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Biden Administration Allows Border Invasion to Continue – Massive Crisis Overwhelms Del Rio Border Sector in Texas

The efforts of the Biden administration to collapse the U.S. immigration system and open the borders to unrestricted illegal alien migration are being extremely successful.  Tens of thousands of illegal border crossers are now assembled in Del Rio, Texas, hometown to the Chief of the U.S. Border Patrol, Raul Ortiz.

The issue has become so overwhelming Ortiz told Houston media, “We’ve never seen a migration population explode so quickly on the immediate border like we saw over the last 72 hours.”  Approximately 13,000 illegal aliens are now encamped underneath the overpass of the international bridge connecting Del Rio, Texas, to Ciudad Acuña in the Mexican state of Coahuila.

Among the invasion forces are massive numbers of Haitians, thousands of them, who previously fled their homeland to South and Central American countries like Brazil and Columbia. After gaining visas to South America they work their way through Panama, Central America and into Mexico where they take organized buses from left-wing open border aid groups and eventually taxi cabs to Del Rio where they walk across the Rio Grande unimpeded.

The Obama administration previously began supporting this network of travel in 2012 during the “unaccompanied alien children” crisis.  However, currently the same system is working in overdrive, because the Obama crew has installed Joe Biden as a disposable figure to facilitate the fundamental change Obama failed to achieve when he was restricted by political backlash.

In the 2021 version of Obama’s operation, the invasion force is no longer limited to children or teenage central American gang members. Now we see entire families of economic migrants, and those who know the U.S. taxpayer will be forced to fund their life in the U.S, flooding the border in extreme numbers.

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Why Did The CDC Stop Recording Vaccine Breakthrough Cases in The U.S. on May 1st? – Today We Got The Obvious Answer, Vaccine Companies Want to Sell Booster Shots

A “breakthrough case” is the term for a person infecting with COVID-19 after they have been vaccinated.  On May 1st the CDC changed the recording and record keeping of COVID-19 breakthrough cases, and stopped tracking them.  The change was announced July 30th {Data Link}.

[…] The Centers for Disease Control and Prevention (CDC) currently monitors hospitalizations and deaths, from any cause, among fully vaccinated individuals with COVID-19, but not breakthrough infections, which it stopped monitoring as of May 1. CDC presents this data in aggregate at the national level but not by state, and there is no single, public repository for data by state or data on breakthrough infections, since the CDC stopped monitoring them. (read more)

At the time the CDC stopped tracking the incidents of vaccinated persons contracting COVID-19 and being hospitalized, many people wondered why?  Obviously if you stop recording vaccinated persons who are hospitalized, it will look like only unvaccinated persons are being hospitalized by the variants in the CDC records.  That skews the data and gives the false impression that only unvaxxed persons are getting infected and/or sick….

…Which is exactly what happened.

The medical industry and media narrative around the COVID-19 Delta Variant was that unvaccinated people in the U.S. were the majority group at risk.  The data supported that narrative because the breakthrough cases were no longer being recorded.   This makes the vaccine approach look better.  The approach of not counting the breakthrough case hospitalizations also makes the pharmaceutical companies look better; their vaccine looks more appealing & more effective.

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FDA Advisory Panel Rejects Pfizer Booster Shots

The Food and Drug Administration (FDA) advisory group who evaluate the efficacy and safety of vaccines have rejected the request for Pfizer booster shots.  However, the White House – desperately trying to push as many needle jabs as possible – was already on track to begin giving booster shots this month.  The implication here is that the White House was not following the recommendations of the FDA or the science.

WASHINGTON DC – A U.S. Food and Drug Administration (FDA) advisory panel voted Friday against approval of Pfizer (PFE)/BioNTech’s (BNTX) third dose for the U.S.

The vote comes after a heated debate in recent weeks over the need for booster or additional shots, which both mRNA companies — Pfizer and Moderna (MRNA) — have advocated for.

Dr. Peter Marks, the FDA’s leading expert on vaccines, touched on the controversy in his introductory remarks. “We know that there may be differing opinions of the interpretation of the data regarding the potential need for additional doses, and we strongly encourage all the different viewpoints to be voiced and discussed regarding the data, which is complex, and evolving,” Marks said.

