My wife and I returned from our honeymoon in may and a few weeks later she started to experience the first signs of what turned out to be M.E. With little awareness it was a struggle for herself, like many others to ever get a diagnosis. But thankfully lorraine was finally diagnosed in January this year. Lorraine has struggled with the condition for over a year now but continues to stray strong through many hard times whether it be with extreme fatigue or disabling pain. With the help of a support group lorraine has been lucky to see some improvement with fatigue but still struggles with very bad pain. I want to raise awareness of this condition for many people who suffer with this, whether they’ve had a diagnosis or not. Please help me raise awareness and your donations will be much appreciated.