Mass Vaccine For Kids

PUBLISHED: 5:06 PM 21 Oct 2021

Biden Regime Ready To ‘Mass’ Vaccinate Kids 5-11: Here’s How You Can Stop It

This is a “rapid” mass vaccine campaign for children aged 5 to 11, which many people argue is designed to kill, steal, and destroy their lives.

Designed to kill. (Source: YouTube Screenshot)

The vaccine is deadly, especially in children. So naturally, the Biden regime is ready to actively push it on them. However, you can fight back.

Conservative Treehouse explained:

All your children belong to us.  And so the United States government announces they are now prepared to trigger the “rapid” mass vaccine campaign for children aged 5 to 11.   The cleaving of American citizens will continue unabated with the current administration helping to divide our nation based on vaccination status.  It is a feature, not a flaw…. fundamental change requires it.

The White House says [Fact Sheet Here] they have secured the shots from Pfizer (after giving enough lead-time for politicians to purchase stock in their portfolios), staged the supplies, organized the logistics to ensure no supply chain issues, reinforced the ramparts and delivered prescripted talking to points to media narrative engineers for deployment against unwilling parents.

The Biden administration announced they have prepared the U.S. healthcare system to aggressively, with as much force and speed as possible, drive the childhood vaccination program.  Leveraging existing partnerships and financial dependencies on government spending, the White House expressed confidence.  They do not anticipate any compliance issues with a forceful national rollout:

WHITE HOUSE – “The Administration has procured enough vaccine to support vaccination for the country’s 28 million children ages 5-11 years old. If authorized by the FDA and recommended by the CDC, the Pfizer-BioNTech vaccine for 5-11 year olds will be a dose and formula specifically for this age group. The vaccine will have packaging available in smaller configurations that will make it easier for physicians’ offices and other smaller, community-based providers to offer the vaccine to kids and their families.

Pending FDA authorization, the packaging configuration will be 10-dose vials in cartons of 10 vials each (100 doses total), delivered in a newly updated product shipper, and the vaccine can be stored for up to 10 weeks at standard refrigeration temperatures and 6 months at ultracold temperatures. And, the vaccine will come with all the ancillary supplies that providers need to serve kids, including smaller needles. The U.S. Department of Health and Human Services (HHS) is working hand-in-hand with states to make this vaccine supply available in communities across the country as rapidly as possible.” (read more)

AP notes: “We’re completing the operational planning to ensure vaccinations for kids ages 5 to 11 are available, easy and convenient,” White House COVID-19 coordinator Jeff Zients said, “We’re going to be ready, pending the FDA and CDC decision.” {link} As for youngsters under 5, Pfizer and Moderna are studying their vaccines in children down to 6 months old, with results expected later in the year.

The progression of the child vaccination program is very foreseeable and predictable.  The rollout will be optional for parents; however, once the optional phase has concluded, likely spring 2022, the political healthcare system will unite with the political education system.

Initially Blue states will mandate vaccination of children to attend school or pre-school.  Then the federal government will step in to apply leverage via threats of education funds being withheld for any non-compliant state.  The 2022 mid-term campaign issue over “universal pre-k” funding will support the federal pressure, and eventually anyone receiving federal subsidies under programs structured to support women, infants and children, will be required to participate.

Young children and adolescents will then be given vaccination passports that will permit them to join with the community of safe kids in parks and venues that target families and younger audiences.

Hey, our vaccination app now shows us the nearest location for our next booster along with healthy tips about eating sustainable algae cakes, bugs ‘n stuff.  How cool is that?

ps.. Small note: The worker mandate math still is not adding up.  In the White House announcement you will find: “Today, 2 in 3 eligible individuals – 189 million Americans – are fully vaccinated.”

The Gateway Pundit added:

The Biden gang is now making plans to give children the vaccine that General Colin Powell took that did nothing to protect him from COVID and may have caused it.  

There are no reasons children ages 5 – 11 should be vaccinated.  They are basically immune to COVID and have higher risks of drowning than dying from COVID.

But this isn’t stopping the Biden gang.  CNN reported earlier today:

The White House on Wednesday unveiled its plans to roll out Covid-19 vaccines for children ages 5 to 11, pending US Food and Drug Administration authorization.

