Everything You Need To Know About THE SHOT But Were Taught To Be Afraid To Ask
Down the Rabbit Hole Volume Five, Part One
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"No one should ever take these jabs ever, under any circumstances, whatsoever." - Dr. Robert Malone, creator of the Messenger RNA injections.
Let’s start here with a clear, succinct overview….
On August 16, 2021, Dr. Sean M. Brooks, Ph.D., gave a quick address before the Southwest Ohio School Board.
First, we’ll look at exactly what he said, which I am including below in transcript format because - surprise, surprise - someone keeps removing his speech from social….
Hmm. I can’t imagine why anyone wouldn’t want you to hear or know about this so that you could… maybe… make an intelligent, educated, informed decision.…
I’ll supply some links for you throughout so you can grab more info on what he’s saying….
I posted this from YouTube originally, but YouTube keeps removing it.
The censorship is already at 1984/Brave New World levels, which should tell you all you need to know about the current scenario and where we would be headed if the people perpetuating this criminal behavior had their way.
Luckily, there are people in this world who will never stand for this.
Rights and freedoms come from the divine, from the universe, from natural law, not from governments deciding they are better than everyone else, convincing people they are in control of us in order to manufacture our consent, and granting us back “permission” to do certain parts and not others of what the universe already allows through our own sovereignty - which our Constitution PROTECTS.
Not that it needs protecting.
It is ours regardless.
But we have a document that does a great job of laying that out for everyone and it would be nice if the people who are tasked with protecting it would do their jobs once in a while instead of systemically dismantling it in favor of special interests, namely lining their own pockets.
I digress, but only because it’s important.
Here’s the speech: https://www.bitchute.com/video/gdnxwUgV1Xf4/
Transcript: “My name is Dr. Sean Brooks, PhD, Oxford. I have 48 publications, including 23 books. I've studied health medicine, anatomy, and physiology for approximately 21 years.
“Dr. Robert Malone, who created the messenger RNA [mRNA] vaccine has said no one should ever take these jabs ever, under any circumstance whatsoever – he created it, and he says, “Don't ever do it!”
“So let me explain what's going to happen to the people who have taken it – they are going to die in the next six months to three to five years for three reasons.
“Number one - You have dramatically decreased your own immune system by 35%. The first jab did it by at least 15%. The second did it by 35%. Now - if you take any booster shot, you will die. That's it. You take a flu shot in the future, you will die.
“The second reason - Antibody Dependent Enhancement [ADE]. And Antibody Dependent Enhancement is what is happening with these jabs with everybody who has taken them - unless of course you've taken a placebo. But there's no way that you would know that.
“So given that fact, Antibody Dependent Enhancement tricks the entire body into believing that the cell that's eating the pathogen is eating it when it isn't, it ends up leading to what's called a cytokine storm, which causes organ failure. That will cause your death - and there's no stopping that. No amount of drugs will stop that.
“The third thing - Blood clotting. Everyone who has taken the jab gets blood clots. If you don't believe me, there's a way you can find out. Take what's called a D-Dimer test. What that does, is that detects blood clotting at the microscopic level. We’re cutting full blood clots out of people right now as I'm talking to you.
“Millions have died from the jabs.
“In your last [SW Ohio School Board] meeting, you advocated for people to take the jabs potentially in the future, along with wearing masks - and I heard parents say the same thing.
“So to the parents who are actually considering jabbing their own children, you're going to sterilize them permanently. People who have taken the jabs are sterilized. 80% of [pregnant] women who have been jabbed have lost their children in the first trimester. You can't have kids.
“You've also injected yourself with the equivalent of HIV. You can now no longer breastfeed, donate blood, donate organs, donate blood plasma, nor bone marrow. If you don't believe me, try to donate blood and blood plasma and find out what happens. You will be denied. Unless of course you live in California, in which case they're allowing people to donate toxic blood with spike proteins in it.
“The jabs create spike proteins. They're in the jabs themselves. And they create it by snapping your RNA in half. You're no longer a human anymore. You're something else - and you're susceptible to countless diseases.
“Now here's what's going to happen in the future - very quickly. I don't know what percentage of your staff is taking the jabs - but your school is going to close - you will not stay open. You will close because they will fall ill and they will die. That will happen in all of your buildings. It will have its way – it’s already happening - Nothing can stop it.” - Dr. Sean M. Brooks, Ph.D.
In Part Two, I’ll fill in some crucial blanks for you. We’ll examine what Dr. Brooks hinted at here but didn’t come out and say….
Amanat, F. (2021). The plasmablast response to SARS-CoV-2 mRNA vaccination is dominated by non-neutralizing antibodies and targets both the NTD and the RBD. MedRxiv. [online] Available from: https://www.medrxiv.org/content/10.1101/2021.03.07.21253098v2
"In this study we profiled vaccine-induced polyclonal antibodies as well as plasmablast derived mAbs from individuals who received SARS-CoV-2 spike mRNA vaccine. Polyclonal antibody responses in vaccinees were robust and comparable to or exceeded those seen after natural infection. However, the ratio of binding to neutralizing antibodies after vaccination was greater than that after natural infection and, at the monoclonal level, we found that the majority of vaccine-induced antibodies did not have neutralizing activity. We also found a co-dominance of mAbs targeting the NTD and RBD of SARS-CoV-2 spike and an original antigenic-sin like backboost to seasonal human coronaviruses OC43 and HKU1. Neutralizing activity of NTD mAbs but not RBD mAbs against a clinical viral isolate carrying E484K as well as extensive changes in the NTD was abolished, suggesting that a proportion of vaccine induced RBD binding antibodies may provide substantial protection against viral variants carrying single E484K RBD mutations.”
