(8 months, 3 weeks ago)
Commons ChamberThe hon. Lady makes a valid point. There is always more that Governments and local authorities can do, and thank goodness for the charity sector. Charities that support people with learning disabilities do great work.
We have a project called Rumbles in Nottinghamshire that runs two cafés, one outside my constituency and one in Ashfield on Sutton Lawn. It has been running for about 15, 16 or maybe 17 years and was set up to help people with learning disabilities. There are a couple of paid staff who train young people with special educational needs or learning difficulties in cooking, cleaning, doing the washing, serving people and operating the till. Those are great skills for young people with learning difficulties. It gets them out of the house, and gives their parents and families some respite. They get out and learn new skills and mix with people, making new friends. It is absolutely brilliant that we have these initiatives locally.
However, we have a slight problem and the Minister might be able to help me with it, because he came to visit the café earlier this year. This service, which is a lifeline to people and their families, faces the axe. This brilliant facility is facing closure after about 17 years in operation. The charity was paying the council a peppercorn rent of just a few hundred quid a year, I believe it was, but the council decided that it is such a good business it wants to put the rent up to £7,000 a year and it also expects the charity to maintain the public toilets next door at a cost of £10,000 a year. The charity has agreed to pay the £7,000 and it has some extra support to do that, but that is still not good enough for the local authority. The local authority does not realise that if this place closes and goes into the private sector, the young people with learning disabilities will have nowhere else to go. If this place goes, they cannot do their training and their work or meet their friends. I hope the Minister might be able to help and steer me in the right direction on how to convince our local authority to keep this lifeline open.
My hon. Friend makes a really good point. Rumbles café—there are several across Nottinghamshire—does fantastic work with young people with learning disabilities, getting them into the workplace and supporting them. Does he agree that it is slightly strange that Ashfield District Council says that the closure of the café and kicking them out of the building is about the money, when only a few years ago the councillors spent five or six times as much to give themselves extra cabinet jobs and put it in their own pockets?
My hon. Friend is quite right—I forgot about this—that just a few years back, this same bunch of councillors created five extra cabinet positions when they first got elected, at a cost of about £60,000 and then created a political officer position at a cost of another £30,000. That is £80,000 or £90,000 there, so their maths do not stack up. In fact, their maths do stack up when it comes to giving themselves hefty pay rises, so maybe they should take a long, hard look in the mirror. I thank my hon. Friend for that intervention.
Rumbles café has helped literally hundreds of people across Ashfield over the years. I want to give a special mention to a lady called Helen Storer. She is 60 years old, bless her, and she lives in Selston. She has special educational needs—she says herself that she has her own difficulties—but she lives independently, on her own. She relies on the support of good neighbours and good friends in the community—it is a cracking community—and she worked at Rumbles. She volunteered there, learned new skills and made friends. She learned how to cook and other life skills, such as how to do housework and stuff like that, and she absolutely loved the place. It brought her on leaps and bounds.
Places like this are a lifeline. It should not be about making huge amounts of money. We should put people before profit in these sorts of situations. Look—it does make money, but it goes back into the caff to help support people to learn those new skills to live independent lives. It has no shareholders, just honest hard-working folk who are doing the best for people with special educational needs in the community.
I have said it before, and sometimes I get a little bit of opposition to trying to get people into work, especially disabled people. It is not cruel to get disabled people back into work. Most people, as we know from Mencap’s own figures, want to work and want to get into the workplace. It is up to us as a responsible society to try to give the support they need to get in the workplace and have a stake in society. I often think about little Jossie and her mum and dad, and the challenges they face. When parents have a little girl of six or seven who has got her difficulties, they are always thinking, “What’s going to happen to that little girl when she leaves school?” They want that little girl to have lots of opportunities. They want her to live independently and to be able to make some of her own decisions and just do the simple things in life—to go out and shop, run the house, budget, have friends and have a social life. That is so important. Not everybody like Jossie can live an independent life, but a lot can, and it is important that as a society we support these people.
