Archive for the ‘Viruses’ Category

“Super-Fast” Lone Star Ticks Showing up in New Places

https://www.lymedisease.org/lyme-sci-super-fast-lone-star-ticks-are-showing-up-in-new-places/

LYME SCI: “Super-fast” lone star ticks are showing up in new places

March 30, 2022

By Lonnie Marcum

The lone star tick (Amblyomma americanum) has been rapidly expanding its range, from the Southern United States into the Northeast and Midwest.

This tick is a major vector of several viral, bacterial, and protozoan pathogens affecting humans, pets, livestock, birds and other wild animals in the United States. In some Midwestern states, it is commonly known as the “turkey tick” due to its association with wild turkeys. (Childs and Paddock, 2003)

Currently, the lone star tick is known to transmit human ehrlichiosis, tularemia, Heartland virus, Bourbon virus, Southern tick-associated rash illness (STARI) and rarely Rocky Mountain spotted fever—one of the deadliest tick-borne diseases in the US.

People bitten by a lone star tick may also develop alpha-gal syndrome—a severe allergy to meat and meat-related products.

A recent crowdsourced science project has documented the largest increase of the lone star tick in decades. Researchers documented new tick encounters in over 300 counties—including six new counties in western states—where these ticks had not been documented before.

TickSpotters program evaluates photos

In a study published in the Journal of Medical Entomology, researchers at the University of Rhode Island (URI) evaluated over 9,500 photos submitted between 2014-2019 to the TickSpotters surveillance program.

To document the changes, researchers first identified the ticks in the submitted photos, then logged the county each was reported from. They used this method to plot the geographic ranges of three medically important U.S. tick species: Amblyomma americanum, Ixodes scapularis and Ixodes pacificus. The last two are the vectors for Lyme disease.

More than 5,000 photographs of the lone star tick were received from over 1,000 counties across the US. Of those, 341 counties had no previous record of lone star ticks. The largest expansion of the lone star tick was seen in Illinois, Indiana, Kentucky, and Ohio.

In addition, the lone star tick was reported in several counties in the western US, a region not typically associated with these ticks. Notably, it was found in six new counties in California, four counties in Colorado and one new county each in Idaho, Oregon and Utah.

“The causative drivers of these upturns are complex, but have a lot to do with increased host availability, warming temperatures, and moisture availability,” researcher Heather L Kopsco, PhD, told Entomology Today,

Female lone star ticks are identifiable by a single silvery-white spot on the center of their back (scutum.) The male lone star tick is slightly smaller, with varied white streaks or spots around the margins of its body.

Finding Heartland virus in Georgia

Another recent study published in the CDC journal “Emerging Infectious Diseases” found lone star ticks infected by Heartland virus in Georgia. The article points out several major knowledge gaps and the complexity of diseases carried by the lone star tick. (Romer et al, 2022)

“Heartland is an emerging infectious disease that is not well understood,” says Emory University’s Gonzalo Vazquez-Prokopec PhD, senior author of the study.

Interestingly, the genetic analysis of the Heartland virus from Georgia shows that it is 2%-5% different from previous genetic sequences of the virus.

“These results suggest that the virus may be evolving very rapidly in different geographic locations, or that it may be circulating primarily in isolated areas and not dispersing quickly between those areas,” Vazquez-Prokopec says.

The Heartland virus wasn’t officially named until 2009. However, the CDC has since found evidence of it in wild animals in at least 13 states, including stored samples from deer dating back to 2001. (Clark et al, 2018)

Because the initial symptoms of these tick-borne viruses resemble the flu, and tests for it are not readily available, it is likely being undetected and underreported in humans.

Quick and aggressive

The lone star tick moves quickly and aggressively, says Thomas Mather, PhD, Director of the TickEncounter Resource Center and co-author of the URI study.

“It is super-fast. It can move from below your knees to the top of your head in a matter of seconds.” Mather says it is the tick most frequently found attached to humans in the South.

The greatest risk of being bitten by the adults exists in early spring through fall. Lone star ticks are found mostly in woodlands with dense undergrowth and around animal resting areas, where they will quest on tall grass and low hanging branches.

