Coronavirus

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Sal the Agorist @SallyMayweather

Myocarditis cases in USA, Ages 12-20:

2019: 16

2020: 9

2021: 2,301

July 3rd 2022
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https://trib247.com/articles/jab-vic...ign=Newsletter

Jab victim Steve Wenger wins congressional support for rights; Doctors afraid

by: WorldTribune.com 07/12/2022 Source: WorldTribune.com

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Steve Wenger

Overcoming debilitating injuries from an adverse reaction after receiving a Covid-19 vaccine, Steve Wenger has become a powerful advocate for vaccine victims’ rights.

On May 18, 2021, Wenger received the Johnson & Johnson vaccine. Less than a month later, he entered the emergency room crawling on his hands and knees. He stayed there three and half months. For two of those months, he became a quadriplegic, ultimately diagnosed with chronic inflammatory demyelinating polyneuropathy (CIDP), a severe form of Guillain-Barré syndrome attributed to the vaccine.

After leaving the hospital, “I had to relearn to walk I had to relearn to dress myself. I had to relearn to do everything that you do in your daily life," Wenger recalls. "It was a long brutal road.”

Shortly after leaving the hospital, Wenger became an advocate for those injured by Covid vaccines.

A face-to-face meeting with his member of Congress, Arizona Republican Rep. Debbie Lesko, led to a number of initiatives including a letter signed by eleven Republican congressmen calling for reforms in the Vaccine Injury Compensation Program (VICP) to include Covid-19 vaccines.
He is working to build a bipartisan coalition to address their needs. He directs those injured by Covid-19 vaccines to React19.org.


The Countermeasure Injury Compensation Program CICP is designed to assist those injured by vaccines not yet recognized by the VICP, according to Wenger. However, the program has been highly unresponsive, Wenger describes, in which cases are determined by bureaucratic functionaries and victims are not allowed legal representation.

“They have paid like eight actual claims over the course of twenty years, out of 7,000,” Wenger says. “All these other claims have been denied. Now all of the sudden, the CICP is getting hit with hundreds of thousands of requests for these Covid vaccines.”

“My mission had become to get those Covid Vaccines moved over the the VICP, which is the Vaccine Injury Compensation Program,” where “your issue actually goes before a judge and you can have a legal team to plead your case,” Wenger says. “And to get myself and everybody who has been affected by this the financial help they need.”

Another part of the problem, is fear among doctors to officially certify Covid vaccine injuries.

“My team of neurologists at Mayo Clinic was phenomenal. Those guys were straight up with me. They would say to my face, ‘What you are dealing with was definitely caused by the vaccine.” No question about it. Definitely caused by the vaccine — timeline, [inaudible], everything just tied back to my vaccine date,” Wenger recounts.

“Would they put that in writing and put their name on it?” Wenger continues, “Absolutely not.”

The result, in his experience, is that news stories on vaccine injuries simply don’t get published, because doctors are afraid to state publicly what they know and share in private. A result is that the public isn’t informed or aware of the risks.

As is typical for severely injured Covid vaccine victims, the financial effects also were devastating. Wenger's medical bills and sudden inability to work wiped out the family savings.

It has been “a financial wrecking ball,” Wenger says. “Our savings is gone. A year ago at this time, I had a ton of money in a bank account—an emergency fund. . . Thank God we had that, but that emergency fund is gone.”

Previously debt free except for mortgage and car payments, Wenger now describes tens of thousands of dollars in credit card debt and medical expenses owed.

Unable to afford the mortgage on their home, the Wenger’s uprooted and moved out of state, where his wife received a higher paying job as the sole earner.

Wenger counts himself lucky.

“I talk to a lot of vaccine injured and while what I went through was a horrific, miserable, nightmarish experience, I credit myself as being lucky, because I had a clear-cut diagnosis.”
For Wenger, the urgency of his work is a consequence of the enormity of the plight: "If you look at the VAERS data (Vaccine Adverse Event Reporting System) for the last twenty years — every adverse event reporting for all those vaccines," Wenger observes, "add them all together and take that number — there were more reports of Covid vaccine adverse events reported in 2021 than every other vaccine for twenty prior years total."

