Tuesday, 29 May 2018

'That's not normal!'

The team are lined up. Georgie and Juliette on each end standing, Simon standing in the middle and Ben and Donsat either side.
Acting on Disability team, 
L-R Georgie, Ben, Simon, Don and Juliette

Just back from a trip to the USA to provide training for a global tech firm. The Sminty team, all five of us, decided to walk the ten blocks from our hotel to our first event in downtown Manhattan. We thought we would make a striking alternative to the famous Reservoir Dogs photo - two men on mobility scooters, two women with hidden disabilities and a man who has Aspergers. 

As we walked I was talking about how polite New Yorkers were, how they move out of the way for wheelchair and scooter users and often say hello or smile. An older lady, wrapped in a thick scarf in sweltering heat, saw us. She stopped and as we passed her, pointed at me and yelled ‘Now that is not normal!’ My fellow scooter user waited a moment and then asked me ‘Well how do you feel about that?’ I paused to process it and then answered, ‘I feel I should be angry or upset but actually I am rather pleased. I now have an opening line for the event we’re about to do’. And so it proved to be. 

This trip had a few firsts for me. I wasn’t alone and had a team of talented people alongside. What was more familiar were the demands, many hours of flying in short space of time, delivering two three hour events in different locations, being New York City and Silicon Valley. Then there was the client: they employ the brightest of people and there was a subtle but evident pressure. Before the trip, they were extremely thorough: scripts and slides had to be approved by many of their people. I'm not used to that.  

Ben and Juliette stand near one another, Juliette has a scrip in hand.
Ben and Juliette on stage
We were delivering Acting on Disability, a form of training using interactive theatre. The actors play out management scenarios, live in front of an audience. As MC, I interrupt the scenes at specific moments to ask the audience for their thoughts, what they think of the manager's behaviour, what could be done better. Whilst writing the scripts, I researched common first names used in the US, what American companies call departments such as UK ‘occupational health’ being 'employee benefits' in the US. Place names were changed, for example we talked about Whole Foods not Sainsburys. This helps the audience to identify and adds to the realism. 

This style of training is highly interactive, it can pack a dramatic punch and more importantly, it is practically helpful. I like it when a member of the audience puts their hand up to say ‘The manager has a point, and yet I can understand what the individual is saying. I’m not sure what to do!’  Many years after such an event I’ve had people tell me ‘I still do that thing suggested in the scene’. 

This performing of complex but relatable situations allows us to develop the skills of the manager, showing how they can navigate their way through what might feel like an impasse. Sometimes making an adjustment ('accommodation' in the US) is simple, but you don’t need training for that. We’re more about the shades of grey, when personalities and assumptions override need and impairment. Making an adjustment can affect other people, it can be complex and awkward to talk about and the question of reasonableness is part of managing disability at work. Individuals can be forthcoming or secretive about a disability. That’s the stuff we like to talk about. 

All of the Sminty team have a disability or impairment. It’s one of our professional rules. So if a character has sight loss or a mental health issue, so does the actor. That can make it hard to find the right skilled people but I constantly search, assess and collect email addresses. The insiders' knowledge they bring adds depth to the scene and delivers the most impactful moments when they step out of character and talk of their real life experiences. 

Simon is on stage, dark background. He is looking to his left with his left hand on chin and has a half smile.
Simon on stage, looking thoughtful and happy
Our team comprised of me, a short person who uses a mobility scooter, someone with cerebral palsy, someone with sight loss, someone with mental health issues and someone with Aspergers and dyspraxia. The trip included three 7 plus-hour flights, multiple transfers and never more than two nights in any one location. A combination of detailed forward planning and open conversations with the team about needs and preferences allowed the trip to pass smoothly. A brilliantly helpful airline in Virgin Atlantic (thank you, thank you!) lovely staff at Yotel in New York (one offered to walk three blocks with me just to hold an umbrella) and Aloft in Silicon Valley (those big rooms, a pool and a robot that delivers items to your room!) Plus, a diverse team where one would support another if needed as we played to our strengths. 

Feedback has been amazing. In New York they’d had the cast of Hamilton and Hilary Clinton visit in recent months, tough acts to follow, especially with the word 'disability' in your title. Satisfaction scores for our events, by asking attendees ‘was this worth attending? would you recommend it?’ were 98%. Being the perfectionist task-master that I can be, I want to know where we lost the 2% but I’m wise enough to know this is pretty good. 

