In today’s news:
CDC approves Moderna and Johnson & Johnson COVID-19 vaccine booster shots.
The Centers for Disease Control and Prevention on Thursday endorsed booster shots of the Moderna and Johnson & Johnson COVID-19 vaccines for tens of millions of Americans.
The green light from CDC Director Rochelle Walensky means that eligible Americans at risk of severe disease can choose any of the three boosters, including the Pfizer shot, now authorized in the United States, regardless of their original shot.
“The evidence shows that all three COVID-19 vaccines authorized in the United States are safe – as demonstrated by the over 400 million vaccine doses already given,” Walensky said in a statement.CDC Press Release 21 October 2021
I take umbrage with, “The evidence shows that all three COVID-19 vaccines authorized in the United States are safe – as demonstrated by the over 400 million vaccine doses already given…”
Safe? Really?! Apparently the CDC’s definition of “safe” is a helluva lot different than mine and my other fellow Patriots.
Case in Point One:
September 10, 2021, WXYZ-TV Channel 7 posted a request on Facebook, asking people who had lost an unvaccinated loved one to COVID-19 to contact them for a story.
The post has received more than 241,000 comments and most are about someone who was injured or died from the COVID shot, or who got severe COVID-19 despite being fully vaccinated.Your Daily Dose of Audra, 09 October 2021
For reference, WXYZ-TV Channel 7 services metropolitan Detroit Michigan (aka Metro Detroit). The Metro Detroit area has a population of roughly 4.3 million people in 6 counties. Interestingly enough, the drive in this heavily blue held area to get residents “vaccinated” has been a massive undertaking. Coincidence?
Jacobs died 13 days after she received the single-shot at a CVS pharmacy on April 8, just five days before federal health agencies temporarily paused the vaccine administration while they examined an unusual blood-clotting disorder.
On Sept. 20, Michigan Medicine pathologist Dr. Michael Caplan completed the autopsy report.
Jacobs “appears to have succumbed” to a “rare but nevertheless documented” complication associated with the viral vector vaccine, cerebral venous sinus thrombosis, he wrote in the summary.
According to Yale Medicine, the condition is characterized by a blood clot in the venous sinuses, part of the brain’s blood drainage system.
According to the CDC, there have been three other confirmed deaths of thrombosis with thrombocytopenia syndrome (TTS) after patients received the Johnson & Johnson vaccine, administered to more than 15 million people in the United States.
Thrombosis occurs when blood clots block blood vessels; Thrombocytopenia is a condition with which patients have low blood platelet counts, the CDC reports. The official number, however, will likely grow.
It does not include Jacobs, and a 37-year-old Washington woman who died on Sept. 7 of TTS after receiving the Johnson & Johnson shot. State officials there said hers was believed to be the fourth such death in the nation.Michigan woman’s death caused by rare Johnson & Johnson COVID vaccine side effect, autopsy report says
Case in Point Two:
As per WebMD.com, the recovery rate for Covid-19 is 97-99.75%. Yet, in the United States the number of deaths is 730,368.
What we need to ask ourselves, WHY is the US’s death rate so high? We are a first world country with advanced technology and modern medicine. The United States only accounts for 4.25% of the world population and yet third world countries’ Covid mortality rates are lower than ours. WHY?
According to the CDC, over 3,143,513 Americans have been admitted to the hospital with COVID-19. Based on these numbers logically we can infer that the majority of Americans whom have died from COVID-19 did so in the hospital.
Hmmm…now THAT is interesting…that brings me to my next point…
Case in Point Three:
What are the therapeutic protocols and guidelines for COVID-19 patients in a hospital?
The spectrum of medical therapies to treat coronavirus disease 2019 (COVID-19) is growing and evolving rapidly, including both drugs approved by U.S. Food and Drug Administration (FDA) and drugs made available under FDA emergency use authorization (EUA). CDC strongly encourages clinicians, patients and their advocates, and health system administrators to regularly consult the COVID-19 Treatment Guidelinesexternal iconpublished by the National Institutes of Health (NIH).
The treatment and management recommendations in these guidelines are based on scientific evidence and expert opinion and are frequently updated. Current clinical management of COVID-19 consists of infection prevention and control measures and supportive care, including supplemental oxygen and mechanical ventilatory support when indicated.
FDA has approved one drug, remdesivir (Veklury), for the treatment of COVID-19 in hospitalized patients aged 12 years and older who weigh at least 40 kg.Therapeutic Options
Remdesivir…I’ve heard of that drug. It was used to treat Ebola in third world countries.
In large-scale clinical trials of anti-Ebola drugs, the mortality rate of patients in the experimental group treated with Remdesivir was 53% (175 patients, 82 survived after 28 days), and the efficacy was significantly lower than that of two monoclonal antibodies MAb114 (35% mortality) and REGN-EB3 (33% mortality).Dose and Safety of Remdesivir, 04 February 2020
…As you can see, they (The NIH) admit that remdesivir causes renal and liver failure! One of the symptoms is “ALT and AST elevations,” which are indications of liver damage. Is that really the drug you want when someone is at risk for a cytokine storm and thrombosis? They even have a monitoring requirement for these side effects. Also, it does have some drug interactions as well…Horowitz: The $cience of remdesivir vs. ivermectin: A tale of two drugs, 18 October 2021
What in the cold fuckery?! 53% mortality rate? The NIH “admit that remdesivir causes renal and liver failure…” yet it is an APPROVED course of treatment for patients hospitalized with COVID-19?
I encourage all of you to click on the hyperlink, Coronavirus Disease 2019 (COVID-19) Treatment Guidelines (straight from the NIH) and SAVE the document as a pdf in its entirety at your leisure. Spoiler alert: the NIH RECOMMENDS Ivermectin as a course of treatment…gasp!
Case in Point Four:
Faux-ci and our federal government are knowingly murdering of Americans and on a mass scale. There is a reason why even though the United States only makes up 4.25% of the population we lead the global in COVID-19 death rates.
Doctor Exposes the Dangers of Remdesivir and other Drugs that are Being Recommended by NIH
Even though the World Health Organization (WHO) is not recommending remdesivir, Dr. Anthony Fauci, the most hated government official in the US, along with his National Institute of Health (NIH) still continues to recommend remdesivir as a so-called treatment for the alleged viral illness COVID19.
On its advisory last updated on August 25, 2021 entitled “Therapeutic Management of Hospitalized Adults With COVID-19”, the NIH openly admits that they are still recommending remdesivir to be used as part of the official medical protocol.
While on its website, the WHO’s advisory last updated November 20, 2020, it was stated:
“WHO has issued a conditional recommendation against the use of remdesivir in hospitalized patients, regardless of disease severity, as there is currently no evidence that remdesivir improves survival and other outcomes in these patients.
This recommendation, released on 20 November, is part of a living guideline on clinical care for COVID-19. It was developed by an international guideline development group, which includes 28 clinical care experts, 4 patient-partners and one ethicist…
…work on this began on 15 October when the WHO Solidarity Trial published its interim results. Data reviewed by the panel included results from this trial, as well as 3 other randomized controlled trials. In all, data from over 7000 patients across the 4 trials were considered.
The evidence suggested no important effect on mortality, need for mechanical ventilation, time to clinical improvement, and other patient-important outcomes.”
So how come this recommendation from the WHO is not being implemented in hospitals?
Why do the NIH and the WHO have different recommendations when they’re supposed to work together in, (let’s say SARS2 has been isolated, purified, and genetically characterized) solving the so-called pandemic?
This even goes back to April, during the early days of the panic-driven psychotic fear-mongering schemes by the COVID industrial complex, which includes Bill Gates and Dr. Anthony Fauci of course, maximized by the power of the media through 24/7 news and propaganda.
So according to Fauci in April 2020, remdesivir “will be the standard care” even though at the same statement he admitted that it’s “not yet been peer-reviewed”.
