Covid vaccines are not effective, they give you AIDS and make you infertile

Here's data from the England health report titled "SARS-CoV-2 variants of concern and variants under investigation in England" - Technical briefing 23- Published on 17 September 2021.This briefing provides an update on previous briefings up to 3 September 2021

Source: assets.publishing.service.gov.uk...

From the article above:

"Deaths within 28 days of positive specimen date"
"All cases: 2,542"
"Dose 1 deaths within 28 days: 149
"Dose 2 deaths within 28 days: 1,613
"Unvaccinated deaths within 28 days: 722"

Considering there are so many jabbed persons now in developed countries, going by your own metrics there ought to be a greater and significant representation of jabbed "unvaccinated" persons vs unjabbed "unvaccinated" persons, if 70-95% of the population in most developed countries received at least one jab by now, which means that the representation of "unvaccinated persons" may be conflated up to 20 times greater than the number actually is.

This would very likely be apparent in statistics of "unvaccinated persons" risk of mortality and morbidity to covid, if the statistics of "unvaccinated" persons only measured persons who have never received a covid injection - and not conflating that data with persons who received a covid injection less than 14 days before subsequent infection with covid.

There are multiple sources of information confirming this, here's one from the CDC itself.

"Persons were considered fully vaccinated ≥14 days after receipt of the second dose in a 2-dose series (Pfizer-BioNTech or Moderna COVID-19 vaccines) or after 1 dose of the single-dose Janssen (Johnson & Johnson) COVID-19 vaccine; partially vaccinated ≥14 days after receipt of the first dose and less than 14 days after the second dose in a 2-dose series; and unvaccinated less than 14 days receipt of the first dose of a 2-dose series or 1 dose of the single-dose vaccine or if no vaccination registry data were available."
† *Among residents of Los Angeles County; excludes Pasadena and Long Beach*

If the vaccine was effective, then you would expect to see way less hospitalisations from vaccinated persons. Full stop, no matter how you try to spin it. It doesn't. Meta-analysis on peer reviewed studies (which is the strongest clinical grade of evidence available) have shown both quercetin and ivermectin to be 70-80% effective at reducing hospitalisations and deaths. Compared to your vax which is 50% effective at best, -50% to -300% effective at worst? I'm not talking about monotherapy studies, but studies where patients take quercetin and ivermectin with zinc (no point taking a zinc carrier without any zinc supplementation if you're deficient in zinc, or during very late stages of the disease the outcomes of patient treatment will obviously be poorer.)

The data shows that people who were vaccinated earlier have a greater risk of developing serious symptoms in later infections. That sounds awfully a lot like Antibody Dependent Enhancement (ADE) to me.


Currently the Pfizer is less than 39% effective due to mutations. From 95% effective down to 39% effective due to mutations within a year:


Here's an interesting video showing lab antibody tests after the first and second jabs. Not someones opinion, this is measurable evidence and data extrapolated from serology lab results, from objective scientific t-cell count tests. This was just a single patient though, so it would be nice if doctors were routinely doing these lab tests. If similar effects are happening to many vaxxed people, then this is a nightmare scenario.

To summarize, he began by showing the patient's pre-jab labs which were normal:

- After the first jab, CD8 cells came back high (lymphocytes). These are the killer T cells.

- After the second jab...

• Granulocytes were high meaning the patient's immune system was responding to tissue damage.

• Lymphocytes (including CD8 and Natural Killer) cells were low -- leaving the patient vulnerable to 'breakthrough' infections.

• CD3-/CD56+CD16+(Natural Killer) cells were low -- they are first responders to viral infections and cancer cells.

All other immune lab scores came back on the lower end of normal, too, after the second jab.

IOW, the patient's adaptive immune system "tanked." This doctor said the patient's lab results point to an auto-immune disorder they did not have prior to the jabs. Why the # would you take this? It's destroying your immune system:A deficiency in an autoimmune response, or a reduced auto-immune response, is an auto-immune deficiency syndrome, otherwise known as AIDS.

"But the vaccine also makes people less transmissible?“

That’s what some studies claimed, yes.

But at what point in time did they measure this effect?

The jabs initially trigger your immune system.

But what if the effect fades and you walk around bar any mucosal protection?