The Biden administration has secured enough vaccine supply to vaccinate the 28 million children ages 5 to 11 who would become eligible for vaccination if the vaccine is authorized for that age group and will help equip more than 25,000 pediatric and primary care offices, hundreds of community health centers and rural health clinics as well as tens of thousands of pharmacies to administer the shots, according to the White House.
“We know millions of parents have been waiting for Covid-19 vaccine for kids in this age group. And should the FDA and (US Centers for Disease Control and Prevention) authorize the vaccine, we will be ready to get shots in arms,” White House Covid-19 response director Jeff Zients told reporters at a White House Covid-19 briefing on Wednesday.
A group known as Sisyphus Complex Solution released the below report related to a meeting between drug companies and the FDA scheduled for next week to discuss mandating vaccines for children:

**URGENT – SUBMISSIONS OF STATEMENT FOR FDA MEETING TO DISCUSS EUA FOR 5 – 11 YEAR OLDS***

DEADLINE – OCTOBER 21st, 2021

***PLEASE FORWARD TO ALL OF YOUR KNOWN CONTACTS (NO RESTRICTIONS ON LOCATION)***

A meeting of the FDA Committee is to be held on Oct. 26th, 2020 to discuss Pfizer-BioNTech’s Emergency Use Authorization (EUA) for administration of their COVID-19 mRNA vaccine to children 5 through 11 years of age.

Responses can be made via: https://www.regulations.gov/document/FDA-2021-N-1088-0001 (please see below for tips as to how to make your response, and you can also view the responses made to date as examples)

WHY ARE WE GENUINELY CONCERNED (nothing to do with ‘anti-vax’)

LISTEN TO THE EXPERTS

Unusual ‘known’ outcomes – MIS-C (specific to children).  Pay close attention to the dates of ‘observations’ between March – June, 2020 for this varied and fatal condition for children.

Take this MIS-C knowledge forward, and apply to ‘Two Different Antibody-Dependent Enhancement (ADE) Risks for SARS-CoV-2 Antibodies’ . Check the Summary which states ‘ADE with mast cells likely plays a role in MIS-C for infants and possibly older MIS-C and MIS-A patients.’

Consider the ‘indications’ from observable data.

Listen to the expert (Dr. Ryan Cole) for additional ‘indications’ of concern here.

Due to these significant risk factors, with no existing burden of proof to guarantee the safety of the children (including acceptance of liability), there can be no legitimate and legally obliged informed consent under the practices administered during this vaccine roll out, and as such requires extensive independent laboratory research to qualify these observable concerns, and further no existing burden of proof is offered to indicate benefit outweighing these evidenced risks. Hence precautionary principle and medical ethics demands the prevention of providing this EUA. Additionally, existing research for early treatment is providing evidence of efficacy, whereby burden of proof must be provided stipulating lower risk than these alternative treatments, taking into consideration the afore mentioned risks associated with ADE and MIS-C.

ADVICE IN MAKING YOUR COMMENTS TO THE FDA

Tips for Submitting Effective Comments.

The comment text box will hold 5000 characters which is about 42 lines, and therefore more substantial evidence is recommended to be presented via the ‘Attach Files’ section. This may include any notarised Affidavit from qualified persons from any nation (please take into account that FDA approvals are being utilised as authorisation across all countries recognising FDA pronouncements).

FOLLOW UP

It is recommended that US Citizens also forward your submissions to your Member of Congress, whereby email addresses can be found here.

You can also inform your US Representative.

Other nationalities are encouraged to contact their representatives to determine the processes, permissions and intended authorisations within your domestic territory.

CONCLUDING STATEMENT

It is highly recommended that all submissions to this process be factually based, and where appropriate demanding of the burden of proof, in conjunction with all standard and legally obliged ethics for both medical treatments and medical practitioners. The evidence provided within our statement of concern is not limited to these concerns (Adverse Reaction reporting systems also indicate a significant risk, including deaths at rates never before witnessed nor allowed to extend into such high numbers – please check for yourselves), so we do strongly advise you seek out not only official narratives, but also independent, credible and qualified information such as via the World Council for Health and Early COVID Care.

“Let the little children come to me and do not hinder them, for to such belongs the kingdom of heaven.” Matthew 19