We are very good at giving benefits away in this country to people, and rightly so—people need that financial support. With rent and council tax support, personal independence payment or disability living allowance, employment and support allowance and other bits and bobs, a single person with learning difficulties can maybe get up to 25 grand a year through the benefits system. I always say that if we can pay somebody on benefits 25 grand a year for being sat at home, surely we can pay them that for going to work, whether the support is from a charity, a Government-funded agency or whatever.
I am going to close on that. Once again, Mr Deputy Speaker, thank you for allowing me to speak tonight. This is a subject close to my heart, and I know from my right hon. and learned Friend the Member for South Swindon (Sir Robert Buckland) that it is close to his heart as well. I look forward to seeing what the Minister has to say.
(1 year, 5 months ago)
Commons ChamberIt is important that we take into account the issues of poverty and regional variations to which the hon. Gentleman refers. They lie right at the heart of all the decisions we have taken. We have come forward in recent times with significant cost of living support measures. My hon. Friend the Member for Mid Sussex (Mims Davies) will be taking through the remaining stages of the Social Security (Additional Payments) (No. 2) Bill this very afternoon to address the people to whom the hon. Gentleman refers.
I do not know whether my right hon. Friend saw my article in The Times a few weeks ago, but it discussed opportunities for towns, such as Mansfield, that have specific local requirements when it comes to tackling economic inactivity, the opportunities of building bespoke local schemes with local employers and training providers, and the opportunities from those relationships on a local level as part of a wider strategy within the region. What is his stance on devolving decision-making powers in this space down to local areas?
My hon. Friend raises a significant and important point. There are areas, particularly around the Work and Health programme, where we have done exactly that. We are engaged in discussions, contingent upon or subsequent to the White Paper that the Department for Levelling Up, Housing and Communities published on levelling up, and in particular with areas such as the west midlands and Greater Manchester, to make sure that we leverage the knowledge, know-how, expertise and all the resources they have at the local level to continue to bring people back into work.
(1 year, 5 months ago)
Commons ChamberThe problem is that the Government are one-trick ponies. They think that that is the answer to getting people back to work, but what we need is a plan to deal with the economically inactive, not just to apply conditions for those receiving unemployment-related benefit on universal credit.
Different parts of the country face different economic needs. In broad-brush terms, in coastal and some former industrial areas, we tend to see lower labour market participation rates and relatively fewer vacancies. In many parts of London and the south-east, we tend to see higher labour market participation, but also relatively fewer vacancies. In major cities such as Birmingham, Leicester, Coventry and Liverpool, we tend to see lower labour market participation, but often higher vacancies. The point is that different economies have different economic needs. Different labour markets have different economic needs. Instead of nationally contracting to deliver one-size-fits-all employment schemes designed from behind a desk in Caxton House, and instead of forcing Mayors—in the words of Andy Street—to go with a “begging bowl” to Whitehall, we should shift power and resources to local communities because, as the leader of Nottingham County Council, the hon. Member for Mansfield (Ben Bradley), said in a very good Red Box article a few weeks ago:
“Local leaders are too often hampered by the Whitehall knows best approach…Employment support programmes are commissioned based on national guidelines, not local needs…Fixing economic inactivity needs a radical pro-devolution mindset.”
I absolutely agree with him.
I thank the right hon. Gentleman for his kind words and for giving way. I should mention that I co-wrote that article with Adam Hawksbee of Onward.
The right hon. Gentleman is absolutely right. He mentioned Mansfield’s statistics and the high levels of economic inactivity. These schemes are best built with local employers and training providers so that they can be bespoke for those needs, with the flexibility that was mentioned earlier; I am sure he would agree with that. Will he join me in calling on Ministers to pilot that in the east midlands when we get our combined authority next year?
Absolutely. Of course, a Labour Government will definitely deliver more resources. I hope that we can pilot that in the east midlands combined authority, as well as in the Leicester area—the hon. Gentleman will know what that is a reference to.