As with every Covid-19 vaccine victim interviewed by Broken Truth, Wenger’s injuries were anticipated by the CDC and FDA back in October 2020, well before release to the public. Guillain-Barré syndrome and CIDP figure prominently in a recovered slide from a presentation by Dr. Tom Shimabukuro, MD, the CDC’s Deputy Director of the Immunization Safety Office.

Screen shots from the FDA’s 161st meeting of the Vaccines and Related Biological Products Advisory Committee, Oct. 22, 2020:

Dr. Tom Shimabukuro, Deputy Director of the Immunization Safety Office, CDC:

Three embedded FDA videos

plus one embedded video that is also viewable on YouTube posted here.

https://www.youtube.com/watch?v=LhFN...e=emb_imp_woyt

20:49 video runtime

https://www.youtube.com/watch?v=LhFN...e=emb_imp_woyt

Adverse reaction to Covid-19 vaccination
Chevydmax04

My journey after receiving the J&J Covid-19 vaccine.

I see that the Whitehouse is still pushing these killer jabs and cannot articulate any rationale that sounds rational. They are pushing now the second booster that does not address BA 5 subvariant of the omicron variant. All the doctors I have listened to say "For people that already got the basic 2 jabs of the main killer jab, whatever you do, 'DON'T get a booster or another booster.' That is the way you can keep from harming yourself further. Notice they are especially pushing getting the second booster now to elder people and teenagers who are immunocompromised. I guess the reason the White House Doc is recommending this is because those people are most likely to be killed or injured by getting the second booster. That sounds like what they would consider to be right thinking.

Then when Fall flu season comes around, they are going to be pushing a brand new "vaccine" that does addresss BA 5 but no telling how many new variants and subvariants they will identify in the Fall.
So expect more gobbledygook advice from the White House in the coming months.

________________________

https://www.beckershospitalreview.co...812G5550689I0J


White House outlines strategy to combat BA.5: 3 COVID-19 updates

Erica Carbajal - 22 hours ago

Officials in President Joe Biden's administration are considering plans to make second COVID-19 boosters available to all adults as part of the White House's larger strategy to combat a rise in cases and hospitalizations driven by the BA.5 omicron subvariant.
Second boosters would become available to all adults pending sign-off from the FDA and CDC, according to several administration officials who spoke on the condition of anonymity, The Washington Post reported July 11. Second boosters are currently available only to people aged 50 and older and those 12 and older who are immunocompromised.
"I know that the FDA is considering this and looking at it ... and I know CDC scientists are thinking about this and looking at the data as well," Ashish Jha, MD, White House COVID-19 response coordinator, said during a July 12 media briefing.
In the mean time, health officials urged people to get their initial booster dose, available to those aged 5 and older, if they have not done so yet.
"If you haven't, don't delay. Do it now," Dr. Jha said, adding that getting a booster now will not prevent people from getting an omicron-specific vaccine in the fall or winter, when they're expected to become available.
Dr. Jha urged those 50 and older to stay up to date with vaccines and get their second booster. "If you have not gotten a vaccine shot in the year 2022 ... please go get another vaccine shot ... it could save your life," he said. CDC director Rochelle Walensky, MD, referenced data underlining the value of a second booster among those 50 and older.
"Those vaccinated with a primary series and only one booster dose ... had four times the risk of dying from COVID-19 compared to those who had a primary series and two or more booster doses," Dr. Walensky said. CDC data shows just 28 percent of people 50 and older have gotten their second booster.
COVID-19 hospitalizations in the U.S. have risen 18 percent over the past two weeks, with a daily average of 37,766 people hospitalized as of July 11. This marks the highest national average for hospitalizations since March and comes as the highly transmissible BA.5 variant accounts for 65 percent of cases, according to the CDC's latest variant proportion update.
"The key feature of BA.5, that we know about, is its immune evasiveness — you can be fully vaccinated and boosted and still have a risk of breakthrough infection," Dr. Jha told The New York Times July 11. "You can be previously infected — even as recent as the last couple of months — and have a very high rate of reinfection." CDC data shows just 28 percent of people 50 and older have gotten their second booster.
Two more updates:
1. The White House released a fact sheet on its strategy to manage BA.5 July 12. Aside from pending plans to expand eligibility for second boosters — which was not explicitly mentioned in the fact sheet — the strategy is similar to plans to combat earlier strains. The White House said it plans to work with stakeholders to drive additional booster and vaccine uptake; increase access and awareness of treatments like Paxlovid; and make free tests and masks widely available.
2. Experts are keeping a close eye on BA.2.75, the latest omicron relative gaining traction in India. In the U.S., three cases have recently been identified on the West Coast. Experts have expressed concern the subvariant could be even more transmissible than BA.5, since it appears to have a large number of mutations that could make it even more adept at evading immune protection. It's still too early to draw hard conclusions about the strain, experts say, adding that information will become clearer over the coming weeks.

