200,000 Unvaccinated Military Members Denied Temporary Restraining Order as Commanders Threaten Those Who Refuse COVID-19 Vaccines

Egregious abuse of power of those in “authoritative” positions.

This article has been cross-posted from globalresearch.ca
Written by Brian Shilhavy / Health Impact News (September 7, 2021)

All Global Research articles can be read in 51 languages by activating the “Translate Website” drop down menu on the top banner of our home page (Desktop version).

Visit and follow us on Instagram at @crg_globalresearch.

***

 

Several military members told Health Impact News today that their commanders are coercing members of their unit to get the COVID-19 shot TODAY (September 7, 2021) or face the consequences of disobeying a direct order.

One member stated that when they went by the local pharmacy in a drug store, there were many military members lined up to get the shots today, fearful of the consequences if they don’t.

And this is in spite of the fact that military officials are saying publicly that service members still have 2 to 3 months to comply, according to Military.com.

Sailors and Marines Have 90 Days to Get Vaccinated or Face Punishment

2 Sep 2021
Military.com | By Konstantin Toropin

Sailors and Marines now have 90 days to get vaccinated against COVID-19 or risk disobeying a lawful order, a violation of the Uniform Code of Military Justice, the maritime branches’ top leaders said in a series ofmessagesreleased Tuesday and Wednesday.

Airmen Have Less than Two Months to Get Fully Vaccinated

7 Sep 2021
Military.com | By Stephen Losey

The Department of the Air Force has set a tight two-month deadline for active-duty troops to be fully vaccinated against COVID-19. Those who don’t get the shot in time could be punished under the Uniform Code of Military Justice.

Airmen and Space Force Guardians must be fully vaccinated – including a two-week period after a final shot – by Nov. 2, the Air Force said in a press release Friday. Air National Guardsmen and reservists have until Dec. 2.

Apparently the military commanders are following their own schedule, regardless of what is being stated publicly by the various branches.

Lawmakers in the U.S. House of Representatives have now proposed legislation that would prevent the military from issuing dishonorable discharges for service members who refuse the COVID-19 vaccine.

Lawmakers Try to Ban Dishonorable Discharges for Troops Who Refuse Mandatory COVID-19 Vaccines

2 Sep 2021
Military.com | By Travis Tritten

House lawmakers have backed legislation prohibiting dishonorable discharges for troops who refuse the COVID-19 vaccine, as the Navy gave its sailors 90 days to get the shot this week and the Army and Air Force were poised Thursday to enforce their own timetables.

Legislation sponsored by Rep. Mark Green, R-Tenn., an Army veteran, requires only honorable discharges for anyone who is separated from the military over refusing to be vaccinated. It was added to the fiscal 2022 defense authorization bill, passed by the House Armed Services Committee on Thursday.

“No American who raises their hand to serve our Nation should be punished for making a highly personal medical decision,” Green said in a statement after the committee vote.

However, service members are telling Health Impact News that this is what some of them are being threatened with, dishonorable discharge, while others have said they have been threatened with demotions and being barred from reenlisting.

Judicial System Again Fails to Protect Constitutional Rights of Citizens by Denying 200,000 Unvaccinated Military a Temporary Restraining Order

On August 17, 2021, two military members filed a lawsuit in federal court in the State of Colorado, claiming that they represented 200,000 service members who were not vaccinated for COVID-19, but that they had previously contracted COVID-19 and recovered, and that therefore there was no need to be vaccinated against COVID-19, as they had “natural immunity.”

On August 24, 2021, Secretary of Defense Lloyd Austin issued a Memorandum for “SENIOR PENTAGON LEADERSHIP COMMANDERS OF THE COMBATANT COMMANDS DEFENSE AGENCY AND DOD FIELD ACTIVITY DIRECTORS” which stated:

I therefore direct the Secretaries of the Military Departments to immediately begin full vaccination of all members of the armed Forces under DoD authority on active duty or in the Ready Reserve, including the National Guard, who are not fully vaccinated against COVID-19. (Source.)

So on August 31, 2021, Todd Callender, counsel for the military Plaintiffs, filed a motion for a Temporary Restraining Order (TRO) to stop this directive from being enforced, which was heard by Judge Raymond P. Moore, who then denied the TRO on September 1, 2021.

The Plaintiffs had expert testimony from an affidavit by Dr. Peter McCullough, stating that “people who have the naturally created antibodies resulting from contracting and recovering from the Virus” should not be vaccinated because “it will do more harm than good.”

Judge Moore rejected his testimony and the evidence provided by the plaintiffs, because it was contrary to what the CDC states.

