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🔥 EXCLUSIVE: ACIP puts HPV vaccine back under the microscope, 20 years after approval MIT professor Retsef Levi will lead a new workgroup to re-examine the HPV vaccine, including its effectiveness, dosing, safety, and long-term population outcomes. LINK 👇👇👇👇 Camus Chief Nerd Jeffrey A Tucker Mary Talley Bowden MD... show more

Maryanne Demasi, PhD

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21,674 Aufrufe • vor 8 Monaten •via X (Twitter)

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🎯Moderna’s success was built on regulatory shortcuts Moderna is scaling back vaccine investment as regulators raise the evidentiary bar, exposing how regulatory shortcuts underpinned approval of its Covid vaccine. STORY LINK 👇👇 Jeffrey A Tucker Camus

🎯Moderna’s success was built on regulatory shortcuts Moderna is scaling back vaccine investment as regulators raise the evidentiary bar, exposing how regulatory shortcuts underpinned approval of its Covid vaccine. STORY LINK 👇👇 Jeffrey A Tucker Camus

Maryanne Demasi, PhD

32,597 Aufrufe • vor 7 Monaten

🛑 The presentation ACIP never heard🛑 Here is an exclusive look at the briefing slides by Charlotte Kuperwasser, PhD that were never presented to ACIP—and have not been made public until now. LINK below 👇👇 Jeffrey A Tucker Retsef Levi Kirk Milhoan React19 - Official Brianne Dressen Stephanie Hook de Garay Jay Bhattacharya, MD, PhD Secretary Kennedy

🛑 The presentation ACIP never heard🛑 Here is an exclusive look at the briefing slides by Charlotte Kuperwasser, PhD that were never presented to ACIP—and have not been made public until now. LINK below 👇👇 Jeffrey A Tucker Retsef Levi Kirk Milhoan React19 - Official Brianne Dressen Stephanie Hook de Garay Jay Bhattacharya, MD, PhD Secretary Kennedy

Maryanne Demasi, PhD

20,256 Aufrufe • vor 6 Monaten

💥EXCLUSIVE: Internal report to federal vaccine advisers calls for urgent recognition of Covid vaccine injuries. The document proposes reforms for diagnosing and treating vaccine-injured patients. It now goes before ACIP on March 18–19 — the first real test of whether the proposals move from paper to policy. LINK 👇 Gain of Fauci Chief Nerd Camus Elon Musk Jeffrey A Tucker React19 - Official MAHA Action Secretary Kennedy Rob Schneider 🇺🇸 Bill Maher Russell Brand

Maryanne Demasi, PhD

146,760 Aufrufe • vor 6 Monaten

"It Is A Myth That Vaccines Are Safe & Necessary...If I Had My Young Children Today, They Would Not Get A Single Vaccine." Dr Pierre Kory, MD "SIDS Occurs At 2, 4 & 6 Months Of Age...Right After Vaccination." "The Gov't Refuses To Do A True Placebo Safety Trial On Any Vaccine." Vaccines have not 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, but vaccines are not safety monitored this way. Hep-B Vaccine: Tested on only 147 infants & children, then monitored for 5 days & granted CDC approval. Hep-A Vaccine: Subjects were monitored for safety, 14 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored for 7 days. Prevnar Pneumonia Vaccine: Study volunteers were monitored for 7 days. MMR Vaccine: Subjects were followed for 42 days. RSV Vaccine: Participants were monitored for 30 days. DTaP & TDaP Vaccines: Subjects were monitored for 14 days. Gardasil HPV Vaccine: Trial participants were surveilled for 14 days. Vaccines have not been safety trialed against a saline placebo. They have all used Aluminum adjuvant or another vaccine as the placebo in clinical trials. Gardasil HPV Clinical Trial: placebo was the Hep-A Vaccine & Aluminum Adjuvant. Hepatitis A Clinical Trial: placebo was the Hep-B Vaccine. Influenza A Clinical Trial: placebo was the Influenza B Vaccine. Meningitis Vaccine Clinical Trial: placebo was the DTaP Vaccine. Pertussis Vaccine Clinical Trial: placebo was the Tetanus & Diphtheria Vaccine. Polio Vaccine Clinical Trial: placebo was Diluted Polio Vaccine. Vaxelis 6 in 1 Vaccine Trial: placebo was the DTaP, Polio, HIB & Hep-B Vaccines. Hepatitis B Clinical Trial: placebo was Aluminum Adjuvant. The countries that have the most infant vaccines on their childhood schedules, have the highest infant mortality. The United States is #1 in infant vaccines & #1 in infant mortality, of all industrialized nations. 97% of infants who die of SIDS, do so within 7 days being vaccinated. 👇Vaccinated Versus Unvaccinated Study👇 👇Vaccine Induced Neurodevelopment Disorders👇 👇Health Outcomes: Vaxxed Versus UnVaxxed👇 Speaker: Dr Pierre Kory, MD Video: @that_barefootgirlv

