Will you take the COVID-19 vaccine?
- Thread starter probyn
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Dude I just traveled
Many countries are no quarantine required already
Trust me I do not have vaccine, don't wear mask, and certainly did not waste a week in quarantine
A source would be useful.
Small portion of partially vaccinated Canadians test positive for COVID-19: PHAC
Roughly 1.3 per cent of Canadians have tested positive for COVID-19 after receiving their first dose of a vaccine, according to the Public Health Agency of Canada (PHAC).
toronto.ctvnews.ca
Many countries are no quarantine required already? Name 3 dozen & what requirements they have to let you in.
Without proof of vaccination (vaccine passport), or getting a needle to test your blood for covid19 infection or covid19 antibodies, or a similar test, as evidence that you are a low risk traveler, what country is going to let people such as you visit without a lengthy mandatory quarantine (assuming such a quarantine is even an option they offer)?
Likewise are such willing to be banned from many businesses, services, transports, etc, locally within their own neighborhood, town, city, province, state or country?
If the blood test option is chosen, how often will it have to be repeated to keep one's status up to date?
Funny how you guys continue to insist on comparing this experimental DNA hack to proven vaccines that a) actually work, and b) went through proper clinical trials.
Still waiting on the sanofi GSK vaccine which is similar to the hepatitis b vaccine
America is in the throes of a pandemic, but not from some Chinese virus. The real threat is Wuhan coronavirus (Covid-19) injections, which are causing young men to suffer heart attacks.
One of them tweeted about how he was perfectly healthy before receiving his first “dose” of the Pfizer jab. Not long after, he found himself in the hospital after suffering a heart attack.
“My cardiovascular system is completely normal & healthy,” wrote Tom Schulz. “But last week I took the Pfizer vaccine and there are reports that it’s been causing heart complications.”
Doctors evaluating Schulz have ruled out most other potential causes of the heart attack. The only common denominator was the Pfizer injection, which even mainstream media outlets are admitting is linked to “heart inflammation” and myocarditis.
Schulz apparently did some research of his own and found that many people, specifically younger men, are suffering similar outcomes post-injection. Even people within his “immediate network,” he says, are experiencing deadly complications.
“‘Low odds of happening’ doesn’t seem too low from where I’m sitting,” Schulz wrote.
Schulz’s doctor says there have been other young men admitted to the same hospital with the same complications. Both the Moderna and the Johnson & Johnson (J&J) injections are causing these problems as well.
“Young men, 18-30 years old, going through mild to severe cardiac events post vaccine,” Schulz writes. “This is scary. It’s official. I have myocarditis.”
www.naturalnews.com
America is in the throes of a pandemic, but not from some Chinese virus. The real threat is Wuhan coronavirus (Covid-19) injections, which are causing young men to suffer heart attacks.
One of them tweeted about how he was perfectly healthy before receiving his first “dose” of the Pfizer jab. Not long after, he found himself in the hospital after suffering a heart attack.
“My cardiovascular system is completely normal & healthy,” wrote Tom Schulz. “But last week I took the Pfizer vaccine and there are reports that it’s been causing heart complications.”
Doctors evaluating Schulz have ruled out most other potential causes of the heart attack. The only common denominator was the Pfizer injection, which even mainstream media outlets are admitting is linked to “heart inflammation” and myocarditis.
Schulz apparently did some research of his own and found that many people, specifically younger men, are suffering similar outcomes post-injection. Even people within his “immediate network,” he says, are experiencing deadly complications.
“‘Low odds of happening’ doesn’t seem too low from where I’m sitting,” Schulz wrote.
Schulz’s doctor says there have been other young men admitted to the same hospital with the same complications. Both the Moderna and the Johnson & Johnson (J&J) injections are causing these problems as well.
“Young men, 18-30 years old, going through mild to severe cardiac events post vaccine,” Schulz writes. “This is scary. It’s official. I have myocarditis.”
Young man suffers HEART ATTACK after getting injected with Pfizer vaccine – NaturalNews.com
America is in the throes of a pandemic, but not from some Chinese virus. The real threat is Wuhan coronavirus (Covid-19) injections, which are causing young men to suffer heart attacks. One of them tweeted about how he was perfectly healthy before receiving his first “dose” of the Pfizer jab...
www.naturalnews.com
G20 Leaders Support Vaccine Passports To Resume International Travel
Tourism ministers from the Group of 20 (G20), the world’s most powerful economies, met virtually today and agreed to back plans for vaccine passports to help the global tourism industry recover.