But Plaintiffs ignore all contrary opinion evidence, including obviously relevant guidance from the Centers for Disease  Control and Prevention (“CDC”) recommending vaccination regardless of whether a person has already had COVID-19 because research has not yet shown people are protected once they recover from the virus.

See Frequently Asked Questions about COVID-19 Vaccination, CDC Website, https://www.cdc.gov/coronavirus/2019-ncov/vaccines/faq.html (last visited Sept. 1, 2021).

The Court is not compelled to view Plaintiffs’ evidence in a vacuum or an echo chamber. As a result, the evidence cited by Plaintiffs coupled with their unsubstantiated insistence on their own natural immunity is insufficient to establish a clear and unequivocal right to a TRO under the circumstances of this case. (Read full opinion here.)

Again, to expect relief from COVID-19 vaccine mandates from the judiciary is just not reasonable. The system is rigged. They will quote the CDC, Anthony Fauci, and a whole host of other corrupt government agencies and leaders to deny facts and keep the COVID-19 narrative going that benefits the Pharmaceutical industry and their Wall Street Billionaires and Bankers.

The judiciary works for these Wall Street Billionaires and Bankers, not for the public.

Mass non-compliance is what is needed now, and while there are signs that those in law enforcement and other government agencies are now forming groups to resist (See: Police, Firefighters In LA Form Group To Resist Vaccine Mandates, for example), where are the military commanders who take seriously the oath they took to protect this country and their citizens??

One of the military members that Health Impact News corresponded with today wrote:

As much as I value my uniform, my time in service and fighting back against such obvious abuses of power I’m coming more and more to the realization that this is the new world order, so to speak.

These vaccines aren’t going away no matter how long or how bitterly we fight this in the courts.

It’s time to tell the system to go **** itself and start figuring out how to best take care of ourselves and our families outside of the system.

Our military leadership has no concern for our wellbeing and they have made it clear that they will punish those who can’t see things from their perspective.

I signed up to defend the Constitution and freedom and now my military leadership is intent on violating both. I’m no longer interested in serving my country in this capacity. It’s time to leave while I can still walk to the door.

*

Note to readers: Please click the share buttons above or below. Follow us on Instagram, @crg_globalresearch. Forward this article to your email lists. Crosspost on your blog site, internet forums. etc.

Featured image: Pfc. Shaniah Edwards, Medical Detachment, prepares to administer the Moderna COVID-19 vaccine to soldiers and airmen at the Joint Force Headquarters, February 12, 2021. (U.S. Army National Guard photo by Sgt. Leona C. Hendrickson – Source.)

CDC, FDA Prepare Mass Distribution of a Merck/Sanofi Six-in-One Vaccine for Kids, Turning Blind Eye to Safety Signals

Egregious oversteps endangering children’s lives.

All Global Research articles can be read in 51 languages by activating the “Translate Website” drop down menu on the top banner of our home page (Desktop version).

Visit and follow us on Instagram at @crg_globalresearch.

***

The FDA approved Vaxelis in late 2018, but only now is the shot being readied for widespread distribution — in Europe, where infants have been given six-in-one vaccines for years (including Vaxelis since 2016), the vaccines have been associated with reports of sudden infant death.

Since the mid-1980s, the number of childhood shots on the Centers for Disease Control and Prevention (CDC) vaccine schedule has more than quadrupled. When parents express reluctance about turning their little ones into perpetual pin cushions, drug makers and doctors have a ready answer — combination vaccines that “simplify” the schedule by decreasing the number of injections administered.

This month marks the U.S. launch of the Merck/Sanofi joint-venture vaccine, Vaxelis, a six-in-one (hexavalent) combination vaccine that contains diphtheria, tetanus and acellular pertussis (DTaP) components as well as components said to protect against polio, Haemophilus influenzae type b (Hib) and hepatitis B.

Public health officials optimistically believe that bundling all of these components into one shot will help close noncompliance loopholes and increase the likelihood that children will complete “all recommended vaccinations.”

Though Vaxelis is the nation’s first hexavalent injection, it joins other four- or five-in-one vaccines already on the CDC schedule. The U.S. Food and Drug Administration (FDA) approved Vaxelis in late 2018 — as a three-dose series for 2-, 4- and 6-month-old infants — but it is only now, two-and-a-half years later, that the shot is being readied for widespread distribution.

Warning signs were ignored

There are numerous warning signs that potent all-in-one vaccines are too much for immature immune systems to handle. Concerning safety signals have emerged not just for hexavalent but also pentavalent (five-in-one) vaccines.

In Europe, where infants have been given hexavalent vaccines for some years (including Vaxelis since 2016), the formulations have produced many troubling reports of sudden infant death.

