I have chronic/ systemic inflammatory response syndrome. From biotoxin mold illness. And other autoimmune. I’m seeing so many people, seems like they have the same problem now. & whatever “ shedding “ is, is a constant challenge now.
I have chronic Lyme Disease. This sounds similar. In fact, I have seen many people talk online about their jab side effects and many of them sound similar to Lyme Disease.
Thanks, P Mac! I will look into it. I've heard of it, but don't know anything about it. I'm always open to treatment options. It's a very difficult road. I'm struggling.
So how can one who is mRNA vaxed measure the amounts of spike proteins in his system, if any? Is the most common indicator of the presence of spikes seeing microclotting as shown on a d-dimer test? Or could one have spikes proteins present without microclotting and with a normal d-dimer test result?
I’ve been asking this same question to no avail. I took two AZ jabs, and want to test for integration. Kevin McKernan has a test kit available to labs. I’ve written to two UK labs to test on my behalf, sadly to date no one has replied. I think these labs are afraid to put their names to this for fear of losing bigger government contracts.
After all, ACE2 is literally the absolute most dangerous receptor if you wanted to design something to attack the human body. It is everywhere."
They wanted to attack the human body through the ACE2 receptor and that is exactly what "they" did spending 15 years testing every sars-cov to find in 2017, a sars-cov in a pangolin, most likely pangolin #8, that had evolved a spike with exceptional ACE2 binding affinity. This was recombined to "create" sars-cov-2 as seen below in an excerpt of my comment. If anyone asks I will post my full comment titled "a ccp/pla 2 front , stealth, "unlimited war", "economic war", bioweapon attack on the west. Front #1) sars-cov-2 + "developed" immune escape variants, front #2) ccp/pla tradecraft + fear-inducing showmanship inducing the west to use ccp/pla slow kill bioweapon spike for its countermeasure mRNA and viral vector produced vaccine antigen."
The following from the March 22, 2020 US "complex" it is a "hide in plain sight" limited hangout, zoonotic origin / wet market infection epicenter inference, mis/dis/mal information, propaganda piece "Emergence of SARS-CoV-2 through recombination and strong purifying selection" (just look at where the authors work) They carefully tell some truth, always make mention of zoonotic evolution while never actually saying sars-cov-2 was zoonotic (plausible deniability) and never mention lab origin.
"We show evidence of strong purifying selection around the receptor binding motif (RBM) in the spike gene and in other genes among bat, pangolin and human coronaviruses, indicating similar strong evolutionary constraints in different host species. We also demonstrate that SARS-CoV-2’s entire RBM was introduced through recombination with coronaviruses from pangolins, possibly a critical step in the evolution of SARS-CoV-2’s ability to infect humans. " "we find significant recombination breakpoints before and after the ACE2 binding site (fig. S2A)," "Specifically, amino acid sequences of the receptor binding motif (RBM) in the C terminal of the S1 subunit are nearly identical to those in two Pan_SL-CoV_GD viruses, with only one amino acid difference (Q498H)—although the RBM region has not been fully sequenced in one of Guangdong pangolin virus (Pan_SL-CoV_GD/P2S)
"Thus, a functional RBM nearly identical to the one in SARS-CoV-2 is naturally present in Pan_SL-CoV_GD viruses. The very distinctive RaTG13 RBM suggests that this virus is unlikely to infect human cells, and that the acquisition of a complete functional RBM (my note; with exceptional human ACE 2 binding ability) by a RaTG13-like CoV through a recombination event with a Pan_SL-CoV_GD-like virus enabled it to use ACE2 for human infection.
note; As this "Research Article" was originally posted to the preprint? server the supplementary data initially contained a spread sheet, subsequently removed, showing on the vertical, line by line, 3533 individual tissue samples taken from a number of sick pangolins. Virus types found in each tissue sample, averaging close to 10 per sample, were listed horizontally - sars-cov was found in sick pangolin #7 and more in sick pangolin #8, more likely the "guilty party" supplying the human ACE 2 binding affinity enhancement identified in sars-cov-2. I expect this spread sheet was removed because someone noticed it actually was a "fine exemplar" of chinese bioweapon research.
When the cia was founded in 1947 its first charge was to round up the japanese and german bioweapon expert war criminals and move them into the US bioweapon program. From then on it's been spies working within bioweapons programs spying on other spies working in these programs. The wuhan lab was obviously a honey trap for this type of research - "no questions asked, cheap we do, to woo you, to the wuhan lab" and, no doubt, they developed innovations of their own. The ccp/pla was obviously able to obtain bioweapon applicable research from a number of sources. A "bioweapon baric" and his UNC gain of function gang developed furin cleavage site, even a moderna patented genetic sequence showed up in sars-cov-2.
a note to myself written while musing one night - "tongue in cheek" or?
Clandestine Services Standard Practice 101 (CSSP101) Handbook
Practice A: Hide in Plain Sight - adapted for "study" (propaganda) publication: Write the truth but Not ALL THE TRUTH. Do not openly, or in any manner direct attention to foundational US research used to create cov2, do not include Ralph S Baric as an author or refer to his or others gain of function work at UNC or our other bioweapon activities. Carefully infer, but do not outright claim natural recombination and avoid any and all reference to lab recombination. Do not in any manner become subject under Admonitions 1 and 2. Remember you worship at the feet of the controller of your funding fauci, who said about lab origin of sars-cov-2 "It is a shiny object that will go away in times."
Admonitions
1) Do not get caught. If caught 1) admit nothing 2) deny everything 3) demand proof - limit speech to insisting there is no proof. Always maintain a " no evidence" position to aid in plausible deniability in the future (when truth comes out).
2) if you get caught and are forced to become a double agent, do so as a triple agent from the start. Do not wait until your double agent status has been "detected by his original sponsor" and you are forced to become a re-doubled agent.
Thank you, for that. Yes, we mustvreview every single angle. I also believe it is a war w several strategies..many old ones, including cloward pavin strategy
Please ignore if you did not ask, on the inner, for the full post
The following is my takeaway "on a Carefully Planned Worldwide Bioweapons Attack" I originally posted this comment to a substack page discussing "DEFUSE"
DEFUSE does provides additional evidence of highly developed PREEXISTING bioweapon development work to enhance sars-cov via the addition of a furin cleavage site undertaken prior to 2018 by the US bioweapon / bioweapon and pandemic countermeasure "complex".
