I remind hon. Members that there have been some changes to normal practice in order to support the new call list system and to ensure that social distancing can be respected. Members should sanitise their microphones using the cleaning materials provided before they use them, and then place those materials in the bin. They should also respect the one-way system around the room. Members should speak only from the horseshoe, and they can speak only if they are on the call list—that applies even if debates are undersubscribed.
Members cannot join the debate if they are not on the list. Members are not expected to remain for the wind-up speeches. I remind hon. Members that there is less of an expectation that they stay for the next two speeches once they have spoken—that is to help manage attendance in the room. Members may wish to stay beyond their speech, but they should be aware that if there are lots of speakers, doing so might prevent Members in the seats in the Public Gallery from moving to the horseshoe.
That this House has considered family visit access in health and social care settings during the covid-19 outbreak.
It is an honour to serve under your chairmanship, Ms McVey. My main focus in speaking today is to highlight the need for improved patient advocacy and adult safeguarding via visitation rights for family members of working-age disabled adults in full-time residential care, including those admitted to hospital. Such patients often cannot speak for themselves and need additional access to family members who are able to advocate and communicate on their behalf.
I applied for the debate because of an awful situation of a mother in my constituency—a mother, much like me or any hon. Member present, who has had to endure a situation that I hope no mother has to face in the future. She is a teacher, a local community advocate, a single mother and someone who has tirelessly fought for her child’s care needs. She was prevented from caring for her son, Jamie, and forced to abandon him to a care home that did not live up to its name. At 21 years old and with no visitors, he was left isolated, bewildered and depressed, often calling out in anguish, “I want my mum. I want my mum.”
Jamie was a warm and affectionate young man who loved touch, kinaesthetic learning and being with people. His mother was denied access to her child, and I cannot begin to imagine what it must have felt like, knowing that her son was denied the care of his family for months—denied a hug, denied the comfort of a warm hand holding his, and denied dignity in his suffering. As a mother, my constituent felt powerless but sure that, had she been able to see him, she would have identified his decline and been able to intervene.
Underfed, Jamie wasted away, getting thinner and thinner in his confusion and isolation. Separated from those he loved and trusted, with multiple bedsores and open wounds left untreated, he began to withdraw within himself and into a catatonic state of unresponsiveness—a young adult with complex disabilities and care needs, left to suffer in silence. By the time his mother was able to see him, it was too late. She reflected on the lack of status that she felt as a mother, which she felt was shared by many family members. It felt to her as though families are often seen as a nuisance or even a threat, and they are sidelined and ignored by some in adult care homes. This mother also felt strongly that some adult care homes do not embrace the care of the whole person.
It might be helpful to colleagues to know that I intend to call the Front Benchers by 3.30 pm at the very latest. I would like to ensure that all colleagues get to speak today.
It is a pleasure to serve under your chairmanship, Ms McVey. I thank my hon. Friend the Member for Beaconsfield (Joy Morrissey) for securing this debate on such a hugely important topic.
Throughout the pandemic I have received devastating correspondence from my constituents, as I imagine all Members have, regarding the inability to see their loved ones in care homes. Although the restrictions placed on care homes are for the protection of the most vulnerable and their carers, the loneliness and isolation that people feel, especially those with dementia, has increased due to covid-19 preventing them from seeing their family and friends.
Although more needs to be done for residents with dementia and other diseases, I welcome the guidance that was provided by the Government last week, which sets out plans on how our care home residents and their families can be reunited. For areas such as mine that have experienced heightened restrictions for more than three months, the measures will help tackle the mental health and wellbeing of care home residents and reunite families.
Prior to those tougher restrictions being imposed in July, the images of family members being able to see one another again were truly heartwarming. The joy in the faces of residents and their families will stay with me for a long time. To have that taken away seems not only heartbreaking but cruel. I truly sympathise with all families and care workers who have had to endure that hardship.
Some care homes in my constituency are extremely limited as to what contact between families they can provide, with either limited window space for window meetings or limited telephones to speak to family members. One care home, which I will not name, has only one phone for residents, and that frequently does not work or is not answered.