Important show. I think is airing live right now but url below will work for replays too.

https://live.childrenshealthdefense....dr-paul-thomas

‘Against The Wind’ Episode 42: FDA + CDC Abandon Science to Get Products Across the Line With Toby Rogers, Ph.D.

‘Against The Wind’ With Dr. Paul Thomas

Science and medicine are at a crossroad and courageous health practitioners are standing up to ensure that humanity and integrity aren’t left behind in the name of “progress.” Dr. Paul Thomas is one of those leading the way and amplifying the voice of brave scientists and health care practitioners who are willing to put their careers on the line to make sure “health” and “care” are restored to healthcare.

*The opinions expressed by the hosts and guests in this show are not necessarily the views of Children's Health Defense

Dachsie comment:

Clear simple explanations of what they are doing and why and how this has been planned for a very long time.
Basically the whole Plandemic and unVirus is a tool to be used to install a totalitarian communistic One World Death and Slavery System for All.

Show host is traveling on the job and there is poor quality video in about the first 20 minutes.

About 1:30:00 video runtime
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https://www.theepochtimes.com/the-un...ent=07-13-2022

https://ecp.yusercontent.com/mail?ur...L78jyvaPHw--~D

July 13, 2022 CrossroadsViews

The ‘Universal Vaccine’ Agenda for Annual Vaccinations and an Endless Pandemic

Crossroads

JOSHUA PHILIPP

Pfizer is developing a “universal vaccine,” which can modify the new mRNA vaccines to fight against new viruses as they emerge. The new type of vaccine isn’t just being developed by Pfizer either, and officials including Dr. Anthony Fauci have touted the vision of the vaccines as being an end-goal of dealing with COVID-19.

The agenda behind universal vaccines goes far beyond COVID-19, however, with Fauci discussing the idea going back as far as 2009. And Pfizer, meanwhile, has also pushed for a similar agenda under the banner of an annual vaccine.

In this live Q&A with Crossroads host Joshua Philipp, we’ll discuss these stories and others, and answer questions from the audience.

Subscribe to the new Crossroads newsletter and stay up-to-date!

* Click the “Save” button below the video to access it later on “My List“.

*Sponsor Special: Up to $2,500 of free silver with American Hartford Gold. Call 877-260-2764, text “JOSHUA” to 6-5-5-3-2, or visit: https://ept.ms/3rshean

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Dachsie comment:

Another attack. They aren't backing down and neither should we.

This is the most clear article I have read about Novavax. See original for full hyperlinks.

Roll the dice -- Anaphylaxis or Autoimmunity.

__________________



https://childrenshealthdefense.org/d...a-6e22549bfb1f


07/13/22
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FDA Authorizes ‘Traditional’ Novavax COVID Vaccine, But Critics Question Safety Claims

The U.S. Food and Drug Administration (FDA) today granted Emergency Use Authorization to the Novavax COVID-19 vaccine. Portrayed as a more “traditional” vaccine that could sway the unvaxxed, some experts said it’s not as “safe” as FDA claims.

By
Julie Comber, Ph.D.

