Category Archives: Flu

Rna In Vax’s ~ Never Before Done ~ Human Guinea Pigs R U

There are 72 common vaccines in the United States.

We have never ever used an mRNA vaccine ever.
We have RNA vaccines. Measles virus is an RNA virus. Polio is an RNA virus.
But the difference is that in those vaccines the virus is part of the vaccine wholly-intact.
When your body generates an antibody against a virus, it is against the outer coating proteins of that virus.

What we’re doing with this new vaccine is we’re taking a little piece of the covid viruses genetics. Specifically, we are taking the code associated with what’s called the Spike Protein. We’re injecting that into the body creating something called a ‘non-neutralizing antibody’ which, in essence, instead of taking that messenger RNA and gobbling it up and making it go away like what happens when you get a measles vaccine and you get a measles and it gobbles it up and it makes it go away, this non-neutralizing antibody actually creates something called antibody dependent enhancement. That’s often referred to as ADE.

An antibody dependent enhancement allows that little piece of messenger RNA to start replicating on its own. And it will. Over and over again, creating these little pieces of proteins inside of our body for our body to create an antibody against.

This is what will Bill Gates meant when he said “yeah, human beings can become their own little vaccine manufacturing machine.”

Because we interject this messenger RNA that binds onto your reverse transcriptase enzymes, and starts replicating itself over and over again creating more antibodies against the spike protein.

Here’s where it gets really interesting..
That spike protein has been shown in 2 other very specific ways to cause injury.

1.) When you create an antibody to that spike proteins..Antibodies are designed and when we write about them in literature we make it look like the letter Y. The two arms of the Y are called FAB fragments and the stem is the FAC fragments FAB are the ones that grab hold of the virus and generally neutralize it.

When you look at the messenger RNA it grabs hold of it but kind of loosely binds it and when this FAC fragment goes over and hooks onto the macrophage that’s supposed to kill it, and it gets taken inside and that messenger RNA gets released.

That’s where it starts to replicate over and over again. It’s like having an on-button but no off-button.

That whole thing, that whole Y mechanism I just described to you has a name. They call it Trojan horse mechanism. They call it this because it allows that virus and that piece of that virus to get inside of your cells, start to replicate, and even get inserted into other parts of your DNA as a Trojan horse.

That is one of three mechanisms.
2.) When you create this antibody, this non-neutralizing antibody, to the messenger RNA, (or that stem/FAC segment to that spike protein) can go into your lungs and attach to the lung tissue and start developing diffuse alveolar damage, which is diffuse injury to the cells inside of your lungs. Where. You. Breath!

It starts to break them down and destroy them. And what those antibodies do is they cause various degrees of puss and bleeding and damage to your lungs.

So, as you get this vaccine, this messenger RNA, you create an antibody, the antibody carries the thing inside of the cells through Trojan horse mechanism the antibody itself goes and starts to damage the lungs.

3.) And the even more sinister thing is that spike protein antibodies can attack your macrophage. Macrophage are a type of white blood cell that gobble up bacteria and bad viruses in your system that aren’t supposed to be there through your FH1 pathway, your hyper-vigilant white blood cells.

We get bacteria into our body all day long from eating, brushing teeth, going to the bathroom, having sex, so those white blood cells just come along and gobble things up and make them go away. There are 2 types of macrophages.

When you get pneumonia or some sort of serious infection the type 1 macrophages are pro-inflammatory and they show up at infection and start creating cytokines and blowing whistles and bringing all the things to try to kill off the infection. They are very aggressive and highly inflammatory, which is what you want!

The type 2 are anti-inflammatory so as you start to recover, the type 2 come in and tell the other guys “shut up we’re here to clean up the mess.” So, they clean up the debris, the dead white blood cells, and all these things.

So both those macrophages work together in concert type 1 -kill off infection and type 2-heal it.
When you’ve got this antibody to the spike protein, which is the full intent and purpose of this entire vaccine, that antibody kills your type 2 macrophages. It attaches to them and inactivates them.

So, in the experimental animals that died of lung infection and inflammation when they sacrificed them..what they found was that all of the lungs were filled up with all of these type 1 pro-inflammatory, highly cytokine types of macrophages and zero type 2 macrophages.
What they did when sacrificing these animals that had not been vaccinated but had been sick, they found that within two days of getting sick without the antibody, without the vaccine, the type 2 macrophages had come into the infection and started cleaning up the mess and started healing it as long as they didn’t have the presence of a spiked antibody.

