British Sign Language Bill Debate
Full Debate: Read Full DebateRosie Cooper
Main Page: Rosie Cooper (Labour - West Lancashire)Department Debates - View all Rosie Cooper's debates with the Department for Work and Pensions
(2 years, 9 months ago)
Commons ChamberI beg to move, That the Bill be now read the Third time.
This is a momentous day for the deaf community. Exactly 19 years ago to the day, British Sign Language was first recognised in a ministerial statement. Sadly for the deaf community, not a lot has changed, so today we have the chance to finally commit that recognition to statute.
Members of the deaf community have been fighting their whole lives for this moment, and many of them are currently in Trafalgar Square watching the debate on a huge display. I realise that the fact that we have got this far is quite astonishing. I have many people to thank for guiding the way and providing useful insights, case studies and reports that have been invaluable in developing the Bill. This has by no means been a solo effort—far from it. I have had help from very many people. Locally, it has been all hands on deck. My specific thanks go to the politics lab group at Edge Hill University in my West Lancashire constituency, who have been helping out by conducting interviews, gathering data and creating a briefing to aid the campaign.
I also want to thank Janice Connolly and everyone at the Merseyside Society for Deaf People. They could not travel here—they could not get coaches to be here—but they are watching this debate at the Deaf Centre in Liverpool. I grew up in that community, running around there, and I owe so much to them all. They have been a huge part of my life. As a child, it was the Friday evening ritual that deaf adults would meet at the Deaf Centre. In those days, it was at Park Way in Princes Park. While the adults socialised, their children, both deaf and hearing, would play together, able to communicate easily and without effort. Being a CODA, a child of deaf adults, gives me a unique position, straddling two worlds with equal access to both. I hope the Bill will bring the hearing and deaf communities together as never before.
I remain incredibly thankful to the Members who have been so supportive of the Bill, both here in the House and in promoting it elsewhere. I echo the words I used on Second Reading in January when I said how fantastic it is that this Chamber is speaking with one voice and that we are doing the right thing.
To come back to this momentous day—one I hope deaf people will celebrate for many years—the recognition of BSL is a landmark acceptance of a language that for far too long as been overlooked and misunderstood. The Bill is a testament to the perseverance of all deaf people and a celebration of deaf culture. We, all of us today, stand on the shoulders of every deaf campaigner who has fought so hard to get us here. Better historians than me can tell that story, but it really is a remarkable one. Every single campaigner who came before or who is still fighting now deserves to be recognised by us today.
In honouring them, I will focus on one campaigner who meant the most to me. That was, of course, my dad. He fought to be treated as an equal human being: to be appreciated and heard based on merit not on deafness. On Second Reading, I spoke of his life experiences and how hard it was for him to show his value and, once he did, how prized and needed his skills were. From that, he was able to provide for his family and enjoy a fulfilled and happy life, which nonetheless, every day, had its communication challenges. He fought for better education for deaf children, and for deaf teachers to teach deaf children. One of my great friends, Mabel Davis, was a very successful deaf headteacher at a school for deaf children. My dad believed that education enabled you to live your best life. He campaigned to make television accessible by using subtitles—what a hard journey that continues to be. On Second Reading, I made reference to Ofcom. It obviously does not read Hansard, because programme subtitles are still dreadful and it is not doing anything about it. Inaccurate rubbish is how I would describe them. I have two hearing aids, so more often than not I prefer to watch TV with subtitles.
To come back to BSL, people assume that BSL is simply sign-supported English and that all deaf people have to do is learn to master the English language. Nothing could be further from the truth. My dad used to say to me, “You can learn a new language; I can’t learn not to be deaf, nor to be hearing.” His words sum up the problem that every deaf campaigner struggles to get across to hearing people who just do not understand the real issue.
That is why this Bill is focused on improving BSL provision. Too often, hearing people have made decisions for deaf people that rely on their conforming to the hearing-centric ways of accessing services. That is just so wrong. Developing guidance for deaf people, integrating BSL into those services, is very important.
There is also a lack of cultural understanding of deaf people and of sign language, which has prevented this change for so long. We are seeing a BSL revolution before our eyes. Deaf people cannot learn not to be deaf, but hearing people can learn BSL, and they are learning. Huge numbers of people are signing up to BSL courses. People at secondary schools and universities are asking to do it, and I am delighted to say that so are Members of this House. Well done.
