It’s hardly newsworthy that medical science is distorted by money. But last week, a case arose that is so blatant, so extreme, and so suspiciously criminal that it should become a rallying point for all of us interested in reform. It involves the two best-respected medical journals in the world, and a finding that immediately affected the lives of thousands of patients around the globe. Two papers purported to be derived from a large, worldwide database, but they were quietly withdrawn when the data was requested by outside reviewers, and none could be produced. Where is the outrage? Where is the passion for reform?
Hydroxychloroquine is a cheap, out-of-patent drug that literally millions of travelers have been using for 65 years for prevention of malaria. It is also taken on a daily basis by hundreds of thousands of lupus patients. Its safety profile and side-effects are well established. Front-line doctors in Wuhan told us early that, in combination with zinc, it was the most effective COVID treatment they knew. It had previously been used with success during the SARS epidemic of 2003. European doctors reported anecdotal success with chloroquine/zinc, and it became standard treatment in France, the Netherlands, and elsewhere [review]. There were about 70 ongoing clinical trials before the two articles appeared.
HCQ has been discouraged by Anthony Fauci and segments of the American medical establishment, and I have wondered if they were compromised by their investments. Fauci is associated, ideologically and financially, with vaccines. The primary competitor for HCQ is Remdesivir, belonging to Gilead Sciences, and selling for $1,000 per dose. Billions of dollars have already been invested in developing a COVID vaccine. That COVID seems to be treatable and that the pandemic is fading with the spring weather is welcome news for world health, but it is devastating for investors in Gilead, Moderna, AstraZeneca, and 20 other companies that are racing to produce a COVID vaccine.
Last month, the two most prestigious medical journals in the world reported large studies by prestigious researchers, based on a large COVID data set from Asia, Europe, and America. The lead author is from Harvard’s Brigham and Women’s teaching hospital. Here is the Lancet article, claiming that hydroquinone is worse than useless. The data appear to show that people treated with HCQ are dying at 3 times the rate of other, similar patients. Here is the New England Journal article, which analyzes comorbidities but does not mention HCQ.
The Lancet paper had been duly peer-reviewed and rushed into print by editors. But seasoned researchers in the field immediately smelled that something must be wrong. How could this huge database of patients exist, crossing four continents and going back to the earliest days of the virus, when no one thought the records would be valuable? How could comparable conditions be established in hospitals from Capetown to Beijing to New York? And how could it be that a drug in use for 65 years have such powerful lethal side-effects that no one had previously identified?
Questioned and challenged to produce the data behind the study, the authors quickly retracted the paper and refused further comment.

“Dr. Desai declined a request from The Times to be put in contact with a hospital or health care facility that provided its data to Surgisphere. He did not respond to inquiries after the retractions.” NYTimes
Nirav Desai is a physician and researcher from Surgisphere, a small Chicago company that claimed to have compiled the impressive database. Both retracted studies were led by Mandeep R. Mehra, a widely published and highly regarded professor of medicine at Harvard, who may end up being the fall guy for this scandal.
But no one is investigating Surgisphere as the source of a criminal fraud. No one is holding the Lancet journal or its editors or reviewers to account. Certainly no one is questioning the broad system funding and publishing the medical research on which the practice of Western medicine is based. To their credit, Science Magazine published this article, hinting at a scandal and beginning to ask the right questions.
This is happening at a time when the medical establishment is making the largest demands ever on our beliefs and our behaviors. We are locked down based on the computer simulation of a compromised researcher, who also did not document the basis of his computation, and whose predictions have proved spectacularly inflated. Why did we trust him, when he had cried wolf twice previously (Ebola, Avian flu)? The liberal-intellectual press and the science journals speak with a unified voice. denouncing anyone who questions vaccines as ‘anti-science’. Every article in Wikipedia and every Google search is plastered with a message that tells us to trust the CDC. The head of Youtube goes on the air to explain why anyone who disagrees with the WHO must have their videos removed.
The largest of the studies evaluating HCQ were discontinued after the Lancet article raised the probability that the studies might be putting lives of experimental subjects at risk. Now they are being re-started, but a fresh scandal has arisen. Dr Meryl Nass has investigated details of the “Soldarity” and “Recovery” trials. She reports that these trials plan to use dosages that are at least 4 times larger than necessary, dosages that have been found to be unsafe in the past, in fact fatal to a few percent of sensitive patients. She does not mention that the trials are leaving out zinc supplementation, which doctors everywhere report to be an essential part of the treatment protocol. The studies have indirect ties to vaccine manufacturers, through the WHO and through the Gates Foundation.
