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Category: Health

  • Matt Hancock – 2020 Statement on Covid-19

    Matt Hancock – 2020 Statement on Covid-19

    The statement made by Matt Hancock, the Secretary of State for Health and Social Care, in the House of Commons on 25 September 2020.

    As the covid-19 incidence rate continues to rise across the country, a suite of local and national actions is required to break the trains of transmission and enable people to maintain a more normal way of life.

    The Government will act swiftly and decisively to limit further spread, reduce disruption and contain local outbreaks. The local action committee command structure has been reviewing the latest evidence, working with local leaders and the scientific community to assess the data and whether further evidence is required.

    The latest data shows a sharp increase in incidence rates per 100,000 population in Leeds, Blackpool, Wigan and Stockport, which are significantly above the national average.

    As a result, we are making regulations which take effect from Saturday 26 September and will impose restrictions on inter-household mixing in private dwellings and gardens in Leeds, Stockport, Wigan and Blackpool. This is in line with measures seen elsewhere in the country, such as Leicester and the West Midlands. People who live in these areas will not be allowed to gather in a private dwelling or garden with any other household unless in a support bubble. People from anywhere else will also not be allowed to gather with another household in a private dwelling or garden in these areas.

    We have also reviewed the position in Leicester, the Borough of Oadby and Wigston, Birmingham, Solihull, Sandwell, Wolverhampton, Bolton, Bradford, Kirklees, Calderdale and the remaining local authorities in Greater Manchester and have decided to maintain their position on the watchlist as areas of intervention, as well as the current restrictions in these areas.

    This will be difficult news for the people living in these areas, profoundly affecting their daily lives. These decisions are not taken lightly, and such measures will be kept under review and in place no longer than they are necessary. There are exemptions to these measures so people can still meet with those in their support bubble. There are other limited exemptions such as for work purposes or to provide care or assistance to a vulnerable person. Through the Health Protection (Coronavirus, Restrictions) (Protected Areas and Linked Childcare Households) (Amendment) Regulations 2020, people may create an exclusive childcare bubble for the purposes of informal childcare for children under 14, helping ease pressure on those living under local restrictions so they can get to work.

    The guidance on gov.uk covering these areas will also be amended to fully reflect these changes.

  • Rosena Allin-Khan – 2020 Comments on NHS Staff Mental Health

    Rosena Allin-Khan – 2020 Comments on NHS Staff Mental Health

    The comments made by Rosena Allin-Khan, the Shadow Minister for Mental Health, on 24 September 2020. Allin-Khan was commenting on statistics published by the NHS showing over 500,000 sick days had been taken in May 2020 alone.

    These statistics must serve as a wakeup call for the Government. At a time when COVID-19 related sickness absences were going down, mental ill health absences were soaring.

    Our health and care staff have sacrificed so much during this pandemic – it demonstrates why Labour’s ‘Care for Carers’ package is so vital. Dedicated mental health support should be available for all health and care staff.

    Since launching the package in June, I have requested meetings with the Government – it is a disgrace that this offer has not been taken up. I urge the Government to reconsider our offer.

    Ahead of winter and a second spike, the Government must learn the lessons of this spring. We must fight for the mental health of those who have supported us so courageously during this crisis.

  • Matt Hancock – 2020 Comments on Launch of Covid-19 App

    Matt Hancock – 2020 Comments on Launch of Covid-19 App

    The comments made by Matt Hancock, the Secretary of State for Health and Social Care, on 24 September 2020.

    We are at a tipping point in our efforts to control the spread of this virus. With infection rates rising we must use every tool at our disposal to prevent transmission, including the latest technology.

    We have worked extensively with tech companies, international partners, and privacy and medical experts – and learned from the trials – to develop an app that is secure, simple to use and will help keep our country safe.

    Today’s launch marks an important step forward in our fight against this invisible killer and I urge everyone who can to download and use the app to protect themselves and their loved ones.

  • Helen Whately – 2020 Speech on Axial Spondyloarthritis

    Helen Whately – 2020 Speech on Axial Spondyloarthritis

    The speech made by Helen Whately, the Minister for Care, in the House of Commons on 17 September, in reply to Tom Randall.