Here's proof that the effects do fade over time. Very strong correlations in data and academic journal articles

Strong data correlation between increased covid cases and vaccination between various countries (comparing infections per million persons per capita to doses per million persons per capita):

Strong data correlation between waning protection of the vaccine and it only offering short lived protection: (Note the parabolic rise in cases post 51% of population vaccinated in Cypress from the start to the end of June 2021)

Risk of myocarditis from covid jabs is 20 to 120 times higher than that which was expected according to the CDC's and Pfizer's own internal documents
(Does the CDC's and Pfizer's own internal documents count as misinformation too?). That's a very high risk profile, and a very bad risk to benefit ratio. Compared to the side effects of HCQ or Ivermectin which have been around for decades, are extremely well studied in terms of known safety, dosage profiles and side effects (compared to no studies on the the long term effects of the jabs and no active placebo/control groups), and both HCQ and Ivermectin are mass prescribed drugs with some of the safest drug profiles of currently prescribed drugs today.

Conclusive proof from peer-reviewed academic journal articles that vaccination is irrefutably linked to reduced Th1 antibody responses in infants, children and adults, and poorer outcomes to all infections vs. unvaccinated persons. (If you care about everyone's health, then you ought to do your due dilligence to read at least this link and read the academic journal articles cited in the post, and you should share it to everyone whom you know and care about):

I encourage everybody to read and share the post in the above link as well as the peer-reviewed academic journal articles which are cited in the above link. The information cited in the above link is entirely based on peer reviewed academic journal literature. Many scientists have no other choice but to post this information on 4chan because it doesn't actively censor information and scientists reputation and livelihood is at risk by speaking out? Many scientists have openly come out and said this. The disclaimer on 4chans website is on there purely for liability reasons, if anyone seeks to discredit the information on the basis of where it is posted (whilst having complete disregard to the actual substance of the post)

One may argue that there being a greater amount of vaccinated hospitalised persons compared to unvaccinated means that the vaccines are unsafe, only in circumstances where the pool of subjects is equal on both sides of the divide (or if the vaccine were 100% effective). Otherwise there will always be a breakeven point once the number of vaccinated people exceeds that of unvaccinated. . The effectiveness of the vaccine was supposedly 90% effective at reducing hospitalizations caused by the initial variant. There's the unknowns of how many people from each group are at what level of risk, what age, etc etc.

Pro jab shills will selectively cherrypick parts of my argument to address, either because of cognitive dissonance or because they're paid, and they will stonewall and not give any response the contentious issues that they have no good reply to, such as the reduced t-cell counts observable in serology tests, which are not disputable, not based in opinion and they are objective measures of health. The serology and antibody lab tests are objective measures of evidence, not opinion based, and they conclusively prove immune system deficiencies post vaccination.

Pro jab shills will fail to address the fact "unvaccinated" individuals in covid statistics contain a large representation of persons who have received covid injections, which immediately invalidates all the assertions you made because the data you based those assertions is based on "unvaccinated" risk, when the "unvaccinated" demographic of persons are conflated with persons who received a jab but were then infected 2 weeks before the jab had time to take full effect.

Shills are pro vaccinating kids when theres neurological issues and birth defects and miscarriages linked to vaccination? When kids have the least likely chance to have poor outcomes of the disease (0.005% or less?) and theres no long term data on their safety? Look how long it took for asbestos related diseases caused by asbestos exposure over 30 years in the past to be analysed and understood, over 30 years. They think giving kids AIDS or a 1 in 300 risk of myocarditis in young boys is worth the risk? for a virus that has a 0.005% chance of death? Source: www.gov.uk...-1 -vaccine-analysis-print

My daughter had covid with symptoms of the flu and nothing else, she was perfectly fine. My grandmother who is nearly 90 years old had it and she survived, so did my aunt contract covid and survive who is a type 2 diabetic and she is bordering obese. They ate well, had sunlight, took vitamin D, Zinc, vitamin C and Quercetin. They also didn't go to a hospital and get ventilated and killed from ventillation tearing their inflammed lungs and preventing them from coughing up phlegm and exosomes which need to come out of the body and lungs, due to an invasive ventilation tube being crammed and obstructing the asophagus, leading to suffocation. So I've lived with it and dealt with it, i'm not just talking out of my asshole.