"It Is A Myth That Vaccines Are Safe & Necessary...If I Had My Young Children Today, They Would Not Get A Single Vaccine." Dr Pierre Kory, MD "SIDS Occurs At 2, 4 & 6 Months Of Age...Right After Vaccination." "The Gov't Refuses To Do A True Placebo Safety Trial On Any Vaccine." Vaccines have not 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, but vaccines are not safety monitored this way. Hep-B Vaccine: Tested on only 147 infants & children, then monitored for 5 days & granted CDC approval. Hep-A Vaccine: Subjects were monitored for safety, 14 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored for 7 days. Prevnar Pneumonia Vaccine: Study volunteers were monitored for 7 days. MMR Vaccine: Subjects were followed for 42 days. RSV Vaccine: Participants were monitored for 30 days. DTaP & TDaP Vaccines: Subjects were monitored for 14 days. Gardasil HPV Vaccine: Trial participants were surveilled for 14 days. Vaccines have not been safety trialed against a saline placebo. They have all used Aluminum adjuvant or another vaccine as the placebo in clinical trials. Gardasil HPV Clinical Trial: placebo was the Hep-A Vaccine & Aluminum Adjuvant. Hepatitis A Clinical Trial: placebo was the Hep-B Vaccine. Influenza A Clinical Trial: placebo was the Influenza B Vaccine. Meningitis Vaccine Clinical Trial: placebo was the DTaP Vaccine. Pertussis Vaccine Clinical Trial: placebo was the Tetanus & Diphtheria Vaccine. Polio Vaccine Clinical Trial: placebo was Diluted Polio Vaccine. Vaxelis 6 in 1 Vaccine Trial: placebo was the DTaP, Polio, HIB & Hep-B Vaccines. Hepatitis B Clinical Trial: placebo was Aluminum Adjuvant. The countries that have the most infant vaccines on their childhood schedules, have the highest infant mortality. The United States is #1 in infant vaccines & #1 in infant mortality, of all industrialized nations. 97% of infants who die of SIDS, do so within 7 days being vaccinated. 👇Vaccinated Versus Unvaccinated Study👇 👇Vaccine Induced Neurodevelopment Disorders👇 👇Health Outcomes: Vaxxed Versus UnVaxxed👇 Speaker: Dr Pierre Kory, MD Video: @that_barefootgirlv

Valerie Anne Smith

262,818 Aufrufe • vor 1 Jahr

"No Vaccine On The Childhood Schedule Has Ever Been Tested Against A True Placebo." Del Bigtree "No Vaccine Has Ever Been Thoroughly Safety Tested." The Hep-B Vaccine Used Injected Aluminum As The 'Placebo...' 'Safety Tested' On 147 Children For Only 5 Days Before Approval. 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. 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. 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. List⏬Of 'Placebos' Used In Vaccine Clinical Trials As Listed From The Package Inserts For Common Vaccines: Hepatitis B Clinical Trial...Placebo Was Injected Aluminum Adjuvant. 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. 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. 👇Hep-B Vaccine Package Insert👇 👇Gardasil HPV Vaccine Package Insert👇 👇Hep-A Vaccine Package Insert👇 Speaker: Alex Clark & Del Bigtree Podcast: Alex Clark

"No Vaccine On The Childhood Schedule Has Ever Been Tested Against A True Placebo." Del Bigtree "No Vaccine Has Ever Been Thoroughly Safety Tested." The Hep-B Vaccine Used Injected Aluminum As The 'Placebo...' 'Safety Tested' On 147 Children For Only 5 Days Before Approval. 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. 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. 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. List⏬Of 'Placebos' Used In Vaccine Clinical Trials As Listed From The Package Inserts For Common Vaccines: Hepatitis B Clinical Trial...Placebo Was Injected Aluminum Adjuvant. 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. 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. 👇Hep-B Vaccine Package Insert👇 👇Gardasil HPV Vaccine Package Insert👇 👇Hep-A Vaccine Package Insert👇 Speaker: Alex Clark & Del Bigtree Podcast: Alex Clark

