Author Topic: Epidemics: Bird Flu, TB, AIDs, Superbugs, Ebola, etc  (Read 324938 times)

ccp

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Re: Epidemics: Bird Flu, TB, AIDs, Superbugs, Ebola, etc
« Reply #1700 on: March 06, 2022, 01:09:47 PM »
"And they actually think there’s going to be 300,000 excess deaths due to — they call it ‘Covid and indirect Covid,’ whatever that means — in the U.S. in 2022. "

I assume this means any deaths that have a corona link.

Guessing this includes
  lack of access to care for medical services due to fear of getting corona,  long wait times,
  suicide from isolation , perhaps prolonged heart lung damage from corona infection, and agree would include
  deaths from the vaccine (the most rare)




Crafty_Dog

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ET: Wuhan Cooties rots the brain
« Reply #1703 on: March 08, 2022, 11:23:56 AM »
Even Mild Cases of COVID-19 Can Lead to Brain Changes: Study
By Zachary Stieber March 8, 2022 Updated: March 8, 2022biggersmaller Print
Mild COVID-19 cases were linked to changes in the brain in a newly published study.

Approximately 785 people underwent a brain scan and about half later tested positive for COVID-19. All the people got a second brain scan, including those who had survived the disease.

Researchers from the Wellcome Centre for Integrative Neuroimaging at the University of Oxford analyzed the scans and found the participants infected with COVID-19 had a greater reduction in the thickness of grey matter, which helps humans perform various functions such as making decisions, and other negative outcomes.

“Despite the infection being mild for 96% of our participants, we saw a greater loss of grey matter volume, and greater tissue damage in the infected participants, on average 4.5 months after infection,” professor Gwenaëlle Douaud, the study’s lead author, said in a statement.

“They also showed greater decline in their mental abilities to perform complex tasks, and this mental worsening was partly related to these brain abnormalities. All these negative effects were more marked at older ages.”

The paper was published in Nature following peer review.

The scans were taken from the UK Biobank, a large-scale medical database that contains information on approximately 500,000 UK residents.

Those whose scans were analyzed were aged 51 to 81. The reason the study did not include younger people is that all participants in the scanning were 40 or older, Douaud told The Epoch Times in an email.

The scans were taken on average 38 months apart.

Epoch Times Photo
The red-yellow regions are the parts of the brain that researchers found shrunk the most in people who contracted COVID-19, compared with a non-infected cohort. (G. Douaud, in collaboration with Anderson Winkler and Saad Jbabdi, University of Oxford and NIH)
Researchers said the two cohorts—people who ended up getting infected and people who did not—were similar in terms of age, sex, and many risk factors.

Participants also engaged in cognitive tests, and the infected group was more likely to experience cognitive decline by the time of the second test.

The brain changes ranged from 0.2 to 2 percent additional change in the infected group.

Researchers described the study as the first in the world to compare images taken before COVID-19 infection with scans after infection.

COVID-19 is the disease caused by the CCP (Chinese Communist Party) virus, also known as SARS-CoV-2.

The study was funded by a Wellcome Trust award.

Limitations of the research include the lack of stratification of severity of the cases beyond the detail of whether they needed hospital care and most participants being white. The study also did not account for vaccination status.

Researchers said that further study is needed to see whether the negative impact can be partially reversed and whether the effects would persist over longer periods of time.


G M

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Re: ET: Wuhan Cooties rots the brain
« Reply #1704 on: March 08, 2022, 01:02:50 PM »
Did these people take the ClotShot?

Even Mild Cases of COVID-19 Can Lead to Brain Changes: Study
By Zachary Stieber March 8, 2022 Updated: March 8, 2022biggersmaller Print
Mild COVID-19 cases were linked to changes in the brain in a newly published study.

Approximately 785 people underwent a brain scan and about half later tested positive for COVID-19. All the people got a second brain scan, including those who had survived the disease.

Researchers from the Wellcome Centre for Integrative Neuroimaging at the University of Oxford analyzed the scans and found the participants infected with COVID-19 had a greater reduction in the thickness of grey matter, which helps humans perform various functions such as making decisions, and other negative outcomes.

“Despite the infection being mild for 96% of our participants, we saw a greater loss of grey matter volume, and greater tissue damage in the infected participants, on average 4.5 months after infection,” professor Gwenaëlle Douaud, the study’s lead author, said in a statement.

“They also showed greater decline in their mental abilities to perform complex tasks, and this mental worsening was partly related to these brain abnormalities. All these negative effects were more marked at older ages.”

The paper was published in Nature following peer review.

The scans were taken from the UK Biobank, a large-scale medical database that contains information on approximately 500,000 UK residents.

Those whose scans were analyzed were aged 51 to 81. The reason the study did not include younger people is that all participants in the scanning were 40 or older, Douaud told The Epoch Times in an email.

The scans were taken on average 38 months apart.

Epoch Times Photo
The red-yellow regions are the parts of the brain that researchers found shrunk the most in people who contracted COVID-19, compared with a non-infected cohort. (G. Douaud, in collaboration with Anderson Winkler and Saad Jbabdi, University of Oxford and NIH)
Researchers said the two cohorts—people who ended up getting infected and people who did not—were similar in terms of age, sex, and many risk factors.

Participants also engaged in cognitive tests, and the infected group was more likely to experience cognitive decline by the time of the second test.

The brain changes ranged from 0.2 to 2 percent additional change in the infected group.

Researchers described the study as the first in the world to compare images taken before COVID-19 infection with scans after infection.

COVID-19 is the disease caused by the CCP (Chinese Communist Party) virus, also known as SARS-CoV-2.

The study was funded by a Wellcome Trust award.

Limitations of the research include the lack of stratification of severity of the cases beyond the detail of whether they needed hospital care and most participants being white. The study also did not account for vaccination status.

Researchers said that further study is needed to see whether the negative impact can be partially reversed and whether the effects would persist over longer periods of time.

Crafty_Dog

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Dr. Peter McCullough: Uh oh
« Reply #1705 on: March 09, 2022, 04:11:04 AM »
Dr. Peter McCullough: Findings From Early COVID-19 Vaccine Studies Potentially Alarming
'This is getting into human chromosomes'
By Beth Brelje March 8, 2022 Updated: March 8, 2022biggersmaller Print
How safe are COVID-19 vaccines? Should everyone be taking them? Are people who get vaccines more likely to get COVID-19? Can genetic material in the vaccines be incorporated into the human genome? These are some of the unknown questions that researchers around the world are currently investigating.

With more initial findings and hypotheses now released to the public, a group of free speech and information advocates last week during a presentation in Pennsylvania gave their “uncensored” take of the current science. They are currently traveling around the United States sharing concerns about how public health policy and debate throughout the COVID-19 pandemic has been handled.

The speakers were Dr. Peter McCullough, a renowned cardiologist whose own research is highly-cited; Dr. Bryan Ardis, a chiropractor; attorney Thomas Renz; and Steve Kirsch, a Silicon Valley philanthropist who supported early efforts searching for COVID-19 treatments in medicines already on the market. They were invited by the “Lions for Liberty,” a group of Penn State University students, faculty, and staff that sprang up in response to the university’s pandemic mitigation policies that require employees to get vaccinated for COVID-19.

The four spoke on numerous occasions; at Toftrees Resort in State College on March 3 and at Hershey Lodge on March 4 before which they testified at the Capitol Building in Harrisburg in a hearing hosted by state Sen. Doug Mastriano, who is a Republican running for governor.

They presented data from peer-reviewed studies, the Centers for Disease Control and Prevention (CDC), and government documents, and expressed their concerns that the COVID-19 vaccines recommended for all Americans were problematic from the start.

“It was clear vaccines weren’t sufficiently tested and important groups were excluded, like pregnant women,” McCullough said in Hershey. “With no data on safety and efficacy, pregnant women were encouraged, then later forced, to take the vaccines.”

He called the results of a newly released study disturbing. The study, titled  “Immune imprinting, breadth of variant recognition, and germinal center response in human SARS-CoV-2 infection and vaccination,” shows that messenger ribonucleic acid (mRNA) from the vaccine stays in the body much longer than expected. Messenger RNA is a single-stranded molecule that carries genetic code, usually from the DNA in a cell’s nucleus, to ribosomes, the cell’s protein-making area.

“It shows the messenger RNA is in the lymph nodes months after the vaccine had been received. This is proven,” McCullough said. “The vaccines are not leaving the body. It’s found in the lymph nodes at 60 days. The thought in the FDA briefing book was that these vaccines were going to be in the body for a day or two, generate immunity, and then be out.”

He cited another paper published in February by a team of researchers led by Associate Prof. Yang De Marinis at the Department of Clinical Sciences of Lund University, Sweden, that shows “reverse transcription” is happening—that is, an enzyme makes a copy of DNA from RNA.

“This is getting into human chromosomes, at least this segment is. If it turns out that the entire code goes into human chromosomes, and if it expresses spike protein within cells—spike protein is an abnormal protein, it is not a human protein— if this protein is expressed within human cells on a regular basis or on demand, and it’s passed from parent cells to daughter cells, and it’s passed to the developing embryo, we’re in trouble.”

Now, the race is on to confirm this finding with additional studies, McCullough said.

“On the CDC website, it says the vaccines don’t change the human genome. This paper that just broke in the last week is strongly suggesting the CDC was gravely wrong,” McCullough said. “We should have had monthly safety reports to America. If we’re going to ask Americans to take an experimental vaccine or investigational vaccine, there should have been a safety report.”

Coming out of the clinical trials, what was reported in the briefing booklet looked OK, McCullough said. Through October, over 220 million people took a vaccine.

The Vaccine Adverse Event Reporting System (VAERS) has now recorded as many as 24,000 reports of people dying shortly after taking a COVID-19 vaccine, over 34,000 reports of myocarditis or pericarditis after taking a vaccine, and 44,000 reports from people permanently disabled with a host of conditions after taking a vaccine. These reports, which can be made by any member of the public, have yet to be definitively linked to COVID-19 vaccines and further research is needed to quantify the risk.

Now, a new study in The Lancet is pointing to potential multi-inflammatory syndrome in COVID-19 vaccinated children, McCullough said. “Some kids are on ventilators. These were perfectly healthy kids and now they’re on the ventilator fighting for their life.”

State Legislation
During the hearing in Harrisburg, a number of COVID-related bills were mentioned.

Mastriano is the prime sponsor of Senate Bill 471, dubbed the Medical Freedom Act, which proposed that the state government shall not impose a vaccination requirement on adults or children without consent. It also proposed to make it illegal for the government to mandate employers to require vaccination of their staff and ensures unemployment compensation for unvaccinated workers. The bill moved out of the Health and Human Services Committee in November, committee chair state Sen. Michele Brooks said at the hearing. She also advocated for her own legislation, Senate Bill 937, which prohibits the state from requiring COVID-19 vaccines for students in kindergarten through grade 12. It is now in the House Education Committee, Brooks said.

