On Sat, Nov 14, 2020, 4:26 PM Gary Kohls <[email protected]> wrote:

>
*To my many online vaccine skeptic colleagues: The current issue of the
> Duluth Reader published a Letter to the Editor from a local Duluth, MN
> Emergency Room physician whose final statement was “*Kohls is
> intellectually dishonest and needs to go”. His arguments concerning  the
> current pandemic will seem plausible to most readers (and also most
> publishers and editors of most newspapers) so I would appreciate some
> outside help from colleagues in refuting his arguments. I have made it a
> policy of mine to not get down in the mud with critics and waste valuable
> time and column space in responding to critics. My experience is that most
> of my critics in the past have been trolls. However this critic (who did
> not identify himself as an ER doc) seemed to make plausible arguments that
> are very much in line with the mainstream Big Pharma, Big Media, NIH, CDC,
> NIAID, FDA  narratives.
>
> Anyway I hope somebody out there might be willing to refute some of the
> statements made by the letter-writer. The email address to use is
> [email protected]. In case anybody wants to mention how the Reader’s
> LTE section for 11/12/2020 was accessed, the web address was
> https://duluthreader.com/articles/2020/11/12/116271-letters-nov-12-2020.
>
> Immediately below is the LTE and below that is the published column that
> Dr Bernhardt criticized (also attached above).
>
> Thanks, Gary
>
>
> _______________________________________________________________________________________________________________________________-
>
>
>
> *Kohls continues to misinform*
>
> Gary Kohls continues his campaign of misinformation and disinformation
> about SARS-COV-2, testing and vaccinations. His November 5th column begins
> with the lie that “the elusive (and therefore dubious) SARS virus has not
> yet been isolated in the lab, much less been reproducibly grown in living
> tissue culture.”
>
> Fact: On January 20, 2020, CDC received a clinical specimen collected from
> the first reported U.S. patient infected with SARS-CoV-2. CDC immediately
> placed the specimen into cell culture to grow a sufficient amount of virus
> for study. On Feb. 2, 2020, CDC generated enough SARS-CoV-2 grown in cell
> culture to distribute to medical and scientific researchers
> <https://www.cdc.gov/coronavirus/2019-ncov/lab/grows-virus-cell-culture.html>
> .
>
> Kohls then proceeds to describe our current situation as an “alleged
> pandemic which has relied on testing with the equally dubious PCR test
> kits...” The test kits are properly described as RT-PCR, which stands for
> Reverse Transcriptase Polymerase Chain Reaction. It’s the PCR portion that
> Kohls has issues with. It is an extensively tested technique for
> identifying short chain sequences of DNA. Kohls claims “the PCR test’s
> inventor has repeatedly asserted that his test CANNOT be used for
> diagnostic purposes.” Fact: PCR and RT-PCR are widely used around the world
> for diagnosis of viral disease. The test is extremely accurate and
> sensitive.
>
> The test inventor, Dr Kary B. Mullis won a Nobel prize for his work. He
> died in 2019 before the pandemic started so he had nothing to say about
> SARS-COV-2. He additionally never said the test could not be used for
> diagnostic purposes. That notion circulated this past summer on Facebook
> and fringe websites – the very places Kohls does his research. There are
> several debunkings of this by responsible organizations such as Reuters
> <https://www.reuters.com/article/uk-factcheck-pcr/fact-check-inventor-of-method-used-to-test-for-covid-19-didnt-say-it-cant-be-used-in-virus-detection-idUSKBN24420X>
> .
>
> Kohls then expresses doubt that asymptomatic people with a positive test
> are truly infected, calling it “conventional wisdom.” Conventional wisdom
> actually did not expect high asymptomatic infection rates based on
> experience with SARS-COV-1. These people go on to develop antibodies so we
> do know they were infected. Kohls must know this.
>
> All of this is in the first four paragraphs of Kohl’s article. It’s clear
> Kohls has no training or expertise in virology or diagnostic testing. He
> then goes on to disparage the proposed vaccine protocols in his typical
> tendentious fashion, taking issue with statisticians who design the trials
> because he knows better. He suspects they’re crooked and own company stock.
