Deaths reported to VAERS as of December 17, 2021.
The VAERs system was established to monitor vaccine safety of FDA approved products.
The EUA genetic vaccines were first administered in the United States on December 14, 2020. Since that time there have been more adverse events and deaths reported for the genetic vaccines than all other vaccines combined over the last 30 years.
Cause for safety concerns was there just a few months after these products were given to people. Given that the genetic vaccines are only EUA, any deaths should have been cause to stop using these products immediately.
#TakeScienceBack
Reference:
https://openvaers.com/covid-data/mortality crossed referenced with United States Department of Health and Human Services (DHHS), Public Health Service (PHS), Centers for Disease Control (CDC) / Food and Drug Administration (FDA), Vaccine Adverse Event Reporting System (VAERS) Accessed at http://wonder.cdc.gov/vaers.html
The VAERs system was established to monitor vaccine safety of FDA approved products.
The EUA genetic vaccines were first administered in the United States on December 14, 2020. Since that time there have been more adverse events and deaths reported for the genetic vaccines than all other vaccines combined over the last 30 years.
Cause for safety concerns was there just a few months after these products were given to people. Given that the genetic vaccines are only EUA, any deaths should have been cause to stop using these products immediately.
#TakeScienceBack
Reference:
https://openvaers.com/covid-data/mortality crossed referenced with United States Department of Health and Human Services (DHHS), Public Health Service (PHS), Centers for Disease Control (CDC) / Food and Drug Administration (FDA), Vaccine Adverse Event Reporting System (VAERS) Accessed at http://wonder.cdc.gov/vaers.html
LetterToHealthcareProfessionals.pdf
134.8 KB
Letter to Healthcare Provider
The healthcare community appears uninformed on many facts regarding COVID-19 genetic vaccination, especially for children.
Being willfully blind of scientific facts is a breach of responsibility by healthcare professionals.
We MUST critically analyze ALL the information before us and do what is best for our children.
Be informed about this critical issue AND share this letter with your doctor or pharmacist.
#TakeScienceBack
The healthcare community appears uninformed on many facts regarding COVID-19 genetic vaccination, especially for children.
Being willfully blind of scientific facts is a breach of responsibility by healthcare professionals.
We MUST critically analyze ALL the information before us and do what is best for our children.
Be informed about this critical issue AND share this letter with your doctor or pharmacist.
#TakeScienceBack
Fact vs. Myth
There have been many myths perpetuated about COVID-19 over the last two years. Myths are statements that have been made that were not backed by science or data. Facts are supported by data and tested by science to be repeatable.
Fight fear with facts.
#TakeScienceBack
References:
1- https://bit.ly/3sKYxmp
2- https://bit.ly/3HCrzZA
3- https://bit.ly/3FEe0rP
4- https://go.nature.com/33TJzjk
5- https://openvaers.com/
6- https://bit.ly/3EZTDnH
7- https://bit.ly/3HybxQn
There have been many myths perpetuated about COVID-19 over the last two years. Myths are statements that have been made that were not backed by science or data. Facts are supported by data and tested by science to be repeatable.
Fight fear with facts.
#TakeScienceBack
References:
1- https://bit.ly/3sKYxmp
2- https://bit.ly/3HCrzZA
3- https://bit.ly/3FEe0rP
4- https://go.nature.com/33TJzjk
5- https://openvaers.com/
6- https://bit.ly/3EZTDnH
7- https://bit.ly/3HybxQn
FDA recently gave Emergency Use Authorization of COVID-19 booster vaccination for children aged 12-15.
The science on the safety concerns for the COVID-19 genetic vaccines is clear.
Informed consent has been lacking. The purpose of informed consent is to provide you with enough information so you can understand the possible risks and benefits of receiving the COVID-19 genetic vaccine and decide whether or not you want to receive the COVID-19 genetic vaccine. Here are trusted, science backed answers to questions about COVID-19 genetic vaccines for children.
Many are still in the dark about the possible safety concerns. Help us fight the fear with facts by sharing this information to bring awareness. The decisions made today, will have lasting consequences.
#TakeScienceBack
The science on the safety concerns for the COVID-19 genetic vaccines is clear.
Informed consent has been lacking. The purpose of informed consent is to provide you with enough information so you can understand the possible risks and benefits of receiving the COVID-19 genetic vaccine and decide whether or not you want to receive the COVID-19 genetic vaccine. Here are trusted, science backed answers to questions about COVID-19 genetic vaccines for children.
Many are still in the dark about the possible safety concerns. Help us fight the fear with facts by sharing this information to bring awareness. The decisions made today, will have lasting consequences.
#TakeScienceBack
The Vaccine Adverse Event Reporting System (VAERS) is a national early warning system to detect possible safety problems after FDA approval of vaccines. VAERS is co-managed by the CDC and the FDA.