One has to ask these questions - why do all the spike protein based (incomplete virus) covid jabs contain adjuvants when the spike protein itself is cytotoxic? Since the spike protein is cytotoxic theres no need to introduce adjuvants to cause inflammation to induce an immune system response, a cytotoxic agent would cause inflammation on its own without the use of adjuvants, which is why adjuvants are used in classical inactivated virus vaccines (because inactivated viruses do not elicit an immune response or inflammation on their own).

The fact graphene oxide adjuvants are used in both the gene-therapy (moderna, pfizer) and adenovirus vector (jj) injections which contains a live activated virus, when the spike protein is cytotoxic, proves the adjuvants are unneccessary and are added to poison us. The clinical trials on Pfizer vaccine compared the jabs containing virus with adjuvants to shots with just adjuvants (graphene oxide). So of course results would look similar in terms of risk profiles when both groups are being poisoned. If the placebo group was honestly conducted, they would have been injected with saline, not shots with just adjuvants. Beyond the fact adjuvants in a live virus vaccine are unneccessary.

Comparing the safety of the Pfizer jab by comparing persons who received a poison shot (graphene oxide) with spike protein (extra poison), to persons who received a poison shot (graphene oxide) without spike protein, is not a good nor a genuine or trustworthy way to conduct a risk assessment on an experimental drug. No other vaccines have ever been approved targeting only half the virus.

Giving your body knowledge of just the spike protein, and not the whole virus, can lead to your body creating an antibody response and map to deal with half the virus, which results in your body being unable to get rid of the actual virus in subsequent infection (since it doesn't know how to deal with the other half of the virus, but your body thinks its seen the virus before so it deploys the vaccine induced antibodies which are suboptimal, instead of your broad spectrum Th1 antibodies which indiscriminately # everything up and memory B cell antibodies which create a new antibody map to a new antigen which the body thinks it has not seen before.

It's the worst outcome of original antigenic sin, and vaccines are supposed to be designed to give you the best outcome of original antigenic sin by giving you the whole completed map to a virus (in classic inactivated complete virus vaccines) - but out of all of the covid vaccines (all the approved ones in western countries) - none contain a complete inactivated virus.

Spike protein based incomplete virus covid 19 injections give your body half the map required to produce antibodies, resulting in suboptimal antibodies which cannot handle strains of the real virus (spike protein injection induced antibodies are just designed to eliminate the spike protein, not the whole virus) which is definitely going to cause your immune response to be suboptimal when you become infected with a live mutated variant - priming your body with the worst outcome possible having regard to original antigenic sin - a person naive to the antigen who has never been infected with a corona virus would likely fare better than someone who has been vaccinated with half the map to create antibodies as you get in the spike protein vector injections, and a person who has been injected with an inactivated complete virus or naturally infected would likely fare better than persons naive to the antigen and those injected with spike protein based injections who can only produce suboptimal antibodies.

So not all vaccines are the same and sinopharm/sinovac is definitely not the same animal that the mRNA vaccines are, in terms of the likelihood of ADE. (inactivated virus vaccines are less likely to cause ADE events since they give your body a correct complete map to create antibodies from the whole antigen rather than just a part of it, even though they are still just as leaky and there is still some risk of ADE from leaky vaccines due to the highly mutable nature of coronaviruses - which is why they were targeted for gain of function research and AIDS proteins were attached onto the corona virus, because corona viruses are highly mutable owing to their recombinant nature (Corona viruses like to attach onto anything that has DNA or RNA)

Since the c19 spike protein which is the viral target for the mRNA and adenovirus vector injections, not the whole covid19 corona virus but just a part of it, being injected with a spike protein based injection rather than a whole complete inactivated virus (sinopharm/sinovac) potentially increases the risk of Transfection causing the corona virus mRNA to overwrite parts of your DNA compared to a whole inactivated coronavirus (which still carries a risk of transfection due to the recombinant nature of corona viruses.)The kicker is that naturally produced mRNA, produced by the body and by viruses through cell hijacking, ordinarilly never leave the cell nucleus, so the virus never has a chance to have the mRNA leave the nucleus and enter the bloodstream to alter your DNA when you're infected naturally. When you inject mRNA and coronaviruses into the bloodstream, the chance of transfection actually increases exponentially.Source: www.thermofisher.com...