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The U.S. Food and Drug Administration (FDA) today granted Emergency Use Authorization (EUA) for the Novavax COVID-19 vaccine for adults 18 and over.

The EUA is for the two-dose primary series targeting the original Wuhan SARS-CoV-2 virus, limiting the vaccine’s use, as about two-thirds of Americans already have completed a primary series of either the Pfizer, Moderna or Johnson & Johnson vaccines.

The Centers for Disease Control and Prevention (CDC) still needs to sign off on Novavax’s vaccine before pharmacies and other healthcare providers can start administering shots.

The vaccine maker’s stock rose 3% earlier today, after Politico reported yesterday that the FDA would likely announce the decision today.

The Biden administration on Monday announced a deal with Novavax to purchase 3.2 million doses of the vaccine.

Under the taxpayer-funded deal — which the U.S. Department of Health and Human Services said was contingent on the vaccine receiving EUA and formal recommendation by the Centers for Disease Control and Prevention — the U.S. government will provide the vaccine to states, jurisdictions, federal pharmacy partners and federally qualified health centers.

Advisors to the FDA last month recommended the agency accept Novavax’s EUA application, but the agency delayed issuing the authorization pending FDA review of the Maryland-based company’s manufacturing process.

Novavax already is available in other countries, including Canada and Australia, under the name Nuvaxovid.

The Novavax vaccine relies on a protein-based technology used for decades, leading some media outlets to portray it as a “traditional” vaccine compared with other COVID-19 vaccines that use newer technologies.

Politico reported last month that FDA committee members expressed interest in making available a vaccine that uses a different technology than the mRNA vaccines widely used in the U.S., “in hopes of convincing unvaccinated holdouts to change their minds.”

According to Politico, Novavax “may appeal to the sliver of the population allergic to components of the messenger RNA vaccines developed by Pfizer-BioNTech and Moderna, or who are skeptical of those shots’ newer technology.”

But according to Dr. Meryl Nass, an internist with a special interest in vaccine-induced illnesses, chronic fatigue syndrome and toxicology, the media’s portrayal of Novavax as a more traditional vaccine is not accurate.

Nass, a member of the Children’s Health Defense (CHD) scientific advisory committee, pointed out that the Novavax shot contains a novel adjuvant, Matrix-M, “so it is not really an old-fashioned shot.”

Nass raised safety concerns specific to the adjuvant, while others voiced concerns about Novavax being linked to heart inflammation and blood clots, and the fact that the vaccine was designed for use against the original Wuhan strain of SARS-CoV-2 — not the various Omicron variants that are dominant today.

How does Novavax differ from other COVID vaccines used in U.S.?

Novavax is a subunit protein vaccine. It uses the spike protein, which it delivers directly to the host cell, from the viral coat of the SARS-CoV-2 virus, as the antigen — the part of the vaccine that provokes an immune response.

The mRNA-based shots — Pfizer and Moderna — use a lipid nanoparticle to encapsulate the mRNA and usher it into the host cell. Then the host cell’s own machinery produces the spike protein.

“Unlike mRNA vaccines, the spike protein is already premade in the Novavax vaccine, said Dr. Diana Florescu, who led the Novavax clinical trial. “It’s a shortcut. All the synthesis happens outside the body and we just give the end product: the spike protein.”

Johnson & Johnson’s Janssen COVID-19 shot is a viral vector vaccine. It also causes cells to produce the spike protein, but in a different way than the mRNA shots. It uses a virus called adenovirus, familiar as a common cause of respiratory infections.

The DNA in the adenovirus is modified so that when it enters the host cell, it causes the cell’s own machinery to produce the spike protein.

The adenovirus is also modified so it cannot replicate itself, which is why it is called a replication-defective recombinant adenoviral vector vaccine.

Adjuvant used in Novavax linked to autoimmune disease

Because Novavax is a protein subunit vaccine, it uses just the spike protein as the antigen rather than the whole pathogen (an inactivated or attenuated virus). Using the whole pathogen would expose the host to the virus’ entire protein coat instead of just one protein.

Protein subunit vaccines are often less immunogenic (less likely to provoke the immune system) than vaccines that use whole pathogens as the antigen, and may not generate a strong enough immune response.