    I congratulate my hon. Friend the Member for Gedling (Tom Randall) on securing this debate and on bringing the House’s attention to the need for earlier diagnosis of axial ​spondyloarthritis. May I say how important it is that he has brought his personal experience to the debate? The House should appreciate the courage he has shown to speak up about his own condition—something that cannot be easy, but that is an example. I feel strongly that all of us bring our own experiences to our work. That is one of the reasons it is important to have a diverse House of Commons. He has brought his own extremely painful experience to bear. I am confident that simply by doing so, he will make a difference for many others who suffer from this painful condition or who may do so in the future.

    My hon. Friend rightly highlighted how critical it is for those with axial spondyloarthritis to get the right diagnosis and get it quickly, and to have their symptoms taken seriously by all healthcare professionals. It is clearly incredibly important to ensure that people can access the right sort of care at the right time, as it can prevent the potentially devastating impact of the condition on quality of life. I very much appreciate from his account and from others I have read how the condition affects people and their loved ones. We must do all we can to reduce the impact on people’s physical and mental health, and I want to do so.

    As my hon. Friend said, axial spondyloarthritis, which may also be referred to as axial SpA or AS, is a form of inflammatory arthritis that most commonly affects the spine. It is a painful long-term condition that currently has no cure. As well as affecting the joints in the spine, it can affect the chest, the pelvis and other joints, ligaments and tendons. Unfortunately, AS is often misdiagnosed as mechanical lower back pain or diagnosed late, leading to delays in access to effective treatments. It is estimated that approximately 220,000 people, or one in 200 of the adult population in the UK, have the condition.

    As my hon. Friend said, the average age of onset is relatively young at 24, with patients having to wait on average eight and a half years before diagnosis at an average age of 32. That is clearly far too long to be waiting for a diagnosis, because left untreated the condition can lead to irreversible spinal fusion, causing severe disability. That makes a rapid referral to specialist care for those with any signs or symptoms crucial to treatment and to preventing those kinds of outcomes.

    I recognise that AS can have a devastating effect on the quality of life of people who sadly go undiagnosed or misdiagnosed for far too long. This must get better. It is clear to me that early diagnosis and treatment are the key to preventing the development of other serious conditions further down the line and to improving the quality of life of those who suffer from this condition.

    We recognise that one major reason for the delays in diagnosing axial SpA is a lack of awareness of the condition among healthcare professionals and the general public. That can take many forms: a lack of awareness of different types of arthritis; a lack of knowledge about the differences between inflammatory and mechanical back pain; or misunderstanding that AS affects similar numbers of men and women. Educational interventions to improve the level of awareness should lead to improvements in earlier diagnosis, and a range of materials are being produced to this effect. For example, an online training module on AS for GPs has been produced by the Royal College of General Practitioners.​

    In June this year, the National Institute for Health and Clinical Excellence published its managing spondyloarthritis in adults pathway, which has been well received by patient groups and charities. This set out recommendations for healthcare professionals in diagnosing and managing axial SpA in adults. It describes how to improve the quality of care being provided or commissioned in this area, both through guidance and via an associated quality standard. I completely agree that we would expect providers and commissioners to be following the guidance and recommendations in this area so that we can improve the overall rate of earlier diagnosis. It is not only important that we have this guidance but that it will be within the pathway that the APPG and my hon. Friend have argued should be put into place in practice.

    Munira Wilson

    While I welcome the guidance and the pathway, what does the Minister suggest can be done to tackle the clinical conservatism that we quite often find among specialists even once the diagnosis is made? In my husband’s case, the rheumatologists said to him, “You are far too young for us to move you on to the more advanced treatments”, so he was living with huge amounts of pain on just very mild painkillers and steroids. It was only because we happen to live in London that we got him re-referred to a world-leading specialist in the field who then put him on anti-TNFs. He is now able to be the primary carer of our two very young, active children, which he could not do otherwise. Not everybody has that luxury, especially if they live in a rural area.

    Helen Whately

    The hon. Member makes a really important point, again drawing from her own personal and family experience, about the importance of awareness of what is the best treatment for this condition. If she would like me to do so, I am happy to take away her specific point and look into how we can address the need for improvement in the treatment, as well as her general point about needing a better pathway. I am also happy to meet my hon. Friend the Member for Gedling, as he requested, to talk further about how we can make more progress on the right treatment for this condition, and awareness of it.

