TMJ 'dysfunction' - Health implications

Florida State Surgeon General, Joseph A. Ladapo, MD, PhD Calls for Halt in the Use of COVID-19 mRNA Vaccines

Tallahassee, Florida. – On December 6, 2023, State Surgeon General Dr. Joseph A. Ladapo sent a letter to the United States Food and Drug Administration (FDA) Commissioner Dr. Robert M. Califf and Center for Disease Control and Prevention (CDC) Director Dr. Mandy Cohen regarding questions pertaining to the safety assessments and the discovery of billions of DNA fragments per dose of the Pfizer and Moderna COVID-19 mRNA vaccines.

The Surgeon General outlined concerns regarding nucleic acid contaminants in the approved Pfizer and Moderna COVID-19 mRNA vaccines, particularly in the presence of lipid nanoparticle complexes, and Simian Virus 40 (SV40) promoter/enhancer DNA. Lipid nanoparticles are an efficient vehicle for delivery of the mRNA in the COVID-19 vaccines into human cells, and may therefore be an equally efficient vehicle for delivering contaminant DNA into human cells. The presence of SV40 promoter/enhancer DNA may also pose a unique and heightened risk of DNA integration into human cells.

[In 1960, it was discovered that Simian Virus 40 (SV40) contaminated up to 30% of the poliovirus vaccines in the US. This contamination arose because the vaccines were produced in monkey kidney cell cultures harbouring SV40 between 1955 and 1963. During this period, approximately 90% of children and 60% of adults in the USA were inoculated for polio and possibly exposed to SV40. Many epidemiologic and molecular pathogenesis studies have been conducted to identify potential cancer risks since this ‘natural’ experiment began. Productive SV40 infection has the potential to initiate malignancy in various target tissues.[2] ]

Back in 2007, the FDA put forth its guidance for regulatory limits pertaining to DNA vaccines in their document entitled, Guidance for Industry: Considerations for Plasmid DNA Vaccines for Infectious Disease Indications. This informative guide highlighted key concerns that surround vaccines utilizing innovative delivery methods when it comes to DNA integration, specifically mentioning that:

• The integration of DNA may theoretically affect an individual's oncogenes, which are responsible for the transformation of a healthy cell into a cancerous one.
• DNA integration may lead to chromosomal instability.
• The Guidance for Industry delved into the biodistribution of DNA vaccines and the possible repercussions that DNA integration could have on unintended parts of the body such as the blood, heart, brain, liver, kidney, bone marrow, ovaries/testes, lung, draining lymph nodes, spleen, and the site of injection.

On December 14, 2023, the FDA provided a written response in which they failed to provide any evidence of DNA integration assessments being conducted to address the risks that they had highlighted in their 2007 guide. Considering the FDA's acknowledgement of the unique risks that DNA integration presents, along with the efficacy of COVID-19 mRNA vaccine's lipid nanoparticle delivery system and the existence of DNA fragments in these vaccines, it is imperative for the safety of human beings to evaluate the risks associated with contaminant DNA integration into human DNA. Unfortunately, the FDA has not offered any evidence to indicate that such risks have been assessed and mitigated. Thus, Florida State Surgeon General Dr. Joseph A. Ladapo made the following statement:

"The FDA's response fails to present any data or evidence indicating that they conducted the DNA integration assessments that they had previously recommended. Instead, they have cited genotoxicity studies, which are not comprehensive enough to accurately evaluate DNA integration risk. Furthermore, they have obscured the distinction between the SV40 promoter/enhancer and SV40 proteins, which are two separate elements."

DNA integration poses an unprecedented risk to human health, including the risk that DNA integrated into the gametes of mRNA COVID-19 vaccine recipients could be transmitted to their offspring. Therefore, if the risks of DNA integration have not been adequately assessed for mRNA COVID-19 vaccines, then these vaccines should not be used in human beings. Health care providers concerned about patient safety regarding COVID-19 should prioritize patient access to non-mRNA COVID-19 vaccines and treatments. I hope that the FDA will, at some point, take its regulatory responsibility seriously, to safeguard human health, including the integrity of the human genome, in the context of COVID-19."

