Archive for the ‘Activism’ Category

CDC Stops Counting ‘Non Severe’ “Vaccinated” COVID Cases Back in May. Lowers PCR for “Vaccinated” in April – Nothing to See Here

https://www.businessinsider.com/risk-of-delta-variant-cdc-stopped-tracking-cases-vaccinated-2021-7

The CDC stopped tracking most COVID-19 cases in vaccinated people. That makes it hard to know how dangerous Delta really is.

Aria Bendix Jul 3, 2021
coronavirus testing
A nurse administers a COVID-19 test at a testing site in Suffolk County, New York, on December 18, 2020.   John Paraskevas/Newsday via Getty ImagesImportant excerpts from article below:
  • The CDC stopped monitoring non-severe COVID-19 cases among vaccinated people in May.
  • It’s hard to assess Delta’s risk without knowing what mild breakthrough cases look like — or whether they’re becoming more common.

Since May 1, the agency has only reported and investigated coronavirus infections among vaccinated people that resulted in hospitalization or death.

In a recent blog post for Harvard Health Publishing, Robert Shmerling, an associate professor of medicine at Harvard Medical School, called the CDC’s decision not to track all breakthrough cases “surprising” and “disappointing.”

The coronavirus is going to stick around forever. Get ready for the new normal.  (See link for article)

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**Comment**

While the article is riddled with inaccuracies, the take-away here is the CDC has STOPPED counting the majority of cases in “vaccinated” people.  I reported on this fact earlier but it bares mentioning again as this decision is muddying all data being used, which is supplying the rhetoric and tyrannical action.  There is no way to know the impact of anything at this point, with data purposely twisted for a predetermined outcome.

BTW: it was done numerous times before:

But the fun doesn’t end here.

In April, the CDC issued new guidance to laboratories recommending reducing the RT-PCR CT value to 28 cycles, but only for those fully “vaccinated” individuals being tested for COVID.

In other words, lowering the CT threshold parameter will lead to missing infectious persons, and will give the illusion that “vaccinated” people aren’t contracting COVID.

The first question you must ask is, why would the CDC do such a thing?  When you understand their MO; the long and sordid history of corruption, conflicts of interest, and rigging variables for their own nefarious purposes – you can quickly surmise why.  They don’t want people to know the full story, because the full story would reveal that these “break-through” cases (getting COVID after being fully immunized) are far more prolific than the CDC wants to admit to – proving the injections are unnecessary and ineffective.

“Breakthrough” cases can also be deadly, with one study showing 6% end in death. As of June 28, the Centers for Disease Control and Prevention (CDC) reports 4,686 breakthrough cases resulting in death and hospitalization.

But these deaths and maimed bodies don’t matter, because it’s all for the greater good.

For some historical perspective, watch how “60 Minutes”covered the 1976 swine flu mass vaccination program which was halted after 4,000 reported adverse events.  In contrast, there are 463,457 adverse events reported after the COVID injections from December 2020 to July, 2021, and less than 1% are typically recorded.

For anyone reading this website, you already understand that the CDC owns the patents on not only the very pathogens, but on the testing which it rigs for its own pre-determined outcome. They’ve been doing this with Lyme/MSIDS for over 40 years and continue to get away with arbitrary testing cut-offs, which keeps thousands from diagnosis and treatment.  They are quite experienced at twisting data.

The inconvenient truths that the injections aren’t effective, safe, or needed isn’t good for Big Pharma, Big Tech, mainstream media, FDA, CDC, NIH, or our government – all of which stand to gain from these lucrative gene-therapy injections that aren’t vaccines.

Important quote:

“By tracking only cases requiring hospitalization or causing death, we may miss the chance to learn how people with ‘milder’ disease are affected by Delta or other variant infections, such as how long their symptoms last and how the infection may disrupt their lives.” Robert Shmerling, associate professor of medicine at Harvard Medical School

But, that is exactly the point.