    Coming back to the overall points about what we can do to improve the treatment, the NHS long-term plan set out our plans to improve healthcare for people with long-term conditions, including axial SpA. That includes making sure that everybody should have direct access to a musculoskeletal first-contact practitioner, expanding the number of physiotherapists working in primary care networks, and improving diagnosis by enabling people to access these services without first needing a GP referral—in fact, going directly to speak to somebody with particular expertise in the area of musculoskeletal conditions. The hon. Member for York Central (Rachael Maskell) intervened to make a point about the demands on physiotherapists. I have asked to be kept updated on progress on delivering the expansion of the number of physiotherapists in primary care networks and, more broadly, on the implementation of the NHS long-term plan. We do indeed need to make sure that we have sufficient physiotherapists to be able to deliver on that. I anticipate that that should have a positive impact on the problem of delayed diagnosis for a range of conditions, and particularly for this specific condition.​

    While better education and awareness of AS should improve the situation, there is clearly more that we can and must do to understand the condition. The National Institute for Health Research is funding a wide range of studies on musculoskeletal conditions, including AS specifically. That research covers both earlier diagnosis and treatment options for the condition, so that we continue to build our understanding of good practice and improve both the treatment and the outcomes for those who have the condition.

    In conclusion, I want to pick up on my hon. Friend’s point about the importance of awareness and the call for an awareness campaign by the APPG, and I should of course commend the National Axial Spondyloarthritis Society for its work in this area. My hon. Friend mentioned that there is clearly a huge amount of public health messaging going out at the moment, but I hope the time will come when we can gain more airtime for this particular condition. However, the fact that we are having this conversation in the Chamber is in itself a step towards raising awareness of the condition, and so, ​too, is all the work that is going on; that is important as well, because along with having the policy and the pathway, we must make sure it is put into practice.

    I congratulate my hon. Friend again on bringing this subject to the attention of the House and on the work he is doing and the effect that this will have. I truly want to support him and to do our best for all who suffer from this condition and may suffer from it in future, to ensure that we achieve much earlier diagnosis and treatment and better outcomes for those with the condition.

    Madam Deputy Speaker (Dame Eleanor Laing)

    I commend the hon. Member for Gedling (Tom Randall) on his courage in bringing such a personal and difficult matter before the House. Many people will not appreciate that that is a difficult thing to do, and I am sure that he will have made a difference to many by what he has done today. [Hon. Members: “Hear, hear.”] I am pleased that those in the Chamber are in agreement.

  • Tom Randall – 2020 Speech on Axial Spondyloarthritis

    Tom Randall – 2020 Speech on Axial Spondyloarthritis

    The text of the speech made by Tom Randall, the Conservative MP for Gedling, on 17 September 2020.

    I am grateful for the opportunity to hold this Adjournment debate. I have been a Member of this House for nine months. One of the great privileges of being a Member of Parliament is the opportunity to sit in this Chamber. The more astute observers might have noticed that I occasionally sit slightly awkwardly on these Benches. I admit that, sometimes, I slouch. One of my waggish Twitter correspondents recently juxtaposed a photograph of me and a photograph of my right hon. Friend the Leader of the House reclining on the Treasury Bench, with the caption,

    “great to see Gedling MP getting comfy in parliament and following in the footsteps of his fellow parliamentarian”.

    I admire the Leader of the House very much—there is much to admire about him—but on this, alas, I do not seek to emulate him. Rather, my awkward posture arises from the condition I have: ankylosing spondylitis.

    Ankylosing spondylitis is one of three sub-types of a type of inflammatory arthritis called axial spondyloarthritis. Axial spondyloarthritis is a chronic inflammation of the spine and joints. It is a painful and progressive long-term condition for which there is no cure. It is unlike conditions such as osteoarthritis, which is often associated with older people and the wear and tear that comes with ageing.

    Axial spondyloarthritis, often abbreviated to axial SpA or AS, tends to present in the late teens or early 20s, with the average onset being just 24. In my own case, I first presented with symptoms at 16. As well as the stiffness and pain that one might expect from an arthritic condition, axial SpA is also associated with a range of complications and comorbidities, including uveitis and psoriasis. But it is perhaps the less visible complications of AS that can be the most debilitating. Many suffer from severe fatigue, as well as flare-ups and stiffness.

