FDA Citizen Petition
Together with Kevin McKernan, Dr Jessica Rose, Dr David Speicher, and Maria Gutschi, Julian Gillespie drafted a detailed Citizen Petition that was filed with the FDA on 20 January by Katie Ashby-Koppens of PJ O’Brien & Associates
.. you can download a copy below or go to the US Regulations.Gov page HERE
The Petition presents just two grounds as the basis for seeking the FDA suspend or revoke the approvals given to the Covid-19 products of Pfizer and Moderna
Freedom of Truth group submission comment
I have put in this submission comment below on behalf of our group and attached the Unmasking the Contamination Crisis piece written by Gaz’s defenders voice to them as some added info which is below.
Each and everyone of us can do similar, please read Julian Gillespie’s substack because it covers a lot of ground on various issues and also highlights that this petition will be handed directly to RFK Jnr if he get selected as Secretary of the HHS.
Our community Freedom of Truth group support this petition because the process of giving approvals for the dispersement and mass injection of millions of people with what is clearly a Gene Therapy technology has been totally compromised and not undertaken as it should have been as described in the petition itself and covering letter. The approvals are not likely legitimate or legal under the flawed procedures.
The harms and deaths that have occurred as a result of these injections which are continueing are unprecedented and the potential for ongoing major health problems including terminal and debilitating illnesses is astronomical and must stop.
We demand for the sake of humanity and for the need to rebuild faith, hope and trust into the health systems that you immediately withdraw these products until they have been through the appropriate scrutiny and independent studies be undertaken to determine the real risks of them including the DNA contamination...before any consideration to bringing them back to market is undertaken.
People are aware of massive health issues and confidence in your organizations credibility is now shattered.. WE are looking for truth and integrity and genuine care of the people.
It is now time to sort this mess out.
Unmasking the Contamination Crisis in mRNA Injectable Drugs: A Public Health Catastrophe in the Making
What if a hidden crisis lay within the COVID-19 vaccines? Shocking DNA contamination levels challenge the "safe and effective" narrative, raising alarming risks regulators refuse to address.
The development of COVID-19 mRNA vaccines was heralded as a marvel of modern science, but a darker truth lies buried beneath the veneer of innovation and triumph. Disturbing revelations have emerged about significant DNA contamination in vaccine lots—contamination that reaches levels up to 470 times the so- called “safe” limit defined by the World Health Organization.
This is not a trivial oversight or a manufacturing hiccup. This is a crisis that directly threatens the health and safety of every individual injected with these drugs.
The alarm bells began to ring loudly when Kevin McKernan first uncovered alarmingly high levels of DNA contamination in early 2023, a finding that has since been corroborated by numerous independent scientists. The most recent revelation comes from a study conducted in a laboratory utilized by the FDA itself, exposing staggering levels of contamination in every analysed vaccine lot.
This discovery, particularly significant because of the FDA’s connection, suggests that the problem may be even worse than initially reported. Methodological limitations raise the possibility that larger, more dangerous DNA fragments capable of disrupting cellular functions remain undetected. Instead of taking responsibility, the FDA—the agency charged with safeguarding public health—has chosen to distance itself from these damning findings.
By denying ownership of the study and refusing to act, the FDA has demonstrated a chilling disregard for public safety, prioritizing perception over accountability.
DNA contamination, even in small fragments, is far from a hypothetical risk confined to theoretical science. These fragments can trigger immune pathways like cGAS-STING,[1] leading to chronic inflammation and immune system dysregulation. The threat of genomic integration—where foreign DNA integrates into human cells—looms ominously, with potentially catastrophic consequences if it occurs in critical regions such as oncogenes or tumour suppressor genes.
This risk is compounded by the lipid nanoparticles (LNPs) used in vaccine delivery, which protect these fragments and enhance their ability to enter human cells. The very mechanism designed to deliver the mRNA payload efficiently may inadvertently pave the way for these fragments to wreak havoc within the human body.
The FDA laboratory’s report indicated that the DNA contamination consisted of non-replicating fragments, which might appear less dangerous at first glance. The probability of genomic integration was estimated at approximately 1 in 10 million cells.
While this figure may sound reassuringly small, the broader context reveals a much more alarming reality. The human body contains roughly 37 trillion cells, meaning that even such a low probability translates to an average of around 3,700 cells per individual potentially experiencing genomic integration.
If foreign DNA integrates into critical genomic regions in just one of these cells,[2] the results could be catastrophic, leading to mutations that may escape immune detection and cause severe health outcomes over time.
When scaled to the billions of vaccinated individuals worldwide, the potential for population-wide health impacts becomes staggering. The sheer number of affected cells across global populations magnifies the risk of rare but severe reactions, challenging the dismissive assurances of safety provided by regulatory bodies.
These are not merely theoretical risks; they are statistically plausible outcomes that demand immediate scrutiny and decisive action. The scale and scope of these potential outcomes should compel regulatory agencies and manufacturers to halt vaccine distribution until these dangers are fully understood and mitigated.
To grasp the implications, consider even a single integration event. If a DNA fragment integrates into a critical genomic region like an oncogene, it could initiate a cascade of cellular changes that lead to cancer. While the immune system is adept at identifying and eliminating abnormal cells, it is not infallible.
A single mutated cell that evades detection could proliferate unchecked, causing devastating consequences. When scaled across billions of vaccinated individuals, even a seemingly insignificant per-cell risk becomes an unthinkably large public health hazard.
This is not speculation. The mechanisms for genomic integration are well-documented in molecular biology. Foreign DNA fragments, if delivered into the cell nucleus—a plausible scenario given the LNP delivery system— can interact with the host’s genetic material. DNA repair pathways, such as non-homologous end joining (NHEJ) and homologous recombination, could potentially incorporate these fragments into the genome.
These are not abstract possibilities; they are established biological processes, with consequences that include genetic instability, oncogenesis, and other severe health outcomes.
Moreover, the ability of the immune system to eliminate mutated cells varies significantly among individuals. People with compromised immune systems, whether due to age, pre-existing conditions, or immuno- suppressive therapies, are particularly vulnerable.
For these populations, the risks of genomic integration and its downstream consequences become even more pronounced. Alarmingly, these vulnerabilities have not been adequately addressed in public discussions, leaving millions unaware of the heightened dangers they may face.
Despite these glaring concerns, regulatory agencies continue to lean on hollow reassurances. The FDA, in its official response to the study, stated that “no safety concerns related to residual DNA have been identified,” citing the billions of doses administered as proof of safety. This reasoning is dangerously flawed. Just as the widespread use of cigarettes once masked their lethal consequences, the mass administration of a product does not inherently validate its safety. The absence of immediate, observable harm does not negate the potential for long-term effects.
The latency period for many diseases, including cancers potentially caused by genomic integration, means that the full impact of this contamination may not become evident for years or even decades.
The FDA’s attempt to distance itself from its own study—conducted under its supervision, in its labs, and using its resources—underscores the depth of this crisis. By dismissing the findings as “not belonging” to the agency, the FDA has chosen to obscure evidence that directly challenges the safety claims of mRNA vaccines. This abdication of responsibility is a betrayal of public trust and a dereliction of the agency’s mandate to protect public health.
The silence from other regulatory bodies, such as the Australian Therapeutic Goods Administration (TGA), is equally damning. Their dismissal of similar findings from independent researchers as “misinformation” reflects a systemic unwillingness to confront inconvenient truths. This coordinated evasion raises serious questions about the integrity of the global regulatory framework and its ability to safeguard public health in the face of mounting evidence of harm.
What makes this silence even more troubling is the unprecedented reliance on mRNA vaccine technology as the foundation for future global health initiatives. If these vaccines are allowed to continue distribution without addressing the contamination crisis, the repercussions will extend far beyond COVID-19. Public trust in vaccines, already fragile in some communities, will be irreparably damaged. The credibility of regulatory agencies, already eroded by inconsistent messaging and lack of transparency, will collapse under the weight of their inaction.
The discovery of significant DNA contamination in mRNA vaccines is not merely a technical flaw; it is a public health catastrophe waiting to unfold. The stakes are too high to allow complacency. These vaccines must be withdrawn from distribution immediately, and a comprehensive investigation must be launched. This investigation must not be conducted by the same regulatory agencies that have already demonstrated their unwillingness to act but by independent entities free from political and financial influence.
Independent and rigorous research must be prioritised to fully understand the scope and implications of DNA contamination. Manufacturing processes must be scrutinised to ensure that such contamination is eliminated in future vaccine production. Transparency from vaccine manufacturers is not optional; it is a moral imperative. Long-term monitoring systems must be established to track the potential late-onset health effects, including cancers and autoimmune disorders, in vaccinated populations.