That’s why they require the use of an adjuvant — in this case, Matrix-M — in addition to the antigen to get a stronger immune response.

However, few adjuvants are both potent and non-toxic enough for clinical use.

The proposed primary series for Novavax is two intramuscular injections 21 days apart at the dose level of 5 µg of the recombinant spike protein and 50 µg of the Matrix-M adjuvant.

Matrix-M, originally called QS-21, was one of the saponins derived from Quillaja saponaria, which is the soap bark tree native to Chile.

Some reports point out that the Matrix-M adjuvant — unlike the polyethylene glycol (PEG) lipid used in mRNA vaccines — is not linked to anaphylaxis (a severe allergic reaction), making it more attractive to people who are allergic to PEG.

But according to Nass, while it’s true that Matrix-M — which is not found in any other vaccines in the U.S. — isn’t linked to anaphylaxis, it is linked to autoimmune diseases.

“While touted as a replacement for the PEG lipid found in the mRNA vaccine, Matrix-M is less likely to cause anaphylaxis but more likely to cause autoimmune diseases,” Nass said.

Nass voiced other safety concerns about Novavax technology, including the use of moth cells.

According to the University of Nebraska Medical Center, where Novavax Phase 3 clinical trials were conducted, the Novavax vaccine uses moth cells to create a nanotechnology version of the COVID-19 spike protein.

Nass said insect cells can be used to grow proteins rapidly. “There is one flu vaccine made the same way: Flublok,” Nass said. Flublok is one of two egg-free flu vaccines licensed for use in the U.S.

“How many insect and viral proteins or other molecules are being injected into you when you get the Novavax vaccine — which is a function of how purified the vaccine is — is unknown,” Nass said.

Novavax still uses the spike protein

The SARS-CoV-2 virus encodes 29 proteins, but Novavax — like Pfizer, Moderna and Johnson & Johnson — chose to target only the spike protein.

As previously reported in The Defender, it is not known if the spike protein itself is safe.

“We have known for a long time that the spike protein is a pathogenic protein,” said Byram Bridle, Ph.D., assistant professor of immunology at the University of Guelph, Ontario. “It is a toxin. It can cause damage to our body if it gets into circulation.”

According to Brian Hooker, Ph.D., CHD’s chief scientific officer, “If you wanted to pick the most toxic protein, you know what represents the highest virulence, the highest amount of damage on the COVID-19 virus? You would pick the spike protein.”

The spike protein “has been consistently shown to create clotting issues in the blood,” Hooker said.

Novavax downplays link to heart issues

According to the briefing document for the Vaccines and Related Biological Products Advisory Committee meeting on June 7, severe local adverse events occurred in 1.2 to 7.2% of Novavax recipients, and systemic adverse events occurred in 2.4% to 12.1% of Novavax recipients.

These adverse events were more frequent after the second dose than after the first dose.

As previously reported in The Defender, there are concerns that Novavax is associated with myocarditis and pericarditis, just like the mRNA vaccines.

Reuters reported that the FDA asked Novavax to “flag” myocarditis and pericarditis as an “important identified risk” in its materials accompanying the vaccine. It is not known if the vaccine maker agreed to do so.

Novavax denied the connection between its vaccine and the reported cases of heart inflammation, claiming that “natural background events” of myocarditis can be expected in any large database.

“Based on our interpretation of all the clinical data supporting NVX-CoV2373 [Novavax]… we believe there is insufficient evidence to establish a causal relationship,” Novavax stated.

Does it work against the Omicron variant?

Like the other COVID-19 vaccines available in the U.S., Novavax’s vaccine was developed against the ancestral Wuhan strain of SARS-CoV-2.

In the FDA’s June 7 briefing document on the vaccine’s efficacy and safety, the FDA stated:

“The study enrollment and efficacy follow-up occurred during December 27, 2020, to September 27, 2021, and mainly when the Alpha variant of SARS-CoV-2 was predominant and prior to the emergence of Delta and Omicron variants.

