US Military is Working on COVID Vaccine and Implantable Microchips

The Pentagon’s Defense Advanced Research Projects Agency (DARPA) is working on a COVID vaccine that will work on all variants and it has developed an implantable microchip that it says will monitor everyone for signs of the virus. Retired Colonel Matt Hepburn, an army infectious disease physician heading up DARPA’s response to the pandemic, appeared on 60 Minutes to demonstrate the technology that he said acts as a ‘check engine light’. He said that DARPA has developed a filter to remove the virus from the blood via a dialysis machine, already approved by the FDA, and that it already has been used on 300 patients. -GEG

The Pentagon’s Defense Advanced Research Projects Agency (DARPA) is working on a COVID vaccine that will work on all variants and has developed an implantable microchip that it says will continuously monitor the human body for signs of the virus.

Retired Colonel Matt Hepburn, an army infectious disease physician heading up DARPA’s response to the pandemic, appeared on 60 Minutes to demonstrate the technology.

Holding up a vial of green tissue-like gel, which contains the chip, Hepburn proclaimed “You put it underneath your skin and what that tells you is that there are chemical reactions going on inside the body, and that signal means you are going to have symptoms tomorrow.”

“It’s like a ‘check engine’ light,” Hepburn added, noting that those with the chip “would get the signal, then self-administer a blood draw and test themselves on site.”

“We can have that information in three to five minutes,” Hepburn continued, adding “As you truncate that time, as you diagnose and treat, what you do is you stop the infection in its tracks.”

Hepburn also declared that DARPA has developed a filter to remove the virus from the blood via a dialysis machine, and that the FDA has approved it, and it has already been used on 300 patients.

Read full article here…




Report: Maddie, a 12-Year Old Girl Enrolled in a COVID-19 Vaccine Trial for Children, Has Severe Injuries

COVID-19 vaccine manufacturers are now conducting clinical trials on children age 6 months to 12 years old. The children are volunteered by their parents who sign them up for the unethical trials. A young woman on Youtube, whose channel is called WhatsHerFace, reported on Facebook posts and her communications with the family of a 12-year old girl named Maddie who was severely damaged after taking part in a COVID-19 vaccine trial. Maddie’s injuries include paralyzation from the waist down, inability to urinate on her own, a bowel obstruction, excruciating pain, fainting episodes and other neurological problems. It was unclear which vaccine, Pfizer, Moderna or Johnson and Johnson, she received.




In World First, Denmark Ditches AstraZeneca’s COVID-19 Shot. Health Minister Faints During Announcement.

Denmark became the first country to stop using AstraZeneca’s COVID-19 vaccine altogether over a potential link to a rare but serious form of blood clot. Many countries in Europe and elsewhere have resumed using the shot, with some restricting it to certain age groups, mostly those aged above 50 or above 60. Denmark suspended the use of the Johnson and Johnson vaccine that has been delayed in Europe over similar clotting concerns.

The head of Denmark’s medicines agency, Tanja Erichsen, collapsed during a press conference on the decision to stop using the Oxford-AstraZeneca COVID vaccine. It was reported that she went to the hospital and has recovered.

* Country stops using vaccine after blood clot reports

* Side-effects “real and serious” – health agency head

* AstraZeneca says it respects Denmark’s decision

* Denmark has also paused use of J&J vaccine (Adds J&J context, Astra comment)

By Nikolaj Skydsgaard and Jacob Gronholt-Pedersen

COPENHAGEN, April 14 (Reuters) – Denmark on Wednesday became the first country to stop using AstraZeneca’s COVID-19 vaccine altogether over a potential link to a rare but serious form of blood clot.

The decision will push back the scheduled conclusion of Denmark’s vaccination scheme to early August from July 25, health authorities said.

But that new timeline assumes it will start using the Johnson & Johnson vaccine, whose rollout in Europe has been delayed over similar clotting concerns and the use of which Denmark has suspended. That shot comprises around a third of the country’s total contracted supply.

Results of investigations into the AstraZeneca-associated blood clots “showed real and serious side-effects,” Danish health agency head Soren Brostrom told a news briefing.

