by CSAAdmin | Sep 29, 2025 | SpA Warrior Stories
▶ Watch: Colin on Life, Setbacks, and Renewed Strength with Psoriatic Arthritis A candid conversation hosted by Brenda Dauder, Executive Director of the Canadian Spondyloarthritis Association. About the Conversation Psoriatic arthritis (PsA) can reshape a...
by CSAAdmin | Sep 29, 2025 | SpA Warrior Stories
▶ Watch: Erin’s Journey with Psoriatic Arthritis A real and powerful story of living, growing, and thriving with psoriatic arthritis. About the Conversation In this video, Brenda Delodder, Executive Director of the Canadian Spondyloarthritis Association (CSA), sits...
by CSAAdmin | Sep 29, 2025 | Advocacy Resources, PsA
On October 19, we join together to recognize National Psoriatic Arthritis Day—a day focused on raising awareness of psoriatic arthritis (PsA) and supporting everyone affected by it. We’re pleased to share resources and personal stories that emphasize the power of...
by CSAAdmin | Sep 29, 2025 | Downloadable PDF, Resources
Track Your Symptoms and Take Control of Your Health Living with spondyloarthritis (SpA) can mean dealing with changing symptoms that affect your mobility, comfort, and quality of life. The Canadian Spondyloarthritis Association (CSA) has created a free, easy-to-use...
by CSAAdmin | Sep 23, 2025 | Blog Posts, Fundraisers
Living with axial spondyloarthritis (axSpA) is a journey that looks different for every patient, but stories like Michael’s highlight both the challenges and the hope that come with a diagnosis. Michael first began experiencing sharp, shooting pains in his back, neck,...
