Safety information - everything you never wanted to know
A list of items to help you decide if vaccines are safe. EDUCATIONAL PURPOSES ONLY. PLEASE CONSULT A PROFESSIONAL FOR MORE INFORMATION to make the best choice for your situation.
TESTING FACTS:
Standard for industry is double blind inert placebo control studies that last at least one year to six years. An inert placebo is something that causes zero side effects in everyone. They test vaccines against other vaccines. That’s not a placebo. They test them for as little as 4 days. That’s not science. It is politics.
Here is a chart showing the control for all the ones on the USA childhood schedule: There are three ways to access this chart. Pick the link that works best for you:
https://icandecide.org/72-vaccine-doses-no-placebo-trials/
https://bit.ly/ICANVaxTrialChart
OPEN VAERS
https://openvaers.com/resources/no-placebo-table?idU=1
***************************************************************************************************HEPATITIS B:
has no control at all. They just tell us, “IT WORKS. Take it because we say so.” The testing for that is 4 and 5 days. DAYS. It takes two weeks for antibodies to form.
Engerix-B:
“All subjects were monitored for 4 days post-adminstration.”
https://www.fda.gov/media/119403/download
Recombivax HB
“…monitored for 5 days …”
https://www.fda.gov/media/74274/download
Why is Hep B given on day one: Does it provide any benefit to newborns?
Minutes of meeting : Immunization Practices Advisory Committee, October 16-17, 1990, Atlanta, Georgia
“The increasing incidence of hepatitis B in the last 8 years has been primarily in adults, but data show that high-risk group immunization of adults is not feasible. The prevailing conclusion is that either infants, preferably, or possible adolescent immunization is the way to control this disease, though it may take 15-20 years to see the effects.”
https://stacks.cdc.gov/view/cdc/77069
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PREVNAR:
Prevnar was tested against an experimental shot. They compared two experimental shots. That proves nothing about the safety of either one.
Prevnar package insert
Go to page 3. They used an investigational (aka experimental shot) called meningococcal group C conjugate vaccine [MnCC]) as the control. That is not valid science.
https://www.fda.gov/media/76076/download
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TESTING FOR 4 DAYS:
Here are a few examples to get you started. This will help you figure out what you are looking for.
HAVRIX Hepatitis A
https://www.fda.gov/media/119388/download
“… adverse reactions and general events were recorded … for 4 days (Days 0 to 3) …”
PEDIARIX Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed, Hepatitis B (Recombinant) and Inactivated Poliovirus […] Combined
https://www.fda.gov/media/79830/download
“… adverse reactions were collected … for 4 consecutive days …”
Recombivax HB
https://www.fda.gov/media/74274/download
“…monitored for 5 days after each dose.”
***************************************************************************************************HOW TO LOOK UP ANY VACCINE ON THE USA SCHEDULE:
This link will take you to a list of every vaccine that is licensed for use in the USA. Click the name, on the next screen click the link for PACKAGE INSERT. This takes you to the FDA drug insert information for the vaccine.
Section 6: This is where you can find clinical trial information and a list of the adverse effects that are caused by the shot. Manufacturers are required to list things here that have a causal relationship with the vaccine. They always brush off vaccine side effects claiming it is correlation rather than causation. This list is causation.
https://www.fda.gov/vaccines-blood-biologics/vaccines/vaccines-licensed-use-united-states
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SECTION 6 OF PACKAGE INSERT:
This lists the adverse events that are CAUSED by that vaccine. This is a federal law.
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?fr=201.57
“Federal law provides that package inserts for vaccine should include “only those adverse events for which there is some basis to believe there is a causal relationship between the drug and the occurrence of the adverse event.” 21 CFR 201.57”
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THIS IS NOT LONG ENOUGH:
Dr Plotkin testified that this is not long enough to find autoimmune issues being caused the vaccines.
Transcript YouTube 1:00:22
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “Dr Plotkin, earlier, you testified that there are two Hep B vaccines in the market, one by Glasko GSK that's Engerix-B, and the other one is by Merck Recombivax HB, right?
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Yes.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “This is the product, the manufacturer insert for Recombivax HB, correct?
