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Dr. Robert Malone, Inventor of mRNA and DNA vaccine tech |

Публикуван в United States of America - Социални взаимоотношения и развлечения - 10 - 31 Jul 21 17:40

Dr. Robert Malone provides us with an in depth discussion on his past of how he invented the mRNA and DNA technology. You are sure to learn a lot in this highly interesting topic.
00:00:00 Intro
00:00:22 Welcoming Dr. Robert Malone
00:00:32 What you invented?
00:01:29 Background
00:05:08 University of California, Davis
00:06:01 Robert Cardi, senior pathologist
00:07:24 Murray B. Gardner
00:09:00 Becoming Biochemist and Molecular Biologist
00:12:19 Davis Pathology Lab, California Regional Primate Research Center
00:13:35 Preston A. Marx, Murray B. Gardner, Bob/Robert Gallo | HIV/AIDS
00:15:11 Science politics
00:16:42 MD Ph.D. program, Chicago
00:19:01 Ted Friedman, UC San Diego | Retroviral Gene Therapy
00:20:58 Inder Verma, Salk Institute
00:23:12 What was the process of the mRNA basis?
00:25:36 What makes a retrovirus retro is...
00:27:47 Packaging sequence of retrovirus RNA
00:31:09 Chloramphenicol Acetyltransferase
00:31:53 Suresh Subramani | Luciferase
00:34:11 Anthony R. Hunter, Judy White
00:36:45 Large-scale preparation of RNA
00:38:45 Gordon Ringgolds new discovery
00:41:06 Phil Feldner
00:42:13 All this led to PNAS Paper
00:43:43 Dan St. Louis | Retroviral Gene Therapy project
00:46:50 Using gene therapy technologies for vaccine purposes
00:48:32 As a Teaching Assistant on an Embryology Lab
00:50:39 Patent disclosure of use RNA as a drug | Consequences
00:54:25 Working at Vical | Karl Y Hostetler, Douglas D. Richman
00:57:04 Collaboration with John Wolfe
00:59:17 Raj Kumar | Science Paper 1990
01:02:10 Patent Disclosure
01:03:35 Leaving Vical
01:04:35 The patents ended up issuing
01:08:29 Covid vaccination: FDA approval timeline | Your involvement
01:11:31 Wuhan Seafood Market virus
01:16:09 Current work
01:18:17 Logic behind drug repurposing
01:29:16 Drug repurpose mitigate the risk
01:33:22 Do you believe in the vaccines currently offered?
01:37:07 Certain vaccines for a specific person? | Risk-benefit ratio
01:45:22 In terms of specific vaccines
01:48:12 Coming to the RNA vaccines
01:53:04 How can the governments say to disapprove of vaccination? | Noble Lie
01:59:40 The idea of enforcing the Noble Lie
02:05:13 Algorithm based fact-checking
02:11:03 Lost our faith in public health | Anti-vaxxers
02:15:39 Can FDA approves the vaccine reformulate the vaccine?
02:22:14 Governments at risk
02:25:42 Is taking Vitamin-D and Zinc daily a great way to combat? | Ivermectin
02:28:43 Concluding statements: 1. Noble Lie
02:30:07 2. Bioethics
02:31:25 3. Evolution of viruses become less pathogenic highly infectious
02:32:44 Media likes oppositional relationship and misses the information
02:35:49 Wrapping Up


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Коментари (10)

