The-Right-Answer

The "Right" Answer

Why the Vaccines are Putting us on Thin Ice


Infection Dynamics

Infections move in wave format, ebbing and flowing - every Corona virus ebbs during summer also, due to higher Vitamin D / Innate Immunity levels - and vaccines to be effective must hit everyone before the flood cycle.

New Child Cases & Deaths

The Childrens Hospital of New Orleans made global news the end of August when it announced an astonishing new outbreak of covid cases and mortalities amongst CHILDREN. Even putting them onto respirators, tragic. We need a WHO team in to examine and ascertain WHY? And to prevent vaccine company interference, because the speculation is that the mRNA vaccines might be causing this.

Psuedo Covid Syndrome

Germany and India have led global research in establishing that both Covid itself, and the mRNA vaccines, trigger or aggravate auto-immune diseases such as MS, or RA, especially in painful, bi-lateral joint flare-ups or sudden, inflammatory bone destruction.

ENGINEERING & ARTIFICIAL INTELLIGENCE

Systems Engineering a Human Covid Cure

We believe we do not need a Product, a vaccine or a pill, to stop the Pandemic, but a Process. It's called natural Innate Immunity. This is the master control or AI-like brain of our entire human OS. Humans are exposed to tens of millions of pathogens very day, and another 9 trillion bacteria, viruses, and fungi live on our skin or in our bodies; our ability to either live in peaceful symbiosis or to resist them and not get ill is derived by our INNATE IMMUNITY. Covid is an Innate pathogen. The vaccines are not Innate in nature - they are the opposite; they are back-end, specialized Adaptive Immune response.


Using an Adaptive response against an Innate Immunity attacker is like putting diesel fuel into a regular vehicle. It might work for a few miles, but internally it's burning up the engine.  This is key to understanding why the Covid vaccines are failing: 1 - they were never the right response; 2 - they interfere with the right response (Innate Immunity). God designed this complexity for us. And if we open our eyes, we'll 'see' the miracle of the pandemic, not just the hardship, and how little distance we have to go to stop the virus:  just 2% of all humans to treat.  And it's GONE. Like anthrax. Or smallpox.  We used Innate antivirals and antibiotics working as antivirals against both.  And the threats vanished. Only AFTER the outbreaks were under control was a smallpox vaccine pursued.

Infections, like oceans, move in waves. There are predictable, mathmatical, ebb & flood currents.


The virus ebbs (goes out) in its original form... comes back (floods) in a much stronger mutation. We have a few weeks, or months, between each flood, or new strong varient. If we wish to vaccinate. If everyone worldwide is not vaccinated during the ebb and before the next flood; then the virus gets stronger, and we - the humans - get weaker. It learns very quickly, in days to weeks, how to beat whatever Regn mRNA mutation the vaccines throw at it. And becomes 'resistent.' We are essentially, condensing into a few months, the years it takes bacteria to turn into super bacteria; and triggering new evoluations of covid into super viral pathogens. With our vaccines. The more we 'improve' them, as with India's new circular RNA vaccine - the worse COVID gets. WE JUST DON'T SEE IT YET.

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Both Delta and Btn 1.1.1.7 emerged at Christmas 2020 -  a few weeks after the mRNA vaccines began to be introduced in India and the UK, respectively. India began clinical dosing of  mRNA vaccine candidate HGCO19, by Gennova, Dec. 11, 2020. And a few weeks later Delta appeared there. In the UK, Moderna and Pfizer began dosing millions of mRNA vaccines, there were massive leaks of the Pfizer vaccine from improper storage, and Btn 1.1.1.7 appeared soon after. Both new strains took 2 -3 months to reach the US and spread globally. If one 'maps' the N protein, ORF and RDB variance locations between the mRNA vaccines and the new mutations, they are almost identical.

(Whereas the historical variance between Corona, Sars, and Mers and Covid19, were not.)

By Christmas 2020, Covid19 had been flying about the world for a year. And there were already some 200 minor variants identified. But the first major, deadly variants - the two new strains that really challenged our immune systems even more, and were more contagious and rapid in spread - only emerged AFTER the mRNA vaccines began to be dosed. Had we left covid19 largely 'alone,' and not intervened with its viral RNA, it is likely that btn 1.1.1.7 and Delta would NOT have emerged.


What would have been, we feel, a better, safer strategy would be the traditional MCM (Medical Countermeasures) US Department of Defense protocol:  1) TREATMENT   2)  CONTAINMENT  3) INNATE IMMUNITY BOOST.


