BATTLE FOR WORLD | August 12, 2020: It now appears that the United States, Britain and allies want to get the most out of surveillance and authoritarian transformation of countries as the coronavirus pandemic runs its course. This implies that the pandemic was put in place for a reason. Lockdown = Lock Step.
And the obstacle that threatens to end the pandemic is the unexpected release of Russia’s safe vaccine using “viral vector” technology exclusive to Russia.
The United States is urging the Russian people not to use the vaccine. This advice is coming from a country that has instigated revolutions in the Ukraine, now Belarus, South America, Venezuela, Cuba, etc. And in the United States boundaries itself a faction war has erupted between three rival groups of elites.
According to the U.S. representatives, the Russian development is nothing more than a fake – full-fledged studies of it, as stated, have not been carried out, and therefore, the vaccine can pose a very serious danger. With the recent documentary released with Dr. Judy Mikovits outing the United States criminal vaccine industry cabal, where vaccines are laced with properties to do other things, refer to the YouTube CENSORED: DOCTORS IN BLACK / PlanDemic, video, here.
What this sounds like, is that the Russian vaccine has no boogieman RNA-code to damage the immune system. It is just a safe vaccine using the already proven to be safe “viral vectors”. This fact Dr. Anthony Fauci is having fainting spells from. But why?
The countries of Europe, in particular in the UK, holds the same point of view, which is: The Russian vaccine can have a very negative effect on the situation with the pandemic. That the vaccine will give a false sense of security, and after the start of mass vaccination, an active increase in frequency will begin. False sense of security sounds like the West wants to implement a regimen of cocktail medications for all?
Russia has said, with the release of the safe Sputnik V vaccine, it will bring the pandemic to an end. This effect, the U.S. sees as negative. That means the U.S. and allies involved want the pandemic to be around as long as possible. And it makes sense, because the longer the pandemic remains, more people get infected and the profit potential increases and whatever else is part of the diabolical plan.
Also, Russia noted that the Sputnik V vaccine was developed for Russia, and if other countries want it they have to enter into negotiations. So Russia did not develop the vaccine to exert enormous profits from it. However, this is what pharmaceutical companies in the United States are expecting to do. And Russia with a safe vaccine interferes with the plan. So the coronavirus pandemic is being exaggerated to exploit future profits from drugs and vaccines being developed in the West under patents. And Russia’s safe vaccine is going to interfere with a lot of patent money.
Things are going to get very nasty regarding vaccine profits and it is going to play out in the media. And President Trump said he cut out the middle-man and the elites who control this pharmaceutical sector of profiteering are very upset at him.
British experts also threw some shade, saying: “This is a rash and unwise decision. It is unethical to vaccinate with an unproven vaccine on a mass scale. Any problem that arises during vaccination in Russia will have disastrous consequences. Both because of its negative impact on health, and because it will further impede the formation of a positive attitude towards vaccines among the population,” – quotes from the publication “InoSMI“.
Readers keep in mind, the ruling elite globalists are the very ones pushing to bash Russia’s vaccine. The same ones who are always manipulating US politicians…to sanction Russia. A faction war has erupted.
COVID-19 vaccine war, pandemic for profit…
BATTLE FOR WORLD | September 15, 2020: Exciting news about an antibody therapy that could be safe and effective in neutralizing the coronavirus COVID-19 is being tested by researchers at the University of Pittsburgh School of Medicine (UPMC) in the United States.
“Ab8 not only has potential as therapy for COVID-19, but it also could be used to keep people from getting SARS-CoV-2 infections,” said the study co-author John Mellors, chief of the Division of Infectious Diseases at the University of Pittsburgh and University of Pittsburgh Medical Center.
And Mellors further adds “Antibodies of larger size have worked against other infectious diseases and have been well tolerated, giving us hope that it could be an effective treatment for patients with COVID-19 and for protection of those who have never had the infection and are not immune”.
The scientists were able to isolate “the smallest biological molecule” that has the ability to “completely and specifically neutralizes” SARS-CoV-2, which is the virus responsible for causing the novel coronavirus.
The neutralizing antibody is 10 times smaller*1 than a full-sized antibody, and was used to create a drug called Ab8 that researchers are hoping have the potential to prevent and treat the virus in human.
The research scientists are reporting that the drug during early testing has proven “highly effective in preventing and treating SARS-CoV-2 infection” in mice and hamsters. The drug has shown signs of no negative side-effects in people due to the fact that it does not bind to human cells, according to the early study.
“Its small size might allow it to be given as an inhaled*2 drug or intradermally, rather than intravenously through an IV drip, like most monoclonal antibodies currently in development,” the report said.
And the scientists say, “We hope that the antibodies we have discovered will contribute to that triumph.”
*1. Maybe the future of medicine lies in the usage of nano(mini)-antibodies to neutralize viruses.
*2. Aerosolized form.
BATTLE FOR WORLD | September 18, 2020: US President Donald Trump announced to reporters on Friday (Sept. 18) that by April 2021 there would be enough supplies of the vaccine for COVID-19 to vaccinate every American. And that the vaccine could begin reaching distribution points in the US soon to treat high-risk persons within a month’s time. The vaccine would be available for free to every American, said the president.
