Hey! I added you, if you don't mind. I'm so relieved to find someone with CFIDS that I can talk to. I've been suffering from debilitating, chronic fatigue for years now and it seems like only recently my family has been taking seriously the fact that it might be CFIDS. My pediatrician kept telling me it was "just stress", and my parents assumed it was something I would "grow out of." The same doctor had the nerve to tell me the illness didn't really exist. We've been getting a lot of testing done lately, but I match the criteria for CFIDS perfectly, and so far nothing has really come up. When were you diagnosed?
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