NHS Funding

Edward Argar Excerpts

Monday 31st October 2016 Commons Chamber

[Mr Hunt]

I am happy to visit the hon. Gentleman’s local hospital, as I have been concerned about it for some time. I know that things have been particularly challenging there in the wake of what happened in neighbouring Mid Staffs, which has created its own pressures on the hospital. I also know that its staff work extremely hard in very challenging circumstances, so, yes, I will visit that hospital.

[Edward Argar (Charnwood) (Con)]

Does my right hon. Friend agree that achieving improvements in public health comes down not simply to the amount of money spent by the Government on it, but to a range of factors, including how it is spent, regulation, education and individuals’ choices?

[Mr Hunt]

I absolutely agree with that. This House should be very proud of the fact that, according to the UN, when it comes to public health this is the fifth healthiest country on the planet—after Iceland, Andorra, Singapore and Sweden, if my memory serves me correctly. That is a record we want to continue.

Community Pharmacy in 2016-17 and Beyond

Edward Argar Excerpts

1st reading: House of Commons
Thursday 20th October 2016 Commons Chamber

[David Mowat]

I am not sure that takes us forward, but it is right to say that spending NHS money on payments of £25,000 to many pharmacies within half a mile of one other is the wrong way to spend money when we need more in cancer drugs funds, in GP surgeries and in accident and emergency—that is what we need to be doing.

[Edward Argar (Charnwood) (Con)]

A large number of rural villages and small towns in my constituency are served by individual local pharmacies, which play an important role in the community. I welcome the Minister’s comments about the access scheme. Will he reassure me that small pharmacies in rural areas such as mine will be among those to benefit from the access protections he has outlined?

[David Mowat]

Yes, I can reassure my hon. Friend on that. Indeed, I can make the specific point that the 25% that make up the largest pharmacies will not be in the access scheme; it is directed more at smaller pharmacies.

Glenfield Hospital Children’s Heart Surgery Unit

Edward Argar Excerpts

Wednesday 19th October 2016 Westminster Hall

[Liz Kendall]

My hon. Friend is absolutely right. We have to think about people’s needs in the round—the need for high-quality surgery; ongoing care and support; and, critically, help for those families for whom this is a terrible, frightening and ongoing experience. Making the east midlands the only place without a heart surgery unit does not make sense.

It does not have to be this way. In its own standards, NHS England says:

“Networks will need to establish systems to ensure that referrals…between centres are managed in such a way as to ensure that each clinician is able to achieve their numbers”.

Its own standards say that people need to work together so that everyone can achieve the best. However, at the moment NHS England is not developing the work. I am a long-standing champion of patient choice, but the current proposals deny choice to patients from across the country who use Glenfield children’s heart surgery unit on an ongoing basis.

[Edward Argar (Charnwood) (Con)]

I pay tribute to the hon. Lady for securing this important debate. The Glenfield children’s heart unit is vital not only to my constituents but, as she said, to people across the east midlands and beyond. She has alluded to the significant progress that the hospital has made in just the past year in driving up the number of referrals and operations. That significant progress gives me confidence that it is on track to meet its target. Will she join me in urging the Minister to press NHS England to pause, look at the excellent clinical outcomes and the progress on increasing referral numbers, and think again, to keep this hugely important children’s heart unit open?

[Liz Kendall]

The hon. Gentleman makes an extremely important point. The clinicians at the unit and the hospital bosses have striven continually to improve patient care. They are not complacent for a second. They bust a gut to keep making improvements. Those improvements will, I am sure, be recognised and acknowledged by the 58 patients in the hon. Gentleman’s constituency who are receiving continuing care at Glenfield. He is right to say that NHS England needs to look in detail at the improvements that have been and are being made. When NHS England came to the centre in September—I was more than a little disappointed that it had not made a visit before it launched its proposals to close the unit—it found that some of its perceptions were wrong.

One important standard for improving care is co-locating—bringing together, in other words—the different children’s services, which includes not just surgery but other heart support, paediatric intensive care and wider services available to children. NHS England initially marked Glenfield down for not having plans to co-locate services. I am afraid that that was completely and utterly wrong. On coming to the centre it discovered that there are indeed such plans. I would like the Minister to confirm that University Hospitals of Leicester trust has plans to complete the co-location of all the services before April 2019, and has secured all the capital budget necessary to build its new children’s services hospital. To put all that at risk when the hospital is trying to improve services would be a big mistake.