Absurdly, none of the clinical studies assessing Vaxelis safety and efficacy conducted fair comparisons against an inert placebo. Instead, in the two U.S. clinical trials for Vaxelis, not only did investigators compare infants receiving Vaxelis to babies who received Sanofi’s five-in-one Pentacel — but babies in both groups also received rotavirus and pneumococcal vaccines at the same time!

In this context, the CDC’s sales pitch to the public — and its claims that side effects are “usually mild” — cannot be considered credible.

Here are some of the other facts missing from the CDC’s communications:

  • In the two U.S. trials six infants died (slide #27) in the Vaxelis group (some after receiving just one dose); one infant also died in the “control” group that received five-in-one vaccines.
  • All six Vaxelis recipients died within six weeks of vaccination. This timing matches other published accounts of infant deaths “clustering” following hexavalent vaccination.
  • The reported causes of death for the infants who received Vaxelis included asphyxia, sepsis, fluid in the brain and sudden infant death syndrome (SIDS). These outcomes correspond to the types of adverse events reported following hexavalent vaccination in Europe.
  • Package inserts for other vaccines on the CDC schedule list similar causes of death, suggesting these fatal Vaxelis outcomes are plausibly associated with vaccination.
  • In the clinical trials, the rate of fever was notably higher in Vaxelis recipients even when compared to children receiving five-in-one vaccines (47% vs. 34%).

Juicing vaccine sales

In the no-liability context enjoyed by vaccine makers in the U.S., combination vaccines are already quite popular. In fact, market watchers and health economists praise the jumbo shots as being a catalyst for positive industry trends and a “key to commercial success.”

 

Thus, financial analysts expect Vaxelis to “garner significant patient share following its [U.S.] launch” — predicting that it will account for almost a third of U.S. DTaP vaccinations by 2028 — or $841 million in annual sales.

These predictions represent good news for Merck and Sanofi, two of the “big four” pharma giants that dominate the childhood vaccine market in the United States. Merck is already doing a booming vaccine business, recently reporting annual sales growth of 14.8% for its pneumococcal vaccine (Pneumovax 23) and 5.4% for its human papillomavirus (HPV) vaccine Gardasil-9.

However, Merck also faces proliferating Gardasil-related lawsuits — including legal actions alleging that the company knew about and ignored life-changing adverse events from the get-go, many of which (when not fatal) have involved autoimmunity and chronic pain. In fact, before the advent of emergency use COVID vaccines (responsible for an alarming escalation of vaccine-related adverse events), Gardasil had had “more side effects reported than all other vaccines combined.”

Sanofi, too, is embroiled in thousands of lawsuits worldwide — notably for its disastrous and sometimes fatal dengue vaccine. As with Merck, this has not dampened overall vaccine sales growth, which continues its strong upward trajectory, likely to be further strengthened by the U.S. Vaxelis rollout.

Although Sanofi has not been a front-runner in the COVID vaccine race, the company is currently running clinical trials for messenger RNA (mRNA) vaccines for both COVID and seasonal influenza.

Aluminum secrecy and grandfathered ingredients

Merck’s proprietary, “super-powered” aluminum adjuvant — amorphous aluminum hydroxyphosphate sulfate (AAHS) — which is believed to play a significant role in Gardasil’s risk profile, is also present in Vaxelis.

After Merck developed AAHS, it began to “preferentially” feature AAHS in its vaccines even though, as Danish scientists outlined last year, the company appears to have disregarded procedures ordinarily required for approval of new adjuvants.

According to the Danes, at the time AAHS appeared, it represented a “new type of aluminium adjuvant with excipients that [had] not been used earlier in [European Medicines Agency] authorised vaccines.” It should have been — but apparently was not — tested against an inert placebo. For this and other reasons, the Danish scientists question the ethical underpinnings of the Gardasil clinical trials.

In noting that Merck also “seems to have prevented independent studies of AAHS,” the Danes repeated a critique aired by world-famous aluminum expert Christopher Exley in 2018. In an extensive discussion of different aluminum-based adjuvants and their immunological mechanisms of action, Exley and co-authors emphasized the importance of studying aluminum adjuvants one by one, as each is “chemically and biologically dissimilar with concomitantly potentially distinct roles in vaccine-related adverse events.”

Concerningly, the Vaxelis liquid suspension is adjuvanted onto not just AAHS, but also another aluminum adjuvant — aluminum phosphate). The package insert disingenuously shorthands the combination of adjuvants as “aluminum salts.”

How this double whammy of aluminum (319 micrograms per vaccine dose) interacts with the vaccine’s six antigens, or Vaxelis’s numerous other ingredients, or the heavy aluminum load in other childhood vaccines is largely unknown.

