Testimony of Deanna McLeod — Part 2 | Allison Inquiry

🎙️ Testimony of Deanna McLeod — Part 2 — Allison Inquiry, September 11, 2026

🔬 Continuation of testimony of Deanna McLeod at the Allison Inquiry, delivered on September 11, 2026.

Evidence evaluation specialist, McLeod presents Ontario data and US registries showing increases in myocarditis (76-87%), pulmonary embolisms (+13%) and certain cancers in women after mRNA vaccination. She questions the accelerated approval framework and regulatory classification of mRNA vaccines. Each claim is that of the witness.

00:00 🎬 Resumption of testimony and administration of oath
01:00 📊 Data on Bell’s palsy and community care, Bell
03:00 🫁 Pulmonary embolisms: increase of 13% in Ontario
05:00 ❤️ Myocarditis and pericarditis: increases of 76% and 87%
07:30 🧪 Regulatory framework and approval within two months
10:30 🧬 mRNA classification: vaccine or gene therapy?
12:30 🎗️ Breast cancer data (Ontario and SEER registry)
15:30 🏥 Hospital capacity and the role of chief medical officers
17:20 🎤 Acknowledgments and conclusion of testimony

🏛️ Political context
🔎 Deanna McLeod testifies before the Allison Inquiry, regarding the response to the COVID-19 pandemic.
📅 This testimony on September 11, 2026, follows a previous appearance, as McLeod was unable to complete her presentation during the first session.
📋 McLeod introduces herself as a specialist in evidence assessment for clinical guidelines, particularly in oncology.

⚖️ Comparison of opinions
📊 McLeod states that Ontario data show statistically significant increases in myocarditis, pulmonary embolisms and certain cancers following mRNA vaccination.
⚖️ She argues that the accelerated approval framework (two months) was insufficient compared to standard norms.
🧬 She distinguishes between regulatory classification (vaccine) and the biological mechanism she describes as gene therapy, arguing that trial standards should have been stricter.
⚠️ These assertions are those of the witness; they were not subject to cross-examination in this excerpt.

📢 Reactions and controversies
🗣️ A commissioner interrupts McLeod to clarify that some patients were unable to access care, nuancing the interpretation of billing data.
⏱️ The limited time (13 minutes allocated) constrained McLeod to expedite her presentation, leaving some points undeveloped.
📌 No partisan debate: this is a technical testimony before a public inquiry.

📜 Legislative and social consequences
📋 The data presented could inform the recommendations of the Allison Inquiry on monitoring adverse post-vaccination effects.
🏥 McLeod calls for a review of the monitoring and regulatory classification of mRNA products.
🔬 Her testimony raises questions about the adequacy of emergency approval frameworks for future products in a public health crisis context.

❓ Key Questions
1️⃣ Will Ontario data from McLeod be reviewed by independent experts in the Allison Inquiry?
2️⃣ Will the accelerated approval framework be revised in light of these testimonies?
3️⃣ Did the classification of mRNA as a "vaccine" rather than "gene therapy" affect trial standards?
4️⃣ What follow-up will the Allison Inquiry give to the data on myocarditis and pulmonary embolisms?
5️⃣ Are the observed increases in cancer attributable to vaccination, pandemic underdiagnosis, or other factors?

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