Now only severe cases will be recorded, to downplay the fact the injections don’t stop infection or death.

Further, they are paying students to persuade people to get the jab and attempting to divide us by blaming the unvaccinated for the pandemic, particularly those who vote conservatively, even though numerous polls and studies have proven this tenant is inaccurate.

Meanwhile, these same corrupt ‘authorities’ are censoring and bad-mouthing cheap, effective treatments that work, so a misinformed public continues to believe their only recourse is to get the dangerous but lucrative COVID shots, our own government developed.

They are also hiding the number of fully “vaccinated” White House staffers who have contracted COVID.
Contracting COVID after being “vaccinated” is an inconvenient truth for the powers that be that must be denied at all costs.

For more:

Category:

Activism, vaccines, Viruses

CDC Quietly Withdraws EUA for COVID PCR Test – It Can’t Distinguish Between COVID & the Flu

https://healthimpactnews.com/2021/cdc-to-withdraw-emergency-use-authorization-for-rt-pcr-test-because-it-cannot-distinguish-between-sars-cov-2-and-the-flu/

CDC to Withdraw Emergency Use Authorization for RT PCR Test Because It Cannot Distinguish Between SARS-CoV-2 and the Flu

by Brian Shilhavy, July 25, 2021
Editor, Health Impact News

The CDC quietly announced last week that it was withdrawing its request to the FDA for Emergency Use Authorization (EUA) of the 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2.

Most of the public is probably unaware that similar to the current COVID-19 injections that are not yet approved by the FDA, but only given Emergency Use Authorization, so too the hundreds of diagnostic tests that supposedly detect COVID-19 are also NOT approved by the FDA, but only authorized via an EUA.

What is the reason the CDC is withdrawing its EUA request for the Real-Time RT-PCR Diagnostic Panel?

In preparation for this change, CDC recommends clinical laboratories and testing sites that have been using the CDC 2019-nCoV RT-PCR assay select and begin their transition to another FDA-authorized COVID-19 test.

CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. (Source.)

Caitlin McFall, writing for Fox News, is the only one in the corporate media I could find that even reported this, and the few reports I found in the Alternative media so far have been mostly inaccurate.

McFall reports:

The Centers for Disease Control and Prevention (CDC) urged labs this week to stock clinics with kits that can test for both the coronavirus and the flu as the “influenza season” draws near.

The CDC said Wednesday it will withdrawal its request for the “Emergency Use Authorization” of real-time diagnostic testing kits, which were used starting in February 2020 to detect signs of the coronavirus, by the end of the year.

“CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives,” the agency said.

The U.S. has reported more than 34.4 million cases of the coronavirus since the pandemic began in 2020 and more than 610,000 deaths.

But while cases of COVID-19 soared nationwide, hospitalizations and deaths caused by influenza dropped.

According to data released by the CDC earlier this month, influenza mortality rates were significantly lower throughout 2020 than previous years.

There were 646 deaths relating to the flu among adults reported in 2020, whereas in 2019 the CDC estimated that between 24,000 and 62,000 people died from influenza-related illnesses.

The CDC urged laboratories to “save both time and resources” by introducing kits that can determine and distinguish a positive test for the coronavirus and flu. (Source.)

So there you have it.

The CDC just basically admitted that many of the COVID-19 cases this past year could not be distinguished from “flu cases.” No wonder flu cases decreased to zero in so many places. See:
Health Officials Admit that Only Those Vaccinated for the Flu are Getting the Flu This Year

The ending of the EUA for the Real-Time RT-PCR Diagnostic Panel will not happen until the end of the year, December 31, 2021, and the CDC recommends that laboratories start transitioning to other types of COVID-19 diagnostic tests that have been given an EUA by the FDA here.

At the time of publication of this article, the FDA has issued 251 EUAs for COVID-19 diagnostic tests since April 1, 2020. The vast majority of them are for the RT-PCR tests, including about 20 that were just issued EUAs since the beginning of this month, July, 2021.