Nymphal ticks quest lower to the ground but also move fast. If you encounter a patch of larvae, you’ll find they may latch on by the hundreds. Tick Encounters recommends using sticky duct tape to remove these larvae as soon as possible.

Expanding range

The range of the lone star tick in North America has increased dramatically over the past 30 years. Large numbers have been recorded as far to the northeast as Maine, as far to the southeast as Florida, as far south as Mexico and as far west as Colorado. Recently, patchy encounters have also been noted in Canada and the West coast.

Diseases carried by lone star ticks

The following is a list of symptoms of diseases caused by the bite of the lone star tick per the CDC.

Alpha-gal Syndrome (AGS)

Reactions can include:

  • Rash
  • Hives
  • Nausea or vomiting
  • Heartburn or indigestion
  • Diarrhea
  • Cough, shortness of breath, or difficulty breathing
  • Drop in blood pressure
  • Swelling of the lips, throat, tongue, or eye lids
  • Dizziness or faintness
  • Severe stomach pain

Symptoms commonly appear 2-6 hours after eating meat or dairy products, or after exposure to products containing alpha-gal (for example, gelatin-coated medications). Personal products that use ingredients containing “hydrolyzed protein,” lanolin, glycerin, collagen, or tallow are particularly problematic.

AGS reactions can differ from person to person and range from mild to severe. Anaphylaxis (a potentially life-threatening allergic reaction involving multiple organ systems) may need urgent medical care.

People may not react after every alpha-gal exposure.

Seek immediate emergency care if you are having a severe allergic reaction.

Bourbon Virus

Scientists are still learning about possible symptoms caused by this virus.

People diagnosed with Bourbon virus disease had symptoms including:

  • fever
  • tiredness
  • rash
  • headache
  • other body aches
  • nausea, and

Patients with Bourbon virus will have low blood counts for cells that fight infection and help prevent bleeding.

There is no medicine to treat Bourbon virus disease. Doctors can only treat the symptoms. For example, some patients may need to be hospitalized and given intravenous fluids and treatment for pain and fever. Antibiotics don’t work against viruses.

Ehrlichiosis

Signs and symptoms of ehrlichiosis typically begin 1-2 weeks after the bite of an infected tick. Left untreated, ehrlichiosis can be fatal. Early treatment with doxycycline is highly effective.

Early signs and symptoms (the first 5 days of illness) are usually mild or moderate and may include:

  • Fever, chills
  • Severe headache
  • Muscle aches
  • Nausea, vomiting, diarrhea, loss of appetite
  • Confusion
  • Rash (more common in children)

About a third of people with ehrlichiosis report a rash, which can look like red splotches or pinpoint dots. This typically develops five days after the fever begins.

Early treatment can reduce your risk of developing severe illness, which can include:

  • Damage to the brain or nervous system (e.g. inflammation of the brain and surrounding tissue (called meningoencephalitis))
  • Respiratory failure
  • Uncontrolled bleeding
  • Organ failure
  • Death
Heartland Virus
  • Most people infected with Heartland virus experience fever, fatigue, decreased appetite, headache, nausea, diarrhea, and muscle or joint pain. Many require hospitalization.
  • Some people also have lower than normal counts of white blood cells (cells that help fight infections) and lower than normal counts of platelets (which help clot blood). Sometimes, liver enzymes are elevated.
  • It can take up to two weeks for symptoms to appear after an infected tick bite.
Rocky Mountain Spotted Fever

Early signs and symptoms are not specific to RMSF. However, the disease can rapidly progress to a life-threatening illness.

Signs and symptoms can include:

  • Fever
  • Headache
  • Rash
  • Nausea
  • Vomiting
  • Stomach pain
  • Muscle pain
  • Lack of appetite

While almost all patients with RMSF will develop a rash, it often does not appear early in illness, which can make RMSF difficult to diagnose. RMSF rash usually develops 2-4 days after fever begins. The appearance of the rash can vary widely. Some rashes look like red splotches and some look like pinpoint dots.