Bannon, S. (2021). Episode 1,129 – Are Vaccines Causing Mutations? Bannon’s War Room. [online] Available from: https://rumble.com/vkg9mf-episode-1129-are-vaccines-causing-mutations.html
Cardozo, T. (2020). Informed consent disclosure to vaccine trial subjects of risk of COVID-19 vaccines worsening clinical disease. National Library of Medicine. [online] Available from: https://pubmed.ncbi.nlm.nih.gov/33113270/
“The specific and significant COVID-19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.”
"COVID‐19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe disease than if they were not vaccinated. Vaccines for SARS, MERS and RSV have never been approved, and the data generated in the development and testing of these vaccines suggest a serious mechanistic concern: that vaccines designed empirically using the traditional approach (consisting of the unmodified or minimally modified coronavirus viral spike to elicit neutralising antibodies), be they composed of protein, viral vector, DNA or RNA and irrespective of delivery method, may worsen COVID‐19 disease via antibody‐dependent enhancement (ADE). This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID‐19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials."
Chossudovsky, M. (2021). Does the Virus Exist? SARS-CoV-2 Has Not Been Isolated? “Biggest Fraud in Medical History.” Global Research. [online] Available here: https://www.globalresearch.ca/does-the-virus-exist-the-sars-cov-2-has-not-been-isolated-biggest-fraud-in-medical-history/5752066
Mercola, J. (2021). Joe Rogan on Breakthrough Cases and Vaccine Passports. Mercola. [online] Available from: https://articles.mercola.com/sites/articles/archive/2021/08/21/breakthrough-cases-and-vaccine-passports.aspx
Nal, R. (2021). Bombshell: Nobel Prize Winner Reveals – Covid Vaccine is ‘Creating Variants.’ Right and Freedoms. [online] Available from: https://rightsfreedoms.wordpress.com/2021/05/24/bombshell-nobel-prize-winner-reveals-covid-vaccine-is-creating-variants
Paulding, T. (2021). Fear porn incorporated. American Thinker. [online] Available here: https://www.americanthinker.com/blog/2021/08/fear_porn_incorporated.html
Rappoport, J. (2021). CDC/FDA confess: they had no virus when they concocted the test for the virus. No More Fake News. [online] Available from: https://blog.nomorefakenews.com/2021/07/29/cdc-fda-confess-they-had-no-virus-when-they-concocted-the-test-for-the-virus
Tseng, C. (2012). Immunization with SARS Coronavirus Vaccines Leads to Pulmonary Immunopathology on Challenge with the SARS Virus. US National Library of Medicine. [online] Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335060/
“Vaccine candidates for preventing SARS have been developed by various groups and include inactivated whole virus, spike (S) protein preparations, virus-like particles (VLPs), plasmid DNA and a number of vectors containing genes for SARS-CoV proteins. Phase I studies in humans have been conducted with a whole virus vaccine and a DNA vaccine. An early concern for application of a SARS-CoV vaccine was the experience with other coronavirus infections which induced enhanced disease and immunopathology in animals when challenged with infectious virus, a concern reinforced by the report that animals given an alum adjuvanted SARS vaccine and subsequently challenged with SARS-CoV exhibited an immunopathologic lung reaction reminiscent of that described for respiratory syncytial virus (RSV) in infants and in animal models given RSV vaccine and challenged naturally (infants) or artificially (animals) with RSV. We and others described a similar immunopathologic reaction in mice vaccinated with a SARS-CoV vaccine and subsequently challenged with SARS-CoV. It has been proposed that the nucleocapsid protein of SARS-CoV is the antigen to which the immunopathologic reaction is directed. Thus, concern for proceeding to humans with candidate SARS-CoV vaccines emerged from these various observations.”
Yahi, N. (2021). Infection-enhancing anti-SARS-CoV-2 antibodies recognize both the original Wuhan D614G strain and Delta variants. A potential risk for mass vaccination? Journal of Infection. [online] Available from: https://www.journalofinfection.com/article/S0163-4453(21)00392-3/fulltext
"In conclusion, ADE (Antibody Dependent Enhancement) may occur in people receiving vaccines based on the original Wuhan strain spike sequence (either mRNA or viral vectors) and then exposed to a Delta variant. Although this potential risk has been cleverly anticipated before the massive use of Covid-19 vaccines, the ability of SARS-CoV-2 antibodies to mediate infection enhancement in vivo has never been formally demonstrated. However, although the results obtained so far have been rather reassuring, to the best of our knowledge ADE of Delta variants has not been specifically assessed. Since our data indicate that Delta variants are especially well recognized by infection enhancing antibodies targeting the NTD, the possibility of ADE should be further investigated as it may represent a potential risk for mass vaccination during the current Delta variant pandemic. In this respect, second generation vaccines with spike protein formulations lacking structurally-conserved ADE-related epitopes should be considered."