Craig Venter of the NIH and Human Genome: Creating Synthetic Life | ” – trying to design what we want biology to do”

Agenda of the Human Genome Project: ” – for manufacturing and operating a complete human being.”

Playing God in Frankenstein’s Footsteps: Synthetic Biology and the Meaning of Life
– [ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837218/ ]

Thanks to a pingback post by the following site: There Is No Pandemic, it led me to a very interesting video featuring a Mr. Craig Venter, delving into an incredibly topical subject – even though the video was made in 2010.

Don’t think synthetic life-forms are possible in vaccines? Or that there’s even an agenda to do this?

Craig Venter, genetic researcher for the NIH and the Human Genome Project, would tell you otherwise…

“operating system”

“all the characteristics of the first species disappear”

“new species emerges from this software”

“making the flu vaccine each year by using these new synthetic techniques”

Click image for archived video. Original source can be found here: [ https://www.theguardian.com/science/2010/may/20/craig-venter-synthetic-life-form ]
“Craig Venter creates synthetic life form”
Full transcript. Some embellishment has been added for emphasis.

Craig Venter: “Well this has been about a 15 year process. It started back in 1995, when we sequenced the first two genomes in history. Including the smallest genome, that of mycoplasma genitalium. And we set out a goal to try and understand what the smallest genome you can have as an operating system, to try and understand the basic components of life. It’s taken us through this long journey. Much longer than we ever anticipated. But that’s what happens when you enter into areas that nobody’s ever been before.

So at first we had to learn how to write the genetic code to synthesize pieces. Because the largest piece that ever has been synthesized other than our work has been only 30,000 letters. The first chromosome we were trying to make was over 500,000. And the one that we ultimately made and report in this paper is over 1,000,000 letters of genetic code. And we start with 4 bottles of chemicals, and the computer code in the computer, the digital code in the computer from DNA sequence. So, just learning how to do the synthesis was mastering a lot of chemistry that has never been done before. And we learned sequentially over the years how to build larger and larger molecules.

In 2003 we reported making a 5,000 letter bacterial virus, 5X174, and how to error correct the pieces. So, we start with pieces of DNA coming off DNA synthesizers; they’re only about 50-80 letters long. That’s pretty much the limit of what you can make with a chemical synthesizer. So everything we make from that has to be putting these little pieces together. Much like having a box of legos and having to assemble them back in the right order to get what you started with. So it’s been progressive over this entire time period. We thought we would have this almost 3 years ago. But we kept running into very significant biological roadblocks.”

Interviewer: “All right. And what do you ultimately hope to do with a method like this?

Craig Venter: “Well, this is an important step, we think, both scientifically and philosophically. It certainly changed my views of definitions of life and how life works. It’s pretty stunning when you just replace the DNA software in the cell, and the cell instantly starts reading that new software, starts making a whole different set of proteins. And within a short while, all the characteristics of the first species disappear. And a new species emerges from this software that controls that cell going forward.

When we look at life forms we see them as sort of fixed entities. But this shows, in fact how dynamic they are. That they change from second to second. And that life is basically a result of an information process, a software process. Our genetic code is our software. And our cells are dynamically constantly reading that genetic code, making new proteins, the proteins make the other cellular components, and that’s what we see. But it’s hard to imagine how dynamic it is until we found, simply by replacing the software, it started making a whole new cell, whatever is defined by that software. So that’s, that’s a pretty important change in how we approach and think about life.

Also this is now the first time where we’ve started with information in the computer, built that software molecule, now over a million letters of genetic code, put that into a recipient cell, and have this process start where that information converted that cell into a new species. So this becomes a very powerful tool for trying to design what we want biology to do.

As leaders of competing genome projects, Francis Collins, director of the National Human Genome Research Institute, and J. Craig Venter, president of Celera Genomics, were recognized, correctly, as the two most important players in the worldwide effort to spell out the 3 billion “letters” of the human genome–the biochemical recipe, encoded in our DNA, for manufacturing and operating a complete human being.

