So the Yale Listen Study said 709 days per their testing of vaxinjured still having continuous spike production (which I am a participant in this study) and show T cell exhaustion etc

Well it’s actually longer than that:

My first injection was 12/23/2020 and I haven’t stopped producing spike and it’s now 02/21/2025

8 months after my 2 Moderna injections I still had large amounts of spike detected per antigen testing- & I’ve never had Covid( results below)

That’s 1,521 days - of continuous spike protein production with NO OFF SWITCH since my first injection & STILL in my body to date

Let that sink in!

(3 years worth of Cytokine 14 panels & S1 immune subset panels below)

I am a documented, confirmed & diagnoses Adverse reaction to MRNA vaccine ( T50.B95A)

2022

6/14 cytokines activated
Vax spike in classical, non classical and intermediate monocytes

2023

11/14 cytokines activated
We cleared all 3 monocyte lines

*Persistence of S1 Spike Protein in CD16+ Monocytes up to 245 Days in SARS-CoV-2 Negative Post COVID-19 Vaccination Individuals with Post-Acute Sequalae of COVID-19 (PASC)-Like Symptoms*

Via: Bruce K. Patterson, Ram Yogendra, Edgar B. Francisco, Emily Long, Amruta Pise, Eric Osgood, John Bream, Mark Kreimer, Devon Jeffers, Christopher Beaty, Richard Vander Heide, Jose Guevara-Coto, Rodrigo A Mora-Rodríguez

doi: doi.org/10.1101/2024.0…

{this is the preprint they refused to publish unless they took the vaxinjured data out- MY DOCTOR WHO DIAGNOSED & SAVED ME IS AN AUTHOR}

• ABSTRACT •
There have been concerning reports about people experiencing new onset persistent complications (greater than 30 days) following approved SARS-CoV-2 vaccines (BNT162b2 (Pfizer), mRNA-1273 (Moderna), Janssen (Johnson and Johnson), and ChAdOx1 nCoV-19 (AstraZeneca))

We sought to determine the immunologic abnormalities in these patients and to investigate whether the potential etiology was similar to Post-Acute Sequalae of COVID (PASC), or long COVID

We studied 50 individuals who received one of the approved COVID-19 vaccines and who experienced new onset PASC-like symptoms along with 45 individuals post-vaccination without symptoms as controls

We performed multiplex cytokine/chemokine profiling with machine learning as well as SARS-CoV-2 S1 protein detection on CD16+ monocyte subsets using flow cytometry and mass spectrometry. We determined that post-vaccination individuals with PASC- like symptoms had similar symptoms to PASC patients

When analyzing their immune profile, Post-vaccination individuals had statistically significant elevations of sCD40L (p<0.001), CCL5 (p=0.017), IL-6 (p=0.043), and IL-8 (p=0.022)

Machine learning characterized these individuals as PASC using previously developed algorithms

Of the S1 positive post-vaccination patients, we demonstrated by liquid chromatography/ mass spectrometry that these CD16+ cells from post-vaccination patients from all 4 vaccine manufacturers contained S1, S1 mutant and S2 peptide sequences

Post-COVID vaccination individuals with PASC-like symptoms exhibit markers of platelet activation and pro-inflammatory cytokine production, which may be driven by the persistence of SARS-CoV-2 S1 proteins in intermediate and non-classical monocytes

The data from this study also cannot make any inferences on epidemiology and prevalence for persistent post-COVID vaccine symptoms

Thus, further studies and research need to be done to understand the risk factors, likelihood and prevalence of these symptoms

Summary: SARS CoV-2 S1 Protein in CD16+ Monocytes Post-Vaccination

• Footnotes •
Abbreviations: PASC, post-acute sequelae of COVID-19; POVIP, post-vaccination individuals with PASC-like symptoms; NCM, non-classical monocytes; IM, intermediate monocytes; CX3CL1, C-X3-C motif chemokine ligand 1; CX3CR1, C-X3-C motif chemokine receptor 1; IL, interleukin; RANTES, regulation on activation, healthy control T-expressed and secreted; CCR, chemokine receptor; IFN, interferon; TNF, tumor necrosis factor; MIP, macrophage inflammatory protein; PBMCs, peripheral blood mononuclear cells; VEGF, vascular endothelial growth factor; LH, long hauler or PASC

• Paper in collection : COVID-19 SARS-CoV-2 preprints from medRxiv and bioRxiv connect.medrxiv.org/relate/content…
• INTRODUCTION •
Despite over 13 billion doses of SARS-CoV2 vaccines being administered to individuals worldwide, there have been concerning reports and publications of persistent adverse effects of the COVID-19 vaccines

These reports suggest that new-onset cardiac, vascular and neurological symptoms commenced within minutes and hours after vaccination and subsequently, were persisting for months and years 1–5

Interestingly, many of these persistent post-vaccine symptoms are similar to symptoms associated with post-acute sequelae of COVID (PASC), or long COVID

We recently reported that the S1 protein subunit of SARS-CoV2 was persistent in both nonclassical (CD14- CD16+) and intermediate (CD14+CD16+) monocytes several months and years after acute infection and could be a possible pathophysiological explanation for PASC

Interestingly, the BNT162b2 (Pfizer), mRNA-1273 (Moderna), Janssen (Johnson and Johnson), and ChAdOx1 nCoV-19 (AstraZeneca) vaccines also deliver a synthetic S1 protein subunit directly into muscle cells to elicit an immunological response

Since there were similarities between PASC and persistent post-vaccination symptoms in individuals who never had a history of COVID infection, we sought to study if persistent S1 proteins were also present in CD16+ monocytes of both groups

One of the challenges in studying individuals with persistent post-vaccination symptoms is the lack of approved confirmatory tests to rule out previous infection or exposure to SARS-CoV2

Hence, we used a combination of patient clinical history, negative anti-nucleocapsid antibody testing and T-detect testing as a way to screen these patients

Here, we report on 50 individuals with symptoms >1 month following vaccination (with either Pfizer, Moderna, Johnson and Johnson or AstraZeneca) that resembled the spectrum of symptoms reported in long COVID or PASC7

We used machine learning to analyze the immune profiles in these individuals

Further, we used high parameter, single cell analysis to determine if S1 protein generated by vaccination persisted in immune cells as previously described

• Per FOIA •

• THE DOD CONTRACT WITH PFIZER •

Have a good day!