With the presence of a spiked antibody it killed them and didn’t allow them to do their job.
So, those are 3 of probably 7 mechanisms of how this vaccine is going to cause a problem.
1.) Antibodies to the spike protein are going to destroy your lungs. 2.) The antibody to the spike protein is going to shut off your M2 anti-inflammatory macrophages. 3.) The antibody to the spike protein is going to loosely bind the virus, or loosely bind the messenger RNA, and drag it inside of your cell through a Trojan horse phenomenon, making it start replicating and having this process go on and on and on because it is an on-button without an off-button.

U.S. government statistics reveal that the flu vaccine is the most dangerous vaccine in America

(Natural News) Even the bestselling flu vaccine is only the fifth most popular vaccine in the United States. Prevnar, the vaccine used to prevent infection caused by pneumococcal bacteria; Gardasil, which supposedly prevents cervical cancer; PENTAct-HIB, given to tiny infants to stave off diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis, and Haemophilus influenzae type b; and Infanrix/Pediarix, a vaccine indicated for active immunization against diphtheria, tetanus, pertussis, infection caused by all known subtypes of hepatitis B virus, and poliomyelitis; are all far more popular than the flu vaccine.

Nonetheless, a report released in 2013 by the Department of Justice, shows that more than half of all claims settled by the National Vaccine Injury Compensation Program, also known as the Vaccine Court, were for injuries caused by the influenza vaccine.

As reported by Health Impact News, during the period covering 16 August to 15 November 2013, 139 claims were settled by the Vaccine Court, 70 of which received compensation. Of these settled claims, 42 – or 60 percent – were for injuries caused by the flu vaccine. The remaining 40 percent were for injuries caused by 11 other vaccines.

The greatest number of injuries by far that were reported as a result of the flu vaccine were for Guillain-Barré Syndrome, or GBS, a condition which the National Institute of Neurological Disorders and Stroke describes as follows:

Guillain-Barré syndrome (GBS) is a disorder in which the body’s immune system attacks part of the peripheral nervous system. The first symptoms of this disorder include varying degrees of weakness or tingling sensations in the legs. In many instances the symmetrical weakness and abnormal sensations spread to the arms and upper body. These symptoms can increase in intensity until certain muscles cannot be used at all and, when severe, the person is almost totally paralyzed. In these cases the disorder is life threatening – potentially interfering with breathing and, at times, with blood pressure or heart rate – and is considered a medical emergency. Such an individual is often put on a ventilator to assist with breathing and is watched closely for problems such as an abnormal heart beat, infections, blood clots, and high or low blood pressure. Most individuals, however, have good recovery from even the most severe cases of Guillain-Barré syndrome, although some continue to have a certain degree of weakness.


Neonatal Hepatitis B Vaccine, The Autism Influencer From Day One Of Life?

Is the U.S.-mandated Hepatitis B vaccine administered to newborn infants within 24 hours of birth the initial ‘impact’ vaccine for ‘programming’ a child’s unfortunate decline into the Autism Spectrum Disorder (ASD)?

The answer to that question is a resounding “YES” according to a 2016 peer review study titled, Neonatal hepatitis B vaccination impaired the behavior and neurogenesis of mice transiently in early adulthood published in the Elsevier peer review journal Psychoneuroendochrinology.

The extensive research on mice brains published above indicates what the CDC/FDA should have found and warned against as part of the licensing procedures for the Hepatitis B vaccine introduced as a recommended infant/childhood vaccine way back in 1991, when “the first dose was recommended to be administered at birth before hospital discharge or at age 1–2 months.” [3]

That apparent default by the ever-increasing-malfeasance being exposed on the part of the CDC/FDA’s either ineptness or reliance upon what’s known as “consensus science,” is proof of the absolute need for the dismantling of a federal U.S. health agency—listed on the U.S. Stock Exchange (NASDAQ) [4]by Congress, who has oversight.



CDC Scandal: Committee that Withdrew Recommendation for Nasal Flu Vaccine Now Recommends it to Experiment on American Public

