Kat Lanteigne
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N.B. neurological syndrome: Researcher, advocates aim to circumvent provinceHealth experts say patients impacted by the N.B. brain syndrome deserve action. 'It is their right to have a scientific investigation,' says BloodWatch co-founder Kat Lanteigne.HealthJan 12, 2022
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Families, advocates question transparency of investigation into N.B. neurological syndromeA man whose father is suffering from the neurological syndrome under investigation says he’s frustrated with a lack of transparency.HealthAug 5, 2021
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