CDC Won’t Release Review of Post-Vaccination Heart Inflammation

The U.S. Centers for Disease Control and Prevention (CDC) will not release its review of post-COVID-19-vaccination heart inflammation.

The CDC has been performing abstractions on reports of post-vaccination myocarditis, a form of heart inflammation, submitted to the Vaccine Adverse Event Reporting System.

But the agency is saying that federal law prevents it from releasing the results.

The abstractions “are considered medical records which are withheld in full from disclosure,” the CDC told The Epoch Times in a recent letter, responding to a Freedom of Information Act request.

One of the exemptions in the act says that agencies can withhold materials that are “specifically exempted from disclosure by statute, if that statute (i) requires that the matters be withheld from the public in such a manner as to leave no discretion on the issue; or (ii) establishes particular criteria for withholding or refers to particular types of matters to be withheld; and (B) if enacted after the date of enactment of the OPEN FOIA Act of 2009, specifically cites to this paragraph.”

The CDC pointed to the Public Health Service Act, which was enacted in 1944, and says that vaccine injury reports and other information that may identify a person shall not be made available to any person except the person who received the vaccine or a legal representative for that person.

The information sought is available through the CDC website without details that would identify patients, the agency also said.

The CDC said that it does not have a formal definition of “abstraction” but that it means the process of reviewing medical records, including autopsy reports and death certificates, and recording data in a database. “Please note that this definition means that any abstracted data, because they originate from medical records, is also considered medical records,” a CDC records officer told The Epoch Times in an email.

Keep reading

FDA Withholds Autopsy Results of Those Who Died After COVID Shots

The U.S. Food and Drug Administration (FDA) has refused a Freedom of Information Act (FOIA) request to release the autopsy results of people whose deaths were reported to the Vaccine Adverse Event Reporting System (VAERS) after receiving a COVID-19 shot. The FOIA request was submitted by The Epoch Times newspaper.1

“VAERS is a centralized vaccine reaction reporting system that was among the safety provisions secured by parents of DPT (diphtheria-pertussis-tetanus) vaccine injured children in the National Childhood Vaccine Injury Act (NCVIA) of 1986,” explains Barbara Loe Fisher, co-founder and president of the National Vaccine Information Center (NVIC). It is jointly operated by the FDA and U.S. Centers for Disease Control and Prevention (CDC).2 3

According to The Epoch Times, the FDA declined to release any autopsy reports of VAERS deaths, even redacted copies, citing FOIA section (8) (A) which allows federal agencies to withhold information from the public if an agency “reasonably foresees that disclosure would harm an interest protected by an exemption,” with the exemption being “personnel and medical files and similar files the disclosure of which would constitute a clearly unwarranted invasion of personal privacy.

Keep reading

‘Positive Association’ Between Vaccine-Related Aluminum Exposure and Persistent Asthma

A study funded by the Centers for Disease Control and Prevention (CDC) has found a “positive association” between vaccine-related aluminum exposure and persistent asthma.

The study (pdf), published on Sept. 28 in the medical journal Academic Pediatrics, sought to “assess the association between cumulative aluminum exposure from vaccines before age 24 months [2 years of age]” and see whether this group of children developed asthma between ages 2 and 5.

Authors of the retrospective cohort study included current and former CDC staffers. They analyzed data from a cohort of 326,991 children who were born between 2008 and 2014 at seven medical care organizations across the United States that participate in the Vaccine Safety Datalink, a network of health groups that collaborate with the CDC in studying vaccine safety.

Results of the observational study showed that children who were vaccinated with most or all of the recommended aluminum-containing vaccines (>3.00 mg aluminum exposure) had at least a 36 percent higher risk of being diagnosed with persistent asthma than kids who got fewer vaccines (≤3.00 mg aluminum exposure).

