Is SV40 Large Tumor Antigen required for SV40 origin of replication activity.
No
Here we detect Pfizer plasmid DNA in a colon tumor biopsy 1 year after vaccination.
And its not small amounts of DNA. Its so much DNA that it can only be explained by plasmid amplification post vaccination or genome integration and amplification.
Over 75% of people over that age of 25 have a significantly calcified pineal gland.
In a 2001 study on fluoride distribution, pineal gland fluoride levels were measured in aged cadavers. Researchers found that:
“There was a positive correlation between pineal F[luoride] and pineal Ca[lcium] (r = 0.73, p<0.02) but no correlation between pineal F and bone F. By old age, the pineal gland has readily accumulated F and its F/Ca ratio is higher than bone.”[3]
They concluded that over time through regular fluorideexposure, “the pineal accumulates fluoride and that this accumulation may be implicated in the pathogenesis of pineal calcification. Given the essential role of the pineal gland and melatonin in regulating wake/sleep patterns, creativity, calmness and spiritual health, these findings have profound implications”
The pineal gland is an endocrine gland whose main function is the biosynthesis and secretion of melatonin, a hormone responsible for regulating circadian rhythms, e.g., the sleep/wake cycle. Due to its exceptionally high vascularization and its location outside the blood–brain barrier, the pineal gland may accumulate significant amounts of calcium and fluoride, making it the most fluoride-saturated organ of the human body. Both the calcification and accumulation of fluoride may result in melatonin deficiency.
In the 1960s a miraculous treatment for chronic pain, traumatic injury, strokes and spinal cord paralysis was discovered that spread across America like wildfire—until the FDA buried it.
Here, 60 Minutes exposed the FDA using the same playbook they used throughout COVID-19.
My thanks to lead authors Ilyes Baghli and Pierrick Martinez for their incredible inspired work, FLCCC’s Dr.Paul Marik for his extensive work on repurposed drugs and every co-author who worked hard to bring this paper to life.
I hope that this peer-reviewed paper lays the groundwork for a brand new future for Cancer Treatment.
Many of you know that I have been helping thousands of Cancer patients with high dose Ivermectin, Mebendazole, and Fenbendazole.
We are already starting to see incredible successes with these repurposed drugs.
Mainstream Oncology collapsed after the rollout of contaminated COVID-19 mRNA Vaccines.
•To maximize profits, the pharmaceutical industry will often identify vulnerable groups who lack the ability to advocate for themselves and refuse pharmaceutical products.
•When the DPT vaccine was first developed over a century ago, it was tested at Irish orphanages. Recently mass graves of those early test subjects were discovered.
•Since the DPT vaccine hit the market, physicians around the world have observed waves of infant deaths following its use, which were often sudden and inexplicable (along with many other severe side effects).
•Numerous data sources correlate increasing childhood vaccination rates with increasing infant deaths. Those deaths played a key role in creating the 1986 National Childhood Vaccine Injury Act. That forgotten data compromises the majority of this article.
•When the COVID lockdowns happened, vaccine safety activists predicted the lockdowns would lead to an unprecedented drop in infant deaths since children were skipping their vaccines. This ended up being exactly what happened, and it was reconfirmed by infant deaths dropping in Florida after the pandemic prompted many parents to begin not vaccinating their children.
More than half of the US peer reviewers for four major medical journals received industry payments between 2020 and 2022, new research shows. Altogether they received more than $64 million in general, non-research payments, with a median payment per physician of $7614. Research payments — including money paid directly to physicians as well as funds related to research for which a physician was registered as a principal investigator — exceeded $1 billion.
A doctor who took his own life left a heartbreaking suicide note saying he had ‘run out of gas’ as he warned of the immense pressure medics are under.
Dr Will West was in the third year of his ophthalmology training at George Washington University School of Medicine and Health Sciences in Washington D.C.
His suicide at the age of 33 devastated his friends and family, as well as those he worked with.
The devoted doctor, who was nicknamed ‘Iron Will’ for his determination, said it was not one single event which had led to his death but highlighted the immense pressure of his residency which his family say prevented him seeking help.
‘To those who will be negatively affected by my actions, I’m so sorry. I have simply run out of gas and have nothing left to give,’ West wrote in the note obtained by the Washington Post.