“We have therefore chosen to continue the vaccination programme for all target groups without this vaccine.”

Astrazeneca said it respected Denmark’s choice and would continue to provide it with data to inform future decisions.

Read full article here…

Gateway Pundit:   https://www.thegatewaypundit.com/2021/04/head-denmarks-health-agency-keels-drops-unconscious-presser-decision-stop-using-astrazeneca-vaccines-happens-vaccinated/




Former Chief Scientist for Pfizer Makes Shocking Revelations, Says New Vaccines Will Skip Clinical Trials

Dr. Mike Yeadon, former Vice President and Chief Scientist of Allergy and Respiratory Research for Pfizer, says the COVID-19 virus has yet to be produced for study, even after more than one year into the ‘pandemic’. He also said the ‘top up’ booster vaccines for variants will be excused from clinical safety studies! He dropped a bombshell when he predicted that those who refuse vaccines will be coerced, and those who are left will be rounded up and thrown into prison camps. He warned that there is no benign explanation for mass vaccination and vaccine passports. [OK, if not benign, then what is the correct adjective? The answer is ‘sinister’.] -GEG

Listen to James Delingpole’s podcast audio interview with Dr. Mike Yeadon at this link:   https://delingpole.podbean.com/e/dr-mike-yeadon-1617215402/

Summary by JW Williams
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Dr. Mike Yeadon, PhD is the former Vice President Chief Scientist of Allergy and Respiratory Research for Pfizer. While Dr. Yeadon supports the COVID vaccine for a very small number of people at risk of dying, such as those over the age of 70 that have other serious health problems, but  he says it should not be given to people who are not in danger of dying. At the 30-minute mark in this interview, he said no one has isolated the virus. Therefore, it cannot be proven to be the cause of Covid-19 or any other illness. He explained that it is no threat to children and, therefore, there is no reason they should take the vaccine.
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He said it is unnecessary for new vaccines to be made for variants because the variants are so similar to the original that vaccines should immunize against the variants as well. Near the 40-minute mark, he made the stunning revelation that ‘top-up’ booster vaccines, updated for variants, are so similar to the original vaccines that they don’t require manufacturers to do clinical safety studies! He said there is no benign explanation for this.
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https://globalbiodefense.com/2021/03/19/why-well-get-covid-booster-vaccines-quickly-and-how-we-know-theyre-safe/
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He warned that there is no medical reason for vaccine passports as he says individuals who take the vaccine are immune and should not be worried if others want to skip the vaccine. He says that the passports will be used to coerce vaccines and to build a centralized database for totalitarian control.
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He dropped another bombshell when he said vaccines could be used to depopulate masses of people, without destroying the environment, while maintaining plausible deniability. He said that the new, gene-based technology should not be given to 100% of the population because it can cause irreversible damage. He went further and stated that those who refuse vaccines will be coerced, and those who are left will be rounded up and thrown into prison camps. He chastised doctors who are giving vaccines because they know that the vast majority of people are not at risk from dying from COVID, but will die from the vaccine, and that there is a bigger agenda at play.
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People cannot believe that such evil exists, but there is no benign explanation. He mentioned Stalin who said that one death is a tragedy, a million a statistic.
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He says that if a sufficient portion of people refuse the vaccine, the plan cannot complete. Don’t be coerced into something you don’t need. Human experimentation is illegal. There are laws against discrimination to protect unvaccinated people.



Nearly 40% Of Marines Refuse COVID-19 Vaccine

A report states that 38.9% of Marines, with an average age of 25, putting them at roughly 0.18% risk of death, are refusing to take the COVID-19 experimental vaccines when they have been given the choice to reject them. None of the COVID-19 vaccines have been proven to prevent people from testing positive for COVID-19, falling ill, or transmitting it. Approximately 75,500 marines have been vaccinated, while 48,000 have declined.

According to the report, 38.9% of Marines – with an average age of 25, putting them at roughly 0.18% risk of death, are refusing to take the jab – which doesn’t prevent one from getting COVID-19, falling ill, or transmitting it. Who could have guessed that extraordinarily fit people with a minimal chance of death don’t want to inject the most rushed vaccine in history.