To uphold transparency and scientific integrity, State Surgeon General Dr. Joseph A. Ladapo will continue to scrutinize the research on these risks and keep Floridians updated. [4][/color]

This is a document released to the physicians and the public:

Approving a vaccine, utilizing novel RNA technology without extensive testing, is extremely dangerous. The vaccine could be a bioweapon and even more dangerous than the original infection".[1]

You can download a pdf file about the risks of developing prion disease through mRNA technology here

Oops! FDA Accidentally Reveals List of Covid Vaccine Side Effects, Including Myocarditis, Autoimmune Disease & Death Despite knowing the dire dangers of this "vaccine" the FDA granted Pfizer emergency use authorization on December 11, 2020, just 2 months after becoming aware of the serious life-threatening adverse effects.[3]

FDA’s draft list of “possible adverse event outcomes,” appeared briefly during a public meeting by the US Food and Drug Administration’s Product Advisory Committee on October 22, 2020 reviewing the safety and efficacy of Covid-19 vaccines:

• Acute disseminated encephalomyelitis
• Acute myocardial infarction
• Anaphylaxis
• Acute respiratory distress syndrome
• Arthritis and arthralgia
• Autoimmune disease
• Convulsions/Seizures
• Death
• Disseminated intravascular coagulation
• Encephalitis/Myelitis/Encephalomyelitis/Meningomyelitis/Meningitis//Encephalopathy
• Guillain-Barr syndrome
• Immune thrombocytopenia
• Kawasaki disease
• Multi-system inflammatory syndrome in children
• Myocarditis/pericarditis
• Narcolepsy/cataplexy
• Stroke
• Transverse myelitis
• Vaccine enhanced disease
• Venus thromboembolism

Despite the long list of known possible side effects, the FDA later granted Pfizer emergency use authorization on December 11, 2020, about two months after the meeting. This was a dastardly act and resulted in untold harm and death upon millions of Americans.

To obtain information about the Pfizer vaccines, the Medical Professionals for Transparency (PHMPT) took the FDA to court. Public Health and Medical Professionals for Transparency (PHMPT), a non-profit organization that first filed a lawsuit against the U.S. Food and Drug Administration (FDA) in the U.S. District Court for the Northern District of Texas last September. Questioning the FDA’s decision to withhold data related to Pfizer and BioNTech’s 2019 COVID-19 vaccine.

FDA loses case! Pfizer forced to disclose vaccine side effects data
US168 Information Network 2022-03-05 02:1

Pfizer lost the court case and was required to disclose all the serious side effects. On March 1, the U.S. Food and Drug Administration (FDA) lost a lawsuit. The court required the FDA to complete the disclosure of 329,000 pages of complete review documents for Pfizer's new vaccine before this summer. Now, the FDA has released the first batch of documents. However, it did not provide any form of interpretation or organization of the document. A total of 150 documents are currently published on its website and are available for free download. However, when it comes to the process of this case, it was full of twists and turns.

In November last year, the PHMPT organization asked the FDA to fully disclose vaccine review data, but the FDA did not respond. Subsequently, the PHMPT organization took the FDA to court. The FDA, however, applied to a federal judge to disclose only 500 pages of relevant documents each month. In other words, it will take a full 55 years, until 2076, to fully disclose the 329,000 pages of information! The PHMPT organization was angry at the time: By 2076, many of the people who manufactured, approved, and vaccinated would have long passed away. "Nine pages of side effects that they wanted to hide for 75 years."“Millions of people will get sick or die from the vaccine, and no one knows what will happen in the years to come.”

The plaintiff believes that the FDA violated U.S. federal law, which states that "once a licence is obtained, data and information about a biological product during the licensing approval process can be immediately publicly disclosed." This is in line with the FDA's commitment to "complete transparency" before and after the approval of the new coronavirus vaccine.

The PHMPT organization is composed of dozens of scholars, professors and public health professionals from well-known universities in the United States. They claim that independent scientists cannot conduct proper analysis until all documents submitted by Pfizer to the FDA for approval of the new corona vaccine are made public. There is no guarantee that critical vaccines that millions of Americans will receive, either voluntarily or required by their employers, will be safe and effective. The lawsuit ushered in major progress. On March 1, the FDA lost the case in the Texas District Court. Starting from that day, numerous review documents related to the "safety and effectiveness" of the Pfizer vaccine must be released. Among the many documents, the most shocking one was the report on the adverse reactions of the Pfizer vaccine, which was nine pages long.

The documents disclosed so far list more than 1,000 adverse reactions, many of which are seen for the first time, including:

• Brain: Dizziness, blurred vision, memory loss, migraines
• Heart: Shortness of breath, chest pain, rapid heart rate, dizziness
• Lungs: Shortness of breath, chest tightness, coughing, wheezing
• Stomach: Nausea, indigestion, abdominal pain, bloating
• Liver: Yellowing skin, dark urine, chronic fatigue, swelling in the legs
• Kidneys: Swelling of hands and feet, shortness of breath, fatigue, frequent urination
• Intestines: Abdominal pain, constipation, diarrhoea, rectal bleeding
• Skin: Rashes, itching, dryness, discolouration
• Eyes: Redness, dryness, blurred vision, floaters
• Ears: Hearing loss, ringing in the ears, earache, dizziness
• Throat: Sore throat, hoarseness, difficulty swallowing, cough
• Nose: Runny nose, sneezing, stuffiness, loss of smell
• Pancreas: Abdominal pain, nausea, weight loss, fatty stools
• Gallbladder: Abdominal pain, indigestion, nausea, dark urine
• Spleen: Pain in the upper abdomen, anaemia, frequent infections
• Bones: Joint pain, bone pain, fractures, loss of height
• Muscles: Muscle aches, cramps, muscle weakness, stiffness
• Bladder: Frequent urination, painful urination, blood in urine, pelvic pain.

