I am still trying to understand why there is such a push to get the jab by Governments, agencies such as the CDC, WHO, NIH the MSM and foundations like Bill and Melinda Gates. I’ve noticed if they try too hard to sell us something, it’s worth questioning. Like the fake Ivermectin story linked here. It’s not like the government has given us any reason to trust them or their motives recently. Some go so far as to say that there is an excess of lying about it.
There is plenty of evidence that the jab it isn’t working the way it was supposed to when considering the Covid re-emergence in Israel, the most vaccinated country in the world. Conversely, there is plenty of evidence that existing medicine proven to be safe are being disparaged, yet they are shown to be effective like HCQ, Zinc, Ivermectin, Z-Pak and so forth.
It makes me ask why is this happening. I think the jab has helped some people with co-morbitdities, but there are more fatalities and side effects from it than all other vaccines combined. It is far past when they have pulled other vaccines because of their danger.
I posted about graphene oxide, a poison and a substance that can make it a bio-weapon. This was my first red flag.
Now, I’m discovering the dangers of pseudouridylyl. This is a discussion about it and what it does.
COVID-19 RNA Based Vaccines and the Risk of Prion Disease (Yes, it can cause diseases that should be rare. This violates the do no harm Hippocratic Oath)
States Dr. Carrie Madej joins journalist Alex Newman to discuss the trans-humanist agenda behind the COVID vaccines…SARS-CoV-2 (the mathematical model) contains a replica of human chromosome 8, which means that the WHO PCR test kits should give a positive result in all people tested. More worryingly, chromosome 8 has to do with human intelligence and fertility. That means it could trigger an autoimmune reaction against a chromosome that codes for two of our most valuable human qualities.
Pfizer and Moderna have also incorporated an artificial nucleoside into the vaccine’s RNA, called pseudouridylyl, or “Psi” for short, which is absolutely out of this world. Dr. Madej says, “Nobody knows the effects of this… It can act like a computer hacking program. It can be like a one-way program, always trying to hack your body… they say they suppress our immune checkpoints so they can put the code in and our body doesn’t destroy it…
The advent of new vaccine technology creates new potential mechanisms of vaccine adverse events. For example, the first killed polio vaccine actually caused polio in recipients because the up scaled manufacturing process did not effectively kill the polio virus before it was injected into patients. RNA based vaccines offers special risks of inducing specific adverse events.
One such potential adverse event is prion based diseases caused by activation of intrinsic proteins to form prions. A wealth of knowledge has been published on a class of RNA binding proteins shown to participating in causing a number of neurological diseases including Alzheimer’s disease and ALS. TDP-43 and FUS are among the best studied of these proteins [2].
The Pfizer RNA based COVID-19 vaccine was approved by the US FDA under an emergency use authorization without long term safety data. Because of concerns about the safety of this vaccine a study was performed to determine if the vaccine could potentially induce prion based disease.
Me——-> A bunch of science discussion here from the same article here to get you thinking whether it is safe for you.
Back to the link.—–>There is an old saying in medicine that “the cure may be worse than the disease.” The phrase can be applied to vaccines. In the current paper the concern is raised that the RNA based COVID vaccines have the potential to cause more disease than the epidemic of COVID-19.
This paper focuses on a novel potential adverse event mechanism causing prion disease which could be even more common and debilitating than the viral infection the vaccine is designed to prevent. While this paper focuses on one potential adverse event there are multiple other potential fatal adverse events as discussed below.
Over the last two decades there has been a concern among certain scientists that prions could be used as bioweapons. More recently there has been a concern that ubiquitous intracellular molecules could be activated to cause prion disease including Alzheimer’s disease, ALS and other neurodegenerative diseases.
This concern originates due to potential for misuse of research data on the mechanisms by which certain RNA binding proteins like TDP-43, FUS and others can be activated to form disease causing prions. The fact that this research, which could be used for bioweapons development, is funded by private organizations including the Bill and Melinda Gates Foundation, and Ellison Medical Foundation [2] without national/international oversight is also a concern.
—–> Back to me trying to put the facts together.
The link I noticed was the use of proteins. Amino Acids are the building blocks of our internal make up (gross generalization here) and proteins are made up of amino acids. They use the word bioweapon again.
The mRNA jab induces a spike protein to create some immunity. It can also be used for other nefarious purposes. I don’t trust that those listed in the first sentence have our best interests in mind. I could get into some conspiracy stuff like population control (and may later if the facts line up enough), a Bill Gates favorite, but let’s stick to the science.
—> More science discussion about protein and the jab now using the link above.
Published data has shown that there are several different factors that can contribute to the conversion of certain RNA binding proteins including TDP-43, FUS and related molecules to their pathologic states. These RNA binding proteins have many functions and are found in both the nucleus and the cytoplasm. These binding proteins have amino acid regions, binding motifs that bind specific RNA sequences.