On the same day, the tourism minister of Canada announced that Canada is working with international partners to develop a standardized vaccine certification, which the majority of Canadians support, according to a recent survey.
Tourism ministers from the Group of 20 (G20), the world’s most powerful economies, met virtually today and agreed to back plans for vaccine passports to help the global tourism industry recover.
On the same day, the tourism minister of Canada announced that Canada is working with international partners to develop a standardized vaccine certification, which the majority of Canadians support, according to a recent survey.
The family of a Michigan woman says she died as the result of complications 11 days after receiving the Johnson & Johnson (J&J) COVID vaccine.
(Article by Megan Redshaw, J.D. republished from LifeSiteNews.com)
Anne VanGeest, 35, died April 19 at Mercy Health Saint Mary’s hospital in Grand Rapids from an acute subarachnoid brain hemorrhage, FOX 17 reported.
“It is with profound sadness that we share the news of Anne’s passing Anne (Annie), who was 35, was a loving mother, wife, sister and daughter,” the family said in a statement provided by Lambert, a Grand Rapids public relations firm that is providing its services to the family pro bono.
VanGeest received the J&J shot on April 8, five days before the Centers for Disease Control and Prevention (CDC) paused the vaccine to investigate reports of potentially dangerous blood clots in women who received the shot.
VanGeest’s family said her headache started on April 16 — eight days after being vaccinated. She died three days later. Her death certificate notes a natural death, specifically from an acute subarachnoid hemorrhage, or bleeding between the brain and tissue around the brain.
Symptoms of the rare blood clots typically develop six to 15 days after getting the shot.
“These initial symptoms are fairly vague and nonspecific,” said Dr. Tom Shimabukuro of the CDC COVID-19 Response. “(It’s) mainly headache, but importantly, the headaches for these started six or more days after vaccination.”
VanGeest’s physician filed a report to the CDC’s Vaccine Adverse Event Reporting System (VAERS).
In an email to the VanGeest family, the CDC confirmed her death had been reported to VAERS, but said the system is not designed to determine whether a reported adverse event was caused by the vaccine.
“When VAERS receives reports of serious illness or death after vaccination, VAERS staff contact the hospital where the patient was treated to obtain the associated medical records to better understand the adverse event,” the CDC said.
According to the CDC website, “the CDC follows up on any report of death to request additional information and learn more about what occurred and to determine whether the death was a result of the vaccine or unrelated.”
The Defender has repeatedly reached out to the CDC since March 8 to determine how investigations into reported deaths are conducted, but have yet to receive a response.
On April 13, the CDC and FDA called for an immediate halt to the use of J&J’s COVID vaccine, marketed under the company’s Janssen subsidiary, while they investigated at least six cases of a rare and serious disorder called cerebral venous thrombosis (CVT).
CVT occurs when a blood clot forms in the brain’s venous sinuses. The clot prevents blood from draining out of the brain. As a result, blood cells may break and leak blood into the brain tissues, forming a hemorrhage.
On April 14, the CDC’s Advisory Committee on Immunization Practices (ACIP) postponed a vote on whether to lift the pause on the J&J vaccine, effectively extending it pending further analysis of data relating to blood clots in people who received the vaccine.
On April 23, the ACIP voted 10 – 4 to recommend lifting the pause of the J&J shot without restrictions or an additional warning about the risk of blood clotting disorders after analyzing 15 cases of rare blood clots, including three deaths, according to a slide presentation shared during the meeting.
The ACIP said the link between blood clots and J&J’s COVID vaccine was “plausible,” but concluded the vaccine’s benefits outweigh the risks. The FDA and CDC voted to lift the pause, but the FDA said it would add a warning label about potentially serious blood clotting disorders.
Denmark health officials announced Monday they would remove the J&J vaccine from the country’s vaccine program after concluding that the benefits of the vaccine do not outweigh the risk of blood clots.
On April 30 Children’s Health Defense queried the VAERS data for a series of adverse events associated with the formation of clotting disorders and other related conditions. VAERS yielded a total of 1,845 reports for all three vaccines from Dec. 14, 2020, through April 23.
Of the 1,845 cases reported, there were 655 reports attributed to Pfizer, 577 reports to Moderna and 608 reports to J&J. However, U.S. health officials only acknowledged 15 blood clot cases associated with the J&J vaccine at the April 16 meeting.