The Hoover Institute senior fellow and adviser on Trump’s coronavirus task force, Scott Atlas, further explained that 100 million doses of a vaccine would be available by the end of 2020, and approximately 700 million doses to be available by the end of the first quarter of 2021, which ends on the last day of March. The United Sates population is approximately 328 million. The vaccine supply count likely includes repeated vaccination due the fact that once inoculated, the antibodies do not last indefinitely. (BattleForWorld: The COVID-19 vaccination will be similar to the repeated flu shots. Did they use the flu shot approach of repeated inoculation to acclimate the masses for the COVID-19 frequency vaccination plan? People will be going to see health practitioners a lot more. And no wonder why in the United States they are setting up doctor’s offices, i.e. MinuteClinics or Care Clinics, in places like Walgreens, CVS pharmacy, Walmart, Costco, etc. They had this all planned out in advance. Under no circumstances is this a coincidence.)
“It’s not a forced vaccination, of course,”* said Atlas, and noted that prioritized individuals will include the elderly and first responders bumped to the front of the line for protection.
(BattleForWorld: *They will implement the term “force vaccination” in other ways by attaching it to requirements: job/work place, state ID, passport, etc.)
Source, Sputnik News.
BATTLE FOR WORLD | September 4, 2020: It what appears to be an information snippet-release moment, the Russian Defense Minister Sergey Shoigu said Friday (September 4) while speaking to the SCO, CIS and CSTO countries, that: Their are countries outside the Shanghai Cooperation Organizations (SCO), the Commonwealth of Independent States (CIS) and the Collective Security Treaty Organization (CSTO) that develop biological weapons and measures must be taken over this threat.
And said that “We have discussed possible measures on mutual aid and establishment of a reaction potential to biological hazard threats, including the military biological activity of non-regional states,” said Shoigu to Defense Ministers.
He then added: The attending Ministers also shared experience in overcoming the coronavirus pandemic aftermath.
(BattleForWorld: Readers, something deceptive is going on, on the world’s stage. Shoigu is alerting to pay attention to bioweapons. You only have to check the countries not associated with the SCO, CIS and CSTO to get some clarity. There are countries outside this association that are gearing up to use bioweapons and may have already done so. Was COVID-19 one of those releases?)
BATTLE FOR WORLD | August 20, 2020: Russia announcing to be the first to develop and register a working and safe vaccine against the coronavirus, but for the globalist pharmaceutical industry, it was taken as unpleasant news, where Big Pharma immediately started to criticize the Russian vaccine achievement out of fear of losing colossal profits.
The U.S. firm, the Association of Clinical Research Organizations, which links a number of large biopharmaceutical companies, including Bayer, AstraZeneca, Novartis and others, has criticized the Russian vaccine achievement. The organization even sent a letter to the Russian Minister of Health Mikhail Murashko, expressing what it says are concerns regarding plans to use the Russian drug, and told the minister trials for the drug was inadequate.
(BattleForWorld: Basically, the U.S. firm is trying to bully Russia to second place status, to let it know that only U.S. biopharmaceutical companies get first place access, because patents are involved for big profits.)
Regarding trials, the Russian Gamaleya Scientific Research Institute of Epidemiology and Microbiology, the one who developed the vaccine, disagreed with the criticism from the U.S. firm, noting that the technical platform used to develop and test the vaccine has been tried and tested and is well understood. The Russian Federal Service for Surveillance in Healthcare also rebuked U.S. Big Pharma’s claims against the Russian vaccine, that it was doing so based on the lack of knowledge regarding results from the research.
Emphasizing that “The vaccine has passed a serious preclinical stage of testing on animals and has shown the ability to develop cellular immunity and humoral specific immunity,” said Elena Smolyarchuk, Head of the Center for Clinical Study of Medicines at Russia’s Sechenov University.
Further adding that “If certain people, or specific companies lose billions of dollars from the Russian vaccine, what kind of reaction do you expect? It seems to me that the reaction is completely normal,” said Alexander Gintsburg, Director of the Gamaleya Scientific Research Institute of Epidemiology and Microbiology.
BATTLE FOR WORLD | September 4, 2020: One of the Russian vaccines test results were published in the leading international scientific journal The Lancet detailing the results from the first two stages of clinical trials.
Two vaccine developers from the Gamaleya Centre, Alexander Gintsburg and Denis Logunov, as well as the CEO of the Russian Direct Investment Fund Kirill Dmitriev, were interviewed by Sputnik News regarding The Lancet article and why it’s of importance to the global scientific community.
The Lancet, the world’s most influential scientific journal, has published the first two stages of clinical trials results less than a month after the Sputnik V COVID-19 vaccine was registered in Russia.
The timely article responds to foreign criticism, providing long-awaited answers to the West that the Russian vaccine development achievement, the world’s first registered coronavirus vaccine, is not only effective but safe.
“In September (2020), a complete study of the vaccine in animals, primates, Syrian hamsters, transgenic mice, in which the vaccine has shown 100% protective efficacy (and results in primates and Syrian hamsters were obtained before clinical trials), will be published. The first results of the ongoing post-registration clinical trial involving 40,000 volunteers will be published in October-November”, said the Gamaleya Centre, the developers of the Sputnik V vaccine.
