Genetic manipulation of humans: Jeff Rense and Jon Rappoport

by Jon Rappoport

February 22, 2017

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(Update: Part-1 here, Part-2 here)

Listen to a brand new conversation between Jeff Rense and Jon Rappoport, on the subject of new vaccines that will permanently change the DNA of humans. This is vital information.

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

24 comments on “Genetic manipulation of humans: Jeff Rense and Jon Rappoport

  1. robertwachsmuth says:

    Mutations going on right now , doesn’t the FDA and CDC Doctors ever come out of there Office to see what their doing to us . MURDER HEALTH CARE SYSTEM Killing My Family Dumping there Bodies . Soylent Green is Real .

  2. winkelr says:

    The RNA viral contamination has been going on for decades and it can cause permanent DNA alteration. See the book “plague”.

  3. Sue says:

    Dr. Harold Buttram discussed, in his book “Vaccinations and Immune Malfunction,” how foreign RNA and DNA from animals in the vaccines has been causing genetic alteration for quite some time. And I read that book at least 30 years ago.

  4. Thank goodness for epigenetics!

  5. Terry Adams says:

    As someone who has what they call “morgellons disease” I fear that I am one of the advanced test cases for this technology.. The things I am extracting from my body are absolutely stunning… (google “terracer’s youtube”).

  6. Michael says:

    One small imperfection in the evil plan- you forgot to blame it all on “government”.

    • Sue says:

      Oh, my dear. The globalist government is very much involved, since the monied corporate interests (and pharma is at the top, but also very much intertwined with other huge industries) are the oligarchy which is now running the world. PLEASE WAKE UP.

  7. Diogenes Shrugged says:

    Jon, you’re implying that muscle injections somehow change a person’s DNA throughout the body, including germ cells. I think you’re wrong about that. I strongly doubt these changes can be passed on to the next generation. You might want to look into that and clarify what you find. Thanks.

    • Sue says:

      Well, here are a few examples to explore:

      Unveiling the Culprit – Is Foreign DNA Contamination the ……

      “Victoria and colleagues have identified the contamination of live viral vaccines for use in healthy children, with viral nucleic acids; the findings have since been confirmed by the vaccine manufacturers and the data reported to the FDA. Contaminating nucleic acids include retroviral sequences from the producer chicken and primate cells. Specifically, Avian leucosis virus (ALV) was present as RNA in viral particles while simian retrovirus (SRV) was present as genetically defective DNA. Rotarix, an orally administered rotavirus vaccine, contained nucleic acids from porcine circovirus-1 (PCV1), virus. Since this report, a second rotavirus vaccine (RotaTeq) has been shown to contain nucleic acids from both PCV1 and PCV2, a pathogen in pigs that is associated with wasting and immunodeficiency. The circumstances in which PCV2 induces disease are discussed below.

      VRM: The Rise of Mutagenic Viruses « Vaccine Resistance …

      ‘Many novel vaccines are produced in animal cell substrates, and emerging infectious diseases may theoretically be transmitted from animals to humans through these vaccines.’ FDA
      ‘Vaccines are increasingly becoming ineffective and causing “immune dysfunction. Additionally, “vaccine antigen responses” may be reprogramming viruses (altering the DNA template of the virus – alterations in the ‘Nucleotide sequencing’ of the primary viral strain) while weakening the immune systems of the most vaccinated individuals.’

      “Virus genomes use either DNA or RNA. Examples of DNA viruses include herpes, chickenpox and smallpox – they replicate in nuclei after infiltrating host cells. RNA viruses, on the other hand, inject their RNA into host cell cytoplasm, where it is then used to synthesize proteins and form replica viruses. RNA viruses include influenza, HIV and Ebola, to name but a few.

  8. DNomer says:

    You people don’t seem to know that modern genetic engineering uses a virus to deliver the gene splice. The virus is superior to the ‘gene gun’ (which was always a joke), and is really the only feasible way to genetically alter people. The virus is a specialized carrier that can actually splice genetic material. Obviously, then your own biology will continue to replicate your new genome. This is not a joke. The Cabal considers all people to be merely biological material, anyway. Take a look at this video (you can skip to 1:15 if you like):

    • Sue says:

      “You people” ? This isn’t a contest. It is about getting to the truth. Many avenues, one answer at the end of all those roads.

