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    • Frank Ziovas
      • Jun 27, 2021
      • 1 min read

    DR. RUBY: MAGNETISM - INTENTIONALLY ADDED TO MRNA SHOT - WARNING LABEL: NOT FOR USE IN HUMANS

    Updated: Jul 28, 2021

    28 JUNE 2021 | Frank Ziovas | Please share and subscribe: help us get the truth out there!

    Follow us on Telegram https://t.me/seetvnews

    Millions are finding out that magnets are now sticking to them after this poison MRNA injection. Listen to what is intentionally being put into their bodies and getting into every cell. This is a Crime Against Humanity (download pdf "Nuremberg 2" https://tinyurl.com/nurnberg2process ) which will lead to catastrophic death around the world. Hospitals are filling up not with Covid patients but with people suffering from horrific side effects from the shot.


    Watch the Full interview with Dr Ruby:

    DR. RUBY: MAGNETISM - INTENTIONALLY ADDED TO MRNA SHOT - WARNING LABEL: NOT FOR USE IN HUMANS


    Magnification is real: Magnetofection is a transfection method that uses magnetic fields to concentrate particles containing nucleic acid and in-utero samples to the target cells of the body.[1] This method attempts to unite the advantages of the biochemical (cationic lipids or polymer atoms) and physical (electroporation, gene gun) transfection methods in one system while excluding their inconveniences (low efficiency, toxicity).[citation needed] In 1978, Marseille-based OZ Biosciencestrademarked in the UK the word Magnetofection.[2](magenti-infection)


    Resources

    Magnetofection - Wikipedia

    Magnetofection - Search Results - PubMed (nih.gov)


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    265 views0 comments
    • Frank Ziovas
      • Jun 27, 2021
      • 3 min read

    “You are a pathetic liar”: CDC senior scientist to CDC's head of immunization

    Updated: Jul 28, 2021

    June 28 2021 | Source: ICAN | SHARYL ATTKISSON

    Your support means everything, please subscribe and share| help us get the truth out there!

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    On August 27, 2014, Dr. Thompson, provided a statement through his attorney that the CDC “omitted statistically significant information” showing an association between the MMR vaccine and autism in the first and only MMR-autism study ever conducted by the CDC with American children. Dr. Thompson, in a recorded phone call, stated the following regarding concealing this association: “Oh my God, I can’t believe we did what we did. But we did. It’s all there. It’s all there. I have handwritten notes.” Dr. Thompson further stated on that call:



    A CDC internal email released through a Freedom of Information Act request reveals just how nasty things got behind closed doors after a CDC senior scientist confessed to covering up a link between vaccines and autism, and implicated his CDC colleagues.


    The email, dated Sept. 2, 2018, was written by CDC's Dr. Willam (Bill) Thompson to Dr. Frank DeStefano, CDC’s head of immunization safety.


    In the email, Thompson responds to an interview DeStefano gave me in 2014. It was after Thompson stunned the scientific community by saying that he, DeStefano, and other CDC scientists committed fraud in a major vaccine-autism study. It was information that upended a decade-and-a-half of government and vaccine industry narratives on the controversy, and stood to impact some of the millions of families in the U.S. who have autistic children.


    According to Thompson, he and his fellow CDC scientists covered up a link between MMR vaccine and autism in African-American boys. “The omitted data suggested that African American males who received the MMR vaccine before age 36 months were at increased risk for autism,” Thompson later testified


    CDC officials disposed of study documents "in a huge garbage can"


    As part of the alleged fraud and coverup, Thompson said he and the other CDC scientists who conducted the research got together and literally trashed study data.


    Thompson first revealed his role in the fraud during a series of phone conversations with the parent of an autistic child. The parent surreptitiously recorded the calls, in which Thompson confessed and said he lived with tremendous guilt.


    When the parent made the recordings public, Thompson admitted to scientific fraud and issued a statement issued through his attorney. “I regret that my coauthors and I omitted statistically significant information,” read the statement, in part. He also described how he says he and his CDC colleagues had a meeting and literally threw documents from the research into a garbage can.

    The coauthors scheduled a meeting to destroy documents related to the study. The remaining four coauthors all met and brought a big garbage can into the meeting room and reviewed and went through all the hard copy documents that we had thought we should discard and put them in a huge garbage can. However, because I assumed it was illegal and would violate both FOIA and DOJ requests, I kept hard copies of all documents in my office, and I retained all associated computer files. Dr. William "Bill" Thompson, CDC Senior Scientist

    CDC would not permit Thompson to do media interviews after he blew the whistle.


    Thompson’s email included the link to my interview with DeStefano and the transcript.


    Listen to the full audio https://soundcloud.com/fomotion/cdc-whistle-blower-full-audio


    The latest information is very concerning.


    It shows the motivation behind decisions is money and not the health and safety of kids or pregnant women. It also illustrates the lengths government bureaucrats are willing to go in order gain the trust of the public.



    References

    https://sharylattkisson.com/2021/06/you-are-a-pathetic-liar-cdc-senior-scientist-to-cdcs-head-of-immunization/

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    • Michael Moore
      • May 24, 2021
      • 4 min read

    Centers for Disease Control and Prevention (CDC). Updated Report (VAERS)

    Updated: Jul 28, 2021

    25 May 2021 Michael Moore | Email: michael.mooore@seetvnews.com

    Please support us by sharing and subscribing; Help us get the truth out there.

