by CSAAdmin | May 29, 2025 | Fundraisers, News, Past Fundraisers
On behalf of the Canadian Spondyloarthritis Association, we want to extend our deepest gratitude to everyone who helped make this year’s Let’s Get Loud for AS Gala such a resounding success. Thanks to your incredible generosity and unwavering support, we raised an...
by CSAAdmin | Apr 29, 2025 | Blog Posts, News, World AS Day
In Canada, the average delay to diagnosis for axSpA remains a staggering 7 to 10 years. On World AS Day, we proudly stand with our global community to raise awareness, celebrate resilience, and amplify the voices of those living with axial spondyloarthritis...
by CSAAdmin | Apr 23, 2025 | SpA Warrior Stories
It took Georgina nearly 30 years to receive a diagnosis, despite having symptoms, a family history of AS, and carrying the HLA-B27 marker. Unfortunately, this isn’t uncommon for many people living with spondyloarthritis. Georgina first started experiencing...
by CSAAdmin | Apr 23, 2025 | News, SpA Warrior Stories
FOR IMMEDIATE RELEASE: From Coast to Coast: Tyler Ashton’s 11,000 km Solo Cross-Canada Ride to Champion Those Living with Spondyloarthritis | Canadian Spondyloarthritis Association Tyler Ashton is on an extraordinary mission. With nothing but his bicycle,...
by CSAAdmin | Apr 2, 2025 | Advocacy Resources, Resources, Special Advocacy Days, World AS Day
Dealing with a New Diagnosisw/ Dr Dayna Lee-Baggley Mindful Eating and Chronic Illness w/ Samantha Holmgren, RD Spondyloarthritis Patient Forumw/ SPARCC World AS Day , observed globally on May 4th, is dedicated to those affected by Axial Spondyloarthritis (axSpA), a...