(2 years, 8 months ago)
Commons ChamberI am delighted, too. I am pleased to announce that more than 112,000 kickstart jobs have been started by young people across the UK. Many young people have found permanent jobs through kickstart, and we continue to work closely with employers to help young people find those long-term employment opportunities. We have helped employers to move kickstart participants into apprenticeships more easily by working with colleagues in the Department for Education to ensure employers receive the incentive payments for doing so.
How has the Department worked with DFE to ensure that people on universal credit who are accessing new training and qualifications through the various Government schemes do not lose their universal credit entitlement as a result?
(3 years, 1 month ago)
Commons ChamberI know that my hon. Friend takes a strong interest in her Jobcentre Plus, as she updated me following her visit. I remind Members that since September 2020, our enhanced DWP youth offer has provided wraparound support for 18 to 24-year-old claimants, providing a 13-week tailored pre-employment course. I am pleased that Stafford JCP is hosting an interactive kickstart event tomorrow; our JCPs do that kind of event and engagement regularly.
I am grateful to my hon. Friend for all her team are doing to support people back into work. In conversations with my local jobcentre staff this week, they reported very positive progress. They asked what opportunities there might be to consider extending kickstart-style schemes or incentives, so they are able to help out-of-work adults as well as young people. I wonder if my hon. Friend could help me to answer their question.
I am proud that our plan for jobs supports people, at any age and at any career stage, who are looking for new opportunities through, for example, our sector-based work academy programmes, our enhanced “50 PLUS: Choices” offer, and the new DWP “Train and Progress”, through which people can train for longer into a growing sector using the flexibilities built in within universal credit.
(3 years, 8 months ago)
Commons ChamberI thank the hon. Lady for her question. I know that she is focused on young people, as am I. She may have heard from the Secretary of State that we are absolutely determined about this and that that work is already embedded; it is part of kickstart. This placement is treated like regular work, so all existing schemes such as Access to Work can be used, and our young people in jobcentres will be able to discuss all the options via the work coach.
Earlier this month, I announced the £170 million covid winter grant scheme to help disadvantaged people, particularly children, through the challenging winter months ahead, with food and essential utility bills over Christmas through to the end of March. The first half of funding for the scheme will reach local authorities in England this week. I am delighted to say that Nottinghamshire has been allocated £2.3 million and South Gloucestershire £569,000.
Does my right hon. Friend agree that it is hugely important for the most vulnerable children—those whose welfare we know is a source of worry for their teachers when they do not see them for weeks—that we can offer the best possible help in the holidays, with proper structured and face-to-face support for those children and their families such as that offered through our holiday activity clubs?
I agree with my hon. Friend and he looks ready and dressed to support a holiday activity fund when the opportunity comes along. Maintaining that important link over the longer holidays can be transformative for children’s health and educational prospects, which is why I was proud to announce earlier this month the £220 million expansion of the programme for the longer school holidays right throughout 2021. This will offer enriching activities such as arts and sports, which will help them to perform better in school, as well as a free nutritious meal while they are there.
(5 years, 10 months ago)
Commons ChamberUrgent Questions are proposed each morning by backbench MPs, and up to two may be selected each day by the Speaker. Chosen Urgent Questions are announced 30 minutes before Parliament sits each day.
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As the hon. Lady knows, support is available in the system. I am sorry to hear about her constituent’s predicament. Of course, the whole point of universal credit is that it is a welfare system that also assists people into work. We have analysis that has been published that makes it very clear that under universal credit people get into work faster, stay in work longer and earn more.
I welcome the move to a system of benefits that no longer traps people out of work. A month into universal credit’s roll-out in Mansfield, staff at my local jobcentre are happy with the way things have progressed. Will the Minister confirm that under universal credit a million people who are disabled will see their regular income increase because of the new system?
I am pleased to hear that universal credit is rolling out in Mansfield and working well. I get a similar message when I go up and down the country. My hon. Friend is absolutely right: 1 million disabled households will on average receive an extra £110 per month as a result of universal credit.
