MMR vaccine from their childhood vaccination schedule. 👇MMR Live Vaccine Package Insert👇 👇MMR Live Vaccine Sheds For 30 Days👇 👇MMR Live Vaccine Causes Epilepsy & Autism👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

106,798 views • 1 year ago

"The Most Damning Of All Evidence Is That The DTaP Vaccine Will Kill You 30X More Than The Disease Itself." Dr Paul Thomas, MD "Whooping Cough Vaccine Primes Your Body To Contract Pertussis Multiple Times, Over & Over, For Life." Safety Tested For Only 14 Days With No Placebo. Pertussis (Whooping Cough) Vaccine is part of the multi vaccination of TDaP &/or DTaP. The Placebos used to 'safety test' the Pertussis vaccine were the Tetanus & Diphtheria vaccines. Tested for only 14 days before US FDA & CDC approval. Warnings: The vaccine does not stop transmission or infection. Whooping cough outbreaks occur within the vaccinated because natural contraction of whooping cough provides lifelong immunity. The risk of a serious adverse event after vaccination is 1 in 25, including SIDS Apnea: SIDS is now being called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. Tetanus Toxoid causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. How The 3 Components Are Grown & Cultured: Tetanus: C. Tetani Toxoid is grown in heated & putrefied Beef Heart Infusion, known as BHI. The tetanus toxin is treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Diphtheria: C. Diphtheriae grown on fetal bovine serum then treated with Formaldehyde. Pertussis: B. Pertussis bacteria grown on dairy casein fermentation broth then treated with glutaraldehyde & formaldehyde. Warning To Those With Dairy & Latex Allergies: Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP & DTaP Vaccines. Many cases of fatal anaphylaxis are caused by this. Ingredients Of DTaP & TDaP Vaccines: Tetanus Toxoid Diphtheria Toxin Pertussis Antigen Polysorbate 80 Formaldehyde Glutaraldehyde Aluminum Adjuvant Neomycin Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Bell's palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder 👇Pertussis Outbreaks Occur In The Vaccinated👇 👇Pertussis Vaccine Does Not Prevent Spread👇 👇Pertussis Vaccine Not Effective Against Infection👇 Speaker: Dr Paul Thomas, MD Video: Children’s Health Defense
1:16

"The Most Damning Of All Evidence Is That The DTaP Vaccine Will Kill You 30X More Than The Disease Itself." Dr Paul Thomas, MD "Whooping Cough Vaccine Primes Your Body To Contract Pertussis Multiple Times, Over & Over, For Life." Safety Tested For Only 14 Days With No Placebo. Pertussis (Whooping Cough) Vaccine is part of the multi vaccination of TDaP &/or DTaP. The Placebos used to 'safety test' the Pertussis vaccine were the Tetanus & Diphtheria vaccines. Tested for only 14 days before US FDA & CDC approval. Warnings: The vaccine does not stop transmission or infection. Whooping cough outbreaks occur within the vaccinated because natural contraction of whooping cough provides lifelong immunity. The risk of a serious adverse event after vaccination is 1 in 25, including SIDS Apnea: SIDS is now being called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. Stated in chapter 21 of the CDC Website for Tetanus...the Tetanus Toxoid-containing Vaccine has never been safety tested nor studied in a vaccine trial. Tetanus Toxoid causes both Brachial Neuritis & Guillain Barré Syndrome. Brachial Neuritis causes paralysis of the shoulder/arm & Guillain Barre' Syndrome causes paralysis of the entire body & carries the same symptoms as polio. How The 3 Components Are Grown & Cultured: Tetanus: C. Tetani Toxoid is grown in heated & putrefied Beef Heart Infusion, known as BHI. The tetanus toxin is treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Diphtheria: C. Diphtheriae grown on fetal bovine serum then treated with Formaldehyde. Pertussis: B. Pertussis bacteria grown on dairy casein fermentation broth then treated with glutaraldehyde & formaldehyde. Warning To Those With Dairy & Latex Allergies: Those with milk & latex allergies are not given informed consent as to the milk casein & latex used in the production of TDaP & DTaP Vaccines. Many cases of fatal anaphylaxis are caused by this. Ingredients Of DTaP & TDaP Vaccines: Tetanus Toxoid Diphtheria Toxin Pertussis Antigen Polysorbate 80 Formaldehyde Glutaraldehyde Aluminum Adjuvant Neomycin Post Marketing Adverse Events: Guillain Barre Syndrome Brachial Neuritis Lymphadenitis Lymphadenopathy Anaphylaxis Myocarditis Injection site tumor Severe back pain & myalgia Encephalitis Bell's palsy Loss of consciousness Paresthesia Angioedema Apnea New onset autoimmune disorder 👇Pertussis Outbreaks Occur In The Vaccinated👇 👇Pertussis Vaccine Does Not Prevent Spread👇 👇Pertussis Vaccine Not Effective Against Infection👇 Speaker: Dr Paul Thomas, MD Video: Children’s Health Defense

