I am about to see a neurologist as my doctor thinks I have me/cfs. I am ill most of the time and get stressed easily this makes me very ill! I am soooo nervous about this neurologist appointment. Has anyone else had to go see a neurologist regarding diagnosis of cfs? What happened at the appointment? If I have an idea what to expect I will stress less and hopefully will be able to get out of bed and attend the appointment! (stupid possible cfs!) I realise that everyone is different I just want some sort of heads up! Can anyone help me out im scared. I have a 9 month old daughter and I hate stressing as she picks up on it. HELP I would appreciate it!
Laura