It appears on its face that these trials are designed to fail, and will kill experimental subjects on the way to “proving” that HCQ is an ineffective treatment. These suspicions can only be amplified by an announcement today from FDA that chloroquine cannot be used for COVID cases. This intrusion into physician autonomy is unprecedented. For as long as FDA has existed, its policy has been to permit physicians to freely prescribe drugs off-label for any condition where the individual physician feels it might be useful.
The institutions in which Americans and Europeans have entrusted their health have betrayed our trust. There are narrow implications for the future of HCQ and treatment of COVID, and then there are broader implications about the need for overhauling the profit incentives in medical research.
Narrow perspective
For those of who dare to look beyond our own noses, a concerted campaign to discredit a good, cheap treatment for COVID is a hint that might help us see past the conventional narrative to make sense of the bizarre global events of the last five months. This is a real virus, a real pandemic, but it is being exploited for a political agenda far larger than the effects of the disease itself.
- Why have death rates been consistently overestimated in public reports?
- Why have hospitals been incentivized to over-report COVID deaths, and to treat patients with ventilators that ?
- Why has CDC failed to recommend simple, inexpensive prevention measures (vitamin D, zinc, immune-enhancing herbs, special measures for nursing homes)?
- Why have our government agencies encouraged shortcutting of safety tests in “warp-speed” vaccine development, while discrediting simple, cheap treatments (intravenous vitamin C, chloroquine/zinc, Artemisia) that work in other countries?
- Why has COVID become cause for bailouts of the financial sector that have little to do with the disease, while working families and small businesses have been forced into bankruptcy?
Many geneticists, including two Nobel laureates, cite evidence that COVID seems to be man-made, the product of genetic engineering (excellent technical summary). But this idea is off the table for discussion, censored by both the scientific community and by the mainstream press (original article, sanitized rewrite). Could it be that the same powerful forces benefiting from the lockdown and social control have power to censor both the scientific establishment and the popular press? These may seem wild speculations, but perhaps they are justified by wild events.
The rules we are asked to follow have been maximally destructive to our economy, our institutions, and our culture, while providing far less life-saving benefit than simpler strategies. Maybe the cultural and social isolation were intended to serve a different purpose than the protection of public health.
Broad perspective
“Two major study retractions in one month have left researchers wondering if the peer review process is broken.” NYTimes
The Times calls them “big blunders” but this is far too charitable. A big blunder is when you publish an article without noticing that a plus sign is really a minus. But when you fail to notice that the database of patient cases you are analyzing doesn’t exist, that is a fraud and not a blunder.
We like to think that medical practice is following medical research as the tail follows the dog. But look at the two economies—$3.5 trillion per year in health care revenues in America vs an NSF budget of only $8 billion spread over every kind of science. It may be too much to expect the dog to wag the tail when the tail is 500 times bigger than the dog.
Meanwhile, medical consumers are voting with their feet. People flock to dietary supplements ($35 billion/year), acupuncturists, chiropractors, and alternative healers. 40% of Americans think that non-standard approaches to cancer are more likely to cure them than chemotherapy and radiation, while most of the purveyors of those alternatives have been driven overseas by aggressive FDA “oversight”.
If the medical science establishment wishes to regain the trust of the American public, they will have to demonstrate that the health of individual patients weighs more heavily in their calculations than the profit motive.
Discussion
98 reader comments
Imported threads are marked Archive. New comments are welcome and moderated for spam.
