I think that the point here is that there are thousands of people whose basic needs will no longer be met. If you are able bodied on Jobseekers allowance, for instance, you receive an amount of money which is considered the minimum amount that you need to live on. If you are disabled, you are getting less than this already, but we carefully budget, learning disabled people have assistance to make sure they can afford what they need. There is a ton of research to say that the price of living for a disabled person is significantly higher than that of an able bodied person, and these cuts are going to make them REALLY suffer.
IMO it's a human rights issue, we have a responsibility to take care of our sick, elderly and vulnerable, but they are becoming more and more isolated at a time when they are also expected to go out and find work. How is a person with mobility difficulties, living in a care establishment, going to get to work if they have no transport?
I know first hand what it's like. I have been a single mum to a severely autistic dd for 9 years and I have lived on a tight budget, trying to give my dd what she needs as well as take care of my son, my home, oh yeah, and myself somewhere along the line. She is now in a residential school and comes home regularly at weekend. Under the new rules she will lose her mobility allowance, meaning that the social interaction that she needs will not be possible when she is home. She will not be able to go anywhere so I can teach her how to cope with the outside world. She has epilepsy, and without the car I would struggle to get her to hospital without an ambulance, or home if she is ok but needs to rest. She has behavioural difficulties which mean that if we have to leave somewhere, we have to leave NOW! I can't do that if we have to go and wait for a bus, she has no sense of danger so could run into the road, or she might push me into the road, leaving her alone and vulnerable.
On top of that, I have to attend regular appointments at her school and residential placement, drive her backwards and forwards between home, resi and school, and be able to get to her in an emergency day or night. So even when she is not with me, I need the car that she is entitled to, or at least the cash to pay for a taxi. Without her mobility allowance I have no way of doing anything.
The rocketing price of fuel is making it hard enough to run a car for her, but I struggle on, to take the car away completely will pretty much mean that my dd will be completely isolated from her friends and family, and I will never be able to see her.
I don't have the answers to the government problems, but that money MUST come from somewhere else, they are infringing on people's RIGHTS here, not just inconveniencing them. If my story doesn't convince you, then have a look at the Mencap website, or the Scope website, or one of the many other major disability charities for more stories of how people will suffer. Then tell me it's fair and right.