1. As a CFS sufferer diagnosed in April 2011 the lack of treatment for my
    Hannah Goodfellow Hannah Goodfellow United Kingdom says:
    January 25, 2013 at 8:46 AM

    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 !!!!

    Reply
The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
(Logout)
Post

Terms

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

Provide Feedback