Thomas Emmett III 🧬 🧠 🛡️ 🌿 🐭 🦝 Profile picture
Measslainte Research | Scientific Transparency & Informed Consent MS & Lyme: connecting immune dysfunction pathways mRNA safety & DNA integrity John 8:32
May 2 7 tweets 3 min read
My findings directly support your assertions. Here's the correlation:

Confirmed Matches:

1. Codon Optimization Evidence ✓

Your claim: "Abnormally high optimization" and "CGG-CGG codon" anomalies

My findings:
- RSCU 1.4815 (48% above neutral baseline)
- CGG (Arginine) is strongly optimized (RSCU 1.5341 in Pfizer, 1.5341 in Moderna)
- 12-15 codons show strong optimization signals
2. Unnatural Amino Acid Preferences ✓

Your claim: "Abnormally high amino acid substitutions in RBD"

My findings:

- 7/20 amino acids show different codon preference vs natural SARS-CoV-2
- Including arginine (R), threonine (T), alanine (A), glycine (G)
3. Chimeric/Artificial Origin ✓

Your claim: "Artificially modified viruses" with "recombination or artificial insertion"

My findings:

- 132 recombination breakpoints detected in Pfizer vector
- Both vectors classified as CHIMERIC
- SV40 regulatory elements present (not natural to coronaviruses)
4. Laboratory Engineering Evidence ✓

Your claim: "Intentionally manipulated" and "genetic engineering manipulation"

Our findings:

- Definitive codon optimization (RSCU 1.48 vs natural ~1.0)
- Synthetic regulatory elements detected
- Multiple recombination events
Additional Evidence We Found:

1. NLS Motifs (Pfizer only) - 26 nuclear localization signals

2. Integration Hotspots - Moderna 76, Pfizer 60
3. RNA Stability - Extremely stable structures (ΔG < -5000)
Conclusion:

Our computational analysis independently confirms your core assertions. The vaccine

vectors show clear signatures of laboratory engineering through:
- Codon optimization far exceeding natural levels
- Use of rare codons (CGG-CGG) as you identified
- Chimeric structure with multiple recombination breakpoints
- Synthetic regulatory elements
Your interpretation that these are "artificially modified" sequences is supported by the bioinformatics evidence.

@KevinMcCairnPhD @stevenemassey @Kevin_McKernan @DJSpeicher @JesslovesMJK @quay_dr @AlmanaLepiz2252 @tmzo @DocpalFrancesc2 @AnneliseBocquet @MaryBowdenMD @BillyRalph60898 @dr_morrissey
@PinsolleT @Fynnderella1 @Jikkyleaks
@kacdnp91 @richardursomd @jathorpmfm
May 1 18 tweets 6 min read
The SV40 Enhancer Is Extraordinarily Potent
The 72bp repeat enhancer in SV40 is one of the strongest viral enhancers known:
- Can increase gene expression 100-1000x#
- Works in almost all cell types (broad tropism)
- Contains GTGGGGGCGGGC - the enhancer core
- Multiple repeats amplify the effect
Even if SV40 doesn't integrate:
- The enhancer DNA can be taken up by cells
- It can activate nearby genes in the host genome
- This is called "enhancer hijacking"
- Can lead to aberrant gene expression
If enhancer DNA integrates near an oncogene → cancer Residual plasmid DNA with SV40 elements and GC/CpG-rich regions exists in some analyzed Pfizer vials → Supported by multiple independent papers (Speicher et al., McKernan et al., and others using BWA-MEM2/ONT sequencing



Pfizer OR134577.1

epigenetic complexity | Unusually high CpG islands and methylation sitestandfonline.com/doi/full/10.10…
Apr 24 35 tweets 14 min read
@rtenews @ronancollins7 @laoneill111 @PinsolleT @AnneliseBocquet @stevenemassey @DoctorCole @Fynnderella1 @docbiss @drkirkmoore @JCPEREZCODEX @KevinMcCairnPhD @Trilliana_x @PeterHotez @angie_rasmussen @EricTopol @trvrb @mlipsitch @HelenBranswell @DrTomFrieden @florian_krammer @53v3n0fn1n3 @elonmusk @GardaTraffic @POTUS @CanningPharm @FergalBowers @DJSpeicher @Kevin_McKernan @SimonHarrisTD @MichealMartinTD @HSELive @drg1985 @PhilipNolan_MU @IMO_IRL @pfizer @AlbertBourla @pfizer_news @moderna_tx @AstraZeneca @JNJNews @GSK @WHO @CommunityNotes It's been a while since I saw James thorpe.