The cash cow for these tests and the hundreds of companies that got rich selling them will now have to move on to the next phase to be able to cash in.

Diagnostic Testing Fraud: Controlling the Masses and Medical Kidnapping

We have been covering the corruption in the medical diagnostic testing field for the better part of a decade now, and we exposed it early on in the COVID-19 Plandemic last year as well.

Here are some of our previous articles from last year exposing the fraud of COVID-19 diagnostic testing.

When we started MedicalKidnap.com back in 2014, we learned that fraudulent diagnostic testing was a common way for doctors and hospitals to order children be removed from their homes.

Often they create false drug test positive results to remove children from their parents.

Alabama Lab Owner Arrested for Falsifying Results of Drug Tests Used to Medically Kidnap Children

The worst offender, by far, in medically kidnapping children by use of a medical diagnostic test, is within the field of radiology and finding “proof” of child abuse simply by looking at x-rays.

This whole field has developed a recent new class of pediatricians “certified” as “Child Abuse Pediatricians,” and the lucrative jobs of these doctors depend on them finding abused children and putting them into the lucrative child trafficking network known as “foster care.”

We have actually published an eBook on this topic, or you can look up individual cases on our MedicaKidnap.com website to learn how this evil system works.

When it comes to diagnosing “influenza,” we have exposed the fraud there as well, as pre-COVID-19 the CDC simply used estimates of cases of the flu, since they cannot verify actual numbers each year by diagnostic testing.

Annual Flu Deaths Scam Unwittingly Exposed and Replaced by the COVID Deaths Scam

So COVID-19 allowed them to just further exploit the fraud of diagnostic testing to create fear and panic, and achieve their goals of enslaving the public and rolling out their experimental mRNA injections.

With this latest announcement by the CDC that they are now going to retire the RT-PCR Diagnostic tests and replace them with other tests that can now test both COVID and influenza, it is pretty easy to see what their game plan is for later this year.

Just about everyone in the U.S. will be able to be tested “positive” for something by this Fall when the flu season starts.

This will be the “Hegelian principle” implementation for 2021. The government creates the problem, and then they create the solution, which we know now is more “vaccines” for everything in life that ails us, and try to punish those who don’t want to play their game.

I’m ready. Are you?

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**Comment**

The CDC often quietly updates its website with inconvenient truth, when it works in their favor.  With COVID, this new information will make it possible for them to now jack the numbers of flu cases since they literally quit counting them making everything COVID.  I’m sure this will also be used to push the flu vaccine, which has never been effective, doesn’t prevent transmission, and actually increases your risk of contracting non-flu respiratory illness by 65%.

But there’s even something more diabolical going on here.

According to Jon Rappoport, the CDC/FDA is essentially confessing that they didn’t have a “virus” to begin with when they concocted the test using contrived samples of the virus. In short, they invented synthetic gene sequences and stated these sequences HAD TO BE close to the sequence of SARS-CoV-2. There is still no proof there is something called SARS-CoV-2. This article shows that the sequence used in PCR testing is present in ALL human DNA which equates C8 as a foreign hostile material and indeed the coronavirus – Covid19 – itself.

Each of the 59 different PCR tests for SARS-CoV-2 told different lies and concocted different fabrications about the genetic makeup of the virus—the virus we didn’t have. Obviously, then, these tests would give unreliable results.

BUT, don’t worry, be happy, because NOW, the CDC and the FDA say, they really do have actual virus samples of SARS-CoV-2 from patients; they have better targets for the PCR test, and labs should start gearing up for the new and improved tests.
In other words, they were lying THEN, but they’re not lying NOW. They were “contriving,” but now they’re telling the truth.