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COVID Politics Takes a Dark Turn, Biden Administration Takes Control of Monoclonal Antibody Drugs in Order to Block Treatments in Red States and Ration Equitable Treatment

When Joe Biden’s Health and Human Services made the announcement earlier this month (LINK) that they were taking full control over Monoclonal Antibody drugs (mAb) in order to begin rationing the highly effective treatment for COVID-19 infection, several people sounded alarm bells as there was the potential for rationing of COVID treatment based on political ideology.   Representative Chip Roy of Texas was one of the first to raise concerns (link).

The change in HHS approach followed republican governor Ron DeSantis of Florida promoting the use of mAb and opening up dozens of treatment centers throughout his state.   Other governors quickly took notice of the effective action plan of DeSantis in Florida and started to follow that path.

As soon as HHS noticed the red state governors were working on a effective treatment alternative to the vaccine approach, HHS appears to have moved in to block it – thereby restricting the treatment pathway in order to enhance the vaccine approach. [HHS Announcement]  Note the alarm word “equitable“:

It took a week for the new HHS restrictions to impact the pre-existing orders.  However, now Alabama is the first state to draw attention to the problem Joe Biden’s administration is creating by rationing mAb treatment and making determinations on which states should be allowed the “equitable use of the available supply“; a fancy term for “rationing” the life-saving treatment based on alignment with the political ideology of the government in control of it.

Newsweek – Albama doctors are concerned about the impact on health care systems after the U.S. Department of Health and Human Services (HHS) decided to temporarily limit monoclonal antibody order. […] Dr. Scott Harris, Alabama’s state health officer, told Newsweek that the shots are key for protecting a person against hospitalization and death … “It can be a lifesaver if given in the first 10 days of symptoms,” Arora said about monoclonal antibodies. “We’re calling on the federal government to help us provide more of this treatment, not less, so we can save lives and keep COVID patients out of the hospital.”

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Outbreak of Measles in Virginia and Wisconsin Afghan Refugee Settlements Forces Pause in New Arrivals

We have actually seen this issue before as a result of the Obama open border policy.  A measles outbreak in Virginia and Wisconsin amid refugees from Afghanistan has caused the U.S. State Department to pause the program for further arrivals.

[…] The Virginia Department of Health initially said Friday that three people who arrived from Afghanistan had been diagnosed with the measles in northern Virginia. The agency said it was informing people who risked possible exposure at places that included Dulles International Airport and two local hospitals. (read more)

Another Study Shows Hospitalization Numbers of COVID Patients in U.S. are Overinflated, Not Drawing Distinction Between COVID Incidental To Admission or Treatment Thereof

Interesting data on SARS-CoV-2 (COVID-19) being released and discussed today.  The first is the release of a study [DATA HERE] indicating that half of all recorded hospitalization cases for COVID-19 are incorrectly being interpreted.

The study of 50,000 VA patients recorded as hospitalized and testing positive for COVID-19, reflects that roughly half of the patients recorded on the dashboard were admitted to the hospital for some other, unrelated, reason and incidentally tested positive for the virus upon admission.  They arrived for treatment for something else, were tested and recorded for COVID, but the treatment was not for any COVID-19 related issue.

An earlier study in May, using the charts of hospitalized pediatric patients found roughly the same thing; 40 to 45 percent of the patients recorded as COVID hospitalizations, when in reality they were in the hospital for something unrelated to COVID.   As noted in the AtlanticFor two separate studies published in May, doctors in California read through several hundred charts of pediatric patients, one by one, to figure out why, exactly, each COVID-positive child had been admitted to the hospital. Did they need treatment for COVID, or was there some other reason for admission, like cancer treatment or a psychiatric episode, and the COVID diagnosis was merely incidental? According to the researchers, 40 to 45 percent of the hospitalizations that they examined were for patients in the latter group.”

In the VA study released today approximately half of the COVID-19 recorded hospital cases had nothing to do with COVID-19. “[T]he study suggests that roughly half of all the hospitalized patients showing up on COVID-data dashboards in 2021 may have been admitted for another reason entirely, or had only a mild presentation of disease.” (link)

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American Medical Bureaucracy, Including AMA, Increase Threats Against Doctors Who Do Not Comply With Forced Vaccination Position

“Nice license you’ve got there Doc, it’d be a shame if something happened to it”…

That is the overwhelming threat message coming from the regulatory boards of the American medical establishment to all doctors operating in the U.S.   The professional threats have increased in direct proportion to the tone of threat from the White House.    The threats are intended to maintain the fear narrative behind COVID-19, and push all medical healthcare providers to carry only one acceptable opinion.

