Dutch Medical Center Succeeds With Creating Flying Syringes

Article posted with permission from the author, Suzanne Hamner

Bill Gates’ dream of transforming mosquitoes into “flying syringes” is now closer to reality than previously thought. If you recall the article at Sons of Liberty Media, “Bill Gates On Board With GMO Mosquitoes To Administer Vaccines Bypassing Informed Consent”, you would know that Gates awarded $100,000 to “Hiroyuki Matsuoka of Jichi Medical University in Japan to do research on genetically modified mosquitoes.” The plan was for Professor Matsuoka to “design” a mosquito that can produce and secrete a malaria vaccine protein into a host’s skin.

Fast forward from that article to today when The Blaze reported “The mosquito research Gates has been funding since 2008 appears to have paid off, turning out flying syringes.”

Researchers at the Bill Gates Foundation-backed Leiden University Medical Center in the Netherlands have joined an international effort to transform mosquitoes into flying syringes. According to a study published late last month in the New England Journal of Medicine, they apparently now have an effective way of using mosquitoes to deliver some protection against malaria in unsuspecting humans — and possibly other payloads in the future as well.

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Is being published in the New England Journal of Medicine supposed to lend some sort of legitimacy to Dr. Frankenstein types of experiments and biological modification of insect life? If you know about the corruption taking place in the scientific medical journal industry, it provides no legitimacy at all. Using the search term “mosquitoes” on The Sons of Liberty Media website produces a plethora of articles by contributors outlining the genetic modification of mosquitoes for various purposes.

The story highlights a 2010 study that actually altered mosquito saliva to deliver leishmania vaccine to mice. Leishmania is a type of parasite normally found in a specific genus of sandflies that causes illness to humans and animals.

Shigeto Yoshida, the lead researcher on a 2010 study that modified mosquitoes’ saliva such that they would deliver leishmania vaccines to mice when sucking their blood, noted that vaccination by insect was “just like a conventional vaccination but with no pain and no cost.”

“What’s more, continuous exposure to bites will maintain high levels of protective immunity, through natural boosting, for a lifetime. So the insect shifts from being a pest to being beneficial,” added Yoshida.

Despite the Japanese geneticist’s optimism, his study acknowledged that “medical safety issues and concerns about informed consent mitigate the use of the ‘flying vaccinator’ as a method to deliver vaccines.”

Robert Sinden, professor emeritus of parasite cell biology at Imperial College London, told Science at the time that in addition to vaccinating people without their informed consent, no regulatory agency would sign off on the initiative.

It’s always informed consent and medical safety issues that prevent mosquitoes from being used as a means of delivering vaccines. Moreover, it seems one professor believes regulatory agencies would not approve the initiative. One shouldn’t be so sure since millions of GMO mosquitoes were released upon populations in the united States despite citizens voicing their opposition. See here, here, and here. It was all courtesy of the US Environmental Protection Agency (EPA). And, the National Institute of Health funded research in 2022 to the University of Washington under Sean Murphy for “proof of concept” mosquito delivery of vaccine technology.

The Dutch researchers at Leiden University Medical Center (LUMC) turned to genetically modifying parasites and using mosquitoes as the vector of delivery.

In an earlier trial, the researchers tested the effectiveness of GA1, a malaria parasite genetically modified to stop developing after roughly 24 hours of infection in humans, but found that it only provided low protective efficacy against malaria. Hoping for a better outcome, the researchers crafted another parasite, GA2, to stop developing around six days following invasion in preclinical humanized mouse models.

The Bill Gates-backed Gavi, also known as the Vaccine Alliance, noted that “because the parasite dies before it infects the blood cells and evolves into its deadly phase, it instead acts as a way of priming the immune system, as a vaccination usually would.”

Afforded a test group of 43 adults between the ages of 19 and 35 who previously had no record of malaria infection, the researchers subjected subjects to 50 bites from GA2-infected mosquitoes, 50 bites from GA1-infected mosquitoes, or 50 bites from uninfected mosquitoes (placebo), in three vaccination sessions at 28-day intervals. Three weeks following their third devouring by mosquitoes, the human test subjects underwent malaria infection with five bites from infected mosquitoes.

