healthimpactnews--2020-12-11--President Trump Threatens to Fire FDA Chief Unless He Approves Pfizer COVID Vaccine Immediately

Multiple news outlets reported today that the White House has informed the FDA that if they do not approve the new experimental Pfizer COVID vaccine by the end of the day today , Friday , December 11 , 2020 , that Stephen Hahn , the head of the FDA , would be fired .
This follows a Twitter storm by the President earlier in the day where he Tweeted : I just want to stop the world from killing itself !
The Swine Flu ( H1N1 ) , and the attempt for a vaccine by the Obama Administration , with @ @ @ @ @ @ @ complete and total disaster .
Now they want to come in and take over one of the “ greatest and fastest medical miracles in modern day history.
” I don ’ t think so !
While my pushing the money drenched but heavily bureaucratic @ US_FDA saved five years in the approval of NUMEROUS great new vaccines , it is still a big , old , slow turtle .
Get the dam vaccines out NOW , Dr. Hahn @ SteveFDA .
Stop playing games and start saving lives !
!
!
Health Impact @ @ @ @ @ @ @ this issue , as we , along with many other organizations , have called upon the FDA to NOT approve the dangerous new Pfizer COVID vaccine that literally thousands of medical doctors and scientists around the world have said is too dangerous to approve , as it will result in deaths , brain injuries , autoimmune diseases , infertility and more .
I posed this question in an article published in October , and I will repeat what I wrote then here : It is important to remember that President Trump did not @ @ @ @ @ @ @ presidents before him .
He was chosen from the Wall Street Billionaires club .
Since the COVID plandemic started earlier this year , over $ 7 TRILLION of federal funds has been allocated to fight “ the virus.
” Most of that is for the multiple vaccines being developed under Operation Warp Speed , which was basically given a blank check to spend as much money as needed to develop COVID vaccines .
It is safe to conclude that more funds have rolled into the bank accounts of Big Pharma this year , @ @ @ @ @ @ @ the years of the history of the U.S. put together .
Not all of the COVID funding went to Big Pharma of course .
The military has received its fair share for its role in distributing the new vaccines when they become available , and what exactly that role is going to be is yet to be seen .
Many other Wall Street corporations got richer over COVID as well , as businesses were chosen based arbitrarily on which ones were “ essential ” and which ones were not , and the entire @ @ @ @ @ @ @ literally overnight .
Did President Trump Really Test Positive for COVID ?
Or was it another Act to Boost Big Pharma ?
Last week it was announced that President Trump tested positive for COVID along with “ mild symptoms.
” He was admitted to Walter Reed hospital .
The same day his condition was announced to the public , it was also immediately announced that the President was being administered a new experimental COVID drug , Regeneron ’ s REGN-COV2 .
Business journals apparently already had press releases ready about the drug , @ @ @ @ @ @ @ went up .
FiercePharma , one the Pharmaceutical companies ’ main marketing trade publications , was one of the first to publish the story : In a bombshell development Thursday , President Donald J. Trump tested positive for COVID-19 , sending shockwaves through the country with just weeks until Election Day .
One unanswered question was how the president ’ s physicians would navigate an uncertain treatment course—and an unproven antibody cocktail from Regeneron is now in the spotlight .
Trump ’ s personal doctor confirmed Friday that the president was treated with @ @ @ @ @ @ @ investigational antibody cocktail for COVID-19 , dubbed REGN-COV2… Trump ’ s early treatment with Regeneron ’ s cocktail was an immediate boon for investors with the drugmaker ’ s stock trading up around $ 20—or 3 % —in after-market hours Friday .
Regeneron does not even have emergency use approval yet .
FiercePharma also reports that Regeneron ’ s CEO Len Schleifer has been a guest at the White House during the pandemic .
Unlike another highly touted COVID-19 hopeful , Gilead Sciences ’ s Veklury ( remdesivir ) , REGN-COV2 has no @ @ @ @ @ @ @ fact that could underscore Trump ’ s relationship with New York-based Regeneron and CEO Len Schleifer , who has been a guest at the White House during the pandemic .
The company said late Friday that Trump ’ s doctors had requested the therapy under its compassionate use program .
An eventual clean bill of health for Trump could go a long way to boosting confidence in Regeneron ’ s therapy , which is already raising hopes of $ 6 billion in sales per year—assuming it can secure the FDA ’ s approval @ @ @ @ @ @ @ being supplied to the U.S. government at $ 24 on average for a two-dose regimen , antibody drugs could be far more expensive , as they are typically priced well into the thousands , Morningstar analyst Karen Andersen told clients last month .
But antibodies could be particularly useful for older adults , whose immune systems may not respond as well to vaccination .
( Full article . )
( Emphasis Added ) Regeneron ’ s co-founders then made the media rounds after the “ free ” publicity they received from the President @ @ @ @ @ @ @ after Regeneron published early data on its antibody cocktail to treat COVID-19 , the world found out the president of the U.S. was taking it .
What followed was a run-up for Regeneron shares , a series of shout-outs from President Donald Trump and a fair share of media appearances for the company ’ s co-founders .
The high-profile attention is a rare public relations bump that can ’ t be bought—and one the company seems at ease leveraging .
It may also be a sign of the COVID-19 times .
Gilead CEO @ @ @ @ @ @ @ TV interviews to talk about remdesivir , the company ’ s antiviral that ’ s still in clinical trials but boasts an emergency use authorization from the FDA .
( Full article .
Emphasis added . )
On October 4 , 2020 , it was announced that Trump had received his second dose of remdesivir , another experimental COVID drug , but one that has already received fast-track approval by the FDA , and has been widely distributed to hospitals .
His doctors reported that President Trump would receive the full 5 doses @ @ @ @ @ @ @ pharmaceutical marketing trade publication , announced on Friday , October 2nd , the same day Trump was admitted to Walter Reed , that sales of Gilead ’ s remdesivir were beginning to slump , and that the company was taking over distribution of the drug now as a result of the slow-down in sales .
The cost for the 5-dose treatment of remdesivir is $ 3,120.00 , and sales are expected to exceed $ 3.5 billion in revenue .
Hydroxychloroquine ( HCQ ) , a drug with no patents due to being in @ @ @ @ @ @ @ for over 35 years and with a cost of about $ 20 per dose , was condemned by U.S. public health officials like Dr. Fauci as supposedly being ineffective in treating COVID .
The efforts to discredit HCQ included publishing fabricated studies to try and “ prove ” that HCQ was not effective against COVID patients .
Gilead ’ s remdesivir was given fast-track approval instead , and demand initially sky rocketed .
But now , apparently the supply of remdesivir exceeds demand .
So whatever you want to believe about the President @ @ @ @ @ @ @ thing is very clear : two pharmaceutical companies with experimental COVID drugs saw their sales and stock value soar .

