>>56956 (OP)
Vaccines are a means of biological warfare. Endocrine disruptors are a means of chemical warfare. Endocrine disruptors and other chemical weapons contaminate the environment and can be phased out if vaccine bio-weapons take their place.
The advantages of vaccines are:
1. Cheaper than endocrine disruptors.
2. Little to no environmental contamination. E.g., A plastic bottle will poison you and the surrounding environment with bisphenol whereas a vaccine will only harm the receiver.
3. Different populations can be targeted for different objectives with tailor-made vaccines. E.g., Some vaccines can destroy reproductive organs while others weaken immune systems.
Vaccines, whether bacterial or not, contain:
Mercury (neurotoxin, endocrine disruptor)
Aluminium hydroxide (hypoxic, neurotoxic)
Squalene (endocrine disruptor)
Saponins (endocrine disruptor, increases heavy metal absorption)
Polysorbate-80/20 (increases heavy metal absorption)
SV-40 cells (cancer)
Formaldehyde (carcinogen, forms plastic in contact with certain lipids)
Octoxynol-9 (spermicide, carcinogen, can be used as a replacement for Nonoxynol-9)
- Octoxynol-9 was previously a common spermicide but was removed from the U.S. market in 2002 after manufacturers failed to perform new studies required by the FDA.
Modern vaccines contain adjuvants so to intentionally cause an exaggerated immune system response, which is usually aluminium, but they also added peanut oil as an adjuvant. The purpose of these adjuvants is to irritate the immune system and make it react to the rest of the vaccine's contents. I.e., instead of a live virus they would use attenuated. Instead of attenuated they would use dead virus. Instead of dead virus they would use virus parts etc. The further down they go the more adjuvants they need to get the body to react to it, because the body sees it as a non-issue whereby a dead virus or virus parts can't infect it.
The problem here is that dendritic cells have no idea how to distinguish between what is causing the fake immune reaction, which often picks up some random ingredient in the vaccine, brings it to the lymph nodes to program long term immunity, resulting in ling long allergy or autoimmune disorder. The adjuvants irritate the entire immune system, which can't tell what is doing it, so the immune system targets incorrect parts as the "problem", and this is where most environmental and nut allergies come from. Injecting heavy metals also bypass the normal methods of entry to the body where it is optimized to remove them, so the safe toxicity arguments are moot.
It's also ignored that no real safety research has ever been done on vaccines. All vaccines are tested against other vaccines instead of a saline solution, and regulators are all captured.
The measles vaccine primes children for sterility and repeated vaccination.
The hepatitis B and HPV vaccines prevents teen pregnancies and increases the rate of endometriosis.
The flu vaccine incrementally weakens the immune system.
Adjuvants cause autoimmune problems and deposit heavy metals into the brain.
Vaccines cause genomic instability, immune/transcriptomic dysregulation, accumulative genetic damage, compounding mutations and clonal expansion. This contributes to infertility and reduces the procreation drive.
The rate of precocious puberty in girls almost exactly matches the rate of autism in boys.
Every infant goes through a process of mini-puberty in the first few months of life. Technically, this starts in the first few hours after birth. E.g., in boys a significant amount of testosterone floods the brain to prime his sexual development. A similar process happens with girls, but they don't get a flood of testosterone and instead get follicle stimulating hormone and luteinizing hormone to aid their development. This has an impact on language organization, laryngeal sound production, and baby babbling, helping the baby make sounds and eventually talk.
Autism is characterized by terrible verbal skills as well as an "overtly male brain", plus an obsession with patterns and systems. Autism is also highly correlated with genital malformation and almost entirely affects males. In girls there is a correlated development issue call precocious puberty, whereby girls go through puberty early at 5-8 years old instead of getting autism.
These interferences (autism in boys and precocious puberty in girls) of mini-puberty only show up later in life. Both interferences started showing up in considerable numbers around the mid-1990s and became obvious around the 2010s.
The hepatitis B vaccine became widespread during the mid-1990s. The hep B vaccine prevents or disrupts the process of mini-puberty in babies. The efficacy of the hep B vaccine is largely dependent on administering it within the first 24 hours post-birth. However, it was most likely designed to sterilize males outright.
These interferences and subsequent hormone deficiencies, and general endocrine disruption, are merely side-effects of what was originally intended. It would also become too suspicious if women were being sterilized, and it would risk total population collapse rather than a controlled demolition.
Note 1:
The hepatitis B vaccine is a recombinant DNA vaccine, also known as chimeric vaccine, it's not a conventional vaccine. It was initially scheduled for 3 doses plus booster shots every 10 to 15 years. After clinical Stage 3 trials and settlements honoured by the US government that reached 4 billion dollars, it was re-scheduled to 1 singular shot, with a booster shot being suggested for heath-service workers.
