Hello all.... As a fellow sufferer for 8 years I do know the range of symptoms that Fibro/ME/CFS brings. But I wonder if all the negativity and moaning on this site actually helps... Yes, it is very painful to move especially after being in bed for several hours, yes, insomnia sucks etc etc. But please wouldn't it sometimes be great to read blogs about good times, helpful health professionals, and supportive famillies. Little things that have proved positive for you, wether that be food, exercise whatever. At the moment anyone reading the blogs on this site must think they have fallen into the doomed depths of despair. Things are not easy I am not playing that down, but come on guys, we are fed, watered, have a roof over our heads and the condition is not terminal. Lets have some positive action too. I expect to be blasted by some readers, but I have also have a right to express my views.
Take care Annie.