A companion bill, SB 1091/HB 1741 would increase access to off-label FDA approved medications in the early stages of COVID-19. This would allow physicians and pharmacists to prescribe and dispense drugs already approved by the FDA for off-label treatment of COVID-19, without penalty from licensing boards. And it would clarify that a pharmacy may not decline to fill a prescription of a COVID-19 early treatment drug based solely on their opinion of the drug. Mastriano is the prime sponsor of this Senate bill and Rep. Dawn Keefer sponsors the House version.

Ardis made a plea to lawmakers at the hearing, on behalf of doctors.

“Please let them practice medicine. Never in the history of the world has there been one protocol for every human. We are all genetically different,” Ardis said. “Please allow doctors, once again, to be protected to practice medicine. They are the only ones that have known the history of their patients. You cannot tell me there’s one solution or protocol for every American who gets a respiratory infection right now; it’s impossible. And then you’re going to take their license from them, destroy their livelihood and then slander them with their reputation, because they’re holding to their oath to do no harm? Please. Put legislation in place that they can never be punished for doing their best to do no harm, to treat their patients.”

Penn State Snubbed Event
Lions for Liberty invited two university policy makers, Penn State President Eric Barron and Provost Nick Jones, to attend the forum. But Barron and Jones were not among the combined 700 attendees.

“It is disconcerting, to say the least, that leadership from the university’s administration were unwilling to attend or engage in either of these events,” Arielle Girouard, Lions for Liberty press secretary told The Epoch Times. “It is unfortunate that one of the nation’s top universities in research, education, and innovation has repeatedly denied our attempts to have a discussion on the science that has driven public health and institutional, including university, policies over the past two years. President Barron acknowledges a growing lack of public trust in higher education. It is hard to see how refusal to engage with credentialed academics and professionals, from both within and outside of the Penn State community, does anything but sow further distrust in the public. Regardless, Lions for Liberty isn’t going anywhere. We are committed to fostering a community, open to all who seek truth, so we may make well-informed decisions regarding our health, among other individual liberties.”

Penn State did not respond to a request from The Epoch Times to explain why they did not attend.

The Association of American Physicians and Surgeons and the Penn State chapter of Turning Point USA co-hosted the speakers with Lions for Liberty.


G M

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Re: Dr. Peter McCullough: Uh oh
« Reply #1706 on: March 09, 2022, 08:12:22 AM »
Nuremberg 2.0 is coming.

Dr. Peter McCullough: Findings From Early COVID-19 Vaccine Studies Potentially Alarming
'This is getting into human chromosomes'
By Beth Brelje March 8, 2022 Updated: March 8, 2022biggersmaller Print
How safe are COVID-19 vaccines? Should everyone be taking them? Are people who get vaccines more likely to get COVID-19? Can genetic material in the vaccines be incorporated into the human genome? These are some of the unknown questions that researchers around the world are currently investigating.

With more initial findings and hypotheses now released to the public, a group of free speech and information advocates last week during a presentation in Pennsylvania gave their “uncensored” take of the current science. They are currently traveling around the United States sharing concerns about how public health policy and debate throughout the COVID-19 pandemic has been handled.

The speakers were Dr. Peter McCullough, a renowned cardiologist whose own research is highly-cited; Dr. Bryan Ardis, a chiropractor; attorney Thomas Renz; and Steve Kirsch, a Silicon Valley philanthropist who supported early efforts searching for COVID-19 treatments in medicines already on the market. They were invited by the “Lions for Liberty,” a group of Penn State University students, faculty, and staff that sprang up in response to the university’s pandemic mitigation policies that require employees to get vaccinated for COVID-19.

The four spoke on numerous occasions; at Toftrees Resort in State College on March 3 and at Hershey Lodge on March 4 before which they testified at the Capitol Building in Harrisburg in a hearing hosted by state Sen. Doug Mastriano, who is a Republican running for governor.

They presented data from peer-reviewed studies, the Centers for Disease Control and Prevention (CDC), and government documents, and expressed their concerns that the COVID-19 vaccines recommended for all Americans were problematic from the start.

“It was clear vaccines weren’t sufficiently tested and important groups were excluded, like pregnant women,” McCullough said in Hershey. “With no data on safety and efficacy, pregnant women were encouraged, then later forced, to take the vaccines.”

He called the results of a newly released study disturbing. The study, titled  “Immune imprinting, breadth of variant recognition, and germinal center response in human SARS-CoV-2 infection and vaccination,” shows that messenger ribonucleic acid (mRNA) from the vaccine stays in the body much longer than expected. Messenger RNA is a single-stranded molecule that carries genetic code, usually from the DNA in a cell’s nucleus, to ribosomes, the cell’s protein-making area.

“It shows the messenger RNA is in the lymph nodes months after the vaccine had been received. This is proven,” McCullough said. “The vaccines are not leaving the body. It’s found in the lymph nodes at 60 days. The thought in the FDA briefing book was that these vaccines were going to be in the body for a day or two, generate immunity, and then be out.”

He cited another paper published in February by a team of researchers led by Associate Prof. Yang De Marinis at the Department of Clinical Sciences of Lund University, Sweden, that shows “reverse transcription” is happening—that is, an enzyme makes a copy of DNA from RNA.

“This is getting into human chromosomes, at least this segment is. If it turns out that the entire code goes into human chromosomes, and if it expresses spike protein within cells—spike protein is an abnormal protein, it is not a human protein— if this protein is expressed within human cells on a regular basis or on demand, and it’s passed from parent cells to daughter cells, and it’s passed to the developing embryo, we’re in trouble.”

Now, the race is on to confirm this finding with additional studies, McCullough said.

“On the CDC website, it says the vaccines don’t change the human genome. This paper that just broke in the last week is strongly suggesting the CDC was gravely wrong,” McCullough said. “We should have had monthly safety reports to America. If we’re going to ask Americans to take an experimental vaccine or investigational vaccine, there should have been a safety report.”

Coming out of the clinical trials, what was reported in the briefing booklet looked OK, McCullough said. Through October, over 220 million people took a vaccine.

The Vaccine Adverse Event Reporting System (VAERS) has now recorded as many as 24,000 reports of people dying shortly after taking a COVID-19 vaccine, over 34,000 reports of myocarditis or pericarditis after taking a vaccine, and 44,000 reports from people permanently disabled with a host of conditions after taking a vaccine. These reports, which can be made by any member of the public, have yet to be definitively linked to COVID-19 vaccines and further research is needed to quantify the risk.

Now, a new study in The Lancet is pointing to potential multi-inflammatory syndrome in COVID-19 vaccinated children, McCullough said. “Some kids are on ventilators. These were perfectly healthy kids and now they’re on the ventilator fighting for their life.”

State Legislation
During the hearing in Harrisburg, a number of COVID-related bills were mentioned.

Mastriano is the prime sponsor of Senate Bill 471, dubbed the Medical Freedom Act, which proposed that the state government shall not impose a vaccination requirement on adults or children without consent. It also proposed to make it illegal for the government to mandate employers to require vaccination of their staff and ensures unemployment compensation for unvaccinated workers. The bill moved out of the Health and Human Services Committee in November, committee chair state Sen. Michele Brooks said at the hearing. She also advocated for her own legislation, Senate Bill 937, which prohibits the state from requiring COVID-19 vaccines for students in kindergarten through grade 12. It is now in the House Education Committee, Brooks said.

A companion bill, SB 1091/HB 1741 would increase access to off-label FDA approved medications in the early stages of COVID-19. This would allow physicians and pharmacists to prescribe and dispense drugs already approved by the FDA for off-label treatment of COVID-19, without penalty from licensing boards. And it would clarify that a pharmacy may not decline to fill a prescription of a COVID-19 early treatment drug based solely on their opinion of the drug. Mastriano is the prime sponsor of this Senate bill and Rep. Dawn Keefer sponsors the House version.

Ardis made a plea to lawmakers at the hearing, on behalf of doctors.

“Please let them practice medicine. Never in the history of the world has there been one protocol for every human. We are all genetically different,” Ardis said. “Please allow doctors, once again, to be protected to practice medicine. They are the only ones that have known the history of their patients. You cannot tell me there’s one solution or protocol for every American who gets a respiratory infection right now; it’s impossible. And then you’re going to take their license from them, destroy their livelihood and then slander them with their reputation, because they’re holding to their oath to do no harm? Please. Put legislation in place that they can never be punished for doing their best to do no harm, to treat their patients.”

Penn State Snubbed Event
Lions for Liberty invited two university policy makers, Penn State President Eric Barron and Provost Nick Jones, to attend the forum. But Barron and Jones were not among the combined 700 attendees.

“It is disconcerting, to say the least, that leadership from the university’s administration were unwilling to attend or engage in either of these events,” Arielle Girouard, Lions for Liberty press secretary told The Epoch Times. “It is unfortunate that one of the nation’s top universities in research, education, and innovation has repeatedly denied our attempts to have a discussion on the science that has driven public health and institutional, including university, policies over the past two years. President Barron acknowledges a growing lack of public trust in higher education. It is hard to see how refusal to engage with credentialed academics and professionals, from both within and outside of the Penn State community, does anything but sow further distrust in the public. Regardless, Lions for Liberty isn’t going anywhere. We are committed to fostering a community, open to all who seek truth, so we may make well-informed decisions regarding our health, among other individual liberties.”

Penn State did not respond to a request from The Epoch Times to explain why they did not attend.

The Association of American Physicians and Surgeons and the Penn State chapter of Turning Point USA co-hosted the speakers with Lions for Liberty.



ccp

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"When Physicians Spread Unscientific Information About COVID-19"
« Reply #1709 on: March 19, 2022, 05:16:03 AM »
https://jamanetwork.com/journals/jama/fullarticle/2789369

FYI
I am not endorsing this
just posting for the board's interest.


ccp

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2nd post
« Reply #1710 on: March 19, 2022, 05:30:21 AM »

Crafty_Dog

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Wuhan Cooties and Diabetes
« Reply #1711 on: March 23, 2022, 02:44:26 AM »
New Research Shows Higher Risk of Developing Diabetes After Covid-19 Infection
Study adds to growing evidence showing increased risk for a range of cardiometabolic conditions after Covid-19

By Sumathi Reddy
Follow
Updated March 21, 2022 7:52 pm ET


A large new study found that people who recovered from Covid-19 within the past year are 40% more likely to receive a new diagnosis of diabetes compared to those who weren’t infected.

The increased risk translates into 1% of people who have had Covid-19 developing diabetes who otherwise wouldn’t have, the study’s author says, resulting in potentially millions of new cases world-wide.

Most of the people with diabetes in the study, published online Monday in the journal Lancet Diabetes and Endocrinology, were diagnosed with Type 2 diabetes, not Type 1. Some researchers say Covid-19 could also be triggering an entirely new type of diabetes in which certain cells mistakenly start to raise, rather than lower, blood sugar.

The study adds to evidence showing an increased post-Covid-19 risk of cardiometabolic conditions, such as diabetes as well as heart and kidney complications. Normally when people think of long-term Covid-19 symptoms, they think of problems such as cognitive issues, fatigue or shortness of breath. But scientists say there are likely different types of long Covid, and one appears to be defined by cardiometabolic problems that arise after Covid-19. So far, the World Health Organization estimates there have been more than 464 million cases of Covid-19, so even small percentages of those people developing long-term complications would be significant.


