Testimony of Deanna McLeod | Allison Inquiry
🎙️ Testimony of Deanna McLeod — Allison Inquiry, September 10, 2026
🔬 On September 10, 2026, Deanna McLeod — founder of an independent research firm and graduate in immunology from McMaster — testifies before the Allison Inquiry.
📊 She states that she analyzed Ontario health data obtained through access to information and presents conclusions suggesting that vaccinated individuals would have had a higher risk of contracting COVID-19 after the arrival of the Omicron variant.
⚠️ She also raises questions about informed consent, effects on fertility, miscarriages, pulmonary embolisms, and chronic fatigue.
📌 These assertions are those of the witness and do not constitute facts established by scientific consensus.
00:00 🎬 Oath and presentation of Deanna McLeod
02:30 🧬 Presentation of the independent research firm
05:00 ⚖️ Regulatory framework and informed consent of physicians
09:00 💉 Analysis of Pfizer clinical trial data
13:30 📊 Ontario data on COVID cases by vaccination status
18:00 🏥 Effects on hospitalizations and the immune system
22:00 🤰 Impacts on reproductive health and pregnancies
27:00 📋 Conclusions and invitation to return to testify
🏛️ Political context
🏛️ The Allison Inquiry is a public inquiry into the management of the COVID-19 pandemic in Canada.
🔬 Deanna McLeod runs an independent research firm founded in 2000; she contributed to the audit of Alberta’s response to COVID-19 (Dyson Report).
📋 The testimony concerns Ontario health data obtained through an access to information request, analyzed in partnership with a clinicians’ alliance.
⚖️ Comparison of opinions
🔬 McLeod asserts that Ontario data show an increased risk of COVID among vaccinated individuals after Omicron, contrary to official public health conclusions.
⚖️ She asserts that the legal framework imposed on physicians has compromised patient informed consent.
📊 She contests the method of counting vaccine status in the first 14 days following injection, arguing that it masks early side effects.
📢 Reactions and controversies
⚠️ These claims by Deanna McLeod do not represent consensus within the scientific and medical community.
🔎 The interviewer interrupted the testimony on several occasions to clarify statements or highlight their implications.
📌 The panel indicated that the slides would be posted online and that the witness could return to complete their testimony, noting the importance placed on their findings by the Allison Inquiry.
📜 Legislative and social consequences
📋 If McLeod’s analyses were validated, they would raise major questions about public health policies related to booster doses.
🏥 Her data suggests an increase in cases of anemia, embolisms, Bell’s palsy, and fertility issues in Ontario following the vaccination campaign.
⚖️ The testimony highlights a debate on the regulatory framework for mRNA vaccines and the lack of mandatory clinical evaluation for formula changes.
❓ Key questions
1️⃣ Were the Ontario data analyzed by McLeod peer-reviewed and independently validated?
2️⃣ Did the legal framework imposed on physicians during the pandemic truly compromise informed consent?
3️⃣ Did public health authorities analyze side effects occurring within 14 days following vaccination?
4️⃣ Were booster doses subjected to sufficient clinical evaluations prior to their distribution?
5️⃣ Will the Allison Inquiry follow up on the recommendations stemming from this testimony?
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