"The exact furin cleavage site found in SARS-CoV-2 is found in another protein, a protein called alpha-ENaC found in humans and studied heavily at the same university (UNC) as one of the PI’s of DEFUSE. "
UNC - University of North Carolina at Chapel Hill home of bioweapon baric and the bioweapon baric gain of function gang.
and then DEFUSE, based on prior knowledge writes its proposal showing that "it" has prior knowledge of the location to place the furin cleavage site to weaponize sars-cov thereby "creating" sars-cov-2. "SARS-CoV-2 has its furin cleavage site at exactly the location proposed in these grants."
It is made obvious by the outworking of events that this US developed furin cleave site and specific technology to insert it was "transfered"/taken/stolen and PRIOR to 2018 delivered to the bioweapon / bioweapon and pandemic countermeasure "complex" of the "chinese" communist party/peoples liberation army - ccp/pla.
From the Abstract of "SARS-CoV-2 and the Secret of the Furin Site" "Here we show genomic fingerprints which are specific of Pangolin-CoVs, Bat-SARS-like (CoVZC45, CoVZXC21), bat RatG13 and human SARS-CoV-2 coronaviruses. This, along with phylogenetic analysis, we found that these species have the same evolutionary origin in the bat, including a genetic recombination of S gene between Pangolin-CoV (2017) and RatG13 ancestors." RatG13 "isolated in 2013".
The following from the March 22, 2020 "US" complex "hide in plain sight" limited hangout, zoonotic origin / wet market infection epicenter, mis/dis/mal information, propaganda piece "Emergence of SARS-CoV-2 through recombination and strong purifying selection" (just look at where the authors work)
"We show evidence of strong purifying selection around the receptor binding motif (RBM) in the spike gene and in other genes among bat, pangolin and human coronaviruses, indicating similar strong evolutionary constraints in different host species. We also demonstrate that SARS-CoV-2’s entire RBM was introduced through recombination with coronaviruses from pangolins, possibly a critical step in the evolution of SARS-CoV-2’s ability to infect humans. " "we find significant recombination breakpoints before and after the ACE2 binding site (fig. S2A)," "Specifically, amino acid sequences of the receptor binding motif (RBM) in the C terminal of the S1 subunit are nearly identical to those in two Pan_SL-CoV_GD viruses, with only one amino acid difference (Q498H)—although the RBM region has not been fully sequenced in one of Guangdong pangolin virus (Pan_SL-CoV_GD/P2S)
"Thus, a functional RBM nearly identical to the one in SARS-CoV-2 is naturally present in Pan_SL-CoV_GD viruses. The very distinctive RaTG13 RBM suggests that this virus is unlikely to infect human cells, and that the acquisition of a complete functional RBM (my note; with exceptional human ACE 2 binding ability) by a RaTG13-like CoV through a recombination event with a Pan_SL-CoV_GD-like virus enabled it to use ACE2 for human infection.
note; As this "Research Article" was originally posted to the preprint? server the supplementary data initially contained a spread sheet, subsequently removed, showing on the vertical, line by line, 3533 individual tissue samples taken from a number of sick pangolins. Virus types found in each tissue sample, averaging close to 10 per sample, were listed horizontally - sars-cov was found in sick pangolin #7 and more in sick pangolin #8, more likely the "guilty party" supplying the human ACE 2 binding affinity enhancement identified in sars-cov-2.
"Furthermore, SARS-CoV-2 has a unique furin cleavage site insertion (PRRA) not found in any other CoVs in the Sarbecovirus group (24), although similar motifs are also found in MERS and more divergent bat CoVs (25) (Fig. S3). This PRRA motif makes the S1/S2 cleavage in SARS-CoV-2 much more efficiently than in SARS-CoV and may expand its tropism and/or enhance its transmissibility (23)"
Sars-cov backbone and sars-cov components were on the bioweapon lab shelves of the "chinese" communist party/people's liberation army (ccp/pla) bioweapon / bioweapon and pandemic countermeasure "complex" from 2013 - a sars-cov virus with a 50% fatality rate when transfected in aerosolized bat feces, this cov-2 supplied the "backbone" for sars-cov-2, and from 2017 a pangoplin sars-cov spike component with exceptional binding to human ACE 2.
Recombination and Strong Purifying Selection using these and using "US" furin cleavage site technology that was used to put the "2" into sars-cov, created the "pandemic" level of human to human transmission shown in sars-cov-"2".
Then this ccp/pla bioweapon complex did what it would do - develop a countermeasure vaccine and do human testing while continuing to bio weaponize their sars-cov-2, most particularly the spike*, with various bioweapon toxin inserts and virulence inhibited toxin inserts and continue to do countermeasure vaccine testing on humans. *note; Whole spike which was by that time well "noised abroad" as the choice coronavirus antigen for coding countermeasure agent mRNA.
From events we may see that during this ccp/pla bioweapon/bioweapon countermeasure development process*, in the March 2018 time frame, a virulence inhibited early sars-cov-2 began to spread across China, Asia Pacific and into areas of Chinese contact in Africa developing widespread immunity to sars-cov-2 in the population of those areas which lasted until the immunity breakthrough and increased virulence changes developed into sars-cov-2 seen in the Delta variant. see The Ethical Skeptic "China’s CCP Concealed SARS-CoV-2 Presence in China as Far Back as March 2018 https://theethicalskeptic.com/2021/11/15/chinas-ccp-concealed-sars-cov-2-presence-in-china-as-far-back-as-march-2018/
*note; The modus operandi MO of a bioweapon/bioweapon countermeasure complex is FIRST DEVELOP THE BIOWEAPON
Then a breakdown of virulence inhibition? or a leak or breakthrough infection? or a DELIBERATE DECISION to release a virulent sars-cov-2 as a stealth bioweapon attack on the west with a "pandemic" in china "GO player" cover story and THE DELIBERATE DECISION made by the ccp/pla to use all means necessary to suppress and stop the spread of covid-19 in China and THE DELIBERATE DECISION made by the ccp/pla to use all means necessary, then, to insure that that initial release sars-cov-2 spread to the world and that certain subsequent variants developed and released in "coincidental" conjunction with ccp/pla vaccine testing in foreign countries also spread, quite possibly, initially via bioweapon encapsulation to produce airborne aerosols particles , South African variant, most virulent Gamma P1 in Brazil, or spread across the world and such as Delta and then the case of Omicron. Omicron with the prion creating spike insert toxin reportedly somehow now removed. The prion creating spike insert toxin present in prior variants and replicated by mRNA in the whole spike "vaccine " antigen.
