MitNak back for the Attack
on the Stack like a Power Pack #2
You can find the original here:
So you can visit his Stack and show your support and comments. For the convenience of us non-Japanese readers, I took his entire post that was translated in my email to cut and past the entire thing here. If I made any errors in transcription I will correct them as quickly as possible.
With apologies, there is just so much genius contained in his post that I will interrupt it with my own amplifications within the text so that people can get the full scope of what he is presenting. His command of this material is extremely impressive.
Hey Kids,
I hate Reaction Videos that people do on youtube because they have no original content of their own.
Sew, lettuce imagine I'm sitting alone in my house close to noon with no sound, silently reading MitNak's latest Stack and get to the line:
"....my thinking that “the army’s beriberi epidemic in Russo-Japan War was caused by Smallpox vaccine developed by Shibasaburo Kitasato..."
And I let out a VERY LOUD: "OHHHHHH..... SHIT !!!!" that ever surprised me as it bounced off the hard walls.
Brilliant. Just freakin' BRILLIANT !!!!!!!!!!!!!!
Then I alternated between anger and giggling like a schoolgirl at whatever was written in japanese as "fuckers" "assholes" and "motherfuckers" being faithfully rendered in my Mother Tongue. You HAVE to love the passion for the Truth that MitNak has!
I finished compling this around 8pm. So I thought MitNak’s work had enough merit to spend an 8 hour day with it.
日本の反ワク運動の現状
Japan's anti-vaccine movement
MITNAK
SEP 9
I had ceased my attempt to keep up with the recent trend. Now, I have a lot of things to do, such as revealing the lie of “original antigenic sin“ which I’m convinced it is BULLSHIT concept, proving that “IgG4-Related Disease = Chronic Serum Sickness“, my thinking that “the army’s beriberi epidemic in Russo-Japan War was caused by Smallpox vaccine developed by Shibasaburo Kitasato“, and investigating Unit 731 for the reason of the truth of certain prion disease…etc.
Lordy… I’ve written 700 page books on all of these topics. I’ll try to wear briefs…
There is a supporting document from 1975 that shows contamination of ALL vaccines by bacteriophage VIRUSES found in Fetal Bovine Serum is IMPOSSIBLE to filter out. I will provide a link to that document in my googledrive only for those who request it by email:
generalportal55@gmail.com
https://apnews.com/article/fact-check-vaccines-monkey-kidneys-aborted-fetal-cells-510729340523
Post misleads on vaccine 'ingredients' | AP News
"Monkey kidneys, aborted fetal cells, fetal bovine serum, polysorbate 80, formaldehyd, thimerosal." But "monkey kidneys," "aborted fetal cells" and "fetal bovine serum" are not ingredients in vaccines. Instead, the post misleadingly refers to the ways some vaccines are produced. Some vaccines are created using viruses.
https://www.thermofisher.com/us/en/home/references/gibco-cell-culture-basics/cell-culture-environment/culture-media/fbs-basics/guide-to-fetal-bovine-serum-vaccine-production.html
Guide to Fetal Bovine Serum in Vaccine Production
Fetal bovine serum (FBS) is the most widely used growth supplement added to in vitro cell cultures. It has been in use for over fifty years, outperforming both synthetic and natural growth supplements. FBS is employed across a variety of research and industrial applications, including vaccine production.
https://www.indiatimes.com/news/india/calf-serum-role-in-making-of-covid-vaccine-explained-543005.html
The Role Of Calf Serum In Making Of COVID Vaccine Explained; Gursharan Bhalla
Updated on Jun 18, 2021, 16:30 IST
There have been some social media posts regarding the composition of COVAXIN where it has been suggested that the vaccine contains the newborn calf serum. The government has clarified that the facts have been twisted and misrepresented in these posts.
"The final vaccine (COVAXIN) does not contain newborn calf serum at all and the calf serum is not an ingredient of the final vaccine product," Union Health Ministry said.
Then, what is the role of the serum in making of the vaccine? Is newborn calf serum used to make Bharat Biotech's Covaxin?
An RTI reply to applicant Vikas Patni suggests so. "The newborn calf serum is used in the revival process of Vero cells, which is further used for the production of coronavirus during the manufacturing of Covaxin," Bharat Biotech in a reply to the Central Drugs Standard Control Organisation (CDSCO) has said. The RTI asked if vaccine producers used fetal bovine serum (FBS) in making coronavirus vaccines.