Some patients who survive severe RMSF may be left with permanent damage, including amputation of arms, legs, fingers, or toes (from damage to blood vessels in these areas); hearing loss; paralysis; or mental disability.

Southern tick-associated rash illness (STARI)

It is not known whether antibiotic treatment is necessary or beneficial for patients with STARI. Nevertheless, because STARI resembles early Lyme disease, physicians will often treat patients with oral antibiotics.

The rash of STARI is a red, expanding “bull’s-eye” lesion that develops around the site of a lone star tick bite. The rash usually appears within seven days of the tick bite and expands to a diameter of three inches or more. The rash should not be confused with much smaller areas of redness and discomfort that can occur commonly at the site of any tick bite.

Patients may also experience fatigue, headache, fever, and muscle pains. The saliva from lone star ticks can be irritating; redness and discomfort at a bite site does not necessarily indicate an infection.

Tularemia

The signs and symptoms of tularemia vary depending on how the bacteria enter the body. Illness ranges from mild to life-threatening. All forms are accompanied by fever, which can be as high as 104 °F.

“Ulceroglandular” is the most common form of tularemia and usually occurs following a tick or deer fly bite or after handing an infected animal. A skin ulcer appears at the site where the bacteria entered the body. The ulcer is accompanied by swelling lymph glands, usually in the armpit or groin.

LymeSci is written by Lonnie Marcum, a Licensed Physical Therapist and mother of a daughter with Lyme. She serves on a subcommittee of the federal Tick-Borne Disease Working Group. Follow her on Twitter: @LonnieRhea  Email her at: lmarcum@lymedisease.org.

References

Childs JE, Paddock CD. (2003) The ascendancy of Amblyomma americanum as a vector of pathogens affecting humans in the United States. Annu Rev Entomol. 48:307-37. doi: 10.1146/annurev.ento.48.091801.112728. Epub 2002 Jun 4. PMID: 12414740.

Clarke, L. L., Ruder, M. G., Mead, D. G., & Howerth, E. W. (2018). Heartland Virus Exposure in White-Tailed Deer in the Southeastern United States, 2001-2015. The American journal of tropical medicine and hygiene, 99(5), 1346–1349. https://doi.org/10.4269/ajtmh.18-0555

Guzmán-Cornejo C et al (2011) The Amblyomma (Acari: Ixodida: Ixodidae) of Mexico: identification keys, distribution and hosts. Zootaxa 2998:16–38

Kopsco HL, Duhaime RJ, Mather TN. (2021) Crowdsourced Tick Image-Informed Updates to U.S. County Records of Three Medically Important Tick Species. J Med Entomol.  11:tjab082. doi: 10.1093/jme/tjab082. Epub ahead of print. PMID: 33973636.

Monzón, J. D., Atkinson, E. G., Henn, B. M., & Benach, J. L. (2016). Population and Evolutionary Genomics of Amblyomma americanum, an Expanding Arthropod Disease Vector. Genome biology and evolution, 8(5), 1351–1360. https://doi.org/10.1093/gbe/evw080

Riemersma KK, Komar N. (2015) Heartland Virus Neutralizing Antibodies in Vertebrate Wildlife, United States, 2009-2014. Emerg Infect Dis. 21(10):1830-3. doi: 10.3201/eid2110.150380. PMID: 26401988; PMCID: PMC4593439.

Romer, Y., Adcock, K., Wei, Z., Mead, D. G., Kirstein, O., Bellman, S….Vazquez-Prokopec, G. M. (2022). Isolation of Heartland Virus from Lone Star Ticks, Georgia, USA, 2019. Emerging Infectious Diseases, 28(4), 786-792. https://doi.org/10.3201/eid2804.211540.

Springer YP, Eisen L, Beati L, James AM, Eisen RJ. (2014) Spatial distribution of counties in the continental United States with records of occurrence of Amblyomma americanum (Ixodida: Ixodidae). J Med Entomol. Mar;51(2):342-51. doi: 10.1603/me13115. PMID: 24724282; PMCID: PMC4623429.