[ https://content.time.com/time/subscriber/article/0,33009,998842,00.html ]

We have a wide range of applications, so at the biotech company that funded the synthetic genomics that Ham Smith and I started a few years back, we have a major deal with ExxonMobil to try and use algae to capture carbon dioxide and make new hydrocarbons that can go into the Exxon refineries. To try and replace taking the oil out of the ground.

There’s no natural algaes that we know that can do this at the scale it’s needed. So we’re going to have to use our synthetic genomic techniques to either heavily modify existing algaes or develop whole new ones from scratch that have all the parameters that we want. These same tools, these same processes can be used for making chemicals, for making food substances, we hope for cleaning up water.

But perhaps the most important immediate application is we’re already working at the Venter Institute and working with Novartis to try and make new vaccines very quickly; we think we can shorten the process by 99% for making the flu vaccine each year by using these new synthetic techniques. But I think it’s going to be one of those situations I tell audiences I talk to that ‘we’re entering a new era we’re limited mostly by our imaginations’.”

Interviewer: “Could you ever use a method like this with a higher organism? Something more complex than bacteria?

Craig Venter: “Well, it’s certainly not in the immediate future. Bacteria have much more simplified genetic systems. They don’t have the same complex regulation that higher organisms have. But there are a number of single cell eukaryotes.

So we’re eukaryotes because we have a nucleus, I think one of the key things we mastered with our studies, particularly since 2003, and we reported the latest results a few months ago in Science at the end of last year, is we can move chromosomes across the branches of life. So we can move from bacteria into eukaryotes, we use yeast for all these processes. We can take the chromosomes out of yeast and move them back into bacteria to create new life forms.

So a next step would be try to make a simplified eukaryote. Yeast is very key for bio-manufacturing, for ethanol production, etc. And if we can have even a more efficient yeast cell, and at the same time, try and understand all its components, I think we’ll be able to make synthetic eukaryotes. Higher animals, multi-cellular systems are, I think, projects for the much more distant future.”

Interviewer: “Actually I have a couple more questions. Just about how we distinguish between any sort of synthetically – organisms with synthetic genomes versus the natural ones? One question I guess would be about containment.”

[Interview cuts out a section]

Craig Venter: ” – we were when we first started down this process, what could be an artifact that could fool us into thinking we had created synthetic life, when in fact it was just a contaminate of the native chromosome? And, where would even a single molecule of native chromosome could fool us into thinking we had created a new cell?

So early on we started designing a process of putting watermarks in the genetic code. We did this in the first chromosome we reported two years ago, basically all of us that helped build the genetic code signed the DNA, coded our names into the chromosome.

With this genome we’ve gone a little bit further; we’ve put 4 major watermarks in. We’ve developed a new code for writing English language, other languages, with punctuation and numbers into the genetic code. In the first watermark we actually have this code that needs to be decoded for people to read the rest. We even have a website built into the genetic code that if people solve it they can let us know that they’ve been able to read it.

“- and that no one may buy or sell except one who has the mark or the name of the beast, or the number of his name.”Revelation 13:17

All the authors of this study over the… certainly the last decade, our names are all encoded in this first genome. And we have three quotations built in there of adding a little philosophy to the genetic code at the same time. Which I think the chance of finding any of these in a naturally occurring genome is about as close to zero as you can get. So we can absolutely prove from the genetic changes, that we’ve been built in to the design of the chromosomes that it’s unquestionably the synthetic DNA that we made, not some natural contaminant.

A containment, that’s a really critical issue, and it’s one of the most important issues to us, and one of the number one questions I get asked in all my litera- all my lectures around the globe. And when we look at molecular biology for the last several decades, we all use e. coli in the laboratory, that genes from multiple species have been put in it over the years – probably tens of millions of experiments. And there’s not been a single accident. And the reason for that is that e. coli has a chemical dependency for growing in the laboratory.

So these are things we can start to build in to the design of synthetic genomes, we can build in suicide genes so they can’t escape. And so we can use artificial amino acids. There’s a number of approaches that we’re developing and other labs are developing to guarantee absolute containment.

And this first proof of principle, we’ve largely copied the mycoides genome, because as a control, if we couldn’t boot up something that was already known, we could never get to the design phase. We deleted 14 genes from this genome, and made all these other genetic modifications. This cell only grows on extremely rich [media(sp?)] on the laboratory.

