https://thehighwire.com/ark-videos/court-decision-forces-cdc-to-release-v-safe-free-text-data/  Video Here (Approx. 28 Min)

Court Win: CDC Must Release V-SAFE ‘FREE-TEXT’ Data

The Attorneys that represent ICAN have won a huge case for transparency around COVID vaccine injuries. A Texas judge has ruled that CDC must produce 7.8 million “free-text field entries” in the V-safe reporting app, which they had previously omitted from a production they were supposed to provide ICAN back in September of 2022. These entries are highly significant because they represent accounts of the victims injuries in their own words, rather than simply checking a box. The CDC must provide 390,000 entries a month, starting Feb 15th, and every month thereafter for the entire year. The productions will be available to download or view at http://www.icandecide.org/vsafe.

POSTED: January 12, 2024

https://childrenshealthdefense.org/defender/federal-judge-cdc-release-v-safe-texts-covid-vaccine-injuries/

01/16/24

Federal Judge Orders CDC to Release V-safe Texts Detailing COVID Vaccine Injuries

In a “huge win for transparency,” a federal judge this month ordered the Centers for Disease Control and Prevention to disclose the entirety of 7.8 million free-text reports detailing adverse reactions submitted by COVID-19 vaccine recipients through the V-safe monitoring app.

 
Article Excerpts:

The judge rejected the CDC’s claims that confidentiality concerns and resource limitations prevented the agency from publicly releasing the trove of first-hand testimonies.

Instead, U.S. District Judge Matthew Kacsmaryk for the Northern District of Texas, Amarillo Division, embraced arguments from the plaintiffs — the nonprofit watchdog group Freedom Coalition of Doctors for Choice — that obscuring the data enabled potentially misleading safety conclusions by hindering full understanding of the vaccines’ impacts.

Prior lawsuits forced the CDC to release superficial, check-the-box summaries of common symptoms generated by the V-safe system. However, the free-text fields that the CDC is now required to release represent the lone channel for reporting serious conditions like myocarditisblood clots or strokes.

The first tranche of nearly 400,000 free-text entries, which the judge ordered to be released by Feb. 15, will be available for public viewing and analysis on the Informed Consent Action Network’s (ICAN) V-safe data page.

The V-safe system was designed to capture survey data from vaccine recipients daily for the first seven days, weekly for the following five weeks, and at three-, six- and 12-month intervals.

Go here for one V-safe entry out of 7.8 MILLION entries:  https://twitter.com/AaronSiriSG/status/1745613099582074922?

“Help me!” yet over 100 days later reported to V-safe “still full disability, … 100+ days of speech, physical therapy and vestibular therapy & more to come … still no response from CDC, no help from public health, no help from FDA…”

“Unlike VAERS, the data in v-safe is gathered from a known and quantifiable universe of individuals. In fact, v-safe has precisely 10,108,273 registered users as of August 2022. These users are asked to answer the same questions. By aggregating answers to identical questions in v-safe, the rate of an adverse reaction can be calculated. That is not possible with VAERS.” ~ Attorney Aaron Siri

(See link for article)

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For more:

https://jamesroguski.substack.com/p/its-time-to-yell-at-the-us-government?

It’s Time To YELL At The U.S. Government

Tell the Office for Global Affairs exactly what you really think of the proposed “Pandemic Agreement.” Submit your written comments by Monday, January 22, 2024. GET IT OUT OF YOUR SYSTEM!

EVERYONE ON EARTH is invited to submit your written comments via email to OGA.RSVP@hhs.gov before 5pm Eastern time on Monday, January 22, 2024 with the subject line:

“Written Comment Re: Implications of Access and Benefit Sharing (ABS) Commitments/Regimes and Other Proposed Commitments in the WHO Pandemic Agreement”

The most recent Negotiating Text of the WHO Pandemic Agreement (Negotiating Text) can be found here:  https://apps.who.int/​gb/​inb/​pdf_​files/​inb7/​A_​INB7_​3-en.pdf

FALSE ASSUMPTION #1:

The Office for Global Affairs (OGA) wants us to answer a series of questions that assume that we want a “Pandemic Agreement” to be negotiated. They assume that we want “rapid creation and equitable deployment of safe and effective vaccines, diagnostic tests, and treatments.”