Valerie Anne Smith

46,282 Aufrufe • vor 1 Jahr

"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

"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 Aufrufe • vor 1 Jahr

"Gardasil HPV Vaccine Targets Millions Of Teens Who Have ZERO Risk From Cervical Cancer." "Children Who Take The Gardasil Vaccine Are 37 Times More Likely To Die From The Vaccine Than They Are To Die From Cervical Cancer." --RFK Jr "The Death Rates In The Gardasil Safety Trials Were 37 Times The Death Rates For Cervical Cancer." Like Most Vaccines, Gardasil HPV Vaccine Was Never Tested Against A True Placebo, A Saline Placebo. The Placebos Used In The Clinical Trials Were Aluminum Adjuvant (AAHS) & The Hep-A Vaccine. Clinical Trial Safety Results Female & Male: 💉40 Deaths post vaccination 💉290 New diagnosed autoimmune diseases 💉25% Fetal death during pregnancy 💉90 Cases of congenital deformity 💉27 Breastfeeding infants had adverse events Gardasil HPV Vaccine Ingredients (3 Doses): 💉HPV L1 Proteins (9 Strains): Including HPV DNA fragments, which act as a 3rd adjuvant, undisclosed on the package insert. Lawsuit against Merck is currently underway. Court documents reveal that Merck was fully aware of an additional adjuvant in Gardasil that was not disclosed to recipients & did not have regulatory approval. 💉Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant: Known Neurotoxin permeating the Blood Brain Barrier to cause diseases such as Autism, Alzheimer's & MS. 💉Polysorbate 80: Weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions, adverse Cardiac Events & The American College of Pediatricians has warned that Gardasil is linked to a condition known as Premature Ovarian Failure. 💉Sodium Borate (Borax): Banned in food in the U.S. & poses harm to the male reproductive system & to the developing fetus. It can cause acute toxic reactions when eaten or inhaled, which raises the question of what reactions might result when it is injected. 💉GMO Yeast Protein: The type of yeast used in Gardasil, Saccharomyces Cerevisiae, causes autoimmune disease by provoking an autoimmune response in the body. 💉L-Histidine: A chemical compound the body uses to make another chemical Histamine. Histamines cause inflammation &, like aluminum & polysorbate 80, they also increase the permeability of blood vessels. Histamines have been found to increase blood clotting by 5 times when combined with surfactants – & death from blood clots is the most common form of death after Gardasil injection. 👇Lawsuit Against Merck For Undisclosed DNA👇 👇Vaccine Placebos Used In Safety Trials👇 👇DNA Fragments Found In Gardasil HPV Protein👇 Video: Children’s Health Defense @MAHAalliance Secretary Kennedy

"Gardasil HPV Vaccine Targets Millions Of Teens Who Have ZERO Risk From Cervical Cancer." "Children Who Take The Gardasil Vaccine Are 37 Times More Likely To Die From The Vaccine Than They Are To Die From Cervical Cancer." --RFK Jr "The Death Rates In The Gardasil Safety Trials Were 37 Times The Death Rates For Cervical Cancer." Like Most Vaccines, Gardasil HPV Vaccine Was Never Tested Against A True Placebo, A Saline Placebo. The Placebos Used In The Clinical Trials Were Aluminum Adjuvant (AAHS) & The Hep-A Vaccine. Clinical Trial Safety Results Female & Male: 💉40 Deaths post vaccination 💉290 New diagnosed autoimmune diseases 💉25% Fetal death during pregnancy 💉90 Cases of congenital deformity 💉27 Breastfeeding infants had adverse events Gardasil HPV Vaccine Ingredients (3 Doses): 💉HPV L1 Proteins (9 Strains): Including HPV DNA fragments, which act as a 3rd adjuvant, undisclosed on the package insert. Lawsuit against Merck is currently underway. Court documents reveal that Merck was fully aware of an additional adjuvant in Gardasil that was not disclosed to recipients & did not have regulatory approval. 💉Aluminum as Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) Adjuvant: Known Neurotoxin permeating the Blood Brain Barrier to cause diseases such as Autism, Alzheimer's & MS. 💉Polysorbate 80: Weakens the blood brain barrier & binds tightly to aluminum. It has been shown to cause Anaphylactic Shock, Hypersensitivity Reactions, adverse Cardiac Events & The American College of Pediatricians has warned that Gardasil is linked to a condition known as Premature Ovarian Failure. 💉Sodium Borate (Borax): Banned in food in the U.S. & poses harm to the male reproductive system & to the developing fetus. It can cause acute toxic reactions when eaten or inhaled, which raises the question of what reactions might result when it is injected. 💉GMO Yeast Protein: The type of yeast used in Gardasil, Saccharomyces Cerevisiae, causes autoimmune disease by provoking an autoimmune response in the body. 💉L-Histidine: A chemical compound the body uses to make another chemical Histamine. Histamines cause inflammation &, like aluminum & polysorbate 80, they also increase the permeability of blood vessels. Histamines have been found to increase blood clotting by 5 times when combined with surfactants – & death from blood clots is the most common form of death after Gardasil injection. 👇Lawsuit Against Merck For Undisclosed DNA👇 👇Vaccine Placebos Used In Safety Trials👇 👇DNA Fragments Found In Gardasil HPV Protein👇 Video: Children’s Health Defense @MAHAalliance Secretary Kennedy