(6 years, 5 months ago)
Commons ChamberWe are debating a number of important statutory instruments, and in the light of the time constraints, I will confine my comments to the measures relating to free school meals.
The benefits of free school meals for those who need them have been set out today and in the past. While it is absolutely right that we debate these new eligibility criteria for free school meals, although it is disappointing that there are no Liberal Democrats in the Chamber, it is also right that we do so with a focus on facts, not inaccurate claims—the Secretary of State made the position clear—that these proposals take away free school meals from children. In fact, as has been set out, it is estimated that by 2022, under the new regulations, about 50,000 more children—more, not fewer—will benefit from a free school meal than under the previous benefit system.
The approach in these regulations not only extends support to more children, but ensures, as my hon. Friend the Member for Fylde (Mark Menzies) made clear, that we target that support at those who most need it and where it will have the greatest impact in changing lives. As he also set out, the Government have always been open and clear that when universal credit was rolled out, there would be new criteria, but that no child currently on free school meals would lose out until 2022, and that those in either primary or secondary school would continue to benefit while in that school.
Much is being made of claims that 1 million children will have free school meals taken from them, but that is simply not accurate. I am not usually one to cite “Channel 4 News”, but on this occasion, like my hon. Friend the Member for Croydon South (Chris Philp), I will quote its FactCheck verdict, which reads:
“This is not a case of the government taking free school meals from a million children who are currently receiving them. It’s about comparing two future, hypothetical scenarios, one of which is more generous than the other.”
Both of them are more generous than the old benefits system.
I will not, because I am conscious of the time.
An issue such as this, which is of real importance to many people, quite rightly excites strong passions and strong arguments, but it is important that we stick to the facts. An Opposition who are unable to muster coherent arguments against actual Government policy are instead taking issue with hypothetical Government policy and scenarios. I am committed to ensuring that disadvantaged young people can get a free nutritious meal at school, and I am sure that that is true of all colleagues on both sides of the House, regardless of where they stand on these two hypothetical scenarios. These measures mean that more people will be able to get free school meals than at present, which is why I will be voting with the Government to extend the eligibility for free school meals.
Opposition Members know that I have been the first to stand up and challenge the Government on universal credit, and the Government have listened. First, at the 2016 autumn statement, we reduced the taper rate from 65% to 63%, which cost the country £700 million but put around £300 into families’ pockets. Secondly, I worked with the Government at the end of last year to secure £1.5 billion of comprehensive improvements: two weeks’ extra housing benefit for those transitioning on to universal credit with housing payments; double the advance payment and twice as long to pay it back; direct payments to landlords; and a slowed-down roll-out. Those were all things that the Opposition asked for, so I am staggered that they are asking us to vote against them today.
For the past two years, I have worked not only with my colleagues, but proudly on a cross-party basis to achieve those improvements. Today is a big wake-up call. These motions are not about improving universal credit, but simply about playing politics. I have seen that for the first time. The Government have taken the time to understand how best to transfer a lump-sum benefit such as free school meals into a tapered system such as universal credit. An earnings threshold is perfectly acceptable to all reasonable people—by the way, we are talking about taxpayers. The only possible improvement I could encourage Ministers to look at is automatic entitlement if there is a disability in the family.
Let us get the facts straight. All reception, year 1 and year 2 children will continue to receive free school meals—full stop. The measures apply only to year 3 and beyond. All those currently receiving free school meals will continue to receive them until the end of their phase of schooling or 2022, whichever is the further away. Labour is creating false headlines by saying that any child will lose. Under the proposals, the Government will focus better on children who are in, or at risk of, poverty. That is, as we have heard, around 50,000 children by 2022.
Conservative Members know that no children will lose their existing entitlement to free school meals or free childcare as a result of our policies. Meanwhile, my jobcentre says that fear of universal credit is the biggest challenge that it faces in the roll-out. Will my hon. Friend comment on where that fear might be coming from?
