SAA receives no government funding and relies on the generous donations from individuals to create and maintain the programs and services aimed at improving the futures of the 3.2 million Americans affected by spondyloarthritis.
John and Maya’s paths first crossed near Rochester, New York at Sunshine Camp—an amazing, week-long escape for children living with muscular dystrophy. They met in…
I am very excited and honored to congratulate the Spondylitis Association of America (SAA) on 30 years of service and support to the Spondyloarthritis Community.…
We hear a few different terms to describe ankylosing spondylitis (AS) and related diseases: Spondyloarthritis, spondyloarthritides and spondyloarthropathy.…
Spondylitis Association of America (SAA): Can you describe the following blood tests and what they look for? Also, how...
A collection of questions about medications answered by SAA Medical Board Member Dr. Lianne Gensler.
Physicians and scientists relentlessly search for clues as to what causes or affects a disease. Is it more common in women or in men? Is...
Barbara Schiller held a dinner at Poor Herbie’s in Madison, NJ to raise funds for SAA and spread awareness of ankylosing spondylitis in her community.…
Does it take you more than 30 minutes to fall asleep at night? Do you wake up during the night and have a hard time…
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