Valerie Anne Smith

62,264 views • 11 months ago

SHINGRIX Shingles Vaccine...Clinical Trials Used No Placebo & 'Safety Tested' For Only 7 Days. Black Box Warning For Guillain Barre Syndrome Causing A 'Polio Like' Paralysis. 50% Of Recipients Experience Severe Systemic Reaction. Vaccine Causes 15X Increased Risk Of Shingles. --- WARNINGS AND PRECAUTIONS --- *⃣ In postmarketing, Guillain-Barré syndrome was observed during the 42 days following vaccination with SHINGRIX & Black Box Warning added in 2021. *⃣ Anaphylaxis & Syncope is associated with SHINGRIX. Emergency procedures & appropriate medical treatment should be administered for cerebral perfusion & anaphylaxis. *⃣ Documented Lupus cases induced by the Shingrix vaccine. ---CLINICAL TRIAL & SAFETY STUDY--- *⃣ GSK Glaxosmithkline Clinical trials for SHINGRIX used diluted SHINGRIX as the placebo. *⃣ Shingrix participants in 'safety studies' were monitored for 7 days post vaccination. Two independent datasets—a general practice dataset (Outcome Health’s Population Level Analysis and Reporting) & a statewide hospital and notifiable conditions linked dataset (Vaccine Safety Health Link)- were analysed. A 15-fold increase in new onset shingles within 21 days post vaccination. ---POST MARKETING ADVERSE EVENTS--- Gout Shingles Arthritis Myalgia Optic Ischemic Neuropathy New onset immune mediated disease Death GI distress Arthralgia Neuropathy Infective pneumonia Influenza Neuralgia Guillain Barre Syndrome Lupus ---DESCRIPTION & INGREDIENTS--- The gE antigen is obtained by culturing GMO genetically engineered Chinese Hamster Ovary cells, the adjuvant suspension component is AS01B. Shingrix contains 5 Phosphates, DOPC, MPL which comes from the cell wall of Salmonella, QS21, Polysorbate 80, Sucrose, Host Cell Protein & DNA. ---NEW NOVEL ANTIGEN USED IN SHINGRIX--- AS01B Adjuvant & QS21 Excipient:Intramuscular injection of free QS21 results in necrosis at the injection site & it is likely that the toxicity of free QS21 that was observed after injection is caused by the binding of QS21 to cellular cholesterol in the membranes of local cells. QS21 binds irreversibly to cholesterol to form a complex, and when QS21 is exposed to erythrocytes it causes pores to form in the lipid bilayer of the cells. Systemic reactions occur in 50% of the recipients. ---NUMBERS NEEDED TO PREVENT NEURALGIA--- The numbers needed to treat to prevent 1 case of neuralgia is 356 patients receiving both doses of Shingrix. ---Waning Efficacy Over Time--- Year 1: 67% Effective Year 2: 50% Effective Year 8: 27% Effective Year 10: 15% Effective Shingles of course is a painful illness, but it can be cured permanently & cleared from the system within 14 days using a natural 3 part protocol. Let me know in the comments or thru DM if you would like my protocol I developed that cured my husband's severe Shingles in 2016. The vaccine is harmful & allopathic antiviral treatments after a shingles diagnosis are toxic to the system & do not heal the root cause as to why you got shingles in the 1st place. Heal, treat the root cause & permanently eradicate the post shingle neuropathy is the best way to deal with shingles. 👇GSK SHINGRIX Package Insert👇 👇SHINGRIX Causes Guillain Barre Syndrome👇 👇SHINGRIX Vaccine Causes Lupus👇 👇SHINGRIX Causes 15X Increase In Shingles👇 Speaker: Dr Jeffrey Barke, MD
2:25

