(8 years, 9 months ago)
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That is a fine intervention, and I agree with the point the hon. Gentleman makes. I was not going to focus particularly on rural issues, but he is absolutely right. I live in a rural area and I know that, particularly in England and Wales, the cuts to public transport and dial-a-bus services have compounded the problem of people being unable to manage when they lose their Motability vehicle, so I agree wholeheartedly with that sentiment.
I congratulate my hon. Friend on securing the debate. My constituent, Claire Ross, is 15 years old. She lives in a rural area and has a brain tumour, meaning that she becomes tired easily. Her Motability vehicle was used to take her to school and to hospital appointments. A recent reassessment removed the component from Claire and now the vehicle sits, unable to be used, at her parents’ house. Does my hon. Friend share my concern for Claire now that the Motability component has been taken away from her, and does he agree that it is shameful of the Government not to respond to my numerous representations on her behalf?
I wholeheartedly agree, and I find it incredible that nobody has responded following my hon. Friend’s inquiries. I think most hon. Members here will have very similar examples from their constituencies, which highlights how unfair the measures are. I will come back to that, which is something the Government really need to take stock of. They should be working tirelessly to support the independence and inclusion of disabled people, using all means possible through Government channels.
An example of the concerns we have heard is highlighted in a briefing paper from Muscular Dystrophy UK. Trailblazers, which comes under the umbrella of that organisation, is a group of young disabled campaigners aiming to tackle the social issues affecting young disabled people, such as their access to higher education, employment, and social and leisure opportunities. These are young people who fully understand the difficulties they face in life. They are campaigning to raise awareness of this issue and to support others. They also know the possible consequences of the new PIP assessment.
One trailblazer commented:
“I suffer from muscular dystrophy and I am still able to walk, although it is difficult. I frequently push myself to live my life as much as I can, despite fatigue and anxiety that comes with it. I am absolutely terrified that one day, be it tomorrow or in a year, I will receive the letter that tells me I need to be reassessed for PIP. As someone who can stand and does not ‘look’ disabled at times, I believe I will have no chance of retaining my car.”
They added:
“If I don’t have my car, I simply would not go out.”
This is a young person who knows how independent they have become since being able to access a car through the Motability scheme. Imagine being aware of the life transformation that they went through and the absolute dread of being forced to return to the pre-car state.