“I am a natural doctor. I have about 1,600 patients, many are vaccinated, just to give you a little backstory about my credibility.
“What I’ve seen so far is all information from physicians, medical physicians, natural physicians and also immunization and virology doctors, things like that and then, also nurses.
“So, what I’m about to share with you is the first vaxxine, the second vaxxine and then the boosters and what it does to you.
“The first vaxxine, as it goes into your body has a small amount of saline and a bunch of ingredients that are very catastrophic to your cellular system.
“What that does to your immune system, which is your deep bone marrow, your thymus gland, your spleen and all other systems associated with your immune system, it decreases your ability to produce white blood cells by 50% from your first vaxxine.
“Then, 8 weeks later, which is white blood cell reproductive system, so your ability to make another generation of white blood cells is 8 weeks, that’s why they set it up 8 weeks later, to hit it again. So, you hit the white blood cell ability while it’s down.
“So now what they do is they decrease the saline in the second one and they increase the harmful ingredients, so now you have a shift in the ingredients…
“And then, what they do is there is a second dose attacks your ability to make white blood cells by an additional 25%.
“So now, you only have the ability to make white blood cells functioning at 25%. So you just wiped out 75% of your military and the ability to make that military.
“Then what they do is they set in the booster. The booster has 81 strands of foreign bacteria that your cells have never come across. You don’t have the antibodies to fight it. You only have 25% of your white blood cell production to be able to fight it, so it’s a losing battle.
“So then what starts to happen is you start to get chronic inflammation that goes to the areas that you had predisposition. So if you are someone with gut health issues, that’s your area that this is going to focus on and you’re going to have inflammation in the gut health.
“If you have tumors or a cancer or if you have, say endometriosis or you have a skin condition, whatever that is, it’s going to inflame that area, because now the body has hit the parasympathetic nervous system, which is the fight or flight and your body is in a chronic inflammatory state with a low immunity and a low immune response.
“Then, you get your second booster. What the second booster has is it has 8 strands of HIV and now, what that does is it completely shuts off your ability to make white blood cells and if you Google what disease it is, it is HIV.
“So now, we have people walking around with no immune system, no ability to make an immune system, 81 strands of foreign bacteria and then, 8 strands of foreign HIV, along with all the other harmful ingredients, and then they remove all the saline from the first and second booster.
“Now, to make matters worse, during this process, 20-30% of the population is going to die, every single series of this process. There’s four series.
“They have 3 more boosters that are coming out and the reason why is because once they’ve made you so that your immune system can’t make white blood cells anymore, you become dependent on the boosters to survive, just like how someone’s life becomes dependent on insulin.
“Big Pharma is looking for people that either die off…for population control and then, those that don’t die off, they will have recurring customers for life, with the boosters so that they have to maintain income and collect the money back from all the funding that they put in to make these vaxxines in the first place.
“So, I hope that was helpful, I hope that you listened to this properly and I hope that you take the time to do your own critical thinking and just give it two to three years.
“Every single animal that participated in this study for any of these vaxxines had a 100% death rate and I encourage you all to just take a moment and look around you and just wait it out.
“And let’s just see, let Nature take it course and let’s just see what happens. Thank you.”
Former Pfizer employee Karen Kingston blew the whistle on Stew Peters Show last month, revealing that the Covid vaxxines are intentionally inducing AIDS and Anthony Facui is profiting from this Democide.
Stockholm University just released a scientific horror. The “spike” protein in the Covid-19 “vaccines” are penetrating the cells of the vaccinated, reaching the cell nuclei, and impairing your cell’s ability to repair damaged DNA.
Pharmaceutical “vaccines” are silencing the genes responsible for DNA repair and deleting them forever in humans.
Johnson & Johnson uses Adenovirus 26 (Ad26) in its vaxxine. J&J openly admits that their Ad26 vector “codes your cells to produce a spike protein”but they don’t tell you they’re also deleting your genes.
The U.S. patent #20140017278 for Adenovirus 26 and 35 Filovirus, openly states that it codes your cells with the Ebola and Marburg chimeric proteins.
“The filovirus antigenic protein is usually a glycoprotein from an Ebola virus or a Marburg virus.”
The J&J Adenovirus 26 vector deletes your E1 gene. The patent also states that it deletes the E1 gene in Humans. This is known as the X Chromosome. The E1 gene is required for accurate and instant repair of damaged DNA. Deletion of this gene is lethal.
E1 gene deletion causes embryonic lethality which means permanent sterility for men and women. It causes Lactic Acidosis in children which is the lack of oxygen in the blood. E1 gene deletion causes rapid cancer growth, Thrombosis, and the coagulation of the blood which leads to clotting. Blood clotting is the main reason people are dying from the Covid vaxxines.
E1 gene deletion causes Mitochondrial DNA-Associated Syndrome which is a process of glucose metabolism deficiency that exists in various diseases such as Alzheimer’s, epilepsy, diabetes-associated cognitive decline, and severe neurological disorders such as Leigh’s Syndrome. There’s a progressive loss of mental cognition and typically results in death within two or three years, usually due to respiratory failure.