Along with all Members, I agree that we need to tackle this pandemic but we also need to be fair in tackling it. I fear that is one factor that we are forgetting. It is more important than ever to use technology to help mitigate some of those issues, but a lack of understanding of how to use technology, on the part of residents and even staff, has prevented it from being fully utilised. What is being done further to mitigate those issues?
I thank the hon. Member for Beaconsfield (Joy Morrissey) for securing the debate and I congratulate her on her moving speech on Jamie’s behalf. I lived in her constituency through my teens, and in fact I stood against her predecessor a long time ago. My mother is still one of her constituents. She is living very much independently, but maybe one day I will need to go to the hon. Member for help with my mother regarding the issue that we are debating today.
I will also place on the record my thanks to those working in the social care sector. Their courageous work during the pandemic, delivering quality care in horrendously difficult circumstances, has not gone unnoticed. The pandemic has been difficult for everyone, but for those residing in care homes, or for those with loved ones living in them, it has been nightmarish. Over 40% of covid-19 deaths have taken place in care homes—more than 26,000 deaths. The combination of fear and isolation, coupled with a dearth of familiar emotional support, is creating a mental health crisis in our care home settings.
Recently, I received this letter from a constituent:
“Dear Alex, my letter is concerning my bedbound 81-year-old mother. who is currently resident at a care home in Leeds North West. My mother, Patricia, has been a resident for many years. Along with many families, we had no contact with mum over the course of the pandemic, apart from a very short video, which lasted around a minute, sent when requested at desperation in the early months of the pandemic.
We requested that should a window room become available, could mum be moved, so we could at least visit her from a safe distance without entering the premises. Six weeks ago, a room did become available and we have been visiting mum at a window since. Today, however, I was contacted by the care home manager to inform me that we can no longer visit mum.
It is a pleasure to serve under you as Chair in this important debate, Ms McVey. I thank the hon. Member for Beaconsfield (Joy Morrissey) for securing it and for sharing the harrowing story of Jamie from her constituency. It will stay with every single person who heard it.
I will begin my remarks, as others have done, by sharing a passage from a letter from a constituent called Penny Hutchinson. Her mother, Yvonne, is living with dementia in a care home in Halifax. She said: “Imagine that you had not seen your mum for eight months because she has been locked away in isolation with no meaningful family contact. Then imagine the huge feeling of relief and elation as restrictions are lifted and the vulnerable are told they no longer need to shield. Now imagine the feeling of complete desolation when you discover that those freedoms and privileges don’t apply to your mum and dad. Add to that the overwhelming feeling of guilt when you try to explain to your loved one why you can’t come in to see her, hold her hand or give her a hug, and that there is no end in sight.” I sent that letter on to the Secretary of State for Health and Social Care because it said more than I could have done on her behalf.
Like Penny’s mum, more than 70% of people living in care homes have a form of dementia. Visits from family members have a really important part to play in the cognitive state of those residents, but instead of being able to be close to loved ones at this anxious time, the best they can hope for is a socially distanced meeting behind plexiglass or outside in this weather. Although that is well intentioned, it can often cause confusion and distress.
Efforts to protect those who are older and clinically vulnerable by managing contact diligently will still of course have to be a priority in the coming weeks as we strive to avoid outbreaks in care homes and manage them where they have occurred. The Alzheimer’s Society has been keen to make it clear that for those with dementia, limiting visits in that way can lead to their symptoms increasing and their condition deteriorating more rapidly, ultimately leading to premature death, so a rebalancing of those risks is required.
It is a pleasure to serve under your chairmanship, Ms McVey. I offer sincere thanks to the hon. Member for Beaconsfield (Joy Morrissey) for securing this vital debate.
It is clear that many MPs have been contacted by worried—often terrified—constituents whose parents, children, relatives or friends are in care homes. I for one have felt utterly heartbroken listening to some of them describing the fear and isolation that they know their loved ones are experiencing, and I, too, have an example—one of many. The mother of my constituent Steph is in a care home. Steph is one of five children and for a long time they have each spent hours on end with their mother. They lovingly held her hands, combed her hair, remembered stories together and reminisced about the past. They were not just visiting their mum; they were providing essential care.