A query in VAERS for subarachnoid brain hemorrhage yielded 31 cases, eight of which were associated with J&J’s COVID vaccine.
Read more at: LifeSiteNews.com
(Article by Megan Redshaw, J.D. republished from LifeSiteNews.com)
Anne VanGeest, 35, died April 19 at Mercy Health Saint Mary’s hospital in Grand Rapids from an acute subarachnoid brain hemorrhage, FOX 17 reported.
“It is with profound sadness that we share the news of Anne’s passing Anne (Annie), who was 35, was a loving mother, wife, sister and daughter,” the family said in a statement provided by Lambert, a Grand Rapids public relations firm that is providing its services to the family pro bono.
VanGeest received the J&J shot on April 8, five days before the Centers for Disease Control and Prevention (CDC) paused the vaccine to investigate reports of potentially dangerous blood clots in women who received the shot.
VanGeest’s family said her headache started on April 16 — eight days after being vaccinated. She died three days later. Her death certificate notes a natural death, specifically from an acute subarachnoid hemorrhage, or bleeding between the brain and tissue around the brain.
Symptoms of the rare blood clots typically develop six to 15 days after getting the shot.
“These initial symptoms are fairly vague and nonspecific,” said Dr. Tom Shimabukuro of the CDC COVID-19 Response. “(It’s) mainly headache, but importantly, the headaches for these started six or more days after vaccination.”
VanGeest’s physician filed a report to the CDC’s Vaccine Adverse Event Reporting System (VAERS).
In an email to the VanGeest family, the CDC confirmed her death had been reported to VAERS, but said the system is not designed to determine whether a reported adverse event was caused by the vaccine.
“When VAERS receives reports of serious illness or death after vaccination, VAERS staff contact the hospital where the patient was treated to obtain the associated medical records to better understand the adverse event,” the CDC said.
According to the CDC website, “the CDC follows up on any report of death to request additional information and learn more about what occurred and to determine whether the death was a result of the vaccine or unrelated.”
The Defender has repeatedly reached out to the CDC since March 8 to determine how investigations into reported deaths are conducted, but have yet to receive a response.
On April 13, the CDC and FDA called for an immediate halt to the use of J&J’s COVID vaccine, marketed under the company’s Janssen subsidiary, while they investigated at least six cases of a rare and serious disorder called cerebral venous thrombosis (CVT).
CVT occurs when a blood clot forms in the brain’s venous sinuses. The clot prevents blood from draining out of the brain. As a result, blood cells may break and leak blood into the brain tissues, forming a hemorrhage.
On April 14, the CDC’s Advisory Committee on Immunization Practices (ACIP) postponed a vote on whether to lift the pause on the J&J vaccine, effectively extending it pending further analysis of data relating to blood clots in people who received the vaccine.
On April 23, the ACIP voted 10 – 4 to recommend lifting the pause of the J&J shot without restrictions or an additional warning about the risk of blood clotting disorders after analyzing 15 cases of rare blood clots, including three deaths, according to a slide presentation shared during the meeting.
The ACIP said the link between blood clots and J&J’s COVID vaccine was “plausible,” but concluded the vaccine’s benefits outweigh the risks. The FDA and CDC voted to lift the pause, but the FDA said it would add a warning label about potentially serious blood clotting disorders.
Denmark health officials announced Monday they would remove the J&J vaccine from the country’s vaccine program after concluding that the benefits of the vaccine do not outweigh the risk of blood clots.
On April 30 Children’s Health Defense queried the VAERS data for a series of adverse events associated with the formation of clotting disorders and other related conditions. VAERS yielded a total of 1,845 reports for all three vaccines from Dec. 14, 2020, through April 23.
Of the 1,845 cases reported, there were 655 reports attributed to Pfizer, 577 reports to Moderna and 608 reports to J&J. However, U.S. health officials only acknowledged 15 blood clot cases associated with the J&J vaccine at the April 16 meeting.
A query in VAERS for subarachnoid brain hemorrhage yielded 31 cases, eight of which were associated with J&J’s COVID vaccine.
Read more at: LifeSiteNews.com
This is good news
nypost.com
Moderna booster effective against COVID-19 variants, company says
Moderna’s COVID-19 vaccine booster may be effective against some of the virus’ variants.
nypost.com
Your insults are very disheartening to us good-natured science-believing folks!
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