According to the FDA, the half life of Hydroxychloroquine IN BLOOD is 537 hours
What this means is that the concentration of hydroxychloroquine in the blood circulation decreases by half every 537 hours.
https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/009768s037s045s047lbl.pdf
If this is the case, then the concentration of drug in the blood would increase exactly as in accordance with the accumulations shown below -
Day 1 : 2400 mg of HCQ
Day 2 : 800 mg of HCQ + 2326 mg = Total of 3126mg
Day 3 : 800 mg of HCQ + 2255mg + 775mg = Total of 3830mg
Day 4 : 800 mg of HCQ + 2187mg + 751mg + 775mg = Total of 4513mg
Day 5 : 800 mg of HCQ + 2120mg + 729mg + 751mg + 775mg = Total of 5175mg
Day 6 : 800 mg of HCQ + 2056mg + 706mg + 729mg + 751mg + 775mg = Total of 5817mg
Day 7 : 800 mg of HCQ + 1993mg + 685mg + 706mg + 729mg + 751mg + 775 mg = Total of 6439 mg
Day 8 : 800 mg of HCQ + 1932mg + 664mg + 685mg + 706mg + 729mg + 751mg + 775 mg = Total of 7042 mg
Day 9 : 800 mg of HCQ + 1873mg + 644mg + 664mg + 685mg + 706mg + 729mg + 751mg + 775mg = Total of 7627mg
So by day 4 the concentration in the blood would be equivalent to that produced by a lethal bolus dose of 4g. Their bodies would have struggled to cope with the dosage on day 4, only to be met with further dosages on days 5-9.
As a result of this criminal behaviour, 396 people died = 25% of the subjects, compared to 0.78% on a low dose.
Despite these findings, the WHO proceeded to carry out studies of HCQ on equally high doses in several countries. The behaviour of the WHO is manifestly criminal, and can only be explained in terms of the vast profits that biopharma stand to make by discrediting an effective and cheap drug, Thousands have died as a direct result of this malpractice.
India’s ICMR, its official medical research agency, had written to the WHO, telling WHO that the hydroxychloroquine doses being used in the Solidarity trial were 4 times higher than the doses being used in India.
https://www.newindianexpress.com/nation/2020/may/29/icmr-writes-to-who-disagreeing-with-hcq-assessment-officials-say-international-trial-dosage-four-ti-2149702.html
They definitely did exceed the toxic dosage and the Solidarity trials commissioned by the WHO continue to do so. Their agenda is to discredit HCQ so it does not detract from profit from Remdesivir and other patented drugs. No need to invoke the spiritual.
https://www.palmerfoundation.com.au/who-and-uk-trials-use-potentially-lethal-hydroxychloroquine-dose-according-to-who-consultant/
There are 155 studies published where Hydroxychloroquine is used to fight Covid19. 100% of the trials were effective when applied early. They all use small dosages. You can see for yourself - c19study.com
There was absolutely no reason for Oxford University to use a giant dose unless they were looking to induce toxic effects from the outset.
If they were genuinely interested in protecting the health of these patients, then why did they exceed the toxic limit with the dosage, and why did they call a halt to the study prematurely - realising that they were inducing toxicity and had to stop?
What is also remarkable is that the WHO took this single study of deliberate overdose and ignored all the 155 positive studies using much smaller doses - then used the negative result of this single study to order a halt to 70 ongoing trials of hydroxychloroquine around the world.
One last time:
They did NOT "exceed the toxic limit with the dosage".
There is NO evidence to support these claims apart from your mis-reading of toxicological data.
But since you seem more interested in conspiracy theories than science:
Why didn't President Trump take hydroxychloroquine when he was sick?
He pushed it for months and months, and in fact all these conspiracy theories can be traced back to his tweets.
Or did he sell out to Big Pharma?
Oh no!
Who's going to save the children from all those blood-drinking, pedophiliac satanists in Hollywood now???
Hydroxychloroquine is potentially lethal at 5g, I agree. But it also has a half life of 22.4 days. Here is the dosing schedule used during the RECOVERY TRIALS
I have added the residual amount from each previous day to the new amount added each day. The result is a massive overdose to twice the lethal amount.