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Yes.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “And the clinical trial experience would be found in section 6.1 correct?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Yes.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “In section 6.1, when you look at the clinical trials that were done pre licensure for Recombivax HB, how long does it say that safety was monitored after each dose?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “um, let’s see, ah five days.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “Is 5 days long enough to detect an autoimmune disorder that arises after 5 days?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Ah, No.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “Is 5 days long enough to detect any neurological disorder that arose from the vaccine after 5 days?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “No.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “There is no control group, correct?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Ah, It does not mention any control group. No.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “If you turn to section 6.2, under immune system disorders, does it say that there were reports of hypers sensitive reactions including anaphylaxis, anaphylactoid reactions, bronchospasms, and urticaria having been reported in the first few hours after vaccination?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Yes.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “Have there been reports of hypersensitivity syndrome?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Yes. That's what states.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “Reports of arthritis?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Um, it is mentioned.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “It also reports autoimmune diseases including systemic lupus erythematosus, lupus-like syndrome, vasculitis, and polyarteritis nodosa as well. Correct?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Yes. That's what it states.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “And also it states that under the nervous system disorders, it states that after that there have been reports of Guillain-Barre syndrome, correct?
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Yes.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “As well as multiple sclerosis, exacerbation of multiple sclerosis, myelitis including transverse myelitis, seizure, febrile seizure, peripheral neuropathy including Bell's palsy, radiculopathy.”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Radiculopathy.”
[Dr. Plotkin corrects Mr. Siri’s pronunciation]
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “Thank you very much. Um, muscle weakness, hypoesthesia, and encephalitis, correct?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Correct.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “These are events that are reported after vaccination and as you've just we've just discussed, in order to establish whether it's causal between the vaccine and the condition, you need a randomly, a randomized placebo-controlled study. But that was not done for the this hepatitis B vaccine before licensure was it?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “No.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “Okay. And given that the vaccine now appears on the CDC’s recommended list, isn't it true that it would now be considered unethical to conduct such a study today?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Um, it would be, yes, it would be ethically difficult.”
https://thehighwire.com/page/1/?s=stanley+plotkin
Full 9 hours of deposition
https://thehighwire.com/ark-videos/the-deposition-of-stanley-plotkin/
Transcript
https://www.lumenfidei.ie/documents/dr-stanley-plotkin-testimony.pdf
***************************************************************************************************HOW LONG SHOULD THEY BE TESTED - DAYS is not long enough:
Duration of Pediatric Clinical Trials Submitted to the US Food and Drug Administration
“Our findings suggest that these pediatric studies may not provide complete safety data across all critical periods of growth and development. This observation may be important because multiple periods of critical pediatric growth and development exist, including marked deceleration in linear growth and weight gain during the first 2 years of life, and initiation of puberty around ages 11 to 13 years, accompanied by acceleration in linear growth that may last for 3 to 4 years.34,35 Although the first 3 years of life are often considered more critical than older ages for brain development, biochemical studies of brain metabolism suggest that high brain metabolic rates characteristic of early childhood may not decline to adult levels until ages 16 to 18 years, suggesting that the school-age and adolescent periods are equally critical periods of brain development.36 Given this information, even the longest trial duration identified in our study (364 weeks/7 years) does not completely evaluate potential critical stages of all pediatric growth and development periods, nor does it begin to characterize the exposure associated with lifelong therapy.”
“Public availability of data on drug efficacy and safety in children may require an additional 6 years.40 “
https://pmc.ncbi.nlm.nih.gov/articles/PMC6526087/
Step 3: Clinical Research - This is the FDA
”Length of Study: 1 to 4 years”
https://www.fda.gov/patients/drug-development-process/step-3-clinical-research
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LIABILITY:
“No vaccine manufacturer shall be liable in a civil action for damages arising from a vaccine-related injury or death associated with the administration of a vaccine after the effective date of this subtitle if the injury or death resulted from side effects that were unavoidable even though the vaccine was properly prepared and was accompanied by proper directions and warnings.”
“No vaccine manufacturer shall be liable in a civil action for damages arising from a vaccine-related injury or death associated with the administration of a vaccine after the effective date of this subtitle if the injury or death resulted from side effects that were unavoidable even though the vaccine was properly prepared and was accompanied by proper directions and warnings.”
Vaccine manufacturers are not liable for injury or death resulting from a vaccine. What other products do you use where the manufacturer can fail to test them and then not be held responsible for injuries and death?