Before getting to the American Medical Association (AMA) statements and guidance, let’s first look at some of the threats from the specialty fields in the system.  Look at the last paragraph of this notification letter from the American Board of Emergency Medicine (ABEM): (Source)

The ABEM specialty portal contains a link for people within the emergency room healthcare field to “report a violation” of the approved messaging.  Should an emergency room physician or healthcare provider (ie. nurse) make any statement that contradicts the governing authority, they will have their certification revoked.   Think about that.

Also, keep in mind, these are threats that only pertain to the delivery of healthcare in the United States, and the position of forced vaccination in America.  This is happening at the same time that other countries are abandoning the ‘exclusive vaccination approach‘, and are instead focusing on using their healthcare systems to keep people alive and healthy.

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Lara Logan Notes the OSHA Shift in Record Keeping that Preceded Joe Biden’s Use of The Agency for Vaccine Enforcement

Lara Logan notes how Joe Biden is using the Occupational Safety and Health Administration (OSHA) as the compliance mechanism to enforce mandatory COVID vaccination as a requirement for continued employment; and contrasts Biden’s announcement against the earlier press release from OSHA in May of this year.  We wrote about it HERE.

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May 22, 2021 – “An interesting about-face from the Dept of Labor and OSHA. Previously OSHA stated that any employer who required vaccinations must report adverse reactions as workplace injuries. However, OSHA is now saying they will not “enforce” that record-keeping requirement until May of 2022.”

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The Ethics of Forced Employment Vaccination by Dr. Julie Ponesse

Canadian professor Dr. Julie Ponesse is an expert in ethics who has been eloquently teaching college students for twenty years.  Her story is one story, a profound story; and it is our story.

It is the story of a world gone mad, and the people within it – strong enough to recognize the brutal insanity.

https://youtu.be/7ZapO8imfuA

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This is the professor I want teaching my grandchildren.  This is the teacher they deserve….

I despise those in power of every stripe who have put our world into this place of darkness. A place devoid of common intellectual sense, created by weakness, and driven by ideological minds with no regard for freedom, humanity or human purpose.  Participation in evil enterprise it itself evil.  My tribe will not participate.  We stand defiant and resolute.

..”In a time of universal deceit, telling the truth is a revolutionary act.”

Welcome to the revolution.

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Australia Bans Ivermectin

If you suspect the extremely heavy-handed Australia/New Zealand COVID-19 mitigation efforts might be a beta-test for just how far a government can go to control the citizens therein, well, this latest development appears to be an affirmation in that direction.

The ruling authority in Australia has just banned doctors from prescribing Ivermectin.  The Advisory Committee for Medicines Scheduling and the Australian National COVID Clinical Evidence Taskforce, have determined that any effort to mitigate COVID-19 with therapeutics will likely diminish the goal of vaccinating the entire population.  Therefore Ivermectin, which has saved thousands of lives and is widely in use in multiple countries including India, is now official banned from use by Australian doctors.  Quite remarkable….

AUSTRALIA – Today, the TGA, acting on the advice of the Advisory Committee for Medicines Scheduling, has placed new restrictions on the prescribing of oral ivermectin. General practitioners are now only able to prescribe ivermectin for TGA-approved conditions (indications) – scabies and certain parasitic infections.  […] These changes have been introduced because of concerns with the prescribing of oral ivermectin for the claimed prevention or treatment of COVID-19. Ivermectin is not approved for use in COVID-19 in Australia. (LINK)

Consider this from Studies within the NIH:

♦ (STUDY – 1) “Moderate-certainty evidence finds that large reductions in COVID-19 deaths are possible using ivermectin. Using ivermectin early in the clinical course may reduce numbers progressing to severe disease. The apparent safety and low cost suggest that ivermectin is likely to have a significant impact on the SARS-CoV-2 pandemic globally.” (LINK)

♦ (STUDY – 2, INDIA) “There were no severe adverse drug events recorded in the study. A 5-day course of ivermectin was found to be safe and effective in treating adult patients with mild COVID-19.” (LINK)

The Australian government is banning a therapeutic treatment with a history of success in order to force the citizens into a situation where they must take the vaccine.   Here comes the black-market.