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BREAKING: INCUBATED PFIZER C19 SHOTS SELF-ASSEMBLE INTO 3D POISONS Pfizer and Moderna incubated material revealed progressive self assembled animated worm-like entities, discs, chains, spirals, tubes, carbon nano tube filaments, ribbons, tapes, three dimensional spirals, beaded chains and right-angle structures containing other artificial entities within them. Researchers Call For An Immediate Global Ban ❤️ THE DR. JANE RUBY SHOW ❤️ https://rumble.com/v5ad4sr-incubated-pfizer-c19-self-assemble-into-3d-poison.html

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Graphene Oxide Nanoparticles are in COVID Vaccines; a new report says they are safe for humans....They are lying! Dr. Peter and Ginger Breggin SciTechDaily calls graphene oxide nanoparticles a “wonder material” that is now “verified safe” in humans by new research.1 It further declares graphene oxide is, in bold, “A revolutionary nanomaterial with huge potential to tackle multiple global challenges could be developed further without acute risk to human health, research suggests.” [Continue reading below] Imagine that—graphene oxide nanoparticles are “without acute risk to human health.” That would suggest it’s harmless in vaccines, at least in the short run. The medical-industrial-military complex seems bent on proving graphene oxide nanoparticles are safe — perhaps because critical researchers have discovered them hidden in COVID “vaccines.”2 The defenders of graphene oxide nanoparticles are handicapped in making safety claims because a motherload of research going back many years finds graphene oxide and nanoparticles in general are harmful to multiple body organs, to cells, and even to life itself across a spectrum of species. The actual research study3 that supposedly proved the safety of inhaled graphene oxide nanoparticles was published in Nature Nanotechnology in 2024. It reports and dismisses the importance of their own findings: That the blood of the volunteers who inhaled graphene nanoparticles consistently caused clotting (thrombosis) when passed through arteries removed from people with pre-existing heart disease. Here is what the research scientists themselves conclude: The magnitude of the greater thrombogenicity after GO [graphene oxide nanoparticles] exposure was relatively mild and would be potentially of limited consequence, even in patients with pre-existing heart disease. Nevertheless, we recommend that characterization of the thrombogenic potential is included in experimental models used to develop risk assessments for graphene materials that may be of higher risk, or to consider higher exposure scenarios. [Emphasis added] The authors have no right to draw such benign conclusions, declaring that it would be safe “even in patients with pre-existing heart disease.” As noted above, the danger signs came from testing the blood of the volunteers who had inhaled graphene oxide on cardiac arteries taken from patients with heart disease. The conclusion should be that it is especially dangerous in patients with pre-existing heart disease. Given the surfacing of this risk in a very small study of humans, no further human studies and no commercial use of inhaled graphene nanoparticles should be allowed until further animal studies investigate this risk. To add to these concerns, thrombosis is one of the tragic outcomes of the COVID genetic jabs, which release graphene oxide nanoparticles into the cells and the blood along with the genetic material. The corruption of science today makes science entirely unreliable, in this case, whether we are reading a commentary in a science magazine or the research study itself. Summarizing the Limits of the Study Ironically, the study is largely worthless except as a warning about the potential clotting dangers of graphene oxide nanoparticles: (1) The study involved only 14 health volunteers, making it virtually useless as a proof of its general safety It takes not 14, but hundreds and preferably thousands of subjects to evaluate the safety of a potentially dangerous substance, already unleashed on the public. Nonetheless, the clotting problem was found in a statically significant number of the 14 volunteers, which make it an especially alarming and valid signal that should produce fears instead of optimism. (2) The authors boast that this is the first respiratory study of its kind, and yet they leap to dangerous conclusions about the safety of the graphene oxide nanoparticles. (3) The authors admit that their graphene oxide nanoparticles are far more “clean” or “pure” than those in commercial use, which makes the study less relevant to real-life use. (4) The authors largely ignore the vast existing literature on harm caused by graphene oxide nanoparticles and nanoparticles in general to living things, including mammals. Earlier Research Warns of Dangers A 2016 review of “graphene-family nanomaterials” (GFN) with 240 scientific citations came to ominous conclusions about their safety, citing numerous mechanisms of harm:4 This review collects studies on the toxic effects of GFNs in several organs and cell models. We also point out that various factors determine the toxicity of GFNs… In addition, several typical mechanisms underlying GFN toxicity have been revealed, for instance, physical destruction, oxidative stress, DNA damage, inflammatory response, apoptosis, autophagy, and necrosis. … and oxidative stress plays a crucial role in these pathways. They note that lung studies are comparatively more available and have threatening results: In conclusion, the lung injury induced by GFNs has been studied in several studies, the results of which have demonstrated inflammatory cell infiltration, pulmonary edema and granuloma formation in the lungs. They also note that the dangers of graphene oxide have not been as well studied in other organs: However, only a few specific studies have evaluated in other organs, such as the liver, spleen, and kidney, and the injury symptoms… nor have the related behavioural manifestations been studied. The developmental toxicity of GFNs may induce structural abnormalities, growth retardation, behavioural and functional abnormalities, and even death. … However, based on studies of other nanomaterials toxicity, long-term GFNs exposure may be an important factor harming health [3 citations]. Therefore, the long-term study of GFNs is necessary. A September 2022 in-depth review of the literature on the toxicity of graphene oxide (GO) concluded:5 One feature that needs more attention is toxicity; it was discovered that the concentration of GO affects whether or not it is physiologically harmful, which restricts its use in the field of medicine. It has been found that there are a lot of animal species for which GO showed some cytotoxic nature. This is one of the aspects that needs more study. GO can be functionalized quite easily. Therefore, there is a need for more research to find ways to reduce its toxicity. A 2024 study reviewed the toxic effect of all kinds of nanoparticles. Using nematodes as an animal model, they found that aging is a serious consequence.6 Graphene and other nanoparticles enter into the cells of the body and can do harm in a wide variety of barely studied mechanisms. More specifically, studies have already documented that graphene oxide and graphene oxide nanoparticles are potentially highly dangerous to humans. Summary and Conclusion The research study we discussed that used 14 volunteers subjected to inhaled graphene oxide nanoparticles actually gives very serious warnings about increased blood clotting but the announcement of the article and the article itself claim to demonstrate the safety of graphene oxide. Meanwhile graphene oxide nanoparticles are being found throughout our environment and, thanks to the COVID genetic vaccines,7,8 in our cells and in our blood stream. Implications for COVID Vaccines Concerning the COVID genetic “vaccines,” for many additional reasons they should have been stopped within days of their release. Indeed, the Johnson and Johnson vaccine was withdrawn from the U.S. because of 9 deaths due to thrombosis,9 while the mRNA vaccines continue being promoted despite more than 18,000 reports of deaths to the CDC and FDA’s VAERS reporting system as of January 26, 2024.10 As we document in our book, COVID-19 and the Global Predators, the government backed the Moderna and Pfizer deadly injections because they were picked as far back as 2010 by Bill Gates as his favorite “vaccine” investments. Potentially hundreds of other vaccines were put out of business by the government picking Gates’ preferences. No one should take these genetic vaccines. And in general, all of us need to be alert and concerned that we are being inundated with nanoparticles and nanotechnology with potentially grave consequences, now and in the foreseeable future. Primary author Peter R. Breggin MD References: 1 https://scitechdaily.com/wonder-material-graphene-verified-safe-in-groundbreaking-human-study/ 2 Here is the actual Pfizer document that mentions graphene oxide on page 7: 125742_S1_M4_4.2.1-vr-vtr-10741.pdf (phmpt.org). Here is an article discussing it: FDA confirms Graphene Oxide is in the Covid-19 Vaccines | Principia Scientific Intl. (principia-scientific.com). One scientist has identified it in all 4 vaccines: Dr. Robert Young Finds Graphene Oxide in All Four Vaccines and Other Disturbing Ingredients | The Liberty Beacon. Also see: https://d6scj24zvfbbo.cloudfront.net/f70819d756ae5bccc8a997b74aa0253a/200000404-ccb3dccb40/Dr-CAMPRA_DETECTS_GRAPHENE_IN_COVID19_VACCINES.