FALSE ASSUMPTION #2:

The proposed negotiating text of the “Pandemic Agreement” that was published on October 30, 2023 is already out of date. A new version is being written as we speak and is due to be available in February 2024. The Office for Global Affairs (OGA) wants us to comment on what is already an old version of the proposed agreement.

THESE ARE FALSE ASSUMPTIONS THAT MUST BE CHALLENGED

My thoughts are best summarized in this video:

https://www.bitchute.com/video/68noiys4ufyP/  and this website: http://ThePeoplesDeclaration.com

FEEL FREE TO COPY MY LETTER AND DECLARATION AND EDIT IT TO MAKE IT YOUR OWN:

My letter to the Office of Global Affairs:

The United States government should develop the software for a GLOBALLY AND PUBLICLY AVAILABLE interactive forum/database for ALL types of health care practitioners to share their clinical experiences and observations IN REAL TIME WITHOUT CENSORSHIP OF ANY KIND regarding all diseases so that everyone on earth can access the wisdom of absolutely all the health professionals in the world for free.

The tens of billions of dollars that might potentially be spent on pandemic prevention, preparedness and response would be much better spent ensuring that safe, potable drinking water and sanitary removal of waste water be provided for everyone on earth.

*****

STOP THESE NEGOTIATIONS

These negotiations are in regards to what is essentially a trade dispute masquerading as a health issue that is beyond the competency of the World Health Organization.

Health care is NOT an enumerated authority of the federal government. You have zero lawful authority regarding health. Health care is an issue that must be controlled by the 50 states as directed by the people of each state.

These negotiations MUST be terminated immediately.

Before any international agreement is to even be considered, a full reckoning of mistakes made, and crimes committed over the past five years MUST occur.

No treaty, agreement, framework convention, amendments to the existing International Health Regulations or any other international instrument is needed, nor is one desired.

Any agreement in the form of an open-ended “Framework Convention” MUST BE REJECTED.

I DO NOT SUPPORT AND I ACTIVELY OPPOSE FURTHER INVESTMENT IN THE PHARMACEUTICAL, HOSPITAL, EMERGENCY, INDUSTRIAL COMPLEX (PHEIC).

The search for “pathogens with pandemic potential” and the plan to build a global laboratory network to facilitate genetic sequencing is a thinly veiled disguise for bioweapons research.

The use of Midazolam, ventilators, Run-Death-Is-Near, Paxlovid, Molnupiravir, and most other pharmaceutical interventions has been an absolute health and financial disaster for everyone except the pharmaceutical industry.

Any discussion of, or any attempt to control or even monitor our unalienable right to free speech must be opposed and destroyed in its entirety. The WHO, the FDA and the CDC are the true source of the “infodemic” and they are the greatest providers of mis, dis and mal information.

The mRNA platform and the coercion used to implement it has been such an absolute disaster that those who promoted and implemented it are guilty of crimes against humanity.

STOP THE SHOTS!

STOP THESE NEGOTIATIONS

EXIT THE WHO

FREQUENTLY ASKED QUESTIONS:

Question: If I submitted an email, but then I thought of something else that I wanted to say, can I submit another email?

Answer: YES.


Question: If I missed the deadline, can I still submit an email after the deadline has passed?

Answer: Yes. Here is what the Office for Global Affairs said: “Comments received after that date will be considered to the extent practicable.”

For more:

https://rumble.com/v459qcz-the-truth-about-lyme-disease-with-lori-dennis.html Podcast Here (Approx. 47 Min)

The Truth About Lyme Disease With Lori Dennis

1/5/24

Lyme disease remains to be, in many ways, a daunting mystery to scientists and doctors across the globe. But rather than shying away from the puzzling aspects to this illness, Lori Dennis has made it her mission to dig into the research and advocate for those affected. In doing so, she has uncovered shocking revelations about the transmission, symptomatology, diagnosis, treatment and prolonged impacts of Lyme. Lori presents a few of her discoveries on ‘Doctors & Scientists’ this week.

Lori Dennis, MA, a registered Psychotherapist in private practice in Toronto, Canada, is the author of Lyme Madness: Rescuing My Son Down the Rabbit Hole of Chronic Lyme Disease.

On this expedition, just like all Lyme sufferers and caregivers, we were forced to become our own microbiologist, neurologist, immunologist, gastroenterologist, infectious disease specialist and so on, in order to map out a treatment plan, all without a GPS.