SHINGRIX Shingles Vaccine...Clinical Trials Used No Placebo & 'Safety Tested' For Only 7 Days. Black Box Warning For Guillain Barre Syndrome Causing A 'Polio Like' Paralysis. 50% Of Recipients Experience Severe Systemic Reaction. Vaccine Causes 15X Increased Risk Of Shingles. --- WARNINGS AND PRECAUTIONS --- *⃣ In postmarketing, Guillain-Barré syndrome was observed during the 42 days following vaccination with SHINGRIX & Black Box Warning added in 2021. *⃣ Anaphylaxis & Syncope is associated with SHINGRIX. Emergency procedures & appropriate medical treatment should be administered for cerebral perfusion & anaphylaxis. *⃣ Documented Lupus cases induced by the Shingrix vaccine. ---CLINICAL TRIAL & SAFETY STUDY--- *⃣ GSK Glaxosmithkline Clinical trials for SHINGRIX used diluted SHINGRIX as the placebo. *⃣ Shingrix participants in 'safety studies' were monitored for 7 days post vaccination. Two independent datasets—a general practice dataset (Outcome Health’s Population Level Analysis and Reporting) & a statewide hospital and notifiable conditions linked dataset (Vaccine Safety Health Link)- were analysed. A 15-fold increase in new onset shingles within 21 days post vaccination. ---POST MARKETING ADVERSE EVENTS--- Gout Shingles Arthritis Myalgia Optic Ischemic Neuropathy New onset immune mediated disease Death GI distress Arthralgia Neuropathy Infective pneumonia Influenza Neuralgia Guillain Barre Syndrome Lupus ---DESCRIPTION & INGREDIENTS--- The gE antigen is obtained by culturing GMO genetically engineered Chinese Hamster Ovary cells, the adjuvant suspension component is AS01B. Shingrix contains 5 Phosphates, DOPC, MPL which comes from the cell wall of Salmonella, QS21, Polysorbate 80, Sucrose, Host Cell Protein & DNA. ---NEW NOVEL ANTIGEN USED IN SHINGRIX--- AS01B Adjuvant & QS21 Excipient:Intramuscular injection of free QS21 results in necrosis at the injection site & it is likely that the toxicity of free QS21 that was observed after injection is caused by the binding of QS21 to cellular cholesterol in the membranes of local cells. QS21 binds irreversibly to cholesterol to form a complex, and when QS21 is exposed to erythrocytes it causes pores to form in the lipid bilayer of the cells. Systemic reactions occur in 50% of the recipients. ---NUMBERS NEEDED TO PREVENT NEURALGIA--- The numbers needed to treat to prevent 1 case of neuralgia is 356 patients receiving both doses of Shingrix. ---Waning Efficacy Over Time--- Year 1: 67% Effective Year 2: 50% Effective Year 8: 27% Effective Year 10: 15% Effective Shingles of course is a painful illness, but it can be cured permanently & cleared from the system within 14 days using a natural 3 part protocol. Let me know in the comments or thru DM if you would like my protocol I developed that cured my husband's severe Shingles in 2016. The vaccine is harmful & allopathic antiviral treatments after a shingles diagnosis are toxic to the system & do not heal the root cause as to why you got shingles in the 1st place. Heal, treat the root cause & permanently eradicate the post shingle neuropathy is the best way to deal with shingles. 👇GSK SHINGRIX Package Insert👇 👇SHINGRIX Causes Guillain Barre Syndrome👇 👇SHINGRIX Vaccine Causes Lupus👇 👇SHINGRIX Causes 15X Increase In Shingles👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

447,289 views • 11 months ago

PREVNAR Pneumonia Vaccine...If People Read The Package Insert, No One Would Get This Injection. No Safety Studies Using A Placebo For All 5 Pneumonia Shots. Warning Of Sudden Death From Apnea Following Injection. 44,240 Shots Are Required To Prevent Only 41 Cases Of Pneumonia. --Ingredients-- Pneumonia Strains conjugated to diphtheria toxoid CRM197 protein: Beef Heart Infusion (BHI) is used as a culture medium to grow diphtheria toxoid, the bacterium that produces diphtheria toxin. The infusion is prepared by suspending minced beef heart in water, heated to boiling & putrid environment allows the diphtheria toxin to grow. The diphtheria toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant: Known Neurotoxin permeating the Blood Brain Barrier to cause diseases such as Autism, Alzheimer's & MS. This vaccine has 8X the toxic limit of aluminum safe for a 7lb infant for direct injection, per FDA own standards of 5mcg/per kg of weight as max aluminum limit. Polysorbate 80: Weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions & adverse Cardiac Events --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of Pneumovax 23 was the HEP-A & HEP-B vaccines. The safety trial 'placebo' used to prove the safety of Prevnar 20 was the Prevnar 13 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 13 was the Prevnar 9 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 9 was the Prevnar 7 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 7 was the DTP-HIB vaccine. --Serious Adverse Events & Post Market Injuries-- Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. The adult, without warning, will stop breathing & the death will be classified as SUDS or SADS, Sudden Unexpected Death Syndrome & Sudden Adult Death Syndrome. Guillain Barre Syndrome(full body paralysis) Lymphadenopathy Cyanosis(cardiac distress) Hypotonia Vascular Disease Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis Systemic Inflammatory Response System(SIRS) 👇Prevnar Package Insert👇 👇Pneumonia Vaccine Serious Adverse Events👇 👇Pneumonia Vaccine/Guillain Barre Syndrome👇 Speaker: Dr Jeffrey Barke, MD
0:59