%20NotOnTheBeeb.co.uk.pdf?ph=995abaf71c 3 Andrews, J.P.M., Joshi, S.S., Tzolos, E. et al. First-in-human controlled inhalation of thin graphene oxide nanosheets to study acute cardiorespiratory responses. Nat. Nanotechnology. (2024). https://doi.org/10.1038/s41565-023-01572-3. First-in-human controlled inhalation of thin graphene oxide nanosheets to study acute cardiorespiratory responses | Nature Nanotechnology 4 Ou, L., Song, B., Liang, H. et al. Toxicity of graphene-family nanoparticles: a general review of the origins and mechanisms. Part Fibre Toxicol 13, 57 (2016). https://doi.org/10.1186/s12989-016-0168-y https://www.sciencedirect.com/science/article/abs/pii/S0013935124000100 5 Yadav S, Singh Raman AP, et al. An Update on Graphene Oxide: Applications and Toxicity. ACS Omega. 2022 Sep 28;7(40):35387-35445. doi: 10.1021/acsomega.2c03171. PMID: 36249372; PMCID: PMC9558614. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558614/ 6 Evaluating the adverse effects and mechanisms of nanomaterial exposure on longevity of C. elegans: A literature meta-analysis and bioinformatics analysis of multi-transcriptome data – ScienceDirect 7 BREAKING: FDA confirms Graphene Oxide is in the mRNA COVID-19 Vaccines after being forced to publish Confidential Pfizer Documents by order of the US Federal Court – The Expose (expose-news.com) 8 Graphene oxide as novel vaccine adjuvant – ScienceDirect 9 FDA puts the brakes on J&J vaccine after 9th clotting death reported | Ars Technica 10 COVID Vaccine Data – OpenVAERS https://substack.com/home/post/p-142282349

Make Meat Great Again! Don’t Let The Globalists Pull This Off Corey Lynn It’s 2023, and most people are scurrying about their days making plans for the Holidays and figuring out whether to serve up a roast, a turkey or a ham. Meanwhile, over 70,000 clowns are toasting champagne at their 5 star hotels in Dubai while thinking they can tell people whether or not a roast, a turkey, or a ham is allowed. While flying around in their private jets, they giggle as they cook up their conspiracy theory on “climate change” to convince people to eat less meat. While they’re dancing with politicians and coercing nations to set new policies and regulations to harm the productivity of farmers and ranchers – our food source – people should be supporting them and stand together in defiance of this nonsense. The funny thing is, while these clowns conspire and celebrate their narrative to save the planet, in part by the absurdity of reducing meat consumption, many of these same clowns are supporters of Merck and were pushing for a vote at Codex to inject cattle, pigs, and poultry with Merck’s toxic steroid-like drug zilpaterol hydrochloride to produce more muscle and less fat. This of course brings a fortune to Merck, while benefiting the bottom line for ranchers who are ok with poisoning their livestock and humans. How’s that for an oxymoron? That’s right, on November 28th, while the clowns sipped champagne on their private jets headed to the COP28 in Dubai to “save the world from climate change” and instruct nations to reduce meat consumption, their counterparts were at FAO headquarters in Rome, Italy, voting to approve this poison. So the question is – do they want to reduce meat consumption or do they want to muscle up the meat and make it more desirable to eat so people devour toxins? Perhaps it’s both. Who can keep track anymore? The cocktails are endless, from GMOs to hormones, antibiotics, DNA and mRNA, or growing meat in a petri dish or 3D printing it. These globalists want to make it so inedible, no one will want to consume meat. According to Scott Tips, President of The National Health Federation, who attends these Codex meetings to fight for the safety of consumers, this is all about money, and by adopting the Codex standard zilpaterol can “flood the world markets unobstructed.” This would allow Merck to force all of the countries who voted against it to open their markets to zilpaterol-tainted meat as well. Most of the western hemisphere has already been using zilpaterol despite