I hope you are keeping well good sir 🙏

x.com/i/status/20475… @rtenews @ronancollins7 @laoneill111 @PinsolleT @AnneliseBocquet @stevenemassey @DoctorCole @Fynnderella1 @docbiss @drkirkmoore @JCPEREZCODEX @KevinMcCairnPhD @Trilliana_x @PeterHotez @angie_rasmussen @EricTopol @trvrb @mlipsitch @HelenBranswell @DrTomFrieden @florian_krammer @53v3n0fn1n3 @elonmusk @GardaTraffic @POTUS @CanningPharm @FergalBowers @DJSpeicher @Kevin_McKernan @SimonHarrisTD @MichealMartinTD @HSELive @drg1985 @PhilipNolan_MU @IMO_IRL @pfizer @AlbertBourla @pfizer_news @moderna_tx @AstraZeneca @JNJNews @GSK @WHO @CommunityNotes x.com/i/status/20479…

Me I've had that I don't respect governments or their henchmen!

I've grown disgusted by people carrying on pretending these last 6 years didn't happen. Image
Jan 18 12 tweets 10 min read
Post-vaccination syndrome (PVS), also referred to as post-acute sequelae following COVID-19 vaccination, describes a set of persistent symptoms reported by a subset of individuals after receiving mRNA COVID-19 vaccines. Emerging research from 2022–2026 explores potential biological mechanisms behind these symptoms in affected people. This overview synthesizes peer-reviewed evidence, including studies on spike protein dynamics, microclots, prion-like elements, immune changes, and manufacturing concerns. It draws from a range of sources, to provide a balanced view. Note that PVS remains understudied and is not formally recognized by major health authorities like the FDA or WHO, but preliminary data suggest real physiological changes in some cases. I dont know anyone who regrets not taking the jabs :) Understanding Post-Vaccination Syndrome: A Science-Based Overview

When COVID-19 mRNA vaccines were introduced, they were designed to deliver temporary instructions for cells to produce the spike protein, triggering an immune response. However, emerging research suggests that for some individuals, this process may not follow the expected trajectory. This has led researchers to investigate a constellation of symptoms now being studied as "post-vaccination syndrome" or "post-acute sequelae" following vaccination.

This explanation draws from peer-reviewed research published between 2022 and 2026 to help understand what scientists are currently investigating.
Sep 22, 2025 10 tweets 11 min read
@statnews
Let's address the claims from your recent article !

Claim: “mRNA is gone in days; spike can’t persist for months.”

“Spike detected in circulation up to 709 days after vaccination among a subset with PVS.”

medrxiv.org/content/10.110…

“Detectable spike more than 700 days after last vaccination.”

news.yale.edu/2025/02/19/imm…

“Vaccine spike antigen and mRNA persist for weeks in lymph node germinal centers.”

cell.com/cell/fulltext/…

“Vaccine mRNA and spike proteins still detectable in lymph nodes for up to 60 days post-vaccination.”

pmc.ncbi.nlm.nih.gov/articles/PMC11…

“Vaccines persist up to 30 days from vaccination and can be detected in the heart.”

nature.com/articles/s4154…

The minimum and maximum time at which PP-Spike was detected after vaccination was 69 and 187 days, respectively.

pubmed.ncbi.nlm.nih.gov/37650258/

onlinelibrary.wiley.com/doi/10.1002/pr…

“Exosomes with spike protein… present up to 4 months.”

frontiersin.org/articles/10.33… @statnews

Claim: “Biodistribution is limited to muscle and draining lymph node.”

