Thank you to Richard Dolan for asking the right questions. ❤️
The CV19 was engineered. We have been conducting corona virus research since the 1930’s:
Coronaviruses were first discovered in the 1930s when an acute respiratory infection of domesticated chickens was shown to be caused by infectious bronchitis virus (IBV). Arthur Schalk and M.C. Hawn described in 1931 a new respiratory infection of chickens in North Dakota. The infection of new-born chicks was characterized by gasping and listlessness. The mortality rate of the chicks was 40–90%. Fred Beaudette and Charles Hudson six years later successfully isolated and cultivated the infectious bronchitis virus which caused the disease. In the 1940s, two more animal coronaviruses, mouse hepatitis virus (MHV) and transmissible gastroenteritis virus (TGEV), were isolated. It was not realized at the time that these three different viruses were related.
Human coronaviruses were discovered in the 1960s. They were isolated using two different methods in the United Kingdom and the United States. https://en.wikipedia.org/wiki/Coronavirus.
Once people began to understand the implications of gain-of-function research there were steps taken to curb some of it shown in this article from Nature, Nov. 12, 2015 https://www.nature.com/news/engineered-bat-virus-stirs-debate-over-risky-research-1.18787
An experiment that created a hybrid version of a bat coronavirus — one related to the virus that causes SARS (severe acute respiratory syndrome) — has triggered renewed debate over whether engineering lab variants of viruses with possible pandemic potential is worth the risks.
In an article published in Nature Medicine1 on 9 November, scientists investigated a virus called SHC014, which is found in horseshoe bats in China. The researchers created a chimaeric virus, made up of a surface protein of SHC014 and the backbone of a SARS virus that had been adapted to grow in mice and to mimic human disease. The chimaera infected human airway cells — proving that the surface protein of SHC014 has the necessary structure to bind to a key receptor on the cells and to infect them. It also caused disease in mice, but did not kill them.
Although almost all coronaviruses isolated from bats have not been able to bind to the key human receptor, SHC014 is not the first that can do so. In 2013, researchers reported this ability for the first time in a different coronavirus isolated from the same bat population2.
The argument is essentially a rerun of the debate over whether to allow lab research that increases the virulence, ease of spread or host range of dangerous pathogens — what is known as ‘gain-of-function’ research. In October 2014, the US government imposed a moratorium on federal funding of such research on the viruses that cause SARS, influenza and MERS (Middle East respiratory syndrome, a deadly disease caused by a virus that sporadically jumps from camels to people).
The latest study was already under way before the US moratorium began, and the US National Institutes of Health (NIH) allowed it to proceed while it was under review by the agency, says Ralph Baric, an infectious-disease researcher at the University of North Carolina at Chapel Hill, a co-author of the study. The NIH eventually concluded that the work was not so risky as to fall under the moratorium, he says.
In a US patent from 2004, US20060257852A1 United States Fig. 18 lists its viral components as:
FIG. 18: Genome organization of Coronaviruses representative of group 1 (HCoV-229E, accession number: AF304460), group 2 (mouse hepatitis virus MHV, accession number: NC—001846), group 3 (avian infectious bronchitis virus AIBV, accession number: NC—001451) and SARS coronavirus. Other completely sequenced coronaviruses used in this study are available at the following accession numbers: porcine epidemic diarrhea virus (PEDV), AF353511; transmissible gastroenteritis virus (TGV), ND—002306; Bovine coronavirus (BCoV): AF220295. Red boxes represent group-specific genes. The position of the leader RNA sequence and poly(A) tract is also indicated in genomes where they are reported. The position of specific IG sequences is indicated by circles of different shades. In the SARS genome, we also find three IG sequences specific for group 2 coronavirus.
Notice the animals these viruses come from. Then pls note:
Although the extent of any risk is difficult to assess, Simon Wain-Hobson, a virologist at the Pasteur Institute in Paris, points out that the researchers have created a novel virus that “grows remarkably well” in human cells. “If the virus escaped, nobody could predict the trajectory,” he says. https://www.nature.com/news/engineered-bat-virus-stirs-debate-over-risky-research-1.18787
Whether ‘it’ got loose or we are looking at a ‘Plan-demic’ there are a couple of sources out there, Doctors and PhD’s who are speaking out, most notably Dr Rashid Buttar and Dr. Judy Mikovits.