Eight months on from the arrival of coronavirus, Steph still cannot touch her mum. People like her all over the country cannot hug their mothers or fathers, children, siblings or friends. They still cannot hold their hands to comfort or reassure them. All that they can do is watch their often rapid decline, for just half an hour at a time, from a distance—perhaps from a structure in a garden, or sometimes through a closed window, or maybe a screen if they are lucky. Like Steph’s mum those vulnerable people are struggling to understand why their children and families cannot be with them. An entire lifetime of love and closeness is ripped away from them and torn apart. For every person affected, every single passing day is a precious day lost.
Now, as winter approaches and, predictably, we are in the second wave, there are still no guidelines in place to protect loved ones from dying not only in loneliness and isolation, but from it. The Government like to talk up their ambition in many other areas. We have all heard of Operation Moonshot, Nightingale hospitals and world-beating apps, but there has been barely a whisper about allowing family carers to be with their loved ones. The announcement of a trial period was welcome, but for many people it created an even greater desperation, because they could not see any end in sight for the enforced separation.
It is a pleasure to serve under your chairmanship, Ms McVey. I, too, thank my hon. Friend the Member for Beaconsfield (Joy Morrissey) for securing this vital debate and opening it so well. I also want to join in with the calls of thanks to the staff across the social care sector who have worked so hard for residents across the country. I send my thoughts and best wishes to all the residents, and their families and friends.
East Sussex has the highest proportion of care homes in the south-east, and yet our county has the lowest covid rate. That suggests that our care homes have stood up to the challenge and done a great job, despite the enormous task that was in front of them.
The challenge before us now is as follows: keeping vulnerable people safe without taking away their right to live their years in dignity, and in the company of family and friends. I have been helped by many residents across my constituency to put that dilemma into words. A contribution from Heathfield sums it up:
“In the care home where my partner resides, they allow two half-hour visiting slots a day. There are forty residents, that will give each resident one half-hour visit every ten days, even so it is still not enough. On each visit the loved one sits at one end of a room, the visitor at the opposite end and the carer in between…My partner’s mental health has remarkably deteriorated in the last few months, apathy and depression are more dominant on each visit. Every time we visit she seems more and more withdrawn and most likely feels abandoned by her loved ones because of the limited visiting.”
Last week, the Government issued revised guidance for visiting arrangements in care homes, to ensure safe access and visits by families and loved ones. The guidance proposed a range of options to create covid-19-secure care home environments and visits, including visits taking place outside and the installation of wall-to-ceiling screens.
It is a pleasure to speak under your chairmanship, Ms McVey. I thank my hon. Friend the Member for Beaconsfield (Joy Morrissey) for securing this important debate.
One of the harshest features of the restrictions that we introduced many months ago to stop the spread of covid has been for our constituents not to be able to visit their loved ones in care homes. I have received—as I am sure has every colleague in this place—many letters expressing the real frustration and angst that they feel because of the restrictions that we have introduced. The updated guidance released last week is welcome, and it attempts to address some of the concerns, but we need to bring an element of humanity and empathy to the guidance. I know that many in this room, and our constituents, will feel that something has gone wrong over the last few months.
I want to talk briefly about a family in my constituency whose situation is very similar to those already raised by other Members. There is a young man whose family live in my Warrington South constituency, but his care home is in Greater Manchester. While we did not have any restrictions in Warrington, he was existing under restrictions in Greater Manchester, and different approaches were being taken. I tried many, many times to speak to the director of public health in Greater Manchester about the issues facing this family. I must say, it was a real nightmare to communicate across different county boundaries and to try to have a one-to-one conversation with someone from the care home and with the people regulating that care home.
The young man did not get to see his parents for about five months in total. That is simply wrong. Not only did the young man not get to see his mum and dad, but mum and dad did not get to see their son. I can only imagine how awful it would be, as a dad, not to see my son for that length of time. I think we do need to think again about the way we have interpreted some of these rules.