This OMICRON ALLOWED TO SPREAD THROUGH CHINA reportedly doing relatively little damage to the people of China whose immune systems it appears were mostly protected from repeated infections and repeated mRMA injections creating toxic whole spike and doing other damage which made Omicron reportedly much more debilitating and killing in the multiple infection / multiple injection "west". And now, in the west, a omicron with a prion initiating site "insert" reported.
imo - All Total, fact + fact + fact, shows a ccp/pla 2 front , stealth, "unlimited war", "economic war", bioweapon attack on the west. Front #1) sars-cov-2 + "developed" immune escape variants, front #2) ccp/pla tradecraft + fear-inducing showmanship inducing the west to use ccp/pla slow kill bioweapon spike for its countermeasure mRNA and viral vector produced vaccine antigen. Induced with terrible deaths for the most vulnerable elderly and comorbid, people filmed dropping dead, staged?,on China streets. Where else in the world did we see this happening before "vaccines"? Apartment doors welded shut, massive spraying and fogging of the streets and public spaces and the phenomenal construction of hospitals in weeks which were shortly to be closed down.. Quite the show. Quite the FEAR FEAR FEAR producing show inducing the west to use "their" long planned "countermeasure" Mrna to now generate the ccp/pla bio-engineered toxic "slow kill" "spike" for its "vaccine" antigen. Infection, injection, infection, injection, infection, injection death and debilitation in the west, China largely protected with widespread prior immunity until delta with actual lock downs and conventional vaccines. "chinese" Go players vs complicit "western" checkers players.
The facts that the surveillance state ccp/pla "china" 100% knew what was circulating person to person in wuhan and 100% deliberately worked to conceal this while working to keep travel open from wuhan to the world and while they looted the "west's" stocks of N95 shows ccp/pla intent at best to "never let a good crisis go to waste" if the release was somehow not deliberate, while providing "pandemic explanation" cover with 2 "red herring" (ethical skeptic) trails 1) zoonotic origin with wet market outbreak center, to be supported by the west's complicit US bioweapon / bioweapon countermeasure / military / industrial / pharma complex, with full knowledge as to the origin of sars-cov-2, as a cover for their own complicit gain of function (gain of effect) "contribution" the furin cleavage site, the "2", the pandemic level of human to human transmission, in sars-cov-2 and other technology transferred to and taken by the ccp/pla and used by the ccp/pla for the lab recombination "creation" of sars-cov-2. Effective zoonotic "cover" for 3 years yet still being debunked leading to
"red herring" (ethical skeptic) trail 2) "ACCIDENTAL" lab release. How long for this to be debunked?
.... . evil here evil there - evil won round "covid"
cloward pavin strategy = the new serfdom for those remaining after depopulation
The reality is good vs evil, Light vs darkness, Freedom and Opportunity leading to a Golden Age on Our Planet Earth vs "their" plan for a total control, genetically engineered, depopulated, dystopian futureless earth.
I asked my Cardiologist in early ‘23 at my annual checkup if he’d order a D Dimer test for me just to see if I had any clotting issues. I didn’t take the jab.
He refused.
Of course, every year I ask the Assistant if they’re seeing jab related problems there and without missing a beat they always say, “No.”
I took my vaxed son to my GP who is fully aware of the vax issues (his wife is vax injured), my GP ordered a d-dimer test for both my son & I (I am unvaccinated). Both our results came back normal. But I don’t know if that means spikes are not present or could still be.
All of that is interesting. Whike working crazy covid in LTC & Hospital & ended up in ED w heart problems. I had an elevated D-dimer. They performed a dopplar scan and we found nothing (in an arm that had been swelling too). They said to carry on.."could be stress". I had read that it could be indicative of cancer also.
Found nothing... interesting. As I told my sister, who had crazy tachycardia after $&!?, they won't tell you if they see anything wrong. Not sure why? Have the parameters of "normal" changed so much that tachycardia is considered normal? Or arm swelling? Or syncope? All chalked up to stress and anxiety. Thank goodness we are all required to have useful health insurance 😏.
Yes, I suppose you’re right. I’m entitled to a second opinion so perhaps there’s someone here who’ll do the right thing. I just know I can’t pre screen that profession and get a straight answer on the phone as any consumer should.
Its a simple blood test. If your cardiologist will not prescribe a d-dimer knowing you got mRNA vaxed & you have a heart condition, get rid of him asap. Not joking. It’s your life.
So a year after Covid infection (not jabbed), mine is down to 0.9 mcg/mL. Doc seems to think this is fine, but I am taking aspirin nonetheless. I figure clot-stoke is more likely than bleed-stroke.
Even our ERs are not using D-dimer which used to be among the standard cardiology tests. D-dimers are elevated so frequently now that they are not useful for the doctor. Troponin is still measured. If your troponin is elevated, you can assume your D-dimer is also elevated. But of course you cannot know the level. "Put on the blinders" seems to be the approach that healthcare has to use.
You can also get a D-dimer test by ordering the test online and getting the blood draw at places like Quest Diagnostics and LabCorp, bypassing the doctor completely. The blood tests I self-order are about the same $$$ out-of-pocket as my insurance co-pay would have been.
As always, you have loaded your readers with information to ponder. Still, I really REALLY need you to answer a question for me as best you can: we all know that the jabs were, in fact, at best, transfections of high- fidelity self- replicating mRNAs. Such or similar transfections have been used in the study of lab animals ( rats) for well over a decade— particularly studying areas of their brains. But to understand the effect of such mRNAs on the area so transfected, the researchers had to kill the rat and dissect the brain within a week or two, before the rats’ immune system completely wiped out the transfected area. So, maybe this is happening with the jabbed? Maybe pseudouridine slows down this inevitable process? Any ideas?
My guess is that vaxed people who received a dead batch jab (zero side affects) will probably be fine. My son’s jab had zero impact on him, did notice anything, & his d-dimer came back very healthy normal. But others in my family received warm batch jabs & were immediately very sick & suffered heart arrhythmia for months.. thankfully zero hot batch jabs in my family but I have read about areas where an entire small town or village all received jabs from one hot batch & families were wiped out ie: 2 of 5 in a given family receiving a hot batch jab died. You can look up the toxicity of your batch at howbadismybatch.com. Most batches have zero deaths but some are loaded with death.
Wow. Thanks for sharing. I do have a friend whose mother and sister died within weeks of each other. Said ot was covid. Interesting. We didn't hear of a lot of covid deaths here- just hse two
The lab leak hoax is another distraction, the only way to create a worldwide pandemic is to clone lots and lots of virus and spread it all over the place.