In the clarification, the government reiterated the well-known use of calf serum, as also serum extracted from other animals, in the development of vaccines. These are needed to grow the disease-causing virus, bacteria or other pathogens in the laboratory, but do not themselves become an ingredient of the vaccine.
These nutrients, like specific sugar and salt molecules, are extracted from tissues of suitable animals like horses, cow, goat or sheep. The virus grows in these nutrient-rich solutions. After that, it goes through several stages of purification that make it suitable to be used in a vaccine. There is no trace of the growth medium after the entire process is over.
According to the website of the Food and Drug Administration of the United States, cow components are used mainly because cows are large animals, easily available, and rich in some of the useful chemicals and enzymes.
“Cow milk is a source of amino acids, and sugars such as galactose. Cow tallow derivatives used in vaccine manufacture include glycerol. Gelatin and some amino acids come from cow bones. Cow skeletal muscle is used to prepare broths used in certain complex media. Many difficult to grow micro-organisms and the cells that are used to propagate viruses require the addition of serum from blood to the growth media,” it says.
=============================================
These Denials By Admission are infantile.
THERE IS NO WAY TO FILTER FOR BACTERIOPHAGES IN THE SERUM OR FINAL PRODUCT.
THERE IS NO WAY TO FILTER FOR DNA OR RNA IN THE FINAL PRODUCT.
THERE IS NO WAY TO FILTER FOR PRI-FUCKING-ONS IN THE FINAL PRODUCT.
Lies, Lies, and DAMNED LIES.
The FDA 'wrote a letter' and 'asked' that vaccine makers try to do a good job...
https://www.fda.gov/vaccines-blood-biologics/bovine-derived-materials-used-vaccine-manufacturing-questions-and-answers
Scientists have found that different bovine tissues contain different amounts of the BSE agent. It is generally believed that the highest amounts of infectivity are found in the brain and spinal cord from animals in the final stages of clinical disease. Some tissues, such as skeletal muscle and milk, have never been shown to have any infectivity. However, the slaughtering and butchering methods used to obtain tissues and prepare materials can affect the amount of infectivity that may be present. Also the production processes used to prepare bovine-derived materials (such as heat sterilization and chemical treatment) may reduce or remove infectivity.
Are these motherfuckers crazy or just serial killers? or both?
PRIONS HANG UPSIDE DOWN IN THE LYMPH LIKE BATS IN YOUR FUCKING ATTIC! THE LYMPHATIC SYSTEM IS EVERYFUCKINGWHERE IN THE BODY SO THAT IS WHY YOU CAN EAT A HAMBURGER AND BE DEAD OF CJD WITHIN DAYS!
“generally believed” is a goddamned RELIGIOUS STATEMENT. Science would laugh these fuckers into the alakline hydrolysis vats.
We ain’t never found no preeyons in milk or meat (outright fucking lie) but if you’re sloppy during choppin’ up Bossy The Cow then’s you’s gunna git some preeyons in yer bergers and mulkshakes…
Exodus 22:18 Thou shalt not suffer a witch [poisoner/sorcerer] to live.
“…heat sterilization and chemical treatment may reduce or remove infectivity.”
”may”? “MAY”? What kind of fucking Science is MAY?
Prions are heat stable to 1560 degrees Farenheit. That’s the melting point of Barium. Aluminum would be a liquid stream flowing down the streets of Maui so Prions would be all-like “y’say sumpin’ dawg?”
What measures have the FDA taken to ensure that people are not exposed to the BSE agent in vaccines?
It is believed that variant CJD was acquired from eating food products containing the BSE agent. However, FDA wants to minimize any chance that the BSE agent could be introduced into biologic products during manufacture. The Center for Biologics Evaluation and Research (CBER) is responsible for regulation of biologic products, including vaccines. In a 1991 letter to manufacturers CBER expressed concern about bovine sourced material. In December 1993 and May 1996 FDA issued letters advising that bovine derived materials from animals born in or residing in countries where BSE had occurred should not be used to manufacture FDA-regulated products intended for administration to humans. A 1993 Points to Consider document ("Points to Consider in the Characterization of Cell Lines Used for the Production of Biologics") stressed the importance of control of sourcing of bovine materials. On April 19, 2000, CBER issued a letter reminding manufacturers that the USDA list of BSE-countries had been expanded to include not only those countries where BSE was known to exist but also those where BSE may exist (FR, January 6, 1998). CBER strongly recommended "that manufacturers take whatever steps are necessary to assure that materials derived from all species of ruminant animals born, raised or slaughtered in countries where BSE is known to exist, or countries where the USDA has been unable to assure FDA that BSE does not exist, are not used in the manufacture of FDA-regulated products intended for administration to humans."