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Jamie entered full-time care at age 13. As a child in a care setting, it was wonderful. The care was holistic and helped support Jamie in every aspect of his daily life and learning. He thrived in that environment, but the change came when he moved into adult social care. Many adult care homes are excellent and highly skilled in supporting adults with complex disabilities, but others—it might be a very small minority—seem reluctant to work with families or to provide adequate levels of transparency and care. It is an ongoing problem, which existed well before the covid pandemic; that has only highlighted these issues.
Disallowing visits or video links that allow families to see and interact with patients takes away a level of scrutiny that makes those already vulnerable chronically so. Depriving vulnerable working-age disabled adults who have complex disabilities and needs, especially those who already struggle with communication, of the love and support of their families is inhumane and cruel. As a society, we lessen our dignity and humanity when we allow our loved ones to perish alone and to wither away and give up on life. Jamie had no voice, so I am here today to speak on his behalf, and on behalf of his mother and grandmother, to make sure that his story is remembered and that other deaths can be prevented this winter.
I welcome the Government’s support for care homes and adult social care during the pandemic and I thank the Minister for reaching out to me the moment that I applied for this debate. She has been incredibly helpful and I thank her for her active participation in finding a solution and justice in Jamie’s case. I thank the Government for their care home support package in March that announced £1.6 billion funding for local government and £1.3 billion to go to the NHS and social care. In April, a further £1.6 billion was announced for local government and for the adult social care action plan and, in September 2020, the Government published “Adult social care: our COVID-19 winter plan 2020 to 2021”, which was shaped and recommended by the adult social care taskforce. The plan set out key elements of national support available for the social care sector for winter 2020; I welcome everything that was outlined in it.
Finally, I welcome the Government’s announcement on visiting guidelines from 5 November. Allowing visitation is so important for patient care, advocacy, safeguarding and mental wellbeing, particularly for disabled vulnerable patients who may not be able to advocate for their own care needs. Allowing family members to visit could save many lives during the winter months and prevent other vulnerable disabled patients from being neglected, abused and left to suffer and die in silence, while restoring a level of compassion, empathy and humanity to patient care both in hospital and in the care home setting.
Now that we are in the second lockdown I ask the Minister and others to consider what lessons we have learned from the excess deaths in care homes and from the adult safeguarding issues raised during the first lockdown. I understand that the main goal of the Department of Health and Social Care is to protect the NHS, particularly during the winter months, but we also need to save the lives of the vulnerable disabled by allowing each patient to have a family member with them as their advocate and carer. That would be aided by the improvement in mass testing in the coming months and the availability of personal protective equipment. This cohort needs a special exemption. A carer would allow for lives to be saved and, with mass testing and the arrival of a vaccine, that could help safeguard many other lives in the future.
If the NHS reaches capacity, as it often does in the peak winter months of January and February, another alternative would be for a family member or carer of the vulnerable patient to care for them directly in a home, a hospital or care home setting. A family member or loved one can also help with caring for the vulnerable person at home, further reducing the burden of care to the NHS. Many of these family members are able-bodied adults who are at a lower risk of developing serious health problems from covid-19 transmission. We also have to allow people to care for those they love.
I welcome the Government’s announcement in the winter care plan that local authorities should work with social care services to reopen safely, especially day services and respite services. Reopening such day centres would allow families to manage a disabled loved one’s care more effectively, while perhaps reducing the need for full-time residential care and lightening the burden on full-time carers who do not have access to vital daycare facilities. The Relatives and Residents Association, which is an advocacy group, reported that helpline callers had been concerned about the standard of care falling as already stretched services face staff shortages and burn-out. Stopping visits from family and friends restricts the ability for oversight and advocacy.
One of the callers to the association’s helpline said that his wife
“starved herself to death. Her death was due to the pandemic but she did not die from the virus itself. It wasn’t coronavirus—it was death due to a refusal to eat. She was isolated and alone.”
Perhaps the Minister could provide clarity as to whether families are now permitted to remove their loved ones from residential care home settings, and what the protocol for that would be, moving forward.