PREVNAR Pneumonia Vaccine...If People Read The Package Insert, No One Would Get This Injection. No Safety Studies Using A Placebo For All 5 Pneumonia Shots. Warning Of Sudden Death From Apnea Following Injection. 44,240 Shots Are Required To Prevent Only 41 Cases Of Pneumonia. --Ingredients-- Pneumonia Strains conjugated to diphtheria toxoid CRM197 protein: Beef Heart Infusion (BHI) is used as a culture medium to grow diphtheria toxoid, the bacterium that produces diphtheria toxin. The infusion is prepared by suspending minced beef heart in water, heated to boiling & putrid environment allows the diphtheria toxin to grow. The diphtheria toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting Bovine Spongiform Encephalopathy also known as Mad Cow Disease. Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant: Known Neurotoxin permeating the Blood Brain Barrier to cause diseases such as Autism, Alzheimer's & MS. This vaccine has 8X the toxic limit of aluminum safe for a 7lb infant for direct injection, per FDA own standards of 5mcg/per kg of weight as max aluminum limit. Polysorbate 80: Weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions & adverse Cardiac Events --Clinical Safety Trials--No True Placebo Used-- The safety trial 'placebo' used to prove the safety of Pneumovax 23 was the HEP-A & HEP-B vaccines. The safety trial 'placebo' used to prove the safety of Prevnar 20 was the Prevnar 13 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 13 was the Prevnar 9 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 9 was the Prevnar 7 vaccine. The safety trial 'placebo' used to prove the safety of Prevnar 7 was the DTP-HIB vaccine. --Serious Adverse Events & Post Market Injuries-- Apnea: SIDS can be called 'Aluminum Adjuvant Apnea.' Aluminum Adjuvants cause apnea, affecting & stopping the breathing center of the brain. The infant, without warning, will stop breathing & the death will be classified as SIDS. The adult, without warning, will stop breathing & the death will be classified as SUDS or SADS, Sudden Unexpected Death Syndrome & Sudden Adult Death Syndrome. Guillain Barre Syndrome(full body paralysis) Lymphadenopathy Cyanosis(cardiac distress) Hypotonia Vascular Disease Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis Systemic Inflammatory Response System(SIRS) 👇Prevnar Package Insert👇 👇Pneumonia Vaccine Serious Adverse Events👇 👇Pneumonia Vaccine/Guillain Barre Syndrome👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

136,945 views • 1 year ago

FDA Approves Meningitis Vaccine 'MenQuadfi' For 6 Week Old Infants. Stamped 'Safe & Effective' Despite Causing 5.3% Serious Adverse Events... 1 Out Of Every 20 Children Were Seriously Harmed Including Death. The 'Placebo' Was Menveo Meningitis Vaccine Causing Harm To 1 in 30... The Licensure & Approval For Meningitis Vaccines Without A Single True Placebo Used: The 1st Meningitis Vaccine, Menomune, was licensed without a proper placebo-controlled trial & was then used as the placebo control to license the next meningitis vaccine, Menactra. This Meningitis Vaccine, Menactra, is then used as the placebo control to license the Meningitis Vaccine, Menveo. And then the Meningitis Vaccine, Menveo, is used as the placebo control to license the new Meningitis Vaccine, MenQuadfi. During the clinical trial, 5.3% of infants receiving MenQuadfi & 3.6% of infants receiving Menveo had a serious adverse reaction. But because these rates were “similar,” this product was deemed “safe” by FDA because it assumes Menveo is “safe.” Serious Adverse Events & Post Marketing Injuries: Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis Death MenQuadfi Ingredients & Tetanus Toxoid Information: (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate The Preparation Of Tetanus Toxoid: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow. Essentially growing toxin on rancid meat. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting 'Mad Cow Disease', Bovine Spongiform Encephalopathy. -Meningitis only affects 6-8 out of every 100,000 people. - Yet the serious adverse events from the vaccine affects 5,300 out of every 100,000 people. 👇MenQuadfi Package Insert👇 👇FDA Definition Of Serious Adverse Event👇 👇Quad Meningitis Vaccine Adverse Events👇 Speaker: Dr Scott Graves
1:54

FDA Approves Meningitis Vaccine 'MenQuadfi' For 6 Week Old Infants. Stamped 'Safe & Effective' Despite Causing 5.3% Serious Adverse Events... 1 Out Of Every 20 Children Were Seriously Harmed Including Death. The 'Placebo' Was Menveo Meningitis Vaccine Causing Harm To 1 in 30... The Licensure & Approval For Meningitis Vaccines Without A Single True Placebo Used: The 1st Meningitis Vaccine, Menomune, was licensed without a proper placebo-controlled trial & was then used as the placebo control to license the next meningitis vaccine, Menactra. This Meningitis Vaccine, Menactra, is then used as the placebo control to license the Meningitis Vaccine, Menveo. And then the Meningitis Vaccine, Menveo, is used as the placebo control to license the new Meningitis Vaccine, MenQuadfi. During the clinical trial, 5.3% of infants receiving MenQuadfi & 3.6% of infants receiving Menveo had a serious adverse reaction. But because these rates were “similar,” this product was deemed “safe” by FDA because it assumes Menveo is “safe.” Serious Adverse Events & Post Marketing Injuries: Guillain Barre Syndrome (full body paralysis) Bell's Palsy (facial paralysis) SIRVA Shoulder Injury (pain & paralysis) Anaphylaxis (risk of sudden death) Infant Apnea Heart Palpitations Syncope (fainting) Fever & Chills Hives Difficulty Breathing Acute Disseminated Encephalomyelitis (ADEM) Arthralgia Convulsions Paresthesia Seizure Transverse myelitis Death MenQuadfi Ingredients & Tetanus Toxoid Information: (A,C,W,Y) Meningitis Strains 55 mcg Tetanus Toxoid Protein Carrier Formaldehyde Sodium Chloride Sodium Acetate The Preparation Of Tetanus Toxoid: Beef Heart Infusion (BHI) is used as a culture medium to grow C. Tetani, the bacterium that produces tetanus toxin. The infusion is prepared by suspending minced beef heart in water & then heated to boiling. The heated putrid environment allows the tetanus toxin to grow. Essentially growing toxin on rancid meat. The tetanus toxin is then treated with formaldehyde to inactivate its pathogenic properties. But some toxoid preparations can still contain undesirable contaminants, which puts you at risk for contracting 'Mad Cow Disease', Bovine Spongiform Encephalopathy. -Meningitis only affects 6-8 out of every 100,000 people. - Yet the serious adverse events from the vaccine affects 5,300 out of every 100,000 people. 👇MenQuadfi Package Insert👇 👇FDA Definition Of Serious Adverse Event👇 👇Quad Meningitis Vaccine Adverse Events👇 Speaker: Dr Scott Graves

