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Life in a mental health unit when you shouldn't be there

Life in a mental health unit when you shouldn't be there and as the general election nears, the podcast combs through proposed Tory benefits cuts.

Emma Tracey speaks to the mother of a 35 year old woman with learning disabilities who has been living in a mental health facility “unnecessarily†for
three years. She says there is no reason for her to be living there and that it's due to lack of appropriate housing and care in the community. We
also hear from autistic author Alexis Quinn who feels let down by the system but is living in her own home now.
Mencap's analysis shows over 2,000 learning disabled or autistic people are inappropriately leading restricted lives in hospital. Dan Scorer from the charity shines some light on the situation as the government again misses its own target to bring down the numbers.

Last week prime minister Rishi Sunak outlined the Conservative's plans to change work and Personal Independent Payments (PIP) benefits if they win the pending general election. Talk of benefits change is always concerning and Drew Hyndman from the Access All team combs through what he said and puts it in perspective.

Activist Shani Dhanda is presently the number one most influential disabled person in the UK according to Shaw Trust's Power 100 list. As the proud Brummy starts a new programme on the ±«Óãtv's Asian Network, she talks to us about her journey to understanding what being disabled means.

Access All was made by Niamh Hughes, Alex Collins, Drew Hyndman, and edited by Damon Rose and Alex Lewis. Recorded and mixed by Dave O'Neill. The Senior Editor is Sam Bonham.

"Alexa, ask the ±«Óãtv for Access All" to play the latest episode. Or subscribe on ±«Óãtv Sounds app or website.

Release date:

Available now

33 minutes

Transcription

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24th April 2024

bbc.co.uk/accessall

Access All – episode 101

Presented by Emma Tracey

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EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I really, really do genuinely wish I knew British Sign Language, BSL, because if I did I would sign to you hello. It’s Access All, I’m Emma, and we have six fabulous new BSL films on the ±«Óãtv Sounds YouTube channel which are highlights of some of the greatest interviews we’ve done over the last couple of months. We’ve got people like Bryony Gordon, Bradley Riches, Molly from The Traitors, they’re all there. So, if you know somebody who loves BSL, who knows BSL and who fancies getting a bit of our podcast tell them to get on to that ±«Óãtv Sounds YouTube channel and have a look at those fabulous films. On with the show.

MUSIC-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Theme music.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Welcome to Access All, the ±«Óãtv’s weekly disability and mental health podcast. I’m Emma Tracey, and this week we are going to be digging down into some of the big disability news stories. And honestly, there have been so many to choose from this week.

ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý The government has consistently missed their targets to reduce the numbers of people with learning disabilities and/or autistic people who are needlessly detained in mental health units. We’ll be talking about that in a moment. We know there’s lots of jitteriness when politicians start talking about changes to benefits, so we will be going through Rishi Sunak’s speech about work related benefits and Personal Independence Payments later. And I also will be sitting down to chat to Shani Dhanda, the most powerful and influential disabled person in the UK according to the Shaw Power 100 list. And she’ll be telling me about her new Motivation show on the ±«Óãtv Asian Network.

ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Don’t forget to subscribe to us on ±«Óãtv Sounds or wherever you get your podcasts from. And do contact me; I love to hear from you. We are accessall@bbc.co.uk.

ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý It’s been a busy week, as I’ve said, in disability news. And one of the stories that we’ve been thinking about is the fact that NHS England has confirmed that nearly 2,050 people with learning disabilities and/or autistic people are still being detained in mental health hospitals when they don’t need to be. The government pledged to bring this number to below 1,445 by the end of March 2024, but obviously this hasn’t happened. And on the line to talk to us about it is Dan Scorer, the head of policy at learning disability charity Mencap. Hi Dan, how are you doing?

DAN-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Hi, I’m good thank you.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, what’s happening here Dan?

DAN-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Well, as you said back in 2019 the government and the NHS set a target to reduce the number of people with a learning disability and autistic people trapped in mental health hospitals, mainly detained under the Mental Health Act, to reduce that number of people by 50% by the end of March just gone. Now, that hasn’t happened; there are still many hundreds of people who are still trapped in mental health hospitals who shouldn’t be. And what we’re seeing across the country is the integrated care systems, the 42 NHS areas across England, the majority are just not making the progress needed, nearly three quarters have not achieved the reduction in the numbers of people that they should have done. And we’re seeing about 30% of areas making no progress or actually going backwards.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And just to put a bit of context into this: the government started making targets for lessening the numbers of people with learning disabilities and/or autistic people in mental health hospitals after the Winterbourne View scandal. Tell us about that scandal, Dan.

