April 29, 2020: A date which will live in Infamy.

We are living through a Medical Holocaust as we speak. In this Medical Holocaust, Hospitals are paid to murder the public with poisons. Anthony Fauci and the rest of his co-conspirators are every bit as evil and worthy of hate than the likes of Adolph Hitler and Joseph Mengele.

Much of the world also “feels” that same Anthony Fauci is an evil man responsible for the death totals around the world, but they can’t quite put their finger on a proof beyond a reasonable doubt. I tend to look at things mathematically. I went back to college for econometrics. There is a proof that Fauci intentionally chose to kill a large number of people by stopping Remdesivir trials early.

The date of April 29, 2020 is right up there with December 7, 1941 and September 11, 2001 to me.

It’s becoming clear that the large majority of “COVID” deaths in 2020 were the direct result of hospital protocols designed to kill patients. Remdesivir was a major part of the death protocol which also included opioids, ventilation, and other methods. It was already known to cause organ failures and high death rates before the COVID-19 pandemic. The motives were simple: to commit murder and profit. These people are sadistic and evil and enjoy killing people. Fauci is a serial killer. Murder is a part of their incentives to commit fraud the same as the massive amounts of money they make from their evil scams.

The “COVID” deaths in the early phases of the Pandemic in China were likely a direct result of Remdesivir or some other deadly hospital protocols, not any virus or bioweapon. Remdesivir had probably been used by Michael Callahan when he was in China. When “COVID” came to the United States, Remdesivir was used again, and once again was a main driver of “COVID” deaths, along with mechanical ventilators, paralyzing agents, and opioids, as described by Dr. Pierre Kory who used these methods extensively to cause death.

There was a major competitor to Remdesivir in the United States in early 2020 - Hydroxychloroquine.

Dr. Zev Zelenko had scoured MedCram in early 2020 looking for information on how to fight COVID. He developed a protocol using Hydroxychloroquine, a “zinc ionophore.” The ionophore allowed zinc pass through the cellular wall into cells. According to Zelenko, once inside the cells, the zinc stopped the modified coronavirus from replicating.

Zelenko had good results using hydroxychloroquine with zinc and sent a letter to the President outlining his successful protocol. President Trump publicly acknowledged Zelenko’s letter and announced that he was taking hydroxychloroquine. Plans were underway to distribute hydroxychloroquine. The Pandemic of Medical Protocols would have been stopped cold.

Meanwhile, there was a lesser-known competitor to Remdesivir and Hydroxychloroquine at the time fighting to become the standard of care - Famotidine. The Famotidine story is a very important story to understand. The Famotidine discovery would ultimately force Dr. Fauci to show his hand. It would force Dr. Fauci to take an action that would prove beyond a reasonable doubt that he intentionally forced Remdesivir into Medical protocols in order to kill large numbers of American citizens.

Dr. Robert Malone claims to have identified Famotidine as a COVID treatment using computer models sometime after receiving the SARS2 virus sequence in early January 2020. Dr. Malone was one of the first people in the United States to contract COVID in late February 2020. He took Famotidine to treat the disease. He said it worked for him. He announced that Famotidine was cure for COVID on LinkedIn in late February.

Famotidine had also been used in China with Malone’s colleague Michael Callahan. Callahan said that COVID death rates were lower in China among a group of people using Famotidine. The dates and results of Callahan’s Famotidine and apparent Remdesivir “treaments” in China remain unpublished and unknown to the public.

Michael Callahan went to Robert Kadlec and pressed for Famotidine trials. Kadlec contacted Tracey Caldwell at Northwell Health. Tracey Caldwell and Northwell Health were already working with Alchem in some capacity on Famotidine. Alchem in Florida was where Robert Malone had identified Famotidine from his computer model.

Kadlec demanded to know if Famotidine was promising for COVID. After receiving the information he requested, Kadlec contracted with Alchem for clinical trials of Famotidine. Alchem in turn subcontracted to Northwell.