<3

(1) ~ A MUST READ THREAD/PART 1 of 2 THREADS (1/25)

** Would you Like “Turbo Cancer” with that? **

~The “Turbo Cancer is a myth” MYTH is a low point, even for big pharma cartel and their pseudoscience cronies~

* By: Arkmedic Substack *

• Today’s article is hopefully going to answer the question about whether "Turbo Cancer”

(a) exists
(b) is a consequence, or possible consequence of the imposition of a genetic vaccine platform on the global population

.@Jikkyleaks. (2) ~ “Turbo Cancer is a Myth: Via Wikipedia” ~

• The first thing that needs clearing up is “where did the Turbo Cancer phrase come from?”

• If you’re in the field you might think this is a made up term, but it really exemplifies the idea of a rapidly progressive cancer, that is progressing or spreading much faster than you would be used to

• Most oncologists know how the cancers they treat progress and so can give you an idea of what to expect

• A prostate cancer in an elderly person for instance would normally take years to progress, so getting growing secondaries in a few months would be unusual

• Similarly for a small breast cancer that was surgically removed or treated with radiotherapy which would be expected to be cured with the first line of treatment

• So you would think “Turbo Cancer” would be embedded in the oncologists lexicon from old, but it isn’t

• In fact the first mentions were coming from Twitter/X the end of 2022 and beginning of 2023:
x.com/search?q=%22tu…

• Here is Dr Charles Hoffe talking about it back in January 2023 as a relatively new phenomenon below:

(1) • OCTOBER TERM, 2012 •

— Syllabus —
NOTE: Where it is feasible, a syllabus (headnote) will be released, as is being done in connection with this case, at the time the opinion is issued

The syllabus constitutes no part of the opinion of the Court but has been prepared by the Reporter of Decisions for the convenience of the reader

~ See United States v. Detroit Timber & Lumber Co., 200 U.S. 321, 337 ~
SUPREME COURT OF THE UNITED STATES

• Syllabus •
ASSOCIATION FOR MOLECULAR PATHOLOGY ET AL. U. MYRIAD GENETICS, INC., ET AL.

CERTIORARI TO THE UNITED STATES COURT OF APPEALS FOR
THE FEDERAL CIRCUIT

No. 12-398. Argued April 15, 2013—Decided June 13, 2013

• Each human gene is encoded as deoxyribonucleic acid (DNA), which
takes the shape of a "double helix."

• Each "cross-bar" in that helix
consists of two chemically joined nucleotides

• Sequences of DNA nucleotides contain the information necessary to create strings of amino acids used to build proteins in the body

• The nucleotides that code for amino acids are "exons," & those that do not are "introns."

• Scientists can extract DNA from cells to isolate specific segments for study

• They can also synthetically create exons-only strands of nucleotides known as complementary DNA (cDNA)

• DNA contains only the exons that occur in DNA, omitting the intervening introns

• Respondent Myriad Genetics, Inc. (Myriad), obtained several patents after discovering the precise location & sequence of the BRCA1 & BRCA2 genes (breast & ovarian cancer genes), mutations of which can dramatically increase the risk of breast & ovarian cancer

• This knowledge allowed Myriad to determine the genes' typical nucleotide sequence, which, in turn enabled it to develop medical tests useful for detecting mutations in these genes in a particular patient to assess the patient's cancer risk

• If valid, Myriad's patents would give it the exclusive right to isolate an individual's BRCA1 & BRCA2 genes & would give Myriad the exclusive right to synthetically create BRCA cDNA

• Petitioners filed suit, seeking a declaration that Myriad's patents are invalid under 35 U.S. C. §101

• As relevant here, the District Court granted summary judgment to petitioners, concluding that Myriad's claims were invalid because they covered products of nature

• The Federal Circuit initially reversed but on remand in light of Mayo Collaborative Services v. Prometheus Laboratories, Inc., 566 U.S. — the Circuit found both isolated DNA & cDNA patent eligible (2) Cite as: 569 U.S. _ - (2013)

• Syllabus •

(c) DNA is not a "product of nature," so it is patent eligible under §101

• cDNA does not present the same obstacles to patentability as naturally occurring, isolated DNA segments

• Its creation results in an exons only molecule, which is not naturally occurring

• Its order of the exons may be dictated by nature, but the lab technician unquestionably creates something new when introns are removed from a DNA sequence to make cDNA Pp 16-17

(d) This case, it is important to note, does not involve method
claims, patents on new applications of knowledge about the BRCA1 & BRCA2 genes or the patentability of DNA in which the order of the naturally occurring nucleotides has been altered Pp. 17-18 689 F 3d 1303, affirmed in part & reversed in part

• THOMAS, J., delivered the opinion of the Court, in which ROBERTS, C. J., & KENNEDY, GINSBURG, BREYER, ALITO, SOTOMAYOR, & KAGAN, JJ., joined & in which SCALIA, J., joined in part

• SCALIA, J., filed an opinion concurring in part & concurring in the judgment

** ~> THE VACCINATED CAN BE PATENTED {OWNED} <~ **

• In a court case in 2013 (Pathology .vs. Myriad Genetics, Inc. in the U.S. the Supreme Court ruled that “you can not patent Human DNA as it was a “ from nature.” •

• BUT at the end of the ruling the Supreme Court DID RULE that “if you were to change a human’s genome by mRNA vaccines (which are being used currently) then the GENOME CAN BE PATENTED.” •

• This means that everyone who has had the vax is now technically “patented” & something that iOS patented is “owned” & will come under the definition of “trans-human.” •

• Those people that are legally identified as “trans-human” do not have access to Human Rights or any rights provided by the state •

• This is because they are not classed as 100% organic or a human •

• Therefore, technically anyone having this vaccine could no longer have any access to human rights •