Leaky vaccines (those which dont prevent transmission) allow mutated strains to escape and infect others too, and mutation is far more likely in a jabbed person since the virus is put under extra evolutionary pressure to mutate into something more virluent to infect a vaccinated and protected host.

The link to infertility

Syncytin-1 is a hormone which is naturally produced by the body, and is responsible for the formation of placenta.

Covid-19 S1 spike protein is a homologue to Syncytin-1, which means that it looks practically the same to the body.

By introducing a cytotoxic spike protein which looks incredibly similar to a hormone responsible to the formation of human placenta, the consequence is that when the body forms antibodies to the covid 19 S1 spike protein antigen, during menstural cycles and pregnancy the production of syncytin-1 will also trigger the same S1 spike protein antibody response from the body, and those S1 spike protein antibodies will interfere with and destroy the naturally produced syncyctin-1, which leads to the early miscarriage of pregnancies, menstural cycles coming far earlier than they should, and infertility through your body being trained to attack placenta owing to the similarity to syncytin-1 and the covid-19 spike protein.

Yes, you read that right. The covid 19 injections train the body to reject and destroy the hormone responsible for the formation of human placenta, leading to permanent infertility, miscarriages, and early and disregulated menstural cycles.

"To summarize, it looks as though pregnant women who are getting the COVID-19 vaccine are at increased risk not only for miscarriage but also for future infertility and having an autistic child. So, please, be careful out there and spread the word.
The best way to treat any disease is to prevent it. These vaccines simply are not decreasing COVID-19 but radically decreasing the health of those who receive it, especially pregnant women that the CDC merely a month ago encouraged to get vaccinated without a shred of safety evidence."
Source for above: www.lewrockwell.com... 5/joseph-mercola/the-many-ways-in-which-covid-vaccines-may-harm-your-health/

Funny title. But yeah it's probably true. Dont you need HIV retrovirus to call it AIDS?
I'd call it immune deficiency

South Park sang it best with “every one got AIDS”

So your saying you can get aids without HIV?

A reply to: PapagiorgioCZ

Immune deficiency is a sequella of HIV.

A deficiency or reduced capacity to have an auto-immune response is an auto-immune deficiency, otherwise known as an auto-immune deficiency syndrome, or AIDS. So no, you don't need to contract HIV in order to develop an AIDS, although Covid-19 was made by recombining a corona virus with HIV protein in order to increase or gain the function of the HIV virus.

Corona virus was chosen for gain of function research (increasing the functions an infectious agent has) due to its highly mutable nature, owing to its recombinant nature of wanting to recombine with everything. That makes it highly mutable and that makes the prospects of making a non-leaky vaccine for corona virus extremely low.

In saying that, ordinarily a person would have to contract HIV and another virus before HIV develops into AIDS, but Covid-19 is an airborne, transmissable coronavirus which was recombined with HIV proteins and xenotropic murine leukemia virus-related virus, which can cause ME-CFS and can lead to AIDS if infected with HIV.

Since Covid-19 and the Covid-19 vaccines both have HIV protein and XMLV protein, then AIDS developing as a morbidity and sequella to Covid-19 infection post-recovery is definitely a possibility. It's known as "long-haul covid" though, not AIDS. But what "long-haul covid" actually is is a reduced immune system, an immune system deficiency (AIDS), which causes latent viruses which were once suppressed by your immune system to reactivate once Covid-19 destroys the protective wall that is your immune system permanently. Jabbed persons will not fare well in the coming flu seasons.

"SARS-CoV-2 Spike Protein Engineered With HIV

According to Mikovits, there’s evidence showing the SARS-CoV-2 spike protein was engineered by integrating HIV and XMRV proteins. XMRV stands for xenotropic murine leukemia virus-related virus, a human retrovirus that is very similar to endogenous retroviruses also found in other mammals.

XMRV has been linked to ME-CFS. HIV, which can cause AIDS, is another human retrovirus (although as mentioned earlier, HIV does not appear to trigger AIDS all by itself. It needs a coinfection.)

“Our endogenous gammaretrovirus is called human endogenous retrovirus-W (HERV-W). HERVW is all the way back in genesis in our original endogenous genome. It’s a gammaretrovirus that expresses only the envelope, because in retroviruses, the envelope alone is enough to cause the disease. That envelope protein is called syncytin. They’re [now] calling it ‘spike protein’ just to throw us all off,” Mikovits says.