My hon. Friend makes a valuable point. That fear is particularly prevalent on social media. There is a saying that a mistruth can travel halfway around the world before the truth has even put its boots on. That is happening with universal credit, aided and abetted by social media. Universal credit is not even in my constituency yet, but I hear from constituents who are worried about it. Oddly enough, I can put their minds completely at rest when I explain it to them.
As I have mentioned, tax credits recipients automatically get free school meals at the moment, which could mean that a family on £50,000 a year receives them. That cannot be right—[Interruption.] People on legacy tax credits who do not have disabilities in their family—those on the old benefit system who are transferring over—can have regular incomes of up to that level. The new system expands the criteria so that we can get to more children who need our support, not fewer.
Although I understand that a key part of any charity’s role is lobbying, I am disappointed in the Children’s Society. Its suggestion that 1 million children will lose free school meals is simply not true. Labour has jumped on that bandwagon, and it has taught me a lesson. There are colleagues from all parts of this House—SNP Members included—whom I trust and respect, and with whom I will continue to work to improve the lives of the most vulnerable in society, but if people think that the Labour party is the answer to tackling poverty, they are being misled. Today—this is a big wake-up call to me—the Labour party has clearly shown that it is prioritising headlines over improving the lives of struggling families. If you want a headline spun, Mr Deputy Speaker, ask the Labour party; if you want a competent job done, ask the Tory party.
(6 years, 5 months ago)
Westminster HallWestminster Hall is an alternative Chamber for MPs to hold debates, named after the adjoining Westminster Hall.
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I beg to move,
That this House has considered support for former miners with pneumoconiosis.
It is a great pleasure to serve under your chairmanship, Mr Bailey. I thank the Minister for being here to respond to the debate and colleagues for their attendance.
It is a privilege to have secured my first Westminster Hall debate on a subject of interest to many of my constituents and many in former coalmining communities across the UK. Mansfield has a proud coalmining history, which ended very recently—just a few years ago—when the nearby Thoresby colliery closed. For decades, the community was built around the industry, and we still feel many of its effects.
I applied for this debate because, although coalminers’ pneumoconiosis is not a terribly widely known illness, it is prevalent within mining communities and should receive greater attention. I have been contacted by a number of constituents and unions about this issue, which I am keen to raise directly with Ministers. I am asking the Department for Work and Pensions to work with the Department of Health and Social Care to review the diagnostic tools that are used to assess miners for signs for pneumoconiosis.
Coalminers’ pneumoconiosis is an occupational lung disease caused by the inhalation of dust from coalmines. It is often known as “black lung” and it causes thousands of death each year worldwide. Inhaled coal dust progressively builds up in the lungs over long periods, leading to inflammation of the lungs, fibrosis and even necrosis. The most common symptoms of pneumoconiosis are coughing and shortness of breath. The risk is generally higher when people have been exposed to mineral dust in high concentrations and if they have been exposed to coal dust for long periods.
Coughing and shortness of breath can, of course, be symptoms of a wide range of illnesses, which is partly why pneumoconiosis is often overlooked by health professionals and others. Even when a former miner presents to their GP with those symptoms, it is not always picked up straightaway. Most miners would recognise that a cough is inherent—part of the territory of working in those conditions—and many would not consider it a symptom of anything more than their career underground. Many therefore do not come forward early enough, and this is where the problem lies. We need to do more to encourage this conversation.
Many former miners who present with such symptoms are simply referred as out-patients to their local hospitals for standard chest X-rays. They will have had these X-rays regularly throughout their time in the industry and most will have been told that they have a clean bill of health on that basis. The trouble is that traditional two-dimensional X-ray films often do not show enough detail to diagnose pneumoconiosis, especially when the patient is in the early stages of the disease. The tell-tale sign of the disease is nodules in the lungs, which can be as small as l mm or 2 mm in diameter. When using X-rays for diagnosis, it is usually possible to pick up on pneumoconiosis only at a later stage, when large masses of dense fibrosis have developed in the lungs. By that stage, there is usually a notable decrease in lung function—in effect, it is too late.