the fact that there has never been a risk assessment done, it’s banned from use in horses because it’s not safe, and Merck actually withdrew it from the market in 2015 before working its way back in. At that time, under Merck’s brand name “Zilmax,” even Cargill and Tyson suspended their purchases of Zilmax-fed cattle in North America. The many-years-long battle against the toxic vet drug came to an end when the Commission voted 88-49 with 11 abstentions to approve zilpaterol MRLs (maximum residue levels). Scott Tips reported that those “speaking against the standard were the European Union, Switzerland, Norway, Russia, Kazakhstan, Turkey, China, Thailand, Saudi Arabia, Qatar, Iran, Iraq, UAE, Algeria, Belarus, Syria, Tunisia, North Macedonia, and Cameroon. Those pushing the standard were the United States, Canada, New Zealand, many African states, and every single one of the Western-hemisphere countries. The UK remained strangely aloof, as if wishing to avoid offending anyone.” Back in the U.S., Rep. Thomas Massie (R-KY) has been trying to get the PRIME Act passed for nearly 6 years, but feels he is beginning to make headway now. If passed, the PRIME Act will make it much easier for local farms to compete with the handful of big meat companies, by allowing safe, local processing options rather than a farmer having to travel for hours to a USDA-inspected processing facility. According to Rep. Massie, “Current law exempts custom slaughter of animals from federal inspection regulations, but only if the meat is slaughtered for personal, household, guest, and employee use (21 U.S.C. § 623(a)). This means that in order to sell individual cuts of locally raised meats to consumers, farmers and ranchers must first send their animals to one of a limited number of USDA-inspected slaughterhouses. These USDA-inspected slaughterhouses are sometimes hundreds of miles away from farms and ranches, adding substantial transportation costs and increasing the chances of locally raised meat co-mingling with industrially-produced meat. The PRIME Act would expand the current custom exemption and allow small farms, ranches, and slaughterhouses to thrive.” While the battle on meat continues, it’s important for everyone to do their due diligence when it comes to shopping for and purchasing meat. According to the USDA, in March they released a proposed rule with new regulatory requirements on those voluntary “Product of USA” labels, whereby the claim can only be used on meat, poultry and egg products if they are derived from animals that are born, raised, slaughtered and processed in the USA. So pay attention to the labels – on all food for that matter. There are some small farms that offer co-ops whereby several people can go in on the ownership of cattle and split the beef. There are also a handful of companies who ship bundles of beef. In either case, it’s always important to confirm how the cattle are raised and processed, and if they are given zilpaterol, antibiotics, hormones, or mRNA. Always support your local farmers, whether it be for meat, vegetables, fruit, raw milk, or other items. They are quite literally our key to survival, unless of course you are able to grow enough food and raise livestock to support your entire family on an annual basis. They deserve our support and respect. Corey’s Digs has done extensive research on an incredible, fully vertically integrated large ranching operation in the U.S. who controls their entire supply chain. It’s quite impressive. The cattle are all pasture raised on over 290,000 combined acres by their own mothers. This is a premium lineage of all Prime and High Choice, with the processing facility being right on the ranch, and the beef is aged for 21 days before shipping. Never ever zilpaterol, antibiotics, hormones, mRNA, or vaccines. They ship a variety of bundles monthly or every other month, along with individual added cuts, straight from the ranch to a customer’s home. The biggest difference is the taste – it’s amazing how delicious Prime beef is without all those toxins. The beef is exclusive to members through Shopping Club Freedom, which boasts hundreds of non toxic products that everyone uses in their daily lives, all of which are patented and produced by this same company right here in the U.S. It’s one heck of a solution to ensure access to healthy products and beef while sticking it to the globalists who want to rule everyone’s life, which is why Corey’s Digs has partnered with them and has been shopping there for over two years now. No one should let these madmen make choices for them or their families. Everyone should support U.S. farmers and ranchers, get behind Rep. Massie’s PRIME Act, and don’t buy the poison these globalists are selling. MAKE MEAT GREAT AGAIN! Subscribe to Corey’s Digs so you don’t miss a Dig! https://www.coreysdigs.com/food-supply-chain/make-meat-great-again-dont-let-the-globalists-pull-this-off/

Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero April 23, 2022 by Dr. Ariyana Love By Dr. Ariyana Love, N.D. In a recent interview with Maria Zeee on Zeee Media, I discussed another very troubling discovery about the mRNA bioweapons technology. Maria Zeee asked me to shed more light on the Doherty Institutes involvement with the US biolabs in Ukraine. Russian reports revealed that 350 cryocontainers with blood serum samples were transferred from the Public Health Centre of the Ministry of Health of Ukraine to a reference laboratory for infectious diseases at the Doherty Institute in Australia. Under the guise of tackling Placental Malaria, the Doherty Institute has been directly involved in research using insects such as mosquitos and tics as bioweapons carriers. The Doherty Institute also developed a “vaccine” that uses a parasite to target the placenta of pregnant women to abort their babies in utero, under the pretext of “antibody research”. During the testing of this novel technology, mosquitos were developed as carriers of a genetically attenuated parasite called the P. falciparum which is the most deadly of the 5 Malaria causing parasites. The World Health Organization (WHO) and the U.S. Government were also directly involved in this research to “immunize” via mosquito bite using radiation-attenuated Sporozoites. In May of 2021, a Bill Gates-funded firm in the wild. Clinical trials conducted by the WHO in 2020, used 11 human volunteers who were “immunized” with more than 1000 bites by irradiated mosquitos infected by Sporozoites (Spz) from the P. falciparum NF54 strain or 3D7/NF54 clone. The female Anopheles mosquito inject a minimum of Sporozoites (Spz) (~ 100) during its bite. It was tested on adolescents, children and infants aged 6 months old. 1 out of the 6 volunteers developed parasitaemia 12 days after exposure. Parasitaemia means parasites in the blood. The parasite “vaccines” use radiation-attenuated Sporozoite, administered under drug coverage. Genetically-attenuated Sporozoite “vaccines” and recombinant protein “vaccines” (RTS,S and R21) and recombinant viral vectors “vaccines” (Chad63 MVA ME-TRAP, CSVAC, ChAd63 METRAP and MVA METRAP with the matrix-M adjuvant) are all used. Sporozoite recombinant proteins, DNA or viral vectored protein fragments (mRNA) and attenuated Sporozoite “vaccines” induce malaria reactive CD4+ and CD8+ T-lymphocyte counts. Radiation-attenuated Sporozoite (RAS), genetically-attenuated parasite (GAP) and Sporozoite are administered under drug coverage, according to the WHO study. Here’s another WHO study from 2021. By 2021, they had a P. falciparum Sporozoite (PfSPZ) “vaccine” as the main candidate containing live, radiation-attenuated, whole, aseptic and metabolically active Sporozoite which have been isolated from the salivary glands of mosquitos infected by P. falciparum. They tested their novel “vaccine” on infants in Kenya. Another study conducted by the NIAID in 2022, used Malian children 6-10 years old and injected them with three doses of the PfSpz “vaccine” to induce an “infection” by “parasitic disease” of a “vector borne disease” using the P. falciparum. Another study in 2021 carried out by the U.S. Government, experimented on 336 infants aged 5-12 months, in Kenya, inoculating them with the P. falciparum “vaccine”. This is not in fact a “vaccine” but a weapons system for the murder of babies in utero and this is a bioweapon which is transmissible to others, according to the WHO research. In addition, the WHO’s P. falciparum research helped in the development of monoclonal antibodies. In fact, the P. falciparum parasite is a critical component in the monoclonal antibodies bioweapon system. Please also see: Monoclonal Antibodies Is Experimental Gene Therapy – Patent Review PATENT The PRIMVAC “vaccine” candidate was in government trials in 2016. By 2020, the PRIMVAC “vaccine” adjuvanted with Alhydrogel was in clinical trials. The Alhydrogel patent shows unsafe levels of aluminum and other heavy metals. A VAR2CSA plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) patent for a synthetic protein was registered in December, 2014. The VAR2CSA “vaccine” is owned by the