In June of 2016 the Center for Disease Control and Prevention (CDC) Advisory Committee on Immunization Practices (ACIP) admitted that the live attenuated nasal influenza vaccine known as “FluMist” was not effective, and was not recommended for the 2016-2017 flu season.
It was also not recommended for the current flu season (2017-2018). The CDC’s own data showed that the nasal vaccine was not effective. The CDC press release in 2016 stated, “This three percent estimate means no protective benefit could be measured.” Shortly after this announcement in 2016, a family in Utah went public with their story, explaining how their 8-year old daughter died from influenza, even though she had been vaccinated with FluMist.
They had trusted the CDC and their flu recommendations, but now they have lost their daughter. Even though the CDC withdrew their recommendation for the failed nasal flu vaccine, FluMist retained its FDA approval and has been available to purchase the past two years. On February 21, 2018, the CDC’s ACIP reversed its decision on FluMist, and voted 12-2 to add FluMist to the CDC’s list of recommended vaccines for the 2018-2019 influenza season. Stat News reports how members of the ACIP expressed concerns about deciding to reverse their decision and recommend it: “
The motion to recommend FluMist passed by a surprising 12-to-2 vote, the outcome of which belies the unease that a number of members of the committee clearly felt about the decision they were making. They faced, in essence, a Catch-22: It has been impossible to generate the type of data that would normally be used to make a decision like this. The only way to see if the problem has been solved is to use the vaccine. But without an ACIP recommendation, the vaccine’s use in the U.S. would remain minimal.”
So the fact is that the effectiveness of FluMist is still not known, but the CDC has no qualms about testing it on the American public to find out.
Read More…


Are Many Modern Diseases Linked to the Failed Mass Swine Flu Vaccination in 1976?

Crohn’s. Lupus. Autism. ADHD. Food allergies. Celiac disease. Sjögren’s syndrome. Polymyalgia rheumatica. Multiple sclerosis. Anklyosing spondylitis. Type 1 diabetes. Vasculitis. Peripheral neuropathy.
The list goes on, and on, and on. We are being increasingly diagnosed with these conditions and diseases of unknown origin, and science has very little to say – why would autoimmune diseases and mysterious diseases of inflammation be so prevalent? When did this increase start?
Something changed dramatically in 1976. What changed was national mass vaccination against influenza.
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Science vs. CDC: Is the Flu Vaccine More Dangerous than the Flu?

CDC’s strategy to use fear to ramp up flu vaccine sales ­­­­requires the agency to exaggerate both flu risks and vaccine efficacy. Pharmaceutical companies and public health officials vastly overstate flu cases and deaths in order to market influenza “as a threat of great proportions.” Simple fact-checking shows that since October 2017, only 14.7% of the almost 447,000 “flu” specimens tested by clinical laboratories working with CDC have tested positive for influenza.
This proportion has remained relatively constant for the past two decades. According to the British Medical Journal’s Peter Doshi, “Even the ideal influenza vaccine…can only deal with a small part of the ‘flu’ problem because most ‘flu’ appears to have nothing to do with influenza.” Actual influenza deaths not only rank lower than the major killers such as heart disease and cancer but also are lower down in the mortality rankings than ulcers and hernias. Incredibly, even though most “flu” is not influenza and flu vaccine effectiveness is as low as 10%, public health authorities keep telling everyone from six months of age on up (including pregnant women) that the flu shot is “better than nothing” and the “best tool we have.”
However, there are many unanswered questions about influenza vaccines that warrant rigorous investigation. Recent peer-reviewed studies suggest that the shots may actually make people more susceptible to serious problems (as with the recently recalled dengue vaccine) and that getting flu shots year after year may be lowering subsequent vaccine effectiveness as well as drastically increasing risks for Alzheimer’s disease.
Getting vaccinated against one strain of influenza may increase risks for other severe respiratory viruses. Unfortunately, most members of the public are not reading this alarming science. The public should make health decisions based on sound science, not scare tactics.
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6 of 7,767 Science Being Ignored As Deaths from the Flu Continue to Mount Among Mass Flu Vaccinated Population Inbox x Vaccine Impact News Unsubscribe 5:04 AM (4 hours ago) to me Vaccine Impact Science Being Ignored As Deaths from the Flu Continue to Mount Among Mass Flu Vaccinated Population


The U.S. is in the midst of one of the worst outbreaks of influenza in years, and in spite of the fact that the CDC is estimating that the flu vaccine is only about 10% effective, there are massive advertising campaigns in place to get the entire population vaccinated for the flu. Media reports are coming in reporting high rates of deaths due to the flu, and the majority of those dying from the flu have been vaccinated.
The flu shot is not without severe risks, risks that are routinely censored in the corporate “mainstream” media, and include paralysis from Guillain-Barré Syndrome, chronic shoulder pain from SIRVA, and death. It is, by far, the most dangerous vaccine in America. Given the fact that health authorities themselves admit that the flu vaccine is not effective, the public should be made aware of these risks.
The bigger question that needs to be considered is: could the lucrative mass flu vaccination program actually be a cause for more severe flu outbreaks, rather than a cure?
Over 300 million doses of the flu vaccine are manufactured each season, representing a huge cash flow for the pharmaceutical industry that they would obviously be hesitant to give up simply because it is not effective, or even if it is an underlying cause of more severe flu outbreaks.
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