    The condition presents itself in a period when most people are at a crucial stage of their lives, looking to build careers, start families and forge social relationships. I well remember my early 20s, when I was starting out in my first job after university, before I was prescribed the treatments that I am on now. When I got home after doing an eight-hour day in the office—something that most people would take in their stride—I crashed out on the bed, completely exhausted from a normal day at work.

    Munira Wilson (Twickenham) (LD)

    I congratulate the hon. Member on securing this important debate. My husband also suffers from ankylosing spondylitis. Like the hon. Member, he started getting symptoms when he was about 20, and it took him about 10 years to get diagnosed. He was exhausted and struggling to work, and there were days when I had to help him put his socks on because he could not bend over. Does the hon. Member agree that the shocking delays in getting a diagnosis have a massive impact on quality of life, as do the difficulties that people have in accessing the right treatment? We need to improve awareness, particularly of the National Institute for Health and Care Excellence guidelines on the treatments available.

    ​Tom Randall

    The hon. Lady is absolutely right. What I and her husband have experienced is sadly not a rare phenomenon.

    The name axial spondyloarthritis will be unknown to many, if not most, people, but it is not uncommon. It affects about one in 200 of the adult population in the UK, or just under a quarter of a million people.

    Jim Shannon (Strangford) (DUP)

    I congratulate the hon. Gentleman on bringing forward this debate. I spoke to him this morning to seek his permission to intervene. He is aware of the massive eight-and-a-half-year delay in diagnosing this awful illness. I read an article in my newspaper back home in May about a young mum in Northern Ireland and her battle. We must all be determined to secure extra funding so that early diagnosis can happen, for adequate research into this life-changing debilitating disease, and for more support groups. In Northern Ireland, we have only two—one in Belfast and one in Londonderry—for a population of 1.8 million spread across the whole Province.

    Tom Randall

    In last night’s Adjournment debate, the hon. Member for Pontypridd (Alex Davies-Jones) said that she felt like a proper MP after the hon. Gentleman intervened on her in an Adjournment debate, and I echo those sentiments. He is completely right about the delay, which I will come on to in a moment, and about the role that support groups can play in showing that people are not alone in having the condition and in providing moral and practical support. I hope that now awareness has been raised, there will be more than two groups in Northern Ireland in due course.

    As I was saying, there are a quarter of a million people with AS, which makes it more prevalent than multiple sclerosis and Parkinson’s combined. Hon. Members may say, “Well, so what?” AS is incurable and it can be managed through medication, physiotherapy or exercise, but what makes it worthy of particular concern and debate is, as outlined earlier, the delay to diagnosis.

    The symptoms of AS can be difficult to diagnose. I was passed between neurologists, geneticists and other specialists as various conditions were ruled out, before a rheumatologist finally diagnosed AS when I was about 20. I was very lucky that I had to wait only a couple of years before getting my diagnosis, but on average, there is a delay of eight and a half years between the onset of AS symptoms and diagnosis in the UK.

    Gareth Bacon (Orpington) (Con)

    I commend my hon. Friend’s bravery in refusing to allow the condition to prevent him from gaining a place in this House and in attempting to draw more attention to the condition. How does the UK compare internationally in terms of the delay that various hon. Members have discussed between the onset of symptoms and diagnosis?

    Tom Randall

    I think in comparable countries such as Germany, France and Italy it is four, five or six years. Certainly, I think the delay to diagnosis in the UK is one of the longest in Europe, and that is something that needs to be remedied. Obviously, during that delay of eight and a half years, the condition can deteriorate considerably. One does not need to be an expert to understand the clinical, economic and human burden of delayed diagnosis.

    ​Andy Slaughter (Hammersmith) (Lab)

    I congratulate the hon. Gentleman on this timely debate. I have the honour to have the National Axial Spondyloarthritis Society based in my constituency, which is why I have some knowledge of the matter and am involved in the all-party parliamentary group on axial spondyloarthritis. I am sure that he will join me in praising its work and the extraordinary expertise that it brings. The danger is that if people do not have that association or contact, as many medical practitioners do not, it is difficult to diagnose, and therefore, heartbreakingly, young people suffer in pain and do not get a diagnosis when they should. Will he praise the NASS’s work and agree that the NHS needs to communicate about it much more widely?