Now we know why Albert Bourla, was able to pronounce quite casually at Davos: "Do you remember what we promised you in LA at our 2019 conference? We promised that by the end of 2023 we shall reduce the world population by 50%. I am pleased to inform you that we have achieved our goal". To this, he got a huge aplomb from his fellow conspirators. He knew about all the adverse effects and was sure to eventually achieve his goals.

According to relevant reports, among the documents released, those marked as priority review requests contained more than 100 pages of anonymous safety-related data tables. Some other documents also included tables of gender, age, and BMI of unidentified participants; some typical drug or vaccine application documents; one document showing Pfizer paid nearly $2.9 million in standard user fees to the FDA; Fast Track designation letter (usually not released); non-clinical confidential summary of vaccine; not randomized to vaccine trial List of anonymous subjects, etc. It is unclear whether the disclosed documents will provide new research results on the safety or effectiveness of the vaccine. But a representative of the non-profit organization said, "Our job is to obtain these documents, and the real situation needs to be analysed by scientists and other professionals."

Once this matter was made public, it immediately aroused heated discussions among netizens on Twitter:
"Of the 46,000 participants in the Pfizer trial, 42,000 had adverse reactions and 1,200 died. FDA rules state that the death of one person within 30 days of receiving an experimental trial drug will end the trial. But this never happened and we need to ask why?

Moderna confirms COVID mRNA Vaccines cause Cancer
By The Exposé on December 2, 2023
Moderna, the pharmaceutical company responsible for developing a mRNA COVID vaccine, has come under fire after revelations emerged that its injection has been found to cause cancer. Billions of DNA fragments were discovered in vials of the vaccine, which were deemed to be extremely dangerous. The startling discovery was made during a hearing on the topic of “Injuries Caused by COVID-19 Vaccines”, which was led by Congresswoman Marjorie Taylor Greene (R-Ga.), where Dr. Robert Malone presented his findings. He explained that Moderna’s patent reveals the presence of billions of DNA fragments and other contaminants that are linked to cancer and birth defects.

Dr. Malone further elaborated that Moderna acknowledges the risks associated with DNA in vaccines, preferring RNA instead. However, their mRNA injection, which has been administered to tens of millions of people, is contaminated with DNA. He stated, “Moderna has a patent on the use of RNA for vaccines. And in that, Moderna explicitly acknowledges that RNA is superior to DNA for vaccine purposes because of problems, including the possibility of insertional mutagenesis that could lead to the activation of oncogenes or the inactivation of tumour suppressor genes.”

Despite this revelation, the FDA claims to have no knowledge of any concerns surrounding the vaccine, even though Moderna’s patent outlines these concerns about DNA and genotoxicity. Moderna is aware that DNA is a contaminant, and it is only present because of the manufacturing process they use. They use DNA to make RNA and then degrade the DNA before purifying the degraded DNA away from the RNA. Unfortunately, the process is not very effective, and as a result, contaminated mRNA vaccines have been distributed to millions of people.

Incredibly, Pfizer’s mRNA jab for COVID was also found to be contaminated with cancer-causing DNA fragments. Researchers in the United States and Canada were able to obtain unopened vials of Moderna’s COVID jab and discovered large numbers of DNA fragments in the RNA preparation. They used standard reconstruction tools to study the circular plasmid DNAs, which were found to contain sequences that were normally not allowed in anything that was going to be used in humans, including an antibiotic resistance gene and Simian Virus 40 promoter sequences. The latter was considered to be particularly dangerous by the FDA and its inclusion in the vaccine could lead to an increased risk of insertional mutagenesis.

Pfizer provided documentation about the contamination to regulators in the US, Europe, and Canada, but regulators deleted the notation about SV40 sequences, apparently to keep it hidden from the public. Dr. Malone pointed out that high-level people at both Moderna and Pfizer had to have been aware of this issue and the potential consequences for vaccine recipients. These consequences could be anything associated with DNA damage, such as birth defects and cancer, being the most notable ones.

The Expose Urgently Needs donations

"France is cancelling mandatory vaccines, wondering if this is related to the data released by Pfizer. The report showed that 1,229 healthy people died from the vaccine."