Our story is by no means unique. Most chronic Lyme sufferers are ill for months, years or even decades before they come to understand the root cause of their dis-ease. Most sufferers consult with a multitude of doctors only to have to figure it out for themselves. ~ Lori Dennis

For more:

Articles by Lori Dennis:

https://www.theepochtimes.com/health/fda-launches-fresh-bid-to-toss-out-high-profile-ivermectin-case-

FDA Launches Fresh Bid to Toss Out High-Profile Ivermectin Case

Attempt comes after appeals court ruled agency likely overstepped its authority in warnings against ivermecton

By Zachary Stieber

1/15/2024

The U.S. Food and Drug Administration (FDA) is seeking to persuade a federal court to dismiss a lawsuit challenging its repeated advisories against using ivermectin to treat COVID-19.

The FDA in a sealed motion asked the U.S. District Court for the Southern District of Texas to dismiss the suit, which was brought by three doctors who allege the FDA’s warnings were illegal.

The late 2023 motion was sealed because exhibits the government cited “include confidential information” from a separate legal proceeding, according to a government brief.

Government lawyers said they would file redacted versions of the motion for public perusal but still haven’t done so.
Attorneys for the doctors said on Jan. 12 that the court should reject the government’s fresh bid to throw out the case.“
The FDA exceeded its authority by repeatedly issuing public directives not to use ivermectin for COVID-19, even though the drug remains fully approved for human use,” they wrote.
(See link for article)
__________________
**Comment**
The hammer needs to come down on the corrupt and dysfunctional FDA.  Anything less allows further tyranny.
The Appeals Court has ruled the FDA exceeded their authorityThis judgement should stand.
The FDA’s argument is that the plaintiffs haven’t suffered injuries traceable to the FDA, but the doctors state they have suffered economic harm, reputational harm, and increased exposure to malpractice liability and forced or untimely resignations due to the FDA’s actions.
Sadly, this is becoming the MO of our government.  I’m sure these doctors are mostly motivated by the illness and death they experienced with their patients due to being handcuffed from utilizing a safe, cheap, and effective medicine for COVID which could have saved lives.
The entire ivermectin saga has been chronicled.

While the FDA has power to authorize or approve drugs for a specific use, doctors are free to prescribe cleared drugs for other “off-label” purposes. Of course “off-label” prescribing of ivermectin was censored and prohibited not only by the FDA but by the AMA and other professional medical groups Pharmacists wouldn’t even fill prescriptions for it.  This is far bigger problem than just the FDA and each of these groups need to be overhauled to limit their power over doctors.

If they get away with it for ivermectin, it could be anything in the future.

Lastly, it must be celebrated widely and loudly that finally a doctor, at great personal cost, was willing to go the distance against our corrupt government and was exonerated.

This poor doctor’s crime?  He advised for time-tested, safe, and inexpensive vitamins & natural remedies for COVID.

Our corrupt and inept government sued him for $508 BILLION dollars.  

The case drug on for over 3 stressful years and he was debanked by 5 banks.  Insurance companies dropped his patient’s ability to use insurance while under his care.  

Knowing they couldn’t win the case, the FTC offered him money in a settlement that would have come with a gag order where he couldn’t discuss the case.  He refused their bribes and is now speaking out on how the government bankrupts dissenters.

No, the ivermectin case can not be dismissed.  There’s too much at stake.

https://anandamide.substack.com/p/spider-webs-in-the-pfizer-closet

Spider webs in the Pfizer closet

Kurtosis and the Mystery ORF

Important excerpts:

Lets just remind the reader that now the EMA, the FDA and Health Canada have acknowledged that SV40 promoters are in fact in the vaccine. Despite some of them accusing us of lab contamination, they now can see the sequence in the data Pfizer gave them. They only decided to look 3 years later after a few billion doses.

What is the Mystery ORF in Green on the opposite strand of Spike? Why was this ORF never disclosed despite the WHO and FDA regulation claiming all ORFs need to be identified? This seems like a major omission as FDA can’t claim this is of no consequence if regulations demand all ORFs be disclosed.

That Mystery ORF’s closest hits is to a protein involved in silk. These silk proteins have many amyloidogenic domains.

I guess we will have to comb through Mass Spec data to see if any of these reverse strand mystery ORFs turn into proteins.We shouldn’t have to do this. We have a failure to disclose by Pfizer of an ORF involved in silk, collagen and fibroin. Mysterious clots are getting pulled from patients arteries.