Valerie Anne Smith

169,254 views • 10 months ago

"Unequivocally...For Every Single Vaccine On The Childhood Schedule...Your Risk Of Dying From The Vaccine Far Exceeds Your Risk Of Death From The Disease." Dr Paul Thomas, MD "If You're Afraid Of Your Child Dying, If That's What You Fear The Most...Do Not Give Them A Vaccine." Full Data---Rounded For Ease Of Reference... Unrounded Raw Data Listed At Bottom Of Post. 🔵Polio: Death From The Disease: 1 in 1 Trillion Death From The Vaccine: 1 in 215K 🔵Diphtheria: Death From The Disease: 1 in 42.5 Million Death From The Vaccine: 1 in 76K 🔵Tetanus: Death From The Disease: 1 in 1.5 Million Death From The Vaccine: 1 in 76K 🔵Pertussis: Death From The Disease: 1 in 2.3 Million Death From The Vaccine: 1 in 76K 🔵Measles: Death From The Disease: 1 in 106.5 Million Death From The Vaccine: 1 in 108K 🔵Mumps: Death From The Disease: 1 in 40.3 Million Death From The Vaccine: 1 in 108K 🔵Rubella: Death From The Disease: 0/ Negligible Death From The Vaccine: 1 in 108K 🔵Varicella: Death From The Disease: 1 in 32.3 Million Death From The Vaccine: 1 in 202K 🔵Hepatitis A: Death From The Disease: 1 in 1.6 Million Death From The Vaccine: 1 in 73K 🔵Hepatitis B: Death From The Disease: 1 in 305K Death From The Vaccine: 1 in 96K 🔵HIB: Death From The Disease: 1 in 1.5 Million Death From The Vaccine: 1 in 46K 🔵Pneumococcal: Death From The Disease: 1 in 236K Death From The Vaccine: 1 in 50K 🔵Meningococcal: Death From The Disease: 1 in 822K Death From The Vaccine: 1 in 141K 🔵Influenza: Death From The Disease: 1 in 136K Death From The Vaccine: 1 in 15K Dr. Paul Thomas, Dr. Kenneth P. Stoller & Stand for Health Freedom, are suing the CDC. The lawsuit accuses the CDC of recommending 72+ vaccine doses for American children without ever testing the cumulative schedule for safety. The Lawsuit... No safety testing: The CDC & FDA has never studied the long term, combined effects of the full childhood schedule. The Institute Of Medicine has issued two decades of warnings, but no accountability or action has resulted. 27 years of silence: By law, HHS must file biennial reports to Congress on vaccine safety efforts. No reports have been issued since 1998. Constitutional violations: The suit charges the CDC with First Amendment violations(silencing dissenting doctors), the Fifth Amendment violations(due process & bodily integrity) & the Administrative Procedure Act violations(arbitrary & capricious rulemaking). The Plaintiffs Seek... Reclassification of all childhood vaccines to Category B. This shifts to shared decision making, which would make medical exemptions far easier to obtain. That rigorous safety studies be required, comparing fully vaccinated vs. unvaccinated children before any return to a mandated schedule. To end retaliation against doctors. Physicians who issue exemptions based on individualized medical judgment, would be protected. If the case is won, this lawsuit will expose the unlawful CDC hyper vaccination program. It will mark a massive victory for families who seek vaccine exemptions & for physicians fighting to practice real 'patient focused' medicine. Full Raw Data---'Unrounded' Complete Numbers... 🔴POLIO: Risk of death from Polio is 1 in 1 Trillion. Risk of death from the Polio Vaccine is 1 in 214,973. 🔴DIPHTHERIA: Risk of death from Diphtheria is 1 in 42,509,839. Risk of death from the DTaP Vaccine is 1 in 76,341. 🔴TETANUS: Risk of death from Tetanus is 1 in 1,506,184. Risk of death from the DTaP Vaccine is 1 in 76,341. 🔴PERTUSSIS: Risk of death from Pertussis is 1 in 2,346,718. Risk of death from the DTaP Vaccine is 1 in 76,341. 🔴MEASLES: Risk of death from Measles is 1 in 106,506,429. Risk of death from the MMR Vaccine is 1 in 108,666. 🔴MUMPS: Risk of death from Mumps is 1 in 40,371,594. Risk of death from the MMR Vaccine is 1 in 108,666. 🔴RUBELLA: Risk of death from Rubella is 0. Risk of death from the MMR Vaccine is 1 in 108,666. 🔴VARICELLA: Risk of death from Chickenpox is 1 in 32,331,860. Risk of death from the Vaccine is 1 in 202,398. 🔴HEPATITIS A: Risk of death from Hepatitis A is 1 in 1,667,135. Risk of death from the Vaccine is 1 in 72,948. 🔴HEPATITIS B: Risk of death from Hepatitis B is 1 in 305,465. Risk of death from the vaccine is 1 in 96,314. 🔴HIB: Risk of death from HIB is 1 in 1,494,710. Risk of death from the HIB Vaccine is 1 in 45,966. 🔴PNEUMOCOCCAL: Risk of death from Pneumonia is 1 in 236,562. Risk of death from the vaccine is 1 in 50,056. 🔴MENINGOCOCCAL: Risk of death from Meningitis is 1 in 821,925. Risk of death from the Vaccine is 1 in 141,124. 🔴INFLUENZA: Risk of death from Influenza is 1 in 135,905. Risk of death from the Flu Vaccine is 1 in 15,702. 👇Dr Paul Thomas, MD "Vax Facts"👇 👇Stand For Health Freedom👇 👇Dr Paul Thomas' Research Data👇 Speaker: PaulThomas Video: @toxins_in_children