The Lancet article highlights the safety of The Sputnik V vaccine as one of the main conclusions cited in the study. Regarding the first and second-stage clinical trial results, the scientists did not find any serious adverse effects from the vaccine based on the evaluated criteria. – Not all candidate vaccines can boast about such results, because some have recorded up to 25% experiencing serious adverse effects.
The Lancet article presented the evidence of the Sputnik V vaccine treatment’s ability to launch and maintain a long-term immune response to the coronavirus in 100% of those vaccinated due to its unique two-stage introduction technology. And Denis Logunov, deputy research director at the Gamaleya Centre, said that a humoral and cellular immune response is achieved, through which is enough to protect a person from COVID-19, observed in 100% of those vaccinated.
“The antibody levels in vaccinated volunteers was 1.4-1.5 times higher than in those who had recovered. For reference, Britain’s AstraZeneca vaccine showed an antibody level roughly equal to the antibody level in those who had had the coronavirus infection”, said Logunov. In addition, all of the volunteers who received the Sputnik V vaccine developed T-cell immunity, represented by both CD4+ and CD8+ cells, making it possible to recognize and destroy coronavirus-infected cells.
One of the western scientific community’s biggest fears about the use of ‘human adenoviral vector vaccines’ – the technology used in Sputnik V – was the ‘pre-existing immunity to adenoviruses’ in some people.
Their concern that ‘the person’s immunity might not allow the required amount of human adenovirus into the body’. This provides as a kind of “taxi” in the vaccine, to deliver the outer shell genetic material of the coronavirus into the cells (important: so that the coronavirus itself does not enter the body with the vaccine, which completely eliminates the possibility of infection).
“We’ve chosen the optimal safe dosage, providing an effective immune response in 100% of those vaccinated, including those who have recently had adenovirus infections. This reduces the urgency of developing new vaccines based on untested platforms”, said Denis Logunov from the Gamaleya Centre.
Unverified platforms that are being used to develop vaccines in some Western companies, which includes mRNA technology (in the Moderna vaccine), and the chimpanzee adenovirus (in AstraZeneca’s vaccine), of which have never been used to create registered vaccines.
And such drugs are badly in need of long-term testing because of concerns about their effect on the body’s reproductive functions or the possible high carcinogenic properties that lead to cancer, said the Gamaleya centre.
Russian scientists refer to studies about the safety of their platform, the vector technology, on which the Sputnik V vaccine is based:
“Since 1953, more than 250 clinical trials have been carried out globally, and more than 75 international articles have been published confirming the safety of vaccines and drugs based on this platform”, said Denis Logunov. Further emphasizing that “Human adenoviral vectors-based drugs have been used for over 15 years. In particular, these are Ebola vaccines and the anti-cancer Gendicine, which has been used in China for over 12 years”.
Gamaleya vs AstraZeneca
Russia is responding to criticism posed by the West about the insufficient number of volunteers for their two-vector vaccine Sputnik V, the scientists noted that they managed to test this system on a wider range of people, and more so than one of the leading vaccine candidates, AstraZeneca, had done.
The British pharmaceutical giant used four times fewer volunteers during the first two-stage trials to gather results about their two-vector vaccine’s effectiveness.
“The number of volunteers involved in testing the Russian Sputnik V vaccine during stages 1 and 2, carried out with two injections, was 4 times higher than the number of people AstraZeneca involved”, said Dmitriev.
The US Food and Drug Administration announced the possibility of using accelerated registration for vaccine candidates due to the current epidemiological situation, the pandemic and high infection rate, without a third phase clinical trial on tens of thousands of volunteers.
And the British authorities are also studying the possibility of a similar approach to the US. At the same time, these countries’ drug regulators, regarding accelerated registration, said it will only be possible for vaccines that have proven their effectiveness and safety.
“To date, the only one meeting these criteria is a human adenoviral vector platform. It has proven its safety through several decades of numerous studies”, emphasized Dmitriev.
Now that The Lancet’s publication of the clinical trial results have been published, Kirill Dmitriev, the CEO of the Russian Direct Investment Fund, has presented a few questions to the United States and British vaccine manufactures regarding their COVID-19 vaccines.
“In turn, Russia can now ask some questions to the international community.
1.) We are calling to publishing official data that would prove the long-term efficacy of chimpanzee adenovirus or mRNA-based vaccines,
2.) the absence of any carcinogenic risks and effects on fertility when used.
3.) We would also like to know why AstraZeneca is pushing for a legal disclaimer for unwanted side effects”.
U.S. questionable vaccine
Source, Sputnik News.
Russia’s Sputnik V COVID-19 vaccine.
News report on the Sputnik V vaccine.
BATTLE FOR WORLD | September 8, 2020: Well, the truth is slowly coming out regarding Bill Gates and Dr. Anthony Fauci’s motives for COVID-19 vaccine in the United States, and Big Pharma for the world. (Russia asks the United States and Britain a few questions about their vaccines, here.)