DAN-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, that scandal was exposed by the ±«Óãtv’s Panorama programme through undercover reporting back in 2011. And that showed the appalling physical abuse, neglect and ill-treatment of people with a learning disability and autistic people at a place called Winterbourne View near Bristol. And a number of staff were charged with criminal offences. Six were jailed for up to two years for the appalling way that they treated people in that setting. And that really shone a light on the number of people with a learning disability and autistic people trapped in these kinds of settings. And after that the government put in place a two-year programme to get people out of these places and support them in the community. And that just didn’t happen. In 2015 NHS England led on another plan that set targets through to 2019 to reduce numbers by 35% to 50%, and again that didn’t happen. And then in 2019 the NHS long-term plan was published committing to that 50% reduction by the end of March just gone, which also hasn’t happened.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, the government is constantly missing their own targets. Why is this happening? Why are they missing the targets? What’s causing this, from your perspective?

DAN-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Well, we’re just not seeing the progress needed across the country in developing the right support in the community. So, we know there are hundreds of people trapped in units for two reasons: they haven’t got the social care support that’s needed in the community, forcing them to come out; and they haven’t got the right housing in place in the community for them. So, there simply just has not been the investment needed in the housing and the specialist staff teams that are needed in communities. So, we’re seeing both people trapped in units and also more people going in because there just aren’t the right early intervention and crisis support services in the community to support people and stop them going into these hospitals.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Well, one of the people you’re talking about there is a lady we’re calling Rose, who’s 35 and has a learning disability. We’re able to speak to Rose’s mum, Sarah. Thank you so much for joining us. Sarah, your daughter has a learning disability, what does that mean for her and her life?

SARAH-ÌýÌýÌýÌýÌýÌýÌýÌýÌý She’s uneven development and her mental abilities didn’t grow at the same speed or at the right time. So, it means that she doesn’t understand a lot of what is said to her. She can talk very well, and people think she is much more able than she is. She’s able in lots of ways but she doesn’t understand a lot of what’s going on. She just needs help with everything she does. She needs guidance and support.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý She’s been in hospital since 2014 and is currently two hours away from you by car. How did she end up in hospital?

SARAH-ÌýÌýÌýÌýÌýÌýÌýÌýÌý She had been in a placement that broke down, a supported living placement she’s been moved to. And when she was there it was fine for a short while, but she didn’t have the level of attention she required, she didn’t have the level of help, and in the end she was moved. We do go and see her, I try to go at least every three weeks.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, she’s two hours away from you now?

SARAH-ÌýÌýÌýÌýÌýÌýÌýÌýÌý Yes.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And what is life like for your daughter Rose in hospital as far as you know, because you’re obviously not able to see her that much?

SARAH-ÌýÌýÌýÌýÌýÌýÌýÌýÌý She’s fine. She’s looked after. But she doesn’t live a life of her own. She has not got the support just with day-to-day living that she would like. It’s a hospital and so she is very institutionalised because there is nowhere for her to go, there is no accommodation available. Everything she does is so regimented I suppose. She can’t do anything on impulse. If she wants to go for a walk she has to wait to get permission; she has to be signed out to do it; she has to have a carer to go with her. She can’t just say, oh I fancy walking down the shop and buying myself a bar of chocolate. She has to get permission and it has to be signed for and she has to, as I say, be accompanied every time. And yes, she does need care, but she doesn’t need that level of restraint.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý You go to see her, what’s it like?

SARAH-ÌýÌýÌýÌýÌýÌýÌýÌýÌý Secure. So, you go through big metal gates to go in. You have to buzz the buzzer first and get permission to go in. She’s brought out to meet me and we go out for lunch with carer. There is nowhere very homely. We sit in what they call the therapy kitchen, which is a table and chairs, and that’s it. It’s not comfy.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And this has been her life for ten years. What are your hopes for Rose, Sarah?

SARAH-ÌýÌýÌýÌýÌýÌýÌýÌýÌý I hoped she would be provided with accommodation and have the 24/7 support that she requires, but from people that are constant and people that she knows, can get to know and build a relationship with, and that she can live her own life and indulge in her hobbies with encouragement.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý What are her hobbies?

SARAH-ÌýÌýÌýÌýÌýÌýÌýÌýÌý Oh, she likes singing. She likes going to church, particularly the sort of church where it’s cheerful and upbeat. She likes painting and drawing. And she likes pottering around outdoors, a bit of gardening. She likes anything physical, any little activities that she can do.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And obviously, you know, to see her family. It must have had a massive impact on all you all of this?

