A lot of people on here seem to think that cuts to disability benefits are a good thing and more disabled people should be able to work well I have had experience of this and it was hell on earth. I was diagnosed with epilepsy at 21, fibromyalgia at 25, chronic kidney disease at 27 and narcolepsy at 35.
when I was 35 (now 40) I gave up working after trying to hold onto jobs. In a nutshell every time I was taken on bosses promised the earth in support but the reality was very different and each boss apart from 1 ended up hating me for no other reason then struggling with disabilities. I was belittled many times, shouted at in front of other staff, one boss even tried to make trouble in the next job I had.
when I was first diagnosed with epilepsy at 21 I was let go on heath and safety grounds after a period of sick leave and I didn’t work till I was 24. I had been there since I was 18
from 24 till 32 I worked in a job that was ok until a new boss took over after 3 years in the job and removed all my adjustments.
from 32 till 35 I worked in a job that gradually wore me down and my old boss tried to cause trouble for me.
So out if 4 bosses 1 worked with me to put in reasonable adjustments, supported me with access to work and was great. 3 were terrible. I honestly think this is how it would be out in the word of employment for many disabled people- out of 4 bosses 1 would be great.
so if anyone wants to ask me about the reality of being disabled and employed and the attitudes toward me then please go ahead
just a little sub note when I did get access to work it actually cost more then my now benefits do as I had a full time support worker.