The United Nations agency social media managers shared a quote on Twitter from Secretary-General Antonio Guterres at a virtual town hall event with women’s civil society organizations in late August where he connected the coronavirus pandemic with “patriarchy,” – the post came under attack.
Guterres said: “The COVID-19 pandemic is demonstrating what we all know: millennia of patriarchy have resulted in a male-dominated world with a male-dominated culture which damages everyone[*1] – women, men, girls and boys,” quoted in the UN tweet sighting a passage from his speech.
(BattleForWorld: [*1] Referring to the endless wars being prolonged by men. [- Mixed Reactions as Trump Slams Pentagon Chiefs For Reluctance to Pull Out of ‘Endless Wars’])
The post drew criticism and outrage for it was interpreted as blaming men for the health crisis[*2] and running with a ‘woke’ left-wing buzzword.
(BattleForWorld: [*2] At the tip of the ruling elites sits seven males. They make a large percentage of the decisions that befalls the Earth.)
(In the Silent Revolution Of Truth, Compilation Edition, Volume 1, “enhanced”, the free PDF book: Download and read about the ‘seven dark ones’, page 1485. The Mighty Ones [the ruling elites] survive in the bunker closet, page 1487. The ‘Council of 7 Men’, page 1489. Implementing genocide to cull the population. They will induce a pandemic using…vaccine to spread fast flu infection, page 1489. Note: Use the page number display located at the top of the page to find the correct page. Free Book, PDF Format – Links: Book Summary | and Download Book – Volume 1)
(In the Silent Revolution Of Truth, Compilation Edition, Volume 2, the free PDF book: Download and read how in the post-COVID era, the countries [of which there are few] who make it their business to take care of their people, will fare better and return back to some form of normalcy, while the rest will be erratic, pages 784 and 790. Note: Use the page number display located at the top of the page to find the correct page. Free Book, PDF Format – Links: Book Summary | and Download Volume 2 Book)
United Nations tweet.
BATTLE FOR WORLD | September 10, 2020: The CEO of AstraZeneca Pascal Soriot in a conference call with investors on Wednesday (Sept 9) revealed that the person who had experienced a severe reaction in its global COVID-19 vaccine trials causing it to pause, showed symptoms related to the rare neurological disorder, spinal inflammatory disorder called “transverse myelitis”.
The participant in the trial was a woman in the United Kingdom, who had suffered symptoms consistent with the disease.
The regulatory board overseeing safety and data components of the vaccine trial has reportedly confirmed that the participant was injected with the British drugmaker, AstraZeneca, COVID-19 vaccine and not a placebo. The vaccine trial was halted after a participant suffered neurological symptoms, diagnosed as multiple sclerosis. AstraZeneca maintains that the event was unrelated to the effects of vaccine.
Sky News reported that the United Kingdom Health Minister Matt Hancock referred to the halt as a “standard process” when something new needs to be investigated and confirmed, and that this was not the first instance of the trial being stopped.
(BattleForWorld: I wonder if this is related to an autoimmune response? Retroviruses are known to trigger such things. There are claims about “transverse myelitis” being reported in acute HIV infection, here. AstraZeneca COVID-19 vaccine, according to the Russians is a chimpanzee adenovirus vaccine. – The documentary released with Dr. Judy Mikovits outing the United States criminal vaccine industry cabal, about vaccines being laced with properties to do other things, refer to the YouTube CENSORED: DOCTORS IN BLACK / PlanDemic, video, here.)
“We addressed the critical problem of pre-existing immunity on the efficacy of Ad-based vaccine carriers by developing vectors derived from chimpanzee-origin Ad viruses termed AdC68 and AdC7 or Pan9 and Pan7, respectively. These vaccine carriers are based on molecular clones18 thereby circumventing risks associated with potential contamination of the vaccines with unidentified pathogens of simian origin”, here. Another article about “chimpanzee adenoviral vectors”, here.
Source, Yahoo News.
BATTLE FOR WORLD | September 8, 2020: The chimpanzee adenovirus vaccine for COVID-19 manufactured by AstraZeneca has been put on pause during the Phase 3 trial after a suspected ‘serious adverse reaction’ by one of the participants in the UK.
AstraZeneca noted that it is “standard review process triggered a pause to vaccination to allow review of safety data,” a spokesperson for the company said on Tuesday (Sept 8) in a Twitter post. Nothing was mentioned on whether the hold was self-imposed or ordered by regulators.
AstraZeneca Twitter post.
BATTLE FOR WORLD | August 28, 2020: The United States on Wednesday (August 26) slapped sanctions on five Russian institutes, and the reason given is that they are developing chemical and biological weapons. The sanctions were imposed to restrict the research institute of the Russian Defence Ministry, which had an important role in developing the first COVID-19 vaccine together with the Gamaleya Institute.
The U.S. sanctions against Russian institutes are aimed at trying to interfere with the marketing of the Russian COVID-19 vaccine, as the U.S. promote their own pharmaceutical companies.
