For those that don’t know, I’m half in limboland with an FND diagnosis which includes CFS and have been referred back to a neurologist, so I still have a question mark against MS.
I applied for Personal Independence Payment back in April and have recently had a letter saying that an assessor will be visiting me next week. In fact, I’m sitting here waiting for them to 'phone me (they tried last night but I was putting my littl’un to bed).
So, does anyone have any tips? I’d like to provide as much information as I can.