Rappoport states virology’s version of “we isolated the virus” to mean they created a soup in the lab containing monkey cells, toxic chemicals, drugs and random genetic material.  Researchers than assume that cells die due to a bit of mucus from a patient they dropped in the soup, therefore the virus must be the killer agent in the mucus – when it very well could be any of the components within the contrived soup.

The “new and improved” tests are nothing more than a money-maker for our corrupt public health ‘authorities’, who own patents on virtually every aspect surrounding COVID, including the spike protein.
They will now continue spinning their narrative utilizing these phoney tests.

Regarding Lyme/MSIDS, the CDC quietly updated their website from previously insisting Lyme can’t be spread congenitally to now admitting it’s possible, but rare.  But, as Lyme advocate Carl Tuttle points out: How can it be rare when nobody’s counting? The timing is impeccable.  Whenever there is a Lyme vaccine in the pipeline, the CDC finally admits how devastating and prolific tick-borne illness is.  I stand firmly with Tuttle that No Lyme vaccine should be considered until persistent infection is recognized.  But this will never happen because if they admit to persistent infection, they are also admitting that a vaccine would be ineffective against it.

The CDC often makes bold proclamations without a shred of evidence.  

For more on the PCR scam:

This completely bogus test has caused irreparable harm.  It’s been used to falsely elevate cases, then used to make the COVID injections appear to be working (by lowering the cycle threshold).  It has been used to make it appear that fully “vaccinated” people aren’t contracting or dying from COVID (called “break-through” cases) when many are, as well as to quarantine people, keep them from working, and causing unsubstantiated fear in the public.

This is not new.  Lyme/MSIDS patients have also been in a war due to faulty, arbitrary testing  that’s been rigged for a pre-determined outcome.

Category:

Activism, Testing, Viruses

Research Consortium Aims to Develop New Drug For Bartonellosis

https://www.lymedisease.org/research-consortium-bartonellosis/

Research consortium aims to develop new drug for bartonellosis

July 15, 2021

Key infectious disease researchers at Tulane University, Duke University and North Carolina State University will collaborate on an initiative to develop a treatment for bartonelloses, a spectrum of vector-borne diseases that can cause debilitating symptoms.

The three-year, $4.8 million initiative funded by The Steven and Alexandra Cohen Foundation, will establish the Bartonella Research Consortium to develop a novel treatment for bartonelloses.

Bartonella are zoonotic, stealth bacterial pathogens that were not known to infect animals or humans prior to the HIV epidemic when immunocompromised patients began showing symptoms of bartonelloses.

Bartonelloses are often self-limiting diseases that can be cleared by the immune systems of healthy individuals. In immunocompromised individuals or as co-infections, they can cause severe neuropsychiatric, cardiovascular, and rheumatological symptoms. Cats and fleas often harbor the pathogen, which increases the likelihood of transmission to humans.

The principal investigators of the consortium support a collaborative approach to the study of complex, poorly understood infectious diseases. By working together to prevent and treat Bartonella infections, they will provide patient-relevant solutions that improve both animal and human health. Targeted antimicrobial strategies to eliminate long-standing Bartonella infections will dramatically improve patient outcomes.

Similarities between Bartonella and Lyme infections

Bartonella symptoms overlap with those of other vector borne organisms such as Borrelia burgdorferi, the bacteria that causes Lyme disease. In some instances, patients have been infected with both Bartonella and Borrelia burgdorferi infections, which can cause an exacerbation of symptoms. 

As often seen in Lyme disease patients, a subset of people with bartonelloses develop chronic symptoms despite prior antibiotic therapy. Treatment failures have been documented with both infections, thus the need for drugs that specifically target and eliminate these bacteria.

Associate Professor Monica Embers, a microbiologist and immunologist at the Tulane National Primate Research Center, focuses on the persistence of tick-borne infectious disease despite antibiotic therapy and will bring her expertise to the consortium.

“There are a lot of similarities between Bartonella and Borrelia infections, both of which are notoriously difficult to detect and treat. Developing targeted treatments has the potential to alleviate a lot of suffering, both in the human and pet populations,” said Embers.