“We are not sure that this is the right step towards cooperation in the fight against the [coronavirus] pandemic, the importance of which, we think, is not disputed even in Washington [DC].” “One gets the impression that it is all about the trivial use of sanctions pressure in the interests of promoting their own companies, now pharmaceutical ones, as is the case with the ongoing promotion of their gas on the European market”. And “This is a continuation of the sort of an addiction to sanctions. Some kind of a Theatre of the Absurd of sanctions. We, of course, categorically reject any statements alleging some of our organisations of involvement or participation in the development of chemical and bacteriological weapons — this is absolute nonsense”, said Russia’s Foreign Ministry spokeswoman Maria Zakharova on Thursday and Friday (August 27 and 28).
(BattleForWorld: Readers, you see what is happening, U.S. Big Pharma is trying to push-out other vaccine makers. It was set from the beginning all along, to use the coronavirus pandemic for profit. Was the pandemic deliberate?
And even though the U.S. has pulled funding from WHO [the World Health Organization], it is going to try and use the organization to give it first preference, to laud its vaccines as more preferred.
While the U.S. is blaming China for the virus, it’s the U.S. who’s pushing to profit big from the virus.)
Source, Sputnik News.
Covid-19 vaccine research.
BATTLE FOR WORLD | September 1, 2020: Finally, after several months of COVID-19 death hysteria media hype in the United States because of Dr. Anthony Fauci, the CDC (Centers for Disease Control and Prevention) has released new data last week showing that many Americans who have died from COVID-19 also had other contributing conditions.
The report highlights that only 6% of deaths have COVID-19 as the only cause mentioned (that’s approximately 9,000), and that 94% of patients who died from coronavirus also had other “health conditions and contributing causes.”
CDC COVID-19 death chart hysteria drama.
BATTLE FOR WORLD | August 31, 2020: On August 12 Russia announced that it was the first country in the world to register a vaccine against the coronavirus COVID-19. The approval of the vaccine before large-scale safety trials prompted disbelief and attacks from the United States and Britain – but now health authorities in those countries say they might do the same as Russia.
On Monday (August 31) director of the Russian Direct Investment Fund, Kirill Dmitriev, told reporters that the fund “notes the desire of the US and British authorities to follow the fast-track registration procedure for coronavirus vaccines that has been applied in the Russian Federation”. And that “The Western world was shocked by Russia’s success and had to go through four stages of accepting the inevitable: denial, anger, depression, and ultimately acceptance. Recent statement show that some of our Western partners already passed the stage of depression and it has now been accepted that Russia’s approach is the correct one.”
The U.S. FDA Commissioner Stephen Hahn told the Financial Times that he is prepared to fast-track the coronavirus vaccine process with emergency use authorization before Phase 3 trials are completed, if the benefits outweigh the risks.
(BattleForWorld: To fast-track vaccines in this way for approval, the manufacturer has to be confident in the science and technology that goes into producing the vaccine. Also keep in mind that the U.S. has exempted vaccine manufacturers from liability. Does this give them a loophole to fast-track vaccine approval?)
While the U.K. government has set out plans to approve a future vaccine using a temporary authorization by the local drugs regulator before getting the approval of the European Medicines Agency that the UK is still a member of.
Source, Sputnik News.
BATTLE FOR WORLD | August 24, 2020: The country of Italy on Monday started human trials of their own potential COVID-19 vaccine, named GRAd-COV2, developed by ReiThera, a Rome-based biotechnology company.
Human trials are being done at Rome’s Lazzaro Spallanzani Hospital, known for its specialization in infectious diseases. 90 volunteers will receive the GRAd-COV2 vaccine. Financing for the trials came from the Lazio administrative region and the Italian Research Ministry.
“We will see if it produces any side effects and if it produces neutralizing antibodies,” Vaia, the Anadolu Agency, who noted that the second phase of the trial will be done in countries showing high infection rates of COVID-19, to include Mexico and Brazil.
(BattleForWorld: The more countries develop their own COVID-19 vaccines, the better, because it ensures and prevents one country from weaponizing their vaccine using politics. Y’all see what US Big Phama and the news media are doing to President Trump regarding COVID-19 treatments?
I think the US is going to manipulate WHO [the World Health Organization], to give it first preference, to laud its vaccines as more preferred.)
Italy’s COVID-19 vaccine developed by ReiThera.
BATTLE FOR WORLD | August 24, 2020: President Trump has announced the emergency authorization of convalescent plasma for COVID-19, a treatment that already has been given to more than 70,000 patients, according to experts familiar with the therapy.
The White House press secretary Kayleigh McEnany in a tweet said: “a major therapeutic breakthrough on the China virus.” – The treatment is convalescent plasma, and several scientists and physicians believe that the therapy might provide some benefit but is far from a breakthrough. It is rich in antibodies proved to be helpful in fighting the coronavirus, and is being used in China, Russia and other countries.
On CBS’s “Face the Nation” on Sunday (August 23), former FDA commissioner Scott Gottlieb said the blood product was already widely available, so the change would be “incremental.” But if it is as Mr. Gottlieb said to be widely available, emergency authorization by the president would not have been necessary. Is Mr. Gottlieb fibbing? Because Dr. Anthony Fauci does not support convalescent plasma therapy or usage of hydroxychloroquine and because of this, stumbling blocks were put in the way to discourage doctors from using them.
