SpA Warrior Stories

Raj’s Story

Raj’s Story

Meet Raj from the UK. He is the Chair of NASS, patient advocate and motivated to not let AS define him. Diagnosed in his early 20’s Raj was told he would likely be in a wheel chair in 10 years. Watch his inspiring video sharing how he set goals, had a plan and...

read more
Bjillian’s Story

Bjillian’s Story

Former Canadian Spondyloarthritis Assocation board member, Bjillian describes her first symptoms and how the pain progression happened. She also describes how she deals with the disease on a daily basis and how it impacts her life.

read more
Dawn’s Story

Dawn’s Story

Canadian Spondyloarthritis Assocation's member Dawn tells her story about how Ankylosing Spondylitis affects her life. She also describes her road to diagnoses and how it made her feel.

read more

Marilyn’s Story

Getting the right diagnosis changed my lifeLike so many Canadians, Marilyn Walsh had her life plans derailed by the devastating effects of arthritis. Fortunately, a proper diagnosis and treatment helped correct years of pain and suffering, and now Marilyn is devoted...

read more

Jen’s Story – Young Adult Feature

My name is Jen and I live in Northeastern Ontario. I am currently 26 years of age and have been diagnosed with two forms of inflammatory arthritis: undifferentiated connective tissue disease and axial spondyloarthropathy with peripheral involvement.It was towards the...

read more

Marie’s Story

In retrospect, I think the first signs of AS started about 25 years ago, when I was about 40 years old. I remember lying on the floor and my back was really stiff when I stood up. I never thought much about it as it would quickly disappear once I walked around. Around...

read more