This is a bit of a vent, cry, shout and things along those lines.
I just discovered today that I’m due an ESA assessment next year.
Why, when I’ve got a progressive disease? Answers not necessarily required.
In 2013 I was due a second assessment, first was 2011.
I went through the route of “unable to attend”.
Doing this meant I ad to prove why not so I contacted my MS nurse.
After this I received a letter saying I’d been awarded esa support group.
I’m scared it’ll be ANOTHER benefit I’ll get less from because “Oh you look well, you don’t seem disabled” situation.
It is soo unfair. I just want to AAAARRRGGGHHH!!!