
Witness Testimony

Keywords from Transcript
media fear messaging, coerced second dose, pharmacist hesitation, ER exemption refusal, grandchild emotional pressure, metallic taste onset, vision loss episode, migraine and tachycardia, rapid muscle atrophy, Guillain-Barre concern, swallowing impairment, neuromuscular admission London, disability denial pre-existing claim, Vaccine Injury Support Program delay, online censorship claims
Included in the Report:
Ms. Julie Pinder
Industrial Worker
Personal Experience
Witness ID:
NCI-W-069
Hearing
Toronto
Ontario
Date:
April 1, 2023
Report
Inquiry into the Appropriateness and Efficacy of the COVID-19 Response in Canada; November 2023
Main Topic
Testimony describing coercion to receive second COVID-19 vaccine dose following adverse reaction to first dose, resulting in progressive neuromuscular decline and muscle atrophy.
One Line Summary
Julie Pinder testified that after experiencing adverse reactions to her first vaccine dose, she felt pressured into a second dose and subsequently developed rapid muscle wasting, neurological impairment, and long-term disability.
Synopsis
Julie Pinder testified that she received her first COVID-19 vaccine dose in March 2021 due to fear generated by media messaging and a desire to “do her part.” Following the first dose, she experienced extreme fatigue, rash, elevated heart rate, calf cramping, and ankle weakness but did not initially associate these symptoms with vaccination. Despite reluctance, she sought a second dose after workplace discussions about mandates and mask removal for the vaccinated, as well as social pressure and comments from political leadership regarding the unvaccinated. A pharmacist initially declined to administer the second dose without medical clearance, but an emergency room physician refused to consider an exemption and warned her she could endanger her grandchild if she remained unvaccinated.
After receiving the second dose, Pinder testified that she developed metallic taste, severe migraine, temporary vision loss in one eye, and progressively worsening neurological symptoms. Within weeks, she began dropping objects, experiencing cognitive impairment, muscle cramping, swallowing difficulty, and rapid visible muscle wasting affecting her limbs, trunk, and neck. She sought care at St. Thomas hospital and later at London Health Sciences Centre, where she was briefly admitted. Although Guillain-Barré syndrome was mentioned, she testified that appropriate diagnostic procedures were not performed at that time. She underwent nerve conduction studies, MRI, CT scans, and genetic testing, but no definitive autoimmune condition was identified.
Pinder stated that one specialist suggested the injury was vaccine-related, but she faced difficulty obtaining formal recognition. Her long-term disability claim was denied on the basis of pre-existing neurological reactions, and she reported delays and barriers in accessing the federal Vaccine Injury Support Program. She testified that she lost her employment, that her husband also suffered cardiac injury after vaccination, and that both financial strain and online censorship compounded their hardship. She expressed concern about pediatric vaccination risks and stated that injured individuals lack meaningful institutional support.
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