The only other place it goes, the mycoides genome is a minor goat pathogen that causes mastitis in goats. We think we’ve eliminated the genes associated with that, but it will not grow outside of the laboratory unless it’s deliberately injected or sprayed into a goat. So, we don’t work with goats, so we think we have pretty good containment systems in the lab.

There’s selectable markers that’s dependent on a specific antibiotic. So these are early attempts, I think. These containment approaches would get far more sophisticated with the next versions of what we and others do.”

Interviewer: “All right. Well, are there any final points you’d like to make before we close?”

Craig Venter: “Well, this is the first synthetic cell that’s been made and we call it synthetic because the cell is totally derived from a synthetic chromosome made from 4 bottles of chemicals on a chemical synthesizer. Starting with information in the computer.

Before we did these experiments starting back in the late 90’s, we asked for a complete bioethical review, knowing we were going into uncharted territory, trying to create new species. The review group at the University of Pennsylvania published the results in Science in 1999. Since then there’s been lots of different review processes around the world. The Sloan Foundation funded my institute, the Venter Institute, along with MIT, and a Washington think tank, to look at the security issues concerning this. That report was published and can be downloaded from JCVI.org.

There’s been ongoing discussions in the U.S. government, in the E.U., the National Academy of Sciences has done reports on this. So I think this is the first incidence in science where the extensive bioethical review took place before the experiments were done. And it’s part of an ongoing process that we’ve been driving, trying to make sure that the science proceeds in an ethical fashion, that we’re being thoughtful about what we do, and looking forward to the implications to the future.”

End of transcript.

So here is undeniable proof, that the folks at the NIH and Human Genome Project have been trying to synthesize organisms for the sole purpose of creating new species/life forms, and using these techniques for vaccines, AND states that these synthetic substances WILL CHANGE DNA.

It all ties back to the NIH and the HUMAN GENOME PROJECT. The theory that the COVID vaccines are an attempt at a worldwide genome experiment project is becoming clearer every single day, backed up with all of the data that has come forward, backed up with all of the studies pointing to this very agenda, backed up with countless interviews, positions and documentations of the likes of Anthony Fauci, Christine Grady, Bill Gates, Craig Venter, Eric Lander, Klaus Schwab, Francis Collins, their institutes and cohorts GAVI, WEF, Bill and Melinda Gates Foundation, NIH, Human Genome Project, World Health Organization, United Nations, MIT, Harvard, etc., etc., etc.

“Venter and colleagues published their paper about creating a bacterial cell controlled by a chemically synthesized genome in the journal Science in May 2010.

“Some of you are asking, why do this? It’s great basic science, but there are some more compelling reasons,” he said, noting that synthetic DNA can be used to develop genomics-based vaccines.

“The National Institutes of Health has funded my institute to create synthetic pieces of every known flu virus, so anytime we need a new vaccine, we can just take these pieces off the shelf, and go through the assembly and have flu vaccine stocks in a very short time,” he said. “In the next year or two, you might get the first synthetic DNA vaccines.”

Web archive version: Synthetic life forms can produce vaccines, gobble up CO2 and more, says expert

Although the below excerpt specifies “intranasal”, there are also endeavors of injectable live attenuated vaccines as well:

“The company’s breakthrough Synthetic Attenuated Virus Engineering (SAVE) platform utilizes a computer algorithm to recode the genomes of viruses and construct live-attenuated vaccines to prevent viral infections or treat solid tumors.”

Web archive version: Codagenix and Serum Institute of India Announce Commencement of First-in-Human Trial of COVI-VAC, A Single Dose, Intranasal Live Attenuated Vaccine for COVID-19

[ https://pubmed.ncbi.nlm.nih.gov/16778323/ ] “Genetically modified live attenuated parasites as vaccines for leishmaniasis” (2006)

[ https://pubmed.ncbi.nlm.nih.gov/28620583/ ] “Engineering of Genetically Arrested Parasites (GAPs) For a Precision Malaria Vaccine” (2017)

[ https://www.niaid.nih.gov/news-events/investigational-malaria-vaccine-gives-strong-lasting-protection ] “Investigational Malaria Vaccine Gives Strong, Lasting Protection” (2021)“The vaccine combines live parasites with either of two widely used antimalarial drugs—an approach termed chemoprophylaxis vaccination.”

