All the latest news and stories about Alzheimer's disease, dementia and the brain.

Mark Breslaw, member of our Lived Experience Partner Program, shares how his personal motto, “Enjoy the ride,” has taken on deeper meaning following his diagnosis. Through family traditions, cherished memories and everyday moments, Mark reflects on choosing joy, connection and presence while navigating uncertainty.

Lived experience partner Don Cheeseman’s shares through his writing an honest and vulnerable perspective on navigating daily life, social interactions and isolation. His story highlights the importance of sharing lived experiences to help others feel less alone and build understanding of dementia.

James Donovan shares his volunteer experience as our support group facilitator, supporting adult children caring for parents living with dementia. Drawing on his professional background and personal connection to dementia, James offers a space where caregivers feel understood, share experiences and support one another. His story demonstrates the meaningful impact of connection and community in the caregiving journey.

The Alzheimer Society of BC and Yukon partners with the Health Design Lab at Emily Carr University of Art + Design and the University of Victoria to bring together biomedical dementia researchers and people affected by the disease to discuss inclusive research practices. Discussions from participants lead to the creation of complementary guides, Collaborative minds.

Learn how the Alzheimer Society of BC and Yukon is helping build communities that are inclusive, supportive and accessible for people living with dementia and their care-partners and how you can join the movement.

Shifting identity may be a normal part of moving forward after a caregiving experience, as these three caregivers have experienced. Rediscovering identity is key. Each of these stories is a reminder that it may take time and patience, but moving forward and re-finding your identity is possible.

Cynthia Wong was diagnosed with Mild Cognitive Impairment (MCI) and a First Link® program participant. She shares how supporting the Telethon for Alzheimer’s can help ensure people living with dementia and their families have access to culturally relevant support and services.

After her mother Hazel was diagnosed with vascular dementia, lifelong Kelowna resident Arlene Hildred became her primary caregiver, navigating the challenges of progressive dementia and long-term care. Arlene reflects on her five years of caregiving as an unexpected gift that brought peace, understanding and a renewed relationship during her mother’s final years.

The Agency recommends public reimbursement for the disease-modifying therapy.

At an important time for our organization and mission, the Alzheimer Society of BC and Yukon is looking for our next CEO. We're seeking a visionary, values-driven leader to guide a talented and dedicated team, advance our ambitious strategy, and strengthen our impact for people affected by dementia across British Columbia and Yukon.