About

Live through my eyes, through the world of a sufferer of immune deficiency and Myalgic Encephalomyelitis (ME) who is offered no treatment and has to live with the fact that our Government are deliberately placing psychiatrists in positions of power to control policy on ME and ensure no biomedical research is under taken to find a cure – hence the promotion of ‘anti science’.

1 Comment (+add yours?)

  1. Erica Verrillo
    Dec 11, 2012 @ 12:19:14

    PLEASE POST!! CFS Treatment Book Giveaway!

    (This is my Christmas gift to the CFS/ME community – no catch, no hidden agenda – just a gift.)

    On December 22nd and December 23rd 2012, Amazon.com will be giving away free copies of Chronic Fatigue Syndrome: A Treatment Guide, 2nd Edition. Dr. Charles Lapp calls this “the book every patient should have.” The book includes over 100 effective treatments, spanning the full range of pharmaceutical and complementary modalities, an in-depth discussion of symptoms with cross-referencing to appropriate treatments, the latest research into the causes and mechanisms of the illness, doctors’ protocols, coping techniques, special sections for managing chemical sensitivities, dietary restrictions and the special needs of children, as well as extensive appendices covering resources, locations of doctors and clinics, local, national and international organizations, and internet ordering information. The book also features over 2600 useful links to further reading, research articles, and patient reviews. Don’t miss out on this opportunity!

    For more information go to: http://www.cfstreatmentguide.com.
    Blog: http://cfstreatment.blogspot.com/

    Reply

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