As some of you know from reading my site, I try to be active in well FMS/CFS activism. I believe that we need to spread awareness about these condition because awareness, in my opinion, will lead to a better understanding (and hopefully more respect from the medical community and a CURE, or at least a treatment option that works. <img src="/images/graemlins/laugh.gif" alt="" />
Regardless, the Million Letter Campaign is set to happen in May of 2005. There's been a few important updates to my article. Please check 'em out and keep this in the back of your mind. I really appreciate it.
Here's the link to the article.
http://www.bellaonline.com/articles/art22495.asp
