1. Hannah Goodfellow Hannah Goodfellow United Kingdom says:

    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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