Although Canada and the US have each reported one case of BSE and the USDA has placed Canada on the list of countries with BSE, FDA has not recommended that manufacturers find a new source for bovine derived materials obtained from these countries for use in manufacture of drugs or biological products. The FDA believes that the control measures in place assure the safety of bovine derived materials sourced from these countries and used in manufacture of vaccines.
Are bovine derived materials from North America used in the manufacture of vaccines?
Yes, bovine derived materials from North America, specifically the US and Canada, are used in vaccine manufacture. Since there has been extensive movement of live cows and cow-derived materials between Canada and the US it is difficult to establish that an animal has not been born, raised or slaughtered in Canada. Moreover, control measures, such as the ruminant-to-ruminant feed ban have been similar in the two countries. Therefore, FDA has not recommended that manufacturers using bovine derived material from Canada replace those materials with materials from countries not on the USDA list of countries that have BSE or are at risk of BSE.
How did the FDA discover that some manufacturers are not universally following letters, Points to Consider (PTC) and guidance documents?
During review of new license applications manufacturers are asked to provide detailed descriptions of the manufacturing process and documentation of source country for all materials of animal origin. In 2000, during review of a license application it was determined that some of the material used during manufacture had been obtained from countries which are on the USDA list of countries which either have or may have BSE. This finding prompted an inquiry of all licensed vaccines.
What is FDA doing now to assure that companies follow guidance, letters, and PTC documents?
The Center for Biologics Evaluation and Research (CBER) has asked licensed vaccine manufacturers to evaluate all bovine sourced material used at any stage of manufacture. Manufacturers have been requested to identify all material of animal origin. For materials of bovine origin CBER has asked manufacturers to identify the source country from which the animals originated, the date the material was obtained and the date the material was used in manufacture of vaccine lots. When it is determined that any bovine-derived component used to make the working seeds or during routine production was obtained from a country on the current USDA list of countries (with the exception of Canada) which either have or may have BSE or from an unknown country, the manufacturer has been asked to change the source of such material. CBER inspects vaccine manufacturers on a routine basis to determine whether sourcing and documentation are consistent with current recommendations contained in letters and guidance documents.
That was me being ‘brief’. That is proof positive that Unit 731, just like Project Paperclip that it was folded into NEVER ENDED. You have the FDA colluding with the USDA as psychologlical warfare divisions to PRETEND to make you ‘safe’ while assuring that their witchy poisons are getting into every fucking thing on the planet.
Back to MitNak:
I’m enough to be involved the excitement of the masses anymore. Even I had a hard time to calm down the anti-vaxxters panic “the WHO’s secret document in 1972 that really doesn’t exist“.
I don’t know what is meant by the sentence on the secret document so I will followup with MitNak and we can address that as a separate Stack.
I’m making the materials for publishing on Dr. Theron Randolph who should be called as “Allergy fundamentalist“ . If you are against vaccination, you should trace the history of allergy. Just End game.
I couldn’t be more pleased with someone than when I read that statement. It shows that MitNak has COMPLETE command of the concepts at work here with such surgical focus that nothing will escape his scrutiny, therefore answers will be the final word on the topic with no distractions.
I would set the theme of material Multiple Chemical Sensitivity referred by Dr. Randolph, but since I mention, it is meaningless unless connect vaccine, so that I was struck with the idea proving “MCS is Vaccine Induced Disease“, where I evoked GULF WAR ILLNESS, but I was bothered with RAND report seems to need paying, which said GWS is NOT psychotic BUT resembles MCS.
I was so excited by this post that I stopped my work-schedule just to respond to it. Unfortunately there are TWO RAND reports on GWS. The first one (the important one) was disappeared not long after I had put out my book ICD-999. I remember in the early 2000s, sitting in the Champaign Illinois Public Library copying and pasting the text from the report by hand on a public computer using their word processor where I had to edit out all of the line-breaks to make a coherent document, with tables transcribed and color coded for my own use THAT IS SAVED ON A 3.5” FLOPPY DISK DRIVE!
Anyone old enough to even remember a floppy disk?
I will make the RAND report available to anyone who emails me.
So, when I was researching whether there are case reports developing FOOD ALLERGY after inoculating current gene recombinant tool, I found the fucking page.
https://www.sciencedaily.com/releases/2021/09/210917161212.htm
“Allergic reactions to the new mRNA-based COVID-19 vaccines are rare, typically mild and treatable, and they should not deter people from becoming vaccinated, according to research from the STANFORD UNIVERSITY School of Medicine.”