• There have been a few legal papers discussing this recently so clarification should be available soon •

supremecourt.gov/opinions/12pdf… supremecourt.gov/opinions/12pdf…

This was disheartening to read and process

Email update from international human rights general secretary

Accountability is coming

Wake up people

With @ReportAdve30828 @negar_harari @Patent_SUN can you post your patents thread please

(1) — miRNA —

• miRNA: What It Is & How It Works • via @GeneticLifehack

~ Key takeaways ~
• miRNAs are small non-coding RNA molecules that regulate gene expression

• miRNAs are important in many different biological processes, including cancer growth, immune response, cardiovascular disease & longevity

• Exposure to environmental factors, such as PFAS, heavy metals & BPA, can alter miRNA levels, which then affects the expression of other genes (2) ~ MicroRNA: Controlling Gene Expression ~
• On Genetic Lifehacks, I write about how your genes make you unique & a little different from everyone else

• Variants in protein-coding genes make us all individuals, requiring slightly different nutrients, responding differently to pathogens & predisposing us to different chronic diseases

• The central dogma of biology is that genes are transcribed into mRNA in the cell nucleus

• This mRNA then travels to the cytosol of the cell where it is translated by ribosomes into the corresponding protein

• Gene –> mRNA –> Protein

• We have around 20,000 protein-coding genes in the human genome, but that’s only a small portion of our DNA.[ref]

• Our DNA also encodes RNAs that aren’t translated into proteins

• These are called non-coding RNA genes

• There are currently more than 7,000 known & named RNA genes

• They are divided up & classified by size & function — microRNAs, transfer RNAs, long non-coding RNAs, circular RNAs, small interfering RNAs, small nuclear RNAs & ribosomal RNAs.[ref]

• MicroRNA, or miRNA, is a small strand of RNA that controls gene expression

• Gene expression here refers to how much of the corresponding protein is made from a gene

• Specifically, miRNAs regulate gene expression post-transcriptionally

Heres the list of 15,000 yall

Let’s go

These people are pro pharma funded and they don’t want Kennedy helping the injured or bereaved

docs.google.com/document/d/13Z… Dear Senator Sign-On Letter
January 13, 2025

Dear Senators,

As public health professionals, scientists and concerned constituents, we are writing to urge you to oppose the nomination of Robert F. Kennedy Jr. for Secretary of Health and Human Services (HHS). Our concerns are three-fold.

First, Mr. Kennedy is unqualified to lead the nation’s health department with a budget of over $1.6 trillion and over 80,000 employees. He has little to no relevant administrative, policy or health experience or expertise that would prepare him to oversee the work of critical public health agencies including the National Institutes of Health, the Centers for Disease Control and Prevention, the Food and Drug Administration, the Centers for Medicare and Medicaid Services and more. It is also essential that the Secretary of HHS fully understand how our health system works in the US, including the recognition that the public health system depends on providing support for state, local, academic and community-based partners working in cities and towns across the country.

Second, the nation’s health department must be led by someone who respects and believes in science - robust basic research, pandemic preparedness and evidence-based approaches to all conditions that threaten Americans’ lives and well-being and are designed to protect us from cradle to grave. Even now, the spread of the H5N1 virus and the first known case of Clade 1 MPox in California, should serve as ample reminders that we can never “take a break” from studying infectious diseases as suggested by Mr. Kennedy at an anti-vaccine conference in November. (Nov. 3, NBC News)

Finally, Mr. Kennedy is well known for his conspiracy-driven theories on vaccines, COVID-19, HIV, and fluoridation. His unfounded, fringe beliefs could significantly undermine public health practices across the country and around the world.

It is unfathomable that President Trump, whose Administration implemented Operation Warp Speed, the historic, rapid development of highly effective vaccines for COVID-19, would now be nominating someone who is decidedly anti-vaccine and could, if confirmed, undermine not only the progress we’ve made in saving lives from COVID-19 but also from life-threatening infectious diseases including polio, tetanus, measles, mumps, seasonal flu and more.

As public health professionals and scientists, we strongly urge you to prioritize science and evidence-based approaches to public health. We need a leader at the helm of HHS who people can trust. Please oppose this dangerous nomination.

Sincerely,

The letter

🚨🚨University of Rochester Covid-19 VACCINE DEATHS & Side effects REPORT🚨🚨

‼️Data through Aug 7, 2021‼️

If this report would have been released- so many lives would have been saved

•1/300 deaths
•1/30 adverse events
•Targeted race and ethnicity as well

🤬🤬

•Pages 1-35• Pages 36-71

💥The layers of the onion are being peeled back yall💥

📌Sustained Vascular Inflammatory Effects of SARS-CoV-2 Spike Protein on Human Endothelial Cells📌

🚨SARS-CoV-2 Spike Protein Induces A Procoagulant State Of The Human Endothelium🚨

💥Abstract💥

•Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has been associated with systemic inflammation & vascular injury, which contribute to the development of acute respiratory syndrome (ARDS) & the mortality of COVID-19 infection•

•Moreover, multiorgan complications due to persistent endothelial dysfunction have been suspected as the cause of post-acute sequelae of SARS-CoV-2 infection•

•Therefore, elucidation of the vascular inflammatory effect of SARS-CoV-2 will increase our understanding of how endothelial cells (ECs) contribute to the short- & long-term consequences of SARS-CoV-2 infection•

•Here, we investigated the interaction of SARS-CoV-2 spike protein with human ECs from aortic (HAoEC) & pulmonary microvascular (HPMC) origins, cultured under physiological flow conditions•

💥We showed that the SARS-CoV-2 spike protein triggers prolonged expression of cell adhesion markers in both ECs, similar to the effect of TNF-α💥

(I’ll post my TNF-A and amyloid fibrin microclot tests below)

💥SARS-CoV-2 spike treatment also led to the release of various cytokines and chemokines observed in severe COVID-19 patients💥

(I’ll put my cytokine panels below)

💥Moreover, increased binding of leukocytes to the endothelial surface & a procoagulant state of the endothelium were observed💥