This type of training might seem risky for the client, for their teams, their reputation. They’re bringing over people from a different country to talk directly about a difficult subject. But sometimes taking the greatest risk gives the greatest reward. I received a lovely compliment  from the individual at the tech firm who asked me over to do this work. I was told during the planning there was concern, even hesitation, about the project. My supporter apparently said ‘It’ll be ok, it’s Simon’. In fact, it wasn't just me, I had a great team alongside me. And thankfully I was told this bit afterwards. 

Thursday, 24 May 2018

Disability training, Abnormally Funny People style

A little while back the great people at Skill Boosters approached me to see if I'd like to make a training video with them. The topic was to be disability, employment and customer service. 

I said I'd be interested, but how about we do it a little differently? I suggested we make it with Abnormally Funny People, the comedy team I'm part of. To my delight, they agreed. I'm pleased to say after a lot of brilliant, creative, hard work, it is ready. 

Below is the promo video. If you want to know more, contact Peter Thorpe, at Skill Boosters 020 3859 4308  peter.thorpe@skillboosters.com 

There are dynamic subtitles included and the next sentence is a link to the transcript if you prefer.  Transcript of Skill Boosters disability training video made with Abnormally Funny People 

Thursday, 22 February 2018

International work

Whilst chatting with a long standing client she exclaimed “Simon, I had no idea about your work internationally. You need to tell people about it!”  

We were attending a meeting at Middlesex University to hear about new research in to how diversity strategies have been implemented in global organisations. I was invited by the British Council, an organisation I've worked with for many years, who had commissioned the research. I was asked to speak outlining my experience and the work I’ve done. This is work I love and have enjoyed immensely over the years. So here we go...

Simon is greeted and shaking hands with a number of Hong Kong people.
Meeting bankers in Hong Kong
I should clarify I specifically work in field of disability rather than the broader diversity arena. I have been working internationally since 2002. Around half of those trips have been because the British Council have asked me to go to a region. The other half has been for a range of organisations including Bank of America, Google, Goldman Sachs, HSBC and McDonalds.  I’ve a long term relationship with Community Business in Asia who ask me to help out from time to time. Finally I’ve chaired international conferences or hosted a Dining with a Difference event for senior leaders. 

Much of this work is speaking, be it a keynote or within a training course but it’s not just that. Dining with a Difference has become something rather special when I'm abroad. I host the dinner, provide structure, take feedback and keep things on track but individual tables are hosted by a local disabled person (whom I've briefed beforehand) and they lead the discussion on their table. It's been amazingly powerful, impactful on the night and a starting gun to longer lasting change. Consultancy projects pop up from time to time, be it writing a disability and employment guide for the Bulgarian government or creating a disability and media organisation with Disability Rights and Education Fund (DREDF) in Berkeley, California. This project was to show US news media how to be more accurate and inclusive when reporting disability stories. I met with the Washington Post at their offices, and was overawed by the journalistic history. As a comedy fan, meeting with television executives at 30 Rockefellar Plaza was a treat.

Enough of the work, tell me where you've been, I hope you're asking?  

Simon in the middle of five Google people, after a dining event
With the Google team in California
Albania, Australia, Austria, Canada, China, Croatia, Denmark, Dubai, Egypt, France, Greece, Hong Kong, Japan, Jordan, Oman, Pakistan, Qatar, Russia, Singapore, South Korea, Ukraine and the USA  Several of these I’ve visited multiple times. 

What have been my observations? 

A different country often means a different cultural view of disability and of disabled people. I try to understand this approach, see where it is strong and useful to progress towards the independence and inclusion of disabled people. I also look for where it’s a hinderance, often where disabled people themselves have not had input. The cultural differences fascinate me, and they can frustrate me. I cannot ignore them, nor assume I have all the answers. If I arrive and expect the same as the UK and don't develop my thinking, I will miss a trick. There’s diversity in disability! 