"We wanted to understand the spectrum of ALLERGIES TO THE NEW VACCINES and understand what was causing them," said the study's senior author, Kari Nadeau, MD, PhD, the Naddisy Foundation Professor in Pediatric Food Allergy, Immunology, and Asthma.
…Of the 22 recipient”, 15 had physician-documented histories of prior allergic reactions, including 10 to antibiotics, nine to foods and eight to nonantibiotic medications. (Some recipients had more than one type of allergy.)
The researchers performed follow-up laboratory testing on 11 individuals to determine what type of allergic reaction they had, as well as what triggered their allergy: Was it one of the inert sugar or lipid ingredients in the bubble, or something else in the vaccine?
The study participants underwent skin-prick tests, in which a clinician injected small amounts of potential allergens -- the lipids, sugars (polyethylene glycol or polysorbates) or entire vaccine -- into the skin. Skin-prick testing detects allergic reactions mediated by a form of antibody known as immunoglobin E, or IgE; these reactions are generally associated with the severest allergies.
None of the recipients reacted on skin-prick tests to the inert ingredients in the vaccines, and just one recipient's skin reacted to the whole COVID-19 vaccine. Follow-up blood tests showed that the vaccine recipients did not have significant levels of IgE antibodies against the vaccine ingredients.
Since the skin tests did NOT EXPLAIN the mechanism of recipients' allergic reactions, the investigators proceeded to another type of diagnostic test. Vaccine recipients provided blood samples for tests of allergic activation of immune cells known as basophils. The blood samples from 10 of the 11 participants showed a reaction to the inert ingredient polyethylene glycol (PEG), which is used in both the Pfizer and Moderna vaccines. In addition, ALL 11 RECIPIENTS HAD BASOPHIL ACTIVATION IN RESPONSE TO THE WHOLE mRNA VACCINE WHEN IT WAS MIXED WITH THEIR OWN BASOPHILS.
All 11 subjects had high levels of IgG antibodies against PEG in their blood; IgG antibodies help activate basophils UNDER SOME CONDITIONS, and this finding suggests the individuals were LIKELY SENSITIVE TO PEG BEFORE RECEIVING THEIR VACCINES.
What are these FUCKERS saying? They were supposed to attempt to know SPECTRUM of allergy after vax, but said “LIKELY SENSITIVE BEFORE RECEIVING VACCINES“???
As much as I would like to interfere with the fraud measuring ONLY IgE by Allergy “test”, beyond of it, they are still lying. The mention of “SOME CONDITIONS” means they are referring to the IgG”4” antibody which is currently under discussion！
Gather ‘round my fellow martial artists as Samurai MitNak and your favorite Drunken Boxer: Patrick-where-did-I-put-my-car-keys Jordan-san have a Master Class on SERUM SICKNESS.
Ag = Antigen
Ab = Antibody
IC = Immune Complex formed by Ag+Ab
What puts this all in perspective is the Jordan Maxim or meme from 2008:
”If you’re not looking for something - you won’t find it.”
The masturbatory fixation on IgE, IgE, IgE!!!!! proves that they are fixated on a case-defintion that excludes Continuum so that they can continue to pretend that something isn’t there or was not seen. Serum Sickness is caused by IC’s implanted under the influence of IgE. Allergy AND Infectious Disease Departments in hospitals and clinics are lumped together - so the fuckers KNOW what is going on. It just takes us to show your their stealth Kara-Te moves. Kara-Te means EMPTY HAND.
Tricky - huh?
The yellow highlighted bit was for when I show that they KNOW how to create kidney damage but OPENLY LIE about it in the Merck Fucking Medical Manual. But that is not what I wanted to showcase here.
“Injected Serum…”
Remember how the Associated Press and the India Times and FDA said that Fetal Bovine SERUM (SERUM SICKNESS…. GET IT?) was used to ‘make’ the vaccines, but ‘wasn’t in the final product’ ?
HOW do they filter it out? How do you get out the PROTEINS that make up the serum because that is what the human body reacts to. NOT the ‘inert’ sugars, NOT the ‘inert’ lipids. Oh… wait…. it was the PEG…. Butt… weight… PEG is NOT A PROTEIN!