C(now) = C(initial) x e-0.03094 x t where t is the time passed in days
PART 3 : RECOVERY TRIAL DOSAGES
Day 1 : 2400 mg of HCQ
Day 2 : 800 mg of HCQ + 2326 mg = Total of 3126mg
Day 3 : 800 mg of HCQ + 2255mg + 775mg = Total of 3830mg
Day 4 : 800 mg of HCQ + 2187mg + 751mg + 775mg = Total of 4513mg
Day 5 : 800 mg of HCQ + 2120mg + 729mg + 751mg + 775mg = Total of 5175mg
Day 6 : 800 mg of HCQ + 2056mg + 706mg + 729mg + 751mg + 775mg = Total of 5817mg
Day 7 : 800 mg of HCQ + 1993mg + 685mg + 706mg + 729mg + 751mg + 775 mg = Total of 6439 mg
Day 8 : 800 mg of HCQ + 1932mg + 664mg + 685mg + 706mg + 729mg + 751mg + 775 mg = Total of 7042 mg
Day 9 : 800 mg of HCQ + 1873mg + 644mg + 664mg + 685mg + 706mg + 729mg + 751mg + 775mg = Total of 7627mg
During the first day each subject was given 2400mg of hydroxychloroquine (HCQ)
On the second day, each subject was given a further 800 mg, and 2326 mg of the first days dosage was still in their system
On the third day they were given a further 800 mg and 2255mg from the first day, and 775 mg from the second day were still in their system
Etc
We can see that by day 9, everyone of the 1500 subjects taking part in the RECOVERY trial was severely overdosed with almost 2 x the lethal dose (if we take the lethal dose as 4g).
1500 people were subjected to this drug regimen. We need to understand what these people went through. Their bodies were weakened by Covid and were struggling to cope with the initial dose. Yet every day a new dose was added which intoxicated them again to an even deeper level. Eventually their bodies just could not cope and 25% of them died.
Standard dosage for rheumatoid arthritis is 600 per day.
In 22 days this adds up to 13200 mg, which is almost twice as much the amount given to the patients in the Covid trial.
RA patients of plaquenil are not dead - they are healthier.
https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/009768s037s045s047lbl.pdf
Seriously dude, why would reserachers deliberately kill of one quarter of their study subjects and then PUBLISH THE DESCRIPTION OF THE MURDER WEAPON?
To achieve their supposedly dubious purposes without detection they could have instead:
1. Given patients a placebo and then claimed that hydoxychloroqione didn't work.
2. Given patients a small dose of hydoxychloroqione and then claimed that it didn't work.
3. Given patients a supposedly lethal amount of hydoxychloroqione and then lied about the dose administered.
Who was going to dispute any of the above?
You think that those 1500 patients - spread out across multiple clinics - knew how the other 1499 fared? And than that they would work out statistical significance to denouce the researchers for occulting the trial's real findings?
Covid is far from a universally fatal disease, so it's not like one (or even 100) of those patients could have jumped up and said:
"Look at me! Hydroxychloroquine works and I am living proof!"
Most patients recover anyway.
It's sad that intelligent people should devote their brains to conspiracies rather than advancing science or producing responsible public health messages.
The Initial dose for Rheumatoid arthritis is 400mg -600mg, (equivalent to 310 to 465 mg base.) The RECOVERY study used 6 times this.
This is followed by a daily dose of 200mg-400mg, (equivalent to 155 to 310 mg base). The RECOVERY study used 4 times this.
All the literature says that we should never exceed 5mg/kg/day to avoid toxic effects. The RECOVERY trial used an initial concentration of 34mg/kg followed by 11mg/kg/day
Even compared to the schedule for Rheumatoid arthritis, the dosage is much greater.
Source : https://www.drugs.com/dosage/hydroxychloroquine.html
I am not alone in making these observations -
https://covexit.com/recovery-covid-19-research-blasted-for-toxic-dosage-towards-oxfordgate/
"I am not alone in making these observations"
You must be in the company of other people who do not understand science, because NO actual malaria expert, rheumatologist, toxicologist etc. ever claimed that the RECOVERY trial tried to murder its patients.
Or even that it used a potentially lethal dose of HC.
Do you really think that every single scientist in the world beloings to the radical left or is on Big Pharma's payroll?
Even those mixing generic drugs in India?
Anyway, it seems that my reply to your comment got lost in the thread, so let's try again:
First, the dosage you suggested for RA is wrong.
The correct dose is:
400-600 mg/day (310-465 mg base/day)
600mg (465 mg base/day) is not the initial dose but your DAILY pill until you can switch to maintenance, hopefully after a few weeks.
At this dosage, you reach the allegedly lethal 5mg within HC's half-life in 14 days, even allowing for time passed.
Problem is, half-life has little to do with acute toxicity, which is determined by SPEED of absorption, which is anything but linear.
"Following ingestion, the drugs are rapidly absorbed from the upper gastrointestinal (GI) tract and slowly redistribute to other compartments, eventually accumulating in erythrocytes, liver, lung, kidney, heart, muscle, and retinal tissue [43]. The combination of rapid absorption, high oral bioavailability, and slow redistribution prompts early peak serum levels post-ingestion which correlate with symptom severity in overdose [41]."