    Tom Randall

    I pay tribute to the hon. Gentleman’s work. He was an active member of the APPG long before I was in this place. On the issues that he identifies, on which I will go into more detail in a moment, he is absolutely right.

    Rachael Maskell (York Central) (Lab/Co-op)

    I am grateful to the hon. Gentleman for bringing forward this debate. Before coming to this House, I was a physiotherapist. I ran an AS group for swimming and exercise and really know the benefits of that. The Chartered Society of Physiotherapy was in touch with me just this week to say that, because of covid, it is experiencing a real shortage of physios for the future and that 2,339 more physios are needed. Does he agree that we need to look back at the NHS work plan to ensure we have the right practitioners in place to support people like him?

    Tom Randall

    Physiotherapy can play a key role in managing the symptoms of AS, and we should all support the work that physiotherapists do with patients.

    Anthony Browne (South Cambridgeshire) (Con)

    I congratulate my hon. Friend on securing the debate on this important issue, and I pay tribute to his bravery in overcoming his condition and ensuring it did not prevent him coming to this House.

    I have a family member, a friend and a constituent who suffer from AS, and I know well the problems with delayed diagnosis. My constituent Frances Reid started having symptoms 10 years ago. She went from doctor to doctor to doctor but did not get diagnosed. She was diagnosed only one year ago, and she now has pains across her entire body and needs joint replacements. She is in so much pain that she wakes up eight to 10 times a night. In contrast, a friend from Canada was diagnosed really early. With treatment and exercise, he leads a full life. What lessons can we learn from countries that have quicker diagnosis and what would my hon. Friend like to see here?

    Tom Randall

    My hon. Friend neatly explains the consequences of delayed diagnosis. A recent systematic review of the available literature found that, overall, patients with a delayed diagnosis of AS had worse clinical outcomes, including higher disease activity, worse physical function and more structural damage compared with patients who had an earlier diagnosis. Those with a delayed diagnosis also had higher healthcare costs and a greater likelihood of work disability, as well as a worse quality of life, including a greater likelihood of depression. Those are the consequences of not giving a prompt diagnosis.​

    We spoke earlier about the National Axial Spondyloarthritis Society, or NASS, which has identified four factors that contribute to delay: a lack of awareness among the public that AS might be the cause of their chronic pain; GPs failing to recognise the features of AS; referral to non-rheumatologists who might not promptly recognise AS; and failure by rheumatology and radiology teams to optimally request or interpret investigations. AS cannot be cured, but reducing the eight-and-a-half-year average delay in diagnosis will lead to better outcomes for those living with the condition.

    The all-party group for axial spondyloarthritis, of which I am a vice-chair, suggests three steps that would help to reduce the delay in diagnosis. The first is the adoption of a local inflammatory back pain pathway to support swift referral from primary care directly to rheumatology. Low levels of referral to rheumatology from primary care represent one of the key barriers to achieving an early diagnosis of AS, and a national audit by the APPG found that 79% of clinical commissioning groups do not have a specified inflammatory back pain pathway in place, despite NICE guidelines recommending that.

    Jerome Mayhew (Broadland) (Con)

    My hon. Friend makes reference to the NICE guidelines and the quality standard on spondyloarthritis not being implemented by 79% of clinical commissioning groups. Does he agree that that simply relates to primary carers referring directly to rheumatology departments, which is not a cost issue but one of professional education?

    Tom Randall

    My hon. Friend is absolutely right, and that neatly leads me on to the APPG’s second proposal. I appreciate that the NHS is rather busy at the moment with public health messaging of one kind or another, but awareness of AS remains low and support for an awareness campaign would help to significantly raise the visibility of the condition not only among the public, but among GPs.

    Thirdly, the APPG suggests encouraging the routine adoption of minimum service specifications across the NHS to help to reassure patients, particularly in the context of covid-19 and the difficulties many patients face in accessing key services during the recent lockdown. I would welcome any opportunity to meet Ministers separately to discuss those proposals in detail, if that were possible.