You can order the chimeric messenger RNA of the Lentivirus and the Adenovirus 5 vectors or Baculoviridae online from Thermo Fischer, for recombinant cross-species genomics (cloning).
Thermo Fischer explains how the Adenovirus 5targets andentersthebronchial epithelial cells(lungs) and deletes the E3 and E4 genes, intentionally inducing Sjögren’ssyndrome which is long-term autoimmunity (AIDS).
Loss of your E4 gene deletes your cognitive function. Deletion of your E3 gene degenerates your brain, causes dementia, gradual loss of memory, judgment, and the overall ability to function.
The knockout of these genes affects the moisture-producing glands of your body. It’s not the “spike protein” that’s causing the blood of the vaxxed to coagulate, it’s the gene silencing (deletion). Without moisture, your blood coagulates and clots. The deletion of these genes also causes gastrointestinal disorders.
Adenovirus 5 also alters the cell signaling pathways and leads to Lymphoma due to destruction to the immune system. This causes cancers to grow and the blood to coagulate.
This is proof positive they’re creating the next “pandemic” with lethal injections that will gradually induce AIDS in the inoculated masses through gene deletion.
The pharmaceutical cartel has not only injected Ebola and Marburg into people but they’re alsotransfecting people’s cells with these catastrophic chimeric pathogens. The vaxxed will battle chronic infections and lifelong disabilities while the cells of the vaxxed continuously replicate with the synthetic genetic sequences of Ebola and Marburg until it kills them unless they detoxify continuously.
The immune system of the vaxxed is depreciating 5% each week according to a recent UK Government study. Everyone who vaxxed age 30 and above, will have no immunity left by Christmas. But that’s not all.
As the cells of the vaxxed replicate Ebola and Marburg “spike proteins” and their cells decay and die, they will shed the chimeric disease throughout the population via transmission. Therefore it’s crucial for the unvaxxed to continuously detoxify as well.
According to a UK government declaration from the NIH, we are presently in a Phase III clinical trial on Humans using the Adenovirus 5 vector to “fight Covid-19” which began on January 22, 2021.
“This is a global phase III clinical trial to evaluate efficacy, safety, immuogenicity of Ad5-nCoV manufactured by Cansino and Beijing Institute of Biotechnology in health adults aged 18 years old and above.”
So the UK Government is partners with the Chinese Communist Party (CCP) to exterminate Humans.
The World Health Organization (WHO) also published on their website that we are in an Ebola Vaccine Stage III Clinical Trial.
WHO published that we are in an Ebola Vaccine Stage III Clinical Trial
Viruses are still anunproven theory. Given the advances in scientific lab equipment and considering that we’re able to observe nanotechnology under microscopy and spectroscopy, would somebody please explain to me why we still can’t identify a virus? Could Germ Theory be the big pharmacopeia lie in modern medicine and Terrain Theorybe the more relevant truth?
Governments enhanced the airborne transmissibility in mammals (Humans) of highly virulent avian influenza strains. The history of making pathogens transmissible goes back at least to the synthesis of viable influenza H1N1from 1918. Incidentally, the 2009 swine flu Pandemicwas also induced by inoculation using the H1N1 vaxxine. So this is nothing new under the sun.
Sinister shadow governments have been weaponizing nature, producing diseases through vaxxine injection and genetically manipulating Humans for at least the past 100 years. But where did they get this technology to do it?
The U.S. National Library of Medicine revealed something rather interesting. The USSR’s ‘invisible anthrax’ is a Gain-of-Function bioweapon created by introducing an “alien gene“ into Bacillus anthracis (bacteria). That’s how they made Anthrax. They used an alien gene and genetically altered bacterial immunological properties to produce a deadly pathogen to Humans. Where did they get an alien gene from? A UFO crash perhaps? Negotiations with other beings? Your guess is as good as mine.
The U.S. Government has been testing this germ warfare technology on its own military troops since the 1950s, using Adenovirus 4, Ad5, and Ad7 vectors with HIV encoding Envelope (clade C.1086). The Ad7 vector delivered in enteric capsules has been used to“vaccinate” U.S. military personnel “against respiratory and gastrointestinal illness”, since the 1970s.
Monkeypox is also made from the same bacterial pathogens as Ebola and Marburg. Ebola and Marburg can kill nine out of ten people it infects. Although this is not really an infection, it’s transfection (human cloning).
Ebola and Marburgcause hemorrhagic fevers (VHF). They simultaneously affect multiple organ systems in the body and may be accompanied by hemorrhage, or bleeding. These pathogens cause high fever, chills, muscle aches, and vomiting. The patients worsen rapidly until they bleed from every orifice in their body, including needle puncture wounds. They usually die within 1-3 days.
Bill and Melinda Gates say on their Gavi website to expect the next pandemic to be a Marburg outbreak. These two psychics or psychos also claim that Ebola and Marburg are carried by African Green Monkeys.