A successful diagnosis is also less likely because of the time that has passed since the pits closed. The doctor they see now, who examines the X-ray, is less likely to have specialist knowledge of the industry and related illnesses. They are also less likely to have seen this disease before, so are perhaps less likely to spot it.
For the best results and the quickest analysis, a CT scan is the most effective diagnostic tool. CT scans show the lungs in three dimensions, which provides far greater detail and allows for a more accurate diagnosis. For many of us, it is surprising to learn that there is not a regular screening programme in place for former coalminers to pick up cases of pneumoconiosis and other lung conditions. Many former miners received their last X-ray at work. When miners retire or are made redundant, their access to regular X-rays simply stops. Former miners then tend not to receive another until they present to their GP with symptoms such as breathing difficulties or a persistent cough. Many fear that they have cancer, and are given a CT scan only to find that it is in fact pneumoconiosis.
It is important to note that the latency period for pneumoconiosis is about 10 years, but can be as long as 15 to 20 years. The lack of regular screening once a miner leaves that environment and retires is clearly a problem. I am aware of several cases in my constituency of miners who received the all-clear for pneumoconiosis after getting old-fashioned X-rays at work, but were subsequently diagnosed with pneumoconiosis after CT scans revealed evidence of the disease.
My hon. Friend is making an excellent point. I have personal experience of lung disease in the family. Both of my grandfathers were miners, and some of their lung issues did not come to the fore until at least a decade after they left the pit. I want to emphasise the importance of what he says: we need to ensure that there is support throughout the process and throughout people’s lives.
My hon. Friend is absolutely right. That is a prime example of why it is important that assessment is ongoing and people who used to work down the mines have access to diagnosis and treatment throughout the rest of their lives.
A few years ago, the Union of Democratic Mineworkers decided to run a test case. The UDM paid for five former miners who had recently been made redundant to have CT scans. The men had all received recent occupational X-rays at the colliery, and each had received the all-clear from those scans, but when the five men went for CT scans, two were diagnosed with pneumoconiosis. Interestingly, two of the other three men were diagnosed with other health issues, which had previously been unseen in the X-rays. Four out of five had conditions that required a CT scan to get a diagnosis. Surely it is clear that former mineworkers are at high risk of many different respiratory health problems, and that a CT scan is the most effective tool for diagnosis.
At present, the reality is that without post-retirement screening for pneumoconiosis, and with standard guidance from the DWP and the Department of Health promoting X-rays for testing, many cases are not picked up until it is too late. It is a sad truth that pneumoconiosis is often noted in a patient’s file for the first time when they receive a diagnosis of lung cancer or other advanced respiratory illness. That is clearly unacceptable.
I agree with much of what the hon. Gentleman is saying. I just want to mention the compensation scheme. When people are deceased, if somebody other than the widow claims for compensation, it is incredibly onerous and expensive and there are many hurdles in the way. Does he agree that that process needs to be simplified and expensive hurdles scrapped?
I agree that it is important that people have access to the compensation that they rightly deserve, and that that should be as simple a process as possible. Key to that is diagnosing the condition in the first place. To get access to that compensation, they have to prove that they have the condition, which has to be diagnosed.
The issue of pneumoconiosis testing has been batted about between the Department for Work and Pensions, the Department of Health and regional clinical commissioning groups for too long. Miners are rightly entitled to compensation and access to benefits as a result of work-related illnesses including pneumoconiosis. The compensation provides lump-sum payments to sufferers and their dependants. The Government have a duty to look after those who suffer from diseases caused by their working environment. Hard-working coalminers deserve their rightful compensation and disability benefits when their working environment has left them with an incurable illness. If individuals are not diagnosed at an early stage, they miss out on not only vital healthcare but the welfare support that they deserve.
To successfully claim compensation, miners must prove that they have pneumoconiosis. Again, this is where we run into issues. The DWP also relies on X-rays to provide evidence of pneumoconiosis for compensation claims. The compensation assessments are problematic. Former miners are frequently tested with digital X-rays, but even the newer technology struggles to pick up on the true condition of the lungs. Often the image is not clear enough to confidently diagnose pneumoconiosis. In such instances, if their claim is denied by the DWP, the miner will lodge an appeal. That takes considerable time and effort, and it will draw on DWP staff time and resources as applications are processed for a second time. In order to appeal the decision, miners may undergo further diagnostic testing, including the all-important CT scan, which is an additional expense and carries an additional exposure to radiation.