💥Transcriptomic profiles of SARS-CoV-2 spike-activated HPMC & HAoEC showed prolonged upregulation of genes & pathways associated with responses to virus, cytokine-mediated signaling, pattern recognition, as well as complement & coagulation pathways💥

•Our findings support experimental and clinical observations of the vascular consequences of SARS-CoV-2 infection & highlight the importance of EC protection as one of the strategies to mitigate the severe effects as well as the possible post-acute complications of COVID-19 disease•

link.springer.com/article/10.100… 💥Introduction💥

•Although severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) primarily infects the respiratory tract, there is evidence that the causative agent of COVID-19 disease directly interacts with the vasculature•

•The observed thrombotic symptoms in severe COVID-19 patients, with arterial & venous thrombosis contributing to their mortality highlight the substantial consequences of SARS-CoV-2 on the endothelium•

💥Beyond the lungs, vascular coagulopathy & inflammation leading to cardiovascular & neurological complications have been reported in kidney, heart & brain💥

•Moreover, preexisting cardiovascular disorders associated with endothelial dysfunction are one of the main comorbidities correlated with severe COVID-19 disease outcomes & deaths•

💥Endothelial cells (ECs) are constantly exposed to plasma components & have a crucial role in maintaining vascular homeostasis, including regulating the coagulation state, as well as local & general inflammation•

•Although direct infection of SARS-CoV-2 of ECs has been described, findings regarding the susceptibility of ECs for infection & the expression of the receptor angiotensin-converting enzyme 2 (ACE2) & transmembrane protease serine 2 (TMPRSS2) are controversial•

💥Several reports described that SARS-CoV-2 particles, including the spike protein, can interact directly with the endothelium, leading to barrier damage & vascular dysfunction•

💥In the lungs, SARS-CoV-2 spike protein alone can induce infection-like injury & vascular inflammatory responses, including increases in endothelial adhesion molecule expression & recruitment of immune cells💥

•Circulating viral particles in the plasma of COVID-19 patients correlated with disease severity, indicating a high incidence of endothelial exposure, also beyond the respiratory tract•

💥Moreover, spike protein present in the plasma can be taken up & deposited in various organs suggesting that systemic spread of SARS-CoV-2 is facilitated by ECs💥

💥Several studies have documented possible mechanisms through which SARS-CoV-2 causes vascular injury & endothelial dysfunction including downregulation of ACE2 and disruption of mitochondrial function💥

💥Others have described that the vascular damage effect of SARS-CoV-2 spike protein is caused by endothelial glycocalyx disruption & engagement of integrins, leading to the activation of TGF-β signaling💥

Robles et al. showed that SARS-CoV-2 spike protein can induce the nuclear translocation of NF-kB, leading to expression of procoagulant/proinflammatory responses of ECs💥

•The presence of biomarkers for systemic inflammation and an increased procoagulant state in the plasma are prominently observed in acute COVID-19 infection•

Moreover, systemic inflammation was still observed when viral infection was cleared in COVID-19 patients, potentially contributing to the multi-organ disorders in the post-acute sequelae of SARS-CoV-2 (PASC), also known as “Long COVID”

•In this context, persistent endothelial dysfunction has been identified as a significant driver of prolonged non-respiratory symptoms PASC•

💥In this study, we investigated the interaction of SARS-CoV-2 spike protein with primary human ECs from 2 anatomical origins: aortic (HAoEC) as well as lung microvascular (HPMC), which were cultured under physiological flow to simulate the vascular environment💥

‼️We showed that SARS-CoV-2 spike protein elicited prolonged inflammatory responses in both the macr & microvascular ECs‼️

•We also investigated pathways mediating the interaction of SARS-CoV-2 spike protein & cellular dynamic of ECs post-interaction elucidating possible persistent effect of SARS CoV-2 on the endothelium•

📍(1)

🐭 UNIVERSAL DECLARATION ON BIOETHICS & HUMAN RIGHTS🐭

🔺(UNESCO)

United Nations Educational, Scientific, & Cultural Organization🔺

📌Foreword:

💥In October 2005, the General Conference of UNESCO adopted by acclamation the Universal Declaration on Bioethics & Human Rights💥

💥For the first time in the history of bioethics, Member States committed themselves & the international community to respect & apply the fundamental principles of bioethics set forth within a single text💥

💥In dealing with ethical issues raised by medicine, life sciences & associated technologies as applied to human beings💥

💥the Declaration, as reflected in its title, anchors the principles it endorses in the rules that govern respect for human dignity, human rights & fundamental freedoms💥

💥By enshrining bioethics in international human rights & by ensuring respect for the life of human beings💥

💥the Declaration recognizes the interrelation between ethics & human rights in the specific field of bioethics💥

💥Together with the Declaration, the General Conference of UNESCO adopted a resolution which calls upon Member States to make every effort to give effect to the principles set out in the Declaration & invites me to take appropriate steps to ensure the follow-up to the Declaration, including its widest possible dissemination💥

💥This brochure constitutes a first tool for the dissemination of the Declaration & is aimed at contributing significantly to knowledge of the Declaration
worldwide & to understanding of the principles set out therein, so human beings everywhere can benefit from the advances of science & technology within the framework of respect for human rights & fundamental freedoms💥

📌Signed,

Koïchiro Matsuura
📍(2)

🐭The General Conference:🐭

💥Conscious of the unique capacity of human beings to reflect upon their own existence & on their environment, to perceive injustice, to avoid danger, assume responsibility, seek cooperation & to exhibit moral sense gives expression to ethical principles💥

💥Reflecting on the rapid developments in science & technology, which increasingly affect our understanding of life & life itself, resulting in a strong demand for a global response to the ethical implications of such developments💥

💥Recognizing that ethical issues raised by the rapid advances in science & their technological applications should be examined with due respect to the dignity of the human person & universal respect for & observance of, human rights & fundamental freedoms💥

💥Resolving that it is necessary & timely for the international community to state universal principles that will provide a foundation for humanity’s response to the ever-increasing dilemmas & controversies that science & technology present for humankind & for the environment💥

💥Recalling the Universal Declaration of Human Rights of 10 December 1948💥

💥the Universal Declaration on the Human Genome & Human Rights adopted by the General Conference of UNESCO on 11 November 1997💥