There have been more deaths reported to VAERS after the COVID-19 genetic vaccines were given than all other vaccines combined over the last 30 years. Since these genetic vaccines have not been fully FDA approved and the safety concern for these genetic vaccines was clear during the first months of them being given, the use of these vaccines should have been halted.
When will the FDA pause the use of COVID-19 genetic vaccines to properly assess the high reports of Adverse Events?
Help us #TakeScienceBack
References:
https://vaersanalysis.info/2021/12/31/vaers-summary-for-covid-19-vaccines-through-12-24-2021/
https://openvaers.com/index.php
There have been more deaths reported to VAERS after the COVID-19 genetic vaccines were given than all other vaccines combined over the last 30 years. Since these genetic vaccines have not been fully FDA approved and the safety concern for these genetic vaccines was clear during the first months of them being given, the use of these vaccines should have been halted.
When will the FDA pause the use of COVID-19 genetic vaccines to properly assess the high reports of Adverse Events?
Help us #TakeScienceBack
References:
https://vaersanalysis.info/2021/12/31/vaers-summary-for-covid-19-vaccines-through-12-24-2021/
https://openvaers.com/index.php
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FEAR -> Pandemics or emergencies can induce high levels of stress triggered by fear.
CORTISOL -> When you experience stress, triggered by fear, your brain sends a response to make hormones, like cortisol.
BODILY HARM -> Accumulation of stress hormones and subsequent inflammation compromise your body's ability to fight disease.
COPING STRATEGIES -> Individuals who adopt positive coping strategies suffer fewer symptoms of depression and anxiety.
Fight fear with facts
Healthy mind, healthy body
#TakeScienceBack
SEE COMMENTS FOR FULL POST
**Telegram's comment glitch fixed
CORTISOL -> When you experience stress, triggered by fear, your brain sends a response to make hormones, like cortisol.
BODILY HARM -> Accumulation of stress hormones and subsequent inflammation compromise your body's ability to fight disease.
COPING STRATEGIES -> Individuals who adopt positive coping strategies suffer fewer symptoms of depression and anxiety.
Fight fear with facts
Healthy mind, healthy body
#TakeScienceBack
SEE COMMENTS FOR FULL POST
**Telegram's comment glitch fixed
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RESET AND BUILD A STRONG FOUNDATION
Republished with permission from Ms. Isabell Wohlfart Mental Trainer Diplomate and inside-out approach coaching with 10 years of experience.
(Highly recommended by the respected Dr. Karl Ehrhard Psychotherapist and Mental Coach in Germany)
We thank Ms. Isabell Wohlfart very much for stepping up and sharing her expert professional opinion.
You can contact her at isabell.wohlfart@t-online.de
We encourage healthcare workers, scientists, and professionals whose voices have been sidelined to come forward so we can allow you to tell your story and share your expertise.
#TakeScienceBack
Republished with permission from Ms. Isabell Wohlfart Mental Trainer Diplomate and inside-out approach coaching with 10 years of experience.
(Highly recommended by the respected Dr. Karl Ehrhard Psychotherapist and Mental Coach in Germany)
We thank Ms. Isabell Wohlfart very much for stepping up and sharing her expert professional opinion.
You can contact her at isabell.wohlfart@t-online.de
We encourage healthcare workers, scientists, and professionals whose voices have been sidelined to come forward so we can allow you to tell your story and share your expertise.
#TakeScienceBack
In a recent study, CDC stated the data supports the safety of C0V1D-19 v@¢¢ination during pregnancy. (https://www.cdc.gov/mmwr/volumes/71/wr/mm7101e1.htm?s_cid=mm7101e1_w#contribAff) Therefore, CDC now recommends C0V1D-19 genetic v@¢¢ination for women who are pregnant, recently pregnant, who are trying to become pregnant now, or who might become pregnant in the future.
However, there is a marked increase in pregnancy loss for those 1mmun1zed with C0V1D-19 genetic v@¢¢ines in the first 20 weeks of pregnancy. Pregnancy is a precarious time not just for the expectant mother but most importantly the developing fetus.
When expectant mothers are told not to drink coffee, eat deli meats, or take ibuprofen why would it be acceptable to inject them with an experimental genetic v@¢¢ine when the risks are unknown?
#TakeScienceBack
References:
(1) https://bit.ly/3pu64m0
(2) https://bit.ly/31qXWuN
(3) doi.org/10.1056/nejmoa2104983
(4) doi.org/10.1056/NEJMx210016
(5) https://bit.ly/3kxj2On
However, there is a marked increase in pregnancy loss for those 1mmun1zed with C0V1D-19 genetic v@¢¢ines in the first 20 weeks of pregnancy. Pregnancy is a precarious time not just for the expectant mother but most importantly the developing fetus.
When expectant mothers are told not to drink coffee, eat deli meats, or take ibuprofen why would it be acceptable to inject them with an experimental genetic v@¢¢ine when the risks are unknown?