31 Jul 21 21:03

Second, the Pfizer and Moderna vaccines contain lipid nanoparticles that are “PEGylated”, meaning the nanoparticles are coated with PEG (polyethylene glycol). [9] PEGs can lead to life threatening anaphylaxis or other conditions such as thrombocytopenia.[10][50] Such reactions are already occurring during the initial rollout and PEGs are the most likely culprit.[11] Approximately 72% of the US population have PEG antibodies, with 8% having highly elevated levels (more than 500 ng/mL), putting them at risk for severe allergic reaction and/or future autoimmune disorders.[12] These reactions were totally predictable, with many experts warning of the danger posed by PEGs[13][14][15][55], yet participants with a history of severe allergic reaction were excluded from the trials, serving to obscure the actual negative impact PEGs will have now that these injections are being given to members of the public who have not been screened for PEG antibodies.[16][53] Also, there is some worrying evidence to suggest that PEGs cross the blood-brain barrier and accumulate in the brain, possibly causing inflammation and/or autoimmune conditions, a fact gleaned from previous animal studies on mRNA vaccines. PEGs were found to be distributed across a spectrum of tissues including the brain.[52] Additionally, nanoparticles (such as PEGylated hydrogel) are known components for state of the art medical interventions, including biosurveillance technology currently being developed by DARPA and companies like Profusa Inc.[17][18][19][20][21] The secretive nature of this technology necessitates a knowledge gap between developers and the general public, so although my research efforts have yet to verify a direct functional relationship between PEGylated nanoparticles used in covid injections and biosurveillance, I personally do not relish the prospect of being injected with such given their association with biosurveillance technology of the military industrial complex.

31 Jul 21 21:06

Third, it is impossible to ascertain long term safety because of the foreshortened timeframe of Operation Warp Speed.[22] Vaccines should be tested for multiple years to adequately assess their longterm effects.[23] Short term safety is questionable too, as much of the data are still unavailable, and the current reports on safety and efficacy essentially amount to self-reported press releases from these companies themselves.[24] Fourth, the efficacy number of 90% for Pfizer and 94% for Moderna is statistically misleading, reporting a relative reduction instead of absolute reduction of risk*. Also, the trials only assessed these vaccines’ ability to prevent mild symptoms and NOT their ability to prevent transmission.[25] If they don’t prevent people from transmitting the virus (especially when safer, cheaper drugs like Ivermectin do) [26][27][58] what’s the point?

31 Jul 21 21:09

Fifth, these are NOT vaccines in the normal sense. They are mRNA vaccines, which utilize a completely different process for achieving disease protection**; mRNA vaccines seek to introduce synthetic messenger RNA into the body in order to “trick” cells into producing immunogens, which then stimulate an immune response.[28] These vaccines are the first of their kind ever to gain authorization.[29] Current vaccinations are essentially an extension of phase 3 of the trials.[30] Because of the lack of long term safety assessment and the new nature of this technology, people are participating in a mass human experiment with no way of knowing the long term health effects these could cause. Many problems from vaccines are known to have an incubatory period and do not manifest until much later, which is why testing needs to occur for multiple years in order to adequately assess risk. [31] One such problem currently being discussed is the mRNA technology’s possible impact on female fertility, as it encourages the production of antibodies against a laboratory stabilized SARS-CoV-2 spike protein that contains a very similar protein crucial for the development of placenta called syncytin-1. This could interfere with the reproductive process by encouraging the immune system to react against syncytin-1, thereby disrupting placental development.[32][71] The vaccines’ impact on fertility is currently unknown as animal reproductive toxicity studies have not been completed.[33]

31 Jul 21 21:12

Sixth, there was a signature for many different problems seen in the various trials and initial rollout for these vaccines, problems that are concurrent with commonly documented vaccine injuries. Injuries reported in the various trials/rollout have included, but are not limited to, anaphylaxis, Bell’s palsy, transverse myelitis, multi-system inflammatory syndrome, flash pulmonary edema, miscarriage, dyskinesia, myalgic encephalomyelitis, idiopathic thrombocytopenia purpura, and death. [34][35][36][37][50][51][56][59]