by Brian Shilhavy
Editor, Health Impact News
Multiple news outlets reported today that the White House has informed the FDA that if they do not approve the new experimental Pfizer COVID vaccine by the end of the day today, Friday, December 11, 2020, that Stephen Hahn, the head of the FDA, would be fired.
This follows a Twitter storm by the President earlier in the day where he Tweeted:
I just want to stop the world from killing itself!
The Swine Flu (H1N1), and the attempt for a vaccine by the Obama Administration, with Joe Biden in charge, was a complete and total disaster. Now they want to come in and take over one of the “greatest and fastest medical miracles in modern day history.” I don’t think so!
While my pushing the money drenched but heavily bureaucratic @US_FDA saved five years in the approval of NUMEROUS great new vaccines, it is still a big, old, slow turtle. Get the dam vaccines out NOW, Dr. Hahn @SteveFDA. Stop playing games and start saving lives!!!
Health Impact News opposes the President 100% on this issue, as we, along with many other organizations, have called upon the FDA to NOT approve the dangerous new Pfizer COVID vaccine that literally thousands of medical doctors and scientists around the world have said is too dangerous to approve, as it will result in deaths, brain injuries, autoimmune diseases, infertility and more.
See our previous coverage:
I posed this question in an article published in October, and I will repeat what I wrote then here:
It is important to remember that President Trump did not come through the political ranks like most presidents before him. He was chosen from the Wall Street Billionaires club.
Since the COVID plandemic started earlier this year, over $7 TRILLION of federal funds has been allocated to fight “the virus.” Most of that is for the multiple vaccines being developed under Operation Warp Speed, which was basically given a blank check to spend as much money as needed to develop COVID vaccines.
It is safe to conclude that more funds have rolled into the bank accounts of Big Pharma this year, 2020, than probably the rest of the years of the history of the U.S. put together.
Not all of the COVID funding went to Big Pharma of course. The military has received its fair share for its role in distributing the new vaccines when they become available, and what exactly that role is going to be is yet to be seen.
Many other Wall Street corporations got richer over COVID as well, as businesses were chosen based arbitrarily on which ones were “essential” and which ones were not, and the entire business landscape in the U.S. changed almost literally overnight.
Did President Trump Really Test Positive for COVID? Or was it another Act to Boost Big Pharma?
Last week it was announced that President Trump tested positive for COVID along with “mild symptoms.” He was admitted to Walter Reed hospital.
The same day his condition was announced to the public, it was also immediately announced that the President was being administered a new experimental COVID drug, Regeneron’s REGN-COV2.
Business journals apparently already had press releases ready about the drug, and the company’s stock immediately went up.
FiercePharma, one the Pharmaceutical companies’ main marketing trade publications, was one of the first to publish the story:
In a bombshell development Thursday, President Donald J. Trump tested positive for COVID-19, sending shockwaves through the country with just weeks until Election Day. One unanswered question was how the president’s physicians would navigate an uncertain treatment course—and an unproven antibody cocktail from Regeneron is now in the spotlight. Trump’s personal doctor confirmed Friday that the president was treated with an 8-gram dose of Regeneron’s investigational antibody cocktail for COVID-19, dubbed REGN-COV2… Trump’s early treatment with Regeneron’s cocktail was an immediate boon for investors with the drugmaker’s stock trading up around $20—or 3%—in after-market hours Friday.
Regeneron does not even have emergency use approval yet. FiercePharma also reports that Regeneron’s CEO Len Schleifer has been a guest at the White House during the pandemic.
Kyle Blankenship reports:
Unlike another highly touted COVID-19 hopeful, Gilead Sciences’s Veklury (remdesivir), REGN-COV2 has no emergency use approvals anywhere in the world—a fact that could underscore Trump’s relationship with New York-based Regeneron and CEO Len Schleifer, who has been a guest at the White House during the pandemic. The company said late Friday that Trump’s doctors had requested the therapy under its compassionate use program. An eventual clean bill of health for Trump could go a long way to boosting confidence in Regeneron’s therapy, which is already raising hopes of $6 billion in sales per year—assuming it can secure the FDA’s approval. Compared with vaccines, which are being supplied to the U.S. government at $24 on average for a two-dose regimen, antibody drugs could be far more expensive, as they are typically priced well into the thousands, Morningstar analyst Karen Andersen told clients last month. But antibodies could be particularly useful for older adults, whose immune systems may not respond as well to vaccination. (Full article.) (Emphasis Added)
Regeneron’s co-founders then made the media rounds after the “free” publicity they received from the President for using their product.
Beth Snyder Bulik, writing for FiercePharma, reported on Oct. 7th:
Just days after Regeneron published early data on its antibody cocktail to treat COVID-19, the world found out the president of the U.S. was taking it. What followed was a run-up for Regeneron shares, a series of shout-outs from President Donald Trump and a fair share of media appearances for the company’s co-founders. The high-profile attention is a rare public relations bump that can’t be bought—and one the company seems at ease leveraging. It may also be a sign of the COVID-19 times. Gilead CEO Daniel O’Day went on multiple TV interviews to talk about remdesivir, the company’s antiviral that’s still in clinical trials but boasts an emergency use authorization from the FDA. (Full article. Emphasis added.)
On October 4, 2020, it was announced that Trump had received his second dose of remdesivir, another experimental COVID drug, but one that has already received fast-track approval by the FDA, and has been widely distributed to hospitals.
His doctors reported that President Trump would receive the full 5 doses.
Interestingly, FiercePharma, the main pharmaceutical marketing trade publication, announced on Friday, October 2nd, the same day Trump was admitted to Walter Reed, that sales of Gilead’s remdesivir were beginning to slump, and that the company was taking over distribution of the drug now as a result of the slow-down in sales.
Angus Liu, writing for FiercePharma, reported:
After a somewhat chaotic initial rollout by the U.S. government, Gilead Sciences is now taking distribution of COVID-19 drug remdesivir into its own hands. Starting Thursday, Gilead will directly sell remdesivir, branded as Veklury, to American hospitals, ending a five-month phase when the U.S. Department of Health and Human services was responsible for allocating it, the company and HHS said. AmerisourceBergen will remain the sole U.S. distributor through the end of the year.
The cost for the 5-dose treatment of remdesivir is $3,120.00, and sales are expected to exceed $3.5 billion in revenue.
Hydroxychloroquine (HCQ), a drug with no patents due to being in the marketplace with a perfect safety record for over 35 years and with a cost of about $20 per dose, was condemned by U.S. public health officials like Dr. Fauci as supposedly being ineffective in treating COVID.
The efforts to discredit HCQ included publishing fabricated studies to try and “prove” that HCQ was not effective against COVID patients.
Gilead’s remdesivir was given fast-track approval instead, and demand initially sky rocketed.
But now, apparently the supply of remdesivir exceeds demand.
FiercePharma reported:
Remdesivir is one of only a few drugs to show signs of benefits in COVID-19 during the early days of the pandemic. But just like the world’s response to the virus, the initial distribution of the antiviral drug was confusing under the feds’ oversight. Some doses went directly to hospitals but not necessarily to those in greatest need, and some hospitals either didn’t receive enough or were left empty-handed, NPR reported in May, weeks after the remdesivir won its emergency use authorization from the FDA. The allocations improved later, but HHS’ methods for earmarking doses remained a mystery. Meanwhile, Gilead quickly worked to ramp up supply, increasing internal manufacturing capacity and signing on contractors. Now, the supply’s exceeding market demand. At the end of June, HHS secured more than 500,000 treatment courses of the drug, which represented nearly all of Gilead’s yield through September. However, states and territories haven’t been accepting their full allocations, and only 32% of the total amount was actually purchased by hospitals from July to September, HHS said Thursday, citing data from its Office of the Assistant Secretary for Preparedness and Response. Now that Gilead’s meeting real-time demand for the drug in the U.S., the HHS and the company decided it’s time for the HHS to bow out and let the company handle commercial sales directly to hospitals. (Full article at FiercePharma).
So whatever you want to believe about the President’s diagnosis with COVID, one thing is very clear: two pharmaceutical companies with experimental COVID drugs saw their sales and stock value soar.


healthimpactnews--2020-12-12--FDA Shuts Down Natural Pain Options

FDA Shuts Down Natural Pain Options

FDA-approved pain medicines are dangerous , but the government is systematically attacking safer , non-addictive natural treatments .
Action Alert !
A recent study in Switzerland found that acetaminophen poisoning increased by 40 % following the approval of 1,000mg doses .
This is just the latest data to indicate the public health problems caused by this commonly used pain drug , which is the active ingredient in Tylenol .
Despite the dangers of FDA-approved pain drugs , the federal government aggressively attacks and censors natural pain medicines like homeopathic treatments , CBD , medical foods , and supplements .
This @ @ @ @ @ @ @ ve written for years about the dangers of acetaminophen .
It is the most commonly prescribed class of drugs despite causing 50 percent of all liver failure in the US .
According to the FDA ’ s adverse event database , acetaminophen has caused more than 100,000 adverse events and more than 78,000 serious adverse events , including 24,000 deaths .
It has also been linked to asthma and hearing loss .
Overdoses involving opioids killed nearly 47,000 people in 2018 alone .
Now consider the federal government ’ s approach to natural @ @ @ @ @ @ @ all injectable homeopathic medicines , which includes Traumeel , a prescription-only homeopathic medicine for pain with an extremely robust safety profile .
Previously , the FDA went after Limbrel , a medical food for the treatment of osteoarthritis .
In a letter to Primus , the FDA stated that 194 adverse event reports for Limbrel were received between 2007 and 2017—about 20 a year .
Then , of course , there ’ s CBD .
The federal government ’ s approach to CBD right now is frankly a mess , and we ’ @ @ @ @ @ @ @ coverage .
In short , hemp and its derivatives have been legalized at the federal level , but FDA laws still apply to products containing hemp , such as supplements , lotions , cosmetics , etc .
Since 2018 , the FDA has been trying to figure out how it will treat these products .
Recall , too , that the agency has approved a CBD drug , and according to FDA rules , this means that CBD can not legally be sold as a supplement .
We ultimately don ’ t know @ @ @ @ @ @ @ .
If history provides any clues , the FDA will protect the drug-approval process and ban CBD supplements .
To add to the confusion , Congress is directing the FDA to release an interim policy ( called a policy of enforcement discretion ) explaining how it will treat CBD products in the marketplace as the agency develops its final regulatory framework .
Will the FDA release an interim policy that allows CBD supplements for the time being before banning them outright when a final policy is released ?
We just don ’ t @ @ @ @ @ @ @ the FDA will not do the right thing , especially when Big Pharma profits are at stake .
It is unconscionable , but unsurprising , that the FDA would reduce access to safe , non-addictive alternatives to dangerous opioid drugs that killed 30,000 people in 2018 alone .
We ’ ve also seen basic information on natural health censored to protect drug industry profits during the COVID-19 pandemic .
This cronyism has to stop .
Action Alert !
Write to Congress and the FDA , telling them to issue a policy of enforcement @ @ @ @ @ @ @ CBD supplements at therapeutic levels and full-spectrum hemp oil .
Please send your message immediately .
By sending this message , you will also be supporting our petition to ungag doctors so that they can share with patients the benefits of supplements and natural treatments for COVID .

by Alliance for Natural Health
FDA-approved pain medicines are dangerous, but the government is systematically attacking safer, non-addictive natural treatments. Action Alert!
A recent study in Switzerland found that acetaminophen poisoning increased by 40% following the approval of 1,000mg doses. This is just the latest data to indicate the public health problems caused by this commonly used pain drug, which is the active ingredient in Tylenol.
Despite the dangers of FDA-approved pain drugs, the federal government aggressively attacks and censors natural pain medicines like homeopathic treatments, CBD, medical foods, and supplements. This needless suffering must end.
We’ve written for years about the dangers of acetaminophen. It is the most commonly prescribed class of drugs despite causing 50 percent of all liver failure in the US. According to the FDA’s adverse event database, acetaminophen has caused more than 100,000 adverse events and more than 78,000 serious adverse events, including 24,000 deaths. It has also been linked to asthma and hearing loss.
Overdoses involving opioids killed nearly 47,000 people in 2018 alone.
Now consider the federal government’s approach to natural pain medicines. The FDA essentially banned all injectable homeopathic medicines, which includes Traumeel, a prescription-only homeopathic medicine for pain with an extremely robust safety profile.
Previously, the FDA went after Limbrel, a medical food for the treatment of osteoarthritis. In a letter to Primus, the FDA stated that 194 adverse event reports for Limbrel were received between 2007 and 2017—about 20 a year.
Then, of course, there’s CBD. The federal government’s approach to CBD right now is frankly a mess, and we’ve sifted through the details in previous coverage. In short, hemp and its derivatives have been legalized at the federal level, but FDA laws still apply to products containing hemp, such as supplements, lotions, cosmetics, etc. Since 2018, the FDA has been trying to figure out how it will treat these products. Recall, too, that the agency has approved a CBD drug, and according to FDA rules, this means that CBD cannot legally be sold as a supplement.
We ultimately don’t know how the FDA will treat CBD supplements. If history provides any clues, the FDA will protect the drug-approval process and ban CBD supplements. To add to the confusion, Congress is directing the FDA to release an interim policy (called a policy of enforcement discretion) explaining how it will treat CBD products in the marketplace as the agency develops its final regulatory framework. Will the FDA release an interim policy that allows CBD supplements for the time being before banning them outright when a final policy is released? We just don’t know, but we should assume that the FDA will not do the right thing, especially when Big Pharma profits are at stake.
It is unconscionable, but unsurprising, that the FDA would reduce access to safe, non-addictive alternatives to dangerous opioid drugs that killed 30,000 people in 2018 alone. We’ve also seen basic information on natural health censored to protect drug industry profits during the COVID-19 pandemic. This cronyism has to stop.
Action Alert! Write to Congress and the FDA, telling them to issue a policy of enforcement discretion that protects consumer access to hemp-derived CBD supplements at therapeutic levels and full-spectrum hemp oil. Please send your message immediately. By sending this message, you will also be supporting our petition to ungag doctors so that they can share with patients the benefits of supplements and natural treatments for COVID.