If planes were not tested, would you fly in them? Would it seem appropriate for anyone to force you to do so?
https://uscode.house.gov/view.xhtml?path=/prelim@title42/chapter6A/subchapter19&edition=prelim
https://www.hrsa.gov/sites/default/files/hrsa/vicp/title-xxi-phs-vaccines-1517.pdf
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FDA LICENSE DOES NOT MEAN IT STOPS INFECTION OR TRANSMISSION:
“… FDA’s authorization and licensure standards for vaccines do not require demonstration of the prevention of infection or transmission.”
Go here and click Download to read the document where the FDA explains this fact:
https://www.regulations.gov/document/FDA-2023-P-0360-0191
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MMR violates guidelines
Medication Administration: Vaccines for Immunizations (Ambulatory) - CE/NCPD
“Two live vaccines should not be given in the same muscle mass.”
https://elsevier.health/en-US/preview/vaccines-immunizations
MMR is three live viruses. It comes in ONE SHOT that is injected into one muscle. Clearly, this goes against the guidelines.
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DO INFANTS BENEFIT FROM VACCINES GIVEN IN THE FIRST YEAR:
These studies say no.
A Prime Time for Trained Immunity: Innate Immune Memory in Newborns and Infants
Infants 6 months and younger don’t get the right immune response and they don’t get to the same level of immunity if they start that early. No matter how many vaccines they get later, they never reach the full level of immunity. The early vaccines appear to prime the immune system improperly.
https://karger.com/neo/article-abstract/105/2/136/327715/A-Prime-Time-for-Trained-Immunity-Innate-Immune?redirectedFrom=fulltext
Maternal antibodies and infant immune responses to vaccines
“Infants are born with immature immune systems, making it difficult for them to effectively respond to the infectious pathogens …”
Research also shows that a child below age 1 has almost no immune memory. That makes it futile to vaccinated them. It is all risk and no reward.
https://www.sciencedirect.com/science/article/pii/S0264410X15010634
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SIDS - Sudden Infant Death Syndrome:
There is evidence being found of an association between vaccines and SIDS.
The Immature Infant Liver: Cytochrome P450 Enzymes and their Relevance to Vaccine Safety and SIDS Research
“Results: CYP450 enzymes exhibit developmental immaturity in infants and genetic polymorphisms—particularly in CYP2D6 and CYP3A5—may affect vaccine excipient clearance. While epidemiological evidence shows temporal clustering of some SIDS cases post-vaccination, causality remains unproven. Inflammation-induced suppression of CYP450 enzymes raise questions about potential metabolic vulnerabilities, which current postmortem protocols often fail to capture.”
https://www.medsci.org/v22p2434.htm
CYP450 = super family = gigantic group of enzymes that plays a major role in detoxifying things from the body.
genetic polymorphisms = some have genetic vulnerabilities
Jefferey Jaxen explains (paraphrased): “When you can’t detox these pathways, inflammation arises which affects the entire body. That causes a cytokine storm. It affects the breathing pathways – the serotonin pathway which is the autonomic nervous system. That causes the baby to stop breathing.”
See The HighWire Episode 427: THE AGENDA EXPOSED, Timestamp 25:27
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VACCINATED MOTHERS DO NOT PASS ANY IMMUNITY TO THEIR BABIES.
This puts every infant at serious risk in that first year. And vaccinating them does not help.
Maternally derived measles immunity in era of vaccine-protected mothers
“By 1984, most women <26 years of age derived their immunity from the vaccine. The measles vaccine elicits lower antibody titers than the natural disease. ~ Yeager et al. 6 have noted a progressive decline in the mean titer in cord sera between 1969 and 1980, an effect to be expected with the arrival of vaccinated girls to the age of motherhood. Many of today's infants receive less antibody at birth and become both susceptible to measles and responsive to the vaccine at an earlier age than was the case a decade ago.”
https://pubmed.ncbi.nlm.nih.gov/3701511/
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POSSIBLE LINK TO SIDS (Sudden Infant Death Syndrome):
The Immature Infant Liver: Cytochrome P450 Enzymes and their Relevance to Vaccine Safety and SIDS Research
“Results: CYP450 enzymes exhibit developmental immaturity in infants and genetic polymorphisms—particularly in CYP2D6 and CYP3A5—may affect vaccine excipient clearance. While epidemiological evidence shows temporal clustering of some SIDS cases post-vaccination, causality remains unproven. Inflammation-induced suppression of CYP450 enzymes raise questions about potential metabolic vulnerabilities, which current postmortem protocols often fail to capture.”
