NVIC Seeing Through the COVID Spin- ; Covid -19 Vaccines can cause injuries , and Death , Long Term Follow-up of Adverse Reactions nearly Impossible


NVIC Seeing Through the COVID Spin. -Analysis by Barbara Loe Fisher

https://articles.mercola.com/sites/articles/archive/2021/05/11/nvic-seeing-through-the-covid-spin.aspx?ui=351b973b51dd8d94b40d43b54c99780f794c82daa03fe9c71f963a4ce91bf507&sd=20101212&cid_source=dnl&cid_medium=email&cid_content=art1HL&cid=20210511_HL2&mid=DM873657&rid=1154453668. - May 11, 2021)

  • COVID-19 vaccines were not designed to, and have not yet been proven to prevent infection and transmission of the new coronavirus in the majority of recipients
  • There is not one credible scientific study published in the medical literature demonstrating that high fevers, chills, headache, joint and muscle aching, disabling fatigue and other symptoms following vaccination are “good” for the body and indicate the body is successfully producing artificial immunity
  • There are no long-term studies evaluating the range of effects at the cellular and molecular level on the biological and genetic integrity of humans who receive the COVID vaccine



Can COVID-19 vaccines cause injuries and death?


According to the U.S. Department of Health and Human Services, adverse events are classified into five grades. The guidelines are as follows:

  • Grade 1 - Considered mild or asymptomatic and no intervention is required
  • Grade 2 - A moderate event but minimal, local or noninvasive interventions are needed indicated. In some situations, certain activities of daily living are limited (shopping, meal preparations, using the telephone).
  • Grade 3 - Considered a severe or medically significant adverse event but not one that is considered  immediately life-threatening. In certain cases, hospitalization, including long-term hospitalization is needed. Grade 3 reactions are disabling and limit a person’s ability to perform activities of daily living (feeding self, bathing, self-care). 
  • Grade 4 - A life-threatening event where urgent intervention is required  
  • Grade 5 - Death related to an adverse event


COVID-19 Vaccines in the U.S.

As of February 27, 2021, the U.S. Food and Drug Administration had authorized three COVID-19 vaccines under Emergency Use Authorization (EUA). Under EUA authority, the FDA Commissioner may permit “unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions caused by CBRN (CBRN = chemical, biological, radiological, nuclear) threat agents when there are no adequate, approved, and available alternatives.”

Adverse Events Following mRNA COVID-19 Vaccine Administration

Health officials have cautioned that symptoms of adverse reactions following COVID-19 vaccination may overlap with those of COVID-19 illness and be difficult to distinguish. However, symptoms of loss of taste or smell, shortness of breath, cough, rhinorrhea or sore throat are not considered common vaccine reactions, and persons experiencing these symptoms post-vaccination may be positive for SARS-CoV-2 or another infection.46

Persons who have pre-existing immunity to SARS-CoV-2 may be at increased risk of severe reactogenicity following mRNA COVID-19 vaccination. In a study pending peer review conducted by the Icahn School of Medicine at Mount Sinai, researchers reported that persons with pre-existing immunity to SARS-CoV-2 who received mRNA COVID-19 vaccines had significantly higher rates of systemic reactions when compared to those who were not immune at the time of vaccination. Systemic reactions included fatigue, headache, chills, fever, joint or muscle pains.47

Thrombocytopenia, a serious blood disorder that causes low platelets which will prevent the blood from clotting, has been reported following mRNA vaccination. In some cases, death has resulted from the bleeding disorder.48 In one case, a 56-year-old obstetrician who developed the condition within three days of receiving the Pfizer-BioNTech COVID-19 vaccine died of a stroke 16 days post-vaccination.49

Long-term follow-up of clinical trial participants to monitor for conditions such as cancer and autoimmune diseases will become difficult, if not impossible, if the vaccine makers hasten to offer their vaccines to the placebo groups. If this occurs, it will completely erase the ability of researchers to compare or evaluate potential long-term differences in health outcomes among the vaccinated and placebo groups. Pfizer and Moderna company executives have both suggested that the COVID-19 vaccine clinical trial participants who received a placebo should be vaccinated.50