healthimpactnews--2020-12-12--Unlike UK, U.S. FDA Allows Pregnant and Nursing Women to Receive Experimental Pfizer COVID Vaccine

The U.S. FDA has given emergency use authorization ( EUA ) to the experimental Pfizer COVID mRNA vaccine , a type of vaccine that has never before been authorized for use in humans .
The FDA ’ s EUA for the Pfizer COVID vaccine follows an emergency use authorization in the U.K. about 10 days ago .
Both governments have issued guidelines for the new vaccines , one set of guidelines for doctors and healthcare providers who will administer the vaccine , and a shorter set of guidelines for “ recipients ” who plan on taking the vaccine .
Even @ @ @ @ @ @ @ from the same company ( Pfizer ) , there are notable differences .
The UK guidelines , issued by the UK Department of Health and Social Care and the Medicines & Healthcare products Regulatory Agency , give strict warnings to doctors NOT to give the vaccine to women who are pregnant or nursing , or to women planning on becoming pregnant , with a warning about potential infertility issues .
Pregnancy There are no or limited amount of data from the use of COVID-19 mRNA Vaccine BNT162b2 .
Animal reproductive toxicity studies have @ @ @ @ @ @ @ BNT162b2 is not recommended during pregnancy .
For women of childbearing age , pregnancy should be excluded before vaccination .
In addition , women of childbearing age should be advised to avoid pregnancy for at least 2 months after their second dose .
Breast-feeding It is unknown whether COVID-19 mRNA Vaccine BNT162b2 is excreted in human milk .
A risk to the newborns/infants can not be excluded .
COVID-19 mRNA Vaccine BNT162b2 should not be used during breast-feeding .
Fertility It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility @ @ @ @ @ @ @ the U.S. FDA ’ s guidelines for doctors ( at the time of this writing ) contain no such warning to not give the Pfizer experimental COVID vaccine to pregnant , lactating , or women trying to become pregnant .
All pregnancies have a risk of birth defect , loss , or other adverse outcomes .
In the US general population , the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 % to 4 % and 15 % to 20 % , respectively .
Available data @ @ @ @ @ @ @ women are insufficient to inform vaccine-associated risks in pregnancy .
Data are not available to assess the effects of Pfizer-BioNTech COVID-19 Vaccine on the breastfed infant or on milk production/excretion .
( Source . )
The FDA ’ s Recipient Guidelines simply tells pregnant and lactating women to discuss it with their healthcare provider .
Nothing is discussed or recommended for women planning to become pregnant , unlike the UK guidelines that tell women not to become pregnant for two months following the second dose , and informing doctors that the future effect @ @ @ @ @ @ @ there are no warnings in the FDA ’ s guidelines for the experimental Pfizer COVID vaccine for pregnant and nursing women , there are plenty of other warnings .
First , they make it very clear that this is an “ unapproved ” vaccine .
From the FDA ’ s Recipient Guidelines : The Pfizer-BioNTech COVID-19 Vaccine is an unapproved vaccine that may prevent COVID-19 .
There is no FDA-approved vaccine to prevent COVID-19 .
HAS THE PFIZER-BIONTECH COVID-19 VACCINE BEEN USED BEFORE ?
The Pfizer-BioNTech COVID-19 Vaccine is an unapproved vaccine .
@ @ @ @ @ @ @ 16 years of age and older have received at least 1 dose of the Pfizer-BioNTech COVID-19 Vaccine .
WHAT ARE THE BENEFITS OF THE PFIZER-BIONTECH COVID-19 VACCINE ?
In an ongoing clinical trial , the Pfizer-BioNTech COVID-19 Vaccine has been shown to prevent COVID-19 following 2 doses given 3 weeks apart .
The duration of protection against COVID-19 is currently unknown .
( Source . )
In short , the FDA is allowing Pfizer to use the American public as lab rats to further study this vaccine .
Warnings in the FDA ’ @ @ @ @ @ @ @ administer Pfizer-BioNTech COVID-19 Vaccine to individuals with known history of a severe allergic reaction ( e.g.
, anaphylaxis ) to any component of the Pfizer-BioNTech COVID-19 Vaccine ( see Full EUA Prescribing Information ) .
Appropriate medical treatment used to manage immediate allergic reactions must be immediately available in the event an acute anaphylactic reaction occurs following administration of Pfizer-BioNTech COVID-19 Vaccine .
Immunocompromised persons , including individuals receiving immunosuppressant therapy , may have a diminished immune response to the Pfizer-BioNTech COVID-19 Vaccine .
Pfizer-BioNTech COVID-19 Vaccine may not protect all vaccine recipients @ @ @ @ @ @ @ Vaccine that have been reported in clinical trials include injection site pain , fatigue , headache , muscle pain , chills , joint pain , fever , injection site swelling , injection site redness , nausea , malaise , and lymphadenopathy ( see Full EUA Prescribing Information ) .
Severe allergic reactions have been reported following the Pfizer-BioNTech COVID-19 Vaccine during mass vaccination outside of clinical trials .
Additional adverse reactions , some of which may be serious , may become apparent with more widespread use of the Pfizer-BioNTech COVID-19 Vaccine .
Serious @ @ @ @ @ @ @ Death ; • A life-threatening adverse event ; • Inpatient hospitalization or prolongation of existing hospitalization ; • A persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions ; • A congenital anomaly/birth defect ; • An important medical event that based on appropriate medical judgement may jeopardize the individual and may require medical or surgical intervention to prevent one of the outcomes listed above .
( Source . )
Since the Pfizer COVID vaccine is supposed to be distributed through the nation ’ s Walgreens and @ @ @ @ @ @ @ these stores have physicians and paramedics standing by to treat the patients who go into anaphylactic shock ?
Or is the military going to be at all of these stores providing medics to handle that ?
To get the latest version of these guidelines , visit the FDA website here .
Everyone should contact their federal representatives in the Senate and the House and demand that the FDA include the same warnings for pregnant and nursing women as the UK guidelines to the same vaccine contain !
UK First to Approve Pfizer COVID @ @ @ @ @ @ @ Says Vaccine Can Make Females Infertile Vaccine Injury Prayer Clinics will be Needed for the Coming Tsunami of Vaccine Injuries Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler , MeWe , and Gab !
If our website is seized and shut down , find us on Parler , MeWe and Gab for further instructions about where to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