    Follow us on Telegram https://t.me/seetvnews


    VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.


    VEARS has issued an updated report on the adverse reactions to the latest mNRA Vaccines or GMO Therapy for humans. This report shows that between Dec. 14, 2020 and April 30, there was a total of 157,277 total adverse events reported to VAERS, including 3,837 deaths — an increase of 293 over the previous week — and a total of 16,014 serious injuries, up 2,467 since last week.


    The number of deaths by ‘vaccination’ is increasing weekly according to Governmental figures.





    According to official figures, 240.2 million COVID vaccine doses have been administered as of April 30. This includes 105 million doses of Moderna, 127 million doses of Pfizer and 8 million doses of the Johnson &Johnson (J&J) COVID vaccine.


    Of the 3,837 deaths reported as of April 30, a quarter occurred within 48 hours of vaccination, 16 percent within 24 hours and 39percent in people who became ill within 48 hours of receiving the vaccination.


    Further, according to the CDC figures, This week’s VAERS data shows:


    • 21% of deaths were related to cardiac disorders.

    • 54% of those who died were male, 44% were female and the remaining death reports did not include gender of the deceased.

    • The average age of death was 75.1 and the youngest deaths reported include two 15-year-olds (VAERS I.D. 1187918 and 1242573 ) and a 16-year-old (VAERS I.D. 1225942). There were other reported deaths in children under 16 that could not be confirmed or contained obvious errors.

    • As of April 30, 805 pregnant women reported adverse events related to COVID vaccines, including 235 reports of miscarriage or premature birth.

    • Of the 1,597 cases of Bell’s Palsy reported, 51% were reported after Pfizer-BioNTech vaccinations, 40% following vaccination with the Moderna vaccine and 131 cases, or 10%, of Bell’s Palsy cases were reported in conjunction with J&J.

    • There were 162 reports of Guillain-Barré Syndrome with 41% of cases attributed to Pfizer, 45% to Moderna and 19% to J&J.

    • There were 44,348 reports of anaphylaxis with 38% of cases attributed to Pfizer’s vaccine, 47% to Moderna and 14% to J&J.


    Despite the above figures, the FDA (Federal Drug Administration) is set to authorize (or authorized) Pfizer vaccine for young teens aged 12 to fifteen by early next week.


    On May 4, The Defender reported the U.S. Food and Drug Administration (FDA) is preparing to authorize use of the Pfizer-BioNTech COVID vaccine in adolescents 12 to 15 years old by early next week and Pfizer is going to ask for the expanded Use Authorization so that children as young as 2 can be forcibly vaccinated.


    ‘According to CDC data, the death rate among adolescents ages 0 to 17 who get COVID and are subsequently hospitalized is 0.7%, with many experiencing either mild or no symptoms at all. The COVID death rate in all adolescent age categories is less than 0.1%, leading some experts to question whether vaccines should be targeted to an age group that so far appears to be mostly spared from severe COVID.


    Just recently a third U.S. male was diagnosed with vaccine-induced blood clots and a woman died from brain hemorrhage after receiving the J&J (Johnson & Johnson) vaccine.

    The Defender, a Children’s Health Defense News service May 6, on May 6th reported ‘doctors at University of Utah Health treated the third male to develop vaccine-induced thrombotic thrombocytopenia in the U.S.’


    ‘The man, under age 50, received J&J’s vaccine in early April. Ten days later he experienced pain in his toes, which then progressed to his thighs. He later began experiencing chest pain. A CT scan revealed a bilateral pulmonary embolism. Physicians discovered low platelets and blood clots in his legs and lungs, leading them to suspect VITT was the cause.’


    On May 4, They also reported a 35-year-old Michigan woman dying from complications 11 days after receiving the J&J’s vaccine. The woman’s family said her headache started on April 16, eight days after being vaccinated. She died three days later. Her death certificate notes a natural death, specifically from an acute subarachnoid hemorrhage, or bleeding between the brain and tissue around the brain.

    The attending physician filed a report to VAERS. In an email to the family, the CDC confirmed her death had been reported to VAERS, but said the system is not designed to determine whether a reported adverse event was caused by the vaccine.’


    ‘Of the 2,808 cases reported, there were 1043 reports attributed to Pfizer, 893 reports to Moderna and 860 reports to J&J — 847 cases more than U.S. health officials acknowledged during the April 23 meeting where it was recommended the pause be lifted on J&J’s vaccine.

    Other countries have rejected some of the vaccines including Denmark rejecting the J&J Vaccine.


    The Danish Health Authority said in a statement “….it had concluded the benefits of using the COVID-19 vaccine from J&J do not outweigh the risk of causing the possible adverse effect in those who receive the vaccine.”


    “Taking the present situation in Denmark into account, what we are currently losing in our effort to prevent severe illness from COVID-19 cannot outweigh the risk of causing possible side effects in the form of severe blood clots in those we vaccinate,” the health authority said.


    The previous month they had halted use of the AstraZeneca vaccine due to the increased risk of blot clots. Other European countries are following suit.


    The Defender has made repeated attempts to contact CDC with questions as, according to their website (CDC) all deaths are followed up. Yet to date there has been a deathly silence.


    https://vaers.hhs.gov/

    https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=CAT&EVENTS=ON&VAX=COVID19

    https://childrenshealthdefense.org/defender/vaers-vaccine-injuries-climb-pfizer-seeks-full-approval/




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