Social Care
We host a debate about social care services for blind and partially sighted people.
When you first register for a certificate of visual impairment and you have informed your local authority that you may need care and support, they have a legal duty, under The Social Care Act, to carry out an assessment. This assessment is designed to evaluate what kind of extra support you need, perhaps it is help around the home or navigating the outside world. But problems seem to occur when a local authority does not have the specialist knowledge of visual impairments in order to diagnose the most suitable help and when newly blind people are not aware of what they are entitled to.
On the programme, we hear from two people who have experienced problems in accessing social care assistance from their local authorities. We discuss rehabilitation, a service which offers visual impairment training, and why certain areas of the UK don't have the necessary specialist support.
Our guests include: Professor Fred Reid, a long time campaigner on behalf of visually impaired people, and honorary professor of history at Warwick University. Simon Labbett, chair of the Rehabilitation Workers Professional Network, and a rehabilitation officer for the blind and John Dixon, the RNIB's policy lead on social care.
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In Touch transcript: 19/10/21
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THE ATTACHED TRANSCRIPT WAS TYPED FROM A RECORDING AND NOT COPIED FROM AN ORIGINAL SCRIPT.Ìý BECAUSE OF THE RISK OF MISHEARING AND THE DIFFICULTY IN SOME CASES OF IDENTIFYING INDIVIDUAL SPEAKERS, THE Â鶹ԼÅÄ CANNOT VOUCH FOR ITS COMPLETE ACCURACY.
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IN TOUCH – Social Care
TX:Ìý 19.10.2021Ìý 2040-2100
PRESENTER:Ìý ÌýÌýÌýÌýÌýÌýÌý PETER WHITE
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PRODUCER:Ìý ÌýÌýÌýÌýÌýÌýÌýÌýÌý BETH HEMMINGS
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White
Good evening.Ìý There’s been much talk about social care in recent months and the need to give it the financial support that it requires.Ìý Most of that talk has been about the kind of care some of us will need towards the end of life and how it can be fairly paid for.Ìý A very justifiable concern and one which has consistently been kicked into the long grass for at least the last couple of decades.Ìý But what has hardly had a mention, from either press or politicians, is the kind of support a disability might make necessary, often coming out of the blue and in the middle of life.Ìý When people think about the sudden or gradual loss of sight, they tend to think about its emotional effect but the truth is that there are a great many practical skills which can be relearned, which can make the process of coping far easier than most people imagine.Ìý And that’s where social care comes in or it should do.Ìý But social care, unlike health care, is not a national service and it depends on local provision.Ìý And that’s where the problems can start.
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We’re going to be discussing why in a moment but Carly and Penelope have been telling me about the difficulties they’ve experienced in getting the help they feel they need.Ìý Penelope was registered visually impaired in June and she was told that the registration would be sent to her local authority and she would be contacted about an assessment in a couple of weeks.Ìý Nothing happened until she contacted the RNIB, an organisation she hadn’t even heard of until then, and only then did things start to move.Ìý She explained why she felt so anxious.
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Penelope
I needed help mainly in the home because when I boil a kettle instead of the hot water going into the cup, it tends to go on the side sometimes.Ìý Even going out to do every day shopping and stuff like that, I can’t see the kerb, I don’t see humps and bumps.Ìý And so, I really needed some kind of guidance which I was told I was going to need, like stick training, which I still haven’t got at the moment.Ìý But things to do in the house, like I can’t have a bath because I can’t get up because I’m also an amputee, so I have to have showers but I haven’t got a rail – a handrail – to hold on to, so my daughter has to come in and help me with certain things like that.Ìý And it was – it got to a stage where I was getting so stressed that I got psoriasis, where my hair dropped out, I started getting lumps in my head etc. etc.
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White
Can I ask you?Ìý How long have you had to wait and have you had an assessment yet?