Now if you listen carefully to this statement by Dr. Fauci, the respected National Institute of Allergy and Infectious Diseases Director and the man who is at the same time being blamed by many doctors and scientists for so many deaths caused by AZT, his recommended drug for AIDS, is playing with words through double-speak, euphemism, and even deliberate lies and deception. For example, he stated:
“We think it’s opening the door to the fact that we now have the capability of treating COVID-19…”
The reason why we’re making the announcement now is something that I think people don’t fully appreciate.
Whenever you have clear cut evidence that you have a drug that works, you have an ethical obligation to immediately let the people in the placebo group know so that they can have access…
We would have normally waited several more days. The data may change, but the conclusion won’t.”
Fauci then added that “the mortality rate trended toward being better in the remdesivir arm, 8% vs. 11%”.
The truth is that remdesivir, along with other drugs that are currently being recommended by the NIH, particularly dexamethasone, an anti-inflammatory and the antibiotic vancomycin, are found to be causing these deaths in hospitals through severe kidney damage and multiple organ failure, resulting to pulmonary edema or the drowning of one’s own lung.
This is the main reason why many patients die and not because of the so-called COVID19 (which is not yet objectively proven to exist anyway) or what they labeled COVID pneumonia (which is still just pneumonia anyway!).
What’s disturbing is the possibility that perhaps, most government health agency right now around the world is recommending this cocktail of organ damaging drugs.
As Dr. Bryan Ardis has revealed, the holistic doctor who’s been exposing the dangers of remdesivir since last year, this drug has “caused acute kidney failure in 35 percent of patients who used the drug within five to ten days”. And when mixed with dexamethasone and vancomycin, it caused acute kidney failure in “up to 45 percent of patients in a span of five days”.
This bleak story on the current protocol given by the NIH while being tolerated by other government agencies is yet another candidate for cover-up. This is really true in many hospitals. Despite high rates of negative effects, particularly severe kidney poisoning, the drugs are still being used and the people are still being treated like mere experimental objects.
As Dr. Ardis explains:
“When you cause acute kidney failure with drugs that they’re using in ICUs … while they have an intravenous drip that is putting water into their body – their abdomen, heart and lungs eventually fill up with water.”
And, as dark as it sounds, he also stated:
“They are using remdesivir the same way that they used gas chambers to destroy people in Germany. This is how they’re doing it, and perpetuating those deaths, using a drug in hospitals.”
All of this, according to Dr. Ardis, results to pulmonary edema, a water accumulating in the lungs. This, unfortunately, is mistakenly diagnosed as COVID pneumonia.
Indeed, there was a trial for remdesivir last year. As Rhoda Wilson of theexpose.uk reported on September 2:
“In June 2020 a trial was published of 61 patients with Covid-19 who were given a 10-day course of remdesivir. The results of that trial noted “12 patients (23%) had serious adverse events. The most common serious adverse events — multiple-organ-dysfunction syndrome, septic shock, acute kidney injury, and hypotension …
Four patients (8%) discontinued remdesivir treatment prematurely: one because of worsening of pre-existing renal failure, one because of multiple organ failure, and two because of elevated aminotransferases, including one patient with a maculopapular rash.”
Meanwhile, in a podcast with Dr. Wolfgang Wodarg, lawyer Reiner Fuellmich, and his team, Dr. Ardis stated that Dr. Fauci recommends remdesivir based on first, the study for ebola in 2018, in which it was never proven effective and safe, and the second study which was sponsored by the same company that manufactures remdesivir.
This started in March 2020, involving 53 COVID patients from 3 countries: Japan, America, and Canada. Dr. Ardis added that the subjects were then given remdesivir for 28 days, based on studies quoted by Dr. Fauci in the links posted at the NIH website.
Dr. Bryan Ardis then explained that aside from remdesivir, there was another drug that Fauci also pulled out because of its highly toxic effects. Meanwhile, the other study quoted has shown that “22% of all 53 patients experienced the 4 lethal side effects”, as mentioned above.Doctor Exposes the Dangers of Remdesivir and other Drugs that are Being Recommended by NIH, September 2021
Stay turned for Part Three…