Pfizer-BioNTech officials have already stated that they will begin offering the vaccine to placebo recipients by March 1, 2021, which is several months earlier than what they had originally planned for.51 By mid- January 2021, Moderna had already begun offering the vaccine to some placebo group participants


SARS-CoV-2 Virus & COVID-19 Quick Facts


 COVID-19 Vaccine

  • More than 200 different types of COVID-19 vaccines are being developed worldwide.23 In December 2020, two experimental mRNA COVID-19 vaccines developed and produced by Pfizer with BioNTech and Moderna with NIAID were granted an Emergency Use Authorization (EUA) by the U.S. Food and Drug Administration (FDA) for distribution and use in the U.S.24 25 As of Apr. 23, 2021, the CDC recommends two doses of the Pfizer COVID-19 vaccine administered to individuals age 16 and older,26 while the Moderna vaccine is approved for two doses administered to individuals over age 18 to prevent severe COVID-19 disease. 27
  • An Emergency Use Authorization (EUA) granted by the FDA to pharmaceutical corporations for distribution of experimental COVID-19 vaccines in the U.S. does not mean that the agency has evaluated all safety and efficacy data and officially approved licensure of the vaccine. The EUA authorizes manufacturers to release an experimental vaccine for voluntary use and the FDA states that vaccine recipients must “have the option to accept or refuse the vaccine.”37
  • As of April 23, 2021, health officials at the World Health Organization (WHO) and U.S National Institutes of Health (NIH) have warned that, while there is evidence that two doses of the Pfizer-BioNTech and Moderna vaccines can prevent symptomatic COVID-19 disease, there is a lack of evidence that the vaccines are effective in preventing infection and transmission of SARS-Cov-2.38 39 40 The Janssen/Johnson & Johnson vaccine was also granted an EUA based on efficacy data that demonstrated evidence for protection against symptomatic COVID-19 disease rather than protection against infection and transmission of the new coronavirus.41
  • As of April 23, 2021, there have been 118,902 reports of adverse events following vaccination with COVID-19 vaccination submitted to the federal vaccine adverse event reporting system (VAERS), including 12,619serious adverse events, 2,435 life-threatening events, 8,149 hospitalizations, and 3,544 deaths. Reported adverse events have included pain at the injection site; fatigue; anaphylaxis; headache; muscle and joint pain; fever; chills;42 swollen lymph nodes; nausea and vomiting;43 immune thrombocytopenia purpura (ITP) (low blood platelets);44 45 Bell’s Palsy;46 cardiac arrest; neurological dysfunction; rheumatoid arthritis; blood clots; heart, kidney and liver failure;47 and death.48 49 50
  • The CDC states that contraindications to receiving COVID-19 vaccines include (1) a history of severe allergic reaction to a previous vaccine dose or any of its ingredients; (2) a history of an immediate allergic reaction of any severity to a previous mRNA COVID-19 vaccine dose or to any of its ingredients. A  polyethylene glycol (PEG) allergy is considered a contraindication to mRNA vaccines, while a polysorbate allergy is considered a contraindication to Janssen vaccine. The CDC states that a person with a contraindication to mRNA vaccination may be able to receive the Janssen vaccine and vice versa provided that precautions are taken. This includes ensuring that the vaccine is administered by a healthcare provider who is equipped to manage severe allergic reactions.51
  • On Mar. 10, 2020, the Secretary of Health and Human Services (HHS) invoked the 2005 Public Readiness and Emergency Preparedness (PREP) Act, after declaring that the COVID-19 pandemic was a public health emergency. As a result, manufacturers of COVID-19 vaccines that have been developed to respond to the SARS-CoV-2 pandemic are considered public health emergency “countermeasures”. The PREP Act shields manufacturers and vaccine providers from liability and vaccine injury compensation claims will be processed by the Countermeasures Injury Compensation Program (CICP)
National Vaccine Information Centre ( NVIC) - Your Health, Your Family Your Choice
- Vaccines may be mixed up when given the second dose
- Placebo  Control group may be given the vaccine 
- Planning to vaccinate everyone will result in no covid-19 unvaccinated population  control group
- Possible Rollout of vaccines certificates/ passports will coheres/ force people to have a vaccine especially when contra-indicated to have a vaccine
- Administration of further biological injections  in the future from different manufactures ( some may close down or stop production) will make it impossible to assess side-effects and unpredictable/ unavoidable ingredients interactions. 
- it is impossible to research if ingredients in covid-19 vaccines will interfere / interact with any other medical treatments  ie.  affect the success rates of  medical treatments  eg.  surgery ( delay post- operative  healing  and risk infection) , radiotherapy, chemotherapy, blood transfusions, transplants or worsen  the side -effects of certain medications  and treatments   
- no studies  and impossible to know  the impact on  fertility , pregnacy and the developing foetus and health of the mother and the future children
- no studies and impossible to predict how it may  affect healing and recovery  from  minor or major accidental trauma and injuries as the covid-19 vaccine has the potential to cause blood problems and could potentially interfere with the normal  function of the healing mechansim and  the immune sytem response to  toxic, chemical, physical and biological insults.
 With so many risks, uncertainties  and unknowns the precautionary measure is paramount for the future of humanity as a species.
There is a reminder and a call for the health professional and scientists to practice / apply  ethics and  never forget. PRIMUM NON NOCERE/ FIRST DO NO HARM 