Dr. Anthony Fauci is not interested in having US doctors use hydroxychloroquine or blood plasma antibodies because they are not treatments under patents. The US President authorizing convalescent plasma with an executive order is overriding Dr. Fauci’s recommendations. And what that says is, Big Pharma corporate interest that Fauci represents and the White House are at war.
Over the many decades corporation-power was being setup to behave like what we’re seeing now, having corporations chip-away at the powers of the US presidency. This is exactly what the social media platforms are doing, including the corporate news media. It’s a sign that the US central government is in decline.
There has been a massive disinformation campaign that stretches from sections of the US government that has been taken over by corporate influence with news media support. Who are blatantly suppressing true information by attacking it with false narratives.
BATTLE FOR WORLD | August 22, 2020: President Trump has sounded the alarm warning the American people, to let them know that the Food and Drug Administration, the FDA, is slow-walking vaccine testing until after the November presidential election.
The president in his tweet said, “The deep state, or whoever, over at the FDA is making it very difficult for drug companies to get people in order to test the vaccines and therapeutics. Obviously, they are hoping to delay the answer until after November 3rd. Must focus on speed, and saving lives!”
Trump’s Twitter post.
But according to the FDA, human trials for a COVID-19 vaccine are currently being carried out. And no vaccine has been produced yet passing all the safety checks necessary for general population use.
President Trump also tweeted in another post referring to the FDA’s decision to revoke emergency authorization of hydroxychloroquine and chloroquine to treat COVID-19 because it was “unlikely to be effective” (BattleForWorld: Blame Dr. Anthony Fauci. He prefers the patented drug Remdesivir – more money.)
Source, The Sun.
BATTLE FOR WORLD | August 22, 2020: In the United States Big Pharma dictates, silencing doctors for using the inexpensive and popular drug hydroxychloroquine to treat the coronavirus COVID-19 illness.
Dr. Mark McDonald speaks out about the cover-up to news site Weberzwayfilms:
Host: Do you believe that the coronavirus is basically something like smaller, like the flu, that we could be OK with?
Dr. McDonald: Well, the virus is real, but the numbers are not. In fact death as of today in the pediatric population from seasonal flu far exceed that from coronavirus. The CDC director himself announced this last week while he was also announcing that suicides have gone up 25% since last year – doubled. Depression has gone up 400% since the same time last year in the child population…
Host: Why do you think YouTube, Instagram and Facebook have silenced you guys?
Dr. McDonald: Because what we are saying is dangerous. It’s dangerous to a coalition of forces – specifically politicians, some media, and special interest groups, such as teachers’ unions, pharmaceutical companies and vaccine makers, to consolidate, grow and maintain their power and their money.
Host: Is hydroxychloroquine even bad?
Dr. McDonald: Hydroxychloroquine has been a safe and effective medication throughout the world for sixty-five years. It was developed from tree bark (BattleForWorld: i.e., cinchona bark) and then turned into “quinine” which was used by the British in India to protect against malaria infections. Today, the synthetic form such as hydroxychloroquine is used throughout the world. It is actually a WHO mandated necessary medication and to keep and to prevent against malaria pandemics. And it’s beings used in the United States for lupus, rheumatoid arthritis (BattleForWorld: e.g., swollen joints, joint pain, leg cramps, leg heaviness, etc.) on a daily basis for decades in patients who take it every single day – women, children, pregnant women, nursing mothers and elderly adults. – Even now in Africa it is considered to be a supplement and sold over the counter in many countries safely and effectively.
Until this year, hydroxychloroquine was consider to be safe for all people. It was only after January of 2020 that hydroxychloroquine became the devil.
Host: Who’s pushing against hydroxychloroquine; who’s behind it?
Dr. McDonald: I think there’s a coalition of forces that are behind the push against hydroxychloroquine. It started in January when Gilead pharmaceuticals announced some benefits to a patented drug called Remdesivir that reduced hospital stay course for those with coronavirus by 3 or 4 days, certainly meaningful, but certainly not curative. As soon as that happened, media, politicians, other special interest groups got onboard with trying to stop hydroxychloroquine from being made available by doctors to their patients and a whole campaign was set against it, including several research publications like the Lancet back in June that published fraudulent data to say that hydroxychloroquine did not work or it killed people – was later retracted [by The Lancet journal].
My belief at this point is that it is all about the election (i.e., presidential 2020) and there are people now in position of power, politicians primarily, who will benefit from, keeping America scared, stuck at home through November. If all Americans had access to hydroxychloroquine the pandemic would essentially end in about 30 days. And if that happens a lot of people (i.e., politicians playing power games) would lose.
Host: And who are you voting for in 2020?
Dr. McDonald: For which office?
Host: The presidency.
Dr. McDonald: I voted for Donald Trump four years ago. I will vote for him again.
BATTLE FOR WORLD | August 20, 2020: The country the United States has hit with a number of sanctions over the years, nonetheless, Cuba is making headway and is about to start testing their own COVID-19 vaccine, according to the official Cuban registry for clinical trials.
