SPONDYLITIS ASSOCIATION OF AMERICA
September 3, 2013
When my doctor told me that I probably has AS, I was mystified as to what that meant. All the information that I initially found told me that I would eventually turn into a bent over, stiff-spined, disabled victim. I am so grateful to SAA for all the current, thorough information that they offer. From their educational articles I learned that this didn't have to be my fate, and from their discussion forums, I got my questions answered by others with the same experiences that I had. The support and valuable conversations I have had there have changed my life, and now, 10 years later I am able to offer words of support to others. SAA is the best!
Ways to make it better...
If I had to make changes to this organization, I would...
Increase the educational marketing, to reach even more people and make others aware of this disease.
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