I am new to this site and after years of suffering on and off with pain, i feel i am now starting to get somewhere. I have had the tests for MS and have now been refered to a rhumatologist. It was my best friend who unoffically cares for me who researched Fibromyalgia and said having looked on the NHS site that all the symptoms and tests and explanations i have had over the years where echoed by many of you. Even symptoms that i have that i just put down to me are echoed on here.
Finally my doctor said at my last reveiw that he thinks the outcome of my results will be Fibromyalgia. I have read alot of posts on here and it is reasuring to know what is to come and that there is support and somewhere to come and talk when things get hard.