The name of the vaccine is “Soberana 01” produced by the state-run biopharmaceutical company the Finlay Institute of Vaccines and will be tested in a phase I trial involving 676 adults between 19 and 80 years old, for its effectiveness and evaluation regarding side effects and toxicity. If results are good the trial will move to phase II to continue to determine if the medication works. Results will be published around February 2021.
In May (2020), Cuba’s leader Miguel Díaz-Canel noted the need to produce a local vaccine to ensure the nation’s “sovereignty.” (BattleForWorld: This has been a repeating theme and implies that at some point, the accessibility of vaccines will be weaponized. Meaning that if you want access to COVID-19 vaccines you will have to do whatever the globalists require. And countries who are unable to develop their own vaccines will be caught in-between faction wars. The country of Jamaica has been subjected to this tussle, where it was told by the U.S. not to use the Cuban interferon medicine to treat COVID-19.)
Over the decades Cuba has created an impressive biotechnology industry that produces vaccines and medications used locally. They have developed a drug to prevent ulcers caused from diabetes, and at the beginning of the coronavirus pandemic, the government aggressively promoted their interferon medication to treat COVID-19. (BattleForWorld: In the United States the FDA due to drug-politics was told to shutdown interferon testing because drug patents were more profitable.)
Cuba’s “Soberana” COVID-19 vaccine.
BATTLE FOR WORLD | August 18, 2020: The coronavirus COVID-19 pandemic keeps twisting and turning. In the latest tracking of the virus, news is being reported that the original virus strain has mutated into something that is less deadly, and that is a good sign, although more infectious.
(BattleForWorld: How can a deadly strain mutated into something less deadly so fast? They are saying it has degraded, appear to be suggesting into something like an influenza. Is this, the new mutation, possible in such a short period? In mid-April when my source had forecast that the quarantine would start lifting, in June there was a rumor – that a mild antidote was released, i.e. aerosolized into the air. The weak antidote implied that the virus would eventually come under control in some mysterious way, just as how the infection was mysteriously spreading fast worldwide. So, eventually, the public would come away with the impression that the virus COVID-19 was a spook, not even knowing about the secret workings to curtail the virus on the private-side with the release of a mild antidote.)
The new mutation, discovered in early February (2020), is called “D614G mutation”, being reported as a common strain of the COVID-19 novel coronavirus found in Europe and North America and also parts of Asia – India, Malaysia and the Philippines, said to be more infectious than other strains. But that, however, it is less deadly, said Paul Tambyah, the president-elect of the International Society of Infectious Diseases.
So basically, the warning is that the new strain was 10 times more infectious, but that the virus mutation was unlikely to reduce the effectiveness of potential vaccines. That means there will be a vaccine push for inoculation replicating the safeguard against something like the seasonal flu – where a yearly vaccine is needed. (BattleForWorld: From the early beginning when President Trump formed the Task Force, this was what Dr. Anthony Fauci was suggesting. How could he have known that in such a very short time, in weeks? Strange.)
COVID-19 – D614G mutation, less deadly, but more infectious.
BATTLE FOR WORLD | August 18, 2020: Another Russian COVID-19 vaccine on the way. The ‘Vector’ virology center in Novosibirsk has announced that an entirely different solution to treat COVID-19 is entering the second stage of clinical trials.
Russia is investigating all the possibilities to potentially fix the coronavirus. Anna Popova, the head of the national health watchdog Rospotrebnadzor, has announced on Monday (August 17) that volunteers were injected with Vector’s experimental vaccine on August 12, and five days later, on August 17, a second group received the vaccine.
“Clinical trials are being carried out today, and all the specially selected volunteers are doing well,” and “Those who received the vaccine have not shown any adverse reactions, and there is not even the slightest reddening at the injection site,” noted Popova.
(BattleForWorld: The COVID-19 vaccine from Vector in Novosibirsk is going to be the game changer!!! This is going to be the “pièce de résistance” of vaccines, period. Using new technology coming from a place known in Russia since Soviet times to be the heart of Russia’s science city, that has developed extraterrestrial-like technologies now being used on the Earth.)
BATTLE FOR WORLD | August 17, 2020: The People’s Daily of China is reporting, citing documents from their National Intellectual Property Administration regulator, that the pharmaceutical company CanSino Biologics Inc has won a patent from Beijing to produce the country’s first COVID-19 vaccine. The patent was issued on August 11.
Now we have two vaccines, from Russia and China, being produced to treat the coronavirus COVID-19.
(BattleForWorld: In the United States two of the ruling elite factions that have taken over the U.S. foreign policy – have the U.S. wasting its money on hording military weapons and also foolishly giving away billions of dollars to countries to keep subterfuge and wars alive. There’s no America first for the American people anymore. It has been, a foreign country first, and maybe America second, if it’s good [i.e. stirring up strife] helping the foreign country. 95% of the United States congress is being blackmailed by a foreign power – hence for all the foreign policy tension, sanctions, government revolutions, etc. All being done by a small group of elites inside the U.S. that has wrapped its claws around the United States. So the United States being first in this and that is over, because it chose to stop investing in its people and chose instead to invest in a foreign country bent on world domination ambition.)
China’s CanSino’s COVID-19 vaccine.