"Intravenous administration of lipid nanoparticles has been the most common route to deliver therapeutic genes to endothelial cells, as these cells are located in the inner surface of blood vessels and are in direct contact with the blood. However, when nanoparticles enter the blood circulation, they are often eliminated by cells of the reticuloendothelial system or preferentially transfect hepatocytes, which prevents nanoparticles from reaching and transfecting endothelial cells [69, 94, 186–189].
ATTN:ADVANCED
"Knowing that lipid nanoparticles can be directed to the pulmonary endothelium by introducing cationic lipids in their formulation established one of the first rational design strategies to target endothelial cells. This finding could accelerate the production of targeted nanoparticles to the endothelium, as most nanoparticles generated prior to this discovery were fabricated with lipids ob..."
While searching my uncles research...
And i would ask comment from Walter so I'll post this there as well AND I would be asking for input from Judy on this as well THOUGH I already know that she is currently covering several of the particular mechanisms mentioned in this paper in her class ("book club") so then my request to the SHiTzus is;
This giant work seems to explain all the currently operative modes of biological destruction but in rabbits. It may be the cypher.
Mahalo Walter. One of the first symptoms that I noticed for myself and that I have had to manage is a particular type of scalp flaking that can be painful (painful itchy) and is essentially persistant. I use T-gel coal tar shampoo which is the only product that works to keep this under control. I wonder how this production of toxic waste from the skull may be related to production of spike at the skull meninges.
I'm not a doctor, but I've read a ton, and I understand mechanics and how things work. There are things that help with the spike proteins specifically Nattokinase, Serrapeptase, & blackseed oil (or Ivermectin if you have it), I think those just help. The only cellular process that can get rid of cells that have been programed to run a muck with mRNA is called Autophagy. Given how D3 would have been a much better defense against covid than the so called vaccines, I'd think it would help your body do its thing in response to the spikes being produced. Were it me, I'd take the listed supplements and plenty of D3 daily. As hard as it is, I'd do at least a 24 hr fast once a week. I'd research autophagy and try to find out if 4 one day fasts per month do the best good, or should I do 2, 2 day fasts per month. Might also want to limit ones eating to just an 8hr window which also helps trigger autophagy each day as well. If I was vaxed, I'd be all over that, and trying to figure out everything about autophagy that I could as my life would likely depend on it. I hope this helps. But that's just my thoughts on what to do about it, for what ever it's worth. If you find good info on autophagy let me know.
When I was trying to heal after a mysterious disease left me unable to use my legs well, I also researched mitochondrial dysfunction and how to aid recovery (I was already studying Nutrition).
One of the things that I believed helped was heat, like from hot summer days outside- get a good sweat in, the garden maybe :)
So, it was heat and lots of antioxidants (clean food). I had read this somewhere and had some result. Eventually, over 2 years, my legs mostly healed- I could walk anyway.
A physician, a woman, who also lost the use of her legs, dx w MS and had to be in a wheelchair for a time. She began researching and developing a diet for recovery. One main ingredient was so organ meat 1 x a wk.She recovered her ability to walk!
I don't remember her name, but surely duckduckgo does!
Personal story: I have not had the jabs, but, (pre-covid) I had Phlebitis following a dog bite on my left calf muscle (non penetrating). I have large ropey varicose veins on that leg. Not only did Natto and Resveratrol stop the Phlebitis, but the vein went flat and never returned to the varicose state. I used the Serrapeptase to clean up the dead tissue after the treatment was done.
When the cia was founded in 1947 its first charge was to round up the japanese and german bioweapon expert war criminals and move then into the US bioweapon program. From then on its been spies working within bioweapons programs spying on other spies working in these programs. The wuhan lab was obviously a honey trap for this type of research. The ccp/pla was able to get bioweapon applicable research from numbers of sources. A bioweapon baric and his UNC bioweapon gang developed furin cleavage site, even a moderna patented genetic sequence showed up sars-cov-2
A note written to myself while "musing" one night. "tongue in cheek" or?
Clandestine Services Standard Practice 101 (CSSP101) handbook
Practice A: Hide in Plain Sight - adapted for "study" (propaganda) publication: Write the truth but Not ALL THE TRUTH "Do not openly, or in a manner direct attention to foundational US research used to create cov2, do not include Ralph S Baric as an author or refer to his or others work. Carefully infer, but do not outright claim natural recombination, limit or avoid all reference to lab recombination. Do not in any manner become subject under Admonitions 1 and 2. Remember you worship at the feat of the controller of your funding fauci. "It is a shiny object that will go away in times."
Admonitions
1) Do not get caught. If caught 1) admit to nothing 2) deny everything 3) demand proof limit speech to insisting there is no proof. Always maintain a " no evidence" position to aid in plausible deniability in the future (when truth comes out).
2) if you get caught and are forced to become a double agent, do so as a triple agent from the start. Do not wait until until your double agent status has been "detected by his original sponsor" and you are forced to become a re-doubled agent.
I have chronic/ systemic inflammatory response syndrome. From biotoxin mold illness. And other autoimmune. I’m seeing so many people, seems like they have the same problem now. & whatever “ shedding “ is, is a constant challenge now.
I have chronic Lyme Disease. This sounds similar. In fact, I have seen many people talk online about their jab side effects and many of them sound similar to Lyme Disease.
I’m very thankful for my integrative medicine doctor, after almost 2 decades of neglect and gaslighting by my insurance dictated disability doctors.
Blair,
Have you looked into Methylene blue to help treat your Lyme? Some pisit that it may also help C19, for the same reasons
Thanks, P Mac! I will look into it. I've heard of it, but don't know anything about it. I'm always open to treatment options. It's a very difficult road. I'm struggling.
You are so right
Have that too but last time I checked, mine was undetectable.
https://cirsnetwork.com/diagnosing-cirs/
This has info & some resources
Thank you, Rosalind!
Here too
So how can one who is mRNA vaxed measure the amounts of spike proteins in his system, if any? Is the most common indicator of the presence of spikes seeing microclotting as shown on a d-dimer test? Or could one have spikes proteins present without microclotting and with a normal d-dimer test result?
I’ve been asking this same question to no avail. I took two AZ jabs, and want to test for integration. Kevin McKernan has a test kit available to labs. I’ve written to two UK labs to test on my behalf, sadly to date no one has replied. I think these labs are afraid to put their names to this for fear of losing bigger government contracts.
After all, ACE2 is literally the absolute most dangerous receptor if you wanted to design something to attack the human body. It is everywhere."