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Penelope
I had to wait until September, where – because of the RNIB, social services recruited a new person and she’s such a lovely lady and as soon as she read my case she phoned me up and she’s ordered me things to help me in the house, like with gadgets to help make my tea.Ìý I don’t see colour, everything is black and white, so she’s ordered me gadgets to tell me what colour my clothes are and stuff like that.Ìý But it took a while and it caused me anxiety and I suffer with depression but it just made my depression worse.Ìý I felt like I was alone, I didn’t care, I didn’t count, I was just another statistic.
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White
Carly, if I can come to you.Ìý Tell me about your own circumstances when you needed help and what happened.
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Carly
After I had children, my eyesight deteriorated dramatically and that’s when I needed help.
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White
Tell me about the kind of help that you felt you needed.
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Carly
Well, at the time, it was just basic things in the house, sort of kitchenware, you know when you’re cooking, chopping veg was becoming difficult.Ìý I was listening to Penelope before, pouring your kettle was always a bit of a disaster as in your bench is covered in hot water.Ìý So, I did get [indistinct word] support out a couple of times and they did offer certain things to help me but nothing that made a difference but at the time nothing really needed to change, it was later on, as things developed and got worse, and I tried to seek help from the local council and nobody would come out and see me.
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White
You asked for help from the local council, how long did you have to wait?
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Carly
Well, I didn’t wait long for the [indistinct word] support, but when I asked for the council they went through everything on the phone and said you can have an assessment but you won’t – because at the time I was living on benefits – you won’t qualify for any extra support because your husband should be helping.Ìý I had two young children, so, obviously, I was struggling with keeping the house tidy.Ìý At the time, that was my major worry.
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White
And what was your feeling about that, when you said that your husband should be doing these things for you or helping you?
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Carly
I think, at the time, I was a bit shocked, it makes me feel a bit isolated.Ìý I wasn’t in a very supportive marriage; he wouldn’t accept my disability.Ìý So, no, that wasn’t an option.Ìý But the whole independence, you feel like you’ve lost everything.
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White
And how much do you know about what your rights are?
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Carly
Well, I probably think I know quite a bit but I probably don’t, because you don’t know what you don’t know do you.
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White
No.Ìý Can I just ask Penelope the same thing – how much did you know about what you were entitled to?
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Penelope
I just feel like my independence has been taken away from me because I’ve always worked, I’ve worked in health and social care, palliative care, end of life and right now I just feel like my independence is being taken away and that’s not me.Ìý But because I haven’t had the support, I feel like I’ve been let down a lot.
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White
Penelope and Carly.
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Well, since raising their cases, we’ve heard from both local authorities involved.Ìý Penelope lives under Lambeth Council, they told us that staffing issues had, unfortunately, resulted in a delay to the specialist sensory assessments undertaken by their rehabilitation officers for visual impairment.Ìý They say: “We apologise for the delay and for any inconvenience caused by delays in contacting people who’ve recently received a certificate of visual impairment.Ìý We are now fully staffed and extra resources have been provided to support clearing the backlog of CVI registrations.â€
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Meanwhile, Carly comes under North Tyneside.Ìý Their Director of Adult Services said: “We’re committed to enabling our residents to live their lives as safely and independently as possible.Ìý We’re very sorry to hear if someone is disappointed with the support they’ve received.Ìý We consider people’s own strengths and the support available to them from their wider networks, alongside any local authority support.â€
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Well, we’ve subsequently heard that Carly has received a call offering her a further assessment of her needs.
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So, a little intervention does no harm.
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But organisations of blind people and rehabilitation officers themselves feel that it’s the local nature of the way help is offered that is often bound to lead to inconsistencies throughout the country.Ìý Well, to discuss this situation and how we got where we are I’m joined by Professor Fred Reid, a long-time campaigner on behalf of visually impaired people and Simon Labbett, Chair of the Rehabilitation Workers Professional Network and a rehab officer for the blind himself.
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Simon Labbett first.Ìý Just explain what should have happened in cases like Penelope’s and Carly’s.
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Labbett
Well, my heart sinks when I hear those two stories but what should happen is you would be entitled, in law, to a specialist assessment.Ìý The RNIB says within 28 days.Ìý So, an assessment carried out by someone who has the knowledge and understanding to probe and ask the right questions.Ìý And from that point on, presumably a referral would be made for vision rehabilitation.Ìý So, that’s what should happen.
