Editorial Note - February 7, 2026
This petition originally called for a moratorium on "all current and future mRNA/modRNA applications." A reader cited the case of a newborn saved by individualized mRNA gene-editing therapy (NEJM, May 2025) — administered with genuine informed consent, full transparency, and no liability shields. That therapy already meets every standard this petition demands. Our evidence points to one thing: mass deployments of the technology among billions of healthy people under coerced consent, suppressed data, and total manufacturer immunity. The language now matches.

Petition To:

1. The Honorable Robert F. Kennedy Jr., Secretary, U.S. Department of Health and Human Services
2. Dr. Marty Makary, MD, Commissioner, U.S. Food and Drug Administration
3. Sen. Bill Cassidy, MD (R-LA), Chair, and Sen. Bernie Sanders (I-VT), Ranking Member, U.S. Senate Committee on Health, Education, Labor and Pensions (HELP)
4. Rep. Brett Guthrie (R-KY), Chair, and Rep. Frank Pallone Jr. (D-NJ), Ranking Member, U.S. House Committee on Energy and Commerce
5. The Honorable Pam Bondi, Attorney General of the United States
6. Dr. Kirk Milhoan, MD, PhD, Chair, and Dr. Robert W. Malone, MD, MS, Vice Chair, CDC Advisory Committee on Immunization Practices (ACIP)
7. Governor Bill Lee (R-TN), Governor Katie Hobbs (D-AZ), and Governor Tim Walz (D-MN)
8. Dr. Peter McCullough, MD, MPH, President, McCullough Foundation
9. Dr. Pierre Kory, MD, President, Front Line COVID-19 Critical Care Alliance (FLCCC)

The Crisis
We are witnessing the largest iatrogenic catastrophe in the history of modern medicine — caused not by a molecule, but by the unprecedented, liability-free mass deployment of an inadequately tested platform on billions of healthy people without genuine informed consent.

Over 700 peer-reviewed studies on Zenodo and more than 3,600 studies catalogued by React19 now document a staggering range of injuries. As of February 4, 2026, peer-reviewed research confirms that mRNA, plasmid DNA, and spike protein persist in the human body for more than 3.5 years post-injection, with potential indefinite shedding onto unvaccinated individuals. The evidence is no longer "emerging." It has arrived. 

The Evidence

The following represents a fraction of documented harms. The full scope is catalogued across 700+ studies in the Zenodo Collection. And React19.org Database.

Cardiovascular: Myocarditis, cardiac arrest, sudden cardiac death, stroke, pulmonary embolism

Neurological: Guillain-Barré syndrome, Bell's palsy, seizures, encephalitis, small fiber neuropathy

Immunological: Autoimmune disorders, IgG4 class switching, viral reactivation (shingles, EBV, CMV)

Hematological: Vaccine-induced immune thrombocytopenia and thrombosis (VITT), cerebral venous sinus thrombosis, sudden death from thromboembolisms

Ocular: Corneal endothelial cell destruction (8.4% irreversible loss within 75 days), retinal vascular occlusion, possibly blindness

Reproductive: Miscarriage, menstrual irregularities, abnormal uterine bleeding

Oncological: Accelerated cancer progression ("turbo cancers"), disrupted tumor surveillance

Mortality: 1,223 deaths in the first 90 days post-EUA (Pfizer Document 5.3.6) — data they wanted to hide for 75 years.

⚠ IMPORTANT NOTE: A December 2025 Stanford study confirmed lipid nanoparticles themselves trigger harmful immune responses — implicating the entire mass-deployed mRNA platform. We invite signers to verify these harms against the 700+ studies in the Zenodo and React19 collections.

The Voices That Matter
Kirk Milhoan, MD, PhD — Chair of the CDC's Advisory Committee on Immunization Practices and a physician who holds no mRNA technology patents — has publicly declared mRNA technology to be "the number one existential threat to humanity.” This is not a fringe activist. This is the government's chief vaccine adviser.

We call upon Robert W. Malone, MD, MS — ACIP Vice Chair and inventor of mRNA transfection technology — to join Dr. Milhoan in publicly supporting this moratorium. The Chair has called modRNA/mRNA technology an existential threat. Your signature would carry singular weight. You are publicly fighting to pull the COVID modRNA “vaccines” from the market. We ask you to go further — and demand a moratorium on mass-deployed products built on this platform.