They wanted to attack the human body through the ACE2 receptor and that is exactly what "they" did spending 15 years testing every sars-cov to find in 2017, a sars-cov in a pangolin, most likely pangolin #8, that had evolved a spike with exceptional ACE2 binding affinity. This was recombined to "create" sars-cov-2 as seen below in an excerpt of my comment. If anyone asks I will post my full comment titled "a ccp/pla 2 front , stealth, "unlimited war", "economic war", bioweapon attack on the west. Front #1) sars-cov-2 + "developed" immune escape variants, front #2) ccp/pla tradecraft + fear-inducing showmanship inducing the west to use ccp/pla slow kill bioweapon spike for its countermeasure mRNA and viral vector produced vaccine antigen."
The following from the March 22, 2020 US "complex" it is a "hide in plain sight" limited hangout, zoonotic origin / wet market infection epicenter inference, mis/dis/mal information, propaganda piece "Emergence of SARS-CoV-2 through recombination and strong purifying selection" (just look at where the authors work) They carefully tell some truth, always make mention of zoonotic evolution while never actually saying sars-cov-2 was zoonotic (plausible deniability) and never mention lab origin.
"We show evidence of strong purifying selection around the receptor binding motif (RBM) in the spike gene and in other genes among bat, pangolin and human coronaviruses, indicating similar strong evolutionary constraints in different host species. We also demonstrate that SARS-CoV-2’s entire RBM was introduced through recombination with coronaviruses from pangolins, possibly a critical step in the evolution of SARS-CoV-2’s ability to infect humans. " "we find significant recombination breakpoints before and after the ACE2 binding site (fig. S2A)," "Specifically, amino acid sequences of the receptor binding motif (RBM) in the C terminal of the S1 subunit are nearly identical to those in two Pan_SL-CoV_GD viruses, with only one amino acid difference (Q498H)—although the RBM region has not been fully sequenced in one of Guangdong pangolin virus (Pan_SL-CoV_GD/P2S)
"Thus, a functional RBM nearly identical to the one in SARS-CoV-2 is naturally present in Pan_SL-CoV_GD viruses. The very distinctive RaTG13 RBM suggests that this virus is unlikely to infect human cells, and that the acquisition of a complete functional RBM (my note; with exceptional human ACE 2 binding ability) by a RaTG13-like CoV through a recombination event with a Pan_SL-CoV_GD-like virus enabled it to use ACE2 for human infection.
note; As this "Research Article" was originally posted to the preprint? server the supplementary data initially contained a spread sheet, subsequently removed, showing on the vertical, line by line, 3533 individual tissue samples taken from a number of sick pangolins. Virus types found in each tissue sample, averaging close to 10 per sample, were listed horizontally - sars-cov was found in sick pangolin #7 and more in sick pangolin #8, more likely the "guilty party" supplying the human ACE 2 binding affinity enhancement identified in sars-cov-2. I expect this spread sheet was removed because someone noticed it actually was a "fine exemplar" of chinese bioweapon research.
What are your thoughts on this? Trudeau basically helped wuhan/China. He hid the documents for years.
Why is no one talking about Trudeau enabling China and perhaps there is more to the story. The timeline is interesting.
https://www.thebureau.news/p/breaking-canadian-spy-suspect-qiu
https://www.lifesitenews.com/news/intel-docs-reveal-top-trudeau-govt-virologist-had-clandestine-relationship-with-communist-china/?utm_source=daily-usa-2024-03-05&utm_medium=email
When the cia was founded in 1947 its first charge was to round up the japanese and german bioweapon expert war criminals and move them into the US bioweapon program. From then on it's been spies working within bioweapons programs spying on other spies working in these programs. The wuhan lab was obviously a honey trap for this type of research - "no questions asked, cheap we do, to woo you, to the wuhan lab" and, no doubt, they developed innovations of their own. The ccp/pla was obviously able to obtain bioweapon applicable research from a number of sources. A "bioweapon baric" and his UNC gain of function gang developed furin cleavage site, even a moderna patented genetic sequence showed up in sars-cov-2.
a note to myself written while musing one night - "tongue in cheek" or?
Clandestine Services Standard Practice 101 (CSSP101) Handbook
Practice A: Hide in Plain Sight - adapted for "study" (propaganda) publication: Write the truth but Not ALL THE TRUTH. Do not openly, or in any manner direct attention to foundational US research used to create cov2, do not include Ralph S Baric as an author or refer to his or others gain of function work at UNC or our other bioweapon activities. Carefully infer, but do not outright claim natural recombination and avoid any and all reference to lab recombination. Do not in any manner become subject under Admonitions 1 and 2. Remember you worship at the feet of the controller of your funding fauci, who said about lab origin of sars-cov-2 "It is a shiny object that will go away in times."
Admonitions
1) Do not get caught. If caught 1) admit nothing 2) deny everything 3) demand proof - limit speech to insisting there is no proof. Always maintain a " no evidence" position to aid in plausible deniability in the future (when truth comes out).
2) if you get caught and are forced to become a double agent, do so as a triple agent from the start. Do not wait until your double agent status has been "detected by his original sponsor" and you are forced to become a re-doubled agent.
I like your writing style and comments. You should put this info you write in an article and post it. : )
I wouldn’t mind saving it too. Lol
I followed you and will be interested to any further articles you do.
Thanks and take care.
Thank You.
Thank you, for that. Yes, we mustvreview every single angle. I also believe it is a war w several strategies..many old ones, including cloward pavin strategy
Please ignore if you did not ask, on the inner, for the full post
The following is my takeaway "on a Carefully Planned Worldwide Bioweapons Attack" I originally posted this comment to a substack page discussing "DEFUSE"
DEFUSE does provides additional evidence of highly developed PREEXISTING bioweapon development work to enhance sars-cov via the addition of a furin cleavage site undertaken prior to 2018 by the US bioweapon / bioweapon and pandemic countermeasure "complex".
"The exact furin cleavage site found in SARS-CoV-2 is found in another protein, a protein called alpha-ENaC found in humans and studied heavily at the same university (UNC) as one of the PI’s of DEFUSE. "
UNC - University of North Carolina at Chapel Hill home of bioweapon baric and the bioweapon baric gain of function gang.
and then DEFUSE, based on prior knowledge writes its proposal showing that "it" has prior knowledge of the location to place the furin cleavage site to weaponize sars-cov thereby "creating" sars-cov-2. "SARS-CoV-2 has its furin cleavage site at exactly the location proposed in these grants."
It is made obvious by the outworking of events that this US developed furin cleave site and specific technology to insert it was "transfered"/taken/stolen and PRIOR to 2018 delivered to the bioweapon / bioweapon and pandemic countermeasure "complex" of the "chinese" communist party/peoples liberation army - ccp/pla.