According to Mikovits, the SARS-CoV-2 virus was created by introducing a mutation into a molecular clone. Vero E6 monkey tissues are known to be infected with SIV and other gammaretroviruses, and the SARS-CoV-2 virus has markers suggesting it was grown in a Vero E6 cell line, she says.

“So syncytin is the gammaretrovirus; it cross-reacts with the mouse and monkey gammaretroviruses. Monkeys, mice all have syncytin. Endogenous viruses express, especially during hormonal cycles. When it’s expressed in the wrong place, like in the brain or the spinal cord, it’s long been associated with the inflammatory disease and the destruction of the myelin sheet in multiple sclerosis (MS).

So, syncytin expressed it in the wrong place gives you the paralytics diseases. We know Parkinson’s is associated with Type I interferon responses. We’re now starting to appreciate that there is low-level expression of our endogenous virome all the time, and that in our innate immune response it’s trying to shape and educate our Type I interferon pathways …

The final and biggest problem is these exosomes, because your body’s exosomes are like your cells’ response to express its regulatory RNAs, small inhibitory RNAs, long-chain non-coding RNA — which Ritchie Shoemaker has long associated with chronic Lyme and ME/CFS — and the TGF-beta I pathway.

TGF-beta I, that’s the master switch to turn on which Type I interferon, which [is needed for] myelopoiesis. But these exosomes are packaging not only RNA that you’re making, but now you’ve dysregulated the methylation so you’ve woken up your endogenous virome, and then syncytin is going to be expressed.”"
Source for above: www.lewrockwell.com...


Here's some more Doctor's speaking out about reduced killer (CD8) T-cell counts post vaccine.

‘What we’re seeing post vaccine is a drop in your killer T cells, your CD8 cells. And what do CD8 cells do? They keep all other viruses in check.’

Also check out Dr. Cole's presentation from the White Coat summit on Vaccines

More evidence on the link to disrupted menstural cycles post vaccination - "COVID-19 vaccine's impact on menstrual cycles needs to be investigated after 30,000 women report changes, says top scientist"

a reply to: natoshis

Well this is interesting, it’s going to take awhile to read everything. Thx for posting


Aha I see you added the song,

a reply to: natoshis

Maybe dumb question but does that also mean kung flu can cause aids?

a reply to: Chalcedony

It's not a dumb question at all.

I know that mRNA from a naturally infected virus has far less chance of causing neurodegenerative diseases and CJD and Alzheimers, since the mRNA cannot cross the blood brain barrier or enter the bloodstream in a natural infection.

I think that being exposed to vaccinated persons shedding spike protein, can prime your immune system to make suboptimal antibodies for just the spike protein which will definitely make you fare off far worse than the virus itself.

It's possible that the spike protein jabs only contain HIV protein, and not the XMLV protein. It's possible that people who have been injected with the spike protein jabs will have HIV in their bloodstream, but that they won't develop AIDS unless they contract covid naturally which also has the XMLV protein which causes the total degradation of the immune system.

If that's the case, then being infected with corona virus naturally may cause a naturally infected person to potentially develop AIDS or "long haul covid" as a morbidity post-recovery, and the fact people who have recovered from covid who have long haul covid are susceptible to latent viruses may very well be because their immune system is gone.
The best chance for keeping your immune system is probably staying away from vaccinated persons, and propylactically treating covid and treating covid as early as possible with zinc, zinc carriers, vitamin C intravenously or high doses of liposomal vitamin C, high doses of vitamin D (8000-10,000 IU daily if sick), an antibiotic if in the progressed stages of the condition to prevent bacterial pneumonia, iron chelates/lactoferretin and curcumin to expell iron from the body caused by spike protein cleaving off the HEMA iron from haemoglobin in the blood, and anti thrombotics such as asprin to prevent strokes when infected, and definitely no ventilation in hospital as the invasive ventilation obstructs your asophagus preventing you from expelling exosomes and phlegm which needs to be expelled when you're sick with covid and it progresses to the bacterial pneumonia stage

The sooner you can kick covid in the butt with good treatment, the less of your immune system it will destroy, even if it destroys some of it. If you are exposed to vaccinated persons, then the shedding of spike protein will prime your immune system with suboptimal antibodies which cannot get rid of the spike protein antigens, leading to immortalised cell monocytes and the death of the immune system when the body starts to produce tyrosine phosphatase PTPN22 (which it does when it cannot expel a foreign infected and immortalised cell monocyte which should normally die within 2 weeks)

I agree with part of the title.