What We Demand
We, the undersigned, demand an immediate and complete moratorium on all mass-deployed mRNA/modRNA vaccine and gene therapy products intended for population-wide administration unless the following conditions are met:

1. Independent Safety Review: A comprehensive, transparent safety review conducted by scientists and physicians with no financial ties to mRNA technology patents, pharmaceutical manufacturers, or government agencies that authorized these products.
2. Full Disclosure: Complete public release of all clinical trial data, adverse event reports, manufacturing quality records, and internal communications related to mRNA product development and authorization.
3. Accountability: A formal congressional investigation into the regulatory failures that permitted mass deployment of a technology now documented to cause widespread, multi-system harm — and into the financial conflicts of interest that may have influenced those decisions.
4. Victims' Registry: Establishment of a national registry for mRNA vaccine injury documentation, with a streamlined compensation process.

A Necessary Distinction
This moratorium targets the mass production and population-wide deployment of mRNA/modRNA products under liability shields, suppressed safety data, and coerced consent. It does not target individualized therapeutic applications — such as personalized gene-editing treatments for patients with rare, fatal genetic disorders — which operate under traditional informed consent, compassionate use oversight, full data transparency, and genuine physician-patient decision-making. These therapeutic applications already meet every standard this petition demands for mass-deployed products. That contrast is the indictment.

Why This Matters Now
This petition launches as newly released Epstein files document a decades-long Gates-Epstein-JPMorgan financial architecture designed to monetize pandemics — operational years before COVID-19. The demand for independent review has never been more urgent. 

HHS Secretary RFK Jr. has already defunded all 22 BARDA mRNA contracts, with $500 million in terminated contracts. Nine states are pursuing moratorium legislation — and three (Tennessee, Arizona, Minnesota) have now introduced bills designating mRNA injections as biological weapons of mass destruction. The McCullough Foundation's latest research confirms mRNA persistence and shedding extend to all mRNA-based products. The momentum is building — no one has yet formally demanded a moratorium on mass-deployed products built on the entire platform.

International momentum has been building since 2024. The Hope Accord — launched in July 2024 by 12 international doctors and scientists — has now gathered over 68,000 signatures, including 2,063 verified physicians, calling for suspension and investigation of COVID-19 mRNA products. Our petition carries that torch forward, demanding a moratorium on the entire mass-deployed platform — not just the COVID shots.

Your Signature Matters
100,000+ signatures create media coverage. 250,000 creates political pressure. One million creates a mandate that no elected official can ignore.

The medical freedom community has the numbers. This is the rallying point.

Sign. Share. Demand accountability.

90-day target: May 4, 2026

Evidence Base:

1. COVID-19 mRNA "Vaccine" Harms Research Collection — 700+ Peer-Reviewed Studies (Zenodo)
2. React19 Science Database catalogs more than 3,600 studies on adverse reactions.
3. Hulscher et al. (Feb 2026): mRNA, plasmid DNA, and spike protein persist 3.5+ years post-injection; indefinite shedding possible (Focal Points)
4. Hulscher, N., "Third U.S. State Introduces Legislation Designating mRNA Injections as Biological Weapons," Focal Points (February 6, 2026)
5. The Pfizer Papers: Pfizer's Crimes Against Humanity, by Naomi Wolf
6. Pfizer Post-Marketing Experience Document 5.3.6 (PHMPT)
7. D2D Adverse Events Categorization by Systems Affected
8. Stanford Medicine Study (December 2025): Lipid nanoparticles trigger harmful immune responses independent of spike protein
9. Turkish Corneal Study (Sumer & Subasi, Ophthalmic Epidemiology, July 2025): 8.4% irreversible corneal endothelial cell loss within 75 days post-Pfizer vaccination
10. DutyToDissent.substack.com: "We the People Demand a Moratorium on mRNA Gene Therapy Technology" (February 6, 2026)
11. DutyToDissent.substack.com: Why This Petition Targets Mass Deployment — Not Safe, Effective Therapeutics" (February 8, 2026)

Who We Are
This petition is initiated by Duty to Dissent (dutytodissent.substack.com), a physician-led publication dedicated to the principle that medical conscience must prevail over institutional conformity.

Read the full context:

We the People Demand a Moratorium — Duty Calls #17
Platform Problem: Why This Petition Targets Mass Deployment

 Updated February 8, 2026: Petition language refined to precisely target mass-deployed products. See Editorial Note above.