“Relevant data to assess effectiveness of NVX-CoV2373 [Novavax] against the Omicron variant and sublineages, including observational data from use in other countries where the vaccine has been deployed, are currently unavailable; however, based on the efficacy estimate in the clinical trial of this vaccine, it is more likely than not that the vaccine will provide some meaningful level of protection against COVID-19 due to Omicron, in particular against more severe disease.”

The FDA briefing document also stated that due to the limited length of follow-up, “it is not currently possible to assess sustained efficacy over a period longer than 2 months.”

Bruce Gellin, chief of global public health strategy at the Rockefeller Foundation, was the lone abstaining vote on the FDA committee that voted to recommend Novavax on June 7.

Gellin said he abstained because the committee wasn’t given data on how the vaccine performs against the current Omicron variants, or for how many months its protection lasts.

Will Novavax convince the unvaxxed?

CNET last month reported that more than two years into the pandemic, a majority of Americans (about 67%) are fully vaccinated against COVID-19, and many have been boosted.

A Kaiser Family Foundation poll found 75% of adult Americans self-report that they are already vaccinated.

Meanwhile, those hesitant or opposed to COVID-19 vaccination seem to be firm and consistent in their opinion, according to the Kaiser poll.

Kaiser has tracked the “public’s attitudes and experiences with COVID-19 vaccinations” since December 2020. During that time, the percentage of American adults who answered the poll and said they would “definitely not” get vaccinated ranged from 12% to 17%.

In April, the most recent month reported, 17% of those polled said they would “definitely not” get vaccinated against COVID-19.

Millions of Americans have already been infected with COVID-19 and recovered. As of February 2022, the overall seroprevalence rate (indicating previous COVID-19 infection) in the U.S., determined by random antibody testing, was 57%.

____



Julie Comber, Ph.D.

Julie Comber is a freelance science reporter for The Defender.

Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. CHD is planning many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured. Your support is essential to CHD’s successful mission.

https://stevekirsch.substack.com/p/s...m_medium=email

Should you get the Novavax vaccine?

Absolutely not! Here are my top 5 reasons why you shouldn't.

Steve Kirsch

5 hr ago July, 14, 2022

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The FDA just approved the Novavax vaccine for COVID under EUA. It won’t be available until the CDC outside committee approves it. The CDC's Advisory Committee on Immunization Practices is scheduled to meet July 19.

I have nothing personally against Novavax. It might turn out to be the safest COVID vaccine to date. But “safest” and “safe” are two different animals: one is relative and the other is absolute.

Here are my top 5 reasons to say “No” to Novavax:

COVID is a disease which is easily treatable. Why would you take a risk on a new product with unknown risks when you don’t need to?

As Andrew Wakefield and others point out, we’ve never had a vaccine where the benefits > outweigh the risk. While this might be the first one, you’ll want to wait for an independent study that proves it.

They have to come clean and admit their issues before we can ever trust them again.

You run the risk of original antigenic sin (OAS) and/or antibody dependent enhancement (ADE). In short, you run the risk of making yourself worse off.

We just don’t know. We don’t know anything about their adjuvant — Matrix M. We don’t know anything about safety. We don’t know if they can manufacture it properly (they are now on their third contract manufacturer).

For further reading, see these 3 excellent articles, all from Substack authors:
Empowered!
Novavax - hope or hype?
I have had more requests to write an article about the Novavax COVID-19 vaccine than about any other topic during the entire manufactured crisis of the past two years. I’ve been holding back until I felt I had enough information to make it worth your while to read. I’ll be adding to this article as more data come in, so check back in on it from time to …
Read more
3 months ago · 41 likes · 46 comments · Robyn Chuter
uTobian
Some thoughts on the FDA's briefing document for the Novavax EUA application
[Updated June 7, 2022. I’ve re-written the section on the cross-over period. My hunch was correct — it essentially wipes out the control group after 49 days. But they did *not* cross over to Moderna and Pfizer, they crossed over to the opposite of whatever they had in the pre-crossover period — placebo or Novavax. It’s a very strange study design that …
Read more
a month ago · 178 likes · 87 comments · Toby Rogers
uTobian
No evidence of effectiveness against Omicron, definitely causes myocarditis, Sounds great! says the FDA's "expert advisory committee"
I. Welcome to the clown show Let’s talk about yesterday’s meeting of the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC): They had ten permanent voting members and TWELVE ringers (aka Temporary Voting Members). The cartel does not leave anything to chance…
Read more
a month ago · 210 likes · 83 com

