Welcome to our virtual community! Start by browsing through the personal stories featured here.
We have organized these stories into two categories: Your Stories – stories sent to us at the Spondylitis Association of America – and selections from The Faces of Ankylosing Spondylitis project.
Tell A Story with SAA Storytellers, Your Stories on Stage! Send Us Your Story Pitch!
Are you interested in being a part of SAA Storytellers, Your Stories on Stage?
SAA is always looking for those in the spondyloarthritis community to tell their story (patients, caregivers, medical personnel, and friends of the community – all are welcome!).
Kristen Ray My journey with Ankylosing Spondylitis (AS) has been very long, my first memories of symptoms starting at around age 6. Back then AS was only considered to be a man’s disease, it wasn’t until the…
My symptoms began when I was 16 in the year of 2014. I would miss weeks of school because the pain was too much to handle. I was called names and a druggie because I was losing…
Co-Founder of Spondylitis Association of America, The first President of the Board of Directors and the first Executive Director In 1983, when I co-founded this organization, there was no information available about AS – not a single…
My memory of that day in 1997 centers around driving home on I-295 in Portland, in the Fore River area; that’s when the words I’d just heard took hold. “You have been diagnosed with ankylosing spondylitis.”