Matt Shelton

A few have asked for a more 30K Ft view of this. If you recall process 1 vs process 2 bait and switch described by @RetsefL and @joshg99… The PCR step in process 1 erases all methyl groups on DNA. Switch to process 2 and you reintroduce not just SV40 and the whole plasmid backbone but now all your residual DNA looks like a foreign invader to your cells as it’s methylated in a manner not seen in humans.

What Suppression Order? Why can't Hipkins talk? I have sent the following Official Information Act request this morning. "Hi On 13 August 2025, Chris Hipkins MP, stated in a radio interview with Mike Hoskings that he was under a suppression order. I request the following information under the Official Information Act 1982: 1. A copy of the suppression order; 2. The details of the legal proceeding that resulted in the suppression order; 3.The name of the party that initiated the court order for the suppression order; 4. The duration of the suppression order. I require the information for a submission to Parliament which is due on 18 September 2025. I look forward to hearing back from you. Kind regards Kirsten Murfitt" @theplatform_nz @NewstalkZB @nzdsos @HopeRising19 @SeanPlunket @samuffindellmp @LobbyForGoodNZ @theplatform_nz

🚨 BREAKING STUDY: mRNA Injections Induce Severe, Long-Lasting Genetic Disruption Linked to Cancer and Chronic Disease 🧪 Using high-resolution RNA sequencing on blood samples, we discovered that COVID-19 “vaccines” SEVERELY disrupt expression of THOUSANDS of genes—triggering mitochondrial failure, immune reprogramming, and oncogenic activation that can persist for MONTHS to YEARS post-injection. 🧬Differential gene expression analysis compared mRNA-injured patients (cancer, adverse events) to 803 healthy controls — revealing widespread transcriptomic CHAOS: ⚠️ Mitochondrial failure – Complex I breakdown, oxidative stress, energy collapse ⚠️ Immune reprogramming – Chronic inflammation, ACE2 suppression, TLR hyperactivation ⚠️ Oncogenic activation – MYC up, p53/KRAS down, DNA repair suppression ⚠️ Cellular stress – Ribosome overload, misfolded protein buildup, proteasome activation ⚠️ Epigenetic remodeling – Chromatin shifts, methylation changes, nucleosome displacement ⚠️ Reverse transcription suggested – Patterns consistent with LINE-1 activity and persistent plasmid DNA, raising concern for potential genomic integration or sustained foreign gene expression To our knowledge, this is the first study to show long-term genetic disruption in people harmed by the COVID-19 "vaccines". It’s time for the immediate withdrawal of these dangerous gene therapies to protect the remaining ~20% of the population still considering booster doses. The landmark study was conducted by scientists from Neo7Bioscience (Dr. John Catanzaro, Dr. Natalia von Ranke, Dr. Wei Zhang, Dr. Philipp Anokin), the University of North Texas (Dr. Danyang Shao, Dr. Ahmad Bereimipour, Minh Vu), the McCullough Foundation (Dr. Peter McCullough and Nicolas Hulscher) and Medicinal Genomics (Kevin McKernan). 📰Synthetic mRNA Vaccines and Transcriptomic Dysregulation: Evidence From New-Onset Adverse Events and Cancers Post-Vaccination. Preprints. 2025;2025072155. doi: 10.20944/preprints202507.2155.v1 @neo7bioscience @Docjohnc @UNTsocial @P_McCulloughMD @McCulloughFund @Kevin_McKernan @MediGenomics