    I will leave the last word to Zoë Clark, who addressed the APPG’s last physical meeting in January. She told attendees how, after getting AS symptoms aged 20, incorrect diagnoses and the impact of her condition left her socially isolated and unable to live independently, at a time when she was trying to complete a demanding four-year master’s degree in osteopathy. She said that living with undiagnosed AS was a frightening time and she ended up having to largely sacrifice her social life, due to the difficulties of balancing her degree with the pain and fatigue she regularly experienced.

    No one should have to wait eight and a half years to find out what is wrong with them. I hope that we can begin to put that right.

  • Matt Hancock – 2020 Comments on Emergency Support from European Union Mobility Package

    Matt Hancock – 2020 Comments on Emergency Support from European Union Mobility Package

    The comments made by a spokesperson for Matt Hancock, the Secretary of State of Health and Social Care, on 18 September 2020.

    This will fund some of the costs associated with the transporting of equipment and items of personal protective equipment (PPE) to the UK from overseas.

    The successful bid for this grant ensures the UK continues to benefit from its own contributions to the EU under the Withdrawal Agreement.

    The EU mobility package is part of the Emergency Support Instrument (ESI). The ESI has an overall budget of €2.7 billion and was activated in April 2020.

    We continue to explore every opportunity for international cooperation to tackle the virus and save lives.

    The UK’s successful bid was £31,024,734 (€34,047,679).

  • Jonathan Ashworth – 2020 Comments on New Coronavirus Cases

    Jonathan Ashworth – 2020 Comments on New Coronavirus Cases

    The comments made by Jonathan Ashworth, the Shadow Secretary of State for Health and Social Care, on 6 September 2020.

    Today’s increase in Coronavirus cases is deeply concerning and a stark reminder that there is no room for complacency in tackling the spread of the virus.

    This increase, combined with the ongoing testing fiasco where ill people are told to drive for miles for tests, and the poor performance of the contact tracing system, needs an explanation from Ministers.

    Matt Hancock must come to the House of Commons tomorrow to set out what is being done to get testing back on track and bring case numbers down.

  • Jonathan Ashworth – 2020 Speech on Covid-19

    Jonathan Ashworth – 2020 Speech on Covid-19

    The speech made by Jonathan Ashworth, the Shadow Secretary of State for Health and Social Care, in the House of Commons on 1 September 2020.

    We are indeed all on the same side in fighting this virus. I hope that the Secretary of State understands that when we raise issues, we do so because we urge the Government ​to improve their response to fighting this virus. This remains a lethal virus that leaves many with serious, debilitating sickness. Everything must be done to drive down and eliminate infections and suppress the virus completely.

    With that in mind, I hope that the Secretary of State can answer a few questions today. I am grateful for advance sight of his statement. First, to avoid a second national lockdown, which we all want to avoid, an effective test and tracing regime is vital. I listened carefully to the figures that he outlined, but he did not tell the House that the numbers going into the system have actually fallen in the past week, from 79% to 72%. This system is not yet world beating.

    Throughout questions the Secretary of State has rejected criticisms of the private sector contractors who are involved in delivering the system, so there is no point in me raising them again, but would it not be better if money was spent on investing in local public health teams, particularly in those areas where restrictions are in place, so that they can do more door-to-door testing, as we have seen, for example, in Leicester? Surely that would be a better use of public funding, for example, than paying for so-called influencers on Instagram to big up test and trace.

    On testing itself, the Secretary of State now supports mass testing as a policy aim. It is something I have been calling for, for some months. It is something the former Health Secretary, the Chair of the Health Select Committee, has been calling for. Indeed, we tried to persuade the Secretary of State of its merits before the summer when we asked him to introduce regular testing of NHS front-line staff. He whipped his MPs to vote against it, but will he now, given that he is in favour of mass testing, introduce regular weekly testing of all front-line NHS workers?

    To move to mass testing means evolving our testing regime from one that provides antibody tests and diagnostic PCR—polymerase chain reaction—tests effectively to a system of mass screening using more rapid, on-the-spot antigen tests. The Secretary of State referred to rapid tests in his statement. Can he tell us when rapid, on-the-spot antigen tests will be rolled out across society and which sectors of the workforce will be first in the queue to access those tests?