Valerie Anne Smith

48,956 Aufrufe • vor 1 Jahr

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

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

318,092 Aufrufe • vor 1 Jahr

"mRNA Vaccines Were Injected Into Milk Bubbles & Fed To Mice...Within 3 Feedings The Mice Were Fully Vaccinated." Dr Peter McCullough "This Proves That Messenger RNA Crosses The GI Tract." "The USDA Has An Entire Array Of Genetic Vaccines That They Are Developing With Merck." Merck Animal Health vaccines & related developments: Companion animals Canine Influenza: Merck has developed & received USDA approval for the NOBIVAC NXT Canine Flu H3N2 vaccine, which uses RNA-particle self replicating spray technology to protect dogs against canine influenza. Feline Leukemia Virus (FeLV): The USDA also approved the NOBIVAC NXT FeLV vaccine, which utilizes the same RNA-particle self replicating spray technology as the canine influenza vaccine. This is toxic for your family pets & you *⃣ when your pet sneezes or gets saliva on you, you receive the vaccine too, thru shedding. Livestock Cattle: Merck offers a range of vaccines for cattle under the BOVILIS name, including enteric disease caused by bovine coronavirus (BOVILIS CORONAVIRUS). Swine: Merck's acquired company, Harrisvaccines, received USDA licensure for its RNA Particle (RP) vaccine platform, allowing for the manufacturing of herd-specific, custom vaccines for various diseases including those impacting swine. Poultry: Merck Animal Health partnered with Cambridge Technologies to be the exclusive sales agent for their autogenous poultry vaccines, including an experimental vaccine for avian metapneumovirus type B, which received USDA approval for manufacturing & sale. This is toxic for livestock & to you *⃣ you will be consuming the self replicating RNA spike protein. Bayer Monsanto Food Crops Big Ag & Bayer/Monsanto are rolling out RNA spray technology on common food crops — without long term studies on health or environmental impacts. Here's a list of crops that could be sprayed with mRNA interference (RNAi) sprays👇🏽 Potatoes Tomatoes Corn Cabbage Cotton Papaya Peas Cucumber Grapes Strawberries Zucchini Soybeans Wheat Chickpeas Rice Barley Lettuce Spinach These will be toxic to vegetables, fruit, our soil & to you *⃣ you will be consuming self replicating RNA spike protein. No mandatory labeling will be required for crops treated with mRNA sprays in the US. 👇Exosome mRNA Vaccine Fed To Mice In Milk👇 👇USDA Approves Merck Spray Family Pet Vaccine👇 👇Expanding Edible Plant Based Vaccines👇 Speaker: Dr Peter McCullough, MD Video: @toxins_in_children

"mRNA Vaccines Were Injected Into Milk Bubbles & Fed To Mice...Within 3 Feedings The Mice Were Fully Vaccinated." Dr Peter McCullough "This Proves That Messenger RNA Crosses The GI Tract." "The USDA Has An Entire Array Of Genetic Vaccines That They Are Developing With Merck." Merck Animal Health vaccines & related developments: Companion animals Canine Influenza: Merck has developed & received USDA approval for the NOBIVAC NXT Canine Flu H3N2 vaccine, which uses RNA-particle self replicating spray technology to protect dogs against canine influenza. Feline Leukemia Virus (FeLV): The USDA also approved the NOBIVAC NXT FeLV vaccine, which utilizes the same RNA-particle self replicating spray technology as the canine influenza vaccine. This is toxic for your family pets & you ⃣ when your pet sneezes or gets saliva on you, you receive the vaccine too, thru shedding. Livestock Cattle: Merck offers a range of vaccines for cattle under the BOVILIS name, including enteric disease caused by bovine coronavirus (BOVILIS CORONAVIRUS). Swine: Merck's acquired company, Harrisvaccines, received USDA licensure for its RNA Particle (RP) vaccine platform, allowing for the manufacturing of herd-specific, custom vaccines for various diseases including those impacting swine. Poultry: Merck Animal Health partnered with Cambridge Technologies to be the exclusive sales agent for their autogenous poultry vaccines, including an experimental vaccine for avian metapneumovirus type B, which received USDA approval for manufacturing & sale. This is toxic for livestock & to you ⃣ you will be consuming the self replicating RNA spike protein. Bayer Monsanto Food Crops Big Ag & Bayer/Monsanto are rolling out RNA spray technology on common food crops — without long term studies on health or environmental impacts. Here's a list of crops that could be sprayed with mRNA interference (RNAi) sprays👇🏽 Potatoes Tomatoes Corn Cabbage Cotton Papaya Peas Cucumber Grapes Strawberries Zucchini Soybeans Wheat Chickpeas Rice Barley Lettuce Spinach These will be toxic to vegetables, fruit, our soil & to you *⃣ you will be consuming self replicating RNA spike protein. No mandatory labeling will be required for crops treated with mRNA sprays in the US. 👇Exosome mRNA Vaccine Fed To Mice In Milk👇 👇USDA Approves Merck Spray Family Pet Vaccine👇 👇Expanding Edible Plant Based Vaccines👇 Speaker: Dr Peter McCullough, MD Video: @toxins_in_children