CYP450 = super family = gigantic group of enzymes that plays a major role in detoxifying things from the body.
genetic polymorphisms = some have genetic vulnerabilities
Jefferey explains (paraphrased): “When you can’t detox these pathways, inflammation arises which affects the entire body. That causes a cytokine storm. It affects the breathing pathways – the serotonin pathway which is the autonomic nervous system. That causes the baby to stop breathing.”
https://www.medsci.org/v22p2434.htm
***************************************************************************************************MEASLES: vaccinated spread it for 800 days:
Measles Vaccine Virus RNA in Children More Than 100 Days after Vaccination
“We report detection and confirmation of MeVV RNA from the respiratory tract of 11 children between 100 and 800 days after most recent receipt of measles-containing vaccine.”
800 days = 2 years, 2, and 10 days
https://www.mdpi.com/1999-4915/11/7/636
The vaccinated are spreading it. So, the claim that we all need to be vaccinated to protect those who aren’t old enough yet or who are immunocompromised or otherwise vulnerable is baloney. The vaccinated are actually spreading it to the vulnerable.
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PERTUSSIS aka whooping cough vaccine:
This vaccine causes linked epitope suppression aka original antigenic sin. That means the vaccine provides immunity to only the 4 or 5 variants that are in the shot. The vaccine stops the vaccinated from ever gaining immunity to the variants that are not in the vaccine. There are somewhere around 3000 variants.
The vaccinated get mild symptoms. They don’t get sick enough to stay home. That means they spread it to everyone. That includes newborns, the elderly, and immunocompromised.
All medical personnel are fully vaccinated. They are spreading it to everyone. A vaccinated person goes to a medical facility due to injury or illness. He or she can end up with whooping cough on top of the original medical issue.
Here is the documentation:
The 112-Year Odyssey of Pertussis and Pertussis Vaccines Mistakes Made and Implications for the Future
“Because of linked-epitope suppression, all children who were primed by DTaP vaccines will be more susceptible to pertussis throughout their lifetimes, and there is no easy way to decrease this increased lifetime susceptibility.”
https://academic.oup.com/jpids/article/8/4/334/5359449?login=false
Video:
Here is a great explanation. Start at timestamp 18:00
https://thehighwire.com/ark-videos/big-pharma-propaganda-exposed/
Find links to notes, studies and videos here:
https://cheryldibiase.substack.com/p/the-highwire-episode-62-big-pharma
Here is where Aaron Siri explains this: timestamp 4:43
https://cheryldibiase.substack.com/p/episode-359-safeguarding-vaccine
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POLIO:
Facts to calm fears.
Poliomyelitis
“The overwhelming majority of infections (95%) are asymptomatic.”
https://hhs.iowa.gov/center-acute-disease-epidemiology/epi-manual/reportable-diseases/poliomyelitis
Mayo Clinic Polio
“Top of Form
About 5% of people with the poliovirus get a mild version of the disease called abortive poliomyelitis.”
“Nonparalytic polio
A more severe form of the disease, called nonparalytic polio, affects about 1% of those infected. While the illness lasts longer than a few days, it doesn't cause paralysis. Besides having more-severe flu-like symptoms, nonparalytic polio symptoms may include:
Neck pain or stiffness
Aches or stiffness in the arms or legs
Severe headache
Paralytic polio
This most serious form of the disease is rare.”
https://www.mayoclinic.org/diseases-conditions/polio/symptoms-causes/syc-20376512
Inactivated poliovirus vaccine IPV (this is the shot used in the USA)
“Disadvantages”
“IPV induces very low levels of immunity in the intestine. As a result, when a person immunized with IPV is infected with wild poliovirus, the virus can still multiply inside the intestines and be shed in the faeces, risking continued circulation.”
“IPV does not stop transmission of the virus”
https://polioeradication.org/about-polio/the-vaccines/ipv/
OPV Oral Polio Vaccine
“… OPV can cause vaccine-associated paralytic poliomyelitis (VAPP).”
https://polioeradication.org/about-polio/the-vaccines/opv/
The oral polio vaccine OPV causes
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VACCINES INCREASE THE RISK OF OTHER ILLNESSES:
Influenza (FLU) shot increases the risk of non-influenza infections.
