A British government report has potentially lifted the lid on why Germany is pulling its citizens out of Portugal.
It is a report that answers the question yesterday by Portugal’s minister of foreign affairs Augusto Santos Silva: “Why are German authorities ignoring the Covid Digital Certificate?”
“People over the age of 50 who have been fully vaccinated are three times more likely to die from the Delta variant than those who haven’t received any vaccines” (this is a headline taken from Swiss online ‘uncut news’ yesterday).
The jabs can precipitate a ‘rare’ but deadly condition known as ADE (antibody dependent enhancement) which basically means that someone who might have naturally developed only a mild illness as a result of contracting Covid-19 could experience severe disease, lasting morbidity and even death as a result of having been vaccinated.
The British government report “SARS-CoV-2 variants of concern and variants under investigation” dated June 25 may explain it (click here).
Pages 13 and 14 explain that of the over-50s attending A&E as a result of contracting the Delta variant between February and June this year, 3,546 were fully-vaccinated (having received both jabs); 976 were unvaccinated.
Almost every organ had high levels, almost. Almost total infestation. Almost like someone injected it!
Boosters push and more explained at bottom.
“The first-ever postmortem study of a patient vaccinated against COVID-19 has revealed that viral RNA was found in every organ of the patient’s body, meaning that the vaccine is either ineffective or the coronavirus actually spreads faster in vaccinated individuals.”
Both. But more Latter. And more fatal. I already covered the jabbed dead versus normal. Jabbed are literally more likely to die from it. MSM is hiding this and going on about symptoms. Dead people have reduced symptoms, can confirm.
“A previously symptomless 86-year-old man received the first dose of the BNT162b2 mRNA COVID-19 vaccine. He died 4 weeks later from acute renal and respiratory failure. Although he did not present with any COVID-19-specific symptoms, he tested positive for SARS-CoV-2 before he died. Spike protein (S1) antigen-binding showed significant levels for immunoglobulin (Ig) G, while nucleocapsid IgG/IgM was not elicited. Acute bronchopneumonia and tubular failure were assigned as the cause of death at autopsy;
however, we did not observe any characteristic morphological features of COVID-19.
Postmortem molecular mapping by real-time polymerase chain reaction revealed relevant SARS-CoV-2 cycle threshold values in all organs examined (oropharynx, olfactory mucosa, trachea, lungs, heart, kidney and cerebrum) except for the liver and olfactory bulb. These results might suggest that the first vaccination induces immunogenicity but not sterile immunity.”
So to save 86 year-olds, for like, six months, we need to damage all young adults and children? Fucking locusts. Are the Bad Boomers in power pushing this a Biblical plague? Maybe the jab itself is more Boomer Doomer than the wild virus.
It makes sense the liver would be clear because the liver’s function is clearing that shit but finding it in the heart? Goner. Dead man walking. Kidney? Suggests liver moved it there. Cerebrum? Yep, zombie.
Maybe the liver pushed it out of the liver, and back into the bloodstream, infecting the brain? Old people and some heavily disease-burdened (like STDs) have thin blood brain barrier.
The cerebrum or telencephalon is the largest part of the brain containing the cerebral cortex, as well as several subcortical structures, including the hippocampus, basal ganglia, and olfactory bulb. In the human brain, the cerebrum is the uppermost region of the central nervous system.Wikipedia
All we need is psychosis and they’re literal zombies. Maybe the psychotic break happens later, once it’s really stewed in the brain juices for a while. It’s written off as dementia in old people so may already be happening. Maybe they get a form of terminal agitation in addition. I do actually know my stuff. When it’s in the basal ganglia you are absolutely screwed. That’s motor control. It’s in the hippocampus possibly explaining the terminally stupid decision to get a second one. It’s damaging memory then, which suggests senility symptoms oncoming. I wonder if it’s more likely to kill small or large amygdala people faster. Likely smaller.
What is the overall effect of this death stick? Advanced cellular senescence? Meaning the average age of death would be those with least lifespan left, presently seen, but that will just keep getting younger and younger and younger. Logan’s Run modRNA mod? So a basic model we assume their remainder lifespan is cut in half. Does this help pension plans and national debt? Well assuming 80 is lifespan (slightly shorter in men, who are dying faster from this…) then a 60yo would die at 70, a 50yo would die at 65, a 40yo at 60, a 30yo at 55, a 25yo at ~50. a 20yo at <50, a 10yo at 45 a 5yo at 40 … etc. Down to school age.