According to the Vaxelis package insert, the vaccine also includes: polysorbate 80 (an ingredient flagged for its propensity to induce hypersensitivity reactions); glutaraldehyde and formaldehyde (problematic chemicals deemed necessary to inactivate pertussis toxin); bovine serum albumin (often harvested from bovine fetuses when female cows are found to be pregnant at slaughter); three different antibiotics (neomycin, streptomycin and polymyxin B); ammonium thiocyanate (also a rust inhibitor, weedkiller and defoliant); and yeast protein (associated, notably in hepatitis B vaccines, with autoimmune reactions).

Regulatory loopholes allow manufacturers to “grandfather” ingredients into new vaccines if the components are already present in other licensed vaccines — regardless of how inadequate the original safety testing may have been.

Thus, Merck and Sanofi perceived no need to test Vaxelis for DNA-damaging or cancer-causing effects, and conducted no studies of the ingredients’ pharmokinetics (i.e., how the substances move “into, through, and out of the body”).

The main cautionary note sounded in the meager Vaxelis patient information sheet is to not give Vaxelis to children if they are “allergic to any of the ingredients.”

For thee and thee … but not for me?

The CDC seems to be particularly interested in ensuring that poor and non-white children get Vaxelis. The agency began laying the groundwork to offer Vaxelis through the Vaccines for Children (VFC) Program — the agency’s vaccine program for the poor — over two years ago, in March 2019.

In September of that year, the CDC followed up with an affirmative vote. Public health departments have been promoting Vaxelis to participating VFC providers since early June 2021.

At its September 2019 meeting, CDC outlined another topic deemed important for discussion in the near future — raising the issue of whether Vaxelis should be “preferentially recommended” for the American Indian/Alaskan Native (AI/AN) pediatric population.

The tenuous rationale, according to the meeting notes, was because, “in the pre-vaccine era” (more than 35 years ago), “Hib disease occurred at a younger age among the AI/AN population compared to the general population.”

Wave of the future?

Judging from its website, the CDC perceives combination vaccines to be the wave of the future, and has signaled its strong endorsement of Vaxelis by incorporating the new vaccine into its 2021 vaccine schedule.

As if exposure to six antigens were not enough, FDA and CDC also say it is okay for healthcare providers to administer the six-in-one shot at the same time as other vaccines.

These agencies’ characterization of the Vaxelis safety profile as “acceptable” indicates they have either not done their due diligence, or are willing to accept a high level of collateral damage in exchange for the “convenience” of six-in-one shots.

However, as the “overwhelmed by guilt” parents of COVID-vaccine-injured teens are increasingly finding out, convenience is poor consolation for life-changing or life-threatening adverse outcomes.

*

Note to readers: Please click the share buttons above or below. Follow us on Instagram, @crg_globalresearch. Forward this article to your email lists. Crosspost on your blog site, internet forums. etc.

Featured image is from CHD

Fact checking is extremely important. I want to reiterate not to take everything at face value; no matter what you read, where you read it from, or who you hear it from. And to be clear, do not rely on “fact checking” websites to give you accurate information either. These are just as likely, (if not even more likely…), to feed false information and false debunking accounts to manipulate the reader. Please take everything into consideration before adhering to a certain narrative – and always keep your mind open to other possibilities.

Fair use disclaimer: Some of the links from this article are provided from different sources/sites to give the reader extra information and cite the sources, but does not necessarily mean that I endorse the contents of the site itself. Additionally, I have tried to provide links to the contents that I used from other sites as an educational and/or entertainment means only; if you feel that any information deserves further citation or request to be clarified, please let me know through the contact page.

Get an Earful

Egregious Medical Tyranny Holds Patient Hostage in a Hospital and Refuses Her Preferred Medical Treatment – Patient DIES Under Their Protocol - Veronica Wolski was denied specific treatment - AND denied the freedom to leave the hospital.
More LIES and CONtradictions About COVID and the Vaccines | How Does Anyone Still Believe the Narrative? - We have been lied to numerous times by top officials. When will the rest of the world wake up?
W.H.O. / Governments Working in Collusion with Big Pharma? | A Necessary Look Back at the Swine Flu Pandemic - STEPPING BACK IN TIME: Another attempt to vaccinate the whole world.
Jerm Warfare Interview with Dr. Zelenko: “These “vaccines”, which I call ‘poison death shots’ “ - "The only reason you'd vaccinate your child is if you believe in child sacrifice."
Scandal Behind the FDA “Fake Approval” of Pfizer Jab - Corruption and collusions behind the Pfizer/FDA "vaccine" efforts.
Our Grave Concerns About the Handling of the COVID Pandemic by Governments of the Nations of the UK - Open letter from several healthcare professions to the UK government/administrators.