Swedish study has demonstrated and confirmed that the mRNA in the Pfizer/BioNTech Covid injections infiltrates cells and transcribes its message onto human DNA within 6 hours, altering our own DNA.
A previous study published in October 2021 from Sweden found the spike protein enters into our cells’ nuclei and impairs the mechanism our cells have to repair damaged DNA. We’ve included this study here as The Highwire made an easy-to-understand video explaining it, including graphics, and so it is a good starting point to help understand the significance of the latest study from Sweden.
https://ce399fascism.wordpress.com/2010/08/06/the-genetic-bomb-paul-virilio-and-sylvere-lotringer/
PV: Yes. Einstein recognized three bombs: the atomic bomb, the cyber bomb, and the genetic bomb. And here we are faced with delirium. The atomic bomb has been a delirium, which we have not been able to leave behind. Then they set off the second frenzy, the cyber bomb, the bomb of information. And now the third bomb, which is beginning, the third delirium, Einstein called it the demographic bomb, but it goes without saying that the demographic bomb is tied to the genetic bomb. It is possible to think that this research is in fact being done to counter demographics, that is, to introduce an under-species and a super-species.
SL: You think we’re heading for catastrophe?
PV: I think the genetic bomb has an apocalyptic dimension to it. The three bombs, moreover, together have an apocalyptic dimension. Not the end of the world, but extermination in the broad sense. You know, contrary to what people think of me, I am not a thinker of the excess. I try to be a kind of periscope of probable catastrophes. What I believe is that these three bombs are developing in parallel. This catastrophic triptych is preparing a universal accident, a total accident whose dimension we cannot even imagine. Each time we invent a technology, whether electronic or biogenetic, we program a catastrophe and an accident that we cannot imagine. When we invented electricity, we didn’t imagine Chernobyl. So, in the research on the living being, on the book of life, we cannot imagine the nature of the catastrophe. We can imagine a monster, OK, but artists have been imagining that since Breughel and Bosch. Since Bosch, the search and programming for monsters has already taken place. I, for my part, believe that the total catastrophe, which these three bombs are programming, is the accident of science. It is no longer science that programs the accidents; it is science that is going to have a permanent accident. You see? The accident of science is that science is going to destroy itself. I believe that just as there was an accident of politics, so to speak, in the 20th century – and what an accident, otherwise we will understand nothing about Auschwitz and the Shoah – so at this very moment an accident of science and knowledge, whose consequences we cannot imagine, is being programmed. The cyber bomb and the genetic bomb are ripe, as they say, pregnant, the two of them, with a scientific catastrophe which we cannot imagine because it is perhaps the catastrophe of science itself.
SL: The genetic manipulation of the human is the accident of science.
PV: In a certain way, the accident of science is an accident that has not yet taken place, even if we can say that the labs – I mean the labs, not extermination, not the gas chambers – the labs at Auschwitz-Birkenau were the prefiguration of this accident. Auschwitz was not only a crime against humanity; it is the beginning of the accident of science. But that drags in the question of art.
Medical News and Perspectives | July 23/30, 2003
JAMA. 2003;290(4):449-450. doi:10.1001/jama.290.4.449
The United Kingdom (UK) has granted a license to Roslin Institute, Edinburgh, Scotland, to create human embryos for stem cell research via parthenogenesis, a “virgin birth” technique that jolts oocytes into a fertilized state without sperm. The license also allows the institute—former home of Dolly the sheep, which died in February—and its lead cloning researcher, Ian Wilmut, PhD, to derive stem cells from embryos created for in vitro fertilization (IVF) .
These nonhuman primate eggs have developed into 8-day-old embryos via a process called parthenogenesis (Science . 2002;295:819) (Photo credit: AAAS)
It is the fourth license for embryonic stem cell research handed out by the government of the United Kingdom, but the first license allowing the creation of human embryos by any means.
Speaking at the National Institutes of Health, Bethesda, Md, Wilmut said that he supports research on all types of stem cells, whether from embryos or adult tissues.
But he added that cloned embryos offer the most promising means for identifying the origins of and treatments for genetic conditions such as amyotrophic lateral sclerosis, or Lou Gehrig disease (JAMA. 2001;285:1691-1693). Embryos created using DNA from individuals with such diseases could provide researchers with an almost unlimited supply of stem cells, each carrying the key genetic defect. Such a pool would allow scientists to undertake more, and more sophisticated, experiments than any other available technology, said Wilmut, who spoke at a conference sponsored by the General Motors Cancer Research Foundation.
INCREASING THE EGG SUPPLY
INCREASING THE EGG SUPPLY
In an interview following his talk, Wilmut said that the aims of the newly licensed research are two-fold: to improve basic stem cell culturing technologies and to increase the supply of human eggs available for research.