Jamie’s care home was in a neighbouring county, but his mother and grandmother lived in my constituency. Buckinghamshire County Council and the NHS are excellent and I worked extremely closely with them during the pandemic and the first lockdown to protect care homes and elderly residents, and to reduce the rate of transmission and death in care homes. I was proud of the work that we all did to protect the elderly in South Bucks.
However, the issue of working-age adults with complex disabilities in residential care facilities completely passed me by in the first lockdown, because many of my residents had additional needs and were at home. They were reliant on day centres and respite care. That was the issue I was seeing, not the issue of the long-term residential care crisis.
I did not learn about Jamie’s treatment during lockdown until the week before his death, when it was too late for me to help. That is why I am raising the matter now. This patient cohort cannot speak or advocate for their own care. They require extensive care and support from care home and hospital staff, and could run the greatest risk of being sidelined during a spike in hospital admissions, when staff resources are spread more thinly and they have to prioritise patient care.
Because these patients require the most care it is important that they have a family member who can be with them as their patient advocate and carer, to help ensure that they make it through these winter months. I welcome the Government’s announcement of a vaccine and I know that, with the highlighting of safeguarding, we can get through these winter months, and that Jamie’s memory will not be forgotten.
There is no greater need than to spend time with one’s loved ones. That need is even stronger for our most vulnerable and we must go further in addressing that need. The Government’s announcement last week was a big step in the right direction, but we need to carry on our journey to tackle the issues of loneliness and mental health.
I will put on the record my thanks to all the care workers across Radcliffe, Prestwich and Whitefield for the immense work that they have undertaken during the pandemic, for the work that they continue to undertake, and for the hardship that they must endure in having to deal with the frustrations and heartbreak that they see on a daily basis.
We are devastated that our family is being so cruelly torn apart. I thought that, as a strong woman, I would be able to deal with the mental impact, but it is destructive. Surely, there are humane options which can keep families together.”
I am thankful to the Minister and to the Government that guidance has now been released that says visiting through screens or windows is allowed, which is welcome news for my constituent. However, for many residents with dementia or other cognitive impairments, the distress that would cause makes it untenable. Similarly, the British winter makes outdoor visits impractical for older and vulnerable visitors.
In addition, the cost of implementing measures that have been suggested to create environments that are safe from covid-19 are to be met by care providers. There is no commitment of additional money, excluding the infection control fund, to cover the costs associated with purchasing screens or visiting pods. Government shortcomings will doubtless result in convenient finger-pointing at individual care homes, which are unable to front the additional costs for safe visiting.
We also need to give family members the same rights as key workers, who are afforded regular access to testing and trained to wear personal protective equipment. The Government must know that that is the best way forward, as they promised a pilot scheme on those lines, but that was nearly a month ago and no date for the pilot has been forthcoming. I look forward to hearing the Minister say when we can expect to see that pilot begin.
The wellbeing of residents must be placed at the forefront of the Government’s plans. That should include a recognition of the important role that social workers play in facilitating providers’ and residents’ decision making about visits. Social workers must be recognised as professional visitors, to ensure that residents’ views and wishes are central to decision making about visits, and to support care providers to explore thoroughly rights and risks alongside all the other factors that must be considered in making bespoke visiting arrangements.
Practice is different across the care sector. Hospices such as the Sue Ryder Wheatfields Hospice in my constituency have given social workers access, unlike many care homes, which have denied them access. Social workers are mentioned briefly in the guidance issued for lockdown, which states:
“Social workers can assist with individual risk assessments, for visits, and can advise on decision-making where the person in question lacks capacity to make the decision themselves.”
But social workers do so much more, and are pivotal in promoting strengths-based human rights models of good practice. Social workers undertake a variety of statutory and non-statutory functions on behalf of public bodies. Recognition of the importance of safe access to care and health settings for social workers as professional visitors is essential. I look forward to hearing the Minister’s comments on this matter.
Residents, staff and the families of those in care homes have been failed by this Government since the beginning of the pandemic. From woefully inadequate PPE—I had to deliver PPE myself to care settings—to inadequate testing, I am afraid that the social care sector has been treated with contempt. On top of a decade of underfunding, that has created a crisis within a crisis that is entirely of the Government’s own making.