Some of the eye opening conversations have included the impact of religion in a country, and how this informs how disabled people are viewed. Some cultures see disability as bad karma, paying for sins in the past. Perhaps the biggest hurdle, and not unique, is the soft bigotry of low expectation*. This is not limited to overseas of course, nor to just non-disabled people's thoughts - it can be the disabled people themselves. If you’ve had a limited education, been excluded, not spent time with independent minded disabled people and been wrapped in cotton wool, or worse, hidden away by a family or in an institution, maybe you won’t think you can do much. 

Simon sitting on some conrete steps, with an Egyptian man wheelchair user and two other people
In Cairo, with some trail-blazers
Then there are the trail blazers. There's a pride and kinship that swells up inside me when I connect with another disabled person in a very different country, and realise they ‘get it’. They’ve learnt to how to achieve change, often in extremely trying and isolating circumstances. Their aim to remove barriers to enable them to participate. They know how to educate people of their abilities. Medicine, religion, charity might try and help, but sometimes hinder. In the meantime, the trail blazers want to get on the bus, get to the University, the shop, the local council meeting, earn a living. They want to be included, be productive and engaged with society. They want to be able to make decisions for themselves. I’m not one who goes in for inspirational fluff, however I have met half a dozen accidental role models who in incredibly difficult circumstances are leading the social and cultural change towards disability in their country. Their brilliance, skill and resilience impresses me no end.   

In the UK we can be a little complacent, or better put, our expectations are high. Nothing is perfect but access has improved, we have funding for adjustments in work, an enviable car scheme to keep us mobile, accessible buses and taxis too and for some, welfare support. We have anti-discrimination legislation, disability is recognised as something that needs legal protection. Slower but ever present, are a multitude of schemes aiming to increase employment and service provision for disabled people. We have funding for our Paralympians and disability art. These existing measures I suspect is why United Nations efforts, such as the Convention on the Rights of Persons with a Disability and the International Day of Persons with Disabilities haven’t gained real traction in the UK, although that is changing. Travel abroad, particularly to the countries that don’t have anti-discrimination legislation or positive action programmes, and the UN efforts become a big deal. They are solid, internationally recognised symbols that can help focus the mind and help individuals to bring about change. 
Eating out in Guangzhou with Fiona

Often, it’s down to individuals interaction with one another that gets things moving in the first place. At a dinner event in Paris one (not disabled) person said to me, ‘Ah, but we’re different here. We don’t like talking about this stuff, it’s awkward. Not like you British people.’ I smiled and said it was the same in the UK, people tend to feel awkward. As I explained to her, my worry is if we never speak of it, will anything change? I quoted a gay Italian friend who spoke about the development of gay rights and he suggested to me, ‘Simon, sometimes you have to make it an issue, and only then can it become a non-issue.’ 

In Tirana, in Albania, I was asked to speak at a theatre with seats for 300 people in the round. Ten minutes before the start time, there were perhaps 30 people there. Of course I was disappointed with the low turn out but from experience I know that a smaller group can mean greater interaction. However, with barely a minute to go, 200 people turned up. As they filled the seats I felt some apprehension, this was a big crowd. In my speech, amongst other things, I suggested putting people in care homes wasn’t the best way. I said the right equipment and technology can improve disabled people’s lives, if they could just access it. The atmosphere turned frosty, almost hostile. Several hands shot up and people angrily disagreed, saying ‘You’re wrong, we care for people, not push them out. That is what our politics stand for!' Or 'Technology isn't the answer. You're cold, and not helping these poor people!’ I acknowledged their points but suggested there were problems with such an approach, as it continued dependency, and asked them if they’ve spoken with disabled people? The atmosphere didn’t improve and I wondered if I might need to make a hasty exit. Luckily, two women who worked with local disabled people stood up and eloquently explained that those they worked with, provided services to, wanted what I was suggesting: independence, equipment that helped. Of course, human help was part of that but the thinking needed to change. I finished my talk and was very happy that many in the audience came over to continue the discussion. I'm still friends with the two women who rescued me. Later that day, I found myself in the front row of a live broadcast of Albania’s version of BBC's ‘Strictly Come Dancing’. Well, I was in the front row but a teenage Albanian pop star turned up and I was bumped to the second row. It was one of my more memorable working days and reminded me of the fun of working abroad, you never know what might happen next. 
Simon on a stage,  in a suit, arms raised mid speech
Charing a conference in Qatar

