Vax Questions
All the questions we have about the Covid vaccines.
This is an effort to consolidate the primary questions surrounding the new Covid vaccines. As I have stated before, I am pro-vax, pro-test, anti-rush.
The Vax Questions generally fall into 4 categories:
Technology itself (mRNA, DNA, etc.)
Risks (Spike protein, LNPs, & processes involved—production, dosing, etc.)
Timing (antigenic escape)
Activation of latent SARS-CoV-2
Vax Basics
Vaccines are a delivery (or production) mechanism of antigens (proteins). Antigens are molecular structures on the surface of viruses that are recognized by the immune system & are capable of triggering an immune response (antibody production). https://en.m.wikipedia.org/wiki/Antigen
Vaccines come in many types:
Vaccines work in different ways. For example, the smallpox vaccine is actually an attenuated vaccinia virus that is very similar to smallpox. So exposure to weakened vaccinia provides immunity to smallpox. https://cdc.gov/smallpox/vaccine-basics/index.html
A disease we are all familiar with, influenza (flu), has many versions of vaccines. Inactivated (flu shot – grown in chicken eggs), live attenuated (nasal spray/mist – egg based), Recombinant, and cell-based (grown in mammal cells) https://cdc.gov/flu/prevent/how-fluvaccine-made.htm
The Technology
Covid-19 Vaccines are in one of two camps:
mRNA
Viral Vector (DNA)
https://cdc.gov/coronavirus/2019-ncov/vaccines/different-vaccines/viralvector.html…
Viral Vectors for dummies: scientists added the gene that makes the spike protein to chimp-adenoviruses which is injected into the human. Cells engulf the adenovirus and, once inside, it transfers its DNA into the cell nucleus. DNA is copied into mRNA. https://nytimes.com/interactive/2020/health/oxford-astrazeneca-covid-19-vaccine.html
The mRNA leaves the nucleus and the cell begins assembling the spike-protein antigen, some of which migrate to the surface of the cell. This, along with the presence of the adenovirus itself (vaccine), kicks off the immune response.
mRNA Vaccines for Dummies: They are kinda like the DNA vaccines but they skip the DNA step and just deliver into your body the mRNA. The mRNA never enters the nucleus of the cell but uses the cell to become a spike-protein factory.
Risks
mRNA technology is very new & has potential risks related to lipid nanoparticles (LNPs), which have confounded scientists for years. They are toxic. Link: Dr. Vanessa Schmidt Krueger’s Q&A about the EMA Committee’s report on BioNTech mRNA vaccine. http://enformtk.u-aizu.ac.jp/howard/gcep_dr_vanessa_schmidt_krueger/
Basic summary of the Q&A:
Contaminants. Vaccines can be mass-produced using different techniques than how they were produced during trials. To lower costs, they will use bacteria DNA to produce the RNA which can vary in quality. BioNTech has admitted that there are contaminants:
Mass production can result in poor quality. Some new batches of BioNTech have only 55% RNA integrity (so basically half is un-viable which cause the cells to produce truncated pieces of the spike protein):
Bacterial DNA contamination. Contamination of the vaccine with bacteria DNA is a small risk, but the net result would be really bad:
Dosing seems suspect. In summary, dosing at 10, 20 or 30 micrograms produced the SAME EFFECT in the body. And yet they are shipping @ 30µg. “the efficacy remains the same regardless of whether 10 µg or 30 µg are used but the side effects increase, that is severe medical malpractice.”
Lipid Nanoparticles and the trouble they cause. LNPs are needed to envelope the RNA so it can enter the cell, but some of them are toxic. You can’t deliver the RNA without using some toxic LNPs. This can result in apoptosis (cell death). Some remain in your body for 4-5 months.
Much of LNP intel is known…in animals. But not so much in humans:
LNPs are toxic to cells and cause apoptosis (cell death):
LNPs breaks DNA strands in animal tests:
Dr. Vanessa Schmidt Krueger covers LNPs in incredible detail. Other things she says:
7.5 years is the normal amount of time to test a vaccine.
RNA is producing the spike protein. “They (the spike) will go away at some point, then we’ll no longer be a genetically modified organism but we are a GMO for as long as they are there.”
