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Objective:Health - Resistance Against Medical Tyranny

O:H header
In this episode of Objective:Health we highlight some of the resistance we've seen to the medical tyranny that has descended on us under the guise of a deadly pandemic. Whether in the form of lawsuits, class action suits, standing up to employers mandating vaccination for their employees, or just everyday citizens resisting mask mandates or quarantine measures, it's heartening to see individuals fighting back, standing their ground and generally resisting the infringement of their rights by an out-of-control authoritarian state.

While governments, corporations or employers in general may believe they have the right to dictate our right to free movement, forced medical procedures, right to employment or rights to free association, there are citizens who have had enough and are fighting back against the monolithic machine attempting to lock us in our homes to die a slow death.

As Benjamin Franklin said "Those who would give up essential liberty, to purchase a little temporary safety, deserve neither liberty nor safety." And while there are those attempting to force that choice on us, the ability to resist has yet to be completely extinguished. Join us on this episode as we look at some of the inspiring stories of ordinary people fighting back.


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Running Time: 00:35:57

Download: MP3 — 32.9 MB


Attention

Extent of brain abnormalities in American children revealed in groundbreaking study

brain child america
© fmajor/Getty Images
CT scan of a child's head.
Early results from a landmark research program designed to observe the brain development and health of American children have just been released, revealing a first glimpse at a dataset both invaluable and, in many ways, disquieting.

The Adolescent Brain Cognitive Development (ABCD) Study is the largest long-term study of its kind in the United States, involving almost 11,700 healthy children aged between nine and ten who are being studied at over 20 research sites across the country.

At the outset of the ABCD Study, this huge, demographically diverse cohort of children had their brains scanned by high-resolution structural magnetic resonance imaging (MRI) machines.

This was to provide a baseline measurement of their developing brains, which will be rescanned at two-year intervals for the duration of the 10-year longitudinal study - helping scientists to understand how the children's brain development might be linked to a huge range of factors, from sleep levels to sport, substance use, time spent playing video games, academic results, and much more.

Comment: See also:


Pills

Top Yale Doctor/Researcher: 'Ivermectin works,' including for long-haul COVID

doctor hospital
A Yale University professor and renowned cancer researcher has pored over the COVID-19 literature and treated several dozen patients. He can remain silent no longer.

Dr. Alessandro Santin, a practicing oncologist and scientist who runs a large laboratory at Yale, believes firmly that ivermectin could vastly cut suffering from COVID-19. Santin joins a growing group of doctors committed to using the safe, generic drug both as an early home treatment to prevent hospitalization and alongside inpatient treatments like steroids and oxygen.

"The bottom line is that ivermectin works. I've seen that in my patients as well as treating my own family in Italy," Santin said in an interview, referring to his father, 88, who recently suffered a serious bout of COVID. "We must find a way to administer it on a large scale to a lot of people."

Comment: See also:


Syringe

3,964 deaths - 162,610 injuries: European database of adverse drug reactions for covid-19 'vaccines'

EuroVigilance
The European database of suspected drug reaction reports, EudraVigilance, is now tracking reports of injuries and deaths following the experimental COVID-19 "vaccines."

Here is what EudraVigilance states about their database:
This website was launched by the European Medicines Agency in 2012 to provide public access to reports of suspected side effects (also known as suspected adverse drug reactions). These reports are submitted electronically to EudraVigilance by national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorisations (licences) for the medicines.

EudraVigilance is a system designed for collecting reports of suspected side effects. These reports are used for evaluating the benefits and risks of medicines during their development and monitoring their safety following their authorisation in the European Economic Area (EEA). EudraVigilance has been in use since December 2001.

This website was launched to comply with the EudraVigilance Access Policy, which was developed to improve public health by supporting the monitoring of the safety of medicines and to increase transparency for stakeholders, including the general public.

The Management Board of the European Medicines Agency first approved the EudraVigilance Access Policy in December 2010. A revision was adopted by the Board in December 2015 based on the 2010 pharmacovigilance legislation. The policy aims to provide stakeholders such as national medicines regulatory authorities in the EEA, the European Commission, healthcare professionals, patients and consumers, as well as the pharmaceutical industry and research organisations, with access to reports on suspected side effects.

Transparency is a key guiding principle of the Agency, and is pivotal to building trust and confidence in the regulatory process. By increasing transparency, the Agency is better able to address the growing need among stakeholders, including the general public, for access to information. (Source.)

Comment: See also:


Eye 1

'Digital Hate' Group CCDH awakens ire of the public in failed attempt to silence & cancel health freedom advocates

quote
After a globally coordinated campaign involving over 100 mainstream media outlets, 12 state attorney generals, and a Congressional hearing, to discredit, defame, vilify and otherwise de-platform a number of prominent health freedom advocates and whistleblowers, thousands of supporters have risen up to speak out against this failed attempt to divert attention from vaccine safety concerns, draconian government regulations, and the growing socio-economic and psychological harms the government's response to COVID has wrought upon millions of citizens.

Soon after two organizations calling themselves the "Center for Countering Digital Hate" and "Anti-Vax Watch" published a document titled, The Disinformation Dozen: Why Platforms Must Act on Twelve Leading Online Anti-Vaxxers on March 24th — which received international media amplification across at least 100 different news outlets — a tidal wave of social media responses inundated their posts on Instagram, Facebook, and Twitter, calling them out for their clearly hypocritical behavior in viciously attacking and defaming 12 prominent health freedom advocates and whistleblowers.

