Will the MSM cover the vaccine damage and deaths that are now being caused.

Will the MSM cover the vaccine damage and deaths that are now being caused.

Here is the $64,000 question for the main-stream-media (MSM), at what point will they start properly investigating the vaccine damage and deaths that are currently being caused. How bad does it need to get do you think? Perhaps MSM is now totally irrelevant because they are part of the narrative and the lies that are being perpetrated on a very frightened and impressionable public, who will do anything to get back to normal.

Background

“First do no harm”, “primum non nocere”,

The famous words attributed to Hippocrates the father of medicine. Prevention of injury and illness is another significant aspect of medical practice. The biggest question in the world today has this most sacrosanct tenet been utterly compromised by those who have the money and intent to corrupt health as we know it and what if it is the pharmaceutical companies themselves have conspired to facilitate for this to happen, in the quest for profit and control. What do you think?

When you look at the heath of the nation in the UK you realise, we are very sick with high levels of obesity, diabetes, autoimmune disease, heart disease and dementia. Who benefits from that do you think, (follow the money)? You don’t make eye watering profits from healthy people, right? When did the pharmaceutical companies care about your health, only when it gives them an opportunity to vaccinate the whole planet with experimental gene therapies and that they are indemnified from prosecution? A truly win-win situation.

Vaccines are safe?

You are being told that the vaccines are safe by the government, your doctor and the pharmaceutical companies who made the vaccine in the first place. And you have decided to believe it, and that is 100% understandable and the reason is, you are probably trusting the information that you are being given.

It is also your decision as to whether you have the vaccine or not, all I am doing is giving you extra information so when you make your decision it is a reasoned, and without peer and MSM pressure, it’s your body, and you need to be very aware of the fact that whatever is injected into your body is 100% irreversible.

I have now received my letter and I quote “we have sent you this letter as experts recommend that people in your age group should be among the first to receive the free NHS coronavirus vaccine”. Nowhere in my letter is there any reference to possible side effects from the vaccine and nowhere does it say this is voluntary.

Do side effects matter to you, what if death was also part of the side effects?

Let’s look at some information.

US data

Here is an US article taken from The Defender - The Children’s Health Defense News dated 19.2.21.

According to new data released today, as of Feb. 12, 15,923 adverse reactions to COVID vaccines, including 929 deaths, have been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) since Dec. 14, 2020.

VAERS is the primary mechanism in the U.S. for reporting adverse vaccine reactions. Reports submitted to VAERS require further investigation before a determination can be made as to whether the reported adverse event was directly or indirectly caused by the vaccine.

The latest VAERS data show that 799 of the deaths were reported in the U.S., and that about one-third of those deaths occurred within 48 hours of the individual receiving the vaccination.

As is consistent with previous VAERS data reports,192 of the reported deaths — or 21% — were cardiac-related. As The Defender reported earlier this month, Dr. J. Patrick Whelan, a paediatric rheumatologist, warned the U.S. Food and Drug Administration in December that mRNA vaccines like those developed by Pfizer and Moderna could cause heart attacks and other injuries in ways not assessed in safety trials.

Of the 929 deaths reported since Dec. 14, 2020, the average age of the deceased was 77.8 and the youngest was 23. Fifty-two percent of the reported deaths were among men, 45% were women and 3% are unknown. Fifty-eight percent of the deaths were reported in people who received the Pfizer vaccine, and 41% were related to the Moderna vaccine.

According to the latest data, 3,126 “serious” adverse reactions have been reported. Adverse reaction reports from the latest CDC data also include:

· 34 miscarriages and pre-term births

· 917 anaphylactic reactions, 70% of which were reported after a Pfizer vaccine and 30% after the Moderna vaccine

· Bell’s palsy (Pfizer 75%; Moderna: 25%)

So far, only Pfizer and Moderna vaccines — approved for emergency use, but not fully licensed — are being used in the U.S.

AstraZeneca’s COVID vaccine, which does not use mRNA technology, was approved for emergency use this week by the World Health Organization, paving the way for some countries to start using it. However, as The Defender reported this week, some nations have said they won’t use it, citing safety and efficacy concerns.

Fierce Pharma reported today that the FDA may reject the AstraZeneca vaccine over concerns relating to efficacy, especially against new COVID variants, and manufacturing issues.

News reports indicate that a growing number of people, including nearly 30% of healthcare workers, now say they don’t want the COVID vaccine, citing safety concerns.

The Washington Post reported this week that nearly a third of military personnel are opting out of the vaccines, and ESPN reported that top NBA players are reluctant to promote the vaccine.

