Vaccines and Immunity: What Does The Real Science Show?

FACT: Vaccines create temporal (short-term) antibodies ONLY. This is the sole requirement from the FDA in order to get approval to sell the vaccine. If you read the vaccine product insert written by the pharmaceutical company that creates the vaccine, it clearly states the increase in temporal antibodies as the basis for proof the vaccine works.

It also gives the percentage of people that had an increase in antibodies after the vaccination. Sometimes this number is quite low in the 50% range, defying any real herd immunity protection theory (more on the myth of herd immunity below).

Antibodies do NOT equal immunity

But science has long known that antibodies alone do NOT create real immunity. Some people with high levels of antibodies can be exposed to an illness and still get sick, while others without antibodies can be exposed and not get sick. Dr. Merrill Chase, nicknamed the Grandfather of Immunology for his pioneering work, did clear-cut research on this issue back in the 1950s. His results are clear: antibody levels don’t determine immunity. More on his work below.

The immune system is a highly complex system and science is still in its infancy understanding how it functions. In fact, immunology textbooks were completely rewritten recently after a University of Virginia study finally proving the link between the gut and the brain through the lymphatic system. Before this 2014 study, immunology books were adamant there was no link.

Doctors are never taught the ingredients in vaccines, the way they disrupt the immune system or the research proving antibodies do not create immunity.

But doctors, who are only trained to promote vaccines and not in the science of vaccination, will never tell you this. In fact, most doctors don’t know since their main sources of vaccine information come from pharmaceutical company representatives paid to sell the vaccine, or the CDC, a government agency that has been called out many times for taking pharmaceutical industry money and collects royalties on vaccines sales.

If vaccines create immunity, why are there multiple cases of outbreaks in vaccinated populations?

Since vaccines are given by injection, they bypass the normal immune pathway and therefore do not trigger the cellular immune system, which science shows to be the main component necessary to create immunity.

As a result, there are numerous reports of outbreaks in fully vaccinated populations, with booster shots not making a difference (studies here). Since there is no benefit of immunity with vaccines, yet the very real risk of side effects and reactions, the question is who really benefits from an outdated vaccine program?

Clearly, vaccines only benefit the pharmaceutical and medical industry, which uses vaccines to create health issues and customers for its prescription drug market and medical treatments. The global vaccine market is worth around $58 BILLION a year with an almost doubling expected in the next decade. As usual, the industry puts profits before patients.

This recent report published by the CDC proves that outbreaks occur in those that are vaccinated…

Click here to read the full report

Creating future customers

So if vaccines don’t create immunity, what do they create? They create future customers for pharmaceutical companies. How? Because the toxic ingredients create health issues and these toxins accumulate in the body causing more issues the more vaccines are received. This is one reason the US vaccine schedule is constantly increasing and now requires 72 vaccines before a child goes to school.

See the current recommended schedule for vaccines here or refer to the CDC website.

Viruses reduce later health issues 

Before childhood vaccines became a huge moneymaker for pharmaceutical companies, these issues were considered “normal” and there was no fear around catching them. Any long-lasting complications were extremely rare (99.9% of cases recovered within a few days with no lasting issues). In fact, many experts argue that childhood illnesses are good for our immune system.

Recently science has discovered that having a childhood illness REDUCES later health issues, like cancer (Studies here). More of the benefits of viruses here.

Herd immunity can only come from naturally caught illnesses — NOT from vaccines. Some people may be old enough to remember that just 20 years ago, measles and chicken pox were benign illnesses that, for centuries, were a rite of passage for children.

Just because it’s contagious doesn’t it mean it’s deadly. In fact, lot of research (studies here) shows a health benefit of these typical childhood illnesses — like reducing cancer risk, lowering risk of heart disease and reducing dementia risk.

