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Author Topic: Official CDC Vax Death Toll: 11,000 (And Counting)  (Read 634 times)

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Offline SeanJohnson

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Official CDC Vax Death Toll: 11,000 (And Counting)
« on: July 18, 2021, 09:54:37 AM »
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  • [Keep in mind these stats, by their very nature, will be grossly underreported, as victims will not always be able to trace deaths to the abortion vax -SJ]



    Nearly 11,000 Deaths After CÖVÌD Vaccines Reported to CDC, as FDA Adds New Warning to J&J Vaccine
    VAERS data released today by the CDC showed a total of 463,457 reports of adverse events from all age groups following CÖVÌD vaccines, including 10,991 deaths and 48,385 serious injuries between Dec. 14, 2020 and July 9, 2021.
    By
    Megan Redshaw

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    Data released today by the Centers for Disease Control and Prevention (CDC) included 463,457 reports of injuries and deaths, across all age groups, following CÖVÌD vaccines — an increase of more than 25,000 compared with the previous week.


    The data comes directly from reports submitted to the Vaccine Adverse Event Reporting System (VAERS), the primary government-funded system for reporting adverse vaccine reactions in the U.S.
    Every Friday, VAERS makes public all vaccine injury reports received as of a specified date, usually about a week prior to the release date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.


    Data released today show that between Dec. 14, 2020 and July 9, 2021, a total of 463,457 total adverse events were reported to VAERS, including 10,991 deaths — an increase of 1,943 over the previous week. There were 48,385 serious injuries reported during the same time period — up 7,370 compared with the previous week.




    In the U.S., 333 million CÖVÌD vaccine doses had been administered as of July 9. This includes: 135 million doses of mσdernα’s vaccine, 184 million doses of pfιzєr and 13 million doses of the Johnson & Johnson (J&J) CÖVÌD vaccine.

    Of the 10,991 deaths reported as of July 9, 22% occurred within 48 hours of vaccination, 15% occurred within 24 hours and 37% occurred in people who became ill within 48 hours of being ναccιnαted.
    This week’s data for 12- to 17-year-olds show:

    Other reports include two 13-year-old boys (VAERS I.D. 1406840 and 1429457) who died two days after receiving a pfιzєr vaccine, three 15-year-olds (VAERS I.D. 1187918, 1382906 and 1242573), three 16-year-olds (VAERS I.D. 1420630, 1225942 and 1386841) and three 17-year-olds (VAERS I.D. 1199455, 1388042 and 1420762).

    This week’s total VAERS data, from Dec. 14, 2020 to July 9, 2021, for all age groups combined show:

    Experts warn of ‘huge risk’ as mσdernα launches CÖVÌD vaccine trials for pregnant women
    mσdernα will study its CÖVÌD vaccine in pregnant women, according to a posting on ClinicalTrials.gov. The observational study, expected to begin July 22, will enroll about 1,000 females over age 18 who will be studied over a 21-month period.


    Women who received a mσdernα vaccine during the 28 days prior to their last menstrual period, or at any time during pregnancy, are eligible.


    The brief summary of the trial states the main goal is “to evaluate the outcomes of pregnancy in females exposed to the mσdernα CÖVÌD-19 vaccine (mRNA-1273) during pregnancy.”


    Currently, the CDC says pregnant women can get a CÖVÌD vaccine. But the agency also acknowledges there is limited data available about the safety of CÖVÌD vaccines for people who are pregnant.
    Tell Schools/Universities Children/Young Adults!
    “Pregnant women are taking what may be a huge risk with the CÖVÌD vaccine,” said Jennifer Margulis, Ph.D., author of “Your Baby, Your Way.” Margulis said in an email to The Defender, there is no evidence CÖVÌD vaccines are safe, but ample evidence suggesting it is dangerous to expose pregnant women and unborn babies to drugs and interventions that can disrupt immunity.


    Lyn Redwood, RN, MSN and president emerita of Children’s Health Defense, said it’s “bass-ackwards to release the vaccine to pregnant women before doing a clinical trial or proper animal studies.”


    FDA added warning to J&J vaccine of ‘serious but rare’ autoimmune disorder
    On July 13, the FDA added a new warning on J&J’s (Janssen) CÖVÌD vaccine to include information pertaining to an observed increased risk of Guillain-Barré Syndrome (GBS) following vaccination.


    According to an FDA news release, GBS is a neurological disorder in which the body’s immune system damages nerve cells, causing muscle weakness or, in the most severe cases, paralysis.


    Based on an analysis of VAERS data, there have been 100 preliminary reports of GBS following vaccination with J&J’s vaccine. Of these reports, 95 were serious and required hospitalization. There was one reported death.


    While the cause of GBS is not fully known, it often follows infection with a virus and has been linked to other vaccines. The FDA concluded the benefits of the vaccine outweigh any danger, but included the proviso in fact sheets about the drug for providers and patients.


    The CDC’s Advisory Committee on Immunization Practices (ACIP) is expected to discuss the GBS cases during an upcoming meeting, the CDC said.


    Coroner says vaccine not to blame for man’s death after pfιzєr— wife not convinced
    A healthcare worker who died four days after his second dose of pfιzєr’s CÖVÌD vaccine was killed by heart disease, according to the Orange County, California coroner.