I congratulate my hon. Friend on bringing this Bill to Parliament. Last week I went to a school in Putney where I found out the sign for Putney. [In British Sign Language: “Putney”.] There is a deaf teacher teaching the hearing pupils British Sign Language. The pupils love those classes, and now they are opening up the ability to communicate throughout our community. It is fantastic to see. I have seen the revolution for myself in Putney, and it is great to see it going on across the country as well.
I thank my hon. Friend for those comments. BSL is such a rich, vibrant, brilliant language, which relies not only on signing but on body language and facial expression. It is great fun. When I was Lord Mayor of Liverpool I got the children to finger-spell 26 letters of the alphabet for sponsorship. The money they raised in sponsorship was used to buy minicoms for deaf people—although mobile phones would soon replace those; none the less in those days that too was a revolution.
Where are we today? Deaf representation in the media is at an all-time high. Just in the last year we have seen a deaf superhero using American Sign Language; Troy Kotsur, a deaf actor, is nominated for an Oscar and last week won a BAFTA, and Rose Ayling-Ellis won “Strictly Come Dancing”. In 1987, all those years ago, Marlee Matlin won the Best Actress Oscar for “Children of a Lesser God”, but it took another 35 years for Troy to become the second person nominated for his role in “CODA”, which stands for “child of deaf adults”—I know, I am one, but sadly I will not be getting an Oscar.
Since 1987, other movies have been roundly criticised for using hearing actors to play deaf roles. A sign of the times is that “CODA” actually cast deaf actors in deaf roles—what recognition! That is magnificent. The times they are a-changing. The country is supporting deaf people, and we cannot let Parliament fall behind. I believe we must capitalise on this revolution by passing the Bill and taking every step we can to push it as far as possible.
My hon. Friend started her speech on Third Reading by paying tribute to all those campaigners who went before her and the magnificent landmark changes that they fought for over the years. It would be remiss of us not to get on the record our thanks to her for bringing this Bill to Parliament and getting it through to Third Reading today, and to wish it Godspeed in the other place.
I thank my hon. Friend for his kind comments. My dad would be really pleased with himself today—not necessarily with me, but with himself.
I congratulate the hon. Lady on bringing such an important Bill before this House, and pay personal tribute to her. I am very moved by what she is saying, especially her comments about her parents.
During the debate on taxis, my hon. Friend the Member for Darlington (Peter Gibson) talked about Bills passing the “mum test”, and the hon. Lady has been making very powerful comments about her dad. In the last years of his life, my dad was profoundly disabled with a debilitating neurodegenerative disease, so he really relied on the support of people, taxis and so on. I humbly suggest to my colleagues that when we talk about the Bills we are considering today, we need to talk about them passing both the mum and the dad test.
Absolutely; I will come on to my mum very soon. As with all those things that happened in the ’60s and ’70s, my dad took pole position; my mum took care of home affairs. As Members will see, she played just as much of a role in me being here today as my dad did, but he was more vocal. People would say that I am my dad’s daughter. He did not care; he would just bowl on and try to get what he needed. My mum would be more diplomatic—go it slowly and get there eventually. Sadly, I got too much of the former and a lot less of the latter, but we are who we are.
Before I discuss the incredibly positive things that I believe this Bill will do, I want to address what could not be included in it. Some campaigners have made the fair point that this Bill does not give specific legal rights to deaf people, or feel it does not go quite far enough. To be absolutely clear, this Bill is not a silver bullet for the deaf community that will cure overnight all the injustices they face. As Members of this House will appreciate, this is a private Member’s Bill, one that has been brought forward by an Opposition MP and was drawn 20th out of 20 in the ballot. There are limitations on private Members’ Bills that have to be accepted, but I am pleased to say that working together with the Minister for Disabled People, we have pushed for this Bill to be as strong as it can be. I am proud of the Bill and proud of the work we did. It is going to make such a difference to the lives of deaf people, and they will be proud of it too. They might want it all today, but they can have nearly all of it soon.
Deaf people have long felt that the one-size-fits-all disability legislation that should have given their language the protection it needs is inadequate and disregards deaf culture and heritage. In bringing forward this Bill, I knew that we could not rewrite or replace legislation; instead, we are opening the door for deaf people to have their voices heard and their language protected. With this Bill, we are planting our feet firmly in an open doorway. There are those in the deaf community who used another analogy—they said, “It’s like being in a lift. We’ve gone in the lift on the ground floor; the only way is up.” I really quite like that analogy, too.