Finally, I want to discuss the impact on other services in Leicester and the region of closing the children’s heart surgery unit. It is extremely important. As I said earlier, NHS England has itself said that it would not put forward proposals to close the unit unless it had done a risk assessment of the costs and benefits, including the knock-on effect on other services. It has not yet done that. I am concerned about two services in particular. Glenfield has a world-leading extracorporeal membrane oxygenation service. Essentially, if someone has a weak heart and needs surgery on it, ECMO enables oxygen to be pumped back into the blood during the operation. Glenfield’s is only the second ECMO service in the world to treat more than 2,000 patients. It conducts 50% of the entire ECMO activity in the UK. It also has the country’s only national patient transport service enabling people who need ECMO to be transferred swiftly from anywhere in the country to Glenfield. The huge benefits of that service were seen during recent flu crises.

Brain Tumours

Edward Argar Excerpts

Monday 18th April 2016 Westminster Hall

[Edward Argar (Charnwood) (Con)]

May I begin by welcoming this long overdue debate? The importance and impact of the issue are impossible to overstate and have been eloquently set out by other right hon. and hon. Members. Of all cancers, brain tumours are the biggest killer of people under the age of 40, with fewer than 20% of those diagnosed surviving beyond five years. Although welcome progress has been made in the treatment of and research into other cancers, with significant improvements in survival rates, sadly, that is not matched in respect of brain tumours. A number of problems remain.

My right hon. Friend the Member for Loughborough (Nicky Morgan) is sadly unable to speak in today’s debate, but her interest in and commitment to this cause are well known. She asked me to mention her constituents Terry and Eileen Smith, who lost their son Michael last November, and David Bird—his wife and daughter came to see my right hon. Friend—who sadly passed away after a very late diagnosis; that came too late for anything to be done.

Those stories are echoed by that of Jake McCarthy, whose family live in Rothley in my constituency. He was a bright, talented 24-year-old who on Christmas eve 2012 lost his life to a brain tumour diagnosed too late. Jake’s family and friends set up the Jake McCarthy Foundation to help to prevent others from experiencing such a tragic loss. The foundation helps to raise awareness of the symptoms and promotes the importance of early diagnosis. So far, it has raised more than a quarter of a million pounds. On 11 June we will see the third annual cycle ride to raise yet more money. Members of Jake’s family who set up the foundation are here today, and I pay tribute to their bravery and the work they have done through the foundation.

[Seema Kennedy (South Ribble) (Con)]

My hon. Friend is speaking powerfully about his young constituent. Does he agree that brain cancers, precisely because they affect children and young adults in the prime of life, disproportionately affect others? I pay tribute to my constituent Adam Bolton, a father of four. An owner of a small business employing 15 people, because of his treatment, he has had to sell his business.

[Edward Argar]

My hon. Friend rightly draws attention to the human consequences of this terrible cancer. It is clear that, while brain cancer is rarer than some, the mortality rate is very high, and awareness of symptoms and swift diagnosis are vital. It is research, however, that holds the key to beating the disease in the long term. Other Members have cited the stark statistic that research into the disease accounts for just over 1% of the £498 million spent on cancer research, and that is truly shocking.

[Alberto Costa (South Leicestershire) (Con)]

Many of my constituents have also raised this important matter with me. Brain Tumour Research in Buckinghamshire has requested not just an increase in funding from Government, but an absolute minimum, on which we can argue for increased funding over the years. Does my hon. Friend agree that that is the right approach?

[Edward Argar]

My hon. Friend is absolutely right. We need to see the amount of funding increased to the £30 million to £35 million proposed in the petition. I was disappointed by the Department’s official response, which essentially appeared to abrogate responsibility for helping to identify and address areas with insufficient funding. I echo my hon. Friend the Member for Mid Derbyshire (Pauline Latham) in asking whether the Minister thinks that the current level of funding is adequate. If it is not, what steps will the Government take not to pass the problem to the voluntary sector, but to take the lead in addressing and filling that gap?

The Petitions Committee was right to state that brain tumour patients have been let down by a lack of leadership from successive Governments. This is not a party political issue; it is about getting it right. I hope that the Minister’s response, as his responses normally are, will be positive, constructive and encouraging. It is through the efforts of Jake McCarthy’s family and friends and people like them across the UK that we are having this debate. We owe it to them and to Jake to rise to that challenge.