About 6 percent of the children with eczema and 2.1 percent of the children without eczema developed persistent asthma in the study. Each additional milligram of vaccine-related aluminum exposure was associated with 1.26- and 1.19-times higher rates of persistent asthma among children with and without eczema, respectively.

Overall, there was a “positive association” between vaccine-related aluminum exposure and persistent asthma, the authors said. They did not conclude that the results suggest any causative link. “[A]dditional investigation of this hypothesis appears warranted,” they added.

Keep reading

Hundreds of Thousands of Americans Sought Medical Care After COVID-19 Vaccination: CDC Data

Hundreds of thousands of Americans sought medical care after getting a COVID-19 vaccine, according to Centers for Disease Control and Prevention (CDC) data released on Oct. 3.

Some 782,900 people reported seeking medical attention, emergency room care, and/or hospitalization following COVID-19 vaccination. Another 2.5 million people reported needing to miss school, work, or other normal activities as a result of a health event after getting a COVID-19 vaccine.

The reports were made to the CDC’s V-safe program, a new vaccine safety monitoring system to which users can report issues through smartphones.

The CDC released the data to the Informed Consent Action Network (ICAN) after being sued over not producing the data when asked by the nonprofit. ICAN posted a dashboard summarizing the data.

“It took numerous legal demands, appeals, and two lawsuits, and over a year, but the CDC finally capitulated and agreed to a court order requiring them to do what they should have done from day one, release the V-safe data to the public,” Aaron Siri, a lawyer representing ICAN in the case, told The Epoch Times in an email.

About 10 million people utilized V-safe during the period of time the data covers: Dec. 14, 2020, to July 31, 2022. About 231 million Americans received at least one vaccine doses during that time.

The V-safe users reported about 71 million symptoms.

The most commonly reported symptoms were chills (3.5 million), swelling (3.6 million), joint pain (4 million), muscle or body aches (7.8 million), headache (9.7 million), fatigue (12.7 million), and general pain (19.5 million).

About 4.2 million of the symptoms were of severe severity.

Keep reading

Pfizer’s “Vaccine” Causes Astonishing Drop in Male Fertility – Men Have Not Been Informed nor Given Their Consent

When the Covid-19 vaccine rollout to the public began in late 2020, medical professionals, public health agencies, and government spokespeople all assured the public that the novel mRNA “vaccines” did not cause negative systematic effects on human bodies. They promised the public, many of whom were sceptical about the safety of a drug brought to market at “warp speed,” that the vaccines were “safe and effective.”

Those who questioned or challenged the “safe and effective” assurances were dismissed as “anti-vaxxers” and accused of wanting to kill others, especially the elderly. Few medical and public health experts spoke out about the need for long-term studies.

This attack on challengers to public health’s all-out push, and the resulting censorship of the emerging problem, resulted in catastrophic harm to male fertility.

The following is extracted from the article ‘Pfizer, FDA, CDC Hid Proven Harms to Male Sperm Quality, Testes Function, from mRNA Vaccine Ingredients’ by Amy Kelly, Program Director for the War Room/DailyClout Pfizer Documents Analysis Project as well as the COO of DailyClout.  Find more by Amy Kelly HERE.

Pfizer’s own documents and other medical studies show:

  1. Pfizer did not test “male reproductive toxicity”. Male reproductive toxicity is defined as adverse effects (negative impacts) related to sexual function and fertility in an adult male.[2]
  2. Pfizer also did not test for adverse effects from vaccinated men’s semen, on the development of their offspring.[3]
  3. mRNA vaccine ingredients travel throughout the body and gather in organs, including in the testes.[4]
  4. mRNA vaccines resulting in “anti-sperm antibodies” – that is to say, antibodies that treat sperm as an “invader”, and damage or kill it – is a known adverse event related to this form of vaccination.[5]
  5. mRNA vaccines cause a staggering drop in semen concentration and total motile count.[6]
  6. By suppressing discussion of this information, public health agencies, medical professionals, and governments globally denied and continue to deny men true informed consent.