And from the epidemiological side:
"Cardiomyopathy is described in case reports of patients presenting with chronic chloroquine and/or hydroxychloroquine toxicity [...] Chronic exposure to cumulative doses of 1277 g and 1843 g of chloroquine and hydroxychloroquine, respectively, over an average of 13 years has been demonstrated to produce this effect."
What this means is that even at a daily dose of 390mg for 13 years, what you may get is cardiomyopathy, not death.
Also, with 1843 g of hydroxychloroquine over 13 years, you reach your potentially lethal dose of 5mg in a few weeks.
Yet, RA patients don't die but keep taking their daily HC dose, maintaining these supposedly fatal serum levels for the following... er... 13 years.
Second, the assertion below is false:
"All the literature says that we should never exceed 5mg/kg/day to avoid toxic effects."
No. The dose for acute malaria is 2g in 48 hours, which for me (an average 167cm X 50 kg) translates into 20mg/kg/day.
In fact, Plaquenil's weight-base dosage suggests 13mg/kg/day + 6.5mg/kg/day within the first six hours, followed by an additional 6.5mg/kg/day at 24 hrs, and followed by yet another 6.5mg/kg/day 48 hrs after the initial dose.
https://reference.medscape.com/drug/plaquenil-hydroxychloroquine-sulfate-343205
Seriously: you cannot extrapolate chronic toxicity from acute toxicity.
Professor Martin Landray was in charge of the RECOVERY study. He was asked “How did you decide on the dosage of hydroxychloroquine?”
His answer was
“The doses were chosen on the basis of pharmacokinetic modelling and these are in line with the sort of doses that you used for other diseases such as amoebic dysentery.”
(Well Hydroxychloroquine is never used to treat amoebic dysentry. His response is retarded)
And the follow-up question was:
“Are there any maximum dosage for HCQ in the UK?”
“I would have to check but it is much larger than the 2400mg, something like six or 10 times that.”
(this answer is not just retarded, it is criminally insane. If people were put on 24000 mg they would be stone dead. Professor Landray should face criminal charges of negligence or deliberate malpractice)
“ … the HCQ dosage used are not dissimilar to that used, as I said, in for example amoebic dysentery.”
Video of interview with Professor Landray
https://www.youtube.com/watch?v=31VEJlRyB2c&feature=emb_logo
They did not exceed the toxic limit at all, you are misinformed.
Read up on acute and chronic toxicity.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369162/
Taking 5gr in one go is NOT the same as taking 5gr over 5 days.
Half-life is irrelevant because it only refers to how long after administration the drug is excreted, and not to where the drug goes and at what speed (this is far from constant), as well as to what it actually does while gallivanting throughout the human body.
Once upon a time this was a science blog. Now it has become a haven for conspiracy theorists who refuse to read the science even when science is shown to them.
Josh, the RECOVERY study administered to an experimental group of 1500 subjects a lethal dose of 2400 mg of HCQ on day 1 and 800 mg on each of the succeeding 9 days. The result was 25% of the experimental group died.
Oxford university published their conclusion that HCQ does not work, and WHO followed immediately with a suspension of HCQ trials regardless of the fact that 152 positive studies of HCQ confirm that it works on ordinary dosages.
By giving them a deliberate overdose, the experimental subjects were effectively murdered, just to discredit a competing drug (HCQ).
I am in deep shock. The treatment of HCQ is very revealing about the true motivations behind the vaccine.
I would recommend that we look at all the existing studies with HCQ and ascertain the LD50 or toxic limit based on all studies done up to date. I have a list of 152 studies on Covid and HCQ.
This can then be used to prove that the RECOVERY study was deliberately negligent and murderous in intent by overdosing all of their subjects. A legal case could then be pursued.
You are confusing chloroquine with hydroxychloroquine:
"Chloroquine is 2-3 times more toxic than hydroxychloroquine."
And:
A *potentially* lethal dose for hydroxychloroquine (see note on the paper) is "ingestion of greater than 5 g."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211615/
Patients received 2400 mg of HYDROXYCHLOROQUINE in the trial, so less than half the dose "associated with fatal outcome."