Steinke J, Platts-Mills T, Commins, S. (2015) The alpha-gal story: lessons learned from connecting the dots. J Allergy Clin Immunol. 135(3): 589-96.

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**Comment**

Great, informative article.  I disagree with the notion that the climate is causing tick movement and proliferation of disease – here’s why:

Ticks will be the last species on the planet besides the IRS.

Category:

Alpha Gal Meat Allergy, Ehrlichiosis, Lyme, research, Rocky Mountain Spotted Fever, Ticks, Transmission, Tularemia, Viruses

FDA Authorizes 2nd Booster for Ages 50 & Up Without Consulting Its Vax Panel & The Fact There’s a 22,000% Increase in Deaths After Shots

https://thenewamerican.com/fda-authorized-second-booster-for-americans-50-without-consulting-with-its-vax-panel

FDA Authorized Second Booster for Americans 50+ Without Consulting With Its Vax Panel

by Veronika Kyrylenko
FDA Authorized Second Booster for Americans 50+ Without Consulting With Its Vax Panel
Plyushkin/iStock/Getty Images Plus

On Tuesday, the FDA authorized Americans who are 50 years of age and older to receive a second booster of the Covid shot from either Pfizer-BioNTech or Moderna. The move comes after the Biden administration, disregarding the most basic “scientific” decorum and procedures, was reported to offer older Americans a fourth dose of the Covid vaccine. By fall, younger Americans will likely be able to get their second booster, too.

The news of the administration’s planning to make yet another dose available to the public was first reported by The New York Times over the weekend.  (See link for article)

Important excerpt:

There’s a troubling caveat in that decision: it seems to have been made by the administration without discussion with the U.S. Food and Drug Administration’s (FDA) and the U.S. Centers for Disease Control and Prevention (CDC) “independent” panels. Meaning, the Biden administration is releasing the fourth vaccine booster without any public deliberation on the matter.

____________________

SUMMARY:

  • Federal public health agencies have been operating under regulatory capture
  • There is no “science” behind the move
  • Vinay Prasad of the Brownstown Institute argues that the advisory committees’ meetings are skipped “because many smart people will disagree with them, and consider their plan reckless and lacking data.
  • August 2021 – two senior FDA regulators resigned from their positions over disagreement with the White House’s pressure to move forward with COVID booster shots without FDA approval, as well as with the CDC’s involvement in the approval process.
  • VRBPAC decided that it was too early to throw its support behind a blanket authorization for booster doses of Pfizer’s COVID shot for people 16 and older and voted against recommending it to the general public.
  • Prasad states that due to it being an election year, Biden’s desire to “keep COVID numbers low” reaffirms the assumption that public health is acting as a political organization not a health organization.
  • COVID shot efficacy is dire: breakthrough infections even about the triple vaxxed has prompted the Pfizer CEO to announce that the immune protection offered by the third dose “is not very good against infections” and “doesn’t last very long,” yet maintains the necessity of taking yet another dose.

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https://healthimpactnews.com/2022/22000-increase-in-deaths-following-covid-vaccines-for-adults-over-50-as-fda-authorizes-2nd-booster-for-this-age-group/

22,000% Increase in Deaths following COVID “Vaccines” for Adults Over 50 as FDA Authorizes 2nd Booster for this Age Group

by Brian Shilhavy
Editor, Health Impact News

March 29, 2022

A sampling of the stories we have covered over the past 15 months on thousands of older adults dying after the COVID Vaccines.

by Brian Shilhavy
Editor, Health Impact News

The FDA announced today that it has issued another emergency use authorization (EUA) for a second COVID booster vaccine for adults over the age of 50, and as young as 12 years old if they are “immune compromised.”

Pfizer had made the request for a second booster shot two weeks ago, but their request was for adults over the age of 65. The FDA, however, lowered that to age 50, and issued the EUA for both the Pfizer and Moderna COVID-19 vaccines.

Fierce Pharma reports:

Amid the ongoing debate over the need for another round of COVID-19 boosters, the FDA has acted quickly on the matter.