Keep reading

Investigation into spikes in newborn baby deaths in Scotland

In September 2021 at least 21 babies under four weeks old died, a rate of 4.9 per 1,000 births. And in March at least 18 died, the equivalent of 4.6 per 1,000 births.

Public Health Minister Marie Todd said: “Every death is a tragedy for the families involved, that is why earlier this year I committed to this review to find out if there is a reason for the increase.

“I appreciate how difficult this time is for anyone affected and I would encourage them to access support if they wish to do so.”

She added information about organisations and help was available on the National Bereavement Care Pathways Scotland and Scottish government websites.

Ms Todd said anything identified would feed into recommendations and actions to improve the quality of care for mother and babies.

Keep reading

Smoking gun? FDA refusing to provide key covid “vaccine” safety analyses, suggesting massive coverup

Government regulators at the U.S. Food and Drug Administration (FDA) say they will not release any of the agency’s Covid-19 “vaccine” safety analyses for independent review because their findings are allegedly part of internal discussions that are protected by law.

Back in July, The Epoch Times submitted a request to the FDA for all analyses performed using a special method called Empirical Bayesian data mining. This method involves comparing adverse events recorded after injection with a Fauci Flu shot to adverse events recorded after injection with some other non-covid vaccine.

Whatever data these analyses produced was used by the FDA to foist Chinese Virus shots on everyone, including infants and toddlers. (Related: Check out our earlier coverage about the FDA’s suspicious secrecy to learn more.)

The operational procedures laid out by the agency and its partner in January 2021 and February 2022 stipulate that the FDA is to perform data mining “at least biweekly,” if not more often than that, to identify adverse events “reported more frequently than expected following vaccination with COVID-19 vaccines.” That data was to come from the official Vaccine Adverse Event Reporting System (VAERS).

Keep reading

Embalmers Have Been Finding Numerous Long, Fibrous Clots That Lack Post-Mortem Characteristics

Several embalmers across the country have been observing many large, and sometimes very long, “fibrous” and rubbery clots inside the corpses they treat, and are speaking out about their findings.

Numerous embalmers from different states confirmed to The Epoch Times that they have been seeing these strange clots, starting from either 2020 or 2021.

It’s not yet known if the cause of the new clot phenomenon is COVID-19, vaccines, both, or something different.

The Epoch Times received additional videos and photos of the anomalous clots, but could not upload them due to the level of gore.

Mike Adams, who runs an ISO-17025 accredited lab in Texas, analyzed clots in August and found them to be lacking iron, potassium, magnesium, and zinc.

Adams’s lab uses inductively coupled plasma mass spectrometry (ICP-MS), triple quadrupole mass spectrometer, and liquid chromatography-mass spectrometry, usually testing food for metals, pesticides, and glyphosate.

“We have tested one of the clots from embalmer Richard Hirschman, via ICP-MS. Also tested side by side, live human blood from an unvaccinated person,” Adams told The Epoch Times.

He found that the clots are lacking key elements present in healthy human blood, such as iron, potassium, and magnesium, suggesting that they are formed from something other than blood.

Keep reading

Pfizer and Moderna Trial Data Shows a Higher Risk of Serious Adverse Events Among Vaccinated Participants, a New Study Finds

peer-reviewed study published two days ago found that both the Moderna and the Pfizer vaccine trial data appeared to have a negative benefit/harm ratio.  One of the authors of the paper is Peter Doshi, an associate editor of the British Medical Journal.

Using a prespecified list of adverse events of special interest (“AESI”) identified by the Brighton Collaboration, the study found a higher risk of serious AESI in the mRNA COVID-19 vaccine group relative to placebo in both the Pfizer and Moderna adult phase III trials.

“These results raise concerns that mRNA vaccines are associated with more harm than initially estimated at the time of emergency authorisation,” the study authors wrote.

Keep reading