The requirements on the Government to produce guidance created by clause 3 of the Bill will be carried out in direct consultation with a non-statutory advisory board. This will be an essential mechanism for deaf people to say, “This isn’t working. This is what would help. This is what needs to change”—and we all accept that a lot needs to change. Since introducing the Bill, I have been contacted by hundreds of deaf people from all over the country, telling me about situations in which a public service has failed them, and I have shared some horrific stories with the Minister. Those stories are truly unbelievable, yet a significant portion of the population faces those issues every day. These are issues that have shaped deaf culture and consequently, I totally admit, make me the person I am today.
Deaf culture is important because it allows individuals to be who they are and live in a way that is unique to them. People who have not been exposed to deaf culture may not know what I mean by that. A simplistic way of starting to talk about it is to say, for example, that deaf people look at each other when they are communicating, but in our hearing culture it is common to look away—to break eye contact. Try keeping up with that if you are trying to lip read! It is impossible. In deaf culture, it is absolutely acceptable to tap another person to gain their attention; it is marked by physical proximity, directness, even thumping on tables and floors—I am not going to go on about that because I will start to recognise my own behaviour. Deaf culture is all about challenging injustices—fighting to be heard and understood through whatever means necessary.
People on the edge of the deaf community sometimes think deaf people are demanding and unreasonable, and sometimes they are, but they need to be—they have to be; they have to challenge in order to be heard. As we know in this place, it is the people who challenge the system who change things, and I am proud to come from a community that does not sit back and complain, but that gets up and challenges perceived injustices again and again and again until they are rectified. That shows why the BSL Bill will be so powerful: if we remove the barriers restricting the potential of deaf people it will be truly amazing to see how much they can and will achieve.
Many years ago my four-year-old niece explained to her young friends, who had never seen people sign before, that her grandparents were actually just the same as them except their ears did not work. When we accept that some people are deaf and accommodate that, rather than just trying to ignore it, deaf people will be able to make so much more of a difference; but before they can make that difference, we must tackle the precise details of the problems deaf people face, and we will tackle that in the guidance accompanying this Bill.
One important matter the guidance must address is the lack of forward planning for BSL use. We must not continually have a system that creates a service for hearing people and then retrospectively and half-heartedly attempts to add the provision of BSL. BSL needs to be a consideration when services are being designed, not an afterthought. This will cut out huge amounts of wasted time and money, because public services have had to scramble to throw some sort of BSL provision together, or, even worse, many do not bother at all. Through this guidance we will start to see the Government becoming proactive in considering deaf people and the need for BSL, specifically with increased and improved interpretation and a wider understanding of BSL as a language.
In every aspect of public service there are failings; I have so many examples to draw on from my own life growing up with my parents, from years of doing casework for my constituents, and from the hundreds of letters I have been sent since introducing this Bill, and, sadly, a lot of these problems are things that a hearing person would never have considered.
In prisons, for instance, frighteningly little is done for deaf people. The isolation a deaf prisoner might experience from not having any other BSL users to talk to, and not being able to watch subtitled TV or make telephone calls, is absolutely terrifying. I have read reports of deaf prisoners committing suicide because they simply could not bear the isolation. This cannot be allowed to happen again and we need to do all we can to stop it. Mental health provision in prisons is already an area of great concern to me; if we add to that the difficulties a deaf person in prison would experience this could be considered a crisis.
As I have said, these are problems that a hearing person would not consider, but a BSL advisory board would be able to draw on its members’ own life experiences to ensure the guidance the Secretary of State issues is much more than just a vague commitment to do more—and it has to be. It will target problem areas and say how they need to be addressed and what needs to be done differently.
I know that a huge focus of the guidance will have to be on education. When I speak to deaf people about what they feel needs to be prioritised, education is more often than not the first thing they mention. Deaf people currently have little faith in the education system. On Second Reading, I explained how my mum would give her three children lessons every day at home, before we were even pre-school age. She would explain, “Because we’re deaf, they’ll think you’re daft.” We had to do those lessons. We had to learn to read and write and to do our sums, and we had to be absolutely proficient before we got to school.
A tale is told that, having had the bit drummed into me that people would think we were not capable because my parents were deaf, when I got to school and found that my classmates could not read and write or do sums as quickly as I could, I came home and expressed, “And they thought we were daft?” I genuinely do not remember that, but the tale is that, when I got home, I could not wait to tell my parents, “It’s not us.” There it goes.