New studies offer clues about who might be more susceptible to long Covid, a term for lingering Covid-19 symptoms. WSJ breaks down the science of long Covid and the state of treatment. Illustration: Jacob Reynolds for The Wall Street Journal
“We’re finding out more and more that it’s not only respiratory problems or brain fog or only fatigue,” says Ziyad Al-Aly, chief of research and development at the VA St. Louis Health Care System and a clinical epidemiologist at Washington University in St. Louis, who led the study. “There are heart manifestations, and clearly diabetes and kidney manifestations.”


Dr. Al-Aly’s group has recently published studies on those broader risks. One showed a higher risk of developing heart problems, including stroke and heart attack, in people who have had Covid-19 than in people who haven’t. Another showed post-Covid-19 patients were more likely to have declines in kidney function or kidney damage as much as six months after infection when compared to patients who hadn’t had Covid-19.

The researchers found only an association between Covid-19 and cardiometabolic conditions, without proving a cause. Some doctors say that new diagnoses of Type 2 diabetes and heart conditions could be influenced by weight gain or decreased activity during the pandemic, although lifestyle changes wouldn’t necessarily explain an increase specifically in people who have had Covid-19.

In the new diabetes study, Dr. Al-Aly and co-researchers analyzed the records of 181,000 Covid-19 patients in the Veterans Health Administration system who were diagnosed with Covid-19 within the past year and compared them to more than eight million people who didn’t have Covid-19.  The VA study didn’t look at diabetes cases by vaccination status.

“When you look at the data on a national scale it’s clearly happening even in people who have no risk factors or very little risk factors,” Dr. Al-Aly said, adding that new diagnoses are happening even in young adults with a healthy weight and no previous history of high blood sugar.



Maren Laughlin, a program director at the National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases, said the study was very well done. Its main limitation, she noted, is that VA patients generally tend to be older and sicker and include more males than the broader population.

It hasn’t been determined why a Covid-19 infection might be leading to new cases of diabetes. One possibility is that the virus might damage the pancreas’s ability to secrete insulin, the hormone that regulates blood sugar. Another theory is that the strong immune response to Covid-19 generates an inflammatory cascade that results in low-grade inflammation, which interferes with insulin secretion and sensitivity.

All types of diabetes share the symptom of high blood sugars, but they are distinct conditions. Type 2 is the most common, and can be associated with diet and exercise. Typically in Type 2, people become resistant to the hormone insulin, which regulates blood sugar. The pancreas struggles to keep up with the body’s increased demand for insulin, leading to higher blood-sugar levels.

Type 1, by contrast, is an autoimmune disease in which the body destroys pancreatic cells that produce insulin. Other types of diabetes include gestational diabetes, which can develop in pregnant women.


The latest study follows other recent research that has found an increased risk of a diabetes diagnosis after a Covid-19 infection, including a January Centers for Disease Control and Prevention report looking at children.

In a March study in the journal Diabetologia, German researchers found that people who had Covid-19 had a roughly 28% increased risk of a new Type 2 diagnosis compared to those who had an acute upper-respiratory infection that wasn’t Covid-19. The researchers compared data from more than 35,000 Covid-19 patients to an equal number of people with infections that weren’t Covid-19. They didn’t find an increased risk for other types of diabetes.

And a February JAMA Network Open study found that people who tested positive for Covid-19 had roughly a two times greater risk of a new Type 2 diagnosis one to five months after their infection compared to those who tested negative for the virus. About 7% of hospitalized adults with Covid-19 received new diabetes diagnoses within five months, compared to 3.6% of adults without Covid-19.

There are many challenges in interpreting the data, says Jason Block, an internal-medicine physician and associate professor at Harvard Medical School who is senior author of the JAMA study. Many people hadn’t been to see a doctor for a while during the pandemic, so they might have had diabetes without knowing it. In addition, steroids—a commonly used medication for severe Covid-19 patients—can temporarily increase blood sugar and might also trigger diabetes in patients at risk for the condition.

There are several possible biological reasons why a diabetes diagnosis might follow a Covid-19 infection. Research has indicated that the virus can infect and damage beta cells in the pancreas so that they produce less insulin.

In one study, researchers found that when they added the coronavirus to beta cell samples, genetic changes occurred in the cells that significantly reduced their ability to make insulin. Instead, to the researchers’ surprise, the cells did something unusual: They started making a different hormone, glucagon, whose function is to increase blood-glucose levels.


“The beta cells lost their cell identity and turned into a different type of cell,” says Shuibing Chen, director of the diabetes program at Weill Cornell Medicine in Manhattan, who led the study.

Dr. Chen says Covid-19 infection appears to be triggering a new type of diabetes that isn’t Type 1 or Type 2. Dr. Chen says her team is studying treatments specifically for Covid-19 patients newly diagnosed with diabetes to see whether they can block the process by which the cells might change.

Stanford researchers in an August study published in the journal Cell Metabolism documented another possible clue to post-Covid-19 diabetes. Lab studies found that the virus selectively targeted beta cells in the pancreas.

“It reduced their viability pretty quickly and reduced their ability to secrete insulin in less than a day,” says Peter Jackson, a professor in the microbiology and immunology department at Stanford University School of Medicine, and senior author on the study. “It’s a strong effect.”

G M

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Re: Wuhan Cooties and Diabetes
« Reply #1712 on: March 23, 2022, 02:49:53 AM »
As always, my question is: did this population take the ClotShot?

New Research Shows Higher Risk of Developing Diabetes After Covid-19 Infection
Study adds to growing evidence showing increased risk for a range of cardiometabolic conditions after Covid-19

By Sumathi Reddy
Follow
Updated March 21, 2022 7:52 pm ET


A large new study found that people who recovered from Covid-19 within the past year are 40% more likely to receive a new diagnosis of diabetes compared to those who weren’t infected.

The increased risk translates into 1% of people who have had Covid-19 developing diabetes who otherwise wouldn’t have, the study’s author says, resulting in potentially millions of new cases world-wide.

Most of the people with diabetes in the study, published online Monday in the journal Lancet Diabetes and Endocrinology, were diagnosed with Type 2 diabetes, not Type 1. Some researchers say Covid-19 could also be triggering an entirely new type of diabetes in which certain cells mistakenly start to raise, rather than lower, blood sugar.

The study adds to evidence showing an increased post-Covid-19 risk of cardiometabolic conditions, such as diabetes as well as heart and kidney complications. Normally when people think of long-term Covid-19 symptoms, they think of problems such as cognitive issues, fatigue or shortness of breath. But scientists say there are likely different types of long Covid, and one appears to be defined by cardiometabolic problems that arise after Covid-19. So far, the World Health Organization estimates there have been more than 464 million cases of Covid-19, so even small percentages of those people developing long-term complications would be significant.


New studies offer clues about who might be more susceptible to long Covid, a term for lingering Covid-19 symptoms. WSJ breaks down the science of long Covid and the state of treatment. Illustration: Jacob Reynolds for The Wall Street Journal
“We’re finding out more and more that it’s not only respiratory problems or brain fog or only fatigue,” says Ziyad Al-Aly, chief of research and development at the VA St. Louis Health Care System and a clinical epidemiologist at Washington University in St. Louis, who led the study. “There are heart manifestations, and clearly diabetes and kidney manifestations.”


Dr. Al-Aly’s group has recently published studies on those broader risks. One showed a higher risk of developing heart problems, including stroke and heart attack, in people who have had Covid-19 than in people who haven’t. Another showed post-Covid-19 patients were more likely to have declines in kidney function or kidney damage as much as six months after infection when compared to patients who hadn’t had Covid-19.

The researchers found only an association between Covid-19 and cardiometabolic conditions, without proving a cause. Some doctors say that new diagnoses of Type 2 diabetes and heart conditions could be influenced by weight gain or decreased activity during the pandemic, although lifestyle changes wouldn’t necessarily explain an increase specifically in people who have had Covid-19.

In the new diabetes study, Dr. Al-Aly and co-researchers analyzed the records of 181,000 Covid-19 patients in the Veterans Health Administration system who were diagnosed with Covid-19 within the past year and compared them to more than eight million people who didn’t have Covid-19.  The VA study didn’t look at diabetes cases by vaccination status.

“When you look at the data on a national scale it’s clearly happening even in people who have no risk factors or very little risk factors,” Dr. Al-Aly said, adding that new diagnoses are happening even in young adults with a healthy weight and no previous history of high blood sugar.



Maren Laughlin, a program director at the National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases, said the study was very well done. Its main limitation, she noted, is that VA patients generally tend to be older and sicker and include more males than the broader population.

It hasn’t been determined why a Covid-19 infection might be leading to new cases of diabetes. One possibility is that the virus might damage the pancreas’s ability to secrete insulin, the hormone that regulates blood sugar. Another theory is that the strong immune response to Covid-19 generates an inflammatory cascade that results in low-grade inflammation, which interferes with insulin secretion and sensitivity.

All types of diabetes share the symptom of high blood sugars, but they are distinct conditions. Type 2 is the most common, and can be associated with diet and exercise. Typically in Type 2, people become resistant to the hormone insulin, which regulates blood sugar. The pancreas struggles to keep up with the body’s increased demand for insulin, leading to higher blood-sugar levels.

Type 1, by contrast, is an autoimmune disease in which the body destroys pancreatic cells that produce insulin. Other types of diabetes include gestational diabetes, which can develop in pregnant women.


The latest study follows other recent research that has found an increased risk of a diabetes diagnosis after a Covid-19 infection, including a January Centers for Disease Control and Prevention report looking at children.

In a March study in the journal Diabetologia, German researchers found that people who had Covid-19 had a roughly 28% increased risk of a new Type 2 diagnosis compared to those who had an acute upper-respiratory infection that wasn’t Covid-19. The researchers compared data from more than 35,000 Covid-19 patients to an equal number of people with infections that weren’t Covid-19. They didn’t find an increased risk for other types of diabetes.

And a February JAMA Network Open study found that people who tested positive for Covid-19 had roughly a two times greater risk of a new Type 2 diagnosis one to five months after their infection compared to those who tested negative for the virus. About 7% of hospitalized adults with Covid-19 received new diabetes diagnoses within five months, compared to 3.6% of adults without Covid-19.

There are many challenges in interpreting the data, says Jason Block, an internal-medicine physician and associate professor at Harvard Medical School who is senior author of the JAMA study. Many people hadn’t been to see a doctor for a while during the pandemic, so they might have had diabetes without knowing it. In addition, steroids—a commonly used medication for severe Covid-19 patients—can temporarily increase blood sugar and might also trigger diabetes in patients at risk for the condition.

There are several possible biological reasons why a diabetes diagnosis might follow a Covid-19 infection. Research has indicated that the virus can infect and damage beta cells in the pancreas so that they produce less insulin.