BATTLE FOR WORLD | August 16, 2020: Russia has revealed that Western research institutions are seeking to lure away (i.e. BUY) scientists from the Gamalei National Research Center for Epidemiology and Microbiology of the Russian Health Ministry, but that the West has not had any success, said the research center’s chief, Alexander Gintsburg.
(BattleForWorld: What this means is that the West is at a disadvantage in the vaccine technology that Russia is using to develop their COVID-19 vaccine. And that implies that the vaccines being developed in the West are inferior.)
The chief further states: “Our researchers have been working at the Gamalei Institute for ten years… Any American or European university can only dream of having such researchers. And they are seeking to lure them away. But they won’t be able to,” aired on the Vesti Nedeli weekly news roundup on the Rossiya-1 television channel.
Director of the National Research Center of Epidemiology and Microbiology, Alexander Gintsburg
BATTLE FOR WORLD | August 16, 2020: Russia has announced that it has started production of the world’s first novel coronavirus vaccine, named Sputnik V, created by the Moscow-based pharmaceutical company the Gamaleya Research Institute of Epidemiology and Microbiology. The vaccine was fast-tracked for approval after proving that it was capable of building up immunity against the virus COVID-19 during limited human testing.
An animation promotional clip for the Sputnik V COVID-19 vaccine showing it in action destroying the virus was released by The Russian Direct Investment Fund, Russia’s sovereign wealth fund.
The CGI video, 38 seconds long, starts out showing the Earth being swallowed up by a giant coronavirus spore. Then, a satellite resembling Sputnik 1, (i.e. the world’s first artificial Earth satellite launched into space by the USSR in 1957), approaches and penetrates the virus, breaking through and flying out, where it then circles around the infected virus-planet, as the giant virus spore is gradually eradicated.
Russia says it expects to produce 500 million doses of the vaccine next year, and has also announced that production and additional clinical trials are expected to take place in other countries .
The Sputnik V vaccine, also known as “Gam-COVID-Vak”, is an adenoviral vector vaccine consisting of two shots, – the second dose is injected three weeks after the first one.
While in the United States Dr. Anthony Fauci who holds several patents to manufacture vaccines and drugs to secure excessive profits for the ruling elites, is in disbelief as Russia announced the first safe COVID-19 vaccine product, now in production.
Animation promotional clip for the Sputnik V COVID-19 vaccine.
BATTLE FOR WORLD | August 15, 2020: Russia has registered the world’s first vaccine as doubts spread abroad, even with recent comments coming from the US president. RT talks to the head of the Gamaleya Institute of Russia, Alexander Gintsburg, for more information on how they managed to get a vaccine developed so quickly.
Many are going to be surprised by the answer. And the question as to be asked: are the research institutes in the West driven purely by patent profits and ego?
Although the vaccine was created in just five months, it “wasn’t made from scratch,” noted Gintsburg. Who explains that “A whole generation of biotechnicians, virologist, immunologists… have been for more than 20 years developing the technology that was used to create this vaccine along with at least six other drugs.” And added that the institute’s work on the Ebola vaccine GamEvac-Combi several years ago was particularly helpful, whose research went into determining things like the composition of the drug and immunization doses.
BATTLE FOR WORLD | August 13, 2020: Russia has registered the world’s first Covid-19 vaccine and is prepared to cooperate with countries interested in developing and producing vaccines and treatment for the coronavirus, said the Moscow representative to the United Nations (UN).
“We are ready for international cooperation with all interested partners in the development and production of vaccines and treatments to ensure a coordinated global response to the spread of Covid-19 and a common victory over the pandemic,” Ambassador Vassily Nebenzia announced to the UN Security Council on Wednesday (August 12).
Western governments have belittle the Russian achievement, demanding to see evidence of the vaccine’s safety, WHILE THEIR OWN pharmaceutical companies have been exempt from liability lawsuits over potential adverse effects. That means the United States is lauding about the safety of vaccine, but yet cannot guarantee it for their own citizens. Why?
Kirill Dmitriev, head of the Russian Direct Investment Fund (RDIF) that funded the vaccine research project, said that a “politicized approach to the Russian vaccine on the part of a number of Western countries endangers the lives of their citizens.” (BattleForWorld: It appears the West does not want the coronavirus pandemic to end soon. Are other motives involved to not want this for their citizens?)
BATTLE FOR WORLD | August 15, 2020: The United States CDC has morphed into a criminal organization doing all sorts of unethical things in the name of science. Over the many decades what they have done with cancer, autism, HIV-AIDS, etc., hiding information from the public, their latest undertaking is politicizing the coronavirus to spread fear with the aim of prolonging the pandemic for profit using drugs and vaccines developed under patents.
The CDC (Centers for Disease Control and Prevention) as well as NIH (The National Institutes of Health) are both in need of overhaul.
Two senior Trump appointees have departed the Centers for Disease Control and Prevention on Friday (August 14), bringing a change to agency that has been heavily scrutinized for its approach to the coronavirus.
The CDC’s chief of staff, Kyle McGowan, and the deputy chief of staff, Amanda Campbell, have both announced their departure from the agency on Friday.
More departures are needed because these organizations have been compromised.