My mum did not trust the system to treat hearing children of deaf parents as capable. I think that, sadly, at the time, she would have thought that deaf children would have even less of a chance than us. That was so very wrong. Of course, that was a long time ago, but while things have improved, many challenges remain. People will simply assume that a deaf student is learning more slowly or struggling when most of the time that is not the case.
My hon. Friend is making a powerful contribution. The nub of what she is saying is that this is a battle for equality: equality of opportunity for children and young people going through education; equality of treatment for deaf people, ensuring that they are treated with respect; equality of access to public services, with deaf people treated like everyone else; and equality of language through communication. Alongside English—the spoken word—British Sign Language is how deaf people communicate. Is it not all about equality?
My hon. Friend is absolutely right. That runs right through the Bill and through my comments. Given an equal opportunity, deaf people can achieve so much. This will make my hon. Friend’s case: I was told about a deaf student whose class was visited by a specialist interpreter. At the end of the day, the teacher told the interpreter that he was amazed, because he had never seen the student talk so much. When the specialist interpreter asked the student why that was, he found that the so-called communicator whom the school employed had only the most basic BSL qualification, so he could not do the job. He could not transmit to the deaf student what the teacher was saying; ergo, the student had the ability but no chance to prove it.
We take simple things like that for granted, but deaf people have to battle that day in, day out. It would be outrageous to think of a hearing person being taught history by someone who had taken only the most basic English lessons, so why do we accept that for deaf people? Why are we allowing deaf students to receive information from their teachers through people who know the bare minimum of BSL and who are not qualified interpreters? We are wasting both taxpayers’ money and the untapped potential of that student.
In the past year alone, we have seen a seismic shift in understanding and acceptance of deaf people and BSL. Continuing to fail them over and over is just not right, and it cannot be ignored any more. It never was right, but at least now people are starting to understand the situation.
With social understanding of the need for BSL inclusion, we must address some shameful and frustratingly obvious oversights.
Throughout the covid pandemic, deaf people have been met with a constant reminder that we are not treating them as equals. Every statement made to the nation, every change in lockdown policy, and every announcement of a support scheme was done without a BSL interpreter on many channels. In fact, interpretation was available on one channel only. We had a simple way to include a sizeable proportion of the population and to prevent people from being left behind, but we failed to do so and must ask ourselves why.
Clause 2 requires the Secretary of State to publish a report on what each Department has done to promote or facilitate the use of BSL in its communications with the public. Any public announcement made without an interpreter or any White Paper released without BSL translation will be reported to the Secretary of State, and that failure will be published for everyone to see. That will be another powerful tool by which each Department will be held to account. Deaf campaigners will be able to compare the guidance from the Secretary of State directly with the published reports. Hiring a registered qualified interpreter for a briefing or to create a BSL translation is an easy commitment with such a minimal cost, so we will soon see Departments make their services and announcements accessible.
That aim is the Bill’s central point: the complete and total inclusion of deaf people. They should be able to watch and understand a national address by the Prime Minister. They should be able to go to a meeting at the jobcentre and talk freely with their adviser. They should be able to have a fully trained and registered qualified interpreter available for them at medical appointments. I have talked at length and could go on and on, but I will not. We are failing at all those things on daily basis, but with the support of Members here today and Members in the other place later, we can start along the road towards fixing such injustices once and for all.
As a nation, we cannot afford to waste the talents of our deaf population. When this Bill becomes law, as I hope it will, I say to the deaf community, and to all those watching at home or in Trafalgar Square or wherever, “Now it is over to you to achieve your potential and to live your best possible lives. That will enrich us all.” I thank the Minister for everything she has done to get Bill legislation through, and I hope that we will agree to give it its Third Reading today, and that it whizzes through the other place. I hope that today will mark the end of the campaign to recognise sign language as a language and the start of the campaign to liberate the potential of every deaf person in this country.
It is a privilege to be here on a Friday to listen to a fantastic speech from my friend the hon. Member for West Lancashire (Rosie Cooper). This place, as you know Madam Deputy Speaker, can be quite confrontational at times, but at other times we come together to right a wrong, and that is what this House has been doing over the past few weeks and today. As a former Disabilities Minister, I congratulate the Minister, because we tried to make this change several times. Promises were made in 2003, and we got things partly in writing, but did it go anywhere? Not really. The Equality Act 2010 did not even mention BSL. When I was Minister, people were worried about costs and this and that, but at the end of the day we are finally here today.
