Disabled Students’ Allowance Scheme

Baroness Thomas of Winchester Excerpts

Thursday 9th December 2021 Lords Chamber

[The Lord Privy Seal (Baroness Evans of Bowes Park) (Con)]

My Lords, the noble Baroness, Lady Thomas of Winchester, wishes to speak virtually. I think this is a convenient point for me to call her.

[Baroness Thomas of Winchester (LD) [V]]

My Lords, a student I know with the hidden disabilities of ADHD and dyslexia has had very good support from Brunel University because she had been told about DSA not at her school but at her diagnosis. Could the Minister encourage all schools to be more proactive in explaining the benefits of DSA?

[Baroness Barran (Con)]

The noble Baroness makes a good point and it is helpful to have a specific example. We work very hard to raise awareness of DSA through multiple channels, but there is still a significant gap between the number of registered disabled students at university and those who access the grant.

Young Carers

Baroness Thomas of Winchester Excerpts

Thursday 23rd March 2017 Lords Chamber

[Lord Nash]

Again, I make the point that the first step is to identify them. The Children and Families Act now places an obligation on local authorities to assess their needs and support them, where they request it. However, we need to do more to identify them in the first place.

[Baroness Thomas of Winchester (LD)]

My Lords, I remind the noble Lord’s department that some young carers do not identify themselves with the words “caring” or “carer” if they care for a disabled parent. The noble Baroness, Lady Grey-Thompson, has confirmed this. They undertake this caring as a matter of course and have done so all their lives. They need to be identified but they may not know the word “carer”.

[Lord Nash]

The noble Baroness makes a very good point. Again, our guidance to schools is helpful in this regard. As I say, the work we are doing with schools and school nurses will, I hope, make sure that all pupils are aware of what the terminology means.

Queen’s Speech

Baroness Thomas of Winchester Excerpts

Wednesday 3rd June 2015 Lords Chamber

[Baroness Thomas of Winchester (LD)]

My Lords, before turning to my remarks on the welfare part of the gracious Speech, I will pay tribute to the former Minister for Pensions, my erstwhile colleague Steve Webb, who played such an important part at the DWP. His knowledge of the complex worlds of both benefits and pensions was unparalleled. I also mention Mark Harper, the most recent Minister for Disabled People, who has now risen to the giddy height of government Chief Whip in another place. He was very good at listening to those of us who are disabled here and I hope that his successor, Mr Justin Tomlinson, will be found similarly approachable by some of us here. After all, this House probably beats the other place in its number of disabled Members—although one must never forget those with hidden disabilities.

Before going on, I declare my usual interest in receiving DLA. The noble Lord, Lord Freud, who I am afraid is no longer my noble friend but I hope is still a friend, will not be surprised that those of us who focus on welfare in this House are understandably fearful of the £12 billion of planned cuts in the unprotected parts of the DWP budget. This will be a recurring theme this afternoon for those of us speaking about welfare, as the noble Lord, Lord Fowler, did. We do not know nearly enough about where these cuts will come. Might this mean taxing or means-testing disability benefits? Even the Times called this a “nightmare policy”. All we know, I think, is that some research was commissioned on this, but I note that it has not been ruled out—as was, two days ago, the limiting of child benefit. We will, almost certainly, have to wait until the Budget next month, and then the comprehensive spending review in the autumn, to find out the full details.

The only policies in this area which have been announced are a reduction in the benefit cap and the freezing of child benefit and a number of working-age benefits and tax credits. What we do not know at this point is what impact these policies will have on some of the most vulnerable families. More of them will have to move out of expensive housing areas such as London, and the pressure on local welfare assistance schemes and food banks is likely to increase.

The whole subject of local assistance schemes, and how they should be taken forward, is worthy of a separate debate, such are the questions it throws up, but there is no time for that today. I commend the Social Security Advisory Committee’s report on this, published recently. I am glad that the Government are keen to get more disabled people into work by halving the gap between disabled and non-disabled people. That is a very ambitious aim and I hope that we hear more about how it is to be achieved. I hope that the noble Lord can give us a commitment not to cut the Access to Work budget, which is surely a key part of getting disabled people into work. I am very pleased to hear that the referral process has been made simpler and that the mental health support services contract appears to be secure. What is now needed is another push to publicise the mental health part of the scheme and the whole Access to Work initiative, but there is no point in this unless the budget is safe.

Under the same heading, I am afraid that I make no apology for mentioning yet again how concerned I am at the move from 50 metres to 20 metres in the personal independence payment assessment, which is extraordinarily harsh and will mean that thousands of disabled people are likely to lose the enhanced rate of mobility allowance, and thus their Motability cars, when the bulk of reassessments start in October. This will surely not help the Government’s stated aim of getting a lot more disabled people into work, and will particularly hit disabled people in rural areas. I know that PIP guidance is now statutory, but I wonder whether that is really making a difference. I am not holding my breath that the descriptor will be changed, as I think it should be. All I can hope is that the healthcare assessors working for Atos and Capita who do the PIP assessments are diligent in reading any supporting letters from a claimant’s doctor, consultant or physiotherapist, and that they closely question the claimant about whether they can walk the short distance in the test even if there is a gale-force wind blowing, an icy surface, or they have to cross a busy road with kerbs—and, of course, whether they can walk this distance, not too slowly, several times a day if necessary.

Lastly, I look forward to the work of the post-legislative scrutiny committee on the Equality Act 2010 as it affects disabled people. Many people think that anything enshrined in law is done and dusted, which is why it is necessary to see exactly how the law is working, and whether some more dusting needs to be done.