by Brian Shilhavy
Editor, Health Impact News
The U.S. FDA has given emergency use authorization (EUA) to the experimental Pfizer COVID mRNA vaccine, a type of vaccine that has never before been authorized for use in humans.
The FDA’s EUA for the Pfizer COVID vaccine follows an emergency use authorization in the U.K. about 10 days ago.
Both governments have issued guidelines for the new vaccines, one set of guidelines for doctors and healthcare providers who will administer the vaccine, and a shorter set of guidelines for “recipients” who plan on taking the vaccine.
Even though these guidelines cover the same vaccine from the same company (Pfizer), there are notable differences.
The UK guidelines, issued by the UK Department of Health and Social Care and the Medicines & Healthcare products Regulatory Agency, give strict warnings to doctors NOT to give the vaccine to women who are pregnant or nursing, or to women planning on becoming pregnant, with a warning about potential infertility issues.
4.6 Fertility, pregnancy and lactation Pregnancy
There are no or limited amount of data from the use of COVID-19 mRNA Vaccine BNT162b2. Animal reproductive toxicity studies have not been completed. COVID-19 mRNA Vaccine BNT162b2 is not recommended during pregnancy. For women of childbearing age, pregnancy should be excluded before vaccination. In addition, women of childbearing age should be advised to avoid pregnancy for at least 2 months after their second dose. Breast-feeding
It is unknown whether COVID-19 mRNA Vaccine BNT162b2 is excreted in human milk. A risk to the newborns/infants cannot be excluded. COVID-19 mRNA Vaccine BNT162b2 should not be used during breast-feeding. Fertility
It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility. (Source.)
Unfortunately, the U.S. FDA’s guidelines for doctors (at the time of this writing) contain no such warning to not give the Pfizer experimental COVID vaccine to pregnant, lactating, or women trying to become pregnant.
11.1 Pregnancy Risk Summary All pregnancies have a risk of birth defect, loss, or other adverse outcomes. In the US general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Available data on Pfizer-BioNTech COVID-19 Vaccine administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy. 11.2 Lactation Risk Summary Data are not available to assess the effects of Pfizer-BioNTech COVID-19 Vaccine on the breastfed infant or on milk production/excretion. (Source.)
The FDA’s Recipient Guidelines simply tells pregnant and lactating women to discuss it with their healthcare provider.
WHAT IF I AM PREGNANT OR BREASTFEEDING? If you are pregnant or breastfeeding, discuss your options with your healthcare provider. (Source.)
Nothing is discussed or recommended for women planning to become pregnant, unlike the UK guidelines that tell women not to become pregnant for two months following the second dose, and informing doctors that the future effect on fertility is “unknown.”
FDA Warnings on the Pfizer COVID Vaccine: Acute Anaphylactic Reactions Expected
While there are no warnings in the FDA’s guidelines for the experimental Pfizer COVID vaccine for pregnant and nursing women, there are plenty of other warnings.
First, they make it very clear that this is an “unapproved” vaccine. From the FDA’s Recipient Guidelines:
The Pfizer-BioNTech COVID-19 Vaccine is an unapproved vaccine that may prevent COVID-19. There is no FDA-approved vaccine to prevent COVID-19. HAS THE PFIZER-BIONTECH COVID-19 VACCINE BEEN USED BEFORE? The Pfizer-BioNTech COVID-19 Vaccine is an unapproved vaccine. In clinical trials, approximately 20,000 individuals 16 years of age and older have received at least 1 dose of the Pfizer-BioNTech COVID-19 Vaccine. WHAT ARE THE BENEFITS OF THE PFIZER-BIONTECH COVID-19 VACCINE? In an ongoing clinical trial, the Pfizer-BioNTech COVID-19 Vaccine has been shown to prevent COVID-19 following 2 doses given 3 weeks apart. The duration of protection against COVID-19 is currently unknown. (Source.)
In short, the FDA is allowing Pfizer to use the American public as lab rats to further study this vaccine.
Warnings in the FDA’s guidelines for doctors:
Contraindications Do not administer Pfizer-BioNTech COVID-19 Vaccine to individuals with known history of a severe allergic reaction (e.g., anaphylaxis) to any component of the Pfizer-BioNTech COVID-19 Vaccine (see Full EUA Prescribing Information). Warnings Appropriate medical treatment used to manage immediate allergic reactions must be immediately available in the event an acute anaphylactic reaction occurs following administration of Pfizer-BioNTech COVID-19 Vaccine. Immunocompromised persons, including individuals receiving immunosuppressant therapy, may have a diminished immune response to the Pfizer-BioNTech COVID-19 Vaccine. Pfizer-BioNTech COVID-19 Vaccine may not protect all vaccine recipients. Adverse Reactions Adverse reactions following the Pfizer-BioNTech COVID-19 Vaccine that have been reported in clinical trials include injection site pain, fatigue, headache, muscle pain, chills, joint pain, fever, injection site swelling, injection site redness, nausea, malaise, and lymphadenopathy (see Full EUA Prescribing Information). Severe allergic reactions have been reported following the Pfizer-BioNTech COVID-19 Vaccine during mass vaccination outside of clinical trials. Additional adverse reactions, some of which may be serious, may become apparent with more widespread use of the Pfizer-BioNTech COVID-19 Vaccine. Serious adverse events are defined as: • Death;
• A life-threatening adverse event;
• Inpatient hospitalization or prolongation of existing hospitalization;
• A persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions;
• A congenital anomaly/birth defect;
• An important medical event that based on appropriate medical judgement may jeopardize the individual and may require medical or surgical intervention to prevent one of the outcomes listed above. (Source.)
Since the Pfizer COVID vaccine is supposed to be distributed through the nation’s Walgreens and CVS retail stores, will all of these stores have physicians and paramedics standing by to treat the patients who go into anaphylactic shock?
Or is the military going to be at all of these stores providing medics to handle that?
To get the latest version of these guidelines, visit the FDA website here.
Everyone should contact their federal representatives in the Senate and the House and demand that the FDA include the same warnings for pregnant and nursing women as the UK guidelines to the same vaccine contain!
See Also:
See Also:


healthimpactnews--2020-12-14--Oregon Pediatrician Publishes Study Comparing His Vaccinated and Unvaccinated Children Then Has His

Oregon Pediatrician Publishes Study Comparing His Vaccinated and Unvaccinated Children Then Has His Medical License Suspended

Dr. Paul Thomas , M.D .
was born in Portland , Oregon , and grew up in Southern Africa .
He has a masters degree in biology , an M.D .
from Dartmouth Medical School , and completed his pediatric residency at the University of California , San Diego .
He is a board-certified fellow of the American Academy of Pediatrics , and also carries board certifications in Addiction Medicine and Integrative Holistic Medicine .
He started the Pediatric After-hours Clinic ( now Pediatric ER ) at Emanuel Children ’ s Hospital , where he also taught medical students and @ @ @ @ @ @ @ the work of Dr. Paul Thomas on Health Impact News many times over the past many years .
He is a champion in the Health Freedom movement , and strongly believes in Informed Consent when it comes to vaccines .
Because Dr. Thomas believes that parents know best when it comes to the care of their children , he has parents in his practice with a wide range of views on vaccines .
Some of the parents of children in his practice do not get vaccines at all , while others do vaccinate @ @ @ @ @ @ @ than what the CDC recommends .
Dr. Thomas does not bully parents into taking his position on vaccines .
He states that if parents want to vaccinate their children , at least he is the kind of doctor that has actually researched vaccines , and not just accepted what was taught in medical school which is not much when it comes to vaccines , other than the Big Pharma mantra that “ all vaccines are effective and safe.
” Dr. Thomas knows first hand that this is not true , and his belief @ @ @ @ @ @ @ their children , they are probably better off in his practice where he can better help them deal with any negative side effects .
The vast majority of doctors who do vaccinate children have no knowledge of vaccine injuries , because they don ’ t even know how to recognize them .
Hence , Dr. Thomas is one the unique doctors in America today who can actually look at the data of his patients over the years , and compare the outcomes of vaccinated children versus unvaccinated children , a study that the @ @ @ @ @ @ @ is just what he did .
Along with James Lyons-Weiler , Ph.D. , they published their study in the International Journal of Environmental Research and Public Health .
The title of the study is Relative Incidence of Office Visits and Cumulative Rates of Billed Diagnoses Along the Axis of Vaccination .
Shortly after he published this study which has great value to the public and parents who want to make informed decisions about the health of their children and vaccination , his medical license in Oregon was suspended , because the study clearly @ @ @ @ @ @ @ much healthier than those who are vaccinated .
Dr. Thomas recently joined Del Bigtree on the Highwire to discuss his study and his current situation in his medical practice .
Here is a copy of the interview from their Bitchute Channel .
Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler , MeWe , and Gab !
If our website is seized and shut down , find us on Parler , MeWe and Gab for further instructions about where @ @ @ @ @ @ @ Behind the Plandemic and Rioting to Usher in the New World Order

Comments by Brian Shilhavy
Editor, Health Impact News
Dr. Paul Thomas, M.D. was born in Portland, Oregon, and grew up in Southern Africa. He has a masters degree in biology, an M.D. from Dartmouth Medical School, and completed his pediatric residency at the University of California, San Diego.
He is a board-certified fellow of the American Academy of Pediatrics, and also carries board certifications in Addiction Medicine and Integrative Holistic Medicine. He started the Pediatric After-hours Clinic (now Pediatric ER) at Emanuel Children’s Hospital, where he also taught medical students and residents from 1988-1993.
We have featured the work of Dr. Paul Thomas on Health Impact News many times over the past many years. He is a champion in the Health Freedom movement, and strongly believes in Informed Consent when it comes to vaccines.
Because Dr. Thomas believes that parents know best when it comes to the care of their children, he has parents in his practice with a wide range of views on vaccines. Some of the parents of children in his practice do not get vaccines at all, while others do vaccinate, although usually at a slower pace than what the CDC recommends.
Dr. Thomas does not bully parents into taking his position on vaccines. He states that if parents want to vaccinate their children, at least he is the kind of doctor that has actually researched vaccines, and not just accepted what was taught in medical school which is not much when it comes to vaccines, other than the Big Pharma mantra that “all vaccines are effective and safe.”
Dr. Thomas knows first hand that this is not true, and his belief is that if parents decide to vaccinate their children, they are probably better off in his practice where he can better help them deal with any negative side effects. The vast majority of doctors who do vaccinate children have no knowledge of vaccine injuries, because they don’t even know how to recognize them.
Hence, Dr. Thomas is one the unique doctors in America today who can actually look at the data of his patients over the years, and compare the outcomes of vaccinated children versus unvaccinated children, a study that the CDC refuses to do.
And that is just what he did. Along with James Lyons-Weiler, Ph.D., they published their study in the International Journal of Environmental Research and Public Health.
The title of the study is Relative Incidence of Office Visits and Cumulative Rates of Billed Diagnoses Along the Axis of Vaccination.
Shortly after he published this study which has great value to the public and parents who want to make informed decisions about the health of their children and vaccination, his medical license in Oregon was suspended, because the study clearly shows that unvaccinated children tend to be much healthier than those who are vaccinated.
Dr. Thomas recently joined Del Bigtree on the Highwire to discuss his study and his current situation in his medical practice.
Here is a copy of the interview from their Bitchute Channel.
See Also:


healthimpactnews--2020-12-13--WARNING! Seniors and Healthcare Workers First in Line to Get the Experimental COVID Vaccine!