Now, with all of that being said, and with this outright admission by Craig Venter about their agenda, I have to bring up one of Richard Fleming’s latest criticism of ALL the doctors that have claimed to find what seems to be graphene oxide, nanobots, and/or parasitic-like organisms in the vaccines.

Firstly, this should have been approached in a more scientific approach to researching the vaccine’s contents.

While the other doctors are investigating these vaccines and are questioning its contents, even inviting other scientists and researchers to help them identify what these substances are, Dr. Fleming is undermining their research and dismissing their conclusions. Even implying, at one point, the mention of “credentials” as to whether or not to take one seriously.

Secondly… isn’t that precisely why we’re in the mess we’re in right now? Because SO many people decided to trust the likes of Anthony Fauci and Francis Collins? Does it matter how many so-called credentials one has to determine their sincerity and integrity or even professionalism? Doesn’t look like it to me. As long as a researcher is honest and looking for the truth, I will take their word over an overpaid “expert” any day. Especially ones who conduct inhumane, atrocious experiments on other living beings.

Then, of course, when addressing anything in a scientific approach, and certainly before reaching concrete conclusions and dismissing any other research (like the fraudulent Lancet paper did, for example…) one must consider ALL variables. Take the following for consideration:

how many vials total did Richard Fleming test?

were they from the same batch, or all different batches? Different brands, or all the same brand?

were all these vials from the same country? – it is becoming more and more apparent that different countries are getting different doses/batches

at what magnification did Fleming conduct his tests compared to all of the other doctors/scientists?

are we considering that some batches/doses will contain certain substances while others consist of saline solutions only – as what has already been theorized?

if different countries are getting different batches, there is a chance that there will be different substances for each country – to perhaps test a wider set of material/organisms and/or to target certain people’s DNA/ethnicity/etc.?

what is the “garbage” and “debris” that Fleming is referencing? “Garbage” has to be something. Was there an attempt to identify these compositions? Or just label them all with the term “debris” and “garbage”?

Fleming also mentions the term “crystalline” on more than one occasion… does he realize that there are indeed nanocrystal-graphene hybrid material that has been synthesized? Does he know every possible thing that can be synthesized or genetically modified using either Venter’s DNA genetic modification technique or the CRISPR technology?

“Nanocrystal-graphene have been proposed as a new kind of promising hybrid for a wide range of application areas including catalysts, electronics, sensors, biomedicine, and energy storage, etc. Although a variety of methods have been developed for the preparation of hybrids, a facile and general synthetic approach is still highly required.”

“A rich library of highly crystalline nanocrystals, with types including noble metal, metal oxide, magnetic material and semiconductor were successfully grown on chemically converted graphene (CCG), which is simultaneously reduced from GO during the synthesis.”

[ https://pubmed.ncbi.nlm.nih.gov/22699842/ ] “Generalized syntheses of nanocrystal-graphene hybrids in high-boiling-point organic solvents”

Is Mr. Fleming aware of all the technological and biological advancements and agendas in the arena of nanotechnology in combination with virus-based particles?

“Genetically modified viruses offer a general route for the production of materials with complex nanoscale detail, for use either directly or as templates. It appears likely that modified viruses will feature prominently in the nanotechnology of the immediate future. The possible commercial exploitation of virus-templated materials includes nanowires, high surface area materials for battery electrodes, detectors, catalytic material, light harvesting devices, quantum dots, and tunable photonic devices.”

[ https://onlinelibrary.wiley.com/doi/abs/10.1002/9783527671403.hlc094 ] “7 Virus Particle-Based Liquid Crystals”

Will Mr. Fleming attempt to identify these so-called “garbage” and “debris” and conduct further studies with a higher magnification, or continue to shoot down other’s legitimate attempts at trying to figure out exactly what these particles are? Notice he never tries to identify what ANYTHING in the vaccine is, other than mentioning “lipid nanoparticles”. Only giving his opinion of what it’s not.