Increased Risk of Noninfluenza Respiratory Virus Infections Associated With Receipt of Inactivated Influenza Vaccine
“We randomized 115 children to trivalent inactivated influenza vaccine (TIV) or placebo. Over the following 9 months, TIV recipients had an increased risk of virologically-confirmed non-influenza infections (relative risk: 4.40; 95% confidence interval: 1.31-14.8). Being protected against influenza, TIV recipients may lack temporary non-specific immunity that protected against other respiratory viruses.”
Relative risk = 440%
TRANSLATION: You may not get the flu but you sure will get other things.
It limited the disease covered by the shot while EXPANDING all the rest.
https://academic.oup.com/cid/article/54/12/1778/455098#google_vignette
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VACCINES CAN MAKE THE VACCINATED MORE SICK: that is called negative efficacy
Effectiveness of the Influenza Vaccine During the 2024-2025 Respiratory Viral Season
“Among 53402 employees, 43857 (82.1%) had received the influenza vaccine by the end of the study. Influenza occurred in 1079 (2.02%) during the study. The cumulative incidence of influenza was similar for the vaccinated and unvaccinated states early, but over the course of the study the cumulative incidence of influenza increased more rapidly among the vaccinated than the unvaccinated.”
“In an analysis adjusted for age, sex, clinical nursing job, and employment location, the risk of influenza was significantly higher for the vaccinated compared to the unvaccinated state (HR, 1.27; 95% C.I., 1.07 – 1.51; P = 0.007), yielding a calculated vaccine effectiveness of −26.9% …”
That means you are 26.9% greater chance of getting sick with flu if you got the vaccine.
“Conclusions This study found that influenza vaccination of working-aged adults was associated with a higher risk of influenza during the 2024-2025 respiratory viral season, suggesting that the vaccine has not been effective in preventing influenza this season.”
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DISEASE ENHANCEMENT:
Some vaccines actually make the disease worse. This is called immune enhancement. So far, this has been documented with respiratory virus vaccines, RSV and Coronavirus (including covid-19 viruses). Here is Dr Hotez explaining.
March 5, 2020
House Science, Space, and Technology Committee Hearing on Coronavirus
[Dr Peter Hotez, House Science, Space, and Technology Committee Hearing on Coronavirus]:
Timestamp 0:23:00 “One of the things that we’re not hearing a lot about is the unique potential safety problem of coronavirus vaccines. Ah, this was ah, first found in the early 1960s with respiratory syncytial virus [RSV] ah, vaccines. And it was done here in Washington with the NIH and Children’s National Medical Center. That some of those kids who got the vaccine actually did worse, and I believe there were two deaths in the consequence of that study. Because what happens with certain types of respiratory virus vaccines, you get immunized and then when you get actually exposed to the virus, you get this kind of paradoxical immune enhancement phenomena… When we started developing coronavirus vaccines and our colleagues, we noticed in laboratory animals that they started to show some of the same immune pathology that resembled what had happened 50 years earlier. We said, ‘Oh, my God. This is going to be problematic.’ … These clinical, ah, trials are not going to go quickly because of that immune enhancement. It’s gonna take time.”
https://www.c-span.org/video/?470035-1/house-science-space-technology-committee-hearing-coronavirus
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VACCINES CAUSE OTHER ILLNESSES TO BECOME DEADLY:
A study comparing villages in Africa found that the vaccinated villages had a tenfold increase in death from temporary illnesses that are not normally deadly.
Screenshot from The HighWire EPISODE 320: THOUGHT POLICE: https://thehighwire.com/ark-videos/thought-police/
The Introduction of Diphtheria-Tetanus-Pertussis and Oral Polio Vaccine Among Young Infants in an Urban African Community: A Natural Experiment
https://pubmed.ncbi.nlm.nih.gov/28188123/
Children ended up dying at 10Xs the rate of those that never received it.
What they pointed out was that up to that point studies were only looking at were the kids being protected against Diphtheria-Tetanus-Pertussis. The vaccine seemed to stop that from happening. But it created other immune issues where the children were dying of malaria and everything else at higher rates. So, the mortality was 10 times the rate.