Thelying CDC claimsthat people can get “Ebola Virus disease” through direct contact with an infected animal (bat or nonhuman primate). They’re taking the absolute piss out of us! Never in the history of medicine has an animal disease infected Humans! The only possible way to make a Human diseased with an animal disease is through cross-species genomics using Adenvirus or mRNA and Nanotechnology.
Polio vaccines used in the late 1950s and early 1960s were intentionally contaminated with a bacterial pathogen called the “Simian Virus” 40 (SV40) present in monkey kidney cells. The Simian Virus is used for infecting Humans.It was “accidentally administered to Humans” through Polio vaxxines.
The “Vaccinia virus” is similar to the “smallpox virus” but it’s not naturally occurring after all. Scientific Direct reported that “vaccinee-to-cattle and cattle-to-human Transmissions occurred on Farms”, proving the transmission of pathogens between animal to human species is being done by genetic engineering and administered through vaxxines.
Knocking out the E1 and E3 genes is necessary when transfecting cross-species in order to make the pathogen replicate. The Vaccinia pathogen has been used on a wide scale to produce many different kinds of chimeric proteins, including HIV-1 and it encodes approximately 250 genes.
Ebola and Marburg are GAIN-and-Loss-of-Function bioweapons and both are created using the “Green Monkey disease“, a chimeric pathogen that you can purchase online!
Adenovirus’ are from human/monkey clone origin and are used with chimeric Lentiviruses, as well as the Filoviruses. Of course, none of these are actual viruses! All the Adenoviruses and messenger RNA (mRNA) are chimeric weapons used to code your cells to reproduce deadly proteins used to both silence genes and program artificial genetic sequences. They are inducing diseases and making up disease names and syndromes to hide the fact that it’s coming from vaxxines!
Ebola, Marburg, and Monkeypox are Gain-of-Function bioweapons created using the “Green Monkey disease”. It’s an Adenovirus made from E. coli bacteria from the decaying flesh of a human/monkey hybrid’s kidney tissue culture. Adenovirus vectors transfect Humans withmonkey DNA, Ebola, and HIV. Adenovirus vectors are transfecting humans with monkey DNA and Human DNA from a Chimpanzee/Human clone to be exact.
There are 49 immunologically distinct types of adenovirus that can cause infection for long-term gene expression. They’re made with Sialic acid which is a group of derivatives of Neuraminic Acid found in animal tissues. Sialic acid is the primary entry receptor used in Adenovirus.
Sialic Acid is an animal DNA from “Species D” Adenovirus which is used in both Adenovirus 5 and Adenovirus 26 (Sinovac and J&J) to transfect Ebola and HIV into Human cells using Sialic acid-bearing glycans (animal DNA) as a primary cell entry receptor. Adenovirus 5 is of“Chimpanzee origin”. There’s that Green Monkey clone again!
Sialic acid proliferates tumor growth and metastases. N-acetylneuraminic acid (Neu5Ac) is made from E. coli bacteria. See the study’s here and here.
Polio vaxxines used in the late 1950s and early 1960s were “contaminated with a virus” or rather a bacterial pathogen called the Simian Virus 40 (SV40) which is present in monkey kidney cells used to grow the vaxxine.
The Pharma death cult is inducing diseases with their vaxxine racket and making up names and syndromes that they can then profit from by “treating” later when people become diseased. What would life be like without the Pharma cartel disabling our children and killing healthy people in the name of science and medicine?
There are no viruses involved in the making of any of the mRNA or Adenovirus vaxxines, only GAIN-and Loss-of-Function chimeric pathogens made from bacteria and other plasmids which Pharma keeps naming “viruses”.
There’s no “spike” from a virus particle being used in any of these vaxxine induced diseases. We should change our language from “spike protein” which is a half-truth with a half-lie and replace it with “chimeric protein” to be medically accurate because that’s what we’re dealing with.
E. coli bacteria are used as the base for all these chimeric diseases because bacteria DNA replicates. They’re also using other plasmids and mixing fungus, yeasts, and “several mammal-based systems” (Human/Chimpanzee clone), then genetically enhancing them to increase lethality.
They’re also using baculovirus-mediated insect cell expression. This means the Pharma cult is transfecting human cells with insect DNA. This could explain the strange mutations and Morgellons.
Marburg issimply Ebolawith Ricinadded to make it more lethal. Both cause hemorrhagic fevers (VHF) and attack multiple organ systems in the body, accompanied by bleeding.
The Pharma death cartel and the Eugenicists already have a PCR kit for “testing” for Marburg disease and a vaxxine to immunize against, called RiVax. The main component of RiVax is “a genetically altered version of a Ricin Toxin.” Ricin is more toxic than Graphene Oxide, by the way.
I think it’s high time people stop trusting our governments, stop relying on government and take our children out of public schools, as Dr. Zev Zelenko said to Alex Jones on Info Wars. Don’t sacrifice your kids to Satan.
My detox protocol works for the vaxxed and the unvaxxed to kill the Micro-plasmids (parasites, transgenic Hydra’s and bacteria) and reverse the coagulation cascade which leads to blood clots.