And with all of the evidence showing that genetically modified organisms is not only highly probable but also incredibly likely, considering the NIH’s many, many, MANY horrific experiments and crimes against humanity (and animal life), and Craig Venter’s ventures, not to mention Bill Gates’ very own admission and extensive funding in this matter, I am ultimately left questioning Fleming’s motives.

Bill Gates: “You know, is there something to worry about with medicines, that is might – some of them might have side effects? Do we need safety testing? I mean and we’re taking things that are… you know, genetically modified organisms and we’re injecting them in little kids arms. We just shoot them right into the vein.”

Bottom line: yes, these vaccines are extremely dangerous. And if the ones in control of pushing these worldwide vaccines are also in control of the Human Genome Project and attempts at re-writing our DNA, our best bet would be to avoid these at all costs and address these as the crimes they are.

Fact checking is extremely important. I want to reiterate not to take everything at face value; no matter what you read, where you read it from, or who you hear it from. And to be clear, do not rely on “fact checking” websites to give you accurate information either. These are just as likely, (if not even more likely…), to feed false information and false debunking accounts to manipulate the reader. Please take everything into consideration before adhering to a certain narrative – and always keep your mind open to other possibilities.

Fair use disclaimer: Some of the links from this article are provided from different sources/sites to give the reader extra information and cite the sources, but does not necessarily mean that I endorse the contents of the site itself. Additionally, I have tried to provide links to the contents that I used from other sites as an educational and/or entertainment means only; if you feel that any information deserves further citation or request to be clarified, please let me know through the contact page.

Featured image by PublicDomainPictures from Pixabay

Studies PROVE That Live Parasites and Parasite Proteins Are Being Used/Tested in Vaccines | Are Parasites the Cause of ALL Illnesses?

At least 650,000 – 800,000 CHILDREN have been injected with a malaria vaccine to test its efficacy.

After investigating parasitic like organisms possibly being used in vaccines – I realized, these studies have been conducted for a LONG TIME. And who knows for how long?

It is a true, real, honest-to-badness endeavor.

Now, a lot of scientists/doctors/virologists/biologists may already know all of this and see nothing wrong with it. I, however, an innocent researcher, never knew that this was a real agenda all in the sake of “curing” people from… well, parasites.

I know. It doesn’t make sense to me – why inoculate someone with parasites, if they are trying to prevent them from the very same parasite they’re being inoculated with?

It reminds me of the flu/COVID shots, actually. Why deliberately inoculate someone with a virus that you’re trying to prevent/immunize them from getting? Especially if they have a chance of acquiring it naturally and producing the more beneficial ‘natural immunity’? Perhaps I just don’t understand the “science”. Or perhaps “science” as we’re being taught to believe it, is full of holes and hidden motives.

Or perhaps, what started out as a benevolent effort to help humankind, became corrupted and twisted into a sinister agenda to perform horrific experimentation on the whole population.

I can’t give you the definitive answer to that. I don’t believe that all scientists are corrupt and have hidden agendas. But I do believe that some do. And I do believe that those “world leaders” and scientists bent on transhumanism/genetic modifications/immortality (for their own people)/depopulation-slavery(for everyone else), has hijacked the scientific/medical/health communities, and are initiating their own forms of control and influence to initiate their “great reset”, which is another way of saying “reset the human race”.

So I shouldn’t have been shocked and surprised to learn that studies of “live parasites” in vaccines is a real thing. I’m not saying they’re used in ALL vaccines, but they are certainly being used in some.

“In a one-two punch, a malaria vaccine in development pairs a shot of the live parasite that causes the disease with a whammy of infection-fighting drugs to immediately quell it.”A malaria vaccine with live parasites shows promise in a small trial

Sure, Jan.

From the same article:

“Adrian Hill, a vaccinologist at the University of Oxford and director of the Jenner Institute who is involved with the R21 malaria vaccine: “If you give people [in Africa] a whopping dose of malaria and then for any reason that drug is expired or it isn’t the right drug or they took it too late — who’s going to take responsibility for that?”A malaria vaccine with live parasites shows promise in a small trial

Another article, unironically on the same date (June 30, 2021) as the previous one, states the following:

“Participants in the study, published on 30 June in Nature1, were given a shot containing live Plasmodium falciparum parasites, along with drugs to kill any parasites that reached the liver or bloodstream, where they can cause malaria symptoms. Participants were then intentionally infected with malaria three months later to test the vaccine’s efficacy.”