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White
And how typical is what actually happened to them, I mean how likely is that to be an outcome around the country?
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Labbett
Well, yeah, three months was cited then, three months is a long time, it can be 12 months and in Lambeth’s case there was indeed a worker in the end, some areas of the country, local authorities don’t have one.Ìý
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White
So, there are some places who do not have rehab officers?
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Labbett
Indeed.Ìý In a local authority they’re normally round about two or three, sometimes more than that but in a few cases, there are no rehab workers.
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White
So, why the difference between what should happen and what did happen?
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Labbett
I think people don’t know what you’re entitled to.Ìý So, when you do struggle, you don’t know that the local authority has a duty to support you or at least to assess you.Ìý And so, when you do make contact, if you finally get around to doing that, you may be talking to someone at the local authority who doesn’t know the service exists in the first place.Ìý I mean a lot of local authorities operate a single point of access, rather than a specialist hotline for visually impaired people.Ìý And unless you ask the right questions, you may not get through that initial screening process.
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White
So, this is lack of specialist knowledge about visual impairment?
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Labbett
It is, lack of specialist knowledge by the employers themselves and lack of knowledge, unsurprisingly, on behalf of people who don’t know what’s out there and why would you know that there’s a specialist service until you come to want one?
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White
Let me bring in Professor Fred Reid.Ìý Now you’ve written a paper on several aspects of this problem for the National Federation of the Blind, including its history.Ìý How did we get to this point?
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Reid
There is a postcode lottery, it really depends where you live what services you get.Ìý And there is a feeling abroad that that’s something that has developed recently, say since the start of 2010 with the notorious austerity cuts.Ìý But actually, the situation has much deeper causes than that.Ìý And the basic cause is that in 1947/48 health was set up under central government, the famous National Health Service, but welfare services were left to local authorities and they ran a patchwork of services for all sorts of people, including blind welfare.Ìý Now that was a situation that was left right up to 1970, when the government of the day legislated for all local authorities to set up a social services department that would bring all the services together.Ìý Each local authority was to submit a plan for integrating all the social services under their care and the government promised large amounts of money annually to build up that degree of universal social services.Ìý And so, from the 1980s onwards, they introduced, what was called, a mixed economy whereby some services were delivered by private organisations, some by voluntary organisations, some by social services themselves.Ìý And the truth is that that situation has been left in spite of many attempts to reform it, including the Care Act of 2014, it’s been left as a patchwork and we’ve got this postcode lottery that we’ve inherited from the past.Ìý There hasn’t been political agreement regulated centrally by central government telling the local authorities how many professional workers they must employ and what standard of service they must deliver, it’s simply left to the local authorities to work their budgets as best they can.
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White
Right.Ìý I want to bring in Simon Labbett.Ìý On this question of a national service, because I think you have doubts about whether a national service, as opposed to a system run locally, is necessarily the right thing.
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Labbett
I think vision rehabilitation is all about people engaging with their communities and I think at a local level that’s the best place to decide what’s needed for an area.Ìý And certainly, I wouldn’t advocate vision rehabilitation goes into the NHS because what we’re talking about here is not a medical model, we’re talking about people learning skills and regaining confidence.Ìý Though it’s not really care either, it’s not welfare, it’s rehabilitation and it’s giving people back skills and self-esteem, so it’s hard to know where it fits in.
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White
Well, I was going to ask you both that.Ìý Originally this was welfare, then it was thought of as rights, which may well be the case, but isn’t it, really, education – the kind of services that people need, blind people need, are ways of relearning skills aren’t they.Ìý I mean, Fred, would that be a better way to look at it?