    As The Defender reported this week, Tim Zook, an x-ray technologist at South Coast Global Medical Center in Santa Ana, was hospitalized Jan. 5 — just hours after being ναccιnαted. Zook’s wife, Rochelle, told the Orange County Register her husband’s health rapidly deteriorated after receiving his second dose of pfιzєr’s vaccine. He died Jan. 9.


    An autopsy report released Wednesday found Zook’s heart was severely enlarged, thicker than normal and dilated. “There is a focus of severe coronary artery disease,” according to the report, which also said Zook’s heart valves showed mild-to-moderate calcium deposits.


    [size={defaultattr}][font={defaultattr}]The autopsy report concluded the official cause of death was “hypertensive and atherosclerotic heart disease with severe cardiomegaly [enlarged heart] and heart failure.”[/font][/size]
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    Rochelle Zook said she is not convinced her husband’s death is unrelated to the vaccine. He was “quite healthy,” she said shortly after her husband’s death. Rochelle Zook preserved samples of her husband’s tissue for future testing, hoping to learn more as data about vaccines emerge in years to come.
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    Woman’s sudden paralysis linked to J&J vaccine

    A Houston woman spent 22 days in the hospital after getting a CÖVÌD vaccine and then developing GBS, ABC 13 reported July 14. After Jamie Walton got the J&J vaccine, she started feeling numbness and tingling in her feet and hands.[/font]

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    “I know my body and I knew something wasn’t right, so I kept trying to go to different doctors and I kept being told, ‘You’re dehydrated. You’re fine,'” Walton said. “One doctor told me I had anxiety.”
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    The otherwise healthy woman ended up paralyzed from the waist down and lost her ability to walk. Walton went to the emergency room twice and met with several doctors before her diagnosis was confirmed. She was hospitalized for 22 days, had to learn how to walk again and do other basic movements. Her case was reported to VAERS.
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    pfιzєr fails to convince FDA on immediate need for boosters

    pfιzєr executives met privately this week with U.S. senior scientists and regulators to press their case for quick authorization of CÖVÌD booster vaccines amid pushback from federal health agencies who last week said the extra doses are not needed.[/font]

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    Officials said after the meeting that more data — and possibly several 
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    more months — would be needed before regulators could determine whether booster shots were necessary, The Defender reported.

    [font={defaultattr}]The meeting was largely seen as a courtesy after pfιzєr’s announcement last week that it would seek Emergency Use Authorization for its booster shot led to unusual pushback from the U.S. Food and Drug Administration (FDA) and CDC.[/font]
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    Woman with ‘life-altering’ injuries after CÖVÌD vaccine teams up with U.S. senators to demand answers

    A Utah woman and two U.S. senators are teaming up to get answers from federal health agencies about life-altering injuries people have experienced after receiving a CÖVÌD vaccine, The Defender reported July 7.[/font]

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    Brianne Dressen, preschool teacher from Utah, was injured after participating in AstraZeneca’s CÖVÌD vaccine clinical trial in November 2020. She accuмulated more than $250,000 in medical bills as a result of injuries she believes were caused by the vaccine.
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    After experiencing severe symptoms and neurological decline, Dressen spent months teaching herself how to walk, eat and form sentences again — all while she traveled in search of answers.
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    Dressen, along with other people who said they were injured by vaccines but “repeatedly ignored” by the medical community, participated last month in a news conference held by Sen. Ron Johnson (R-Wis).
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    Following the news conference, Johnson and Utah Sen. Mike Lee wrote a letter to the CDC and FDA after the agencies ignored requests for assistance and answers from families injured by CÖVÌD vaccines.
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    Lee and Johnson said widespread lack of acknowledgement of adverse events following receipt of a CÖVÌD vaccine has made it nearly impossible for some individuals to obtain the medical treatment they need, and that risks must be disclosed to the medical community and general public.
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    In the letter, Lee and Johnson asked the FDA and CDC about the adverse events suffered during clinical trials, disclosed in the FDA’s Emergency Use Authorization Memorandum for the pfιzєr, mσdernα and Johnson & Johnson vaccines, as well as reported injuries from the U.S. AstraZeneca trial.
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    They also asked the CDC whether it is working with physicians and researchers at the FDA, National Institutes of Health or other medical research bodies to provide the various individuals who experienced adverse effects vaccine treatment and care.
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    130 days and counting, CDC ignores The Defender’s inquiries

    According to the CDC website, “the CDC follows up on any report of death to request additional information and learn more about what occurred and to determine whether the death was a result of the vaccine or unrelated.”[/font]

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    On March 8, The Defender contacted the CDC with a written list of questions about reported deaths and injuries related to CÖVÌD vaccines. We have made repeated attempts, by phone and email, to obtain a response to our questions.
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    Despite multiple phone and email communications with several people at the CDC, and despite being told that our request was in the system and that someone would respond, we have not yet received answers to any of the questions we submitted. It has been 130 days since we sent our first email to the CDC requesting information.
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    Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.
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    Rom 5: 20 - "But where sin increased, grace abounded all the more."


    Offline Incredulous

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    Re: Official CDC Vax Death Toll: 11,000 (And Counting)
    « Reply #1 on: July 18, 2021, 03:38:47 PM »
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  • Translated, that would mean the actual world death count exceeds 200K souls.
    "Some preachers will keep silence about the truth, and others will trample it underfoot and deny it. Sanctity of life will be held in derision even by those who outwardly profess it, for in those days Our Lord Jesus Christ will send them not a true Pastor but a destroyer."  St. Francis of Assisi