Conspiracy conspiracy conspiracy.
Have studies been done to see how lupus patients (or others who regularly use HCQ) fare when exposed to COVID-19?
No discussion of Dr. Vladimir “Zev” Zelenko is complete without mentioning his awards:
https://www.physiciansweekly.com/the-skeptical-scalpel-awards/
Anyhow, I really like keto so far, although I'm experimenting with trying
to set my own spin. It's essential to be flexible with your daily diet, even if you're locked into some
thing like"keeping carbohydrates low". I don't want to be the person eating out with
friends that orders something weird off the menu, or nothing at all, although I want to lose
weight. It is just flat out not worth it,
if you ask me if your diet comes at the cost of your joy.
xoxo Anyhow just wanted to say. Stuff like this helps
keep me and allow me to stay on track. I hope that you continue to
develop, and people that want this can find it!
Thanks and Fantastic luck again. That is all GREAT. Been doing my best to attempt to do quality study,
so stuff like this helps. Anyone else think the
biggest problem people have with weight loss comes from them not putting in the
job first? Like I do you wish to start losing weight ASAP,
but you have to be inclined to do a little research.
I am sorry to say you are just likely going to have issues, if you do not do your part.
To clarify something:
True, not all COVID patients experience hypoxia.
Is it also true that:
Not all *symptomatic* COVID patients experience hypoxia? (If so, what are their symptoms, which in the worst cases become serious enough to cause death?)
The other NIG cause of death and disability is the so called "coagulopathy": development of blood clots in the blood vessles of the lung, heart, brain, kidney: all of which can be fatal. This is being treated by prophylactic or therapeutic doses of low molecular weight heparin. After getting better and leaving the hopsital, anti-coagulant therapy is continued for at least 45 days, often using Rivaroxaban.
BIG, not NIG, in the post above. Typo!
It has been widely conceded that the COVID-19 death count has been artificially inflated by a number of factors, such as institutions recording the cause of death as COVID-19 whenever the patient tested positive for the disease regardless of comorbidities, or where no test was administered but the symptoms of the dying person merely suggested COVID-19. Apparently there is no reliable standard practice commonly enforced for confirming death by COVID-19? And is it true that the existing PCR tests return false positives for COVID-19 by giving a positive result for other coronaviruses not just COVID-19? If any or all of this is true, then the COVID-19 death counts (and case counts) may be wildly inflated, yet are being used to generate so much fear and cause unprecedented global lockdowns that will cause families to lose their homes, destroy small businesses, throw millions into poverty, etc.
If this is the case, I have a question for the medical professionals. I have read that if a COVID-19 patient is symptomatic, a key symptom is hypoxia, i.e. a blood problem not a lung problem such as pneumonia and that this what is "new" about COVID-19 and what distinguishes it from other coronaviruses and/or a common flu. True? If so, is there a simple test for this hypoxia condition that should be required along with existing tests to verify this condition before the patient could be declared COVID-19 positive? Would this help clean up the data?
My apologies if this is a stupid question....it's coming from a layman.
There's a very simple test for hypoxia. You can get a pulse oxymeter from the drug store for under $50 and put it on your finger and have a result in about 15 seconds. The reason this is not required for diagnosing COVID is (1) not all COVID patients experience hypoxia, and (2) as you note, diagnosing COVID has become highly politicized.
The doctor's perfect record of success with HCQ (a/k/a, "the drug
that Pres. Trump touted") earned him a front-page hit-piece in the
New York Times, which speared him not with any scientific evidence
to "debunk" his claims, or any testimony by unhappy patients (there
being none of either), but with the jeer that he'd become a "right-wing
star" for "touting" HCQ.
https://www.nytimes.com/2020/04/02/technology/doctor-zelenko-coronavirus-drugs.html
Recall that Dr. Didier Raoult, who's also used the drug successfully
to treat COVID-19, has been under ferocious government attack in
France, which Big Pharma doth bestride like a colossus:
https://asiatimes.com/2020/03/why-france-is-hiding-a-cheap-and-tested-virus-cure/
MCM
From Dick Atlee:
I think this is the answer — or at least the strongest answer — to the
people who tell me that advocating the use of hydroxychloroquine (HCQ)
to treat COVID-19 is tantamount to killing people.