    • Michael says:

      Oh you people…YOU PEOPLE!
      *Tuht* You friggin people.
      I know who you people are…your not, those people, your not even ‘WE THE PEOPLE’, your … ‘you peeple”
      U people…. you peeep hole, your pronoun wrong. *triggering*
      Your…I don’t even want to say, it salt in my mouth…*phttuee* I won’t say again….GAWD!
      This is not a joke…get with it pee-eep-paul.

    • DNomer says:

      I see that some of you wish to focus on my use of the phrase ‘you people’, but I hope you will focus on the important points. The proposed weapon discussed in the Pentagon briefing room shown in the short video that I linked is spread via an aerosol, such as an air-burst munition carrying the virus. The people would probably ‘get sick’ to a certain extent as the virus spreads inside them, but the real intent is for them to survive and carry the new DNA.

      Jon makes an important point in his discussion that a vaccine is just a mixture of viruses, and no one is testing this to see which viruses and how they operate — certainly not the CDC nor the FDA. So there is a real threat that these special gene-splicing viruses could be included in vaccines and no one would have a clue.

      My understanding, however, is that this virus-based delivery mechanism is fraught with problems, and there is no near-term threat that actual improved people would come out of it as Mr. Rense exclaims. The likelihood of messing a person up is MUCH higher than making him into Superman. Pentagon staffers would probably yawn if some Afghani peasants got somewhat sick, or even very sick from such an aerosol, if they even found out. But if a rich person got sick from some ‘treatment’ that was supposed to be really helpful, there would be much less yawning.

  9. Deborah says:

    It IS already happening. Bye, Bye Africa. Scientists created HepB->HIV->AIDS. I can’t imagine this boding well from Africa. BM Gates gave Farzan $6M, 6mo after the NYT article, to create the first Vax.

    One month before the NY Times published “Protection Without a Vaccine”, this article was published 29Feb15
    “Anti-HIV Molecule May Lead to Vaccine and Long-Acting Treatment”

    Quote: “researchers injected a NEW GENETIC THERAPY into four monkeys infected with SIV (HIV’s simian cousin.”
    -To develop the therapy, the researchers took a molecule with antibody-like properties that latches onto the CD4 receptor and connected it with a short protein fragment that attaches to the adjacent CCR5 receptor. Next, they fashioned genetic instructions for the manufacture of this fused molecule, which they named eCD4-lg, and put that code into a benign virus that was designed to integrate the instructions into human cells. The idea is to get the human body to produce the SIV-fighting molecule indefinitely. The molecule is meant to work by attaching to the CD4 and CCR5 receptors in a claw-like shape, thus blocking the virus from connecting to the immune cell, thwarting its attempts at infection from the first step. ~end
    *More on Ecd4-ig below.

    9Mar15 NYT Publishes “Protection Without a Vaccine:
    “By delivering synthetic genes into the muscles of the [experimental] monkeys, the scientists are essentially RE-ENGINEERING THE ANIMALS TO RESIST DISEASE.”
    “’The sky’s the limit,’ said MICHAEL FARZAN, an immunologist at Scripps and lead author of the new study.”
    “The first human trial based on this strategy — called immunoprophylaxis by gene transfer, or I.G.T. — is underway, AND SEVERAL NEW ONES ARE PLANNED.”
    “I.G.T. is altogether different from traditional vaccination. It is instead A FORM OF GENE THERAPY. Scientists isolate the genes that produce powerful antibodies against certain diseases and then synthesize artificial versions. The genes are placed into viruses and injected into human tissue, usually muscle.”~end

    Six months later, on 23Sep15, Michael Farzan, the immunologist quoted above, was granted $6Million by BM GATES FOUNDATION to develop a revolutionary HIV/AIDS ALTERNATIVE VAXINE

    Scripps Florida Scientists Awarded $6 Million to Develop Alternative HIV/AIDS Vaccine
    JUPITER, FL – September 23, 2015 – Scientists from the Florida campus of The Scripps Research Institute (TSRI) have been awarded up to nearly $6 million from the Bill & Melinda Gates Foundation to develop a revolutionary HIV/AIDS ALTERNATIVE VACCINE that has demonstrated great potential in animal models.

    The research, to be led by TSRI Professor Michael Farzan, will be supported by four years of funding—the first grant awarded by the Gates Foundation to a Scripps Florida scientist.

    “I’m grateful to the Gates Foundation for its strong support of our research and for its continued commitment to eradicating HIV/AIDS throughout the world,” Farzan said.