Hepatitis B has a statistically 0% contraction rate in uncircumcised infants. The hepatitis B recombinant DNA vaccine and the vitamin K injection are claimed to treat problems (infection in the case of hep B and haemorrhage in the case of vit K) caused by circumcision. The only way for an infant to contract hepatitis B would be during circumcision. The only way for a child to have a vitamin K deficiency is after circumcision or rare delivery complications.
Note 2:
The hepatitis B vaccine became forced at birth because homosexuals kept dying from it, but they refused to get the shot, so the government mandated that everyone get it.
Why are boys 4x more likely to be autistic than girls?
The blood brain barrier in women is stronger than that of men. Men are physically stronger in terms of their skeletal structure and muscularity, women are stronger in their ability to handle poison and toxins, an adaptation necessary to shield children in the womb. Women are also more biologically resilient to candidiasis (they have yeast in their meat flaps) and other forms of digestive dysbiosis. More of the heavy metals in the vaccine adjuvants crosses the blood brain barrier of boys than girls because of this difference, hence the increased rate of boys with autism and/or the side-effects of these vaccines that are merely being diagnosed as autism.
Other than the usual vaccines, unleashing a pandemic can install justification and coercion for a more particular vaccine. The pandemic may be fake, or it may be real, and your choices will be to risk contracting whatever is out there or to take the vaccine that's also designed to maim and/or kill, which is assuming you have a choice.
Another vector of attack can be via plant crops, especially via grain. For example, the yearly flu is from chemicals put in grain supplies, and any new flu afflictions will come via poisons added to the grain and legume supplies.
COVID and/or the vaccines could have been a racially tailored attack on Europeans/Whites via their foetal ovarian formation.
The female foetus will develop eggs, and these require a specific protein, −KTS, which is an isomer of WT1, to begin to form. This process is delicate and time critical. Interrupting it with the vaccine leaves the foetus fully formed, but the eggs are not fully formed as they are made completely sterile thanks to the vaccine in question. 10-12 years from these most recent mass injections against COVID, the number of teenage and early 20s pregnancies will drop to record lows, then a few years later alarm bells will ring as women in general won't be able to get pregnant.
The "side-effect" involving heart issues may have been due to the vaccines' interaction with fast conduction tissue.
If this also causes cellular instability in germline cells, catastrophic outcomes will become visible after a few decades, such as x20-30 cancer incidence growth, <0.5 birth rates etc.
Research into the mRNA vaccine and how it could affect ovary development in human foetuses is required.
Natural immunity is the gold standard of immunity, for immunity can only be achieved via your own immune system. If natural immunity isn't the best possible immunity, then none of the theory behind any vaccine makes sense.
When encountering a virus naturally, you are exposed to all possible antigenic sites from inside and outside the virus at all stages of its development. One of the keys to inducing immune memory is a broad spectrum of antigenic sites, and the only way to get this completely is from natural immunity, thus from a wide variety of antibodies to all parts of the virus via natural infection.
The miniscule spectrum of vaccine induced antibodies created in response to proteins alone have no chance of inducing robust and long-lasting immunity, only natural immunity can do that, hence endless booster shots.
Vaccines only hinder or prevent a natural process of the alleged problem from becoming endemic and harmless. And herd immunity isn't real, your immune system isn't shared. Mass vaccination means putting the majority at risk to theoretically protect the minority.
In natural conditions the strain that out-competes isn't the most lethal, it's the least. The least lethal strain is eventually present in most of a given population, who interact with other people and transmit the virus. The most lethal strain kills people and limits transmission, which is regardless of how vaccines leave a vacuum for more lethal strains to proliferate. This is why Ebola is not at risk for causing an epidemic, because Ebola kills too quickly. Therefore, a virus can't be more contagious and more deadly. If a virus is more contagious it will also be less deadly.
Leaky vaccines put evolutionary pressure on more lethal strains to dominate to the point of their lethality limiting their spread, and they're still more lethal than the strain that would have dominated without a leaky vaccine. That's why death rates started to rise again just after mass vaccination.
Vaccines of the past took a neutered virus sector and taught your body how to defend against that (dead) virus. The mRNA teaches your body using lipid nanoparticle inserted mRNA sequences to produce a cytotoxic spike protein, which destroys living tissue when it comes into contact with it and spreads throughout the body.
The virus causes you to make spike proteins as viruses attached to them. Your body then goes into a hyperimmune response to purge the virus attached spike proteins. With the vaccine the body makes the spike proteins indefinitely and doesn't associate them with a virus at all. This creates an entirely different immune response in that the virus is not associated with it, whereas natural infection creates a more robust response to all the proteins of the virus.