SARAH-ÌýÌýÌýÌýÌýÌýÌýÌýÌý Yes, it is very difficult to see the family. And in fact she can’t see her nieces except now that she can come here for an afternoon. So, if they are down here from Yorkshire then she can come over to see her brother and her nieces at that point.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Has she met her nieces? Has she been able to see her nieces?

SARAH-ÌýÌýÌýÌýÌýÌýÌýÌýÌý She has done now, yes. But for the first two or three years of their lives she couldn’t even see them because they’re not allowed into the hospital.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý We’re going to hear now from Alexis Quinn who’s autistic and spent more than three and a half years in a mental health facility before escaping. How long we’re you in hospital for?

ALEXIS-ÌýÌýÌýÌýÌýÌýÌýÌý Just shy of four years.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Right. That’s a long time, isn’t it?

ALEXIS-ÌýÌýÌýÌýÌýÌýÌýÌý It’s a very long time. And I think again, you know, hospital staff when you are admitted to a hospital they’re often not a specialist or they don’t have training in autism and so, again, those sensory sensitivities that I was experiencing in the community were heightened in hospital. Most public know that autistic people need routine, structure, predictability, and hospitals are the opposite: they’re chaotic, they’re noisy, they’re sensory driven. And so as soon as I was admitted everything just got a whole lot worse, which was unimaginable for me at the time. I thought I was going somewhere for some care and some treatment, you know, and where I might experience some understanding, and in fact it was the very opposite. And so what happened is I got stuck in a cycle of sensory overload, I’d have a meltdown, six to ten men would hold me on the floor, they’d pull my pants down, they’d inject me with powerful sedative medication and then they’d take me to a room where I’d be locked in. And I wouldn’t know when I would get out, so I could be there for days, weeks, months even. And that cycle just kept repeating. And when I was allowed out I would have this anxiety about when the next sensory overload would come.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, they continued to see your reactions as mental health related rather than as reactions from an autistic person to being in this setting?

ALEXIS-ÌýÌýÌýÌýÌýÌýÌýÌý I think what we have is a situation where staff aren’t trained in autism, and we have a situation where there’s gross understaffing. And so where you’ve got 18 very distressed people on a ward all creating, you know, sensory chaos, noise, unpredictability you have a situation that can’t be managed very effectively with probably one nurse and a couple of healthcare assistants.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý What would have been appropriate for you? What could have prevented this from happening?

ALEXIS-ÌýÌýÌýÌýÌýÌýÌýÌý What I would say is that I needed help and support, some psychology to understand what was going on for me; I needed some autistic specific occupational therapy, probably some speech and language; and I might have needed somebody to come into my house and just give me a bit of a hand with what was going on. I don’t think it would have cost very much money. At the time I was a teacher. You’re looking at a situation really which was perfectly manageable had the right support been available at the right time.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý That was Alexis Quinn telling her story. Now, Dan Scorer from Mencap, learning disability charity, and Sarah, mum of Rose who is in a mental health hospital, are still with me. What needs to happen to change things for people like Rose?

DAN-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý We need to see the investment in every part of the country in the housing and support in the community so that people like Rose and hundreds of others like her can be released from these institutions where they should not be. They do not need to be there; there is no therapeutic or other benefit from them being there. They, like anyone else, should be able to live their lives in the community with the support they need.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And what is a community place? What does that look like for someone who might have been in hospital for ten years?

DAN-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, we’re talking about people living in an ordinary house on an ordinary street, with the staff support, the care staff they need, potentially around the clock if they have that level of support need; take part in activities, take part in their interests; living a life, a free life in the community like all of us expect to; not having to ask permission to leave, living behind locked doors. This is the kind of life everyone expects to lead.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And we’re not talking about money today, but often someone’s place in the community would be a lot cheaper than their place in hospital?

DAN-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý That’s possible over time. Fundamentally this is about over half a billion pounds a year being spent on buying the wrong kind of care.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Dan Scorer and Sarah, thank you so much.

ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I think you listeners knew we were going to talk about this story this week. Yes, of course, it’s the speech Prime Minister Rishi Sunak made late last year where he laid out some of the issues he sees as being in the benefits system. And I tell you what, our reporter Drew Hyndman is here to help me understand what he said and talk about what he means. Drew, thank you for being here. There are a lot of jitters amongst disabled people when politicians start talking about changes to benefits, particularly Personal Independence Payments. What did the Prime Minister actually say in his speech?