#TakeScienceBack
References:
(1) https://bit.ly/3pu64m0
(2) https://bit.ly/31qXWuN
(3) doi.org/10.1056/nejmoa2104983
(4) doi.org/10.1056/NEJMx210016
(5) https://bit.ly/3kxj2On
For decades, expectant mothers have been considered a vulnerable group to be shielded from potential harms of research for the sake of their fetuses’ health. The first trimester is the riskiest time for the developing fetus.
As of January 23, 2022, a total of 3,692 cases of miscarriage have been reported through the CDC VA3R5 (2).
More safety studies are needed before authorizing these v@cc1nes for use in expectant mothers as it’s premature to recommend them given what preliminary studies have shown when they were administered during the first trimester.
Help us #TakeScienceBack
References:
1- https://bit.ly/3nDykmo crossed referenced with United States Department of Health and Human Services (DHHS), Public Health Service (PHS), Centers for Disease Control (CDC) / Food and Drug Administration (FDA), Va¢¢ine Adverse Event Reporting System (VA3R5) Accessed at https://bit.ly/3FIzhA0
2- https://bit.ly/3nHAzEZ
NOTE: Typos intended. Some original to the report from the source, some to avoid censoring.
As of January 23, 2022, a total of 3,692 cases of miscarriage have been reported through the CDC VA3R5 (2).
More safety studies are needed before authorizing these v@cc1nes for use in expectant mothers as it’s premature to recommend them given what preliminary studies have shown when they were administered during the first trimester.
Help us #TakeScienceBack
References:
1- https://bit.ly/3nDykmo crossed referenced with United States Department of Health and Human Services (DHHS), Public Health Service (PHS), Centers for Disease Control (CDC) / Food and Drug Administration (FDA), Va¢¢ine Adverse Event Reporting System (VA3R5) Accessed at https://bit.ly/3FIzhA0
2- https://bit.ly/3nHAzEZ
NOTE: Typos intended. Some original to the report from the source, some to avoid censoring.
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Phases of Clinical Trials
PRECLINICAL
The drug or treatment is tested first in the laboratory, then in animals. Preclinical studies are important for eliminating potential vaccines that are either toxic or do not induce protective immune responses.
Length of Study: up to 10 years
PHASE 1
The purpose of Phase 1 is to ensure that the treatment is safe in humans and to determine how and where it distributes within the body. This testing takes place with a small group of healthy volunteers, usually 15 to 50.
Length of Study: Several months
PHASE 2
The purpose of a Phase 2 Clinical Trial is to determine the right dosage and effectiveness in treating that particular disease. This testing takes place with a larger number of volunteers who have the disease, up to 100.
Length of Study: Several months to 2 years
Continued in comments
PRECLINICAL
The drug or treatment is tested first in the laboratory, then in animals. Preclinical studies are important for eliminating potential vaccines that are either toxic or do not induce protective immune responses.
Length of Study: up to 10 years
PHASE 1
The purpose of Phase 1 is to ensure that the treatment is safe in humans and to determine how and where it distributes within the body. This testing takes place with a small group of healthy volunteers, usually 15 to 50.
Length of Study: Several months
PHASE 2
The purpose of a Phase 2 Clinical Trial is to determine the right dosage and effectiveness in treating that particular disease. This testing takes place with a larger number of volunteers who have the disease, up to 100.
Length of Study: Several months to 2 years
Continued in comments
A 12-year-old boy dies 5 days after receiving his C0V1D genetic vaccine. He died of septic shock and Meningococcal meningitis.
Genetic vaccines were approved by the FDA for emergency authorization use on children ages 5 and older over, with booster now being recommended.
As of January 28, 2022, the death of 91 children aged 0-18 have been recorded in VA3RS in relation to the C0V1D genetic vaccines (1). Children have higher death rates in car crashes than from C0V1D. (2)
Ask yourself, is this medical treatment necessary for healthy children?
#takescienceback
1 - openvaers.com
2 - https://bit.ly/3qHZ1qM
Genetic vaccines were approved by the FDA for emergency authorization use on children ages 5 and older over, with booster now being recommended.
As of January 28, 2022, the death of 91 children aged 0-18 have been recorded in VA3RS in relation to the C0V1D genetic vaccines (1). Children have higher death rates in car crashes than from C0V1D. (2)
Ask yourself, is this medical treatment necessary for healthy children?
#takescienceback
1 - openvaers.com
2 - https://bit.ly/3qHZ1qM
Ethical Science Council is looking for feedback on topics of interest for future posts. Please help us by voting for which topic would be of most interest to you or you would like to learn more about.
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Immunity
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Health and Nutrition
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Survey Topics:
Immunity
Adverse Events
Health and Nutrition
Treatment Options
Government and Pharma Accountability
Other (fillable)
https://www.survio.com/survey/d/X0O3U9O7K2D5Z2P0L