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Dachsie comment:

"You can’t trust the FDA, CDC, or drug companies. "
Yes, we know and they know the trust is gone and the only way that medicine, healthcare, public health policies and biological and medical science can work is in a free country where it is possible for trust to operate as it should.

We know they know they can lie and have lied increasingly about everything from the beginning including whether there ever was a pandemic and the exact nature of the alleged pandemic disease. Instead of fixing real errors and problems, they just change the definitions, quietly on the sly.

The command-coerce-compliance model is the only game they have left and death and destruction is the only outcome of that model.

Thanks to and many prayers for Dr. Toby Rogers and all the brave scientists and doctors and healthcare providers and truth seekers and spreaders.
Discipline is the price of freedom and the One Who is Truth is the only Way.

BIDEN ADMIN THREATENS PHARMACIES

The Biden administration sent a memo late Wednesday to over 60,000 pharmacies across the country warning them that they are legally obligated under federal law to fill orders for contraceptives and abortion-causing drugs regardless of patients' pregnancy status. “Under federal civil rights law, pregnancy discrimination includes discrimination based on current pregnancy, past pregnancy, potential or intended pregnancy, and medical conditions related to pregnancy or childbirth,” reads the memo.
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Dachsie comment:

The "Biden administration" has no business telling what prescriptions for medicines pharmacies should fill or not fill.

Doctors should be able to prescribe medicines that they think are best for their patient's health, of course observing proper regulations. and expect the prescriptions to be filled.

Ivermectiin and hydroxycloroquine are safe and effective medicines and pharmacies should fill these properly prescribed medicines by doctors, and these medicines actually have something to do with health not harm.

https://trib247.com/ar
A new documentary, "Infertility: A Diabolical Agenda", details how the World Health Organization (WHO) intends to produce an anti-fertility vaccine in response to perceived overpopulation, and that such vaccines have been used — without people’s knowledge or consent — since the mid-1990s.

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Documentary exposes plan by WHO to reduce global population via vaccines
by: WorldTribune.com 07/13/2022 Source: WorldTribune.com


The documentary, produced by Dr. Andrew Wakefield and Children’s Health Defense, "illustrates the depopulation agenda is not a conspiracy theory. It’s reality, and it’s happening worldwide," Dr. Joseph Mercola noted in a July 11 report on the documentary for The Defender.

"The human papillomavirus (HPV) vaccine and the COVID-19 shots also have adverse impacts on fertility that are being ignored," Mercola noted.

The WHO "has been caught more than once deliberately deceiving women into thinking they were vaccinated against tetanus, when in fact they were being sterilized. This is an ethical and moral low that is hard to beat," Mercola added.

Wakefield, in an interview with The Defender, said the documentary presents a “very important story, and it’s a story that I’d been aware of for some years. I think a lot of people heard about this intentional infertility vaccine program being conducted, primarily in women in developing countries. But it had gone into abeyance so I hadn’t paid due attention. I should have paid more attention to it, because people had asked me over the years, ‘Do you think there is a population control agenda?’ …

“The allegation had been that the World Health Organization, under the guise of a neonatal tetanus prevention program, had been deliberately sterilizing women [in Kenya] — either using a vaccine to abort existing pregnancies or to prevent future pregnancies. They had done this under the guise of protecting children rather than actually reducing the population.”

Wakefield said it is no secret that the WHO had been working on an anti-fertility vaccine since the 1970s.

Papers were published, and the WHO itself even admitted it.

"The real issue here is that of informed consent," Mercola wrote.

The documentary details how, in 1995, the Kenyan government launched a WHO vaccination campaign against tetanus among women of childbearing age.

