Thank you Kevin. Much better than peer review, as you have stated, reproducing your results at a number of different labs is the best validation. It's painfully obvious that the shots need to be stopped immediately. Are any "leaders" paying attention? Peace.
Thank you for this report. Do they know what does the DNA code for?
Not expecting any response here, never got one from this substack author. Not sure if asking about the -Pro-Pro- sequencing section, which should be ONLY in the genetically modifying injections replacing the natural -Lys-Val- dipeptide (in the official NIH published data), is maybe inappropriate or who knows what the real reason for no answer is... This answer would tell us though, if there are any naturally covid infected individuals with a Spike different than the injected one...
My layman's understanding is that it will vary across the board as there are lots of tiny variable snippets, so which "switches" get turned on will vary from batch to batch but also epigenetically from person to person because of variables like lifestyle, toxicity, susceptibility, location, stressors, etc.
Then also the effects of the "other" contaminants, like the bacterial components is also unknown.🤷♀️
But I'm likely oversimplifying and as I said, I'm not an expert. Thankfully, Substack is full of awesomely clever individuals (like A) that are happy to correct in respectful and non- condescending ways😉
"The EMA set limits for dsDNA contamination at less than 330ng/mg RNA. This is roughly 1 part per 3,030 mRNA molecules. It is not clear how they set these standards. For instance, a shot containing 34 trillion mRNAs with a 1 part per 3,000 plasmid contamination rate would equate to over 10 billion antibiotic resistant plasmids being transfected per patient.
The sequencing evidence we now have on hand confirms that most of this DNA is in-fact the expression plasmid DNA, complete with spike protein, SV40 mammalian expression promoters, aminoglycoside antibiotic resistance and high copy origins of replication that are compatible with both mammalian expression and bacterial amplification."
I have a very dystopian mindset: the suspicion arises that the plasmids will render old 20th century medical therapies impotent. Thus, the gene therapy pathway is forced upon us. Covid-19 was the Grand Debut.
They have the assays available to run the pathology on blood and tissues. However those have to be run by labs which have certifications to do that kind of work. It’s going to require doctors ordering that pathology and a lab willing to run the tests and using the right assays to detect it. That is the goal, to find out if integration has occurred in people suffering post vax pathologies.
Is there a connection between dna plasmids and plasmonics used for nanotechnology communications in the terahertz band? If so, will you please explain it, Kevin?
Are you prohibited from speaking about this as a result of NDAs signed while you worked on the Human Genome Project?
Will you please comment on the Internet of Nano Things which are embedded in both intelligent face masks and genetic injections (Lipid Nano Particles?)
One timeseries per state for all BNT162b1/2 trial doses that were administered pre-rollout.
I can supply data with conserved information for product type, dosage and county of investigator as well if anyone is interested. In that case write me(at)pervaers.com
One thing to always consider. The data process being used to 'bulldoze' a desired by them but undesirable thing for most of us, is just that. The bulldozer method. jam it in hope it sticks and the worst possible thing happens. Yet, 8 billion people will demonstrate the falsehood of that approach. Human bodies are clever and most, despite evidence to the contrary, do not want to be eliminated. Push and they wobble but they do not fall down. stimulating conversation though. and lots of avenues for disaster !
Of which: 35,324 died 2.3% | 37,538 life-threatening 2.4% | 65,896 permanently disabled 4.2% | 5,432 possible miscarriage or stillbirth 0.3%
NOTE: VAERS receives reports for only a small fraction of actual adverse events. (Source: CDC)”
Hence my thanks, and thanks to Dr. Buckhaults & students, Dr. Lee and especially to Kevin.
VAERS is not up to date, and seems to suffer from some UI/UX input issues and maybe data input/verification challenges. Maybe the contracted verifiers are working from home.
VAERS, such as it is, provides me a few clues about what to watch for. Kevin’s vaccine sequencing is another set of dots.