An acquired immune deficiency, can be acquired from things other then HIV. I have also heard it said numerous times it does have a portion of the HIV virus genetic material coded into it as well. Just a small section.

As for the part about effectiveness.... They are working as designed...

a reply to: natoshis

So basically the pharma industry has performed the scam of the millennium.They have legislated that you must have a shot that will cause you to require their meds for the rest of your life.

a reply to: natoshis

So, less than are dying of covid? Shocking. But now those numbers are significant because they feed your narrative? Tell us more...

How the immortalisation of cell monocytes causes the production of auto-immune hormone tyrosine phosphatase PTPN22 which causes the immune system to shut down when it cannot destroy foreign antigens and infected monocytes become immortalises (see picture below)

ibb.co...

Source for below: archive.4plebs.org...

"Prometheus project initiative(PPI) is 2 days into its partially declassified state and is entering:
>The Qualified Subjects Warning Phase.
This is to issue a warning and inform all Subjects who Qualified to continue their existence past the year 2030.
>QRD on Prometheus project:
>In ~1920 a 100 year long project was initiated with the intent of reducing the world population by 95%, completed by the year 2030.
>Considering all projected threats emerging by the year 2030 it was paramount to filter the population and separate the compromised and mentally unstable subjects from those who would prove to be resistant to external psychological effects, thus ensuring their loyalty to the host authority.
>For these reasons a program of mental training was developed and initiated - the so called "liberal civil rights movement" "sexual minorities liberation" "sexual revolution" etc. The goal of this program was to expose the population to an incredible amount of psychologically and mentally degrading behavioral incentives in order to stimulate a stable positive response in as many subjects as possible, causing them to adopt the "liberal" pattern as the basis for their behavior, consequentially presenting themselves as easily manipulated and mentally weak in resisting psychological attacks in the future warfare scenarios.

>In the early 2000s the PPI entered the phase of preparing for active depopulation campaign which was to be initiated in 2019 and be complete its final phase by 2030
>Scripps Research Institute was issued orders to prepare the framework for introducing the active depopulation agent using the front of immunology research.
www.scripps.edu...
www.pnas.org...
Have fun googling about Scripps Research institute and relatedinvolved personas.
>The news about protein PTPN22 was made public in 2016.
>Protein PTPN22 is the protein responsible for the deactivation of the immune system in a human organism.
>In laymen's terms if a human organism produces high levels of PTPN22 as a result of not finding a defense against a foreign organism, it would cause a shutdown of the immune system in a human organism causing a rabid deterioration and a collapse of body functions resulting in a swift death.

Hello good guy in government/Q anon/Dove of Oneness
Operation Dark Winter laid the groundwork for BASIS labs such as those affiliated with Fort Detrick (true origin of covid-19) and Dugway Proving Grounds to release an apocalyptic virus that will, as the unknowing shills have told us, kill 1/3 of the global population, in accordance with Agenda 21, the Georgia Guidestones, and the Population Council. The nobles all vaccinated themselves against it, right under our noses. Their vaccines were not to the harmless covfefe. We will blame the vaccinated for causing mutations; the vaccinated will blame the unvaccinated; the real virus outlined in Dark Winter will not be detected, just the epsilon variant of the two-year cold, all the deaths blamed on the latter by submissive and cowed scientist shills. "We detected epsilon variant in half of the 1/3 population who died. This means the epsilon variant is difficult to detect." (Real virus, likely some kind of chickenpox, will not be detected at all; on the off-chance it is, a scientist will be told to disregard it, and he will obey unquestioningly). It's likely few of the paid propagandists who # this board up with bots for a living will be inoculated. You're going to die with the rest of us, despite helping with this plan by blaming chinks and Fauci. None of you have mentioned Operation Dark Winter because you're all controlled ops, at best promoters of a modified hangout that seeks to blame random jews instead of the transatlantic anglo-jewish oligarchy truly responsible."