Italian health minister Roberto Speranza, under investigation for homicide over vaccinations
November 23, 2024
Former Italian health minister Roberto Speranza is under investigation for homicide after emails revealed that from the very start of the vaccinations he knew the shots were killing people. He gave orders to local health authorities to conceal deaths and serious side effects to reassure Italian citizens of their safety and to not jeopardize the vaccination campaign. The story has been reported on both German and Italian news networks.

However, the truth is, that when the news broke about this, it was after the Public Prosecutor had already asked the court to archive the accusation — that is, to close it as not worthy of consideration. In fact, during the administration in which Speranza held the office of Minister of Health, immunity was granted to all government officials, to kill with impunity.

Originally, the reports said "The Rome public prosecutors' office is investigating Roberto Speranza, the Italian governments' health minister, during the time of covid measures. He was responsible for the vaccination campaign. The investigations are the result of complaints related to the Italian Medicines Agency - AIFA. Emails from the Italian medicine's agency the former director of AIFA Nicola Magrini is also under investigation. The publication of these internal emails revealed that they had been aware of the dangers of the covid vaccination from the start. The accusation is that the responsible minister and the head of the drug authority knowingly and deliberately exposed the unsuspecting Italian population to this risk. Yes, they encouraged Italians to get vaccinated.

Vaccination was even made mandatory for certain professional groups. Consequently, then the side effects, including fatal ones, came to light the investigations are for murder, serious bodily harm and more because Speranza and magrini evidently gave instructions to the local health authorities to conceal the deaths and serious side effects that occurred immediately after the vaccination campaign started in order not to jeopardize the vaccination campaign and to reassure the Citizens about their safety. The responsible minister and the head of AIFA, are now expected to answer for these actions according to the complaints from the police unions and the financial police as well as from the private organization. 'Listen to me' which represents 4,200 people damaged by Vaccines in Italy. Police officers and teachers were subjected to mandatory covid vaccination.

Here is the former health minister Roberto Speranza proudly announcing vaccination statistics in Italy: (photo)
"We have now reached a massively significant percentage of vaccinated people in Italy, 89.41% therefore currently in Italy just over 10% of the population remains unvaccinated. Well, today, Roberto Speranza is under investigation for lies he allegedly told about Vaccines. Among the crimes he is accused of are ideological falsehood and murder. The minister Roberto Speranza, along with Nicola Magrini, the former general manager of AIFA are both registered in the investigative records of the Rome prosecutor's Office."

Last week, the House of Representatives of the Philippines passed a resolution to investigate over 260,000 unexplained excess deaths in 2021 and 67,000 unexplained excess deaths in 2022. The next day, they were hit by an earthquake.

U.K. government data reveals young people are DYING of cancer at “explosive” rates, following the vaccine push.

The latest government data from the United Kingdom has caused alarm among oncologists and medical experts, as it reveals a sharp increase in the number of teenagers and young people succumbing to rapidly metastasizing and terminal cancers since the emergence of the Wuhan coronavirus. The 45-page analysis was conducted by Edward Dowd, a former Wall Street hedge fund manager and COVID-19 researcher. Dowd's report identified a "sharp reversal of decades of mortality data," highlighting a significant increase in excess deaths in 2022, which he deemed highly statistically significant.

Dowd's study established a baseline of normal cancer death rates from 2010 to 2020 that remained consistent until late 2021, when there was a significant increase in cancer death rates in the U.K. after the COVID-19 vaccine rollout. Dowd's research aimed to identify patterns observed in trends in cancer post-2020, and he noted that the report was one of the first to do so.

The surge in cancer cases has led some medical experts to suggest that COVID-19 vaccines may be contributing to the spike in cancer rates. Health Canada confirmed that Pfizer COVID-19 injections contain SV40 DNA sequence that can cause cancer. Medical expert Dr. McCullough warned that receiving multiple mRNA COVID "vaccines" could promote "turbo cancer," while pancreatic cancer rates have skyrocketed as COVID jabs and boosters send toxic spike protein prions into vital organs, including the pancreas, fuelling turbo cancer. The worrying trend underscores the need for further research into the long-term effects of COVID-19 vaccines.

References:
REF:[1] Classen JB. COVID-19 RNA-Based Vaccines and the Risk of Prion Disease. Microbial Infect Dis. 2021; 5(1):
[2] Dang-Tan, T., M Mahmud, S., Puntoni, R. et al. Polio vaccines, Simian Virus 40, and human cancer: the epidemiologic evidence for a causal association. Oncogene 23, 6535–6540 (2004). https://doi.org/10.1038/sj.onc.1207877
[3] Oops! FDA Accidentally Reveals List of Covid Vaccine Side Effects, Including Myocarditis, Autoimmune Disease & Death
[4] FL Surgeon General Urges A Halt To COVID Vaccines
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