I thought there was something to the idea of ‘public trust.’ And I had other good reasons back then for not being on Twitter all the time. No crystal ball. A spouse in the midst of a cascade of serious health issues unrelated to vaccines.
In one of the FDA meetings on vaccine approval Albert Bourla (Pfizer CEO) was asked by a member of the FDA committee if they ever checked what happened when the endogenous HERV-K reverse transcriptase was also being expressed (typically in frequently dividing tissue like cancer or embryos). He laughed at the question, which was weird because it clearly is going to occur at some rate. It may be negligible, but they needed to check this.
I'm not willing to go back through the hours and hours worth of meetings to find it, maybe the one before approval for children. Perhaps there are transcripts somewhere I haven't found. Anyway, if you can skip the reverse transcriptase step it will obviously be even more likely to happen.
Sorry to sound like a conspiracy theorist, but can you shed some light on the findings of this article? In general I take articles from The Expose with a pinch of salt, but the official documents supposedly released by Pfizer ( in less than 75 years!) seem to imply that graphene oxide was used in the manufacturing process and therefore could feasibly be a contaminant in the vaccines in the way that the DNA is. I’ve seen other doctors/PhDs saying that the things visible are just cholesterol crystals.
Have you noticed, or looked for, anything else in your vaccine vials.
With regard to supposed nanotechnology in the vials, I’m not convinced yet as I have been told these could be salt crystal formations or maybe fragments from machinery used in manufacturing.
I did however stick a magnet to the arm of my mother after a Pfizer and that of a friend after a Moderna and don’t know how to explain that!
Thanks for any further light you can shed on these matters.
1) Expired Lots: Were the new new lot vials expired? What are possible issues with using expired vaccine? Plasmids should only degrade over time, not appear from nowhere, correct?
2) qPCR Kit Used/COI: Can you do your testing again with another manufacturer's qPCR kit to eliminate that potential conflict of interest?
The criticisms of your results appear to be weak, and it should be easy to eliminate them with a few additional steps.
Pfizer has moved the expiration dates of these vaccine continually. There is a Substack below called kleptoplastic conniptions that shows how one can assess if an expired lot has experienced decay. It’s worth reading to see that this is a non issue.
2)Dr. Sin Lee designed his own primers and Sanger sequenced the amplicons with his own polymerases.
If our PCR kits had the contamination, the NTCs would not be clean.
This has been controlled for and Dr. Lee has made his own amplicons
Thank you for your reply, Kevin. I read your article "Kleptoplastic Conniptions" and it answered all of my questions. I think it should silence reasonable critics. But far too many have abandoned reason.
Looking at the people around me who have been vaccinated, most of them look fine now!
Out of 1000 people inoculated with this experimental gene therapy drug, biologic, how many and what percentage of people are likely to die within 10 years from cancer, immunodeficiency, brain disease, etc.?
Which article done by Dr. Phillip Buckhaults is about their test on the BNT162b2 vials? He doesn't have any paper that talks about such on his page in the link.
Thank you Kevin. Much better than peer review, as you have stated, reproducing your results at a number of different labs is the best validation. It's painfully obvious that the shots need to be stopped immediately. Are any "leaders" paying attention? Peace.
Thank you for this report. Do they know what does the DNA code for?
Not expecting any response here, never got one from this substack author. Not sure if asking about the -Pro-Pro- sequencing section, which should be ONLY in the genetically modifying injections replacing the natural -Lys-Val- dipeptide (in the official NIH published data), is maybe inappropriate or who knows what the real reason for no answer is... This answer would tell us though, if there are any naturally covid infected individuals with a Spike different than the injected one...
My layman's understanding is that it will vary across the board as there are lots of tiny variable snippets, so which "switches" get turned on will vary from batch to batch but also epigenetically from person to person because of variables like lifestyle, toxicity, susceptibility, location, stressors, etc.