[Sir Edward Leigh (in the Chair)]

We have 15 more speakers. If they all stick to about four minutes, we should get everyone in. Members of the public have written to their MP and their MP is here. They want to hear their MP speak, so I know that everyone will try to keep to their four minutes from now on and not take too many interventions.

Dementia and Alzheimer’s Disease

Edward Argar Excerpts

Tuesday 12th April 2016 Westminster Hall

[Edward Argar (Charnwood) (Con)]

I pay tribute to the hon. Member for Strangford (Jim Shannon) for securing this important debate and for his long-standing focus on the issue. Last September when I was able to secure a debate on this subject I was very grateful to him for attending, and for his eloquent words, and I want to reciprocate today.

The subject is one of great significance—a significance that grows every day as our population ages and our life expectancy grows. It is an issue that is personally hugely important to me. I have supported the Alzheimer’s Society for many years, and recently in the House I co-hosted with the hon. Member for Oldham East and Saddleworth (Debbie Abrahams) a dementia friends session for Members and staff. I am very grateful for all the work that she does on this issue.

Dementia is incredibly cruel. It can take a person away from us, even while they are still with us. As the hon. Member for Strangford and my hon. Friend the Member for Aldridge-Brownhills (Wendy Morton) set out, the basic facts are stark. My hon. Friend in particular drew attention to the challenge of early-onset dementia, which can often be forgotten, and we must remember the specialist services and support that people with early-onset dementia need and cater for them.

This is not a party political point. The Labour party should be very proud of its record in government on this subject, and I believe that this Government and this Prime Minister can rightly be proud of ours. We have heard a lot about the importance of awareness and understanding, care and treatment and research. My hon. Friend the Member for North West Hampshire (Kit Malthouse) was characteristically modest in talking about the Dementia Research Institute. The one thing he omitted to say was that it was his idea, and he should be rightly proud of what he has set in motion.

The aspect of this important issue that I want to focus on is the organisations and individuals who do so much to care for and support those with dementia. Setting aside for a moment the human impact of dementia, the estimated cost of dementia is £23 billion per year, with a large proportion of that effectively met by families and voluntary carers. We must remember the army of 670,000 all too often unsung heroes who help and care for people with dementia, as well as organisations such as Age UK and the Alzheimer’s Society, of which I am a member, and local councils and CCGs.

Last year, I had the pleasure of visiting the Poppies Memory Café in Syston, and later this month I will visit the Thrummy Drummer dementia support group in Thurmaston. Both do vital work in supporting those with dementia in Charnwood and providing respite to carers. Alongside the excellent support services in my constituency that play such a vital role for those with dementia and those who care for them, there is another service that is sadly under threat as we speak today. The CCG recently took the decision to cease funding the service based in the Birstall resource centre in School Lane in my constituency, which Age UK has run for many years. It provides a vital lifeline for 19 people with severe dementia and respite for their families and carers, with a further eight people waiting for referrals. The service is not only much valued but extremely well used in Birstall. The removal of CCG funding will cause the service to close, which will have a devastating impact. A glance at the CCG board papers suggests that the decision is not financial; its budget has actually increased.

It is deeply disappointing that the CCG has taken that decision. While I am grateful to the CCG for the time it has taken to set out its views to me, I remain unconvinced of their logic. The reality is that that service is of huge importance to everyone. I suggest that its closure would be a tragedy for those who use it and that the CCG is taking a short-term view in closing it; costs to the NHS will go up in the long term. I would like to take this opportunity to say that it is time for the CCG to pause, think again, accept that it has got this wrong and reverse the decision.

Dementia Care Services

Edward Argar Excerpts

Wednesday 9th September 2015 Westminster Hall

[Edward Argar (Charnwood) (Con)]

I beg to move,

That this House has considered dementia care services.

It is a pleasure to lead this debate—the first in my name since my election—under your chairmanship, Mr Davies. It is also a pleasure to debate with a Minister whose commitment to this cause is well known, on a subject of such importance. Indeed, its importance grows daily.

I am particularly pleased to see my hon. Friend the Member for Wealden (Nusrat Ghani) next to me. I hope that she plans to speak in this debate, because her work in her constituency on this subject, and the depth of her knowledge, is well known and will be of great benefit to the House.