In one study, researchers found that when they added the coronavirus to beta cell samples, genetic changes occurred in the cells that significantly reduced their ability to make insulin. Instead, to the researchers’ surprise, the cells did something unusual: They started making a different hormone, glucagon, whose function is to increase blood-glucose levels.


“The beta cells lost their cell identity and turned into a different type of cell,” says Shuibing Chen, director of the diabetes program at Weill Cornell Medicine in Manhattan, who led the study.

Dr. Chen says Covid-19 infection appears to be triggering a new type of diabetes that isn’t Type 1 or Type 2. Dr. Chen says her team is studying treatments specifically for Covid-19 patients newly diagnosed with diabetes to see whether they can block the process by which the cells might change.

Stanford researchers in an August study published in the journal Cell Metabolism documented another possible clue to post-Covid-19 diabetes. Lab studies found that the virus selectively targeted beta cells in the pancreas.

“It reduced their viability pretty quickly and reduced their ability to secrete insulin in less than a day,” says Peter Jackson, a professor in the microbiology and immunology department at Stanford University School of Medicine, and senior author on the study. “It’s a strong effect.”

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Re: Epidemics: Bird Flu, TB, AIDs, Superbugs, Ebola, etc
« Reply #1713 on: March 23, 2022, 03:10:48 AM »
A very good question and one not to be pushed under the carpet.

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Re: Epidemics: Bird Flu, TB, AIDs, Superbugs, Ebola, etc
« Reply #1714 on: March 23, 2022, 07:34:32 AM »
Newly Released Pfizer Documents Reveal COVID Jab Dangers
Joseph Mercola
Joseph Mercola
 March 22, 2022 Updated: March 23, 2022biggersmaller Print
What really happened in the first 90 days of the jab rollout? How many adverse events and different health problems? How many deaths? The first tranche of documents were released March 1, 2022, and it proves beyond any shadow of a doubt—we’ve been sold down the river!

Story at-a-glance
A small batch of documents released by the U.S. Food and Drug Administration in mid-November 2021 revealed that in the first three months of the COVID jab rollout, Pfizer received 42,086 adverse event reports that included 1,223 deaths
The first really large tranche of Pfizer documents — some 10,000 pages — was released by the FDA March 1, 2022. Included are nine pages of recorded side effects, about 158,000 different health problems in all
An initial review of case report forms (CRFs) reveal significant data collection errors and anomalies
Problems included patients entered into the “healthy population” group who were far from healthy; serious adverse event (SAE) numbers that were left blank; sample barcodes that were missing; at least one death of a patient the day before being listed as being at a medical checkup; and second doses that were administered outside the three-week protocol window. There also are questions as to whether participants were properly observed for an adequate amount of time; plus adverse events were listed as “not serious” despite extended hospital stay and much more
A majority of the CRFs in this release were from Ventavia-run trial sites. Ventavia is currently facing a lawsuit brought by Brook Jackson, a former Ventavia regional director. Jackson was fired shortly after she brought concerns about potential data falsification and poor laboratory management to the attention of the FDA and higher-ups in the company
In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the U.S. Food and Drug Administration to obtain the documentation used to approve Comirnaty, including safety and effectiveness data, adverse reaction reports and lists of active and inactive ingredients.

When, after a month, the FDA still had not responded to the FOIA request, the PHMPT sued.1 Pfizer and the FDA asked the judge to give them 75 years to release all the documents (doling out just 500 pages per month)2 but, fortunately, the judge ruled that they have to release them at a rate of 55,000 pages per month.

COVID Jab Supporter Gets Red-Pilled
In mid-November 2021, the FDA released the first 91 pages,3,4 which alone revealed the FDA has been aware of shocking safety issues since April 30, 2021. For nurse educator John Campbell, featured in the video above, these documents appear to have served as a “red pill,”5 waking him up to the possibility that the jabs may be far more dangerous than anyone expected, but he didn’t get around to reviewing them until now.

Cumulatively, through February 28, 2021, Pfizer received 42,086 adverse event reports, including 1,223 deaths. The latest tranche of Pfizer documents also includes a whopping nine pages of recorded side effects — 158,000 in all!
In his video, Campbell reviews the documents listed as “5.3.6. Postmarketing Experience,” which were originally marked “confidential.” They reveal that, cumulatively, through February 28, 2021, Pfizer received 42,086 adverse event reports, including 1,223 deaths.

As noted by Campbell, “It would have been good to know about this at the time, wouldn’t it?” referring to the rollout of the jabs. Campbell has been fairly consistent in his support of the “safe and effective” vaccine narrative, but “This has just destroyed trust in authority,” he says.

To have 1,223 fatalities and 42,086 reports of injury in the first three months is a significant safety signal, especially when you consider that the 1976 swine flu vaccine was pulled after only 25 deaths.

Now, the number of doses shipped has been redacted under a FOIA redaction code that stands for “Trade secrets and commercial or financial information obtained from a person and privileged or confidential.” Why would the number of doses shipped be confidential?

Campbell is clearly bothered by this redaction, as you cannot calculate the incidence rate or side effects if you don’t know what the denominator is. As noted by Campbell, that number cannot be proprietary. It’s being withheld for some other reason (and I just stated what that might be).

Even without knowing the underreporting factor, Campbell is appalled by the number of reported side effects. It is very clear that this information red-pilled Campbell. For an overview of the types of side effects recorded, check out Campbell’s video. I’ve already reviewed that in previous articles.

Here, we’ll move on to the first really large tranche of Pfizer documents, which was released March 1, 2022. In all, the FDA has some 450,000 pages of data from Pfizer’s COVID jab trials, and we now have just over 10,000 of those pages. You can find them all on PHMPT.org.6

Findings From Early Review of Case Reports
March 7, 2022, investigative journalist Sonia Elijah published a review of her initial findings on Trial Site News,7 having glossed through some of the thousands of newly-released documents.

Her review centers primarily on the case report forms (CRFs). These are documents used in clinical research to record standardized data from each patient, including adverse events. As such, they’re a crucial part of the clinical trial process.

A majority of the CRFs in this release were from Ventavia-run trial sites. Ventavia is currently facing a lawsuit brought by Brook Jackson, a former Ventavia regional director. Jackson was fired shortly after she brought concerns about potential data falsification and poor laboratory management to the attention of the FDA and higher-ups in the company.

Her testimony was published November 2, 2021, in The British Medical Journal — the oldest and most prestigious medical journal in the world — by investigative journalist Paul Thacker.8 Facebook fact checkers actually tried to “debunk” this BMJ article and censored it.

In her review of the CRFs, Elijah found a number of errors and anomalies that seem to corroborate Jackson’s claims, including the following:9

Patients entered into the “healthy population” group who were far from healthy — For example, one such “healthy” participant was a Type 2 diabetic with angina, a cardiac stent and a history of heart attack.
Serious adverse event (SAE) numbers were left blank — Ventavia site No. 1085 has a particularly large number of missing SAE numbers.
Missing barcodes for samples collected — Without those barcodes, you can’t match the sample to the participant.
Suspicious-looking SAE start and end dates — For example, the so-called “healthy” diabetic suffered a “serious” heart attack October 27, 2020. The “end” date is listed as October 28, the next day, which is odd because it was recorded as serious enough to require hospitalization.
Also, on that same day, October 28, the patient was diagnosed with pneumonia, so likely remained hospitalized. “This anomaly raises doubt as to the accuracy of these recorded dates, potentially violating ALOCA-C clinical site documentation guidelines for clinical trials,” Elijah writes.

Unblinded teams were responsible for reviewing adverse event reports for signs of COVID cases, and to review severe COVID cases — Yet in some cases they appear to have dismissed the possibility of an event being COVID-related, such as pneumonia. This despite the fact that Pfizer’s protocol (section 8.2.4) lists “enhanced COVID-19” (i.e., antibody dependent enhancement) as a potential side effect to be on the lookout for. As noted by Elijah:
“Inadvertently, this could have led to bias, as the unblinded teams would have been aware which participants were assigned the placebo and those who received the vaccine. They might have been under pressure by the sponsor for the trial to go a certain way and for events like ‘COVID Pneumonia’ to be classified simply as pneumonia.”

Impossible dating — The diabetic who suffered a heart attack followed by pneumonia (which may have been unacknowledged COVID pneumonia) died, and the date of death is listed as the day before the patient supposedly went for a “COVID ill” visit.
Clearly, it’s impossible for a dead person to attend a medical visit, so something is wrong here. The clinical investigator note states: “There cannot be a date later than date of death. Please remove data from the COVID illness visit and add cough and shortness of breath as AEs (adverse events).” “What kind of pressure was being exerted here?” Elijah asks.

Adverse events listed as “not serious” despite extended hospital stay — In one case, the participant fell and suffered facial lacerations the day after the second dose and was hospitalized for 26 days, yet the fall was not reported as serious.
Other anomalies in this particular case include listing the fall as being caused by a “fall” unrelated to the study treatment, and the facial laceration being the result of “hypotension” (low blood pressure). The SAE number is also missing for the facial lacerations.

Elijah writes, “Doubts can be raised over the credibility of this information given the fall and facial lacerations were intrinsically related. So, if facial lacerations were due to ‘hypotension’ then the fall should be due to that too.” Might low blood pressure be an effect of the experimental shot? Possibly. Especially when you consider the patient fell the day after being given the second dose.

Even more suspicious: the causality for the fall was recorded as “related” (to the treatment) on the serious adverse event form, but listed as “not related” on the adverse event CRF. A note states, “Please confirm correct causality.”

Dismissing brand new health problems as unrelated to the treatment — For example, in one case, a female participant with no medical history of impaired kidney function was diagnosed with kidney stones and severe hypokalemia, requiring hospitalization, one month after her second dose. Yet despite her having no history of kidney problems, both events were dismissed as “not related” to the study treatment and no further investigation was done.
In closing, Elijah writes:10

“All the evidence gleaned over a limited time appears to back up whistleblower Jackson’s claims of poor trial site data management and raises questions as to how Ventavia conducted the Pfizer clinical trials.

The errors and anomalies in the CRFs also allude to her claims that the clinical research associates were not trained adequately, with many having had no prior clinical experience history. If such egregious findings are true at these sites, could they manifest at other trial sites around North America and beyond?”

Enormous List of Side Effects
The latest tranche of Pfizer documents also includes a whopping nine pages of recorded side effects — 158,000 in all! The picture below speaks louder than anything I can say about this list.

pfizer list release
Enormous Gap Between What We’ve Been Told and Reality

The Pfizer documents reveal an enormous gap between what we were told about the jab and what the FDA and Pfizer actually knew about it. In a recent article published by The Defender,11 Dr. Meryl Nass asks, “Pfizer, FDA documents contradict official COVID vaccine safety narrative — Is this fraud?”

As noted by Nass, what we’re told in the media is one thing, and what these documents reveal is another. And, importantly, the content of these documents “tell us what information Pfizer and the FDA are willing to stand by.” They also establish what the legal requirements for emergency use authorization and licensing.