Beyond the pandemic, long-term reform of the social care system is urgently needed. But for now, at the very least families should be able to see their loved ones, so I urge the Minister for Care to press forward with the pilot, to ensure that it begins as quickly and safely as possible.
I want to put on the record my thanks to Calderdale’s director of public health, Debs Harkins, who has worked tirelessly throughout the pandemic alongside her colleagues, including the director of adult services and wellbeing, Iain Baines. They have both met Penny and others to try to make progress.
Before I move on to the solutions, I want to point out that when I received a response to Penny’s letter from the Minister’s civil servants, it said: “The Government’s guidance for visiting arrangements for care homes published on 22 July allows for local decision making based on the assessment of the director of public health and the care provider. Further details can be found at the gov.uk website by searching for ‘visiting care homes during coronavirus’.”
I followed that link, and at the time it stressed that:
“For local areas with a high local COVID alert level (high risk or very high risk)”—
Halifax has been in tier 2 equivalent restrictions since July—
“visiting should be limited to exceptional circumstances only”,
such as end-of-life care. That gives no discretion for directors of public health, and puts them in an impossible position with family members desperate to see loved ones. Some clarity on decision making for visits would be incredibly welcome.
I imagine that everybody in this debate feels that the situation is far from acceptable—we have heard from many hon. Members already—so what would make a difference? I have been pleased to see news this week of mass testing, rapid testing and vaccines being developed at pace. We must ensure that residents of care homes, those working in care homes and designated family members are the first in line to access them as they become available. Treating designated family members as key workers would be a logical step. It would not overwhelm the system and would ease the distress of so many care home residents and their families.
We all know that social care workers have been among the many heroes of this crisis. They have carried themselves with dignity, honour and respect in the face of unimaginable pressures. However, as they tell us, not even they can provide full care to their residents without the support of family members. For those with dementia, family visits are not privileges or luxuries but a vital part of their care and treatment. Therefore, it seems appropriate to consider measures such as this—the shadow Minister has also been calling for it—which would ease the considerable pressures that social care workers have been placed under and the mental anguish faced by separated families. We must work together to reach a better settlement for care home staff, residents and their family members.
When this is all over, we will bring the economy back from the brink, but there will be some opportunities that we will never get again. Let us not regret not doing everything possible when we had the chance.
Last week I co-ordinated a group of 40 MPs from across the House who wrote to the Secretary of State with a real plan. It would allow a designated family or friend carer to have the same key worker status as someone paid to work in a care home. They would have the same access to tests and PPE, and the same access to their loved ones. A number of groups have been calling for various measures of that kind for some time. They include the National Care Forum, Age UK, One Dementia Voice and the British Association of Social Workers. We are pleased to give them and the people they represent our full backing and a strong voice today.
I want to be clear: care workers have been magnificent throughout the pandemic, but the care that our families give is no less important for health and wellbeing. The cruel 30-minute time limit on visits must be scrapped, and care homes must have protection from legal action if covid is introduced to a home by a designated visitor. Those are the same protections that have been agreed for the NHS. Time is running out. With every day that passes, isolation, loneliness and deterioration grow for many of the most vulnerable in society, and friends and family carers experience more anguish. They pass another day of separation from their loved ones as they slip away faster, and more painfully, than they should.
It is often said that the true test of a country is how it treats its most vulnerable. For as long as the Government hold out and do not implement the plan I have described, they are failing that test, and failing the thousands of families who experience anguish every single precious day.
I recognise that we have now liberated care home visits, compared with the last lockdown. I also recognise the dilemma for the Minister, because she has been a target for some. We try to do the right thing by residents, and yet here we are saying, “Open up!” If we do so, we need to protect the Minister—the onus, if we take more risk, is based on a cross-party decision.
I hope I am not overdramatising, but some of the measures read to me as more akin to a prison visit than a care home visit. They are also costly, in a system that is already financially constrained. Furthermore, the measures could be avoided with the introduction of testing for designated family and friends.