In the original description of herd immunity, the protection to the population at large occurred only if people contracted the infections naturally. The reason for this is that naturally-acquired immunity lasts for a lifetime. The vaccine proponents quickly latched onto this concept and applied it to vaccine-induced immunity. But, there was one major problem – vaccine-induced immunity lasted for only a relatively short period [if at all] and then this applies only to humoral immunity.

This is why they began to suggest boosters for most vaccines, even the common childhood infections such as chickenpox, measles, mumps, and rubella.

What this means is that at least half the population, have had no vaccine-induced immunity against any of these diseases for which they had been vaccinated very early in life. In essence, at least 50% or more of the population was unprotected for decades.

We have all lived for at least 30 to 40 years with 50% or less of the population having vaccine protection. So even in theory, herd immunity has not existed in this country for many decades and no resurgent epidemics have occurred. Vaccine-induced herd immunity is a lie used to frighten doctors, public-health officials, other medical personnel and the public into accepting vaccinations.”

Click here to read the full article

Transmission of measles among a highly vaccinated school population–Anchorage, Alaska, 1998.

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://www.ncbi.nlm.nih.gov/m/pubmed/30793754/

Induction of secretory immunity and memory at mucosal surfaces

There is a considerable disparity with regard to migration of memory/effector cells from mucosal inductive sites to secretory effector sites and systemic immune organs. Also, although immunological memory is generated after mucosal priming, this may be masked by a self-limiting response protecting the inductive lymphoid tissue in the gut. The intranasal route of vaccine application targeting nasopharynx-associated lymphoid tissue may be more advantageous for certain infections, but only if successful stimulation is achieved without the use of toxic adjuvants that might reach the central nervous system.
https://www.ncbi.nlm.nih.gov/m/pubmed/17067945/

The innate immune response differs in primary and secondary Salmonella infection.

These studies provide a coherent view of innate immunity to oral Salmonella infection, reveal novel sources of IFN-gamma, and demonstrate that immune status influences the nature of the innate response.
https://www.ncbi.nlm.nih.gov/m/pubmed/12370380/

Immune Response That Begin Within Cells Lining Our Mucous Membrane Are Fighting Off More Illnesses Than We Know on: ‘An innate antiviral pathway acting before interferons at epithelial surfaces’

Suggests an unfamiliar layer of defense begins its work even before your first immune response becomes active. The newly discovered mechanism protects you with little fanfare or fuss, and occurs within the cells of your mucous membrane — the moist tissues lining your nose, mouth, lungs, and urinary and digestive tracts.
In other words, your immune system begins its fight at the point where viruses normally get in.

https://www.medicaldaily.com/immune-response-begin-within-cells-lining-our-mucous-membrane-are-fighting-more-363992
https://www.nature.com/articles/ni.3319

Normal structure, function, and histology of mucosa-associated lymphoid tissue.

“The mucosa-associated lymphoid tissue (MALT) initiates immune responses to specific antigens encountered along all mucosal surfaces. MALT inductive sites are secondary immune tissues where antigen sampling occurs and immune responses are initiated.”
https://www.ncbi.nlm.nih.gov/m/pubmed/17067945/

Chemokines and the Tissue-Specific Migration of Lymphocytes

Constitutively expressed epithelial chemokines may help determine the character of local immune responses and contribute to the systemic organization of the immune system.
https://www.sciencedirect.com/science/article/pii/S1074761301002618

Variability in Humoral Immunity to Measles Vaccine: New Developments.

Despite the existence of an effective measles vaccine, resurgence in measles cases in the USA and across Europe has occurred, including in individuals vaccinated with two doses of the vaccine. [This study further shows that humeral immunity (antibodies) don’t equal immunity.]
https://www.ncbi.nlm.nih.gov/m/pubmed/26602762/

Failure of inactivated influenza A vaccine to protect healthy children aged 6-24 months.

“Inactivated influenza vaccine did not reduce the attack rate of influenza A infection in 6-24 month old children.”
https://www.ncbi.nlm.nih.gov/m/pubmed/15056235