    Will the Secretary of State also look at introducing saliva testing, which is being used in Hong Kong, for example, and will he ensure the quick turnaround of tests? I wonder whether he has seen the study from Yale that suggests that saliva testing could be as sensitive as nose and throat swabs. What is his attitude towards pooled testing, which would surely increase the capacity in areas of low prevalence? Does he have a plan to introduce pooled testing? Will he allow GPs to carry out testing or, at the very least, to arrange a test for their patients directly? They currently have to ask their patients to log on to the national system, which is causing huge delays.

    On local lockdowns, the Secretary of State said that he wants to involve MPs and elected officials. What process will be used to properly consult local Members of Parliament? What can MPs expect? When a decision has been made to put a local area into restriction, will he publish the specific evidence behind that decision? ​Why is it, for example, that our constituents in Leicester are not able to gather in private gardens? Can he publish the scientific evidence for that decision?

    In Trafford, we have seen infections increase. The local authority leader and the director of public health felt that restrictions should continue, but the hon. Member for Altrincham and Sale West (Sir Graham Brady) felt that they should be lifted. Why did the Secretary of State overrule the advice of the director of public health and instead endorse the representations of the chairman of the 1922 committee? There was a similar story in Bradford, and in Bolton, where restrictions are due to be lifted tonight, infections are increasing. Is it still his plan to lift restrictions tonight in Trafford and Bolton, even though infections are increasing compared with last week, when he made his initial decision?

    The Secretary of State is right: in the end, a vaccine is our best hope to stop this pandemic. Vaccines save hundreds of millions of lives every year, and I repeat my offer to work with him on a cross-party basis to promote uptake and challenge the poison of anti-vax myths, including those that we witnessed at the irresponsible and dangerous demonstration this weekend in Trafalgar Square. We will work constructively with him on the proposals he brings to the House. Does he share my concerns about those leaders, such as Putin and Trump, who are trying to short-cut testing to rush out a vaccine, undermining safety and efficacy, potentially damaging millions of lives and giving succour to the anti-vax movement?

    Finally, health protection is built upon good population health. Poverty makes people sick. Ending cuts and tackling deprivation as a determinant of ill health is vital to improving and protecting people’s health. But the Secretary of State is now embarking on a risky, distracting restructuring of Public Health England in the middle of a pandemic. Tory MPs like to blame Public Health England—it is such rotten luck that these decent, hard-working, competent Ministers are always let down by the people who work for them—but is not the reality that this restructuring will sap morale and focus and should wait until the end of the pandemic? The UK has suffered the highest per capita death rate of any major world economy. To get through this winter safely, our NHS and public health services need resources, and staff need personal protective equipment, fair pay, security and support. I hope he can deliver that.

  • Matt Hancock – 2020 Statement on Covid-19

    Matt Hancock – 2020 Statement on Covid-19

    The statement made by Matt Hancock, the Secretary of State for Health and Social Care, in the House of Commons on 1 September 2020.

    With your permission, and indeed your encouragement, Mr Speaker, I would like to make a statement on coronavirus. The latest figures demonstrate how much progress we are making in our fight against this invisible killer. There are currently 60 patients in mechanical ventilator beds with coronavirus—that is down from 3,300 at the peak—and the latest daily number for recorded deaths is two. However, although those figures are lower than before, we must remain vigilant. I said in July that a second wave was rolling across Europe and, sadly, we are now seeing an exponential rise in the number of cases in France and Spain—hospitalisations are rising there too. We must do everything in our power to protect against a second wave here in the UK, so I would like to update the House on the work we are doing to that end.

    To support the return of education, and to get our economy moving again, it is critical that we all play our part. The first line of defence is, and has always been, social distancing and personal hygiene. We will soon be launching a new campaign reminding people of how they can help to stop the spread of coronavirus: “Hands, face, space and get a test if you have symptoms.” Everyone has a part to play in following the social distancing rules and doing the basics. After all, this is a virus that thrives on social contact. I would like to thank the British public for everything they have done so far, but we must continue and we must maintain our resolve.

    The second line of defence is testing and contact tracing. We have now processed over 16 million tests in this country, and we are investing in new testing technologies, including a rapid test for coronavirus and other winter viruses that will help to provide on-the-spot results in under 90 minutes, helping us to break chains of transmission quickly. These tests do not require a trained health professional to operate them, so they can be rolled out in more non-clinical settings. We now have one of the most comprehensive systems of testing in the world, and we want to go much, much further.