INCREASING THE EGG SUPPLY
Roslin will immediately begin collecting embryos donated by patients from IVF clinics, which typically create several excess embryos per pregnancy attempt. The second route to boosting the egg supply, parthenogenesis, is much more technically challenging, said Harry Griffin, PhD, acting director at Roslin.
INCREASING THE EGG SUPPLY
The process involves gathering immature eggs from donors undergoing surgery for nonfertility-related reasons and then coaxing them to maturity in the laboratory. If successful, Roslin scientists will try to glean stem cells from the parthenotes (embryos grown from unfertilized eggs).
INCREASING THE EGG SUPPLY
Roslin’s agenda is the latest in a long line of advances involving parthenogenesis. Decades ago, scientists discovered that some plants and lower animals, including insects and corals, reproduce via the technique. Because the oocytes do not complete meiosis, they contain a full complement of the parent’s chromosomes—a clone.
INCREASING THE EGG SUPPLY
SUCCESS IN PRIMATES
Then in 1936, Gregory Pincus, MD, one of the scientists involved in developing the first birth control pill, induced parthenogenesis in rabbit eggs via temperature change and chemical agents. In 2001, Michael West, PhD, and colleagues at Advanced Cell Technology (ACT), Worcester, Mass, announced the creation of human parthenotes, although many scientists expressed skepticism about the embryos’ usefulness, as they died shortly after creation. A year later, though, a team led by ACT scientists and Kent Vrana, PhD, professor of physiology at Wake Forest University School of Medicine, obtained embryonic stem cells from monkey parthenotes, an advance that sparked a wave of enthusiasm (Science. 2002;295:819).
SUCCESS IN PRIMATES
Roslin is the latest institute to ride that wave, and Wilmut expressed confidence that parthenogenic human embryos will eventually provide a rich source of stem cells for research. But constructing a steady supply of stem cells is just the first step in the research pipeline. Once collected, the cells need to be fed and kept stable.
SUCCESS IN PRIMATES
Because current stem cell lines rely on mouse “feeder” cells, in theory, Wilmut said, unknown viruses in animal feeder cells could find their way into the human cells, a concern that the US Food and Drug Administration has also raised. To avoid that possibility, scientists at Roslin are developing techniques that would rely instead on human feeder cells or, even more ambitiously, on completely cell-free media. That is, the embryonic stem cells would grow in a rich soup of organic compounds.
SUCCESS IN PRIMATES
According to an abstract posted on the Web site of the UK’s Human Fertilization and Embryology Authority (HFEA), the agency that grants stem cell research licenses, Roslin now has permission to pursue this goal, too (http://www.hfea.gov.uk/aboutHFEA/researchLicenses.htm).
TO CLONE, OR NOT TO CLONE
TO CLONE, OR NOT TO CLONE
Like Roslin, the other three UK licensees—Guy’s Hospital, London; the Institute of Stem Cell Research at the University of Edinburgh; and the London Fertility Centre—are culturing stem cells from donated IVF embryos.
TO CLONE, OR NOT TO CLONE
Under a sweeping 1990 law, the HFEA regulates all IVF and human embryo research in the United Kingdom; a 2001 update to the HFEA banned all reproductive cloning and mandated that any artificially created human embryos must be destroyed within 14 days. In March, the House of Lords ruled that despite challenges from antiabortion groups, the HFEA holds the authority to license research involving embryo creation via parthenogenesis and cell nuclear replacement, although cloning for reproductive purposes remains off limits.
TO CLONE, OR NOT TO CLONE
Wilmut did not say if Roslin would pursue a license to attempt the more controversial nuclear replacement technique, the method used to create Dolly. In nuclear replacement, genetic material from an adult cell is transplanted into an oocyte, which is stimulated and begins embryonic development—a procedure that succeeds only rarely. While parthenogenesis allows cloning of reproductive-aged females, nuclear replacement could, hypothetically, clone any person, alive or dead (if viable DNA can be recovered).
TO CLONE, OR NOT TO CLONE
While tightly controlled in the United Kingdom, cloning research in the United States is largely unregulated. Bills outlawing the creation of cloned embryos for reproduction—and also for research, depending on the bill—have stalled in the US Congress, leaving the cloning landscape wide open for private companies. However, restrictions apply to researchers receiving federal funds, who may work with a handful of approved but largely uncharacterized embryonic stem cell lines and are not allowed to create cloned human embryos (JAMA. 2003; 289:1092).
https://ce399.wordpress.com/2012/06/14/uk-licenses-human-embryo-creation-jama-72003/
Say we slip energy use wise to 1700 A.D.. Could NZ support her population? The thought strayed in this afternoon with the fog that collapse could crash deeply. We shop in the Marina grocery store with a view of the Bay and Golden Gate. Got thinking about inventory. Completely out of choices in the Egg department-not restocked. Meats looked thin.