While the VAERS database numbers may seem sobering, according to a U.S. Department of Health and Human Services study, the actual number of adverse events is likely significantly higher. VAERS is a passive surveillance that relies on the willingness of individuals to submit reports voluntarily.

According to the VAERS website, healthcare providers are required by law to report to VAERS:

· Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccination

· An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine

The CDC says healthcare providers are strongly encouraged to report:

· Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event

· Vaccine administration errors

However, “within the specified time” means that reactions occurring outside that timeframe may not be reported, in addition to reactions suffered hours or days later by people who don’t report those reactions to their healthcare provider.

Vaccine manufacturers are required to report to VAERS “all adverse events that come to their attention.”

Historically, however, fewer than 1% of adverse events have ever been reported to VAERS, a system that Children’s Health Defense has previously referred to as an “abject failure.”

UK Data, taken from the GOV.UK website

Coronavirus vaccine - weekly summary of Yellow Card reporting

The Yellow Card scheme is a mechanism by which anybody can voluntarily report any suspected adverse reactions or side effects to the vaccine. It is very important to note that a Yellow Card report does not necessarily mean the vaccine caused that reaction or event.

This report covers the period 9 December 2020 to 7 February 2021.

As of 7 February 2021, for the UK

• 24,207 Yellow Cards have been reported for the Pfizer/BioNTech

• 20,428 have been reported for the Oxford University/AstraZeneca vaccine

• 113 have been reported where the brand of the vaccine was not specified.

In the week since the previous summary for 31 January 2021 we have received a further 3,882 Yellow Cards for the Pfizer/BioNTech vaccine, 8,680 for the Oxford University/AstraZeneca vaccine and 41 where the brand was not specified. A higher number of doses of the Oxford University/AstraZeneca vaccine were administered in the last week than the Pfizer/BioNTech vaccine .

For both vaccines the overall reporting rate is around 3 to 4 Yellow Cards per 1,000 doses administered.

For both vaccines, the overwhelming majority of reports relate to injection-site reactions (sore arm for example) and generalised symptoms such as ‘flu-like’ illness, headache, chills, fatigue (tiredness), nausea (feeling sick), fever, dizziness, weakness, aching muscles, and rapid heartbeat. Generally, these happen shortly after the vaccination and are not associated with more serious or lasting illness.

These types of reactions reflect the normal immune response triggered by the body to the vaccines. They are typically seen with most types of vaccine and tend to resolve within a day or two. The nature of reported suspected side effects is broadly similar across age groups, although, as was seen in clinical trials and as is usually seen with other vaccines, they may be reported more frequently in younger adults.

Severe allergy

On 9 December 2020, the MHRA issued preliminary guidance on severe allergic reactions after the Pfizer/BioNTech vaccine due to early reports of anaphylaxis. Following further detailed review, this advice was amended on 30 December to the current advice. This advice is that people with a previous history of severe allergic reactions to any ingredients of the vaccine should not receive it. People who receive the vaccine should be monitored for at least 15 minutes afterwards.

Widespread use of the vaccine now suggests that severe allergic reactions to the Pfizer/BioNTech vaccine are very rare and have been reported at a rate between 1 and 2 cases per 100,000 doses administered. Similar reporting was seen in the United States with the same vaccine. Anaphylaxis can also be a very rare side effect associated with most other vaccines.

Following very substantial exposure across the UK population, no other new safety concerns have been identified from reports received so far.

Conclusion

• The increases in number of ADR reports reflects the increase in vaccine deployment as new vaccination centres have opened across the UK

• The number and nature of suspected adverse reactions reported so far are not unusual in comparison to other types of routinely used vaccines

• The overall safety experience with both vaccines is so far as expected from the clinical trials

• Based on current experience, the expected benefits of both COVID-19 vaccines in preventing COVID-19 and its serious complications far outweigh any known side effects

• As with all vaccines and medicines, the safety of COVID-19 vaccines is being continuously monitored

My Observation

There is a significant difference in the data that is being published between the US and the UK, which I need to further investigate. The US data is showing significant numbers of deaths and serious side effects, and also when it is being estimated that fewer than 1% of adverse events have ever been reported to VAERS.

Does the US vaccine damage data now coming in thick and fast as we roll out the vaccination program worry you? Does it make you think twice about having the vaccination?

Let us be clear these vaccines have not been approved; they have been released on emergency dispensation without animal studies. The vaccines are in stage 3 trials and will not be completed until the end of 2022. Those people that are accepting the vaccination are therefore part of a worldwide experiment.