    Next, we come to contact tracing. NHS Test and Trace is consistently reaching tens of thousands of people who need to isolate each week. As I mentioned in answer to a question earlier, the latest week’s data shows that 84.3% of contacts were reached and asked to self-isolate, where contact details were provided. Since its launch, we have reached over 300,000 people, who may have been unwittingly carrying the virus. Today, we also launch our new system of pay to isolate. We want to support people on low incomes in areas with a high incidence of covid-19 who need to self-isolate and are unable to work from home. Under the scheme, people who test positive for the virus will receive £130 for the 10-day period they have to stay at home. Other contacts, including, for instance, members of their household, who have to self-isolate for 14 days, will be entitled to a payment of £182. We have rolled out the scheme in Blackburn with Darwen, Pendle and Oldham, and we will look to expand it as we see how it operates on the ground.​

    The third line of defence is targeted local intervention. Over the summer, we have worked hard to integrate our national system with the local response, and the local action that we are taking is working. In Leicester, as the hon. Member for Leicester South (Jonathan Ashworth) knows well, as a local MP, in Luton and in parts of northern England, we have been able to release local interventions, because the case rate has come down. We also now publish significantly more local information, and I put in place a system for building local consensus with all elected officials, including colleagues across this House, wherever possible. Our goal is that local action should be as targeted as possible. This combination of social distancing, test and trace and local action is a system in which we all have a responsibility to act, and this gives us the tools to control the virus while protecting education, the economy and the things we hold dear.

    Meanwhile, work on a vaccine continues to progress. The best-case scenario remains a vaccine this year. While no vaccine technology is certain, since the House last met, vaccine trials have gone well. The Oxford vaccine continues to be the world leader, and we have now contracted with six different vaccine providers so that whichever comes off, we can get access in this country. While we give vaccine development all our support, we will insist on safety and efficacy.

    I can update the House on changes to legislation that I propose to bring forward in the coming weeks to ensure that a vaccine approved by the Medicines and Healthcare Products Regulatory Agency can be deployed here, whether or not it has a European licence. The MHRA standards are equal to the highest in the world. Furthermore, on the development of the vaccine, which proceeds at pace, I will shortly ask the House to approve a broader range of qualified clinical personnel who can deploy the vaccine in order of clinical priority, as I mentioned in questions. As well as the potential vaccine, we also have a flu vaccination programme—the biggest flu vaccination programme in history—to roll out this year.

    Finally, Mr Speaker, in preparation for this winter, we are expanding A&E capacity. We have allocated billions more funding to the NHS. We have retained the Nightingale hospitals to ensure that the NHS is fully prepared, and we published last month updated guidance on the protection of social care. As well as this, last month, figures showed a record number of nurses in the NHS—over 13,000 more than last year—and record numbers of both doctors and nurses going into training. We are doing all we can to prevent a second peak to prepare the NHS for winter and to restore as much of life and the things we love as possible. As schools go back, we must all remain vigilant and throughout the crisis we all have a role to play.

    This is a war against an invisible enemy in which we are all on the same side. As we learn more and more about this unprecedented virus, so we constantly seek to improve our response to protect the health of the nation and the things we hold dear. I commend this statement to the House.

  • Lisa Nandy – 2020 Comments on US Not Helping in Global Vaccine

    Lisa Nandy – 2020 Comments on US Not Helping in Global Vaccine

    The comments made by Lisa Nandy, the Shadow Foreign Secretary, on 2 September 2020.

    This is an extraordinary attack on the World Health Organisation in the midst of a global pandemic and a deeply concerning setback in the search for a vaccine.

    This kind of ‘vaccine nationalism’ risks hampering the fight against the spread of Covid-19 and ultimately delaying the development, manufacture and distribution of a vaccine. This is a global fight that demands a coordinated international response.

    It is becoming increasingly clear that the UK government is either unwilling or unable to exert influence across the Atlantic, and that the ‘deep friendship… and special relationship’ heralded by the Foreign Secretary is becoming increasingly one-sided.

    The UK must now show global leadership, begin building alliances with our democratic partners around the world and work collaboratively to prevent a national scramble for a vaccine.