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Reid
There’s a lot of merit in that.Ìý And by the way I’m not in favour of giving vision rehabilitation to the National Health Service.Ìý But there is a kind of medical component in it, in that many people suffer great psychological trauma as they go through the sight loss journey and the great thing about having specialist workers is in part for this very important reason of this psychological trauma, they can’t just bounce back in six weeks, like you get over a fracture, it’s not like that.Ìý Or they may be sunk in depression over just the trauma of losing their sight and not being able to see their children.Ìý This is a hugely complicated area and it needs highly skilled, highly trained professional workers.Ìý And I agree with what Simon says about locality being the point where it should be delivered but there has to be an agreed standard of what resources are provided to deliver it.
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White
I should say, at this point, we did invite the Minister for Social Care to join this debate, she wasn’t available but the Department of Health and Social Care told us: “We want everyone who needs it to have access to high quality and compassionate care.Ìý Local authorities are responsible for assessing eligibility and individual care packages.Ìý We have supported them with over £6 billion to tackle the impact of Covid-19, as well as almost £2.4 million for adult social care.Ìý The £5.4 billion announced last month, as part of our social care reform plans, includes investment in the Disabled Facilities Grant, to enable people to live independently in their own homes.â€
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Labbett
Can I just say there, eligibility doesn’t come into this, rehabilitation is a requirement in the Care Act and it is not a question of eligibility.Ìý If you can reduce or delay the costs of care then you should be looking at early intervention and rehabilitation is just that, so it’s a cost saving measure.
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White
Simon Labbett, Professor Fred Reid, thank you both very much indeed.
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So, what are the prospects of change?Ìý Well, for the past three years John Dixon has been policy lead on social care at the RNIB, before that he was cabinet member for health and social care with Cardiff Council.Ìý Now you’re attempting to make some changes to deal with some of this, particularly the lack of rehab officers, and there is a care bill going through parliament at the moment.Ìý What are you actually proposing, what are you trying to do?
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Dixon
Vision rehabilitation it is not what we call a regulated service, so while it’s a statutory service it’s something that every local authority in the UK has to provide, it’s not regulated, so no one checks whether it’s being provided or not.Ìý The changes RNIB wants to make to the Health and Care Bill would be to make rehabilitation services more widely and vision rehabilitation, more specifically, regulated services, so, for the first time, we would have inspections, we would have standards, we would have reports, we would have a consequence for failure if local authorities aren’t providing properly.Ìý But it’s quite easy to overlook a service that you feel is a nice to provide, rather than I must provide this service and I think that’s the difference that this would make.
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At the moment, no one knows what’s going on.Ìý If we look at rehabilitation more widely then these are critical services that we need, as a country, to recover from covid.Ìý So, regulation, for me, is an obvious no brainer.
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White
Some might think after what we’ve heard and indeed you’ve said it, that it’s almost a Cinderella service, that this is just tinkering at the edges.Ìý What about this idea that the only total answer to this is a national social care service run along the same lines as the NHS?
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Dixon
I mean that’s what they’re looking at in Scotland and my guess would be that if they’re thinking about in England as well then they’ll let that play out in Scotland and see what happens there.Ìý There are plusses and minuses.Ìý It is attractive superficially because you would have national standards, you would, presumably, have reports that were going from across the country to the Secretary of State.Ìý But, on the other hand, my worry is that a national care service could end up being the servant of the NHS, purely there to get beds clear to reduce transfers of care, completely forgetting about the rehabilitation element of it as well, which is getting away from the original point of social care, which is to maximise people’s independence.Ìý It’s not just about bringing someone food on a tray in their living room, it’s about encouraging them, giving them the tools to get up into the kitchen and make the food themselves.
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White
John Dixon, thank you very much indeed.
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And that is it for today.Ìý We’ve issued an open invitation to the Minister for Social Care to appear on In Touch to answer some of the questions raised in this programme, we look forward to seeing her.Ìý We also look forward to your views on social care, you can email intouch@bbc.co.uk, leave a voice message on 0161 8361338 or just go to our website bbc.co.uk/intouch.Ìý
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From me, Peter White, producer Beth Hemmings and studio managers Carwyn Griffith and Jonathan Esp, goodbye.
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- Tue 19 Oct 2021 20:40Â鶹ԼÅÄ Radio 4
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News, views and information for people who are blind or partially sighted