There was a problem for Anthony Fauci with the trial, however. A huge problem. Hydroxychloroquine was also going to be included in the study. Under pressure from the Trump Administration, The FDA issued an EUA for Hydroxychloroquine on March 28, 2021. Although the EUA was limited to hospitalized patients only, as opposed to dispensed to the public as a preventative measure, Alchem/Northwell’s Famotidine trials were going to include Hydroxychloroquine as a standard of care.

Between Hydroxychloroquine and Famotidine, the results would have been spectacular compared to the death rates of “COVID.” The real cause of “COVID” deaths were Remdesivir and related protocols all along. Simply stopping the Remdesivir protocols death program would have stopped “COVID.” If you compare Hydroxychloroquine, zinc, and Famotidine to the lack of Remdesivir, opioids, and ventilators, of course you will see a huge difference in death rates. The Pandemic would have ended.

So Fauci and company had to find a way to stop the Famotidine/Hydroxychloroquine trials. They conspired to replace Hydroxychloroquine with Remdesivir in the Famotidine trials. It was imperative to Fauci and co that people continue to die in the trials to keep the impression of an untreatable and novel disease.

Alchem was awarded their contract for Famotidine trials on April 14, 2020. The trials were to test Famotidine against a “standard of care.”

A Multi-site, Randomized, Double-Blind, Comparative Trial of the Safety and Efficacy of Standard of Care (SOC) Plus Famotidine vs SOC Plus Placebo for the Treatment of COVID-19 in Hospitalized Adults. The overall objective of the study is to evaluate the clinical efficacy of COVID-19 treatments consisting of standard of care (SOC), vs SOC with high dose famotidine in patients hospitalized and meeting radiologic criteria for COVID-19 disease.

Two weeks later, on April 28, 2020 Robert Malone tweeted a “press release” about the trials.

“Press Release: A Multi-site, randomized, Double-Blind, Comparative Trial of the Safety and Efficacy of Hydroxychloroquine and Famotidine for the Treatment of COVID-19 in Hospitalized Adults.” Dr. Malone has since removed the “press release” from his own website.

Dr. Malone’s 2021 CV states that he designed the Famotidine/Hydroxychloroquine trials.

• Developed and wrote initial clinical trial design for a comparative trial of the safety and efficacy of hydroxychloroquine, and the combination of hydroxychloroquine and famotidine for the treatment of COVID-19 in hospitalized adults.

Reiterating, Hydroxychloroquine was to be the standard of care in the Famotidine trials. The FDA had issued an EUA for HCQ on March 28, 2020. In his April 28, 2020 tweet, Dr. Malone confirmed that the SOC to be used in the Famotidine trials would be Hydroxychloroquine. It would be apparent soon that one or the other or both of the substances in combination would safely and effectively treat COVID.

The next day, April 29, 2020, a date which will live in infamy, Dr. Anthony Fauci shut down Remdesivir clinical trials early. Fauci announced that the trials were a success. In reality, “COVID” patients in Remdesivir trials were dying at a much higher death rate than in Hydroxychloroquine trials also underway, and Fauci knew it. This is his guilt. This is the proof. All that’s left to do is organize all the data and communications into a court case.

On May 1, the FDA issued an EUA for Remdesivir. The standard of care to be used in the clinical trials of Famotidine was changed to Remdesivir.

On 29 April 2020, the National Institute of Allergy and Infectious Diseases (NIAID) announced that Remdesivir was better than placebo in reducing time to recovery for people hospitalized with advanced COVID-19 and lung involvement. In an earlier study of adult patients admitted to a hospital for severe COVID-19, Remdesivir was not associated with statistically significant clinical benefits. In that study, Remdesivir was not associated with a difference in time to clinical improvement. Although not statistically significant, patients receiving Remdesivir had a numerically faster time to clinical improvement than those receiving placebo among patients with symptom duration of 10 days or less. Remdesivir was stopped early because of higher numbers of adverse events compared to placebo. Because of these studies the FDA stated on 1 May 2020, that it is "reasonable to believe" that known and potential benefits of Remdesivir outweigh its known and potential risks, in some specific populations hospitalized with severe COVID-19.

Given the refinement of standard of care to include Remdesivir and no longer hydroxychloroquine, we have edited the study protocol to reflect this new standard of care.

