Pfizer’s “Vaccine” Causes Astonishing Drop in Male Fertility – Men Have Not Been Informed nor Given Their Consent

When the Covid-19 vaccine rollout to the public began in late 2020, medical professionals, public health agencies, and government spokespeople all assured the public that the novel mRNA “vaccines” did not cause negative systematic effects on human bodies. They promised the public, many of whom were sceptical about the safety of a drug brought to market at “warp speed,” that the vaccines were “safe and effective.”

Those who questioned or challenged the “safe and effective” assurances were dismissed as “anti-vaxxers” and accused of wanting to kill others, especially the elderly. Few medical and public health experts spoke out about the need for long-term studies.

This attack on challengers to public health’s all-out push, and the resulting censorship of the emerging problem, resulted in catastrophic harm to male fertility.

The following is extracted from the article ‘Pfizer, FDA, CDC Hid Proven Harms to Male Sperm Quality, Testes Function, from mRNA Vaccine Ingredients’ by Amy Kelly, Program Director for the War Room/DailyClout Pfizer Documents Analysis Project as well as the COO of DailyClout.  Find more by Amy Kelly HERE.

Pfizer’s own documents and other medical studies show:

  1. Pfizer did not test “male reproductive toxicity”. Male reproductive toxicity is defined as adverse effects (negative impacts) related to sexual function and fertility in an adult male.[2]
  2. Pfizer also did not test for adverse effects from vaccinated men’s semen, on the development of their offspring.[3]
  3. mRNA vaccine ingredients travel throughout the body and gather in organs, including in the testes.[4]
  4. mRNA vaccines resulting in “anti-sperm antibodies” – that is to say, antibodies that treat sperm as an “invader”, and damage or kill it – is a known adverse event related to this form of vaccination.[5]
  5. mRNA vaccines cause a staggering drop in semen concentration and total motile count.[6]
  6. By suppressing discussion of this information, public health agencies, medical professionals, and governments globally denied and continue to deny men true informed consent.

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National Guardsman with religious objection given COVID-19 vaccine instead of flu shot

Aformer National Guardsman who sought a religious exemption to the military COVID-19 vaccine mandate was given the mRNA shot instead of an inoculation for the flu “accidentally,” according to the service. 

After refusing the COVID vaccine multiple times and requesting a religious exemption to the mandate, former Maine National Guard Specialist Mathew Bouchard was given the mRNA shot instead of the flu vaccine months before he was to leave the service, he told Just the News on Thursday. 

Bouchard, who served in the military for six years, said he first filled out a COVID vaccine refusal form in April 2021, then again in November when he was ordered to get the flu shot, despite the fact that he was leaving the military two months later. 

When he went to get the flu vaccine, Bouchard filled out the refusal form for the COVID vaccine and then completed a form for the flu shot. 

There were two separate lines for vaccinations, one for COVID and the other for the flu, and there were two separate noncommissioned officers (NCOs) administering the vaccines. While Bouchard was in the flu shot line, the NCO in the COVID line said that anyone needing the flu vaccine could go to his line to get it. Bouchard asked the NCO if he should be doing this, and the NCO changed his mind, so Bouchard went back to the flu shot line. 

Both Bouchard and his attorney, R. Davis Younts, mentioned that it was unusual for the NCO in the COVID vaccine line to offer the flu shot because there are supposed to be different NCOs to give different vaccines. One NCO isn’t supposed to give two different vaccines. There are also not supposed to be two different vaccines at the same table. 

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Pfizer CEO pulls out of testifying to EU Parliament COVID panel

Pfizer Chief Executive Albert Bourla has pulled out of an appointment to testify before the European Parliament’s special committee on COVID-19, at which he was expected to face tough questions on how secretive vaccine deals were struck.

The decision follows an audit report into the EU’s vaccine procurement strategy published earlier in the month that raised new questions about contact between Bourla and European Commission President Ursula von der Leyen that preceded a multibillion-euro vaccine contract.

The head of the U.S. pharmaceutical giant, the largest supplier of COVID-19 vaccines to the EU, was scheduled to appear before the panel on October 10. The committee is meeting with key officials involved in the EU’s vaccine procurement process to draw lessons on how to respond to future pandemics. Other pharmaceutical executives have addressed the committee, including the CEO of Moderna and senior officials from AstraZeneca and Sanofi.

The committee’s chair, Belgian MEP Kathleen Van Brempt, told POLITICO she “deeply regrets” the decision taken by Pfizer.