Nobody would die before 35 except anomalies. Do we see this? Why try to deny those unless pattern?
Anomalous deaths would be acute advanced senescence. Intention may be largely chronic. They can blame global warming.
So, yes. That’s very neat. A lot of younger fertile people getting it would die around menopause/manopause. Hence, perfect economic efficiency is achieved. The aging (genetic void) population dies off as soon as reproduction is achieved. We’d need at least ten years to see if average lifespan has gone down (80 to 70). Assuming this simple model. Younger Boomers and Gen Xers are the ones to watch. A reversal of lifespan is unprecedented. This is the slowest kill model and explains the push until 2023*. We’ll begin to notice by then en masse. This is why new techs need a decade PLUS of human trials. They look at lifespan.
*MPs love the book Nudge. Has the NHS guaranteed treatment for genomic ‘vaccine’ damage? No. Nobody is talking about this. Experimental subjects are considered consenting adults, so may not be eligible for NHS treatment.
Add in a sterilising effect especially in men, STD transmission, and the guidestones would be about right.
If that basic of the most basic models is correct, then the kids currently injected will die shortly after their feckless parentals. Remember, saving the NHS also means fewer old people burdening it like lampreys. They could come out later and thank you for your willing participation, since you did technically save the NHS – by dying younger. Experiments are permitted to legally deceive you, so long as they debrief you. In 2023.
By accelerating aging population, that’s very eugenic technically but deeply wrong re family. Surplus of orphans. Pedo paradise. Adult IQ would be higher (and GDP shoot up) since the morons would’ve happily skipped along for the euthanasia, children in tow.
The average age is 80-something now because they have no remainder, so it becomes weeks, not years. It fits.
And there’s no known time limit on shedding those synthetic SPs, secondhand smoke-like. At a certain uptake, society may be fumigating itself. Birth rates already have tanked. We may need a leper colony. They could be lifelong biohazards. They could easily test their exhalation at different points post-experimental injections. PE majors have a tube you breathe into, they could easily do it. The fact they don’t means they know the result would make them hated. Could be like the Island 2005 film.
The basal ganglia are a group of subcortical nuclei, meaning groups of neurons that lie below the cerebral cortex. The basal ganglia is comprised of the striatum, which consists of the caudate nucleus and the putamen, the globus pallidus, the subthalamic nucleus, and the substantia nigra The basal ganglia are primarily associated with motor control, since motor disorders, such as Parkinson’s or Huntington’s diseases stem from dysfunction of neurons within the basal ganglia. For voluntary motor behavior, the basal ganglia are involved in the initiation or suppression of behavior and can regulate movement through modulating activity in the thalamus and cortex. In addition to motor control, the basal ganglia also communicate with non-motor regions of the cerebral cortex and play a role in other behaviors such as emotional and cognitive processing.
If it retarded them, I doubt any of us would notice.
An earlier coronavirus vaccine paper: why boosters and well, all of this really
Vaccines against infectious bronchitis of chickens (Gallus gallus domesticus) have arguably been the most successful, and certainly the most widely used, of vaccines for diseases caused by coronaviruses, the others being against bovine, canine, feline and porcine coronaviruses. Infectious bronchitis virus (IBV), together with the genetically related coronaviruses of turkey (Meleagris gallopovo) and ring-necked pheasant (Phasianus colchicus), is a group 3 coronavirus, severe acute respiratory syndrome (SARS) coronavirus being tentatively in group 4, the other known mammalian coronaviruses being in groups 1 and 2. IBV replicates not only in respiratory tissues (including the nose, trachea, lungs and airsacs, causing respiratory disease), but also in the kidney (associated with minor or major nephritis), oviduct, and in many parts of the alimentary tract–the oesophagus, proventriculus, duodenum, jejunum, bursa of Fabricius, caecal tonsils (near the distal end of the tract), rectum and cloaca (the common opening for release of eggs and faeces), usually without clinical effects. The virus can persist, being re-excreted at the onset of egg laying (4 to 5 months of age), believed to be a consequence of the stress of coming into lay. Genetic lines of chickens differ in the extent to which IBV causes mortality in chicks, and in respect of clearance of the virus after the acute phase. Live attenuated (by passage in chicken embryonated eggs) IBV strains were introduced as vaccines in the 1950s, followed a couple of decades later by inactivated vaccines for boosting protection in egg-laying birds. Live vaccines are usually applied to meat-type