On the verge of having his Famotidine discovery tested to be a cure for the so-called COVID-19 Pandemic, Dr. Robert Malone resigned from Alchem.

On April 14, the federal government awarded a $20.7 million contract to Malone’s employer, Alchem, and its subcontractor, Northwell, for a trial to assess the safety and effectiveness of “the combination of hydroxychloroquine and famotidine for the treatment of moderate to severe COVID-19 disease,” according to a brief summary of the award.

Malone resigned as Alchem’s chief medical officer a week later, citing what he described as a difficult work environment. He has since been critical of Callahan and the project. Meantime, the trial has been paused indefinitely because of a dearth of new patients in New York.

“The Northwell trial is just a zombie at this point,” Malone said. “Completely irrelevant, except in a negative sense.”

The resignation of Dr. Malone from Alchem appears almost certainly to be a direct result of Fauci changing the standard of care from Hydroxychloroquine to Remdesivir, although Dr. Malone has never stated that objection in public.

It’s been 3 years now. Dr. Malone has described himself as a “whistleblower.” But he has kept that whistle in his pocket when it comes to the reasons behind his resignation from Alchem. There is no way to look at this and say that Dr. Malone could not have prevented a tremendous amount of deaths by blowing his whistle on why Fauci changed the standard of care in a study that Malone was involved in back on April 29, 2020. I’m sure it is a heavy burden for him to bear. The only Salvation I can thing of, if there is any, is to blow that whistle on Remdesivir, Fauci, and everything I’m saying here. If I can figure it out, I know he can too. He lived it.

I said before that Fauci was a serial killer. Malone said of Fauci: “responsible for hundreds of thousands of deaths from AZT, Remdesivir, and SARS-CoV-2.” So I don’t know what’s stopping him from using his whistle. He can prove Fauci’s guilt, fast. Again, he live it, and has all the expertise in the world.

An Attorney General could prove it fast too, using the clinical trials statistics, depositions, and communications from within the conspirator group. The truth is inherit in all of that information. Meanwhile, the Medical Holocaust continues.

Dr. Anthony Fauci intentionally chose a deadly product as a “standard of care.” To create a statistical deception of a “benefit” from the use of Remdesivir, they used the deadly compound in both the control and test groups. Let me make this simple for you like I said I would.

Let’s say you want to prove that injecting gasoline into someone’s veins will cure COVID. I’m assuming that Gasoline is deadly and would not cure COVID. Using the deceptions allowed in the clinical trials model, you can easily meet the low standard of proof to show a benefit from Gasoline.

Just take two groups and divide them equally. Give one group Gasoline + Famotidine. Give the other group Gasoline Only. Then, go around and make sure more patients are dying in the Gasoline Only group. Presto, Famotidine is beneficial for COVID, because less died from COVID in the group using Famotidine. It’s that simple. It will be that obvious in the data if and when the public ever gets all of it and honest statisticians ever take a look at it.

The reality is that Gasoline and Remdesivir were killing patients in both groups, not COVID, and that their “cures” are really poisons. “Lies, damned lies, and statistics” was the first lecture I heard in Econometrics. I was sitting in that same classroom when I heard about 9/11, another form of deception, where CNN overlaid images of planes crashing into the World Trade Center, and CIA/Mossad demoed the towers. You can research Pearl Harbour in detail and discover how the US not only knew of the impending air raid from Japan, but also took steps to provoke the air raid. I know those statements take a lot to back up and I haven’t done that here, but like I said before, I put April 29, 2020 in the same sentence as December 7, 1941 and September 11, 2001, and I meant what I said.

In the case of the Northwell Famotidine/Remdesivir trials, they were killing patients with ventilators, opioids, and the like to create the statistical deception they wanted. That’s provable. That’s murder. That’s illegal.

So that’s what they did. Fauci’s forced through an EUA for a poison that causes higher death rates than if you don’t use it all.

I hope I’ve made my point. Next time you tell someone, Anthony Fauci is a mass murderer, and they say “prove it,” tell them this if you like. Anthony Fauci abused the clinical trials process to approve Remdesivir as a standard of care that he 100% knew would cause a great number of deaths compared to Hydroxychloquine. On April 29, 2020.

Charles Wright