Rushed Vaccines Have Bad Results
A successful vaccine has never been developed for any of the many strains of coronaviruses, due to the nature of the virus itself; and vaccinated people can have a higher chance of serious illness and death when later exposed to another strain of the virus, a phenomenon known as ‘virus interference.’
Similarly, a vaccine for the common cold has never been delivered.
Most takers of the Moderna and Pfizer vaccines are unaware of the dangers of the experimental vaccines they are taking, an explicit violation of the Nuremberg Trials Code which requires fully informed consent of subjects in medical experimentation.
These new vaccinations have not had the typical 3-5 years of safety testing and are considered experimental. Some private medical insurance will not pay for injury or death.
While vaccine makers insist any COVID-19 vaccine reaching the market will have undergone rigorous testing, the way trial protocols are designed suggests these vaccines will not have a significant impact on infection rates, hospitalizations or deaths.
Shockingly, preventing infection with SARS-CoV-2 is not a criterion for success in these vaccine trials. The only criterion for a successful COVID-19 vaccine is a reduction of symptoms shared by both COVID-19 and the common cold.
In AstraZeneca’s case, the interim analysis includes 50 vaccine recipients. The vaccine will be a success if 12 or fewer develop symptoms after exposure to SARS-CoV-2, compared to 19 in the 25-person control group.
At least two cases of transverse myelitis (severe inflammation of the spinal cord) has been documented in AstraZeneca’s trial, and the company temporarily halted its trial in September 2020. In October, Johnson & Johnson also paused its trial due to an undisclosed “unexplained illness” in one of its participants.
If the vaccine cannot reduce infection, hospitalization or death, then it cannot end the pandemic, which means everyone who takes the vaccine will be doing so in vain.
The Gates Foundation has on many occasions rushed vaccinations to poor countries such as India and Africa. The foundation has faced numerous lawsuits for:
Permanently crippling children treated for Polio, some who died because they could not breath
Permanently sterilizing women without their knowledge or consent
For illegally tested vaccines on tribal children
Ethical violations: pressuring vulnerable village girls into the trials, bullying parents, forging consent forms, and refusing medical care to the injured girls.
Causing the death of many who were vaccinated
Robert Kennedy Jr. is the Vaccine Being Rushed?
Are Vaccines that are Rushed Thru Testing Safe?
Quickly created vaccinations have a higher chance of causing an adverse reaction which could be temporary and minor, painful and debilitating enough to keep the person from working, or even cause disability and death.
The 2020 corona virus outbreak infected many people but without making them sick or they recovered fully and are now immune. There is no guarantee of any long term protection, prevention of spreading the virus, or guarantee of health.
Some of the largest sectors to have gained during the pandemic are big pharma, privately owned hospitals and HMOs due to CARES act payouts.
There simply hasn't been sufficient time to properly test the so-called "vaccines" being distributed right now. The vaccine manufacturers know this and are calling the experimental gene therapy a "vaccine" – that is a crime for which they have no liability.
COVID19 vaccine trails have been rigged to pass efficacy tests.
The trials are merely testing reduction of common cold symptoms.
Side effects are common. In cases, they have been deadly.
Why would you consciously not demand answers to these dangerous scenarios?
1. Vaccination - The Silent Epidemic(2013)
2. The Greater Good - (2011)
3. Shots In The Dark -(2009)
4. Vaccination The Hidden Truth -(1998)
5. Vaccine Nation - (2008)
6. Vaccination - The Truth About Vaccines -
7. Lethal Injection - http://bit.ly/1URN7BJ
8. Bought - (2015)
9. Deadly Immunity - (2005)
10. Autism - Made in the USA(2009)
11. Beyond Treason - (2005)
12. Trace Amounts - (2014)
13. Why We Don't Vaccinate -
“I'm just beside myself with anger over this synthetic gene therapy, this chemical poison, and what they're doing worldwide,” Mikovits says. “We're already seeing deaths from this shot. It's illegal. It shouldn't be done. It should be stopped right now. It should have never been allowed to happen, yet we see it being forced on the most vulnerable populations.”
https://patient.info/forums/discuss/shingles-and-flu-shot-619064?page=4 - Shingles as a side effect to flu vaccines - followed by a push to vaccinate for shingles
https://beforeitsnews.com/health/2021/03/20-countries-now-suspend-experimental-covid-injections-are-you-hesitant-3038567.html 20 Countries Now Suspend Experimental COVID Injections - Are You Hesitant? Tuesday, March 23, 2021
https://www.bitchute.com/video/1SHUTGFX4K5b/ - Dr. Christine Northrup interview with Nicholas Veniamin discussing vaccination dangers from childhood to covid.
https://patient.info/forums/discuss/shingles-and-flu-shot-619064?page=4 Reports of Shingles outbreaks after receiving Influenza Vax
Important Notes & Ramifications
Deeper Dive: The Problem With Synthetic RNA
Dr. Joseph Mercola
The messenger RNA (mRNA) used in many COVID-19 vaccines are not natural. They’re synthetic. Since naturally produced mRNA rapidly degrades, it must be complexed with lipids or polymers to prevent this from happening. COVID-19 vaccines use PEGylated lipid nanoparticles, and PEG is known to cause anaphylaxis.2 Lipid nanoparticles may also cause other problems.