“It may come as a shock, but what the FDA said when it issued both the EUA and the license for Pfizer’s vaccines was very different from what you heard from the Centers for Disease Control and Prevention (CDC), the media and other sources,” Nass writes.12

CDC Guidance Contradicts Comirnaty Label
She also lists several instances where CDC statements to the public clearly contradict statements on the Comirnaty label. For example:13,14

• While the CDC initially claimed that anaphylactic reactions to the jab occur at approximately the same rate as other vaccines, they’ve since removed that claim, and both the CDC and the Comirnaty label now states that administration of Comirnaty is limited to facilities that can medically manage anaphylactic reactions.

“This is not the case for other vaccines,” Nass says, adding that research from Harvard hospitals reveal the rate of anaphylaxis in employees who got the COVID jab was 50 to 100 times higher than the rate claimed by the CDC, which calculates that rate based on reports in the Vaccine Adverse Event Reporting System (VAERS). Interestingly enough, this matches up with what we believe to be the underreporting factor for VAERS might be.

• While the CDC claims post-jab myocarditis is mild and resolves quickly, the Comirnaty label clearly states that “Information is not yet available about potential long-term sequelae.”

• The CDC recommends the COVID jab for pregnant women, yet the label states that “available data on Comirnaty administered to pregnant women are insufficient to inform vaccine associated risks in pregnancy.”

• The CDC, FDA and mainstream media contend that the COVID jab cannot cause cancer or fertility problems, yet the Comirnaty label clearly states that “Comirnaty has not been evaluated for the potential to cause carcinogenicity, genotoxicity, or impairment of male fertility.” If it has not been evaluated, how can they claim to know that it cannot cause these kinds of problems — especially considering the list of reported side effects, above?

• Even though the stated purpose of mass vaccination is to create “herd immunity,” the FDA did not require Pfizer to assess whether the jab could protect against asymptomatic infection or prevent transmission of SARS-CoV-2.

What Was It All For?

With each passing week, the cracks in the official COVID narrative keep multiplying and widening. It’ll be interesting to see what finally breaks the proverbial dam.

Pfizer CEO Albert Bourla is now out there pushing for a fourth shot,15 saying a second booster will be “necessary for most,” as three shots not only can’t protect against variants, but they rapidly wane in strength. For those same reasons, Americans must expect to get an annual booster each fall.

Under normal circumstances, that should have ripped the wool off of people’s eyes, but the COVID brainwashing has been so successful, many still can’t see just how badly they’ve been lied to. I believe the final salvo that will wake up the masses will either be revelations about harms, or the realization of what the planned social credit system would actually mean for the average American.

In 2018, Pfizer proudly partnered with a Chinese Communist Party (CCP) payment platform, Alipay, which was used to implement an early Chinese version of vaccine passports, called the “Internet + Vaccination” initiative, aimed at creating “Disease awareness via mobile devices.”16

According to the U.S. State Department, Alipay is a “tool” used by the CCP in its build-up of “technology-facilitated surveillance and social control” network, also known as a social credit system. The same sort of system is now being rolled out in other parts of the world, including the U.S., so it’s interesting to note Pfizer’s involvement with that early digital vaccine passport initiative.

Mid-March 2022, Bourla gave an interview with Washington Post Live (above), admitting the decision to use mRNA technology in the creation of a COVID “vaccine” was “counterintuitive,” as Pfizer has “good experience” with several other vaccine technologies, but only two years’ worth of experience with mRNA, which had never been used in a commercially available medicine before.

In the end, Bourla may come to regret that decision, as it has turned out to be an incredibly lethal one. Although I guess it will depend on whether he’s ever held to account for those choices.

Originally published March 22, 2022 on Mercola.com

Sources and References
1 The Defender, Nov. 19, 2021
2 Newsmax, Dec. 8, 2021
3, 6 PHMPT.org Pfizer documents
4 thekylebecker.substack.com, Nov. 21, 2021
5 Steve Kirsch Substack, March 11, 2022
7, 9, 10 Trial Site News, March 7, 2022
8 The BMJ 2021; 375:n2635
11, 13 The Defender, March 15, 2022
14 Meryl Nass Substack, March 14, 2022
15 NY Post, March 13, 2022
16 The National Pulse, Dec. 29, 2021


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Re: Epidemics: Bird Flu, TB, AIDs, Superbugs, Ebola, etc
« Reply #1716 on: March 27, 2022, 12:36:10 AM »
FK!!!





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We know the ClotShot isn't effective...
« Reply #1721 on: April 04, 2022, 02:48:43 PM »


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Numerous health problems likely due to vaxxes
« Reply #1724 on: April 06, 2022, 08:00:59 AM »
https://www.theepochtimes.com/numerous-health-problems-more-likely-due-to-covid-19-vaccines-than-coincidence-vaers-data-analysis_4380017.html?utm_source=Top5&utm_campaign=top5-2022-04-06&utm_medium=email&est=9cmgapl14acNyL%2Bb7VTRp5P9%2BC2FgCvjvQ1bpWCvIEVlIHj18jjfCL3GzM4ZMoDuq%2B5j

Numerous Health Problems More Likely Because of COVID-19 Vaccines Than Coincidence: VAERS Data Analysis
By Petr Svab April 3, 2022 Updated: April 5, 2022biggersmaller Print
Various health problems reported by people after receiving one of the COVID-19 vaccine shots are more likely to have been caused by the vaccines than to be coincidental, according to an analysis of data from the Vaccine Adverse Event Reporting System (VAERS).

VAERS has been flooded with more than 1 million reports of various health problems and more than 21,000 death reports since the introduction of the vaccines in late 2020. Some experts and public officials have downplayed the significance of the reports, noting that just because a health problem occurs after getting the vaccine doesn’t mean the problem was caused by it.

However, a deeper analysis of the data indicates that many of the adverse effects are more than just a coincidence, according to Jessica Rose, a computational biologist who’s been studying the data for at least nine months.

“The safety signals being thrown off in VAERS now are off the charts across the board,” Rose told The Epoch Times.

There are multiple ways to parse the data in order to flesh out whether the causal link between an adverse event and the vaccination is real or illusory. For example, multiple COVID-19 vaccines come in two doses. A random adverse event unrelated to the vaccine should be dose-agnostic. A stroke randomly coinciding with a vaccination shouldn’t be picky about which dose it was.

In the VAERS data, however, a number of the reported problems are dose-dependent. Myocarditis in teenagers is reported several times more often after the second vaccine dose than after the first dose. Following a vaccine booster shot, in contrast, the frequency is significantly lower than after the first dose, Rose found.

Epoch Times Photo
A graph showing age against the absolute number of myocarditis reports filed to VAERS according to doses 1, 2, and 3 of the COVID-19 vaccines. (Jessica Rose)
Other researchers and health authorities have already acknowledged that the shots are associated with an elevated risk of myocarditis, especially in teenage boys, although they usually also say the risk is low.

Yet dose-dependency shows up in the VAERS data for other problems as well, including fainting and dizziness, which are more common after the first dose.

Epoch Times Photo
A graph showing age against the absolute number of syncope (fainting) reports filed to VAERS according to doses 1 and 2 of the COVID-19 vaccines. (Jessica Rose)
Rose acknowledged that statistical analysis seldom provides definitive answers. For instance, there could be some unknown factor that leads to more reports of unrelated health events after the first or second vaccine dose. In her view, however, the data leans away from such a conclusion.

Previous research shows that the majority of VAERS reports are filed by medical staff, who shouldn’t fail to report adverse events based on which dose is being administered. To Rose, it seems more likely that if people suffer health problems after an injection of a novel substance and if the problems substantially change between the first and the second shot, the substance probably had something to do with it.

“In lieu of being able to explain this happening for any other reason, it satisfies the dose-response point quite well, in my opinion,” she said of the myocarditis results.

As for why the reports dropped after the vaccine “booster” shots, Rose said she hasn’t found a definitive explanation. It could be that people who didn’t feel well after the first two shots would think twice about getting more. As such, those most at risk for an adverse reaction would be less likely to get the booster.

She arrived at the results after she evaluated the VAERS data from the perspective of the Bradford Hill criteria—a set of nine questions that are used by epidemiologists to determine whether any given factor is likely the cause of an observed health effect. She said she found evidence to answer all of the questions positively.

Rose encountered resistance in the establishment science circles when she first tried to publicize her analyses. Last year, right before her paper on VAERS myocarditis data was printed, the publisher pulled the paper for unclear reasons.

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Wuhan Vax far more dangerous than advertised
« Reply #1725 on: April 06, 2022, 08:04:00 AM »
second

https://www.theepochtimes.com/covid-jab-is-far-more-dangerous-than-advertised_4381781.html?utm_source=Top5&utm_campaign=top5-2022-04-06&utm_medium=email&est=X7uELVMk2OQATVCqV8jYHnZLNSFPbFuNb1M3jh2EIxrmVsQlqJQTh1y9jPJQKwDhjAlo


COVID Jab Is Far More Dangerous Than Advertised
And that's for those over the age of 65.
BY JOSEPH MERCOLA TIMEAPRIL 4, 2022 PRINT
October 26, 2021, Global Research published an interview with Dr. Peter McCullough, in which he reviews and explains the findings of a September 2021 study published in the journal Toxicology Reports.



STORY AT-A-GLANCE
According to a September 2021 analysis, based on conservative, best-case scenarios, the COVID shots have killed five times more seniors (65+) than the infection
In younger people and children, the risk associated with the COVID shot, compared to the risk of COVID-19, is bound to be even more pronounced
Data show higher vaccination rates do not translate into lower COVID-19 case rates
50% of reported deaths after COVID-19 “vaccination” occur within 24 hours; 80% occur within the first week. According to one report, 86% of deaths have no other explanation aside from a vaccine adverse event. A Scandinavian study concluded about 40% of post-jab deaths among seniors in assisted living homes are directly due to the injection
The study in the journal Toxicology Reports, states: (1)

“A novel best-case scenario cost-benefit analysis showed very conservatively that there are five times the number of deaths attributable to each inoculation vs those attributable to COVID-19 in the most vulnerable 65+ demographic.

The risk of death from COVID-19 decreases drastically as age decreases, and the longer-term effects of the inoculations on lower age groups will increase their risk-benefit ratio, perhaps substantially.”

“A novel best-case scenario cost-benefit analysis showed very conservatively that there are five times the number of deaths attributable to each inoculation vs those attributable to COVID-19 in the most vulnerable 65+ demographic.

The risk of death from COVID-19 decreases drastically as age decreases, and the longer-term effects of the inoculations on lower age groups will increase their risk-benefit ratio, perhaps substantially.”

McCullough has impeccable academic credentials. He’s an internist, cardiologist, epidemiologist and a full professor of medicine at Texas A&M College of Medicine in Dallas. He also has a master’s degree in public health and is known for being one of the top five most-published medical researchers in the United States, in addition to being the editor of two medical journals.