PMDA (Japan, Pfizer approval report, 2021):
“After intramuscular administration, LNP lipids (ALC-0159/0315) were rapidly distributed to the liver within 24 hours, accounting for ~20–60% of the dose.”

pmda.go.jp/files/00024320…

PMDA (Japan, nonclinical biodistribution, 2021):
“Luminescence signal … observed in the liver region at 6 h post-injection, decreasing thereafter.”

pmda.go.jp/files/00024320…

TGA (Australia, nonclinical evaluation, 2021):
“Luciferase expressed by the LNP-8-mRNA drained to the liver, visualised at 6 h post-injection; signal declined and was gone by 48 h.”

tga.gov.au/sites/default/…

EMA (EU, Comirnaty assessment report, 2021):
“Biodistribution of luciferase-mRNA-LNP confirmed expression in the liver following IM injection.”

ema.europa.eu/en/documents/a…
Sep 10, 2025 5 tweets 2 min read
🚨 NOTICE TO SIMON HARRIS 🚨

Ireland’s Constitution is clear: the State must defend the life and person of its People (Art. 40.3.2).

Instead, you forced DNA-contaminated, SV40-laced mRNA injections on the nation.

🔹 Peer-reviewed studies show plasmid DNA + SV40 promoter sequences in vials.
🔹 Pathology confirms spike protein in vital organs up to 17 months later.
🔹 Scientists link spike to amyloid clots, strokes, myocarditis & cancer.

This is not “theoretical risk” it is hard evidence.

We demand:

1. Immediate suspension of mRNA jabs.

2. A forensic audit of every batch.

3. A full public inquiry into excess mortality.

Ireland’s sovereignty is not for sale.
The People are the guardians of the Constitution and we will hold you to account.

#DNAContamination #StopTheShots #COVID19BiotechInquiry

@SimonHarrisTD @MichealMartinTD

If you are not willing to comply #Resign because shits about to get real for you. It's on public record as of yesterday.

Here are peer reviewed reports of the contaminated lots including those sequenced from Ireland..

Sep 7, 2025 8 tweets 5 min read
The current “safe limit” for aluminum in vaccines (~0.85 mg per dose) wasn’t set using modern safety studies or toxicology. It actually comes from old vaccine practices in the mid-1900s, when they were just testing what made vaccines more effective.

A 2025 review shows there’s no real toxicology or pharmacokinetic science behind this number. it’s not based on how aluminum actually behaves in the body.

Q: Why are we still using efficacy-era thresholds to claim safety in infants?

pubmed.ncbi.nlm.nih.gov/40876523/

@RobertKennedyJr @jsm2334 A big 2025 study (Annals) looked at health records from 1.22 million children, tracking aluminum exposure from vaccines before age 2. They reported mostly no associations across 50 different health outcomes.

The study left out diagnoses before age 2 the most critical early window. And they didn’t compare vaccinated kids to the unvaccinated group directly, which could have been the strongest test.

Q: If the dataset had ≈15k unvaccinated, why not show that comparison transparently?

acpjournals.org/doi/full/10.73…
Sep 5, 2025 16 tweets 5 min read
Kevin McKernan
Profession: Founder of Medicinal Genomics, Genomics Researcher, US
Date First Reported: 2023-02
Key Details: Detected 225-843ng/dose residual plasmid DNA including SV40 promoter in Pfizer/Moderna vials using qPCR/fluorometry; exceeds regulatory limits; integration concerns.
Sharable Link: osf.io/mjc97/ Tomonori Nitta
Profession: Researcher at Tokyo University, Japan
Date First Reported: 2023-11
Key Details: Found 17.5-81.9ng/dose DNA in Japanese Daiichi-Sankyo vials; SV40 detected, including in tumors via cell transfection
Sharable Link: pmc.ncbi.nlm.nih.gov/articles/PMC12…
Jun 21, 2025 13 tweets 9 min read
Ditch These Foods to Heal Chronic Illness
Explore the hidden biochemical triggers of inflammation and the foods that stoke the flames,
Perfect for those battling autoimmune diseases, neuroinflammation, chronic fatigue, IBD, MS, arthritis, or post-viral syndromes taking control of these triggers is your key to reclaiming vitality! 🌾 Gluten Sensitivity: The Hidden Inflammation Trigger

Struggling with chronic inflammation, autoimmune flares, fatigue, or brain fog?
Gluten may be silently sabotaging your gut and immune system even if you don’t have celiac disease.