Only two weeks after Pfizer and its partner BioNTech asked the agency for an emergency use authorization (EUA) for a second round of COVID-19 boosters in people 65 and older, the FDA has granted the nod. The new FDA authorization covers those who have already been boosted with any COVID vaccine and are either 50 and older or 12 and older if they are immunocompromised.

At around the same time on Tuesday morning, Moderna said the FDA had granted its application for a second booster. The Moderna nod covers adults over 50 who have been boosted once, plus immunocompromised adults over 18. Moderna applied for a second booster on March 17. (Full article.)

Do you think the FDA looked at the data in their Vaccine Adverse Event Reporting System (VAERS) regarding COVID-19 vaccines for this age group to see if there were any concerns before authorizing a second booster shot for this age group?

Not likely.

As we have previously reported, the FDA does no safety oversight on these vaccines, but simply takes the drug manufacturers’ word for it, allowing them to police themselves. See:

Just Released Documents by Pfizer Show BioNTech Paid FDA $2,875,842.00 “Drug User Fee” for COVID-19 Vaccine Approval

So we will review the data on this age group in VAERS as a service to the public.

Here is what VAERS is reporting for people over the age of 50 following COVID-19 vaccines. (Source

There are currently 14,752 deaths recorded in VAERS for people over the age of 50 following a COVID-19 vaccine, covering a period of 15 months. That’s an average of 983 deaths a month for this age group.

Here are the results for this age group for the previous 30 years following ALL vaccines in VAERS. (Source.)

There were 1,590 deaths recorded following ALL vaccines for the previous 30 years for people older than 50. So if we divide that number by 360 months we get a monthly average of 4.4 deaths.

So we have seen a 22,000% increase in deaths for people over the age of 50 following COVID-19 vaccines, and the FDA just authorized another booster for those who are left in this age group.

But who cares? The corporate media owned by Big Pharma wants everyone to worry about Russia instead right now, while the FDA’s crimes go unpunished and they continue to produce and distribute more deadly shots.

Here is a video I put together last September when the FDA approved the first booster for seniors, which includes whistleblower testimonies from those who saw people die after taking the COVID-19 vaccines.  This is on our Bitchute Channel. (Approx. 20 Min)

This is simply euthanasia and mass murder, and they are getting away with it.

For more:  https://madisonarealymesupportgroup.com/2020/12/21/warning-3150-injuries-in-1st-week-of-covid-vaccines-among-american-healthcare-workers-pregnant-women-included/

Category:

Activism, vaccines, Viruses

Devastation of CARES Act & Media Propaganda Exposed. Former Media Exec States UK Warned Media Not to Challenge Official COVID Narrative. Current Lawsuit Against Biden Admin

https://rumble.com/vyuseu-heroes-taking-down-evil-journalist-april-moss-goes-nuclear-exposes-vaxx-hos.

The CARES Act Literally Hand-Cuffs Doctors From Doing Their Jobs

Media outlets mass-produce propaganda to control society, silencing those who dare to disrupt their narratives. Award winning journalist and ex-CBS Detroit employee, April Moss joined the Stew Peters Show Monday to expose Big Tech and Big Pharma’s collusion to kill the unvaccinated, the compliance of the media, nurses, doctors, and more.

Moss’s upcoming documentary, ‘Bad Medicine’ exposes how the media is killing thousands with the help Big Pharma, and the damage done so far. Visit FreedomMed.org to find clinics and doctors near you that prescribe ivermectin and effective treatments against the plandemic.

For appropriate COVID treatment:

For more:

Creating a “National Pandemic Emergency” provided justification for such sweeping actions that override individual physician medical decision-making and patients’ rights.

The CARES Act provides incentives for hospitals to use treatments dictated solely by the federal government under the auspices of the NIH. These “bounties” must paid back if not “earned” by making the COVID-19 diagnosis and following the COVID-19 protocol.  Government employees making the rules happen to have patents on nearly every aspect of COVID including the FDA approved treatments.