The public deserves more than platitudes and reassurances. They deserve accountability. They deserve transparency. And most importantly, they deserve safety. Anything less is a betrayal of trust on a global scale. The DNA contamination crisis is not just a failure of science; it is a moral failing of the systems designed to protect us. The risks are real, the dangers are undeniable, and the cost of inaction is too high to bear. It is time to confront this crisis with the urgency and integrity it demands. The lives of billions depend on it.
1. The cGAS-STING pathway is part of the body’s natural defence system. It helps detect stray pieces of DNA that shouldn’t be outside the cell’s nucleus—like DNA from viruses, bacteria, or damaged cells— and signals the immune system to respond. This process starts when a protein called cGAS senses the foreign DNA and creates a signal molecule that activates another protein called STING. Together, they trigger the production of chemicals that alert the immune system to fight off infections or repair damage. However, if this system gets over-activated, it can cause problems like long-term inflammation or autoimmune diseases. In the case of vaccine contamination, this pathway might react to leftover DNA fragments, potentially causing unexpected immune reactions.
2. Even a single cell with a critical DNA mutation can potentially lead to serious health issues like cancer. If the mutation occurs in important parts of the DNA, such as those controlling cell growth (oncogenes or tumor suppressor genes), the cell can begin to replicate uncontrollably. While the immune system usually identifies and destroys such abnormal cells, some can evade detection and cause complications. Considering the human body has trillions of cells, even a very low chance of mutation can result in a significant number of affected cells, especially when viewed at a population level.
Authored by Gaz’s a defenders Voice
Potoroo gathering Sunday 23rd Feb
We are finally having a gathering for the first time this year at Potoroo... without any specific speakers just and open mic session for anyone and everyone to have rap about where they see us at this point of time...
Obviously plenty to talk about with the show that keeps giving, hopefully by then RFK will be confirmed as Secretary of Human Health Services, and may he hit ground running like the Trumpster... we’ll just have to wait and see... OMG the Trumpet has trumped everyone with some positives...but also some outrageous stuff, I suppose what else would you expect.. I can’t stop shaking my head in belief and disbelief...
I hope RFK is more balanced and not to compromised... everyone knows his understanding of health and vaccines is comprehensive, so we must live in hope he will make some solid steps in the right direction..
Narooma group Gathering at the Golf club on Sunday the 16th Feb
Lunch at 12noon, meeting from 1pm, open discussion..
Please call Marilyn to confirm numbers 0244721835 or just roll up anyway
Incredible post on Cobargo Bermagui Facebook Noticeboard page
put up by Orida Armour Lushmoor who has been badly vaccine damaged and is asking if others have been also, the responses are amazing lots of people coming out revealing their injuries including deaths of loved ones... Lots of support from the people but nothing from authorities.. Orida and her husband have been fighting for some assistance but have continually been fobbed off, in Orida’s words
“ Over the past 18 months I have written hundreds of emails to politicians at all levels about the jabs. I can confirm there is resounding silence, non engagement, belittling or expert political circular speak. Kristy McBain still will not meet with me. I must have well over 12 written requests. She said she would, both in writing and through phone calls. Nothing.
Kristy and a number of her staffers have confirmed that her office are sending jab injured local constituents away without representation or care. I can confirm, as a multiple medically diagnosed jab injured Australian, there is no compunction, desire or morality by the major parties or government departments to care, support or represent.” Orida
Have a look at the post and the comments because they are amazing I think to see the comments you have to join the Noticeboard...
Orida and her husband have joined our group and are wanting to attend our upcoming gathering, they are trying to get some traction and move things along , so please come along and support them.
Here is MP Russel Broadbent giving the issue some air in Parliament mentioning Orida
Also tomorrow.. if you can, go and show support to this worthy cause.
Grand Jury Indictment Gathering in Canberra tomorrow Saturday 8th February at Magna Carta Place, Canberra 2600
12.00 picnic commences 12.30 Speakers address the people 1.00 People’s Court Grand Jury You will be able to connect via a link to be part of this rally in spite of where you may reside. The link is not ACTIVE yet for security reasons
HERE IS WHERE YOU GO TO FIND THIS LINK – SO KEEP CHECKING FOR ITS ACTIVATION – IT IS UNDER THE VIDEO
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