Dementia is incredibly cruel; it can take a person away from you even while they are still with you. It is estimated that there are around 850,000 people with dementia in the UK; that 21 million people have a family member or close friend with dementia; and that a third of people over 65 will develop it. The majority of those 850,000 people are over 65, but an estimated 17,000 people below that age have dementia. In my constituency of Charnwood, it is estimated that just over 1,000 people have dementia. All of this—put aside the human consequences for a moment—is estimated to cost around £23 billion per annum, with a huge proportion of that being met by families, either through care that they engage or through the free hours of care that the 670,000 voluntary carers provide. The challenge before us is huge.

Significant progress on dementia has been made in this country in recent years. However, while we as a society have made significant strides in improving our longevity and our ability to fix and patch up our physical selves through the medical profession, our understanding of and care for the mind have fallen behind somewhat. Dementia poses a massive financial challenge to our country, as people live longer—a good thing, but a partial consequence is an increase in the number of dementia cases.

The last Labour Government should be rightly proud of their work in bringing forward the first national dementia strategy, and I pay tribute to them, through the shadow Minister, for that far-sighted step. It is a baton that the current Government, and particularly this Prime Minister, have seized with vigour; there has been the Prime Minister’s challenge on dementia 2012, the G8 dementia summit, and the Prime Minister’s 2020 challenge. All this is hugely positive, and dementia is an issue on which there is considerable consensus in all parts of the House, and among all the parties represented within it. However, we must not think for one moment that we have done enough, nor lose the momentum built up thus far.

[Jim Shannon (Strangford) (DUP)]

I congratulate the hon. Gentleman on bringing this matter to the House for consideration. A great many of us across my constituency of Strangford and the whole of the United Kingdom of Great Britain and Northern Ireland know people who suffer from dementia. Just last week, I had the opportunity to go to what is referred to as a memory café, which is organised by the Alzheimer’s Association, which is a wonderful organisation. I met some wonderful people, as well as their carers and families. Does he recognise the good work that the Alzheimer’s Association does? Does he feel that now is the time to not only raise awareness of Alzheimer’s but commend the Alzheimer’s Association for its work?

[Edward Argar]

In addition to the hon. Gentleman’s many talents, which are well known in this House, he appears to be a mind-reader, as I was about to come on to that subject, having visited a similar memory café on Monday. He is absolutely right to highlight and pay tribute to the work of such places. On Monday, I went to the Syston community centre, where our local Alzheimer’s Society group was holding its regular Poppies memory café session for about 30 carers and people with dementia. As I am sure the hon. Gentleman did on his visit to his local memory café, I met some amazing people and it was a fantastic session. My memories of that session, and the lessons I learned from it, remain with me; I continue to reflect on them. However, across the UK, including in my region—the east Midlands and Leicestershire—the access to and coverage of such vital services remains patchy; that was a message I got loud and clear from the people I spoke to. As I suggested, that session left me in no doubt about the vital role of dedicated and passionate carers, including the amazing people whom the hon. Gentleman and I met, in helping people with dementia.

[Graham Evans (Weaver Vale) (Con)]

I am most grateful to my hon. Friend for securing this debate, and he has made some powerful points. I would like to share with him some things that we are doing in Cheshire, and indeed in Weaver Vale. Dementia awareness is so important. My staff have received dementia awareness training, so that we can identify people with dementia. Also, our local town centres are dementia-friendly, which is significant. It enables people to come out as families and they are made most welcome in town centres, such as that of Northwich. Does my hon. Friend agree that town centres across the country should be dementia-friendly?

[Edward Argar]

Yet again, it appears that another hon. Member has the facility of reading minds and anticipating speeches, because I was about to say that there remains too little understanding of dementia in our communities, despite the progress made, and dementia-friendly communities and workplaces can play a hugely important role in supporting both those who have dementia and those who care for them.

I encourage the Minister to push all Government Departments to become dementia-friendly workplaces, and to keep talking about dementia and raising awareness of it. I also encourage her to keep the NHS talking about it. I know that other hon. Members—not least the shadow Minister, the hon. Member for Oldham East and Saddleworth, who is chair of the all-party group on dementia and possibly the only dementia champion in this House—will continue to raise these issues, as the shadow Minister has done over many years.

