VIDEO MODERNA VACCINE NEWS EXPOSED - Magnetism INTENTIONALLY Added to Vaccine to Force mRNA Through Entire Body

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Tobi

Active Member
Jan 29, 2021
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Los Angeles california

VIDEO MODERNA VACCINE NEWS EXPOSED - Magnetism INTENTIONALLY Added to Vaccine to Force mRNA Through Entire Body

wow, I'm sending this one out for sure! last time I "accidently" posted something on facebook about the vaccine. my 12 year old daughter wrote about just this. Her journalism teacher called it fake news and she almost flunked the class. I posted it to alert any parents about the dangers of vaccinating your kids. surprisingly mostly positive responses, but a few Bad haters. One wrote "she must be a trump supporter." no kidding stupid
 

Jean Clink

Active Member
Jan 29, 2021
111
66
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My friend's son put a magnet on a piece of CHICKEN and the thing stuck to it.... Her son and his friends (unvaccinated) had magnets stick to them.
 

Timothy Bair

Senior Member
Feb 17, 2021
1,242
1,725
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timothybair.wordpress.com
wow, I'm sending this one out for sure! last time I "accidently" posted something on facebook about the vaccine. my 12 year old daughter wrote about just this. Her journalism teacher called it fake news and she almost flunked the class. I posted it to alert any parents about the dangers of vaccinating your kids. surprisingly mostly positive responses, but a few Bad haters. One wrote "she must be a trump supporter." no kidding stupid
NOTE: THE "INFORMED CONSENT" REQUIREMENTS

"Informed Consent of Emergency Use Authorization Products
Since an Emergency Use Authorization (EUA) means the products are investigational and experimental only, products approved for emergency use are prohibited from being mandated by federal law, and an individual must consent to the use of the experimental product. An EUA is very specific: “…individuals to whom the product is administered are informed … of the option to accept or refuse the product …” 21 U.S.C. §360bbb-3 “Authorization for medical products for use in emergencies”
• (e) (conditions of authorization)
• (1) unapproved product
• (A) required conditions
• (ii) appropriate conditions designed to ensure that individuals to whom the product is administered are informed
• (III) of the option to accept or refuse administration of the product
1. “The FDA has an obligation to ensure that recipients of the vaccine under an EUA are informed, to the extent practicable under the applicable circumstances, that FDA has authorized the emergency use of the vaccine, of the known and potential benefits and risks, the extent to which such benefits
and risks are unknown, that they have the option to accept or refuse the vaccine, and of any available alternatives to the product.”7
At the regular August 2020 CDC Advisory Committee on Immunization Practices (ACIP) weekly meeting held at the CDC in Atlanta Georgia, the CDC-ACIP Executive Secretary Amanda Cohn, MD stated:8 "I just wanted to add that, just wanted to remind everybody, that under an Emergency Use Authorization, an EUA, vaccines are not allowed to be mandatory. So, early in this vaccination phase, individuals will have to be consented and they won't be able to be mandated.” (Emphasis added)"


 
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Timothy Bair

Senior Member
Feb 17, 2021
1,242
1,725
113
timothybair.wordpress.com
My sister got the AztraZenca and she has the magnetism thing on the site of the vaccine months ago. Not just Moderna and Pfizer??? What about that? Help
DID SHE GIVE INFORMED CONSENT?


NOTE: THE "INFORMED CONSENT" REQUIREMENTS

"Informed Consent of Emergency Use Authorization Products
Since an Emergency Use Authorization (EUA) means the products are investigational and experimental only, products approved for emergency use are prohibited from being mandated by federal law, and an individual must consent to the use of the experimental product.
An EUA is very specific: “…individuals to whom the product is administered are informed … of the option to accept or refuse the product …” 21 U.S.C. §360bbb-3 “Authorization for medical products for use in emergencies”
• (e) (conditions of authorization)
• (1) unapproved product
• (A) required conditions
• (ii) appropriate conditions designed to ensure that individuals to whom the product is administered are informed
• (III) of the option to accept or refuse administration of the product
1. “The FDA has an obligation to ensure that recipients of the vaccine under an EUA are informed, to the extent practicable under the applicable circumstances, that FDA has authorized the emergency use of the vaccine, of the known and potential benefits and risks, the extent to which such benefits
and risks are unknown, that they have the option to accept or refuse the vaccine, and of any available alternatives to the product.”7
At the regular August 2020 CDC Advisory Committee on Immunization Practices (ACIP) weekly meeting held at the CDC in Atlanta Georgia, the CDC-ACIP Executive Secretary Amanda Cohn, MD stated:8 "I just wanted to add that, just wanted to remind everybody, that under an Emergency Use Authorization, an EUA, vaccines are not allowed to be mandatory. So, early in this vaccination phase, individuals will have to be consented and they won't be able to be mandated.” (Emphasis added)"

AFLDS WHITE PAPER: CIVIL LIBERTIES SURROUNDING MEDICAL EXPERIMENTATION



§360bbb–3a. Emergency use of medical products​


 
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Scout9

Well-known Member
Feb 13, 2021
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VIDEO MODERNA VACCINE NEWS EXPOSED - Magnetism INTENTIONALLY Added to Vaccine to Force mRNA Through Entire Body

My former sister-in-law was dx with Guillen's BS two + decades ago. I am not sure what the precipitating variable was, and even though she was very sick for a period of time; she made a full recovery. Perhaps there is hope afterall.
 

RMT

Well-known Member
Feb 19, 2021
642
702
93
My former sister-in-law was dx with Guillen's BS two + decades ago. I am not sure what the precipitating variable was, and even though she was very sick for a period of time; she made a full recovery. Perhaps there is hope afterall.
Are you talking about Guillain-Barré syndrome? Glad there was a successful recovery.

A big % of the public is positive for Guillain-Barré. Testing can't tell you WHEN you had or contracted it, just that you had it. Dr Judy Mikovits has said it is caused from vaccines - it's caused by a latent retro virus from contaminated vaccines that simmers in one's body and attacks when one's immune system isn't in good shape.

Viruses grown for human vaccines are grown in monkey, mice and other animal tissue used by virologists. The tissue used is contaminated with each animal's own viruses - like the bats.
So with each vaccine injected into our bodies, we are getting all these viruses that are specific to the animal tissue it was grown in. Many vaccines also contain aborted fetal tissue that was NEVER tested prior to use along with dog dna, army worm dna...look it up, you be shocked. Why do we need another species' dna in our body?
 
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RMT

Well-known Member
Feb 19, 2021
642
702
93

VIDEO MODERNA VACCINE NEWS EXPOSED - Magnetism INTENTIONALLY Added to Vaccine to Force mRNA Through Entire Body

Love Dr Ruby & Stew Peters. Excellent reporting. Iron Oxide damages cells.

Look up Iron chelation therapy - used to prevent iron-mediated injury to cells.
 

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