A small but important victory happened when I visited Oman. I met with a Facilities Manager for an international bank. He arrived, sat down letting out a weary sigh. He started by explaining to me I didn’t understand the country. Specifically he told me that the system worked differently there, there were bank branches in remote mountainous regions and wheelchair access wasn’t at the top of his priority list. He was resistant, reluctant and couldn’t wait for our meeting to be over so he could get back to his real work. Between you and me, these are the people I quite like. They tell me exactly what they’re thinking and what’s important to them. I can work with these people. It’s the ones that nod, weakly smile and say a few platitudes that are harder. I can’t quite remember what I said to him, I know I acknowledged his position and the local differences. However, within thirty minutes he had completely changed and became an evangelist, wanting to change things. I like to think somewhere in Oman there’s a remote, high on a hill, lonely branch of a bank that now has good wheelchair access.  I might not have changed the world but such changes may mean the world to someone. 

*A quote from Susan Daniels, a US civil servant and disability campaigner.

Tuesday, 10 October 2017

Disability: To some it identifies what's wrong in the world, to others it represents what's wrong with themselves.

In the summer of 2017 I hosted an event for the Business Disability Forum in London. Below is the significantly modified speech I made there. It's a thought piece really, me trying to work something out. It got people talking and I'd love to hear what you think. 

Hello, my name is Simon Minty, I am your host this evening. If you don’t know me, I’ve been an associate to the Business Disability Forum for twenty years. 

Asda supermarket sign with three symbols of a man, woman and wheelchair user with the words Not every disability is visible and Accessible Toilet
Asda toilet sign - disability is very broad these days but
have those identifying as so, kept pace?
It’s great that you are here and great that you do the job you do. I suspect some of you came to this disability or diversity role by accident, or maybe it was on purpose as it looked interesting? Maybe some of you are directly affected so have a personal interest. Dare I suggest, maybe one or two of you are after an award from the Queen! I know most of us do this work because we want to see change. Working with the Forum, such change is about improving how organisations operate in the workplace and how they interact with their disabled customers. 

After several years in banking, I became professionally involved in disability equality. Luckily for me, the changes needed were pretty clear plus there was new equality legislation to help. Skilled, knowledgable and confident people, (many of whom had visible impairments and identified as disabled) advised on how things could improve. If you were around in the early noughties, you had legally enforceable rights and were part of the conversation and informed the plan.

It wasn't all rosey. Then as now, a lot of disabled people (legally at least) prefer to keep quiet, they're embarrassed and don't want to be treated differently. The law didn't even come in to it. More significantly, they didn't see themselves the same as those who used a wheelchair or a guide dog. They were something separate and different. 

A round street sign with a red edge, inside it has multiple stick people all the same. Underneath the sign is a notice saying May contain hidden disabilities
Many people have conditions that are a disability
under the law but the condition is not visible.
In the last few years, there has been an increased openness about non-visible conditions, be it mental health, neurological or long term health conditions. That's great! But many affected people don’t speak so they don't get the assistance that could make their life easier or them more effective. They remain fearful of the word 'disability' and use a lot of mental energy trying to avoid it. So it makes me wonder, does anything unite the visibly disabled and those with something invisibleit?  

It's hard to give a straight answer. I think there is but it's complex and nuanced. It might be a perception of the self, a feeling, noticing you might be treated differently. Or, you behave differently to fit in. It's knowing you think about something that no one else does (except for those with exactly the same thing who get it instinctively). I think the fear of a loss of independence is part of it. 

Why am I asking what do we have in common? Does it matter?

A man sits underneath a white horse shaped animal. He is half way through painting black stripes on it.
Is it a horse or a zebra?
As we focus more on non-visible disabilities, we don’t have an agreed unifying model across all disabilities. Plus ca change! That's not unique and other strands of equality don't all agree on everything. The differences might be greater than the commonality but there is commonality. If the plan for those who can, is to hide it, will that just re-enforce the stigma? How do we reduce the shame for those who actually need a little help? They don't have wear a t-shirt but surely in 2017 they should be able to speak for themselves.