Links and Notes can be found here: https://cheryldibiase.substack.com/p/the-highwire-episode-320-thought at Timestamp 57:20
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ENTIRE CHILDHOOD SCHEDULE TESTING:
There are no studies showing the entire childhood vaccine schedule is safe. How can we be sure that the schedule is not causing other problems like in Africa?
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AUTISM:
The claim is that the relationship between Autism and vaccines has been studied. Here are two experts testifying. Under oath they have to admit that there are no studies.
DR PLOTKIN:
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “There's only one condition for which they couldn't find any evidence one way or another on whether it caused, whether the vaccine causes that condition, correct?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Right.”
[Aaron Siri, ESQ, Lead counsel ICAN legal team]: “And that was -- what was that condition?”
[Dr Stanley Plotkin; World’s Leading Authority on Vaccines]: “Autism.”
https://thehighwire.com/page/1/?s=stanley+plotkin
Full 9 hours of deposition
https://thehighwire.com/ark-videos/the-deposition-of-stanley-plotkin/
Transcript
https://www.lumenfidei.ie/documents/dr-stanley-plotkin-testimony.pdf
DR EDWARDS:
[Aaron Siri, Lead Counsel, ICAN legal team]:
“In your opinion, did the clinical trails relied upon to license the vaccines that Gates received, many of which are still on the market today, were they designed to rule out that the vaccine causes autism?”
[Dr Kathryn Edwards, World-Leading Vaccinologist, “The Godmother of Vaccines”]:
“No. You badgered me into answering the question the way you want me to. But, I, I think that, that’s probably the answer.”
[Aaron Siri, Lead Counsel, ICAN legal team]:
“Is it, Is that your accurate and truthful testimony?”
[Dr Kathryn Edwards, World-Leading Vaccinologist, “The Godmother of Vaccines”]:
“Yes.”
Go to timestamp 16:13 to read a transcript of her testimony.
https://cheryldibiase.substack.com/p/the-highwire-episode-383-hidden-games
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VACCINE SAFETY WHITE PAPER:
Introduction To Vaccine Safety And Policy In The United States
https://icandecide.org/article/introduction-to-vaccine-safety-and-policy-in-the-united-states/
White Paper
https://icandecide.org/wp-content/uploads/2019/09/VaccineSafety-Version-1.0-October-2-2017-1.pdf
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VACCINE DEBATE ICAN VS HHS:
ICAN Vaccine Safety Debate
https://icandecide.org/vaccine-safety-debate/
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SOMETHING TO SHARE WITH LEGISLATORS AND SUCH:
An Introduction to Vaccine Safety
https://icandecide.org/article/an-introduction-to-vaccine-safety/
https://icandecide.org/wp-content/uploads/2023/08/INTRO_TO_VAX_SAFETY_2023.pdf
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GETTING CHILDHOOD ILLNESSES has benefits:
HEART DISEASE:
Association of measles and mumps with cardiovascular disease: The Japan Collaborative Cohort (JACC) study
“Measles and mumps infections were associated with decreased risks of mortality from cardiovascular disease.”
“A higher number of infections was associated with a lower risk of mortality from cardiovascular disease.”
“Methods: 43,689 men and 60,147 women aged 40–79 years at baseline (1988–1990) completed a lifestyle questionnaire, including their history of measles and mumps, and were followed until 2009. Histories of infections were categorized as having no infection (reference), measles only, mumps only, or both infections. Hazard ratios (HR) for mortality from CVD across histories of infections were calculated.”
CVD = cardiovascular disease
“Men with measles only had multivariable HR (95% confidence interval) of 0.92 (0.85–0.99) for total CVD, those with mumps only had 0.52 (0.28–0.94) for total stroke and 0.21 (0.05–0.86) for hemorrhagic stroke, and those with both infections had 0.80 (0.71–0.90) for total CVD, 0.71 (0.53–0.93) for myocardial infarction, and 0.83 (0.69–0.98) for total stroke.”
HR (95% confidence interval) = 1.0 would be normal rate.
Measles only: There is an 8% reduction of cardiovascular disease in those who have measles only. Mumps only: There is a 48% reduction in cardiovascular disease and reduction of 79% in hemorrhagic stroke in those who had mumps only.