Immortalised cell monocytes are a result of the body not being able to destroy the covid-19 spike protein antigen
(likely due to suboptimal antibodies caused by exposure to the vaccine either directly or by exposure to shedding from a vaccinated person, but you can take nicotine and CBD oil to induce monocyte cell apoptosis)

Source for below: archive.4plebs.org...

"Here are some actual FACTS about the vaccine and COVID-19 with sources. Save the post, save your loved ones.

COVID-19 is a virus that contains two spike proteins, S1 and S2. The virus itself does some harm, which is different than than the damage the spike proteins do.

So, lets talk about the virus first. The virus functions similar to malaria mechanical function inside the blood. It rips the hemes off of your hemoglobin, making your blood not be able to transport oxygen to your organs. This is why COVID causes organ failure, and low oxygen levels. This is also why Hydroxychloroquine works against it, it prevents your hemes from being torn off your hemoglobin. When your hemoglobin is ripped apart, you end up with free floating hemes that are toxic as well as radical Iron particles in your blood that your liver must remove, and when your liver gets overloaded, it is processed in the lungs, resulting in lungs becoming inflamed and filled with fluid. This is also why ventilators don't work, people are breathing fine, they are low on oxygen because they are low on hemoglobin, and no amount of mechanical breathing can increase the amount of oxygen the blood can absorb without hemoglobin. chemrxiv.org...

Now, on to the spike proteins. When you get infected with COVID, the spike proteins go around infecting certain cells and injecting viral RNA (set of temporary instructions) and duplicating the virus. It takes about 1 week for your body to recognize the virus is bad and evoke a immune response. When your body does this, it sends a bunch of monocytes to kill the infected cells. The spike proteins are eaten by the Classical Monocytes and SHOULD be destroyed inside of them, and then the monocyte will undergo apoptosis (die). This is working for the S2 protein, but not the S1. The S1 protein is being eaten by Classical Monocytes, but it is making the Monocytes change into Intermediate, and Non-Classical monocytes, and the S1 protein is NOT BEING DESTROYED in them, so they are refusing to undergo apoptosis. A monocyte should only live for 1 day to 1 week, but the Non-Classical Monocytes with the S1 protein in them are not dying for up to 15 months or more. Dr. Bruce Patterson is leading the research on this. www.youtube.com...

So, even after your body has killed off COVID-19 inside of you, you have a bunch of monocytes presenting the S1 protein. These monocytes with the S1 protein can pass through the blood-brain barrier, and go anywhere in your body. They are causing vasodilation (increased size of blood vessels) throughout peoples body, inflammation of blood vessels, and nano clotting, especially in the capillaries. These nano clots and inflammation can cause heart attacks, fatigue, and all sorts of other problems. This is what is called Long Haul COVID.

So, remember, what the virus does, and what the spike proteins do are 2 different things. But, your body only responds by creating antibodies that will recognize and destroy the spike proteins (which neutralizes COVID's ability to replicate within the body, thus killing COVID). But the spike protein symptoms (vasodilation, inflammation, and nanoclotting) are not what the virus does (destroying hemoglobin).

NOW, to the vaccine. The vaccine injects either an adenovirus, or graphene oxide (toxic to humans in high doses, but processed by an enzyme from the lungs in 2-3 weeks usually) into your body. phys.org...

The vaccine either had spike proteins in it (Pfizer and Moderna) or causes your cells to begin producing spike proteins via mRNA (Pfizer, Moderna, J&J, Astrazeneca, all of them but Novavax). This causes your body to have an immediate immune response and begin producing antibodies against the spike proteins. This does make your body effectively immune to COVID if it worked properly. But it doesn't for 1 reason. The S1 spike proteins being eaten by your Classical Monocytes are being turned into Non-Classical monocytes (which should die in 1 week or less normally) that are not undergoing apoptosis, and therefore never dying. These S1 presenting monocytes are going throughout the body and causing serious damage, and hurting your immune system. www.biorxiv.org...

IF YOU COULD FORCE YOUR NON-CLASSICAL MONOCYTES TO UNDERGO APOPTOSIS, the vaccine would work properly. Bruce Patterson suggests using several drugs in his protocol to achieve the goals. Ivermectin kills the virus, Statins prevent the S1 protein presenting Monocytes from attaching to your cells, and several drugs (including nicotine) can induce monocyte apoptosis. When the S1 presenting Non-Classical monocytes undergo apoptosis, the S1 protein is destroyed, and the nano clotting, inflammation, etc. go away. This is also why smokers have been shown to test positive for COVID symptoms 80% less than the general population, the nicotine effectively renders them immune to the effects of the S1 protein, and thus most of COVID's symptoms. www.webmd.com...