“The Navy and Marine Corps are providing substantial educational information broadly, and working with commands to ensure Marines, Sailors, and beneficiaries have accurate information regarding the safety and efficacy of the vaccines to encourage individuals to get immunized,” said Marines spokesman, Capt. Andrew Wood, in a statement to The Hill, adding “We continue to make the vaccine available to Marines, Sailors, civilians, contractors and authorized beneficiaries based on the prioritization schedule listed in the [Department of Defense] population schema.”

According to the data, approximately 75,500 marines have been vaccinated, while 48,000 have declined. The overall acceptance rate is 61.1%. The figures include active-duty, reserves, and the Individual Mobilization Augmentee Marines, according to the CNN report.

The rate of declined vaccines was as high as 57% at Camp Lejeune in North Carolina.

Read full article here…




Midwin Charles: 47-Year-Old MSNBC Legal Analyst Dead After Experimental mRNA COVID Shot

Brooklyn defense attorney and television commentator Midwin Charles is dead 37 days after receiving at least one experimental COVID shot. Ms. Charles posted the trendy “I’m vaccinated” announcement on Twitter on March 1, and her family announced her death on April 6, just over a month after her first experimental shot. It is unknown if she received a second injection. This article points out that Ms. Charles was very active on social media, averaging 25 tweets per day since May 2009, but that number kept decreasing and was reduced to one on March 24, one on March 25, one was tweet was deleted on March 26, and then no more. Her second dose of experimental mRNA would have been due around March 21-22.

Midwin Charles was best known for being a legal analyst on MSNBC and CNN. This video shows segments of her criticizing people for not wearing masks, social distancing, etc.

Brooklyn defense attorney and television commentator Midwin Charles is dead after what appears to be several days of suffering after receiving at least one experimental COVID shot.

Ms. Charles posted the trendy “I’m vaccinated” announcement on Twitter on March 1.

The tweet is still live as of publishing. It is also archived.

Her next tweet jokes about her “death causing peanut allergy” and that her insurance did not cover the EpiPen costs.

She then retweeted a North Carolina professor talking about “black vax hesitancy.” An analysis of her tweet activity thereafter indicates that her health started deteriorating three weeks later.

Ms. Charles, 47, was always very active on Twitter. She averaged about 25 tweets per day since May 2009. Ms. Charles was even more active last month. She averaged 39 tweets/retweets per day from March 10 to March 20, according to Social Blade.

Read full article here…




FDA Suspends Experimental Johnson and Johnson COVID Shot Linked to Fatal Blood Clots

The FDA announced today that it was suspending the use of the Johnson and Johnson experimental COVID vaccine.  The CDC & FDA are reviewing data involving six reported US cases of a rare and severe type of blood clot in individuals after receiving the vaccine. Doctors said that an extremely rare immune response triggers the blood clots by sending signals in patients’ blood to clot. While they said they hadn’t seen complications with other vaccines, Dr. Marks said the US believes the problem in the Johnson and Johnson and AstraZeneca vaccines is “related” to the adenovirus platform.

The FDA announced today that it was recommending a pause in the use of the Johnson and Johnson experimental COVID vaccine “out of an abundance of caution.”

From their Twitter account:

Today FDA and @CDCgov issued a statement regarding the Johnson & Johnson #COVID19 vaccine. We are recommending a pause in the use of this vaccine out of an abundance of caution.

As of 4/12, 6.8m+ doses of the J&J vaccine have been administered in the U.S. CDC & FDA are reviewing data involving 6 reported U.S. cases of a rare & severe type of blood clot in individuals after receiving the vaccine. Right now, these adverse events appear to be extremely rare

Treatment of this specific type of blood clot is different from the treatment that might typically be administered.

CDC will convene a meeting of the Advisory Committee on Immunization Practices (ACIP) on Wednesday to further review these cases and assess their potential significance. FDA will review that analysis as it also investigates these cases.

Until that process is complete, we are recommending this pause. This is important to ensure that the health care provider community is aware of the potential for these adverse events and can plan due to the unique treatment required with this type of blood clot.

