The incompetent lettered government agencies supposedly concerned about your health will try to scare you with statements like “The Nipah virus has a 40% to 75% mortality rate”. What that means is, severe symptomatic infections without appropriate treatment can have a 40% to 75% mortality rate. And then they say there are no treatments, which is a lie.
It’s important to know that to be infected by the Nipah virus, it must be IN you, not ON you. They will test for the presence of the virus outside of you, on your mucosal linings, in your snot, spit, sweat, urine and feces. Testing positive does not mean you are infected, but it will scare the crap out of people who don’t understand how the immune system protects them. The virus must get inside of you to affect you. It gets inside by attaching to cellular receptors called Ephrin 2 or EPHB2 receptors. These receptors do not exist on your skin or mucosal linings. So, how does it get in? It enters through breaks in the skin or breaks in the mucosal linings. In other words, this is a direct contact transfer, not a respiratory transfer like the Sars-CoV-2 virus was. Based on the mode of transmission alone, any outbreaks have been and will be small and localized.
Ok, let’s say the virus gets in you through breaks in your skin or mucosa. Now what happens? If it got in your blood, the virus could attach to EPHB2 receptors along the linings of your blood vessels and heart. If it got in your interstitial fluids between cells and tissues, it could attach to the same receptors on nerve cells. The same receptors also exist on heart muscle cells.
Once attached to the receptors, the cells can take in the genetic material of the virus and make more copies. This replication process is inhibited by zinc inside of the cells. This is because the Nipah virus is an RNA virus that uses RNA polymerase to replicate, and zinc inhibits the actions of RNA polymerase. While this is happening, cells of the immune system, specifically natural killer cells and cytotoxic T-cells will destroy the cells that have the viral replication going on.
In people with healthy immune systems, the virus will be eliminated quickly, and sometimes symptoms never even develop. The more tissue that gets damaged by the immune response, the more severe the symptoms will be. What this means is, some people will encounter the Nipah virus, develop immunity, and never even know it. Some people with immune suppression will develop severe symptoms, and those are the cases that have high mortality rates without appropriate treatment. Even the WHO admits, “Nipah virus infection in humans causes a range of clinical presentations, from asymptomatic infection (subclinical) to acute respiratory infection and fatal encephalitis.”
They will try to convince you that injecting something into your body to create a protein that is on the Nipah virus will result in antibodies that will protect you from developing severe symptoms. This procedure will not protect you from getting infected. They already admitted there is no protection against infection by mRNA shots as evidenced from covid injection outcomes. But they will still try to convince you it’s a good idea because it will protect you from severe disease.
It's a bad idea, and here’s why: The proteins that are created by the mRNA shot are bioactive. That means the proteins can be released from the cells that made them, circulate, and attach to the cellular receptors we already discussed. When whole viruses attach to receptors, they are taken in by the cells. When the bioactive proteins attach to receptors, they are not taken in by the cells, they just sit there, firmly attached. This will cause an inflammatory immune response that will destroy those cells. Since an mRNA injected person has absolutely no idea how many viable strands of mRNA they will get, how many proteins their body will make, nor where they will go, nor how long they will make them, the results could be catastrophic.
Also, since the mRNA injection is only creating one protein that is just a small part of the virus, the resultant antibodies will be suboptimal and can worsen the symptoms in some people that get infected due to antibody dependent enhancement (ADE). I explain ADE in this video: https://drkevinstillwagon.substack.com/p/the-mechanisms-of-two-types-of-antibody
So, what’s a person to do? Just know that most people have built in protection against infection and there is no need to panic. Do everything you can to further prevent infections, like common sense and good hygiene. Proper levels of exercise, vitamin D and C are known to help prevent infections because of their support of that mucosal protective barrier. Zinc with quercetin supplementation won’t necessarily prevent infections but can help slow RNA viral replication. If a person does start developing severe symptoms after an infection, superior lifesaving monoclonal antibodies have already been developed and can be administered. Monoclonal antibodies should never be used as a prophylactic, only as a treatment. They can’t prevent infections; they only treat severe infections.
The Nipah virus can be weaponized by modifying it in laboratories with CRISPR technology. They can insert a new attachment genetic code that uses human respiratory epithelial receptors that are on the outside of you instead of the EPHB2 receptors that are inside of you. This makes it more transmissible. If this happens, you will know for sure it came from a lab, not from nature. Do not panic even if that happens as most of us have cellular mucosal protection against infection. The real threat is injecting something into your body that ultimately destroys that cellular protection. Injections are the true weapons.
Thank you for the very clear explanation about bioactive proteins.
great article thanks for the warning.