Welfare Reform (People with Disabilities)

Debate between Natalie McGarry and Chris Evans

Tuesday 30th June 2015 Westminster Hall

[Natalie McGarry (Glasgow East) (SNP)]

Thank you for the opportunity to speak in this debate, Sir Roger. I thank the hon. Member for Oldham East and Saddleworth (Debbie Abrahams) for making a necessary and pertinent examination of what is happening in the welfare state, with particular regard to disabilities. As the SNP spokesperson on disability, this is a matter of great importance to me.

We have had some good speeches today, and I particularly welcome the conversation about the narrative that we spin around disability. The general election was particularly bruising, and for disabled people to hear parties talk not about being the party of people with disabilities, but about hard-working people, with the inference that people who are not in work are not hard-working and do not aspire to be, damages the debate. Today in the Chamber, my SNP colleagues are debating the Committee stage of the Scotland Bill, in particular welfare and disabilities. Many of the amendments in our name are aimed at ensuring that the Scotland Bill delivers more devolution and does not devolve further austerity and shackle the Scottish Parliament to further Tory attacks on the welfare state. They are the result of extensive consultation with civic Scotland and work done in partnership with other organisations.

Just this morning, 12 of Scotland’s leading third sector organisations published a letter in The Herald, timed to coincide with today’s debate and ahead of the emergency Budget next week, expressing grave concerns about the severe detrimental impact of the Government’s austerity measures on low and middle-income families. In particular, they highlight the threat to tax credits and other support that would fall within universal credit and say to us, here in this House, that as, we begin the process of defining the shape of Scotland’s social security system, we need to

“understand how high the stakes are”.

It is incumbent on every one of us—not just those from Scotland—to listen to those voices. The groups that have put their heads above the parapet on this matter are some of Scotland’s largest and most influential civil society organisations, including Citizens Advice Scotland, Barnardo’s Scotland, the Child Poverty Action Group in Scotland, the Church of Scotland, Inclusion Scotland, One Parent Families Scotland, Oxfam Scotland, the Scottish Trades Union Congress and the Trussell Trust. These organisations bear on their shoulders much of the burden of mopping up some of the worst effects of austerity on the most vulnerable in our society.

The UK Government’s programme of welfare reform has had a devastating impact on too many people across the country. In Scotland, the Scottish Government estimate that UK Government welfare cuts have reduced welfare funding in Scotland by almost £2.5 billion in 2015-16 alone. That estimate comes before the additional planned welfare cuts of perhaps £12 billion across the UK, which can only have a further devastating impact on communities across Scotland and the UK. Where will those cuts be made? How much more can be cut?

What is absolutely clear is that people with disabilities are disproportionately impacted by welfare reform, which fits in perfectly with a pattern whereby the UK Government’s cuts programme hits the most vulnerable in our society hardest, punishing them for the reckless damage done to the economy by the few at the top. Further planned cuts can only cause greater and sustained damage, driving yet more households into poverty and desperation. The roll-out of the personal independence payment has been riddled with delays and errors, which have caused a great deal of distress and hardship for people with disabilities. BBC News reports that 78,700 people are currently waiting to hear whether they can claim PIP, 3,200 of whom have waited more than a year to have their claims processed and 22,800 have waited more than 20 weeks. In June 2015, a High Court judge ruled in favour of two PIP claimants who had had their applications delayed by around nine months, to the detriment of their health and financial security.

[Chris Evans (Islwyn) (Lab/Co-op)]

Is the hon. Lady as concerned as I am by the Motor Neurone Disease Association finding that, accompanied with the move to PIP and universal credit, people with MND are now expected to attend face-to-face assessments, despite clear medical evidence that such assessments have a severe impact on their condition?