ZeroHedge News published some notes regarding the call:

The health officials who spoke on today’s call started by reiterating details about the decision to halt the J&J shared with the press earlier. Officials said they would update doctors with new vaccine “fact sheets” designated certain medications that could be associated with higher risks of blood clots.

After they said they were only seeing symptoms in patients who received the JNJ vaccine, the first question from the press (asked by an FT reporter) was: what about AstraZeneca? In Europe, governments have been imposing age limits on who can receive the AstraZeneca jab for similar reasons.

Officials responded by brushing the AZ question aside, before saying they hoped the halt would last for only a few days. Pressed about what’s causing the clots, doctors said that an extremely rare immune response triggers the blood clots by sending signals in patients’ blood to clot. While they said they hadn’t seen complications with other vaccines, Dr. Marks said the US believes the problem in the JNJ and AZ vaccines is “related” to the adenovirus platform, though he didn’t offer much in the way of details.

At one point, Dr. Marks said “the real thing that is so notable here is not just the cerebral blood clods…it’s their occurrence together that makes a pattern, and that pattern is very very similar to what was seen with another vaccine.”

A reporter for CNN mentioned that they were being told that this was something being “looked into” earlier, and Schuchat explained that the CDC had first looked into how best to advise the health-care community to treat and respond.

The FDA left open the possibility that new cases of blood clots could be brought to its attention. The FDA will actively search for vaccines. New guidance to be issued will help educate doctors and other health-care professionals about risk factors that could put patients at risk of the autoimmune reaction.

After offering examples of symptoms that would be on the list of potential warning signs, Dr. Marks was pressed to open up a bit more about symptoms after a doctor who was on the call asked him about specific symptoms seen by these patients. The doctor noted that listing “headaches” on a list of suspect symptoms or “abdominal pain” could lead to a lot more tests and doctor visits. At this, Marks seemed to have trouble putting a figure on the background rate of blood clots, and other questions about the prevalence of symptoms that could be seen on the FDA’s list.

“This is going to translate to a lot more doctors visits for people like me,” the doctor said.

The press briefing was ended soon after. Of course, it’s not difficult to understand why the FDA was starting to feel uncomfortable. A wave of patients being told to seek emergency care as a precaution could push ER occupancy rates higher again. Suddenly, the numbers will be telling us that we are back in the worst of the COVID pandemic.

Read the full article at ZeroHedge News.

Read full article here…




CDC Data Shows Number of COVID Vaccine Injuries Surpasses 50,000, According to VAERS

The CDC released data from the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccines that showed a total of 50,861 total adverse events were reported, including 2,249 deaths, between December 14, 2020, and March 26, 2021. A total of  136.7 million COVID vaccine doses had been administered. Other vaccine injuries include 341 pregnant women reporting adverse events, 578 cases of Bell’s Palsy, and 2,578 reports of anaphylaxis.

Data released today by the Centers for Disease Control and Prevention (CDC) on the number of injuries and deaths reported to the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccines revealed steadily rising numbers, but no new trends. VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.

Every Friday, VAERS makes public all vaccine injury reports received to the system as of Friday of the previous week. Today’s data show that between Dec. 14, 2020, and March 26, a total of 50,861 total adverse events were reported to VAERS, including 2,249 deaths — an increase of 199 over the previous seven days — and 7,726 serious injuries, up 631 over the same time period.

Of the 2,249 deaths reported as of March 26, 28% occurred within 48 hours of vaccination, 19% occurred within 24 hours and 43% occurred in people who became ill within 48 hours of being vaccinated.

In the U.S., 136.7 million COVID vaccine doses had been administered as of March 26.