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"Unequivocally...For Every Single Vaccine On The Childhood Schedule...Your Risk Of Dying From The Vaccine Far Exceeds Your Risk Of Death From The Disease." Dr Paul Thomas, MD "If You're Afraid Of Your Child Dying, If That's What You Fear The Most...Do Not Give Them A Vaccine." Full Data---Rounded For Ease Of Reference... Unrounded Raw Data Listed At Bottom Of Post. 🔵Polio: Death From The Disease: 1 in 1 Trillion Death From The Vaccine: 1 in 215K 🔵Diphtheria: Death From The Disease: 1 in 42.5 Million Death From The Vaccine: 1 in 76K 🔵Tetanus: Death From The Disease: 1 in 1.5 Million Death From The Vaccine: 1 in 76K 🔵Pertussis: Death From The Disease: 1 in 2.3 Million Death From The Vaccine: 1 in 76K 🔵Measles: Death From The Disease: 1 in 106.5 Million Death From The Vaccine: 1 in 108K 🔵Mumps: Death From The Disease: 1 in 40.3 Million Death From The Vaccine: 1 in 108K 🔵Rubella: Death From The Disease: 0/ Negligible Death From The Vaccine: 1 in 108K 🔵Varicella: Death From The Disease: 1 in 32.3 Million Death From The Vaccine: 1 in 202K 🔵Hepatitis A: Death From The Disease: 1 in 1.6 Million Death From The Vaccine: 1 in 73K 🔵Hepatitis B: Death From The Disease: 1 in 305K Death From The Vaccine: 1 in 96K 🔵HIB: Death From The Disease: 1 in 1.5 Million Death From The Vaccine: 1 in 46K 🔵Pneumococcal: Death From The Disease: 1 in 236K Death From The Vaccine: 1 in 50K 🔵Meningococcal: Death From The Disease: 1 in 822K Death From The Vaccine: 1 in 141K 🔵Influenza: Death From The Disease: 1 in 136K Death From The Vaccine: 1 in 15K Dr. Paul Thomas, Dr. Kenneth P. Stoller & Stand for Health Freedom, are suing the CDC. The lawsuit accuses the CDC of recommending 72+ vaccine doses for American children without ever testing the cumulative schedule for safety. The Lawsuit... No safety testing: The CDC & FDA has never studied the long term, combined effects of the full childhood schedule. The Institute Of Medicine has issued two decades of warnings, but no accountability or action has resulted. 27 years of silence: By law, HHS must file biennial reports to Congress on vaccine safety efforts. No reports have been issued since 1998. Constitutional violations: The suit charges the CDC with First Amendment violations(silencing dissenting doctors), the Fifth Amendment violations(due process & bodily integrity) & the Administrative Procedure Act violations(arbitrary & capricious rulemaking). The Plaintiffs Seek... Reclassification of all childhood vaccines to Category B. This shifts to shared decision making, which would make medical exemptions far easier to obtain. That rigorous safety studies be required, comparing fully vaccinated vs. unvaccinated children before any return to a mandated schedule. To end retaliation against doctors. Physicians who issue exemptions based on individualized medical judgment, would be protected. If the case is won, this lawsuit will expose the unlawful CDC hyper vaccination program. It will mark a massive victory for families who seek vaccine exemptions & for physicians fighting to practice real 'patient focused' medicine. Full Raw Data---'Unrounded' Complete Numbers... 🔴POLIO: Risk of death from Polio is 1 in 1 Trillion. Risk of death from the Polio Vaccine is 1 in 214,973. 🔴DIPHTHERIA: Risk of death from Diphtheria is 1 in 42,509,839. Risk of death from the DTaP Vaccine is 1 in 76,341. 🔴TETANUS: Risk of death from Tetanus is 1 in 1,506,184. Risk of death from the DTaP Vaccine is 1 in 76,341. 🔴PERTUSSIS: Risk of death from Pertussis is 1 in 2,346,718. Risk of death from the DTaP Vaccine is 1 in 76,341. 🔴MEASLES: Risk of death from Measles is 1 in 106,506,429. Risk of death from the MMR Vaccine is 1 in 108,666. 🔴MUMPS: Risk of death from Mumps is 1 in 40,371,594. Risk of death from the MMR Vaccine is 1 in 108,666. 🔴RUBELLA: Risk of death from Rubella is 0. Risk of death from the MMR Vaccine is 1 in 108,666. 🔴VARICELLA: Risk of death from Chickenpox is 1 in 32,331,860. Risk of death from the Vaccine is 1 in 202,398. 🔴HEPATITIS A: Risk of death from Hepatitis A is 1 in 1,667,135. Risk of death from the Vaccine is 1 in 72,948. 🔴HEPATITIS B: Risk of death from Hepatitis B is 1 in 305,465. Risk of death from the vaccine is 1 in 96,314. 🔴HIB: Risk of death from HIB is 1 in 1,494,710. Risk of death from the HIB Vaccine is 1 in 45,966. 🔴PNEUMOCOCCAL: Risk of death from Pneumonia is 1 in 236,562. Risk of death from the vaccine is 1 in 50,056. 🔴MENINGOCOCCAL: Risk of death from Meningitis is 1 in 821,925. Risk of death from the Vaccine is 1 in 141,124. 🔴INFLUENZA: Risk of death from Influenza is 1 in 135,905. Risk of death from the Flu Vaccine is 1 in 15,702. 👇Dr Paul Thomas, MD "Vax Facts"👇 👇Stand For Health Freedom👇 👇Dr Paul Thomas' Research Data👇 Speaker: PaulThomas Video: @toxins_in_children