DREW-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, the Prime Minister focused on three things: fit notes, the work capability assessment and PIP, Personal Independence Payments. The essence of the speech was he wants more people to be working. At the moment about half the people who have work limiting conditions, as they’re called, are unemployed long term, and about half of those are in work. He wants to increase the number of people who are in work, and also have the people that are in work working more hours per week.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Let’s talk about Personal Independence Payments. It’s something that many, many disabled people receive, whether they’re in work or not in work, because it’s not relating to whether you’re employed or not, is it?

DREW-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý No. So, it stood out in the speech because, unlike the work capability assessments and the fit notes, it’s not to do with your ability to work, it’s to do with whether you meet the criteria that you are assessed with. So, you are given this money to help with the extra cost that you may incur from being disabled.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Drew, you asked people to tell you what they use their Personal Independence Payment for because we know it’s really, really important to a lot of people and close to their hearts. What did they tell you?

DREW-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah, so I put a tweet out late last night before the recording, and had a couple of replies. Very grateful to those people. I woke up to an overwhelming response, about 140 people, and there was a whole list. The common ones that were coming up were: prescription charges because you often have extra medication; taxis because public transport isn’t accessible; repairs and insurance for mobility aids, which is obviously an ongoing cost after the initial outlay of that aid; increasing utility bills, either to charge or run a piece of equipment, but also to make sure that temperatures are kept at the right level for certain conditions; and also things like private medical care a lot of people were saying.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Oh, interesting.

DREW-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Because of the length of NHS waiting lists, and also the NHS doesn’t offer every medication, every kind of care, and so a lot of people were saying that they use it to pay for private things like physiotherapy and stuff like that.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý That’s really, really interesting. And of course you asked because Rishi Sunak was talking about potentially changing Personal Independence Payments.

DREW-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, he says he’s worried about it being misused, and he also thinks that people with, say, mental health conditions maybe don’t need the same level of payout as those who are physically disabled. He’s proposing several things, and this is going up for consultation – these changes aren’t set in stone – he’s proposing things such as instead of cash payments offering people access to talking therapies and under support.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And what are disability charities saying about Sunak’s proposals?

DREW-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý They’ve reacted pretty strongly. Scope called it a full-on assault on disabled people. The charity Sense said that he was portraying disabled people as shirkers. We also spoke to Dan Scorer from Mencap from earlier in the programme and he had this to say in response:

DAN-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, we’re extremely worried by what the government have been saying about potentially reducing the numbers of people in future that will be eligible for Personal Independence Payment, which is so vital in terms of going some way to meeting the extra costs that disabled people face.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And of course we did contact the government about these proposals, and a spokesperson from the Department for Work and Pensions said:Ìý

DWP-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Our welfare reforms will modernise the support available for those who need it the most, ensuring the welfare system changes lives for the better. Our £2.5 billion Back to Work plan will help over a million people, including those with disabilities and long-term health conditions to break down barriers to work. This includes helping almost 400,000 extra people access mental health treatment through NHS talking therapies.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Of course Rishi Sunak has announced all these things, which would only go through any further if he gets in to power. We are in an election year. What are the other parties saying about what he’s been proposing?

DREW-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, the other major parties in England and Wales haven’t released their policies on disability benefits just yet for the upcoming elections, but there has been some pretty broad criticism, much like the disability charities. Labour have claimed that the focus should be on NHS waiting lists, and this was echoed by the Lib Dems who even called the speech desperate. And the Greens added that the government shouldn’t be blaming people who are ill. So, all of them saying that the focus should be on NHS waiting lists rather than people claiming benefits.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý It is an election year, Drew, and Rishi Sunak seems to be saying things here that disabled people are not going to want to hear. Is he thinking about the disabled vote? You know, disabled people vote too.

DREW-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yes, they do. And you can only speculate, but there are roughly 3 million people who claim PIP, but there are about 16 million disabled people in the UK as a whole. So, even as a sort of disabled constituency the number of people affected by changes to PIP or the work capability assessment is relatively small. So, as a voting pool it isn’t necessarily going to alienate every single voter. And indeed for people on PIP it may not factor into every single one of their decisions when it comes to taking a part at the ballot box.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý But it might appeal to people who worry that there are things that need to change about benefits?

DREW-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yes, and Rishi Sunak pointed out, based on projections, that the PIP spending will increase by 50% in the coming years if nothing is done to change it. And so for some people that is a concern, the amount that we spend on benefits and balancing that with taxation levels for people that are in work.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Drew, thank you for explaining all this to me and laying it out so clearly.

ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Now for something completely different. As you know, here on Access All we like to chat to the movers and the shakers of the disability world, so it made complete sense to have Shani Dhanda on the podcast. She is top of the Shaw Trust Power 100 disability list. Here’s our chat:

ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Shani Dhanda.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Hi [laughs].

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Hi. Are you the most powerful disabled person in the UK right now?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Ah, it feels like such a scary title!

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý [Laughs].

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý No, I don’t think so. I think, you know, it’s definitely a joint effort, right? It’s lovely to be recognised though by the Shaw Trust. It’s a very big title with I feel like a lot of responsibility, if that makes sense.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah. And now you are the new host of the Motivation show on ±«Óãtv Asian Network.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I am, and I’m so excited about it!

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Why are you so excited? What’s so exciting about it?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I have always contributed as a guest to lots of shows, and now it just feels amazing to be on the other side, and I think perhaps be the first visibly disabled presenter.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý On the Asian Network?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I think so.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Well, I think so too. Let’s hear a clip of you on the Asian Network:

[Clip]

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý It’s Shani on Asia Network Motivation. And today’s show is all about setting boundaries. Let’s kick things off by highlighting the importance of setting them. Boundaries aren’t just about saying no; they’re about creating space for what truly matters in your life. It’s like drawing a line in the sand and saying this is what I stand for and this is what I won’t tolerate. A few boundaries I…

[End of clip]

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Oh, don’t fade out! I want to hear the rest of the boundaries.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý [Laughs].

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý That’s so interesting. I want to talk to you about boundaries, because that clip was from the show just before this recording and you focused on boundaries. How important is it for disabled people to set boundaries?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I think it’s something that’s so important that, you know, most people don’t prioritise, whether you’re disabled or not. And I think my life has been so much more healthier in so many ways [laughs] as a result of putting boundaries in place, you know. I mean healthier in all its forms: my emotional health, my mental health and my physical health. But it isn’t something easy to do.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, what boundaries, other than the phone notifications, do you put in place?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I’m not afraid to say no if I don’t want to do something, if I don’t want to go somewhere, or if I’m no longer able to. And I spent a lot of time feeling really bad about those things. But if I physically can’t then I can’t.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And in the studio on ±«Óãtv Asian Network you get to drive the desk, you said you play your own music and everything, what adaptations did they put in place for you?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Well, as soon as I walked into the studio the desks were height adjustable.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý What?!

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Which blew my mind away. I didn’t know that. So, that really massively helped.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Is that in our radio station? I don’t think that’s in many radio stations. I’ve never seen an adjustable desk in a radio studio.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I know. I think it’s in the newer ones.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah, our studio manager, Dave, says he has seen it.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Ah.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And why are they adjustable then?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I think it’s because so many different people use them, and I guess people want to sit or stand. And it’s just an example of when you give people flexibility it will suit most people’s needs.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, it’s actually kind of ironic because it’s because lots of deejays like to stand up that the desk is adjustable, and it’s worked well for you.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Absolutely. I think that’s been the biggest thing that has helped. But also the team have been brilliant, and I haven’t needed many other adjustments really.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý That’s great. and it’s quite important, isn’t it, for disabled people, but for someone who’s of South Asian origin and disabled as well, to be in these mainstream places? Like you’ve been on Rip Off Britain, you did a cameo in EastEnders.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Obviously being on the Shaw Power 100 is important, and being in disability space is important. But how important is it to be in the kind of mainstream spaces too?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I think that’s where we get to really influence change. But it is also a bit of a unique, and a little difficult as well, a bit of a difficult space to occupy because the first thing immediately people notice about me is that I have a short stature. So, I feel like people do make assumptions, and then I get pigeonholed into only talking about disability related topics or covering disability related stories. And that’s something that I really love about the Asian Network Motivation show, it’s nothing to do about disability [laughs].