31 Jul 21 21:16

Seventh, and perhaps most importantly, the movement toward potential vaccine mandates or other coercive policies violates humanity’s most universally accepted principles of human rights and medical ethics, especially for a medical intervention with so many known and unknown safety/efficacy concerns. The absolute bedrock of medical ethics is the right to informed consent, as individuals must be made fully aware of all the potential benefits and risks associated with a medical intervention, while still maintaining the right to decline that intervention should they so choose.[41] Mandates or coercive measures fundamentally violate historical safeguards humanity has put in place to protect us from the ever present threat of medical tyranny, including the Nuremberg Code, the United Nations’ International Covenant on Civil and Political Rights, and UNESCO’s Universal Declaration on Bioethics and Human Rights.[42][43][49] Such would also be in violation of the Hippocratic Oath, for not only do oath keepers pledge first to do no harm, but also to treat the needs of the patient.[44] This implies that a doctor’s duty primarily pertains to the needs of the individual before the needs of the collective, a vital distinction made by Hippocrates and understood for nearly 2 millennia.[45][46] Privileging the needs of the collective is a “fallacy of misplaced concreteness”.[47] While individual need is directly apprehensible and consensual, collective need is an abstract, subjective concept not easily defined. And yet who usually gets to define this concept? Such is most often defined by those in power with the most means to influence institutional narratives, turning medical professionals who treat the needs of the collective according to this definition into mere extensions of that power at the expense of individual informed consent.

31 Jul 21 21:19

* Regarding the reporting on the reduction of relative risk instead of absolute risk, in the phase 3 trial of the Pfizer vaccine, for example, 22,000 people were vaccinated and 22,000 were given placebo, for a total of 44,000 trial participants. Of those 44,000, just 170 were clinically diagnosed as having covid-19 post-vaccination. Of those 170, it was reported that 8 received the vaccine and 162 received the placebo. From this ratio it was inferred that the vaccine would prevent 154 out of 162 from getting the disease for an efficacy of greater than 90%. But even as the British Medical Journal explained, “A relative risk reduction is being reported, not absolute risk reduction, which appears to be less than 1%.”[39] The supposed sterling efficacy touted by both Pfizer and Moderna are great for instilling confidence in their product, yet they were based on figures derived from only a small fraction of trial participants (just 0.38% of total participants in the Pfizer trial, and the same misleading statistical reporting seen in the Moderna trial as well).[40] ** Labeling the mRNA technology employed by Pfizer and Moderna a “vaccine” stretches the term’s definition beyond reasonable limits. Although it is claimed that such an intervention fulfills the purpose of vaccination by encouraging antibodies against an infectious disease, such does not contain any attenuated biologics typical of traditional vaccination, nor has it been proven to prevent infection, transmission, or community circulation; it may be more accurate, therefore, to label such as a “synthetic pathogen delivery device” constituting a form of “gene therapy”.[57]

01 Aug 21 00:04


01 Aug 21 14:38

when studying the #Covid “vaccines”(see below*😉 many things about them are very concerning... Links at pastebin dot com /qTZB6D5h First of all, up until this point there has never been a successful vaccine for coronaviruses in humans due to a problem typical of coronavirus vaccine development called antibody dependent enhancement or ADE.[1] In preliminary animal trials for previous coronavirus vaccines (SARS and MERS), animals were vaccinated and seemed to exhibit a robust antibody response, but upon exposure to the wild virus, they developed a paradoxical immune enhancement leading to severe organ inflammation (especially lungs), and many died.[2][3][61][63][64][65] Paradoxical immune response in respiratory virus vaccines has also taken place in human trials, which occurred during testing of the failed RSV vaccines of the 1960s.[4][69] Alarmingly, there are some statistical indications of ADE in covid vaccine trials, but there is no way to know for sure because many key signifiers of ADE weren’t specifically addressed.[5][66][67] Due to emergency protocol, the usual method of testing animals prior to humans was bypassed, limited animal testing occurred in parallel with humans, and the potential for ADE was not comprehensively assessed.[6][7][54] Historical precedent would suggest, however, that ADE is a distinct possibility, and we may not know the true negative effects until years from now when vaccinated persons are exposed to SARS-CoV-2 or genetically similar versions of coronavirus.[8][62][68][70]

02 Aug 21 01:26
the player


02 Aug 21 04:22
Winston Hopeless Smith

I have my vaccine and am delighted to do so and will vax my kids etc Ignore anti vax hogwash for the conspiracy driven dribble it it