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Genetically Modified Mosquitoes Vaccinate a Human

A box full of genetically modified mosquitoes successfully vaccinated a human against malaria in a trial funded by the National Institutes of Health (NIH).

The study involved about 200 hungry mosquitos biting a human subject’s arm. Human participants placed their arms directly over a small box full of the bloodsuckers.

“We use the mosquitoes like they’re 1,000 small flying syringes,” said researcher Dr. Sean Murphy, as reported by NPR.

Three to five “vaccinations” took place over 30-day intervals.

The mosquitoes gave minor versions of malaria that didn’t make people sick, but gave them antibodies. Efficacy from the antibodies lasted a few months.

“Half of the individuals in each vaccine group did not develop detectable P. falciparum infection, and a subset of these individuals was subjected to a second CHMI 6 months later and remained partially protected. These results support further development of genetically attenuated sporozoites as potential malaria vaccines,” researchers concluded.

Carolina Reid was one of twenty-six participants in the study.

“My whole forearm swelled and blistered. My family was laughing, asking like, ‘why are you subjecting yourself to this?’”

Reid enjoyed her experience so much that she says she wants to participate in as many vaccine trials as she can. For this research, each participant received $4,100 as an incentive.

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The Gates Foundation is Researching How to Manipulate You Into Taking ‘Future’ COVID Vaccines.

The Bill and Melinda Gates Foundation is now funding studies on how to best manipulate people to receive “future” COVID-19 vaccines – including “targeted” messaging and financial compensation – despite studies continuing to show links between the vaccine and myocarditis.

Researchers supported by the Gates Foundation published a study aimed at curbing vaccine hesitancy titled “Overcoming Vaccine Hesitancy for Future COVID-19 and HIV Vaccines: Lessons from Measles and HPV Vaccines.”

Released on August 11th, researchers carried out a “narrative review of studies on interventions to address measles and human papillomavirus vaccine hesitancy” to cross-apply the lessons learned towards future vaccines.

Researchers explicitly reference making people more likely to receive “future” COVID-19 vaccines as their primary goal, concluding that “the most successful interventions directly targeted the population for vaccination.”

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Good News for You Dumb People: YouTube Thought Police Think for You, Big Tech’s Bots Look After Your Best Interests

There’s an interesting moment in a recent YouTube video posted by Dr. John Campbell, a nurse educator who shares informational videos about the latest SARS-CoV-2 and other science on his educational channel. After reviewing government data, Campbell pauses for several seconds and scratches his head. A few beats later he mumbles an apology to the audience, confessing that his head felt a little itchy.

There was no hint from the deadpan tone that Campbell was doing anything other than scratching an itch. But, as some of his over 2.45 million loyal subscribers have boldly pointed out in the comment section, in recent videos Campbell seems darker than usual, almost depressed. Indeed, the nurse educator appears to be doing a lot of hand-wringing and head scratching lately.

It seems, however, that Campbell cannot openly share his concerns with his audience without putting his channel in jeopardy. In order to continue to post videos on YouTube, as he explored in that same head-scratching video, he must censor himself or risk being de-platformed.

YouTube Censors Vaccine Safety and Efficacy Information

YouTube has written guidelines against making videos that discuss vaccine safety, efficacy, and necessity.

This “vaccine misinformation policy” reads: “YouTube doesn’t allow content that poses a serious risk of egregious harm by spreading medical misinformation about currently administered vaccines that are approved and confirmed to be safe and effective by local health authorities and by the World Health Organization (WHO). This is limited to content that contradicts local health authorities’ or the WHO’s guidance on vaccine safety, efficacy, and ingredients.”

The policy applies to vaccine safety, vaccine efficacy, and even information about vaccine ingredients (pdf).

In fact, YouTube will actively delete any content that suggests that vaccines may cause chronic side effects, “outside of rare side effects that are recognized by health authorities.”

This includes YouTube videos posted by medical doctors, scientists, academic researchers, and even patients who have themselves suffered from side effects.

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‘Stunning’: The Real Reason Health Officials Won’t Let Independent Scientists Examine mRNA Vaccine Vials

A 14-minute video (below) that has been overlooked for nearly two years has now resurfaced, exposing stunning information about the COVID-19 jabs and why health officials don’t want individual vaccine vials examined by independent scientists.

The reason, it turns out, is because the vials are all different — and the mRNA in the shots “is not intact.” Both of these pose potentially serious problems.