From the Abstract of "SARS-CoV-2 and the Secret of the Furin Site" "Here we show genomic fingerprints which are specific of Pangolin-CoVs, Bat-SARS-like (CoVZC45, CoVZXC21), bat RatG13 and human SARS-CoV-2 coronaviruses. This, along with phylogenetic analysis, we found that these species have the same evolutionary origin in the bat, including a genetic recombination of S gene between Pangolin-CoV (2017) and RatG13 ancestors." RatG13 "isolated in 2013".
The following from the March 22, 2020 "US" complex "hide in plain sight" limited hangout, zoonotic origin / wet market infection epicenter, mis/dis/mal information, propaganda piece "Emergence of SARS-CoV-2 through recombination and strong purifying selection" (just look at where the authors work)
"We show evidence of strong purifying selection around the receptor binding motif (RBM) in the spike gene and in other genes among bat, pangolin and human coronaviruses, indicating similar strong evolutionary constraints in different host species. We also demonstrate that SARS-CoV-2’s entire RBM was introduced through recombination with coronaviruses from pangolins, possibly a critical step in the evolution of SARS-CoV-2’s ability to infect humans. " "we find significant recombination breakpoints before and after the ACE2 binding site (fig. S2A)," "Specifically, amino acid sequences of the receptor binding motif (RBM) in the C terminal of the S1 subunit are nearly identical to those in two Pan_SL-CoV_GD viruses, with only one amino acid difference (Q498H)—although the RBM region has not been fully sequenced in one of Guangdong pangolin virus (Pan_SL-CoV_GD/P2S)
"Thus, a functional RBM nearly identical to the one in SARS-CoV-2 is naturally present in Pan_SL-CoV_GD viruses. The very distinctive RaTG13 RBM suggests that this virus is unlikely to infect human cells, and that the acquisition of a complete functional RBM (my note; with exceptional human ACE 2 binding ability) by a RaTG13-like CoV through a recombination event with a Pan_SL-CoV_GD-like virus enabled it to use ACE2 for human infection.
note; As this "Research Article" was originally posted to the preprint? server the supplementary data initially contained a spread sheet, subsequently removed, showing on the vertical, line by line, 3533 individual tissue samples taken from a number of sick pangolins. Virus types found in each tissue sample, averaging close to 10 per sample, were listed horizontally - sars-cov was found in sick pangolin #7 and more in sick pangolin #8, more likely the "guilty party" supplying the human ACE 2 binding affinity enhancement identified in sars-cov-2.
"Furthermore, SARS-CoV-2 has a unique furin cleavage site insertion (PRRA) not found in any other CoVs in the Sarbecovirus group (24), although similar motifs are also found in MERS and more divergent bat CoVs (25) (Fig. S3). This PRRA motif makes the S1/S2 cleavage in SARS-CoV-2 much more efficiently than in SARS-CoV and may expand its tropism and/or enhance its transmissibility (23)"
Sars-cov backbone and sars-cov components were on the bioweapon lab shelves of the "chinese" communist party/people's liberation army (ccp/pla) bioweapon / bioweapon and pandemic countermeasure "complex" from 2013 - a sars-cov virus with a 50% fatality rate when transfected in aerosolized bat feces, this cov-2 supplied the "backbone" for sars-cov-2, and from 2017 a pangoplin sars-cov spike component with exceptional binding to human ACE 2.
Recombination and Strong Purifying Selection using these and using "US" furin cleavage site technology that was used to put the "2" into sars-cov, created the "pandemic" level of human to human transmission shown in sars-cov-"2".
Then this ccp/pla bioweapon complex did what it would do - develop a countermeasure vaccine and do human testing while continuing to bio weaponize their sars-cov-2, most particularly the spike*, with various bioweapon toxin inserts and virulence inhibited toxin inserts and continue to do countermeasure vaccine testing on humans. *note; Whole spike which was by that time well "noised abroad" as the choice coronavirus antigen for coding countermeasure agent mRNA.
From events we may see that during this ccp/pla bioweapon/bioweapon countermeasure development process*, in the March 2018 time frame, a virulence inhibited early sars-cov-2 began to spread across China, Asia Pacific and into areas of Chinese contact in Africa developing widespread immunity to sars-cov-2 in the population of those areas which lasted until the immunity breakthrough and increased virulence changes developed into sars-cov-2 seen in the Delta variant. see The Ethical Skeptic "China’s CCP Concealed SARS-CoV-2 Presence in China as Far Back as March 2018 https://theethicalskeptic.com/2021/11/15/chinas-ccp-concealed-sars-cov-2-presence-in-china-as-far-back-as-march-2018/
*note; The modus operandi MO of a bioweapon/bioweapon countermeasure complex is FIRST DEVELOP THE BIOWEAPON
Then a breakdown of virulence inhibition? or a leak or breakthrough infection? or a DELIBERATE DECISION to release a virulent sars-cov-2 as a stealth bioweapon attack on the west with a "pandemic" in china "GO player" cover story and THE DELIBERATE DECISION made by the ccp/pla to use all means necessary to suppress and stop the spread of covid-19 in China and THE DELIBERATE DECISION made by the ccp/pla to use all means necessary, then, to insure that that initial release sars-cov-2 spread to the world and that certain subsequent variants developed and released in "coincidental" conjunction with ccp/pla vaccine testing in foreign countries also spread, quite possibly, initially via bioweapon encapsulation to produce airborne aerosols particles , South African variant, most virulent Gamma P1 in Brazil, or spread across the world and such as Delta and then the case of Omicron. Omicron with the prion creating spike insert toxin reportedly somehow now removed. The prion creating spike insert toxin present in prior variants and replicated by mRNA in the whole spike "vaccine " antigen.
continued as a reply
This OMICRON ALLOWED TO SPREAD THROUGH CHINA reportedly doing relatively little damage to the people of China whose immune systems it appears were mostly protected from repeated infections and repeated mRMA injections creating toxic whole spike and doing other damage which made Omicron reportedly much more debilitating and killing in the multiple infection / multiple injection "west". And now, in the west, a omicron with a prion initiating site "insert" reported.
imo - All Total, fact + fact + fact, shows a ccp/pla 2 front , stealth, "unlimited war", "economic war", bioweapon attack on the west. Front #1) sars-cov-2 + "developed" immune escape variants, front #2) ccp/pla tradecraft + fear-inducing showmanship inducing the west to use ccp/pla slow kill bioweapon spike for its countermeasure mRNA and viral vector produced vaccine antigen. Induced with terrible deaths for the most vulnerable elderly and comorbid, people filmed dropping dead, staged?,on China streets. Where else in the world did we see this happening before "vaccines"? Apartment doors welded shut, massive spraying and fogging of the streets and public spaces and the phenomenal construction of hospitals in weeks which were shortly to be closed down.. Quite the show. Quite the FEAR FEAR FEAR producing show inducing the west to use "their" long planned "countermeasure" Mrna to now generate the ccp/pla bio-engineered toxic "slow kill" "spike" for its "vaccine" antigen. Infection, injection, infection, injection, infection, injection death and debilitation in the west, China largely protected with widespread prior immunity until delta with actual lock downs and conventional vaccines. "chinese" Go players vs complicit "western" checkers players.