So, now, does the vaccine work, and why is COVID and its variants killing people still? Simply put, as your body is introduced to more and more COVID virus (or vaccines) your body begins building a larger and larger reservoir of very harmful S1 presenting Non-Classical Monocytes, that will eventually kill you. So, if you had COVID, you have a reservoir already. If you get the vax, now you have even more. If you get a second vax, or encounter people with COVID, you get even more and more, until you die, unless you do something to induce apoptosis in your Non-Classical Monocytes.

So yes, the vaccine is not useless, it does immunize people against COVID, but it destroys their immune system by creating a reservoir of S1 protein presenting Non-Classical Monocytes that reduce the body's ability to produce antibodies to fight off future COVID infection. If you induce apoptosis in your monocytes, then the vaccine works, and is not overly dangerous. As it is right now, the vaccine is immunizing people against COVID, but then putting their body in a state that it can't fight off COVID, as well as many other pathogens. In addition, the vaccine can kill you, either immediately (via blood clotting), or long term via your reservoir of S1 presenting Monocytes. But COVID can do the latter if you are exposed to enough viral load, even over months or years.

TL;DR Buy some Ivermectin and Nicotine Lozenges and you can survive COVID-19 without vaxx or any side effects."

My next question, How/why could all these completely separate, private, competing drug makers come to the same conclusion independently on their own that using HIV proteins in these drugs is a good idea? Wtf


BTW congratulations you broke the record for longest time without a pro vaccine troll coming along and decrying your point of view with bulls###. Hats off have a beer on me 🍻

originally posted by: Brotherman
My next question, How/why could all these completely separate, private, competing drug makers come to the same conclusion independently on their own that using HIV proteins in these drugs is a good idea? Wtf

There are a handful of families that own them, and all the banks too. Rothschilds comes to mind. They are Satanists. They think the Earth belongs to them, and them alone.

originally posted by: Brotherman
My next question, How/why could all these completely separate, private, competing drug makers come to the same conclusion independently on their own that using HIV proteins in these drugs is a good idea? Wtf

Because the virus is HIV protein attached to an airborne pathogen, so in order to vaccinate against it you have to vaccinate yourself against HIV. (That's probably the "good reason" which sounds reasonable and nice, the "real reason" is probably because they want to reduce the human population down to 500 million in line with the 1st and 10th Georgia Guidestone outlines. Making us all infertile also falls perfectly in line with the 2nd Georgia Guidestone outline.)

But it's an activated virus, not an inactivated one. So you're technically injecting yourself with an activated HIV protein.

My theory is that the autopsies performed on vaccinated persons, which have shown that there are some metallic like parasitic organisms which can survive even after the death of the host (that is not normal, ordinarily parasites require heat and energy from the host to survive) could be an explanation towards how and why covid infected cell monocytes become immortalised.

Theres a lot of evidence emerging that Covid may actually be caused by CHAGAS parasite "Trypanosoma cruzi" or another called "Polypodium hydriforme" which is an immortal, alien like parasite which can exist in sub zero temperatures. Hence why all the FUD and dismissing ivermectin and HCQ which are both extremely potent anti-parasitic drugs.

Anons have identified the “tentacled” organism described by Dr Carrie Madej from the Moderna vaxx as this endocellular parasite called Polypodium hydriforme

Stew Peters and Dr. Carrie Madej reveal living creatures inside the vax/gene therapy

Links between "Trypanosoma cruzi" parasite and Covid-19

Parasite Pill PDF

a reply to: natoshis

So when does zombification start happening? That’s really the bottom line.

a reply to: natoshis

When I saw the Title of your thread, I kinda went "Here we go", AIDS, this should be good.

Forgive me, I was wrong.

Excellent thread and I have heard there is a "chunk" of AIDS within Covid. I'm not sure about that, so, I don't mention it usually (absolutely would NOT surprise me, though).

Again, excellent thread with great info, all in one place, and nicely laid out.

SnF for the great info.