According to the study, eight of the nine participants in the GA2 group received effective protection against the malaria infection. Only one of eight participants in the GA1 group received protection, and none of the participants in the placebo group received protection.

The Dutch researchers now seek to replicate their results in a larger human trial.

The Gates Foundation provided LUMC with $1,578,317 in grants for this “experiment”.

Who were these 43 ignorant idiots that would subject themselves to this kind of experiment? Now, these 43 individuals are walking around with who knows what floating in their bloodstream, possibly donating blood and having children. How did they modify the malaria parasite and with what? What are the unintended consequences – or intended depending on how you look at it? What medical safety issues have been identified?

From the study (page 5 of the PDF or 1917 of the NEJM):

The most common local adverse events that were considered by the investigators to be related to the trial intervention were erythema and pruritus after mosquito bites, some of which were treated with antihistamines or topical corticosteroids. In stage A, erythema was reported by 19 participants (95%) and pruritus by 17 participants (85%) (Fig. S1A and Table S1 in the Supplementary Appendix); in stage B, erythema and pruritus were reported by 23 (100%) and 22 participants (96%), respectively (Fig. S1B through S1D and Table S3). The most common systemic adverse event considered by the investigators to be related to the trial intervention was myalgia (in 4 participants [20%]) in stage A and headache (in 2 participants [9%]) during the immunization phase of stage B. Adverse events that were not considered by the investigators to be related to the trial intervention are summarized in Table S2 and Table S4. [These tables could not be located in the provided printing of the study.]

Two participants had elevated levels of troponin T (18 and 19 ng per milliliter; upper limit of the normal range, 14 ng per milliliter); the investigator assessed these elevations to be unrelated to the trial intervention. Another patient had elevated results of liver-function tests that were considered by investigator to be related to antihistamine use.

On the same page in the box at the top on the lefthand side, this little caveat appeared.

All participants were treated with a curative regimen of atovaquone–proguanil, 28 days, at the latest, after their final exposure (blue circles). [Emphasis mine.]

Atovaquone-proguanil is a combination drug sold under the brand name Malarone to treat or prevent malaria. Malarone has some serious adverse events. One is liver damage, which is sometimes indicated by elevated liver-function tests. Cardiac events such as a racing heart are possible side effects of Malarone. Interesting that two participants had elevated levels of troponin which is a preferred marker for myocardial necrosis. Nothing to worry about here per the investigators. Who knows whether this drug was used to “mask” certain adverse events of introducing genetically modified parasites via mosquito into human guinea pigs.

If these “scientists” were so confident in their mosquito vector delivery of genetically modified parasites to prevent malaria, why were all participants given a drug with serious adverse events at the conclusion of the 35-day observation period? Why not use a drug with a better safety record? Three come to mind.

Gates is close to his “dream” of releasing mosquitoes containing GMO malaria parasites onto the world – with the approval of the “scientific” academic Frankenstein morons. Gates also admits the future may be dependent on mRNA injections as well as these GMO malaria parasite-containing mosquitoes for a “malaria-free future”.

Bill Gates, the man with no college degree in anything, is buying scientists with handsome swaths of greenbacks to carry out “experiments” that would truly frighten Dr. Frankenstein and his monster. What is wrong with scientists today? That’s the million-dollar question when it comes to scientists and medical doctors. We are now living in an “anything goes” world of gruesome experiments conducted on the human race.

Friends, encourage everyone in the US and abroad to stop participating in these trials, experiments, and pseudoscience research for medications, injections, vector-delivered “vaccines”, and anything sounding like it is out of the Twilight Zone. Regulatory agencies, any international NGO, or some president of a country is not going to stop this. You can by refusing to participate. The measly amount of incentive they might offer you is not going to be enough should you experience a serious adverse event. Just ask those who were injured during the trials for the mRNA gene therapy bioweapon CONvid-1984 shot.

Article posted with permission from Sons of Liberty Media