B.C. Dementia Care Crisis: Family Doctors Need More Support
B.C. Dementia Care Crisis: Family Doctors Need More Support

For most families, dementia care doesn't begin with a specialist appointment. It starts with a spouse noticing something different, a son questioning a mother's driving safety, or a daughter trying to explain in a 15-minute appointment that her father is repeating questions, missing medications, and becoming frightened.

Family Doctors on the Front Line

Family physicians are often the first to respond to family concerns and begin difficult conversations about memory loss, safety, medications, and future planning. They become a steady point of contact for families navigating a progressive and life-altering disease, particularly in rural communities with limited specialist access, according to Cathryn France in an opinion piece published June 23, 2026.

That role is only going to grow. More than 85,000 people in British Columbia are living with dementia, and that number will rise as the population ages. Dementia is already one of the most complex and resource-intensive health conditions facing the province, yet much of the challenge falls on family physicians trying to provide care within systems built around short, episodic appointments.

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Physician Agreement Falls Short

B.C.'s renewed physician master agreement recognizes several important pressures in the health-care system, including rural practice, maternity care, psychiatry, and after-hours services. Those priorities matter, France writes, but the agreement does not explicitly prioritize dementia and geriatric care, which is also critical given B.C.'s rapidly aging population.

As dementia progresses, the family doctor's role becomes more complex. A single appointment may involve reviewing medications, assessing safety, responding to changes in behaviour, supporting an exhausted caregiver, and helping families make difficult decisions about what comes next. These are not one-issue visits, but emotional, time-intensive conversations that often require follow-up.

Yet much of primary care is still organized around brief visits and single concerns. Dementia diagnosis and care don't fit that model, France argues.

What Better Support Could Look Like

B.C. has established and subsequently improved the longitudinal family physician payment model to support complex, continuing needs. But dementia care still requires more time, co-ordination, caregiver support, and connection to community services than the system fully recognizes.

France suggests that better support might include longer appointments, caregiver consultations, home visits, and stronger co-ordination with home and community care. It could also include enhanced funding models that support the primary care memory clinic model, where physicians work with other health professionals to assess, diagnose, and support people living with dementia. Dementia-specific quality incentives—including advance care planning, medication reviews, and reducing avoidable hospitalization—would help make time-intensive dementia care more sustainable while improving outcomes for patients, families, and the health-care system.

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