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The FDA approved the mRNA genetic experiment on August 23, 2021 and gave them 14 days to provide a complete list of ingredients being used in the jab. This forces them to admit whether or not their experiment includes graphene oxide, as well as Adverse Event Symptoms (AES).
FDA approval also takes these companies out of the “emergency” category and makes them liable and subject to lawsuits. Now that millions of people have already received the jab, those adversely affected will have grounds to sue Big Pharma for using them as guinea pigs.
- Do we have evidence Pfizer has not come clean over what is in the vials? Yes. The VAERS database shows an incredible diversity of AEs. How do we explain heart inflammation in young children, which might shorten their lives, or congestive heart failure immediately? Or how pregnant woman can kill their babies through breastfeeding, who have thrombocytopenia or thrombosis? Others have zero side effects whereas some have dead arm within 12 hours and can attach magnets to their bodies? None of this makes sense. The normal rate of miscarriage is 20%, but now it’s 80% in some women. How do we explain acute respiratory distress or CNS disorders such as Guillain-Barré syndrome? Normally, when a product comes out, there may be a serious AE that appears, such as heart inflammation, which means the product is recalled just because of that single symptom. The DIVERSITY of these AEs is not consistent with a consistent product.
- Pfizer does not have a website up: A website is ALWAYS ready to go long before a new product is launched after approval. So you’d expect one such as ‘comirnaty.com’ complete with marketing slogans and package insert information. That there isn’t one is a red flag. It suggests that Pfizer knows they’re going to be held accountable for intentionally harming people with the product AS THE MANUFACTURER. What they don’t want is charges being brought against them AS THE MARKETER. Providing they don’t put marketing materials out there, they’ll avoid a whole slew of multi-billion dollar lawsuits. Right now, they are not a marketer, so who is? Public health agencies (FDA, CDC, NIH) and the MSM. These have been the marketers to date. They have been the propagandists misleading the public.
- Has Pfizer violated criminal laws? Yes. As a manufacturer, they have not reported all the serious AEs and deaths through particular reporting channels available to them to the FDA. This is intentionally misinforming the FDA and the American people, so criminal charges will be filed. They do have 2 weeks to come clean as to the ingredients. A lot of information has been withheld until now, which can be construed as intentionally misleading people.
Here is a 9-minute video where Ann Vandersteel interviews former Pfizer Biotech Analyst, Karen Kingston.
We have been told that FDA approval means government can now force us to take their jab. The opposite is the case. It is being removed from an “emergency measure” back into the “normal” process, where constitutional rights have to be respected.