By Heidi H. Sampson
The CDC’s Newest Vaccine Surveillance System, V-Safe, was rolled out December 2020 at the exact same time the Covid 19 shots were rolled out. Up to that point, VAERS (Vaccine Adverse Events Reporting System), a passive system created in 1986 by the CDC put in place after the National Childhood Vaccine Injury Act was implemented. By the CDC’s own admission VAERS is not as effective for a surveillance system as it requires people to submit information once they have been injured or experienced an adverse event following a vaccine.
The V-SAFE Surveillance is different. It is a detailed tracking system spanning one full year, Dec 2020 – Jan 2021. This system incorporated three distinct categories for collected data;
- The 1st Week after the shot requiring a reporting symptom with a Check-the-box format.
- 1st -6th weeks after the shot, they collected information from the “V-Safe Covid Adverse Health Impacts” also included a Check-the-box format.
- The final data was gathered for an entire 12 months after the shot. This incorporated a free text entry online survey format.
The CDC had about 10 million participants of a broad cross section of people, who signed up for V-Safe at the same time they received their first COVID 19 injection. At this point in time, these were the very first, the eager and excited participants to receive this new novel vaccine. Many also claimed this was their civic duty.
Do you remember between Dec 2020 to May 2020 when the preliminary vaccine rollout occurred? We saw images of people standing in long lines waiting to get their shot. We saw the elderly, the frontline workers, health care workers and other essential workers. People were desperate to be first in line to receive their shots. Many people were actually trying to manipulate the special right to be first in line. Most of these people were enthusiastically embracing this newly rolled out, experimental shot.
5-6 months after the shots rollout occurred, it’s important to keep remember that at that time:
- No one was mandated to receive it
- No one was coerced
- No one was bullied
- No one was kicked out of school
- No one was fired from their job
The CDC collected information from 10,108,273 people for 12 months then compiled their results. It’s highly likely, the CDC did not expect the results they received. They clearly were not willingly to make this data public. FOIA (Freedom of Information Act) requests to the CDC were ignored several times. Two federal law suits later, the CDC was ordered to release their “Check-the-box” data.
The first data set collected basic information addressing soreness, redness, swelling at the site etc. 60-80% had the general symptoms supporting CDC’s position about these symptoms indicated the vaccine was doing its job. It is interesting to note however, the symptoms that were NOT on that list to check: Myocarditis, Pericarditis, Chest Pain, Transverse Myelitis, Blood Clotting, etc.
It appears THE CDC WAS NOT HONEST OR FORTHCOMING!
Interestingly, prior to the Dec 2020 rollout, the CDC already had their V-Safe protocol to guide the design of their forthcoming surveillance program. This initial protocol was far more comprehensive. The CDC actually had already identified potential symptoms and conditions of concern.
The following publications clearly indicated concerns:
- July 2020 – New England Journal of Medicine, “An mRNA Vaccine against SARS-CoV2-Preliminary Report”
- Oct 2020 – “Post approval Vaccine Safety Surveillance for Covid 19 Vaccines in US”
- Oct 30, 2020 – “CDC post-authorization post-licensure safety monitoring of Covid 19 vaccines”
Even more revealing, in Nov 2020, one month prior to launching V-Safe, the CDC published “Adverse Events of Special Interest Pre-specified Medical Conditions” document. Guess what was included? Myocarditis, pericarditis, blood clotting, chest pains, transverse myelitis, Acute myocardial Infarction, Anaphylaxis, Guillain Barre Syndrome, Kawasaki Disease, Multisystem Inflammatory Syndrome in children and adults, pregnancy and prespecified conditions, seizures, convulsions, stroke, etc.
In hind sight, these are all the symptom we have been seeing on the rise since the Covid 19 shot was rolled out and ultimately forced upon the population.
However, oddly enough, just one month later the released version of the V-Safe forms excluded these troubling conditions from their ‘check-the-box’ data collection process. The CDC knew the critical information before Dec 2020. They knew the Covid 19 shot could cause life altering conditions including deadly side-effects. Yet they removed those conditions from their surveillance system.
The Second “Check-the-Box” System, “V-Safe Covid Adverse Health Impacts” contained three Questions
- Were you unable to perform normal activities?
- Did you miss work or school?
- Did you require medical attention?
This second system covered the first 6 weeks after the shot.
Of note, it is important to understand, it generally takes at least a week to begin expressing adverse reactions to a vaccine.
These more than 10 million people, who were first in line, who were the eager enthusiasts, the believers in this shot, wanting it to work, they wanted it to be safe and effective. They believed it was a good thing and therefore would have no incentive to make up their stories. Unfortunately, to their surprise, the results contradicted their initial presumptions.
So, what did the data collection actually capture? Keep in mind, this is the CDC’s own unfiltered data and can be found here: V-Safe Data – ICAN – Informed Consent Action Network (icandecide.org)
7.7% or 782,013 people needed medical attention:
- Of those 7.7% – 70% need to be hospitalized or went to ER or Urgent Care
- Approximately 30% used Telehealth
- On average, each person needed medical attention 2-3 times
- Additionally, 13% of individuals reported not being able to work or go to school,
- About 12% were unable to perform normal activities
THIS MEANS 33% of unique individuals were affected by HEALTH IMPACTS. That’s 3.3 million individual people HARMED with a total of 6.5 million Health Impact Reports were submitted to the CDC.
The 3rd Data Set which the CDC has recently been ordered to release is its free-text entries in the V-Safe’s online survey. 7.8 million free text entries will be released in small batches and they tell a much more detailed story. The initial batch released in February revealed symptoms such as chest pain, heart palpitations and shortness of breath, more than a thousand reports of tinnitus, hundreds of reports of menstrual disturbances and approximately 54 reports of miscarriage following vaccination, as well as other reports of medical problems. Since this information was presented 2 more batches of free-text entries have been released and can be found in the link above.
FOLKS – This is a ALARMING – IT’S A LOUD SIGNAL, A RESOUNDING ALARM!!
People in large numbers are being harmed.
WHERE IS OUR CONSUMER PROTECTION? OH, THAT’S RIGHT …. THERE IS NONE!
Since 1986, the National Childhood Vaccine Injury Act gave all vaccine manufacturers total immunity from legal action.
CONSUMER PROTECTION LAWS DO NOT APPLY TO THIS “VACCINE”
THE DATA ARE IN – IT IS NOT SAFE AND EFFECTIVE!
Until the Federal Government removes the liability shield from the Vaccine Manufacturers, the Covid 19 shot MUST be removed from the Maine market.




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