With the FDA giving emergency use authorization ( EUA ) for the experimental Pfizer COVID mRNA vaccine , doses are currently in route to all 50 States and U.S .
Territories .
In most of these states it is being reported that the first doses will be given to the elderly in nursing homes or assisted care facilities , and to healthcare workers .
The general public will probably not see these in the retail outlets , such as Walmart , Walgreens and CVS , until later this month .
Media reports in the Pharma-funded corporate media are downplaying or @ @ @ @ @ @ @ poses , and they are also in many cases erroneously reporting that this is an FDA-approved vaccine .
But as we reported yesterday , where I linked to the actual guidelines published by the FDA right off of their own website , the FDA is making it very clear that these are unapproved vaccines .
See : Unlike UK , U.S. FDA Allows Pregnant and Nursing Women to Receive Experimental Pfizer COVID Vaccine In addition , the FDA guidelines for recipients state : Nobody , at least at this point , should be @ @ @ @ @ @ @ to receive this vaccine .
And no employer should be requiring it either .
Resist the Plandemic and New World Order Agenda !
For those of you who have chosen not to be brainwashed by the propaganda being broadcast by the Big Pharma-owned corporate media 24/7/365 , you know by now that this is NOT a real pandemic , but a very well organized “ Plandemic.
” We have a page in our COVID Information Center with articles and films proving that this is a Plandemic that has been in the works for @ @ @ @ @ @ @ main person who has been master-minding this Plandemic working together with other Globalists around the world to reach their ultimate goal with this Plandemic : The vaccination of every person on the planet , and a drastic reduction of the world ’ s population .
This is NOT a “ conspiracy theory , ” as Bill Gates announced this himself at the very beginning of the Plandemic , and he has also stated over the years many times that he sees vaccinations as necessary to reduce the world ’ s population .
See @ @ @ @ @ @ @ for World ’ s Population of 7 Billion – Was This the Plan All Along ?
If you have family members or loved ones in nursing homes or assisted care facilities , you need to contact these facilities IMMEDIATELY and make sure that they do NOT have your consent to administer this vaccine to your loved ones , especially if you have any kind of medical power of attorney for them .
Do NOT assume that they will NOT give this experimental vaccine to your elderly loved one without your approval !
More @ @ @ @ @ @ @ statement of medical care upon admittance to that facility that allows them to administer vaccines and other medical products without your approval .
If at all possible , get your senior loved one to sign a statement of REFUSAL TO RECEIVE THE PFIZER COVID VACCINE , and if you have medical power of attorney , you sign it as well .
Remember , the Pharma-owned corporate media has already begun trying to condition the public to accept DEATHS and other reactions from this experimental vaccine to be “ normal , ” especially among @ @ @ @ @ @ @ Don ’ t Be Alarmed ’ if People Start Dying After Taking the COVID Vaccine When COVID was first being reported in the U.S. back in March and April this year , tens of thousands of seniors lost their lives , not necessarily from COVID , but because of the way they were treated , where in many cases they were put on ventilators which ended up collapsing their lungs and killing them .
The fear being driven by the media , along with isolating them from their family members who are their @ @ @ @ @ @ @ of their deaths , all of which were blamed on “ the virus.
” See : Dr. Vernon Coleman : Your Government Wants You Dead – BANNED from YouTube Everyone needs to understand that American culture is now dominated by a eugenics mindset that has no value for Senior citizens , who are seen as a financial burden to the healthcare system , especially now during COVID .
Don ’ t Let Medical Bureaucrats Bully You if you Work in Healthcare !
When this vaccine was first rolled out in the UK less @ @ @ @ @ @ @ the NHS medical staff suffered severe anaphylactic reactions after being injected with the Pfizer experimental COVID vaccine .
This is what allegedly prompted the FDA to issue warnings about allergies and anaphylactic shock .
See : Life-Threatening Reactions to Pfizer COVID Experimental Vaccines Results in Warnings to People Who Have Allergies If you work in healthcare , don ’ t risk your life for this vaccine , even if it means losing your job !
Seeing doctors and nurses get sick and not be able to work which in turn will put more @ @ @ @ @ @ @ fits very well into the Globalists ’ plans at this point , because they will NOT blame it on the vaccine , but on COVID .
Remember , there is currently NO LAW that requires anyone to receive this vaccine .
If you are suspended or lose your job over refusing to be injected , contact your union if you have one , or band together and hire a good attorney , because there is no legal basis to refuse anyone in healthcare employment based on compliance with an unapproved , experimental vaccine @ @ @ @ @ @ @ and Safe Treatments Already Exist !
This is the real tragedy that our nation and other nations around the world are facing right now .
There are literally tens of thousands if not hundreds of thousands of doctors and medical professionals around the world who are being censored for their effective COVID treatments .
See : Doctors Around the World Issue Dire WARNING : DO NOT GET THE COVID VACCINE !
!
Older , safer drugs such as hydroxychloriquine and Ivermectin are being used by thousands of doctors with a near 100 % @ @ @ @ @ @ @ Scandal page and read about the Frontline Doctors , and also listen to Dr. Pierre Kory M.D .
who testified before the U.S. Senate last week about all of the doctors in his group that are successfully treating COVID patients with older drugs .
“ I Can ’ t Keep Watching Patients Die Needlessly !
” Medical Professor Testifies to Congress that COVID Cure Already Exists with Ivermectin The reason the FDA refuses to issue emergency use authorizations ( EUAs ) for these older drugs to be used on COVID is that it @ @ @ @ @ @ @ ’ s COVID vaccine and other new drugs recently all ILLEGAL !
And since President Trump and the Federal Government has decimated the U.S. economy and closed down almost 50 % of America ’ s small businesses so that TRILLIONS of dollars could be given to the Big Pharma Billionaires on Wall Street to develop these vaccines and new drugs , we know that it is impossible for them to promote these older drugs that are cheaper , safer , and much more effective .
They should all be arrested for Crimes Against @ @ @ @ @ @ @ media has the American public fixated on the election results and the current power struggle to take over the White House , where no matter who ends up as President of the United States , Operation Warp Speed will continue full speed ahead to carry out the Globalists ’ eugenics and Great Reset agenda .
Unlike UK , U.S. FDA Allows Pregnant and Nursing Women to Receive Experimental Pfizer COVID Vaccine Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on @ @ @ @ @ @ @ If our website is seized and shut down , find us on Parler , MeWe and Gab for further instructions about where to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

by Brian Shilhavy
Editor, Health Impact News
With the FDA giving emergency use authorization (EUA) for the experimental Pfizer COVID mRNA vaccine, doses are currently in route to all 50 States and U.S. Territories.
In most of these states it is being reported that the first doses will be given to the elderly in nursing homes or assisted care facilities, and to healthcare workers.
The general public will probably not see these in the retail outlets, such as Walmart, Walgreens and CVS, until later this month.
Media reports in the Pharma-funded corporate media are downplaying or ignoring altogether the risks that this vaccine poses, and they are also in many cases erroneously reporting that this is an FDA-approved vaccine.
But as we reported yesterday, where I linked to the actual guidelines published by the FDA right off of their own website, the FDA is making it very clear that these are unapproved vaccines. See:
In addition, the FDA guidelines for recipients state:
WHAT IF I DECIDE NOT TO GET THE PFIZER-BIONTECH COVID-19 VACCINE?
It is your choice to receive or not receive the Pfizer-BioNTech COVID-19 Vaccine. Should you decide not to receive it, it will not change your standard medical care.
Nobody, at least at this point, should be coercing you or anyone in your family to receive this vaccine. And no employer should be requiring it either.
Resist the Plandemic and New World Order Agenda!
For those of you who have chosen not to be brainwashed by the propaganda being broadcast by the Big Pharma-owned corporate media 24/7/365, you know by now that this is NOT a real pandemic, but a very well organized “Plandemic.”
We have a page in our COVID Information Center with articles and films proving that this is a Plandemic that has been in the works for years now.
Bill Gates is the main person who has been master-minding this Plandemic working together with other Globalists around the world to reach their ultimate goal with this Plandemic: The vaccination of every person on the planet, and a drastic reduction of the world’s population.
This is NOT a “conspiracy theory,” as Bill Gates announced this himself at the very beginning of the Plandemic, and he has also stated over the years many times that he sees vaccinations as necessary to reduce the world’s population. See:
Protect Your Senior Family Members!
If you have family members or loved ones in nursing homes or assisted care facilities, you need to contact these facilities IMMEDIATELY and make sure that they do NOT have your consent to administer this vaccine to your loved ones, especially if you have any kind of medical power of attorney for them.
Do NOT assume that they will NOT give this experimental vaccine to your elderly loved one without your approval! More than likely you signed some sort of statement of medical care upon admittance to that facility that allows them to administer vaccines and other medical products without your approval.
If at all possible, get your senior loved one to sign a statement of REFUSAL TO RECEIVE THE PFIZER COVID VACCINE, and if you have medical power of attorney, you sign it as well.
Remember, the Pharma-owned corporate media has already begun trying to condition the public to accept DEATHS and other reactions from this experimental vaccine to be “normal,” especially among seniors. See:
When COVID was first being reported in the U.S. back in March and April this year, tens of thousands of seniors lost their lives, not necessarily from COVID, but because of the way they were treated, where in many cases they were put on ventilators which ended up collapsing their lungs and killing them.
The fear being driven by the media, along with isolating them from their family members who are their main advocates, also contributed to many of their deaths, all of which were blamed on “the virus.” See:
Everyone needs to understand that American culture is now dominated by a eugenics mindset that has no value for Senior citizens, who are seen as a financial burden to the healthcare system, especially now during COVID.
Don’t Let Medical Bureaucrats Bully You if you Work in Healthcare!
When this vaccine was first rolled out in the UK less than two weeks ago, some of the NHS medical staff suffered severe anaphylactic reactions after being injected with the Pfizer experimental COVID vaccine. This is what allegedly prompted the FDA to issue warnings about allergies and anaphylactic shock. See:
If you work in healthcare, don’t risk your life for this vaccine, even if it means losing your job! Seeing doctors and nurses get sick and not be able to work which in turn will put more stress on the hospitals is something that fits very well into the Globalists’ plans at this point, because they will NOT blame it on the vaccine, but on COVID.
Remember, there is currently NO LAW that requires anyone to receive this vaccine. If you are suspended or lose your job over refusing to be injected, contact your union if you have one, or band together and hire a good attorney, because there is no legal basis to refuse anyone in healthcare employment based on compliance with an unapproved, experimental vaccine.
Nobody Needs this Vaccine! Effective and Safe Treatments Already Exist!
This is the real tragedy that our nation and other nations around the world are facing right now. There are literally tens of thousands if not hundreds of thousands of doctors and medical professionals around the world who are being censored for their effective COVID treatments. See:
Older, safer drugs such as hydroxychloriquine and Ivermectin are being used by thousands of doctors with a near 100% cure rate. Visit our COVID Hydroxychloroquine Scandal page and read about the Frontline Doctors, and also listen to Dr. Pierre Kory M.D. who testified before the U.S. Senate last week about all of the doctors in his group that are successfully treating COVID patients with older drugs.
The reason the FDA refuses to issue emergency use authorizations (EUAs) for these older drugs to be used on COVID is that it would make the EUAs issued to Pfizer’s COVID vaccine and other new drugs recently all ILLEGAL!
And since President Trump and the Federal Government has decimated the U.S. economy and closed down almost 50% of America’s small businesses so that TRILLIONS of dollars could be given to the Big Pharma Billionaires on Wall Street to develop these vaccines and new drugs, we know that it is impossible for them to promote these older drugs that are cheaper, safer, and much more effective.
They should all be arrested for Crimes Against Humanity, but instead the Pharma-owned corporate media has the American public fixated on the election results and the current power struggle to take over the White House, where no matter who ends up as President of the United States, Operation Warp Speed will continue full speed ahead to carry out the Globalists’ eugenics and Great Reset agenda.
See Also:
See Also:


healthimpactnews--2020-12-15--Coca Cola Tests COVID-19 Positive In Austrian Parliament