chickens at 1 day of age. In experimental situations this can result in sterile immunity when challenged by virulent homologous virus. Although 100% of chickens may be protected (against clinical signs and loss of ciliary activity in trachea), sometimes 10% of vaccinated chicks do not respond with a protective immune response. Protection is short lived, the start of the decline being apparent 9 weeks after vaccination with vaccines based on highly attenuated strains. IBV exists as scores of serotypes (defined by the neutralization test), cross-protection often being poor. Consequently, chickens may be re-vaccinated, with the same or another serotype, two or three weeks later. Single applications of inactivated virus has generally led to protection of <50% of chickens. Two applications have led to 90 to 100% protection in some reports, but remaining below 50% in others. In practice in the field, inactivated vaccines are used in laying birds that have previously been primed with two or three live attenuated virus vaccinations. This increases protection of the laying birds against egg production losses and induces a sustained level of serum antibody, which is passed to progeny. The large spike glycoprotein (S) comprises a carboxy-terminal S2 subunit (approximately 625 amino acid residues), which anchors S in the virus envelope, and an amino-terminal S1 subunit (approximately 520 residues), believed to largely form the distal bulbous part of S. The S1 subunit (purified from IBV virus, expressed using baculovirus or expressed in birds from a fowlpoxvirus vector) induced virus neutralizing antibody. Although protective immune responses were induced, multiple inoculations were required and the percentage of protected chickens was too low (<50%) for commercial application. Remarkably, expression of S1 in birds using a non-pathogenic fowl adenovirus vector induced protection in 90% and 100% of chickens in two experiments. Differences of as little as 5% between the S1 sequences can result in poor cross-protection. Differences in S1 of 2 to 3% (10 to 15 amino acids) can change serotype, suggesting that a small number of epitopes are immunodominant with respect to neutralizing antibody. Initial studies of the role of the IBV nucleocapsid protein (N) in immunity suggested that immunization with bacterially expressed N, while not inducing protection directly, improved the induction of protection by a subsequent inoculation with inactivated IBV. In another study, two intramuscular immunizations of a plasmid expressing N induced protective immunity. The basis of immunity to IBV is not well understood.
Serum antibody levels do not correlate with protection, although local antibody is believed to play a role.
Adoptive transfer of IBV-infection-induced alphabeta T cells bearing CD8 antigen protected chicks from challenge infection. In conclusion, live attenuated IBV vaccines induce good, although short–lived, protection against homologous challenge, although a minority of individuals may respond poorly. Inactivated IBV vaccines are insufficiently efficacious when applied only once and in the absence of priming by live vaccine. Two applications of inactivated IBV are much more efficacious, although this is not a commercially viable proposition in the poultry industry.
However, the cost and logistics of multiple application of a SARS inactivated vaccine would be more acceptable for the protection of human populations, especially if limited to targeted groups (e.g. health care workers and high-risk contacts). Application of a SARS vaccine is perhaps best limited to a minimal number of targeted individuals who can be monitored, as some vaccinated persons might, if infected by SARS coronavirus, become asymptomatic excretors of virus, thereby posing a risk to non-vaccinated people.
Looking further into the future, the high efficacy of the fowl adenovirus vector expressing the IBV S1 subunit provides optimism for a live SARS vaccine, if that were deemed to be necessary, with the possibility of including the N protein gene.
“We have documented the pharmacokinetics and biodistribution of lipidots, synthetic 55-nm-diameter lipid nanoemulsions with potential applications for diagnostics and drug delivery. After intravenous injection in healthy mice, lipidots are stable in blood and taken up preferentially in liver, adrenals, and ovaries, where they release their lipidic cargo. Lipidots depict an original biodistribution, not previously reported for other inorganic or organic nanoparticles, toward organs involved in steroid hormone synthesis and storage (adrenals and ovaries) and localize to precise sites in these organs, suggesting potential applications for imaging and drug delivery.”
A friend suggested the Pfizer one may be ‘safe’ because rich areas are buying it. That was Boomers avoiding the heart effects reported from AZ, possibly to push them to the others, none of them are safe. Potassium is also used in lethal injections, to stop the heart. It’s in Pfizer. Talk about red herring. Watch deaths from heart disease in, say, the next three years.