The facts that the surveillance state ccp/pla "china" 100% knew what was circulating person to person in wuhan and 100% deliberately worked to conceal this while working to keep travel open from wuhan to the world and while they looted the "west's" stocks of N95 shows ccp/pla intent at best to "never let a good crisis go to waste" if the release was somehow not deliberate, while providing "pandemic explanation" cover with 2 "red herring" (ethical skeptic) trails 1) zoonotic origin with wet market outbreak center, to be supported by the west's complicit US bioweapon / bioweapon countermeasure / military / industrial / pharma complex, with full knowledge as to the origin of sars-cov-2, as a cover for their own complicit gain of function (gain of effect) "contribution" the furin cleavage site, the "2", the pandemic level of human to human transmission, in sars-cov-2 and other technology transferred to and taken by the ccp/pla and used by the ccp/pla for the lab recombination "creation" of sars-cov-2. Effective zoonotic "cover" for 3 years yet still being debunked leading to
"red herring" (ethical skeptic) trail 2) "ACCIDENTAL" lab release. How long for this to be debunked?
.... . evil here evil there - evil won round "covid"
cloward pavin strategy = the new serfdom for those remaining after depopulation
The reality is good vs evil, Light vs darkness, Freedom and Opportunity leading to a Golden Age on Our Planet Earth vs "their" plan for a total control, genetically engineered, depopulated, dystopian futureless earth.
Thank.you, for your diligence in reporting.
Is any of this detectable by lab work? Or are the labs in on the scam too? How would one know this is happening?
I asked my Cardiologist in early ‘23 at my annual checkup if he’d order a D Dimer test for me just to see if I had any clotting issues. I didn’t take the jab.
He refused.
Of course, every year I ask the Assistant if they’re seeing jab related problems there and without missing a beat they always say, “No.”
Right.
Get a new cardiologist!
I took my vaxed son to my GP who is fully aware of the vax issues (his wife is vax injured), my GP ordered a d-dimer test for both my son & I (I am unvaccinated). Both our results came back normal. But I don’t know if that means spikes are not present or could still be.
All of that is interesting. Whike working crazy covid in LTC & Hospital & ended up in ED w heart problems. I had an elevated D-dimer. They performed a dopplar scan and we found nothing (in an arm that had been swelling too). They said to carry on.."could be stress". I had read that it could be indicative of cancer also.
Strange though. I have not been.@#$%%
Found nothing... interesting. As I told my sister, who had crazy tachycardia after $&!?, they won't tell you if they see anything wrong. Not sure why? Have the parameters of "normal" changed so much that tachycardia is considered normal? Or arm swelling? Or syncope? All chalked up to stress and anxiety. Thank goodness we are all required to have useful health insurance 😏.
Not sure if you’re using anything to help like lumbrokinase, nattokinase, EDTA, etc.
I’m doing that just as a precaution. For what it’s worth, I really like Dr. Ed Group at Global Healing. You may want to check him out.
Yes, I suppose you’re right. I’m entitled to a second opinion so perhaps there’s someone here who’ll do the right thing. I just know I can’t pre screen that profession and get a straight answer on the phone as any consumer should.
Its a simple blood test. If your cardiologist will not prescribe a d-dimer knowing you got mRNA vaxed & you have a heart condition, get rid of him asap. Not joking. It’s your life.
I didn’t get the ClotShot, fyi.
Glad to hear that!
Can you provide the D-dimer range for "normal"? I want to see if it is different than it was years ago. Thank you.
Less than 0.5 mcg per mL is normal
So a year after Covid infection (not jabbed), mine is down to 0.9 mcg/mL. Doc seems to think this is fine, but I am taking aspirin nonetheless. I figure clot-stoke is more likely than bleed-stroke.
Even our ERs are not using D-dimer which used to be among the standard cardiology tests. D-dimers are elevated so frequently now that they are not useful for the doctor. Troponin is still measured. If your troponin is elevated, you can assume your D-dimer is also elevated. But of course you cannot know the level. "Put on the blinders" seems to be the approach that healthcare has to use.
You can order your own blood tests online and go to the lab for the blood draw. The one I used is mymedlab.com
Thanks!
Insurance dictates. One can request self-pay, which is ridiculous these days.
That was my assumption.
You can also get a D-dimer test by ordering the test online and getting the blood draw at places like Quest Diagnostics and LabCorp, bypassing the doctor completely. The blood tests I self-order are about the same $$$ out-of-pocket as my insurance co-pay would have been.
Not to be a Debbie downer but I read somewhere that D dimer will not show micro clotting. All hearsay of course.
Yeah, I heard that, too. That’s why I assume I have it and am using lumbrokinase, nattokinase, liquid EDTA from Global Healing, etc.
What more can any of us really do?
If they’re spiking our water, meat and vegetables, misting our air…well, you get the point.
Exactly. They're coming at us from all directions so it's difficult to navigate. I'm leaning on my innate wisdom more and more.
As always, you have loaded your readers with information to ponder. Still, I really REALLY need you to answer a question for me as best you can: we all know that the jabs were, in fact, at best, transfections of high- fidelity self- replicating mRNAs. Such or similar transfections have been used in the study of lab animals ( rats) for well over a decade— particularly studying areas of their brains. But to understand the effect of such mRNAs on the area so transfected, the researchers had to kill the rat and dissect the brain within a week or two, before the rats’ immune system completely wiped out the transfected area. So, maybe this is happening with the jabbed? Maybe pseudouridine slows down this inevitable process? Any ideas?
THANKS FOR ALL YOU DO!
My guess is that vaxed people who received a dead batch jab (zero side affects) will probably be fine. My son’s jab had zero impact on him, did notice anything, & his d-dimer came back very healthy normal. But others in my family received warm batch jabs & were immediately very sick & suffered heart arrhythmia for months.. thankfully zero hot batch jabs in my family but I have read about areas where an entire small town or village all received jabs from one hot batch & families were wiped out ie: 2 of 5 in a given family receiving a hot batch jab died. You can look up the toxicity of your batch at howbadismybatch.com. Most batches have zero deaths but some are loaded with death.
