The former head of the CIA Counterterrorism Center has suggested that counterinsurgency tactics used by the military in Iraq and Afghanistan should be applied to ‘domestic extremists’ inside the US.

NPR reports that Robert Grenier, who directed the CIA’s Counterterrorism program from 2004 to 2006, declared “We may be witnessing the dawn of a sustained wave of violent insurgency within our own country, perpetrated by our own countrymen.”

In an op-ed for The New York Times last week, Grenier suggested that “extremists who seek a social apocalypse … are capable of producing endemic political violence of a sort not seen in this country since Reconstruction.”

Source: Summit News

During the election year, President Trump warned that a new administration would be coming to take away the 2nd amendment!  Well, we are not even 2 weeks into the Biden administration and the House has just submitted a new resolution — HR 127 — and within the resolution is the STRICTEST measures ever proposed.  [ Read the bill for yourself ]

Highlights:

The Attorney General, through the Bureau of Alcohol, Tobacco, Firearms and Explosives, shall establish a system for licensing the possession of firearms or ammunition in the United States, and for the registration with the Bureau of each firearm present in the United States.

Within 3 months of the resolution being passed …

REQUIRED INFORMATION.—Under the firearm registration system, the owner of a firearm shall transmit to the Bureau—

“(A) the make, model, and serial number of the firearm, the identity of the owner of the firearm, the date the firearm was acquired by the owner, and where the firearm is or will be stored; and

“(B) a notice specifying the identity of any person to whom, and any period of time during which, the firearm will be loaned to the person.

Then … every gun owner will need to obtain a license and then complete a criminal background check, psychological evaluation, complete a 24-hour training course, and finally carry gun insurance (appears to be $800 a year!).  Of course, your license can be denied or revoked if you are found to be declared ‘psychologically unfit’ for any number of reasons.

And the kicker … if you are found in violation of this new law … the smallest fine was $5,000 up to $150,000 and up to 25 years in jail!

H.R.127 – 117th Congress (2021-2022)_ Sabika Sheikh Firearm Licensing and Registration Act _ Congress.gov _ Library of Congress [PDF]

View the bill on Congress.Gov

Glenn Beck nails the New York Times!  The NYT is suggesting Biden appoint a “reality czar”.  A dystopian reality … because a ‘truth czar’ would be plagiarizing George Orwell’s 1984’s “Ministry of Truth!”

How the Biden Administration Can Help Solve Our Reality Crisis – The New York Times

American Frontline Doctors just dropped an eye-opening paper! [Source]

In conclusion, AFD suggests that the Covid-19 experimental vaccine should not be distributed to those under 50, and in doing so, is reckless.

In medicine, the guiding principle is “First, do no harm.” Widely distributing a COVID-19 experimental vaccine before adequately addressing and clinically evaluating the above concerns is reckless. This is especially true in adults under 50 years old who have an infection survival rate of about 99.98%, and even lower in those without high-risk comorbidities. While “first, do no harm” may not be a guiding principle for politicians or health authorities, it still resides in the forefront of the minds of frontline physicians.

America’s Frontline Doctors’ holds that it is unethical to advocate for the vaccine to persons under 50. The risk and safety evidence based upon trials cannot be justified in younger persons. It is therefore prohibited. If pharmaceutical companies, private businesses or the government mandate or coerce persons to comply with unethical policies for which there is substantial evidence of likely harm, and indeed a person is harmed, that person’s grievances must be adjudicated in light of the future defendant’s knowingly willful misconduct and AFLDS will do everything within its power to assist such plaintiffs. While we sincerely hope this will never be the case, and we are taking all measures to reduce that possibility, should that unfortunate situation come to pass, we expect to assist hundreds of thousands of patients in class action lawsuits.

American Frontline Doctors just dropped an eye-opening paper! [Source]

In this segment, we begin to understand the unique relationships with Big-Tech with the Pharma companies.

