I'm starting a full time education course in September, am on full rates PIP and ESA. It's going to be tough, because my physical and mental health have left me pretty much housebound for the last two years.
I know I couldn't work though, I just don't have the consistency to be reliable enough for a job, I might be able to manage a day or two (and now I have to find a way to manage three) of carefully organised activity with support (thank you ALS), knowing I can back out when I can't cope with it.
My physical ability is severely limited too, I can stand and sit for a bit, but I can't lift anything heavy, or hold a pen, or bend to pick anything up, so a lot of jobs available at my qualification level (none) are pretty much not things I could do.
Heck I could probably get a job, it's just consistency again that I'd cope with, my physical health fluctuates a lot, sometimes I'm well enough to push through the pain and fatigue for a bit, but other times, I'll get an infection that would last for a few weeks and leave me bed bound. I'd be letting people down a lot, and right now I don't think that is the right thing to do.
The college is an attempt to begin training to find a way to work alongside my disability, and something to try to counteract my current mental health issues. It's also for fun. I am able to achieve it because of these benefits, life before would basically have been stuck at home, not able to manage pain, poor mental health, and absolutely no quality of life. I am thankful that there is some support to allow me to enjoy life and struggle a lot less.
I know my best friend, who has been disabled for life with cerebral palsy, who has pretty poor mobility as it affects her lower half, and has mental health difficulties due to brain damage, has stewarded events when well enough, she also spends weekends away at LARP events when she is able. She's still disabled and would find working difficult, much to her frustration as she loves to work, but has found it getting harder and harder as she now has arthritis in her spine due to the pressure from spasticity in her legs, because she walks and refused to use a wheelchair.
We have both worked and had to stop because our health has worsened and we are both looking for ways to work again with our disabilities as they are now, whilst also being parents and having a decent quality of life.
What I mean by this is that on the outside it might look like they're doing really well, but the effort put into looking like they are doing well doesn't show, and they know best what they can and can't do, so if they've been assessed and awarded these benefits, unless you know for sure they are faking it (and I have no idea how anyone can) I wouldn't judge them.