This week’s VAERS data show:

  • 19% of deaths were related to cardiac disorders.
  • 45% of those who died were male, 43% were female and the remaining death reports did not include gender of the deceased.
  • The average age of those who died was 77.7 and the youngest death was an 18-year-old.
  • As of March 26, 341 pregnant women had reported adverse events related to COVID vaccines, including 104 reports of miscarriage or premature birth.
  • Of the 578 cases of Bell’s Palsy reported, 63% of cases were reported after Pfizer-BioNTech vaccinations — almost twice as many as reported (36%) following vaccination with the Moderna vaccine. Seven cases of Bell’s Palsy were reported with Johnson & Johnson (J&J) vaccine (1%).
  • There were 2,578 reports of anaphylaxis, with 53% of cases attributed to the Pfizer-BioNTech vaccine, 44% to Moderna and 3% to J&J vaccine, which was rolled out in the U.S. on March 2.
  • Using a broadened search for any reference to anaphylaxis in chart notes resulted in 15,193 reports, with 52% of cases attributed to Pfizer’s COVID vaccine, 45% to Moderna and 3% to J&J. With each vaccine, nearly 42% of anaphylactic reports occurred in people aged 17-44.

© 4/2/2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

Read full article here:  https://childrenshealthdefense.org/defender/covid-vaccine-injuries-vaers-cdc/




Two Young Adults Die Following Johnson and Johnson Experimental Vaccinations

Health Impact News says that he Johnson and Johnson vaccine is an adenovirus vaccine, and there are currently no approved adenovirus vaccines in the market. The news site says that Johnson and Johnson is now testing their experimental vaccine on the public as part of their Phase 3 trials after receiving an emergency use authorization.

Benjamin Goodman, 32, took the Johnson and Johnson Covid-19 vaccine, got a severe headache, and fell asleep. He was awakened by seizures and died in the early morning, less than 24 hours after taking the jab. He reportedly took the vaccine because he was worried about travel passes/ vaccine passports being used in New York. Desiree Penrod, a 25-year old pre-schoolteacher, took the same Johnson and Johnson vaccine in early March. She wrote on Facebook, “The vaccine is killing me today. My arm hurts, beyond exhausted, headache, stomach cramps and earaches. Multiple people told me that I looked pale today. Yesterday, I was fine but today it’s taking its toll on me.” Facebook flagged her post with a message about Covid-19 vaccines undergoing thorough testing procedures before being approved, dismissing Penrod’s complaints over the effects of the injection. She died six days later. Desiree had a pre-existing seizure disorder and had a seizure the day before she got the vaccine. It is unknown whether she received true informed consent about the risk of the shot as the Johnson & Johnson Clinical Trial reported that there were more seizures in the vaccine group than in the placebo group (4 seizures vs. 1 seizure).

Reports are now surfacing of people dying following the recently authorized Johnson and Johnson experimental COVID shots here in the United States.

The Johnson and Johnson experimental COVID “vaccine” is an “adenovirus” vaccine, and like the experimental mRNA “vaccines” from Pfizer and Moderna, there are currently no approved adenovirus vaccines in the market, although the military has used experimental adenovirus vaccines that are not FDA approved.

So by getting the FDA to issue an EUA, which they did on February 27th, Johnson and Johnson can now test their experimental vaccine on the public as part of their Phase 3 trials.

The vaccine is being produced in Belgium, by the same company that in the past produced the anthrax vaccine that destroyed the lives of so many military personnel.

Read full article here…

From Circle of Mamas:

Desiree Penrod was only 25 years old. She had a pre-existing seizure disorder and according to her Facebook page, she had a seizure on Monday, March 8th, one day before she got the vaccine.

She got the Johnson & Johnson vaccine, Janssen, on Tuesday, March 9th, and the very next day began feeling very unwell.

By Wednesday, March 11th, when she made her final Facebook post, she was very ill. She was found deceased in her home on March 17th.

Link: https://circleofmamas.com/health-news/25-year-old-desiree-penrod-dies-after-johnson-and-johnson-vaccine/




Another Italian Professor is Dead Following the AstraZeneca COVID Injection

The Italian press has reported on the AstraZeneca Covid injection-related deaths of two young professors, Ilaria Pappa from Ischia, Italy, and Zelia Guzzo from Gela, who died 12 days following taking the jab. There will be a criminal investigation into her medical records and the AstraZeneca vaccine. Earlier this month, another investigation was launched into AstraZeneca when a 57-year old music teacher died following the Covid injection. -GEG

As mass vaccination campaigns with experimental COVID injections now move on to the next demographic populations after beginning with senior citizens in assisted care facilities, and the healthcare workers in those facilities, the next targeted groups are educators.