You only have a limited number of t-cells to fight off infection via your immune system, and nearly all of them are too busy fighting off the never-ending supply of spike proteins that their mutated cells are producing. This is allowing trivial infections, such as the chickenpox virus, to make breakthrough infections no matter how old you are. Also, there is no such thing as an mRNA virus.
What is happening and will continue to happen is the immune system destroying any cells displaying the altered spike protein, causing an assortment of ailments.
https://www.npr.org/sections/goatsandsoda/2017/06/28/534403083/mutant-strains-of-polio-vaccine-now-cause-more-paralysis-than-wild-polio
https://www.npr.org/sections/goatsandsoda/2022/04/26/1092867458/vaccine-derived-polio-is-on-the-rise-a-new-vaccine-aims-to-stop-the-spread
Unless all vaccines are fraudulent, then vaccines are a question of cost-benefit with unknown costs and (mostly) minor benefit of reducing a near-zero risk to nearer-zero.
The hepatitis B recombinant DNA vaccine and the vitamin K injection are claimed to treat problems (infection in the case of hep B and haemorrhage in the case of vit K) caused by circumcision. The only way for an infant to contract hepatitis B would be during circumcision. The only way for a child to have a vitamin K deficiency is after circumcision or rare delivery complications. Also, the hepatitis B vaccine became forced at birth because homosexuals kept dying from it, but they refused to get the shot, so the government mandated that everyone get it.
Polio (poliomyelitis), smallpox vaccines, etc. were developed long after the outbreak, after most people had already gained natural immunity. The history of polio is extremely suspicious, in that most statistically listed cases were probably the seasonal flu, and the number of cases may have been exacerbated by a combination of arsenic based pesticides (such as DDT) on crops and lead poisoning, rather than a virus spread via feces.
Smallpox, which has been rebranded as chickenpox, is poisoned tissue below the skin, in which case the body evacuates it straight through the skin. There's no contagion.
Shingles has increased due to the chicken pox and measles vaccines. Also, older people often have a recurring case of shingles or chickenpox as their immune system weakens.
The oral rotavirus vaccine can only be given to under 9-month-olds, which is entirely suspicious.
Diphtheria, tetanus, rubella and mumps are non-issues, but as vaccines they are combined.
Measles has a high spread rate, but it is low risk. Also, naturally contracting Measles-Mumps-Rubella (MMR) and Varicella as a child prevents a deadlier infection as an adult.
Pertussis (whopping cough) has a vast number of cases and is nicknamed the "100-day cough" because it lasts so long, which is what most parents give their children.
Hepatitis A, B, C, Prevnar (for pneumococcal), and act-Hib (for meningitis) offer some benefit, but they also come with more risks.
If you want pertussis or measles, then you have to get them together, but Japan produces a split MMR vaccine.
In the United States, some parents defer to the 1980 vaccine regimen with four vaccines against six diseases:
1. Tuberculosis (Bacille Calmette-Guérin / BCG vaccine).
2. Diphtheria, tetanus, and pertussis (DPT or DTP vaccine).
3. Poliomyelitis (polio).
4. Measles.
- Tetanus has a fairly high rate of complications (seizures being common).
Other parents are now going with this vaccination and nothing else:
1. Diphtheria-Tetanus-Pertussis (DTaP/IPV or dTaP/IPV vaccine) with a-cellular pertussis & pneumococcal conjugate.
- Content difference between Tdap (for older children and adults) and DTaP (for infants and young children) remains uncertain.
- There are cases of children having hypotonic-hyporesponsive episodes due this 3-in-1 vaccine.
The logical choice is to only vaccinate against permanent injury or death, which means very few vaccines if any.
This may leave:
1. Diphtheria.
2. Tetanus.
3. Rabies (or only in the case of).
At the very least, look at the total/gross ingredients of each vaccine (assuming they can be verified), including what they're grown in, weigh up how deadly the disease is and the chance of catching it, then decide for yourself.
If you vaccinate:
Never vaccinate anyone if they are even slightly ill.
Never vaccinate infants, only upon childhood, puberty or post-puberty.
One vaccine at a time with one-month breaks (at minimum) between shots.
- However, consider that non-Europeans (and their proliferation) are re-introducing all kinds of diseases.
Personally, all vaccines are fraudulent even if some vaccines offer a degree of benefit. Vaccines are one of many vectors fundamentally designed to maim, de-fertilize and kill. In isolation each bio-weapon is sufficiently covered by plausible deniability, but in totality they are ruinous. Unvaccinated and uncontaminated immune systems paired with sanitation, hygiene, nutrition, and middle to low population densities are responsible for eradicating disease, not vaccines.