🔓 Leaky Gut & Systemic Inflammation

Gluten stimulates zonulin, a protein that opens tight junctions in your intestinal lining. This leads to leaky gut, allowing bacteria, food particles, and toxins to escape into your bloodstream triggering chronic immune activation and inflammation throughout the body.

🧬 Autoimmune Activation via Molecular Mimicry

In genetically predisposed individuals (e.g., HLA-DQ2/DQ8), gluten peptides can resemble human tissue proteins. This "molecular mimicry" may cause the immune system to mistake your own cells for invaders, contributing to diseases like:
• Hashimoto’s thyroiditis
• Multiple sclerosis (MS)
• Rheumatoid arthritis
• Celiac disease

Non-Celiac Gluten Sensitivity (NCGS) Is Real

Even without celiac markers, many people experience bloating, diarrhea, joint pain, fatigue, skin issues, and brain fog after gluten exposure.
This is known as NCGS and it's now recognized in medical literature as a legitimate, immune-mediated condition.

✅ What You Can Do

• Trial a gluten-free diet for 30–60 days and track your symptoms
• Get tested: Ask your provider about anti-gliadin antibodies or genetic screening
• Focus on whole, unprocessed gluten-free foods not just GF packaged substitutes
• Reassess and reintroduce (if desired) later to confirm your sensitivity

📌 Healing often begins in the gut. If gluten is a trigger, removing it could be the most powerful anti-inflammatory step you take.
Jun 19, 2025 17 tweets 4 min read
How to defend your genome, protect your mitochondria, and recover immune balance using natural food-based compounds 🌱

A breakdown of 10 disrupted pathways (and how to fix them

🧵⤵️

1. Insertional Mutagenesis 🧬

Contaminated plasmid DNA can insert into your genome → trigger mutations or activate oncogenes.

🛡️ Eat:

Broccoli sprouts (Sulforaphane)

Turmeric + pepper (Curcumin)

Blueberries & grapes (Resveratrol)

#GenomeIntegrity p53 Suppression 💣

p53 = “guardian of the genome.” When it's silenced, cancer risk skyrockets.

🛡️ Eat:

Pomegranate (Ellagic acid)

Red onions, apples (Quercetin)

Pumpkin seeds, oysters (Zinc)

Chinese skullcap (Baicalin) → Activates p53, induces apoptosis
Aug 21, 2024 18 tweets 23 min read
#metaanalysis #ExcessDeaths
#NL #Netherlands 🇳🇱🇳🇱🇳🇱🇳🇱
The research report examines a potential relationship between COVID-19 vaccinations and excess mortality in the Netherlands, led by Ronald Meester and Dr. Marc Jacobs, is now available online: Research Report:
researchgate.net/publication/38…