U.S. Government. The CDC is also involved in this VAR2CSA bioweapons development. STERILIZATION OF THE NATIONS Children’s Health Defence reported in August that the Covid-19 injections are dangerous for mothers and babies. According to former Chief Scientist of Pfizer, Dr. Mike Yeadon, the injected ingredients is building up in the ovaries and attacking the placenta of pregnant women. A preliminary findings of mRNA Covid-19 vaccine safety in pregnant persons found that 4 out of 5 pregnant women are loosing their unborn baby to spontaneous abortions. A recent report released in March of this year, shows that fetal deaths due to “covid vaccines” are almost 2,000% greater than deaths associated with other vaccines. Below are a few highlights from the WHO study Plasmodium falciparum pre-erythrocytic stage vaccine development that I want to draw your attention to. RECOMBINANT VIRAL VECTOR “VACCINES” “Viral vectors represent promising tools for vaccine development, because they enable intracellular antigens to be expressed by increasing the ability to generate robust cytotoxic T-lymphocyte responses and proinflammatory interferon and cytokine production without the need for an adjuvant. However, there is great concern regarding their genotoxicity due to possible viral genome integration; this has led to many efforts aimed at finding a high level of safety and efficacy.” “Several viral, bacterial, and parasite vectors have been used in anti-malarial vaccine candidates; currently, many clinical trials are exploring their advantages to increase their potential and accelerate their use in vaccines.” CHAD63 MVA ME-TRAP “This anti-malarial vaccine was developed using chimpanzee adenovirus 63 (Chad63) and modified Vaccinia virus Ankara (MVA) into which were inserted genes encoding the thrombospondin-related adhesion protein (TRAP) multiple epitope (ME) chain.” “The ME-TRAP hybrid is thus a 2398 base pair (bp) insert encoding a single 789 aa-long peptide, covering the complete P. falciparum TRAP sequence, fused to a chain of 20 malaria T- and B-cell epitopes (14 targeting MHC class I, 3 MHC class II and 1 murine).” PCR “A trial involving adults in Senegal to assess vaccine efficacy using a polymerase chain reaction (PCR) assay was able to detect > 10 parasites/μl blood. PCR was positive for 12 out of 57 participants vaccinated with ChAd63 ME-TRAP with a booster dose of MVA ME-TRAP and 13 out of 58 control patients who received an anti-rabies vaccine were positive by PCR, giving 8% efficacy (which was not statistically significant). They thus grouped the results with the 67% efficacy obtained in a study in Kenya and, using Cox regression, showed 50% overall vaccine efficacy in both populations.” CSVAC “CSVAC, a vaccine from Chad63 and MVA to encode the P. falciparum CS protein, continued such line of research into plasmid DNA anti-malarial vaccines; the CS insert was a codon-optimized cDNA encoding the CS protein truncated at the C-terminal extreme thereby lacking 14 C-terminal aa and thus omitting the GPI anchor.” FUTURE DIRECTIONS “Nanovaccinology” with Self-Assembling Protein Nanoparticles (SAPNs)… The next major challenge concerns the host’s genetic variability and parasite proteins’ interaction with the human immune system.” “The choice of antigen to be used is quite complicated due to factors such as the parasite’s complex life-cycle involving two reproduction cycles (sexual and asexual), different development stages and two hosts (the Anopheles mosquito and human beings). All this can be added to the multiple invasion routes described so far for each of its target cells (hepatocytes and/or erythrocytes), the parasite’s ability to modify its gene expression and the genetic variability between P. falciparum circulating strains.” “The next major challenge concerns the host’s genetic variability, particularly major histocompatibility class II (MHCII) complex molecules exerting their mechanism by synthesizing proteins encoded by the HLA-DR regions β1*, β3*, β4* and β5* where the HLA-DR β1* region encodes more than 1500 genetic variants grouped into 16 allele families called HLA-DRβ1*01, *03, *04, *07, etc. Parasite proteins’ interaction with the human immune system should be analysed by predicting B and T epitopes (using NetMHCIIpan 3.2 or other predictors).” UPDATE: 6/6/2022 Please see: Pfizer’s mRNA Vaccine Goes Into Liver Cells and Is Converted to DNA: Study https://ambassadorlove.blog/2022/04/23/malaria-parasites-in-vaccines-target-placenta-kill-babies-in-utero/

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