A recent survey showed that 25% of 18 to 25-year-olds are keen to learn and understand more about dementia, as opposed to only 15% of those aged 55-plus; that was a 2012 YouGov survey, so it is relatively recent. While it is encouraging that young people are keen to understand and learn more about dementia, those figures are still far too low.

[Jim Shannon]

One thing that I became aware of after visiting the memory café last week and speaking to some of the people there—by the way, the Big Lottery Fund was one of the funders of that café, so it is doing good work—is that the age of those being diagnosed with dementia and Alzheimer’s is starting to fall. There are some people in the 40-to-50 bracket who have dementia, which worries me. Does the hon. Gentleman feel that there is anything we can do to raise awareness of that issue?

[Edward Argar]

The hon. Gentleman makes a valid point. Just last Saturday, I was at a gala in Anstey, which is a village in my constituency, and a man came up to talk to me about this issue. He said that a lot of emphasis is put on those in their 60s or 70s who develop dementia, but he told me about a lady who had developed it very early in life, which creates a whole new set of challenges around children, paying mortgages and the support that should be in place but is not always there. I will come on to the support that is or is not in place shortly.

The second part of the picture is about diagnosis and care. Diagnosis rates have improved. In 2011-12, only 45% of people with dementia received a formal diagnosis, but Department of Health figures suggest that the figure is now up to 59%, which is real progress. I know that 66% was the target set for the end of this year, but can I encourage the Minister to go that little bit further and press for a 75% target for diagnoses by 2017? That is ambitious but achievable, and if we do not set ambitious targets we will not achieve them.

However, diagnosis is only the start. Too many people tell of being diagnosed and then receiving no information or support, or only very limited information or support. In a recent Age UK survey, 89% of those surveyed said that they did not feel they had enough information about dementia. We need to improve GPs’ understanding of dementia care; many GPs are fantastic, but that is not universal. We need to ensure that after a diagnosis, people and their families receive information on “What now?”, as well as support. What steps do the Government propose to take to create minimum mandatory standards to ensure that everyone with a diagnosis receives swift signposting and advice from dementia advisers and a proper support package for them and their carers, possibly through the NHS outcomes framework?

We all know—all the research shows this—that once someone is diagnosed with dementia, if they are to continue to lead a full life, it is best for them to be able to live independently at home with their family, but if they are to do that, we must ensure that carers are cared for and supported, and that support plans are in place—as much for the carers as for any individuals with dementia. A recent pilot in Norfolk on the use of Admiral nurses—they are the dementia equivalent of Macmillan nurses, and although they are sadly rather less well known, they do a fantastic job—saved more than £400,000 and provided a strong local support service for carers and people with dementia. What consideration have the Minister and the Department given to how that might be made more widely available? What support can be given to local authorities in that respect?

We are all aware of the funding pressures faced by local authorities—not least my own, Leicestershire. It gets one of the lowest per-head funding settlements in the country, and I hope that that can be reviewed and revisited in this Parliament, with rural councils being given a fairer share. While I would not presume to burden the Minister with responsibility for dealing with the local government finance settlement as well, what progress has been made nationally on developing integrated dementia care pathways, which can go some way to alleviating financial pressures?

While care and support to stay independent at home are key, there are times when people with dementia have cause to be admitted to hospital, and here the picture is by no means universally good. According to a recent survey, 41% of hospitals do not include dementia awareness training in staff inductions, and only 36% have a care pathway in place. Many people with dementia still have real problems when they are admitted to acute care. More research into the quality of personalised care for those with dementia, particularly in hospitals, would be immensely valuable. It is estimated that a quarter of hospital beds are occupied by people with dementia, although they might not necessarily have been admitted for dementia. On average, such people have a 20% longer hospital stay than others.

While some hospitals have made progress in having dementia-friendly wards, it simply is not enough. We should have hospitals that are dementia-friendly in their entirety. We often hear of instances of people with dementia not having that noted on their hospital records, meaning that no allowance has been made for it. We also hear of carers and partners not being allowed to stay with relatives with dementia in hospital, which often leads to acute anxiety and distress among those patients at being in an unfamiliar environment without any familiar faces around them. I hope that Simon Stevens and the NHS can look at that.