Dr. Stephen K. Karanja, former chairman of the Kenya Catholic Doctors Association, became suspicious of the program when he learned that involuntary sterilization programs posing as tetanus programs had occurred.

Also in 1995, the Catholic Women’s League of the Philippines won a court order halting a UNICEF tetanus program that was using tetanus vaccine laced with hCG. Anti-hCG-laced vaccines had also been found in at least four other countries.

"This anti-hCG-laced tetanus vaccine perfectly matched the anti-fertility vaccine the WHO had announced in 1993," Mercola noted.

The paper trail reveals that by 1976, WHO researchers had successfully conjugated, meaning combined or attached, human chorionic gonadotropin (hCG) onto tetanus toxoid, used in the tetanus vaccine. As a result, when given to a woman, she develops antibodies against both tetanus and hCG.

HCG is a hormone that is produced as soon as the sperm enters the egg and the embryo begins to form. In response to this signal, the woman’s ovaries then produce progesterone, which maintains the pregnancy to term. The conjugated vaccine effectively ends and prevents pregnancy as her own immune system will immediately attack and destroy the hCG as soon as it forms.

The WHO abandoned the 1995 campaign without explaining why. But, in 2014, "they were back with a neonatal tetanus program," Mercola wrote. "Girls and women, 15 to 49 years of age, were instructed to get vaccinated with a series of five injections, six months apart. Suspiciously, this is the exact schedule required for the anti-fertility vaccine to produce sterility. Regular tetanus prevention requires only one injection every five to 10 years, and under no circumstance would you need five of them."

The Catholic Church collected three sample vials directly from clinics during the 2014 campaign and had them tested by three independent laboratories. As feared, they contained hCG. Another six vials were then collected and tested. This time, half were found to contain hCG.

When the Catholic Church went public with the findings, urging girls and women to not comply with the vaccination campaign, the Kenyan government went on the defensive, insisting there was nothing wrong with the vaccine.

Wakefield noted: “They used the media to demonize the Catholic Church and insinuate there had been deliberate contamination of these samples with hCG to produce the result they wanted. That’s where it remained until — and this is where it gets really interesting and where the film really comes into its own — our cameras were invited back into the laboratory where these tests were done … [and] the truth was revealed.

“It came down to a resolution of this key question of who was lying and who was being honest? Who was cheating, who was not? It’s really an extraordinary story that woke me up to the importance of this issue. There is an extraordinary prophetic statement at the end from the late Dr. Karanja, OBGYN from Africa. who was at the heart of all of this.

“He said, ‘When they are finished with Africa they’re coming for you.’ ”

Mercola pointed out that "it’s important to realize that no study has ever proven that any of the vaccines on the childhood vaccination schedule are safe, especially when given in various combinations." That includes the Covid vaccines.

As noted by Wakefield, vaccine manufacturers and people like Dr. Anthony Fauci present " 'an almost kindergarten-like approach' to safety."

The blanket statement given is that vaccines in general, and the Covid shots in particular, are “safe and effective,” and that they have no adverse effects on reproduction and fertility.

"This, despite the fact they’ve done no reproductive studies at all," Mercola wrote. "Women who hear such assurances will assume the necessary studies HAVE been done when, in fact, that’s a complete lie. The reality is, that you cannot find evidence of harm if you’re not looking for it."

In some of the Covid vaccine trials, "they actually used a completely inert placebo (although some vaccine makers used another vaccine). But then note what happened," Mercola noted. "Before the trial was over, they unblinded everyone and offered the jab to everyone in the placebo group, effectively eradicating the control group altogether! Then, they tried to bury the data under red tape for 75 years. Thankfully, a sensible judge didn’t let them get away with it."

Wakefield added: “They [Pfizer] knew there were problems. They had identified the problems doing the appropriate study, at least to start with, until they gave the crossover group the vaccine. Then they tried to hide the data because they knew it revealed the seriousness of the adverse reactions to their vaccine. The court overruled them and now those data are being analyzed, and they are terrifying.”

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watch that video here...

https://infertilitymovie.org/a-diabolical-agenda/


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