> He doesn’t like the risk reduction statistics in particular but doesn’t
> tell the reader that continuing information is accrued from vaccinated
> people far beyond the phase three trial.
>
> On the date of publication of Kohl’s article there were 123,718 newly
> diagnosed Covid-2 cases and 1,154 deaths. The world needs an effective
> vaccine as soon as safely possible. Some risk attaches to any new vaccine
> and can only be discerned by trials and follow up. The world also needs
> accurate information. Robert Boone, that’s your responsibility. Se fi
>
> Greg Bernhardt – Duluth
>
>
> ____________________________________________________________________________________________________________________________
>
>
>
> *The Flawed Covid-19 Vaccine Testing Programs at Moderna, Pfizer, Johnson
> & Johnson and AstraZeneca *
>
>
>
> *Bu Gary G. Kohls, MD – November 1, 2020 (1803 words)*
>
>
>
> *There doesn’t appear to be much difference between the testing protocols
> of the dozens of pharmaceutical companies that are working on developing a
> vaccine for the elusive (and therefore dubious) SARS virus that has not
> actually yet been isolated in the lab, much less been reproducibly-grown in
> living tissue cultures. *
>
>
>
> *The evidence for the existence of the new SARS-CoV-2 virus in any given
> patient has mostly been assumptive in the current alleged pandemic which
> has relied on testing with the equally dubious PCR test kits that have been
> manufactured by any number of fly-by-night outfits which are making
> unreliable test kits. *
>
>
>
> *The “case” incidence and death statistics of the current alleged pandemic
> must therefore be also regarded as dubious because the PCR test’s inventor
> has repeatedly asserted that his test CANNOT be used for diagnostic
> purposes.  *
>
>
> *However, the aggressively Big Pharma/Big Media-promoted “conventional
> wisdom”  says that if the PCR test turns out to be positive (even if the
> PCR-positive individual is totally asymptomatic, always wore the masks and
> never ever developed Covid symptoms) that subject must be assumed to be so
> infectious that he must be quarantined for weeks. If the subject does not
> comply with the quarantine order, he or she can– in certain jurisdictions –
> be arrested and imprisoned. *
>
>
>
> *What should be of concern to thinking people is the fact that some of
> these pharma companies (not to mention that many of the PCR test kit
> manufacturers) are indeed just “start-ups” - like the National Institutes
> of Health’s (and Anthony Fauci’s) favorite vaccine company Moderna, whose
> business only involves vaccine development - not manufacture.*
>
>
>
> *Yet Moderna is deeply involved in the race for FDA approval, and its
> stock price has sky-rocketed on hopes that it might massage its test
> results enough to get its Covid-19 vaccine approved (or at least be given
> Emergency Use Authorization [EUA] by the FDA). *
>
>
>
> *Despite its sky-high stock price ($67 per share as of October 30, 2020),
> Moderna has yet to earn a single penny from the sale of any of its handful
> of experimental vaccines. It has, not surprisingly, developed its protocol
> for testing its 2-dose experimental Covid-19 vaccine that is essentially
> the same as the announced protocols of Johnson & Johnson, AstraZeneca and
> Pfizer’s Covid-19 vaccines in that half of the approximately 30,000
> volunteers that they have amassed will be injected with two doses of its
> active vaccine (each of which contains uncertain-to-be-safe ingredients).
> The other half will be injected with a placebo. (Interestingly, in the
> past, some vaccine-testing companies have added a tissue-toxic ingredient
> that will cause injection-site symptoms presumably so that the placebo
> group won’t know if they got the vaccine or not.)*
>
>
>
> *There are reportedly any number of start-up and established
> pharmaceutical corporations world-wide that are also trying to be the next
> block-buster vaccine-seller on the planet, but NONE of them, much less the
> four experimental vaccine companies listed below, have been following
> time-honored methods of testing its experimental drugs and vaccines on lab
> animals, a serious breach of protocol that has become the “new normal” in
> order to comply with President Trump’s Operation Warp Speed, agenda which
> Trump has been pushing in order to produce a vaccine – any vaccine - before
> his re-election bid is decided!! *
>
>
>
> *Of course, the fast-tracking (aka, “short-circuiting”) of normal vaccine
> safety and efficacy studies has been condemned by all ethical scientists
> that don’t have economic or professional “conflicts of interest” that
> guarantee profitable results from the dangerous pseudoscientific
> pro-vaccine stances that Big Pharma shills like those in the Trump
> administration and the current HHS, NIH, CDC, NIAID and FDA has taken over
> the past 10 months.  *
>
>
>
> *Conditional, tentative, Emergency Use Authorization (EUA) from the
> already corporate-compromised FDA is likely to be granted even if the data
> that is presented to the FDA regulatory commissions are flawed and/or
> statistically insignificant – which means that the vaccine has not been
> proven to be safe and effective, especially in the long-term, which, by
> definition, can’t be safely assessed for many years. Sadly, the members of
> most standard “regulatory” commissions are often corporate shills that have
> ulterior motives.*
>
> *There are 30,000 volunteers in each drug company’s study groups and they
> are essentially healthy, essentially middle-aged, eager and “patriotic”
> volunteers. Half of the 30,000 will be injected with a series of two
> immunologically-active vaccines. The other 15,000 members of the group will
> get two shots of a placebo that is supposed to be immunologically-inactive.
> None of the 30,000 will be informed as to which group they are in.*
>
>
>
> *The approximately 30,000 total human guinea pigs that signed up for the
> Moderna study will be monitored until a paltry 53 of the 30,000 volunteers
> gets positive (and very dubious) PCR test results! The 53 may not have -
> and may never develop - SARS signs and symptoms for them to be included in
> the study!*
>
> *Of course, false-positive PCR tests are extremely common and can happen
> to anybody, especially people who have had a common cold, which is often
> caused by simple, benign coronaviruses.*
>
>
>
> *The designers of the Moderna study – just like the other drug companies
> that are in the race – will argue that their study should be considered
> relevant, reportable to the FDA as theoretical proof of effectiveness but
> they cannot claim that their vaccine is either safe or effective long-term.
> *
>
>
>
> *However, these short-term studies can only be partially relied upon for
> short-term safety and effectiveness if 13 or fewer of the 53 PCR-positive
> “cases” occurred in the vaccinated population while at the same time 40 or
> more of the positive PCR “cases” occurred in the placebo group. What won’t
> be discussed will be the fact that over 14,900 of both the placebo group
> and the vaccine group also didn’t have positive PCR tests Covid-19
> symptoms! *
>
>
>
> *It is totally appropriate for legitimate doubters of America’s Big
> Pharma-co-opted drug and vaccine regulatory agencies to ask the question,
> “What kind of Big Pharma-influenced, profit-oriented, junk science is
> behind the studies that are being hastily approved by the likes of the
> obviously co-opted HHS, NIH, CDC, NIAID and FDA? *
>
>
>
> *It is also totally appropriate for the public to have full information
> about what kind of coercive pro-vaccine influence is coming from such Trump
> appointees as his HHS director (and non-physician) Alex Azar, who came into
> Trump’s administration from a $2 million dollar per year CEO post at Big
> Pharma/Big Vaccine giant Eli Lilly. Azar also is part of Trump’s Operation
> Warp Speed, which is the impetus behind the fast-tracking of vaccine
> development, which is certain to be a disaster.*
>
>
>
> *There will surely be dubious conclusions coming from all of the other
> provably untrustworthy pharmaceutical corporations that are in the race to
> develop an Emergency Use Authorized-vaccine that will not have been proven
> to be either safe or effective long-term – but will certainly be
> unaffordable. *
>
>
>
> *Suspiciously, the major investment partner of start-up Moderna is
> actually the US government regulatory and funding body called the National
> Institutes of Health (including the CDC and the NIAID) which reportedly has
> a 50% financial stake in the company. *
>
>
>
> *One can safely assume that – given the corrupt capitalist system that has
> thoroughly taken over our nation - that every Moderna shareholder (even our
> government bureaucracies) will do everything they can do to promote its
> products. *
>
>
>
> *One must suspect also that these government agencies and their buddies in
> the corporate world are doing everything they can to keep the sheeple from
> noticing the most important data points in the studies discussed. *
>
>
>
> *And one of those bits of information is that at least 29,800 of the
> 30,000 volunteers in Moderna’s vaccine trials, will likely not become
> infected whether the got the placebo or the vaccine. What could easily
> happen long-term is that a significant number of the 15,000 in the vaccine
> group, are at risk of developing disabling chronic illnesses such as
> autoimmune disorders. *
>
>
>
> *What About the Vaccine Trials of** Pfizer, **Johnson & Johnson,
> AstraZeneca, et. al.?*
>
>
>
> *The other significant statistical realities that won’t be pointed out in
> the corporate-controlled medical journals (or the corporate-controlled
> media) are the concepts of “Actual Vaccine Efficacy” and “Relative Vaccine
> Efficacy”, which are akin to the likewise purposely hidden-from view Actual
> Risk Reduction (AAR) and Relative Risk Reduction (RRR) that are often
> ignored in drug efficacy trials. *
>
>
>
> *For Moderna, 13 positive PCR tests in the 15,000 member vaccine arm of
> their trial 13/15,000 = 0.00086) is an arbitrarily chosen data point that,
> when compared to the placebo trial may represent some sort of significance.
> 0.00086 is an obviously miniscule number that is the same as a percentage
> figure of 0.086 %. *
>
>
>
> *And 40 or more positive PCR tests in Moderna’s placebo group of 15,000
> subjects (40/15,000 = 0.0027) likewise represents a similarly miniscule
> percentage figure of 0.27 %. Subtracting 0.086 % from 0.27 % will obtain
> the “actual” miniscule benefit of being vaccinated (0.086 %) with Moderna’s
> potentially toxic vaccine vs. receiving the presumably innocuous placebo.*
>
>
>
> *However, the falsely-inflated “relative” vaccine effectiveness numbers
> means that in calculating the Moderna results takes the fraction 13/40
> (which = 0.325 in decimal terms, and which is 32.5% in percentage terms.
> The corporation’s mathematicians, in the standard method of calculating
> relative risk reduction (RRR), subtracts the 0.325 from “1”, resulting in a
> decimal number of  0.675 (which, in percentage terms is 67.5%). *
>
>
>
> *So Moderna statisticians – who may, incidentally, own shares in the
> company - will then report to his bosses at corporate headquarters the
> “relative” effectiveness rate of 67.5 %, which the bosses will receive as
> positive, whereas it is a actually a deceptively inflated figure when it is
> put side-by-side with the actual vaccine effectiveness number of 0.184.*
>
>
>
> *­­*Note that *Pfizer’s* experimental vaccine trial also uses the PCR
> positivity number of 32 in the 30,000 group, 25 in the 15,000 placebo
> group, and 7 in the 15,000 vaccine group as starting statistical analysis
> points.
>
>
>
> Using those numbers, *Pfizer’s* statisticians are actually reporting out
> the falsely-inflated Relative Risk Reduction/Relative Vaccine Effectiveness
> numbers (rather than the Actual Risk Reduction (ARR) numbers to America’s
> easily propagandized press corps and medical professionals, who can be
> relied upon to report – over and over again – the inflated benefits to
> their listeners, viewers and patients.
>
>
>
> Predictably,* Johnson & Johnson* is also using the same mathematical
> trickery as the other Gang of Four, using as their arbitrary PCR-positivity
> break-points the following numbers: 77 PCR-positive tests among the 30,000
> total group; 59 PCR-positive tests in the 15,000 person placebo group,
> and17 PCR-positive tests in the 15,000-person vaccine group.
>
>
>
> *AstraZeneca* is doing the same, just using slightly different numbers of
> PCR-positivity: 50 in the 30,000 group, 38 in the15,000 placebo group and
> 12 in the 15,000 vaccinated group.
>
>
>
> What we seem to have is well expressed in my version of Mark Twain’s
> famous quote: *“There are 3 (or 4) kinds of lies: Lies, Damned Lies,
> Statistics and Covid Statistics”. *
>
>
>
> Discuss.
>
>
>
>
>
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