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706272/pdf/nihms-1019221.pdf
Immediate Hypersensitivity to Polyethylene Glycols and Polysorbates: More Common Than We Have Recognized; J Allergy Clin Immunol Pract; 2019 May-Jun;7(5):1533-1540.e8.; doi: 10.1016/j.jaip.2018.12.003.Epub 2018 Dec 14.The mechanism for macrogol hypersensitivity has been poorly understood. Anti-PEG sIgG has been detected in patients receiving PEG-conjugated protein therapeutics, but was not studied in unconjugated macrogol anaphylactic cases, while anti-PEG sIgE has not been directly measured in any human studies. Our findings of skin test reactivity and coexisting polyethylene glycol-directed sIgE and sIgG antibodies suggest an IgE mediated Type I hypersensitivity could be possible in clinical reactions to unconjugated macrogols. These cases may represent a separate phenotype of immediate hypersensitivity from what has been previously shown during reactions to PEG-asparaginase and other PEGylated compounds. Of note, the absence of binding between patient IgG antibodies and lower MW PEGs also coincided with the tolerance of PEG 300 in both skin and oral challenges in vivo, supporting the involvement of antibodies specific for higher MW PEGs in the clinical reactions. The stronger reactivity of the patient samples against PEGs of higher molecular weight suggests that sensitization and risk of future reactions may depend partially on the molecular weight of PEG antigen exposures, and suggest that PEG may act as the primary antigen even when not conjugated to drug molecules. Detection of sIgE directed against PEG required use of the more sensitive Meso Scale Discovery electrochemiluminescence method and polysorbate-free testing reagents.
I know that to most people that nonsense above just might as well be Japanese or ancient Sanskrit. So let me Drunken Boxing Jordan FarmBoy this stuff for you:
Immediate Hypersensivity = Allergy = IgE
More Common Than We Have Recognized = We don’t know what the fuck we’re doing, we don’t know what the fuck is going on, but we’ve successfully covered it up until COVID.
Conjugated = PEG hooked to a drug or vaccine component = easier to provoke an allergic response to.
Unconjugated = free non-protein-linked goo that still fucks with your immune system.
High Molecular Weight = PEG is a polymer. It can be a small clump of goo, or a large clump of goo. The HMW goo fucks with your immune system more than the LMW goo does. This is akin to when you go in for any kind of CAT scan and they ask you if you are allergic to Iodine. YOU CAN’T BE FUCKING ALLERGIC TO IODINE. At best any Halogen like Chlorine from bleach or a swimming pool or Iodine can be a Hapten, that, when linked to a protein, can fuck with your immune system. But what REALLY blows out your kidneys is the HIGH MOLECULAR WEIGHT CONTRAST MEDIA THAT IS FUCKING PLASTIC.
When has anyone in healthkill ever said that that simply?
When have they ever offered something as simple as NAC N-Acetyl Cysteine 24-hours before a scheduled use of Dye or immediately in an emergcency situation to protect your kidneys? Practically never. They KNOW what is going on because I’m just a goddamned Farm Boy whose Karate is better than their best because I KNOW what is going on. If a stupid Farm Boy can figure this out then they are engaged in lethal fraud.
Corn Clusion: We poked the shit into people and Low! and Hold Bees! they done reacted to it! People have already been primed for reaction to PEG by previous exposure in FOOD and Drugs and Vaccines. They pretend that they don’t know why. They pretend that they are tyring to blame the IgG but they find the IgE which is a reverse of the Serum Sickness scam where they cite maingly IgG but downplay the IgE that is ALWAYS PRESENT BECAUSE THE IMMUNE SYSTEM IS NOT A SINGLE CAR PART THAT OPERATES IN ISOLATION. Immunity is a dynamic system that operates in contiuum and has MEMORY so previous insults LIKE THE FUCKING SKIN TEST will prime the body for DELAYED hypersensitive reactions just like Richet demonstrated when he REPEATEDLY injected toxins to get the host to destroy its own tissue.
But I never finished the Merck citation:
"The standard example of drug hypersensitivity is serum sickness, which is an ALLERGIC REACTION..."
".... specific IgG Abs that form soluble complexes with the Ag to cause an immune complex (type III) reaction; IgE Abs and consequently an IgE-mediated reaction are also produced.
LITTLE EVIDENCE EXISTS FOR AN IgG immune complex mechanism in serum-sickenss-type reactions caused by low-mol-wt drugs."