In this country, they don’t give you even the illusion of choice, it’s largely based on age and supposed availability. There is no safe one.
The lipids preferentially allow the modRNA to ‘slip into the cell’ of those organs, as the enclosed PDF plainly states.
nb The effects described in Malice or Mistake? in the brain are prion–like, they needn’t be actual prions.
Given the potential for adverse effects, potentially fatal ones, it is completely inappropriate and unacceptable that EMA permits these products, which hold only emergency use authorisations, to be administered to younger (<60y) people who are healthy, as they are at unmeasurable risks from SARS-CoV-2.
Of equal importance, you are bound by duty to investigate whether reasons exist for the waves of deaths that have occurred following “vaccination” of elderly residents in care and senior homes. Or are you asserting that dangers of “vaccine”-derived thrombotic events are limited to younger individuals? If not, restricting their use solely in one age group — as decided upon in Germany — equates with nothing less than monstrous, condoned genocide of the other.
In closing, failure to inform “vaccine” recipients of the risks and negligible benefits outlined here represents serious violations of medical ethics and citizens’ medical rights. Those violations are especially grave as all the risks we describe can be expected to increase with each re-vaccination, and each intervening coronavirus exposure. This renders both repeated vaccination and common coronaviruses dangerous to young and healthy age groups, for whom — in the absence of “vaccination” — COVID-19 poses no substantive risk.
Misleading populations into accepting investigational agents such as the gene-based COVID-19 “vaccines”, or coercing them through “vaccine passports”, constitutes clear and egregious violations of the Nuremberg Code. The Nuremberg Code mandates voluntary informed consent “without the intervention of any element of force, fraud, deceit [or] duress”. https://history.nih.gov/display/history/Nuremberg+Code
Might post-injection distribution of CoViD vaccines to the brain explain the rare fatal events of cerebral venous sinus thrombosis (CVST)?
The pharmacovigilance data confirmed the CVST incidences with all genetic vaccines (viral or non-viral vector), however, the regulatory authorities in their recent investigations reported that the CVST was unusually accompanied with thrombocytopenia in subjects injected with CoViD-19 viral vector vaccines (such as AstraZeneca and J&J/Janssen) than those injected with mRNA vaccines. We, therefore, looked at the preclinical studies of these vaccines to ascertain their biodistribution to body tissues (for instance brain) beyond the injection site for a possible explanation of the rare fatal clots formed in the brain. The biodistribution of ChaAdOx1 in mice confirmed the delivery of vaccine into the brain tissues.
The vaccine may therefore spur the brain cells to produce CoViD spike proteins that may lead to an immune response against brain cells, or it may spark a spike protein-induced thrombosis.
This may explain the peculiar incidences of the fatal CVST observed with viral vector-based CoViD-19 vaccines. It is anticipated that other vaccines using similar technology such as AstraZeneca/Oxford (Chimp adenoviral vector), J&J/Janssen (Human adenoviral vector 26), CanSinoBio (Human adenoviral vector 5), and Sputnik V (Human adenoviral vectors 26 and 5), may also lead to the same safety concerns.
Gene therapies, putting the mental in experimental.
All the talk of antibodies is void, as, the ex-Pfizer guy pointed out, antibodies are null and void to the question, and killer cells work on viruses biologically. Those aren’t in the blood. Your body has to make them organically. So the vaccine doesn’t work…. on them. Begging the question, does it work? Well…. people who’ve had it have still got it, so no. Empirically speaking no, it doesn’t work. There wouldn’t be a high rate of people with at least one dose in hospital or morgue if it did. Why don’t we see the morgue figures, actually? We all know why. Shouldn’t a pandemic also tell us morgue admissions?
Damage to FSH and LH could make someone permanently infertile including women. Those are key for supporting a pregnancy. Infertility in women can be indicated. Children of Men is set in England….
The characteristic sloughing of the endometrium caused by fucking with hCG levels is called a decidual cast. It’s the reason some women (not all) with endometriosis can miscarry so often. They’ve weaponised it.
h/t Anonymous Conservative for gene therapy (convid) link, where I still comment sometimes to clarify, despite obstacles in my personal life preventing me from posting much here for personal safety.