( Primum non nocere (Classical Latin: [ˈpriːmũː noːn nɔˈkeːrɛ]) is a Latin phrase that means "first, do no harm". The phrase is sometimes recorded as primum nil nocere.[1][better source needed]

Non-maleficence, which is derived from the maxim, is one of the principal precepts of bioethics that all students in healthcare are taught in school and is a fundamental principle throughout the world. Another way to state it is that, "given an existing problem, it may be better not to do something, or even to do nothing, than to risk causing more harm than good." It reminds healthcare personnel to consider the possible harm that any intervention might do. It is invoked when debating the use of an intervention that carries an obvious risk of harm but a less certain chance of benefit"
Source : https://en.m.wikipedia.org/wiki/Primum_non_nocere


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Der Zauberlehrling - By Johann Wolfgang van Goethe

The poem begins as an old sorcerer departs his workshop, leaving his apprentice with chores to perform.
Tired of fetching water by pail, the apprentice enchants a broom to do the work for him — using magic in which he is not yet fully trained.
The floor is soon awash with water, and the apprentice realizes that he cannot stop the broom because he does not know how.
Not knowing how to control the enchanted broom, the apprentice splits it in two with an axe, but each of the pieces becomes a new broom and takes up a pail and continues fetching water, now at twice the speed. When all seems lost, the old sorcerer returns, quickly breaks the spell and saves the day.
The poem finishes with the old sorcerer's statement that powerful spirits should only be called by the master himself.
( Source: https://www.goodreads.com/book/show/10105737-der-zauberlehrling)


Dr. Stefan Lanka: The history of the infection theory (English transcript)

"Goethe tried to warn of the 2006 influence pandemic, and also of AIDS and of the swallowing of Tamiflu. He did this in Faust I, not in the first edition, that went through censorship, not in the second, but in the third or fourth edition he included this essential passage, in which he describes how even back then a single doctor killed thousands of people:

First he describes in alchemist’s language, how the Tamiflu and chemotherapy of his time was produced: organic mercury compounds, mixed with sirup, Latwergen stands for sirup mixtures, and these will be the hellish Latwergen in alchemistic language and how they were produced. Here are the important lines:

Here was the medicine: the patients died.

No one asked: who recovered?

(Here was the Tamiflu, the patients died (will die?)

And no one asked: who recovered? No one asked: is the theory correct? Does the virus exist at all? )

So we roamed, with our hellish pills,                                                    

Among the valleys and the hills,

Worse than the pestilence (plague) itself we were.

And we’ll treat the black plague also, a political disease just as AIDS, influenza, SARS, BSE, just as small pox, the collective term of leprosy, from which black plague was derived, and also the collective term of polio.

I myself have poisoned thousands: that’s quite clear:

And now from the withered old must hear

How men praise shameless murderers.  

Goethe. He has not been taken seriously ’till today.

Whenever there is a tsunami or an earthquake, I think to myself: Goethe is speaking again. For he warned and this warning was dismissed."

( Source: https://abruptearthchanges.com/2017/11/17/dr-stefan-lanka-the-history-of-the-infection-theory/)