In an Aug. 31 Substack article, Steve Kirsch explains:

“Even if you are getting 100% intact mRNA which would be really rare, you’re still not getting anything that resembles the virus. So the efficacy as far as PROTECTING you will be next to nothing.

“However, what it will do very effectively, if you got reasonably intact mRNA, is to cause you significant harm. You are playing a game of chance with your immune system and what is in the bottle.”

The video notes that members of the European Parliament were only allowed to read the contracts with the drug makers after they’d been heavily redacted. Why the heavy-handed secrecy, even toward legislators?

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Smoking gun? FDA refusing to provide key covid “vaccine” safety analyses, suggesting massive coverup

Government regulators at the U.S. Food and Drug Administration (FDA) say they will not release any of the agency’s Covid-19 “vaccine” safety analyses for independent review because their findings are allegedly part of internal discussions that are protected by law.

Back in July, The Epoch Times submitted a request to the FDA for all analyses performed using a special method called Empirical Bayesian data mining. This method involves comparing adverse events recorded after injection with a Fauci Flu shot to adverse events recorded after injection with some other non-covid vaccine.

Whatever data these analyses produced was used by the FDA to foist Chinese Virus shots on everyone, including infants and toddlers. (Related: Check out our earlier coverage about the FDA’s suspicious secrecy to learn more.)

The operational procedures laid out by the agency and its partner in January 2021 and February 2022 stipulate that the FDA is to perform data mining “at least biweekly,” if not more often than that, to identify adverse events “reported more frequently than expected following vaccination with COVID-19 vaccines.” That data was to come from the official Vaccine Adverse Event Reporting System (VAERS).

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CDC Director Admits Agency Gave False Information on COVID-19 Vaccine Safety Monitoring

The director of the Centers for Disease Control and Prevention (CDC) has acknowledged publicly for the first time that the agency gave false information about its COVID-19 vaccine safety monitoring.

Dr. Rochelle Walensky, the agency’s director, said in a letter made public on Sept. 12 that the CDC did not analyze certain types of adverse event reports at all in 2021, despite the agency previously saying it started in February 2021.

“CDC performed PRR analysis between March 25, 2022, through July 31, 2022,” Walensky said. “CDC also recently addressed a previous statement made to the Epoch Times to clarify PRR were not run between February 26, 2021, to September 30, 2021.”

Walensky’s agency had promised in several documents, starting in early 2021, to perform a type of analysis called Proportional Reporting Ratio (PRR) on reports submitted to the Vaccine Adverse Event Reporting System, which it helps manage.

But the agency said in June that it did not perform PRRs. It also said that performing them was “outside th[e] agency’s purview.”

Confronted with the contradiction, Dr. John Su, a CDC official, told The Epoch Times in July that the agency started performing PRRs in February 2021 and “continues to do so to date.”

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‘Unethical’ and up to 98 Times Worse Than the Disease: Top Scientists Publish Paradigm-Shifting Study About COVID-19 Vaccines

A team of nine experts from Harvard, Johns Hopkins, and other top universities has published paradigm-shifting research about the efficacy and safety of the COVID-19 vaccines and why mandating vaccines for college students is unethical.

This 50-page study, which was published on The Social Science Research Network at the end of August, analyzed CDC and industry-sponsored data on vaccine adverse events, and concluded that mandates for COVID-19 boosters for young people may cause 18 to 98 actual serious adverse events for each COVID-19 infection-related hospitalization theoretically prevented.

The paper is co-authored by Dr. Stefan Baral, an epidemiology professor at Johns Hopkins University; surgeon Martin Adel Makary, M.D., a professor at Johns Hopkins known for his books exposing medical malfeasance, including “Unaccountable: What Hospitals Won’t Tell You and How Transparency Can Revolutionize Heath Care”; and Dr. Vinayak Prasad, a hematologist-oncologist, who is a professor in the UCSF Department of Epidemiology and Biostatistics, as well as the author of over 350 academic and peer-reviewed articles.

But among this team of high-profile international experts who authored this paper, perhaps the most notable is Salmaan Keshavjee, M.D., Ph.D., current Director of the Harvard Medical School Center for Global Health Delivery, and professor of Global Health and Social Medicine at Harvard Medical School. Keshavjee has also worked extensively with Partners In Health, a Boston-based non-profit co-founded by the late Dr. Paul Farmer, on treating drug-resistant tuberculosis, according to his online biography.

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