It's an interview with a doctor whose protocol for the drug is now being
used in many countries which have seen hospitalization and death rates
drop as a result. I'd heard of him, but with my interest in the fraud and
deliberately-designed-to-fail studies of the drug, I foolishly hadn't paid
attention to what he's been doing for the last four months.
The interview was just broadcast this afternoon, and hasn't been broken out
yet from the longer program, but you can hear it (all 40 minutes, unless
you can pull yourself away before that) at
https://www.youtube.com/watch?v=RzqcN6ybfkE&t=2505
He is Dr. Vladimir Zelenko, from Monsey, in upstate New York. He is a very
dour, straightforward, no-nonsense-or-hype doctor whose success speaks
for itself.
The thing that most intrigued me about the many interesting insights
uncovered in this interview was the clear mechanism for how the drug
combination of HCQ and zinc works, with azithromycin as a protection
against respiratory complications. (Note: I've also seen AZT described as
interfering with viral attachment to a cell's ACE-2 receptors).
Zinc is the virus killer, or rather the preventer of the virus's ability to
reproduce in a cell, through inhibition of the RNA polymerase enzyme
required for that process
(ref:https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1001176).
But zinc on its own can't get into the cell to run that interference. HCQ's
job is as an "ionophore" to open a channel for the zinc to enter the cell
(ref:
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0109180)
where it can disable the virus's "replication and transcription complex"
(RTC). Zelenko refers to these three components of his protocol thusly:
HCQ is the gun, zinc is the bullet, and azithromycin is the bulletproof vest
protecting the patient.
He also added clarity to why Trump is being invoked so often in attacks on
HCQ. Having Zelenko's HCQ protocol adopted would mean essentially an end
to the pandemic, which would be a win for Trump. It would also open up the
economy, also a win for Trump. So those who want Trump defeated can't
afford to have HCQ widely used. He's not a Trump fan, he's just being
realistic. Which shows us yet another way in which politics is deadly.
It seems evident that this protocol is a true game-changer in this present
situation. It doesn't require hospitalization for administration, and it is
extremely inexpensive ($20 for the full treatment). It is saving lives in
every country in which it is officially sanctioned, or where doctors are at
least not forbidden to use it. Whether we'll be so fortunate here in the
U.S. remains very much to be seen.
Loved the video of Dr. Vladimir Zelenko,
It got me thinking...
The variation from country to country in infections and deaths makes no sense to me.
One thing that I think is missing is how dietary differences in cultures may affect Covid-19 infection and death rates.
Per Dr. Zelenko:
1) A zinc Ionophore allows zinc to enter a cell.
2) A zinc Ionophore plus zinc pushes zinc into the cell, preventing virus replication.
3) Getting zinc into the cells in the first 5 days was critical to controlling infection.
In my opinion:
If a culture naturally consumes lots of foods high in zinc Ionophores and zinc, it may create a natural barrier to virus replication.
Examples of zinc Ionophores:
1) Hydroxychloroquine
2) EGCg found in green and white teas (more on the wiki page).
3) Quercetin found in red onions and kale (more on the wiki page).
What if a person drank green tea regularly for the week preceeding exposure?
How much zinc would be waiting in the cell for the virus?
What I would expect is that countries that drink green or white tea daily would have a low number of infections and deaths.
That is what appears to be the case from what I can see.
The same could go for Hydroxychloroquine used to treat Lupus or R.A. on a daily basis. They should also see a build-up of cellular zinc.
The high zinc levels in the cells might help explain the early reports of low infections in the Lupus group.
I know most of us are tired of the virus and are ready to get back to our lives.
I have a suggestion:
What if people just started drinking green tea from now on as a preventative?
We might see a drop in the trends.
From the above video, in the case where Dr. Zelenko is trying to stop a pre-existing infection before day six, a high dose of zinc Ionophore with an external source of zinc would seem to be critical for maximum benefit; that's where Dr. Zelenko uses Hydroxychloroquine and zinc. He also adds an antibacterial to prevent the further complication of pneumonia.
The above comments are for informational and speculative purposes only.
Japan should be a good place to study the benefits of a diet high in zinc and ionophores, as green tea is a popular and traditional drink and sushi/sashimi is high in zinc as most seafood is. I have been supplementing with zinc and vitamin D and often drink matcha tea but will get some quercetin and add that to my regime. If it may help and likely has no downside, why not?