The national dementia strategy and the Prime Minister’s challenges on dementia for 2015 and 2020 set out an array of targets and objectives. The key to success, however, will be proper implementation to deliver clear and focused outcomes that are measured, monitored and reported. Will the Minister update the House on the implementation plan to achieve the objectives that we all welcome, and to ensure that dementia care gets its share of the very welcome additional funding that the Government have pledged to the NHS as a whole? Specifically, as we look at how to improve care and support, 37 NHS vanguard sites are piloting new care models, but only three make specific mention of dementia. Will she consider adding to that number? The National Institute for Health and Care Excellence is updating the 2006 clinical guidelines on dementia. That work is due to be completed in September 2017. Will she make representations to NICE on updating the dementia quality standard as part of that? It is an important tool in driving up NHS standards in this area.

The third and final part of tackling dementia is research. We have seen some encouraging early signs over the summer that finding a way of slowing down the progress of dementia might be that little bit closer. There is still a long road ahead for that research, but it is a reminder of the importance of a continued focus.

[Kit Malthouse (North West Hampshire) (Con)]

As a Dementia-Friendly Hampshire ambassador—I am not quite a champion, but an ambassador—I welcome the debate and remind my hon. Friend of the Government’s commitment just before the election to creating a dementia research institute somewhere in the UK within the next five years. Does he agree that it would be helpful if the Minister updated us on the funding envelope for that, and the implementation plan for it over the next four and a half years, given that time is running out for its creation? I have to declare a slight interest, as the idea was fermented at City Hall. I may have had a hand in it, and therefore have a stronger motive to see it come to fruition.

[Edward Argar]

I am grateful to my hon. Friend, and I am beginning to think that I must be careful about what I think, because yet again a Member has touched on a paragraph I was about to begin. He is absolutely right. The Government’s dementia research funding now stands at £66 million. That is double what it was in 2010, but we need to be clear that we must not stop there. I was pleased that earlier this year the Government reaffirmed their commitment to doubling the dementia research spend by 2025. That is vital, and I know that Members on both sides of the House, in the spirit of constructive support, will help to hold the Government to that. Will the Minister commit to collating information on that spend centrally, and to publishing it annually, so that we can track progress? Coming to my hon. Friend’s point, I would be grateful if the Minister updated the House on the plans for a dementia research institute to drive forward research in a truly world-leading way. I pay tribute to my hon. Friend for the work he did in City Hall, and as a Deputy Mayor, in pushing that agenda forward.

Finally and most importantly—I declare an interest as a member of the Alzheimer’s Society—I pay tribute to such organisations as the Alzheimer’s Society, Alzheimer’s Research UK, Age UK and myriad others for the work they and their members do to ensure that we in this House and society never forget this cause, and that we continue to support the tens of thousands of people with dementia—and the voluntary carers, who are the real heroes and heroines. We have a duty to recognise what they do, and to do everything we can as a country to support them. I look forward to the Minister’s comments on what we can do to support carers.

I will close by quoting from a moving and powerful article by Alice Thomson about her father’s dementia. It was published in The Times this summer. She said:

“Old age shouldn’t be seen as a humiliation but more as the other bookend to your childhood; a time when you can rely on the help and patience of others to reach the end but can also still be a central part of family and community life”.

I echo those words and ask the Minister, the Government, all of us and society as a whole to continue to rise to the challenge and to make that a reality for all those who have dementia in this country.

[Philip Davies (in the Chair)]

It may be helpful if I point out that for hour-long debates, we need 20 minutes for the Front Benchers: five minutes each for the two Opposition Front Benchers and 10 minutes for the Minister. If the Minister leaves any time at the end, Mr Argar may get a few seconds to wind up. I will be going to the Front Benchers no later than 5.10 pm. As I understand it, three Members are seeking to catch my eye to make a speech. I will not impose a time limit, but if they think of taking seven minutes each, that would give everyone a fair crack of the whip.

Oral Answers to Questions

Edward Argar Excerpts

Tuesday 7th July 2015 Commons Chamber

[Alistair Burt]

My right hon. Friend is correct. The damage that has been done over many years by not regarding mental ill health as seriously as it should be regarded, and by not having that parity of esteem, has been immense. The campaigns that have been launched against stigma, often fronted by brave people—including some in this House—have done much to correct that, but he is correct to say that the campaign against stigmatisation must continue.

[Edward Argar (Charnwood) (Con)]

The first NHS point of contact for many people with mental health issues is often their GP. Does my right hon. Friend agree that it remains vital that GPs and primary care staff have proper understanding and training in mental health care, and more broadly that such training forms a greater part of medical qualification and training?