Then also the effects of the "other" contaminants, like the bacterial components is also unknown.🤷♀️
But I'm likely oversimplifying and as I said, I'm not an expert. Thankfully, Substack is full of awesomely clever individuals (like A) that are happy to correct in respectful and non- condescending ways😉
Kevin told us in the very first substack on the issue: https://anandamide.substack.com/p/curious-kittens
"The EMA set limits for dsDNA contamination at less than 330ng/mg RNA. This is roughly 1 part per 3,030 mRNA molecules. It is not clear how they set these standards. For instance, a shot containing 34 trillion mRNAs with a 1 part per 3,000 plasmid contamination rate would equate to over 10 billion antibiotic resistant plasmids being transfected per patient.
The sequencing evidence we now have on hand confirms that most of this DNA is in-fact the expression plasmid DNA, complete with spike protein, SV40 mammalian expression promoters, aminoglycoside antibiotic resistance and high copy origins of replication that are compatible with both mammalian expression and bacterial amplification."
" and more work is needed to understand its clinical significance given this DNA contaminant is likely packaged in transfection ready LNPs."
https://asm.org/Articles/2023/January/Plasmids-and-the-Spread-of-Antibiotic-Resistance-G
I have a very dystopian mindset: the suspicion arises that the plasmids will render old 20th century medical therapies impotent. Thus, the gene therapy pathway is forced upon us. Covid-19 was the Grand Debut.
I appreciate your comment very much, thanks.
Kevin, is it possible to test someone for transfection with dsDNA contaminants (i.e. via sequenced biopsy or something along those lines)?
They have the assays available to run the pathology on blood and tissues. However those have to be run by labs which have certifications to do that kind of work. It’s going to require doctors ordering that pathology and a lab willing to run the tests and using the right assays to detect it. That is the goal, to find out if integration has occurred in people suffering post vax pathologies.
Is there a connection between dna plasmids and plasmonics used for nanotechnology communications in the terahertz band? If so, will you please explain it, Kevin?
https://m.youtube.com/watch?v=wktdC-
Are you prohibited from speaking about this as a result of NDAs signed while you worked on the Human Genome Project?
Will you please comment on the Internet of Nano Things which are embedded in both intelligent face masks and genetic injections (Lipid Nano Particles?)
I didn’t sign any NDA for the HGP and your receipt free accusational tone gets you blocked.
The video you suggested was pulled down.
Maybe some analyst here appreciates this:
https://substack.pervaers.com/USA_Misc/Trial_Doses.json
One timeseries per state for all BNT162b1/2 trial doses that were administered pre-rollout.
I can supply data with conserved information for product type, dosage and county of investigator as well if anyone is interested. In that case write me(at)pervaers.com
Dr. König from the MMD Lab also proved it. I don't have details on the procedure, only the results: https://t.me/HolgerFischerRA/8672
One thing to always consider. The data process being used to 'bulldoze' a desired by them but undesirable thing for most of us, is just that. The bulldozer method. jam it in hope it sticks and the worst possible thing happens. Yet, 8 billion people will demonstrate the falsehood of that approach. Human bodies are clever and most, despite evidence to the contrary, do not want to be eliminated. Push and they wobble but they do not fall down. stimulating conversation though. and lots of avenues for disaster !
My first shot, on 2/3/21, was batch EL6232, FWIW. I can sort of put a face on EL6232, even though everyone’s mileage will vary.
For EL9262 as of this writing on July 16, 2023,
at matchyourbatch.org via the VAERSAWARE site:
“1,556,050 events reported through May 5, 2023
Of which: 35,324 died 2.3% | 37,538 life-threatening 2.4% | 65,896 permanently disabled 4.2% | 5,432 possible miscarriage or stillbirth 0.3%
NOTE: VAERS receives reports for only a small fraction of actual adverse events. (Source: CDC)”
Hence my thanks, and thanks to Dr. Buckhaults & students, Dr. Lee and especially to Kevin.
VAERS is not up to date, and seems to suffer from some UI/UX input issues and maybe data input/verification challenges. Maybe the contracted verifiers are working from home.
VAERS, such as it is, provides me a few clues about what to watch for. Kevin’s vaccine sequencing is another set of dots.