Authors Defend Their Paper
Not surprisingly, the Toxicology Reports paper has received scathing critique from certain quarters. Still, corresponding author Ronald Kostoff told Retraction Watch that the criticism has actually been “an extremely small fraction” of the overall response, which by and large has been overwhelmingly positive and supportive. Kostoff went on to say: (2)

“Given the blatant censorship of the mainstream media and social media, only one side of the COVID-19 ‘vaccine’ narrative is reaching the public. Any questioning of the narrative is met with the harshest response …

I went into this with my eyes wide open, determined to identify the truth, irrespective of where it fell. I could not stand idly by while the least vulnerable to serious COVID-19 consequences were injected with substances of unknown mid and long-term safety.

We published a best-case scenario. The real-world situation is far worse than our best-case scenario, and could be the subject of a future paper.

What these results show is that we 1) instituted mass inoculations of an inadequately-tested toxic substance with 2) non-negligible attendant crippling and lethal results to 3) potentially prevent a relatively small number of true COVID-19 deaths. In other words, we used a howitzer where an accurate rifle would have sufficed!”

COVID Jab Campaign Has Had No Discernible Impact
Certainly, data very clearly show the mass “vaccination” campaign has not had a discernible impact on global death rates. On the contrary, in some cases the death toll shot up after the COVID shots became widely available. You can browse through covid19.healthdata.org (3) to see this for yourself. Several examples are also included at the very beginning of the video.

This trend has also been confirmed in a September 2021 study(4) published in the European Journal of Epidemiology. It found COVID-19 case rates are completely unrelated to vaccination rates.

Using data available as of September 3, 2021, from Our World in Data for cross-country analysis, and the White House COVID-19 Team data for U.S. counties, the researchers investigated the relationship between new COVID-19 cases and the percentage of the population that had been fully vaccinated.

Sixty-eight countries were included. Inclusion criteria included second dose vaccine data, COVID-19 case data and population data as of September 3, 2021. They then computed the COVID-19 cases per 1 million people for each country, and calculated the percentage of population that was fully vaccinated.

According to the authors, there was “no discernable relationship between percentage of population fully vaccinated and new COVID-19 cases in the last seven days.” If anything, higher vaccination rates were associated with a slight increase in cases. According to the authors: (5)

“[T]he trend line suggests a marginally positive association such that countries with higher percentage of population fully vaccinated have higher COVID-19 cases per 1 million people.”

The Kostoff Analysis
Getting back to the Toxicology Reports paper, (6) which is being referring to as “the Kostoff analysis,” McCullough says the analysis is definitely making news in clinical medicine. The paper focuses on two factors: assumptions and determinism.

Determinism describes how likely something is. For example, if a person takes a COVID shot, it’s 100% certain they got the injection. It’s not 50% or 75%. It’s an absolute certainty. As a result, that person has a 100% chance of being exposed to whatever risk is associated with that shot.

On the other hand, if a person says no to the injection, it’s not 100% chance they’ll get COVID-19, let alone die from it. You have a less than 1% chance of being exposed to SARS-CoV-2 and getting sick. So, it’s 100% deterministic that taking the shot exposes you to the risks of the shot, and less than 1% deterministic that you’ll get COVID if you don’t take the shot.

The other part of the equation is the assumptions, which are based on calculations using available data, such as pre-COVID death statistics and death reports filed with the U.S. Vaccine Adverse Event Reports System (VAERS).

Mortality Data
As noted by McCullough, two reports have detailed COVID jab death data, showing 50% of deaths occur within 24 hours and 80% occur within the first week. In one of these reports, 86% of deaths were found to have no other explanation aside from a vaccine adverse event. McCullough also cites a Scandinavian study that concluded about 40% of post-jab deaths among seniors in assisted living homes are directly due to the injection. He also cites other eye-opening figures:

The U.S. Center for Disease Control and Prevention reports having more than 30,000 spontaneous reports of either hospitalizations and/or deaths among the fully vaccinated
Data from the Centers for Medicare & Medicaid Services show 300,000 vaccinated CMS recipients have been hospitalized with breakthrough infections
60% of seniors over age 65 hospitalized for COVID-19 have been vaccinated
COVID Shots Are ‘Failing Wholesale’
“When we put all these data together, we have clear-cut science that the vaccines are failing wholesale,” McCullough says. The shots are particularly useless in seniors.

Again, based on a best-case conservative scenario, seniors are five times more likely to die from the shot than they are from the natural infection. This scenario includes the assumption that the PCR test is accurate and reported COVID deaths were in fact due to COVID-19, which we know is not the case, and the assumption that the shots actually prevent death, which we have no proof of.

All things considered, you are FAR better off taking your chances with the natural infection, as McCullough says. The Kostoff analysis also does not take into account the fact that there are safe and effective treatments.

It bases its assumptions on the notion that there aren’t any. It also doesn’t factor in the fact that the COVID shots are utterly ineffective against the Delta and other variants. If you take into account vaccine failure against variants and alternative treatments, it skews the analysis even further toward natural infection being the safest alternative.

FDA and CDC Should Not Run Vaccine Programs
While the U.S. Food and Drug Administration and the CDC claim not a single death following COVID inoculation was caused by the shot, they should not be the ones making that determination, as they are both sponsoring the vaccination campaign.

They have an inherent bias. When you conduct a trial, you would never allow the sponsor to tell you whether the product was the cause of death, because you know they’re biased.

“We have actually fulfilled all of the Bradford Hill criteria. I’ll tell you right now that COVID-19 vaccine is, from an epidemiological perspective, causing these deaths or a large fraction.” ~ Dr. Peter McCullough
What we need is an external group, a critical event committee, to analyze the deaths being reported, as well as a data safety monitoring board. These should have been in place from the start, but were not.

Had they been, the program would most likely have been halted in February, as by then the number of reported deaths, 186, already exceeded the tolerable threshold of about 150 (based on the number of injections given). Now, we’re well over 17,000. (7) There’s no normal circumstance under which that would ever be allowed.

“The CDC and FDA are running the [vaccination] program. They are NOT the people who typically run vaccine programs,” McCullough says. “The drug companies run vaccine programs.

When Pfizer, Moderna, J&J ran their randomized trials, we didn’t have any problems. They had good safety oversight. They had data safety monitoring boards. The did OK. I mean I have to give the drug companies [credit].

But the drug companies are now just the suppliers of the vaccine. Our government agencies are now just running the program. There’s no external advisory committee. There’s no data safety monitoring board. There’s no human ethics committee. NO one is watching out for this!

And so, the CDC and FDA pretty clearly have their marching orders: ‘Execute this program; the vaccine is safe and effective.’ They’re giving no reports to Americans. No safety reports. We needed those once a month. They haven’t told doctors which is the best vaccine, which is the safest vaccine.

They haven’t told us what groups are to watch out for. How to mitigate risks. Maybe there are drug interactions. Maybe it’s people with prior blood clotting problems or diabetes. They’re not telling us anything!

They literally are blindsiding us, and with no transparency, and Americans now are scared to death. You can feel the tension in America. People are walking off the job. They don’t want to lose their jobs, but they don’t want to die of the vaccine! It’s very clear. They say, ‘Listen, I don’t want to die. That’s the reason I’m not taking the vaccine.’ It’s just that clear.”

Bradford Hill Criteria Are Met — COVID Jabs Cause Death
McCullough goes on to explain the Bradford Hill criterion for causation, which is one of the ways by which we can actually determine that, yes, the shots are indeed killing people. We’re not dealing with coincidence.

“The first question we’d ask is: ‘Does the vaccine have a mechanism of action, a biological mechanism of action, that can actually kill a human being?’ And the answer is yes! because the vaccines all use genetic mechanisms to trick the body into making the lethal spike protein of the virus.

It is very conceivable that some people take up too much messenger RNA; they produce a lethal spike protein in sensitive organs like the brain or the heart or elsewhere. The spike protein damages blood vessels, damages organs, causes blood clots. So, it’s well within the mechanism of action that the vaccine could be fatal.

Someone could have a fatal blood clot. They could have fatal myocarditis. The FDA has official warnings of myocarditis. They have warnings on blood clots. They have warnings on a fatal neurologic condition called Guillain-Barré syndrome. So, the FDA warnings, the mechanism of action, clearly say it’s possible.

The second criteria is: ‘Is it a large effect?’ And the answer is yes! This is not a subtle thing. It’s not 151 versus 149 deaths. This is 15,000 deaths. So, it’s a very large effect size, a large effect.

The third [criteria] is: ‘Is it internally consistent?’ Are you seeing other things that could potentially be fatal in VAERS? Yes! We’re seeing heart attacks. We’re seeing strokes. We’re seeing myocarditis. We’re seeing blood clots, and what have you. So, it’s internally consistent.

‘Is it externally consistent?’ That’s the next criteria. Well, if you look in the MHRA, the yellow card system in England, the exact same thing has been found. In the EudraVigilance system in [Europe] the exact same thing’s been found.

So, we have actually fulfilled all of the Bradford Hill criteria. I’ll tell you right now that COVID-19 vaccine is, from an epidemiological perspective, causing these deaths or a large fraction.”

Zero Tolerance for Elective Drugs Causing Death
There may be cases in which a high risk of death from a drug might be acceptable. If you have a terminal incurable disease, for example, you may be willing to experiment and take your chances. Under normal circumstances however, lethal drugs are not tolerated.

After five suspected deaths, a drug will receive a black box warning. At 50 deaths, it will be removed from the market. Considering COVID-19 has a less than 1% risk of death across age groups, the tolerance for a deadly remedy is infinitesimal. At over 17,000 reported deaths, which in real numbers may exceed 212,000,(8) the COVID shots far surpass any reasonable risk to protect against symptomatic COVID-19. As noted by McCullough:

“There is zero tolerance for electively taking a drug or a new vaccine and then dying! There’s zero tolerance for that. People don’t weigh it out and say, ‘Oh well, I’ll take my chances and die.’ And I can tell you, the word got out about vaccines causing death in early April [2021], and by mid-April the vaccination rates in the United States plummeted …

We hadn’t gotten anywhere near our goals. Remember, President Biden set a goal [of 70% vaccination rate] by July 1. We never got there because Americans were frightened by their relatives, people in their churches and their schools dying after the vaccine.

They had heard about it, they saw it. There was an informal internet survey done several months ago, where 12% of Americans knew somebody who had died after the vaccine.

I’m a doctor. I’m an internist and cardiologist. I just came from the hospital … I had a woman die of the COVID-19 vaccine … She had shot No. 1. She had shot No. 2. After shot No. 2, she developed blood clots throughout her body. She required hospitalization. She required intravenous blood thinners. She was ravaged. She had neurologic damage.

After that hospitalization, she was in a walker. She came to my office. I checked for more blood clots. I found more blood clots. I put her back on blood thinners. I saw her about a month later. She seemed like she was a little better. Family was really concerned. The next month I got called by the Dallas Coroner office saying she’s found dead at home.

Most of us don’t have any problem with vaccines; 98% of Americans take all the vaccines … I think most people who are still susceptible would take a COVID vaccine if they knew they weren’t going to die of it or be injured. And because of these giant safety concerns, and the lack of transparency, we’re at an impasse.