A pioneering once-a-day pill that regenerates nerve cell connections damaged by ALS has been FDA-approved for ongoing clinical trials. The drug is now being given to those with ALS and could be a watershed moment in the treatment of the fatal disease.
Amyotrophic lateral sclerosis (ALS), or Lou Gehrig’s disease, affects nerve cells in the brain and spinal cord, called motor neurons, that control voluntary muscle movements like walking, talking, and breathing. As the neurons die and can’t send messages to the muscles, loss of muscle control worsens over time and is eventually fatal.
The US Food and Drug Administration (FDA) has approved several drugs that help manage symptoms or slow the disease’s progress, but there’s no current treatment that reverses the progression of ALS. In short, there’s no cure. That’s where Spinogenix, Inc. comes in.
Spinogenix, a clinical-stage biopharmaceutical company, has developed SPG302, a unique once-a-day pill that regenerates the gaps, called synapses, between neurons to restore communication. Following promising results from clinical trials to evaluate the drug’s safety, the FDA has approved the company’s Investigational New Drug (IND) application, paving the way for further trials.
It is a ‘self-amplifying mRNA vaccine, also known as an ‘sa-mRNA vaccine’, which properly is a ‘gene therapy injection’ and not really a vaccine.
A self-amplifying mRNA shot, as the name implies, contains the equipment needed to make more of itself once it enters cells. You do this by not only injecting the mRNA for the antigen of interest (such as one that encodes the coronavirus spike protein) but also mRNAs that get translated into replicase proteins that will in turn produce more of the mRNA species. Picture sending someone a sheet of paper with some important information on it, and then imagine that you’ve sent them a whole pile of copies of that sheet so they can distribute them. Now imagine sending them a bunch of sheets of material that can assemble themselves into a working photocopier and crank out more sheets when they do. That sounds weird and ridiculous, but hey, that’s biology for you. It’s very, very strange down there in the cell.
Long story short, it turns out that sa-mRNA vaccines are much like mRNA vaccines . . . only worse. Whereas the mRNA vaccines required you to keep returning to the doctor’s office every few months for another booster, the sa-mRNA vaccines will be self-amplifying. That means they’ll not only be hijacking your cells’ machinery to create whatever “protein of interest” Big Pharma wants, they’ll also create replicase proteins that will manufacture more of the mRNA that will make even more of that “protein of interest.”
For those of us who managed to avoid falling for the largest propaganda campaign in modern history and who recognize that the mRNA vaccine is itself a bioweapon that has already injured and/or killed vast numbers of people, this new sa-mRNA technology should be very concerning. Why? Because not only does it come with all the same dangers of regular mRNA vaccines, but it presents the additional risks associated with the random, uncontrolled self-amplification process.
I am filing this under both ‘medical science’ and ‘anti-science’ because the sa-mRNA platform does have medical promise, but is nowhere near safe enough to give to whole populations now. ABN
Japanese Member of Parliament Ryuhei KawadaWe are addressing this press conference from the standpoint that the replicon vaccine should be halted. Therefore, we have decided to hold this emergency press conference. This self-replicating immune agent, scheduled to start regular vaccinations from October 1st, ought to be halted, and I strongly advocate for this action. Additionally, we must ensure thorough investigation and verification to provide relief to mRNA vaccine victims who have suffered significant harm. This must be systematically carried out. Instead of merely discarding unused vaccines, we should facilitate research by passing them on to researchers for analysis. I intend to make these demands to the Prime Minister and the Ministry of Health, Labour and Welfare.
Professor Dr. Seiji Kojima of Nagoya University:Compared to those who are unvaccinated, the mortality rate is five times higher if you get vaccinated twice. The purpose of receiving vaccination is indeed to reduce the mortality rate, but ironically, the rate was five times higher after receiving the vaccine.
Prof Murukami of Tokyo Science University:“Japan is planning a large-scale rollout of self-amplifying vaccines, which are considered hazardous materials…”
“…by the beginning of next month, Japan has the potential to trigger a worldwide disaster”.“The vaccines do not seem to be effective. They do not work. They lack efficacy. mRNA vaccines have resulted in many deaths, injuries, and victims.”
American Buddhist Net 