There are over 40 known Bartonella species or subspecies and at least 17 have been associated with a spectrum of disease symptoms. Although Bartonella remain neglected in human and veterinary medicine, more recent evidence supports an important role for these bacteria in a variety of diseases.

Funding for this research initiative combines the strengths of research laboratories located at Duke University, North Carolina State University and Tulane University.

Principal investigators include Drs. Edward B. Breitschwerdt, Monica E. Embers, Timothy A Haystead and Ricardo G. Maggi. During the next three and a half years, these established investigators and their highly skilled research teams will develop a novel drug for the treatment of bartonelloses.

SOURCE OF PRESS RELEASE: Tulane University

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For more:

Category:

Activism, Bartonella, Psychological Aspects, research, Treatment

Why the FDA is Attacking NAC Supplements – TAKE ACTION

https://anh-usa.org/why-the-fda-is-attacking-nac-supplements/

Why the FDA is Attacking NAC Supplements?

JULY 15, 2021
CATEGORY: STOP CRONY HEALTHCARE

N-acetyl-L-cysteine (NAC) has been on the market as a supplement for decades—why is the FDA attacking it now? Action Alert!

A few weeks ago, we told you about the FDA’s recent actions threatening NAC supplements—products which the FDA has allowed on the market for decades. The question is, why now, after all these years, is the FDA doing this? Digging a bit deeper, it seems obvious that the FDA is clearing the market of affordable NAC supplements in an effort to eliminate competition for NAC drugs that could be coming to market in the next few years. If our suspicions are correct, this would be another outrageous example of the FDA doing Big Pharma’s dirty work. We cannot let it happen.

To briefly recap how we got here: In a slew of warning letters sent last year, the FDA targeted a number of supplement companies marketing “unapproved” cures for hangovers—which the agency absurdly considers to be a “disease.” Some of these products contain NAC. In the letters to those companies, the FDA states that NAC does not meet the legal definition of a supplement because it was approved as a drug in 1963; according to federal law, any substance approved as a drug before it was sold as a supplement cannot be sold as a supplement. All of this means that the status of NAC as a supplement is currently in dispute.

So, why is the FDA threatening NAC now, during a pandemic when a new FDA commissioner hasn’t even been appointed? For starters, a drug company is investigating NAC as a treatment for a rare genetic disorder that damages the myelin sheath, which insulates nerve cells in the brain. The Phase 1 trial was completed in March 2020.

But that’s just the beginning. A search through the government’s clinical trials database shows considerable interest from the pharmaceutical industry in NAC. There are 17 trials looking at NAC, in both drug and supplement form, in the treatment of COVID. Additionally, there are over 50 trials looking at NAC for a variety of other conditions, including: autism spectrum disorder, obsessive compulsive disorder, alcohol abuse disorder, rhinosinusitis, bronchiolitis, cardiac arrhythmia, and more.

Note that NAC drugs are currently available in generic form since it is off-patent, but a company could bring a new branded NAC drug to market if it was proven effective for an additional indication.

Given these facts, it seems reasonable to assume that the FDA is setting the stage for a new NAC drug to come to market by removing the competition from much cheaper NAC supplements. We called it when the FDA pulled a similar move a few years back when they went after brain health supplements, trying to clear the market for a new Alzheimer’s drug—culminating in the recent approval of an Alzheimer’s treatment that many experts think is not effective. CBD supplements may face a similar fate if Congress does not force the FDA’s hand by legalizing CBD in dietary supplements.

It is critically important to maintain access to affordable NAC supplements. In a recent interview with the Life Extension Foundation, Dr. Daniel Amen noted that NAC “has shown promising results in people with bipolar disorder, schizophrenia, OCD, and addictions. It can also decrease inflammation and may help delay brain atrophy in Alzheimer’s disease.” NAC protects the body from toxins, is a selective immune system enhancer, and helps remove free radicals, which contribute to neurogenerative diseases and aging. In Europe, NAC is a prescription medicine used to reduce congestion.