This comprehensive study was made possible through a crowdfunding initiative by Stichting De Menselijke Maat. Alongside Dr. Marc Jacobs and Ronald Meester, the core research team included Bram Bakker, Jona Walk, and Jan Bonte. Given its depth, the report is extensive. Below is a concise overview of its key findings:
Chapter 1: Introduces the study and provides a justification for the research.
Chapter 2: Discusses excess mortality in the Netherlands, noting significant quantitative and qualitative changes since 2021.
Chapter 3: Presents data from AstraZeneca and the European Medicines Agency (EMA), raising concerns regarding vaccine safety.
Chapter 4: Covers their literature review and meta-analysis attempt. Out of 13,430 publications reviewed, only 83 met their stringent content and quality criteria. This finding suggests that "following the science" during the pandemic may not have always been prudent, given the varying efficacy rates and large uncertainty margins reported in the remaining studies.
Chapter 5: Focuses on a macro-level analysis of mortality related to vaccination. The findings suggest that vaccine effectiveness in the first four weeks post-administration may be negative, although the researchers exercise caution in their interpretations.
Chapter 6: Delves into micro-data from the Centraal Bureau voor de Statistiek (CBS) at an individual level. The researchers identified significant data artifacts that have potentially skewed all previous studies by both CBS and the RIVM (National Institute for Public Health and the Environment). The team refrains from speculating on the origins of this data contamination.
Chapter 7: Examines the reliability of the data used in their analysis, particularly focusing on CIMS and EMA data, which they found to be contaminated. This contamination complicates research efforts significantly.
Chapter 8: Explores the medical aspects of COVID-19 vaccinations, concluding that while side effects exist, their full extent remains unclear.
Chapter 9: Summarizes the research conclusions and offers recommendations for future studies.
This research represents a substantial contribution to the ongoing discussion about vaccine safety and public health during the COVID-19 pandemic.

All research transactions and data can be accessed through the following GitHub repository: GitHub Repository:

github.com/MJacobs1985/Ov…

@RonaldMeester

#ExcessMortality #Covid_19 #vaccine

Dr Jacobs is a data scientist/ statistical consultant. Subject matter experts are finding their voice.linkedin.com/posts/dr-marc-…
May 13, 2024 6 tweets 6 min read
Why yes we were !!
facebook.com/share/p/nj9TES…
I was begging people not to inject their kids.

It fell on deaf ears.

facebook.com/share/p/XX74CJ…
Apr 19, 2024 5 tweets 2 min read
@OrlaFeely @UCD_Research @ucddublin @UCDMedicine

What's great about prion seeding?Did you know that the spike protein has 30 amyloidogenic motifs?But please continue to congratulate the mass murder of the West. Shipman doesn't hold a candle to Fauci
Image @OrlaFeely @UCD_Research @ucddublin @UCDMedicine Make sure to congratulate him for #AIDS too.

Apr 19, 2024 4 tweets 2 min read
It's becoming a massive issue amongst the jabbed.

mRNA ribosomal frameshifting can occur when there's a shift in the reading frame during translation,
potentially leading to altered protein production.
frameshifting, could potentially contribute to the misfolding of proteins and thus indirectly play a role in prion formation

#SV40 #dsDNA packaged in #LNPs.

What could go wrong ?Image @EPRC_official @UCD_Research @EdinburghUni @Cambridge_Uni

This comprehensive presentation, Kevin delves into the intriguing world of toxic peptides, amyloids, and prions, exploring their relevance to genetic vaccines and the SARS-CoV-2 virus. Broken into concise sections, he examines the potential implications and emphasize the importance of informed consent. This thread is a valuable resource worth saving. Kevin discusses the inflammatory and amyloidogenic effects of small sequences called epitopes, which can cause memory dysfunction in mice. They also mention a study that found the introduction of gene transfection technologies containing the spike protein can induce amyloidogenic cascades. Kevin highlights a 200% increase in the diagnosis of CJD in France after the rollout of vaccination programs, suggesting a potential link. They discuss the loss of cognitive function associated with exposure to the spike protein and propose that amyloidogenic disease processes may underlie long-haul COVID-19 symptoms. DR McCairn mentions the role of viral infections in facilitating intercellular aggregate dissemination and shares examples of misfolding prion amyloidogenic diseases

rumble.com/v3w8rjx-savims…Image
Apr 18, 2024 7 tweets 5 min read
The characters in this story are made up.

Amyloids and prions are real as are the neurological damage that comes with them.

The Tale of Misfolded Proteins: A Cascade Unleashed
Chapter 1: The Transfection Experiment
In a dimly lit laboratory, Dr. Evelyn Sterling, a brilliant geneticist, embarked on a groundbreaking experiment. She aimed to understand how transfections—introducing foreign DNA into cells—could trigger unexpected consequences. Her lab assistant, Alex, watched with anticipation as Dr. Sterling prepared her materials.

Dr. Sterling: “Alex, today we explore the intricate dance of proteins within cells. Our focus: amyloids and prion-like misfolding.”

Alex: “Fascinating! But why transfections?”

Dr. Sterling: “Because transfections can disrupt the delicate balance. Imagine a peaceful pond—the proteins are like water molecules. Transfections are like tossing a stone into the pond. Ripples form, and the entire ecosystem reacts.”

Chapter 2: The Misfolded Dance
Dr. Sterling transfected human cells with a modified gene encoding an amyloid precursor protein. As the cells absorbed the foreign DNA, the protein synthesis machinery went to work. But something went awry—the protein folded incorrectly.

Dr. Sterling: “Alex, observe. This misfolded protein is like a rogue dancer at a ball. It disrupts the choreography.”

Chapter 3: The Cascade Unleashed
The misfolded protein triggered a cascade. It interacted with other cellular proteins, distorting their shapes. Like dominoes falling, this led to more misfolding. The once-harmonious cellular ballet turned chaotic.

Dr. Sterling: “Alex, see how the misfolded protein recruits others? It’s like a rogue dancer pulling others into a frenzied waltz.”

Chapter 4: The Amyloid Aggregation
The misfolded proteins aggregated, forming amyloid plaques. These sticky clumps clogged cellular pathways, disrupting communication. Neurons struggled to function, leading to memory loss and cognitive decline.

Dr. Sterling: “Alex, these amyloids are like tangled shoelaces—cells stumble, and diseases emerge.”

Chapter 5: The Prion Twist
Dr. Sterling introduced another twist—the prion-like behavior. She transfected cells with a prion protein gene. The prion protein, once misfolded, acted as a template. It induced neighboring proteins to mimic its shape.

Dr. Sterling: “Alex, prions are like contagious dancers. They teach others their twisted steps.”

Chapter 6: The Infection Spreads
The prion-like misfolding spread. Neurons transformed, losing their normal function. Alex watched as the cells became ghostly, their connections severed.

Dr. Sterling: “Alex, this is how prion diseases propagate. Like a macabre dance, they infect neighboring cells.”

Epilogue: A Pathway Unveiled
Dr. Sterling’s research revealed the intricate pathways of protein misfolding. Transfections, like stones in a pond, set off cascades. Amyloids and prion-like diseases emerged, leaving a trail of disrupted cells.

And so, in the quiet of her lab, Dr. Sterling whispered, “We’ve glimpsed the secrets of life’s dance—a choreography both beautiful and treacherous.” Mechanisms of protein-folding diseases at a glance

journals.biologists.com/dmm/article/7/…
Apr 16, 2024 5 tweets 3 min read
The Spike protein of SARS-CoV-2 is PRION-LIKE and amyloid! What does that mean?

You all know about Alzheimer's, Parkinson's, Creutzfeldt-Jakob... these are degenerative pathologies induced by peptides or proteins with a particular conformation (a structure in space): beta sheets. These beta sheets cause the proteins or peptides to aggregate, stick together, until they form insoluble and degenerative films. These degenerative plaques can be visualized in the brain through medical imaging. And these lesions are irreversible.

The thing is, these misfolded peptides/proteins will also act as aggregation nuclei. A bit like the mother-of-pearl of an oyster is deposited around a grain of sand serving as a nucleus. It's a bit the same principle. Proteins or peptides will be able to bind to the primary pathological aggregate. These proteins or peptides are initially normal! But they will become pathological upon contact with the "degenerative nucleus" (cf. Slide "Non-Canonical PRION Disorders").
So, the Spike of the SARS-CoV-2 virus is amyloid... and can therefore form beta conformation fibril deposits (in beta sheets). These amyloid sequences are distributed almost throughout the length of the Spike (cf. Slide "Gain of Function with PRION Disorders").