    Farzan brings an innovative approach to combating HIV. The approach works by coaxing muscle cells into producing inhibitor proteins that block key sites on the virus’s surface used to attach and invade human immune cells—fooling the virus into thinking it is binding to a human cell.

    Unable to attach to cells, and unable to reproduce, the virus simply floats impotently in the blood stream.

    Farzan and colleagues’ breakthrough research received worldwide attention when announced earlier this year in the journal Nature. When the drug candidate, called eCD4-lg, was tested in the laboratory and in animal models, the results were so powerful and universally effective that they suggested the compound’s potential to serve the role of an alternative HIV/AIDS vaccine. The drug candidate offered complete protection of animal models against the virus for up to one year.

    “Our compound eCD4-Ig is the broadest and most potent entry inhibitor described so far, effective against all strains tested,” Farzan said. “At the end of our research, we expect to have enough evidence to develop a firm foundation to fully evaluate its potential as an alternative vaccine.”

    There are approximately 35 million people living with HIV-1—more than 25 million in sub-Saharan Africa—and more than two million new infections annually.

    About The Scripps Research Institute
    The Scripps Research Institute (TSRI) is one of the world’s largest independent, not-for-profit organizations focusing on research in the biomedical sciences. TSRI is internationally recognized for its contributions to science and health, including its role in laying the foundation for new treatments for cancer, rheumatoid arthritis, hemophilia, and other diseases. An institution that evolved from the Scripps Metabolic Clinic founded by philanthropist Ellen Browning Scripps in 1924, the institute now employs more than 2,500 people on its campuses in La Jolla, CA, and Jupiter, FL, where its renowned scientists—including two Nobel laureates and 20 members of the National Academy of Science, Engineering or Medicine—work toward their next discoveries. The institute’s graduate program, which awards PhD degrees in biology and chemistry, ranks among the top ten of its kind in the nation. For more information, see

    • Deborah says:

      Who will OWN the rights to GE’d Humans?
      You can’t own a patent for something NATURE creates.
      MonSatan genetically engineered seed so they could ‘own’ those foods/seed. They don’t reproduce.
      This caused devastation in India- 250K farmers have committed suicide, due to failed corps and staggering debt. BM GATES responsible for spreading MonSatan seed to India and Africa, along with other atrocities- Vaxines, Disease Vectors (mosquitoes)…

      Monsanto is seeking patents not only on methods of breeding, but on ACTUAL BREEDING HERDS OF PIGS AS WELL AS THE OFFSPRING that result.
      “If these patents are granted, Monsanto can legally prevent breeders and farmers from breeding pigs whose characteristics are described in the patent claims, or force them to pay royalties,” says Then. “It’s a first step toward the same kind of corporate control of an animal line that Monsanto is aggressively pursuing with various grain and vegetable lines.”
      According to Then, “I couldn’t believe this. I’ve been reviewing patents for 10 years and I had to read this three times. Monsanto isn’t just seeking a patent for the method, they are seeking a patent on the actual pigs which are bred from this method. It’s an astoundingly broad and dangerous claim.”
      Take patent application WO 2005/017204. This refers to pigs in which A CERTAIN GENE SEQUENCE RELATED TO FASTER GROWTH is detected. This is A VARIATION ON A NATURALLY OCCURRING SEQUENCE — Monsanto didn’t invent it.
      It was first identified in mice and humans. Monsanto wants to use the detection of this gene sequence to screen pig populations, in order to find which animals are likely to produce more pork per pound of feed. (And that will be Monsanto Brand genetically engineered feed grown from Monsanto Brand genetically engineered seed raised in fields sprayed with Monsanto Brand Roundup Ready herbicide and doused with Monsanto Brand pesticides, of course).

      •Claim 16 asks for a patent on: “A pig offspring produced by a method …”
      •Claim 17 asks for a patent on: “A pig herd having an increased frequency of a specific …gene…”
      •Claim 23 asks for a patent on: “A pig population produced by the method…”
      •Claim 30 asks for a patent on: “A swine herd produced by a method…”
      This means the pigs, their offspring, and the use of the genetic information for breeding will be entirely owned by Monsanto, Inc. and any replication or infringement of their patent by man or beast will mean royalties or jail for the offending swine.

  10. passiton873 says:

    GMO Humans! All part of the agenda!

  11. Anders Pilgaard says:

    I really wish this conversation would be uploaded again by Jeff Rense, I can’t find it on youtube

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