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https://thehighwire.com/videos/tv-exec-reveals-shocking-censorship-of-media/  Video Here (Approx. 17 Min)

Former British broadcasting executive, Mark Sharman, recently spoke out about the incredible failures of the media during Covid. Journalists were warned not to question the official government line in their reporting.

https://thenewamerican.com/u-k-warned-media-not-to-challenge-official-covid-narrative-says-former-media-exec

U.K. Warned Media Not to Challenge Official Covid Narrative, Says Former Media Exec

by Michael Tennant
U.K. Warned Media Not to Challenge Official Covid Narrative, Says Former Media Exec
RistoArnaudov/iStock/Getty Images Plus

During the beginning stages of the Covid-19 pandemic, the British government threatened the media with penalties for reporting anything other than the official line, turning journalists into “cheerleaders for the government,” a former U.K. news executive said last week.

Mark Sharman, a former executive at ITV News and Sky News, told GB News that the U.K.’s Office of Communications (Ofcom) issued a bulletin to broadcasters in early 2020.

“It was a warning to basically say, ‘Do not question the official government line [on Covid-19],’” he said.

“Now, to be fair to them,” he continued, “they said, ‘You can have opposition voices on, but presenters must intervene if there’s any danger of harmful misinformation.’”

That, of course, means anything that contradicts the official narrative, no matter how rooted in evidence or how reliable its source may be.

Ofcom meant what it said. The agency is empowered to impose a variety of sanctions on broadcasters that violate its dictates, up to and including revoking a broadcaster’s license, and it has done so repeatedly over the last two years. However, as Sharman pointed out, most of the penalties were meted out to smaller outlets that couldn’t fight back.  (See link for article)

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Please go here to learn of how our government pays the media directly, puts “informants” in the national media and other institutions, uses reporters for information, and plants news stories.

SUMMARY:

  • Exec admits the current media environment has caused the biggest assault on freedom of speech and democracy he’s known in his lifetime.
  • The UK is far from alone.  There is a worldwide narrative and anyone dissenting is censored, branded as giving “false” or “misinformation,” and called “conspiracy theorists”.
  • The exec also admitted that “vaccine” injuries are not being covered in the media.
  • He states the “vaccine” damaged suffer twice from the actual injury but then again by doctors who don’t accept their plight.
  • He states the media has let the public down for not holding the government accountable – particularly over the injections, as well as not asking questions about the government doing secret deals with Pfizer, the FDA wanting to hide Pfizer’s data for 75 years, the government spending 500 million pounds on COVID shot advertising, as well as the fact the world’s biggest companies are owned by BlackRock & Vanguard – subsidized by the Gates Foundation and which in turn owns about 35 billion pounds worth of Pfizer stock.
  • The Big Tech/Big Media approach to COVID has now set a precedent that will be with us for years to come due to one-sided coverage, censorship, and cancel-culture tactics.
Only a few media outlets have apologized over their biased, singular coverage and they are both foreign:

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https://thenewamerican.com/lawsuit-biden-admin-pressuring-big-tech-to-censor-users/

Lawsuit: Biden Admin Pressuring Big Tech to Censor Users

by Veronika Kyrylenko
Lawsuit: Biden Admin Pressuring Big Tech to Censor Users
tylim/iStock/Getty Images Plus

The U.S. Surgeon General and the Department of Health and Human Services (HHS) of the Biden administration have directed social-media platforms, including Twitter, to suppress alleged “misinformation” about Covid, alleges a federal lawsuit filed on March 24.

The New Civil Liberties Alliance (NCLA), a conservative civil-rights group, filed the lawsuit in an Ohio federal court on behalf of social-media users Mark Changizi, Daniel Kotzin, and Michael Senger.