💥and the International Declaration on Human Genetic Data adopted by the General Conference of UNESCO on 16 October 2003💥

💥Noting the United Nations International Covenant on Economic, Social & Cultural Rights & the International Covenant on Civil & Political Rights of 16 December 1966💥

💥the United Nations International Convention on the Elimination of All Forms of Racial Discrimination of 21 December 1965💥

💥the United Nations Convention on the Elimination of All Forms of Discrimination against Women of 18 December 1979💥

💥the United Nations Convention on the Rights of the Child of 20 November 1989💥

💥the United Nations Convention on Biological Diversity of 5 June 1992💥

💥the Standard Rules on the Equalization of Opportunities for Persons with Disabilities adopted by the General Assembly of the United Nations in 1993💥

💥UNESCO Recommendation on the Status of Scientific Researchers of 20 November 1974💥

💥UNESCO Declaration on Race & Racial Prejudice of 27 November 1978💥

💥UNESCO Declaration on the Responsibilities of the Present Generations Towards Future Generations of 12 November 1997💥

💥UNESCO Universal Declaration on Cultural Diversity 2 November 2001💥

💥the ILO Convention 169 concerning Indigenous & Tribal Peoples in Independent Countries of 27 June 1989💥

💥the International Treaty on
Plant Genetic Resources for Food & Agriculture which was adopted by the FAO Conference on 3 November 2001 & entered into force on 29 June 2004💥

💥the Agreement on Trade Related Aspects of Intellectual Property Rights (TRIPS) annexed to the Marrakech Agreement establishing the World Trade Organization which entered into force on 1 January 1995💥

💥the Doha Declaration on the
TRIPS Agreement & Public Health of 14 November 2001💥

💥& other relevant international instruments adopted by the United Nations & the specialized agencies of the United Nations system💥

💥in particular the Food & Agriculture Organization of the United Nations (FAO)💥

💥& the World Health Organization (WHO)💥

💥What do this video and these pictures all have in common?💥

They are all of the amyloid fibrin microclots that are growing inside of US

Confirmed via testing in myself while still alive, then confirmed via clot analysis via extraction during embalmer process, and now via microscope

That’s not the bad part- ITS IN THE UNVAXED AS WELL- i’ve been trying to tell you there are literally no more pure bloods

Prions yall- look em up!

this is not good 😭😭

with @NestCommander and @CharlesRixey

💥ATTENTION💥

- IF YOU ARE UNVAXED AND NEVER HAD COVID- They need your sample

- IF YOU ARE UNVAXED AND HAD COVID- They need your sample

- IF YOU ARE VAXED - They need your

~ WE are bringing the world the Science in real time with full transparency and ethics and also not govt funded ~

💥PLEASE SHARE/ every single person deserves and needs to know the truth 💥

DO THE RIGHT THING YALL

“What’s done in the dark always comes to light”

Tik toc. Til toc- TIMES UP CRIMINALS- ITS TIME FOR SOME ACCOUNTABILITY STAT 💜🐭

‼️‼️💥NEW STUDY DONE IN HUMAN CELLS CONFIRMS DNA QUANTIFICATION METHODS, SHOWS PERSISTENCE & EXOSOMAL SHUTTLING (SHEDDING) :

Read About Testing & Treatment Protocol💥‼️‼️

~via: @BelknapM Substack💜

~LNPs (lipid nano particles) dump ModRNA (Modified Ribonucleic Acid) payload into cells & the ModRNA makes spike protein by using the cell’s “machinery” (Ribosomes- are macromolecular machines, found within all cells, that perform biological protein synthesis (messenger RNA translation)

•AS DESIGNED : Spike is released from cells, cleaved from membranes & exported in FULL form

•Per @JesslovesMJK, Ulrike Kämmerer, Verena Schulz and Klaus Steger have just published what might be the paper of the century entitled:

“BioNTech RNA-Based COVID-19 Injections Contain Large Amounts Of Residual DNA Including An SV40 Promoter/Enhancer Sequence”

•It got through peer review on December 3, 2024 and it confirms much of what has already been evidenced and answers many questions lingering in the background

💥Let’s unpack their results💥 2-)

•We demonstrate successful transfection of nucleoside-modified mRNA (modRNA) biologicals into HEK293 cells and show robust levels of spike proteins over several days of cell culture

•Secretion into cell supernatants occurred predominantly via extracellular vesicles enriched for exosome markers

•We further analyzed RNA and DNA contents of these vials and identified large amounts of DNA after RNase-A digestion in all lots with concentrations ranging from 32.7 ng to 43.4 ng per clinical dose

•This far EXCEEDS the maximal acceptable concentration of 10 ng per clinical dose that has been set by international regulatory authorities

•Gene analyses with selected PCR primer pairs proved that residual DNA represents not only fragments of the DNA matrices coding for the spike gene, but of all genes from the plasmid including the SV40 promoter/enhancer and the antibiotic resistance gene

💥MASSIVE SPIKE PROTEIN PATHOGENICITY RESEARCH LIBRARY PUBLISHED💥

via: @NicHulscher

~A comprehensive list of over 250 peer-reviewed studies demonstrating SARS-CoV-2 Spike protein harms has just been published by Erik Sass and Dr. Martin Wucher~SARS-CoV-2 Spike Protein Pathogenicity Research Library

zenodo.org/records/142692… •This enormous body of research demonstrating that Spike protein is a highly toxic substance confirms that the COVID-19 injectable products are fundamentally unsafe for human use

•Moreover, these data further amplify the rationale for Spike protein detoxification:
cureus.com/articles/20765…

🧵•(1)

💜I-PREVENT Vaccine Injury💜

{An approach to post-vaccine cardiovascular & cancer care}

~via : @Honest_Medicine

🚨Disclaimer🚨

~Note: {This document is primarily intended to assist healthcare professionals in providing appropriate medical care for patients who have received a COVID-19 vaccine}