Moving on to ADE and Cytokine Storms. When they have tried these mRNA vaccines in the past there have been examples of vaxers encountering the disease post-vax and having a miserable time. It is a concern for SAR-CoV-2
https://www.nature.com/articles/s41564-020-00789-5
This was published in a 2012 paper about RSV vaccine attempts. A couple of compelling quotes: “RSV lung disease was enhanced by the PRIOR vaccination” & “This combined experience provides concern for trials with SARS-CoV vaccines in humans.”
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0035421
There are a host of other concerns about the vaccines that need to be addressed:
Is the spike protein produced by the vaccination process significantly different than the natural spike protein? Some have suggested the natural spike is “folded” but “unfolded” in it's vaccine form and that the unfolded spike crosses the blood-brain barrier.
Does the spike protein leave the injection site and enter the circulatory system. “Free” spike proteins were apparently not considered as a part of the initial trial and not anticipated.
Are these free spike proteins and LNPs collecting in tissues and organs? There are reports of both the spike and LNPs collecting in the ovaries.
How long to the free spike proteins and LNPs remain in your body?
What about graphene (oxide) toxicity?
Are people actually shedding spike protein to others? Not just in breast milk but through the air to people around them?
Is a spike only vaccine a good thing. SARS-CoV-2 is more than just a spike protein. Creating a vaccine around just that component of the pathogen might not be a good idea.
Timing
Immune Escape. Geert Vanden Bossche (among others) is concerned about the TIMING of a mass vaccination DURING a pandemic and its potential impact on Viral Immune Escape (Antigenic Escape) https://mcusercontent.com/92561d6dedb66a43fe9a6548f/files/bead7203-0798-4ac8-abe2-076208015556/Public_health_emergency_of_international_concert_Geert_Vanden_Bossche.01.pdf…
He is Pro-Vax but believe that prophylactic vaccines should not be administered in the heat of a pandemic because the vaccine temporarily lowers your immune response WHILE the virus is circulating which could lead to the virus escaping the immune response.
Immune escape creates a population problem; not just an individual problem. Similar to using the wrong antibiotics in bacterial infections which results in superbugs. Immune escape will drive resistance to the vaccines.
Another concern he has: Long-live antibodies from the Vaccines have high specificity and out-compete our natural antibodies – and they will continue to do so. A huge problem. Natural antibodies have “broad protection” – it doesn’t matter what variant of SARS-CoV-2 you get.
Was able to find three responses to GVB’s immune escape hypothesis. One somewhat supportive and two challenging his claims. Great read here:
https://dryburgh.com/vanden-bossche-theory-fact-or-fiction/
Dr Robert Malone, Bret Weinstein and Steve Kirsch give us a very helpful 15 minutes of discussion on everything from LNPs and free spike protein to immune escape. Worth your time (~15 mins):
https://www.bitchute.com/video/84K04msS2qUQ/
Another quick dive opinion on just the spike protein is Dr. Bryam Brindle (~8 mins):
https://www.bitchute.com/video/g1IfHVKr17Bx/
And Doloris Cahill has opinions (~2 mins):
https://www.bitchute.com/video/reWEmMgskaHc/
Dr. Peter McCullough has gone from vax proponent to recommending it to NO ONE (~25 mins)
https://rumble.com/embed/vhjd7q/?pub=4
Let’s see how long this YouTube video lasts (~9 mins):
Activation of Latent SARS-CoV-2
We may be seeing this phenomenon in East Asia right now—which only makes sense if you believe that SARS-CoV-2 was present prior to when the Chinese first announced it (Dec 2019).
Hypothesis: a person had Covid in the past (maybe 12-24 months) then receives the vaccine. The presence of the spike protein kicks off the reactivation of a dormant Covid infection. Now the person has the Covid infection again!
This process is not totally foreign, in fact there is some chatter about the Covid vaccines kicking off reinfections of other diseases like shingles. Tough to know for sure without studies.
Is it possible that a latent response from the vaccines could result in a dengue-type second-infection ADE response? That is just speculation but might be worth watching in the future.
Excellent summation
Glad to see you have a substack, I followed you on twitter but I kept getting banned.
I would look into the book Turtles All The Way Down, Vaccine Science and Myth. Vaccine trials are very dodgy, not using inert placebos, but comparing them to a previously approved vaccine, "all the way down" to when they were approved without proper trials. They are likely no0t as safe as we are led to believe.