Seeing the neurologist today. Rather nervous as I have absolutely no idea what to expect. The nerves are stopping me from sleeping - it’s 5am already and I’ve had no sleep. I am going to be in a bad way by the time my appointment rolls around.
Every part of me aches. My chest feels like I’m being physically pinned down.
I have an appointment at the job centre to discuss the decision ATOS have made but ATOS haven’t even bothered to get in touch with me. I have no idea what their decision is, if they’ve even made it. I sent my form to them almost three months ago now.
I’m not even sure if I can get out of bed, let alone head to the job centre. Screw this.
Does any one else have respiratory problems with their cfs? When I get really bad I find it hard to breathe/start wheezing and I don’t know if others suffer from that or how common that is.
Wtf is with the porn in the cfs tag?
Silly body, I know it’s ME Awareness Day but I’m already pretty aware, how about not making me feel sicker?
She has the strength of 1.5 kittens!
She can move at the speed of a tortoise with a limp!
She can do almost nothing!
It’s all in a day’s work for
dun dun dun
CHRONIC FATIGUE GIRL!