An Austrian parliamentary member exposed the defectiveness of the government ’ s COVID-19 tests by demonstrating in the parliament how a glass of Coca Cola tested positive for COVID-19 .
In footage from the meeting in Vienna Friday , FPO General Secretary Michael Schnedlitz brings a glass of Coca Cola to the podium , from which he proceeds to collect drops to use on an antigen rapid test being used on a mass scale .
After going to the lectern and starting his speech , the politician sprinkled few drops of cola on corona rapid test .
Three minutes later @ @ @ @ @ @ @ Cola was COVID-19 positive .
After demonstrating a positive result , Schnedlitz goes on to slam the tests as a waste of taxpayer resources .
“ Mr .
President , we are likely to have a problem now , we have a positive corona test in parliament , namely this cola triggered a positive corona test .
I don ’ t know how to deal with it now !
With things like this you are throwing tens of millions of euros in tax money out of the window instead of providing real protection @ @ @ @ @ @ @ homes , instead of investing money in our hospitals .
The corona mass tests are worthless !
This was also shown by a simple experiment in parliament , in which a cola had a positive result !
But this black-green government spends tens of millions in tax money on precisely these tests.
” Earlier , the Tanzanian President John Magufuli growing suspicious of the World Health Organization ( WHO ) , decided to investigate the claims of the tests himself .
He sent the WHO samples of a goat , a papaya and @ @ @ @ @ @ @ which came COVID-19 positive .
Because of such massive COVID-19 false positive cases scandal , the Australian Government has scrapped a billion dollar coronavirus vaccine agreement with Australian biotech company CSL Limited to supply 51 million doses of a Covid-19 vaccine being developed by the University of Queensland after several trial participants returned false positive HIV test results .
It should be noted that the Portuguese appeals court has ruled that PCR tests are unreliable and that it is unlawful to quarantine people based solely on a PCR test .
A video clip @ @ @ @ @ @ @ with Dr. Kary Mullis , the man who developed the PCR test which is being used today to allegedly detect the COVID virus , has gone viral the past few days .
Speaking about how Anthony Fauci was falsely using the test back then to test for HIV , he criticizes Anthony Fauci who “ doesn ’ t know anything about anything ” and his refusal at the time to debate him about the HIV hoax .
Dr. Kary Mullis died in 2019 , just weeks before the COVID Plandemic was launched .
@ @ @ @ @ @ @ : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler , MeWe , and Gab !
If our website is seized and shut down , find us on Parler , MeWe and Gab for further instructions about where to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

by GreatGameIndia.com
An Austrian parliamentary member exposed the defectiveness of the government’s COVID-19 tests by demonstrating in the parliament how a glass of Coca Cola tested positive for COVID-19.
In footage from the meeting in Vienna Friday, FPO General Secretary Michael Schnedlitz brings a glass of Coca Cola to the podium, from which he proceeds to collect drops to use on an antigen rapid test being used on a mass scale.
After going to the lectern and starting his speech, the politician sprinkled few drops of cola on corona rapid test. Three minutes later the test showed a result: Coca Cola was COVID-19 positive.
After demonstrating a positive result, Schnedlitz goes on to slam the tests as a waste of taxpayer resources.
“Mr. President, we are likely to have a problem now, we have a positive corona test in parliament, namely this cola triggered a positive corona test. I don’t know how to deal with it now! With things like this you are throwing tens of millions of euros in tax money out of the window instead of providing real protection for old people’s and nursing homes, instead of investing money in our hospitals. The corona mass tests are worthless! This was also shown by a simple experiment in parliament, in which a cola had a positive result! But this black-green government spends tens of millions in tax money on precisely these tests.”
Earlier, the Tanzanian President John Magufuli growing suspicious of the World Health Organization (WHO), decided to investigate the claims of the tests himself. He sent the WHO samples of a goat, a papaya and a quail for testing, all of which came COVID-19 positive.
Because of such massive COVID-19 false positive cases scandal, the Australian Government has scrapped a billion dollar coronavirus vaccine agreement with Australian biotech company CSL Limited to supply 51 million doses of a Covid-19 vaccine being developed by the University of Queensland after several trial participants returned false positive HIV test results.
It should be noted that the Portuguese appeals court has ruled that PCR tests are unreliable and that it is unlawful to quarantine people based solely on a PCR test.
Read the full article at GreatGameIndia.com.
A video clip from an older interview several years ago with Dr. Kary Mullis, the man who developed the PCR test which is being used today to allegedly detect the COVID virus, has gone viral the past few days.
Speaking about how Anthony Fauci was falsely using the test back then to test for HIV, he criticizes Anthony Fauci who “doesn’t know anything about anything” and his refusal at the time to debate him about the HIV hoax.
Dr. Kary Mullis died in 2019, just weeks before the COVID Plandemic was launched.
See Also:


healthimpactnews--2020-12-14--Planned Surveillance and Control by Global Technocrats: A Big-Picture Look at the Current Pandemic B

“ Planned Surveillance and Control by Global Technocrats : A Big-Picture Look at the Current Pandemic Beneficiaries , ” a peer-reviewed article by Children ’ s Health Defense , has been accepted for publication in the journal , International Journal of Vaccine Theory , Practice and Research .
The journal was launched in 2020 by John W. Oller , Jr. , Ph.D. ( editor-in-chief ) and Christopher A. Shaw , Ph.D. ( senior editor ) “ to make independent research , free from constraints of monetary , political , or any other undisclosed influence , about vaccine theory and practice @ @ @ @ @ @ @ Health Defense article , which will appear in the journal by year ’ s end , assesses how the pandemic has facilitated a financial , tech , biopharmaceutical and military-intelligence push for centralized , technocratic control .
Global financial patterns and pronouncements point to a seismic overhaul of governance and financial systems that is playing out beneath the surface of the Covid-19 pandemic , reaching far beyond the health domain .
Increased centralized control has the potential to create an unbridgeable chasm between a tiny handful of winners and a majority of losers @ @ @ @ @ @ @ the technocratic and financial forces and agendas at play , this rapid review identifies some of the pandemic ’ s principal beneficiaries across the interwoven financial , tech , biopharmaceutical , and military-intelligence sectors , assessing developments in the context of the accelerating global push for technocratic consolidation and control .
The evidence suggests that Trojan horse coronavirus vaccines may challenge bodily integrity and informed consent in entirely new ways , transporting invasive technologies into people ’ s brains and bodies .
Technologies such as brain-machine interfaces , digital identity tracking devices , @ @ @ @ @ @ @ central banking goal of replacing currencies with digital transaction and identification systems and creating a global control grid that connects the world population to the military-pharma-intelligence cloud of the global technocrats .
Moreover , using vaccines as a delivery vehicle for surveillance technologies cancels any legal liability .
President Dwight Eisenhower ’ s farewell speech at the end of his 8 years in office , on January 17 , 1961 , where he warned about the danger of the technocrats .
One quote : Today , the solitary inventor tinkering in his shop @ @ @ @ @ @ @ scientists .
In laboratories and testing fields in the same fashion , the free university , historically the fountain head of free ideas and scientific discovery , has experienced a revolution in the conduct of research .
Partly because of the huge cost of research , a government contract becomes virtually a substitute for intellectual curiosity .
For every old blackboard there are now hundreds of new electronic computers .
The prospect of domination of the nation ’ s scholars by federal employment , project allocations , and the power of money is @ @ @ @ @ @ @ be regarded .
Yet in holding scientific research and discovery in respect , as we should , we must also be alert to the equal and opposite danger that public policy could itself become the captive of a scientific technological elite .
Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler , MeWe , and Gab !
If our website is seized and shut down , find us on Parler , MeWe and Gab for further instructions about where @ @ @ @ @ @ @ Behind the Plandemic and Rioting to Usher in the New World Order