“Several malaria vaccines are in development. The most advanced — RTS,S — has been given to more than 650,000 children as part of a pilot programme in three African countries to assess its safety and efficacy, as well as the logistics of rolling it out.

Another vaccine, called R21, was recently shown to be up to 77% effective in a trial of 450 young children, and a larger study is under way.

Both of these use the same malaria protein, called circumsporozoite protein, to trigger immune responses. That protein decorates the outside of the sporozoite form of the parasite, the stage in its life cycle when it first enters the human body from the salivary glands of infected mosquitoes.

Vaccine made of live malaria parasites shows early success

So let me get this straight… They are trying to combat malaria, by pumping you full of live parasites that causes malaria, in order to cure/immunize against… malaria…?

Does this make sense to anyone? Wouldn’t it be more prudent to use, say, a highly efficacious anti-parasitic drug – like, oh… I don’t know… Ivermectin, perhaps, if/when a parasitic infestation occurs?

[ https://pubmed.ncbi.nlm.nih.gov/31948767/ ] “Ivermectin as a novel complementary malaria control tool to reduce incidence and prevalence: a modelling study”

Why deliberately inundate someone with parasites just to “possibly” immunize them from the very same thing? Then that leaves the very real dilemma… what if the immunization doesn’t work, and you’re left with a body full of parasites? Does anyone really want to take this chance? I can understand testing the correct dosage of Ivermectin to combat the amount of parasitic infestation, but no – it’s “Jump right to vaccines! Even though we don’t know if this will work either, let’s just go ahead and infect hundreds of thousands of innocent lives with live parasites and/or parasite proteins! What could possibly go wrong?”

And how HORRIFIC to be testing vaccines on children! Regardless if the vaccine has a live parasite or if it’s a protein from the parasite that HELPS them get infected… it is still an outrageous proposal to deliberately inoculate them and TEST the vaccine on them! And then are we to conclude that they are going to be deliberately infected with malaria (more parasites) to test the vaccine efficacy in later weeks/months?

650,000 babies and children?! Are you kidding me? In what world is this okay? This is outrageous and should automatically be labeled a crime against humanity. Maybe they wouldn’t be infested with malaria if they weren’t INTENTIONALLY INJECTED WITH A MALARIA VACCINE to begin with. All in the supposed “proposed” hope of “curing” them from malaria? Am I the only one who finds this absolutely ridiculous and atrocious? How about we stop experimenting on human lives and parasites to begin with? Perhaps if mad scientists weren’t genetically modifying everything under the sun, we wouldn’t be having these issues.

[ https://pubmed.ncbi.nlm.nih.gov/29077880/ ] “Repetitive sequences in malaria parasite proteins”:

“Five species of parasite cause malaria in humans with the most severe disease caused by Plasmodium falciparum.

We discuss the diverse roles of low-complexity repetitive sequences throughout the parasite life cycle, from mediating protein-protein interactions to enabling the parasite to evade the host immune system.”

Now why would they want to enable the parasite to evade the host immune system…?

And going back to Ivermectin, touted a “wonder drug” (which is also used as a prophylactic treatment), is there something to be said for an anti-parasitic drug that not only works against parasites, but also works wonders on SEVERAL different ailments? Or… could it be possible that all ailments are caused by parasites?

Blood clots, heart attacks, strokes, encephalitis, lung disease, pneumonia, kidney issues, gout, lupus, etc., etc., etc., etc. A few examples that help lend credence to this theory are presented below (embellishments have been added for emphasis):

Arthritis:

[ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003687/ ] “Toxoplasmosis seroprevalence in rheumatoid arthritis patients: A systematic review and meta-analysis”:

“Toxoplasmosis is a cosmopolitan infection caused by an intracellular obligatory protozoan, Toxoplasma gondii. Infection to this parasite in immunocompetent patients is usually asymptomatic, but today it is believed that the infection can be a risk factor for a variety of diseases, including rheumatoid arthritis (RA). RA is an autoimmune disease and the most common type of inflammatory arthritis that is a major cause of disability.”