“After reading hundreds of testimonies, the Instagram user learned many women experienced desidual casts, the lining of the uterus falling out. A quick Google search of the term showed a spike in search results in January 2021, when the Covid-19 vaccines were being introduced.”
Endometriosis is a regenerative medical issue which involves the appearance of endometrial tissue outside the uterine cavity, causing pelvic discomfort to be felt by the patient and in some cases, infertility. It has been discovered that the progesterone treatment used for endometriosis oftentimes leads to the formation of a decidual cast.
One of the most common contraceptives, forced on minors in the UK. They’re even telling virgins they ‘need’ it ‘just in case’, I had personal experience of shutting down those lies as a teen. I’m not taking shit with side effects and no longitudinal studies on fertility because my doctor assumes I’ll magically turn into a whore. That’s just insulting. Their only excuse after that was ‘period pains’ ….yes they were STILL trying to push it….. I was like…. I’ll stick to Ibuprofen, thanks? Progesterone causes PMT so if you’re wondering why so many modern women are bitchy….. it’s the progesterone only pill. I’ve had to drop friends after they started taking it. They became raging banshees. They suddenly hated men too. Pretty sure most SJWs are on it. Men on xenoestrogens exhibit PMT like symptoms, also those on steroids. So it isn’t just women being poisoned.
So HCG issues + progesterone = …….
Without endometriosis, it still occurs
The use of consolidated oral preventative pills may prompt the formation of decidual casts. There have been cases of dysfunctional uterine draining where the patient was prescribed a monophasic oral preventative, and an extensive decidual cast was discovered amid the treatment regimen. The same will happen in cases of treating oral pills for an adolescent menorrhagia. Medroxyprogesterone acetic acid derivation (DMPA) is an injectable type of prophylactic which has been demonstrated to cause the development and conveyance of decidual casts as well.
Things the men commenting on this wouldn’t know. Use it wisely.
1995 evidence of precedent for deceptive vector of transmission, official contamination reportage and hence, UN contravention of genocide law established in the 1940s, section (d) and (c):
“PIP: A priest, president of Human Life International (HLI) based in Maryland, has asked Congress to investigate reports of women in some developing countries unknowingly receiving a tetanus vaccine laced with the anti-fertility drug human chorionic gonadotropin (hCG). If it is true, he wants Congress to publicly condemn the mass vaccinations and to cut off funding to UN agencies and other involved organizations. The natural hormone hCG is needed to maintain pregnancy. The hormone would produce antibodies against hCG to prevent pregnancy. In the fall of 1994, the Pro Life Committee of Mexico was suspicious of the protocols for the tetanus toxoid campaign because they excludedallmalesandchildren and called for multipleinjections of the vaccine in onlywomenofreproductiveage. Yet, one injection provides protection for at least 10 years. The Committee had vials of the tetanus vaccine analyzed for hCG. It informed HLI about the tetanus toxoid vaccine. HLI then told its World Council members and HLI affiliates in more than 60 countries. Similar tetanus vaccines laced with hCG have been uncovered in the Philippines and in Nicaragua. In addition to the World Health Organization (WHO), other organizations involved in the development of an anti-fertility vaccine using hCG include the UNPopulationFund, the UN Development Programme, the World Bank, the PopulationCouncil, the RockefellerFoundation, the US National Institute of Child Health and Human Development, the All India Institute of Medical Sciences, and Uppsala, Helsinki, and Ohio State universities. The priest objects that, if indeed the purpose of the mass vaccinations is to prevent pregnancies, women are uninformed, unsuspecting, and unconsenting victims.”
“Vaccines are under development for the control of fertility in males and females. This review discusses developments in anti-fertility vaccines at the National Institute of Immunology, New Delhi, India. A single injection procedure for the sterilization or castration of male animals depending on the site at which the injection is given, has passed through fieldtesting and is expected to be on the market in the nearfuture. Vaccines inducing antibodiesagainstthehuman chorionic gonadotropin have gone through phase I trials with satisfactoryresults. A vaccine producing a consistentlybioeffectiveantibody response against gonadotropin-releasing hormone is ready for phase I/II clinical trials in patients of carcinoma of prostate after due experimentation in animals and toxicology studies. Research to identify sperm antigens for incorporation into second generation vaccines is in progress.”
Control, like farm animals. Single injection for castration of male animals possible.