Briefcase

Masks are experimental medical devices that must be optional, according to law

mask medical mask
© Rattankun Thongbun/Getty Images
Just like the COVID vaccines, use of masks (instead of respirators) to block transmission of a virus was only authorized as experimental use. As such, according to law, it must be optional. If we are going to passively allow governors and governments to make this medical device mandatory, what is to stop them from making the vaccine mandatory?

As I've mentioned before, both the FDA and OSHA have made it clear over the years that only respirators, not masks, are considered valid PPE to block transmission of a respiratory virus. Which is why mask manufacturers must continue to place a disclaimer on their labels that the product does not work for airborne viruses. The CDC is lying to the public and giving them a false sense of security by suggesting masks are valid medical devices for COVID. That is why the FDA was forced to use an Emergency Use Authorization - the same process used for the vaccines - to approve masks as medical devices to be used as source control to reduce the spread of COVID on April 24, 2020.

Comment: See also:


Donut

Krispy Kreme will give you a free doughnut every day this year — if you've been vaccinated

krispy kreme donuts
In case you needed another reason to get your COVID-19 vaccination, Krispy Kreme is sweetening the deal — it's giving free doughnuts to anyone with proof of vaccination, all year long.

Starting Monday, any customer with a valid COVID-19 vaccination card will receive a free Original Glazed doughnut at participating locations nationwide. The iconic doughnut shop specifies that any guests who have received at least one of the two shots of the Moderna or Pfizer vaccine, or one shot of the Johnson & Johnson vaccine qualify for the promotion.

All you need to show is your vaccination card to redeem your doughnut — a vaccine sticker is not valid.

Comment: Did the irony that a company selling bottom-of-the-barrel processed garbage would be offering freebies to people undergoing an undoubtedly detrimental health procedure just get completely missed?

See also: Vaccine Marketing: U.S. businesses offering freebies to vax recipients despite ongoing reports about side effects


Donut

Vaccine Marketing: U.S. businesses offering freebies to vax recipients despite ongoing reports about side effects

donut
COVID-19 vaccines are still considered to be experimental and some recipients have experienced horrible side effects from taking it. This includes actor/lawyer/writer/comedian, Ben Stein. Some recipients have also died after taking it, leading many European countries to suspend certain versions.

So despite all the public service announcements and government pressure to take the shot, there are people who still don't want it - even health care workers.

Kroger isn't mandating COVID shots but is offering $100 to employees who take them. Some businesses are also offering other incentives to customers.

Comment: Back in 2014 the WHO engaged in a similar campaign to 'shape the public's behavior toward vaccination' Read more: WHO wants to market vaccines like soda & burgers
In October 2014, the WHO's Strategic Advisory Group of Experts (SAGE) published an extensive report on vaccine hesitancy, looking at different approaches to help shape the public's behavior toward vaccination.24 The report specifically explored marketing strategies employed by other organizations such as the International Food and Beverage Alliance (IFBA), which includes companies like Coca Cola Company, Pepsico and McDonalds...

According to newspaper columnist Lawrence Solomon, "The World Health Organization Working Group recommended that this fact-free, emotion-laden Coca-Cola style marketing strategy be urged on the international "pro-vaccination lobbies." He added, "Aided by this 'Keep It Simple, Stupid' strategy, WHO is hopeful that the marketing wizardry that works for the food and beverage giants will help the pro-vaccination movement overcome the public's reluctance to vaccinate."24



Arrow Down

Common cold suppresses covid-19 infection

cold sneeze


There follows a guest post by Lockdown Sceptics' regular Guy de la Bédoyère.


Just when you thought the Covid madness couldn't take any more twists, here comes another one but you'd better brace yourself. The BBC's Science Correspondent James Gallagher has a startling revelation that the common cold (the rhinovirus) can suppress COVID-19 because it's so tough the SARS-CoV-2 virus gets pushed out of the way to make room for it. The news comes from the Journal of Infectious Diseases.

Here's the summary:
Human rhinovirus triggers an innate immune response that blocks SARS-CoV-2 replication within the human respiratory epithelium. Given the high prevalence of human rhinovirus, this interference effect might cause a population-wide reduction in the number of new COVID-19 infections.

From a host's perspective, HRV [Human Rhinovirus] infections, which are usually associated with mild disease, stimulate an antiviral response that prevents infections by more severe (and sometimes lethal) viruses such as SARS-CoV-2.

Comment: See also:


Syringe

AstraZeneca cherry-picked data, misrepresented vaccine's efficacy, independent medical board alleges

vaccine jab astrazeneca
© Daniel Leal-Olivas/AFP via Getty Images
A health worker administers a dose of the AstraZeneca vaccine at a coronavirus vaccination location in London on Tuesday.
An independent panel of medical experts overseeing AstraZeneca's coronavirus vaccine trial accused the pharmaceutical company of cherry-picking favorable data, The New York Times reported.

The Data and Safety Monitoring Board (DSMB) alleged that AstraZeneca misrepresented the results of its coronavirus vaccine trial when it announced Monday morning that the vaccine had 79% efficacy at preventing symptomatic coronavirus, according to the NYT. The panel wrote a sharply-worded letter to the British pharmaceutical company and U.S. health officials hours after the results were released, triggering the National Institute of Allergy and Infectious Diseases (NIAID) to issue a statement expressing concern.

The DSMB's letter said AstraZeneca calculated its efficacy rate based on data that was "most favorable for the study as opposed to the most recent and most complete," the NYT reported.

Comment: While the above is undoubtedly true, its interesting that AstraZeneca is getting all the press for its problems, while the big players like Pfizer and Moderna are seemingly getting a pass (despite problems). Could it be that there's a subtle push toward the mRNA vaccines by making the non-mRNA ones look bad?

See also: