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.
20 years ago, I was out of medical options for my ankylosing spondylitis. It was before the biologics came out and I had life threatening consequences to the existing medicines. I needed a new plan. At my…
In March of this year, the SAA had the opportunity to exhibit at a medical conference for Primary…
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...
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