CHINA WARNS THE US NOT TO ATTEMPT A VACCINE

Vaccines are NEVER part of an emergency response to any public health emergency. Not since smallpox. And Delta is a great example of why - we never want to de-stabalize an emergency situation to make it more volatile than it already is. Not only were the vaccines the wrong answer due to timing - they would take over a year, possibly several years, to be ready and distributed - they were the wrong answer in terms of potential volatility of a very dangerous virus that China had warned the US since 2014, NOT to attempt to use a vaccine against. Chinese scientists had warned repeatedly, the US and OTAN (NATO), that covid19 used its N protein to disable, or bypass the human Innate Immune system. And that any tampering with ANY covid protein or RNA would trigger more deadly consequences.


WHY THE VACCINES WERE THE WRONG ANSWER, AT THE WRONG TIME

They were not an immediate, urgent response to an urgent need. They did NOTHING to help those suffering and dying with covid19, the entire first year and a half of the pandemic. At best, vaccine impact began to be seen in the US sometime in late May to June 2021. But 4.4 million had already died worldwide by then, and 2 to 3 times that number, suffered with the virus. And devastating impact to families and economies. Had we thrown instead, aggressive treatment at the virus; and begun immediately to fund and prioritize CURE R&D, the pandemic probably would have been contained by early to mid-summer 2020. The vaccine emphasis entirely derailed any Treatment and Cure work; until Europe - with its Horizon programme - and Asia, with independent efforts, primarily out of Japan, Korea and China  - began to refocus on Treatment and Cure work in spring 2021.


  1. Vaccines are only, or mostly, effective against Adaptive pathogens; but Covid19, or any Corona virus, is Innate. The two types of pathogens work entirely differently inside the human host, making vaccines a poor choice agianst Covid. Our Innate Immune system is our strongest, "Always On,' parent immunity. It is with us from birth, and does not need antibodies. It also is more sophisticated and complex in mechanism than simple mRNA manipulation: it blocks viral attackers including Covid19 through a host of intertwined mechanisms: cellular surface glycoprotein changes; ACE 2 and TMPRSS2 inhibitors, ph control, aminos and enzymes and GHF and other molecular level changes; and miRNA and ORF changes - much more granular than the mRNA vaccine alterations. Our bodies have been blocking viruses and beating them for thousands of years.
  2. Mature, sophisticated viral families like Corona, one of the oldest viruses on earth, with the largest RNA strand,  mutate or morph quickly in response to new threats. Hepatitis is capable of morphing from enveloped to naked and back again - as enveloped, it is easily destroyed by soap or solvents; but as naked it is not. Covid19 is believed capable of dropping its S spike protein and using only its N and M, or E; or of even hiding inside of microphage or bacterial hosts, to infect human hosts. In 2014 China identified the Corona N protein as the primary difference between Sars, Mers, and Corona determining deadliness. In Covid19, the N protein and ORF variance, as well as minor RDB variance, are believed the main determinants of whether adults will die - whether the virus can bypass their Innate Immunity and infect them with great enough microbial load.


IMPACT OF THE NEW MUTATIONS ON CHILDREN

Except for America, Covid19 has historically spared children by virtue of their stronger Innate Immunity (not their Adaptive Immunity) defending them against the viral N protein. That's why the Btn 1.1.1.7 and Delta infections of children, was alarming. It marked a significant mutation. If such mutation arose, as is speculated, from introduction of the mRNA vaccines, that is tragic. If vaccines introduced to protect adults, are killing our children. Because until btn 1.1.1.7 and delta, children never died of Covid. Rarely were sick from it. The only change introduced, worldwide, was the mRNA vaccine. In India, they are now introducing a 'circular' RNA vaccine - which holds the possibility of even more disastrous effect and trigger even more dangerous mutation. Covid19 itself is already proven capable of both circular RNA adaptation; and of beating the Rgn mRNA vaccine targets.


Whatever man throws at it in terms of mutated RNA, the virus beats.


VACCINES WILL ONLY WORK AGAINST A PANDEMIC IF THEY ARE INSTANTLY DOSED.. WORLDWIDE

Due to the wave pattern of infection dynamics in a large pathogen spread or outbreak; a vaccine, which is a 'subtle' influence taking weeks to being to work, can only be effective if EVERYONE in the total risk population is dosed in a small-enough timeframe to beat the viral reaction to a new host environment threat - which is to mutate as aggressively as possible. When not threatened, Corona and Covid19 virus mutations are rapid but mild and insiginficant in variance. When the mRNA vaccines began to threaten them, they dramatically changed RNA sequence and the gap between Corona and Delta (N, Orf, other) dramatically increased. 