Blood Clots:

[ https://www.news-medical.net/news/20200413/Study-looks-into-how-malaria-parasite-evades-the-immune-system.aspx ] “Study looks into how malaria parasite evades the immune system”:

The parasite causing the most severe form of human malaria uses proteins to make red blood cells sticky, making it harder for the immune system to destroy it and leading to potentially fatal blood clots. New research at the Crick has identified how the parasite may control this process.”

Central Nervous System Disorders:

[ https://www.verywellhealth.com/parasitic-infections-of-the-central-nervous-system-2488670 ] “Parasitic Infections of the Central Nervous System”:

“Trypanosomiasis, also called sleeping sickness, is caused by the protozoan parasites Trypanosoma brucei gambiense or Trypanosoma brucei rhodesiense. Like malaria, the parasite is spread by an insect host.

 

After a period of time, sometimes years, the parasite spreads from the blood to the brain, leading to meningoencephalitis and swelling. A headache, difficulty thinking, personality changes, and movement disorders such as tremor or ataxia (lack of coordination) can result.

Heart Attack / Myocardium / Pericardium:

[ https://heart.bmj.com/content/103/9/651 ] “Cardiac manifestations of parasitic diseases”:

The heart may be affected directly or indirectly by a variety of protozoa and helminths. This involvement may manifest in different ways, but the syndromes resulting from impairment of the myocardium and pericardium are the most frequent. The myocardium may be invaded by parasites that trigger local inflammatory response with subsequent myocarditis or cardiomyopathy

Pneumonia

[ https://thorax.bmj.com/content/66/6/528 ] “Parasitic infections of the lung: a guide for the respiratory physician”:

“Parasitic infections of the lung occur worldwide among both immunocompetent and immunocompromised patients and may affect the respiratory system in a variety of ways. This review provides an update on the presenting symptoms, signs, investigation and management of diseases affecting the lung caused by protozoa, nematodes and trematodes. The clinical presentations and radiographic findings of several of these diseases may mimic tuberculosis and malignancy. It is important to consider parasitic infections in the differential diagnosis of such lung diseases. If identified early, most parasitic diseases that affect the lung are curable with medical or surgical treatments.”

Seizures & Strokes (Gastrointestinal Complications)

[ https://www.verywellhealth.com/parasitic-infections-of-the-central-nervous-system-2488670 ] “Parasitic Infections of the Central Nervous System”:

“Paragonimiasis is a parasitic infection with a flatworm which may enter the body through eating undercooked crab or crayfish. It is rare in the United States, though several cases have been reported in the Midwest. Most commonly it is found in East Asian countries.

The parasite does not often affect the central nervous system but the parasite may reach the brain either through the bloodstream or through the foramina at the base of the skull. The adult form of the parasite both releases inflammatory substances and tunnels through tissues, which can result in headaches, seizures, and strokes.”

[ https://www.verywellhealth.com/symptoms-and-complications-of-chagas-disease-4163007 ] “Symptoms of Chagas Disease”:

“The symptoms of Chagas disease, an infection caused by a protozoan parasite called Trypanosoma cruzi (T. cruzi), resemble those of the flu—at least at first. When the acute phase of the disease resolves, however, the T. cruzi parasite can persist in the body for many years, even in people who appear entirely healthy. Many years later, often after decades, a chronic form of Chagas disease can develop, producing cardiac problems, gastrointestinal problems, or both.”

The Rod of Asclepius

“The probable medical origin of this ancient Greek symbol with a snake wrapped around a staff is the ‘worm theory’ that dates back to about 1500 BC. It was a description of treatment for the parasitic Guinea worm written on papyrus, said to be among the first ancient Egyptian medical documents. Ancient physicians probably used signs with a worm on a stick to advertising the worm treatment service they offered.”The Rod of Asclepius Symbol – History And Meaning

Perhaps the reason that Ivermectin is such a potent medicine against multiple illnesses and viruses, is because every ailment is caused by one parasite or another (or a combination of them).

