SAA’s Advocacy Committee invites you to join our efforts to effect positive change by taking an active role. Stay informed, raise awareness, and contact your elected representatives!
Join in and become an advocate for people living with spondylitis. Together, we can work to increase public awareness, improve access to health care, increase federal research funding to cure spondylitis and influence public policies that impact the spondylitis community.
The Spondylitis Association of America (SAA) is the leading nonprofit organization in the United States, dedicating its resources to the active support of people living with spondylitis. We strive to bring about increased awareness, education, and research to ensure a better life for all those affected by spondylitis.
Strategic Priorities:
Promoting earlier diagnosis and treatment of spondylitis
Promoting public awareness and education about spondylitis
Improving access to appropriate quality health care and medication for all people living with spondylitis
Increasing federal funding for spondylitis & arthritis research
Affecting public policy that impacts the lives of people living with spondylitis
Committee Members
Dr. Robin Dore, MD
Victoria Greenberg
Dr. Mark Haupt, MD
Victoria Killian
Dr. Erin Arnold, MD
Sal Marx
Christy Taylor Gentry
Daniel Wilson
Sara Shaw
Staff
Richard Howard, MBA
Lisa K. Magno
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