Anyone have a good CFIDS letter to explain to friends?

Discussion in 'Fibromyalgia Main Forum' started by Bacci, May 14, 2003.

  1. Bacci

    Bacci New Member

    I have been wanting to do my part in awareness by sending a mass email to all my friends and family. It is amazing how after five years, most of them still don't get it (and none of them have any interest in taking the initiative to research it). So, I was wondering if anyone out there had a good letter or research item that explains CFIDS, it's unknown causes, it's symptoms, treatments etc in a few pages or less? I have seen a few go through here, but not quite what I have been looking for. I am trying to avoid writing it myself because it's too exhausting!

    I'd be interested to see anything you might have.

    Thanks so much!!!