Just wondering about that. I've been writing a letter to my family trying to explain the little I know so far about this MTHFR stuff (I haven't sent it yet) , and now I don't even know what to tell them - "Here's where you COULD HAVE gotten affordable testing". Understandably, I see the importance of sharing this info with others who are in my same gene pool, who might REALLY avoid some nasty health consequences with just a little bit of the right information. Are there other companies/sites where they could still get this done? Here or out of the country (since this might be a necessity in the immediate future!) It doesn't seem clear at all what the status of 23andMe is currently, or might be in the future. This is probably fodder for a different post, but I am really ticked off about this seeming witch hunt by the FDA. I can practically smell the big money and influence behind all this. God forbid us citizens actually get inexpensive, and important health information about ourselves. (!!!!) Thanks!