Look forward to the “drop of testosterone levels”. At least you got to drink some bitch tits beer with the ‘boys’. Don’t come crying to me. You wanted to be ‘male animals’.
I iz TRYING to halp youz. So your dick doesn’t drop off.
“The vaccinations are expected to produce antibodies against spike proteins of SARS-CoV-2. However, spike proteins also contain syncytin-homologous proteins, which are essential for the formation of the placenta in mammals such as humans. It must be absolutely ruled out that a vaccine against SARS-CoV-2 could trigger an immune reaction against syncytin-1, as otherwise infertility of indefinite duration could result in vaccinated women.”
And castration in the men? Why aren’t men studied for this?….
comment “But we all on here already figured this out.
Here is the deal with vaccines and I will spell it out so you all understand.
1.) The method is using the mrna form of vaccine and TBH you cannot test it on an animal because you are changing the DNA of an individual. SO THERE IS NO REASONABLE WAY TO TEST THIS BUT ON HUMANS.
2.) The combinations are endless to what they can do with this so you use a strict batch control process and that is being recorded because that way you can carry out multiple tests on a compliant population with indemnity from being sued. SO YOU ONE SET MAY DEVELOP EXTRA ARMS AND ANOTHER THERE BALLS MAY DROP OFF.
3.) The prize is to record all the good effect batches ignoring the negative ones so enhanced fighting of cancer etc. or maybe even living longer, stonger joints etc. Now you have the recipe for a better outcome for elites who inject themselves.
We are no more than a f%^king lab rats for these people who will profit from people suffering.
That people is what they are up to under the cloak of curing the virus and the great reset. Who would not want to live with good health forever the hard part is the process needs live human experiments to sort the wheat from the chaff. This will help those elites living on this planet after agenda 2030 is completed.
Well that is what this is looking like to me … remove the indemnity protection … you want lab rats you pay for them in full and the cost would be astronomical because of all the combinations. Get it?””
We live under socialism, since the gov won’t let you sue their corporations.
comment “The people who freak out about eating genetically modified foods are the same ones who can’t wait to get an injection that will genetically modify their own immune system.” whole body actually no longer human, rna will re-code whole body over time so short term studies won’t catch it mark of the beast, later to cause boiling flesh type pain predicted in Rev
assuming it’s a thing
as the body tears itself apart
“The next purpose it has is to keep us blind from noticing when the second agenda arrives. The second agenda is when we encounter the mark of the beast.
The first agenda, although still in plain sight, has already been defeated by the second agenda. But to fully understand how events will play out, we need to look at how the first agenda accomplished dominion over the people of world.” read it in link above
“The real mark will be based upon Biblical truth and actual historical events leading up to a worldwide quantum currency reset.
People usually conjure up fantastical ideas that one day, the entire world is going to turn upside down and everyone will immediately know that the end is here. That’s exactly what the enemy wants us to believe.”
changing guards, same boss
“The mark of the beast will be freely chosen by each individual, not forced upon them.”
of any item, smartphones would be my bet
it’s an interesting read
“It’s been documented that in 1729, Saint Germain was working on the establishment and funding of a new world monetary trust. The Saint Germain world trust now contains the majority of the wealth that will be distributed to the world once the new financial reset takes place.
Today, Saint Germain’s world trust prosperity program is known as NESARA and GESARA.
NESARA stands for National Economic Security and Reformation Act. It applies only to the United States.
While GESARA, the Global Economic Security and Reformation Act, applies to the rest of the world.
For centuries, elite families who “follow the light” (or the agenda of the second beast, the beast of the land) have been contributing to this world trust. Saint Germain specifically stated that the money in his world trust would be used in the future for prosperity and humanitarian purposes.
Now, after over 250 years of contributions by the rich and elite followers-of-light, and compounding interest, Saint Germain’s world trust is over one Quattuordecillion dollars. That is a one with 45 zeros behind it.”
missing money went where?
enough for now
can’t say too much
ZH comment “All they have to do is get the women to take it and the population is sterilized. Perfect genocide.” Well they forced HPV onto minors….
comment “He is suggesting that we will get a 1918 type impact when everyone is vaccinated. The virus does not go away and the young and healthy start dropping dead..” Like I’ve said before, Spanish Flu was vaccine-led in death count, all the work-vaccinated dropped dead but less of the old. So the ‘weak immune’ hypothesis is evidently false.