I say to the campaigners in Trafalgar Square, around the country and, indeed, around the world—what we are doing here today will set a precedent for other countries—that disabled people who are deaf or hard of hearing have dreams and aspirations just like anyone else, but those have been held back because we did not understand their language, but expected them to understand ours. No one who is deaf or hard of hearing wants to be deaf or hard of hearing, although I fully understand the community spirit among those people: it has made them what they are today. It has certainly made my friend the hon. Member for West Lancashire who she is today, thanks to mum and dad, I suggest.
We are lucky: we are the ones who can do something about this. As we talk about the different ways in which the Bill will help and will bring BSL more into the open, I have to say not just how amazing it is that in 18 years I have entered every private Member’s Bill ballot and never got anywhere—some would say “Thank goodness for that”, perhaps not least the Front Benchers—but how astonishing it is for a Member to come 20th in the ballot and to bring a Bill that has been tried before, indeed tried by Ministers before, to this point. That has happened because Members on both sides of the House and on the Treasury Bench have worked to make it happen. I have been on the receiving end of some of the lobbying that has suggested that we could have gone further, but we have gone further than I ever dreamt we could go in a private Member’s Bill. We are right on the line between what we can get and what we could not get, and this has been achieved because our efforts have been co-operative.
Perhaps at this stage there is a message for the other House, because the Bill will clearly proceed to the other House. That message should be “Do not delay it, do not try to amend it, do not play party politics with it—just get the damn thing through so it can be given Royal Assent”—a subtle hint from, probably, every Member in this House.
Those who are watching the debate here today may be wondering, “Where is everybody?” This is a day for private Member’s Bills, and this Bill will go through today. Many Members had to be in their constituencies for important events to which they were committed, and I fully understand that: indeed, I shall have to disappear to my own constituency after the debate. The fact that not many Members are here does not mean that other Members are not interested. This Bill is going to go, thank goodness, to the other House, and I say again, subtly, “Hurry up, get this Bill through, because we do not want to lose it.”
I want to say a little about why the Bill is so important. My friend the hon. Member for West Lancashire touched on education. Like the hon. Member for Putney (Fleur Anderson), I have spoken to young people in colleges. They want to learn BSL. When I asked some of them whether, if I came back in two years, they would like me to find that they had taken an O-level or an A-level in the subject, they answered yes, to a man and to a woman. Why has it taken so long for this place, and the education system, to acknowledge the existence of a whole group out there who want to communicate with deaf people? We are not talking about a one-way street.
We all know the figures. About 80,000 people who are deaf or hard of hearing use BSL, and a total of about 180,000 people use it, but for many more people it could open up many new experiences, and the ability to communicate with a community that they may not really understand at present. They could start with basic BSL, and then progress further. As MPs, we can communicate with our constituents in that way. I sent a message out on Facebook the other day. I had an interpreter for my—half a minute? Five minutes? Who knows? It probably seemed a lifetime to anyone who was watching it. The feedback from people who were not from that community was fascinating. They did not understand why people were not lipreading, for instance, or they asked, “Why do people not look at you more carefully?” or “Why do you not speak more slowly?” The answer to that is “Because they are deaf.”
I have spoken before, on Second Reading, about the military community. Sadly, back in the days when I was in the service, hearing defenders were almost unheard of, which is probably why one of my ears is defective—it was affected by all the explosions that went off when I was in the armed forces. The community has said, “We want to learn”, but they have been prevented from doing so. They could not take up the subject, because there was nothing in the curriculum that allowed them to do so—hint, hint to the Education Department, which, I am sure, will be listening.
As the hon. Member for West Lancashire mentioned, we have also gone through covid. When covid hit this country and the world, deaf people not only could not understand what the Prime Minister was saying, depending on what channel they were on, but had to go for their vaccinations. I was lucky enough to be able to volunteer at my local vaccination centre, and several people who were deaf came in. Some of them had interpreters with them—normally family—but others were completely lost in a service that was theirs, free at the point of delivery. They were being vaccinated to protect them, and they were just petrified because no one had taken the time to think whether they needed that extra bit of support. I do not think of it as an extra bit of support—I have banged on about this for years and years, perhaps not quite as much as the hon. Lady, but I have banged on about it, and it is great that we have got to where we are today.