Binding to certain RNA sequences when the proteins are in the cytoplasm is believed to causes the molecules to fold in certain ways leading to pathologic aggregation and prion formation in the cytoplasm [2]. The current analysis indicates Pfizer’s RNA based COVID-19 vaccine contains many of these RNA sequences that have been shown to have high affinity for TDP-43 or FUS and have the potential to induce chronic degenerative neurological diseases.Zinc binding to the RNA recognition motif of TDP-43 is another mechanism leading to formation of amyloid like aggregations [9].
The viral spike protein, coded by the vaccine RNA sequence, binds ACE2 an enzyme containing zinc molecules [8]. This interaction has the potential to increase intracellular zinc levels leading to prion disease. The initial binding could be between spike proteins on the surface of the cell transfected by the vaccine and ACE2 on the surface of an adjacent cell.
The resulting complex may become internalized. Alternatively, the interaction could initially take place in the cytoplasm of a cell that makes ACE2 and has been transfected with the vaccine RNA coding for the spike protein. The interaction is quite concerning given the belief that the virus causing COVID-19, SARS-CoV-2, is a bioweapon [10,11] and it is possible that the viral spike protein may have been designed to cause prion disease.
The ingredient that causes it is pseudouridylyl.
What are prion diseases?
Prion diseases comprise several conditions. A prion is a type of protein that can trigger normal proteins in the brain to fold abnormally. Prion diseases can affect both humans and animals and are sometimes spread to humans by infected meat products. The most common form of prion disease that affects humans is Creutzfeldt-Jakob disease (CJD).
Prion diseases are rare. About 300 cases are reported each year in the U.S. (me here, this is normally, but the jab can induce it, read on)
Types of prion diseases include:
- CJD. A person can inherit this condition, in which case it’s called familial CJD. Sporadic CJD, on the other hand, develops suddenly without any known risk factors. Most cases of CJD are sporadic and tend to strike people around age 60. Acquired CJD is caused by exposure to infected tissue during a medical procedure, such as a cornea transplant. Symptoms of CJD (see below) quickly lead to severe disability and death. In most cases, death occurs within a year.
- Variant CJD. This is an infectious type of the disease that is related to “mad cow disease.” Eating diseased meat may cause the disease in humans. The meat may cause normal human prion protein to develop abnormally. This type of the disease usually affects younger people.
- Variably protease-sensitive prionopathy (VPSPr). This is also extremely rare, it is similar to CJD but the protein is less sensitive to digestion. It is more likely to strike people around age 70 who have a family history of dementia.
- Gerstmann-Sträussler-Scheinker disease (GSS). Extremely rare, but occurs at an earlier age, typically around age 40.
- Kuru. This disease is seen in New Guinea. It’s caused by eating human brain tissue contaminated with infectious prions. Because of increased awareness about the disease and how it is transmitted, kuru is now rare.
- Fatal insomnia (FI). Rare hereditary disorder causing difficulty sleeping. There is also a sporadic form of the disease that is not inherited.
What causes prion disease?
Prion diseases occur when normal prion protein, found on the surface of many cells, becomes abnormal and clump in the brain, causing brain damage. This abnormal accumulation of protein in the brain can cause memory impairment, personality changes, and difficulties with movement. Experts still don’t know a lot about prion diseases, but unfortunately, these disorders are generally fatal.
—-> Don’t miss the word protein
Now I ask myself, why are they trying to give us a 3rd jab? Did the first two not work or not work enough? Is there something more behind the scenes? More discussion now about long term effects of vaccines.
—-> more from the link above
Vaccines have been found to cause a host of chronic, late developing adverse events. Some adverse events like type 1 diabetes may not occur until 3-4 years after a vaccine is administered [1]. In the example of type 1 diabetes the frequency of cases of adverse events may surpass the frequency of cases of severe infectious disease the vaccine was designed to prevent.
Given that type 1 diabetes is only one of many immune mediated diseases potentially caused by vaccines, chronic late occurring adverse events are a serious public health issue.
In Summary for now
As always, decide for yourself and do your own research. I think all the pressure to get jabbed stinks and I’m trying to find out why. There is a pattern and an underlying reason they are pushing it instead of using safe, cheap and effective cures, proven to work. TPTB don’t want to use it and are still pushing the jab on us by saying it is safe. I’ve now listed two ingredients that are poisonous to humans and what they can do to you.
I may write more (if I’m allowed, I’ve notice an uptick from China and unusual places that censor stuff they don’t like) and may tie all of my posts together. There is a theme developing that I hope to develop. It’s already there for those of you who think like a detective and connect the dots.
There is enough that doesn’t make sense to continue sticking this poison into us while ignoring the obvious cure.
Think about it.
