8 Facts You Didn’t Know About The Vaccines

1) It’s not a vaccine. It’s an experimental cell reprogramming injection.

A vaccine contains some type of microorganism designed to create an immune response.  But, what is in those syringes isn’t a microorganism. It’s a type of reprogramming technology.

The injections contain mRNA. The “m” stands for messenger because mRNA carries instructions from the DNA to the parts of your cells that make the substances we need to stay alive. 

Once you get the injection, nanoparticles punch holes in your cells and deliver the mRNA that was made in a drug company lab.  These instructions then tell your body to make parts of the Covid-19 virus.

What is in the injection hijacks your cells and turns them into virus makers.  Our bodies were never designed to be turned into virus production machines.   

It’s like a computer hack for your cells. Instead of your DNA being the only source of instruction for your cells, now messages from a drug company will instruct your cells what to do.

They call it a vaccine, but it’s not.  It’s an experimental injection that reprograms your cells.

2) According to the FDA and the vaccine makers, the experimental injection may cause convulsions, stroke, heart attack, and death and therefore should be monitored for these side effects.

The Vaccines and Related Biological Products Advisory Committee met on October 22, 2020. A 27 page document was presented by Dr. Steve Anderson who is the Director of the Office of Biostatistics & Epidemiology of the Center for Biologics Evaluation and Research (CBER). The CBER is the Center within FDA that regulates biological products for human use.

In this document he listed the possible side effects that should be monitored with the rollout of the Covid Vaccines.  The list included:

Guillain-Barré syndrome, Acute disseminated encephalomyelitis, Transverse myelitis, Encephalitis/ myelitis/ encephalomyelitis/, meningoencephalitis/meningitis/ encepholapathy, Convulsions/seizures, Stroke, Narcolepsy and cataplexy, Anaphylaxis, Acute myocardial infarction, Myocarditis/pericarditis, Autoimmune disease, Deaths, Pregnancy and birth outcomes, Other acute demyelinating diseases, Non-anaphylactic allergic reactions, Thrombocytopenia, Disseminated intravascular coagulation, Venous thromboembolism , Arthritis and arthralgia/joint pain, Kawasaki disease, Multisystem Inflammatory Syndrome in Children, Vaccine enhanced disease.

Here’s slide from the presentation:


Even the manufacturers state their injections can cause things like thrombosis.  Thrombosis is when blood clots block veins or arteries.  This can be deadly.

Here’s a quote from Jannsen (Johnson & Johnson)

“Reports of adverse events following use of the Janssen COVID-19 Vaccine under emergency use authorization suggest an increased risk of thrombosis involving the cerebral venous sinuses and other sites (including but not limited to the large blood vessels of the abdomen and the veins of the lower extremities) combined with thrombocytopenia and with onset of symptoms approximately one to two weeks after vaccination. The reporting rate of thrombosis with thrombocytopenia following administration of the Janssen COVID-19 Vaccine has been highest in females ages 18 through 49 years; some cases have been fatal.”


Johnson & Johnson also admits “Reports of adverse events following use of the Janssen COVID-19 Vaccine under emergency use authorization suggest an increased risk of Guillain-Barré syndrome during the 42 days following vaccination.”

Guillain-Barré Syndrome is a disease where your body’s immune system attacks your nerves. It can also be fatal.

Moderna says their vaccine increases the risk of myocarditis (inflammation of the heart) and pericarditis (inflammation of the tissue that surrounds the heart).

They also said that 1.5% of vaccine recipients experienced chills that were so bad they required medical intervention in people under 64.  For people 65 of age and above, Moderna says that 2.9% of the people who got their vaccine got grade 3 headaches that were deemed “significant”, 5.6% got grade 3 myalgia (muscle pain) that prevented the person’s daily activity, 3.3% got grade 3 arthralgia (joint pain) that prevented the person’s daily activity, and .5% got a fever between 102.1 degrees F and 104.0 degrees F.

For Johnson & Johnson, 1.4% of vaccine recipients age 18-59 got grade 3 myalgia (muscle pain) defined as “(Requiring) bed rest and/or results in loss of work, school, or cancellation of social activities; use of narcotic pain reliever.”

Johnson & Johnson all tells us that there were “Numerical imbalances, with more events in vaccine than placebo recipients…”  This means that the people who got their vaccine had more side effects.  What were these side effects?  According to the manufacturer they were, “Thromboembolic events, Deep vein thrombosis, Pulmonary embolism and Transverse sinus thrombosis with thrombocytopenia.”  However, the manufacturer states that a causal relationship couldn’t be determined.  This means that the company would not take responsibility for these side effects. 

But people who got the Johnson & Johnson vaccine were only monitored for 28 days. 

According to Moderna “Lymphadenopathy-related events that were not necessarily captured in the 7-day e-diary were reported by 1.1% of vaccine recipients and 0.6% of placebo recipients. These events included lymphadenopathy, lymphadenitis, lymph node pain, vaccination-site lymphadenopathy, injection-site lymphadenopathy, and axillary mass, which were plausibly related to vaccination.”

3) Tens of thousands of people who got the experimental injection are getting very sick and dying after the shot

So far, the experimental injection has already injured and killed thousands of people.

The government’s VAER’s database (Vaccine Adverse Event Report System) has identified 15,000 deaths and 7000,000 injuries associated with the Covid vaccines. People who are getting the vaccines are getting very sick and some are dying after getting the shots.  

But these numbers could be 100 times as much.