The argument against the use of CT scans usually focuses on two elements. One is the cost of the scans compared to that of X-rays, and the other is increased exposure to radiation. In reality, if coalminers with suspected pneumoconiosis do not receive a scan the first time, they are often exposed to repeated X-rays over a long period and then eventually a CT scan anyway—often when their condition has deteriorated. That is more time- consuming in the long run, ultimately costs more and can involve increased exposure to harmful radiation.
In this debate, I am asking not for a radical change to the testing programme for all lung-related compensation and disability claims, but simply an acknowledgment that former coalminers are at high risk of lung conditions and that the diagnosis of pneumoconiosis, particularly in the early stages, inevitably requires a CT scan rather than an X-ray. There is a clear argument that the Department should consider CT scans as the definitive gold standard for the investigation process in pneumoconiosis claims.
There is a real possibility that thousands of former mineworkers are living with pneumoconiosis, but have no idea that they have the disease. Their occupational X-rays may have showed nothing and, even if they raise health concerns with their GP years later, there is every possibility that they will again receive only an X-ray, which does not show enough detail to diagnose the condition.
The UDM is based in my constituency. I recently met Jeff Wood, the national president, and Ian Gill, the social insurance officer, who work on pneumoconiosis claims. They explained to me in great detail a number of cases that they have personally seen where miners suffered for years without an official diagnosis. It is easy to sit in Parliament and look at issues on paper, but it is important to remember that there are real people behind those studies, and real families who would benefit from a relatively small and easy policy change.
Any former miners who have had unnecessary delays in receiving their diagnosis should receive the compensation and benefits that they are entitled to. I ask the Minister to work with the Department of Health and Social Care to bring about change and to ensure that people who are entitled to support for pneumoconiosis can access it at the earliest opportunity.
There are several clear benefits to the DWP working with the Department of Health and Social Care to replace standard X-rays with CT scans. Earlier diagnosis for patients will allow them to make the necessary lifestyle changes to improve their overall health.
The hon. Gentleman is right to say that when producing new proposals, policies or guidelines, Ministers should consult with the trade unions—not only the Union of Democratic Mineworkers but the National Union of Mineworkers.
Of course, it is important that everyone involved is encouraged to talk to GPs and to the Government. I am sure that we can do more with that. I mention the UDM simply because it brought the issue to my attention.
We can achieve earlier access to compensation and benefit support from the DWP. There are potential cost savings for the NHS, because an initial CT scan will help to avoid repeated X-rays, GP appointments and out-patient visits, as well as helping the patient to be healthier and less reliant on those services. There will also be a reduction in the number of appeals to the DWP for compensation claims, because the evidence will be provided in the first instance, and a potential reduction in future disability claims, because sufferers will be able to take action sooner to improve their lung function and overall health before it deteriorates.
The DWP needs to take the lead on what is, of course, a work-related disease. In an ideal world, former mineworkers would be offered additional testing at their GP and local health clinics. We need national action because, once again, we face a postcode lottery in terms of the support offered to miners. Some areas fare considerably better than others.
In Mansfield, we are lucky that the unions offer support to former miners. There are also other areas of the country where former miners receive brilliant help and support. In Rotherham, the BreathingSpace community service helps people with a wide range of respiratory conditions. It provides a number of health services but, importantly, also helps individuals and families to access welfare and benefits advice. That is an example of unified working across departments, with benefits advice available in a healthcare setting. As ever, the most successful programmes are those that offer a joined-up approach.