This version of the Merck Medical Manual was 1992. The PEG Allergy paper that I cited above that claimed they didn’t know shit about shit was electronically registered in 2018. That’s 26 years of not knowing shit about shit, unless they just never read the Merck Manual because they were too busy reading modern articles that also had the express purpose of covering up this shit for ANOTHER 26 YEARS…
Being a Farm Boy I am intimately aware of the smell of shit and you can’t cover up that smell…
Back to MitNak:
Bimodal IgG4-mediated human basophil activation. Role of eosinophils; Beauvais, F., Hieblot, C., Burtin, C., & Benveniste, J. (1990); The Journal of Immunology, 144(10), 3881–3890. https://doi.org/10.4049/jimmunol.144.10.3881
The role of IgG4 antibodies in allergic disorders is suspected. Yet, their presence on human basophil membrane has not been demonstrated and the mechanism of the degranulation induced by anti-IgG4 antibodies remains unclear.
As previously reported, we observed that monoclonal anti-IgG4 (10 to 100 micrograms/ml) induced histamine release in the presence of D2O from leukocytes of normal and atopic subjects. The release was accompanied by a decrease of the number of toluidine blue-positive basophils (TB+). Histamine release and TB+ decrease were also observed with lower concentrations of anti-IgG4 (1 to 100 pg/ml).
Since basophil activation assessed by TB+ decrease was more sensitive than histamine release, we thus used the former method to further study the mechanisms of the anti-IgG4- vs anti-IgE-induced basophil activation. Basophil activation by anti-IgG4 at 1 to 100 pg/ml, but not by anti-IgG4 at 10 to 100 micrograms/ml or anti-IgE, required the presence of polymorphonuclear cells.
Furthermore, anti-IgG4-stimulated purified eosinophils, but not neutrophils, released basophil-activating factors identified as cationic proteins from eosinophils. Thus, the human basophil can be activated by anti-IgG4 via two different mechanisms according to the antibody concentration. At high concentrations (10 to 100 micrograms/ml) basophil activation does not require the presence of polymorphonuclear cells whereas at lower concentrations (1 to 100 pg/ml) the presence of eosinophils is necessary.
We propose that in the latter concentration range, basophil activation is a two-step process: 1) release by anti-IgG4 of eosinophil cationic proteins that 2) will, in turn, activate human basophils. This study lends support to the role of IgG4 and eosinophils in anaphylactic reactions.
It means that IgG4 antibody can activate basophils under the presence of eosinophils. That asshole scholars on anti-vax pretend justice optimistically while saying things that “IgG4 is the evidence of immune tolerance“is because they “TREAT“ “ALLERGY“ by means of “DESENSITIZATION THERAPY“ which is “REPEATEDLY ANTIGEN ADMINISTRATION”. But as I mentioned above, I convince that the presence of IgG4 is the evidence of “The transition towards form of CHRONIC SERUM SICKNESS“.
You, dear Reader, have no idea what a sense of satisfaction that I get from reading our Japanese Friend deconstruct these LIES and the creative use of the label: “Asshole Scholars”. I have a very visual imagination and can picture academic awards for the Best Asshole… or Asshole Of The Year.
Butt - I digress…
Just so y’all know (I had to look it up myself…)
https://www.ncbi.nlm.nih.gov › pmc › articles › PMC6102618
IgG4-related disease: why is it so important? - PMC
IgG4-related disease (IgG4-RD) is a recently defined systemic inflammatory and fibrous condition of unknown etiology and multiple clinical presentations. Characteristic features include elevated serum IgG4 levels in approximately 70% of patients; diffuse lymphoplasmocytic infiltrates rich in IgG4 (+) cells; a "storiform" fibrosis pattern ...
It’s all a Shuck & Jive/Bait & Switch, which is why I wrote the 500-page 50-year Anniversary edition of the 1972 WHO Memos. It explains ALL of these lies.
But we’ll still break it down for all of you Martial Arts Practitioners out there with the basics.
As MitNak perfectly outlines you CANNOT evaluate allergy outside of the context of vaccines. This includes his excellent observation that Chemical ALLERGY falls into the same category. When ‘clinical researchers’ cite Systemic Inflammation you know that they are either total idiots or covering up for what I exposed in the 1972 WHO Memo book. When they take you down the road of JUST the Judy Chop (IgE), or JUST the Karate Chope (IgG), or JUST the Ninjee Chop (IgG4) you know that they are purposely trying to deflect your attention to harm you with no consequences for them, by prevening you from tracing the harm all the way back to the source in West Virginia (so to speak). This called Moving Goalposts. They want to keep you from ever discovering their lies so they focus on IgE or IgG and when that isn’t good enough they bring up different subgroups of each. But there are never conclusive or actionable results from their endless studies and they always need “more study” and always need “more money”.