Judy got banned and thrown in jail for proving that: Molecular biologist Dr. Judy A. Mikovits was thrown in jail after discovering evidence that deadly retroviruses are transmitted through vaccines given to humans. From<https://web.archive.org/web/20190806111747/https://explainlife.com/scientist-jailed-after-discovering-deadly-viruses-are-delivered-through-vaccines-2841/.
Here is the first in a series of videos (1-4) That go deep into what is happening, in regular people terms. I highly recommend these for an understanding of the total picture from that angle.
Part 1 of 4 – Roundtable Discussion with Dr. Judy Mikovits | Dr. Rashid A Buttar. https://youtu.be/Leg75TPfLIQ
IMO we have very human, very nasty people capable of long range planning and orchestrating this whole debacle, the evidence exists out there, including implicating Fauci and Gates connected to the WHO and various other organizations (funded by guess who?) where prohibited research went on that is so expertly hidden in a deep morass of scientific research papers and facilities that to quote them would make me look like an uneducated ass for trying. There are those who have made these connections and it isn’t pretty. (see the above video) All I can do is yank the articles written by knowledgeable people about the white papers written on the evolution of this virus. What I will say, my out on the twig speculation is, that I agree with Dr. Judy Mikovits that the virus is two pronged. What we are seeing is an already implanted virus we all have – the entire planet, the common cold and it is the regular, original flu. We carry the signature of it in our immune system by way of antibodies. The key to the current eruption is the modified SARS2 with increase gain of function. When it meets the already inherent corona antibodies, it creates a reaction that has been called the cytokine storm. If you are immune compromised or are toxic from the common meds they give old people to combat old people diseases – (which are from increased toxicity) then your system has no way to expel the massive release of the toxins from your cellular tissue and you become over whelmed. Think asthma, only throughout your entire body.
To complicate this even further radio waves in the 30-300 MHz range have been shown to interfere with the ability of blood plasma to carry hemoglobin which transport oxygen throughout the body and is why some people have considered ozone therapy and barometric chambers as a palliative treatment.
Further, radio frequency in the above mentioned values can increase cell wall permeability making an easier ingress of the virus into its target cells.
Most of the studies on biological effects of radio frequencies identified the ability to regulate calcium ion channels as the main mechanism affecting oxidative stress .
Is Calcium Efflux Good or Bad?
Radio frequency (RF) has been demonstrated to induce calcium ion efflux , where RF is observed to pump ions through channels and pores bound in bilipid membranes . Yet interestingly, the effects of calcium efflux through the activation of voltage‐gated calcium channels (VGCCs) is not one-sided.
Martin L Pall in 2013, published a paper on how various electromagnetic frequencies can activate voltage‐gated calcium channels (VGCCs) which often resulted in rapid increase of intracellular calcium ions, nitric oxide and sometimes dangerous free radicals like peroxynitrite. However, the results of the activation of VGCCs can be either therapeutic or pathological .
If all of the infected cells opened at the same time due to an EMF environmental frequency (such as 5G – whoa), pouring the viral bits into your interstitial fluid water ways and your lymph system could not handle them because they were already carrying a heavy load of pharmaceutical and environmental toxins and struggling to rid your system of them, then you would have a cascade collapse of systems in the body.
There is quite a plan going on here, whether it be from ET’s or our own skanky psychopaths. IMO this is a huge plan of decades building each piece into our lives and environments and we are about to see how successful this will be. Don’t forget that stress and fear are huge immune compromisers!
With all that said there is also an interesting cross over in the plasma energy field and cellular mechanics that became apparent to me listening to an interview on The Higherside Chats :Kosh | EVOs, Plasma Energy, UFOs, & The SAFIRE Project concerning the structure of EVO’s. Thank you for mentioning this person to the Higherside…. https://youtu.be/-ovICZkHibA
And in the end
The love you take
Is equal to the love you make
Love to you all.