The Department of Defense of the federal government has contracted with Google and Oracle to track vaccinated persons. In the document entitled “From the Factory to the Frontlines,” the Department of Health and Human Services (HHS) and the Department of Defense (DOD) stated that, because Warp Speed vaccine candidates use new unlicensed vaccine production methods that “have limited previous data on safety in humans . . . the long-term safety of these vaccines will be carefully assessed using pharmacovigilance surveillance and Phase 4 (post-licensure) clinical trials.”  The vaccination effort itself (OWS) is being managed by the military with the DHS and NSA as opposed to what is usually done, which is civilian health agencies. Law enforcement and DHS officials are not to be prioritized and the CDC Advisory Committee on Immunization Practices has identified “critical populations” including ethnic minorities and the mentally challenged. [Page 27-28]

American Frontline Doctors just published an eye-opening paper! [Source]

In this segment, AFD describes the conflict of interest from Vaccine Developers!

When the worldwide government response to COVID-19 swept the globe, there was a rush to manufacture vaccines. What is mostly unknown is that pharmaceutical companies are shielded from paying anything to people who may be hurt by their vaccines. This is a unique carve-out and financial benefit that caused the pharmaceutical industry to explode to many times its former size in the 35 years since this deal was struck.

Since 1986, when pharmaceutical companies could no longer be sued when anything goes wrong with a vaccine, there has been a huge increase in vaccines and simultaneously much less caution than there should be when recommending a biological agent to millions of perfectly healthy people. “National Childhood Vaccine Injury Act” of 1986” said that nobody can sue pharmaceutical companies for any vaccine injury. 42 USC §300aa-11. So in 1986 there were 11 vaccines but fast forward to now there are 53 (1986: polio, DTP, MMR and that was it) and hundreds more planned. In that time the vaccine market went from $1 billion to $44 billion (that $1B would be worth $2.24B today) and it is obvious that pharmaceuticals are incentivized to make more and more vaccines.

Pharmaceutical companies are now worth $1.3 trillion.” \ They are 2.5x Big Tobacco which is $500 billion/year65 and nearly 100x the NFL.  Over the past twenty years, pharmaceutical companies have spent $4 billion to lobby Congress which is more than aerospace, defense and oil/gas industries combined.\

American Frontline Doctors just dropped an eye-opening paper! [Source]

Precise language is an important way to combat disinformation. There are no COVID-19 vaccines. The correct terminology is that there are experimental COVID-19 vaccines, also known as investigational COVID-19 vaccines. Multiple types of vaccines are being tried; here is an overview of the categories. The ones closest to mass distribution are the mRNA vaccines.

One reason we must call this what it is, which is experimental, is because the American public has been primed to receive this biological agent simply because the word experimental has gone missing. Almost no normal person would volunteer to be the first to receive an experimental drug unless they were very sick and there were no alternatives. With COVID-19 the vast majority of people do not get very sick, and there are many alternative treatments. We must insist on using the correct language of experimental vaccine.

The other reason we must call this what it is, experimental, is because having an experimental status has important legal implications. These agents are being distributed under an EUA (emergency use authorization) which determines how future harm to patients will be compensated.  [ Page 17 ]

American Frontline Doctors just dropped an eye-opening paper! [Source]

The mechanism of action of the experimental mRNA vaccines includes a possible autoimmune rejection of the placenta. In layman’s terms, the vaccine may permanently interfere with a woman’s ability to maintain a pregnancy. The vaccine companies themselves acknowledge the possibility of ill effects on a pregnancy on the vaccine bottle, which says the following: “it is unknown whether COVID-19 mRNA VaccineBNT162b2 has an impact on fertility. And women of childbearing age are advised to avoid pregnancy for at least two months after their second dose.”  – [Page 15]

Scientists who developed the vaccine wanted to suspend the release of the vaccine … because of lifelong infertility!

Many scientists already agree the risk is much too high to release these experimental vaccines to the public at large. On December 1, 2020, the ex-Pfizer head of respiratory research Dr. Michael Yeadon and the lung specialist and former head of the public health department Dr. Wolfgang Wodarg filed an application with the European Medicine Agency responsible for European approval, for the immediate suspension of all SARS CoV-2 vaccine studies, in particular the BioNtech/Pfizer study on BNT162b.  One of the biggest reasons they cited was the possibility of lifelong infertility as described above and copied here. [page 24]