We have seen multiple reports, for example, in the U.S. of entire school districts having to close down following a mass COVID injection campaign, as so many people get sick after the injections that there have not been enough employees in some school districts to hold classes right away following these massive injections.

Last week, I was informed of 3 deaths among faculty following COVID injections in one school district in Portland. But with nothing printed in the media and social media accounts silenced, I could not get collaborating evidence to publish those stories.

The Italian press, however, has now reported another death following the AstraZeneca COVID injection, a young professor from Gela, Italy. This follows our report from last week about 31-year-old Ilaria Pappa, a professor from Ischia, Italy, that The COVID Blog reported.

The professor from Gela is 37-year-old Zelia Guzzo. The Italian news publication quotidianodigela.it reports:

Zelia didn’t make it. After 12 days the professor died.

Only a miracle could have saved her, changing a clinical picture that already last week had appeared irreversible. Shortly before eight o’clock last night it was ascertained that for Zelia Guzzo, 37 years old, there was nothing more to do.

The 37-year-old teacher leaves her husband, also a teacher, and a young son. A tragedy that has shocked the family and all the colleagues where Zelia worked and was appreciated.

Twelve days ago the young woman had felt ill and had been forced to hospitalization first in the hospital, then urgently to Sant’Elia of Caltanissetta. Conditions made very serious because her condition was affected by a cerebral hemorrhage.

Three weeks ago she had received the Astrazeneca vaccine as well as all teachers in the province.

She had been breathing artificially for a week.

The prosecutor’s office of Gela has already started the first investigations to determine the possible causality with the vaccine she had received on March 1. A huge tragedy, which left in shock not only those who knew Zelia but the whole city.

Read full article here…




CDC Data Shows Almost Twice As Many Vaccine-Related Deaths in First 3 Months of 2021 than All Vaccine Deaths Combined over the Past Ten Years

The number of US deaths related to vaccines in 2021 in less than 3 months totals 1,755, which is almost double the number of deaths that were recorded over the past decade, with a total of 994 deaths. Although the percentage of individuals who have died from the COVID-19 ‘vaccine’ is minuscule (less than 0.003%) deaths in 2021 already are 71 times the average for the past decade. -GEG

There are more US deaths related to vaccines in 2021 in less than 3 months than there were the entire past decade. 

The number of deaths related to vaccines this year has absolutely skyrocketed.  According to the CDC’s own data, in 2021 in less than 3 months, we have already seen over 1,750 deaths due to vaccines in the US.

Read full article here…




New Mexico: First Court Case Against Mandatory Vaccination

New Mexico: Attorney Ana Garner represents her client Isaac Legaretta, an officer at the Doña Ana County Detention Center and former Marine, who is suing the county over its new policy for first responders to receive the COVID-19 vaccinations or face termination. As the first case of its kind, it may set a new standard for legal precedent regarding mandatory vaccination. There is a federal statute that requires that the recipient of a medical product with emergency use authorization must be fully informed and must consent because it is experimental. Garner has another lawsuit that challenges not only the Governor of New Mexico, but the emergency itself. If there ever was an emergency, it no longer exists, because the death counts are grossly inflated, PCR tests are meaningless, and asymptomatic transmission is a myth. -GEG

Watch video at Bitchute:  https://www.bitchute.com/video/ebHhNssHgQMd/

In this interview, which was initially banned by YouTube before it was even published (but now reversed), Spiro is joined by Attorney Ana Garner of New Mexico. Garner represents her client Isaac Legaretta, an officer at the Doña Ana County Detention Center and a military veteran, who is suing the county over its new policy for first responders to receive the COVID-19 vaccinations or face termination.

Attorney Garner explains the significance of this case and what is at stake, as it is the first of its kind and may set a new standard for legal precedent regarding mandatory vaccination. Garner says she is prepared to take this case to the Supreme Court if necessary.

Spiro and Ana Garner also discuss another case of hers that is ongoing currently. A case that challenges not only the Governor of New Mexico, but the emergency itself.

Read full article here…