In the past twenty years, for some the word 'disability' helped identify barriers. Now some reject it, it's not about them. In the 90s, the word 'handicapped' was replaced by 'disability'. We may move on to a new word but is the word is the main issue? To some it identifies what's wrong in the world, to others it represents what's wrong with themselves. Can Harry Potter save us here? In the books, characters say 'He Who Must Not Be Named' as they were scared. (Spoiler alert) Harry Potter was one of the few who did say the name 'Voldermort' and Harry was the one who defeated him. I think it's a state of mind more than a word. I worry we may be setting ourselves adrift in to individual units. We must allow for our individuality, but I think finding, celebrating a commonality is desirable too.     
A photo of Simon, who is short statured, talking to someone. Simon is in a brown suit and shirt and smiling.
Simon Minty, a disabled person
and many other things.

I hope amongst the many challenges facing us in this field of work, we continue with one of the aims of the Business Disability Forum, to allow people to be themselves at work or out living their lives, to reduce the stigma of disability, but not to run away from it. 

Business Disability Forum is unique, we’re unique, let’s not be nervous, let’s be proud. 

Thursday, 22 June 2017

Complacency or the long game?

My local dentist is a five minute walk from my home. I use my mobility scooter when I visit as it's too far to walk and this way, I don't have to worry about parking. This week, I went for a check up and for the first time, there were three ramps in place on arrival. 

The back story: in 2010 I sent my dentist a strongly worded letter explaining their three steps meant access for people using wheels, i.e. me, wasn't good and I made some suggestions. They invested in a portable ramp so I could get in. I would call the dentist when I was approaching and they would come out and put the ramp down. I'd go up to the first platform and wait whilst they put the same ramp on the next step and so on. It was a bit of a palaver but just about worked. It took time but I'm rarely in a rush to climb in to the dentist's chair. This week, to have enough ramps for me to go straight in was the warmest welcome I've had there. My smile was bright before seeing the hygienist.  

I posted a photo of the new ramps in situ on Facebook, Twitter and Instagram and received numerous likes. There were a number of comments too, ranging from the pun filled 'glad they ramped up their service' to the somewhat missing the point 'nice tiles'. There was one from a colleague who asked 'is it 20 years since it became the law?'

Indeed it is, and it has been seven years since my strongly worded letter. This made me ponder, had I become complacent? I'm a disability consultant for goodness sake. Why didn't I push them further, or consider a case under the access to goods and services provisions of the Equality Act? Alternatively, why hadn't I taken my custom elsewhere and shown them the power of the disabled / purple pound? Should I have contacted some of my activist friends to ask them to hold a demo and embarrass the dentist in to action?

The reality is a combination of make do and mend but also playing the long game. The first ramp in 2010 was the minimum: adequate but legally arguable as less favourable treatment or a lower standard of service. If I'd gone to court I might have won and things changed but it would have been tough and maybe costly. If I'd taken my custom elsewhere, I suspect their single ramp would have gone in a cupboard and nothing would have changed. Instead, I just kept going back, calling them each time I was approaching, reminding them every time they needed another ramp. My continued presence was pressure. The problem was I only went once or twice a year, so they had long stretches of not being reminded.  

Today though, it's in place and it's great! It's not just me either, it will help plenty of other people including the gazillions of parents with buggies where I live. It shouldn't have taken so long. Some people won't wait that long, some can't wait that long. The long game came good this time but it won't always. 

(Scroll down below the pic for more)

It's a long narrow entrance with graduated steps with level platforms in-between. There are three ramps over the black and white tiles. At the bottom of the steps, so on the pavement, the receptionist doing a happy dance.
Above is a photo of the three ramps in place and the receptionist doing a happy dance. 
Finally, below two links to the recent BBC Ouch podcast which I co-host. There's the show I'm calling 'Life' in which we interview the chap who had booked a date with death in Switzerland but because of the kindest of a stranger, he postponed it. Yep, sometimes help is incredibly urgent. Or if you prefer, a quirky, and utterly enjoyable to make, interview with a comedian who is losing his sight so has made a show about it. 
BBC Ouch talk show  - Life
BBC Ouch talk show - Comedy

Sunday, 9 April 2017

Embolden travel and conversations


Simon in front of the Golden Buddha at the temple of Wat Traimit, Bangkok

Simon in front of the Golden Buddha
at the temple of Wat Traimit, Bangkok

I visited Thailand in March after years of hesitation assuming it would be too hard to get around with a mobility scooter, not to mention emotionality tiring if people overreacted to a short man wandering around. Although not easy, access was ok for me and people weren't especially interested. We spent a few days in Bangkok visiting Royal Palaces, street markets and a terrifying rooftop bar! Then we went to Khau Lak for sunshine and beach time. The world is smaller, difference is everywhere and thankfully most people were polite and helpful. A few couldn't resist taking out their phones to take a photo of me and for once, I decided not to try to control this and gradually I started to not even care. The photo to the right was taken with permission, and I don't think I could look more like a tourist if I'd tried.

Disability and comedy

A new book about disability and comedy has been published, featuring contributions from the Abnormally Funny People team. It's titled 'Seriously FunnyDisability and the Paradoxical Power of Humor'. The publishers notes say the book is 'Exploring a paradox, Shawn Bingham and Sara Green show how humor has been used both to challenge traditional views of disability and to reinforce negative stereotypes and social inequalities. Seriously Funny ranges from ancient Greek dramas to medieval courts jesters to contemporary comedy, from stage performances to the experiences of daily life. Rich with insights into issues of identity and social stratification, it offers an eye-opening perspective on attitudes toward disability across the ages.'

For your listening pleasure

Soon after coming back from Thailand, I was in the studio recording two podcasts. Maybe it was the holiday, maybe it was the guests or maybe the topics, but both shows are rather special in their own different ways. If you fancy a change from your current reading or want something to listen to in the car, whilst keeping fit or on the commute, why not give them a try?

BBC Ouch show discusses T4 in disability history, when the Nazi's killed disabled people. There's fantastic music from Holy Moly & The Crackers.

BBC Ouch talkshow  'Behind the Scenes'

L-R Nicola Werenowska, Stephen Unwin, Kate Monaghan, Simon Minty in the BBC Radio studio.

BBC Radio Studio L-R Nicola Werenowska, Stephen Unwin, Kate Monaghan, Simon  

The Phil & Simon Show talks identity politics, is there creep of the 'non-disableds' talking on behalf of disabled people? When should someone share? And if that's not enough, it ventures in to the minimum wage and learning disabled people debate. Inevitably, voices are raised and tables are thumped.

The Phil & Simon Show  'Where Angels Fear to Tread'

L - R Phil Friend and Simon Minty taken with a selfie stick with a bookshelf in the background.

L - R Phil Friend and Simon 

Saturday, 4 March 2017

Happy Talk

A brief update, promoting the two podcasts I co-host.

First up, BBC Ouch with my co-host Kate Monaghan. This month was a lot of fun to record, we were in a mischievous mood and our guests joined in. We talk serious stuff though, diets to 'cure' your impairment, ADHD, ADD, chimps with Down Syndrome. OK, that last one wasn't as serious.

Secondly, The Phil & Simon Show with my co-host and former business partner, now great friend, Phil Friend. We grapple with the latest disability and wider world issues with varying success. My favourite bit is Phil's reaction when I tell him I'm reading Andrew Neil's book, which finishes around 1997 when Tony Blair becomes Prime Minister. My mum's impartial and piercingly accurate review of this show was 'I see why you call it the PHIL & Simon Show as Phil talks a lot and you try and get a word in.'

You can subscribe to both via iTunes or Audioboom. And do leave a comment or get in contact as it's great to hear from listeners.

Next blog will report back on my trip to Thailand. Excited, what an amazing thing to do, apprehensive, will I be able to get around?

Pic of Natasha Lipman, Simon Minty and Kate Monaghan in BBC Studio
L-R Natasha Lipman, Simon Minty, Kate Monaghan

Friday, 9 December 2016

Walking on Sunshine

The hip is working well. I did trip over the other day... As I was walking, I felt my trousers slipping down a little. I reached behind to pull them up forgetting that my walking stick was in the same hand. The stick got caught between my shins and down I tumbled. There was a weird sensation in my new hip, just for a moment. Almost like a twang but much softer. As someone who has poor balance tripping is perfectly normal to me and my well honed skills of arms out, fall in to a press up position prevented any physical harm. I got up and thirty seconds later all was fine. This new walking lark is amazing and complicated.