Measles & mumps: If you had both, there is a 20% reduction in cardiovascular disease and 29% reduction in heart attacks aka myocardial infarction and 17% reduction in total stroke.
Screenshot from The HighWire Episode 413: THE TRUTH ABOUT MEASLES
This is all that data averaged out.
CVD = cardiovascular disease
MI = myocardial infarction
How many deaths are there in the USA from cardiovascular? For 2024 is was 941,652. If we round it up to 1 million, that’s one million people who died last year.
If you had measles and mumps as a child and didn’t get vaccinated, 200,000 people would be saved PER YEAR. 200,000 deaths avoided by catching measles and mumps if we skipped the vaccines. So we save 600 people from dying from measles while allowing 200,000 per year to die of cardiovascular disease.
https://pubmed.ncbi.nlm.nih.gov/26122188/
There is a really excellent explanation of this here: Timestamp 1:36:25
https://thehighwire.com/ark-videos/the-truth-about-measles/
Find links and notes here:
https://cheryldibiase.substack.com/p/the-highwire-episode-413-the-truth
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CANCER:
Acute infections as a means of cancer prevention: opposing effects to chronic infections?
“In contrast to many chronic infections that are known to be associated with an increased cancer risk, this review of epidemiological studies provided support for an antagonism between acute infections and cancer.”
https://pubmed.ncbi.nlm.nih.gov/16490323/
Screenshot from The HighWire Episode 413: THE TRUTH ABOUT MEASLES
Ovarian cancer: Chicken pox = 30% reduction. Measles = 50% reduction. Mumps = 35% reduction. Rubella = 35% reduction.
Multiple caners: Chicken pox = 34% reduction. Measles = 39% reduction. Mumps = 17% reduction. Rubella = 28% reduction.
18,000,000 new cancer diagnoses each year. 30% reduction means 6 million people every year would not get cancer.
6 million people per year are getting cancer because we vaccinated them as children.
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Do childhood diseases affect NHL and HL risk? A case-control study from northern and southern Italy
“Measles was negatively associated with NHL, particularly follicular B-cell NHL. Our findings provide additional support to the hypothesis that infections by most common childhood pathogens may protect against HL or, at least, be correlated with some other early exposure, which may lower the risk of HL in adulthood. In addition, our study shows that measles may provide a protective effect against NHL.”
https://pubmed.ncbi.nlm.nih.gov/16406019/
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Infantile Hodgkin's disease: remission after measles
https://pubmed.ncbi.nlm.nih.gov/4574047/
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Febrile infectious childhood diseases in the history of cancer patients and matched controls
“The number of FICD decreased the cancer risk, in particular for non-breast cancers.”
https://pubmed.ncbi.nlm.nih.gov/9824838/
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Allergic disease and atopic sensitization in children in relation to measles vaccination and measles infection
“Conclusion: Our data suggest that measles infection may protect against allergic disease in children.”
https://pubmed.ncbi.nlm.nih.gov/19255001/
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Frequency of allergic diseases following measles
“Conclusion: The results of this study indicate that findings of allergic disease are less frequent in children with a history of measles.”
https://pubmed.ncbi.nlm.nih.gov/16854347/
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Measles infection and Parkinson's disease
“A reduced risk of Parkinson's disease was associated with most childhood viral infections.”
https://pubmed.ncbi.nlm.nih.gov/4061437/
***************************************************************************************************WHO WORLD HEALTH ORGANIZATION ADMITS VACCINES ARE NOT SAFE OR EFFECTIVE:
These two shows detail the “WHO Vaccine Safety Summit”. The WHO got together to try and figure out how to improve confidence in vaccines. During the two day meeting, they shared some devastating facts about how UNSAFE the entire vaccine program is, the fact that none of them are properly tested, and that they view human beings as “target populations” regardless of the serious risks. It is worth watching. The first one is the original from January 2020. That was right after this summit. The second one is an updated version from Thanksgiving 2024.
The HighWire Episode 400: W.H.O.’S TO THANK Links & Notes
https://thehighwire.com/ark-videos/w-h-o-s-to-thank/
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VAXXED MOVIES:
https://vaxxedthemovie.com/
Available free here
https://thehighwire.com/ark-videos/vaxxed-from-cover-up-to-catastrophe/
VAXXED II
https://live.childrenshealthdefense.org/chd-tv/videos/vaxxed-2/
VAXXED III