(See link for article)

**Comment**

Pfizer falsified their Western blots. The shots are vastly contaminated with far more than just cancer causing Green monkey cells (SV40).  Adverse events & deaths are off the charts, including IgG4 class switches which tells the immune system to ignore the toxic Spike protein as though it were an allergen. The shots (and even the virus itself) introduce amyloidogenic and prionogenic proteins into the brain and may be infecting people with Creutzfeldt-Jakob and other similar neurodegenerative diseases that arise in protein conformation abnormalities. Yet, the clot-shot train rambles on.  Source

_________________

https://anamihalceamdphd.substack.com/p/spider-silk-polymer-sprayed-via-geoengineering

Spider Silk Polymer Sprayed Via Geoengineering Operations From California – Darkfield Microscopy Analysis

Image: Spider silk specimen as received

I recently did an interview with Reinette Senum, during which she asked me if I would help with furthering the investigation of “Spider Silk” found in Jamestown, California, suspected to come from geoengineering operations. Kathryn Saari had already done Infrared Spectra for Qualitative Analysis. The conclusion was that this is natural spider webs.

Polymers have been sprayed via geoengineering operations for decades. I have shown multiple previous examinations of similar white environmental filaments. Optically they absolutely do not look like spider webs for they are much thicker and more durable. The above conclusion that this is “natural spider silk” is unsatisfactory to me.

However spider silk is a polymer has been deployed and developed since 2002 Nexia Delivers Recombinant Spider Silk by a Canadian Biotechnology company, Nexia.  The method to produce the silk fibres was developed by Nexia in conjunction with the US Army Soldier Biological Chemical Command (SBCCOM). SBCCOM’s Natick Soldier Center has been working with Nexia under a Cooperative Research and Development Agreement (CRADA) since May 1999.

Nexia was later sold to PharmAthene, Inc, a privately held biotechnology company focused on the development of biodefense therapeutics.

I will discuss the very revealing use of spider silk proteins, which are polyamides, the same proteins that we found creating the rubbery clots in humans in detail in another post.  (See link for article)

______________

SUMMARY:

  • The deployment of spider silk proteins used in nanotech and biotech applications has been going on for over 20 years and are self assembling polymers also used for transdermal vaccine delivery, biosensing applications, brain computer interface, creation of synthetic neurons and synthetic biology.  Please read this:   https://madisonarealymesupportgroup.com/2022/04/04/the-chilling-reason-they-wont-declare-the-pandemic-over-creation-of-the-pandemic-treaty/
  • Chemical analysis has revealed dangerous endocrine disruptors (phthalens)
  • Self assembly from nano scale to macro scale requires metals as a catalyst and these environmental fibers contain large amounts of metals.
  • We are inhaling these polymers & they are replicating in our body.
  • Morgellons has been described as biosensing tech that detects resonant DNA frequency and allows it to be accessed via microwave frequency.
  • This tech is in the COVID shots, food and water supply and air
  • The spider filaments appear to contain Quantum Dot like structures (also found in the COVID jab)
  • Aluminum nanoparticle fallout from climate engineering operations is building up in snow, soils and runoff waters. Testing reveals levels of aluminum so astronomically high that the meltwater can only be considered completely contaminated. This 7 minute video contains important GeoengineeringWatch.org footage. The testimony revealed in this video is from a highly degreed former USFS government scientist.
  • Here is the 2022 patent for 3D graphene oxide nanoparticles for cloud seeding.
    • Graphene oxide which some call the new glyphosphate 2.0, has been found in the COVID shots, masks, and PCR swabs (more than 99% of the Pfizer shot is graphene and has been found in all the shots tested including Pfizer, AstraZeneca, J&J, and Moderna).
    • Due to a federal court order, the FDA confirms this despite ‘fact checkers’ false claims.
    • Former Pfizer employee, Karen Kingston, states graphene oxide is in the shots but is not listed directly on the patents because its use is a trade secret.  It is the main ingredient in ‘pegylated lipid hydrogel and is made by SINOPEG in China.
    • Graphene oxide disrupts the immune system, causes blood clots and inflammation, blocks detox pathways, is magnetic, can be activated via 5G, passes the blood, brain, barrier, and is a chemical warfare agent, created by Dr. Mylo Canderian, Ph.D. in 2015.
    • There are medical doctor-made documentaries claiming to show the phenomenon of  undeclared MAC addresses coming from people, and even dead people (2021 onwards) from graveyards!

For more: