I am all for "Being in the Know" but in reading some group responses on the 23andme website it is clear many are new to Spondylitis. I have learned more in groups and forums in the last two years than I have known in the last nearly 30 years since my diagnosis.

Here's wishing more of the medical community takes heart to DNA studies as well. smile as what you don't see is not always what you don't have!