by Children’s Health Defense
“Planned Surveillance and Control by Global Technocrats: A Big-Picture Look at the Current Pandemic Beneficiaries,” a peer-reviewed article by Children’s Health Defense, has been accepted for publication in the journal, International Journal of Vaccine Theory, Practice and Research.
The journal was launched in 2020 by John W. Oller, Jr., Ph.D. (editor-in-chief) and Christopher A. Shaw, Ph.D. (senior editor) “to make independent research, free from constraints of monetary, political, or any other undisclosed influence, about vaccine theory and practice freely accessible.”
The Children’s Health Defense article, which will appear in the journal by year’s end, assesses how the pandemic has facilitated a financial, tech, biopharmaceutical and military-intelligence push for centralized, technocratic control.
Here’s the article:
Abstract
Global financial patterns and pronouncements point to a seismic overhaul of governance and financial systems that is playing out beneath the surface of the Covid-19 pandemic, reaching far beyond the health domain.
Increased centralized control has the potential to create an unbridgeable chasm between a tiny handful of winners and a majority of losers.
To foster an integrated analysis of the technocratic and financial forces and agendas at play, this rapid review identifies some of the pandemic’s principal beneficiaries across the interwoven financial, tech, biopharmaceutical, and military-intelligence sectors, assessing developments in the context of the accelerating global push for technocratic consolidation and control.
The evidence suggests that Trojan horse coronavirus vaccines may challenge bodily integrity and informed consent in entirely new ways, transporting invasive technologies into people’s brains and bodies.
Technologies such as brain-machine interfaces, digital identity tracking devices, and cryptocurrency-compatible chips would contribute to the central banking goal of replacing currencies with digital transaction and identification systems and creating a global control grid that connects the world population to the military-pharma-intelligence cloud of the global technocrats.
Moreover, using vaccines as a delivery vehicle for surveillance technologies cancels any legal liability.
Read the full study at Children’s Health Defense.
President Dwight Eisenhower’s farewell speech at the end of his 8 years in office, on January 17, 1961, where he warned about the danger of the technocrats. One quote:
Today, the solitary inventor tinkering in his shop has been overshadowed by task forces of scientists. In laboratories and testing fields in the same fashion, the free university, historically the fountain head of free ideas and scientific discovery, has experienced a revolution in the conduct of research. Partly because of the huge cost of research, a government contract becomes virtually a substitute for intellectual curiosity. For every old blackboard there are now hundreds of new electronic computers. The prospect of domination of the nation’s scholars by federal employment, project allocations, and the power of money is ever present, and is greatly to be regarded. Yet in holding scientific research and discovery in respect, as we should, we must also be alert to the equal and opposite danger that public policy could itself become the captive of a scientific technological elite.
Watch the full speech:
See Also:


healthimpactnews--2020-12-15--Cornell University Makes Flu Vaccination Mandatory – but Only for White Students

This news report is another example of how vaccines are not about “ health ” or “ disease prevention , ” but part of the eugenics movement for social engineering and population control .
Cornell Offers Exemption to Flu Vaccine for ‘ People of Color ’ Because of “ historical injustices and current events , ” Cornell University will grant an exemption from the requirement for all students to get a flu vaccination for “ people of color.
” Most of us are far too logical to follow the reasoning of this exemption .
Apparently , because of “ systemic @ @ @ @ @ @ @ United States , “ individuals from some marginalized communities may have concerns about needing to agree to such requirements.
” For example , historically , the bodies the of Black , Indigenous , and other People of Color ( BIPOC ) have been mistreated , and used by people in power , sometimes for profit or medical gain .
It is understandable that the current Compact requirements may feel suspect or even exploitative to some BIPOC members of the Cornell community .
Additionally , recent acts of violence against Black people by law @ @ @ @ @ @ @ or powerlessness .
Yes , but what does any of this have to do with not getting a flu shot ?
Police are not giving the flu shot .
Why should that matter ?
At the same time , we know that long-standing social inequalities and health disparities have resulted in COVID-19 disproportionately affecting BIPOC individuals .
Higher percentages of individuals from these communities become infected with COVID , and the health outcomes related to infection are often more serious .
Away from campus community , BIPOC individuals are not as likely to @ @ @ @ @ @ @ health care .
The systems , services , and policies being implemented at Cornell seek to address these inequalities as well as the differential impacts .
Huh ?
What does getting sick from COVID because you ’ re a “ person of color ” have to do with the flu ?
The flu and COVID are two different diseases .
In fact .
because a weakened immune system makes any person — colorful or not — more susceptible to COVID-19 , shouldn ’ t people of color demand they get flu shots first @ @ @ @ @ @ @ problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler , MeWe , and Gab !
If our website is seized and shut down , find us on Parler , MeWe and Gab for further instructions about where to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

Comments by Brian Shilhavy – Editor of Health Impact News
This news report is another example of how vaccines are not about “health” or “disease prevention,” but part of the eugenics movement for social engineering and population control.
Cornell Offers Exemption to Flu Vaccine for ‘People of Color’
by Rick Moran
PJ Media
Excerpts:
Because of “historical injustices and current events,” Cornell University will grant an exemption from the requirement for all students to get a flu vaccination for “people of color.”
Most of us are far too logical to follow the reasoning of this exemption. Apparently, because of “systemic racism and health inequities” in the United States, “individuals from some marginalized communities may have concerns about needing to agree to such requirements.”
Further,:
For example, historically, the bodies the of Black, Indigenous, and other People of Color (BIPOC) have been mistreated, and used by people in power, sometimes for profit or medical gain. It is understandable that the current Compact requirements may feel suspect or even exploitative to some BIPOC members of the Cornell community. Additionally, recent acts of violence against Black people by law enforcement may contribute to feelings of distrust or powerlessness.
Yes, but what does any of this have to do with not getting a flu shot? Police are not giving the flu shot. Why should that matter?
At the same time, we know that long-standing social inequalities and health disparities have resulted in COVID-19 disproportionately affecting BIPOC individuals. Higher percentages of individuals from these communities become infected with COVID, and the health outcomes related to infection are often more serious. Away from campus community, BIPOC individuals are not as likely to have access to preventive services or quality health care. The systems, services, and policies being implemented at Cornell seek to address these inequalities as well as the differential impacts.
Huh? What does getting sick from COVID because you’re a “person of color” have to do with the flu? The flu and COVID are two different diseases. In fact. because a weakened immune system makes any person — colorful or not — more susceptible to COVID-19, shouldn’t people of color demand they get flu shots first instead of getting an exemption?
Read the full article at PJ Media.
See Also:


healthimpactnews--2020-12-15--Vaccinated Israelis to Receive “Free Movement” Waivers as 50% to 75% are Unwilling to take Experimen

Vaccinated Israelis to Receive “Free Movement” Waivers as 50% to 75% are Unwilling to take Experimental COVID19 Vaccine

Health Ministry says holders of ‘ green passports ’ will be able to attend public events and eat at restaurants ; recent polls reveal 50 % to 75 % of Israelis are unwilling to take the jab over concerns it had been developed too fast Israelis who choose to get vaccinated against coronavirus will receive “ free movement ” waivers , allowing them to bypass certain health restrictions , the Health Ministry has said .
Prime Minister Benjamin Netanyahu said last week that Israel will begin administrating coronavirus vaccinations on December 27 and that Israel was ready to vaccinate 60,000 @ @ @ @ @ @ @ of the Pfizer vaccine arrived in Israel last week via special charter flights .
The so-called “ green passports ” will be handed out only after the second shot is administered since Pfizer vaccine requires two jabs in order to be effective .
Holders of the passports will be able to attend public events and eat at restaurants among other things , Health Ministry Director-General Chezy Levy told Channel 12 on Sunday .
They will also not be required to enter mandatory quarantine after contact with a confirmed patient or after returning from @ @ @ @ @ @ @ Those travelling will also not be required to take a mandatory COVID-19 test before leaving the country .
Having problems receiving our newsletters ?
See : How to Beat Internet Censorship and Create Your Own Newsfeed We Are Now on Parler , MeWe , and Gab !
If our website is seized and shut down , find us on Parler , MeWe and Gab for further instructions about where to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

Health Ministry says holders of ‘green passports’ will be able to attend public events and eat at restaurants; recent polls reveal 50% to 75% of Israelis are unwilling to take the jab over concerns it had been developed too fast
by Ynet News
Excerpts:
Israelis who choose to get vaccinated against coronavirus will receive “free movement” waivers, allowing them to bypass certain health restrictions, the Health Ministry has said.
Prime Minister Benjamin Netanyahu said last week that Israel will begin administrating coronavirus vaccinations on December 27 and that Israel was ready to vaccinate 60,000 people a day. Thousands of doses of the Pfizer vaccine arrived in Israel last week via special charter flights.
The so-called “green passports” will be handed out only after the second shot is administered since Pfizer vaccine requires two jabs in order to be effective.
Holders of the passports will be able to attend public events and eat at restaurants among other things, Health Ministry Director-General Chezy Levy told Channel 12 on Sunday.
They will also not be required to enter mandatory quarantine after contact with a confirmed patient or after returning from a “red country” abroad.
Those travelling will also not be required to take a mandatory COVID-19 test before leaving the country.
Read the full article at: Ynet News.
See Also:


healthimpactnews--2020-12-15--The COVID mRNA Vaccine and the Commercial Conquest of the Planet: The Plan