The HIV inserts, gp120, are also amyloidogenic...

What's impressive is that the Spike produced after anti-COVID injections presents the SAME AMYLOID SEQUENCES! In fact, through imaging, we have been able to highlight amyloid deposits at the injection site.

But, SARS-CoV-2 is NEUROTROPIC regardless of the symptomatology! It targets the central nervous system. And it is believed that long COVID may be due to these neurotropic and amyloid properties... Fibrin clots, and coagulation disorders as well, may be due to amyloid fragments of the Spike circulating in the blood. Well, yes, our immune system, by attacking the Spike, will release amyloid sequences...

In short! The Spike is a PRION-LIKE and amyloid molecule...

To the wise listener!

Translation from french 🇫🇷

#Prions #Amyloids & more
Apr 1, 2024 21 tweets 6 min read
Luc Montagnier's last paper, in peer review when he died:

"We present 26 cases of Creuzfeldt-Jacob Disease, all diagnosed in 2021 with the first symptoms appearing within an average of 11.38 days after a Pfizer, Moderna, or AstraZeneca COVID-19 injection"

#TheyKnew

May he rest in peace 🕊️ijvtpr.com/index.php/IJVT…Image
Flashback : June 2021 - Dr. Richard Fleming shares Luc Montagnier’s discovery that spike proteins may contain genetic sequences from HIV... VAIDS is real... #GP120 #Prions & more.
Mar 23, 2024 5 tweets 3 min read
Dr. Ryan Cole Showcases the 'Genetic Clotting Disorder' That's Suddenly Surging in the Population

Throwback to March 22.

@SimonHarrisTD were you the acting health minister during COVID?

These issues haven't gone away.
General election now we don't want someone elected on the 15th count. @rtenews @SimonHarrisTD On September 2, 2021, at 08:30 hrs, Fine Gael's Simon Harris announced plans to establish "popup vax hubs" inside colleges starting September 6th, 2021, to administer COVID vaccines to young people. You did this?

You need to step down.
@SimonHarrisTD

oireachtas.ie/en/debates/deb…


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Feb 23, 2024 5 tweets 2 min read
Accumulated profits at
The website firm soar to nearly €1.7m Underlining a buoyant year for the business, the firm’s cash funds during 2023 increased from €1.22m to €1.52mRIP.ie Company behind records profits of €208,492 for 2020

Curse all you Antivaxxer coffin dodgers 😂

RIP.ie
m.independent.ie/business/irish…
Feb 18, 2024 11 tweets 3 min read
2021-10-16 12:10 hrs
FINE GAEL's REGINA DOHERTY PLOTS TO INCITE HATRED AGAINST HEALTHY FREE PEOPLE IN IRELAND WHO REFUSE TO TAKE mRNA DEATH JABS

WANTED - FOR GRAVE CRIMES AGAINST PEOPLE IN IRELAND


#StopTheJab
#DoNotGetAnyCovidVax
#DoNotGetAnyFluVax
#StopMedicalApartheid
#BigPharma #BigLockdown #MedicalTerrorism #Genocide
#StopVaccineBioWeapons
#OurPeopleAreBeingButchered
#RTE_is_the_Virus
#NEWSTALK_is_the_variant
#FreePeopleIrelandt.me/liberty_stream… @FineGael @ReginaDo @LeoVaradkar Hey Regina,

#IrelandisFull #eiReExit #IREEXIT Image
Feb 12, 2024 6 tweets 2 min read
Program Death ligand ☠️☠️☠️

The increase in PD-L1 expression may reduce the anti-tumor activity of the immune system and increase the risk of cancer progression or recurrence, especially in patients with pre-existing malignancies or immunosuppression.

The paper recommends that cancer patients should be monitored closely after vaccination and that PD-1/PD-L1 inhibitors, a type of immunotherapy that blocks the PD-L1 protein, may be considered as an adjuvant therapy.

That's messed up, as the sick are being gaslit by fools on top of being experimented on.

#turbocancer.

It gets darker the more you look.