I am due to go to an out-patient’s appointment next week. No one has asked me whether I am deaf or visually impaired. These things are not asked of people. I find it astonishing that we are, quite rightly, offering services to people, whether it be in education, in the jobcentre or in any other Government-run service—forget about the private sector—and we are just missing the target.
I just want to endorse the comments of my friend, the right hon. Gentleman, by making a very quick point. My father, who is profoundly deaf—born deaf and with no hearing whatsoever—was in hospital and was seen by a senior registrar, who said, “Mr Cooper.” The lady who was visiting my dad said, “He’s deaf”. The registrar raised their voice and said, “Mr Cooper!” The lady said, “He’s deaf”. The doctor walked right up to his ear, leaned in and said loudly, “Mr Cooper!” Now, if medical professionals themselves are not joining the dots, we have an awful lot of work to do.
My hon. Friend has touched on a very good point. This Bill is not the silver bullet; it is a method of getting somewhere. The hard work will start once the other place gets its finger out. I will, if I may, come back to that story in a second.
We are concentrating on Government Departments, but there is a whole private sector out there, on which the hon. Lady touched, that is missing out on some profits and on people enjoying their services. Clearly, that consultant was not dim, which is what I was described as when I was at school, because I am dyslexic—apparently if you were dyslexic back in the early ‘60s and ’70, you were dim. He was not dim, but he is ignorant—ignorant of what the condition is all about. Clearly, by the sound of it, he was not an ear, nose and throat specialist. I think the House will understand where I am coming from when I say that it is not a lack of intelligence, but a lack of understanding and compassion. “Compassion” sounds like an old-fashioned word, but I thought that was what the health service was supposed to be about. Interestingly, my mother, who was a nurse for some 40 years, would tell me that, in many cases, compassion was the best healer, compared with some of the other methodologies.
As we look at the Bill, we should say to ourselves, “We must draw a line in the sand.” That is quite important and it should have happened years ago. We can talk about the 2003 Act, and about leaving BSL out of the 2010 Act, which I have already done, but, as I have said, we need to draw a line in the sand now. Some of the stars of stage and screen have needed to help us increase public awareness, because, sadly, that is the sort of society in which we live. As everyone here can see, I am an expert in ballroom dancing—I think not! But even I watched “Strictly Come Dancing” towards the end because it sent out such a fantastic message to society that we all have the same dreams and aspirations, which I alluded to earlier.
The hard work starts now—I am sorry, Minister, that I am no longer on the Front Bench; I truly wish that I was sitting there now to support the Bill as it goes through. The Minister and I have had many a conversation about the Bill and, as I have said, this is where the hard work starts. The expectation from the deaf community, which will cheer you to the rafters when you go to the rally later today—sorry, Madam Deputy Speaker, not you, although I am sure they will be cheering you to the rafters. I have only been here for five minutes so you will have to let me off. The deaf community will cheer the Minister to the rafters later, but they will not cheer us if we do not deliver. It does not matter who is in Government; this is a long process. It has taken us this long to get here, but they expect us and the panel to deliver.
Let me touch on the membership of the panel, which is massively important because it will be the voice of the deaf community. I said, I think in Committee or perhaps on Second Reading, that this process should not be completely one-sided. It is absolutely right that the deaf community expect to be on the panel so that we can hear from them, but we have to try to get the balance right so that expectations can be measured and so that we can try to fix this when it goes wrong, although we will not be able to do so there and then. The membership of the panel is very important and should include not just the Minister and members of the different charities and the deaf community.
In conclusion, I am as proud as punch that the Bill will pass through this House today—I am somehow convinced that it will. It has taken a while and the expectation will be high, but let us meet that expectation and allow these people to live their dreams.
With the leave of the House, I should like to make a few very short remarks.
A Bill similar to mine failed in 2014. Deaf people have waited for this for so long. We are on the point of delivering a huge difference for each and every one of them. For goodness sake, I can almost feel deaf people across the country, and in Trafalgar Square saying, “We are here, we are at the point, stop nitpicking and move on! Please, House of Lords, no amendments—there is no time for them! Give us our voice! for God’s sake, please stop it—just move on!” This is not quite British Sign Language, but it is very simple. On behalf of all those deaf people, all those organisations for the deaf, all the individuals who have helped this House and, please God, the other place—thank you. [In British Sign Language: “Thank you.”]
Question put and agreed to.
Bill accordingly read the Third time and passed.
Congratulations, Rosie. You rightly have your place in history for providing a brighter future for many generations to come.