~Note: {Patients should always consult a trusted healthcare provider before embarking on any new treatment}
•There is very limited data on the clinical features, pathogenetic mechanisms, and pathological findings of patients who have had delayed complications related to the COVID-19 vaccine

•In addition, there is no published guidance on how to avoid these complications

•This guidance is, therefore, based on our assessment of the likely pathogenic mechanisms underlying these delayed complications (spike protein-related disease) and the limited available autopsy data
🚨Post-vaccine cardiovascular events and cancer🚨
•The vast majority of serious adverse events following vaccination occur in the two weeks immediately following a dose of the vaccine

•Therefore, we previously suggested that patients who developed no adverse events in the 2 to 3 weeks following vaccination had ‘dodged a proverbial bullet’ and did not require specific interventions to prevent vaccine injury
•However, evolving data suggests this approach may not be optimal, for two reasons

🚨First, some patients who otherwise had no adverse events from the vaccine appear to have delayed acute cardiac events (often leading to sudden death)

•This appears to peak between 4 to 6 months after the vaccine but may extend for at least one year

🚨Second, there has been evidence of an emergence of “turbo” and relapsed cancers in the months following vaccination
•The approach to preventing these serious disorders is unclear and the developers and manufacturers of these ‘vaccines’ obviously did not develop an ‘antidote’

•Nevertheless, we have developed this document to attempt to limit these complications and reassure those who have been vaccinated
•Essentially, both cardiac and cancer-related complications are related to the persistence of spike protein

•Therefore, any intervention that reduces the persistence and the ‘load’ of spike protein will likely be beneficial
•The cause of the increased risk of cancers is less clear, however spike protein-induced alteration in the function of tumor suppressor genes, immune depression, altered mitochondrial function, and other metabolic pathways may be involve 🪡•(2)

🚨Delayed Sudden Cardiac Death🚨
•Sudden cardiac death has been recognized within weeks of the COVID-19 mRNA vaccination, likely due to an arrhythmia triggered by an acute myocarditis, and/or a catecholamine surge and coagulative myocardial necrosis
•More recently, delayed cardiac complications following COVID-19 vaccination have received
attention in the “alternative media”

•This devastating fatal condition has been ignored by the medical establishment

•Typically, these are otherwise healthy individuals without features of the “vaccine injury syndrome” who “die suddenly” — usually 4 to 6 months after the last dose of the COVID-19 vaccine.

•However, the duration of the window for sudden death is unknown and likely extends up to 1 year or longer

•As mentioned, many of these patients are otherwise healthy with no obvious risk factors or history of cardiac disease
•To date, the pathogenesis and pathology of this syndrome have not been reported in peer-reviewed publications

•However, an unpublished autopsy of patients who died unexpectedly following vaccination demonstrated :

🚨endothelial inflammation (most prominently in the heart, lungs, and brain), endothelial damage, rupture of atheromatous plaques, complex formation of amyloid-spike protein fibrin in vessels as well as platelet aggregates and thrombi leading to acute coronary events🚨

🚨lymphocytic vasculitis w/ medial necrosis & the dissection of large vessels (aorta, coronary artery) was found🚨

🚨Expression of spike protein (and not nucleoprotein) was detected at high concentrations in the endothelium of capillaries, small arteries, and veins, as well as within the myocardium, aorta, and brain and aggregated in blood clots🚨
🚨These findings suggest that spike protein-induced endothelialitis, with activation of clotting and medial necrosis of the blood vessel, are the major pathologic events leading to sudden death🚨

•It is important to emphasize that the pathology of this syndrome differs significantly from that of the typical finding of atherosclerotic coronary disease

•However, it is unknown if these patients had underlying coronary artery disease (or risk factors for coronary artery disease) and the acute spike-related endotheliitis served to accelerate this process

•It should be noted that subclinical atherosclerosis is common in Westernized populations

•In the PESA study, subclinical atherosclerosis was highly prevalent in middle-aged individuals, with nearly half of the participants classified as having intermediate or generalized disease
•As this catastrophic disorder is not recognized and has not been studied by the medical establishment, the true incidence and risk factors for sudden cardiac death remain unknown

•Ideally, these asymptomatic patients would be risk stratified, with the initiation of prophylactic measures in the moderate to high-risk groups

•Unfortunately, there is little data to allow for risk stratification

•There are however two potential approaches to risk stratification, and these could be combined

•The first is based on the lot number of the vaccine

•It has been well established (from the VAERS data itself) that certain lots of the vaccine are associated with a much higher risk of adverse events than others; the adverse event rate of “hot” lots is increased one thousand-fold

•Presumably, these “hot” lots have a much higher concentration of mRNA, which translates into a much higher load of spike protein

•The load of spike protein appears to be a major factor predicting the development of serious adverse events to the vaccine

🚨Patients can check if they received a bad lot at the following website: 👇
howbad.com

🚨🚨Finally an answer on the mysterious white clots that embalmers @r_hirschman & @OlooneyJohn and others have been finding during the embalming process🚨🚨

~It confirms what i already knew from my testing with hematologist, @jfvaughnmd09 Dr Jordan Vaughn- where i was diagnosed with amyloid fibrin microclots- graded a 3.5/4- moderate and widespread, with endothelial casts from my vax as it was proven via nucleocapsid testing that ive never had the “virus”~

~these white clots are in the living and it is playing a huge factor in the amount of blood clots, heart attacks, strokes, VITT etc from what we’ve witnessed in the injured community from our own medical results and injuries~

~per @r_hirschman :

•Mike Adams @HealthRanger did an ICP-MS of the clots also in 2022

•Dr Ryan Cole @drcole12 has also done histology of the clots and said they were amyloid like

•Since then, I have met several other researchers from here in the United States and abroad

•They have replicated the ICP-MS, done amino analysis and histological stains

🚨🚨On Monday I traveled to a lab and met with Dr Phillip Triantos @PTriantos in order to connect with a person who could do a special stain called Thioflavin-T, which is used to identify Amyloid🚨🚨

•It tested positive‼️

•It is estimated is that the clots are 70 to 80 percent amyloid

•This is very concerning because if you research amyloid and amyloidosis it is scary