I thought there was something to the idea of ‘public trust.’ And I had other good reasons back then for not being on Twitter all the time. No crystal ball. A spouse in the midst of a cascade of serious health issues unrelated to vaccines.
So thanks again, Kevin.
In one of the FDA meetings on vaccine approval Albert Bourla (Pfizer CEO) was asked by a member of the FDA committee if they ever checked what happened when the endogenous HERV-K reverse transcriptase was also being expressed (typically in frequently dividing tissue like cancer or embryos). He laughed at the question, which was weird because it clearly is going to occur at some rate. It may be negligible, but they needed to check this.
I'm not willing to go back through the hours and hours worth of meetings to find it, maybe the one before approval for children. Perhaps there are transcripts somewhere I haven't found. Anyway, if you can skip the reverse transcriptase step it will obviously be even more likely to happen.
By "it" I mean incorporation into the genome of whatever cells it enters.
https://www.2ndsmartestguyintheworld.com/p/fda-confirms-graphene-oxide-is-in?utm_medium=email
Sorry to sound like a conspiracy theorist, but can you shed some light on the findings of this article? In general I take articles from The Expose with a pinch of salt, but the official documents supposedly released by Pfizer ( in less than 75 years!) seem to imply that graphene oxide was used in the manufacturing process and therefore could feasibly be a contaminant in the vaccines in the way that the DNA is. I’ve seen other doctors/PhDs saying that the things visible are just cholesterol crystals.
Have you noticed, or looked for, anything else in your vaccine vials.
With regard to supposed nanotechnology in the vials, I’m not convinced yet as I have been told these could be salt crystal formations or maybe fragments from machinery used in manufacturing.
I did however stick a magnet to the arm of my mother after a Pfizer and that of a friend after a Moderna and don’t know how to explain that!
Thanks for any further light you can shed on these matters.
Is it possible to move away from the use of bacterial fermentation-based production of the expression vectors to a cleaner process ?
https://www.labiotech.eu/in-depth/enzymatically-produced-cell-free-synthetic-dna-mrna-manufacturing/
Addressing criticisms:
1) Expired Lots: Were the new new lot vials expired? What are possible issues with using expired vaccine? Plasmids should only degrade over time, not appear from nowhere, correct?
2) qPCR Kit Used/COI: Can you do your testing again with another manufacturer's qPCR kit to eliminate that potential conflict of interest?
The criticisms of your results appear to be weak, and it should be easy to eliminate them with a few additional steps.
Pfizer has moved the expiration dates of these vaccine continually. There is a Substack below called kleptoplastic conniptions that shows how one can assess if an expired lot has experienced decay. It’s worth reading to see that this is a non issue.
2)Dr. Sin Lee designed his own primers and Sanger sequenced the amplicons with his own polymerases.
If our PCR kits had the contamination, the NTCs would not be clean.
This has been controlled for and Dr. Lee has made his own amplicons
Thank you for your reply, Kevin. I read your article "Kleptoplastic Conniptions" and it answered all of my questions. I think it should silence reasonable critics. But far too many have abandoned reason.
Anandamide, I also have a question!
Looking at the people around me who have been vaccinated, most of them look fine now!
Out of 1000 people inoculated with this experimental gene therapy drug, biologic, how many and what percentage of people are likely to die within 10 years from cancer, immunodeficiency, brain disease, etc.?
https://doorlesscarp953.substack.com/p/cancer-rates-following-global-nuclear
Which article done by Dr. Phillip Buckhaults is about their test on the BNT162b2 vials? He doesn't have any paper that talks about such on his page in the link.
Hit his Twitter account. He’s tweeting about the data
Thank you.
boy oh boy! good to see someone strongly supporting the mrna vax do his own research. has he published his opinions on the contamination??
I haven’t been following this work. Can you offer a summary of what the near or far term conclusions mean?
Go to the archive list and read upwards from this one https://anandamide.substack.com/p/curious-kittens