If that is true, it makes one wonder why Ivermectin is so highly condemned in the medical/science community. Not all of the medical/science community, of course. It only seems to be the organizations who are incredibly politically and financially charged to do so. Who also just happen to work in conjunction with the huge alphabet government agencies, as well as the big tech / big pharma, and the mainstream media.

Hm… nothing suspicious there, right? And it’s not enough that the places who suffer the most from these diseases are also the ones selected for “investigational/experimental” trials of the very vaccines supposedly touted to immunize against the disease.

Now one could say, “Well, that’s the whole point. The whole country is suffering from this awful disease. So of course they’d want to cure them from it. So they’ll be the ones getting the injections. Duh!”

However, if you really dig into the history and the motives of those doing the “curing”, you will come to realize that they have no altruistic reason for doing so (despite what they say) and instead these “philanthropists” end up making BILLIONS of dollars for doing so. To add onto that, the REAL stories of painful and horrific side effects and deaths caused by these vaccines go mainly unheard of – kind of like how those who have taken the COVID vaccine and have suffered adverse side events are being censored and banned and IGNORED in the mainstream media and in hospitals worldwide. Their accounts also largely being wiped out from big tech platforms.

Now doesn’t it make you wonder, if they can wipe out all of these accounts and silence this awful widespread detrimental effects of the COVID vaccines, can you imagine how many MORE victims of vaccines that were touted as “miraculous cures” (just like the COVID vaccine…) that were inoculated in other countries, never got a chance to tell their stories? Since most of them were from poorly developed countries, and have a different language from the English speaking community, and don’t have common access to the internet… The only story we hear are the ones doing the vaccinating. And of course, according to them, it’s going “fabulously”.

So do you really believe that a known eugenicist, whose father worked with developing Planned Parenthood – the founder who was Margaret Sanger, who outrightly declared her desire to “wipe out the unfit” – that ranged from anyone who was poor, useless eater, African-American, mentally ill, disabled… do you really believe that this BILLIONAIRE, whose history is also connected with Jeffrey Epstein – a convicted child predator/child-trafficker – actually CARES about the human race so much to cure them all with a vaccine?

Bill Gates / United Nations

I smell a

Or, in the case of this post, a parasite.

And again you have to wonder, if Ivermectin is highly effective against parasites and cures many ailments… and the COVID vaccines (and other vaccines) have live parasites in them… then what is the real reason for the high suppression and smear campaign against using Ivermectin? So much so, that it has been banned in many places and some doctors ARRESTED and/or threatened with legal action and a revoke on their license for prescribing it to their patients, although it has been on the market FOR YEARS and approved as a safe medicine?…

Well, I leave that for you to contemplate.

For additional reading:

[ https://pubmed.ncbi.nlm.nih.gov/16778323/ ] “Genetically modified live attenuated parasites as vaccines for leishmaniasis”
[ https://pubmed.ncbi.nlm.nih.gov/30295650/ ] “CRISPR/Cas9 Gene Editing to Make Conditional Mutants of Human Malaria Parasite P. falciparum”
[ https://newatlas.com/science/crispr-gene-edited-parasite-leishmaniasis-vaccine/ ] “CRISPR-gene-edited parasite leads to unique new vaccine”
[ https://www.bu.edu/articles/2021/malaria-vaccine-approved-by-world-health-organization/ ] “Malaria Vaccine—the First Ever to Immunize against a Parasitic Infection—Gets Green Light from WHO”

Fact checking is extremely important. I want to reiterate not to take everything at face value; no matter what you read, where you read it from, or who you hear it from. And to be clear, do not rely on “fact checking” websites to give you accurate information either. These are just as likely, (if not even more likely…), to feed false information and false debunking accounts to manipulate the reader. Please take everything into consideration before adhering to a certain narrative – and always keep your mind open to other possibilities.

Fair use disclaimer: Some of the links from this article are provided from different sources/sites to give the reader extra information and cite the sources, but does not necessarily mean that I endorse the contents of the site itself. Additionally, I have tried to provide links to the contents that I used from other sites as an educational and/or entertainment means only; if you feel that any information deserves further citation or request to be clarified, please let me know through the contact page.

Featured image by Jeremytitus from Pixabay (with slight alteration)

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