Valerie Anne Smith

135,747 views • 9 months ago

"It's A 200 Year Myth That Vaccines Are Safe, Effective, Necessary & Harmless...Every One Of Those Statements Are Lies." Dr Sherri Tenpenny "Not Even One Vaccine Has Ever Been Proven to Be Safe." "If You Don't Die Within 72 Hours Of Injection...The US FDA Approves It As Safe." 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. 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 Neomycin Chinese Hamster Ovary (CHO) Rhesus Monkey (LLC-MK2) Cocker Spaniel Kidney (MDCK) African Green Monkey (VERO) Human Harvested Kidney Human Harvested Lung Live Viruses E. Coli Tetanus Toxoid Every Single⏬Vaccine Safety Trial Period Is Listed In The Package Insert Under Section 6.1, Which States How Long The Trial Participants Were Observed To 'Prove Safety Of The Vaccine' Before Given CDC & FDA Approval. Think the vaccines have gone thru a long robust safety trial to prove they are 'safe & effective'? All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, not vaccines... Hep-B Vaccine: Administered to 147 infants & children who were monitored for 5 days, then granted approval. Gardasil HPV Vaccine: Safety was evaluated using vaccination report card (VRC)- aided surveillance for 14 days. Hep-A Vaccine: Test subjects were followed for safety for 14 days. Influenza A Vaccine: Participants were monitored for adverse events for 28 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored daily for 7 days. DTaP & TDaP Vaccines: Participants were monitored for 14 days. Chicken Pox Vaccine: Subjects were observed for adverse reactions for 42 days. Shingles Vaccine: Test subjects were followed for 7 days. Prevnar Pneumonia Vaccine: Participants were monitored for 7 days. RSV Vaccine: Safety monitored for 30 days. MMR Vaccine: Participants were followed for 42 days. 👇Vaccine Excipient Summary List👇 👇Vaccinated Versus Unvaccinated Study👇 👇Vaccine Induced Neurodevelopment Disorders👇 Speaker: Dr Sherri Tenpenny Video: D. Alec Zeck
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"It's A 200 Year Myth That Vaccines Are Safe, Effective, Necessary & Harmless...Every One Of Those Statements Are Lies." Dr Sherri Tenpenny "Not Even One Vaccine Has Ever Been Proven to Be Safe." "If You Don't Die Within 72 Hours Of Injection...The US FDA Approves It As Safe." 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. 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 Neomycin Chinese Hamster Ovary (CHO) Rhesus Monkey (LLC-MK2) Cocker Spaniel Kidney (MDCK) African Green Monkey (VERO) Human Harvested Kidney Human Harvested Lung Live Viruses E. Coli Tetanus Toxoid Every Single⏬Vaccine Safety Trial Period Is Listed In The Package Insert Under Section 6.1, Which States How Long The Trial Participants Were Observed To 'Prove Safety Of The Vaccine' Before Given CDC & FDA Approval. Think the vaccines have gone thru a long robust safety trial to prove they are 'safe & effective'? All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, not vaccines... Hep-B Vaccine: Administered to 147 infants & children who were monitored for 5 days, then granted approval. Gardasil HPV Vaccine: Safety was evaluated using vaccination report card (VRC)- aided surveillance for 14 days. Hep-A Vaccine: Test subjects were followed for safety for 14 days. Influenza A Vaccine: Participants were monitored for adverse events for 28 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored daily for 7 days. DTaP & TDaP Vaccines: Participants were monitored for 14 days. Chicken Pox Vaccine: Subjects were observed for adverse reactions for 42 days. Shingles Vaccine: Test subjects were followed for 7 days. Prevnar Pneumonia Vaccine: Participants were monitored for 7 days. RSV Vaccine: Safety monitored for 30 days. MMR Vaccine: Participants were followed for 42 days. 👇Vaccine Excipient Summary List👇 👇Vaccinated Versus Unvaccinated Study👇 👇Vaccine Induced Neurodevelopment Disorders👇 Speaker: Dr Sherri Tenpenny Video: D. Alec Zeck

Valerie Anne Smith

90,914 views • 11 months ago