•Amyloid is simply miss folded proteins

•The good news is that now that I know what this is, and sharing it with the world, doctors can start testing people for signs of amyloid in their blood

🚨For amyloid fibrin microclot testing like i had below contact: 👇

•Dr Jordan Vaughn @jfvaughnmd09
MedHelp Alabama - for immunoflourescence Microscopy- A PPP stained with Tht

•my results are below👇👇
Sample results:👇👇

•The COVID-19 pandemic is one of the most manipulated infectious disease events in history, characterized by official lies in an unending stream lead by government bureaucracies, medical
assoc, medical boards, the media, & international agencies

•We have witnessed a
long list of unprecedented intrusions into medical practice, including attacks on medical experts,
destruction of medical careers among doctors refusing to participate in killing their patients & a massive regimentation of health care, led by non-qualified individuals with enormous wealth, power & influence

•For the first time in American history a president, governors, mayors, hospital admins and federal bureaucrats are determining medical treatments based not on accurate scientifically
based or even experience based information, but rather to force the acceptance of special forms of care & “prevention” including remdesivir, use of respirators and ultimately a series of essentially untested messenger RNA vaccines

•For the first time in history medical treatment protocols are not being formulated based on the experience of the doctors treating the largest number of patients successfully, but rather individuals & bureaucracies that have never treated a single patient including Anthony Fauci, Bill Gates, EcoHealth Alliance, the CDC, WHO, state public health officers & hospital admin

•The media (TV, newspapers, magazines, etc), medical societies, state medical boards and the owners of social media have appointed themselves to be the sole source of information concerning this so-called “pandemic”

•Websites have been removed, highly credentialed & experienced clinical doctors & scientific experts in the field of infectious diseases have been demonized, careers have been destroyed & all dissenting information has been labeled “misinfo” & “disinfo”even when sourced from top experts in the fields of virology, infectious diseases, pulmonary critical care & epidemiology

•These blackouts of truth occur even when this information is backed by extensive scientific citations from some of the most qualified medical specialists in the world

•Neither Anthony Fauci, the CDC, WHO nor any medical governmental estab has ever offered any early treatment other than Tylenol, hydration & call an ambulance once your lips are blue

•Not only have these medical orgs & federal lapdogs not even suggested early treatment, they attacked anyone who attempted to initiate such treatment with all the weapons at their disposal: loss of license, removal of hospital privileges, shaming, destruction of reputations & even arrest •A good example of this outrage against freedom of speech & providing informed consent info is the recent suspension by the medical board in Maine of Dr. Meryl Nass’ medical license and the ordering of her to undergo a psychiatric evaluation for prescribing Ivermectin and sharing her expertise in this field

•This behavior by a medical licensing board is reminiscent of the methodology of the Soviet KGB during the period when dissidents were incarcerated in psychiatric gulags to silence their dissent

~OTHER UNPRECEDENTED ATTACKS~

•Another unprecedented tactic is to remove dissenting doctors from their positions as journal editors, reviewers& retracting of their scientific papers from journals, even after these papers have been in print

•Until this pandemic event, I have never seen so many journal papers being retracted, the vast majority promoting alternatives to official dogma, especially if the papers question vaccine safety

•Normally a submitted paper or study is reviewed by experts in the field, called peer review

•These reviews can be quite intense and nit picking in detail, insisting that all errors within the paper be corrected before publication

•So, unless fraud or some other major hidden problem is discovered after the paper is in print, the paper remains in the scientific literature

•We are now witnessing a growing number of excellent scientific papers, written by top experts in the field, being retracted from major medical & scientific journals weeks, months & even years after publication

•A careful review indicates that in far too many instances the authors dared question accepted dogma by the controllers of scientific publications, especially concerning the safety, alternative treatments or efficacy of vaccines

•These journals rely on extensive adverting by pharmaceutical companies for their revenue

•Several instances have occurred where powerful pharmaceutical companies exerted their influence on owners of these journals to remove articles that in any way question these comp products

•Worse still is the actual designing of medical articles for promoting drugs and pharmaceutical products that involve fake studies, so-called ghostwritten articles

•Richard Horton is quoted by the Guardian as saying “journals have devolved into information laundering operations for the pharmaceutical industry.”

•Proven fraudulent “ghostwritten” articles sponsored by pharma giants have appeared regularly in top clinical journals, such as JAMA, and New England Journal of Medicine, never to be removed despite proven scientific abuse& manipulation of data

•Ghostwritten articles involve using planning companies whose job it is to design articles containing manipulated data to support a pharmaceutical product & then have these articles accepted by high-impact clinical journals, that is, the journals most likely to affect clinical decision making of doctors

•Further, they supply doctors in clinical practice with free reprints of these manipulated articles

•The Guardian found 250 comp engaged in this ghostwriting business

•The final step in designing these articles for pub in the most prestigious journals is to recruit well recognized medical experts from prestigious institutions, to add their name to these articles

•These recruited medical authors are either paid upon agreeing to add their name to these pre-written articles or they do so for the prestige of having their name on an article in a prestigious medical journal

•Of vital importance is the observation by experts in the field of medical publishing that nothing has been done to stop this abuse

•Medical ethicists have lamented that because of this widespread practice “you can’t trust anything.”

•While some journals insist on disclosure information, most doctors reading these articles ignore this info or excuse it & several journals make disclosure more difficult by requiring the reader to find the disclosure statements at another location

if you have received these vax with the lot/batch #

i highly advise you get checked for integration bc those numbers are just astounding

👇👇

PFIZER
LOT/batch #s

• GH9715
•FW1374
•343961B
•ACB5517
•FP1972

that’s gonna affect at least 3-4 future generations just there @Kevin_McKernan
@DJSpeicher
@Jikkyleaks

any more lots you need me to distribute so ppl are aware

📢🚨DMSO Could Save Millions From Brain and Spinal Injury🚨📢

via @MidwesternDoc
t.co/n8ri07dGAP

• The decades of evidence showing DMSO revolutionizes the care of many "untreatable" circulatory and neurologic conditions

•Story at a Glance👇

•DMSO is a remarkably safe chemical that protects cells from otherwise fatal stressors (e.g., freezing, burning, shockwaves, ischemia

• Since the heart, brain, and spinal cord are particularly vulnerable to injury, DMSO can produce miraculous results for those conditions

•The usage of DMSO completely transforms the management of strokes (including brain bleeds), heart attacks, and spinal cord injuries

•As I will show here, had the FDA not sabotaged DMSO’s adoption, in addition to countless lives being saved, millions could have been protected from a lifetime of disability or paralysis

•DMSO has many other remarkable properties👇

•For example, it stabilizes proteins, and thus treats many challenging protein disorders (e.g., amyloidosis and numerous genetic disorders

•Many conditions DMSO treats are typically considered to be incurable

•In this article, I will focus on DMSO’s remarkable utility for the conditions that respond best to intravenous DMSO (e.g., a variety of circulatory disorders like varicose veins or Raynaud’s) and complex neurological disorders (e.g., Down Syndrome, Developmental Delay, ALS, Alzheimer’s, Parkinson’s), along with how to administer IV DMSO and DMSO stroke protocols

•If I were stranded on a desert island or knew the world was ending and I could only bring a few therapies with me, one of them, without a doubt, would be DMSO

•This is because:👇

•It treats a wide range of severe illnesses which are often otherwise incurable and frequently fatal or lead to a lifetime of permanent disabilit

•It effectively treats acute injuries and rehabilitates chronic musculoskeletal disorders (e.g., arthritis

•Because of this, it’s one of the best “pain medicines” out there and has allowed many to get their lives back

•It has a variety of unique properties that open up a completely different dimension to how medicine can be practice

•It is one of the safest medically active substances in existence

•Remarkably, in the 1960s, this was recognized and DMSO took the nation by storm (e.g., people everywhere were clamoring for it, gas stations would often advertise they sold it, and tens of thousands of research studies were conducted by enthusiastic scientists around the globe)

•Now however, outside of it being a laboratory chemical or an alternative therapy some people use for joint pain, few are even aware of DMSO’s existence

•This was due to the FDA waging a multi-decade long war against DMSO (despite widespread outcry from Congress and the public), which I believe was arguably the worst thing the FDA has ever done to the country

•Since I am uniquely positioned to present many of the forgotten sides of medicine to the public, I’ve long felt the DMSO story needs to be told

•Simultaneously however, since there is a wealth of data on this topic, I wanted to ensure I honored the importance of this subject and accurately present it

•For this reason, I’ve spent the last three months reading and arranging thousands of pages of literature

•Since there is so much to say on this topic, this series will be broken into a few parts

•In the first installment, I will cover the key properties of DMSO and the challenging conditions where it provides the most profound benefits •What is DMSO?

•Dimethyl sulfoxide, as the name implies, is comprised of two methyl groups and an oxygen atom bonded to sulfur

•This simple chemical and its breakdown products exist in nature (e.g., they can be found in small amounts in milk, tomatoes, tea, coffee, beer clams, and cooked corn, while the salty smell of the ocean is, in part, due to microalgae near the surface creating dimethyl sulfoxide—some of which also makes it into the rain)

•In the body, DMSO is then oxidized or reduced, with the oxidized form (more commonly known by the name :

•methylsulfonylmethanethe or MSM—a common joint healing supplement) being the primary fate of it, while the reduced form DMS (which naturally exists in trace amounts in the body) is the more notorious metabolite because it is responsible for DMSO’s characteristic “side effect,” a distinctive garlic or clam-like odor (or taste) that is excreted through the mouth and skin which certain individuals have difficulty tolerating (and forcing certain longterm DMSO users to creatively arrange their social life)

•This effect typically lasts a few hours, but in certain cases can last up to 72 hours, and appears to be reflective of the overall health of the body (since as people detox, their DMSO odor decreases)

•Note: one school of thought in integrative medicine (e.g., Dr. Mercola is a strong proponent of this model) argues that insufficient oxidation, which leads to a build-up of reduced molecules in the body (termed reductive stress) is a root cause of many illnesses (e.g., the mitochondria cannot function properly if the electron transport chain is reduced)

•The susceptibility to the DMSO odor is one of the best illustrations I have found of this model, particularly since there are many reports showing that concurrently taking chlorine dioxide (an oxidizing agent) eliminates it (as does a user’s overall health improving over time)

•Likewise, some DMSO users and one study have found that when DMSO was taken at the same time as alcohol (another oxidizing agent), the odor was reduced, whereas when alcohol was given an hour after DMSO, the opposite occurred (which touches upon the fact DMSO can sometimes cause excessive drowsiness if combined with a sedative)

•Due to its relatively small size, having both a polar and non-polar half, being able to form hydrogen bonds slightly stronger than those found between water molecules, and not releasing protons, DMSO has two remarkable properties:

•It acts as a near-universal solvent (e.g., it interacts with a vast range of biomolecules and can easily mix with any concentration of water)

•It’s able to pass through biological membranes without damaging them(something to my knowledge, nothing else can do

•Because of this, DMSO will rapidly enter the body (including the brain) regardless of its route of administration (e.g., within 5 minutes after going on the skin it can be found in the blood, and within an hour it can be found within the bones), but simultaneously does not accumulate within the bodyafter prolonged use (and virtually none remains a week after administration)

•Note: in one study of rats, radio-labeled DMSO was found to enter all tissues of the body within 30 minutes (with the highest levels seen in the plasma, kidney, spleen, lung, heart, and testes and the lowest in the lens of the eye), with DMSO levels declining to minimal levels after 24 hours, while another study found orally administered DMSO reached a peak blood level in 4 hours and was undetectable after 120 hours, while MSM appeared in the blood after 48 hours and disappeared after 400 hours (with another human study finding similar results)

•DMSO in turn, has an almost endless amount of uses as it can be applied in almost any manner (e.g., it is frequently applied through the skin—although less is absorbed in this manner than the other routes of administration)

😭😭😭😭😭 please pray for this sweet girl💜💜

she had reaction to : meningitis, pneumonia and tetanus vax all given at once😭😭

she’s getting worse😭