We’ve got a very labor-constrained market. We’ve got people walking off the job. We’ve got planes that aren’t going to fly, and it’s all because our agencies are not being transparent and honest with America about vaccine safety.”

Early Treatment Is Crucial, Vaxxed or Not
As noted by McCullough, the vast majority of patients require hospitalization for COVID-19 is because they’ve not received any treatment and the infection has been allowed free reign for days on end.

“To this day, the patients who get hospitalized are largely those who receive no early care at home,” he says. “They’re either denied care or they don’t know about it, and they end up dying.

The vast majority of people who die, die in the hospital; they don’t die at home. And the reason why they end up in the hospital, it’s typically two weeks of lack of treatment. You can’t let a fatal illness brew for two weeks at home with no treatment, and then start treatment very late in the hospital. It’s not going to work.

There’s been a very good set of analyses, one in the Journal of Clinical Infectious Diseases … that showed, day by day, one loses the opportunity of reducing the hospitalization when monoclonal antibodies are delayed … No doctor should be considered a renegade when they order FDA [emergency use authorized] monoclonal antibody. The monoclonal antibodies are just as approved as the vaccines.

I just had a patient over the weekend, fully vaccinated, took the booster. A month after the booster she went on a trip to Dubai. She just came back, and she got COVID-19! … I got her a monoclonal antibody infusion that day. [The following day] she started the sequence of multidrug therapy for COVID-19. I am telling you, she is going to get through this illness in a few days …

Podcaster Joe Rogan just went through this. Governor Abbott was also a vaccine failure. He went through it. Former President Trump went through it. Americans should see the use of monoclonal antibodies in high risk patients, followed by drugs in an oral sequenced approach. This is standard of care!

It is supported by the Association of Physicians and Surgeons, the Truth for Health Foundation, the American Front Line Doctors, and the Front Line Critical Care Consortium. This is not renegade medicine. This is what patients should have. This is the correct thing! …

If we can’t get the monoclonal antibodies, we certainly use hydroxychloroquine, supported by over 250 studies, ivermectin, supported by over 60 studies, combined with azithromycin or doxycycline, inhaled budesonide … full-dose aspirin … nutraceuticals including zinc, vitamin D, vitamin C, quercetin, NAC … we do oral and nasal decontamination with povidone-iodine.

In acutely sick patients we do it every four hours, [and it] massively reduces the viral load … Fortunately, we have enough doctors now and enough patient awareness, patients who … understand that early treatment is viable, is necessary, and it should be executed.”

Originally published Nov 18, 2021 on Mercola.com

References
(1) Toxicology Reports September 2021; 8: 1665-1684

(2) Retraction Watch October 4, 2021

(3) Covid19.healthdata.org

(4) European Journal of Epidemiology September 30, 2021

(5) European Journal of Epidemiology September 30, 2021

(6) Toxicology Reports September 2021; 8: 1665-1684

(7) OpenVAERS Data as of October 15, 2021

(8) SKirsch.io/vaccine-resources

Views expressed in this article are the opinions of the author and do not necessarily reflect the views of The Epoch Times

Crafty_Dog

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9/21 Dr. Makary
« Reply #1726 on: April 06, 2022, 08:21:09 AM »
third

Natural immunity to covid is powerful. Policymakers seem afraid to say so.
People making decisions about their health deserve honesty from their leaders.
Image without a caption
By Marty Makary
Marty Makary is a professor at the Johns Hopkins School of Medicine and Bloomberg School of Public Health, editor-in-chief of Medpage Today, and author of “The Price We Pay: What Broke American Health Care — and How to Fix It."
September 15, 2021 at 12:45 p.m. EDT

President Biden visits the Viral Pathogenesis Laboratory at the National Institutes of Health in February, with Anthony S. Fauci, director of the National Institute of Allergy and Infectious Diseases, and NIH director Francis Collins listening. (Evan Vucci/AP)



CORRECTION
A previous version of this article erroneously said Spectrum Health is in Detroit. It is in Grand Rapids, Mich. The article has been corrected.

It’s okay to have an incorrect scientific hypothesis. But when new data proves it wrong, you have to adapt. Unfortunately, many elected leaders and public health officials have held on far too long to the hypothesis that natural immunity offers unreliable protection against covid-19 — a contention that is being rapidly debunked by science.

More than 15 studies have demonstrated the power of immunity acquired by previously having the virus. A 700,000-person study from Israel two weeks ago found that those who had experienced prior infections were 27 times less likely to get a second symptomatic covid infection than those who were vaccinated. This affirmed a June Cleveland Clinic study of health-care workers (who are often exposed to the virus), in which none who had previously tested positive for the coronavirus got reinfected. The study authors concluded that “individuals who have had SARS-CoV-2 infection are unlikely to benefit from covid-19 vaccination.” And in May, a Washington University study found that even a mild covid infection resulted in long-lasting immunity.

Coronavirus vaccines work. But this statistical illusion makes people think they don’t.

So, the emerging science suggests that natural immunity is as good as or better than vaccine-induced immunity. That’s why it’s so frustrating that the Biden administration has repeatedly argued that immunity conferred by vaccines is preferable to immunity caused by natural infection, as NIH director Francis Collins told Fox News host told Bret Baier a few weeks ago. That rigid adherence to an outdated theory is also reflected in President Biden’s recent announcement that large companies must require their employees to get vaccinated or submit to regular testing, regardless of whether they previously had the virus.

ADVERTISING


Downplaying the power of natural immunity has had deadly consequences. In January, February and March, we wasted scarce vaccine doses on millions of people who previously had covid. If we had asked Americans who were already protected by natural immunity to step aside in the vaccine line, tens of thousands of lives could have been saved. This is not just in hindsight is 20/20; many of us were vehemently arguing and writing at the time for such a rationing strategy.

One reason public health officials may be afraid to acknowledge the effectiveness of natural immunity is that they fear it will lead some to choose getting the infection over vaccination. That’s a legitimate concern. But we can encourage all Americans to get vaccinated while still being honest about the data. In my clinical experience, I have found patients to be extremely forgiving with evolving data if you are honest and transparent with them. Yet, when asked the common question, “I’ve recovered from covid, is it absolutely essential that I get vaccinated?” many public health officials have put aside the data and responded with a synchronized “yes,” even as studies have shown that reinfections are rare and often asymptomatic or mild when they do occur.

The tide may finally be shifting, as pressure has grown on federal officials. Last week on CNN, Anthony S. Fauci, the nation’s top infectious-disease specialist, hinted that the government may be rethinking its stance on natural immunity, saying, “I think that is something that we need to sit down and discuss seriously.” Some large medical centers, like Spectrum Health in Grand Rapids, Mich., have already announced they will recognize natural immunity for their vaccine requirements. Some Republican governors have picked up on public frustration over how the scientific guidance is inconsistent with the data, with Florida Gov. Ron DeSantis accusing the Biden administration of “not following science” by crafting its vaccine mandate without taking into consideration “infection-conferred immunity.”

Booster shots won’t stop the delta variant. Here’s the math to prove it.

The current Centers for Disease Control and Prevention position about vaccinating children also dismisses the benefits of natural immunity. The Los Angeles County School District recently mandated vaccines for students ages 12 and up who want to learn in person. But young people are less likely to suffer severe or long-lasting symptoms from covid-19 than adults, and have experienced rare heart complications from the vaccines. In Israel, heart inflammation has been observed in between 1 in 3,000 and 1 in 6,000 males age 16 to 24; the CDC has confirmed 854 reports nationally in people age 30 and younger who got the vaccine.


A second dose of the two-shot mRNA vaccine like that produced by Pfizer and Moderna may not even be necessary in children who had covid. Since February, Israel’s Health Ministry has been recommending that anyone, adult or adolescent, who has recovered from covid-19 receive a only single mRNA vaccine dose, instead of two. Even though the risk of severe illness during a reinfection is exceedingly low, some data has demonstrated a slight benefit to one dose in this situation. Other countries use a similar approach. The United States could adopt this strategy now as a reasonable next step in transitioning from an overly rigid to a more flexible vaccine requirement policy. For comparison, the CDC has long recommended that kids do not get the chickenpox vaccine if they had chickenpox infection in the past.

The incorrect hypothesis that natural immunity is unreliable has resulted in the loss of thousands of American lives, avoidable vaccine complications, and damaged the credibility of public health officials. Given the recent mandate announcement by the White House, it would be good for our public health leaders to show humility by acknowledging that the hypothesis they repeatedly trumpeted was not only wrong, but it may be harmful. Let’s all come together around the mounting body of scientific literature and real-world clinical experience that is telling us not to require the full vaccine regimen in people who recovered from covid in the past. Public health officials changing their position on natural immunity, after so much hostility toward the idea, would go a long way in rebuilding the public trust.

G M

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Re: 9/21 Dr. Makary
« Reply #1727 on: April 06, 2022, 08:34:58 AM »
How are you going to "soft kill" the population if you let them avoid the ClotShot?



third

Natural immunity to covid is powerful. Policymakers seem afraid to say so.
People making decisions about their health deserve honesty from their leaders.
Image without a caption
By Marty Makary
Marty Makary is a professor at the Johns Hopkins School of Medicine and Bloomberg School of Public Health, editor-in-chief of Medpage Today, and author of “The Price We Pay: What Broke American Health Care — and How to Fix It."
September 15, 2021 at 12:45 p.m. EDT

President Biden visits the Viral Pathogenesis Laboratory at the National Institutes of Health in February, with Anthony S. Fauci, director of the National Institute of Allergy and Infectious Diseases, and NIH director Francis Collins listening. (Evan Vucci/AP)



CORRECTION
A previous version of this article erroneously said Spectrum Health is in Detroit. It is in Grand Rapids, Mich. The article has been corrected.

It’s okay to have an incorrect scientific hypothesis. But when new data proves it wrong, you have to adapt. Unfortunately, many elected leaders and public health officials have held on far too long to the hypothesis that natural immunity offers unreliable protection against covid-19 — a contention that is being rapidly debunked by science.

More than 15 studies have demonstrated the power of immunity acquired by previously having the virus. A 700,000-person study from Israel two weeks ago found that those who had experienced prior infections were 27 times less likely to get a second symptomatic covid infection than those who were vaccinated. This affirmed a June Cleveland Clinic study of health-care workers (who are often exposed to the virus), in which none who had previously tested positive for the coronavirus got reinfected. The study authors concluded that “individuals who have had SARS-CoV-2 infection are unlikely to benefit from covid-19 vaccination.” And in May, a Washington University study found that even a mild covid infection resulted in long-lasting immunity.

Coronavirus vaccines work. But this statistical illusion makes people think they don’t.

So, the emerging science suggests that natural immunity is as good as or better than vaccine-induced immunity. That’s why it’s so frustrating that the Biden administration has repeatedly argued that immunity conferred by vaccines is preferable to immunity caused by natural infection, as NIH director Francis Collins told Fox News host told Bret Baier a few weeks ago. That rigid adherence to an outdated theory is also reflected in President Biden’s recent announcement that large companies must require their employees to get vaccinated or submit to regular testing, regardless of whether they previously had the virus.