Historically, and affirmed by current new studies out of Russia, Germany, and Israel; if  a vaccine is to work against a pathogen with rapid mutation cycle, the vaccine must dose all impacted populations within a very rapid timeframe, such as 1 to 3 months. *This was the formal teaching in most graduate medical programmes, until 2021. However, if we look at the rapidity of response to the Pfizer and Moderna vaccines in the UK and to the HGCO19 in India, humans had only a few WEEKS to kill all of the virus (or rather, to make every human host it would encounter inhospitable so that it could not continue to reproduce and migrate), before the new strains appeared.


And despite vaccine company claims of efficacy against Delta; Israeli and other non-US findings show only 39% efficacy by the mRNA vaccines against Delta, after 2 doses of vaccine. UK, Canadian, Belgium and WHO studies had already dropped mRNA efficacy to 66% against any Covid strain. Only in the US was a '95% efficacy' claimed. Not any other nation worldwide has believed or documented this. And interestingly -- the US, which claims the highest vaccine efficacy -- continues to have the highest infection and death rates. And now, the highest worldwide CHILD infection and death rates. Calling into question, mRNA efficacy claims. 

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If we are already down to 39% efficiacy with Delta; and as US hospitals all over the Washington DC metro are testing patients for Delta whether they are vaccinated or not, saying, "We are seeing many patients fully vaccinated, dying of Covid;" that represents a 25% drop in efficacy from Covid19 to Delta, for the mRNA vaccines. IF the next mutation followed this pattern it would drop overall efficacy to 15% - 20% fully vaccinated. And child mortalities would be expected to increase even more, in the US.


SUMMARY

Reading medical and clinic studies and reports from OUTSIDE the US gives us a radically different perspective than watching our mainstream US media or reading only what our US Federal Agencies release. But mathmatical and AI modeling never lies: we cannot change math or physics simply by spending more on marketing. The mRNA vaccines are not working to STOP the pandemic. And progressing slowly toward higher saturation levels, worldwide, is only doing what our earliest mathmatical / AI models predicted: it is triggering more and more dangerous mutations; and now it appears to be killing children. OR raising child infection and mortality rates in the US, at least.


VACCINES INCREASING COVID DEATH RATES

In other nations, we see the introduction of the vaccines bring with them waves of new or increasing Covid19 infections and deaths. Vietnam is one of the best and most tragic examples: for months, Vietnam used a combination of physical containment (distance, travel and mask rules) and holistic medicine/ exercise and nutrition to keep its pandemic death rates at 0%. The same in areas of Africa, other parts of Asia, and Australia. But in late July, when Vietnam bowed to external (largely US, not WHO) pressure and began to vaccinate, its covid19 infection and death rates soared:



Vietnam Covid19 death rates as of July 14, 2020 - 0%

Vietnam begins to introduce the Covid19 vaccines, onto a zero% covid death rate.

Within a month, Vietnam surges to the third highest Covid19 death rate worldwide. At only 14% vaccinated.

As the US hits 'herd immunity" - 60% vaccinated - its own Covid19 death rates continue to surge. Especially amongs children.


WHY is the US so Much Worse than the Rest of the World? Black children in Africa are not dying in droves of Covid. Why in the US? Is it our mRNA Vaccines?

The late summer - September outbreak of child and infant Covid19 cases in New Orleans and other US citiesis tragic, but alarming because it is so DIFFERENT from the rest of the world. This entire pandemic, the US, despite our lead in medical and technology and STEM sophistication; also leads in covid19 infections and mortality. Why? This tragic sight above was unheard of, worldwide, all pandemic. What happened in the US? (Except our 'herd immunity?")


Why do we lead the world in child infections and mortality for a virus that traditionally spares children? Is this a new mutation? Is it caused by our higher mRNA vaccine rate? Or is it a new strain not yet identified? Who in the US is supervising NIH, HHS, Pfizer and Moderna? What agency or individual(s) with no financial ties to or profit from the mRNA vaccines, is asking and researching objectively and rapidly, these critically important questions?


In clinical studies and AI modeling, the vaccines shut off or suppress the child's natural Innate Immunity. Just as in adults, they trigger or even cause severe auto-immune disorders. We have - especially children - our own natural Innate Immunity that was fighting off Covid19 successfully for 98 - 99% of 8 billion humans. All we had to do was replenish that Innate Immunity in that small % of humans getting sick. NOT IN OUR CHILDREN. WHO WERE HEALTHY. The US, led by NIH/ Dr Fauci, decided against any Innate Immunity Boost, or Treatment, or Cure. And decided that "only' a vaccine would be used against Covid19.


Even if a child did not receive a vaccine to harm them; they are harmed by the raging mutations the mRNA vaccines are causing. Covid19 did not mutate dangerously at all, until we started dosing the vaccines.


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