Valerie Anne Smith

102,870 Aufrufe • vor 1 Jahr

Dr. Mary Talley Bowden sounds alarm on COVID shots: "9 million children vaccinated despite EUA status—They need to be pulled off the market now!" Dr. Mary Talley Bowden, a respected physician, is raising urgent concerns about the COVID-19 vaccines, calling for their immediate removal from the market. Based on her clinical experience, 7% of her new patients over the two years following the vaccine rollout sought treatment for severe injuries linked to the shots. "I’ve never seen anything like this with any other product," she states, emphasizing that no other medication would remain on the market with such a safety profile. According to the Vaccine Adverse Event Reporting System (VAERS), which Dr. Bowden notes is significantly underreported, 38,000 deaths have been associated with the COVID shots. Under normal FDA protocols, a drug linked to just 5 deaths would receive a black box warning, and 50 deaths would prompt its withdrawal. Yet, the FDA has not only failed to act but has doubled down, adding the shots to the childhood vaccine schedule. Shockingly, 9 million American children have received the latest version, despite the shots remaining under Emergency Use Authorization (EUA) for infants as young as 9 months. Dr. Bowden is appalled that these vaccines remain mandatory in some states, nursing programs, and even for organ transplants. "How can we let people die unless they get the shot?" she asks. Texas has banned COVID vaccine mandates, but many institutions nationwide continue to enforce them. She demands immediate action: the FDA must pull the shots, and accountability is essential to restore public trust. "If nothing happens, it’s a festering wound, and trust will never return," she warns. Despite her close monitoring, Dr. Bowden sees no indication that the government or HHS is addressing this crisis, with their focus shifted to unrelated issues like food quality.

Camus

26,853 Aufrufe • vor 1 Jahr

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

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

138,055 Aufrufe • vor 1 Jahr

Please help our Covid Vaccine Injured via React 19. Sharing my story with React19 - Official has been one of the hardest and most meaningful things I've ever done. If my experience can help even one person feel less alone, it's worth it. Learn more here: We appreciate a share across your social medias, donation or both. Right now, a generous donor has made it possible that all donations received get doubled, increasing the HOPE we can provide, SAVING lives just like mine. All of you make it possible and we are appreciative beyond words. Brianne Dressen Mary Talley Bowden MD Molly Rutherford, MD Dr Clare Craig Liz Churchill Dr. Lynn Fynn-derella Children’s Health Defense Chief Nerd The HighWire Del Bigtree Nicolas Hulscher, MPH “Sudden And Unexpected” Camus Bret Weinstein Brian O'Shea 🇺🇸 JD Vance Doc Pete Chambers Jeffrey A Tucker Jeff Dornik Champagne Joshi Stand for Health Freedom Peter A. McCullough, MD, MPH® Rand Paul Senator Ron Johnson Bret Weinstein Joe Rogan Bernie Moreno Marty Makary MD, MPH A Midwestern Doctor The Disrespected Trucker Wide Awake Media Dr. Dawn Michael Nick Petosky Robert Scott Bell Kevin McKernan The Vigilant Fox 🦊 Nurse Lioness Sense Receptor The Megyn Kelly Show Retsef Levi Robert W Malone, MD Elon Musk Warner Mendenhall MAHA Action Dr. Ben Tapper Ann Forti Anna Matson John Rich🇺🇸 Russell Brand

The Coerced Nurse

15,800 Aufrufe • vor 10 Monaten

"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

"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

62,758 Aufrufe • vor 1 Jahr

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

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 Aufrufe • vor 1 Jahr