According to the lawsuit, all three garnered “tens of thousands of followers” on Twitter and other social-media platforms by actively criticizing restrictions imposed by governments and public-health authorities in response to Covid. As a result, the three have been unlawfully censored. (See link for article)

SUMMARY:

  • A “coordinated and escalating public campaign” on censorship started when White House Press Secretary Jen Psaki announced the president believes social media platforms have a responsibility to “stop amplifying untrustworthy content, disinformation, and misinformation,” regarding COVID, the injections, and elections.  DHS went so far as to brand dissenters as “terrorists.”
  • Pressure amplified in July when Surgeon General Vivek Murthy and HHS started “ordering” social media companies to remove certain posts and ban the perps of “misinformation.” Please see Murthy and Woodcock’s conflicts of interest.
  • The lawsuit contains detailed quotes from admin officials showing they contemplated penalties against social media platforms that allowed “misinformation.”
  • Plaintiffs were suspended and punished from Twitter for simply tweeting that COVID shots don’t stop transmission and that masks don’t work and can be harmful (all of which is true).
  • On March 3, 2022 Murthy went further by demanding tech platforms turn over “information about sources of COVID ‘misinformation’ by May, 2022.
  • Plaintiffs state that no statute endows the Surgeon General with the authority to direct social media companies to censor individuals or viewpoints. Murthy is either misconstruing or violating statutes and articles of the Constitution.
  • Plaintiffs state the administration is not simply colluding but instrumentalizing tech platforms to silence differing opinions which violates free speech.
  • The administration also likely violates the 4th amendment by demanding platforms turn over info about users to the government that the government deems problematic.
  • Murthy’s and HHS’s actions likely exceed their powers under APA and the directives should be found unlawful and invalid.
  • Twitter, Facebook and Youtube have all announced bans on “false claims” about COVID-related matters that go against claims from public health “experts” who just happen to be on a government payroll and own patents on virtually every aspect of COVID.  Youtube’s parent company Google, is directly invested in the AstraZeneca/Oxford COVID “vaccine,” and is also partnered directly with the U.S. military’s DARPA program.

Interestingly, a study has shown that Big Tech censorship of “extremism” actually increases radicalization.

Category:

Activism, Treatment, Viruses

Shocking New COVID Shot Side Effects

https://thehighwire.com/videos/shocking-new-covid-vaccine-side-effects/ Video Here (Approx. 13 Min)

Welcome to the next generation of “vaccine” harms being reported. From mouth blisters to debilitating nervous system disorders, scientists are continuing to report troubling side effects from COVID-19 vaccines.

POSTED: March 25, 2022

Hour long video of adverse events after COVID shots. People dropping and spasming uncontrollably.

Another 20 Minute compilation of athletes, reporters, musicians and others collapsing after shots.

For more:

Category:

Activism, vaccines, Viruses

Researcher Blows Whistle on Data Integrity Issues in Pfizer’s COVID Shot Trial

**UPDATE April, 2022**

As they say: “Follow the money”.

More and more is trickling out about Pfizer including whistleblowers stating the shot is a bioweapon, data was falsified, internal emails tried to cover up fetal cell usage, that it copies the mRNA spike protein into human DNA, has caused increased COVID in young kids, and the suspicious coincidence that the 2022 Oscars were sponsored by Pfizer, the company that just happens to have a new Alopecia drug coming out very soon, and the Rock/Smith distraction. Seems everything today is “brought to you by Pfizer.”

https://thevaccinereaction.org/2022/03/researcher-blows-whistle-on-data-integrity-issues-in-pfizers-covid-vaccine-trial/

http://

Researcher Blows Whistle on Data Integrity: Pfizer COVID shot

Brook Johnson was fired for exposing problems with the integrity of Pfizer’s trial data

For researchers who were testing Pfizer’s vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety. A regional director who was employed at the research organization Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson , emailed a complaint to the US Food and Drug Administration (FDA). Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails.

My name is Brook Johnson. I was fired in September of 2020 for being a whistleblower. I was working on Pfizer’s phase III […] trial on their COVID-19 vaccine. My first day on the job was the 8th of September, and from the very beginning I noticed irregularities, things that were questionable. I would bring up the concerns to my managers and it was always… ‘We’re understaffed, we’re really trying hard to make this work.’ At one point, when I was going through e-mails, there were e-mails from ICON begging Ventavia to follow up on severe adverse events that had been reported. There were several e-mails about mislabeled specimens—blood specimens—and nasal swabs.

Read the full investigation: Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial https://www.bmj.com/content/375/bmj.n…

For more:

Category:

Activism, vaccines, Viruses