I urge the DWP to support that joined-up approach. Ideally, the DWP and the Department of Health and Social Care will agree that a CT scan is the most effective way to diagnose pneumoconiosis. I ask the Minister to commit to a review into whether her Department’s assessments for pneumoconiosis compensation can use CT scans as the default diagnostic tool. I hope the DWP will work with the Department of Health and Social Care to make that happen. It is a relatively simple change, which should not be too hard to implement but could make a real difference to thousands of former mineworkers and their families.
I understand that the UDM recently met my right hon. Friend the Member for Portsmouth North (Penny Mordaunt) when she was a Minister at the DWP, and she expressed sympathy with its campaign. I hope the new Minister will also be inclined to give the issue the immediate attention it deserves.
It is appalling that former miners are suffering unnecessarily and missing out on the compensation and access to benefits that they deserve. There is a postcode lottery and inconsistent access to CT scans. A national system led by the DWP in co-operation with the Department of Health and Social Care could deliver more effective testing and better results. That could help to cut costs, reduce waiting times and most importantly, provide the best support to individuals at the earliest opportunity.
This is not an abstract discussion. The disease affects large numbers of former miners, including people in my constituency, daily, and their families suffer too. It is a progressive disease, but if sufferers are diagnosed at an early stage, they can receive care and support quickly, and access the compensation and benefits that they deserve. We must not let our former coalminers down.
(6 years, 7 months ago)
Commons ChamberIt is a pleasure to follow the heartfelt advice of the hon. Member for Makerfield (Yvonne Fovargue). It is clear that the world of personal finance can be hard to navigate. Without consolidated guidance, anybody could run into difficulties. That is why I welcome the Bill and the certainty it will provide, replacing a complex array of support services for different areas with a simple process for seeking advice.
There have long been calls to consolidate the financial advice services currently available in the UK, and I regularly signpost constituents to those organisations. The problem, however, is that constituents’ problems are rarely simple, and an individual experiencing financial hardship because of issues with their pension may benefit from more holistic financial advice. A single and well-publicised point of access for financial advice would certainly be of huge benefit to my constituents and provide timely and professional assistance to people across the country who encounter difficulties. I look forward to a strong marketing strategy to promote the service to my constituents, ensuring that everybody is aware of the opportunity to get help. Without such a strategy to raise awareness, it will be a waste of time.
I welcome the news that the Government have consulted extensively on the measures, that they are widely supported and that we already have a framework for financial advice that is fit for purpose. StepChange has commented on how important that is for social justice and for supporting families, including many in Mansfield who are just about managing.
Having heard a number of horror stories about the mismanagement of financial claims, I am also pleased that there is now a simpler way of seeking support when an insurance or other claim fails to go to plan. This simpler form of financial assistance is key in educating service users and promoting a sustainable and resilient population. I hope that the measure is met with approval from not just my constituents but people across the country. It sends a clear message to the companies involved that individuals will be held accountable for their business practices, and to consumers that we are on their side.
Finally, cold calling is a particular blight for older people in Mansfield, with many elderly constituents describing to me a feeling of intimidation because of daily calls asking them to make a claim for an accident that they probably have not had, or because of unsolicited scams and financial advice that they do not want. I am delighted that clause 4 makes provision for the Secretary of State for Work and Pensions to ban cold calling, in effect putting those unscrupulous companies on notice and protecting vulnerable people. Like my hon. Friend the Member for Croydon South (Chris Philp), I too have been plagued by calls following a minor car accident, asking me to submit a false claim for whiplash—an injury that I never had. In fact, I could probably run through 20 or 30 numbers that I have saved on my mobile phone under “PPI” or “Car Crash Scam” to alert me not to answer calls from them. The impact of the high level of such fraudulent claims can only have a huge and detrimental effect on insurance premiums, preventing people, particularly young people, from being able to afford to drive, so it is absolutely right that we take action.
The Bill represents an opportunity for the Government to provide more support and easily accessible financial assistance to the public, and delivers on our manifesto commitment to offer respite from debt. It is a real step forward for millions who are struggling with debt or who are having problems making financial claims. That is more evidence, if it were needed, that this Government and the Conservative party are supporting vulnerable people and promoting financial security.