Community Voices
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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. 

We’d love your story as well! Send it to us at Programs@spondylitis.org

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!).

ByKristen Shields

Kristen Shields

Hello, my name is Kristen and I’m 31.  I’ve debated for a long time about a sharing my story because I wondered how I was going to tell it? Who would relate? Would anyone benefit from hearing…

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ByCandace Jackson

Candace Jackson

The pain and stiffness of this disease, and the severity of my other conditions (I also have Ulcerative Colitis, fibromyalgia, and severe Gastroparesis) have prevented me from continuing to work in my dream vocation as a hospital…

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ByYaakov Lewi

Yaakov Lewi

My name is Yaakov Aharon Lewi which is Hebrew for Jacob Aaron Levi. I am 42 years of age. Not only does my name have a religious meaning but it's a family legacy going back thousands of…

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ByKristin Cornelius

Kristin Cornelius

Part of sharing my story is also admitting I don’t have it all figured out. Yeah, I love to be in control, but as anyone who fights this condition knows you don’t always have the last word.…

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ByRose Bigham

Speaking at an FDA Public Meeting on Chronic Pain

This week I flew out to Baltimore (from Seattle! Looong flight!) to attend a public meeting at FDA…

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ByM.J. Rowan

Face 2067

My experience with Rheumatologists wasn’t great. I remember one saying “we don’t know what causes it, 30% of people will have chronic RA, 30% of people will only have one flare, 30% of people will have it…

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