Tolerance = body is being occupied or insulted but it IGNORES IT. This is a BAD THING.
Immunity = body is in the process of becoming occupied or insulted but it is KICKING THE INVADER’S ASS.
Desensitization = a very tricky situation where the actions that the Professional Liars take can be Induced Tolerance, IMMUNOSUPPRESSION, or relaxing Over-reactions to normal antigens or molecular mimicks (tree pollen/fruit crossovers, etc). Mostly it is an artificial dampening effect that rarely removes the ROOT CAUSE.
For all sorts of ‘allergies’ they attempt to SUPPRESS the overt reaction by drugs like steroids or the ‘repeated antigen administration’ often in low doses (not at all homeopathy but a similar approach) to ‘train’ the body to just shut up. But all of this comes with the dangers of provoking more immune responses to the point of delayed hypersensitivity where the threshold of antigens and/or stimulation is exceeded and the body starts attacking itself as in the case of Richet’s experiments that led to the invention of the words: Prophylaxis and Anaphylaxis. Any time you feel swollen anything, or numb anything you are very close to a lifethreatening situation. So I take even mild allergy like watery eyes and sneezing quite seriously, because as you have seen ALL four hypersentitivity pathways are engaged all the time because it is a CONTINUUM NOT a single thing at a single time from a single stimulus.
It is actually chilling to see someone else other than me speak of Chronic Serum Sickness with knowledge and authority despite me living with this revelation well before my first book in 2008 because I started the investigation that led to the Merck Manual discovery in the early 2000s:
”Surprisingly, glomerulonephritis, so prominent in expermental serum sickness in animals, is rarely a problem.”
The lying bastards built a BILLION DOLLAR industry on Dialysis and Kidney transplants.
Do you see why I heap high praise on MitNak yet rage against the armchair idiots that claim they have ‘done their own research’ when the ‘research’ out there is a complete fraud? The primary finding of Serum Sickness induced in test animals is destroyed kidneys! But it doesn’t happen in humans! Isn’t that a surprise?
A Look Back at Pirquet & Schick’s Influential Serum Sickness Study. The Rheumatologist; Ruth Jessen, H. (2020, 11/12).
The BioMarin group extensively monitored patients taking pegvaliase, recording clinical data, measurements of antibody titers of multiple isotypes and specificities, assessments of enzymatic neutralization, immune complexes and biomarkers for complement activation.
…Some patients receiving therapeutic anti-sera in the early 20th century received repeated doses when they were thought to be re-exposed. However, administration of the foreign serum was not chronic, in contrast to ongoing treatment with pegvaliase. This ongoing administration creates its own hazards and challenges, as it does for pegloticase.
As Dr. Atkinson explains, “They were able to treat these patients for several years. Despite having low C3, low C4, and despite antibodies developing, they got away with it.
“The antibodies kind of leveled off. Despite giving more antigen, the majority of the patients sort of plateaued. Because they didn’t GET ANY IgE ANTIBODIES, it’s not an acute allergic reaction, which would be another thing to consider.”
He concludes, “So I think IT IS A FORM OF CHRONIC SERUM SICKNESS.”
Thus, this brings consistency to what Stanford motherfuckers were saying. The facts: IgE was NOT detected but IgG was done, of which the level was persistent and made basophils activated, nevertheless the patients still had allergic reactions.
It is interesting to see a ‘doctor’ put Chronic Serum Sickness in print 12 years after a Farm Boy did.
What a Data Dog has to pay attention to is what compartments they were sampling to come up with their titers of immunoglobulins. We saw from all of the previous papers that an IgG/Antigen complex is not pathogenic until it is potentiated by IgE that then allows it to implant in tissue. So is the IgE indetectable because it was tissue bound therefore not demonstrable in the blood? Did they do any biopsies of tissue looking for the IgE? Were they using a sensitive enough test to discover it since the PEG article said “Detection of sIgE directed against PEG required use of the more sensitive Meso Scale Discovery electrochemiluminescence method and polysorbate-free testing reagents.” ? So are these just small children playing with big toys who can’t find their own asses with both hands and a GPS? or are they PURPOSELY failing to find what they don’t want to see?
THE PRODUCTION OF EXPERIMENTAL NEPHRITIS BY REPEATED PROTEID INTOXICATION; Longcope, W. T. (1913); Journal of Experimental Medicine, 18(6), 678–702. https://doi.org/10.1084/jem.18.6.678
This is the oldest report of chronic serum sickness to the extent of which I searched.