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Now, we’ve talked about Shani the broadcaster and Shani, a little bit about the advocate, we’ll talk a little bit more about that later. So, tell me a little bit about your early life before you became famous, Shani Dhanda [laughter]. Where were you born? Where did you grow up? What was life like for you?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Okay, cool. So, I’m a really proud Brummie. I attended a special needs primary school, absolutely loved it. You know, when people ask me, ‘Why did you go to a special needs primary school?’ it’s because that was the only option for me to have an education at that time.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, was that the only place you were offered, your parents were offered?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And your parents were probably like my parents, they didn’t know…

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Exactly.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý … much about disability or special school or mainstream school.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I went to a special school as well, and they weren’t given any other information other than that.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý That’s right, yeah.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, you end up in this big secondary school in Birmingham.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, there’s probably lots of diversity. But you’re a disabled South Asian teenager, female in this massive secondary school. What were the complexities there at school and at home really?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I wasn’t allowed to go on a Year 9 trip, a residential trip, because they told me that the insurance wouldn’t cover me. I didn’t know that they weren’t allowed to say that and that I was essentially being discriminated against. But I didn’t know about the Equality Act and neither did my parents or probably anybody around me at that time. So, there were those kinds of instances where I look back and I think wow, if only I knew what I know now [laughs].

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý What I know now, yeah.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý But I really enjoyed it. I was a popular student. I didn’t know if I’d ever get any GCSEs, but I scraped by. I got 11 GCSEs which I’m still so proud of that [laughs].

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah. And what about being a disabled person in your family_ and in your community?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah, so disability faces an even further sense of stigma in the South Asian community. I was brought up in a really big community, and my family are very sociable so I’m very lucky that my parents never just decided to leave me at home or keep me atÌý home, because many of the parents in my community did and have. But what that meant is I didn’t know any other disabled people in my community, so there were definitely times of loneliness because yes, like, your family are with you but they don’t quite get it.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý And how did it change? How did it go from you not expecting what you deserved and not knowing to fight for things? When did you start advocating for yourself?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, if you had met me at 20 I hated my disability identity. At 16 I really struggled to get a job, and I didn’t even get an interview until I removed any mention of my condition from my covering letter, and this was after applying for over 100 jobs. So, I had gone through lots of different challenges. I think my early 20s I was just like well this is crap, there’s nothing.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Kind of rock bottom.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah, really rock bottom actually.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý So, you had no job, you didn’t know what to do.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý I did have a job but it took me very, you know.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Okay. What did you do?

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý [Laughs] my first job was selling photography packages. It was telesales. I was so bad at it!

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Oh really? You’re not a salesperson? You are a salesperson, you totally are!

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Oh, but I was naïve then, I didn’t know what I was doing. But anyway I got the job, I got the experience, that was great. I got to earn some money. It’s expensive being disabled. And I just wanted to be like my peers, you know, and enjoy my life while I was at college. So, yeah, I really hated my disability identity. Stumbled across the Social Model by accident and it changed my life.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Okay, explain the Social Model.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý The Social Model talks about how you may be born with a condition or an impairment or you may acquire one throughout your life, but the majority of the disabling factors in life are barriers and bias that we face in society, that could be physical barriers, attitudinal barriers, cultural barriers. And it just really made sense. I was like, yeah, it’s not my fault that I’m the height of a four year-old and therefore everybody blames me for the things that I can’t do; it’s because people haven’t thought about my needs. I very visibly live at lots of different intersections, I’m a South Asian disabled woman. And for a very long time people kept telling me, oh you’re hard to reach, you're under-represented, you’re this, you’re that, almost making me feel guilty about the things that make me who I am. And it took me a really long time to unlearn that and realise that those are the things that are my greatest strengths. I don’t buy this that people are under-represented; I think we are over-excluded.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Oh, I like it, over-excluded.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Yeah, let me explain what I mean. So, I’m South Asian, the South Asian community is the second largest population in this country, the issue isn’t that there’s not enough of us. There’s loads of us. The disability community we make up a quarter of the population one in four people, but the issue isn’t that there’s not enough of us. There’s loads of us! And, you know, being a woman, there’s loads of them around too. So, I think for me it’s the simple flipping of the narrative.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Dr Shani Dhanda it’s been an absolute pleasure to speak to you.

SHANI-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý Thank you.

EMMA-ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý You’ve just heard Shani Dhanda. Brilliant. That’s your lot, people. Please contact me. I love to hear from you. You can tell me anything, but this week particularly I’d love to hear about what help and support you’ve had in exams or what you’ve been asking for, what your children have been asking for. Or if you’re like me and it’s been decades since you’ve been in that exam hall, tell me what was around when you were a disabled kid, tell me what you got: how much extra time; how many people were in your exam room; did you have someone sitting right there for you the whole time; did it make any difference. We want to talk about that next week so we’d love to hear from you.

ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý We are on WhatsApp. Just pop the word Access before your message and send it to 0330 123 9480. We are on email accessall@bbc.co.uk. And we are ±«ÓãtvAccessAll on the socials. Thanks for listening and see you next week. Bye.

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