ADVERTISING


Downplaying the power of natural immunity has had deadly consequences. In January, February and March, we wasted scarce vaccine doses on millions of people who previously had covid. If we had asked Americans who were already protected by natural immunity to step aside in the vaccine line, tens of thousands of lives could have been saved. This is not just in hindsight is 20/20; many of us were vehemently arguing and writing at the time for such a rationing strategy.

One reason public health officials may be afraid to acknowledge the effectiveness of natural immunity is that they fear it will lead some to choose getting the infection over vaccination. That’s a legitimate concern. But we can encourage all Americans to get vaccinated while still being honest about the data. In my clinical experience, I have found patients to be extremely forgiving with evolving data if you are honest and transparent with them. Yet, when asked the common question, “I’ve recovered from covid, is it absolutely essential that I get vaccinated?” many public health officials have put aside the data and responded with a synchronized “yes,” even as studies have shown that reinfections are rare and often asymptomatic or mild when they do occur.

The tide may finally be shifting, as pressure has grown on federal officials. Last week on CNN, Anthony S. Fauci, the nation’s top infectious-disease specialist, hinted that the government may be rethinking its stance on natural immunity, saying, “I think that is something that we need to sit down and discuss seriously.” Some large medical centers, like Spectrum Health in Grand Rapids, Mich., have already announced they will recognize natural immunity for their vaccine requirements. Some Republican governors have picked up on public frustration over how the scientific guidance is inconsistent with the data, with Florida Gov. Ron DeSantis accusing the Biden administration of “not following science” by crafting its vaccine mandate without taking into consideration “infection-conferred immunity.”

Booster shots won’t stop the delta variant. Here’s the math to prove it.

The current Centers for Disease Control and Prevention position about vaccinating children also dismisses the benefits of natural immunity. The Los Angeles County School District recently mandated vaccines for students ages 12 and up who want to learn in person. But young people are less likely to suffer severe or long-lasting symptoms from covid-19 than adults, and have experienced rare heart complications from the vaccines. In Israel, heart inflammation has been observed in between 1 in 3,000 and 1 in 6,000 males age 16 to 24; the CDC has confirmed 854 reports nationally in people age 30 and younger who got the vaccine.


A second dose of the two-shot mRNA vaccine like that produced by Pfizer and Moderna may not even be necessary in children who had covid. Since February, Israel’s Health Ministry has been recommending that anyone, adult or adolescent, who has recovered from covid-19 receive a only single mRNA vaccine dose, instead of two. Even though the risk of severe illness during a reinfection is exceedingly low, some data has demonstrated a slight benefit to one dose in this situation. Other countries use a similar approach. The United States could adopt this strategy now as a reasonable next step in transitioning from an overly rigid to a more flexible vaccine requirement policy. For comparison, the CDC has long recommended that kids do not get the chickenpox vaccine if they had chickenpox infection in the past.

The incorrect hypothesis that natural immunity is unreliable has resulted in the loss of thousands of American lives, avoidable vaccine complications, and damaged the credibility of public health officials. Given the recent mandate announcement by the White House, it would be good for our public health leaders to show humility by acknowledging that the hypothesis they repeatedly trumpeted was not only wrong, but it may be harmful. Let’s all come together around the mounting body of scientific literature and real-world clinical experience that is telling us not to require the full vaccine regimen in people who recovered from covid in the past. Public health officials changing their position on natural immunity, after so much hostility toward the idea, would go a long way in rebuilding the public trust.


ccp

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G M

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Re: 4th shot good for only 4 to 6 weeks
« Reply #1730 on: April 07, 2022, 07:42:08 AM »
It still works to produce clots, heart inflammation and cancer after that time period, right?


https://news.yahoo.com/second-covid-booster-shot-extends-012300452.html

 :-o

ccp

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Re: Epidemics: Bird Flu, TB, AIDs, Superbugs, Ebola, etc
« Reply #1731 on: April 07, 2022, 09:03:32 AM »
look at the "science "

 :-P

ccp

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pelosi positive
« Reply #1732 on: April 07, 2022, 09:08:55 AM »
https://www.newsmax.com/newsfront/pelosi-covid-house/2022/04/07/id/1064723/

with of course the usual

"I am fully vaccinated and boosted!" comment
and "thank god for the vaccine"

the one she laughed about when trump wanted to push it through by the end of the yr

we are all praying for her safe recovery.  :wink:




ccp

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G M

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Re: CDC covid vaccine on fertility
« Reply #1737 on: April 20, 2022, 07:36:10 AM »
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/planning-for-pregnancy.html

This site can’t be reachedThe webpage at https://www.cdc.gov/coronavirus/2019-ncov/vaccines/planning-for-pregnancy.html might be temporarily down or it may have moved permanently to a new web address.

Memory-holed?



Crafty_Dog

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Re: Israel study shows correlation of heart issues with vax
« Reply #1741 on: April 30, 2022, 06:43:41 AM »


https://www.nature.com/articles/s41598-022-10928-z

I'm so old, I remember when the left was anti-GMO food products. Now they want people to become GMOs at government gunpoint.




DougMacG

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Re: Israel study shows correlation of heart issues with vax
« Reply #1744 on: April 30, 2022, 04:52:39 PM »


https://www.nature.com/articles/s41598-022-10928-z

I'm so old, I remember when the left was anti-GMO food products. Now they want people to become GMOs at government gunpoint.

The GMO irony is quite good.  We don't want that in our beef, corn or tomatoes but we would do it to ourselves?

Speaking of disinformation, I consented to a jab that was 95% effective against 'alpha' when, unbeknownst to me, the threat was now delta. I don't like relying on old data. Then got infected with Omicron 6 months later. Meanwhile, a relatively young close relative died of an unexplained blood clot. I don't like unexplained.

It's not a vaccine.  It's a crapshoot.
« Last Edit: April 30, 2022, 05:11:34 PM by DougMacG »

G M

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Re: Israel study shows correlation of heart issues with vax
« Reply #1745 on: May 01, 2022, 10:38:08 AM »


https://www.nature.com/articles/s41598-022-10928-z

I'm so old, I remember when the left was anti-GMO food products. Now they want people to become GMOs at government gunpoint.

The GMO irony is quite good.  We don't want that in our beef, corn or tomatoes but we would do it to ourselves?

Speaking of disinformation, I consented to a jab that was 95% effective against 'alpha' when, unbeknownst to me, the threat was now delta. I don't like relying on old data. Then got infected with Omicron 6 months later. Meanwhile, a relatively young close relative died of an unexplained blood clot. I don't like unexplained.

It's not a vaccine.  It's a crapshoot.

https://www.ushmm.org/information/exhibitions/online-exhibitions/special-focus/doctors-trial/nuremberg-code

1. The voluntary consent of the human subject is absolutely essential.

This means that the person involved should have legal capacity to give consent; should be so situated as to be able to exercise free power of choice, without the intervention of any element of force, fraud, deceit, duress, over-reaching, or other ulterior form of constraint or coercion; and should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision. This latter element requires that before the acceptance of an affirmative decision by the experimental subject there should be made known to him the nature, duration, and purpose of the experiment; the method and means by which it is to be conducted; all inconveniences and hazards reasonably to be expected; and the effects upon his health or person which may possibly come from his participation in the experiment.

The duty and responsibility for ascertaining the quality of the consent rests upon each individual who initiates, directs or engages in the experiment. It is a personal duty and responsibility which may not be delegated to another with impunity.

G M

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Re: Israel study shows correlation of heart issues with vax
« Reply #1746 on: May 01, 2022, 10:42:07 AM »
https://imgflip.com/i/6ejdmq



Quote from: G M link=topic=1148.msg145437https://firehydrantoffreedom.com/Themes/default/images/bbc/img.gif#msg145437 date=1651426688


https://www.nature.com/articles/s41598-022-10928-z

I'm so old, I remember when the left was anti-GMO food products. Now they want people to become GMOs at government gunpoint.

The GMO irony is quite good.  We don't want that in our beef, corn or tomatoes but we would do it to ourselves?

Speaking of disinformation, I consented to a jab that was 95% effective against 'alpha' when, unbeknownst to me, the threat was now delta. I don't like relying on old data. Then got infected with Omicron 6 months later. Meanwhile, a relatively young close relative died of an unexplained blood clot. I don't like unexplained.

It's not a vaccine.  It's a crapshoot.

https://www.ushmm.org/information/exhibitions/online-exhibitions/special-focus/doctors-trial/nuremberg-code

1. The voluntary consent of the human subject is absolutely essential.

This means that the person involved should have legal capacity to give consent; should be so situated as to be able to exercise free power of choice, without the intervention of any element of force, fraud, deceit, duress, over-reaching, or other ulterior form of constraint or coercion; and should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision. This latter element requires that before the acceptance of an affirmative decision by the experimental subject there should be made known to him the nature, duration, and purpose of the experiment; the method and means by which it is to be conducted; all inconveniences and hazards reasonably to be expected; and the effects upon his health or person which may possibly come from his participation in the experiment.

The duty and responsibility for ascertaining the quality of the consent rests upon each individual who initiates, directs or engages in the experiment. It is a personal duty and responsibility which may not be delegated to another with impunity.


G M

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Re: Israel study shows correlation of heart issues with vax
« Reply #1748 on: May 01, 2022, 05:06:51 PM »
https://raconteurreport.blogspot.com/2022/04/vaers-finger-counting.html

https://imgflip.com/i/6ejdmq



Quote from: G M link=topic=1148.msg145437https://firehydrantoffreedom.com/Themes/default/images/bbc/img.gif#msg145437 date=1651426688


https://www.nature.com/articles/s41598-022-10928-z

I'm so old, I remember when the left was anti-GMO food products. Now they want people to become GMOs at government gunpoint.

The GMO irony is quite good.  We don't want that in our beef, corn or tomatoes but we would do it to ourselves?

Speaking of disinformation, I consented to a jab that was 95% effective against 'alpha' when, unbeknownst to me, the threat was now delta. I don't like relying on old data. Then got infected with Omicron 6 months later. Meanwhile, a relatively young close relative died of an unexplained blood clot. I don't like unexplained.

It's not a vaccine.  It's a crapshoot.

https://www.ushmm.org/information/exhibitions/online-exhibitions/special-focus/doctors-trial/nuremberg-code

1. The voluntary consent of the human subject is absolutely essential.

This means that the person involved should have legal capacity to give consent; should be so situated as to be able to exercise free power of choice, without the intervention of any element of force, fraud, deceit, duress, over-reaching, or other ulterior form of constraint or coercion; and should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision. This latter element requires that before the acceptance of an affirmative decision by the experimental subject there should be made known to him the nature, duration, and purpose of the experiment; the method and means by which it is to be conducted; all inconveniences and hazards reasonably to be expected; and the effects upon his health or person which may possibly come from his participation in the experiment.

The duty and responsibility for ascertaining the quality of the consent rests upon each individual who initiates, directs or engages in the experiment. It is a personal duty and responsibility which may not be delegated to another with impunity.

G M

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