During the last two years there have been under observation at the Presbyterian Hospital occasional cases of nephritis, characterized by exacerbations of general edema, fever, albuminuria(※proteinuria), and, in a few instances, urticaria and eosinophilia, which in these particular attacks, have a close resemblance to serum disease. It was through the suggestion made by other workers, and derived from a study of these cases, namely, that nephritis might in certain instances be dependent for its origin upon an anaphylactic state, that the present investigation was undertaken.
Comparatively little attention has been paid to the anatomical alterations that may take place during anaphylactic shock, and almost no observations have been made upon the effects of repeated non-fatal anaphylactic shock upon the animal tissues. It is known that man may develop a hypersensitiveness, or allergy, as von Pirquet calls it, to some food stuffs, among which may be mentioned egg-white, fruits, and shell-fish, and under these circumstances it is possible that he may be subjected from time to time to many nonfatal attacks of intoxication by the proteins of these substances. It is important, therefore, to determine if in animals artificially sensitized to foreign protein, repeated intoxications of these foreign proteins may cause injurious effects upon the body.
…There is, therefore, a certain amount of evidence to show that during anaphylaxis some of the body cells may be injured, and a few observations tend to support the idea that this injury may be followed by a reaction on the part of the fixed and migratory body cells. A series of experiments, therefore, was planned to determine if, during repeated anaphylactic shocks in animals, ANY PERMANENT INJURY might be done to the body cells, PARTICULARLY THE KIDNEY, and whether there might be any reaction visible microscopically on the part of the tissues to such repeated intoxications.
It is undeniable that this preparation is a biological weapon for mass-producing kidney disease: if disguising IgG4 for IgG and alledging "immunization," there will be a lot of robots that does not appear to be sick, but can be controlled whether to kill by any biological switch.
Good Grief! this article predates the WHO Memos by 59 years.
The Truth Is Out There as they say on the X-Files.
”Charles-Robert Richet, French physiologist who won the 1913 Nobel Prize for Physiology or Medicine for his discovery of and coining of the term anaphylaxis, the life-threatening allergic reaction he observed in a sensitized animal upon second exposure to an antigen.”
”In his experiments, Richet injected a dog with sea anemone toxin in an attempt to protect it. Even though the dog had previously tolerated the toxin, after re-exposing it three weeks later, the dog developed anaphylaxis.”
So even back then they were demonstrating that immune reaction was a continuum between Allergy, Delayed Hypersensitivity/Arthus Reaction, Serum Sickness, and Contact Dermatitis. 110 years later and we see that academia is the official scrubber of such knowledge, PURPOSELY covering it up to protect their secrets so that they can continue to harm humans while claiming they don’t know what is happening.
It is important that vaccines are called bioweapons because that is what allied me with Rebecca Carley back in 2008 who was saying it years before I met her while all of the White-Coated Whitebread shills that are prominent today didn’t bother to pick up the phrase until the Covid scam which, by then, was too late. I guess even shills can get scared enough to tell the truth when they find that their Masters will eat them too.
It is very heartening to see ANYONE in Japan take up this stance outside of MitNak and his group.
Finally, although his views are different from mine, please forgive me to introduce the Japanese brave professor claiming for the world using the word “biological weapon”.
https://twitter.com/You3_JP/status/1700012408893534451
They established the organization studying vaccine injury.
https://jsvrc.jp
Please do whatever you can to support the work of MitNak and share his substack in all languages and countries you have available to you.
I spent 8 hours on this Stack and almost 4 more preparing the supporting documents. Through it all, even though I had notes I STILL forgot to mention that where the articles refer to Shellfish Allergy as part of what is provoked by vaccines, that unless shellfish allergy is from the sulfates that they use on the seafood as an antibiotic, then primarily the allergy is to the chitin, which is the same protein that will be in the Bug Food that they want to force on everyone.
So there will be untold harm and suffering and since this is an anaphylactic reaction: Death.
All planned to the minute degree.
Time for a Purge.
It took me LONGER to read this then it did for you to type it. Most of it went over my head...
The take away for me, is that they have made us Allergic to LIFE as we had known it. So, they are commencing to terraform our meat suit into something more dis-eased & borg ready s we'll beg for the future of having no body to feel suffering & finally transhumanism.
Probably why so many folks are Un-Aliving themselves Now ,before that cyborgness comes into play.
I may have read into it a bit......