NAC is also a precursor to glutathione, one of the body’s most important antioxidants. Glutathione plays crucial roles in nutrient metabolism and the regulation of many cellular events (such as gene expression, protein synthesis, cell proliferation, and more); glutathione deficiency contributes to oxidative stress, which is implicated in the development of many diseases: Alzheimer’s, Parkinson’s, liver disease, HIV, heart attack, cancer, stroke, and diabetes.

Note that acetaminophen depletes glutathione, so those who regularly take it should consider, in consultation with an integrative doctor, supplementing with NAC to replenish glutathione levels. In fact, NAC is routinely used in hospitals to counteract acetaminophen toxicity.

NAC is far too important to be threatened by the FDA, especially under such dubious circumstances.

Recently, the FDA announced that, by the end of June 2022, it plans to release drafts or final versions of a number of policies, and among them is the “new dietary ingredient” (NDI) guidance (“new supplement” guidance, in plain English).

It is no exaggeration to say that this is the most dangerous threat to supplements we’ve seen in decades. 

We must continue to vehemently oppose the guidance as currently written and demand that substantial changes are made before the final version is released. It is especially dangerous given that we are in a pandemic situation that is constantly evolving, with scientists warning of viral variants that evade vaccine-induced immunity.

Action Alert! Write to the FDA and tell them not to threaten NAC supplements. Please send your message immediately. 

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For more:

Category:

Activism, Supplements

Wisconsin Physician Fired Over COVID Book

https://www.medpagetoday.com/special-reports/exclusives/93266

Mayo Physician Fired Over COVID Book

— “I’m still in shock I was terminated for this”

by Amanda D’Ambrosio, Enterprise & Investigative Writer, MedPage Today June 24, 2021

A photo of Steven Weiss, MD, and his book: Carnage in America: COVID-19, Racial Injustice, and the Demise of Donald Trump

After publishing a book about his experience on the front lines during the COVID-19 pandemic, a physician was fired from his position at the Mayo Clinic this month, he confirmed to MedPage Today.

Steven Weiss, MD, an internist who practiced at the clinic’s Eau Claire, Wisconsin location for 32 years, stated that he was terminated because he identified himself as an employee of the Mayo Clinic in his new book, called Carnage in America: COVID-19, Racial Injustice, and the Demise of Donald Trump.

According to a June 4 termination letter shared with MedPage Today, Mayo Clinic administrators told Weiss, 62, that his actions violated the health system’s publishing policy, as he did not submit his manuscript to the institution for review before it was printed.

(See link for article)

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**Comment**

You may not like this doctor’s opinion, you may not even agree with it, but the increasing censorship of medical practitioners spells impending doom for free speech & medicine.

This doctor was fired under a “without cause” provision because there was no misconduct, incompetence, negligence, or violation of his employment contract. He simply was fired for not asking “mother may I,” before writing a book on his medical experience.

You can tell by the statements by the administrators that this was all about their fear that people think they support a certain political party.  Weiss discussed the influence of politics, religion, and culture on Americans’ perception of COVID-19, and faulted the administration at the time for the pandemic response.  While there was some negative information on Mayo, Weiss states, “I offered lavish praise in places, too.”

Expect more of this.

Lyme/MSIDS treating doctors have been persecuted for over 40 years due to the fact they disagree with mainstream medicine’s handling of it. Orders in medicine come from the top down and start with the CDC/IDSA‘s abysmal Lyme treatment guidelines that are ineffective, unscientific, and extremely biased.  Wisconsin doctors have come under scrutiny many times for daring to depart from the accepted narrative that Lyme is hard to get and easy to treat.  The reality of thousands of patients proves this to be nothing more than mythology.

Category:

Activism