In 2017, Stat News discussed Moderna’s challenges in developing an mRNA-based drug for Crigler-Najjar, a condition that can lead to jaundice, muscle degeneration and brain damage:
“In order to protect mRNA molecules from the body’s natural defenses, drug developers must wrap them in a protective casing. For Moderna, that meant putting its Crigler-Najjar therapy in nanoparticles made of lipids.
And for its chemists, those nanoparticles created a daunting challenge: Dose too little, and you don’t get enough enzyme to affect the disease; dose too much, and the drug is too toxic for patients.
From the start, Moderna’s scientists knew that using mRNA to spur protein production would be a tough task, so they scoured the medical literature for diseases that might be treated with just small amounts of additional protein.
‘And that list of diseases is very, very short,’ said the former employee … Crigler-Najjar was the lowest-hanging fruit. Yet Moderna could not make its therapy work ... The safe dose was too weak, and repeat injections of a dose strong enough to be effective had troubling effects on the liver in animal studies.”
However, if they call their drugs vaccines, they can bypass the safety studies. All of a sudden, they expect us to believe that all of these safety issues have been resolved? Another problem is related to how long the mRNA remains stable in your system. It’s encased in nanolipid to prevent it from degrading too rapidly, but what happens if the mRNA degrades too slowly, or not at all?
The idea behind mRNA vaccines is that by tricking your body into creating the SARS-CoV-2 spike protein, your immune system will produce antibodies in response. But what happens when you turn your body into a viral protein factory, thus keeping antibody production activated on a continual basis with no ability to shut down?
In addition, your body sees these synthetic particles as non-self and much of the perpetual antibody response will be autoantibodies attacking your own tissues.
“Normally, messenger RNA is not free in your body because it's a danger signal. As a molecular biologist, the central dogma of molecular biology is that our genetic code, DNA, is transcribed, written, into the messenger RNA. That messenger RNA is translated into protein, or used in a regulatory capacity … to regulate gene expression in cells.
So, taking a synthetic messenger RNA and making it thermostable — making it not break down — [is problematic]. We have lots of enzymes (RNAses and DNAses) that degrade free RNA and DNA because, again, those are danger signals to your immune system. They literally drive inflammatory diseases.
Now you've got PEG, PEGylated and polyethylene glycol, and a lipid nanoparticle that will allow it to enter every cell of the body and change the regulation of our own genes with this synthetic RNA, part of which actually is the message for the gene syncytin …
Syncytin is the endogenous gammaretrovirus envelope that's encoded in the human genome … We know that if syncytin … is expressed aberrantly in the body, for instance in the brain, which these lipid nanoparticles will go into, then you've got multiple sclerosis.
The expression of that gene alone enrages microglia, literally inflames and dysregulates the communication between the brain microglia, which are critical for clearing toxins and pathogens in the brain and the communication with astrocytes.
It dysregulates not only the immune system, but also the endocannabinoid system, which is the dimmer switch on inflammation. We've already seen multiple sclerosis as an adverse event in the clinical trials, and we're being lied to: ‘Oh, those people had that [already].’ No, they didn't.
We also see myalgic encephalomyelitis. Inflammation of the brain and the spinal cord, which is [associated with] exogenous gammaretroviruses, the XMRVs.”
These High-Risk Groups Should Avoid COVID-19 Vaccine
According to Mikovits, research shows 4% to 6% of Americans have already been infected with XMRV gammaretroviruses via contaminated vaccines and blood supply for more than three decades, which is driving a number of chronic health conditions. Now, these synthetic gene therapies (the so-called COVID-19 vaccines) will further add to the chronic disease burden by triggering myalgic encephalomyelitis.
Anyone with an inflammatory disease like rheumatoid arthritis, Parkinson's disease, chronic Lyme disease, anybody with an acquired immune deficiency from any pathogens and environmental toxins, those are the people who will be killed, murdered, by this vaccine. ~ Judy A. Mikovits, Ph.D.
Making matters worse, the synthetic mRNA also has an HIV envelope expressed in it, which can cause immune dysregulation. “This is a nightmare,” Mikovits says. “I'm angry, as this should never be allowed.”
As we discussed in previous interviews, SARS-CoV-2 has been engineered in the lab with gain-of-function research that included introducing the HIV envelope into the spike protein.
Mikovits’ hypothesis is that those who are most susceptible to severe neurological side effects and death from the COVID-19 vaccines are those who have previously been injected with XMRVs, borrelia, babesia, mycoplasma, through contaminated vaccines, resulting in chronic disease. (Her book, “Plague of Corruption,” details the science and history of XMRVs, which is a fascinating read.)
“Yes, absolutely,” she says. “That's one of our hypotheses. But also, anyone with an inflammatory disease like rheumatoid arthritis, Parkinson's disease, chronic Lyme disease, anybody with an acquired immune deficiency from any pathogens and environmental toxins.
Those are the people who will be killed, murdered, by this vaccine, and Anthony Fauci knows it … I can't even sleep [because of] how evil this is. This is so deadly, I can't scream it loud enough from the rooftops.”
The chart below lists 35 diseases associated with XMRV infection. If you have any of these, you may want to think long and hard before you line up for an mRNA COVID-19 vaccine, as your chances of severe side effects or death are likely far higher than someone who does not have any of these diseases.