I want the Government to consider the following seven measures: regular testing for at least one designated family member and all visiting health professionals; the vaccine—when ready, as we hope it will be—to be prioritised for care home residents, and given to the designated family member and the staff of the care setting when given to the resident; a recognition that with testing and PPE, safe and closer contact can be permitted, and that we have learned from the devastating impact of the first lockdown; additional funding to support care providers to create covid-19-secure environments to enable members of the wider family to visit; national and local monitoring, and a reporting process for any blanket decision to ban visits; an acceptance that virtual technology, as good as it is, cannot replace human in-person interaction; and, finally, for providers at a local level actively to promote the safe visits.
This Friday, I will partake in my regular care home quiz with the residents at Ardath in Bexhill. Sadly, we cannot be physically together, but will join on Zoom. Our quiz master, the remarkable resident Georgie Farrow, always sets a tough challenge for me and brings laughter to the room. That residential care setting, like many others I visit, demonstrates the love, fun and spirit that can exist. It is vital that we do not lose that ethos while rightly seeking to keep residents safe.
We should not shy away from the real danger. In seeking to protect vulnerable residents, we might not only diminish their quality of life, but end up prematurely ending it altogether. The ingredients of love, care and protection, which loved ones deliver, are vital to keep vulnerable people alive and with a life. On that note, I very much hope that the Government and all of us, across parties, will work together as one to give more life into our care homes.
I want to recognise—we cannot forget it—how badly the first wave hit care homes. Therefore, everything I have just said is tempered against the fact that far too many elderly residents passed away as a result of covid-19. Some of the most awful conversations I have had in the past 12 months were with family members—daughters, sons, wives and husbands—who had lost a loved one in a care home.
At the beginning of the coronavirus pandemic, there were around 66,000 deaths of care home residents, and around 19,500 were covid-related. That means around 30% of all deaths in care homes were related to covid-19. Therefore, it is no surprise that we have had to put measures into place to try to protect residents in care homes, but they are not prisons; they are care homes—the clue is in the word “care”. Care is not just about protecting someone from a virus, but about ensuring that their mental health is maintained.
At the same time, we all know that being able to offer more visits will help everyone’s mental health and wellbeing. That is why we need to look further than the visits that are being carried out today. We need to be able to define the importance of the therapeutic impact that visits can have or, equally, how the suspension of visiting can damage the mental health of individuals and their families.
Dementia or Alzheimer’s disease was the most common pre-existing condition found among those people who sadly died as a result of covid-19 within care homes—around 50% of all deaths. For people who suffer with dementia, a lack of social contact not only is bad for their mental health, but has a significant impact on the progression of that dementia. This is a real priority for those who care for people suffering with dementia. Family and friends must play a significant role in the care of those people. Interpreting their needs and providing that personal care is incredibly important, but also very challenging in very difficult circumstances.
I welcome the announcement of a pilot scheme to enable informal carers to be given key worker status, and I am looking forward to the Minister giving us more details on that. The introduction of the lateral flow rapid tests for Warrington—10,000 being given to Warrington this week—is very welcome. I am encouraging the director of public health in Warrington to make sure that she is in touch with care homes, to ensure that those family members who need to get into care homes can get those frequent tests.
I will finish with a brief mention of a constituent who wrote to me earlier this week—a gentleman who, I think it is fair to say, is in his mature stage of life—to say that he had purchased a piece of technology and had installed it in a window in his wife’s care home. He told me that it was similar to the system used in a post office, with a microphone and a speaker, and it made a world of difference to him and his wife. He could now do a visit in complete safety, with no risk whatsoever. The window remains sealed, but he does not have to shout or practise sign language. He has been able to share his ideas with other people in the care home, and other visitors and relatives have taken on board his ideas and introduced them in other care homes.
I finish by paying tribute, and recording my thanks, to those who work in care homes in Warrington South. They have done an incredible job over the last 12 months. I also thank the members of the social care team in Warrington who look after elderly residents in their own homes by going into a home every day to ensure that they are well cared for.
There are many issues that we need to tackle for families and people in care, and I hope the Minister can take back to the Department some of the things that we have talked about today, so that it can come forward with some more ideas.