When SAA was founded in 1983, there was no support network, no educational materials geared to spondylitis patients, not even a single pamphlet for people affected by spondylitis, a group of related rheumatic diseases that primarily affect the spine and other joints. Nearly 2.7 million Americans are living with the disease.  SAA was the first and remains the largest resource in the U.S. for people seeking information on spondylitis.  Our focus is on research, patient advocacy, education and support, as well as raising awareness about this group of diseases.

Our mission at the Spondylitis Association of America is to be a leader in the quest to cure Ankylosing Spondylitis and related diseases, and to empower those affected to live life to the fullest.  There are more than 100 types of arthritis. For more than 35 years, SAA has focused on just one - yours. So that no one has to face spondylitis alone.

Spondylitis Association of America

Cassie Shafer

Paula Olsiewski

Kristine Eskandari Mph, Ches

Sean Ewert

Richard Howard, MBA

Diann Peterson, CFRE

The Advocacy and Engagement team at the Spondylitis Association of America focuses on empowering patients and advocating for their needs through community outreach, education, and support initiatives. This team works to raise awareness about spondylitis while engaging with patients, family members, and healthcare providers to promote access to resources and foster a strong support network. By developing programs and coordinating volunteer efforts, they aim to enhance the overall experience of those affected by spondylitis and advocate for research and policy changes that benefit the community.

Advocacy and Engagement

About

Team members

Other teams at Spondylitis Association of America

Leadership Team