Wow. Thanks for sharing. I do have a friend whose mother and sister died within weeks of each other. Said ot was covid. Interesting. We didn't hear of a lot of covid deaths here- just hse two
The lab leak hoax is another distraction, the only way to create a worldwide pandemic is to clone lots and lots of virus and spread it all over the place.
More here; https://truthaddict.substack.com/p/lab-leak-zoonotic-spillover-or-deliberate
International Military games Wuhan October 2019????
Crimson contagion...
ATTN:INTERMEDIATE
"Intravenous administration of lipid nanoparticles has been the most common route to deliver therapeutic genes to endothelial cells, as these cells are located in the inner surface of blood vessels and are in direct contact with the blood. However, when nanoparticles enter the blood circulation, they are often eliminated by cells of the reticuloendothelial system or preferentially transfect hepatocytes, which prevents nanoparticles from reaching and transfecting endothelial cells [69, 94, 186–189].
ATTN:ADVANCED
"Knowing that lipid nanoparticles can be directed to the pulmonary endothelium by introducing cationic lipids in their formulation established one of the first rational design strategies to target endothelial cells. This finding could accelerate the production of targeted nanoparticles to the endothelium, as most nanoparticles generated prior to this discovery were fabricated with lipids ob..."
While searching my uncles research...
And i would ask comment from Walter so I'll post this there as well AND I would be asking for input from Judy on this as well THOUGH I already know that she is currently covering several of the particular mechanisms mentioned in this paper in her class ("book club") so then my request to the SHiTzus is;
This giant work seems to explain all the currently operative modes of biological destruction but in rabbits. It may be the cypher.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9897626/
Wow! This is the gift that keeps giving, for sure.
Thank you, Walter, for widening our knowledge.
What is your take on nicotine patches as a way to displace the spike protein?
Mahalo Walter. One of the first symptoms that I noticed for myself and that I have had to manage is a particular type of scalp flaking that can be painful (painful itchy) and is essentially persistant. I use T-gel coal tar shampoo which is the only product that works to keep this under control. I wonder how this production of toxic waste from the skull may be related to production of spike at the skull meninges.
Strange! I've had covid but not the sh*t. I also have that, and a LOT of hair loss!
Yep
Could be psoriasis? Lots of ppl with skin issues.
I think it's different. It seems different than psoriasis but maybe the spike is involved in both.
D3 stat.
D3 For spike removal? Anything else?
I'm not a doctor, but I've read a ton, and I understand mechanics and how things work. There are things that help with the spike proteins specifically Nattokinase, Serrapeptase, & blackseed oil (or Ivermectin if you have it), I think those just help. The only cellular process that can get rid of cells that have been programed to run a muck with mRNA is called Autophagy. Given how D3 would have been a much better defense against covid than the so called vaccines, I'd think it would help your body do its thing in response to the spikes being produced. Were it me, I'd take the listed supplements and plenty of D3 daily. As hard as it is, I'd do at least a 24 hr fast once a week. I'd research autophagy and try to find out if 4 one day fasts per month do the best good, or should I do 2, 2 day fasts per month. Might also want to limit ones eating to just an 8hr window which also helps trigger autophagy each day as well. If I was vaxed, I'd be all over that, and trying to figure out everything about autophagy that I could as my life would likely depend on it. I hope this helps. But that's just my thoughts on what to do about it, for what ever it's worth. If you find good info on autophagy let me know.
Good info. Thx.
When I was trying to heal after a mysterious disease left me unable to use my legs well, I also researched mitochondrial dysfunction and how to aid recovery (I was already studying Nutrition).
One of the things that I believed helped was heat, like from hot summer days outside- get a good sweat in, the garden maybe :)
So, it was heat and lots of antioxidants (clean food). I had read this somewhere and had some result. Eventually, over 2 years, my legs mostly healed- I could walk anyway.
A physician, a woman, who also lost the use of her legs, dx w MS and had to be in a wheelchair for a time. She began researching and developing a diet for recovery. One main ingredient was so organ meat 1 x a wk.She recovered her ability to walk!
I don't remember her name, but surely duckduckgo does!
I started feeding my dog just cooked heart meat, and eggs. He lost a few pounds, and has way more energy. So real food is important, that's for sure.
Nattokinase, Resveratrol, Serrapeptase and more depending on who is listing.
Personal story: I have not had the jabs, but, (pre-covid) I had Phlebitis following a dog bite on my left calf muscle (non penetrating). I have large ropey varicose veins on that leg. Not only did Natto and Resveratrol stop the Phlebitis, but the vein went flat and never returned to the varicose state. I used the Serrapeptase to clean up the dead tissue after the treatment was done.
What is the therapy you recommend? I take Resveratrol for Lyme Disease.
When the cia was founded in 1947 its first charge was to round up the japanese and german bioweapon expert war criminals and move then into the US bioweapon program. From then on its been spies working within bioweapons programs spying on other spies working in these programs. The wuhan lab was obviously a honey trap for this type of research. The ccp/pla was able to get bioweapon applicable research from numbers of sources. A bioweapon baric and his UNC bioweapon gang developed furin cleavage site, even a moderna patented genetic sequence showed up sars-cov-2
A note written to myself while "musing" one night. "tongue in cheek" or?
Clandestine Services Standard Practice 101 (CSSP101) handbook
Practice A: Hide in Plain Sight - adapted for "study" (propaganda) publication: Write the truth but Not ALL THE TRUTH "Do not openly, or in a manner direct attention to foundational US research used to create cov2, do not include Ralph S Baric as an author or refer to his or others work. Carefully infer, but do not outright claim natural recombination, limit or avoid all reference to lab recombination. Do not in any manner become subject under Admonitions 1 and 2. Remember you worship at the feat of the controller of your funding fauci. "It is a shiny object that will go away in times."
Admonitions
1) Do not get caught. If caught 1) admit to nothing 2) deny everything 3) demand proof limit speech to insisting there is no proof. Always maintain a " no evidence" position to aid in plausible deniability in the future (when truth comes out).
2) if you get caught and are forced to become a double agent, do so as a triple agent from the start. Do not wait until until your double agent status has been "detected by his original sponsor" and you are forced to become a re-doubled agent.
Oh good gosh. Ate there no good men anymore?
We, with God, are more than "they".
Didn’t notice anything *
"slow kill" stealth bioweapon - agent spike