As a CFS sufferer diagnosed in April 2011 the lack of treatment for my disease is disgusting. Only treatment offered is CBT, being told by my therapist to fill out a activity log, use a step-o-meter and log how many steps I take a day. Also being told that maybe CFS WAS a virus but its NOT now its my brain thats giving incorrect signals. So I need to increase my activity. I feel this is discrimination - I'm in my house virtually housebound day after day after day. Cant even walk upstairs, make a meal, feel like I've got flu, swollen glands, terrible memory, loss of my independence and job and the pain is unbearable. PLEASE PLEASE give us something !!!!
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