Mounting Evidence: mRNA Vaccine Technology Radically Disrupts The Human Genome Recent data from two patient groups—one with serious injury and one with rapid-onset cancer following mRNA vaccination—reveals a disturbing molecular pattern. Our RNA sequencing of Group 1 and Group 2 patients post-mRNA injection uncovered catastrophic disruption of gene regulation, protein synthesis, immune balance, and genomic stability. What we found ends the debate! This mRNA vaccine platform forces a reprogramming of the cell using: •Foreign RNA transcripts •Artificial regulatory domains (5′/3′ UTRs) •Nucleoside-modified bases (Ψ) that evade detection •Lipid nanoparticles that cross into immunologically and destabilizes your cellular architecture. We compared: •Group 1: Patients with severe systemic syndromes following mRNA exposure •Group 2: Patients with aggressive, treatment-resistant cancers emerging post-injection •Control group: Unexposed healthy individuals (Never had COVID Infection and not mRNA vaccinated) Datasets of 803 healthy people The disruption in transcriptomic control and cell identity was undeniable. Group 1 (Post-Vaccine Injury): •Mitochondrial disassembly (loss of Complex I activity, PINK1 repression) •Proteasome collapse (possible spike accumulation and misfolding) •Translation blockade at ribosomes •Endothelial dysfunction (angiogenic suppression, adhesion molecule overexpression) •Immune activation in a self-targeting loop (↑CD28, CCR7, SELL) Group 2 (New-Onset Cancer): •Nucleolar hypertrophy (↑rRNA, ↑MYC, ↑nucleolin expression) •Tumor suppressor inactivation (↓TP53, ↓KRAS, ↓Wnt) •Aberrant DNA methylation and chromatin remodeling •Chronic immune dysregulation and exhaustion In both groups, we observed: •ACE2 gene silencing → Angiotensin II overload → NF-κB/ERK-driven cancer signaling •Spike chaperone overload (↑HSP90, ↑calnexin) → unfolded protein response •Ribosomal frameshifting → defective protein translation •Persistent synthetic RNA → unresolvable transcriptional instability. The cell enters an irreversible stress and survival loop. it's not off-target toxicity. It is systemic mimicry of host genetic regulation: •Hijacking of host microRNA pathways •Subversion of normal mRNA decay and splicing •Disruption of polyadenylation and nuclear export •Imitation of endogenous regulatory RNA signatures. We detected molecular signatures consistent with: •Alzheimer’s and ALS-related protein misfolding •Parkinsonian mitochondrial stress •Autoimmune T-cell confusion •Oncogenic transcription patterns •Endocrine and metabolic collapse This is not rare. It is reproducible across patients with adverse events. And the most dangerous mechanism of all: Evidence of LINE-1 retroelement activation was present. This means: •High Risk of reverse transcription of synthetic mRNA is occurring •Genomic integration under cellular stress is plausible •This may accelerate somatic mutation and transformation into cancerous clones In Group 2, this correlates with de novo tumor emergence post-vaccine. Somatic mutation patterns and oncogenic signatures mirror viral and retroelement-driven tumorigenesis, indicating aberrant genomic coding embedded within the host DNA. The human cell becomes: •A spike initiated destructive protein-producing machine •A cytokine amplifier •A misfolded protein sink •A genomic landmine The consequences are now undeniable: widespread harm and death following the rushed deployment of mRNA technology. Still branded the crown jewel of vaccine innovation, this platform’s genomic hazards are deliberately ignored—sacrificing truth, safety, and lives for financial gain. Neo7Bioscience will release: •REViSS scores •GSEA enrichment maps •Case comparisons showing synthetic mRNA-induced oncogenic acceleration The data speaks! No more coverup! Paper forthcoming: neo7bioscience.com/contactus

Tawny Buettner, RN, observed a tenfold increase in the rate of myocarditis post-vaccine rollout, and a third of the boys who were diagnosed with the condition developed scarring of the heart.

🚨 EXPOSED: Trans Industry Targets Autistic People: Colorado Autistic Man Sven Scharpen Explains If you're autistic, neurodiverse, on the spectrum, or have family members who are, this one's for you. From @sven_scharpen & I, with love. Link to full vid below. @letkidsbekidsnz

The largest ever study (QoVax) comparing COVID injected to non-injected patients has been stopped without explanation and Queensland Health is on track to destroy all of its samples and evidence. Losing the last evidence that could inform a truly objective assessment of the effects of the injections wouldn't just be a tragedy, it could be a crime. I'm putting Queensland Health bureaucrats on notice. Do not destroy these samples and evidence, allow the study to complete so that the data can be shared for all Australians.

The largest ever study (QoVax) comparing COVID injected to non-injected patients has been stopped without explanation and Queensland Health is on track to destroy all of its samples and evidence. Losing the last evidence that could inform a truly objective assessment of the effects of the injections wouldn't just be a tragedy, it could be a crime. I'm putting Queensland Health bureaucrats on notice. Do not destroy these samples and evidence, allow the study to complete so that the data can be shared for all Australians.

Another major announcement expected: The exact timing of the announcement wasn’t clear, though it was expected in the coming days. "The Department of Health and Human Services, led by Secretary Robert F. Kennedy Jr., is expected to remove the Centers for Disease Control and Prevention’s recommendations for those groups around the same time it launches a new framework for approving vaccines, the people said." #covid

Scroll all the way to the bottom for the poll. stuff.co.nz/politics/3606306…

March 14, 2025 🤯🤯🤯 Japanese House MP Ryuhei Kawada calls for the temporary suspension of mRNA vaccines after a shockingly high number of deaths (more than 2,000 deaths) voluntarily reported! ---------------------------- Voluntary reports from medical institutions to the Ministry of Health, Labour and Welfare alone indicate that there are more than 2,000 deaths! There are more than 2,000 deaths, that’s the situation. Instead of turning a blind eye to this part, the Ministry of Health, Labour and Welfare should immediately review the evaluation criteria. That’s what should be done. If that cannot be done, then at the very least, why can’t they make the decision to temporarily suspend periodic vaccinations? Why can’t the Ministry of Health, Labour and Welfare make that call? Isn’t there any thought of pausing and stopping for a moment? ----------------------------------

Heartfelt statement sent to reporters from Dr Dave Weldon following withdrawal of his nomination for CDC (1/4):