The two companies ’ BNT162b2 has become the first COVID-19 vaccine allowed in the Western world as drug regulators in the U.K. doled out an emergency use authorization on Wednesday , ahead of decisions by the U.S. and Europe , which are expected soon .
For the broader vaccine world , the Medicines and Healthcare products Regulatory Agency ’ s decision means the world now has the first mRNA shot authorized for widespread use , opening up a brand-new chapter for vaccine development .
( FiercePharma Vaccine Trade Publication , December 2 , 2020 ) The COVID Vaccine and the @ @ @ @ @ @ @ Plan For the past 30 years , I ’ ve written about the dangers and ineffectiveness of vaccines , including the new COVID vaccine .
I ’ ve written about cutting edge nanotechnology research and its use , in vaccines , as implanted sensors , which would surveil body and brain processes in real time , and also send instructions to the body and brain .
I ’ ve written about the absurdity of basic vaccine theory ; the unproven notion that the body needs a “ rehearsal , ” in order to @ @ @ @ @ @ @ I ’ ve written about how vaccines , in suppressing the immune system and its full inflammatory response , also suppress the outward signs of diseases , thus presenting a false picture of conquest of those diseases—when in fact the overall health and vitality of the body are reduced .
I ’ ve written about how criminal word games are played .
For example , vaccines causing brain damage in children are shunted into a category called “ autism ” ; and then , researchers claim autism is a separate disease with a @ @ @ @ @ @ @ about the destructive effects of a hundred years of wall-to-wall promotion of the one-disease-one-germ lie .
I ’ ve written about DNA vaccines permanently altering the genetic makeup of the recipients .
I ’ ve written about vaccines used to cause miscarriages in women when they later become pregnant .
But this article is about something else .
It ’ s about the dawn of a new pharmaceutical era , which was born the moment the Pfizer/BioNTech COVID vaccine was approved .
This marks the first time RNA technology deployed in a drug @ @ @ @ @ @ @ finish line and conditionally certified as safe and effective—which it is not .
But no matter .
Bill Gates and other elite planners and money titans have won what for them is a great victory .
Because RNA vaccines are much faster , easier , and cheaper to produce than traditional vaccines .
Instead of years in the making , they can be developed in months .
Whole lists of so-called diseases—West Nile , Bird Flu , Zika , Swine Flu , SARS—can now be brought to soaring profits by making RNA vaccines @ @ @ @ @ @ @ only that , a whole parade of older vaccines—hepatitis , measles , seasonal flu , diphtheria , whooping cough , tetanus , etc.
, can be recast with brand new updated RNA versions .
Researchers can pretend to discover a whole slew of “ new viruses ” that require RNA vaccines jammed into the marketplace in record time .
Don ’ t forget the domesticated animal market ; RNA vaccines for every conceivable invented purpose sold to big corporations that operate cattle , pig , chicken , and fish “ factories.
” We @ @ @ @ @ @ @ of dollars .
More dollars than Amazon dreams of .
This is why the Pfizer RNA COVID vaccine is first in line , and why the Moderna RNA vaccine is next .
Quick , easy , and cheap RNA technology will mean endless numbers of new vaccines .
And therefore , a day will come when every person routinely takes a DNA test to establish a profile , and every profile will be fitted to customized sets of vaccines .
In the same way that cosmetics are designed for every shade of skin @ @ @ @ @ @ @ every DNA profile .
The whole apparatus will be a highly dangerous and ineffective hoax , but what else is new ?
Vaccines have been a hoax since the beginning .
We ’ re talking about MONEY .
So much money , pharmaceutical companies will be bankrolled directly by governments , after a currency reset makes new money invented out of thin air replace the old “ thin air money.
” Patients will receive all these vaccines “ for free.
” Governments will pay the vaccines companies .
UNLESS THESE LUNATICS ARE STOPPED @ @ @ @ @ @ @ the vaccines—no matter what .
If you think the futuristic vaccine-world I ’ m describing could only be a fantasy , what would masks , distancing , lockdowns , and planetary destruction of national economies have been called 15 years ago ?
Think of past vaccines as giant clunky IBM computers sitting in empty rooms…and future vaccines as cell phones carried by billions of people .
Because RNA technology opened the door to faster , easier , and cheaper production .
What remains the same—past , present , and future—is FREEDOM .
The @ @ @ @ @ @ @ mean it , come hell or high water .
CODA : What could be more awkward and foolish than the Pfizer regimen for their COVID vaccine ?
A first shot followed by a later booster .
I don ’ t care how many apps and reminders are built into this system .
The fall-off from the first shot to the second will be enormous .
People will opt out , after they experience severe adverse effects from the initial injection .
They ’ ll forget to show up according to the prescribed schedule @ @ @ @ @ @ @ the Pfizer and Moderna clinical trials of their vaccines were only designed to prevent mild illness—a cough , or chills and fever .
Not serious illness .
Not hospitalization .
Not death .
And cough , chills , and fever cure themselves .
No need for a vaccine .
But none of this makes any difference to the vaccine kings .
They and their public health colleagues can easily rig COVID case numbers in a downward direction—and then claim the success of the vaccine is the reason and the cause .
No , @ @ @ @ @ @ @ approval of the vaccine was planting the flag of RNA technology in the marketplace .
This is the equivalent of building the first railroad tracks , digging the first big canals , flying the first air freight carriers .
New markets , new products , new customers , new money .
Marry these with a vast weakening of human vitality and a strengthening of control over populations , through vaccination , and you have the fascist Holy Grail .
Resistance and revolt are not luxuries .
Having problems receiving our newsletters ?
See @ @ @ @ @ @ @ Create Your Own Newsfeed We Are Now on Parler , MeWe , and Gab !
If our website is seized and shut down , find us on Parler , MeWe and Gab for further instructions about where to find us .
Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

Pfizer and BioNTech have made history.
The two companies’ BNT162b2 has become the first COVID-19 vaccine allowed in the Western world as drug regulators in the U.K. doled out an emergency use authorization on Wednesday, ahead of decisions by the U.S. and Europe, which are expected soon.
For the broader vaccine world, the Medicines and Healthcare products Regulatory Agency’s decision means the world now has the first mRNA shot authorized for widespread use, opening up a brand-new chapter for vaccine development.
(FiercePharma Vaccine Trade Publication, December 2, 2020)
The COVID Vaccine and the Commercial Conquest of the Planet: The Plan
by Jon Rappoport
NoMoreFakeNews.com
For the past 30 years, I’ve written about the dangers and ineffectiveness of vaccines, including the new COVID vaccine.
I’ve written about cutting edge nanotechnology research and its use, in vaccines, as implanted sensors, which would surveil body and brain processes in real time, and also send instructions to the body and brain.
I’ve written about the absurdity of basic vaccine theory; the unproven notion that the body needs a “rehearsal,” in order to prepare for the “real disease.”
I’ve written about how vaccines, in suppressing the immune system and its full inflammatory response, also suppress the outward signs of diseases, thus presenting a false picture of conquest of those diseases—when in fact the overall health and vitality of the body are reduced.
I’ve written about how criminal word games are played. For example, vaccines causing brain damage in children are shunted into a category called “autism”; and then, researchers claim autism is a separate disease with a genetic cause.
I’ve written about the destructive effects of a hundred years of wall-to-wall promotion of the one-disease-one-germ lie.
I’ve written about DNA vaccines permanently altering the genetic makeup of the recipients.
I’ve written about vaccines used to cause miscarriages in women when they later become pregnant.
But this article is about something else.
It’s about the dawn of a new pharmaceutical era, which was born the moment the Pfizer/BioNTech COVID vaccine was approved.
This marks the first time RNA technology deployed in a drug or vaccine has been dragged across the finish line and conditionally certified as safe and effective—which it is not.
But no matter. Bill Gates and other elite planners and money titans have won what for them is a great victory.
Because RNA vaccines are much faster, easier, and cheaper to produce than traditional vaccines.
Instead of years in the making, they can be developed in months.
And this means…bonanza.
Whole lists of so-called diseases—West Nile, Bird Flu, Zika, Swine Flu, SARS—can now be brought to soaring profits by making RNA vaccines to “prevent them.”
And not only that, a whole parade of older vaccines—hepatitis, measles, seasonal flu, diphtheria, whooping cough, tetanus, etc., can be recast with brand new updated RNA versions.
Researchers can pretend to discover a whole slew of “new viruses” that require RNA vaccines jammed into the marketplace in record time.
Don’t forget the domesticated animal market; RNA vaccines for every conceivable invented purpose sold to big corporations that operate cattle, pig, chicken, and fish “factories.”
We’re talking about trillions and trillions of dollars. More dollars than Amazon dreams of.
This is why the Pfizer RNA COVID vaccine is first in line, and why the Moderna RNA vaccine is next.
Quick, easy, and cheap RNA technology will mean endless numbers of new vaccines. And therefore, a day will come when every person routinely takes a DNA test to establish a profile, and every profile will be fitted to customized sets of vaccines.
In the same way that cosmetics are designed for every shade of skin tone, vaccines will be designed for every DNA profile.
The whole apparatus will be a highly dangerous and ineffective hoax, but what else is new? Vaccines have been a hoax since the beginning. We’re talking about MONEY.
So much money, pharmaceutical companies will be bankrolled directly by governments, after a currency reset makes new money invented out of thin air replace the old “thin air money.” Patients will receive all these vaccines “for free.” Governments will pay the vaccines companies.
UNLESS THESE LUNATICS ARE STOPPED.
Unless the people rebel and refuse the vaccines—no matter what.
If you think the futuristic vaccine-world I’m describing could only be a fantasy, what would masks, distancing, lockdowns, and planetary destruction of national economies have been called 15 years ago?
Think of past vaccines as giant clunky IBM computers sitting in empty rooms…and future vaccines as cell phones carried by billions of people.
Because RNA technology opened the door to faster, easier, and cheaper production.
What remains the same—past, present, and future—is FREEDOM.
The natural right to say NO. And mean it, come hell or high water.
CODA: What could be more awkward and foolish than the Pfizer regimen for their COVID vaccine? A first shot followed by a later booster.
I don’t care how many apps and reminders are built into this system. The fall-off from the first shot to the second will be enormous. People will opt out, after they experience severe adverse effects from the initial injection. They’ll forget to show up according to the prescribed schedule.
As I’ve detailed, the Pfizer and Moderna clinical trials of their vaccines were only designed to prevent mild illness—a cough, or chills and fever. Not serious illness. Not hospitalization. Not death. And cough, chills, and fever cure themselves. No need for a vaccine.
But none of this makes any difference to the vaccine kings. They and their public health colleagues can easily rig COVID case numbers in a downward direction—and then claim the success of the vaccine is the reason and the cause.
No, commercially speaking, the point of gaining approval of the vaccine was planting the flag of RNA technology in the marketplace.
This is the equivalent of building the first railroad tracks, digging the first big canals, flying the first air freight carriers.
New markets, new products, new customers, new money.
Marry these with a vast weakening of human vitality and a strengthening of control over populations, through vaccination, and you have the fascist Holy Grail.
Resistance and revolt are not luxuries.
They’re necessities of life.
Read the full article at NoMoreFakeNews.com.
See Also: