October 15, 2025 • 12:00–1:00 pm ET

Join us for an informal lunchtime session where Linda Wilhelm and Therese Lane share their journeys as patient partners in research and policy. They’ll reflect on:

• Where they started, and where they are today
• The different roles patient partners can play
• Equity, diversity, and inclusion in research and healthcare
• Lessons from advocacy, lived experience, and national initiatives

After a short presentation from Linda and Therese, the conversation will open up for your questions. This is a relaxed Q&A-style event designed to be interactive and engaging. We’re also exploring creating an infographic highlighting key insights from the discussion (no one will be identified) – all attendees will receive a copy afterward.

About the speakers

Linda Wilhelm

Linda has lived with rheumatoid arthritis for over 30 years and is a long-time patient advisor, advocate, and leader. She is the President of the Canadian Arthritis Patient Alliance (CAPA), a grassroots, patient-driven national organization. Linda was a member of the Canadian Pain Task Force, advising the federal government on patient-centred care, and has been an active advocate for treatment access and quality of care across Canada for more than two decades.

Therese Lane

Therese brings her lived experience with arthritis and pain since her teens into diverse research and healthcare roles. She volunteers with CAPA, co-chairs the Equity, Diversity, and Inclusion Committee of CIHR’s Chronic Pain Network, and is a member of the Clinical Trials Ontario College of Lived Experience. Therese has partnered on multiple research projects, including the PLAN Project, and is passionate about addressing inequities in pain treatment and the stigma faced by those with addiction and mental health issues.

How to participate:

• Format: Short presentations + open Q&A
• Bring your questions: Submit them in advance when you register, or share them live during the session
• Audience: Patient partners (new and experienced), researchers, clinicians, policymakers—anyone interested in patient engagement

Register now to receive the Zoom link and submit your questions in advance!