T he COVID-19 pandemic provoked a rapid shift in ambulatory health care delivery toward telemedicine to enable health care access and reduce the risk of viral transmission. [1][2][3] The transition was abrupt, with accompanying challenges owing to limited telemedicinerelated technology and training for physicians and other health care workers. 3,4 In Quebec, within the month of July 2020, an unprecedented 1.5 million telemedicine consultations occurred in family medicine, the large majority among physicians with no prior experience with this modality of care. 5 The ubiquitous uptake of telemedicine was accompanied by both enthusiasm and caution -enthusiasm about its postpandemic utility in triaging and managing patients with nonurgent conditions, and facilitating access especially among remote populations, 6 and caution regarding clinical, organizational, professional, economic, legal and regulatory complexities, including the potential of medical errors, duplication of visits and issues with patient confidentiality. [7][8][9][10] In Quebec, several family doctors serving high-needs, multicultural and low-income patient populations observed their absence among those receiving telemedicine during the initial waves of the pandemic. Of concomitant concern was evidence indicating growing racialized inequities in COVID-19-related health care and health outcomes. 11,12 Technological, socioeconomic and cultural factors limiting access to primary care, including telemedicine, are possible explanations that require research and policy attention. 10 Although a substantial body of literature has explored physicians' perceptions and needs surrounding telemedicine [13][14][15][16][17] and challenges of providing virtual care during the pandemic, 4,[18][19][20][21] comparatively little attention has focused on the perspectives of patients, much less socially vulnerable patients.