For those that don`t know, Tiegan, our daughter, has been suffering with ME now for the last 11 years. It has been getting progressively worse to the point that she is completely bedbound, unable to lift her head, communicate, tolerate light or sound or touch and has been tube fed for the last 4 years, unable to eat, drink or swallow. We hope to raise more awareness for this devastating, misunderstood neurological condition. Do you want to join me in making a difference? I'm raising money in aid of ME Association, and every donation will help. Thank you in advance for contributing to this cause which means so much to me. More information about ME Association: The ME Association supports people with Myalgic Encephalopathy (M.E.)/Chronic Fatigue Syndrome through all stages of their illness.