A report that received zero media attention was published by Harvard Pilgrim Health Care, Inc. It states that, “Fewer than 1% of vaccine adverse events are reported.”

This finding was submitted to the Agency for Healthcare Research and Quality (AHRQ) at the US Department of Health and Human Services (HHS).

This suggests that there may be a hundred times as many injuries and deaths related to vaccines than what is reported in VAERS.

The reasons for the low reporting rate (approximately 1 percent) were investigated and found to include:

“[A] lack of clinician awareness, uncertainty about when and what to report, as well as the burdens of reporting: reporting is not part of clinicians’ usual workflow, takes time, and is duplicative.”

This illuminating report concluded that:

“Low reporting rates preclude or slow the identification of ‘problem’ drugs and vaccines that endanger public health. New surveillance methods for drug and vaccine adverse effects are needed.”

The study concluded that with electronic medical records used by most health care organizations today, there is already built-in functionality to capture vaccine injury data.

Guess what happened when the researchers asked the CDC to run a test to see how easy it would be to capture data about vaccine side-effects? The CDC was not interested.

The report says:

“Unfortunately, there was never an opportunity to perform system performance assessments because the necessary CDC contacts were no longer available and the CDC consultants responsible for receiving data were no longer responsive to our multiple requests to proceed with testing and evaluation.”

Let’s think about that.

A study funded by the US government finds that the current system to collect vaccine side-effects (VAERS) captures only about 1 percent of vaccine injuries. The study then suggests how to make VAERS much more accurate, but the CDC was not “responsive to our multiple requests…” They were not interested.


Lazarus, Ross. “Electronic Support for Public Health–Vaccine Adverse Event Reporting System (ESP:VAERS).” AHRQ Digital Healthcare Research. Last modified December 1, 2007.

4) The experimental injection contains nanoparticles, industrial chemicals and PEG. Some people are allergic to PEG and the injection can cause an anaphylactic reaction.

The vaccines contain experimental lipid nano-particles such as:  (4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis (ALC-3015) AND 1,2-distearoyl-snglycero-3-phosphocholine (DPSC).  Very little is known about these substances.

The injections also contain industrial chemicals such as: potassium chloride, monobasic potassium phosphate, dibasic sodium phosphate dehydrate.  Some of these ingredients have been used in fertilizers.

In addition, the injections contain: polyethylene glycol or PEG: polyethylene glycol (PEG) lipid conjugate.  (2- hexyldecanoate),2-[(polyethylene glycol)-2000]-N,N-ditetradecylacetamide (ALC-0159) in Pfizer. (2-hexyldecanoate), 2 [(polyethylene glycol)-2000]-N,N-ditetradecylacetamide in Moderna. 

A significant percentage of the population is allergic the PEG and that may explain so many sudden deaths after getting injected.

According to Science Magazine:

PEG has never been used before in an approved vaccine, but it is found in many drugs that have occasionally triggered anaphylaxis—a potentially life-threatening reaction that can cause rashes, a plummeting blood pressure, shortness of breath, and a fast heartbeat. Some allergists and immunologists believe a small number of people previously exposed to PEG may have high levels of antibodies against PEG, putting them at risk of an anaphylactic reaction to the vaccine.”

In fact Moderna admits “Severe allergic reactions, including anaphylaxis, have been reported following administration of the Moderna COVID-19 Vaccine during mass vaccination outside of clinical trials.”

Johnson & Johnson warns “Appropriate medical treatment to manage immediate allergic reactions must be immediately available in the event an acute anaphylactic reaction occurs following administration of the Janssen COVID-19 Vaccine…In clinical studies, severe allergic reactions, including anaphylaxis, have been reported following administration of the Janssen COVID-19 Vaccine.”

There is no commercially available blood test for PEG allergy so you can’t find out if you are allergic to PEG or not.

5) The companies making the “Covid Vaccines” (Experimental Injections) have no financial responsibility when their injections hurt or kill someone

Covid vaccine companies are not financially responsible when their vaccine hurts or kills someone.  They cannot be sued. They have liability protection from something called the PREP Act. Congress gave it to them.

If you are injured by the vaccine you are on your own.  The vaccine maker is not responsible.

6) The experimental injection is not needed

The vaccine and the risks associated with getting it are totally unnecessary because there are safe and effective ways to prevent and treat Covid right now.  One is called Ivermectin.  There are others. Doctors are using them today and they work.

7) Not tested for DNA Damage

The vaccines were NOT tested to see if they cause cancer or damaged our DNA.

No carcinogenicity or genotoxicity studies were performed on any of the Covid vaccines to determine if they cause cancer.   

8) Vaccine may or may not work

Thousands of people who have received the experimental injections have been diagnosed with Covid afterwards.  This should not be surprising as the manufacturers tell us this.

Moderna says: “The Moderna COVID-19 Vaccine may not protect all vaccine recipients.”

Johnson & Johnson says: “The Janssen COVID-19 Vaccine may not protect all vaccinated individuals.”

There are thousands of people who still get Covid after getting the shots.  In fact, the drug companies’ own data shows that the vaccines are barely effective.  For example, here are the actual numbers from Pfizer:

18,198 people got the vaccine and 18,190 did not get Covid. 

18,325 got the placebo and 18,163 did not get Covid. 

The difference between the vaccinated and unvaccinated was less than 1%. 

The manufacturer also tells us:

“Data are limited to assess the effect of the vaccine against transmission of SARS-CoV-2 from individuals who are infected despite vaccination.”

In other words, they don’t know if “vaccinated” individuals will spread Covid.