Work is busy. I've run a lot of training events with media organisations such as All3Media, Endemol Shine and Warner Bros, some via Indie Training Fund. Really enjoyable courses, either discussing employment and adjustments or getting deep in to portrayal of disability on TV with people who make the shows. Those I met know how to do it, sometimes they just need more confidence or clarity. Had an enjoyable international afternoon with Facilities Managers from the British Council Estates team discussing how they can make their premises more accessible in very different countries.

In November, there was a big conference on branding, advertising, design and media at Kings Place and I was chuffed to be asked to speak at it. Soon after, I spent the day with Channel 4 execs as part of a talent day (thank you 104 Films and Laurence Clark). Great to hear about the different strands, marketing methods and eye opening too as to how it works and what they want - disability wise? Drama and comedy. We go back in January aiming to present some ideas.

Come December and I hosted an event for Purple Space for the launch of their Purple Stories guide, on how to tell your story. The event was packed which is a testament to Kate Nash and her success in bringing people to together and ongoing development of staff networks.

The podcasts come thick and fast. BBC Ouch every month of course and I'm now on their team page which is kinda cool. It was also a technological nightmare to do (thanks for perservering Beth). Plus there's the shooting from the hip, post expert, post truth, unscripted mutterings of me and good friend Phil Friend. One listener said the show should be re-titled Grumpy Old Men do Disability, fair point.

Links below and a pic of me getting ready for 'purple talk'.

Simon, sitting down, is wearing a back suit and purple shirt. His left hand is cupped as to mime talking.
Simon Minty at Purple Space event 8th Dec 2016

BBC Ouch   Sisters Together for Ever

This disability talk show was all about siblings of someone with a disability. What's is it like for the one without?

Phil & Simon Show   Everybody Knows

Phil and Simon, good friends, differing politics, a shared commitment to disability equality discuss Trump, Brexit, British judiciary, genetic screening and using a disability to cover up a character trait you don't want. There's a discussion of the already missed Leonard Cohen's lyrics.

Thursday, 22 September 2016

Hip Hip Away....

On 18th July 2016, I had a total hip replacement operation. I had been avoiding surgery for ten years mostly as I knew anaesthetic for people with my form of dwarfism (SEDc) can have complications. I was lucky to find a fantastic surgeon, a top notch anaesthetist and awesome orthopaedic surgical care practitioner. That was nine weeks ago... I now have better mobility and the original pain has gone. It gets better each day.

During my rehabilitation I stopped working, however, I did record a couple of podcasts. Forgive my crowing but both shows are a treat! Maybe that's because I was the nice side of the operation and therefore euphoric....or maybe it's the medication. What happens is all sorts of half formed thoughts  fly from my mouth and the lovely people I do the shows with work their magic. I hope you enjoy them.

BBC Ouch (59 mins) 

- losing it with 'I live in a bucket' news story 
- when the little voice in your head is Louis Walsh
- that some wear a badge to say they need help whilst others (like me) are offered help all the time

BBC Ouch show link  (opens in a new window) 

BBC Ouch Disability Talk logo
BBC Ouch Disability Talk logo

Phil & Simon Show no. 5    (41 mins) 

- Olympics and the Daily Mail
- my surgery and recovery 
- Asda (supermarket) new toilet signage
- a dodgy joke at the end...it's not the BBC you see 

Phil and Simon Show link   (opens in a new window)

Black and white x-ray of Simon's hips, showing thin thigh bones

X-ray of Simon's hips. Sorry, you can't un-see this!

Simon is on the left, Phil on the right and a microphone is on the table in between them
Phil and Simon

If you've read this far, thank you. As well as the euphoria of being alive post op, I've also been a bit melancholy which I guess is natural. One way I 'enjoy' the downside is to listen to sappy music. I'm old enough to remember this when it came out and I still think it is a belter of a song. Surely we all can relate to the lyrics, about someone you once loved. So here it is, Air Supply's All Out of Love. Turn it up loud!

Thursday, 14 July 2016

The Winner Takes It All... Phil & Simon Show no. 4

The latest Phil and Simon Show is out.

We chat about post-Brexit UK, music to listen to when you're having an MRI scan, Chilcot and the Iraq Inquiry, accessible motor homes, Aspergers, the disabled employment gap, our next Prime Minister and hip surgery. In about 35 mins. We have no boundaries. 

Hope you like it and thank you for listening.