Levi just posted this article from San Diego News Network on the media thread. Chronic fatigue patients fight a ‘lazy’ label, advocate for awareness But you don't look sick: San Diegans suffering from mysterious and misunderstood chronic fatigue syndrome battle daily life I thought it was a great article. Oh rats – another letter to write(email below)! It’s over 1,000 words I’d guess. Uses 2 patient egs – and starts with a man. Very well written and easy to read, good photos. The approach is one of starting with negative reactions that are common, then giving the info that dispels the myths + builds empathy. Eg Then Kim McCLeary is quoted numerous times and there’s a cfids link. Maybe they’re starting to step up! Then xmrv is mentioned in the middlish (I don’t get her cfs me distinction) Definitely worth the energy for a full read, I’d say. Final note – I like all the tags she put at the end (see below) – from what I remember of page optimizing, this article is going to get a lot of hits because she did that. Happy reading! islandfinn By Jennifer Reed, SDNN Jennifer Reed is SDNN’s health and wellness editor. She can be reached at email@example.com Tags: AIDS, Bob Deering, CDC, Centers for Disease Control and Prevention, CFIDS, CFS, chronic fatigue and immune dysfunction syndrome, chronic fatigue syndrome, disability, Epstein-Barr virus, fibromyalgia, flu, K. Kimberly McCleary, lupus, Mexican Hairless Xolo, multiple sclerosis, myalgic encephalomyelitis, Nancy Gordon, science, SDNN, University of Nevada in Reno, Whittemore Peterson Institute, XMRV This entry was posted on Saturday, November 14th, 2009 at 8:42 am and is filed under Health, Lifestyle. You can follow any responses to this entry through the RSS 2.0 feed. You can skip to the end and leave a response. Pinging is currently not allowed.