“We have a multi generational indoctrination that is 200 years old of; safe and effective, safe and effective…
I have been saying now for five years they will never make this mandatory, but they will make it unbelievably difficult to live, that the vast majority of people will roll over…
…”People listen to this closely”
Vaccines always have been a method of mass destruction,
a method of depopulation,
a method for creating customers for life…
https://www.brighteon.com/2622bcc4-ccbf-4a5a-b98d-31334a47dd61
REQUIRED VIEWING! Dr. Sherri Tenpenny gives VERY important information! Hyper-immune response in test animals for previous attempts at coronavirus vaccines, like SARS and MERS, has been a persistent problem. All is well for awhile, until the animals are exposed to the wild mutated virus….
The following transcript and information was graciously and generously provided to us by Theresa Dunford, website: https://sacredconnections.co.uk/index.php/holy-land-of-scotland/
Thank you Thersa and Barry for your service to spreading freedom and truth!
Partial transcript of Dr Tempenny’s interview in which she details the affects of the mRNA vaccines. Shocking!!
The Coronavirus ‘vaccine’.
Dr. Sherri Tenpenny explains (first 20 mins transcribed here, with some repeated sentences left out for ease of reading. Theresa has done her best for accuracy, but recommend also listening yourself):
“A vaccine is a molecule that is injected into our body that generates an antibody. This does that, but the antibodies that it generates are going to be deadly and its going to take somewhere between 4-14 months before we see the full ravage of what is going to happen to people who are vaccinated. We have never used messenger RNA in any vaccines. We have mRNA vaccines, i.e. the measles, polio vaccines are RNA vaccines, but in those vaccines the virus is part of the vaccine, wholly intact, so when your body generates an antibody its against the outer coating protein of that virus. What we are doing with this new virus, we are taking a little piece of that virus’s genetics, specifically associated with what’s called the spike protein, and we are injecting that into the body and creating a non neutralising antibody. A non neutralising antibody, which in essence, instead of taking that messenger RNA, gobbling it up and making it go away, this non-neutralising antibody creates something that’s called an antibody dependent enhancement. They refer to that as ADE, which allows that little piece of messenger RNA to start replicating on its own over and over again, creating these little pieces of virus spike proteins inside our body for our body to create an antibody again.
That spike protein has been shown in two other specific ways to cause injury. No. 1, when you create an antibody to that spike protein – antibodies are designed, and when we write about them, we make it look like a letter Y and the two arms of the Y they call them FAB fragments and the stem down at the bottom, the bottom part of the Y, is the FAB fragment. These are the ones that grab hold of the virus and generally neutralise it. When you look at the messenger RNA it grabs hold of it but kind of loosely binds it, and when this FAB fragment goes over and hooks onto the macrophage that is supposed to kill it, and it gets taken inside, that messenger RNA gets released and that’s where it starts to replicate over and over again. It’s like having an on button but no off button. They call this whole mechanism the Trojan horse mechanism because it allows a piece of that virus to get inside your cells, start to replicate and even get inserted into other parts of your DNA as a Trojan horse. That’s one of three mechanisms.
The second mechanism is when you create this non neutralising antibody to 16:10] the messenger RNA, that spike protein can go into your lungs and attach to your lung tissue and start developing what they call diffused alveoli damage, which is diffused injury of the cells inside your lungs where you breathe. It starts to break them down and destroy them and what those antibodies do is that they cause various degrees of pus, bleeding and damage to the lung. As you get this vaccine, this messenger RNA, you create this antibody. The antibody carries the thing inside the cells according to the Trojan horse mechanism. The antibody goes to start to damage lungs; and the spike protein anitibodies can attack your macrophages.
There are two types of macrophages, type 1 and type 2. Type 1 are a type of white blood cell that gobble up the viruses and bacteria in your system that aren’t supposed to be there. When you get pneumonia, or some serious type of infection, the type 1 macrophages are pro inflammatory. They start creating cytokines [Cytokine storm and cytokine release syndrome are life-threatening systemic inflammatory syndromes involving elevated levels of circulating cytokines and immune-cell hyperactivation] to try and fight off the infection. Very aggressive and highly inflammatory, which is what you want. The type 2 macrophages are anti-inflammatory. As you start to recover, the type 2 macrophages clean up the dead debris tissue, the dead white tissue cells. Type 1 and type 2 macrophages work in concert. Type 1 kill off the infection, type 2 heal it.
When you’ve got this antibody to the spike protein, which is the full intent and purpose of these vaccines, that antibody kills your type 2 macrophages. It attaches to them and inactivates them. So in the experimental animals [injected with the vaccine] that actually died of lung infection and inflammation, what they found was that their lungs were filled up with these type 1, highly inflammatory, cytokine types of macrophages and zero type 2 macrophages. …”
For more iformation: https://vaxxter.com/covid-vaccines-part-2/(link is external)
Dr. Tenpenny’s website: https://www.drtenpenny.com/ (link is external)
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Dr Vernon Coleman MB ChB DSc FRSAAstraZeneca is one of the world’s biggest pharmaceutical companies and it is planning to produce a vaccine for covid-19. Here are just a few facts about the company which those expecting to have their vaccine should know…1) In 2014, AstraZeneca agreed to pay $110 million to settle two lawsuits brought by the state of Texas, claiming that it had fraudulently marketed two drugs. The Texas Attorney General, when he announced the settlements, said the company’s alleged actions were ‘especially disturbing because the well-being of children and the integrity of the state hospital system were jeopardised’.2) The company has paid $350 million to resolve 23,000 lawsuits.3) The company has been charged with illegal marketing, including corrupt data in studies for marketing a drug to children, a sex scandal and a poorly run clinical trial that could have compromised patient safety and data reliability.4) Research for one drug made by AstraZeneca originally included 30 children but only eight children completed the trial and the researcher who conducted the trial concluded that it was inconclusive. However, the study was published anyway and led to a national recommendation that the drug be used as the leading choice for children. Other studies which showed that the drug produced harmful results were never published and were covered up. A company email revealed: ‘Thus far, we have buried trials 15,31,56. The larger issue is how do we face the outside world when they begin to criticise us for suppressing data.’ After years of investigations AstraZeneca paid a $520 million fine in the US and paid $647 million to settle global lawsuits.5) The company has had a number of other lawsuits but you’ve probably got the picture.6) AstraZeneca appears to be among the main contenders to make the covid-19 vaccine which governments are so excited about and which we are told will be the answer to all our prayers.7) Drug companies, governments and doctors are going to be given indemnity so that they cannot be sued if they do something bad.8) AstraZeneca is so confident that its vaccine will receive authorisation that it has already started making billions of doses. The WHO says it is the leading candidate for the billions in profit that lie ahead.Copyright Vernon Coleman September 2020