At the CSA, we are filled with gratitude. Every day, we witness the incredible strength, compassion, and determination of our members, volunteers, healthcare professionals, and partners across the country. You are the heart of this movement—sharing your stories, supporting each other, and pushing for change.
Yet we know that in Canada, too many people still wait 7 to 10 years for a diagnosis. That’s far too long. We need more awareness among healthcare providers, earlier referrals, and equitable access to specialists and imaging—especially for those in rural and underserved communities.
That’s why we’re relentless with our advocacy efforts—calling on decision-makers, policy makers, and healthcare systems to take bold steps to:
- Increase disease awareness among both the public and healthcare professionals to shorten the diagnostic journey,
- Bridge the gap in health equity for diverse and underserved communities impacted,
- Equitable access to new treatment options for people living with spondyloarthritis, as up to 50% become resistant to their treatments within five years,
As we stand with the global axSpA/AS community, we recommit to building a future where no one is left behind. A future where care is timely, equitable, and rooted in patient needs.